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

HERC2

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs75046782	snp	A/G	0.040671	0.13668	intron-variant	HERC2	GRCh38.p7	15:28244770	AAAAAACCATGTTCA[A/G]TGTCCTGGGGCTGTT	8924
rs75055945	snp	C/T	0.00716266	0.059414	intron-variant	HERC2	GRCh38.p7	15:28295115	AAAACACTGATAACA[C/T]CAAGTGCTAACAAAG	8924
rs75108944	snp	A/C	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28127318	GGGAGTCAGCCAAGA[A/C]CCCCACATGCAAGGG	8924
rs75131382	snp	C/G	0.0010242	0.0226064	missense, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28299453	CTGTTCCAGTGTATA[C/G]AATTTCTCCATCTTT	8924
rs75158826	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28226522	AAAGAACAGTCCTCA[A/G]CAAGTGGTATTGAAA	8924
rs75159657	snp	C/T	0.0507089	0.150941	intron-variant	HERC2	GRCh38.p7	15:28124956	GGATGCAGCATGTGA[C/T]AGGAGCACACTTTGC	8924
rs75165924	snp	C/T	0.278664	0.248351	intron-variant	HERC2	GRCh38.p7	15:28135112	ATGGTGTCAATTGTG[C/T]GTTCTTTCTTCCTCA	8924
rs75175732	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28136858	TTTGAAACAAACAAT[C/G]AGAATTAACCAACGA	8924
rs75181529	snp	C/T	0.499904	0.00693167	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272290	CAGCAAGGGCAAAAG[C/T]GGGGCGCTGGTGCCC	8924
rs75202996	snp	C/T	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28193103	AAATGAGTCAAGAAA[C/T]AACTTTTTAAATACA	8924
rs75215902	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28191574	TGACCTGTGTGCCCA[C/T]GAGGTGCCTCCACGC	8924
rs75224447	snp	G/T	0.288386	0.247035	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321716	GAGACCTTGAGAATG[G/T]ACGGTCACAGGAAGC	8924
rs75283132	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28288223	TACATTTTACCATTA[C/T]GGGCCCTTAAGGTTT	8924
rs75293770	snp	G/T			missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28175552	TCGTGCATGTGGCTG[G/T]CGGGGCCCTGCACTG	8924
rs75306408	snp	C/T	0.0463947	0.145069	intron-variant	HERC2	GRCh38.p7	15:28267647	TTGGCATACATGTAC[C/T]ACACGATACGCATTA	8924
rs75306855	snp	C/G	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28192390	CAGGGAACAACAGCA[C/G]ATTAATATATTTCCA	8924
rs75311985	snp	C/G/T	1.66574e-05	0.0028859	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28192126	GGTATTTTGTGGCCG[C/G/T]TCTGGAAAACAGCTG	8924
rs75336642	snp	A/G	0.161267	0.233723	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28300111	CACAAACACACACAC[A/G]TGCATGTGCTCTGAA	8924
rs75343239	snp	C/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28268092	TTCCTGTAAAAATAA[C/T]ATATGGTTCAAGAAA	8924
rs75362608	snp	A/G	0.0345262	0.126772	intron-variant	HERC2	GRCh38.p7	15:28127099	CCAGAGAGACTCCTC[A/G]GGTGTCTGGAAAGTG	8924
rs75376116	snp	C/G	0.0111196	0.0737302	intron-variant	HERC2	GRCh38.p7	15:28161800	GTAATAGTTAAAATA[C/G]CATAGTATCAGAACC	8924
rs75411849	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28164537	TGAAATGTACCTACC[A/T]TTTTTTTTTATGAGG	8924
rs75419499	snp	C/T	0.103794	0.20279	intron-variant	HERC2	GRCh38.p7	15:28262349	TGCAGAGACTCCCAT[C/T]CTCTCTGCCTGCACC	8924
rs75431715	snp	A/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28189845	AAACTTTTTTAAAAA[A/T]TGAATGGTTAACTAC	8924
rs75482451	snp	A/T	0.0162398	0.0886349	intron-variant	HERC2	GRCh38.p7	15:28259254	CGCACATCACCAAGC[A/T]CGACGAAATTTTTGT	8924
rs75501824	snp	G/T	0.264906	0.249555	intron-variant	HERC2	GRCh38.p7	15:28232207	CAGTAATCAATACTG[G/T]TCAATAAGCAGGTTT	8924
rs75558189	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28165879	TCTAGCCCTGTCACC[A/C]AAACAGCAACAAGCA	8924
rs75579680	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28228144	TAAAAAAAAAAAAAA[A/G]GAAAAGAAAAGAAAA	8924
rs75620448	snp	C/G/T	0.0267983	0.112679	intron-variant	HERC2	GRCh38.p7	15:28113346	ATTTCCGCAAGACTC[C/G/T]GTCACGCTCCCTCTC	8924
rs75694916	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28272745	GGGCTCTCTCTCTTT[A/T]CCTTTTCTTCACTTC	8924
rs75738011	snp	A/G	0.0260105	0.111035	intron-variant	HERC2	GRCh38.p7	15:28265245	AAGCAAGCAGATACC[A/G]TAGCATCAGACTACA	8924
rs75755165	snp	A/C	0	0	intron-variant	HERC2	GRCh38.p7	15:28173793	GAGACCCTGTCTACA[A/C]AAAAAAAAAAAAAAA	8924
rs75777342	snp	G/T	0	0	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28320726	TAGATTGGGTGTAAA[G/T]AATTGTCTATCGAAA	8924
rs75779539	snp	C/T	0.046775	0.145601	intron-variant	HERC2	GRCh38.p7	15:28268394	CTGGACACACTTCTG[C/T]GCTCCATCCTGTTTA	8924
rs75829304	snp	A/G	0.0168055	0.0901129	intron-variant	HERC2	GRCh38.p7	15:28164453	ATGACATTCCAGAAC[A/G]TAACTCACTGAAGGA	8924
rs75851564	snp	A/C	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28148036	AGCAAGACTGTGTCT[A/C]CAAAAAAAAAAAAAA	8924
rs75878335	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28171203	TGACATGGCAGTTTT[A/T]TTTGTAATAGTCAAA	8924
rs75883862	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28148513	GTAATTCAAGAGAAC[A/G]TCCTGCAAAACAGAC	8924
rs75893088	snp	C/T	0.36597	0.221475	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272956	CAAGTGCTGGTCCTG[C/T]AGGGGGATGCTTCCT	8924
rs75909135	snp	C/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28224854	AAGAAAAGTGGAAAA[C/T]TTACAAGTATATGAA	8924
rs75921437	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28186851	CGAACATGTACACAC[A/G]GTTAGAGCTCCTTTA	8924
rs75964737	snp	A/G	0.16559	0.235319	intron-variant	HERC2	GRCh38.p7	15:28273038	ATGCAGGAACAAAGC[A/G]ACCTCCAGAAAGACA	8924
rs75968637	snp	A/C	0	0	intron-variant	HERC2	GRCh38.p7	15:28298589	TCACGAGGTCAGGAG[A/C]TCGAGACCATCCTGG	8924
rs75973130	snp	A/G	0.259951	0.249802	intron-variant	HERC2	GRCh38.p7	15:28279217	AGATCTCCAACTCCC[A/G]ACCTGAGGTGATCCG	8924
rs76005419	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28232553	ATTCCATCTCAAAGA[A/G]AAAAAAAAAAAAGAA	8924
rs76034206	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28149094	CGAGAACATCACCAA[A/G]AACAGCCACACGAAC	8924
rs76071020	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28189096	AGTCTCAAAAAAAAG[A/G]AAAGAAAATTCCCAT	8924
rs76083033	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28114543	CCTGAAAAACACACA[C/T]GTCCACACAACCACG	8924
rs76131506	in-del	-/CAA	0.261884	0.249717	intron-variant	HERC2	GRCh38.p7	15:28173378	TCTTAAGATACTATT[-/CAA]CAATTTAAAAAGAAT	8924
rs76160479	snp	C/T	0.040671	0.13668	intron-variant	HERC2	GRCh38.p7	15:28247044	TAACCCTTGTCCTTG[C/T]GCTCTTTCTGTATCA	8924
rs76191755	snp	G/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28115281	TTTTTTTTTTTTTTT[G/T]CTACTCAAAGGTGGT	8924
rs76197309	snp	A/T	0	0	upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28322457	TCACGCCGCGGCGGG[A/T]GGTGGCGCTCACACT	8924
rs76212527	snp	A/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28151770	GTTCATAATAACATT[A/T]AAAAAAAAAACAGGT	8924
rs76228202	snp	C/T	0.263809	0.249618	intron-variant	HERC2	GRCh38.p7	15:28228815	CTGAATACTCTGGTG[C/T]CCTATTCCATTCCTT	8924
rs76266110	snp	A/G			intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299627	GTATTCGATCATTTG[A/G]TAATAAAATCAATGA	8924
rs76283289	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28293623	TATTTACCTACTTCA[A/G]TTTCACACCAATTGC	8924
rs76287873	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28150515	CGAGAATATCACCGA[A/G]AACAGCCACATGAAC	8924
rs76296532	snp	A/G	0.0235391	0.105903	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28201492	TACAGCATAATCATC[A/G]TTACTCAAGAAATCA	8924
rs76297514	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28187127	AACAGACCTTTCATC[A/G]TTTTTAAAACATAAA	8924
rs76309464	snp	A/C	0.106278	0.204558	intron-variant	HERC2	GRCh38.p7	15:28173504	TTATAGTAAGCTGTA[A/C]AACATGCAAACTGGT	8924
rs76328475	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28167056	AAATGTGACAACCAC[C/T]ACAGTAATAATGGAT	8924
rs76333042	snp	A/C	0.0463947	0.145069	intron-variant	HERC2	GRCh38.p7	15:28261100	ATCTGCTTTGCTTTA[A/C]TATTAAGCACAATTC	8924
rs76342700	snp	A/G	0.0232847	0.105357	intron-variant	HERC2	GRCh38.p7	15:28262068	GCTGCCCACCCCTGA[A/G]AGAAGAGAACCCTAA	8924
rs76361530	in-del	-/A	0.266273	0.24947	intron-variant	HERC2	GRCh38.p7	15:28155091	CCTACAAAGCACATG[-/A]AACTCATCCTTTTTT	8924
rs76377083	snp	A/G	0.0818113	0.184966	intron-variant	HERC2	GRCh38.p7	15:28167057	AATGTGACAACCACC[A/G]CAGTAATAATGGATT	8924
rs76461120	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28192943	CCCTTTTTTTTTTTC[C/T]AACAGATTGCAACTC	8924
rs76507515	snp	A/C	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28244164	GCAAGACCCTTGCCT[A/C]AAAAAAAAAGGTAAC	8924
rs76512054	snp	G/T	0.264906	0.249555	intron-variant	HERC2	GRCh38.p7	15:28167201	TCCAGTGGAGAAACT[G/T]GGCAGAGACCCTTAA	8924
rs76517692	snp	A/G	0.264084	0.249603	intron-variant	HERC2	GRCh38.p7	15:28170276	GAATGAGTCTACCCA[A/G]TTTCAAAAGTTGTAA	8924
rs76539705	snp	A/G	0.0422008	0.138995	intron-variant	HERC2	GRCh38.p7	15:28291466	CTGAATATCCACACC[A/G]AAGGGATAATAGTGG	8924
rs76590799	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28138700	CATGCCGGCTAACAC[A/G]TCCATTTTGCAGTCC	8924
rs76613150	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28156229	TCTTTTGGCTTAGGA[C/T]TGACTTGGCAATGCG	8924
rs76637202	snp	C/T	0.0072337	0.0597036	intron-variant	HERC2	GRCh38.p7	15:28269208	GGACAGACCCTGCCC[C/T]GCAAGGGAACACTGC	8924
rs76642379	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28126505	ATCCATCAATGAGTG[A/G]ATAAAGAAAATGTGG	8924
rs76642809	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28298760	GAGATCGCGCCACTG[C/T]ACTCCAGCCTCAGCA	8924
rs76653853	snp	C/T	0.263535	0.249633	intron-variant	HERC2	GRCh38.p7	15:28226051	TAAAAACAGAATATA[C/T]GGGAACACTACCCAG	8924
rs76654715	snp	C/T	0.259951	0.249802	intron-variant	HERC2	GRCh38.p7	15:28256743	GGAACTACAGGCGCC[C/T]GCCACCACAACTGGC	8924
rs76698844	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28161649	AGTTCCTCAGGTGCA[C/T]TAGCCATATTTCAGT	8924
rs76704029	snp	C/T	0.278664	0.248351	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28301027	TCTCTCAGAACCATT[C/T]CCCAATAAAAGACGC	8924
rs76711552	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28273071	ATGCTTACAATCACA[C/G]TAACACATTTACTAC	8924
rs76735000	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28176022	AGGCCTGACACACCA[C/T]CCACAGCCAGTCCAG	8924
rs76758673	snp	G/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28134365	AGTTCTAGCAGCTTT[G/T]TGTAAATACCACCAG	8924
rs76837607	snp	G/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28290313	CACACTTTTTTTTTT[G/T]GAGATGTAGTCTCGC	8924
rs76860236	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28151766	ATGAGTTCATAATAA[A/C]ATTAAAAAAAAAAAC	8924
rs76866518	snp	A/C	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28195055	AGTGAGACTCCGTCT[A/C]AAAAAAAAAAAAAAT	8924
rs76886525	snp	C/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28187758	CATGTCATTTTATTG[C/T]TGCCTCATTCAAATC	8924
rs76890926	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28267211	GGCACAGGTGCTCAC[A/G]GGGACAGCCCAATGA	8924
rs76901743	snp	A/C	0.0471551	0.14613	intron-variant	HERC2	GRCh38.p7	15:28278785	CAAAGTCACTATCAC[A/C]GTCAAATAAAGCCAG	8924
rs76925493	snp	C/T	0	0	intron-variant	HERC2	GRCh38.p7	15:28209942	TTGAATACATTATCT[C/T]TTTTTTTTTTTTTTT	8924
rs76925859	snp	G/T	0.293294	0.246223	intron-variant	HERC2	GRCh38.p7	15:28291869	AAGATCACGCCACTG[G/T]ACTCCAGCCTGGGCG	8924
rs76959019	snp	A/C	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28187898	CCTGCTGTGGTACTG[A/C]CAACATTCCTCCATC	8924
rs76978789	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28243357	AGATTTCTTAAGGCC[A/C]AAAATGAACAACCAT	8924
rs77000329	snp	C/T	0.0737376	0.17729	intron-variant	HERC2	GRCh38.p7	15:28129573	CTCCCGAAACCCAGG[C/T]TCCCAGACACCAGCA	8924
rs77013448	snp	A/G/T	0.0011694	0.0241525	intron-variant	HERC2	GRCh38.p7	15:28191064	ATTTCCACCTAGGAA[A/G/T]AAATGGGTAAAGAAT	8924
rs77019455	snp	C/G	0.301681	0.2446	intron-variant	HERC2	GRCh38.p7	15:28210603	ATTCCCAGCAGCAGC[C/G]TGTTCATGGAGTGCG	8924
rs77042691	snp	C/T	0.0926964	0.194308	intron-variant	HERC2	GRCh38.p7	15:28164042	CTGAGCTTGTGGAAA[C/T]GGGAAAGGCCCTTGT	8924
rs77046420	snp	C/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28194627	GCCACTGTGCCTGGC[C/T]GATCCTTTGACATTT	8924
rs77047768	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28147210	CTCTCGCTTTATATC[C/T]AGTCCACCAGCAAAT	8924
rs77076593	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28167039	ATAAATGTGAACAAT[A/G]AAAATGTGACAACCA	8924
rs77093318	in-del	-/T	0.257176	0.249897	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174230	ATTTTCATTCCAGCA[-/T]GTATAAATCGCATGA	8924
rs77104128	snp	A/C	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28292255	AAAAAAAAAAAAAAC[A/C]AGGCAAAGTATTTGA	8924
rs77126521	snp	A/C/T			intron-variant	HERC2	GRCh38.p7	15:28219250	AGTGGGGCGACCAGA[A/C/T]GCTCATGCAGCCCGC	8924
rs77182473	snp	G/T	0.0832709	0.186283	intron-variant	HERC2	GRCh38.p7	15:28272497	ACAAATACTTGGGAT[G/T]TGAAAGGAAACTAAA	8924
rs77197927	snp	A/G	0.00636936	0.0560724	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28301460	CTGATAGGGACTCCT[A/G]ACCAAATTTATAATA	8924
rs77234772	snp	A/C	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28148985	AAAATTACCAAAAAA[A/C]CACACACGGCTCCTA	8924
rs77273635	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28180533	CCAGAGTTGGGGGAA[C/T]GGGAGGATAAAGACA	8924
rs77327675	snp	A/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28162741	AAAAATACAAAAAAA[A/T]TTAGCCGGGCATGGT	8924
rs77399744	snp	A/C	0.0782157	0.181632	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272346	CCTGTGCCCCGCTGT[A/C]CCACAGCTGAAGCAA	8924
rs77416688	snp	A/T	0.293037	0.246268	intron-variant	HERC2	GRCh38.p7	15:28287082	CTTTTCTGTATAATT[A/T]TTTTCATAATAAAAC	8924
rs77452472	snp	C/T	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314382	AGGGAAGTGGGAAAG[C/T]GAGACAAGGAGATCA	8924
rs77474090	snp	A/C	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28126432	AAGATACTTGCACAC[A/C]CATGTTTATAGCAGT	8924
rs77474499	snp	A/C	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28140068	GTGAGACTCTGTCTC[A/C]AAAAAAAAAAAGAAG	8924
rs77500635	snp	A/G	0.105569	0.204058	intron-variant	HERC2	GRCh38.p7	15:28124411	TATTCTGTCCAGTTT[A/G]ACTGTAAAAAAAATT	8924
rs77519763	snp	C/T	0.161596	0.233848	intron-variant	HERC2	GRCh38.p7	15:28199169	AAAAAGAATTTCATC[C/T]AGCACCCAGAGTGCA	8924
rs77572354	snp	C/G	0.256897	0.249905	intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28315576	AAGGCAGGTGGATCA[C/G]GAGCTCAGGAGTTCA	8924
rs77631111	snp	C/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28183226	TATTTTTTGTTTGTT[C/T]TGAGACAGGGTCATG	8924
rs77631264	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28244788	TCCTGGGGCTGTTTT[C/T]CTCAGGACAACTGCT	8924
rs77634745	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28146413	GTAGAAACAGTGAAA[C/T]TAAAACCACATTTAA	8924
rs77652858	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28167047	GAACAATGAAAATGT[A/G]ACAACCACCACAGTA	8924
rs77671033	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28122161	AAAGAAATCGGGAGT[A/G]CCTGGGGTGAAGACA	8924
rs77714588	snp	A/T	0.166506	0.235645	intron-variant	HERC2	GRCh38.p7	15:28236269	CTTATTATTATTATT[A/T]TTATCATCATCAGCT	8924
rs77725074	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28195576	CATTACGCTAAACAC[A/T]AAAGGATAAATCTTA	8924
rs77730423	snp	A/G	0.0611083	0.163768	intron-variant	HERC2	GRCh38.p7	15:28239239	CTGCAGATCGAAATT[A/G]GTGACATACAACTAA	8924
rs77741988	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28280989	CATCTCCTAAACAGA[A/G]AAAAACACTAGCCAT	8924
rs77770808	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28272777	GGGACATGGTTCTCC[A/G]TACAGAGTACCACAT	8924
rs77775950	snp	A/T	0.040671	0.13668	intron-variant	HERC2	GRCh38.p7	15:28247833	CTGAAAGTTTCCATT[A/T]CTGACAAGAGCCTAA	8924
rs77805166	snp	A/C	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28144275	CCCGGGTTTCACAAG[A/C]TAGGTACCACCCCAT	8924
rs77819576	snp	C/G	0.0111196	0.0737302	intron-variant	HERC2	GRCh38.p7	15:28268763	TACGGGGCCGGCTCT[C/G]CAGCCCTTCCCACCC	8924
rs77820448	snp	A/G	0.0402882	0.136092	intron-variant	HERC2	GRCh38.p7	15:28219231	AAAGCACCGGCATCT[A/G]TGGAGTGGGGCGACC	8924
rs77829148	snp	G/T	0.0178098	0.0926698	intron-variant	HERC2	GRCh38.p7	15:28268065	ATATTAGGAAGAAAC[G/T]GCTGACTTTTGTTCC	8924
rs77854840	snp	A/G	0.0607341	0.163335	intron-variant	HERC2	GRCh38.p7	15:28112958	TCCATTTTCATTTCT[A/G]TAAAGACTCAAGAGG	8924
rs77865049	snp	C/T	0.0235564	0.10594	synonymous-codon, downstream-variant-500B	HERC2	GRCh38.p7	15:28174498	CGCCACACTGTGGGA[C/T]GACCCACAAGCCACG	8924
rs77898096	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28298808	CCCCCCCAAAAAAAA[A/G]AAGAAGAAGAAATAC	8924
rs77925277	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28273338	CAGTTTCAATGACGT[A/G]TAAGACTATACCAGT	8924
rs77926013	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28192953	TTTTCCAACAGATTG[C/T]AACTCAGCATAAAAT	8924
rs77932478	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28192931	GTTTTTGGGTTTCCC[C/T]TTTTTTTTTTCCAAC	8924
rs77947354	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28183741	CAGGTATCACTTTTT[C/T]CACACATTATATACT	8924
rs77966553	snp	C/T	0.0341408	0.126114	intron-variant	HERC2	GRCh38.p7	15:28166961	TAGGTAGAAGACAGA[C/T]GGATGAGAAGGGAAA	8924
rs78043650	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28129417	CCAGGGTTTCCATCA[G/T]GGCTGATCACACAGG	8924
rs78061362	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28280972	AATATTTATCAGCAG[A/C]ACATCTCCTAAACAG	8924
rs78065044	snp	C/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28124286	CAAAGGCACACGGGG[C/G]CCAGTGTGGCATCCA	8924
rs78104319	snp	A/C	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28140067	AGTGAGACTCTGTCT[A/C]AAAAAAAAAAAAGAA	8924
rs78127342	snp	A/C	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28227482	AGAAAAAAAAAAAAA[A/C]CACAAAAAATAGTGT	8924
rs78143828	snp	A/G	0.0236746	0.106192	intron-variant	HERC2	GRCh38.p7	15:28282156	GGAAGCCTGGACTTC[A/G]TCTCCAGCTGCCAGC	8924
rs78194002	snp	A/G	0.00733862	0.0601286	intron-variant	HERC2	GRCh38.p7	15:28135452	AAAGACAAATAGAAT[A/G]TTGAAATAATTTTTT	8924
rs78238504	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28306864	TTTGAAGACACAGTC[A/T]CACTCTGTCACCCAG	8924
rs78257327	snp	A/T	0	0	intron-variant	HERC2	GRCh38.p7	15:28230527	AACATCATTCACTAT[A/T]AAAATCATACACTTA	8924
rs78316732	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28241421	CTACTGACAGGAACA[A/T]AAAATGGTGCAGCCA	8924
rs78374687	snp	C/T	0.0422008	0.138995	intron-variant	HERC2	GRCh38.p7	15:28262779	TTTCTAATGACAGTC[C/T]ATTCATGGAATGTCA	8924
rs78375407	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28114491	ACAGATCAGCAATAG[C/T]TGGAGCCAAATCCAT	8924
rs78406210	snp	A/G	0.00716266	0.059414	intron-variant	HERC2	GRCh38.p7	15:28295544	GCTGGGATTACAGGC[A/G]TGCATCACCATGCCC	8924
rs78433806	snp	A/T	0	0	intron-variant	HERC2	GRCh38.p7	15:28278112	TAAAAAAAAAAAAAA[A/T]TTGGCCAGGTATGGT	8924
rs78460234	snp	A/G	0.0129061	0.0792873	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28248591	TACTTTCTCCTGGAT[A/G]AAGTTTACTAATAAG	8924
rs78481711	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28176025	CCTGACACACCATCC[A/C]CAGCCAGTCCAGGCA	8924
rs78497478	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314864	AGACTCCCTCTCAGG[A/G]AAAAAAAAAAAAAAA	8924
rs78564243	snp	A/G	0.0422008	0.138995	intron-variant	HERC2	GRCh38.p7	15:28282364	ACCACGATGAAAGAT[A/G]TTGGAATAATGTGGC	8924
rs78635135	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28246665	TAAATGCAGGCATGC[C/T]GATCAGCAAAGAAGA	8924
rs78640972	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28165309	AGCCAAGATCGGAGG[G/T]TGGTTATCTAAGGGG	8924
rs78661407	snp	A/C	0.0174175	0.0916809	intron-variant	HERC2	GRCh38.p7	15:28182151	TATTGACAGTCTATA[A/C]TTTTCATTTATGCAC	8924
rs78664853	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28197698	GGAGGTTGCAGTGAG[C/T]CAAGATGGCGCCACT	8924
rs78680559	snp	A/C	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28148038	CAAGACTGTGTCTCC[A/C]AAAAAAAAAAAAAGA	8924
rs78696453	snp	A/G	0.0136895	0.0815924	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28174504	ACTGTGGGACGACCC[A/G]CAAGCCACGCGTGTG	8924
rs78699119	snp	C/T	0.295854	0.245759	intron-variant	HERC2	GRCh38.p7	15:28237855	CCAAAGTTTAACCTC[C/T]TTTCTTGTGGAACAC	8924
rs78703276	snp	C/T	0.000613339	0.0175012	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213913	AATCACAGCCAGGAC[C/T]GCCATGAGGCCCCCC	8924
rs78712637	snp	A/C	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28193361	AAAATTAAGAACTTA[A/C]TGAGTAAGTTTAGAA	8924
rs78725931	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28298775	TACTCCAGCCTCAGC[A/G]ACAGAGCAAGACTCC	8924
rs78766958	in-del	-/T			intron-variant	HERC2	GRCh38.p7	15:28124565	GGCTGGCATGAACAT[-/T]CAAGGTTCTTTTGAG	8924
rs78809959	snp	C/T	0.0737376	0.17729	intron-variant	HERC2	GRCh38.p7	15:28121292	CAGCCCAGGTACCCA[C/T]GAAAGCATCACTTCT	8924
rs78820178	snp	A/G	0.5	0	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321194	GCGCACGATCTACAA[A/G]AACAGCCATAAAGAC	8924
rs78851824	snp	A/C	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28246611	ACTAAAAAAAAAAAA[A/C]AAAGGTGAAAGGGCA	8924
rs78863461	snp	C/G	0.0422008	0.138995	intron-variant	HERC2	GRCh38.p7	15:28281759	AGTGAAAGACTGAAA[C/G]GTAAAGCAGTGCCCC	8924
rs78873895	snp	A/C	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28246610	AACTAAAAAAAAAAA[A/C]CAAAGGTGAAAGGGC	8924
rs78897550	snp	G/T	0	0	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174115	AGTACAGTGCCTGTA[G/T]CTCTCAGGCAGTTAT	8924
rs78902536	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28228145	AAAAAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAG	8924
rs78970358	snp	C/T	0.0126979	0.078662	intron-variant	HERC2	GRCh38.p7	15:28186834	ACGGGATGTGTGAGA[C/T]ACGAACATGTACACA	8924
rs78980176	snp	C/T	0.263535	0.249633	intron-variant	HERC2	GRCh38.p7	15:28188324	GAGGCAGGTGGATCA[C/T]GAAGTCAGGAGATCG	8924
rs78995226	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28129415	GCCCAGGGTTTCCAT[A/C]AGGGCTGATCACACA	8924
rs78999460	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28192401	AGCAGATTAATATAT[C/T]TCCAAAGAAAACAAA	8924
rs79012563	snp	C/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28266639	GGCTGGATCTCAAGA[C/T]ATCTGCTAAGTCAAA	8924
rs79064135	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28163529	ATCAAAAAGGGATGA[C/T]TTAAGCTATAAAGAA	8924
rs79087600	snp	C/T	0.264632	0.249571	intron-variant	HERC2	GRCh38.p7	15:28228648	CAAGAATAAACGTAA[C/T]GCAGAAAGCACGGGC	8924
rs79096404	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28147408	CTCCTGAGCTCAAGC[A/G]AGCTCCTGCCTAGGC	8924
rs79097182	snp	C/T	0.259951	0.249802	intron-variant	HERC2	GRCh38.p7	15:28266851	GTGGTGACCCAACTG[C/T]GTGCACTTGTCAAAA	8924
rs79099923	snp	C/T	0.158962	0.232835	intron-variant	HERC2	GRCh38.p7	15:28236271	TATTATTATTATTTT[C/T]ATCATCATCAGCTGT	8924
rs79104239	snp	C/T	0.00557542	0.0525036	downstream-variant-500B	HERC2	GRCh38.p7	15:28110577	GCCAGTGCTAAACAT[C/T]GTGTCCCTGAATAAA	8924
rs79120569	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28278351	TGGCCCCACTGCCCT[A/G]GGCAACAGTGAGACC	8924
rs79141613	snp	C/T	0.0138799	0.0821421	intron-variant	HERC2	GRCh38.p7	15:28219477	GGCCAGCACCACATC[C/T]GCCCTCAGGGACAGG	8924
rs79155556	snp	G/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28153386	GGGTGGAGCGCAGTG[G/T]CTCACACTTGTAATA	8924
rs79164713	snp	A/C	0.261332	0.249743	intron-variant	HERC2	GRCh38.p7	15:28298484	AGTGGACACCATCCC[A/C]ATTCATTCCACAAAA	8924
rs79203714	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28187512	AATTTTTTGTATTTT[C/T]AGTAGAGACAAGGTT	8924
rs79245957	snp	A/T	0	0	intron-variant	HERC2	GRCh38.p7	15:28245560	TCAAAAAAAAAAAAA[A/T]ATATATACACACACA	8924
rs79256199	snp	A/G	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28289859	AGAGGATGACACGCC[A/G]CAGTGAAAGGACGAC	8924
rs79286671	snp	A/G	0.302435	0.244439	intron-variant	HERC2	GRCh38.p7	15:28289538	ATGCCTCCCCAGCAC[A/G]ATGGAGATACTCCTG	8924
rs79340143	snp	A/C	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28199147	GTGAGACCCCATCTC[A/C]AAAAAAAAAAAGAAT	8924
rs79380392	snp	C/T	0.0607341	0.163335	intron-variant	HERC2	GRCh38.p7	15:28164073	CAGTGCCAGGGACTC[C/T]CACCGCTTCCGACCC	8924
rs79399455	snp	A/G	0.17224	0.237599	intron-variant	HERC2	GRCh38.p7	15:28273033	AGTGGATGCAGGAAC[A/G]AAGCAACCTCCAGAA	8924
rs79450508	snp	A/T	0	0	intron-variant	HERC2	GRCh38.p7	15:28141253	AACTTTTTTTTTTTT[A/T]AATTTAAAGATTATA	8924
rs79476584	snp	A/C	0.265727	0.249505	intron-variant	HERC2	GRCh38.p7	15:28154785	TATTTTTTTATTATA[A/C]TTTAAGTTCTAGGGT	8924
rs79487420	snp	A/C	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28249258	CCACCTTGAGCCCTT[A/C]CTCGCAAGCAGCACT	8924
rs79487803	snp	A/G	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28187308	AGTATATATCACTGA[A/G]TTAAGGAGGTCTGGT	8924
rs79489308	snp	A/T	0	0	intron-variant	HERC2	GRCh38.p7	15:28259810	AAAGAAAAAAAAAAA[A/T]TACAAAAATTAGCCA	8924
rs79489815	snp	C/T	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28173519	CAACATGCAAACTGG[C/T]CTGCCACGGTGGCTC	8924
rs79527789	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28139638	ATGAATAGGATCTCC[A/C]AAAAATCTAAAACAA	8924
rs79534430	snp	A/C	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28199148	TGAGACCCCATCTCA[A/C]AAAAAAAAAAGAATT	8924
rs79567998	snp	G/T			missense	HERC2	GRCh38.p7	15:28124182	AGCAGCAGCAGACGG[G/T]TCCTCAGCGCAATGA	8924
rs79570268	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28240062	TTGTAGGGTTTTTTT[A/T]TAAATCCTTATCATT	8924
rs79576603	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28308791	AATCATTTCAACTGA[A/T]GCTAAAAAAAATTTG	8924
rs79591282	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28189376	TTAGTTTCTGGTTTG[G/T]CTAAAGTAAAAACAT	8924
rs79612398	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28293772	AGCACTGCTATGCAG[A/G]GGCACTGTGACTGAT	8924
rs79719798	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28259507	AAAAAGGACGGAACA[C/T]ATGCCAATATTTTGT	8924
rs79758916	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28253005	CTGTGCTCGGCTGCC[A/T]GACCCAACCTGCCAG	8924
rs79819039	snp	C/G/T	0.498844	0.0331566	intron-variant	HERC2	GRCh38.p7	15:28272400	GGCTAAAGGAGAAAA[C/G/T]ATATTTATTCTAGTA	8924
rs79840202	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28145926	CTTTTGAAGAAGCTC[C/T]GCAGTATGCCAACCA	8924
rs79846789	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28251488	AGTAAAAAAAAAAAA[A/C]AAAAAAACACATAAA	8924
rs79860193	snp	C/T	0.000181322	0.00951988	missense, synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28280099	GAGGCAGAGAAATAC[C/T]GCTGCTTTTCCACTT	8924
rs79864421	snp	G/T	0	0	intron-variant	HERC2	GRCh38.p7	15:28194082	CCTTTTTTTTTTTTT[G/T]TGAGACAGAATCTCC	8924
rs79868153	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28273940	CACATTATCTATAAG[A/G]CTTCAAACCAAGCAC	8924
rs79910337	snp	C/T	0.0524604	0.153226	intron-variant	HERC2	GRCh38.p7	15:28200038	ATTTTACCTTAATGA[C/T]TTCCTTAGAGGCCCC	8924
rs79933035	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28188647	GCAAGTGCTCCTGAA[A/G]TAAGACCATGACTAG	8924
rs79971187	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28141263	TTTTTTAATTTAAAG[A/T]TTATACAAAAATATC	8924
rs79979051	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28272094	ATCTGACTCGCTGCT[A/G]TTACCACCAAACACA	8924
rs79981270	snp	G/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28256904	CCAGCCCAGATCATG[G/T]TTTTTAAGACTCGCG	8924
rs80005868	snp	A/C			missense	HERC2	GRCh38.p7	15:28132214	GGTCTGGGCATCTCC[A/C]CTGCCACAGGCGATG	8924
rs80018962	snp	C/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28188788	TTCTATTTTTGTTTA[C/T]ATGTTAGAAAAAACC	8924
rs80043087	snp	G/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28154877	CCCATTAACTCATCA[G/T]TTACATTAGGTATAT	8924
rs80049267	snp	A/G	0.0962929	0.197165	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111411	GAAAGAAAGGAGAAA[A/G]AAAAAAAATCGATTG	8924
rs80122566	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28189375	CTTAGTTTCTGGTTT[G/T]GCTAAAGTAAAAACA	8924
rs80171019	snp	A/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28259811	AAGAAAAAAAAAAAA[A/T]ACAAAAATTAGCCAG	8924
rs80182548	snp	C/T	0.0437281	0.141251	intron-variant	HERC2	GRCh38.p7	15:28242743	GTTTTATTCCAGAAA[C/T]GGAAGGTTGAGTCAA	8924
rs80193027	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28291447	CATGCAAGGAAAAAA[A/C]ACCCTGAATATCCAC	8924
rs80225126	snp	C/T	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28181900	TCCACCCACAACAAG[C/T]CCTGCAGAGAATAAG	8924
rs80231418	in-del	-/AG	0.258288	0.249863	intron-variant	HERC2	GRCh38.p7	15:28261986	GGCCTGCTTCTGTGA[-/AG]ACACTGGTGTTGGAA	8924
rs80249838	snp	C/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28201171	CTCAGCCACCCTTCA[C/G]ACCCTGTAGGCTTTG	8924
rs80302374	snp	C/G	0.0115144	0.0749975	intron-variant	HERC2	GRCh38.p7	15:28120721	TTATAACCTATAATC[C/G]GATGTATCATCAAAT	8924
rs80337157	snp	C/T	0.00398564	0.0444627	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28315270	ACAGGGAATTCACAC[C/T]CACACTCGCCACACC	8924
rs80340439	snp	A/G	0.499276	0.019009	intron-variant	HERC2	GRCh38.p7	15:28272393	AACATTTGGCTAAAG[A/G]AGAAAAGATATTTAT	8924
rs80344102	snp	A/G	0.261884	0.249717	intron-variant	HERC2	GRCh38.p7	15:28288390	AATTAGCCAGGTGTG[A/G]TGGCGTATGCCTGTA	8924
rs80345552	in-del	-/AAA			intron-variant	HERC2	GRCh38.p7	15:28259808	AAAAAGAAAAAAAAA[-/AAA]TACAAAAATTAGCCA	8924
rs80350074	in-del	-/A	0.26326	0.249648	intron-variant	HERC2	GRCh38.p7	15:28164537	TGAAATGTACCTACC[-/A]TTTTTTTTTATGAGG	8924
rs111229832	snp	A/G	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28272039	AGTGCTCACTGATCC[A/G]AGTCTTCTCCACAAA	8924
rs111232039	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28148791	ACCGAGAGCATCACC[A/G]AGAACGGCCACACGA	8924
rs111239439	snp	A/T	0.0185938	0.0946107	intron-variant	HERC2	GRCh38.p7	15:28281712	AAACGACATGAAGAA[A/T]ACTGAATTGCACACT	8924
rs111241258	snp	A/G	1.64735e-05	0.00286993	synonymous-codon	HERC2	GRCh38.p7	15:28167693	CCTCTTCACCTCTTT[A/G]GTTTTGGTCATGGTT	8924
rs111243072	snp	A/T	0.0463947	0.145069	intron-variant	HERC2	GRCh38.p7	15:28235793	GGCGTGTCCTACCCA[A/T]CACTGCATCCTGAAC	8924
rs111245444	in-del	-/T	0	0	intron-variant	HERC2	GRCh38.p7	15:28119627	CAAGGCTAATTTTTG[-/T]ATTTTTTGTAGAGAT	8924
rs111246683	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28220703	TGCCCTGGTCCTTCC[A/G]TGGCTCCCAGCAGAC	8924
rs111259013	snp	A/C	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28200223	CAAAAATGAAGAAAC[A/C]CTGTCTCTACTAAAA	8924
rs111261207	snp	C/T	6.63185e-05	0.00575802	intron-variant	HERC2	GRCh38.p7	15:28114586	TGCTATTTATGTCAA[C/T]GCAACAGAGACGGAT	8924
rs111263444	snp	C/G/T	9.99357e-05	0.00706816	synonymous-codon	HERC2	GRCh38.p7	15:28124109	TCCAGTTTCGTCGAG[C/G/T]GAGCCTTCCAGGTCG	8924
rs111269832	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28168835	AAAACTGCCAAACAT[A/G]AAAACCAGACCAGAA	8924
rs111273106	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28310273	CAACATGGCAAAACC[A/G]CATTTCTACCAAAAA	8924
rs111298329	in-del	-/C	0	0	frameshift-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28233177	TCTCGAATTATCTTT[-/C]TGAGCTATCCTCCTC	8924
rs111321877	snp	G/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28266075	ATTTAGACCAGCATA[G/T]CATCAGGCCAGTTTC	8924
rs111330403	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28293410	AGGCAGGAGAATGGC[A/G]TGAACCCGGGAGGCA	8924
rs111334430	snp	A/G	0.26271	0.249677	intron-variant	HERC2	GRCh38.p7	15:28227252	TGTGCTCCAGCCTAG[A/G]CGACGGAGTGAGACT	8924
rs111343186	snp	A/G	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28219251	GTGGGGCGACCAGAC[A/G]CTCATGCAGCCCGCT	8924
rs111355943	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28145938	CTCTGCAGTATGCCA[A/C]CCATGACCTTACACG	8924
rs111390855	snp	A/G	0.0422008	0.138995	intron-variant	HERC2	GRCh38.p7	15:28291281	CCAGGCTGGAGTGTA[A/G]AGGCACAATCATAGA	8924
rs111396335	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28296286	CAAGACCAGCCTGAC[C/G]AAGATGGTGAAACTC	8924
rs111400032	snp	A/G	0.0150606	0.0854603	intron-variant	HERC2	GRCh38.p7	15:28248368	GCAACAAAATTAAAA[A/G]TATTAACGAGGCTAT	8924
rs111412987	snp	C/T	0.00755907	0.0610114	intron-variant	HERC2	GRCh38.p7	15:28235815	ATCCTGAACACCTCG[C/T]ATGGTAACTGCACCA	8924
rs111421882	snp	A/G	0.0460142	0.144533	intron-variant	HERC2	GRCh38.p7	15:28225995	CTGGTCAACTCTACC[A/G]AAGATTTAAAGCAGA	8924
rs111425631	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28205156	AAAGAAGAGAACAAC[A/G]ACTCTCCATCAGAAT	8924
rs111426019	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28225720	AAAAAAAAAAAGAAA[A/G]AAAAAAAAGAAGATG	8924
rs111433258	snp	A/G	0.482384	0.0921818	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174015	ACATATTCCAAAGTC[A/G]ATCAAAATGCATACT	8924
rs111435660	snp	C/T	0.0850919	0.187897	intron-variant	HERC2	GRCh38.p7	15:28194996	GGGAGGTGTCAGTTA[C/T]AGTGAGCCAGGATCG	8924
rs111439917	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28122118	CAGACCGGGGAGGGG[A/G]AACAAGGTCCTGGCT	8924
rs111446662	snp	C/T	0.0329836	0.124112	intron-variant	HERC2	GRCh38.p7	15:28143605	GTGCCCACCACCACG[C/T]CCATCTAATTTTTTG	8924
rs111458470	in-del	-/TAG	0.49306	0.0584955	intron-variant	HERC2	GRCh38.p7	15:28289407	ATGCACCTTATAACA[-/TAG]TTCTCAAATACATGA	8924
rs111460644	snp	A/C	0.00716266	0.059414	intron-variant	HERC2	GRCh38.p7	15:28139232	GCTTCTGATGAGCAG[A/C]ATAGGGCAAGAACTG	8924
rs111485817	snp	A/G	0.0150606	0.0854603	intron-variant	HERC2	GRCh38.p7	15:28242153	GAATGGTAGTTGCCA[A/G]GTGCTAGGGAAAATT	8924
rs111487180	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28200939	AAAACATAATTAGAT[C/T]TTTAAAGTTTGATGG	8924
rs111491095	in-del	-/A	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28206677	CTCTACTAAAAATAC[-/A]AAAACATTAGCTGGG	8924
rs111491764	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28223196	CAGTAAAACTTCCCA[A/G]TGGATTTGAAAATAG	8924
rs111512902	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28160726	CTCATGCTCGGTGCA[C/T]TGCACCCACTGTCCT	8924
rs111529497	snp	A/G	0.00716266	0.059414	intron-variant	HERC2	GRCh38.p7	15:28181490	AGTTCAAATGAATGA[A/G]TTCTAACTTTATTTC	8924
rs111536212	snp	A/C	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28225871	ACACATTCCTAAAAA[A/C]ATAAATTACCCGAAC	8924
rs111536790	snp	C/T	0.160609	0.233472	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299969	GAGGCAGGAGAATTG[C/T]TTGAACCCAGGAGGC	8924
rs111545605	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28149548	GAACGTCACCGAGAA[C/T]GGCCACACCAACATA	8924
rs111553059	snp	A/C	0.0333695	0.124785	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28317972	CACTTAAAAAAGAAC[A/C]CAAAAATAGAAACTG	8924
rs111578321	snp	C/T			missense, downstream-variant-500B, nc-transcript-variant	HERC2	GRCh38.p7	15:28186601	TTGCCTTTCTCATCC[C/T]CCTCCTCTTCATTAT	8924
rs111583334	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28209875	AGGTATTTTGGTGTC[C/T]ACAGTTTTTCAACAC	8924
rs111584549	snp	C/G	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28268840	CCAGAGCCGATGCAG[C/G]GGCAGGGCAGGCTAG	8924
rs111585294	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28149613	CTCCTAACCGAGAAC[A/G]TCACCGAGAACGGCT	8924
rs111594547	snp	C/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28150652	ACACACGGCTCCTAA[C/T]CAAGAACATCACCAA	8924
rs111597953	snp	C/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28293403	GAGGCTGAGGCAGGA[C/G]AATGGCGTGAACCCG	8924
rs111615508	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28168068	CTATTAATATTCACA[A/G]CAGGTCACATGAACC	8924
rs111645850	snp	A/G	0.5	0	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317139	TGTGTTGGCCAGGCT[A/G]GAGTGCAATGGCATG	8924
rs111651790	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28228669	AAGCACGGGCAATTA[C/T]TTTAAACATCTAACT	8924
rs111653838	snp	A/G	0.0486741	0.148216	intron-variant	HERC2	GRCh38.p7	15:28224249	GGATTTCACTTTGTC[A/G]CCCAGGCTGGAGCCC	8924
rs111656069	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28218961	GACCTCCCAAACTGT[C/T]ATCTTTTCTGCTTTG	8924
rs111659731	snp	A/G	0.158632	0.232706	intron-variant	HERC2	GRCh38.p7	15:28153423	CTTTGGGAGGTCGAG[A/G]CAGGCAGATCACTGG	8924
rs111664452	snp	C/T	0.0123036	0.0774623	intron-variant	HERC2	GRCh38.p7	15:28203427	AGTGACAGGTTTCAT[C/T]CTAAAAGTTTAAAAT	8924
rs111681126	snp	A/C	0.0129362	0.0793774	intron-variant	HERC2	GRCh38.p7	15:28256049	CATTCCCTCCCAACA[A/C]CCTGACCCATGCCCT	8924
rs111686544	in-del	-/A	0.367913	0.220446	intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28316059	CCTCTTCCGCTGTTT[-/A]AAAAAAAAAAAAAAT	8924
rs111688119	snp	C/G			intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28301649	GCAAAAAAAAAAAAG[C/G]CATTTTTAATTAAAA	8924
rs111701273	snp	A/T	0	0	intron-variant	HERC2	GRCh38.p7	15:28138052	AGCTAATCCAGAGCT[A/T]GCTAACTGTCTTCAA	8924
rs111702544	snp	C/T			intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313043	GGATTTGGGAAGAGG[C/T]CCAACTCCAAGGCTT	8924
rs111712835	snp	A/G	0.00517822	0.0506191	intron-variant	HERC2	GRCh38.p7	15:28113449	CGGGTGGAGGGACGC[A/G]CTCAGAGTGCACTCC	8924
rs111715441	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28148659	CGGCCACACGAACGC[A/G]CATTCTAGTAACACT	8924
rs111731751	snp	A/G	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28250591	CTCGCCAGCATGTAA[A/G]TAACGATCTACTCTG	8924
rs111732702	snp	G/T	0.0399052	0.1355	intron-variant	HERC2	GRCh38.p7	15:28303577	TTTTTTTTTTCTATT[G/T]CTGTGAAGAATGTCA	8924
rs111748297	in-del	-/TC	0.0501905	0.150254	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174336	GCACAATTAAATAAA[-/TC]TATAAGGTTGCTGTA	8924
rs111758471	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28272635	CATGAAAGTTCTAGG[A/G]TCTTAAATTCATGGA	8924
rs111763627	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28293668	TCCCAATGCTTGTGT[A/G]TCCATGGGAAAAGGG	8924
rs111772797	snp	A/G	0.0146672	0.084371	intron-variant	HERC2	GRCh38.p7	15:28225677	CACTCTGGCCTGGCA[A/G]GAGAGCAAGACTCCG	8924
rs111791369	snp	C/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28225980	CAAAGAAAAGCTTAG[C/G]TGGTCAACTCTACCA	8924
rs111793452	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28132050	GGGGCCCTGGGGGCC[C/T]GACTGCGGTGAGCTG	8924
rs111806215	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28293418	GAATGGCGTGAACCC[A/G]GGAGGCAGAGCTTGC	8924
rs111806385	snp	A/T	0.5	0	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318642	AAAAAAAAAGTATTG[A/T]ACAATTAAACTGTTT	8924
rs111819804	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28226992	TTAAAAAGGAGAAAC[A/G]GGCTGGGCGCAGTGG	8924
rs111843121	snp	C/G/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28309154	TCAGATGAAATGTTC[C/G/T]AGAAATATCTACTAA	8924
rs111923642	snp	A/C	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28149423	CATACATTCTAGTAA[A/C]ATTACCAAAAAAACA	8924
rs111955823	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28281776	TAAAGCAGTGCCCCT[C/G]CCCTTCTCAGGGCAT	8924
rs111964648	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314408	GATCAATGAAGCAAC[A/G]GTATGCAGTATATGA	8924
rs111967469	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28200063	TAAAATCAGGTCATA[A/G]GAGTGGGCCTCTGAC	8924
rs111973847	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28232475	AATCGTTTGAACCTG[C/G]GAGGCGGAGGTTGCA	8924
rs112029462	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28295385	CCCAGCCCACAGCCT[C/T]TTTGTGTATGGTCTG	8924
rs112046478	snp	A/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28293662	AGTGAGTCCCAATGC[A/T]TGTGTATCCATGGGA	8924
rs112048244	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28274606	CAATTCTGTGTTTCA[C/T]GGCTGTCACATGAGC	8924
rs112061942	snp	C/T	0.165853	0.235413	intron-variant	HERC2	GRCh38.p7	15:28229036	ATTTTGAAGTTTTGT[C/T]TAAAATCTGAGAAAG	8924
rs112077326	snp	C/T	0	0	intron-variant	HERC2	GRCh38.p7	15:28164954	TCTGTAGGACATATT[C/T]TCTGCCAGCAGTAAC	8924
rs112104080	in-del	-/C/CCTAGTGAAAACATATTTATTC	0.491723	0.0638722	intron-variant	HERC2	GRCh38.p7	15:28272409	GAAAAGATATTTATT[-/C/CCTAGTGAAAACATATTTATTC]CTAGTAAAAACAGAT	8924
rs112117630	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28248995	GCCTATGGAGCTGCG[C/T]GCAGTGGTCCAAACT	8924
rs112135184	snp	C/G	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28252081	TAAACATACTTAAGT[C/G]CTTCCTAATAACGGA	8924
rs112150401	snp	A/G	0.0345262	0.126772	intron-variant	HERC2	GRCh38.p7	15:28159541	GCTACTGAAGTGTGT[A/G]CATTTGTCACGTAGT	8924
rs112152022	snp	A/C	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28146016	GAGGCAGGGCCCATC[A/C]GACAGGGATGTGGTA	8924
rs112162082	snp	A/C	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28164100	ACCCAGCATGGGAAC[A/C]GCTGTGACCCTGTGC	8924
rs112164417	snp	A/G	0.0345262	0.126772	intron-variant	HERC2	GRCh38.p7	15:28143791	CCAACTCCTCTCAAC[A/G]ATTTAGAGGTTTAGA	8924
rs112211554	snp	C/G/T	0.0150606	0.0854603	intron-variant	HERC2	GRCh38.p7	15:28242127	GTAGTCAAATTCAGA[C/G/T]ACAGAAAGTAGAATG	8924
rs112218092	snp	A/C	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28231418	ATGATGGGACTTGCG[A/C]GGGACCACTTGTTTT	8924
rs112219184	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28255022	TGTACACAGCACAAC[C/T]GTGGCAGCTCTACAT	8924
rs112222559	snp	C/T	0.227959	0.249026	intron-variant	HERC2	GRCh38.p7	15:28206591	GTAATCCCTGCACTT[C/T]GGGAGGCCAAGGCGG	8924
rs112230913	snp	C/T	0.5	0	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28246035	ACTGAGCAGAAGCAC[C/T]ATAGAAACTACTAGT	8924
rs112233715	snp	A/G	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28187982	TACTTTTTATTGCCT[A/G]AACGACCTGCTCAAA	8924
rs112234619	snp	G/T	0.264632	0.249571	intron-variant	HERC2	GRCh38.p7	15:28156743	TTGAATACCCTTTAT[G/T]TCTTTCTCCTGCCTG	8924
rs112238395	snp	C/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28145609	ACAGCCACGCCCATT[C/T]TCTGGCATCCAGTCT	8924
rs112250452	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28232642	TTTATAATTTCTAAG[A/C]ATTTTTATTCAAATT	8924
rs112275498	in-del	-/CCC	0	0	intron-variant	HERC2	GRCh38.p7	15:28175466	ATGACCCCCACGTCC[-/CCC]AAGTCAGGATGGCAC	8924
rs112285115	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28231581	ACACTGTTGCTGGGA[G/T]AGCTAAGCACATCCA	8924
rs112306125	snp	C/T	0.0154538	0.0865337	intron-variant	HERC2	GRCh38.p7	15:28218892	TAGAGTGCAACGGCA[C/T]GATCATAGCTCACTG	8924
rs112312024	snp	A/C	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28125279	CCACCACACACAGCA[A/C]CAACGCTCCCTGCCC	8924
rs112325915	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28149441	TACCAAAAAAACACA[C/T]GCGGCTCCTAACCGA	8924
rs112329737	snp	C/T	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28149365	TACCAAAAAAACACA[C/T]GCGGCTCCTAACCGA	8924
rs112334454	snp	A/G	0.0225045	0.103662	intron-variant	HERC2	GRCh38.p7	15:28211282	CACACTGTCCGTGAC[A/G]AAGGGCTTGCCTTTC	8924
rs112349115	snp	A/C	0.0513262	0.151752	intron-variant	HERC2	GRCh38.p7	15:28149435	TAAAATTACCAAAAA[A/C]ACACATGCGGCTCCT	8924
rs112350311	snp	A/C	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28149587	TAAAATTACCAAAAA[A/C]ACACACGCGGCTCCT	8924
rs112365065	in-del	-/CTGT	0.443453	0.160017	intron-variant	HERC2	GRCh38.p7	15:28253179	CATTTTTACACAACA[-/CTGT]CTGACCGTTTTGGCT	8924
rs112366901	snp	A/T	0.0112675	0.0742078	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299536	CAATGATAAACGAGA[A/T]AAGCTTACAGAGTGC	8924
rs112367079	snp	A/G	0.0422008	0.138995	intron-variant	HERC2	GRCh38.p7	15:28309960	GGAACCAAAACATAC[A/G]ACTTTTGGTAAAAAT	8924
rs112371820	snp	C/T	0.0120326	0.0766259	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299561	GAGTGCTCACACTCA[C/T]ATTGCAATTTTTAAA	8924
rs112372165	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28256405	AATAAAAGTCAATTT[C/T]AAGTATTATTTAAAT	8924
rs112385654	snp	C/T	0.00239699	0.0345362	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233196	GCTATCCTCCTCCAA[C/T]GGGGCAAAGAACTTA	8924
rs112388783	in-del	-/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28192930	TCCCTTTTTTTTTTT[-/T]CCAACAGATTGCAAC	8924
rs112394338	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28154919	ATCCCTCCCCCCTCC[C/T]CCCACCCCAAAACAG	8924
rs112394537	snp	C/T	0.0185938	0.0946107	intron-variant	HERC2	GRCh38.p7	15:28226749	AGAGAAACAGATAAA[C/T]TGAACTTCATCAAAA	8924
rs112398965	snp	C/T	0.0505692	0.150756	intron-variant	HERC2	GRCh38.p7	15:28173363	AATTGCATTTGTTTA[C/T]CTTAAGATACTATTC	8924
rs112402788	snp	C/T	0.00716266	0.059414	intron-variant	HERC2	GRCh38.p7	15:28165865	ACACATATTCATTCT[C/T]TAGCCCTGTCACCCA	8924
rs112432022	snp	A/C	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28149359	TAAAATTACCAAAAA[A/C]ACACACGCGGCTCCT	8924
rs112432344	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28240266	TACTAAAAATACAAA[A/T]AATTAGCCGGGCGTG	8924
rs112442914	in-del	-/AT	0.0372196	0.131242	intron-variant	HERC2	GRCh38.p7	15:28114542	TCCTGAAAAACACAC[-/AT]GTCCACACAACCACG	8924
rs112479399	snp	C/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28181608	ACAGAGAGTGCCTCT[C/G]GGCAATAAAATTTAG	8924
rs112483884	snp	C/T	0.5	0	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174184	TTACCTGATCATAAA[C/T]ACAAGAATCAGCAAC	8924
rs112489315	snp	A/G			synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28234208	GCTGCAGTGGTCCTC[A/G]TCTTTCTCCTCGTTG	8924
rs112492297	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28135911	AAATTCCAAATTCAG[A/G]AAACATATTGTGAAA	8924
rs112493824	snp	A/T	0.5	0	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28215329	TGCATGTGTTTAATT[A/T]AAAAAGAATTATTTT	8924
rs112497281	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28149565	GCCACACCAACATAC[A/G]TTCTAGTAAAATTAC	8924
rs112503973	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28209130	TGGCATATCTATAAA[C/T]GGATATACATAGCAA	8924
rs112524735	snp	G/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28200218	CCTGACAAAAATGAA[G/T]AAACACTGTCTCTAC	8924
rs112527277	snp	A/G	0.0955749	0.196603	intron-variant	HERC2	GRCh38.p7	15:28302318	CCTCCAGTTCTATCC[A/G]TGTTGTTGCAAACGG	8924
rs112527396	in-del	-/T	0.333952	0.235483	intron-variant	HERC2	GRCh38.p7	15:28257746	ACAAAATACATATAC[-/T]TTTTTTTTTTTTTGA	8924
rs112532327	snp	C/T	0.0463947	0.145069	intron-variant	HERC2	GRCh38.p7	15:28303790	TTAGTTTTATTCCTA[C/T]GTATTTTACTTTATT	8924
rs112534866	snp	A/G	0.0341408	0.126114	intron-variant	HERC2	GRCh38.p7	15:28271881	GCTGGTACCAAACAG[A/G]GTGACAGCTCAGGTG	8924
rs112545943	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28128859	AGGTTCCTTGCTGGC[G/T]GAGCTATTCCCAGCT	8924
rs112547919	snp	A/G/T	0.000177432	0.00941736	intron-variant	HERC2	GRCh38.p7	15:28238817	TTGATCAATCAACAG[A/G/T]TAAAATGAAAAGAAC	8924
rs112555271	snp	C/T	0.0154538	0.0865337	intron-variant	HERC2	GRCh38.p7	15:28217377	ACACACCATCACACT[C/T]GCAACACAAACGCTC	8924
rs112561649	snp	G/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28207148	TCTGATTCTTTCTCT[G/T]TTCTTGAGATGGAGT	8924
rs112563047	snp	C/T	0.200182	0.244986	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174216	TACTTTCTTCTAAAA[C/T]TTTCATTCCAGCATG	8924
rs112575585	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28149417	CACCAACATACATTC[C/T]AGTAAAATTACCAAA	8924
rs112585884	snp	A/G	5.01375e-05	0.00500662	intron-variant	HERC2	GRCh38.p7	15:28124998	CCACCCAACCTGCCC[A/G]GACTCACCTGTGCAG	8924
rs112586966	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28127392	GGGAGTGGCCAAATC[A/G]CCAGAAAAGAAAGGA	8924
rs112608670	snp	C/T	4.98277e-05	0.00499113	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28255963	TCAATCATGAATCGA[C/T]GACCTGGACTTATGT	8924
rs112609812	snp	A/G	0.0410537	0.137264	intron-variant	HERC2	GRCh38.p7	15:28306234	TTTTATTGCGTTGAG[A/G]TGTGTTCCTTCTATA	8924
rs112616073	snp	A/C/G	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28279062	GCTGGCACAATCTCC[A/C/G]CTCACCGCAACCTCC	8924
rs112634055	in-del	-/AT	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28245638	CATATATGTACACAC[-/AT]ATATATATACACACT	8924
rs112638158	snp	G/T			missense, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28321364	TGTCAAACCCCACCT[G/T]TATATCTGTTTTCAA	8924
rs112646124	snp	G/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28198287	TCAACACTTGTTTTC[G/T]GTTTTGTGTGCTTGA	8924
rs112658698	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28176329	TAAGTAAAAAGAGGA[C/T]ACGTCACAATCACGC	8924
rs112676833	snp	C/T	0.0737376	0.17729	intron-variant	HERC2	GRCh38.p7	15:28134984	GACCTGTTTAATATA[C/T]TTTATATGGTGGTTT	8924
rs112682346	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314755	AATCCCAGCTACTCC[A/G]GAGTCTGAGGCAGGA	8924
rs112686221	snp	C/T	0.5	0	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317121	TTTGAGATGGAGTCT[C/T]GCTGTGTTGGCCAGG	8924
rs112710179	snp	A/G	0.00716266	0.059414	intron-variant	HERC2	GRCh38.p7	15:28268140	TATGAGAGACAGGGT[A/G]AACTGTTTGTGAATG	8924
rs112716923	snp	A/C	0.0193772	0.0965046	intron-variant	HERC2	GRCh38.p7	15:28289108	AACTGAAAACGCCAG[A/C]GATGATAGATTTAAA	8924
rs112717220	snp	A/C	0.0463947	0.145069	intron-variant	HERC2	GRCh38.p7	15:28225858	CTAGATAAAATGGAC[A/C]CATTCCTAAAAACAT	8924
rs112718643	snp	A/G	0.00517822	0.0506191	intron-variant	HERC2	GRCh38.p7	15:28132587	CAACGGTGGCAAACC[A/G]CCCCCATCTGACAGC	8924
rs112730805	snp	A/C	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28205126	AGCAACCACAGAAAA[A/C]AGACATTTCATGAAA	8924
rs112733594	snp	A/G	0.00762663	0.0612793	intron-variant	HERC2	GRCh38.p7	15:28230326	GTGCTACATGCTATG[A/G]TTCTATTCAGCCAAC	8924
rs112744794	snp	A/G	0.5	0	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318638	AAAAAAAAAAAAAGT[A/G]TTGTACAATTAAACT	8924
rs112772439	snp	A/C	0.0399052	0.1355	intron-variant	HERC2	GRCh38.p7	15:28252452	AAGAACTTAGAAAAG[A/C]ACCTCTGGAAAATGC	8924
rs112787947	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28229940	AATATAAATAATGCT[C/T]ATAGGTTTAAATTGG	8924
rs112794030	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28298998	GGGTGTATACAAGCA[G/T]CCATTTTTTTAAACC	8924
rs112796668	snp	C/G	0.084728	0.187577	intron-variant	HERC2	GRCh38.p7	15:28223005	GATTTTGCTCTGTGT[C/G]CCTTCACTGTAATAA	8924
rs112800122	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214339	AGGGAAAGGAGACGG[C/T]TACCCACCTCTAAGT	8924
rs112809169	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28245562	AAAAAAAAAAAAAAA[A/T]ATATACACACACACA	8924
rs112826053	in-del	-/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28290303	AGCAGCAAAACACAC[-/T]TTTTTTTTTTGAGAT	8924
rs112830316	snp	A/G	0.0119404	0.076339	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214823	AAAAGAAAATTTATA[A/G]CGACAAGCATTAAAA	8924
rs112843833	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28207286	ACTACAGGCACACGC[C/T]ACCACGCCCGGCTAA	8924
rs112849629	snp	C/T	0.0460142	0.144533	intron-variant	HERC2	GRCh38.p7	15:28279532	TGACACAGAGCCAGG[C/T]GCAGTGTCTCATGCC	8924
rs112893411	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28256875	GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCC	8924
rs112897904	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28177139	GTTCCTACAACAAGA[C/T]GAAATCAGCTCTCTA	8924
rs112897946	in-del	-/A	0.452719	0.146304	intron-variant	HERC2	GRCh38.p7	15:28251476	TTAGTCACATTAAGT[-/A]AAAAAAAAAAACAAA	8924
rs112899498	snp	G/T	0.0821764	0.185298	intron-variant	HERC2	GRCh38.p7	15:28172349	AAGAACAAAGCTAAA[G/T]AACTCTTGCAACCTG	8924
rs112900193	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28239077	ATGCAGTTAAATTAG[A/G]AATAGGTTTTCAAAA	8924
rs112903633	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28228140	GCTTTAAAAAAAAAA[A/G]AAAAGAAAAGAAAAG	8924
rs112904971	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28150227	CGAGAATGGCCACAT[A/G]AACGTACGTTCTAGT	8924
rs112906191	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28159025	GGATATGAAATTCTG[A/G]GTTGAAAATTCTTCT	8924
rs112907826	snp	C/T	0.0505692	0.150756	intron-variant	HERC2	GRCh38.p7	15:28140246	CGCTCCATCTGCACC[C/T]GCTCCAGTCTTGATC	8924
rs112911866	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28147843	GAGTTTGAGACAAGA[C/T]TGGGCAACACAGAGA	8924
rs112934782	snp	C/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28209552	GTTTCACCGTGTTAG[C/G]CAGGATGGTCTCGAT	8924
rs112940814	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28216034	TTTTTAGAGAAGGGC[C/T]CTCACTGTGTTTCCC	8924
rs112945646	snp	C/T	0.0463947	0.145069	intron-variant	HERC2	GRCh38.p7	15:28262563	CACAATGCACACTCA[C/T]GGTCTCAGTGTGCCT	8924
rs112949024	snp	C/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28272556	TTGACACCAAGACTT[C/T]AGCACAAGACATCGC	8924
rs112955425	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28246181	AAATGTTTGTCCTTT[A/G]GCATATTTCTAAAGA	8924
rs112973969	snp	A/C	0.00716266	0.059414	intron-variant	HERC2	GRCh38.p7	15:28187653	TATGGAGTTTTTTGA[A/C]AAACATATCCGCATT	8924
rs112980995	snp	A/G	0.000148737	0.00862243	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28246779	GTAAGCCACCTCCGC[A/G]AAGTGCCGCCAGCTG	8924
rs112985539	snp	G/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28295213	AAGGTAGACACCTTG[G/T]GTCACAGAATACAGA	8924
rs113010617	snp	A/T	0.0275645	0.114116	intron-variant	HERC2	GRCh38.p7	15:28296181	CAAAGGACAAAAAAA[A/T]TCATCAAATGTGGGC	8924
rs113016494	snp	A/T	0.084364	0.187256	intron-variant	HERC2	GRCh38.p7	15:28184091	AGCTACTTGGGAGGC[A/T]GAGGTGGGAGAATCA	8924
rs113016718	snp	C/T	0.0310256	0.120624	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28174567	GGGCTTCCTGTTAAC[C/T]GTGGTCGTGCCATTG	8924
rs113016891	snp	C/T	0.00716266	0.059414	intron-variant	HERC2	GRCh38.p7	15:28151899	CAACTAACTACAGGA[C/T]GAAGGGAAATGCCTC	8924
rs113023122	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28133962	AAGTTGATTTGACTA[C/T]TCTAGGCCATCTGCA	8924
rs113026948	snp	A/G	0.0418186	0.138422	intron-variant	HERC2	GRCh38.p7	15:28271869	GTTAAGGCGGGAGCT[A/G]GTACCAAACAGAGTG	8924
rs113047450	snp	C/T	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28124333	CAATTGTTTCAAATA[C/T]AGAGAAGCACTATGG	8924
rs113060100	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28232426	GTGCCTGTAGTGCCT[A/G]TAATCCCAGCTACTT	8924
rs113065902	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28235534	AAGATCCTCCTTCCC[C/T]GCAAGCCTTCTGCGA	8924
rs113099644	snp	A/G	0.046775	0.145601	intron-variant	HERC2	GRCh38.p7	15:28256740	GCTGGAACTACAGGC[A/G]CCCGCCACCACAACT	8924
rs113103290	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28262712	AGTCATTTTGTAATA[A/G]ACACCCACTTTCCAA	8924
rs113104459	snp	A/G	0.000798403	0.0199641	intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28315917	CGCCCTCTGATCGCC[A/G]ATCACCTCTGAGACC	8924
rs113105786	snp	C/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28117478	GGCCCGGCAGCACCA[C/G]CCTGGCACGGACCAT	8924
rs113143748	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28112200	GAGGAGCAATTAATT[C/T]CTAGAACTTGGAGTA	8924
rs113149522	snp	A/C	3.29788e-05	0.00406058	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28280093	CCACAGGAGGCAGAG[A/C]AATACCGCTGCTTTT	8924
rs113164386	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28304626	ACCTCAGCCTCCCAA[A/G]GTGCTGGGATTACAG	8924
rs113166392	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28294658	TATTCAAACAAGCCA[A/G]TCACATCTTCCCATG	8924
rs113179127	snp	C/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28293761	GCCAACTGGGAAGCA[C/G]TGCTATGCAGAGGCA	8924
rs113186899	snp	C/T	0.00716266	0.059414	intron-variant	HERC2	GRCh38.p7	15:28113867	CTGACACTGGGCTCA[C/T]CTCGTCCAGCCGACA	8924
rs113192919	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28129229	TGTATTATGGCAAGA[A/G]GACACAGAGTAAGAC	8924
rs113212089	snp	C/G/T	0.0466111	0.145376	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214640	AGGGCACAGGGAAGG[C/G/T]AGACGGCCACCCACC	8924
rs113243370	in-del	-/AC	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28217223	TCCCCTCACACTCAC[-/AC]TCATGCCTCCCTCAT	8924
rs113245635	snp	C/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28306881	ACTCTGTCACCCAGG[C/G]TGGAGTGCAGTAACA	8924
rs113250375	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28265207	GATCTCACTTAGGAA[C/T]ACAAACATAAAACCA	8924
rs113285955	snp	C/G	0.185155	0.241444	intron-variant	HERC2	GRCh38.p7	15:28217001	GACACAAGCAAAATG[C/G]TCACATTCACTCACA	8924
rs113289431	snp	C/T	3.75721e-05	0.00433412	intron-variant	HERC2	GRCh38.p7	15:28190895	GGCTCAATGCTAGTA[C/T]AGAAATGGCCAAGTC	8924
rs113294881	snp	C/T	0.0854556	0.188216	intron-variant	HERC2	GRCh38.p7	15:28143048	TTTATTATGTTGGTA[C/T]TAACTCTTCTAAAAA	8924
rs113312238	in-del	-/AT/CA	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28245673	ATACACACACACACA[-/AT/CA]TACATAAACACACAT	8924
rs113317087	snp	A/G	0.100944	0.200705	intron-variant	HERC2	GRCh38.p7	15:28173493	TATGATTCTATTTAT[A/G]GTAAGCTGTACAACA	8924
rs113328328	in-del	-/A	0.0542392	0.155492	intron-variant	HERC2	GRCh38.p7	15:28182524	AGGCTAACCAAACGG[-/A]AAAAAAAAAAGAAAA	8924
rs113336457	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28230578	AAATACTTAGATTTA[C/T]ATGAAGGACAAATAT	8924
rs113337976	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28233958	AAACCCTCCAAATAA[G/T]ACATGAAACAAAGTC	8924
rs113341207	snp	A/G	0.000139512	0.00835085	intron-variant	HERC2	GRCh38.p7	15:28113031	CACCCACCGTCGGCC[A/G]ACATCAGCCCAGGGC	8924
rs113343980	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28309808	TACAAGCTGCCAAAT[C/T]TGTGTTTGGTAACTT	8924
rs113344580	snp	A/T	0.5	0	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214883	ATTTTTTTATTTTTT[A/T]TTTTTTTGAGACAGA	8924
rs113370191	snp	C/T	0.0252325	0.109451	intron-variant	HERC2	GRCh38.p7	15:28223789	CTGATCAGGGCAGGC[C/T]GCAAATATAGACAGA	8924
rs113408811	snp	A/G	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28240246	ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA	8924
rs113427095	snp	A/G	0.00455775	0.0475195	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28174594	ATTGCCCTGCTGGCC[A/G]TGGTCGTTGTCACCC	8924
rs113452024	snp	C/T	0	0	intron-variant	HERC2	GRCh38.p7	15:28206608	GGAGGCCAAGGCGGG[C/T]GGATCACAAGGTCAG	8924
rs113454991	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28178844	AACAACGGAGCAGGA[A/G]CAAAGGCCGCCCCGC	8924
rs113455813	snp	A/G	0.5	0	synonymous-codon	HERC2	GRCh38.p7	15:28169633	ATTACTGGCAGCAGA[A/G]GAATCAGCATCTGAA	8924
rs113467788	snp	C/G	0.0402882	0.136092	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318416	TGGATCACTTGAGGT[C/G]AGGAGTTCAAAACCA	8924
rs113503298	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28237288	CCAAGTAACAGCAGA[C/T]ACCACATAAACCCAC	8924
rs113505002	snp	A/T	0.262159	0.249704	intron-variant	HERC2	GRCh38.p7	15:28200456	GGGCCATCACCAGAA[A/T]CCAGCCAAGCTGGTA	8924
rs113506340	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28198262	AAGCAAAGGAACACT[C/T]TATCTTTCTTCAACA	8924
rs113508270	snp	A/C	0.00260863	0.036021	intron-variant	HERC2	GRCh38.p7	15:28177559	GCAGGGAACAGAAAG[A/C]CCACAGCATAGCTAG	8924
rs113514666	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28144526	TGTTCTGTTCCACGC[C/T]TCAGCAGGGCCTGTG	8924
rs113522541	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28225867	ATGGACACATTCCTA[A/G]AAACATAAATTACCC	8924
rs113556450	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28267802	CATGACTTCACTCAT[C/T]TCAAGCTCTGCACTG	8924
rs113563945	snp	G/T	0.00716266	0.059414	intron-variant	HERC2	GRCh38.p7	15:28159930	AGATGTCCTTTCTGT[G/T]TGTTAGTTTTCCTTC	8924
rs113579135	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28207283	GGGACTACAGGCACA[C/T]GCCACCACGCCCGGC	8924
rs113612253	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28289643	ATTCGCTAAGAGAAG[C/T]GTCCTTATCTATGAA	8924
rs113615621	snp	C/T	0.00755907	0.0610114	intron-variant	HERC2	GRCh38.p7	15:28206559	AGACTCTAGGTTGGG[C/T]GCGGTGGCTCACGCG	8924
rs113616035	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28149593	TACCAAAAAAACACA[C/T]GCGGCTCCTAACCGA	8924
rs113623981	snp	C/T	0.0998734	0.199905	intron-variant	HERC2	GRCh38.p7	15:28150136	AACCGAGAACATCAC[C/T]GAGAATAGCCGCACA	8924
rs113630512	snp	C/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28272580	ACATCGCCTTCTGCT[C/G]ATAAGAAAGACCAGT	8924
rs113634395	snp	A/G			missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202451	TGCACCACGATCGGC[A/G]GAGCGGGAACGGGCG	8924
rs113638813	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28293667	GTCCCAATGCTTGTG[C/T]ATCCATGGGAAAAGG	8924
rs113650950	snp	A/G	3.42226e-05	0.00413644	intron-variant	HERC2	GRCh38.p7	15:28142189	TGTTACACTATAGCT[A/G]AATAATGTTTTTGCA	8924
rs113652197	snp	C/T	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28294718	CTACAAAATGTGCCT[C/T]CCACAGCCCCTCGTG	8924
rs113668723	snp	C/T	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28256916	ATGTTTTTTAAGACT[C/T]GCGTCCATTATTAGT	8924
rs113703140	snp	A/C	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28188023	TACCATTTCAGAGGA[A/C]ATACAGCTTGACCAC	8924
rs113713295	snp	A/C			intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28300634	CATGACCAGCCTGGC[A/C]AACATGGTGAAACCC	8924
rs113713636	in-del	-/A	0.277867	0.248442	intron-variant	HERC2	GRCh38.p7	15:28151769	CATTAAAAAAAAAAA[-/A]CAGGTCACCTTCAAG	8924
rs113718111	snp	C/T	0	0	intron-variant	HERC2	GRCh38.p7	15:28293669	CCCAATGCTTGTGTA[C/T]CCATGGGAAAAGGGA	8924
rs113718147	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28272584	CGCCTTCTGCTCATA[A/G]GAAAGACCAGTTAAG	8924
rs113719609	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28227621	ACATAGTTGTACCAT[A/T]TGACCCTGTAATTCC	8924
rs113720762	snp	A/T	0.5	0	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317113	TTTTTTTTTTTGAGA[A/T]GGAGTCTTGCTGTGT	8924
rs113745151	snp	C/T	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28286444	TTCATTCCAGGAATG[C/T]AAAGTGGGTTCAACA	8924
rs113748196	snp	A/G	0.0150606	0.0854603	intron-variant	HERC2	GRCh38.p7	15:28244202	CTTTAACCTAAACCT[A/G]GAAACAACTTACATT	8924
rs113749651	snp	A/G	0.0154538	0.0865337	intron-variant	HERC2	GRCh38.p7	15:28261787	AAACACCATATGGGC[A/G]CACAAAACTCTCAGT	8924
rs113752481	snp	A/G	0.00755907	0.0610114	intron-variant	HERC2	GRCh38.p7	15:28241689	GCTGGGCATGGTGGC[A/G]CACGCCTGTAGTCCC	8924
rs113757064	snp	C/G	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28205119	TACGAAAAGCAACCA[C/G]AGAAAAAAGACATTT	8924
rs113778860	in-del	-/ATAG	0	0	intron-variant	HERC2	GRCh38.p7	15:28270243	CTCTTTTTATTTATT[-/ATAG]TATAGATAGATAGAT	8924
rs113780734	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28228805	ATGTTGCTCTCTGAA[C/T]ACTCTGGTGCCCTAT	8924
rs113781720	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28248831	AAATTAATATCACAA[A/C]CACAGATCATACATG	8924
rs113792637	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28155693	GTAGATTGCAAAAAT[C/T]TTCTCCCATTCTGTA	8924
rs113826561	snp	A/G	0	0	intron-variant	HERC2	GRCh38.p7	15:28307418	AAAATTATGGGTTTG[A/G]TTAGCTCCTTCTTTT	8924
rs113827416	snp	C/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28290178	CAGTAAGCCAACCTT[C/G]TGTGTTAGTTCAACT	8924
rs113833163	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28244951	CTAGAACCATAGAAA[A/G]CATGGTGACTTAGAT	8924
rs113833510	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28225513	CCATCCTGGTCAACA[C/T]GGTGAAACCCCGTCT	8924
rs113839970	snp	C/T	0	0	intron-variant	HERC2	GRCh38.p7	15:28180692	GGTCCTCTGTATCCA[C/T]AGGTTCCACGTCCAT	8924
rs113843059	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28146580	CAATTTGTTTTGTGC[A/G]GTCACTCCCGGGCAG	8924
rs113845630	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28264039	AAAAAAAAAAAAAAA[A/C]AAACAAAAACAAAAA	8924
rs113864171	snp	A/G			intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313633	CATATACCTTTACTC[A/G]TCTGCAAATATTTGA	8924
rs113888441	snp	A/C	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28255705	TCACAATTAAATCAT[A/C]TCTCAATAATTTTGT	8924
rs113889502	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28240036	TTAATCTTATAGACA[A/G]GATAATGATATTGTA	8924
rs113893512	snp	A/C	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28218957	CCTCGACCTCCCAAA[A/C]TGTCATCTTTTCTGC	8924
rs113914279	in-del	-/G	0	0	intron-variant	HERC2	GRCh38.p7	15:28269133	ATACAATAAACAGAA[-/G]CTTTGTCAATCTTCA	8924
rs113914919	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28261563	TCCTAGGAACTTACC[A/G]TAAGTTAACATCAGC	8924
rs113920882	snp	A/C	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28148671	CGCACATTCTAGTAA[A/C]ACTACCGAAGAAACA	8924
rs113921795	snp	A/G	0.203575	0.245652	intron-variant	HERC2	GRCh38.p7	15:28206610	AGGCCAAGGCGGGTG[A/G]ATCACAAGGTCAGGA	8924
rs113933794	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28147864	AACACAGAGAGACTC[A/G]TCTCCACAAAAAATA	8924
rs113942559	snp	A/G	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28268920	ATGAAAACATGCCAC[A/G]TCCCAATTTGCCACT	8924
rs113948356	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28191440	TTAGAGAAAAGTCTC[A/G]CTCTAAGACTCAGAA	8924
rs113957516	snp	A/G	0.5	0	intron-variant	HERC2	GRCh38.p7	15:28282867	AACTAGGGAGGCGGC[A/G]GTTGCAGTGAGCCGA	8924
rs113967675	snp	A/G	0.040671	0.13668	intron-variant	HERC2	GRCh38.p7	15:28304426	AGGCTGGAATATAGC[A/G]GCACAATCTCAGCTC	8924
rs113970029	snp	C/T	0.0236746	0.106192	intron-variant	HERC2	GRCh38.p7	15:28257316	GCAGCTGCTGGTCTG[C/T]TCCACAGGAGTCACC	8924
rs113981350	snp	A/G	0.0524604	0.153226	intron-variant	HERC2	GRCh38.p7	15:28193798	TATTTTTAAAGTGGT[A/G]AAAGAAAACACCTAG	8924
rs114034003	snp	A/G	0.0232847	0.105357	intron-variant	HERC2	GRCh38.p7	15:28271012	ACAGTTATACTATAC[A/G]TCTATATATTTATGC	8924
rs114053641	snp	A/G	0.0174175	0.0916809	intron-variant	HERC2	GRCh38.p7	15:28271929	CCCAGTACATAGGAA[A/G]GACCAACAAAGCAGG	8924
rs114073425	snp	A/C	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28281616	CTCCCTGGAAAGGCA[A/C]AGGGTGGCGCACACT	8924
rs114097653	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111326	TCAGAGTAAAATTAA[C/T]TGAAATATTTATAAT	8924
rs114135590	snp	C/G	0.0267878	0.112589	intron-variant	HERC2	GRCh38.p7	15:28178053	GTGAGTTCCTGCCAA[C/G]TCCTGGGCTTTGAGA	8924
rs114203647	snp	A/G	0.0325976	0.123435	intron-variant	HERC2	GRCh38.p7	15:28227975	GGAGTGAGGACTGAT[A/G]GCTAAATGGTGTGCA	8924
rs114213935	snp	C/T	0.0150606	0.0854603	intron-variant	HERC2	GRCh38.p7	15:28240667	GAAAGAAGAAGGCAA[C/T]AATAAAGAGTATGGC	8924
rs114260536	snp	C/T	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28166012	TTATTGAGCCTGGAA[C/T]TTTGTGTTGTGCCAA	8924
rs114378649	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28289776	TGTATAAACTATCTG[A/G]CTACAAAAGGGAAAC	8924
rs114391497	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28113456	AGGGACGCGCTCAGA[A/G]TGCACTCCCTTCAGT	8924
rs114414918	snp	C/T	0.00517822	0.0506191	intron-variant	HERC2	GRCh38.p7	15:28283414	AAAATATTTTTTAAA[C/T]AATGAAAAGAACCAT	8924
rs114433057	snp	A/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28136688	TAAATGAAGCTTTAC[A/G]GGAACACGGCCACAC	8924
rs114446281	snp	G/T	0.00442816	0.0468452	intron-variant	HERC2	GRCh38.p7	15:28117259	AGGAGGCACCGTGCA[G/T]GGGCCCCTCCCTGGT	8924
rs114448863	snp	C/T	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28114993	ACCCAAGGAGCTGAA[C/T]GAAGAATTCACAATT	8924
rs114449560	snp	C/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28153872	GAAGGCAACGGAGCC[C/T]GGTGGGAGGGGCGGG	8924
rs114469338	snp	C/G	0.0818113	0.184966	intron-variant	HERC2	GRCh38.p7	15:28173751	GAAGCTGCAGTGAGC[C/G]AAAATCGTGCCACTG	8924
rs114471411	snp	C/T	0.0267878	0.112589	intron-variant	HERC2	GRCh38.p7	15:28118869	GCATGCTACCCTGAA[C/T]GGGAAGGAGCCACCT	8924
rs114532098	snp	A/G	0.00141949	0.0266032	synonymous-codon	HERC2	GRCh38.p7	15:28144138	AGGGACGATGCTTCT[A/G]TTAGAGGCAAGGTTG	8924
rs114537025	snp	C/T	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28150729	CGGCTTCTAACTAAC[C/T]GAGAACATCACCGAG	8924
rs114574996	snp	C/T	0.046775	0.145601	intron-variant	HERC2	GRCh38.p7	15:28268240	CTGGCCAAGGCTGCA[C/T]GGGGTCAAGAAGAAC	8924
rs114694773	snp	A/G	0.0425829	0.139564	intron-variant	HERC2	GRCh38.p7	15:28168300	GCCAAAAATCTAAGC[A/G]GGAGGCACAGAAACA	8924
rs114724919	snp	A/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28295510	GTTCAAGTGATTCTC[A/G]TGCCTCAGCCCCCAA	8924
rs114732733	snp	A/G	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28171429	AAGGAGAAGATGAGA[A/G]TCAAGCATTATCTTC	8924
rs114735992	snp	A/G	0.00138422	0.0262715	intron-variant	HERC2	GRCh38.p7	15:28265766	CGGTTACTAAGTCCT[A/G]TAAGAGGCCACCTCC	8924
rs114757660	snp	C/T	0.0232847	0.105357	intron-variant	HERC2	GRCh38.p7	15:28266688	CCATACACTGTATGG[C/T]TTTGTTATATTAAAT	8924
rs114770696	snp	A/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28177814	AAATCAAAATTTAGA[A/T]GAAAAAAGTAAAAAT	8924
rs114771721	snp	A/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28225352	AAAAATAACAAAACC[A/G]AAAGTTTGGTTTCTG	8924
rs114774002	snp	A/C	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28185954	AATGAATAAATACAA[A/C]AACAGTCATCATCAC	8924
rs114790826	snp	A/G	0.00993419	0.0697739	intron-variant	HERC2	GRCh38.p7	15:28248489	TAGGATGGACACGTC[A/G]AAAAGCCTAAAGTAA	8924
rs114875495	snp	A/C	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28178131	TCCTTACCAACAGAA[A/C]CCCCATGTTAAAGTG	8924
rs114893914	snp	C/T	0.0463947	0.145069	intron-variant	HERC2	GRCh38.p7	15:28291550	CTTTTATAATCTATA[C/T]ATTTTTATAAGAAAT	8924
rs114933713	snp	A/C	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28290025	GTTCAAAGAGGACGG[A/C]CCTGCAGGAGTTGCA	8924
rs114933928	snp	A/G/T	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28184360	TGTGGGAACATCCCA[A/G/T]TTGGGTGGCAGCCCT	8924
rs114972391	snp	A/C	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28283857	AATCTGATAAGTGTT[A/C]ATATATACACAGGTT	8924
rs114983518	snp	A/T	0.0471551	0.14613	intron-variant	HERC2	GRCh38.p7	15:28239210	GAAAATGTGTTCAAT[A/T]AATAATCAAAATACT	8924
rs114998715	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28115053	AAAGTTACAGCAACT[A/G]GCTAGCAAGGGTTCC	8924
rs115025302	snp	C/T	0.395289	0.203448	intron-variant	HERC2	GRCh38.p7	15:28205253	CTCTACACGGCCTTC[C/T]AGTTGTTCACACTCG	8924
rs115030034	snp	A/G	0.00223222	0.0333336	intron-variant	HERC2	GRCh38.p7	15:28293070	GCTTTTCAGAATGCC[A/G]TACCATTAGTCTCTG	8924
rs115138127	snp	A/G	0.0138799	0.0821421	intron-variant	HERC2	GRCh38.p7	15:28120053	GGTGCACTCAATCGC[A/G]GGGGTTAGACAACGC	8924
rs115152254	snp	A/G	0.0482946	0.147699	intron-variant	HERC2	GRCh38.p7	15:28252140	AATAAAAATTAAACA[A/G]ATAAAATATTCAGTG	8924
rs115208173	snp	C/T	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28149991	GAACATCACCGAGAA[C/T]GGCCACACGAACACA	8924
rs115246798	snp	C/T	0.0543475	0.155628	intron-variant	HERC2	GRCh38.p7	15:28289727	AAATCCATGGACTTA[C/T]GGGACATGGCTCCCT	8924
rs115258068	snp	C/T	0.0168055	0.0901129	intron-variant	HERC2	GRCh38.p7	15:28137422	TGTGGCAACCCTACA[C/T]TGATCAAGTCTATCG	8924
rs115281054	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28112697	TTGGAACCCAAAGCA[A/C]AACCCTTGTTCTCAA	8924
rs115292133	snp	A/G	0.00395047	0.0442677	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265859	GGCCCCAGGTGTACA[A/G]CTCCCCCTCGGCAGT	8924
rs115300781	snp	C/T	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28153954	GACAGGAGGGACCGC[C/T]GACCCCAACACAGCT	8924
rs115304007	snp	C/T	0.040671	0.13668	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28301040	TTTCCCAATAAAAGA[C/T]GCTAGGGCTCTAGGG	8924
rs115316008	snp	A/T	0.0341408	0.126114	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214875	AGATTGTTATTTTTT[A/T]ATTTTTTATTTTTTT	8924
rs115523399	snp	G/T	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28131961	TGGAACGAAGGTAAA[G/T]AGGAGGTTAAAGTGC	8924
rs115579022	snp	A/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28134127	CCTTCACGACTTTAG[A/G]TTTTTTAAAAATTAT	8924
rs115681399	snp	C/T	0.0150606	0.0854603	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313694	TAAACATCTATTGAA[C/T]GTAGGACAACATATA	8924
rs115710012	snp	C/G	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28205128	CAACCACAGAAAAAA[C/G]ACATTTCATGAAAAA	8924
rs115734997	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28286451	CAGGAATGTAAAGTG[G/T]GTTCAACAGTCAAAA	8924
rs115740455	snp	C/T	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28263418	ACAAAGTCCTGACTC[C/T]TACTAGCCTGGGCTC	8924
rs115742016	snp	A/G	0.0337553	0.125452	intron-variant	HERC2	GRCh38.p7	15:28163656	ATACGCTAGGGAATC[A/G]TTTACAAACTAAATT	8924
rs115851654	snp	A/T	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28247035	GAAGCCTGTTAACCC[A/T]TGTCCTTGCGCTCTT	8924
rs115853542	snp	C/T	0.00874735	0.0655527	intron-variant	HERC2	GRCh38.p7	15:28180242	CCATATTCAGTACAG[C/T]TCCATGTTGTAGCCT	8924
rs115860188	snp	C/T	0.00208488	0.0322195	intron-variant	HERC2	GRCh38.p7	15:28117325	GCCGTCTGGGGCGCT[C/T]GACTGTGGACACCCG	8924
rs115879094	snp	A/G	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28281967	CCCTTGAGCACCCAC[A/G]TGCCCTTCTCCCTGA	8924
rs115886865	snp	C/T	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28188013	CCTCAAGATCTACCA[C/T]TTCAGAGGAAATACA	8924
rs115906603	snp	A/C	0.0422008	0.138995	intron-variant	HERC2	GRCh38.p7	15:28272619	TCAAAGAGCACATTT[A/C]CATGAAAGTTCTAGG	8924
rs115909976	snp	A/G	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28244335	AACCAAAAGGTACGT[A/G]CCGTCTAGTTCCACT	8924
rs115916528	snp	C/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28189139	GTACAGCAAAGGCCA[C/T]GCTTAAGATGCAGTG	8924
rs115987105	snp	A/C	0.0228947	0.104514	intron-variant	HERC2	GRCh38.p7	15:28204171	ATCCAGAATGAAATA[A/C]GAATTCTCACATATG	8924
rs116026942	snp	A/G	0.0130921	0.0798413	intron-variant	HERC2	GRCh38.p7	15:28175441	ATTTCAACAGGACGA[A/G]GGCCGTGTCATGACC	8924
rs116048528	snp	C/T	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28291160	CAAGATAATAGCATA[C/T]GCACTTTGTCTGGCC	8924
rs116059806	snp	A/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28145524	AAACCCACGCCCACT[A/G]GGACCATACCATTTC	8924
rs116096912	snp	A/G	0.00211682	0.0324643	synonymous-codon	HERC2	GRCh38.p7	15:28113594	CTCCAGTTCGTAGCC[A/G]GTGAACAGAGAGAGG	8924
rs116142884	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28315048	AGAAAAAATGTGCTG[A/G]CTCCTATGTTACTGC	8924
rs116159174	snp	A/G	0.279018	0.24831	intron-variant	HERC2	GRCh38.p7	15:28205246	AGGACAACTCTACAC[A/G]GCCTTCCAGTTGTTC	8924
rs116161639	snp	C/T	0.0479149	0.147179	intron-variant	HERC2	GRCh38.p7	15:28292730	TAAAAATGGTTAAAA[C/T]GGTAAGTTTTATGGT	8924
rs116163635	snp	A/T	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28142125	GTGTTATTTTCTTTG[A/T]TATTCCTTGGCAAGC	8924
rs116176048	snp	A/G	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28185793	ATGCAGACTCTCAAG[A/G]CTGTATGCACTTCTT	8924
rs116228740	snp	A/G	0.00835141	0.0640778	intron-variant	HERC2	GRCh38.p7	15:28167523	GCAGTGACAGGGACC[A/G]TGTCCTGCGGCATTC	8924
rs116242992	snp	A/G	0.0980852	0.198549	intron-variant	HERC2	GRCh38.p7	15:28289443	AACCTGCAGAGCTGA[A/G]AGAAAATAATCCATA	8924
rs116263822	snp	A/G	0.0142736	0.0832652	intron-variant	HERC2	GRCh38.p7	15:28131835	ACCAGGAGGCTCCAC[A/G]GTGCCCGGATGATCC	8924
rs116330182	snp	A/G	0.0414363	0.137845	intron-variant	HERC2	GRCh38.p7	15:28220111	ATTCCACCAGGCCTC[A/G]GCTCACTCGCTCAGA	8924
rs116330555	snp	A/T	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28291165	TAATAGCATACGCAC[A/T]TTGTCTGGCCTACTG	8924
rs116331597	snp	A/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28240759	CGTATTTGGTCATAC[A/G]ATTTTTGACATGGGA	8924
rs116370737	snp	A/G	0.0168055	0.0901129	intron-variant, utr-variant-5-prime, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28312760	ACCTAAACGTGCCCA[A/G]TAGATTTTCAACTTT	8924
rs116388574	snp	C/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28285936	TTGGGCAAAATGGAC[C/T]TATTCCTCAAATAAT	8924
rs116390824	snp	C/T	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28135310	ATACGGGTAAGCCTT[C/T]GTATTGGAACATAAA	8924
rs116392926	snp	A/T	0.155325	0.23138	intron-variant	HERC2	GRCh38.p7	15:28277464	AATCCACAATTATCT[A/T]AAAAAAAAAAAAAAG	8924
rs116461479	snp	C/T	0.00874735	0.0655527	intron-variant	HERC2	GRCh38.p7	15:28228600	TCTGACTAATAAGCA[C/T]TGACACCCACCTACA	8924
rs116485971	snp	C/T	0.0150606	0.0854603	intron-variant	HERC2	GRCh38.p7	15:28276385	AAGGGCACTGGGTAC[C/T]TGGAAGATGGAAATC	8924
rs116557875	snp	A/T	0.0107246	0.0724382	intron-variant	HERC2	GRCh38.p7	15:28291153	CTACATGCAAGATAA[A/T]AGCATACGCACTTTG	8924
rs116613720	snp	C/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28281091	CATGAAGCACATTTA[C/T]GGACATATTTTAGAG	8924
rs116632344	snp	A/T	0.0111196	0.0737302	intron-variant	HERC2	GRCh38.p7	15:28162013	GTGGCTAAAAAATGT[A/T]AACAATACATGAAAT	8924
rs116633332	snp	C/T	0.00676609	0.0577691	downstream-variant-500B	HERC2	GRCh38.p7	15:28110741	ACAAGCAGCCCAAAC[C/T]GTGTACCATGGCTGC	8924
rs116634664	snp	A/G	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28116110	GTGCACAGAGCTTCC[A/G]ACGGTCCACCACCGT	8924
rs116640531	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28294013	TGTATCTCAATCGGT[A/G]AAAGACACGATATCC	8924
rs116644369	snp	G/T	0.395289	0.203448	intron-variant	HERC2	GRCh38.p7	15:28205256	TACACGGCCTTCCAG[G/T]TGTTCACACTCGGCA	8924
rs116734224	snp	A/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28150264	ACCGAAGAAACACAC[A/G]CGGCTTCTAACCGAG	8924
rs116772198	snp	C/T	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28154691	CAGTTTCCTCATCCA[C/T]ATATAAAGGTAACCC	8924
rs116801679	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28114922	TCAAGTGCATCTCGA[A/G]GCTGCAAGTGCATGG	8924
rs116842964	snp	C/T	0.0618563	0.164627	intron-variant	HERC2	GRCh38.p7	15:28150759	GAATGGCCACACGAA[C/T]GTATATTCTAGTAAA	8924
rs116879078	snp	C/T	0.0146672	0.084371	intron-variant	HERC2	GRCh38.p7	15:28118342	TAGAGGCTGTCTGCA[C/T]TCAGAGGCTGCAGAA	8924
rs116886437	snp	A/C	0.00835141	0.0640778	intron-variant	HERC2	GRCh38.p7	15:28134589	TAACTACAACCTAAG[A/C]TCTAGGTTAACAGAG	8924
rs116891237	snp	C/T	0.0569829	0.158885	intron-variant	HERC2	GRCh38.p7	15:28150472	ACATTCTAGTGAAAT[C/T]ACCAAAAAAACACAC	8924
rs117007668	snp	A/G	0.0225045	0.103662	intron-variant	HERC2	GRCh38.p7	15:28126276	GCTATCTGTGAAAAC[A/G]CGTTGTGATGGAAAG	8924
rs117084492	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28184029	CTCATTTCTACAAAA[A/G]AAATACAAAAAATTA	8924
rs117133134	snp	A/G	0.0236746	0.106192	intron-variant	HERC2	GRCh38.p7	15:28289570	GAAATAAAGCCAGTC[A/G]CTGGAGCTGATCTCC	8924
rs117197523	snp	A/G	0.107341	0.205301	intron-variant	HERC2	GRCh38.p7	15:28216117	AATAGCTGGGACTAC[A/G]GGCATTTTTAAAACC	8924
rs117201485	snp	A/G	0.0256215	0.110247	intron-variant	HERC2	GRCh38.p7	15:28268158	CTGTTTGTGAATGAA[A/G]GAACAGTGGTGTGGG	8924
rs117219845	snp	C/T	0.216649	0.247765	intron-variant	HERC2	GRCh38.p7	15:28137613	CACACCCATAGAAGA[C/T]GGTGAACTTAAACGA	8924
rs117307132	snp	G/T	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28119683	GGTCTCAGACTCCTA[G/T]GCTCAAGCAATCCAT	8924
rs117325217	snp	C/T	0.0399052	0.1355	intron-variant	HERC2	GRCh38.p7	15:28289631	TAAATGACTGGTATT[C/T]GCTAAGAGAAGTGTC	8924
rs117411594	snp	C/T	0.00936635	0.0677906	intron-variant	HERC2	GRCh38.p7	15:28274900	CGCCACACCAGGGAC[C/T]GTACCTGATCGCCAG	8924
rs117427560	snp	A/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28146031	CGACAGGGATGTGGT[A/T]CATACATCACAGATA	8924
rs117437554	snp	A/C/G	0.00676661	0.057772	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28174513	CGACCCACAAGCCAC[A/C/G]CGTGTGATCTTCTGG	8924
rs117483108	snp	C/T	0.0644444	0.167538	intron-variant	HERC2	GRCh38.p7	15:28205199	AACAGCGGAAGGTCT[C/T]TTTTTGTACAACAGT	8924
rs117504827	snp	A/G	0.0228947	0.104514	intron-variant	HERC2	GRCh38.p7	15:28256919	TTTTTTAAGACTCGC[A/G]TCCATTATTAGTGCA	8924
rs117505242	snp	C/T	0.0588605	0.161139	intron-variant	HERC2	GRCh38.p7	15:28149281	TTCTAGTAAAATTAC[C/T]GAAAAAACACACGCA	8924
rs117587984	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28240819	CCTTTTCAATGCATG[A/G]TACTGGGAAATCCAG	8924
rs117624692	snp	A/G	0.105214	0.203807	intron-variant	HERC2	GRCh38.p7	15:28225014	GGGCAATTATACTAT[A/G]AAAGTCTGCATTTAC	8924
rs117663995	snp	C/T	0.0260105	0.111035	intron-variant	HERC2	GRCh38.p7	15:28256962	TTTAAAATATTTCAC[C/T]GAACAGGCTAAAACC	8924
rs117694443	snp	C/G	0.0165278	0.0893908	intron-variant	HERC2	GRCh38.p7	15:28265526	CAGGGTGGGTGGCCT[C/G]GTGAGGCCCACTGTA	8924
rs117702353	snp	C/T	3.30098e-05	0.00406249	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28269362	GGCCAGGCCTTCGCA[C/T]TGGATTGGACCAATC	8924
rs117743506	snp	A/G	0.0256215	0.110247	intron-variant	HERC2	GRCh38.p7	15:28265314	CAAGAGTGGCCGAAC[A/G]TTAAGAAATGTAATA	8924
rs117744568	snp	A/C	0.0252325	0.109451	intron-variant	HERC2	GRCh38.p7	15:28253546	ATTGAAAAGGGTCTG[A/C]TCTTTATTCTAACAT	8924
rs117759466	snp	C/T	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28183140	TCGTCTCCTGTCCTT[C/T]CCAGAGGGCTTGCTC	8924
rs117760720	snp	C/T	0.00874735	0.0655527	intron-variant	HERC2	GRCh38.p7	15:28166077	TGCCAGAAGAACACA[C/T]AAAATTCTACCAACT	8924
rs117772627	snp	C/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28133847	CCATTGATGTATCTG[C/T]CTCTCTCTTTTTGCC	8924
rs117802902	snp	A/G	0.00123598	0.0248287	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28248654	AAGCAGATCTTTCAC[A/G]ACTGTGTTGCTCAAA	8924
rs117902599	snp	A/C	0.0618563	0.164627	intron-variant	HERC2	GRCh38.p7	15:28254288	ACTCTGTCACACACA[A/C]AAAAAAAAGTAAATA	8924
rs117928600	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28116222	AAGTCTTTTCTTTTT[C/T]TTTTTTTTTTTTTTT	8924
rs118021417	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28118737	CAGCCTTCCTGGCTC[C/T]GTGCTGGTGTCCTGT	8924
rs118112076	snp	C/G	0.0192598	0.0962234	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229540	AAGTAAGAAATTCTT[C/G]CTCGCCAGTTTTAAA	8924
rs118141530	snp	A/G	0.0283406	0.115616	intron-variant	HERC2	GRCh38.p7	15:28289636	GACTGGTATTCGCTA[A/G]GAGAAGTGTCCTTAT	8924
rs137872802	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28142691	ATCATTTCTTGAGAT[A/T]TTTTCATATTTGACT	8924
rs137879939	snp	A/C/G/T	0.000347973	0.0131868	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28179217	CAGAGAACGAAGGAA[A/C/G/T]CTTTATCTACAACAG	8924
rs137892609	snp	G/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28139535	GAGCTGGAGGACGGA[G/T]CTATGCTGCATCCAG	8924
rs137897453	snp	C/T	0.0193772	0.0965046	intron-variant	HERC2	GRCh38.p7	15:28160081	ATGTTGCTGTCTGAT[C/T]GTTCCTCTGGAAGTT	8924
rs137905339	snp	C/T	0.0221141	0.102801	intron-variant	HERC2	GRCh38.p7	15:28220033	AAGGCAGGTGGCAGG[C/T]GGGGTGTGCTTGGGC	8924
rs137912927	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28171192	CTGTATATGAATGAC[A/G]TGGCAGTTTTATTTG	8924
rs137918449	snp	C/T	0.00583412	0.0536938	synonymous-codon	HERC2	GRCh38.p7	15:28113185	GAAGGACTCCATCAC[C/T]TCCCAGAACCACTGG	8924
rs137943010	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28254259	TAGCACTCCGGCCTG[G/T]GCAACAAGAGCGAAC	8924
rs137946111	snp	C/G	6.84404e-05	0.0058494	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28198765	CATCTAACCATCATT[C/G]CCACCTAGAATTAAA	8924
rs137965017	snp	A/G	1.65231e-05	0.00287424	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28299448	TGATTCTGTTCCAGT[A/G]TATACAATTTCTCCA	8924
rs137996896	snp	C/T	0.0422008	0.138995	intron-variant	HERC2	GRCh38.p7	15:28282762	CATGGTGAAACCTCA[C/T]CTCTATTAAAAATAC	8924
rs138009549	snp	C/T	0.0111196	0.0737302	intron-variant, utr-variant-5-prime	HERC2, LOC107987422	GRCh38.p7	15:28317649	GTCAGGAGTTAGAGA[C/T]GGTGGCAGAAGAGAG	8924
rs138016143	snp	A/G	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28179804	ACACGTTAAAAAGTA[A/G]AAGAATAAATGTTAA	8924
rs138027454	snp	A/G	0.0111196	0.0737302	intron-variant	HERC2	GRCh38.p7	15:28156195	TTGAGGTCAGGTAGC[A/G]TGATGCCTCCAGCTT	8924
rs138047448	snp	G/T	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28193019	AGATAGTCACTAACC[G/T]TTACCAAGTAGCTCA	8924
rs138051310	snp	A/G	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28251443	GTGAGGCTCCATCTC[A/G]GGGGAAAAAAATTGT	8924
rs138059246	snp	A/G	0.00171224	0.0292094	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214246	GCGAGGCCTGCGGGC[A/G]CACCCTGCGCCGCCT	8924
rs138063419	snp	A/T	0.000691654	0.0185836	missense	HERC2	GRCh38.p7	15:28130268	GAACATGGTCATCTG[A/T]TCCATGGCCCAACCT	8924
rs138130604	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28136695	AGCTTTACGGGAACA[C/T]GGCCACACCCACTCA	8924
rs138137820	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28183976	GCAGATTCCTTGAGC[C/T]CAGGAGTTGGAGACC	8924
rs138177581	snp	C/T	0.000461582	0.0151848	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28228308	GCTGCAGGGTGAGCA[C/T]GCTGAGCATCACCAG	8924
rs138196137	snp	A/G	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28126826	AGAGCTTATTCATGT[A/G]ACCAAACACCACCTG	8924
rs138210389	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28272110	TTACCACCAAACACA[C/T]ACACGCCAGAGAAAA	8924
rs138262025	in-del	-/G			intron-variant	HERC2	GRCh38.p7	15:28271898	GACAGCTCAGGTGAC[-/G]GTGCCCTGCACAGAG	8924
rs138268928	snp	C/T	0.0197687	0.0974348	intron-variant	HERC2	GRCh38.p7	15:28152212	TCAGCAGATCCAGGC[C/T]GCAGTGAAGCCCGCC	8924
rs138275638	snp	A/G	0.000230875	0.0107417	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265842	CCGGCCGTAGTTCCC[A/G]CGGCCCCAGGTGTAC	8924
rs138275754	snp	A/G	0.000158046	0.00888808	synonymous-codon	HERC2	GRCh38.p7	15:28132148	CCGGCCGAGCTTGCC[A/G]TAGTCCCCGTCCCCC	8924
rs138283346	snp	A/G	0.0119091	0.0762411	intron-variant	HERC2	GRCh38.p7	15:28143070	TTCTAAAAAAACTAA[A/G]AAAAAAAAGCTTATC	8924
rs138289458	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28209168	TTCTGTTTACTTATC[A/G]TTTTCATATTTCCAC	8924
rs138301091	snp	A/C/G	1.6571e-05	0.0028784	missense, downstream-variant-500B	HERC2	GRCh38.p7	15:28174484	TCCACAGTTGTCCAC[A/C/G]CCACACTGTGGGACG	8924
rs138309699	snp	A/G	0.0422008	0.138995	intron-variant	HERC2	GRCh38.p7	15:28235682	GCCTTTCTTCTCCCA[A/G]AACCACGTATGAACG	8924
rs138338453	snp	A/G	0.000247143	0.0111135	missense	HERC2	GRCh38.p7	15:28143877	ATGCTCCATACCAAA[A/G]CTCTTGTTTCCCCAT	8924
rs138341710	snp	G/T	6.59196e-05	0.00574068	missense	HERC2	GRCh38.p7	15:28114775	TGTCTCGGATGTACA[G/T]GAGTCCAGGAATAAA	8924
rs138353244	snp	C/T	0.0134861	0.0810011	intron-variant	HERC2	GRCh38.p7	15:28149602	AACACACGCGGCTCC[C/T]AACCGAGAACATCAC	8924
rs138389747	in-del	-/AC			intron-variant	HERC2	GRCh38.p7	15:28205284	GCATCTCCCAGCATG[-/AC]TGCTCTCAAGTTGCT	8924
rs138391773	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28224174	ACACACACAGAGAGA[C/G]AGAGAAACAGACAGA	8924
rs138393107	snp	C/G	0.0107246	0.0724382	intron-variant	HERC2	GRCh38.p7	15:28164517	AATATCTTTAGTCTT[C/G]AGATTGAAATGTACC	8924
rs138399706	snp	C/T	0.0182019	0.0936463	intron-variant	HERC2	GRCh38.p7	15:28225120	AGGCCAGGTGTGGTG[C/T]CTCACACCTGTAATC	8924
rs138410846	snp	A/G	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28288651	AGGAGTTCAAGGCGA[A/G]CCTGGCAAACACAGT	8924
rs138425641	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28258109	TCTCCAATCACAATG[A/G]TATTAAACTAGAAAT	8924
rs138439776	snp	C/G	0.0162398	0.0886349	intron-variant	HERC2	GRCh38.p7	15:28201194	AGGCTTTGCACCCAT[C/G]TCACCTTCTCATTGC	8924
rs138443634	snp	C/T	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28258225	CTGTAATCCAAACAC[C/T]TTGGGAGGCCAAGGC	8924
rs138445418	snp	C/T	0.000254952	0.0112877	missense, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28293019	CTTGGTTCGACACTA[C/T]CATCTGCAGAATTAA	8924
rs138471464	snp	C/G	0.0138799	0.0821421	intron-variant	HERC2	GRCh38.p7	15:28283607	CTGGAACTTCTGGAA[C/G]GAGGAGATGACAAGC	8924
rs138484055	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28118992	AAGGCCTGACACCAC[A/G]CACGGTGGCTCACGC	8924
rs138489725	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28293835	AAAGCTGAGAAAAAT[C/G]ACTTTAGGCCACTGA	8924
rs138491318	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28286333	AGTACAAAGTACAGA[A/G]CAATATATATACAGA	8924
rs138500036	snp	A/G	0.0209421	0.100162	intron-variant	HERC2	GRCh38.p7	15:28307490	TTTTCTACTTTTTTG[A/G]TTTTCCTCTTAGTAC	8924
rs138515312	snp	A/C	0.0441095	0.141807	intron-variant	HERC2	GRCh38.p7	15:28173597	TGAGCTCAGGAGTTC[A/C]AGACCAACCTGAGCA	8924
rs138520526	snp	C/T	0.000629452	0.0177293	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28254462	AAATGTTGAGGCATT[C/T]GCTTCCTGTTCATCA	8924
rs138535006	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28144595	GGCACTACGTGGACA[A/T]GTGCACGTGTCCCTG	8924
rs138538227	snp	A/G	0.0115144	0.0749975	intron-variant	HERC2	GRCh38.p7	15:28268395	TGGACACACTTCTGC[A/G]CTCCATCCTGTTTAG	8924
rs138555162	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28143024	CCATTTGTTTCTACC[A/G]TCAAATGTTTTATTA	8924
rs138559354	snp	C/T	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28200154	ATAATCCCAGCACTT[C/T]GGGAGGCCAAGGCAG	8924
rs138567063	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28275490	CCACCCTATGGGGCA[C/T]TGCCCTCTTCTGACG	8924
rs138576430	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28134399	CTCTGCATAAACAAT[A/G]TTTTCTGCAAAAAAG	8924
rs138594015	snp	A/G	9.88386e-05	0.00702919	missense	HERC2	GRCh38.p7	15:28114631	AGTTTATCGCCAGCC[A/G]CACGTACTCCGCGCG	8924
rs138605797	snp	A/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28219830	GCCATGTGAAGCTTC[A/T]CATGTCTTTTAGGAA	8924
rs138614414	snp	A/T	0.0107246	0.0724382	intron-variant	HERC2	GRCh38.p7	15:28279144	TTACAGGCATGAGCC[A/T]CCAAGCCCCGGCTAA	8924
rs138636407	snp	A/C/G	3.29762e-05	0.00406045	missense, synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213889	GCGCAGGCGACCATC[A/C/G]ATGCCTCCAATCACA	8924
rs138650689	snp	C/T	0.00172422	0.0293111	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28228242	GCAGTGCCGTCTGCG[C/T]GAGGGCCAGCATGCC	8924
rs138651333	snp	C/T	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28193260	AATAACTATGCTTAC[C/T]GTGTTCAAAAAGATA	8924
rs138659705	snp	A/G	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28149992	AACATCACCGAGAAC[A/G]GCCACACGAACACAC	8924
rs138666696	snp	A/G	0.0402882	0.136092	intron-variant	HERC2	GRCh38.p7	15:28211731	AATTTCGGACATGTG[A/G]TGATTTGCATGCACT	8924
rs138699937	snp	A/G	0.000743243	0.0192631	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28236979	GGCACATTCAATCTC[A/G]ACAGGAGACAGCGGT	8924
rs138705900	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28151894	TTGAACAACTAACTA[C/T]AGGATGAAGGGAAAT	8924
rs138708972	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28243219	TGCCCATGGAAAAAA[A/C]GTGACATGTGACCCC	8924
rs138725743	snp	C/T	0.00728044	0.0598934	missense	HERC2	GRCh38.p7	15:28113673	TGCTCATCAAATTCA[C/T]GGAGTCTGGAAGAAA	8924
rs138748705	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28276112	AATCACTTAAACCTG[A/G]GAGACAAAGGTTGCA	8924
rs138768597	snp	A/C			intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28320197	TTGACCCATTGCAAC[A/C]TCCACCTCCCGGGTT	8924
rs138770130	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28209594	GTGATCTGCCCGCCT[C/T]AGCCTCCCAAAGTGC	8924
rs138794144	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28290129	TAAATAATCAGGTAC[A/G]GGTAAGATCTCTGAG	8924
rs138814061	in-del	-/TTG	0.00716266	0.059414	intron-variant	HERC2	GRCh38.p7	15:28278486	CTTTGTATTTTTTTA[-/TTG]TTGTGTTGTTTTTTA	8924
rs138817251	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28133598	TACATTCATGACTAT[A/G]GTTCATTTTGAATTA	8924
rs138827571	snp	C/G	0.000561362	0.0167441	synonymous-codon	HERC2	GRCh38.p7	15:28142298	CACAGCAACACGGGA[C/G]GCCATGCAGTACCTC	8924
rs138844150	snp	C/T	0.0633504	0.166319	intron-variant	HERC2	GRCh38.p7	15:28159926	GTGTAGATGTCCTTT[C/T]TGTTTGTTAGTTTTC	8924
rs138844489	snp	C/T	0.0821764	0.185298	intron-variant	HERC2	GRCh38.p7	15:28184730	AGCCGGGCATGGCGG[C/T]GTGCACCTGTAGTCC	8924
rs138855889	in-del	-/TG			intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28301732	ACTAGTTGTATGTAT[-/TG]GTGTATATATATATA	8924
rs138881353	snp	A/G	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28156662	TTAGGCTGAGACGAT[A/G]GGGTTTTCTAGATAT	8924
rs138887223	snp	A/G	0.000247115	0.0111129	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28201535	TACGTCTGGCTCTCC[A/G]TCACAACAGCACCAG	8924
rs138904231	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28171890	CTGTCCTGGCTAACA[C/T]GGTGAAACCCCGTCT	8924
rs138909869	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28127721	GCTAATCATCTTCTT[C/T]TGCCAGAGCAAGGAA	8924
rs138923800	snp	G/T	0.0532157	0.154195	intron-variant	HERC2	GRCh38.p7	15:28206626	ATCACAAGGTCAGGA[G/T]ATCAAGACCATCCTG	8924
rs138924365	snp	A/G	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28282997	GGGACTGGATGGGAC[A/G]GGATGGGAAGGGAAG	8924
rs138928794	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28264290	TACGTAAATGAGTGG[C/T]ATGCCTGCATGCCAA	8924
rs138944296	in-del	-/A	0.0119091	0.0762411	intron-variant	HERC2	GRCh38.p7	15:28189331	AAGATATCTTTTACG[-/A]ATGATAATCTCCATT	8924
rs138954615	snp	C/T	0.000263552	0.0114764	synonymous-codon	HERC2	GRCh38.p7	15:28167783	GGCTGAGGGGGCCGA[C/T]GGAGTCACTGCAGAG	8924
rs138960481	snp	C/T	0.000798403	0.0199641	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28198452	ACAGAGGCTTTGACC[C/T]GCACTTTATCACCAA	8924
rs138980831	snp	A/T	0.24449	0.249939	intron-variant	HERC2	GRCh38.p7	15:28230790	TCTTTCAGGCCATGC[A/T]GTCTGTCGCAAATAC	8924
rs138981669	snp	A/G	0.00517822	0.0506191	intron-variant	HERC2	GRCh38.p7	15:28123392	AGAGATGCCCCTACC[A/G]TATGGTAATTAGCCC	8924
rs138986321	snp	A/G	0.0185938	0.0946107	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314632	GAGGCCAAGGCGGGC[A/G]GATCATGAGGTCAGG	8924
rs139023234	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174313	CACTACAACCTCTAA[C/T]TGTGTTGGCACAATT	8924
rs139027864	snp	A/T	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28309912	ATTTTTTCTGTTCAC[A/T]TCACTAACAGGATAA	8924
rs139031320	in-del	-/GATG	0.280256	0.248162	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314723	AAATTAGCCAGGAAT[-/GATG]GATGGTACACGCCTG	8924
rs139032363	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28185721	TTTCAGTAATTCTGA[C/T]TTCTGTACGTATGGC	8924
rs139078765	snp	A/G/T	0.000405738	0.0142376	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28268596	GTTTCTGGAGGCAAG[A/G/T]CCTTGGACCAGCTGT	8924
rs139087469	snp	G/T	3.29875e-05	0.00406112	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28248644	AAATCCAATGAAGCA[G/T]ATCTTTCACGACTGT	8924
rs139145104	snp	C/G	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28291033	GGTTCTTTGAAAAAA[C/G]TCAAATTGATAACTT	8924
rs139160402	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28312976	CTAAACTGAAGCTCA[C/G]AAGGCCAATGACTTG	8924
rs139163401	snp	C/T	4.94393e-05	0.00497164	missense	HERC2	GRCh38.p7	15:28168451	TCAGTCTGTCTTCGA[C/T]ATCAACAGCCAGCAT	8924
rs139167008	snp	A/C	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28204470	ACTAAATATACAAAA[A/C]TTAGCCAGGCGTGGT	8924
rs139168653	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28269167	ATCAAACGCCTTAAA[C/G]AAACACCAGAGCTTG	8924
rs139177072	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28150537	CACATGAACGTATAC[C/T]CTAGTGAAATCACCG	8924
rs139192448	in-del	-/T	0.0825414	0.185628	intron-variant	HERC2	GRCh38.p7	15:28161253	ACTTACATTTAATGA[-/T]TTTTTTTTTTAAATA	8924
rs139202561	snp	A/G	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28243897	AACAGATGTAAGAAT[A/G]TTAACGTATTGGCAG	8924
rs139207881	snp	C/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28287357	CAAGGCTGCCAGGTA[C/G]AGAGTCGGTTCTGCG	8924
rs139212661	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28289235	TACACATACACAAAG[G/T]TTGAAAGTGAAAAAA	8924
rs139252313	snp	A/C	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28137748	AGGCCACTTAATAAC[A/C]CTACAGTGGCCTCTA	8924
rs139266323	snp	C/T	0.00517822	0.0506191	intron-variant	HERC2	GRCh38.p7	15:28145777	ACAAGCACCCAAAGA[C/T]GGTCCTGACCTGTCC	8924
rs139271571	snp	C/T	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28168243	CCAATTCCACTTAAG[C/T]ACTTTAAAAGCTCCT	8924
rs139274538	snp	C/T	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28227781	ATGAACAAAATGTTA[C/T]ATATTCATACAATGA	8924
rs139292388	snp	A/G	0.000230924	0.0107428	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28186702	ATGGATTTTACAATC[A/G]ATTCCTGAGCTCCTG	8924
rs139294698	snp	A/G	0.00835141	0.0640778	intron-variant	HERC2	GRCh38.p7	15:28260138	AGAGCTCAGGAGTTC[A/G]AGACCAGCCTGGGCA	8924
rs139302085	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28178359	GACCAGCACTCCTCA[C/T]AGACACAGCCCTGCT	8924
rs139302358	snp	G/T	0.00716266	0.059414	intron-variant	HERC2	GRCh38.p7	15:28145417	AGCAGCTCAGGGATG[G/T]CCCATAAAGGCTTTC	8924
rs139330135	snp	A/G	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28120199	TATTTATGTGAGGAC[A/G]TGACTGACGTACAGC	8924
rs139334721	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28276336	CCTGAATAATGCACC[A/G]GGAGCTCAGAGAGGA	8924
rs139335991	snp	A/G	0.238433	0.249732	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28174600	CTGCTGGCCGTGGTC[A/G]TTGTCACCCCAAGCA	8924
rs139346881	snp	C/T	0.000248519	0.0111444	synonymous-codon	HERC2	GRCh38.p7	15:28144174	GAAGTCTAACAGACA[C/T]GTCACCAAGTCCATG	8924
rs139351974	snp	C/T	0.00159667	0.0282096	synonymous-codon	HERC2	GRCh38.p7	15:28135561	CAGGGCAAGGCAGTG[C/T]TTTCCTCCAGAGTTC	8924
rs139371726	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28116456	TCCTGACCTCAGGCA[A/G]TCTGCCTGCCTCAGC	8924
rs139377848	snp	A/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28212175	GAGGTGAACACAGAC[A/T]TCTCTTCCGGGATAA	8924
rs139389826	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28272470	TAAAAGCAAATAGCT[A/G]GATAGAAGTGAACAA	8924
rs139396404	snp	C/T	0.0174175	0.0916809	intron-variant	HERC2	GRCh38.p7	15:28271316	TTGCAAATTAAATCA[C/T]AGTTCTAATTCTTCT	8924
rs139445742	snp	C/T	0.0103295	0.0711199	intron-variant	HERC2	GRCh38.p7	15:28128906	TTCCCCAGCCCTGTT[C/T]CTCCACGAAAGCCAG	8924
rs139464094	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28281130	AGTAACAAGTTAGAA[C/T]ACACATTCTAACTAG	8924
rs139477811	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28125317	GGTGTTGACCTAGTT[G/T]TCAACTTTACATATG	8924
rs139495382	snp	A/G	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28129608	GCCAAGCCTGCAGCA[A/G]GTCTGTCTAAGGACA	8924
rs139517177	snp	C/G	0.0154538	0.0865337	intron-variant	HERC2	GRCh38.p7	15:28218260	CTGGGGCAGAGCCCT[C/G]AAGCAGCTTCCCCCT	8924
rs139539730	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28246599	GAACTGTCAGTAACT[-/A]AAAAAAAAAAACAAA	8924
rs139541182	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28297672	CAATTTGTCAAATGC[C/T]GGAGAAACATCAGGC	8924
rs139567504	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28247823	CTACTGAAACCTGAA[A/G]GTTTCCATTACTGAC	8924
rs139574599	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28119658	GGGGTTTTATCACGT[C/T]GCCCAGGATGGTCTC	8924
rs139574855	snp	G/T	0.000214142	0.0103453	missense	HERC2	GRCh38.p7	15:28111845	TCGTCGCTGCTGTCG[G/T]CGGCGGCTGGCTCTC	8924
rs139596817	snp	C/T	4.94246e-05	0.0049709	missense	HERC2	GRCh38.p7	15:28125082	GAGCCACAGGCCACA[C/T]GGTTGACCTTCTTAC	8924
rs139604016	snp	G/T	0.0189856	0.0955633	intron-variant	HERC2	GRCh38.p7	15:28181235	TTCATCACAACCGTG[G/T]AACACCGACTCTGTC	8924
rs139607332	snp	A/G	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28208058	AGAACAGAACAGCCA[A/G]TCCAATTCCCAGGCT	8924
rs139608578	snp	A/G	0.000278428	0.0117956	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274446	GAGGTCCGCATCCTC[A/G]CCTGGGCGCACACAC	8924
rs139612007	snp	A/G	0.000247091	0.0111123	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265670	CCCACACGCCACATC[A/G]ATGACCTTCAGTCCT	8924
rs139612195	snp	C/T	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28289048	GCCCCGCAGCTCAGG[C/T]AGTGTAATACCATTT	8924
rs139621924	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28215922	GCTCCTTTACAAATA[C/T]ATTGCAGTTTGTAAA	8924
rs139632748	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28278027	TTGGGAGGTCAAGGC[A/G]AGAGGGTTGCTTGAG	8924
rs139657402	snp	A/C/T	0.000168046	0.00916497	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28275000	CCTTTGCCCGCAGGC[A/C/T]GGGAACTGCAGACGA	8924
rs139691351	snp	A/G	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28162138	AGTTCCAGACCAGCC[A/G]GGCCAACATGGTGAA	8924
rs139703599	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28115675	GCAACACCCACATCA[C/T]AGGTCTAGGCCCTTC	8924
rs139710407	snp	C/G	0.0482946	0.147699	intron-variant	HERC2	GRCh38.p7	15:28308500	TCATCTGCAAACAAG[C/G]ATAATTTGACTTCTT	8924
rs139712645	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28260442	GACTGAACTGCCTTC[C/G]CCTACAGTCAGGATC	8924
rs139713317	snp	A/G	0.00188172	0.0306156	synonymous-codon	HERC2	GRCh38.p7	15:28115513	GCTCAGGGGACTCCC[A/G]GTTCGGATGGCAATG	8924
rs139718674	snp	C/T	1.82091e-05	0.00301732	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256231	GGCCAGGGTCACCAC[C/T]GTCTGCTTCAGGCTG	8924
rs139722186	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28161513	AGCCCACGGCCTTTA[C/T]GACTGATCAGTCCTA	8924
rs139727205	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28148384	AGAAAGTACTTGAAA[G/T]AGAAAGTAACCAACA	8924
rs139728053	snp	C/T	0.000898912	0.0211813	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28175530	CCCCGAGTCCGTGAC[C/T]GCCAGGCAGTGCAGG	8924
rs139738926	snp	C/T	0.158632	0.232706	intron-variant	HERC2	GRCh38.p7	15:28158486	ATCCCTTTACCATTA[C/T]GTAATGGCCTTCTTT	8924
rs139741548	snp	A/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28198993	CTCTACCAAAAATAC[A/G]AAAATTAGCCAGACG	8924
rs139758763	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28195168	GAATATACTAATAAT[A/G]GATTTAAATGAGTCA	8924
rs139794567	snp	A/G	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28284078	TTTTGTGCATGAAAC[A/G]AAGTTCGTGCTAAGT	8924
rs139813405	snp	C/T	0.000330573	0.0128521	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28257115	CTCTTTCTCCTGGGG[C/T]GGGGGCCAGTCCGCG	8924
rs139836062	snp	A/G	0.0275645	0.114116	intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28315612	AGCCTGGGCAACATG[A/G]TGAAACCCCATCTCT	8924
rs139846899	snp	C/T	4.96077e-05	0.0049801	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265946	GCTTTCCAGAGAAGG[C/T]GGAGATCACCTTAGG	8924
rs139868155	snp	C/G	0.000381949	0.0138141	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28255977	ACGACCTGGACTTAT[C/G]TTCACTTCATTGCCT	8924
rs139873521	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28185016	TAAGTGAACTGGTAT[A/T]GTCCCTATTTAATTA	8924
rs139874505	snp	C/T	0.0174175	0.0916809	intron-variant	HERC2	GRCh38.p7	15:28271765	TGGCAAAATCCAACT[C/T]GTACTTGACATGTAA	8924
rs139878123	snp	C/T	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28158213	AGAATGTATATTCTA[C/T]TGATTTGGGGTGGAG	8924
rs139905498	snp	C/T	0.0399052	0.1355	intron-variant	HERC2	GRCh38.p7	15:28206659	TAACACGGTGAAACC[C/T]CATCTCTACTAAAAA	8924
rs139914558	snp	C/T	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28116066	TCCTCAGCACGTGGC[C/T]GGGGCTGGCTCTGCC	8924
rs139926094	snp	C/T	0.00755907	0.0610114	intron-variant	HERC2	GRCh38.p7	15:28252533	ACTTCCATGTTCTCA[C/T]TGATTCTTAATTAAC	8924
rs139926428	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318397	TTCCGGAGGCCGAGA[C/T]GGGTGGATCACTTGA	8924
rs139933691	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28148883	AGAACGGCCACACAA[A/G]CGTATATTCTAGTAA	8924
rs139945694	snp	A/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28204008	CACAACCAGGGCTAA[A/G]GGCAAATACAAAATC	8924
rs139953376	snp	C/T	0.0049311	0.0494088	missense	HERC2	GRCh38.p7	15:28146276	TGACGCCGTCCATGA[C/T]TGTGAGAGGGTCGTG	8924
rs139970998	snp	A/G			missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28201544	CTCTCCGTCACAACA[A/G]CACCAGTAGACTGCA	8924
rs139973203	snp	A/G	0.00252273	0.035426	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28175634	CAGAGCCGTGGCCCA[A/G]TCTGAAGTAATCCCC	8924
rs140027229	snp	C/T	0.00241358	0.0346549	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202356	AAGTACCAGGCAAGC[C/T]GGATGCATTCCCGGA	8924
rs140047493	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28306214	GTGTGTCAGCTGTAT[A/G]TGGCTTTTATTGCGT	8924
rs140060040	snp	A/C/G	0.000142236	0.00843205	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28215682	ACCTTCATGAGCAGC[A/C/G]TGATCCACTGCGGGG	8924
rs140073033	snp	C/T	6.60415e-05	0.00574599	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229535	GATGGAAGTAAGAAA[C/T]TCTTGCTCGCCAGTT	8924
rs140087429	snp	A/G	0.00115251	0.0239776	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28237018	TGCCAAATACGAAGC[A/G]TGTAATCCGAGAAGC	8924
rs140130849	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28244390	AATTAAAATGATGTT[A/G]GGTAGGGACAAGAAC	8924
rs140140499	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28137507	TAATTCTTGAAATAT[C/T]TTAAACTTTTTCATT	8924
rs140153389	snp	A/G	0.000199697	0.00999043	synonymous-codon	HERC2	GRCh38.p7	15:28117116	AGACTTGGTGCCGTC[A/G]GGGCCGGCCAGCCCG	8924
rs140162856	snp	C/G	0.0189249	0.0954164	intron-variant	HERC2	GRCh38.p7	15:28177371	CTCAAGAGTATCAGT[C/G]AGAAACAGTTTCTTA	8924
rs140167298	snp	C/T	9.90001e-05	0.00703493	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28191190	CAGCAGGATCTACGA[C/T]CATTTTTAATCTATG	8924
rs140173670	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28238421	AAAACAAAAAATGCA[C/T]AATCAAAGGAAATTC	8924
rs140184560	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28222758	TGTCTGTACAAACAA[C/T]GTGGTCTGTGCTGAA	8924
rs140192558	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28280782	GAGTGTGGTGACGCA[C/T]GCCTGGAATTCCAGC	8924
rs140198092	snp	A/G	0.0626037	0.165477	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321535	ACTCCCGAAAGCCAG[A/G]AAAGAAAAAAGAGAG	8924
rs140207712	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28266243	ACAATAGGCTAGGCG[C/T]GGTGGCTCACACCTG	8924
rs140234305	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28112854	TGTATTCTGGGGATG[G/T]CCAGATACATTTTTA	8924
rs140257470	snp	C/G	0.0115144	0.0749975	intron-variant	HERC2	GRCh38.p7	15:28170831	AAGCCAATTAGAAAA[C/G]GGCATGAAGACATAT	8924
rs140275392	snp	C/T	0.0146672	0.084371	intron-variant	HERC2	GRCh38.p7	15:28288033	AGCCACTTATTCCTA[C/T]TTTATACATGAGAGG	8924
rs140277325	snp	A/G	0.0103295	0.0711199	intron-variant	HERC2	GRCh38.p7	15:28205330	GATCTCTGCCAGGGA[A/G]ACTGGAAACACAACC	8924
rs140281490	snp	C/T	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28262118	TCTCACACTGCCTTT[C/T]CCCTTCTTCCTACTT	8924
rs140289168	snp	A/G	1.64827e-05	0.00287073	missense	HERC2	GRCh38.p7	15:28163191	AGCTTGAGCAGGTCT[A/G]CCACCACACGAGTGT	8924
rs140317570	snp	A/G	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28246680	TGATCAGCAAAGAAG[A/G]CACTTTAGCTTTCAT	8924
rs140326285	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28189201	GGTCAGCTGGGGGCA[C/T]GCAGGTTAGGTCAGG	8924
rs140328183	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28150715	AGAAAAAACACACGC[A/G]GCTTCTAACTAACCG	8924
rs140338897	snp	C/T	0.00172987	0.0293589	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28233497	CACTGACTTAGGCAA[C/T]GTTCTGTGCTTTACT	8924
rs140343776	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28278457	GAATTAGATGTTATA[C/T]TGTATTGTTTTTTCT	8924
rs140345440	snp	C/T	0.000793349	0.0199009	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28246776	AATGTAAGCCACCTC[C/T]GCGAAGTGCCGCCAG	8924
rs140360543	snp	A/C	0.0379877	0.132479	intron-variant	HERC2	GRCh38.p7	15:28294772	CCCCCGTGTGGCATG[A/C]GGTGTCCCCCACCCC	8924
rs140366877	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28185981	TCACAGTGCTCAGAT[A/G]AAATAAGGAATTGAG	8924
rs140374990	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28244320	GGGGTGAAGCTCAGA[A/C]ACCAAAAGGTACGTA	8924
rs140379541	snp	A/G	0.000197684	0.00993996	synonymous-codon	HERC2	GRCh38.p7	15:28125147	GGCATTGGTGGTTCC[A/G]TCTCCCAGTTGTCCC	8924
rs140397287	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28307131	TGAGCCACCACGCCC[A/G]GCCTGCAAACTTATC	8924
rs140440992	snp	A/G	0.000704875	0.0187601	missense, downstream-variant-500B	HERC2	GRCh38.p7	15:28174460	TCGTGGACAGAGGGC[A/G]TGGCCACATCCACAG	8924
rs140479764	snp	A/T	0.0225045	0.103662	intron-variant	HERC2	GRCh38.p7	15:28133897	TACTGCAGCTATAAA[A/T]GAGGCTTAAGTCAGG	8924
rs140482685	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28292508	GTGGAAAACAGTTTA[C/T]TGCTTCCTCAAACAG	8924
rs140487401	snp	A/G/T	0.000131813	0.0081174	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28176694	CCACTCACCTTCATC[A/G/T]GTCAGAGCCAGGGTC	8924
rs140505159	snp	A/G	0.0107246	0.0724382	intron-variant	HERC2	GRCh38.p7	15:28219415	GGGAGGCTGAGGGAG[A/G]AAGCAGCGACTGGTG	8924
rs140509239	snp	A/C	0.21809	0.247955	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28238757	TTTCTACAGTTCTGA[A/C]CTGTAAAAAATGACT	8924
rs140526067	snp	C/T	0.0460142	0.144533	intron-variant	HERC2	GRCh38.p7	15:28235499	CAAAGGTCCACCCAA[C/T]GGGGGGCTGTATGGA	8924
rs140550308	snp	A/G	0.00303239	0.0388201	intron-variant	HERC2	GRCh38.p7	15:28233591	TTAAAAGAAGGGCAG[A/G]GATGAATATGTACCT	8924
rs140551267	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28191835	ACTTATAAATTAAAA[C/T]ATAACGTGAGTACTG	8924
rs140556070	snp	A/C/G	0.000126475	0.00795136	missense, synonymous-codon, downstream-variant-500B, nc-transcript-variant	HERC2	GRCh38.p7	15:28186582	TGGTTCTCACCTTCC[A/C/G]CTGTTGCCTTTCTCA	8924
rs140561562	snp	A/C	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28250055	GGTTCCAGACCCACC[A/C]CACCCGCCCCGTTGA	8924
rs140589552	snp	C/T	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28183479	CAGCCTCCTAAAGTG[C/T]TGGGATTACAGGTGG	8924
rs140591259	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28274707	GGGTGGGGGTGCATA[C/T]ACTCTCTTTTTTTTC	8924
rs140591282	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28187759	ATGTCATTTTATTGT[C/T]GCCTCATTCAAATCA	8924
rs140601065	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28245785	TAGAAATGGCAAATC[C/T]TCCTTTGTAAAGTAT	8924
rs140630729	snp	C/T	0.00109518	0.023375	missense, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28292977	TCTTTTTTCTCTTTG[C/T]CATTCAGATCTTCTT	8924
rs140659289	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28257433	ACACTATCAGCTTCC[A/G]ATTTTCCCACCCATT	8924
rs140664117	snp	C/T	0.000477889	0.0154504	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28177498	CAGTTAAAGCCGTCG[C/T]GTGCCGGCCACCTGC	8924
rs140671115	snp	C/G	0.000721324	0.0189774	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28196296	AAAAATCAAAGTCAT[C/G]ACAGTTTCTGCATTT	8924
rs140684385	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28285548	GAAAGAGCTACAGTG[A/G]GTGATGAGAAATTTA	8924
rs140701444	snp	A/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28143471	TATTTTTTTTGAGAT[A/G]GAGTCTCGCTCTGTC	8924
rs140708332	snp	C/T	0.000181209	0.00951691	missense	HERC2	GRCh38.p7	15:28124218	ATCTCCTGCAGGTGA[C/T]TGTACTCCATGGGGA	8924
rs140717581	snp	A/G	0.02016	0.0983543	intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28312637	ATTCATAAAAAAAAT[A/G]AAATAAAATAAAGAA	8924
rs140734101	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28117574	GAACTCCAAAAGCAG[C/T]TCCCCCAGCAGACCA	8924
rs140740119	snp	C/T	0.0295035	0.117819	intron-variant	HERC2	GRCh38.p7	15:28173750	GGAAGCTGCAGTGAG[C/T]CAAAATCGTGCCACT	8924
rs140746857	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28200106	GGGTCTTTATAAGAA[A/G]AGACTCCAGGATGGG	8924
rs140760345	snp	A/G	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28149342	ACCAACATACATTCT[A/G]GTAAAATTACCAAAA	8924
rs140763368	snp	C/T	0.0205511	0.0992634	intron-variant	HERC2	GRCh38.p7	15:28210368	TCTAGCTCCTGACCT[C/T]GTGATCCGCCGCCCG	8924
rs140777239	snp	C/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28172558	ATACAACTGAAACAA[C/G]TGGACAATCATGCCA	8924
rs140781510	snp	C/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28285172	CCAAGATATAGAATT[C/G]AACATCACCATCAAT	8924
rs140787364	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28232802	TTTAGAAGAATGGCA[A/G]TAAGTTTAAATGTTC	8924
rs140798342	snp	A/G	0.0115144	0.0749975	intron-variant	HERC2	GRCh38.p7	15:28144530	CTGTTCCACGCCTCA[A/G]CAGGGCCTGTGAGAG	8924
rs140828208	snp	C/T	1.64749e-05	0.00287005	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28262958	ATAACGAACATGTTC[C/T]TCTGTTCCATGTCCA	8924
rs140828476	snp	A/G	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28265124	ACAATACTGAAAGAC[A/G]AGTCATTTCTAAAAT	8924
rs140828528	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28228078	CGCTGAATTGTGACG[A/T]TAAAATGGTACACTT	8924
rs140835326	snp	A/G	0.000131794	0.00811661	synonymous-codon	HERC2	GRCh38.p7	15:28141772	GTCTTGCTCTCTTTT[A/G]AAAATGTCATGGCTC	8924
rs140836021	snp	C/T	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28142765	ACTGCACATGACAAC[C/T]CTCAGTGGCTCTTTC	8924
rs140836045	snp	C/T	0.0271762	0.113356	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174025	AAGTCAATCAAAATG[C/T]ATACTTTAAATAGGT	8924
rs140839645	snp	G/T	0.000154696	0.00879342	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28222203	TCTTCCTCAACGTTG[G/T]CACAACTGGGGCCTG	8924
rs140850840	snp	G/T	0.0444908	0.142359	intron-variant	HERC2	GRCh38.p7	15:28303199	TGGTGAGAGATAGCG[G/T]TCTAGTTTCATTTTT	8924
rs140874625	snp	C/T	0.0158469	0.0875917	intron-variant	HERC2	GRCh38.p7	15:28311771	AGACCCCTGCCCAGA[C/T]CTGAAAGCACTCTAA	8924
rs140886629	snp	C/G	0.030278	0.119257	intron-variant	HERC2	GRCh38.p7	15:28164311	AAGGGGAAAATGACC[C/G]AACCAGTGGACCCTG	8924
rs140887093	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28235410	ATCTTCTGGCAAGCA[A/G]TGAGCCTTGAGGAGG	8924
rs140907462	snp	A/G	1.68863e-05	0.00290566	missense	HERC2	GRCh38.p7	15:28124146	GGGATGCAGGGGCAG[A/G]AGAGCTCGGAGAGGT	8924
rs140925883	snp	C/G	0.00835141	0.0640778	intron-variant	HERC2	GRCh38.p7	15:28266662	AAGTCAAAGATGCCA[C/G]AAACAAAATACCATA	8924
rs140931800	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28272527	ACTAAAGCCGTGGTA[A/G]TTAAATCACTGAATT	8924
rs140932450	snp	A/G	0.00594771	0.0542077	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272283	ACCTTTGCAGCAAGG[A/G]CAAAAGTGGGGCGCT	8924
rs140957718	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28224172	ACACACACACAGAGA[C/G]AGAGAGAAACAGACA	8924
rs140962140	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28274113	TAGTCAGAGTATCAT[A/C]AATCAAATCGCCTGA	8924
rs140964368	snp	A/G	0.00319424	0.0398361	intron-variant	HERC2	GRCh38.p7	15:28217096	TGCTCGCACTCAATC[A/G]CACACTTACACACTT	8924
rs140970441	snp	A/G	0.0138799	0.0821421	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317381	GGCGTGAGCCACCGC[A/G]CCCAGCCGAAGTGAC	8924
rs140970725	snp	A/G	0.000816769	0.020192	synonymous-codon	HERC2	GRCh38.p7	15:28132779	GCCAGCAGCAACATC[A/G]ACCACTTCAATTCCT	8924
rs140996437	snp	C/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28192571	CCCCATCAAAGACAA[C/G]TAGTAAAGCCAGACA	8924
rs141043009	snp	C/T	0.47588	0.107137	intron-variant	HERC2	GRCh38.p7	15:28272436	AGATTAACTTCTTTT[C/T]TTCACAGTTGATCAA	8924
rs141044048	snp	C/T	0.00159617	0.0282053	intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28320152	ACAGTTTTGCTCTCA[C/T]TGTCCAGGCTGGAGT	8924
rs141080770	snp	A/G	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314291	ATAAAGACTTCTATC[A/G]TGAAAGAAGAGCCTG	8924
rs141102128	snp	A/T	0.0162398	0.0886349	intron-variant	HERC2	GRCh38.p7	15:28187576	GACCTCAGGTGATCC[A/T]CCTGCCTCAGCTTCC	8924
rs141106054	snp	C/T	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28245705	TATTTGGTTAATATA[C/T]ACATATATGACCCAA	8924
rs141145226	snp	A/G	0.00017943	0.0094701	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28230454	TAAATCACTCTCTTC[A/G]TTTCCAATTTTTTCT	8924
rs141168199	snp	A/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28300132	GTGCTCTGAAAAGAT[A/T]AACCAAAAGCAAGTA	8924
rs141168688	snp	C/T	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28282342	AATTTTAAACAGTTA[C/T]AGAAATACCACGATG	8924
rs141203755	snp	C/T	0.000153988	0.00877328	missense	HERC2	GRCh38.p7	15:28113136	TCGTCCGGCCCCAGA[C/T]GAAGCGAAGGAAAAG	8924
rs141210218	snp	A/G/T	4.97701e-05	0.00498828	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28192107	GGCTGCTGTGGCAAC[A/G/T]CTTCAGCTGTTTTCC	8924
rs141212514	snp	C/T	0.0146672	0.084371	intron-variant	HERC2	GRCh38.p7	15:28132852	AAAAGTCACCAAATA[C/T]AATGGAAACACATTT	8924
rs141249707	snp	C/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28127057	CAAGGCTCATGTTCT[C/G]TGGAGACACCATCAG	8924
rs141284841	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28155902	TGGTTTTAGGTCTAA[C/T]ATTTAAGTCTTTAAC	8924
rs141318794	snp	C/T	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28128554	ATTCATCCATGAGCC[C/T]CTTCCCTCAATGAAA	8924
rs141325407	snp	A/G	0.000132216	0.00812961	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28299424	AGGAGGGAGCTCTCC[A/G]TTCTGGGTTGATTCT	8924
rs141330793	snp	G/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28185292	CTCATGTCACACGCT[G/T]CAGAGTACTTAGAGC	8924
rs141367564	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28309527	TTTTTCCATCCCCCC[A/G]CACCGTCCTGAAGGG	8924
rs141371319	snp	A/G	0.158302	0.232576	intron-variant	HERC2	GRCh38.p7	15:28217656	TCGGAACCTCAGAAT[A/G]TGATCTTATTTAATG	8924
rs141376862	snp	A/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28163831	TTCTCATTACCACTC[A/G]TGTACTTCCCATTCC	8924
rs141395778	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28259688	GGCCAGGCACAGTGG[C/G]TCACACCTGTAATCC	8924
rs141410978	snp	C/T	0.479188	0.0998651	intron-variant	HERC2	GRCh38.p7	15:28272431	AAAACAGATTAACTT[C/T]TTTTCTTCACAGTTG	8924
rs141413472	snp	A/G	0.00874735	0.0655527	intron-variant	HERC2	GRCh38.p7	15:28286699	CAGACCTATTTACAC[A/G]GCAGAGAGAATCATT	8924
rs141437532	snp	C/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28119476	TTGTTTGCTTTGAGA[C/T]AGTGTCTGGCTCTGT	8924
rs141441362	snp	C/T	0.126372	0.217293	missense, downstream-variant-500B	HERC2	GRCh38.p7	15:28174473	GCGTGGCCACATCCA[C/T]AGTTGTCCACGCCAC	8924
rs141454016	snp	C/T	0.0232847	0.105357	intron-variant	HERC2	GRCh38.p7	15:28196894	AGGACATTTTGGTTT[C/T]TAATTACACCAAGTC	8924
rs141457389	snp	A/G	4.94303e-05	0.00497119	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28177448	TCCAAGTTTTCCATC[A/G]TCACCTTCGCCCCAC	8924
rs141460418	snp	A/C	0.0150606	0.0854603	intron-variant	HERC2	GRCh38.p7	15:28254074	GGATCACCTGAGGTC[A/C]GGAGTTCAAGACAAG	8924
rs141460915	snp	A/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28211467	CCAAGTTGCTGAAGT[A/T]TCAGCCGCTTTCACT	8924
rs141472056	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28272069	ACAAGTGACCTCCCA[C/T]ACCTGTCTCATCTGA	8924
rs141495562	snp	A/C	0.000445416	0.0149168	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265911	CCCGCAAGCGATGTG[A/C]ACCACGTGCTTCCCG	8924
rs141500764	snp	C/T	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28255524	TACTATATAGTTATA[C/T]TGCTGCGACACTCAG	8924
rs141528436	snp	A/G	6.59294e-05	0.00574111	synonymous-codon	HERC2	GRCh38.p7	15:28144081	GTGGCATTTACCTAG[A/G]GCACTCAGCTGTGCA	8924
rs141538748	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28304122	AGTGAGCCGAGATTG[C/T]GCCATTGCTTTCCAG	8924
rs141541560	snp	A/C	0.0189856	0.0955633	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314644	GGCGGATCATGAGGT[A/C]AGGAGTTCAAGACCA	8924
rs141546380	snp	A/G	0.0821764	0.185298	intron-variant	HERC2	GRCh38.p7	15:28173565	GCACTTTGGGAGGCC[A/G]AGATGGGAGGATCAC	8924
rs141552873	snp	A/G/T	0.00024728	0.0111167	synonymous-codon, missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28268494	GCCCAGCCGTCCGCC[A/G/T]TCCCCACAGCCCCAG	8924
rs141555005	snp	A/G	0.00636936	0.0560724	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318245	AAAAGTGATGTGACT[A/G]ACACCTCTTAGCTCT	8924
rs141562067	snp	A/G	0.000675381	0.0183639	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265718	CATCGGAATGGCCTC[A/G]TCCTCACTGGAGCCT	8924
rs141650481	snp	C/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28199708	AAGACCTAACCCACC[C/G]AACCCTGCTTGCCTG	8924
rs141653387	snp	C/T	0.16028	0.233346	intron-variant	HERC2	GRCh38.p7	15:28200391	CAGAGCGAGACTCTG[C/T]CTCAAAAAACAAACA	8924
rs141674276	snp	C/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28157593	ATCAGTGGTGATATC[C/T]CCTTTATCATTTTTT	8924
rs141677977	snp	A/G	0.000649886	0.0180145	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272230	GTGCATGTCGCCCTC[A/G]GAGTGGGGTGCATCC	8924
rs141693645	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28193991	GAGAGAAATTACAAA[A/G]TATGCAGAAAAATCT	8924
rs141732765	snp	C/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28288812	GAGATTGTGCCATTA[C/G]ACTCCAGTCTGGGCA	8924
rs141737904	in-del	-/ACAAAA	0.184521	0.241273	intron-variant	HERC2	GRCh38.p7	15:28225260	TGTCTCAAAACAAAG[-/ACAAAA]ACAAAAACAAAAAAA	8924
rs141739498	snp	C/T	0.000153988	0.00877328	missense	HERC2	GRCh38.p7	15:28111770	TCCCCATCTTAGTGT[C/T]CTGTTAAATAATCTT	8924
rs141745504	snp	A/G/T	0.0138898	0.0822601	intron-variant	HERC2	GRCh38.p7	15:28118738	AGCCTTCCTGGCTCC[A/G/T]TGCTGGTGTCCTGTG	8924
rs141748146	snp	C/T	0.00835141	0.0640778	intron-variant	HERC2	GRCh38.p7	15:28150792	TACTGAAAAAACACA[C/T]GTGACTTCTAAGGGG	8924
rs141754911	snp	A/G	0.000115309	0.00759218	synonymous-codon	HERC2	GRCh38.p7	15:28114644	CCGCACGTACTCCGC[A/G]CGGTTGTCCAGGGTG	8924
rs141776886	snp	A/G	0.0134861	0.0810011	intron-variant	HERC2	GRCh38.p7	15:28153152	TGAGGTCAGGAGTTC[A/G]AGATCAGCCTGACCA	8924
rs141788947	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28149520	CAAAAAAACACACGC[A/G]GCTCCTAACCGAGAA	8924
rs141794098	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28150455	AACGGCCACACGAAC[A/G]TACATTCTAGTGAAA	8924
rs141799399	snp	C/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28210694	CTTTGGTCTGGGGTG[C/T]GGCCTGGGAGTCTGC	8924
rs141801098	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28247045	AACCCTTGTCCTTGC[A/G]CTCTTTCTGTATCAT	8924
rs141808831	snp	A/G	0.0107246	0.0724382	intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28320406	GGCGTGAGCCACTGC[A/G]CCCGGCCACGCAACA	8924
rs141810701	snp	C/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28290881	AAAATCTAAAGTCAA[C/T]GATCTAAGCCTTTGC	8924
rs141819591	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28232059	ACTGCTGTGACTTCC[A/G]GATCCAGAGCACCCC	8924
rs141830027	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28289829	TGTGCAGTGAGAGGA[C/T]GACACACCTCAGTGA	8924
rs141837923	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28310538	GCCCCTGAAGTTTAA[C/G]TAGTGAATGGAAAGG	8924
rs141839082	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28208995	TCAAAAAATGTTTTT[C/T]TCTATTAAAAGTGAC	8924
rs141842156	snp	A/G	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28243314	CAATAAAACTTTTAA[A/G]GTGTAAAAGAAAATC	8924
rs141847559	snp	C/G	1.65671e-05	0.00287807	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233765	GTCAAATGGCACTGC[C/G]TACAGTACCTTTCTA	8924
rs141856716	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28283855	ACAATCTGATAAGTG[C/T]TCATATATACACAGG	8924
rs141867398	snp	A/G	0.0611083	0.163768	intron-variant	HERC2	GRCh38.p7	15:28291798	TAGTCCCAGCTACTC[A/G]GAAGGCTGAGGCAGG	8924
rs141876361	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28272465	AAAAATAAAAGCAAA[C/T]AGCTGGATAGAAGTG	8924
rs141878003	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28238902	AGAAATACATACCTA[A/G]CTCTGAAACTAATAC	8924
rs141881243	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28179336	TTATGCACTGTGTAA[C/T]ATTTCACTCAACCAC	8924
rs141882847	snp	A/G	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28240381	TGAGATCACGTCACT[A/G]CACTCCCGCCTGGGC	8924
rs141887299	snp	A/C	0.0256215	0.110247	intron-variant	HERC2	GRCh38.p7	15:28239374	CTCAAAAAAAGAAAA[A/C]CTGAGTGGTGGTCAC	8924
rs141913704	snp	A/G	1.97799e-05	0.00314476	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202198	GCATCTGAGAGCTCC[A/G]TGACCTGTATGTCGG	8924
rs141958604	snp	A/G	0.000150571	0.00867541	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28255896	TGCAGTAATGGCTGC[A/G]TGTAAGGCTGACTCC	8924
rs141961459	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28278388	TCAAAACAAACAAAC[-/A]AAAAAAAATCATCTC	8924
rs141965027	snp	C/T	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28280626	ACAAAAGAAGTTGGC[C/T]GGGCACAGTGGCTCA	8924
rs141966348	snp	A/G	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28145158	CAGGCCAGGGGCCAT[A/G]GGGACATTTCCCGGG	8924
rs141969705	snp	C/T	0.000658696	0.018136	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213806	AACTGCACGGTGATT[C/T]TGCCCTTTGGGGTGA	8924
rs141981089	snp	A/C/G	0.000154772	0.00879567	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28215694	AGCGTGATCCACTGC[A/C/G]GGGAGCTGAGGGCGC	8924
rs142005623	snp	A/C			intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28319130	TCCTTACGGTAAAAC[A/C]CCACCATTCATTCCT	8924
rs142016910	snp	C/T	0.0123036	0.0774623	intron-variant	HERC2	GRCh38.p7	15:28149928	GAACAGCCACACGAA[C/T]GCACATTCTAGTAAA	8924
rs142034055	snp	A/T	0.000714303	0.018885	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28220498	TGAGGGCTGTGCAGC[A/T]GCCGGCAGCTCTGCC	8924
rs142039662	snp	C/T	0.00874735	0.0655527	intron-variant	HERC2	GRCh38.p7	15:28175981	ACATCTTTCTCAAGC[C/T]GCCTCGGGTCATGAC	8924
rs142046335	in-del	-/GA	0.0345262	0.126772	intron-variant	HERC2	GRCh38.p7	15:28175206	ACCAATTCTCTAAAG[-/GA]AAGTCTTGCTAATAT	8924
rs142047751	snp	C/G	0.0130921	0.0798413	intron-variant	HERC2	GRCh38.p7	15:28262015	GAACACTGCCAGGTC[C/G]ACCTACTTCAAATAC	8924
rs142055786	snp	C/T	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28185045	TAATATCTACAGATG[C/T]AATCAGTTTGAACTA	8924
rs142059352	snp	A/G	0.00366195	0.0426329	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272215	CATCATGACACTCAC[A/G]TGCATGTCGCCCTCG	8924
rs142063906	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28243001	CTAAGAAAAAGGCAA[A/G]GAGGTACACTGTCAC	8924
rs142069556	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28309038	TGTCTGCTTTTAGTA[A/T]CAAGGTTTGAATTTT	8924
rs142071453	snp	C/G/T	4.94352e-05	0.00497143	synonymous-codon	HERC2	GRCh38.p7	15:28141444	TACCTTCCCATCAGC[C/G/T]GTCACAGCAAAGAGG	8924
rs142072884	snp	A/G	0.00172	0.0292753	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28228253	TGCGTGAGGGCCAGC[A/G]TGCCGGAATTGAGCA	8924
rs142085566	snp	A/G	6.58946e-05	0.0057396	synonymous-codon	HERC2	GRCh38.p7	15:28121367	GCGGTTCAGCTCCAC[A/G]ACGGGGCCATGCTGA	8924
rs142093288	snp	A/G	0.00152575	0.0275781	intron-variant	HERC2	GRCh38.p7	15:28198567	ATTTTGTCTCTAAGA[A/G]AAAACAAAAGCACTG	8924
rs142140993	snp	C/T	3.31137e-05	0.00406887	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28186656	CCAAATCTTCCTCTT[C/T]TGCACGGATCCGTCC	8924
rs142143055	snp	C/T	0.0111196	0.0737302	intron-variant	HERC2	GRCh38.p7	15:28173885	TTAAATTGGTGCATA[C/T]GGCAGGAAGGAGGGA	8924
rs142146918	snp	C/G	0.0115144	0.0749975	intron-variant	HERC2	GRCh38.p7	15:28236151	ACCACAGGGTAGACG[C/G]GTAGAGATTCCTGCA	8924
rs142149022	snp	A/G	1.6918e-05	0.00290839	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28270848	GAAACTCTCATTGGG[A/G]CTCAGAGGGCCAGAC	8924
rs142169064	snp	C/G	3.29457e-05	0.00405854	missense	HERC2	GRCh38.p7	15:28141611	TGCCACCAGCAGAGA[C/G]AGTCCAGTCATCTGG	8924
rs142176594	snp	C/G	0.14665	0.227637	intron-variant	HERC2	GRCh38.p7	15:28306564	GTCTGGTTTTGGTAT[C/G]AGGGTAATATTGGCC	8924
rs142200907	snp	C/T	0.0115144	0.0749975	intron-variant	HERC2	GRCh38.p7	15:28139047	AGTGGAGTCTAAAGA[C/T]GTGACTTAATAGACT	8924
rs142208951	snp	C/G	0.0119091	0.0762411	intron-variant	HERC2	GRCh38.p7	15:28309995	AGCTGGTGGGGGAGA[C/G]GTAAACTCCTTCCAA	8924
rs142209264	snp	C/T	0.000298745	0.0122182	synonymous-codon	HERC2	GRCh38.p7	15:28163127	CATGCCGGAAAGCAC[C/T]GCGGAGAGCACATCC	8924
rs142210854	snp	C/T	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28281016	CCATTATTTTCATGT[C/T]ACAAAACCAAATTCA	8924
rs142247584	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28278577	ACAGACACAGAGAGC[C/T]AACTGTAATGTGATT	8924
rs142247617	snp	A/G	0.0119091	0.0762411	intron-variant	HERC2	GRCh38.p7	15:28308974	AGGATATTTGCATCA[A/G]TATTCATCAGAGACA	8924
rs142254143	snp	A/G	0.000280609	0.0118417	missense, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28292917	CATACCCAGCTGTCC[A/G]GAATTGACTTGGCCC	8924
rs142254746	snp	C/T	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28228730	CTCTGTCATGCTGCA[C/T]GATGGGCCTACCCCC	8924
rs142354999	snp	G/T	0.000773987	0.0196569	synonymous-codon	HERC2	GRCh38.p7	15:28111961	CTTGCAGGAATACCT[G/T]GGCAGCTTCAGCAAG	8924
rs142355405	in-del	-/A	0.101301	0.200969	intron-variant	HERC2	GRCh38.p7	15:28276759	AACAAAAACAAAAAC[-/A]AAAAAAAAACTACTC	8924
rs142366957	snp	G/T	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28195849	TTAAGTTATATATAT[G/T]TTGCCACAATGACAA	8924
rs142369597	snp	A/G	0.00517822	0.0506191	intron-variant	HERC2	GRCh38.p7	15:28292098	GCCAGGCATGGTGGC[A/G]GACACCTGTAATCCC	8924
rs142370918	snp	C/T	0.0232847	0.105357	intron-variant	HERC2	GRCh38.p7	15:28253432	CATCCACCTGCTTAT[C/T]AGTAAGAATCTTTTT	8924
rs142379282	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28126631	AAAGTAACTCAGGAA[C/T]GGAAAACCAAACCAT	8924
rs142397100	snp	A/C	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28138385	ATATTTTGTTAGGGG[A/C]TAATGCAGCTGATGA	8924
rs142399136	snp	A/G	0.114176	0.209885	synonymous-codon, downstream-variant-500B	HERC2	GRCh38.p7	15:28174441	AGTCTGGAAGAGGAC[A/G]GGCTCGTGGACAGAG	8924
rs142429456	snp	A/G	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28139713	ATCTATCCAAAGAAT[A/G]TAAGTTTGTTTAATA	8924
rs142436616	snp	C/T	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28168788	TTACTCTGGATCCTA[C/T]TTATTTGAAAAACCA	8924
rs142451695	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28155335	AGATCCCTGAGGAAT[C/T]GCCACACTGTGTTCC	8924
rs142465162	snp	C/T	0.00517822	0.0506191	intron-variant	HERC2	GRCh38.p7	15:28137373	CCTTGCTTTACTGTA[C/T]CTCGCAGATACTGTT	8924
rs142465883	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28167942	GGGCTGTTTAGAATG[C/T]TCCAGATTTTACAGA	8924
rs142475971	snp	A/G	0.0463947	0.145069	intron-variant	HERC2	GRCh38.p7	15:28249750	CTCCCGGGTTAAAGC[A/G]ATTCTCCTGCCTCAG	8924
rs142484179	snp	A/G	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28149218	TACCGAAAAATACAC[A/G]CAGCTCCTAACTGAA	8924
rs142510054	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28180555	ATAAAGACAGAAAAA[C/T]GTAGACAGCTGCTGG	8924
rs142517992	snp	A/G/T	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28240147	CCAATCAGAGGGCGC[A/G/T]GTGGCTCACGCCTGT	8924
rs142538716	snp	C/T	0.00795532	0.062565	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318300	CAGTGAAGGAAAACA[C/T]GGTGATTCAATCACT	8924
rs142553001	snp	C/T	0.000331592	0.0128719	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28238645	TGTCTGGAAGTCCTT[C/T]ATATCATACACCTTC	8924
rs142557336	snp	C/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28182115	TCAAAAATGTTTATT[C/G]TAGGGAAGGCAAGAT	8924
rs142558967	snp	C/T	0.00795532	0.062565	intron-variant, utr-variant-5-prime	HERC2, LOC107987422	GRCh38.p7	15:28317761	AATGGCACAGAACTA[C/T]GCACACACATTGTAC	8924
rs142562377	snp	A/G	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28240730	AGAATGGAGACCCCA[A/G]AAACAATCCATCACG	8924
rs142573451	snp	A/G	0.0376037	0.131863	intron-variant	HERC2	GRCh38.p7	15:28122825	ATGCTGCTGCCCACC[A/G]CTCCCCTACCACACA	8924
rs142576846	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28177738	AACTCTAGAAAGAAT[C/T]TGCAAAGAGGCAAAA	8924
rs142594573	snp	C/T	0.0422008	0.138995	intron-variant	HERC2	GRCh38.p7	15:28207894	CGATGTGTAAACAAG[C/T]GGTGTGTCTGTGTTC	8924
rs142615958	snp	C/G	0.000694008	0.0186151	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214773	GTCCCATGATGGAAG[C/G]ACTGCTTGCAACAAA	8924
rs142622963	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28224170	ACACACACACACAGA[C/G]AGAGAGAGAAACAGA	8924
rs142629847	snp	A/G	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28281799	CAGGGCATCCCCACC[A/G]AGCCACCCTTCAGGC	8924
rs142674130	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28252259	GCTCAAACAGCATAG[C/T]TGCAGGTCAAACAGG	8924
rs142723943	snp	C/T	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28193336	ACTAGAACTGATAAA[C/T]TGAATAATTAAAATT	8924
rs142734218	snp	A/G	0.0130921	0.0798413	intron-variant	HERC2	GRCh38.p7	15:28276220	AAAAAAAAAAAAAGA[A/G]GGTTGTTATAGAAGG	8924
rs142744030	snp	C/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28189249	CAATGCTTCGTATTT[C/T]TCATGTACATGACAT	8924
rs142749105	snp	A/C/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28247718	CAGGCGTGAGCCACC[A/C/G]CACCCAGCCTCCTAC	8924
rs142753406	snp	A/C	0.000316511	0.012576	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28177099	GCTTGGTTTTCAGGG[A/C]CTCGATCAGCCTTGG	8924
rs142779606	snp	A/G/T	1.64738e-05	0.00286995	synonymous-codon	HERC2	GRCh38.p7	15:28111847	GTCGCTGCTGTCGTC[A/G/T]GCGGCTGGCTCTCCT	8924
rs142860322	snp	C/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28152236	GCCCGCCAGATCAAA[C/G]GCCGGGGCCTCAACA	8924
rs142864451	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28120060	TCAATCGCGGGGGTT[A/G]GACAACGCAGAAGCC	8924
rs142872459	snp	A/T	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28215369	TCTTAAGACAATTAC[A/T]CTACAAATTCTGTGA	8924
rs142880342	snp	C/T	0.000872722	0.020871	missense	HERC2	GRCh38.p7	15:28143910	TTTTCTCCAAGCAGC[C/T]TATTTATGTTAATTG	8924
rs142882696	snp	C/T	0.000188539	0.00970741	synonymous-codon	HERC2	GRCh38.p7	15:28115441	TACCTCACTGAGGTC[C/T]GCGATGGTGAGGCTC	8924
rs142888399	snp	A/G	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28223334	TTCTCCTCCAGGTGG[A/G]CGGGAAAAAGACCCA	8924
rs142902862	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28156734	TTGTTCTAATTGAAT[A/G]CCCTTTATTTCTTTC	8924
rs142912223	snp	C/T	0.0232847	0.105357	intron-variant	HERC2	GRCh38.p7	15:28225646	GAGGTTACAGTGAGC[C/T]GAGACTGTGCCACTG	8924
rs142950889	snp	A/C/T	3.29795e-05	0.00406065	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28248653	GAAGCAGATCTTTCA[A/C/T]GACTGTGTTGCTCAA	8924
rs142952871	snp	C/G	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28236437	CTGGGATTACAGGCA[C/G]CCGTCACCACGCCCA	8924
rs142954116	snp	C/T	0.040671	0.13668	intron-variant	HERC2	GRCh38.p7	15:28307770	TCATTCTTCTGCATA[C/T]GAATATCAAGTTTTC	8924
rs142954693	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28273698	AAGAAGGCACAGTGC[G/T]GACCTCTGCAAGGAG	8924
rs142982823	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28140404	TTCATTTAGAGACTA[C/T]GGCACTCTATAAAGA	8924
rs142987386	snp	A/G/T	0.00993419	0.0697739	intron-variant	HERC2	GRCh38.p7	15:28199077	GCTTGAGCCTGGAAG[A/G/T]TGGAGGTTACAATGA	8924
rs143008158	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28165977	ACACAACTGATTCCT[A/G]TGTTGGAGCATAAAA	8924
rs143019486	snp	A/G	0.0103295	0.0711199	intron-variant	HERC2	GRCh38.p7	15:28306196	TTCAGTATGATACTA[A/G]CTGTGTGTCAGCTGT	8924
rs143054068	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28258441	CATGTCATTGCACTC[C/T]GGCCTGGGCAATAAG	8924
rs143067341	snp	A/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313009	CAAAGGCCACACAAC[A/T]CTGAGGCTGTGAGAG	8924
rs143077671	snp	C/G	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28269617	GGTAAGATGAAGCAA[C/G]TGAACAGGTTATTTT	8924
rs143089436	snp	A/C	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28113926	ATGCACACCCCAAGA[A/C]GCCACTCTCAGTACC	8924
rs143094546	snp	A/G	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28173527	AAACTGGTCTGCCAC[A/G]GTGGCTCCTGCCCAT	8924
rs143102919	snp	G/T	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28235824	ACCTCGCATGGTAAC[G/T]GCACCAGGCAACTGT	8924
rs143130515	snp	C/T	0.00253033	0.0354791	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28238168	CCGGGTGTCTTCAAA[C/T]TGCAAAGCAGCTTCC	8924
rs143153426	snp	C/T	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28287824	CGCCTCCTGGGTTCA[C/T]GCCATTCTCCTGCCT	8924
rs143184270	snp	A/G	0.0425829	0.139564	intron-variant	HERC2	GRCh38.p7	15:28156659	ATTTTAGGCTGAGAC[A/G]ATGGGGTTTTCTAGA	8924
rs143193197	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28289164	AAAAAACAGAGGTTG[C/T]CAGGGTGAATAAAGA	8924
rs143198833	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28170570	TCTTTTAGAGAAAAA[C/T]AGGAGACAGTCTTTA	8924
rs143204989	snp	A/G	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28228838	CATTCCTTCCATTTC[A/G]AATATAAAAGTTATG	8924
rs143209042	snp	A/C	0.000153988	0.00877328	missense	HERC2	GRCh38.p7	15:28113650	TTCCTTCCCGAACAG[A/C]AGCCACCTGCTCATC	8924
rs143218676	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313893	ACTGAGAAGCAAAAC[A/G]GAGCTTCTGAGAGAC	8924
rs143221795	in-del	-/GG			intron-variant	HERC2	GRCh38.p7	15:28242228	CTAGAGATGAGTGGC[-/GG]GGTGATGGCTATTAA	8924
rs143228339	snp	A/T	0.0193772	0.0965046	intron-variant	HERC2	GRCh38.p7	15:28292287	TAGACATTTCTCCAG[A/T]GAATGTATACAAATG	8924
rs143242604	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28242750	TCCAGAAACGGAAGG[C/T]TGAGTCAACATTTGA	8924
rs143247137	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28114445	CAGAGTAATAAATAC[C/T]GACCCTGATCACAAA	8924
rs143285731	snp	G/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28159248	AGGAGTATCTTTGTG[G/T]CATTCTCTGTACTTC	8924
rs143290070	snp	A/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28147506	TTAAAAATTAGCTGG[A/G]CACGGCCTATAGTCC	8924
rs143291915	snp	C/T	3.29799e-05	0.00406065	missense	HERC2	GRCh38.p7	15:28130561	GGGATCCGCATTCCA[C/T]TTTAACTACTCCAAG	8924
rs143324593	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28208973	AATGTCTTTCAATAG[C/T]AGGAGATCAAAAAAT	8924
rs143329606	snp	A/G	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28266866	CGTGCACTTGTCAAA[A/G]CCCATCCAACTCTAC	8924
rs143333992	snp	A/G	0.0667028	0.170006	intron-variant	HERC2	GRCh38.p7	15:28206630	CAAGGTCAGGATATC[A/G]AGACCATCCTGGGTA	8924
rs143349479	snp	G/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28282989	GACGGGACGGGACTG[G/T]ATGGGACGGGATGGG	8924
rs143358156	snp	C/T	9.88386e-05	0.00702919	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28237002	ACAGCGGTGTGCTCA[C/T]TGCCAAATACGAAGC	8924
rs143372480	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28185778	CAGATCAATGCTCCA[A/G]TGCAGACTCTCAAGG	8924
rs143388037	snp	A/C/G	0.00123626	0.0248317	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265869	GTACAGCTCCCCCTC[A/C/G]GCAGTGATGGCCGCA	8924
rs143429293	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28116113	CACAGAGCTTCCGAC[A/G]GTCCACCACCGTCAG	8924
rs143434952	in-del	-/C			intron-variant	HERC2	GRCh38.p7	15:28145332	GGTGGTGTACTACAC[-/C]TAAGATCTACAGGAT	8924
rs143456847	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28275777	GACAGAGCAAGACTC[C/T]ATCTCAAAAAAAATA	8924
rs143465745	snp	A/C	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28149003	CACACGGCTCCTAAC[A/C]GAGAACATCACCGAG	8924
rs143474180	snp	A/G	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28209827	TTGAATGGCACCATG[A/G]TATCACACTGTATGG	8924
rs143505356	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28146485	AGACAAGCATCTCAG[A/G]CTGACCACTCTTTCC	8924
rs143514317	snp	A/C	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28208159	ACTTTCAATTGATTT[A/C]TTTCATCCTCAGCAG	8924
rs143523248	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28279362	AAGCATCTAAACTAG[C/T]TGGGCATTAAACATT	8924
rs143530683	snp	A/T	3.33272e-05	0.00408197	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28245885	AGACGCCGTACCCAT[A/T]ATGCCAGGCCAGGCT	8924
rs143548700	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28222922	AGGGCAGTTAAGCTC[A/G]TCCTGTGTGGATCCT	8924
rs143552086	snp	C/G	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28188775	GTTCCAGCATACTTT[C/G]TATTTTTGTTTACAT	8924
rs143557450	snp	C/T	0.00287973	0.0378361	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28246821	GCTGGCGGCCACAGG[C/T]AGTATATCTCCAATG	8924
rs143576992	snp	C/T	0.000399281	0.0141238	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274306	CCCGTCACGACGGAC[C/T]TGAGGAACCTGGTCG	8924
rs143577354	snp	C/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28275706	GAGAATGGTGTGAAC[C/T]TGGGGGGTGCAGCTT	8924
rs143590945	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28219289	CTTTGGGATGAGGAG[A/G]TGTGTGGCAAATGAG	8924
rs143619308	snp	C/T	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28277825	TACAACATGTACAGT[C/T]GTCCCTTGGTATCTG	8924
rs143635277	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28123586	TCTCTACACATTCAG[A/G]CACGGACCTTCGAGG	8924
rs143639066	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28178759	CCTAGAGATTTACAT[C/T]ATCCAATTTTTATTC	8924
rs143646022	snp	A/C	0.00517822	0.0506191	intron-variant	HERC2	GRCh38.p7	15:28302909	ATTCTGGTTATTAAT[A/C]CTTTGTCAGATGGGT	8924
rs143657629	snp	A/C	0.0402882	0.136092	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28215134	CACCTGCCTCGGCCT[A/C]CCAAAGTGCTGGGAT	8924
rs143659671	snp	C/T	0.0205511	0.0992634	intron-variant	HERC2	GRCh38.p7	15:28310248	CTCAGGAGTACAAGA[C/T]CAGCCTGAACAACAT	8924
rs143704278	snp	C/T	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28136777	CCAAAGCTGAAAATA[C/T]CATTGTGCCCTTTAC	8924
rs143706639	snp	A/C/G	0.000297133	0.0121858	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28192030	GGATGCCTGGTTCAC[A/C/G]GAGGACGACACATTC	8924
rs143710331	snp	A/G	4.97896e-05	0.00498922	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233538	CAAGTGCACCTGCAT[A/G]AACTAAAGATAATGC	8924
rs143740086	snp	A/G	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28134941	GCTTCCCAAAGTGCT[A/G]GGATTACAGGCGTGA	8924
rs143746586	snp	A/G	8.24817e-05	0.00642137	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28196545	GGAAAGTCGACAATG[A/G]TATCTTTTCCATTGG	8924
rs143748011	snp	C/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28188945	ATACAAAAATTAGCT[C/G]GGTGAGGTGGTGGGC	8924
rs143768975	snp	C/T	0.046775	0.145601	intron-variant	HERC2	GRCh38.p7	15:28307734	TTTTTAACTTTTATA[C/T]GGCAAAAGAGGAATC	8924
rs143785919	snp	C/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28172290	GCTCATTTTAAGTTA[C/T]ATGGAAATGCAAAGG	8924
rs143785979	snp	A/G	0.0178098	0.0926698	intron-variant	HERC2	GRCh38.p7	15:28209579	CGATCTCCTGACCTC[A/G]TGATCTGCCCGCCTT	8924
rs143832423	snp	A/G	1.64757e-05	0.00287012	synonymous-codon	HERC2	GRCh38.p7	15:28143894	TCTTGTTTCCCCATC[A/G]TTTTCTCCAAGCAGC	8924
rs143873550	snp	C/T	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28160574	GCCATTTGCTAAGAC[C/T]GTTGGAAAAGCACAG	8924
rs143874388	snp	A/G	3.29891e-05	0.00406122	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28268491	ATGGCCCAGCCGTCC[A/G]CCGTCCCCACAGCCC	8924
rs143878740	snp	C/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28137641	CGATAAATGTGTATG[C/T]TCTGATTGCTCCGCC	8924
rs143881631	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28244289	TATGGCAATAAAAAT[G/T]AAAGAACTCAATAAC	8924
rs143907789	snp	G/T	0.0988009	0.199095	intron-variant	HERC2	GRCh38.p7	15:28206766	TGAACCTGGGAGGCG[G/T]AGCTTGCAGTGAGCT	8924
rs143912271	snp	A/G	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28264905	GACAAGGTCTGTCCC[A/G]TCAATGGCAGCAGGA	8924
rs143915369	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28289893	TCTGAGAGGAAGACA[C/T]ACCTCAGTGAGAGGA	8924
rs143948512	snp	C/G	1.65526e-05	0.00287681	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28257079	AAGTCGTAGAAGATT[C/G]AGCGTTGCCACGGCC	8924
rs143956101	snp	C/T	0.00018123	0.00951745	synonymous-codon	HERC2	GRCh38.p7	15:28135621	AATGGATTCAAGCAA[C/T]GTTGGGGTGGACACC	8924
rs143963667	snp	A/G	0.000329935	0.0128397	missense	HERC2	GRCh38.p7	15:28144772	CATCCCCTGGGATGC[A/G]CAGCTCGCTGGACCA	8924
rs143985555	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28291233	ATTAACCCCAAATAC[A/G]AATTTTTTTTTAAGA	8924
rs143995167	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28128089	CACAACCCGAATCTA[C/T]GCAGAAACATCGCAA	8924
rs144004939	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28271400	GGGCATGGTGGCTCA[C/T]GCCTGTAATCCCAGC	8924
rs144012187	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28272483	CTGGATAGAAGTGAA[C/G]AAATACTTGGGATTT	8924
rs144017712	snp	C/G	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28209762	ATAACTGGGGGTCTT[C/G]GAACTCATCCCCATG	8924
rs144018228	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28289258	TGAAAAAAGCTAAAC[C/T]TGGCAAACACACCAC	8924
rs144023617	in-del	-/AC			intron-variant	HERC2	GRCh38.p7	15:28245681	CACACACATACATAA[-/AC]ACACATATATTTGGT	8924
rs144040698	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28208657	ATCGACAAACCCTGA[A/G]CTCCAAGCAATGCAG	8924
rs144052444	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28269743	CAGGGTCACCATTTT[A/G]TGCTTTAGCAGGCAA	8924
rs144068123	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174251	AATCGCATGAGAGCA[C/T]ACCATAATTCTTCTG	8924
rs144098545	snp	C/T	0.00012744	0.00798146	intron-variant	HERC2	GRCh38.p7	15:28114851	CTCACGGCTCATCTC[C/T]ATCCCAGACTCCAGT	8924
rs144110009	snp	C/G	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28173661	AACAAAAATTAGCCA[C/G]GCATGGTGACATGTG	8924
rs144135464	snp	A/G	0.000153988	0.00877328	synonymous-codon	HERC2	GRCh38.p7	15:28132184	CCAGACAGTGTCGTC[A/G]TCTGTGAGGCAGAGG	8924
rs144159781	snp	A/G	0.000267438	0.0115606	intron-variant	HERC2	GRCh38.p7	15:28116998	CAGGTGCTCCAGCAC[A/G]TGGCAAGTTCTCACC	8924
rs144205240	snp	C/T	0.0444908	0.142359	intron-variant	HERC2	GRCh38.p7	15:28250308	CGGCAAGGATGCGCC[C/T]TCACTGGGCTCACCA	8924
rs144218321	snp	C/T	0.000280008	0.011829	missense	HERC2	GRCh38.p7	15:28111873	CTCCTGTAAGTGCGA[C/T]GCGAGCGTAGTCATC	8924
rs144239940	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28286462	AGTGGGTTCAACAGT[C/G]AAAAATCAATGTAAC	8924
rs144247777	snp	A/G	0.0142736	0.0832652	intron-variant	HERC2	GRCh38.p7	15:28278074	CAGCCCGGGCAACAT[A/G]GCAAAACCCAATCTA	8924
rs144252804	snp	C/G	0.0256215	0.110247	intron-variant	HERC2	GRCh38.p7	15:28153644	CGACAGAGAGAGACT[C/G]TGTCTCGAAAAAAGA	8924
rs144291917	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28150742	ACCGAGAACATCACC[A/G]AGAATGGCCACACGA	8924
rs144315891	in-del	-/A	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28282063	AGTGGGTGAGAAAAT[-/A]CACAAACCATGGACA	8924
rs144332072	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28186047	CACTCAAAAATTACA[A/G]GACTGAAGACTAATC	8924
rs144338429	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28244359	TTCCACTTATATGAA[A/G]TCCGAGAACAGACAG	8924
rs144395500	snp	A/C/G	3.29904e-05	0.00406132	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28228358	ATGGTCCCCAGGCTC[A/C/G]GTCCTGACGGGTTCT	8924
rs144400285	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28284495	AACTATATGTTGTCC[A/G]TAAGAAAGTGACTTC	8924
rs144412623	snp	C/G	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28276602	TAGCCGGGTGTGGTG[C/G]TGCATGCCTATAGTC	8924
rs144413909	snp	G/T	9.89789e-05	0.00703418	intron-variant	HERC2	GRCh38.p7	15:28201561	ACCAGTAGACTGCAA[G/T]AAATAAATACATTCA	8924
rs144426894	snp	A/C	6.6189e-05	0.0057524	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28179203	AGCTGACAGTGTCTC[A/C]GAGAACGAAGGAACC	8924
rs144441666	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28287242	AAAAAACAGAAAAAG[A/T]AATGAAAGGAATAGG	8924
rs144448409	snp	C/T	0.00333882	0.0407218	intron-variant	HERC2	GRCh38.p7	15:28135733	CATCAGTTTTTAATC[C/T]CAATATCCCCTAAAT	8924
rs144486937	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28130792	GTGACTGACAGCACA[C/T]CCGTTGGCACACTGT	8924
rs144493203	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28161748	ACAAAGTCCTACAGA[C/T]CCAGTGCTACCAAAT	8924
rs144496043	snp	C/T	0.000266307	0.0115361	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274948	AAAGGCAAAAGACAG[C/T]GCCGCTCGGGATCCC	8924
rs144499198	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28222499	CCCCAAAAAAGCAAA[A/G]TAACTAAGTTAGAAA	8924
rs144504965	snp	C/T	1.66471e-05	0.00288501	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28238140	GGCCAACACAAAACG[C/T]GTGCATGGATTCCCG	8924
rs144517461	snp	C/T	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28225472	GGGAGCTGAGGTGGG[C/T]GGATCGCGAGGTCAA	8924
rs144522189	in-del	-/AAATTA			intron-variant	HERC2	GRCh38.p7	15:28173867	GATCTCTAGTGACAG[-/AAATTA]AATTGGTGCATACGG	8924
rs144534723	snp	G/T	0.0256215	0.110247	intron-variant	HERC2	GRCh38.p7	15:28158535	TGGTTTAAAGTCCGT[G/T]TTATCAGAGACTAGG	8924
rs144539287	snp	C/G	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28218807	CAGTTTTAGGTTCAC[C/G]CAAAATTGAAAGTAC	8924
rs144548621	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28308450	CTAATCATTTTCTTG[C/T]GGAGTCTTTAGGTTT	8924
rs144571647	snp	A/G	0.0115144	0.0749975	intron-variant	HERC2	GRCh38.p7	15:28144532	GTTCCACGCCTCAGC[A/G]GGGCCTGTGAGAGCA	8924
rs144576032	snp	C/G	0.077417	0.180873	intron-variant	HERC2	GRCh38.p7	15:28205099	AAACCAAAGATAATA[C/G]AAAATACGAAAAGCA	8924
rs144665653	snp	C/G	1.67638e-05	0.0028951	intron-variant	HERC2	GRCh38.p7	15:28143001	AATCCAGGTGCCGGG[C/G]AGGCTGACCATTTGT	8924
rs144669539	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28264731	AGCTTAGACCTTACA[A/G]AACTTTTAACCGGGA	8924
rs144692976	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28272713	GTTCCCAGGCTAGAA[A/C]ACTGAGCATAAAACA	8924
rs144701799	snp	A/G	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28140882	AGAAATACATCTAAC[A/G]AGTGATGTGCAAATA	8924
rs144714842	snp	C/T	0.0162398	0.0886349	intron-variant	HERC2	GRCh38.p7	15:28235441	AGGGAAGGAAGCAGA[C/T]ACCTCAGAGGGCACC	8924
rs144739988	snp	A/T	0.0821764	0.185298	intron-variant	HERC2	GRCh38.p7	15:28172812	GATTCACCTGTGAAG[A/T]GAATAAAATGACAAG	8924
rs144750809	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28306466	TGTGTTGTTGAATTC[A/G]GTTTGCTGGTATTTT	8924
rs144750946	snp	A/C	0.00172585	0.0293249	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28228240	GCGCAGTGCCGTCTG[A/C]GTGAGGGCCAGCATG	8924
rs144751758	snp	A/G	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28116049	CCCGAGGCAGTCTCC[A/G]GTCCTCAGCACGTGG	8924
rs144752287	snp	C/T	0.0123036	0.0774623	intron-variant	HERC2	GRCh38.p7	15:28233041	AGCAGGTAGAAATGT[C/T]ACATGGAATCAACAG	8924
rs144753096	snp	C/T	0.0225045	0.103662	intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28320177	TGGAGTGCAATGGCA[C/T]GATCTTGACCCATTG	8924
rs144755113	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28243040	CTCCACAATGCACTA[C/T]AGGTCCTAGCAAGTG	8924
rs144780847	snp	G/T	5.29684e-05	0.00514601	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28218606	GACAAAGAGTCTGCA[G/T]TAAGTTAATAGTGCT	8924
rs144785028	snp	C/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28183152	CTTCCCAGAGGGCTT[C/G]CTCCTTCCACCTTGC	8924
rs144787505	snp	C/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28140184	AGAAGGAAACATGCC[C/T]AATCTGATCAAGGGC	8924
rs144798127	snp	A/G	0.000883488	0.0209991	intron-variant	HERC2	GRCh38.p7	15:28274884	GGGAAGCAGAACAAC[A/G]CGCCACACCAGGGAC	8924
rs144844220	snp	A/T	0.000153988	0.00877328	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229220	AAATTTGGCACTGGC[A/T]TCCATCAAAACATTT	8924
rs144844826	snp	C/T	3.32425e-05	0.00407678	missense	HERC2	GRCh38.p7	15:28116704	GCACGGGTGCTCTGG[C/T]GGCCGGGCTGAGCAG	8924
rs144845979	in-del	-/ATACACACACACACAC			intron-variant	HERC2	GRCh38.p7	15:28245565	AAAAAAAAAAAATAT[-/ATACACACACACACAC]ACACACACACACACA	8924
rs144854380	snp	A/G	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28273177	AGAGATTATAAGTGT[A/G]CAATTAGCTTACACA	8924
rs144859954	snp	C/T	0.0252325	0.109451	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28301339	AGAATAGCCTGAACC[C/T]AGGAGGCCAAGGTTG	8924
rs144864205	snp	A/G	0.0142736	0.0832652	intron-variant	HERC2	GRCh38.p7	15:28231486	ATGGGCACTGCCTGC[A/G]TATGTGACTGGCCCC	8924
rs144893913	snp	C/G	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28287535	CTAGGTGAGGGGAAA[C/G]AAGGAGAAAGGCAAA	8924
rs144912188	snp	A/G	0.000199243	0.00997907	missense	HERC2	GRCh38.p7	15:28113577	GGTCGGCATACCATC[A/G]TCTCCAGTTCGTAGC	8924
rs144924451	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28208710	GACTCGCCACTTTCA[C/T]TCCTCTCCTCCTGGT	8924
rs144935873	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28132907	ATTAAATACCTCTCA[A/G]TCTACACCTTCCTAA	8924
rs144946505	snp	C/T	0.0535932	0.154675	intron-variant	HERC2	GRCh38.p7	15:28289340	AACAAAGAATGTCAC[C/T]GGAGATAAAGGGGGT	8924
rs144974679	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316755	TATCAAGATACTCAT[A/G]TTTATACTTTTTTTA	8924
rs145007566	snp	A/G	0.0364509	0.129988	intron-variant	HERC2	GRCh38.p7	15:28169169	AGGGGATGCTAAGTC[A/G]TCTTAGACATCACTA	8924
rs145043009	snp	A/C/T	0.000643628	0.0179278	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28270722	CGGAGAGCTACACAG[A/C/T]GGAGGCATACAGGGC	8924
rs145048438	snp	A/C	0.00755907	0.0610114	intron-variant	HERC2	GRCh38.p7	15:28127532	GTATTGTTTACATTA[A/C]TATTCCCTGGCTTTG	8924
rs145050992	snp	C/T	0.0103295	0.0711199	intron-variant	HERC2	GRCh38.p7	15:28261401	CTGATATTTAAAACA[C/T]TGTTTCTATTTAAAC	8924
rs145071428	in-del	-/CA	0.430732	0.172731	intron-variant	HERC2	GRCh38.p7	15:28147644	AGCTTTTCTGAATCT[-/CA]CACCTCATTCTAAAA	8924
rs145076740	snp	C/G/T	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28129326	CCCACAGGAGCCACA[C/G/T]AGGACGAGCTTAACT	8924
rs145096796	snp	A/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28230754	AGCTCTTCCTCAAGT[A/G]CCAGAGAGTGAACAT	8924
rs145115376	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28125328	AGTTGTCAACTTTAC[A/G]TATGACCTAGACATG	8924
rs145116712	in-del	-/AAG	0.00856621	0.0648824	intron-variant	HERC2	GRCh38.p7	15:28167668	CACAATACAAAGTTA[-/AAG]AAGAACGCCTCTTCA	8924
rs145116746	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28263804	TGGGAGGCCAAGGCG[A/G]GCGGATCACTTGAGC	8924
rs145118418	snp	A/G	0.000275962	0.0117433	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28230386	GGTGATTTAATTGCA[A/G]TGGGTCTCTTGTCCA	8924
rs145124534	snp	A/T	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28278528	TTCCAATATTTTCGA[A/T]CCATAGTTGGTTGAA	8924
rs145124816	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28120938	AAACACAAGCAGCCC[C/T]ACAGGACCCTATTCC	8924
rs145160340	snp	C/T	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28216964	GCACTCACACCTATA[C/T]TGTTATAACCTCCCA	8924
rs145190727	snp	C/T	0.000314052	0.0125271	synonymous-codon	HERC2	GRCh38.p7	15:28169645	AGAAGAATCAGCATC[C/T]GAAGGCACGCCTATA	8924
rs145192492	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28242514	CTTCTTCCTGAATTA[C/T]AGCTTCTTTATTAGT	8924
rs145193373	snp	C/T	0.000601815	0.0173362	synonymous-codon	HERC2	GRCh38.p7	15:28113122	GGTCCTGGGCAGCCT[C/T]GTCCGGCCCCAGACG	8924
rs145199355	snp	G/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28173483	GTATATGCTGTATGA[G/T]TCTATTTATAGTAAG	8924
rs145199873	snp	C/G	0.00478752	0.0486913	intron-variant	HERC2	GRCh38.p7	15:28138106	AGAAGGCTGCTGAAG[C/G]AAAGTCTGAAGGTAA	8924
rs145200204	snp	A/C	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28228521	TTTGAAACCCACTGA[A/C]ATTTCTTCTGCATGG	8924
rs145221325	snp	C/T	0.0236746	0.106192	intron-variant	HERC2	GRCh38.p7	15:28308607	TAACAGTGGCCACAC[C/T]GAGCATCCTTGTCAT	8924
rs145223332	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28228064	AATGTATTTGATACC[A/G]CTGAATTGTGACGTT	8924
rs145255977	snp	A/G	0.000578211	0.0169933	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28175617	TTTCCGCACGTGCAC[A/G]TCAGAGCCGTGGCCC	8924
rs145261792	snp	A/G	0.00036254	0.0134588	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28246812	AGAAGCAATGCTGGC[A/G]GCCACAGGCAGTATA	8924
rs145270847	snp	C/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28307288	TTAGCCTGCCTGAAG[C/G]CTTGTCAATTTATCT	8924
rs145281467	snp	A/G	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28281701	ATAGTTATTTAAAAC[A/G]ACATGAAGAATACTG	8924
rs145306715	snp	C/T	0.143622	0.226238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316580	TTTGAAAACAAAAAT[C/T]GTTCTATTGAGGCAC	8924
rs145326839	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28154836	TTTGTTACATATGTA[C/T]ACATGTGCCATGTTG	8924
rs145346452	snp	A/G	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28171057	GCCATTCTGGAAAAC[A/G]GCTTGGCAGTTTCTT	8924
rs145357309	snp	G/T	0.000148673	0.00862058	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28299433	CTCTCCGTTCTGGGT[G/T]GATTCTGTTCCAGTG	8924
rs145370046	snp	C/G	0.00714142	0.0593271	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28211013	ACACCTGTGTGAACA[C/G]TTCCAGTCTCCTGAA	8924
rs145385813	snp	C/T	0.00716266	0.059414	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111368	CACAGTTATTTCCAA[C/T]ATACAATCAAGACGA	8924
rs145392874	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28262265	TCATAGTTTTGATGG[C/T]CCCCACCCCAACTTC	8924
rs145413211	snp	A/G	0.000153988	0.00877328	missense	HERC2	GRCh38.p7	15:28114720	CTTGGCACTGTGAAG[A/G]GCAGGCTCATGGCTT	8924
rs145429679	snp	C/T	0.00835141	0.0640778	intron-variant	HERC2	GRCh38.p7	15:28295483	CCTCCCAGGTTCAAG[C/T]GATTCTCCCAAGTTC	8924
rs145436238	snp	C/T	0.000182808	0.00955879	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272241	CCTCGGAGTGGGGTG[C/T]ATCCTTCCTGCAAAT	8924
rs145438661	snp	C/T	0.00183124	0.0302038	synonymous-codon	HERC2	GRCh38.p7	15:28168425	TCTCTTTTCTTGCCA[C/T]GGATTTGGACTCAGT	8924
rs145457557	snp	C/T	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28266151	CTAACACCTCCATGA[C/T]TTTTTGTTCAGTTGG	8924
rs145472930	snp	C/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28163620	GGAATGAAGCTGCAT[C/T]CTGTATAATCTACCC	8924
rs145475397	snp	A/G	0.0103295	0.0711199	intron-variant	HERC2	GRCh38.p7	15:28204018	GCTAAGGGCAAATAC[A/G]AAATCATTAGAAAGC	8924
rs145481625	snp	G/T	6.67947e-05	0.00577866	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28220605	ATCCGTCCTCTCCCA[G/T]CTCACCAATCACGCG	8924
rs145504068	snp	G/T	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28150884	TCCAGAAAAACTACC[G/T]TTCAAATTTGAAGGA	8924
rs145512084	snp	A/T	0.00218925	0.0330126	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28237063	CTCTGTGTCTATCAG[A/T]GGTGAAGAGAGACTC	8924
rs145517892	snp	C/T	0.0509478	0.151255	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214522	CACAGGGAAGGGAGA[C/T]GGCCACCCACCTCTG	8924
rs145533055	snp	A/G	0.00835141	0.0640778	intron-variant	HERC2	GRCh38.p7	15:28118122	AATGAACTTGTCTGC[A/G]TGCCACACACACGGC	8924
rs145535698	snp	C/T	0.000230597	0.0107352	missense	HERC2	GRCh38.p7	15:28130208	AGCCAGTGGCGATGG[C/T]GATGACTTTCTTCCC	8924
rs145556849	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28244434	ATCAGAAGTAAGGTG[A/G]CGATGACCACACAGC	8924
rs145571215	snp	A/G	0.000230639	0.0107362	synonymous-codon	HERC2	GRCh38.p7	15:28141757	CTGCACAAGTTGTTC[A/G]TCTTGCTCTCTTTTA	8924
rs145594989	snp	A/G	0.006278	0.0556739	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28234279	AGATGGATGACTGAA[A/G]CCATTCTGGAAAATG	8924
rs145604050	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28272442	ACTTCTTTTCTTCAC[A/G]GTTGATCAAAAATAA	8924
rs145653832	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28303216	CTAGTTTCATTTTTC[C/T]GCATATGGGTGTCCC	8924
rs145664364	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28149015	AACCGAGAACATCAC[C/T]GAGAACGGCCGCACA	8924
rs145690303	snp	C/T	0.0418186	0.138422	intron-variant	HERC2	GRCh38.p7	15:28293933	AACTAACCTTAACCT[C/T]GAAGTGTAAACACGT	8924
rs145714900	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28163008	CACAAGATCACCGGT[A/G]ATCCATAGCAGCTCT	8924
rs145720174	snp	A/G	0.0607341	0.163335	intron-variant	HERC2	GRCh38.p7	15:28223085	CCAACCATCAAACCT[A/G]GGGGTGGTCTTGGAG	8924
rs145724005	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28245751	GATTATCTCCATTTT[C/T]TACTTATACTACCAT	8924
rs145730767	snp	A/G	0.000642287	0.017909	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213853	TTCTCCAAACTCATC[A/G]TGCATAACTTGACCG	8924
rs145735763	snp	G/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28246189	GTCCTTTAGCATATT[G/T]CTAAAGAATTATCTT	8924
rs145739307	snp	A/C	0.0103295	0.0711199	intron-variant	HERC2	GRCh38.p7	15:28256472	ACTAAAAAAACTCTT[A/C]CCCACAATAGTTGAG	8924
rs145747085	snp	C/T	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28276002	GACCAGCCTGGCCAA[C/T]ATGACGAAACCCTGT	8924
rs145747102	snp	A/G	0.0260105	0.111035	intron-variant	HERC2	GRCh38.p7	15:28307444	CTTTTCTAGTTCTTT[A/G]AGATGTATCATTAGG	8924
rs145759817	snp	A/G	0.000395837	0.0140628	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28177024	GGCCCCAGGTGTACA[A/G]TTCTCCGCTGGATGT	8924
rs145772629	in-del	-/A	0.159951	0.233219	intron-variant	HERC2	GRCh38.p7	15:28180670	AGTGAAAAATAAAAT[-/A]ACAGTTGGTCCTCTG	8924
rs145776637	snp	C/T	0.0103295	0.0711199			GRCh38.p7	15:28258207	GGGCGCAGTGGCTCA[C/T]GCCTGTAATCCAAAC	8924
rs145776845	snp	C/T	0.0228947	0.104514			GRCh38.p7	15:28286085	GAACTCACTGGATAA[C/T]TCCATCAAACATTAA	8924
rs145795772	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28291730	CTCCTATAACCCAAA[A/G]CAAAAACCTCAATTA	8924
rs145801935	snp	G/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28186066	TGAAGACTAATCATA[G/T]GGAAATTCTAGCGAT	8924
rs145826647	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28280743	AACCCCTTCTCTACT[-/A]AAAAAAAAATACAAA	8924
rs145855928	snp	C/T	0.000200538	0.0100114	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28220591	CTGGACTCTTATCCA[C/T]CCGTCCTCTCCCAGC	8924
rs145883454	snp	G/T	0.000699662	0.0186907	missense, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28292993	CATTCAGATCTTCTT[G/T]CTTTGTTCCACTTGG	8924
rs145904322	snp	C/T	0.021333	0.101051	intron-variant	HERC2	GRCh38.p7	15:28303991	GCCCATGTGGTGAAA[C/T]CCTGTCTCTACTAAA	8924
rs145939887	snp	A/G	0.0119091	0.0762411	intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28315604	TCAAGACCAGCCTGG[A/G]CAACATGGTGAAACC	8924
rs145945796	snp	C/G	0.189576	0.242588	intron-variant	HERC2	GRCh38.p7	15:28224168	ACACACACACACACA[C/G]AGAGAGAGAGAAACA	8924
rs146002368	snp	A/G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28180987	AAATCCACGGATACT[A/G/T]AGGGATGACTATGCA	8924
rs146004481	snp	A/G	0.0295035	0.117819	intron-variant	HERC2	GRCh38.p7	15:28240235	CATCCTGGCTAACAC[A/G]GTGAAACCCCATCTC	8924
rs146044137	snp	C/T	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28175352	AGGCAGATACACCAG[C/T]GGGCAAAAGGAACAG	8924
rs146056234	snp	A/G	0.000399281	0.0141238	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256221	CCGCACTGCTGGCCA[A/G]GGTCACCACCGTCTG	8924
rs146061268	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28306203	TGATACTAGCTGTGT[A/G]TCAGCTGTATATGGC	8924
rs146069329	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28282276	CGCCTAACAACATGT[C/T]CTATTGAGAAAGTCA	8924
rs146090836	snp	A/G	0.000659547	0.0181477	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28202233	GTCCAGCAGCCACCC[A/G]ACCAAGGCTTCCACA	8924
rs146099155	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28124321	GGATTCTGAAAACAA[C/T]TGTTTCAAATACAGA	8924
rs146102419	snp	C/T	0.00874735	0.0655527	intron-variant	HERC2	GRCh38.p7	15:28179713	AGGACAGCTAGCTCC[C/T]TTGTGGGGGTGAAAG	8924
rs146124179	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28167568	AAGATGCTAACAAGT[A/G]GACAGCCGAGGTGAA	8924
rs146138275	snp	A/C	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28258525	AACAATTCTCAAGAG[A/C]AATTATAAAATATTT	8924
rs146149348	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28196109	CACTCTACAGAATTA[C/T]TGTATACATAGGAAC	8924
rs146159039	snp	C/G/T	0.00013179	0.0081166	synonymous-codon, missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28201512	TCAAGAAATCAGCTC[C/G/T]TTTTTTGTACGTCTG	8924
rs146165102	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28307860	CGAAAATGAGTTCAC[C/T]GTAGATGTGCGGATT	8924
rs146178395	snp	C/T	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28240382	GAGATCACGTCACTA[C/T]ACTCCCGCCTGGGCG	8924
rs146190898	in-del	-/AA	0.0372196	0.131242	intron-variant	HERC2	GRCh38.p7	15:28243589	GAATTGGCACTTCAC[-/AA]AAGAGAATTTCCAAC	8924
rs146191030	snp	A/C	1.65157e-05	0.0028736	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28268568	CATCAGAATGGGCAG[A/C]AATTTTTACAATGTT	8924
rs146210350	snp	C/G	6.59055e-05	0.00574007	synonymous-codon	HERC2	GRCh38.p7	15:28144695	TGGCATGATGGGATA[C/G]ACGGTGAAGCGCCAG	8924
rs146210640	snp	A/G	5.0166e-05	0.00500804	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274294	GAAAGAACTCACCCC[A/G]TCACGACGGACCTGA	8924
rs146213654	snp	A/G/T	0.00014832	0.0086105	synonymous-codon	HERC2	GRCh38.p7	15:28168449	ACTCAGTCTGTCTTC[A/G/T]ATATCAACAGCCAGC	8924
rs146224816	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28165673	TTAGCCAGGTATGGT[A/G]GTGCATGCTTGTAGT	8924
rs146229042	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28193126	TAAATACAATGTCCA[A/G]TACATAATGACACAT	8924
rs146233668	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28120135	CAAACTGAAGCCATC[A/G]TCCAAGGTAGGGAAA	8924
rs146246766	snp	A/G	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28211972	AAACTCAGGAGAGCC[A/G]CATTCTACAACCGAA	8924
rs146303265	snp	A/G	0.00121837	0.0246516	missense	HERC2	GRCh38.p7	15:28167781	GAGGCTGAGGGGGCC[A/G]ACGGAGTCACTGCAG	8924
rs146304086	snp	A/G	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28281027	ATGTTACAAAACCAA[A/G]TTCAATATAAAAACG	8924
rs146329700	snp	A/C/T	3.30078e-05	0.00406239	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28228287	GGTCGAGGTTGTTTG[A/C/T]GCCGTGCTGCAGGGT	8924
rs146332822	snp	C/T			synonymous-codon	HERC2	GRCh38.p7	15:28111796	ATCTTGTGTAGAGTC[C/T]GAAGCAAAGGAGTCG	8924
rs146342296	snp	A/G	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28149929	AACAGCCACACGAAC[A/G]CACATTCTAGTAAAA	8924
rs146366728	snp	C/T	0.000814705	0.0201665	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28198757	CTCGGCAGCATCTAA[C/T]CATCATTCCCACCTA	8924
rs146369890	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28255591	TATCCTGGCTGCAAG[G/T]GCCAAGGGCACAGGG	8924
rs146380611	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28252851	TTTCAAAATTTCACT[A/G]TGCGTCTACTAAGTT	8924
rs146406729	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28194807	ATGCATGTAACCCCA[A/G]CACTTTGGGAGACTG	8924
rs146406865	snp	A/G	0.0126979	0.078662	intron-variant	HERC2	GRCh38.p7	15:28283388	AAACCATGGAGCCCA[A/G]CTGAAAGTACAAAAT	8924
rs146412689	snp	C/T	0.0134861	0.0810011	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313737	AACAGGTTCCTAGAA[C/T]AATTAGAAAGGTCAG	8924
rs146414784	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28271715	AATTAAACCAAAGCA[A/C]GATATTGGAATGCCT	8924
rs146428168	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28173486	TATGCTGTATGATTC[C/T]ATTTATAGTAAGCTG	8924
rs146443288	snp	C/T	0.00517822	0.0506191	intron-variant	HERC2	GRCh38.p7	15:28266481	GATCGCCCCATTGCA[C/T]TCCACCTTGGGTAAC	8924
rs146468308	in-del	-/G	0.157311	0.232183	intron-variant	HERC2	GRCh38.p7	15:28277479	AAAAAAAAAAAAAAA[-/G]GGGCTTTTTTAAAAT	8924
rs146474931	snp	C/T	0.00636936	0.0560724	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299659	TTACTGAATTAGTGA[C/T]TTAATCATTTTACAT	8924
rs146478729	in-del	-/CT			intron-variant	HERC2	GRCh38.p7	15:28132049	GGGGCCCTGGGGGCC[-/CT]CGACTGCGGTGAGCT	8924
rs146504253	snp	A/G	0.000625819	0.0176782	synonymous-codon, downstream-variant-500B	HERC2	GRCh38.p7	15:28174447	GAAGAGGACGGGCTC[A/G]TGGACAGAGGGCGTG	8924
rs146521940	snp	A/G	1.64928e-05	0.00287161	synonymous-codon	HERC2	GRCh38.p7	15:28146247	CTTACCTGACCGCAC[A/G]GAGACGATCCTGTTG	8924
rs146529814	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28144469	TCCACACCAGGTGAG[A/G]AGGAGTGTGAGCCTG	8924
rs146536754	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28301831	TTTTGAGACGGATCT[C/T]GTTCTGGCACTAAGC	8924
rs146541207	snp	C/T	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28158560	ACTAGGATTGCAACT[C/T]CTGCCTTTTTTTGTT	8924
rs146550637	snp	C/T	0.0263992	0.111815	intron-variant	HERC2	GRCh38.p7	15:28155836	ACATGAAGTCCTTGC[C/T]CATACCTATGTCCTG	8924
rs146554193	snp	C/T	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28253377	GAGGCAATGATAGAA[C/T]CAGTTTTAAAAATAA	8924
rs146558015	snp	C/G	0.000941798	0.0216798	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28192070	ACCATGCGGGACCAG[C/G]TGTCCAGCAGCATGC	8924
rs146600895	snp	C/T	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28138660	GAGCTCTGATGAACA[C/T]GTACAAAGAGATTAA	8924
rs146607491	snp	A/C	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28135802	TTACCACATAGAAAT[A/C]AAATTTAAAGTTAAA	8924
rs146646815	snp	C/T	5.06958e-05	0.00503441	missense	HERC2	GRCh38.p7	15:28132102	GAATGGGAAATACCT[C/T]CATAGGCACTTTACA	8924
rs146655174	snp	A/T	0.0505692	0.150756	intron-variant	HERC2	GRCh38.p7	15:28289195	AGCAAGACCTAATTA[A/T]ATGATACCTGAAAGA	8924
rs146658589	snp	A/T	0.0341408	0.126114	intron-variant	HERC2	GRCh38.p7	15:28146554	AAGGCCAGAAAACAC[A/T]TCCACTTGGCCAATT	8924
rs146661344	snp	C/T	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28208269	CATATTTTTTTCAAA[C/T]GCACCACTCACTATT	8924
rs146672468	snp	C/T	0.00835141	0.0640778	intron-variant	HERC2	GRCh38.p7	15:28205106	AGATAATAGAAAATA[C/T]GAAAAGCAACCACAG	8924
rs146673561	snp	A/G	0.00116912	0.0241494	synonymous-codon	HERC2	GRCh38.p7	15:28141459	CGTCACAGCAAAGAG[A/G]GTCTGTTCCCCTCCG	8924
rs146692741	in-del	-/CCC	0.024191	0.107286	intron-variant	HERC2	GRCh38.p7	15:28175464	TCATGACCCCCACGT[-/CCC]CCAAGTCAGGATGGC	8924
rs146693131	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28276192	CTCCATCTCAAAAAA[A/C]AAAAAAAAAAAAAAA	8924
rs146727015	snp	A/C	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28116280	GTGCAATGGTACGAT[A/C]TCAGCTCACTGCAAC	8924
rs146741301	snp	C/T	1.65839e-05	0.00287953	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28246053	AGAAACTACTAGTTC[C/T]GGAAGGAGAACACCT	8924
rs146760133	snp	A/G	0.00136638	0.0261021	synonymous-codon	HERC2	GRCh38.p7	15:28125129	CAACCGAGGCCTCTG[A/G]ATGGCATTGGTGGTT	8924
rs146769359	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28112308	TGTGGATGCGGGGCG[A/G]CCTGGCTGGCGGAGG	8924
rs146777193	snp	A/G	0.000380282	0.0137839	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28238681	AATCACAGTCCAGAA[A/G]CCTCCATCTTTATTA	8924
rs146778562	snp	C/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28277866	GTACCAGGCTTGCCC[C/G]ACCCTGGCTCCATAC	8924
rs146793547	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28187721	CCAATATGCTACAGT[A/G]ATCAAACTTTTCTGA	8924
rs146803901	snp	A/G	0.00993419	0.0697739	intron-variant	HERC2	GRCh38.p7	15:28219375	AGGCCCCAGGCAGGG[A/G]GCCAGGCCTGCTTCC	8924
rs146814399	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28303179	TTTGATGTGATTTTC[A/G]TATATGGTGAGAGAT	8924
rs146826633	snp	C/T	0.000400695	0.0141487	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274353	CAGCCACACAGAGGA[C/T]ACGGTGCTCTCGTCA	8924
rs146834211	snp	C/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28311996	GGTAGCACTGGGAAG[C/G]AAGAGGATAGGCCAG	8924
rs146849552	snp	C/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28158357	AGTCTCCCATTATTA[C/T]TGTGTGGGAGTCGAA	8924
rs146864624	snp	A/G	0.00130344	0.0254955	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28196288	CGTTTCACAAAAATC[A/G]AAGTCATCACAGTTT	8924
rs146883683	snp	A/G	0.201911	0.245331	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202416	CGATGTTCCTTCTGG[A/G]AAATCCCATCTCCAT	8924
rs146891575	in-del	-/C			intron-variant	HERC2	GRCh38.p7	15:28116222	AAGTCTTTTCTTTTT[-/C]TTTTTTTTTTTTTTT	8924
rs146902740	snp	A/G	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28145275	GGCCCAGAGTAGGCC[A/G]CCCTCGAGGGAGCAG	8924
rs146915810	snp	C/T	0.0236746	0.106192	intron-variant	HERC2	GRCh38.p7	15:28236423	AGCCTCCCGAGTAAC[C/T]GGGATTACAGGCACC	8924
rs146925222	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28254133	TACTAAAACTACAAG[A/G]TTAGTCGGGTGTGGT	8924
rs146961430	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28122345	TCTTGGCCAAGGAGG[C/T]AATCGTGCCTTCTTT	8924
rs146969415	snp	A/G	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28212503	TAACTTGCTTCCAGC[A/G]AGGTTCACCAACTGA	8924
rs147008949	snp	A/G	0.00993419	0.0697739	intron-variant	HERC2	GRCh38.p7	15:28164078	CCAGGGACTCCCACC[A/G]CTTCCGACCCAGCAT	8924
rs147020516	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28219863	GCTAAGAAATGTCAC[A/G]AAACCTCCTCCCGCA	8924
rs147020948	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28256963	TTAAAATATTTCACC[C/G]AACAGGCTAAAACCC	8924
rs147029333	snp	A/G	0.000148445	0.00861397	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265833	ATGGCCCAGCCGGCC[A/G]TAGTTCCCGCGGCCC	8924
rs147029741	snp	A/G	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28239151	TTATAAAATACACTT[A/G]TAAGTAACCCAAAAT	8924
rs147030097	snp	C/T	0.0456336	0.143994	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316791	TGATCGTTTTTATTT[C/T]TTTTGAGACGGATTC	8924
rs147032710	in-del	-/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28271691	AAAAAAGACTGCCAA[-/T]AATAGAAAAATTAAA	8924
rs147040169	snp	A/C	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28289832	GCAGTGAGAGGACGA[A/C]ACACCTCAGTGAGAG	8924
rs147046423	in-del	-/AC	0.0854556	0.188216	intron-variant	HERC2	GRCh38.p7	15:28201946	CCCTTCAGTAGTGAA[-/AC]ACAGCTTTGTTCTGT	8924
rs147059020	snp	G/T	1.83748e-05	0.00303101	missense	HERC2	GRCh38.p7	15:28142359	CAGCAAGGCAGAGTG[G/T]CCAGCTCCAGGTCAC	8924
rs147073138	snp	A/G			intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314684	ACATGATGAAACCCC[A/G]TCTCTACTAAAAATA	8924
rs147074935	snp	C/G	3.2962e-05	0.00405954	missense	HERC2	GRCh38.p7	15:28163227	GCAATCAGCAGACTG[C/G]TGAACTCATCCAAGG	8924
rs147075762	snp	A/G	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28118894	CCACCTCTGGCACCC[A/G]GGGCCGTGGCTGAGC	8924
rs147103414	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28160430	CTCAAGCCTCAGCAA[C/T]GGTGGACGCCCCTCC	8924
rs147112020	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28149595	CCAAAAAAACACACG[C/T]GGCTCCTAACCGAGA	8924
rs147116947	snp	A/G	1.64906e-05	0.00287142	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28254406	GACTCACAGATCCCC[A/G]TATTAATAAGGTCTT	8924
rs147124122	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28242480	ATAGATGGAAACTAA[C/T]GGGTTGCATGGGACC	8924
rs147131648	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28134964	AGGCGTGAGCCACCA[C/T]GCCGGACCTGTTTAA	8924
rs147133601	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28189177	AGGAATGGTACAGTC[C/T]AGTTCTTTGGTCAGC	8924
rs147141413	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28129433	GGCTGATCACACAGG[C/T]ACCCCCTGCCTGGCG	8924
rs147143267	snp	G/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28185978	TCATCACAGTGCTCA[G/T]ATAAAATAAGGAATT	8924
rs147176669	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28242539	ATTAGTAAAGGGGTG[A/G]TGGTTATCAATAACA	8924
rs147194008	snp	A/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28284268	ACACTCTAAAACACT[A/G]CAGATAAAATAGAAT	8924
rs147216292	snp	C/T	0.000148813	0.00862464	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28182508	CAGCCTTCTTTCTAA[C/T]GAGGCTAACCAAACG	8924
rs147247785	snp	C/T	0.0391387	0.134304	intron-variant	HERC2	GRCh38.p7	15:28172449	TCAATGAAACAGTAC[C/T]GAGAGTCCAGAAATA	8924
rs147259778	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28265123	CACAATACTGAAAGA[C/T]GAGTCATTTCTAAAA	8924
rs147271386	snp	C/T	0.0023933	0.0345097	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111370	CAGTTATTTCCAATA[C/T]ACAATCAAGACGACT	8924
rs147277187	in-del	-/CACT			intron-variant	HERC2	GRCh38.p7	15:28217217	CCAGTAATCCCCTCA[-/CACT]CACTCATGCCTCCCT	8924
rs147284172	snp	A/G	0.0829062	0.185956	intron-variant	HERC2	GRCh38.p7	15:28206914	TACTCGCAAGGCTGA[A/G]GCAGGAGAATTGCTT	8924
rs147301001	snp	G/T	0.145978	0.227331	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28300578	CCGTAATCCCAGCAT[G/T]TGGCAGGCCAAGGCA	8924
rs147323805	snp	A/G	3.61873e-05	0.00425351	synonymous-codon	HERC2	GRCh38.p7	15:28132667	CCAGCTTCGGCTTCA[A/G]CTGGTCCTCACTGTC	8924
rs147353313	snp	C/G	0.0103295	0.0711199	intron-variant	HERC2	GRCh38.p7	15:28153673	GAAAAAGAAAAAAAA[C/G]TAGTTGGAAGGCTCC	8924
rs147356364	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28252283	AAACAGGCCAGTCTC[A/G]GTGCACGGGAACATT	8924
rs147365988	snp	A/G	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28247720	GGCGTGAGCCACCAC[A/G]CCCAGCCTCCTACAT	8924
rs147389120	snp	C/T	0.0260105	0.111035	intron-variant	HERC2	GRCh38.p7	15:28297009	ACTTGCTTGCGGGCA[C/T]ACGCACGAAAGATAA	8924
rs147402446	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28260348	AGCTTCTAAAACGGG[A/G]AATTAAAGACACTCC	8924
rs147412909	in-del	-/ACGC	0.0633504	0.166319	intron-variant	HERC2	GRCh38.p7	15:28148654	AGAACGGCCACACGA[-/ACGC]ACGCACATTCTAGTA	8924
rs147414523	snp	A/G	1.66768e-05	0.00288758	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274972	GGATCCCACTCTGGC[A/G]AGCCCCTCCACACCT	8924
rs147430539	snp	C/T	0.0418186	0.138422	intron-variant	HERC2	GRCh38.p7	15:28134730	TTTTTTGAGATGGAG[C/T]CTCGCTCTGTTCCCC	8924
rs147440206	snp	A/G	0.0107246	0.0724382	intron-variant	HERC2	GRCh38.p7	15:28128708	CAGCCCGGCTGGCTT[A/G]AACAACACACACTTA	8924
rs147450103	snp	A/G	5.40945e-05	0.00520042	synonymous-codon	HERC2	GRCh38.p7	15:28132139	GCTGCCTCCCCGGCC[A/G]AGCTTGCCGTAGTCC	8924
rs147451109	snp	C/G	0.031825	0.122064	intron-variant	HERC2	GRCh38.p7	15:28206643	TCAAGACCATCCTGG[C/G]TAACACGGTGAAACC	8924
rs147458915	snp	G/T	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28143699	GATCCGCCCACCTCA[G/T]CCTCCCAAAGTGGTG	8924
rs147460118	snp	C/T	0.0119091	0.0762411	intron-variant	HERC2	GRCh38.p7	15:28203692	CAGGGGCTGGGGTCC[C/T]GGCCTGGCAGAGTAA	8924
rs147470408	in-del	-/C	0.157972	0.232445	intron-variant	HERC2	GRCh38.p7	15:28136628	TACAACAGGAGTTGG[-/C]AAATTATGGCCCATG	8924
rs147494330	snp	A/T	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28286738	TTTAGATAGTTACTA[A/T]GAGTTTACTCCCCTA	8924
rs147496332	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28236010	TGGTCTGGTAAAAAC[A/G]CAGTCCTCAAGTAGA	8924
rs147519395	snp	A/G	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28229238	CATCAAAACATTTCG[A/G]ATGTTCTGTACAGCC	8924
rs147535565	snp	A/G	6.58935e-05	0.00573955	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28237013	CTCATTGCCAAATAC[A/G]AAGCGTGTAATCCGA	8924
rs147572052	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28149430	TCTAGTAAAATTACC[-/A]AAAAAACACATGCGG	8924
rs147576051	snp	C/T	0.000153988	0.00877328	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213783	CGCGACACGTCCGCA[C/T]GTCAGAGAACTGCAC	8924
rs147592737	snp	A/G	0.00631422	0.0558323	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28220459	TCACCCACCAGAGTC[A/G]TCCTCTGTGTCCGAA	8924
rs147606351	snp	A/G	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28282192	GGTGAAGCACGCCCT[A/G]TCCCTGCCAGAGCAG	8924
rs147609746	snp	A/G	0.0103295	0.0711199	intron-variant	HERC2	GRCh38.p7	15:28138703	GCCGGCTAACACATC[A/G]TTTTTTCTGCAGCCA	8924
rs147610835	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28195868	CCACAATGACAAATA[C/T]AATAAAAGGTATATA	8924
rs147620932	snp	A/G	0.0524604	0.153226	intron-variant	HERC2	GRCh38.p7	15:28228539	TTCTTCTGCATGGAT[A/G]CAAGAATAAACGTAA	8924
rs147639343	snp	C/T	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28307302	GGCTTGTCAATTTAT[C/T]TTTTAGAAAAACCAA	8924
rs147649447	snp	G/T	0.0119091	0.0762411	intron-variant	HERC2	GRCh38.p7	15:28308754	TAAGAGATTTTATCA[G/T]GAAAGGATGTTGAAT	8924
rs147678868	snp	A/G	1.65979e-05	0.00288074	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272251	GGGTGCATCCTTCCT[A/G]CAAATGATGCTCTGG	8924
rs147680647	snp	A/G	0.000461163	0.0151779	synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28280139	ATTCTCCTGAAAAAC[A/G]GTTCTATTCAAGGCA	8924
rs147681848	snp	C/T	0.00103728	0.0227501	synonymous-codon	HERC2	GRCh38.p7	15:28167711	TTTGGTCATGGTTTC[C/T]GCAATGATGCTTGCG	8924
rs147697168	snp	A/G	9.99367e-05	0.00706812	synonymous-codon	HERC2	GRCh38.p7	15:28169654	AGCATCTGAAGGCAC[A/G]CCTATAAGAGGAAAA	8924
rs147705404	snp	A/G	0.00262175	0.036111	missense	HERC2	GRCh38.p7	15:28168546	GAGGGGCACTCCACC[A/G]GGGCGATCATGGCGG	8924
rs147713966	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28122361	AATCGTGCCTTCTTT[C/T]GGTTAGGGGTGGGCT	8924
rs147744460	snp	C/T	0.0479149	0.147179	intron-variant	HERC2	GRCh38.p7	15:28291883	GTACTCCAGCCTGGG[C/T]GACAGAACAAGACTC	8924
rs147802077	snp	A/G	5.00981e-05	0.00500465	missense	HERC2	GRCh38.p7	15:28113123	GTCCTGGGCAGCCTC[A/G]TCCGGCCCCAGACGA	8924
rs147808773	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28150756	CGAGAATGGCCACAC[A/G]AACGTATATTCTAGT	8924
rs147819421	snp	C/T	0.0115144	0.0749975	intron-variant	HERC2	GRCh38.p7	15:28204387	AGCACTTTGGGAGCC[C/T]GAGGAGGGCGGATCA	8924
rs147819916	snp	C/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28163801	GGTTCATTGAAAACA[C/T]CATACATAAAAGTCT	8924
rs147829521	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28199845	GAGAGAGGAAGATGT[C/T]AGCCACAAGGAAGCC	8924
rs147841039	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28254056	TGGGAGGCCAAGGCG[A/G]GCGGATCACCTGAGG	8924
rs147849888	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28282315	ACCAAGAACCAGGAA[A/G]ATCTAAAACCAAATT	8924
rs147859430	snp	A/T	0.029116	0.117091	intron-variant	HERC2	GRCh38.p7	15:28284571	TGCAAACATTACTGA[A/T]AGGACAGCAGAAGTT	8924
rs147892890	snp	C/T	0.000214159	0.0103457	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265706	CCCGGCTACCAGCAT[C/T]GGAATGGCCTCGTCC	8924
rs147913506	snp	G/T	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28141151	GTTGAGGCAGGAGAA[G/T]CACTTGAACTCAGGA	8924
rs147916081	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28199624	GGTCTAGATGATGAC[A/G]CTAATGCCTACTGGA	8924
rs147924778	snp	A/G	0.0193772	0.0965046	intron-variant	HERC2	GRCh38.p7	15:28149368	CAAAAAAACACACGC[A/G]GCTCCTAACCGAGAA	8924
rs147927194	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28244365	TTATATGAAGTCCGA[A/G]AACAGACAGAATTAA	8924
rs147935013	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28183247	CAGGGTCATGCTCTG[C/T]CACTCAGGCTGGAAT	8924
rs147936809	snp	A/G	0.0558544	0.157504	intron-variant	HERC2	GRCh38.p7	15:28241588	TCACTTTGGGAGGCC[A/G]AGGTGGGCAGATCAC	8924
rs147955000	snp	G/T	0.046775	0.145601	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316763	TACTCATGTTTATAC[G/T]TTTTTTATCTACTGA	8924
rs148005149	snp	C/T	0.00016621	0.00911467	synonymous-codon, missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28280073	TTATTGTTACCTTTT[C/T]TTGTCCACAGGAGGC	8924
rs148040734	snp	A/G	0.0063281	0.0558928	intron-variant	HERC2	GRCh38.p7	15:28152667	TCCCCGCTGGGGCCA[A/G]CCCCTGTACCTGGTA	8924
rs148047861	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28164182	CCAGAGGAAGATCGA[A/G]AGCCAGGGAAGTGCC	8924
rs148050334	snp	A/G	8.63774e-05	0.00657124	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28222185	TGAGCAGAAGCATTC[A/G]TATCTTCCTCAACGT	8924
rs148052069	snp	C/T	0.00102354	0.0225992	intron-variant	HERC2	GRCh38.p7	15:28246911	ACCTTGAAGAAGGAT[C/T]GAGAAATTTTCATTT	8924
rs148058774	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28275740	GTGAGCCAAGATCGC[A/G]CCACTGCACTCCAGC	8924
rs148064412	snp	C/T	0.00835141	0.0640778	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28315097	TGCAAATACAACCAA[C/T]TGTTCAGCCAGCACA	8924
rs148073915	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28310287	CACATTTCTACCAAA[A/G]ATACAAAAAATTAGC	8924
rs148092853	snp	C/T	0.00250424	0.0352966	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28178939	GAGAGCTGTGATCTG[C/T]CGTGGGATGGGCACC	8924
rs148097787	snp	A/G	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28264884	AAGCAGAAACAACAC[A/G]GCTCTGACAAGGTCT	8924
rs148118843	snp	A/G	0.0399052	0.1355	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317218	GCCTCAACCTCCCAA[A/G]TAGCTGGGATTACAA	8924
rs148127955	snp	A/T	0.0236746	0.106192	intron-variant	HERC2	GRCh38.p7	15:28307746	ATATGGCAAAAGAGG[A/T]ATCTAGCTTCATTCT	8924
rs148135506	snp	C/T	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28145017	CACGCATTCAGCCCC[C/T]GTACCAGGTACCCAG	8924
rs148150960	snp	A/G	0.000461673	0.0151863	missense	HERC2	GRCh38.p7	15:28167817	GTCACTGCGTCCTCA[A/G]AGGAAACAATCTAGT	8924
rs148190038	snp	C/T	0.0310518	0.120672	intron-variant	HERC2	GRCh38.p7	15:28170624	TACTTAGACTTGACA[C/T]CAAAAGTATGATCTA	8924
rs148211311	snp	A/G	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28220359	CAGGTGCGTCCTGAC[A/G]TCCCATTCTAAGGCC	8924
rs148216822	snp	A/G	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28304115	AGGTTGCAGTGAGCC[A/G]AGATTGCGCCATTGC	8924
rs148221386	snp	C/T	0.00993419	0.0697739	intron-variant	HERC2	GRCh38.p7	15:28255387	CCTTCAATAGGAGAA[C/T]GAACAAACAGTACTA	8924
rs148225341	snp	C/T	0.000445342	0.0149155	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28196546	GAAAGTCGACAATGA[C/T]ATCTTTTCCATTGGC	8924
rs148250469	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28128138	TGTGCTACAAAATAA[C/T]TGGTGTCAAGTTGCA	8924
rs148253301	snp	A/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28185239	TTCTGTCTATATAAC[A/G]TGCTCAACAGCGGCA	8924
rs148263834	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28217634	TGTCCCCCAACTTCA[C/T]ATACATTCGGAACCT	8924
rs148280094	snp	C/T	1.70043e-05	0.0029158	intron-variant	HERC2	GRCh38.p7	15:28273052	CAACCTCCAGAAAGA[C/T]AGCATGCTTACAATC	8924
rs148285968	snp	C/T	0.00755907	0.0610114	intron-variant	HERC2	GRCh38.p7	15:28139259	ACTGGAGTGTGGTCA[C/T]TTCTGTGATTCAGTT	8924
rs148287389	snp	A/G	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28286600	AAAATAGCAACAAAC[A/G]GGAACTTCATCATCT	8924
rs148304532	snp	A/C	0.00755907	0.0610114	intron-variant	HERC2	GRCh38.p7	15:28149792	GTATATTCTAGTAAA[A/C]TCACCGAAAAAACAC	8924
rs148314808	snp	C/T	6.5987e-05	0.00574362	synonymous-codon	HERC2	GRCh38.p7	15:28130571	TTCCACTTTAACTAC[C/T]CCAAGACCAGTAAGA	8924
rs148315960	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28242957	CATCATACTTTGTGT[C/G]TGAAATCTGGAAAGC	8924
rs148331498	snp	C/T	0.0154538	0.0865337	intron-variant	HERC2	GRCh38.p7	15:28292437	GTGTTGGTGAGGGTG[C/T]GGAGAAATGGGAACC	8924
rs148344532	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28114082	CCAGGACTACCCCCA[C/T]CAGAGCCCACAGGGC	8924
rs148348282	snp	C/T	0.0825414	0.185628	intron-variant	HERC2	GRCh38.p7	15:28173564	AGCACTTTGGGAGGC[C/T]AAGATGGGAGGATCA	8924
rs148357712	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28208974	ATGTCTTTCAATAGC[A/T]GGAGATCAAAAAATG	8924
rs148359600	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28267112	TATGTTCCTATGATG[G/T]ATGACATTTTCTTGA	8924
rs148362399	snp	A/G	0.000560769	0.0167353	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265899	ACTGTAAGTGCTCCC[A/G]CAAGCGATGTGCACC	8924
rs148365790	snp	C/G	4.94246e-05	0.0049709	missense	HERC2	GRCh38.p7	15:28143985	GCCCACATTCTGTGA[C/G]TGGCAGCTGAAATGA	8924
rs148401310	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28149165	CTAACCGAGAACATC[A/G]CCAAGAATGGCCACA	8924
rs148411249	snp	C/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28181596	GCTCACGTGAACACA[C/G]AGAGTGCCTCTGGGC	8924
rs148414166	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28240677	GGCAATAATAAAGAG[C/T]ATGGCACTGGACAGA	8924
rs148416305	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28137298	TCTGATACGGTTCAC[A/G]ATGATCCCTGCTTCT	8924
rs148448878	in-del	-/CACC			intron-variant	HERC2	GRCh38.p7	15:28224146	TTATACACACACACA[-/CACC]CACACACACACACAC	8924
rs148451375	snp	C/G/T	0.0505437	0.150726	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28202176	ATACTCGTCGGACAC[C/G/T]GTGTCTGCATCTGAG	8924
rs148456855	snp	C/T	0.00126777	0.0251451	synonymous-codon	HERC2	GRCh38.p7	15:28169522	TGTAAGAATATGTGA[C/T]AAGGCCTGCTGTTTG	8924
rs148465917	snp	A/G	0.0414363	0.137845	intron-variant	HERC2	GRCh38.p7	15:28237721	CAATATATAAATTCT[A/G]TGTGTTCGTGAATAC	8924
rs148503135	snp	A/G	0.00367774	0.042724	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28215708	CGGGGAGCTGAGGGC[A/G]CCGCATACCTGCGGC	8924
rs148537831	snp	C/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28256592	CAACCTCCACCCCGC[C/G]CCAACAATCTGCACC	8924
rs148569037	snp	A/G	0.00263907	0.0362294	intron-variant	HERC2	GRCh38.p7	15:28186792	AGACTCTGTAGAATC[A/G]AGCATATTAGATCCT	8924
rs148575153	snp	C/G	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28140226	CCCCACTGGAAGCCT[C/G]GGAACGCTCCATCTG	8924
rs148590388	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28273695	TGCAAGAAGGCACAG[G/T]GCTGACCTCTGCAAG	8924
rs148608734	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28121165	TAAAGAAACACACTG[A/C]CATTCCTGGAAGCCC	8924
rs148626879	snp	C/T	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28160983	TTATGGTAATTCACC[C/T]TGATTTCATCTCTTA	8924
rs148628168	snp	A/G	0.000675414	0.0183644	synonymous-codon	HERC2	GRCh38.p7	15:28135630	AAGCAATGTTGGGGT[A/G]GACACCGACTCTGTC	8924
rs148632780	snp	G/T	0.26326	0.249648	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28320810	AAATCAAAAAATTAG[G/T]ATCTAAGGCCAACAT	8924
rs148652936	snp	A/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28269768	AGGCAAAATCCCAAA[A/G]GCCCACACACAAGGC	8924
rs148673711	snp	C/T	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28209804	AAGACTATATAAGTA[C/T]CATCATTTTGAATGG	8924
rs148695818	snp	C/T	0.0123036	0.0774623	intron-variant	HERC2	GRCh38.p7	15:28290828	ATGCTTAGAGGGAAA[C/T]TTATATTATAGTTTT	8924
rs148711194	snp	A/G	0.000263544	0.0114762	synonymous-codon	HERC2	GRCh38.p7	15:28111880	AAGTGCGATGCGAGC[A/G]TAGTCATCTGTGTCT	8924
rs148716523	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28201967	CTTTGTTCTGTGCCC[A/G]GCAATACCATAGGTT	8924
rs148731297	snp	C/T	0.000889181	0.0210666	synonymous-codon	HERC2	GRCh38.p7	15:28111940	GAGCTTCTCCTCCAG[C/T]ACCTGCTTGCAGGAA	8924
rs148738885	snp	A/T	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28253428	TTTGCATCCACCTGC[A/T]TATTAGTAAGAATCT	8924
rs148744533	snp	C/G	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28207266	CAGCCTTCCCTGTAG[C/G]TGGGACTACAGGCAC	8924
rs148786700	snp	A/G	0.00261777	0.0360837	synonymous-codon	HERC2	GRCh38.p7	15:28167810	AGAGGGGGTCACTGC[A/G]TCCTCAGAGGAAACA	8924
rs148787940	snp	A/G	3.2993e-05	0.00406145	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28228368	GGCTCGGTCCTGACG[A/G]GTTCTCATTGGTGAT	8924
rs148791571	snp	C/T	0.0170251	0.090679	intron-variant	HERC2	GRCh38.p7	15:28249349	GGTGCCCAAAGAGCA[C/T]GGCAGCGAAGAAAGT	8924
rs148799279	snp	C/G	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28258751	AAAGCAGAAATCAAT[C/G]AGATTGAAAGCAAAA	8924
rs148823452	snp	G/T	5.0114e-05	0.00500545	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28220621	CTCACCAATCACGCG[G/T]CCTAGGCCTGGAGGA	8924
rs148841475	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28307583	CTGTTTAATTTCACT[A/C]TTAATTTCTTCACTG	8924
rs148842793	snp	C/T	0.000364142	0.0134885	intron-variant	HERC2	GRCh38.p7	15:28144819	CCTGCGGGAGGAAAG[C/T]GCACCCCGGGGTTAG	8924
rs148897405	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28284660	GGGCACAGTGGCTCA[C/T]GCCTGTAATCCTAGC	8924
rs148898479	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28219849	GTCTTTTAGGAACAG[C/T]TAAGAAATGTCACGA	8924
rs148929519	snp	A/G	9.90034e-05	0.00703505	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28177049	GGATGTGAGGGCTGC[A/G]CTGTGCGAGCTCCCA	8924
rs148941369	snp	C/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28215089	TCACTATGTTGGCCA[C/G]GCTGGTCTCAAACTC	8924
rs148946208	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28163439	CAGATTAAGAAACGA[C/T]GGCCCCTAAAATCTC	8924
rs148963117	snp	C/T	6.64673e-05	0.00576448	synonymous-codon	HERC2	GRCh38.p7	15:28142313	GGCCATGCAGTACCT[C/T]CGGAACCAGGCCCAC	8924
rs148989098	snp	C/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28130755	CACTTAATCTCAGCA[C/T]TCTCAGGAGGCAGGC	8924
rs149010273	snp	A/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28178716	GGCAAAGAACTTGAT[A/T]TAGCAGCAATAACTA	8924
rs149062367	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28208741	CCACCACCAGCAAAG[C/T]GCTTGTCTGCTGGCA	8924
rs149104014	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28169379	AGCATTTAAAGACAA[C/T]AATACAACATTCTTG	8924
rs149108694	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28251527	TAATAATGGCCAGGC[A/G]CGGTGGCTCACGCCT	8924
rs149112375	snp	A/G	0.0111196	0.0737302	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299846	CACGGGGGATCAGGA[A/G]TTTGAGACCAGCCTG	8924
rs149114088	snp	C/T	0.077417	0.180873	intron-variant	HERC2	GRCh38.p7	15:28205097	GAAAACCAAAGATAA[C/T]AGAAAATACGAAAAG	8924
rs149116523	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28261434	TTAGCAAAATATTCT[A/G]TTTTTCCTTCCTGGT	8924
rs149125645	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28242619	ATTACAAGGAAAATG[A/C]GATGCAAAATCTAGA	8924
rs149140322	snp	C/T	0.000307953	0.0124049	missense, utr-variant-5-prime, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28280258	GCTCTTTAACCAGCA[C/T]AGAAAGACACTCCTT	8924
rs149188455	snp	C/T	0.000101319	0.00711682	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28211121	TTCAACTGCTGGCAC[C/T]GCAGCAGGTCCAGGT	8924
rs149202743	snp	A/T	0.0352966	0.128072	intron-variant	HERC2	GRCh38.p7	15:28289347	AATGTCACTGGAGAT[A/T]AAGGGGGTCAAATTT	8924
rs149204675	snp	A/G	0.00541344	0.0517438	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28238663	ATCATACACCTTCCC[A/G]TCAATCACAGTCCAG	8924
rs149219304	snp	A/C	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28149624	GAACATCACCGAGAA[A/C]GGCTGCACGAACGTA	8924
rs149220102	snp	G/T	0.00279162	0.0372561	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316697	TATTTCTACATGTCA[G/T]CTATCAACTGGATTA	8924
rs149233552	snp	A/G	0.0134861	0.0810011	intron-variant	HERC2	GRCh38.p7	15:28215965	AATTCAAAGTGAGAA[A/G]TGGAAGGCAGCTTTT	8924
rs149248554	snp	A/G	3.29826e-05	0.00406082	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28178960	GATGGGCACCGTCCC[A/G]CTGGAAATGCCCAGC	8924
rs149266177	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28165218	AGGGTGACCATGGAG[A/G]ACCATGGAGGCAGAC	8924
rs149277774	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28258120	AATGGTATTAAACTA[G/T]AAATCATGAACAGAA	8924
rs149280444	snp	C/T	0.00016655	0.009124	missense	HERC2	GRCh38.p7	15:28144206	ATGGACAGGAGAGGA[C/T]GCAGCGGTCAGAGAG	8924
rs149304806	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28314995	GTTATAAAAGAGCAC[A/G]TACGGCCCACATAAA	8924
rs149309405	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28188774	GGTTCCAGCATACTT[C/T]CTATTTTTGTTTACA	8924
rs149338352	snp	C/T	5.01274e-05	0.00500612	missense	HERC2	GRCh38.p7	15:28115539	CAATGCCCAGCAACA[C/T]ACCTGATCATTCAGG	8924
rs149339003	in-del	-/TG	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28201626	AAAAAGAAATAAGTC[-/TG]TGAAATCTATAATAT	8924
rs149377534	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28128081	CAAAGACACACAACC[C/T]GAATCTACGCAGAAA	8924
rs149382677	snp	G/T	0.0111196	0.0737302	intron-variant	HERC2	GRCh38.p7	15:28209643	CCACCGCGCCAGGCC[G/T]ATATATCATTTATAT	8924
rs149409263	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28278098	CAATCTATACAAATT[-/A]AAAAAAAAAAAAAAA	8924
rs149432276	snp	G/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28123435	CTTGTCAAGCTGCTT[G/T]CCAGAAACTAACCCA	8924
rs149437745	snp	C/T	0.000329641	0.012834	missense	HERC2	GRCh38.p7	15:28167809	CAGAGGGGGTCACTG[C/T]GTCCTCAGAGGAAAC	8924
rs149438210	snp	A/G	0.0126979	0.078662	intron-variant	HERC2	GRCh38.p7	15:28264642	TACTCAAGGCAGTTT[A/G]CTCAACATATCATCG	8924
rs149447662	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28243981	AGGAGTTTGAGACCA[A/G]CCTGGGCAACAGAGG	8924
rs149481621	snp	A/G/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28254271	CTGGGCAACAAGAGC[A/G/T]AACTCTGTCACACAC	8924
rs149493788	snp	A/G	0.000198568	0.00996217	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256208	GTGCTCAGCACGCCC[A/G]CACTGCTGGCCAGGG	8924
rs149498499	snp	A/G	0.00074209	0.0192482	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214752	GTCCCTCGCCCTTTC[A/G]GTCTTGTCCCATGAT	8924
rs149570373	snp	C/G	0.153665	0.230694	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28312939	CAAAAGAGGCAGTAA[C/G]AGGCTCACTTTTTGT	8924
rs149592795	snp	C/T	0.214932	0.247528	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28174549	TAAGCCTTGCACGAG[C/T]GTGGGCTTCCTGTTA	8924
rs149613949	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28276567	TGGCAAAACCCCATC[C/T]CTACTAAAAATACAA	8924
rs149634318	snp	A/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28143115	GGAAAAAAGCTAAAA[A/G]AACATAAACACTGAA	8924
rs149637097	snp	G/T	0.000593296	0.0172132	intron-variant	HERC2	GRCh38.p7	15:28201440	ATCGAGGCTCCAGCT[G/T]AAGACAATTACTCAC	8924
rs149646235	snp	C/T	0.0425829	0.139564	intron-variant	HERC2	GRCh38.p7	15:28235688	CTTCTCCCAAAACCA[C/T]GTATGAACGTCTCCA	8924
rs149655254	snp	C/T	0.000396125	0.0140679	synonymous-codon	HERC2	GRCh38.p7	15:28125045	GGCGGGCTTGCTGGT[C/T]GACCAGGCGAGGGTA	8924
rs149697483	snp	C/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28129926	AGATGCAGGCGCGCG[C/T]CACCATGCCCAGCTA	8924
rs149701493	snp	C/T	0.00716266	0.059414	intron-variant	HERC2	GRCh38.p7	15:28210560	ACTCATTTCCTCAGA[C/T]GCCCATTAGATGGCT	8924
rs149707599	snp	G/T	0.000543474	0.0164755	synonymous-codon	HERC2	GRCh38.p7	15:28141629	TCCAGTCATCTGGTC[G/T]CCTACAATACACATC	8924
rs149743423	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28173326	CAGCCCAAACATTCA[C/T]CAACAGATAAATGGA	8924
rs149755238	snp	A/C/G	0.000824837	0.0202913	missense, synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265917	AGCGATGTGCACCAC[A/C/G]TGCTTCCCGGCCTGC	8924
rs149756942	snp	A/C/G	0.000218544	0.010451	synonymous-codon	HERC2	GRCh38.p7	15:28168560	CGGGGCGATCATGGC[A/C/G]GCCGGCATCAGGGCC	8924
rs149759750	snp	A/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28162596	CACAAATCAGTTATA[A/T]AACAGGTAAAGGGGC	8924
rs149764593	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28245717	ATATACATATATGAC[A/C]CAAATTTCTTCTGAT	8924
rs149772210	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28256455	GTATTTTTAAAAACT[A/G]GACTAAAAAAACTCT	8924
rs149777328	snp	A/T	0.0460142	0.144533	intron-variant	HERC2	GRCh38.p7	15:28293862	CTGACAATGTCAAGT[A/T]TCAGTCAAAAACAAC	8924
rs149788129	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28284234	TAGAAAAGCCACTAA[A/G]GAAGCTATACAAAAA	8924
rs149792686	snp	A/G	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28115850	ACGGGAGTGTCCTCC[A/G]GGGAGCTACAGCCCT	8924
rs149796121	snp	C/T	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28199225	GGAAGAGAAACTCTT[C/T]AGAACACTGTCTGGC	8924
rs149809183	snp	A/G	0.00044524	0.0149138	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28176754	GATTACTCTGTGACC[A/G]AGAAGGACTTTCACC	8924
rs149831257	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28291465	CCTGAATATCCACAC[C/T]GAAGGGATAATAGTG	8924
rs149946385	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28287411	CAGAGCTTCCAAGTA[A/C]ACCCTCTTCATTAAA	8924
rs149949217	in-del	-/C/CC			intron-variant	HERC2	GRCh38.p7	15:28165292	CCACGGAGTGGGGGA[-/C/CC]CAGCCAAGATCGGAG	8924
rs149949999	snp	A/C/T			intron-variant	HERC2	GRCh38.p7	15:28245564	AAAAAAAAAAAAATA[A/C/T]ATACACACACACACA	8924
rs149950976	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28120235	ATTAAACACTCTGAC[A/G]TCAGTGAAGAGACCA	8924
rs149962152	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28150642	CCAAAAAAACACACA[C/T]GGCTCCTAACCAAGA	8924
rs149969678	snp	A/G	8.66829e-05	0.00658285	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28269281	GGCCTGTGTGTACAC[A/G]CGGCCATTGCGTGAC	8924
rs149972439	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28195343	GCTCAGGCCTGTAAT[C/G]CCAGCTACTCAGGAG	8924
rs149981900	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28281425	CTGCTGCTTACTAGC[C/T]TGGAGGCCAGCAGCC	8924
rs149998328	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28308236	ATGTCTTTCATCAGC[A/G]TTTTAGAGTTTTCAT	8924
rs150008593	snp	A/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28228027	TACAACTAGACAGTG[A/G]TGATGACTCTAGAAA	8924
rs150024899	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28190745	CTCTGCTACCAAAGA[C/G]AGTGAGAATGAAATT	8924
rs150026812	snp	C/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28248268	GCATTCCATAGCACA[C/T]GGAACAAATCTGATA	8924
rs150040527	snp	C/T	0.00597247	0.0543191	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316192	ACTGCTACTGTACTC[C/T]AACCTGGGCAACAGA	8924
rs150090772	snp	A/C	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28258080	TAAAAGAAATGAAAT[A/C]ATATACAGTTTGTTC	8924
rs150101715	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28285445	AACTTCTAAATAATC[C/T]ATGGATCAAAGAGGA	8924
rs150109705	snp	A/C	0.0107246	0.0724382	intron-variant	HERC2	GRCh38.p7	15:28118093	AGAATGACAGGAGCC[A/C]CAGTTGCCTGTAGAA	8924
rs150129817	snp	C/T	0.0193772	0.0965046	intron-variant	HERC2	GRCh38.p7	15:28159707	TCGGAGAAGTTTGAT[C/T]GTCTGAAGCCTTCCT	8924
rs150131561	snp	C/T	1.65051e-05	0.00287267	synonymous-codon	HERC2	GRCh38.p7	15:28141835	CATTAATTCACGAAT[C/T]TTCTTAGCCACCTAA	8924
rs150132959	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28219506	GGGTTCCAGGTGCCA[C/T]ATACATCGCTCCTAA	8924
rs150136396	snp	G/T	0.0150606	0.0854603	intron-variant	HERC2	GRCh38.p7	15:28303206	AGATAGCGGTCTAGT[G/T]TCATTTTTCTGCATA	8924
rs150142651	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28253889	ATTGCTAGAACCCAG[A/G]AGGCAGAGGTTGCAG	8924
rs150143589	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28292645	ACACAGTGAGATTCT[C/G]TCTCTAATTAGTCAA	8924
rs150220154	snp	A/G	0.000115383	0.00759462	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265619	AGAGCTCTACGTACC[A/G]TTCTCAGTGACAGCC	8924
rs150231163	snp	A/C	0.0402882	0.136092	intron-variant	HERC2	GRCh38.p7	15:28239853	GATCACAGGGAGAGG[A/C]GGGCCTGGAGCCATG	8924
rs150231377	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28290125	TTACTAAATAATCAG[A/G]TACGGGTAAGATCTC	8924
rs150246661	snp	A/G	0.211212	0.246973	intron-variant	HERC2	GRCh38.p7	15:28206616	AGGCGGGTGGATCAC[A/G]AGGTCAGGATATCAA	8924
rs150255483	in-del	-/T			intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28186377	TTTTAATGGTATTTT[-/T]CTAAATATAATGTGT	8924
rs150263639	in-del	-/C			intron-variant	HERC2	GRCh38.p7	15:28185204	TAACCTGATTTATTA[-/C]CAGAACTACTACCCC	8924
rs150268966	snp	A/G	0.0126979	0.078662	intron-variant	HERC2	GRCh38.p7	15:28123115	AGAGATGGTCTTTCC[A/G]TTAAACACAAGCCTG	8924
rs150278319	snp	A/G	0.0225045	0.103662	intron-variant	HERC2	GRCh38.p7	15:28151346	AGGTGGCATGTGTCT[A/G]TACTCCTAGCTACTC	8924
rs150280398	snp	C/T	0.0700422	0.173537	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214935	TGGAGTGCAGTGGCA[C/T]GGTCTCGGCTCACTA	8924
rs150283778	snp	C/G	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28288294	TCTTTGGGAGGCCGA[C/G]GTGGGTGGATCACCT	8924
rs150287021	snp	C/T	0.0236746	0.106192	intron-variant	HERC2	GRCh38.p7	15:28139388	GACGCTCTATGGACA[C/T]GTGGCAAAGGGCTGA	8924
rs150289465	snp	C/T	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28197428	TCATTAGCACATTTC[C/T]ATTTCTTAAATTCAG	8924
rs150293247	snp	A/C	0.0551013	0.156571	intron-variant	HERC2	GRCh38.p7	15:28282743	TTGAGACCAGCCTGG[A/C]CAACATGGTGAAACC	8924
rs150336362	snp	C/G/T	0.0279526	0.114869	intron-variant	HERC2	GRCh38.p7	15:28309451	TTATAGTTTTGGTCT[C/G/T]GAAATCTATTTGGTC	8924
rs150341586	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28192709	AGATGACGCACACCA[C/T]GGATCAGAGGCTGCT	8924
rs150343365	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28251216	TGGAGGCCAAGGCGG[A/G]CAGATTACCTCAGGT	8924
rs150346860	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28278507	TGTTGTTTTTTATTG[C/T]TTTTCTTCCAATATT	8924
rs150351679	snp	G/T	0.00914312	0.0669923	intron-variant, utr-variant-5-prime	HERC2, LOC107987422	GRCh38.p7	15:28317635	ACAGATTAGTGGTTG[G/T]CAGGAGTTAGAGATG	8924
rs150363648	snp	A/G	0.363969	0.222539	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272900	AGCCCTCACCTCAGC[A/G]TGCCTCTCTGCACAG	8924
rs150374233	snp	A/G	6.63416e-05	0.00575903	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213943	CACTTCAGGGTTCTC[A/G]GAGTCGGGGAAGTAG	8924
rs150434899	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28134314	AACTTTTATTTATTG[A/G]TCTTCTATCCCGCAA	8924
rs150456865	snp	A/G	0.0825414	0.185628	intron-variant	HERC2	GRCh38.p7	15:28173568	CTTTGGGAGGCCAAG[A/G]TGGGAGGATCACTTG	8924
rs150458870	snp	A/C	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28235624	CTGTGTTTTCTGCCC[A/C]GAATGCTCCCTCATG	8924
rs150489412	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28126764	ATTGGGTACTGTGTA[C/T]ACTACTTGGGTGATG	8924
rs150490465	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28183930	CAGTAGCTCACACCT[A/G]TAATCCTAGCACTTT	8924
rs150494948	snp	A/G	0.0486741	0.148216	intron-variant, utr-variant-5-prime, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28312753	CTGACTTACCTAAAC[A/G]TGCCCAGTAGATTTT	8924
rs150495603	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28268343	GTAGTGTCCTGCTCC[A/C]TCCCAGCGCTACATG	8924
rs150504660	snp	C/T	0.046775	0.145601	intron-variant	HERC2	GRCh38.p7	15:28247481	TCGCCCAGGCTGGAA[C/T]GCAATGGTCTGATCT	8924
rs150517241	snp	A/G/T	4.95585e-05	0.00497763	synonymous-codon	HERC2	GRCh38.p7	15:28168509	CATCGCAGATGCGTC[A/G/T]GAAGGGGCCGCCGAG	8924
rs150536114	snp	C/G	0.0103295	0.0711199	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318355	GAACAGGCCGGGCGC[C/G]GTGGCTCACGCCTAT	8924
rs150568801	snp	A/T	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28265480	CCGGGCCTCTTCCCC[A/T]ATGCCACTGAGCCCC	8924
rs150587720	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28124761	TGCTATGTTGTCCAG[A/G]CTGGTCCTGAACTCC	8924
rs150593330	snp	C/T	2.2799e-05	0.00337624	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274436	GCTCACTGCAGAGGT[C/T]CGCATCCTCGCCTGG	8924
rs150598535	snp	C/T	0.0119091	0.0762411	intron-variant	HERC2	GRCh38.p7	15:28153369	AAACAAAAAAAGTCA[C/T]TGGGTGGAGCGCAGT	8924
rs150604303	snp	C/G	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28115343	ACTGAGATTAGGCCA[C/G]AGTTCACAGCCTGAC	8924
rs150607268	snp	A/G	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28140539	TCTTTTTTTGGGGGC[A/G]GAGACAGAATCTCAC	8924
rs150608324	snp	C/T	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28283871	TCATATATACACAGG[C/T]TGAGTGTCCCTTATA	8924
rs150617349	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28209590	CCTCGTGATCTGCCC[A/G]CCTTAGCCTCCCAAA	8924
rs150619151	snp	A/G	0.0460142	0.144533	intron-variant	HERC2	GRCh38.p7	15:28232328	CAGGCAGATCACGAG[A/G]TCAGGAGATCAAGAC	8924
rs150636762	snp	A/G	1.66899e-05	0.00288871	missense	HERC2	GRCh38.p7	15:28115478	GCCAGCTGCTTCCAG[A/G]CAGGCTCGGCAAGGT	8924
rs150646625	in-del	-/CATT			intron-variant	HERC2	GRCh38.p7	15:28217005	CAAGCAAAATGCTCA[-/CATT]CACTCACACGCATTC	8924
rs150658264	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28171778	TAACAAAAGACAAGC[A/C]AAACCTATACAATAG	8924
rs150661322	snp	A/G	0.162581	0.234218	intron-variant	HERC2	GRCh38.p7	15:28194129	GGAGTGCAGTGGCAC[A/G]ATCTCGGCTCACTGC	8924
rs150675000	snp	C/T	0.000232492	0.0107792	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28255968	CATGAATCGACGACC[C/T]GGACTTATGTTCACT	8924
rs150708287	snp	A/C	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28235465	GGGCACCACAGGCAG[A/C]CCAGCACCCAGCACT	8924
rs150755150	snp	A/G/T	0.00398691	0.0444912	intron-variant	HERC2	GRCh38.p7	15:28135171	TTTAGTATCACGCAC[A/G/T]TTACACAAAATGCCA	8924
rs150756285	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28189320	TTCTTGGATTAAAGA[C/T]ATCTTTTACGAATGA	8924
rs150771724	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28150488	ACCAAAAAAACACAC[A/G]CAGCTTCTAACCGAG	8924
rs150776592	snp	C/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28236180	CACACTTTTTAGCTT[C/T]CTCTGCAGCAACAGA	8924
rs150808318	snp	C/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28185293	TCATGTCACACGCTG[C/T]AGAGTACTTAGAGCA	8924
rs150809483	snp	C/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28271083	CACGCATACACAACA[C/T]TGACTGCGCATGTAT	8924
rs150811076	snp	G/T	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28243332	GTAAAAGAAAATCTG[G/T]GTAAGAAAAAGATTT	8924
rs150817329	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28168029	GTTTTGCAAAGTCAA[A/G]CACATTCATATTTTC	8924
rs150820502	snp	C/T	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28227663	TATAATCAAAAGAAC[C/T]AGAAACAAGCATTCA	8924
rs150830180	snp	C/T	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28259930	CTGAGATTGCACCAA[C/T]GCACTCCAGTCTGGG	8924
rs150853451	snp	A/G	0.000644527	0.0179401	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28186662	CTTCCTCTTCTGCAC[A/G]GATCCGTCCCAGCAG	8924
rs150862359	snp	A/C	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28211533	CCCACTAGCTCTTTA[A/C]CTGATGAAGATGGCA	8924
rs150868499	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28143055	TGTTGGTACTAACTC[C/T]TCTAAAAAAACTAAA	8924
rs150870569	snp	A/G	0.00874735	0.0655527	intron-variant	HERC2	GRCh38.p7	15:28304328	AAACAAGAATAACTT[A/G]GCATCTTCATTTCCA	8924
rs150880836	snp	C/T	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28276229	AAAAGAGGGTTGTTA[C/T]AGAAGGATCTCCCCA	8924
rs150922267	snp	C/T	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28285139	TACAGCTGATAAAAT[C/T]AGAAGACAGAAAAGC	8924
rs150928831	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28200047	AAGGAAGTCATTAAG[A/G]TAAAATCAGGTCATA	8924
rs150930758	snp	C/T	0.00514721	0.0504689	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28257189	GCTGCTCAAAAGTCA[C/T]TGAGCAGATGTCCAC	8924
rs150934480	snp	A/C	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28149229	ACACGCAGCTCCTAA[A/C]TGAAAACATCACCGA	8924
rs150935913	snp	A/C	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28210300	CACCGTGCCCAGCTA[A/C]TGTTTTGTATTTTTA	8924
rs150945963	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28240926	CCTAAAAATAAGTGC[C/T]AAAACTATAAAATTC	8924
rs150956191	snp	A/G	7.06165e-05	0.00594165	missense	HERC2	GRCh38.p7	15:28124191	AGACGGTTCCTCAGC[A/G]CAATGATGGGGATCT	8924
rs150960375	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28272441	AACTTCTTTTCTTCA[C/T]AGTTGATCAAAAATA	8924
rs150976719	snp	C/T	0.000135738	0.00823715	intron-variant	HERC2	GRCh38.p7	15:28112074	ATTAGAAATTGAGTA[C/T]GGCTGCAGTTTACTT	8924
rs150977682	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28173059	TGAGATACCACCATA[C/T]GTCTATCAGTATAAC	8924
rs150982483	snp	C/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28253830	AGCCAGGTGTGGTTG[C/T]GGACGCCTGTAGTCC	8924
rs150992740	snp	A/G	1.64942e-05	0.00287173	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28260860	GCTTGGTCACGCGCA[A/G]GGTGTCAAAGTGCTG	8924
rs151037651	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28274027	CACTCAAACCTCTAC[A/G]AATGACTGATGGCCA	8924
rs151050244	snp	A/C	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28192281	TGAAAGGAGTTAATA[A/C]ATGCCACAAATGGTT	8924
rs151098733	in-del	-/T	0.159951	0.233219	intron-variant	HERC2	GRCh38.p7	15:28182678	AAGCATGTACAGGAG[-/T]TAAGTCCTCTGGAGG	8924
rs151115059	snp	A/G	0.000118657	0.00770159	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28215732	CTGCGGCGTGAGAGC[A/G]ATGCTCCGCACAAAC	8924
rs151122646	snp	G/T	1.64792e-05	0.00287042	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28177427	CCCTTACATTCTGCT[G/T]AAGTGTCCAAGTTTT	8924
rs151122884	snp	A/G	0.00755907	0.0610114	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314253	AACAGAACAGACCAA[A/G]AGTAGATCCTGAAAA	8924
rs151132515	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28309061	TGAATTTTTAATGAC[G/T]TATTTTGTGGCCTAA	8924
rs151141156	snp	C/T	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28228870	CTCACTTTTCCTCCA[C/T]AAAACCAATCCAATC	8924
rs151147091	snp	C/T	0.0626037	0.165477	intron-variant	HERC2	GRCh38.p7	15:28177340	CTATTCTATTCTAAT[C/T]TTCTGCAAAATAATT	8924
rs151151355	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28262101	AGTCCATCTGATGTA[C/T]CTCTCACACTGCCTT	8924
rs151156359	snp	C/T	0.00609565	0.0548696	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214073	CTGAGAACACAAACC[C/T]ACCCCTTCGGAAGGC	8924
rs151157361	snp	C/G	1.65359e-05	0.00287536	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229586	TCCAGGCGAACCTCT[C/G]CTCTCTCCAACTGCA	8924
rs151179905	snp	C/T	0.00518367	0.0506455	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272248	GTGGGGTGCATCCTT[C/T]CTGCAAATGATGCTC	8924
rs151192877	snp	A/G	0.0460142	0.144533	intron-variant	HERC2	GRCh38.p7	15:28223505	TCCTTTAGCCTAGCC[A/G]CTACTTTAGGGCCCC	8924
rs151195958	snp	A/C	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28278297	CTGAGGTGGGAGAAT[A/C]ACTTGAGCCCAGGAG	8924
rs151203423	in-del	-/AG			intron-variant	HERC2	GRCh38.p7	15:28272756	AAGGTAAAGAGAGAG[-/AG]CCCTGGGACATGGTT	8924
rs151205330	snp	A/G/T	0.000265355	0.0115157	missense	HERC2	GRCh38.p7	15:28163128	ATGCCGGAAAGCACC[A/G/T]CGGAGAGCACATCCC	8924
rs151256890	snp	A/G	0.00379308	0.0433838	missense, downstream-variant-500B	HERC2	GRCh38.p7	15:28174458	GCTCGTGGACAGAGG[A/G]CGTGGCCACATCCAC	8924
rs151271682	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28319836	AAAAACACTTTATTA[C/T]GTAAAGTCCTTTACT	8924
rs151286764	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28159259	TGTGGCATTCTCTGT[A/G]CTTCCTGAATTTTAA	8924
rs151294573	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28276736	GCGAGACTCTGTCTC[-/A]AAAAAAAAAACAAAA	8924
rs151303132	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28126658	CCATATGTTCTCATG[A/C]GATGAGGATGCAACG	8924
rs151314175	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28217181	TGACTTACACTTACA[C/T]TGGGTGTCTCATTCG	8924
rs151323226	in-del	-/GG/GGCAGTGTTTGTA	0.439502	0.163061	intron-variant	HERC2	GRCh38.p7	15:28262669	CCTGCCACAGAAAGT[-/GG/GGCAGTGTTTGTA]CAACTCAACAGGTTT	8924
rs151325729	snp	A/G	1.65236e-05	0.00287429	missense	HERC2	GRCh38.p7	15:28112008	ACTCAGGGAGGAAGT[A/G]GTCTGGAGGGTTGTA	8924
rs151325790	snp	A/G	0.0107246	0.0724382	intron-variant	HERC2	GRCh38.p7	15:28298518	GAAGAAATACTTGCC[A/G]GGCACGGTGGCTCAC	8924
rs151331392	snp	C/T	3.3184e-05	0.00407319	missense, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28292972	CTTCATCTTTTTTCT[C/T]TTTGTCATTCAGATC	8924
rs151333414	snp	A/G	0.0260105	0.111035	intron-variant	HERC2	GRCh38.p7	15:28289593	TGATCTCCCCAGAAC[A/G]CTGAGACTGGCTTCT	8924
rs151334920	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28137653	ATGTTCTGATTGCTC[C/T]GCCAACCAGCTGTTC	8924
rs180680885	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28153756	GACAATAGCTTCATT[C/T]TACACCAAGACAAGA	8924
rs180690224	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28133358	ATTTTGGCTATCAGA[C/T]CTTAGTCAGATTATA	8924
rs180699401	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28162298	AGATTGCGCCACCGC[A/G]CTCCAGCCCGGGTGA	8924
rs180703467	snp	A/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28170688	AAATTAAACACTTTC[A/G]TTCTATGAAAGGAAA	8924
rs180707264	snp	A/G	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28211782	GAATGGGAGATCCAG[A/G]GTTGAAAGTGCTTAC	8924
rs180721777	snp	A/G	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28147903	TTAGCCAAGTGTGGC[A/G]GCACAAGCCTGTAGT	8924
rs180723987	snp	A/G	0.000548114	0.0165456	intron-variant	HERC2	GRCh38.p7	15:28121458	AACAGACAAAATTTA[A/G]AATCTGATATGGAAA	8924
rs180725722	snp	A/C	0.0130921	0.0798413	intron-variant	HERC2	GRCh38.p7	15:28193687	GAAAACAAAAAGACT[A/C]TCTGAAAAGCAGACG	8924
rs180970316	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28295448	TTTTGAGACAGAGTC[C/T]TGACTCACCACAACC	8924
rs180980327	snp	A/C	0.00398564	0.0444627	intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28315605	CAAGACCAGCCTGGG[A/C]AACATGGTGAAACCC	8924
rs181032968	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28229024	GTCTCCTGCTAAATT[C/T]TGAAGTTTTGTTTAA	8924
rs181036399	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28266186	CGATGCCAAACATGG[C/T]ACCCAGTAGAAATAT	8924
rs181048464	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28222856	GGAAACCCTGGGCCT[A/G]GAGTCTCTATCCAGC	8924
rs181050358	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28204168	AGAATCCAGAATGAA[A/G]TAAGAATTCTCACAT	8924
rs181054971	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28183630	AGGTGCTAAGGAATT[A/G]CTGCTTCTGTGTTTG	8924
rs181059205	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28258168	AAAATTAAACAACAT[A/G]CTTAATAATCCATGG	8924
rs181061349	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28251047	AAAAAGTCACATGCA[A/G]CAAGGATGAAGACAC	8924
rs181065084	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28240590	ACAGATTACAAAAAC[A/C]TCACAGTGCTAATAA	8924
rs181069637	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28266430	TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG	8924
rs181071196	snp	C/T	0.0138799	0.0821421	intron-variant	HERC2	GRCh38.p7	15:28275415	CCTGGCTCGCCCCAG[C/T]TCCGGCGTCCTCCAC	8924
rs181074674	snp	A/G	0	0	intron-variant	HERC2	GRCh38.p7	15:28285459	CCATGGATCAAAGAG[A/G]AAGTCTCAAGGGAAA	8924
rs181105039	snp	A/G	0.0368353	0.130617	intron-variant	HERC2	GRCh38.p7	15:28194476	TCGGGAGGCTGAAGC[A/G]GGAGAATGGCATGAA	8924
rs181109929	snp	A/C	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28211855	GAGGGGAGAAAACTC[A/C]AGAAGAGTGGGCAGA	8924
rs181123694	snp	A/G	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28171948	GGCGTGGTGGCAGGT[A/G]CCTGTGGTCCCAGCA	8924
rs181132967	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28230115	AGCACTGTTTCTGGA[A/G]CAAAGAATATATTTA	8924
rs181142318	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28286324	CCTAAAGACAGTACA[A/G]AGTACAGAACAATAT	8924
rs181148293	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28251239	CCTCAGGTTGGGAGT[A/T]CAAGACCACCCCAGC	8924
rs181149277	snp	C/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28307134	GCCACCACGCCCGGC[C/G]TGCAAACTTATCTAT	8924
rs181160345	snp	A/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28296129	TCTACATAAAAAACA[A/T]TTATGCTCTGCTTTC	8924
rs181163721	snp	C/G			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316178	CAGTGAGCTGAGATA[C/G]TGCTACTGTACTCCA	8924
rs181171908	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28275550	TAAGCTTTTCACTAC[C/T]TGTGTATGTTAATTT	8924
rs181186906	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28154393	GGCAGGACACAGAAA[C/T]AGCCATCTTGCCAAC	8924
rs181227855	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28119250	AATACAAAAAAAAAA[A/T]TTAGCCTGGCATGGT	8924
rs181238578	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28146587	TTTTGTGCGGTCACT[C/T]CCGGGCAGACTTTCC	8924
rs181242508	snp	C/G	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28150124	CACACGGCTCCTAAC[C/G]GAGAACATCACTGAG	8924
rs181244209	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28197285	AAAACTATACACATA[A/C]TTATTTCTCATGCAA	8924
rs181251417	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28158445	TGCATAGATATTTAG[G/T]ATAGTTAGTTCTTCT	8924
rs181257414	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28128008	CCAAGCAACTGTAGT[A/G]AGCATCATCAGCAAG	8924
rs181258303	snp	C/G	9.8881e-05	0.0070307	intron-variant	HERC2	GRCh38.p7	15:28176632	ATATACTTCAGGCCA[C/G]CGTTTCATATCATTC	8924
rs181266464	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28217301	CCACTTCACCTGAAT[A/G]TAGTCACCTGCCCAC	8924
rs181277629	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28245127	GTCTTCCCATTATCA[A/G]TCTCTGCCTCCTGAG	8924
rs181304088	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28279416	CAAAACAAAATAAAA[C/T]GTATACAACGTTCAG	8924
rs181313774	snp	C/G	0.00795532	0.062565	intron-variant, upstream-variant-2KB, downstream-variant-500B	HERC2, LOC107987422	GRCh38.p7	15:28319511	AATCACTTGCATTCG[C/G]GAGGCGGAAGTTGCA	8924
rs181317223	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28134771	GCAGTGGCGCAATCT[C/T]GGCTCACTGCAACCT	8924
rs181346369	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28209183	ATTTTCATATTTCCA[C/T]GGCAATAAACATATA	8924
rs181353642	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28166346	AAGGGAGAGTAGGAA[G/T]AAGCCCTGTGGTACT	8924
rs181370275	snp	A/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28161664	CTAGCCATATTTCAG[A/T]GTGCAGTGGCCATAT	8924
rs181379122	snp	A/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28225937	GTAACAAGTAAAGAG[A/T]TTGAATCAGTAATTA	8924
rs181386031	snp	C/G/T	0.00358891	0.0422285	intron-variant	HERC2	GRCh38.p7	15:28262617	ACCACACAGAGGGAA[C/G/T]CCTTACTGAGTCCAG	8924
rs181399139	snp	C/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28139593	AATAAATGTGTGTGA[C/G]ACAGTACATTACATG	8924
rs181399939	snp	A/G			intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28300788	AGATTATGTCACTGC[A/G]CTCCAGCCTGGGTAA	8924
rs181476446	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28114471	ACAAAATAAGCTTTA[C/T]ACCCACAGATCAGCA	8924
rs181485938	snp	C/T	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28189342	TACGAATGATAATCT[C/T]CATTGTTGATTTAAT	8924
rs181499986	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28197694	GGGCGGAGGTTGCAG[C/T]GAGTCAAGATGGCGC	8924
rs181503279	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28158842	AGCATTGATGGTCTT[C/T]ACAATTTGGCATGTT	8924
rs181609721	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28140925	CTTTTGCATACATGA[C/T]GTATTTTCAAAATAA	8924
rs181623686	snp	A/C	1.65452e-05	0.00287616	intron-variant	HERC2	GRCh38.p7	15:28177383	AGTCAGAAACAGTTT[A/C]TTATTAGCAAATGAG	8924
rs181625743	snp	C/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28310251	AGGAGTACAAGACCA[C/G]CCTGAACAACATGGC	8924
rs181686318	snp	C/T	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28269492	ACAATAAAAAAAGGC[C/T]GGGAGTAACACTGAG	8924
rs181689516	snp	C/T	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28226320	GGGACCCAAAGTAGC[C/T]AAAATCATCTTGAGA	8924
rs181712725	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28263389	GTTTTCTTTTTGTTT[C/T]CATTCCATGAAAAAC	8924
rs181716838	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28289941	AGGATTACACACCTA[A/G]GTGAGAGGACCACAC	8924
rs181718307	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28247411	CTTCAGTTTTTCTGT[C/T]TACATGGTTCTTTTT	8924
rs181820405	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28300149	ACCAAAAGCAAGTAC[C/T]AATGACTACCTACGG	8924
rs181822662	snp	C/T	0.00597247	0.0543191	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318433	GGAGTTCAAAACCAA[C/T]CTGGCCCACATGGTG	8924
rs181841094	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28208516	AGCAGGTGTATCACC[C/T]GAAGGTCAATGCTTA	8924
rs181843697	snp	A/T	0.261056	0.249755	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28301699	ATCTTTTTTTTTTTT[A/T]AAACTTCTGTGGATA	8924
rs181847799	snp	G/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28177808	CACGAAAAATCAAAA[G/T]TTAGATGAAAAAAGT	8924
rs181861263	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28142142	ATTCCTTGGCAAGCG[A/C]AATTTTTCTGTGTCT	8924
rs181861441	snp	C/T	0.00755907	0.0610114	intron-variant	HERC2	GRCh38.p7	15:28225524	AACACGGTGAAACCC[C/T]GTCTCCACTAAAAAT	8924
rs181863131	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28159700	CTTTAGCTCGGAGAA[G/T]TTTGATCGTCTGAAG	8924
rs181870320	snp	G/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28218925	GCTTTGACCTCGCAG[G/T]GTAAGCAGTCCTCCC	8924
rs181876512	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28244407	GTAGGGACAAGAACT[C/T]AGTATAAGATGATCA	8924
rs181882760	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28279120	CCTCAGTCTCCCAAG[C/T]AGCTGGGATTACAGG	8924
rs181883010	snp	A/G	0.00225013	0.0334664	intron-variant	HERC2	GRCh38.p7	15:28198328	ATACTAAGTACACAT[A/G]CGTTAATGAAAAGTT	8924
rs181886834	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28236225	GACAACCACTCACAG[C/T]TGTTTCTACCTGATT	8924
rs181889482	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28251661	AAAAATCAGCAAGGC[A/G]TGGTGGTGTACGCCT	8924
rs181902578	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28266772	CTGGAGGTAGGAAGG[A/G]GGCATCAACTCAAAG	8924
rs181907424	snp	C/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28307487	AGTTTTTCTACTTTT[C/T]TGATTTTCCTCTTAG	8924
rs181907640	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28287014	GTGGGATAATGCCAG[C/T]GGCACAGTCTCAGGT	8924
rs181915583	snp	A/C	0.0107246	0.0724382	intron-variant	HERC2	GRCh38.p7	15:28115089	TGCAGCCGAGGCACA[A/C]CACAGCCATGGGGAA	8924
rs181962501	snp	A/C/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28161997	TCAAAATAAATCCCA[A/C/G]GTGGCTAAAAAATGT	8924
rs181963647	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28253982	ATAAATATTAAAAAA[A/T]AATAATAAGTACATA	8924
rs181969141	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28182844	ATTCCAAGCCATGGA[A/C]ACAGACGCACAGCTG	8924
rs181970345	snp	A/C	0.00835141	0.0640778	intron-variant	HERC2	GRCh38.p7	15:28289973	CCTCAGTGAGAGGAC[A/C]ACACACCTCAGTGAG	8924
rs181970987	snp	A/C	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28147618	CTCCAACCTGGGCGA[A/C]AAAGTGACAAAGCTT	8924
rs181990497	snp	A/G	0.0429648	0.14013	intron-variant	HERC2	GRCh38.p7	15:28203601	AATCAGCAATAAAAC[A/G]AGTACAACCCCTGAC	8924
rs181995476	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28222672	CTGCAGGCTGGCCCT[C/T]GGCTGGAGTCTGGAT	8924
rs182014451	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28188742	TAAATGTTGAAGCTG[G/T]GTGACAGGTTTGTGA	8924
rs182020458	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28120366	TTGTAATCAACATCA[C/G]GGTAAAAATCATGTG	8924
rs182076659	snp	C/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28279802	TGGGTGACAGAGCAA[C/G]ACATTGTCTCTCCAA	8924
rs182101689	snp	C/T	0.00835141	0.0640778	intron-variant	HERC2	GRCh38.p7	15:28149859	CACACGAACGCACAT[C/T]CTAGTAAAATTACCA	8924
rs182117225	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28137056	AACAACAATAATGTC[C/T]ATGGCAGAGGGGAAT	8924
rs182137752	snp	C/T	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28218271	CCCTCAAGCAGCTTC[C/T]CCCTCACAGCCCCAG	8924
rs182147961	snp	C/T	0.00120141	0.0244798	intron-variant	HERC2	GRCh38.p7	15:28274260	CAGGCCAGCTGTCTG[C/T]GTGCAGAAGGCAAGA	8924
rs182155601	snp	A/C	0.0150606	0.0854603	intron-variant	HERC2	GRCh38.p7	15:28253789	CAATATTTTGAAACC[A/C]CGTCTCTACTAAAAA	8924
rs182159054	snp	A/G	0.00438332	0.0466095	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28315258	AACGTTCATACCACA[A/G]GGAATTCACACCCAC	8924
rs182210492	snp	C/T	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28240404	GCCTGGGCGAAAGAG[C/T]GAGACTCCGTCTAAA	8924
rs182218013	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28172444	ATAAATCAATGAAAC[A/T]GTACTGAGAGTCCAG	8924
rs182247010	snp	C/T	0.0111196	0.0737302	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316931	ACAGGCACGTGCCAC[C/T]ACACCCAGCTAATTT	8924
rs182258953	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28290328	TGAGATGTAGTCTCG[C/T]TTTGTCACCCAGACT	8924
rs182260337	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28310949	AGGTGAGGTGGCACG[C/T]ACCTATAGTCCCAGC	8924
rs182260846	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28270289	CAGACAGACATGTAA[C/T]ATAGATATATAATAT	8924
rs182264302	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28310843	AGCACTTTGGGAGGC[C/T]GAAGCGGGTGGATCA	8924
rs182283035	snp	A/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28224371	GGACCATAGGCACAC[A/T]CCACTATGCCCAGCT	8924
rs182298755	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28242714	TCCATATGACCAATA[C/T]CATGAGCAAAGTAGT	8924
rs182299450	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28233085	CTCTGAAATCACAGA[A/T]CCAATGTGGCAGGGT	8924
rs182305793	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28277674	TTAGCACCTACCGCC[A/G]ACCCGTACATAACAC	8924
rs182308961	snp	C/T	0.00874735	0.0655527	intron-variant	HERC2	GRCh38.p7	15:28260119	CCAAGGCAGGCAGAT[C/T]GCTAGAGCTCAGGAG	8924
rs182311491	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28297525	CTGATGAGAAGTGCT[A/G]TATTAAATATAAACC	8924
rs182327777	snp	A/C/G	0.00756609	0.0611252	intron-variant	HERC2	GRCh38.p7	15:28236377	CTCACTGCAACCTCC[A/C/G]TCTCCTGGGTTCAAG	8924
rs182385364	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28165901	CAACAAGCACACAAA[G/T]GGCCCAGATCTTGAC	8924
rs182419242	snp	A/C	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28231007	TGGGCAACACAAAGC[A/C]AGCAAGAGGTAGAAT	8924
rs182440569	snp	G/T	0.00398564	0.0444627	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174075	TTATAACTGAATAAA[G/T]CTGTTAAAAAATACA	8924
rs182445663	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28148743	TGAACGCGCATTCTA[A/G]TAAAACTACCGAAGA	8924
rs182462952	snp	C/G	0.00716266	0.059414	intron-variant	HERC2	GRCh38.p7	15:28122155	ACACTAAAAGAAATC[C/G]GGAGTGCCTGGGGTG	8924
rs182466382	snp	C/T	0	0	intron-variant	HERC2	GRCh38.p7	15:28155102	ACATGAACTCATCCT[C/T]TTTTATGGCTGCATA	8924
rs182472232	snp	A/C	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28194906	ACTAAAAATACAAAA[A/C]TTAGCCAGGCATGGT	8924
rs182477473	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28195051	ACAGAGTGAGACTCC[A/G]TCTCAAAAAAAAAAA	8924
rs182478007	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28154847	TGTACACATGTGCCA[C/T]GTTGTTGTGCTGCAC	8924
rs182540215	snp	A/C/T	0.000619232	0.0175852	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214254	TGCGGGCGCACCCTG[A/C/T]GCCGCCTCAGCGTGG	8924
rs182546543	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28282876	GGCGGCGGTTGCAGT[A/G]AGCCGAGAACGTCCA	8924
rs182553882	snp	C/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28232084	CACCCCTCGCATTCA[C/G]ACAGGCTGTTATGGT	8924
rs182555979	snp	A/G	0.100588	0.200439	intron-variant	HERC2	GRCh38.p7	15:28195675	ACCAGGGTTGGGGTA[A/G]GGGGAAGTAGGGCAG	8924
rs182557913	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28298776	ACTCCAGCCTCAGCA[A/G]CAGAGCAAGACTCCT	8924
rs182565914	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28252898	GACAGCAGGCCCACC[C/T]CACGCCACAGGCCCA	8924
rs182578737	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28288265	AAAACTTTTTTCTGG[C/T]CAGCCATGGTGGCTC	8924
rs182581546	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28267614	TTACAACACTGTCAG[A/G]GTTGGGCTGTTCTGA	8924
rs182619621	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28174868	CTTAATATTAATCCA[A/G]TTCTGCTTTGTTGCA	8924
rs182673016	snp	A/G			downstream-variant-500B	HERC2	GRCh38.p7	15:28110829	AGATGGGGCTGGGGA[A/G]GAAGTCGGAGGAAAC	8924
rs182674530	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28267181	TGACCTACTAGTTTG[C/T]AAAATACACACAGTG	8924
rs182682801	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28168656	AGCACAGGAAGTGGA[A/G]AGGCAGGGCTAGCAC	8924
rs182691673	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28152134	TATGGGCCTCCGAAT[C/T]GGGCAGCACCTTGCA	8924
rs182696278	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28219635	GCCCCGAGCCCAGAC[A/G]GTGCGCTATGGCATA	8924
rs182696485	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28199443	CTGGTCATCTTTATA[A/C]ATATCAGAACACCAA	8924
rs182697208	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28307548	TATGCTGTGTTGCCA[C/T]TGCCATTTGTTTCAA	8924
rs182706041	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28255098	CCCAACACTTTGGGA[A/G]GACAAGGTGGGGGGA	8924
rs182709728	snp	A/C	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28237697	TGTCGATACCTGGAA[A/C]GCTAATCCCAATATA	8924
rs182719428	snp	A/G	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28270563	CCTTCAACTGCAAAC[A/G]CGTTTAAAAACCACA	8924
rs182737785	snp	C/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28128311	AACTGGCTGGCAGGA[C/T]GAGCCTCCCTGTTTG	8924
rs182741939	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28150235	GCCACATGAACGTAC[A/G]TTCTAGTAAAATTAC	8924
rs182750302	snp	C/T	1.6543e-05	0.00287597	intron-variant	HERC2	GRCh38.p7	15:28130115	CCTTCATGCTCAACC[C/T]TCTTAGATTCACAGG	8924
rs182751447	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28178117	CTCATTCTCCCCCTT[C/T]CTTACCAACAGAACC	8924
rs182757838	snp	C/T	0.0414363	0.137845	intron-variant	HERC2	GRCh38.p7	15:28207903	AACAAGTGGTGTGTC[C/T]GTGTTCCCATAAAAA	8924
rs182765901	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28231906	CCACAGGAAACTCTA[A/G]AAGTGACAGTGTGGG	8924
rs182769207	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28164584	ACACACACAAACACA[G/T]AAAATATGTCTAGAA	8924
rs182785149	snp	C/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28264562	ATAGCAGCACAGCAG[C/G]GACACTTCCCTACAA	8924
rs182831965	snp	C/G	0.154993	0.231244	intron-variant	HERC2	GRCh38.p7	15:28304163	AGAGTGAGACTCCAT[C/G]TCAAAAAAAAAAAAA	8924
rs182840654	snp	A/G	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28258695	ACTAGAAAAAGAACA[A/G]AGTGAACGCAAAACA	8924
rs182874358	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111565	TTGGAAGTCGAGCGT[C/T]CACAGTGTTCCACGC	8924
rs182914120	snp	C/T	0.0126979	0.078662	intron-variant	HERC2	GRCh38.p7	15:28155614	TTGTTGATGGGGTTG[C/T]TTTTTTCTTGTAAAT	8924
rs182921540	snp	C/T	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28223224	TAGGAGCGCTAACCC[C/T]AGGAGAGTAGGCTAG	8924
rs182934485	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28185247	ATATAACGTGCTCAA[C/T]AGCGGCACAGGGCAG	8924
rs182960492	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28252338	ACGGGCACTGCCCTC[A/G]TGAGAACAAAGGACC	8924
rs182962673	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28287351	CCCCTTCAAGGCTGC[C/T]AGGTAGAGAGTCGGT	8924
rs183004530	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28267895	CATCCCTCATTTAAA[C/T]CTAATGCCAAAGTTC	8924
rs183007422	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28149314	TCCTGAGAACATCAC[C/T]GAAAATGGCCACACC	8924
rs183015438	snp	C/T	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28189534	ATAGTTTGCCAATTT[C/T]TTCACTTATTAGCAC	8924
rs183025263	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28209429	CCTCACTGCAAGCTC[C/T]GCCTCCCGAGTTCAC	8924
rs183027475	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28187362	TTTTGAGATGGAATC[C/T]TGCTTGTTGCCCAGG	8924
rs183028589	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28288803	CAGTGAGCTGAGATT[C/G]TGCCATTACACTCCA	8924
rs183029473	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28166766	GGAGTCCCAGTGACC[A/G]AGTCCCAGTGACCAG	8924
rs183033297	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28308238	GTCTTTCATCAGCGT[C/T]TTAGAGTTTTCATTA	8924
rs183035374	snp	A/G/T	0.000455304	0.0150815	intron-variant	HERC2	GRCh38.p7	15:28116966	CCTGTGGGCTCAGGC[A/G/T]ACCACTGCCGGGGAC	8924
rs183045194	snp	A/C	0.00755907	0.0610114	intron-variant	HERC2	GRCh38.p7	15:28249593	GGGACCAGAGTCTGC[A/C]ATGCCAACCCACCAA	8924
rs183049400	snp	A/C	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28210225	TGTAAGCTCCGCCTC[A/C]CGGATTCATGCCATT	8924
rs183051135	snp	C/G	0.00353271	0.0418793	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28213988	CTAGTGCAGACCAAA[C/G]AGCGAGCTCGACAGA	8924
rs183072631	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28308126	GGGATTGCACTGAAT[C/T]GGTAGATTGCTTTGG	8924
rs183106063	snp	A/G	0.000399281	0.0141238	missense	HERC2	GRCh38.p7	15:28144160	GCAAGGTTGAGTCGG[A/G]AGTCTAACAGACACG	8924
rs183107400	snp	G/T	0.00835141	0.0640778	intron-variant	HERC2	GRCh38.p7	15:28200313	GGCAGGAGAATGGCA[G/T]GAACCCGGGAGGCGG	8924
rs183120284	snp	A/G	1.65277e-05	0.00287464	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28248713	ACATCTTTCAATCTG[A/G]CTACAGTCTGAGAAG	8924
rs183124845	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28241113	GAGTGAAACAGCAAC[C/T]GAAAGAATGCAAAAC	8924
rs183136785	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28281328	CATTATAAGGGAATT[G/T]TAAGTTACCTCCCAC	8924
rs183143409	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28220333	AGGCTCCGAGGACAG[A/T]GCGCCAGCTGCAGGT	8924
rs183143615	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28263791	AATCCCAGAACTTTG[C/G]GAGGCCAAGGCGGGC	8924
rs183143974	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28290997	ATGAAAAAGAAAACA[A/G]AATCAATAAAACCAA	8924
rs183153494	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28301913	CAAGGGTTTCTCCTG[C/T]CTCAGCCTCCAGAGT	8924
rs183159223	snp	A/C	0.00716266	0.059414	intron-variant	HERC2	GRCh38.p7	15:28311280	GACCAGCCAAAGCAA[A/C]ACGGTGAAACTCGGT	8924
rs183179528	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28163437	AACAGATTAAGAAAC[A/G]ACGGCCCCTAAAATC	8924
rs183195579	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28205041	GGGGTGGGCGGGGTG[G/T]GCCACCATTGTATAC	8924
rs183210001	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28137616	ACCCATAGAAGACGG[C/T]GAACTTAAACGATAA	8924
rs183262458	snp	A/C	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28163762	ACTGGCATTAACACA[A/C]TATCCAGTCTCTCTC	8924
rs183283016	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28241940	GTCATCAACTGATGG[A/T]TGGACAGCAAAATGT	8924
rs183284907	snp	C/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28191631	ATGTGCAACACAAAT[C/T]TGCTAGACTATACTA	8924
rs183312297	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28227495	AAACACAAAAAATAG[C/T]GTTGGCAGGGAAGCA	8924
rs183318872	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28116165	AGTCAACAGCACCTC[A/G]TTCGCTTCCACAATG	8924
rs183349386	snp	C/T	0.00874735	0.0655527	intron-variant	HERC2	GRCh38.p7	15:28160228	TCAGGTCTCAAACTC[C/T]GTTCTGGGAGAACCA	8924
rs183358230	snp	A/G	0.00517822	0.0506191	intron-variant	HERC2	GRCh38.p7	15:28149022	AACATCACCGAGAAC[A/G]GCCGCACAAACGTAC	8924
rs183363165	snp	A/C	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28122858	AGCTCCCACCCATGC[A/C]CCGCTCACAGCCTGC	8924
rs183379321	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28253258	CCACCTCCTCCTAGT[C/G]TGGCCTTCCAAAATA	8924
rs183389163	snp	C/G	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28277182	AGCAGTTAAGGTGGG[C/G]AGAGAAGACGTGAAT	8924
rs183405709	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316752	ATTTATCAAGATACT[C/T]ATGTTTATACTTTTT	8924
rs183546134	snp	C/T	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314478	TATGTAGGAGCCATT[C/T]TTATTTCCTTTAATT	8924
rs183551562	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28238290	AGGAGAAACAGTGAA[C/T]AGGAAATAAGTTAGG	8924
rs183560064	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28271076	TGCTGTACACGCATA[C/T]ACAACATTGACTGCG	8924
rs183585292	snp	A/G	0.0115144	0.0749975	intron-variant	HERC2	GRCh38.p7	15:28193776	AAACCAAATTGCAAT[A/G]GAATACTATTTTTAA	8924
rs183591081	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28211827	AGCAGCAATCGTAGG[C/T]CTGTGGGAGCAAGAG	8924
rs183596087	snp	A/G	0.00028622	0.0119594	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256192	GGCGGCCGACTGCAC[A/G]GTGCTCAGCACGCCC	8924
rs183596266	snp	A/T	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28171641	GAAGCTCACTTTTTT[A/T]AAAAAAAAAAGCAAT	8924
rs183600456	snp	A/G	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28160401	TTCAGCTTCCGGGCC[A/G]CTTTGTTTACCTACT	8924
rs183601499	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28240144	AATCCAATCAGAGGG[C/T]GCAGTGGCTCACGCC	8924
rs183604957	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28273123	TGTATTTTTAATATT[C/T]AGGATCAAGTTTCTG	8924
rs183618879	snp	C/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28200091	GACACAACAGGACTA[C/G]GGTCTTTATAAGAAG	8924
rs183633250	snp	A/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28296316	CCATCTTTATTAAAA[A/T]TACAACAATTAGCTG	8924
rs183643899	snp	A/C/T	0.014286	0.0834106	intron-variant	HERC2	GRCh38.p7	15:28291777	GGGTGTGGTGGTGCA[A/C/T]GCCTGTAGTCCCAGC	8924
rs183691260	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28226935	TTGGTACACTTATAT[A/C]GTGCATTTATTGGTA	8924
rs183714730	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28196974	AATAACATGAAGACT[C/T]CTTTCGTCCTTTGAT	8924
rs183724784	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28215414	TAGTTGCAGGATTTA[C/T]CACTTAAGAGAAAAG	8924
rs183731464	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28176163	TTCAGCAGAAGAAAC[C/T]GTTCCCATAAATCTC	8924
rs183741469	snp	A/T	0.0111196	0.0737302	intron-variant	HERC2	GRCh38.p7	15:28255626	TTCCGGGTAACGGGA[A/T]TGGTCTACATGAGGA	8924
rs183775782	snp	G/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28139111	ATTTGTGTGACATGC[G/T]TTGCGAAGACACTTG	8924
rs183785353	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28255438	TCCCAATAATAAAAA[A/C]GAAGTCACAATACAC	8924
rs183789118	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28157757	TAGTTCTGCTCTGAT[A/C]TTAGTTATTTTTTGC	8924
rs183800730	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28190206	TTTTTTTTTTAGTAG[A/T]GACGGGGTTTAACTG	8924
rs183808592	snp	A/C	0.0463947	0.145069	intron-variant	HERC2	GRCh38.p7	15:28218209	TGACACCTCTACAAG[A/C]CGAGGAACGCTAAAG	8924
rs183809229	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28150966	AGAGTCCACTTCAGA[C/T]CCCACGAGGACCAGT	8924
rs183816064	snp	C/T	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28253701	GAACAGTGGCTTACG[C/T]CTGAAATCCCAACAC	8924
rs183821495	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28235987	CTGAAATATAACTGA[C/T]TTGAGCCTGGTCTGG	8924
rs183827563	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28145517	ACCAGAAAAACCCAC[A/G]CCCACTGGGACCATA	8924
rs183832501	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	HERC2, LOC107987422	GRCh38.p7	15:28317730	AGTAGTAGTTACATT[C/T]ACAGACCCTTGATAG	8924
rs183832553	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28268998	CGTCAAATGAGTTTA[A/C]ACGTGGAAATGAGTT	8924
rs183842097	snp	A/G	0.021333	0.101051	intron-variant	HERC2	GRCh38.p7	15:28289575	AAAGCCAGTCGCTGG[A/G]GCTGATCTCCCCAGA	8924
rs183842269	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28309254	GTCCAATGCTGAAAG[C/T]GGAGTGTTGAAGCCT	8924
rs183845694	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28244483	CAGAGAAATGAGTCC[A/G]AGTTTGGGAGGGTCC	8924
rs183850867	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28220022	GAGGAAAGGTAAAGG[C/T]AGGTGGCAGGTGGGG	8924
rs183852827	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28179747	GCAACACTATGATCC[C/T]AGCTAGGCTAATGTA	8924
rs183857014	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28279209	TGTTGGTCAGATCTC[C/T]AACTCCCGACCTGAG	8924
rs183863366	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28261765	TCTCAGAAGCTTAGA[A/C]AACAATAAACACCAT	8924
rs183864117	snp	A/G	8.27e-05	0.00642986	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272293	CAAGGGCAAAAGTGG[A/G]GCGCTGGTGCCCTGG	8924
rs183873313	snp	C/T			intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28300301	TAAATCATAAAAAAG[C/T]GAAACCTACAACTGG	8924
rs183874824	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318515	CACCCGTAGTCCCAG[A/C]TACTCGGGAGGCTGA	8924
rs183875178	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28197350	TGCCACGGATTTGAT[C/T]TGGAATCTCAATAGT	8924
rs183882194	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313425	ACCTTGTGATCCACC[C/T]GCCTCGGCCTGGGAT	8924
rs183918710	snp	A/C/G	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28209565	AGCCAGGATGGTCTC[A/C/G]ATCTCCTGACCTCGT	8924
rs183946227	snp	A/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28136633	CAGGAGTTGGCAAAT[A/T]ATGGCCCATGTGCCA	8924
rs183953183	snp	A/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28128584	ATGATTAAAGGGTGC[A/T]TGCTTATATAATTCA	8924
rs184002112	snp	C/T	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28167993	ACATAGCCACTACCA[C/T]CCCCAGTCAGGCCTA	8924
rs184035203	snp	A/C	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28149352	ATTCTAGTAAAATTA[A/C]CAAAAAAACACACGC	8924
rs184039988	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28164770	ATAAATAAATTGGGG[A/G]GAAATAAATCATATT	8924
rs184091739	snp	C/T	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28259216	TCTCCTGCCTTAGCC[C/T]CCTGAGTAGCTGGGA	8924
rs184094413	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28126016	AGGGTTTCACCATGT[A/G]GGTCAGGCTGGTCTC	8924
rs184215449	snp	A/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28285584	CTAAATAAATGATAT[A/T]TTAGAAACTTGGAAA	8924
rs184348384	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28251171	AATGTGGCCAGGTGC[A/G]GTGGCTCACACCTGT	8924
rs184378639	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28306350	TTTTTATCCTTCATT[A/C]TATTGATATGATGTA	8924
rs184402941	snp	A/T	0.00676609	0.0577691	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314749	GCCTGTAATCCCAGC[A/T]ACTCCGGAGTCTGAG	8924
rs184405901	snp	C/T	1.75508e-05	0.00296228	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28268605	GGCAAGGCCTTGGAC[C/T]AGCTGTGGGGCCTAA	8924
rs184411145	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28308720	TTATGTTGAGGTATG[C/T]TTCTTCCATAACCAG	8924
rs184453960	snp	C/T	0.000149146	0.00863428	intron-variant	HERC2	GRCh38.p7	15:28229420	AACATTTTGTTGCCA[C/T]AGCTACCTTAATTAA	8924
rs184469644	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28266242	TACAATAGGCTAGGC[A/G]CGGTGGCTCACACCT	8924
rs184501086	snp	A/G	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28188437	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	8924
rs184505743	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28225318	AGATTAGAGCAGCCA[C/T]AAATTAAATAGAGAA	8924
rs184507886	snp	A/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28208170	ATTTCTTTCATCCTC[A/T]GCAGGTTTAAAATTA	8924
rs184514967	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28260508	CTTCACACTGCAAGT[C/T]CTGGCCAGGGCAATC	8924
rs184521279	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28243906	AAGAATGTTAACGTA[C/T]TGGCAGGAGCGCTGG	8924
rs184528231	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28289273	TTGGCAAACACACCA[C/T]GCAAACACCAAATCA	8924
rs184558965	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28260256	AACACACTAAAGAAG[C/G]AAAACTGCATGACCA	8924
rs184578708	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28160704	GCGATGCCTCGCCCT[A/G]CTTCAGCTCATGCTC	8924
rs184582032	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28181026	AAAGATAAAAACACA[C/T]ACCTGTAGACTATGC	8924
rs184603655	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28187837	TTTAGTGGAGTTGGT[C/T]TACTTGTCCTGCAAA	8924
rs184614465	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28114068	GCCCAGGACACCTGC[C/T]AGGACTACCCCCACC	8924
rs184620263	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28225569	TGGGCGTGGTGGCGC[A/G]TGCCTGTAGTCCCAG	8924
rs184624000	snp	C/T	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28253522	CCTCCAACTTCTCCT[C/T]TCACCTATATTGAAA	8924
rs184638535	snp	C/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28145660	CTGCATTACCTGGCC[C/G]TTTACAGGAAACACT	8924
rs184640036	snp	C/T	0.0178098	0.0926698	intron-variant	HERC2	GRCh38.p7	15:28158532	TGGTGGTTTAAAGTC[C/T]GTTTTATCAGAGACT	8924
rs184646214	snp	A/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28224833	AATGAAATGAGAAAT[A/T]AAAAAAAGAAAAGTG	8924
rs184647895	snp	C/T	0.000496204	0.0157434	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28192083	AGCTGTCCAGCAGCA[C/T]GCCTGGCTGGCTGCT	8924
rs184648113	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28146607	GCAGACTTTCCTACT[A/G]CAACCACACTCCCCT	8924
rs184648730	snp	A/G	0.00301352	0.0386998	intron-variant	HERC2	GRCh38.p7	15:28117249	ATGCACGAGGAGGAG[A/G]CACCGTGCATGGGCC	8924
rs184654245	snp	C/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28210326	TTTTAGTAGAAATGG[C/G]GTTTCACCATGTTAG	8924
rs184672268	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28282996	CGGGACTGGATGGGA[C/T]GGGATGGGAAGGGAA	8924
rs184673232	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28265080	CTCCACAACGCCAGA[A/G]ACACACAAGATGCCA	8924
rs184703875	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28277956	GTGCACATCCTCCAG[C/T]ATAATTTAAATCATC	8924
rs184712768	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28169364	TGACTTACAACATAC[A/C]GCATTTAAAGACAAT	8924
rs184712993	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28120100	CCTTGCCTACAAGCT[A/G]TAATGTTTATGATGC	8924
rs184718485	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28153092	GGCACGGTGGCTCAC[A/G]CCTGGAATCCCAGCA	8924
rs184728154	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28112379	CAGCCCAACTTTGAC[C/T]CCTACAGATTAAGAT	8924
rs184745026	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28139836	GAGGCCAAGGTGGTC[A/G]GATCACAAGGTCAGG	8924
rs184750726	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28306147	TCCGTGTCTTGTTCC[A/G]GATCTTAGAGGAAAG	8924
rs184750836	snp	A/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28284312	AAGTAAACCACAGAG[A/T]GCCAGGAAGAACCAA	8924
rs184781242	snp	A/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28243109	GACACAAGCATAGAC[A/T]ATCACTTGGTTCAGA	8924
rs184781732	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28146068	GTATTTAAAAGTATG[A/G]GAAAGAGGCAAGCAA	8924
rs184786339	snp	A/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28208031	GCTGTCACTGCTCAT[A/T]GGGCTGAGTGCAGAA	8924
rs184791219	snp	C/G	1.64787e-05	0.00287038	intron-variant	HERC2	GRCh38.p7	15:28176656	ATCATTCCTACCCAC[C/G]CAGAAGCACAGAATC	8924
rs184795932	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28181643	ATTTGCTTTGTGGCT[C/T]CTCAGCCAGGAGACA	8924
rs184891587	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28119139	GGGTGCGGTGGCTCA[C/T]GCCTACAGCACTTTG	8924
rs184920667	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28201253	CTCCTACCCCTTTAC[C/T]GTAGTCTGTTCTTTC	8924
rs184923106	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28161252	GAACTTACATTTAAT[G/T]ATTTTTTTTTTAAAT	8924
rs184939820	snp	A/G	0.00517822	0.0506191	intron-variant	HERC2	GRCh38.p7	15:28165462	ATATTGGTGTGAACC[A/G]GTGGTTTTCCATGTA	8924
rs184960952	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28149530	CACGCGGCTCCTAAC[C/T]GAGAACGTCACCGAG	8924
rs185078913	snp	G/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318053	ATTCTGGACTTATGC[G/T]CAAAGACATGCGCCT	8924
rs185187094	snp	C/T	0.0471551	0.14613	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299925	AGGCGTGGTGGCGGG[C/T]GCCTGTAATCCCAGC	8924
rs185221652	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28304399	CTGAGATGGAGTCTT[A/G]CTCTGTAGCCCAGGC	8924
rs185222186	snp	A/C	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28240650	AGCAGATTAAACCCT[A/C]AGAAAGAAGAAGGCA	8924
rs185225951	snp	C/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28274144	AAAGCTGAGAACCCA[C/G]ACCCGGAATCACAGC	8924
rs185232918	snp	C/T	0.0111196	0.0737302	intron-variant	HERC2	GRCh38.p7	15:28275462	GCCGCGGGTGAAGCC[C/T]TGCGTGCTTGACCCA	8924
rs185235348	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28258192	TCCATGGGTCAGGCC[A/G]GGCGCAGTGGCTCAC	8924
rs185245116	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28232420	TGGCGGGTGCCTGTA[A/G]TGCCTATAATCCCAG	8924
rs185251527	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28295700	ACCACGCCCGGCCAC[C/T]GTATTTTATAGTTTT	8924
rs185255590	snp	A/G	0.000399281	0.0141238	intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28315736	TGCGCAGGCTGAAGC[A/G]CAAAAGAAGAAAGAT	8924
rs185284884	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28166485	CCTAACCAAAGACAC[G/T]CAGTAACAATTAGCT	8924
rs185287797	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28161714	CCAGATGGCTCCGGT[C/G]CAGAACATTTCCACA	8924
rs185293415	snp	G/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28189498	TTTTTTCAGATAAAT[G/T]CAATATTATCTTTCA	8924
rs185307537	snp	A/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28201864	AATGGCTACCGAAGA[A/T]CATGAGATGTTTGAA	8924
rs185309589	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28240342	AGAATGGCATGAACC[C/T]GGGAGACAGAGCTTG	8924
rs185344891	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28150190	GAAAAAAACGCACGC[G/T]GCTGCTAACCGAGAA	8924
rs185345698	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28256884	ACAGGCGTGAGCCAC[C/T]GCGCCCAGCCCAGAT	8924
rs185349577	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28293232	GGCGTGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	8924
rs185359175	snp	A/G	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28131599	CTTGAGTGGAGCAGA[A/G]CCGCCGACCCCACCA	8924
rs185364388	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28128164	TTGCAAGAAGCCCAG[A/G]AAGACGAGGAAGTGA	8924
rs185376877	snp	C/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28228841	TCCTTCCATTTCGAA[C/T]ATAAAAGTTATGTCT	8924
rs185381644	snp	A/G	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28199016	GCCAGACGTGGCGGT[A/G]CATGCCTGTGGTCCC	8924
rs185385999	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28219255	GGCGACCAGACGCTC[A/G]TGCAGCCCGCTTGGC	8924
rs185388345	snp	A/C/G	0.000115506	0.00759873	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28182496	ATTCCAGCCCAGCAG[A/C/G]CTTCTTTCTAATGAG	8924
rs185410604	snp	G/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28222557	AAAAACAAAGATAAC[G/T]ACCTAAATATCTAAC	8924
rs185413238	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28115360	GTTCACAGCCTGACC[A/G]GACCCGCAGAACAGA	8924
rs185413863	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28153405	ACACTTGTAATACAA[C/G]CACTTTGGGAGGTCG	8924
rs185441708	snp	C/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28177951	CTCTTCCCAAAACAC[C/G]TCAGCTTATGCTCTT	8924
rs185450262	snp	C/T	0.00874735	0.0655527	intron-variant	HERC2	GRCh38.p7	15:28143009	TGCCGGGGAGGCTGA[C/T]CATTTGTTTCTACCG	8924
rs185450859	snp	G/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28193007	TAAGGTAAGCCCAGA[G/T]AGTCACTAACCTTTA	8924
rs185456492	snp	A/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28160180	GGCTACTCGGGGGTC[A/T]GGGACCCACTTGAGG	8924
rs185510334	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28153893	GAGGGGCGGGAATCA[A/G]GAACCATCAAGCCGC	8924
rs185515154	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28133824	GTTTCTGGATTCCCT[A/G]TTCTGCTCCATTGAT	8924
rs185528999	snp	A/C	0.0111196	0.0737302	intron-variant	HERC2	GRCh38.p7	15:28264035	CAAAAAAAAAAAAAA[A/C]AAACAAACAAAAACA	8924
rs185547854	snp	A/C	0.000399281	0.0141238	missense	HERC2	GRCh38.p7	15:28169618	TGCACCACTTATTTT[A/C]TTACTGGCAGCAGAA	8924
rs185549587	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28219649	CGGTGCGCTATGGCA[A/T]AGCCTCTTCCAGCCC	8924
rs185562168	snp	C/T	0.000399281	0.0141238	missense	HERC2	GRCh38.p7	15:28132825	ACACGAGGGCGGTCA[C/T]ACGGACTGCAAAAAA	8924
rs185565434	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28210640	CGCGCATTTGAAGAA[C/T]CAGCTTAGGTTCTAC	8924
rs185577121	snp	C/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28138417	TATATTAGTTGAATT[C/T]ATTGAAGTCAATGCT	8924
rs185591866	snp	A/G	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28175103	TAAGCCAGTCATAGC[A/G]TATGCTTCTCCAAGC	8924
rs185688083	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28156389	TTCCTATCCATGAGC[A/G]TGGAATGTTATTCCA	8924
rs185692138	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28126899	ACATAAAAAAAGAAC[A/G]TGCCGTTTCTGTTCA	8924
rs185710498	snp	G/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28295136	GCTAACAAAGACACA[G/T]ACCAAGAGAAATGTT	8924
rs185734046	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28196098	CTCACTGTACTCACT[A/C]TACAGAATTACTGTA	8924
rs185789588	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28248070	CCTCAGGGATTATCC[A/C]AAGTCTGCAGGTGAG	8924
rs185793704	snp	C/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28289952	CCTAAGTGAGAGGAC[C/T]ACACACCTCAGTGAG	8924
rs185797469	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28280508	AAGAAACTGAGGCAC[C/G]AAGTGGTTAAGCAAC	8924
rs185797961	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28310264	CAGCCTGAACAACAT[A/G]GCAAAACCACATTTC	8924
rs185803651	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28263653	CATAAAGGGATAAAA[C/T]GCAATTGCAAAAGTA	8924
rs185845098	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28189581	AATGAATCAGTGTAT[C/T]ATGAAATAGTTCCAT	8924
rs185848227	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28255194	ATCACAAAACTAGCC[A/G]GGCATGGTGACATGT	8924
rs185853632	snp	A/C	0.0295035	0.117819	intron-variant	HERC2	GRCh38.p7	15:28209446	CCTCCCGAGTTCACA[A/C]CATTCTCCTGCCTCA	8924
rs185858405	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28237729	AAATTCTATGTGTTC[A/G]TGAATACATAGGAAG	8924
rs185860718	snp	A/G	1.64838e-05	0.00287083	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28270726	GAGCTACACAGCGGA[A/G]GCATACAGGGCGTAG	8924
rs185865505	snp	A/G	0.00153085	0.0276239	missense	HERC2	GRCh38.p7	15:28167767	TAAAAGGCCGAGCGG[A/G]GGCTGAGGGGGCCGA	8924
rs185878778	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28310992	TGAGGCAAGGGAATT[A/G]TTTGAACCTGGGAGG	8924
rs185881412	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28290618	TTGAAATCACAGAAT[A/G]TGTTCTCTGACTACA	8924
rs185894807	snp	A/G	0.00755907	0.0610114	intron-variant	HERC2	GRCh38.p7	15:28287372	GAGAGTCGGTTCTGC[A/G]AAAGCTCTGTACCTG	8924
rs185917522	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28230938	CAAAATAATATACTT[C/T]TTTTAATTTTTAAAA	8924
rs185926901	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28148342	AATAGGAAAAAAGGA[A/G]GAAATTTTAAAAAAA	8924
rs185929479	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28212216	GGAGAAGAGGGTGTG[A/G]GCCATGGGGTTCTTC	8924
rs185931548	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28251240	CTCAGGTTGGGAGTT[A/C]AAGACCACCCCAGCC	8924
rs185933810	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28185408	TCCAAAGCGCCTTGG[A/G]AATGTTAACAACATA	8924
rs185936147	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28307612	TGACCTGTTGGTCAT[C/T]CAGGAGCATATTGTT	8924
rs185943000	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28286558	AAATGACAAAATTCA[A/G]TACTCATGAATGATA	8924
rs185945098	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28266607	GGAATGAATTACCCA[C/T]ACACCCAACCCAACA	8924
rs185947371	snp	A/G	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28222901	CACCTGACACAGCTC[A/G]GTGCCAGGGCAGTTA	8924
rs185947513	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28184473	CAATCAAGTATCTAG[C/T]TTTTCTTTCGACAAT	8924
rs185962561	snp	C/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28307136	CACCACGCCCGGCCT[C/G]CAAACTTATCTATTT	8924
rs185968239	snp	A/G	0.0107246	0.0724382	intron-variant	HERC2	GRCh38.p7	15:28310844	GCACTTTGGGAGGCC[A/G]AAGCGGGTGGATCAT	8924
rs186012571	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28267294	AAAGGTTATCTCCAG[C/T]TTCTGCCATCTGCAC	8924
rs186045950	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28162315	TCCAGCCCGGGTGAA[A/G]GAGACTGTCTCAAAA	8924
rs186048262	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28270422	AAGGTGGGAGGGCCT[A/G]GGGCTGTGGATAAAG	8924
rs186055658	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28121513	CATAGTTTTGTTTAA[A/C]ATCTGTGTTGAAGAC	8924
rs186060513	snp	C/G/T			intron-variant	HERC2	GRCh38.p7	15:28166194	CCAATATTGCTATAA[C/G/T]ATCCAAACCAAAGAC	8924
rs186068026	snp	C/G/T			intron-variant	HERC2	GRCh38.p7	15:28127545	TACTATTCCCTGGCT[C/G/T]TGTCCACTGAGGAGG	8924
rs186079796	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28208772	TCTGTCTGCCACAGC[C/T]TTCAAAGGCTGCCCG	8924
rs186082927	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28204425	AGGAGTTCGAGACCA[C/G]CCTGGCCAACATGGT	8924
rs186168406	snp	C/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28254640	TGGCTAATGCACACA[C/G]CTACCCACAGGCCCC	8924
rs186176563	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28290326	TTTGAGATGTAGTCT[C/T]GCTTTGTCACCCAGA	8924
rs186188300	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28226117	TAAAACAATAAAATA[C/T]TGCTGAAAGAAATTA	8924
rs186189888	snp	C/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28149973	CACACGGCTCCTAAC[C/T]GAGAACATCACCGAG	8924
rs186192173	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28263231	CGAAAAATTTTAAAT[G/T]ACTGCAAATAATATA	8924
rs186226064	snp	C/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28189058	TGCCACTGCACTCCA[C/G]CCTGGGCGACAGAGT	8924
rs186292239	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28240413	AAAGAGCGAGACTCC[A/G]TCTAAAAACAAAAAT	8924
rs186293966	snp	A/C	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28203617	AGTACAACCCCTGAC[A/C]CCGAGAAGCCTGCAT	8924
rs186294487	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28222673	TGCAGGCTGGCCCTC[A/G]GCTGGAGTCTGGATC	8924
rs186296662	snp	C/T	0.000612014	0.0174824	intron-variant	HERC2	GRCh38.p7	15:28257293	CAATCTAAAATGAAT[C/T]TCCAAATGCAGCTGC	8924
rs186301625	snp	C/T	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28209374	TTTGAGACAGAGTCT[C/T]GCTCTGTCACCCAGG	8924
rs186317765	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28120381	GGGTAAAAATCATGT[A/G]TTAATACAAAGGTAC	8924
rs186328140	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28245594	ACACACACACACACA[C/T]ACACACACACAGATA	8924
rs186338370	snp	G/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28162181	CTAAAAATACAAAAA[G/T]TAGCCAGGCATCGTG	8924
rs186344794	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28183135	AGTCCTCGTCTCCTG[C/T]CCTTCCCAGAGGGCT	8924
rs186347142	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28147816	CCAGCTGGGAGGACT[A/G]CTTGAGCCCAGGAGT	8924
rs186432818	snp	A/G	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28287049	AATATGTGCGTGCGC[A/G]CTGTAAAATTCTTTC	8924
rs186439528	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28307516	AGTACTGCTTTAACT[A/G]TATCCCACAGATTTC	8924
rs186461427	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28141107	GCCAGGTGTGGTGGC[A/G]GGCGCCTATAATCCC	8924
rs186463434	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28114490	CACAGATCAGCAATA[A/G]TTGGAGCCAAATCCA	8924
rs186515141	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28301011	GGCACCCAGATTTTG[A/G]TCTCTCAGAACCATT	8924
rs186528132	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28277754	CTCCTATTACCAAAT[A/G]GGTAGGAATCTCATC	8924
rs186531508	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28260165	GGCAACATAGTGAAA[C/T]CGTATCTCCAAAAAA	8924
rs186550430	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28297587	ATCAAAAGCACTAAA[C/T]AGAGTGAAAGAAGCC	8924
rs186554478	snp	A/C			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317017	CCTGACCTCAGCCTC[A/C]CAAACTGCTAGGATT	8924
rs186594592	snp	C/T	0.00874735	0.0655527	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321854	CCCCACAGCAGGGCG[C/T]GTGCGTGAAACAAAA	8924
rs186655998	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28253852	CTGTAGTCCCAGCTA[C/G]TTGGGAGGCTGAGGC	8924
rs186657727	snp	C/T	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28239867	GAGGGCCTGGAGCCA[C/T]GTTGTTGGGAGAAAG	8924
rs186663694	snp	A/C/T	0.000150355	0.0086694	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28220587	CCCACTGGACTCTTA[A/C/T]CCATCCGTCCTCTCC	8924
rs186663936	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28263968	AGTTTGCGGCGAGCC[A/G]AGATTGCACCACTGC	8924
rs186666716	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28255784	AAAAGTTTAGAGTTT[C/T]ACTGTTTTCAGTTAT	8924
rs186670067	snp	A/C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28281555	TGGATATGCTCTCCA[A/C/T]GGGACAGGAGGGCCT	8924
rs186671439	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28303741	GCATCACTGTTTTAC[A/G]GTTTTCGTGGTAGAG	8924
rs186706253	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28195503	CAGTGGAATATTATT[C/T]AGCCATTAAAAAGGA	8924
rs186708756	snp	A/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28231975	TCTCTCCCTCATGCC[A/G]AGGCAGCCTGTCTCC	8924
rs186709682	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28177650	ACTCAACAGGATCAA[C/G]AGCGGAGTTAGCAGG	8924
rs186711885	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28150338	TTACTGAAAAAACAC[A/G]CGGCTTCTAACAGAG	8924
rs186719700	snp	C/T	0.000398268	0.0141059	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28213997	ACCAAACAGCGAGCT[C/T]GACAGAGACACTCAC	8924
rs186723990	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28279487	TGGCTGGCTTCCACA[A/G]TTACTGACAGAAAAA	8924
rs186726525	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28200562	TGTGTTATAGCCAAC[G/T]GAGCTAAGACAAGGG	8924
rs186735146	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28160950	ATGCAATAAACTTAT[G/T]AAAAATAATAATAGT	8924
rs186736087	snp	A/G	0.00835141	0.0640778	intron-variant, upstream-variant-2KB, downstream-variant-500B	HERC2, LOC107987422	GRCh38.p7	15:28319512	ATCACTTGCATTCGG[A/G]AGGCGGAAGTTGCAG	8924
rs186736199	snp	C/T	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28218350	TTTCTACTGTGTAAG[C/T]CCCCAAGTTTGTATA	8924
rs186741824	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28181241	ACAACCGTGGAACAC[C/T]GACTCTGTCCTTGAA	8924
rs186756767	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	HERC2	GRCh38.p7	15:28110633	TTTTGCCTCAATCTG[A/G]TAGTCTTCAGCTCAA	8924
rs186764681	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28275637	AAAAATCATCCTGTA[C/T]AAGAGAGAAAAGGCT	8924
rs186775657	snp	A/G	3.65831e-05	0.00427671	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174390	AAGATACAAATCTGT[A/G]TTACCTAAATAGGAA	8924
rs186780640	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316449	GTTCTAGACCAGCCC[A/G]GACAACAAAGAAAGA	8924
rs186788941	snp	C/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28137223	ATTGACACAGAGGGG[C/T]TATATTTCAAACCTT	8924
rs186790432	snp	A/G	0.0696718	0.173152	intron-variant	HERC2	GRCh38.p7	15:28155586	GAAGTGTCTGTTCAT[A/G]TCCTTCGCCCACTTG	8924
rs186843024	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28241768	GAGGTTGCAGTGAGC[C/T]GAGATCACACCACTG	8924
rs186871869	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28135769	AATTCATAAACCTAA[A/T]CCATGCTTTAGACAT	8924
rs186872885	snp	G/T	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28269706	TTAAATACTAATATA[G/T]TTTTAAATGCTCAAA	8924
rs186921638	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28172204	GTGAATCCATCCTTT[C/T]CACATTGACTTACAG	8924
rs186922866	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28128426	ATGTACTTCCAACTG[A/G]TTTGCTTCCAACTGT	8924
rs186939457	snp	A/G	0.0821764	0.185298	intron-variant	HERC2	GRCh38.p7	15:28159219	AATTATGTGTCTTGG[A/G]GTTGCTCTTCTCGAG	8924
rs186956780	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28197804	TTAGAACATTTCACA[A/G]AATAACTGACAGGAC	8924
rs186964907	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28236250	CTGATTGAGTCTCAC[C/T]ATCCTTATTATTATT	8924
rs186977469	snp	G/T	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28296206	GTGGGCCGGGCATGG[G/T]GGCTCACACCTGTAA	8924
rs186988044	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28131119	ATTGCTCTCATATGT[A/G]AGTTCTTATATTTAA	8924
rs186990526	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28194981	GAATTGCTTGAGCCC[A/G]GGAGGTGTCAGTTAC	8924
rs186994742	snp	A/G	0.00835141	0.0640778	intron-variant	HERC2	GRCh38.p7	15:28154882	TAACTCATCATTTAC[A/G]TTAGGTATATCTCCT	8924
rs187002261	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28168812	AAAACCAGAGTAATG[A/G]CAGGTGAAAAACTGC	8924
rs187026963	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28231438	CCACTTGTTTTTGCA[C/T]TGGGGCACTGGAGTC	8924
rs187027574	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28152309	GATATACACGTGGGT[A/C]ACAGAAGCTGTCCAG	8924
rs187052735	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28223227	GAGCGCTAACCCCAG[A/G]AGAGTAGGCTAGATT	8924
rs187063888	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28258811	ATTGTTCTTTGAAAA[C/G]ATCAACAAAATTGAA	8924
rs187118903	snp	C/T	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28154409	AGCCATCTTGCCAAC[C/T]TGGCAAGGGCAGTTT	8924
rs187141386	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314503	TTAATTTCCTAAAAA[A/G]AGAAAAACATATATT	8924
rs187163163	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28298795	AGCAAGACTCCTTCC[C/T]CCCCAAAAAAAAGAA	8924
rs187177994	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28172568	AACAACTGGACAATC[A/G]TGCCAAAAAAAGCCT	8924
rs187221033	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28251757	GTGAGCCAAGATTAT[A/G]CAACCGCACTCCAGC	8924
rs187225254	snp	A/G	0.0316913	0.121825	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213946	TTCAGGGTTCTCGGA[A/G]TCGGGGAAGTAGTCC	8924
rs187234399	snp	A/C/G/T	0.00048542	0.0155734	intron-variant	HERC2	GRCh38.p7	15:28274480	TCAGAGGAGCCCCCC[A/C/G/T]ACTCCCCTCACTCTC	8924
rs187259796	snp	A/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28136667	CAGGCCCATCATTTC[A/T]TTCTGTAAATGAAGC	8924
rs187321552	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28191734	ACATCCTCTATCAAG[G/T]GGTCAGTTAGATAAA	8924
rs187326346	snp	A/G	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28210227	TAAGCTCCGCCTCCC[A/G]GATTCATGCCATTCT	8924
rs187351366	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28145522	AAAAACCCACGCCCA[C/G]TGGGACCATACCATT	8924
rs187352645	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28160501	TGTGCTAGCAATGAG[C/T]GAGGCTCCGTGGGCG	8924
rs187363692	snp	C/G	0.00229568	0.0338019	intron-variant	HERC2	GRCh38.p7	15:28117196	GAGGCCGCTGCCGCA[C/G]CAGGAAGCACACAGT	8924
rs187376071	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28266819	TGGAAGCGATGGGAG[C/T]GCCCCATGTCTTGAT	8924
rs187400504	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28250187	CCACTTGCCCCCGTG[G/T]CTCACACCAGAAAAA	8924
rs187405359	snp	C/G/T	0.00478244	0.0486902	intron-variant	HERC2	GRCh38.p7	15:28283262	CCAAACTAAGACATA[C/G/T]AATAATCAAACTCCA	8924
rs187406945	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28265422	GAACGGCGGCAGCTG[A/C]TAACCAGCTGAGAGG	8924
rs187420014	snp	C/T	0.0232847	0.105357	intron-variant	HERC2	GRCh38.p7	15:28304400	TGAGATGGAGTCTTG[C/T]TCTGTAGCCCAGGCT	8924
rs187456374	snp	A/G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28210379	ACCTCGTGATCCGCC[A/G/T]CCCGCCTCGGCCTCC	8924
rs187468429	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28228551	GATGCAAGAATAAAC[A/G]TAACGCAGAAAGCAC	8924
rs187468861	snp	A/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28192325	TATAGTTACACCAAT[A/T]TATGAGATGAAGTCC	8924
rs187488319	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28122168	TCGGGAGTGCCTGGG[A/G]TGAAGACAGCAGGGC	8924
rs187523143	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28187492	ACTTGCCACCACACC[C/T]GGCTAATTTTTTGTA	8924
rs187531783	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28267780	TCTCAAGGGACACAA[C/G]TGCAGTCATGACTTC	8924
rs187533877	snp	A/G	0.0107246	0.0724382	intron-variant	HERC2	GRCh38.p7	15:28149315	CCTGAGAACATCACC[A/G]AAAATGGCCACACCA	8924
rs187539364	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28288454	TTTGAACCCAGGAGG[C/G]AGGCAGAGGCTGCAG	8924
rs187540211	snp	C/T	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28224441	TGCCCAAGTTGGTCT[C/T]AAACTCCTGAGCTCA	8924
rs187540578	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28308175	CAATATTGATTCTTC[C/T]AATCCATGAAGATGA	8924
rs187543527	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28252367	CCCACAACAGGAACC[C/T]TAGACTCACCCCCTG	8924
rs187558335	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28186970	TCAAGATGTCTACCT[A/G]AGGCATGAGACACTC	8924
rs187564179	snp	A/G	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28206572	GGTGCGGTGGCTCAC[A/G]CGTGTAATCCCTGCA	8924
rs187564391	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28156728	TTCCTCTTGTTCTAA[C/T]TGAATACCCTTTATT	8924
rs187573354	snp	A/C	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28138665	CTGATGAACATGTAC[A/C]AAGAGATTAAAGTTG	8924
rs187585476	snp	A/G	0.000620925	0.017609	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214255	GCGGGCGCACCCTGC[A/G]CCGCCTCAGCGTGGA	8924
rs187592572	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28232324	GAGGCAGGCAGATCA[C/T]GAGGTCAGGAGATCA	8924
rs187625631	snp	A/G	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28272581	CATCGCCTTCTGCTC[A/G]TAAGAAAGACCAGTT	8924
rs187636034	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314245	TAGAAGTCAACAGAA[C/T]AGACCAAGAGTAGAT	8924
rs187655419	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28168246	ATTCCACTTAAGCAC[G/T]TTAAAAGCTCCTTTA	8924
rs187673417	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28209623	GCTGGGATTACAGGC[A/G]TGAGCCACCGCGCCA	8924
rs187673817	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28248993	GCGCCTATGGAGCTG[C/T]GCGCAGTGGTCCAAA	8924
rs187714753	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28129142	GTGTTGGGGTTCCCC[A/G]GACCGCCCCACGCTC	8924
rs187750734	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28136030	TCTACTATATGCAAA[A/T]CTCTGACAATAACAG	8924
rs187786529	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28160229	CAGGTCTCAAACTCC[A/G]TTCTGGGAGAACCAC	8924
rs187791579	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28164606	TGTCTAGAAGAATTG[C/T]TAAGGAAGAAAATCA	8924
rs187806634	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28208012	ATCATCCTGATTCAG[A/G]TCTGCTGTCACTGCT	8924
rs187808579	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28242823	ATGATCAAGTAATGC[A/G]GGAAAAGCATGTGAT	8924
rs187851665	snp	G/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28124734	CTGACTAATTTTGTA[G/T]AGACAGGGTTTTGCT	8924
rs187864126	snp	A/G	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28116195	GTTGGTGAAAGGCAC[A/G]ATCAATATTAAAAGT	8924
rs187910629	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28292166	CCTGGGAGGTGGAGA[C/T]TGCAATGAGCCAAGA	8924
rs187911624	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28224166	ACACACACACACACA[C/G]AGAGAGAGAGAGAAA	8924
rs187921635	snp	C/G	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28259363	GCCTCCCAACGTGCT[C/G]GGATTACAGGCGTGA	8924
rs187925017	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28190775	TTGTTTCCTTTTCAA[C/G]CTGAACTGATAAGCA	8924
rs187928884	snp	A/G	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28242229	CTAGAGATGAGTGGC[A/G]GTGATGGCTATTAAA	8924
rs187929236	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28277281	AATTGCAAAGAAATA[C/T]ACACACAATTGAGAG	8924
rs187931862	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28117669	TGAGTGCCTCAGCCA[A/G]GACCAGCCCTTCCCC	8924
rs187933713	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28151138	CTGATGTTGGCAGTA[C/T]TGAAATTATATCCTA	8924
rs187941786	snp	A/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28317978	AAAAAGAACACAAAA[A/T]TAGAAACTGTAGGAA	8924
rs187965538	snp	A/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28227381	TAAAGAAGCTCAATG[A/T]CATTCATCATTAGTG	8924
rs188005024	snp	C/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28235506	CCACCCAACGGGGGG[C/T]TGTATGGACACCAAG	8924
rs188008582	snp	A/C	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28308549	CTTTTATTTCTTTCT[A/C]TTGTCTGATTGCTCT	8924
rs188013639	snp	A/G	0.0460142	0.144533	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28215424	ATTTACCACTTAAGA[A/G]AAAAGCAGGTAAACT	8924
rs188023287	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28253622	TTTTTGAGATCCTTG[C/T]GCTAGATTTCACTAT	8924
rs188057138	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28139291	CACAGGACCGGGGCT[C/T]TGTCTCCTCCACTCT	8924
rs188061492	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28158083	AGTTCTAGTTTGATG[A/G]CACTATGGTCTGAGA	8924
rs188067331	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28113337	CACCCTGGCATTTCC[A/G]CAAGACTCCGTCACG	8924
rs188082077	snp	A/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28304250	GCAATTTTACTGAAT[A/T]TATCAGTTCTAATCA	8924
rs188083338	snp	G/T	0.00755907	0.0610114	intron-variant	HERC2	GRCh38.p7	15:28197138	TGTTTTTATGTAACA[G/T]GAGAAGCTCTAGGAA	8924
rs188086401	snp	A/G	0.00152033	0.0275292	intron-variant	HERC2	GRCh38.p7	15:28144809	CCACTCTCGGCCTGC[A/G]GGAGGAAAGCGCACC	8924
rs188091754	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28127589	GACGCCTCAATAGCA[A/G]TGAGCACACCCATCA	8924
rs188095334	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28279305	CAAAAGCAACTCTTG[C/T]AATAAAAGAATAAGA	8924
rs188097422	snp	C/T	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28300313	AAGCGAAACCTACAA[C/T]TGGCAACAAGCAAAT	8924
rs188099614	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28176343	ACACGTCACAATCAC[A/G]CCGGGTGAGCCTGGG	8924
rs188102340	snp	G/T	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28179616	GTGTATTCCTTCTAC[G/T]TTTTTGTTTTTTAAG	8924
rs188103441	snp	A/G	0	0	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318719	ATTAGAGGTTGCTGG[A/G]TGTAGGGCCCTAGGC	8924
rs188144902	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28227984	ACTGATGGCTAAATG[A/G]TGTGCATTTATAGTG	8924
rs188156491	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28264904	TGACAAGGTCTGTCC[C/T]GTCAATGGCAGCAGG	8924
rs188220622	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28299017	TTTTTTTAAACCTCA[A/G]TGGGGACTCTGAAAC	8924
rs188227648	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28291456	AAAAAAAACCCTGAA[C/T]ATCCACACCGAAGGG	8924
rs188250057	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28133196	TACCATCTGGCCCTA[C/T]AAGGAAAGTTTGCAC	8924
rs188286778	snp	C/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28162211	GGCGCATGCCTGTAA[C/T]CCCAGCTACTCAGGA	8924
rs188291973	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28220224	GTGCACACATGAGAG[G/T]AAAATGCAGAAAGTC	8924
rs188293855	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28180702	ATCCATAGGTTCCAC[A/G]TCCATGAATTCAACC	8924
rs188327822	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28255445	AATAAAAAAGAAGTC[A/G]CAATACACACAACAG	8924
rs188329387	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28222811	CTTCGTATGCGCCAG[C/G]AAGGGGGTGCCCGTG	8924
rs188331043	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28203634	CGAGAAGCCTGCATG[C/T]AAGACGCGCATTTAA	8924
rs188392023	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28243544	AAAAAGAAAAAAAGA[A/C]AACCAGATAGAAAAA	8924
rs188424047	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28278736	CTTGTTTCTTTCTGC[C/T]TCCCGTACCTTCTAT	8924
rs188435833	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28174987	ATTTTTCAAGTAAGT[A/T]GCTTCTTGGCCTTAT	8924
rs188437953	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28137654	TGTTCTGATTGCTCC[A/G]CCAACCAGCTGTTCT	8924
rs188449927	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28249712	AGTGCAGTGACATGA[C/T]CTCAGCTCACTGCAA	8924
rs188453719	snp	A/G	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28282908	TGCACTCCAGCCTGG[A/G]AAACAGGGAGAGACT	8924
rs188498396	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28269021	AATGAGTTTACAAAC[A/G]GGAATCTCACGATTA	8924
rs188516674	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28310132	CAACATAGCAAGACC[A/G]TCTCTACAAAAAAAT	8924
rs188516951	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28289719	CATACCTAAAATCCA[C/T]GGACTTACGGGACAT	8924
rs188564747	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28200152	CTATAATCCCAGCAC[C/T]TTGGGAGGCCAAGGC	8924
rs188590191	snp	C/G	0.0107246	0.0724382	intron-variant	HERC2	GRCh38.p7	15:28238379	TTGCCTGGGCCAACT[C/G]AGAACTTGAAATGAG	8924
rs188595900	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28123165	ACACGTGAAAGTAAA[A/G]TGAATGTACCAGTCC	8924
rs188602957	snp	C/T	0.00716266	0.059414	intron-variant	HERC2	GRCh38.p7	15:28271384	TGCCAAATAATAGGC[C/T]GGGCATGGTGGCTCA	8924
rs188644107	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28273803	CCTTAACAAAAATGC[A/G]TAGCACCCAAGACCA	8924
rs188652571	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28256420	CAAGTATTATTTAAA[C/T]AGACAATTTCTCAGT	8924
rs188667044	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28292625	GTATAAGACCAGCCT[A/G]GGCAACACAGTGAGA	8924
rs188686376	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28260338	ATTTTTTAGAAGCTT[A/C]TAAAACGGGGAATTA	8924
rs188700387	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28154292	CTTAGTAAATATTAT[A/G]TATTAACAAACTAAT	8924
rs188714487	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28155861	GTCCTGAATGGTATT[C/G]CCTAGGTCTTCTTCT	8924
rs188718550	snp	C/T	0.0919752	0.193722	intron-variant	HERC2	GRCh38.p7	15:28194255	TATTTTTAGTACAGA[C/T]GGGGTTTCACCGTGT	8924
rs188728677	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28211852	CAAGAGGGGAGAAAA[C/T]TCAAGAAGAGTGGGC	8924
rs188733108	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28171794	AAACCTATACAATAG[A/G]CCGGGTGCGGTGACT	8924
rs188736991	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28240156	GGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC	8924
rs188752526	snp	C/T	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28195696	AGTAGGGCAGTTAAA[C/T]TGCTTAATGGGTACA	8924
rs188761487	snp	C/T	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28286696	TCCCAGACCTATTTA[C/T]ACGGCAGAGAGAATC	8924
rs188765547	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28307146	GGCCTGCAAACTTAT[C/G]TATTTCTTCCACGTT	8924
rs188787231	snp	C/T	6.58946e-05	0.0057396	missense	HERC2	GRCh38.p7	15:28111846	CGTCGCTGCTGTCGT[C/T]GGCGGCTGGCTCTCC	8924
rs188948864	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28196682	ATTTGTTTTTTACAA[A/G]GAGTCTACCTTTTAG	8924
rs188959122	snp	A/C/G	3.29768e-05	0.00406048	intron-variant	HERC2	GRCh38.p7	15:28233617	TACCTCAGGTTAGTC[A/C/G]AGGAATCTGCAGTGT	8924
rs188965350	snp	G/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28296552	TGCCATGTACTTAGC[G/T]TTTCTTAGAGCACCT	8924
rs188967407	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28268214	GGGATGCAGTTTGAG[C/T]AGATAGAAGGCTGGC	8924
rs188973574	snp	C/T	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28120305	CAAGAGTTTCGTGTC[C/T]TAATTCAAAATGCCC	8924
rs188976476	snp	C/T	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28253702	AACAGTGGCTTACGC[C/T]TGAAATCCCAACACT	8924
rs188984769	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28236022	AACACAGTCCTCAAG[C/T]AGAATGCTGTTCCCT	8924
rs189006849	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28182608	CCTCAAGCACTCAAA[A/G]TTTTATGGTTACTTT	8924
rs189014389	snp	A/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28147308	TTCTTTAAATTTCTA[A/T]CATGAAGTAATAGCT	8924
rs189018416	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28161939	GCAACCGGTTTACCA[C/T]CTAGGAAAAAAAGTA	8924
rs189036456	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28225922	AATCTGAATAGACCC[A/G]TAACAAGTAAAGAGA	8924
rs189044639	snp	C/T	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28189339	TTTTACGAATGATAA[C/T]CTCCATTGTTGATTT	8924
rs189052531	snp	C/T	0.0352966	0.128072	intron-variant	HERC2	GRCh38.p7	15:28289364	AGGGGGTCAAATTTA[C/T]AAATATGATGTAAAA	8924
rs189071048	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28261940	TACCAGGACCCAACG[A/C]ACTACAGCCCCCACA	8924
rs189091088	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28208065	AACAGCCAATCCAAT[C/T]CCCAGGCTCCAATCT	8924
rs189102617	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28150079	GAACGGCCACACAAA[C/T]GCACATTCTAGTAAA	8924
rs189124426	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28126502	CCCATCCATCAATGA[A/G]TGGATAAAGAAAATG	8924
rs189150386	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28165013	AATTAAAAATAAAGT[A/G]TTTGCCCTCAAGGTG	8924
rs189158441	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28187969	ACACACTAACAATTA[C/T]TTTTTATTGCCTAAA	8924
rs189158689	snp	A/C	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28149404	CCGAGAACGGCCACA[A/C]CAACATACATTCTAG	8924
rs189177547	snp	A/C	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28112550	GACACATGCTGGGAA[A/C]AGTGGACCCCATCGA	8924
rs189179913	snp	A/T	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28210924	CCTATGTCCATTTTT[A/T]TGAACTGATTATTCA	8924
rs189188214	snp	C/G	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28170014	ATACAAAACAACAAA[C/G]AGAAAAGATGTTCAC	8924
rs189199416	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28250975	GTACGTACATCCTTA[C/T]TACAAATCTGCTGTA	8924
rs189224810	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214874	CAGATTGTTATTTTT[C/T]TATTTTTTATTTTTT	8924
rs189252569	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316828	TCTCACCAGGCTGTA[A/G]TGCAGTGGCGCGATC	8924
rs189256496	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28253278	CTTCCAAAATAATGC[C/T]CACCATTCTTTCACA	8924
rs189310319	snp	C/T	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28209159	AATGTGCTTTTCTGT[C/T]TACTTATCATTTTCA	8924
rs189339365	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28244852	GATGGTCTAAAACAC[G/T]AGAAGAAAAAAAGCC	8924
rs189354860	snp	A/C	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28309039	GTCTGCTTTTAGTAT[A/C]AAGGTTTGAATTTTT	8924
rs189389394	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28166310	CATATAAAAGCATTA[C/T]ACACCAAAAAAATAT	8924
rs189405646	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28119213	CCAGCCTGGCCAACA[C/T]GGTGAAATTGTCTCT	8924
rs189423206	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28257806	GAGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	8924
rs189423490	snp	G/T	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28306174	AAAGGCTTTCAGTTT[G/T]TCACCTTTCAGTATG	8924
rs189426686	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28240483	AATCAAAAATACAGA[A/G]AAGTATGAGAGGGGA	8924
rs189430848	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28275193	CTTTTGTAAAGGAAA[A/G]GTTTTCTCTTTAAGA	8924
rs189450547	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28295423	GGAAAGTATTTTACT[A/T]TTGTTGTTCTTTTGA	8924
rs189491219	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28228986	AAATGTAAAAATGTT[A/T]TACTAGAGTACTTCA	8924
rs189497233	snp	A/G	0.0029723	0.0384359	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265947	CTTTCCAGAGAAGGC[A/G]GAGATCACCTTAGGC	8924
rs189534542	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28153690	AGTTGGAAGGCTCCC[A/G]ACACACACAACACTT	8924
rs189562718	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28303893	TGATTTGGCCGGGCA[A/C]AGTGGCTCATACCTG	8924
rs189566479	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28260543	CGGGAAAAGACATAA[A/G]AGGCGAGCAGACTGG	8924
rs189570551	snp	C/T	0.00517822	0.0506191	intron-variant	HERC2	GRCh38.p7	15:28244243	AGTAGAATGAATAGG[C/T]TGTTGTATATTCAAA	8924
rs189578893	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28279069	CAATCTCCGCTCACC[A/G]CAACCTCCACCTCCC	8924
rs189588973	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299953	AGCTACTCACGAAGC[G/T]GAGGCAGGAGAATTG	8924
rs189638547	snp	C/T	0.0119091	0.0762411	intron-variant	HERC2	GRCh38.p7	15:28188475	AGTGAACCCGGGAGA[C/T]AGAGCTTGCAGTGAG	8924
rs189643232	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28225493	GCGAGGTCAAGAGAT[C/G]GAGACCATCCTGGTC	8924
rs189649220	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28208233	AAACAAACCCACATA[C/T]TCCACATTCTACTGG	8924
rs189655212	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28254901	TTGTTCAAATGTAAA[C/T]GGCAAAGCCACTTGG	8924
rs189676038	snp	G/T	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28270429	GAGGGCCTGGGGCTG[G/T]GGATAAAGGGGAGCT	8924
rs189685533	snp	A/C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28146145	ACTTCCATGAGAATA[A/C/T]GAAGGCAGCATTCTG	8924
rs189705195	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28160182	CTACTCGGGGGTCAG[A/G]GACCCACTTGAGGAG	8924
rs189709742	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28266244	CAATAGGCTAGGCGC[A/G]GTGGCTCACACCTGT	8924
rs189711649	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28178011	TACAACCTGCCTCAG[A/G]ATTAAAGGCATGACC	8924
rs189732283	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28306761	TCATTACCTGTTATT[A/G]GTATGTTCAGGTTCT	8924
rs189738667	snp	C/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28237651	ACTGTTTTAAGCCCT[C/G]CCCTAATGGCATTTA	8924
rs189744494	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28199094	GGAGGTTACAATGAG[C/G]CAAGATCACACAACT	8924
rs189745596	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28219531	TCCTAACAGGCCTAC[A/G]CAGTAGGGAACACTT	8924
rs189764770	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28161334	ACTAAAGCCAAAAAT[C/G]CTAATAGGCACAGAA	8924
rs189854600	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28136894	TTTCACTAAAGTAAA[C/T]TGAGAAAGATATGCT	8924
rs189865148	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28222641	CTGGCCCGAGATACA[A/G]CCTCAGACAGGGTTG	8924
rs189875557	snp	A/G	0.000132216	0.00812961	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28257128	GGCGGGGGCCAGTCC[A/G]CGGAACCATCCATCC	8924
rs189882144	snp	A/G	0.0479149	0.147179	intron-variant	HERC2	GRCh38.p7	15:28293366	GCCGTGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT	8924
rs189893622	snp	A/C	0.0707826	0.174302	intron-variant	HERC2	GRCh38.p7	15:28154914	ATGCTATCCCTCCCC[A/C]CTCCCCCCACCCCAA	8924
rs189909211	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28153351	CGAGCGAGACTGCGT[C/G]TCAAACAAAAAAAGT	8924
rs189963471	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28251181	GGTGCAGTGGCTCAC[A/G]CCTGTAATCCCAACA	8924
rs189971709	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28286294	CATTTTAAGAAGCTA[A/G]TATTAGGTACTGTAC	8924
rs189990971	snp	A/C/T	0.0001491	0.00863305	intron-variant	HERC2	GRCh38.p7	15:28176810	AATCACGCACAGGCA[A/C/T]GGAGAAAGCAATGGA	8924
rs189994163	snp	C/T	0.00716266	0.059414	intron-variant	HERC2	GRCh38.p7	15:28181937	GTGTATGCGCACACA[C/T]GTGCATTCTGCTTGT	8924
rs190019465	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28218248	AAACTCCAGAAGCTG[C/G]GGCAGAGCCCTCAAG	8924
rs190054009	snp	A/C/T	0.000798403	0.0199641	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28315074	ACTGCCACCTCTTCT[A/C/T]AATGAGCTGCAAATA	8924
rs190065162	snp	G/T	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28226257	AATCCCAATGGTCTT[G/T]TTTGCAGATATGGAA	8924
rs190074078	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28139927	AAAAAGATTAGCCAG[A/G]CGTGGTGGCGGGCGC	8924
rs190108888	snp	A/G	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28203393	CTAGGGTTTTGCAGC[A/G]AAGTCTGGGTAACTT	8924
rs190110869	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28240402	CCGCCTGGGCGAAAG[A/G]GCGAGACTCCGTCTA	8924
rs190137930	snp	A/C	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28274190	AAAACAGGTGAAAAA[A/C]CAACCTACTAGGCTT	8924
rs190154005	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28169389	GACAATAATACAACA[C/T]TCTTGGAGACATCTG	8924
rs190157403	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28131905	CCTTACTCCCTCTAG[G/T]CCCTCCACACACTTT	8924
rs190157987	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28290688	AAATACTTGGAAATG[A/T]AATAACAATTTCCAA	8924
rs190233239	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28271043	AGCATATAAACTGAC[C/T]GTGTAAATGTCTAAA	8924
rs190241478	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28255286	GCTGCAGTGAGCCAA[C/T]ATCAGGTCACTGCAT	8924
rs190248824	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28197414	GTTCCTAATTCCCAT[C/T]ATTAGCACATTTCCA	8924
rs190253138	snp	C/T	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28158570	CAACTCCTGCCTTTT[C/T]TTGTTTTCCATTTGC	8924
rs190261507	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28225121	GGCCAGGTGTGGTGC[C/G]TCACACCTGTAATCC	8924
rs190294700	snp	A/G	0.00716266	0.059414	intron-variant	HERC2	GRCh38.p7	15:28295789	GGACTTCATCTTTTC[A/G]TGTCCATAAATAAAG	8924
rs190302570	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28252867	TGCGTCTACTAAGTT[C/T]GTTTTTCTGGTTGTG	8924
rs190309185	snp	A/G	0.00398564	0.0444627	intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28315758	AAGAAAGATGAGGCA[A/G]AGGTCCAAGTAAACC	8924
rs190315485	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28267602	TGTCTGAATCCCTTA[C/T]AACACTGTCAGGGTT	8924
rs190315809	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28266767	AGGAACTGGAGGTAG[C/G]AAGGGGGCATCAACT	8924
rs190331264	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28114267	GGCTGCTCTGTGTCA[C/T]TCAAGCAGCCTGGAG	8924
rs190347462	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28285075	AATAGAACTGAAAGG[A/G]GAAAAAGACATTTAT	8924
rs190352521	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28174676	TCAGGACATTTTCTT[C/T]AATGTAATTTTTACT	8924
rs190360831	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28137280	CTGTGCTAGCAGTCT[A/G]CCTCTGATACGGTTC	8924
rs190365595	snp	C/T	0.143959	0.226396	intron-variant	HERC2	GRCh38.p7	15:28155594	TGTTCATATCCTTCG[C/T]CCACTTGTTGATGGG	8924
rs190366601	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28122442	AGCCTAAGAACTCCA[A/G]GCCCTGAAGGCAGGA	8924
rs190366987	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28315374	GCGGAGACTGGAGCC[A/G]AAGGGCGGCTCACAG	8924
rs190369651	snp	A/C/T	0.000496569	0.0157494	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214008	AGCTCGACAGAGACA[A/C/T]TCACGGAGCTGCCCA	8924
rs190376512	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28231000	TAGTCCATGGGCAAC[A/C]CAAAGCAAGCAAGAG	8924
rs190385331	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28195660	GTTAGATTCAAGGTT[A/G]CCAGGGTTGGGGTAA	8924
rs190385531	snp	G/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28232020	GTTCCTGCATGCCTG[G/T]GTTAAAGGAATCGCA	8924
rs190388120	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28258195	ATGGGTCAGGCCGGG[C/T]GCAGTGGCTCACGCC	8924
rs190392407	snp	C/T	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28212691	AATGCCACACATACC[C/T]GTAAGCCTTTTATAG	8924
rs190392733	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28163642	AATCTACCCATAAGA[C/T]ACGCTAGGGAATCGT	8924
rs190394450	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28251254	TCAAGACCACCCCAG[C/T]CAACATGGGGAAACC	8924
rs190397400	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28185784	AATGCTCCAATGCAG[A/C]CTCTCAAGGCTGTAT	8924
rs190440697	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28310510	ATTAAAAAGTGAGCC[A/G]AAAACATTCAGGGCC	8924
rs190512230	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28150200	CACGCGGCTGCTAAC[C/T]GAGAACATCACCGAG	8924
rs190514565	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28270262	AGATAGATAGATAGA[C/T]AGATAGACAGACAGA	8924
rs190520435	snp	A/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28128290	CAGGCGGGGTGGGGG[A/T]GTGTGAACTGGCTGG	8924
rs190532797	snp	A/G	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28209383	GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC	8924
rs190537487	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28166729	GGAGTCCCAATGACC[A/G]GGTCCCAGTGACCAG	8924
rs190546268	snp	C/G	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28165737	ACCAGGAGGTTGAGG[C/G]TGCAGTGAGCCAAGA	8924
rs190547314	snp	A/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28189500	TTTTCAGATAAATTC[A/T]ATATTATCTTTCATT	8924
rs190555977	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28127098	TCCAGAGAGACTCCT[C/T]GGGTGTCTGGAAAGT	8924
rs190607185	snp	A/C	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28227413	AATGCAAATCAAAAT[A/C]ACAATGAGACACCAC	8924
rs190611576	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28264414	CCTGAACACAGAGAT[C/T]GGAGCATGCATTTCC	8924
rs190615553	snp	A/C/G	0.00358891	0.0422285	intron-variant	HERC2	GRCh38.p7	15:28290327	TTGAGATGTAGTCTC[A/C/G]CTTTGTCACCCAGAC	8924
rs190709873	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28115597	GGATGACAAAACTTC[C/T]CGCTCACTCACACAC	8924
rs190771969	snp	C/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28253878	GAGGCAGGAGAATTG[C/G]TAGAACCCAGGAGGC	8924
rs190774027	snp	A/C	0.00517822	0.0506191	intron-variant	HERC2	GRCh38.p7	15:28289961	GAGGACCACACACCT[A/C]AGTGAGAGGACAACA	8924
rs190775928	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318204	ACCAATCACATCAGA[C/T]TACAAGTACTTTCAC	8924
rs190797133	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28277299	ACACAATTGAGAGCA[C/T]GTAAAACTGGGAAAA	8924
rs190804198	snp	C/T	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28147902	GTTAGCCAAGTGTGG[C/T]AGCACAAGCCTGTAG	8924
rs190805880	snp	A/C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28173886	TAAATTGGTGCATAC[A/C/G]GCAGGAAGGAGGGAG	8924
rs190807270	snp	A/C	0.0138799	0.0821421	intron-variant	HERC2	GRCh38.p7	15:28296652	AGGAAGAAGAGGTTA[A/C]AACTTTTTAAAATAT	8924
rs190807390	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28149826	TGACTTCTAACCAAG[A/G]ACATCGCCGAGAACA	8924
rs190823527	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316890	CAAGCGATTCTCCTG[A/C]CTCAGCCTCCTGAGT	8924
rs190847031	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28294841	CATCTGTCCAGTGTC[A/G]GTGTCCTACGTTCAG	8924
rs190848982	snp	A/C/G	0.00597598	0.0543831	intron-variant	HERC2	GRCh38.p7	15:28249144	AGAAAGAACAAACAC[A/C/G]GTGTCATTATTTTTT	8924
rs190853221	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28209644	CACCGCGCCAGGCCT[A/C]TATATCATTTATATT	8924
rs190872408	snp	A/G	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28310897	CCCGGCTAACACAGC[A/G]AAACCCCATCTCTAC	8924
rs190881857	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28259495	TTATAGAAAATGAAA[A/G]AGGACGGAACACATG	8924
rs190882562	snp	C/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28281619	CCTGGAAAGGCACAG[C/G]GTGGCGCACACTGTG	8924
rs190897866	snp	C/T	0.000399281	0.0141238	missense	HERC2	GRCh38.p7	15:28144101	TCAGCTGTGCACAAG[C/T]TGCCAGCGAGGCCGC	8924
rs190944264	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28280987	CACATCTCCTAAACA[C/G]AGAAAAACACTAGCC	8924
rs190947770	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28263738	GTGAATTGCTAAAAA[A/C]CAGAATTGTTAGGCT	8924
rs190965718	snp	A/G			intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28301769	TATATATATATATAT[A/G]TATATATATATGGGT	8924
rs191013995	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28226710	TGGCTTTTTGGATAC[A/G]ATATCAAAAGCATAG	8924
rs191024223	snp	C/T	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28209494	GACTACAGGCACCTG[C/T]CACCACGCCCAGCTA	8924
rs191032535	snp	C/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28248197	CCCAGCTGGCTCCCC[C/G]ATGTGACATATGAAT	8924
rs191065983	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28195011	CAGTGAGCCAGGATC[A/G]CGCCACTGCACTCCA	8924
rs191094895	snp	A/T	0.0162398	0.0886349	intron-variant	HERC2	GRCh38.p7	15:28200642	AGATAAGGCATACAA[A/T]CTTGGTTGTATCCAA	8924
rs191109043	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28181267	TTGAAGTGAAAACTC[C/T]ATGTAAGGCAGTGAG	8924
rs191109490	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28120403	CAAAGGTACAGGAAC[A/C]AAGAATTTGTTCTTC	8924
rs191119271	snp	A/G	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28221895	CCCTTCGGCTGCTCG[A/G]GAACCAACACCTGTG	8924
rs191131631	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28239953	CAAAATTACCACCTA[A/C]AAAAGGCATTTTTGA	8924
rs191144009	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28179730	TGTGGGGGTGAAAGA[C/G]AGCAACACTATGATC	8924
rs191150267	snp	C/G	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28219776	ACTGCGGTGCTTCCG[C/G]AGGCAGCCCCAGCCT	8924
rs191168370	snp	C/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28279648	ACACACACACACACA[C/T]ACAAATTGTTTTTAT	8924
rs191176297	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28320182	TGCAATGGCATGATC[C/T]TGACCCATTGCAACC	8924
rs191208270	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28177796	TTATGTTAAATACAC[A/G]AAAAATCAAAATTTA	8924
rs191221988	snp	A/G	0.000399281	0.0141238	synonymous-codon	HERC2	GRCh38.p7	15:28141528	GGGAGTGGGAACTTT[A/G]ACTTTTGCGCCTTCA	8924
rs191227419	snp	C/T	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28159340	AGAGTGTTTTCCAAC[C/T]TGGTTCCATTCTCCC	8924
rs191271844	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28308087	TTTTCTGTTTCTGTG[A/G]AGAATGTCATTGGTA	8924
rs191284314	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28204893	GTAACAGATGTATAA[C/T]AGTATTTCCAGAAAA	8924
rs191286935	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28129856	ATCTTGGCTCACTGC[A/C]ACCTCCACCTCCCGG	8924
rs191316917	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28151323	GGAATCAGCATATTA[A/G]CCAGGCAAGGTGGCA	8924
rs191317474	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28241020	CACCAAAAGCAGTGC[A/G]GGCAACAAAAGGAAA	8924
rs191369623	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28162970	AGTGCTCCTAACCTG[C/T]AGTCTACTAGGATGA	8924
rs191379778	snp	G/T	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28121657	CCGGGCAAGAGGCAG[G/T]TCCCTCAGGAAACTA	8924
rs191391112	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28263327	GCAAACGAAATCTAG[A/G]TGACACTTGAGGTTG	8924
rs191391788	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28223666	AAACTGGGGGAATTT[C/T]TCATTTTGCATAGCT	8924
rs191395695	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28258819	TTGAAAAGATCAACA[A/G]AATTGAAAAACTCTA	8924
rs191396674	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28199983	CCCCCCCACCAAAAT[G/T]CATGAAGTCCCAACT	8924
rs191404708	snp	A/G	0.000483393	0.0155391	intron-variant	HERC2	GRCh38.p7	15:28238227	ACTGAGCTGAAACAA[A/G]AAGGGAAAAAGCAAC	8924
rs191412206	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28296230	CCTGTAAACCCCACA[C/T]TTTGGGAGGCCGAGG	8924
rs191439764	snp	A/G	0.0123036	0.0774623	intron-variant	HERC2	GRCh38.p7	15:28194591	AAAACAAAACAAAAC[A/G]AAACAAAAAAACAGG	8924
rs191440168	snp	C/T	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28272618	CTCAAAGAGCACATT[C/T]ACATGAAAGTTCTAG	8924
rs191449967	snp	A/T	0.0150606	0.0854603	intron-variant	HERC2	GRCh38.p7	15:28154771	TTATTTTATATATAT[A/T]TTTTTTTATTATACT	8924
rs191450346	snp	G/T	0.0107246	0.0724382	intron-variant	HERC2	GRCh38.p7	15:28292446	AGGGTGTGGAGAAAT[G/T]GGAACCTTAGTATAC	8924
rs191488022	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28287398	ACCTGTGAGCAAGCA[C/G]AGCTTCCAAGTAAAC	8924
rs191528712	snp	A/C	0.0256215	0.110247	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314654	GAGGTCAGGAGTTCA[A/C]GACCAGCCTGGCCAA	8924
rs191538279	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28222929	TTAAGCTCGTCCTGT[C/G]TGGATCCTGTGGAAG	8924
rs191538419	snp	A/G	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28184731	GCCGGGCATGGCGGC[A/G]TGCACCTGTAGTCCC	8924
rs191611146	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28273825	CCAAGACCAGAGTTC[A/G]TGTTTTTCTTACACA	8924
rs191618548	snp	C/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28292684	GCTGGGCAACAATGT[C/G]AATATACTTCATGCC	8924
rs191620196	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28148725	TCACCGAGAACGGCT[A/G]CATGAACGCGCATTC	8924
rs191626850	snp	C/T	0.00041479	0.0143952	intron-variant	HERC2	GRCh38.p7	15:28144846	TTAGCTTCACTCCAT[C/T]ATCCAATCAACACAA	8924
rs191629642	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28241786	GATCACACCACTGCA[C/T]TCCAACCTGGGCGAC	8924
rs191666535	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28276182	CAGAGCAAGACTCCA[A/T]CTCAAAAAACAAAAA	8924
rs191679170	snp	C/T	0.00318978	0.0398085	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316650	CCAGTCCTAAAAACG[C/T]CAATGAAGACTCCCA	8924
rs191681006	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	HERC2, LOC107987422	GRCh38.p7	15:28317717	CATAGGAAATTGTAG[C/T]AGTAGTTACATTTAC	8924
rs191686746	snp	A/G	0.0372196	0.131242	intron-variant	HERC2	GRCh38.p7	15:28289365	GGGGGTCAAATTTAC[A/G]AATATGATGTAAAAA	8924
rs191692853	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28268984	CTGTCTGGCCCCAAC[A/G]TCAAATGAGTTTACA	8924
rs191703323	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28249772	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGAATTA	8924
rs191707625	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28172296	TTTAAGTTATATGGA[A/G]ATGCAAAGGGCCTAC	8924
rs191738894	snp	A/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28168857	AGACCAGAATGAGAC[A/T]CTGGCTCTCCCTGAG	8924
rs191754102	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28131230	CAATGGCATCGGGAC[A/G]TCCTGCTCCAGCCCC	8924
rs191758579	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28235572	TCTCGAAAGCAGCAG[A/G]AGAGCCCTGCTCCTC	8924
rs191759042	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28152467	TGCCTGATTATCATG[A/C]AGCTAAACATTTACT	8924
rs191762219	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28136070	ATACCCATAAAAGAA[A/C]ACAAATACATTTTAA	8924
rs191771746	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28191841	AAATTAAAACATAAC[G/T]TGAGTACTGACAGGT	8924
rs191775893	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28228063	AAATGTATTTGATAC[C/T]GCTGAATTGTGACGT	8924
rs191776428	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28253659	ATGAAAACCAATAAT[C/G]ACCTACTAAAATACA	8924
rs191780316	snp	G/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28210234	CGCCTCCCGGATTCA[G/T]GCCATTCTCCTGCGT	8924
rs191782844	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28297641	TGATTCCATGTATGG[A/C]GTTCTAGAACAGGCG	8924
rs191871930	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28124790	CCTGAGTTCAAGCAA[C/T]CCGCCCACCTTGGCC	8924
rs191910494	snp	C/G	0.0193772	0.0965046	intron-variant	HERC2	GRCh38.p7	15:28160232	GTCTCAAACTCCGTT[C/G]TGGGAGAACCACTAC	8924
rs191921453	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28116497	GCTAGGGTTATAGGC[A/G]TGAGCCACCGCGCCT	8924
rs191942261	snp	A/G	0.0321182	0.122587	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213949	AGGGTTCTCGGAGTC[A/G]GGGAAGTAGTCCTCT	8924
rs191952361	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28252033	TCATAAAATACACAG[A/T]TGACGAAGTAGACTC	8924
rs191959893	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28165090	GGGGAGCGCCTCAGC[A/G]GGCTGGGGAAGGCAT	8924
rs191963971	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28287241	AAAAAAACAGAAAAA[G/T]AAATGAAAGGAATAG	8924
rs191964585	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28188285	CGGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT	8924
rs191979915	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28149499	CATACATTCCAGTAA[A/C]ATTACCAAAAAAACA	8924
rs191981772	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28253212	TGCCAAGGTTAGCCT[C/T]TGTTCACAGGCTGAC	8924
rs191993981	snp	A/C	0.00993419	0.0697739	intron-variant	HERC2	GRCh38.p7	15:28232339	CGAGGTCAGGAGATC[A/C]AGACCATCTTGGCCA	8924
rs191995535	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28267876	CTGGGTTGGTGTGTA[C/T]ATACATCCCTCATTT	8924
rs192002078	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28225231	GTACTTCGGCCTGAA[A/G]GAAAAGTAAGACCCT	8924
rs192002103	snp	C/G	0.0107246	0.0724382	intron-variant	HERC2	GRCh38.p7	15:28208122	CATGTTCCCTATAAC[C/G]TCTACTATTAATTGA	8924
rs192035757	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28312017	GATAGGCCAGACCTT[C/G]TCTTTCTGAGTGACA	8924
rs192036782	snp	C/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28126775	TGTACACTACTTGGG[C/T]GATGGGAGCACCCAC	8924
rs192054604	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28197827	GACAGGACAAGTTTA[A/C]AGAACACGAACATCA	8924
rs192062862	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28167968	ACAGAGGTAACATGG[G/T]GCCCACCAGACATAG	8924
rs192113572	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28128578	AATGAAATGATTAAA[A/G]GGTGCATGCTTATAT	8924
rs192147777	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28161210	CATCAGAGCTTTAAC[A/G]TTTCAGAATTTCAGA	8924
rs192189471	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28307547	GTATGCTGTGTTGCC[A/G]TTGCCATTTGTTTCA	8924
rs192208338	snp	A/C	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28191616	CACAACAGCACTCCA[A/C]TGTGCAACACAAATT	8924
rs192216921	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28118909	GGGGCCGTGGCTGAG[A/C]CAGAGCAGCCCCCAG	8924
rs192262189	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28231876	CTTGAAACAACACAC[A/G]ATAAATCTATAAACC	8924
rs192266486	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28266973	GTGGATGGAATGAAG[C/T]CAGCACTCTGCAATC	8924
rs192311539	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28308222	TTGTGTCTTCTTTAA[A/T]GTCTTTCATCAGCGT	8924
rs192313154	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28288586	TCACACCTATAATCC[C/T]ATAATCCCAGCACTT	8924
rs192314563	snp	C/T	0.00517822	0.0506191	intron-variant	HERC2	GRCh38.p7	15:28243641	AGGTATCAAACCTCA[C/T]TAATAATCTAGAAAA	8924
rs192354916	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28149174	AACATCACCAAGAAT[A/G]GCCACACGAACGCAC	8924
rs192403364	snp	A/G	0.00014145	0.00840863	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28218667	CCTTTCAGTTTGTTC[A/G]GCTTCTAAAAAAAAT	8924
rs192408943	snp	C/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28189982	CAACAGTATACATAG[C/T]ACAAAAATATCTTTT	8924
rs192450449	snp	C/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28138693	TTGTTTTCATGCCGG[C/T]TAACACATCATTTTT	8924
rs192453078	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28206814	CTCCAGCCTGGGCGA[C/G]AGACCAAGACTCGGT	8924
rs192454340	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28157469	CTTCCTGGTTTAGTC[C/T]TGGGTGGGTGTATGT	8924
rs192466492	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28112916	TCATAACATTTTGAG[C/T]CTTCACATCAGAGAA	8924
rs192475281	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28224273	GGAGCCCAGGCTGGA[A/G]TGCAGTGGCTTTATC	8924
rs192486507	snp	C/T	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28176087	TTTACAAGAAACACA[C/T]GTTAACTTTTTCAGG	8924
rs192494731	snp	C/T	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28150436	AACCGAGAACATCAC[C/T]GACAACGGCCACACG	8924
rs192515338	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28306265	ACCAGTTTTTTGGGG[A/G]TTTTTATCATGAAAG	8924
rs192524205	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28284070	CTTAATAATTTTGTG[C/G]ATGAAACAAAGTTCG	8924
rs192525758	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28304675	GGCCTTTCTCTCTCT[C/T]ATCTGACTCCTCTAG	8924
rs192567408	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28228779	TGTTCCATCTGTCTA[C/T]AGGACTTAGCATGTT	8924
rs192580108	snp	C/T	0.0138799	0.0821421	intron-variant	HERC2	GRCh38.p7	15:28250496	GAGCCATAATCAAAA[C/T]GTGTAATTCTGATGG	8924
rs192607416	snp	A/G	1.66927e-05	0.00288895	synonymous-codon	HERC2	GRCh38.p7	15:28168551	GCACTCCACCGGGGC[A/G]ATCATGGCGGCCGGC	8924
rs192610320	snp	C/T	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28145630	CATCCAGTCTGCATG[C/T]TGTTATGACAGAGGC	8924
rs192615001	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28160698	GGTGAGGCGATGCCT[C/T]GCCCTGCTTCAGCTC	8924
rs192616604	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28146030	CCGACAGGGATGTGG[C/T]ACATACATCACAGAT	8924
rs192627690	snp	A/C	0.103438	0.202533	intron-variant	HERC2	GRCh38.p7	15:28222411	AGGATGAAATACATA[A/C]ATATCCTAGGAAGAT	8924
rs192631087	snp	C/T	0.00373351	0.0430443	intron-variant	HERC2	GRCh38.p7	15:28117222	ACAGTCGGGGATATG[C/T]GGCACTGGCGAATGC	8924
rs192634922	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28200297	CTACTCGGGAGGCTG[A/C]GGCAGGAGAATGGCA	8924
rs192640058	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28282909	GCACTCCAGCCTGGG[A/G]AACAGGGAGAGACTC	8924
rs192649056	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28181008	TGACTATGCATATAA[C/T]GTAAAGATAAAAACA	8924
rs192649881	snp	C/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28256548	TGGAAAGCTCAAGAT[C/G]AGCAGAAGAGCTAAA	8924
rs192692925	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28182281	GTAATTTGATAATGT[A/C]TTTTAGTTCGTGTAA	8924
rs192719109	snp	C/T	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28309211	AGTTTGATGTTTCTT[C/T]GTTAATTTTGTCTGG	8924
rs192725099	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28123693	AGTGGGGACTTGCCA[C/T]AGCCACAAGGCCAGG	8924
rs192738215	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28208026	GGTCTGCTGTCACTG[C/T]TCATTGGGCTGAGTG	8924
rs192739149	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28242872	ATAGTTAAAACTGCA[A/T]CACAAAGCAGCAACA	8924
rs192752360	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28277827	CAACATGTACAGTCG[C/T]CCCTTGGTATCTGTA	8924
rs192776913	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28164758	TGCCTATGTCTCATA[A/G]ATAAATTGGGGGGAA	8924
rs192814684	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28195931	CCACATGCCATGCAA[C/T]TAAACACTTACTAGT	8924
rs192832002	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28112198	ACGAGGAGCAATTAA[C/T]TCCTAGAACTTGGAG	8924
rs192841898	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28156320	CATTGGTAGCTTGAT[A/G]GGGATGGCATTGAAT	8924
rs192865930	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28265057	CCCTGCTGATTATAA[C/T]GGAAAGACTCCACAA	8924
rs192870037	snp	C/T	0.0107246	0.0724382	intron-variant	HERC2	GRCh38.p7	15:28201792	TAATCCTACGAATAA[C/T]TTACTCAGGTCAGAA	8924
rs192874099	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28240161	CAGTGGCTCACGCCT[A/G]TAATCCCAGCACTTT	8924
rs192877053	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28304282	TTTTTGGTGGAGTTT[C/T]CAGGTTTTTCCAAAT	8924
rs192937662	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28224599	TCACTGTGACTTTGA[C/T]AACTGGCCCTGCAGC	8924
rs192955826	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28260167	CAACATAGTGAAACC[A/G]TATCTCCAAAAAAGA	8924
rs192977767	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28260344	TAGAAGCTTCTAAAA[C/T]GGGGAATTAAAGACA	8924
rs192978492	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28187757	TCATGTCATTTTATT[C/G]TTGCCTCATTCAAAT	8924
rs192982529	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28149330	GAAAATGGCCACACC[A/G]ACATACATTCTAGTA	8924
rs192992102	snp	C/T	0.000624046	0.0176531	intron-variant	HERC2	GRCh38.p7	15:28299395	AACACTAGTTAAAGG[C/T]CCTTACCTTTTCTAG	8924
rs192999801	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111381	AATATACAATCAAGA[C/T]GACTCACGACACTTG	8924
rs193014113	snp	C/T	0.000103514	0.0071935	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214257	GGGCGCACCCTGCGC[C/T]GCCTCAGCGTGGACT	8924
rs193019282	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28175008	TTGGCCTTATAGAAT[C/T]ATAAAGTAAAATTCA	8924
rs193059156	snp	G/T	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28138283	AACAGGCTTTCAACG[G/T]AGATGGAACAACCGT	8924
rs193064633	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28253364	TAATATGTAAAGTGA[A/G]GCAATGATAGAACCA	8924
rs193065529	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28289197	CAAGACCTAATTATA[C/T]GATACCTGAAAGAAA	8924
rs193094548	snp	A/C	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28215086	ATTTCACTATGTTGG[A/C]CAGGCTGGTCTCAAA	8924
rs193112195	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28210418	AGGGATTACAGGCAT[G/T]AGCCATTGTGCCCGG	8924
rs193112759	snp	A/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28239116	AAAATAAATAAAAAA[A/T]TCATCCACATATTTG	8924
rs193135445	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28132318	GAAGGCTTGCCACAG[A/G]ACTGGCTTCACAACA	8924
rs193197860	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28278806	ATAAAGCCAGCACTC[C/G]TAACACAAAATATAA	8924
rs193199701	snp	C/T	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28317979	AAAAGAACACAAAAA[C/T]AGAAACTGTAGGAAA	8924
rs193238528	snp	C/G	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28308712	GGCTTTTATTATGTT[C/G]AGGTATGTTTCTTCC	8924
rs193244818	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28164336	ACCCTGGAAACCACA[A/C]CACTCTGATTTAGGA	8924
rs193247355	snp	A/G	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28196832	GTAATGAGCACATGG[A/G]GGTTCATTGTAAACT	8924
rs193270950	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28192988	TCAATCAATGAATGC[C/T]GATTAAGGTAAGCCC	8924
rs193271582	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28255487	GAAAATCATTCTCCA[A/G]GGCAAAGCAAGAAAG	8924
rs193272953	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28291737	AACCCAAAACAAAAA[A/C]CTCAATTAAAAAATG	8924
rs193285177	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28153404	CACACTTGTAATACA[A/G]GCACTTTGGGAGGTC	8924
rs193287494	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28220314	GGGAGCTTATTTAAA[C/T]TGCAGGCTCCGAGGA	8924
rs199498558	snp	C/G			intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28213263	GCACTTGGGCTACAT[C/G]AAAATAATGTAAATG	8924
rs199500960	snp	C/T	3.2994e-05	0.00406152	missense	HERC2	GRCh38.p7	15:28116767	TCCCGTTGGGTGTCA[C/T]GATCAGCAGGGGCGT	8924
rs199522451	snp	A/G	0.00011108	0.0074517	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28186540	ATCCAGGAATGTAGC[A/G]GGAGGTAAGTGAGCA	8924
rs199523105	snp	C/T	1.64953e-05	0.00287182	missense	HERC2	GRCh38.p7	15:28144769	ACTCATCCCCTGGGA[C/T]GCGCAGCTCGCTGGA	8924
rs199528088	snp	C/G/T	1.65029e-05	0.00287248	intron-variant	HERC2	GRCh38.p7	15:28201565	GTAGACTGCAAGAAA[C/G/T]AAATACATTCAAACA	8924
rs199577464	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28232531	TCCAGCCTGGCGACA[A/G]AGCAAGATTCCATCT	8924
rs199593384	snp	C/T	3.58712e-05	0.00423489	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28215681	GACCTTCATGAGCAG[C/T]GTGATCCACTGCGGG	8924
rs199595462	snp	A/C	2.32924e-05	0.00341257	intron-variant	HERC2	GRCh38.p7	15:28268637	GAAGGAAAAATACGA[A/C]GAAAAGTAGTCATCA	8924
rs199598391	snp	C/T	0.00199792	0.0315431	synonymous-codon	HERC2	GRCh38.p7	15:28113209	CCACTGGATCAGCGA[C/T]GCGGAAGGCTCGATG	8924
rs199600891	snp	A/G	0.00299545	0.0385843	intron-variant	HERC2	GRCh38.p7	15:28202317	CGGGAACCCACACAT[A/G]CACAAGCAGAGGCCA	8924
rs199631891	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28294710	TGTTCTTACTACAAA[A/T]TGTGCCTCCCACAGC	8924
rs199632947	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28192635	TATCAGAATTCAGGA[A/G]AAAATAAAGAATTAC	8924
rs199634438	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28294373	AAAGGAAGCCATGAC[A/G]AGGCACATCATAATC	8924
rs199647215	snp	A/G	0.000971985	0.0220238	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214082	CAAACCCACCCCTTC[A/G]GAAGGCCTTCCCACA	8924
rs199648519	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28292231	CCAAACTCCATCTCC[A/C]AAAAAAAAAAAAAAA	8924
rs199653634	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28276753	AAAAAAAAACAAAAA[G/T]AAAAACAAAAAAAAA	8924
rs199666827	snp	A/G	0.00199792	0.0315431	intron-variant	HERC2	GRCh38.p7	15:28163298	ATCCTAAGTCAAATG[A/G]CATCCAACAATTAAC	8924
rs199669003	in-del	-/ATA			intron-variant	HERC2	GRCh38.p7	15:28289406	CATGCACCTTATAAC[-/ATA]ATTCTCAAATACATG	8924
rs199674395	snp	A/T			intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28316059	ACCTCTTCCGCTGTT[A/T]AAAAAAAAAAAAAAT	8924
rs199682651	snp	A/G	0.00199792	0.0315431	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28176713	AGAGCCAGGGTCTGC[A/G]CGTCTCTACTCCCAC	8924
rs199686180	snp	C/T	4.94882e-05	0.0049741	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28269398	GGCATAGTATTTCCA[C/T]CCTATTAACCCCCAA	8924
rs199705204	in-del	-/TGGTGGCA			intron-variant	HERC2	GRCh38.p7	15:28240280	AAAATTAGCCGGGCG[-/TGGTGGCA]GGCGCCTGTAGTCCC	8924
rs199713563	snp	C/G	1.6473e-05	0.00286988	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213793	CCGCATGTCAGAGAA[C/G]TGCACGGTGATTTTG	8924
rs199725508	snp	A/T	0.00299544	0.0385843	intron-variant	HERC2	GRCh38.p7	15:28178817	GTAAGGACACCAATT[A/T]GGGCTTTGGTTAACA	8924
rs199728389	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28294333	AGACTGAAGAATCTG[C/T]ACAAAGCCCACACAA	8924
rs199738357	in-del	-/T			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316492	AAAAAAAATTTTTTT[-/T]GCTGCAAAATGCTCT	8924
rs199790436	snp	A/G	0.000236759	0.0108777	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274438	TCACTGCAGAGGTCC[A/G]CATCCTCGCCTGGGC	8924
rs199791213	snp	A/G	0.000536373	0.0163676	intron-variant	HERC2	GRCh38.p7	15:28182380	GCCCCACCCTGCTGG[A/G]TCCCAGGGAGCAGGC	8924
rs199801737	snp	A/G	5.00196e-05	0.00500073	intron-variant	HERC2	GRCh38.p7	15:28245874	AAACTCCTTTAAGAC[A/G]CCGTACCCATTATGC	8924
rs199808089	in-del	-/ATGG			intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314728	AGCCAGGAATGATGG[-/ATGG]TACACGCCTGTAATC	8924
rs199815300	snp	A/G	1.6861e-05	0.00290348	intron-variant	HERC2	GRCh38.p7	15:28112070	AGTGATTAGAAATTG[A/G]GTACGGCTGCAGTTT	8924
rs199817337	snp	A/C/T			intron-variant	HERC2	GRCh38.p7	15:28217214	CACCCAGTAATCCCC[A/C/T]CACACTCACTCATGC	8924
rs199825741	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28273287	ATTTATCTCATTATC[A/C]AAAACATAAGTAGAA	8924
rs199828625	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28206174	TTAAGAAAATATACA[C/T]CTAGAAAAAAAGTGT	8924
rs199840908	snp	A/G	4.95029e-05	0.00497484	intron-variant	HERC2	GRCh38.p7	15:28177533	TTCACAGACACACGG[A/G]TTGCCAAAGGGCAGG	8924
rs199844052	in-del	-/T/TT	0.0182019	0.0936463	intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28312626	CAGAGACCCTATTCA[-/T/TT]TAAAAAAAATAAAAT	8924
rs199850400	snp	C/T	0.000132301	0.00813223	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28179191	TACCACATTCAAAGC[C/T]GACAGTGTCTCAGAG	8924
rs199854908	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28147437	AGTTAAAGACAGGCC[C/T]GGACAACAGGCTATA	8924
rs199857737	in-del	-/T	0.0150606	0.0854603	intron-variant	HERC2	GRCh38.p7	15:28208508	CCTTCCTAGCAGGTG[-/T]TATCACCCGAAGGTC	8924
rs199863569	snp	A/G			intron-variant, upstream-variant-2KB, downstream-variant-500B	HERC2, LOC107987422	GRCh38.p7	15:28319438	ATACAAAAATTAGTC[A/G]GGCATGCATGGTGGC	8924
rs199866264	in-del	-/A			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321295	ATACCCTAAAAAAAA[-/A]GCCTTACACGAGAAA	8924
rs199869075	snp	C/T	0.000247091	0.0111123	intron-variant	HERC2	GRCh38.p7	15:28141671	TGCCATGGGCAAGAA[C/T]AATGCACACAGCCTC	8924
rs199876765	snp	C/T	0.00197546	0.031366	intron-variant	HERC2	GRCh38.p7	15:28206229	AAACTGTCAAGGCTG[C/T]ATGGCTGTACCTCAA	8924
rs199898039	snp	C/T	7.19282e-05	0.00599658	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256203	GCACGGTGCTCAGCA[C/T]GCCCGCACTGCTGGC	8924
rs199900591	snp	C/T	0.000131948	0.00812136	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265881	CTCGGCAGTGATGGC[C/T]GCACTGTAAGTGCTC	8924
rs199904662	snp	C/T	3.33072e-05	0.00408075	missense	HERC2	GRCh38.p7	15:28115527	CGGTTCGGATGGCAA[C/T]GCCCAGCAACACACC	8924
rs199907206	in-del	-/GGGAT	0.157311	0.232183	intron-variant	HERC2	GRCh38.p7	15:28282966	GGGAAGGGACAGGAA[-/GGGAT]GGGATGGGACGGGAC	8924
rs199912491	snp	G/T	3.55095e-05	0.00421349	intron-variant	HERC2	GRCh38.p7	15:28237128	GCTGGAAAAATAAAT[G/T]TCATCATCAATCTGA	8924
rs199921141	snp	C/T	3.48268e-05	0.00417279	intron-variant	HERC2	GRCh38.p7	15:28191920	ACAAGGCAAAACCAT[C/T]GGTGTGAAAGTGCCC	8924
rs199925329	snp	C/T	0.00199792	0.0315431	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28220593	GGACTCTTATCCATC[C/T]GTCCTCTCCCAGCTC	8924
rs199934844	in-del	-/G	0.079395	0.18274	intron-variant	HERC2	GRCh38.p7	15:28272875	CCCCAAAGCGTTCCC[-/G]GTCTGCGGCAGCCCT	8924
rs199946987	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28136126	CACAAGGGAAAAAAC[A/C]CCTTTTTTTTTTTTA	8924
rs199951842	snp	A/G	0.499929	0.00593906	intron-variant	HERC2	GRCh38.p7	15:28272164	AGTCTTGCTTTAAAA[A/G]TAACTAGACTCGAGT	8924
rs199972946	in-del	-/T			intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28301446	CAGCTGTTCAAAGAC[-/T]GATAGGGACTCCTGA	8924
rs200004044	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28147325	ATGAAGTAATAGCTT[A/C]AAGTTTAAAAATGCT	8924
rs200021106	snp	A/T	8.26822e-05	0.00642917	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28257179	AGGAGATCCAGCTGC[A/T]CAAAAGTCATTGAGC	8924
rs200047478	snp	A/G	0.0071029	0.0591693	missense	HERC2	GRCh38.p7	15:28132789	ACATCGACCACTTCA[A/G]TTCCTCTCAGAGACT	8924
rs200053388	snp	A/C	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28195060	GACTCCGTCTCAAAA[A/C]AAAAAAAAATTAAAA	8924
rs200063806	snp	C/T			upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28323454	TGCCCAGGCTGGTCT[C/T]GAACTCCTGGGCTCA	8924
rs200075924	snp	A/G			intron-variant, upstream-variant-2KB, downstream-variant-500B	HERC2, LOC107987422	GRCh38.p7	15:28319642	AAATGTGTAACAAGG[A/G]CCAAGTACTGTGTAT	8924
rs200084694	snp	C/G	0.497721	0.0336815	missense, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28321416	CTGGGCAGCCAAACA[C/G]AAAGATTCAGAGGGC	8924
rs200086275	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28117191	AGCGTGAGGCCGCTG[C/T]CGCAGCAGGAAGCAC	8924
rs200111473	snp	A/G/T	8.24184e-05	0.00641897	intron-variant	HERC2	GRCh38.p7	15:28130456	GGTGCACATACCCCA[A/G/T]TAAAAATCTGGTTTT	8924
rs200113640	in-del	-/T			intron-variant	HERC2	GRCh38.p7	15:28161254	ACTTACATTTAATGA[-/T]TTTTTTTTTAAATAT	8924
rs200121672	snp	A/C	0.000399281	0.0141238	missense	HERC2	GRCh38.p7	15:28163198	GCAGGTCTACCACCA[A/C]ACGAGTGTCATCCGC	8924
rs200138073	snp	A/G	0.00199792	0.0315431	intron-variant	HERC2	GRCh38.p7	15:28260773	CAAGCTCTATATTCA[A/G]TACCTGGGCAGGCCC	8924
rs200144914	snp	A/G	0.000148308	0.00861	intron-variant	HERC2	GRCh38.p7	15:28176639	TCAGGCCAGCGTTTC[A/G]TATCATTCCTACCCA	8924
rs200146721	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28174718	AACGCGTATGCCACG[A/G]TAGTTGAAAGAATTG	8924
rs200158883	snp	C/T	0.000399281	0.0141238	missense	HERC2	GRCh38.p7	15:28167760	ACTGGGATAAAAGGC[C/T]GAGCGGAGGCTGAGG	8924
rs200167844	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28245568	AAAAAAAAATATATA[C/T]ACACACACACACACA	8924
rs200168470	snp	C/T	1.66676e-05	0.00288679	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274963	CGCCGCTCGGGATCC[C/T]ACTCTGGCGAGCCCC	8924
rs200181265	snp	A/C/T	0.000626762	0.0176919	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28228290	CGAGGTTGTTTGCGC[A/C/T]GTGCTGCAGGGTGAG	8924
rs200194207	snp	C/T	0.000101187	0.0071122	intron-variant	HERC2	GRCh38.p7	15:28168398	ACATTGCTTTAGATT[C/T]GCTTTTACCTCTCTC	8924
rs200204354	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28306574	GGTATCAGGGTAATA[C/T]TGGCCTTCTACAATA	8924
rs200216580	snp	A/G	0.000364003	0.0134859	intron-variant	HERC2	GRCh38.p7	15:28229618	AATATCAATGCATAC[A/G]GTTAAGTGTTATGTA	8924
rs200220947	snp	A/C/T	0.000347454	0.0131763	missense	HERC2	GRCh38.p7	15:28125032	GTTTGCCAGCACTGG[A/C/T]GGGCTTGCTGGTCGA	8924
rs200226171	snp	A/G	0.00199792	0.0315431	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214062	CTAAATTAATTCTGA[A/G]AACACAAACCCACCC	8924
rs200236318	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28294321	ATAAACCCAGGCAGA[C/T]TGAAGAATCTGCACA	8924
rs200252817	snp	A/T			synonymous-codon	HERC2	GRCh38.p7	15:28135567	AAGGCAGTGCTTTCC[A/T]CCAGAGTTCACAGCT	8924
rs200255984	snp	C/T	1.65217e-05	0.00287412	missense, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28299428	GGGAGCTCTCCGTTC[C/T]GGGTTGATTCTGTTC	8924
rs200259544	snp	G/T	9.92014e-05	0.00704208	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28238690	CCAGAAGCCTCCATC[G/T]TTATTATGGTTCTCC	8924
rs200259885	in-del	-/TA			intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28301733	CTAGTTGTATGTATG[-/TA]TGTATATATATATAT	8924
rs200263043	snp	A/G	0.000391539	0.0139863	intron-variant	HERC2	GRCh38.p7	15:28132640	CCGGCCTCTGCACAC[A/G]GCGCCTCCTCACCAG	8924
rs200281947	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28127122	GGAAAGTGTGACGCC[C/T]GCGTGGTCAAGGGCA	8924
rs200294738	snp	A/G	0.00199792	0.0315431	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265702	TAAGCCCGGCTACCA[A/G]CATCGGAATGGCCTC	8924
rs200302507	in-del	-/T	0.0554779	0.157039	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316485	CTCTACAAAAAAAAA[-/T]TTTTTTTGCTGCAAA	8924
rs200317563	in-del	-/TAGA			intron-variant	HERC2	GRCh38.p7	15:28270245	AGATAGATAGATAGA[-/TAGA]CAGACAGACAGACAT	8924
rs200326715	snp	C/T	5.02837e-05	0.00501391	intron-variant	HERC2	GRCh38.p7	15:28142977	AACAGAACAGTATTC[C/T]ATCGCAGGAATCCAG	8924
rs200331656	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28308912	CTTGGTCACAATGAA[C/T]GATCTTTCTAACGTA	8924
rs200333054	snp	C/T	0.000533921	0.0163302	intron-variant	HERC2	GRCh38.p7	15:28256020	GAAAGTGTGTGCCAA[C/T]TTGAGTGAAACGCCA	8924
rs200336266	snp	C/T	1.64735e-05	0.00286993	missense	HERC2	GRCh38.p7	15:28114658	CGCGGTTGTCCAGGG[C/T]GATGTGTGTGTGCTT	8924
rs200336581	snp	C/T	1.6941e-05	0.00291036	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274364	AGGACACGGTGCTCT[C/T]GTCAAAGAGCGAGGC	8924
rs200344133	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28147288	CTGACTAGAAATACC[C/T]TTTGTTCTTTAAATT	8924
rs200350753	in-del	-/AA			intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174311	GGCACTACAACCTCT[-/AA]TTGTGTTGGCACAAT	8924
rs200367191	in-del	-/CA			intron-variant	HERC2	GRCh38.p7	15:28217220	TAATCCCCTCACACT[-/CA]CACTCATGCCTCCCT	8924
rs200371467	snp	C/T	0.000137625	0.00829419	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28222200	ATATCTTCCTCAACG[C/T]TGTCACAACTGGGGC	8924
rs200377671	snp	A/G	3.32347e-05	0.00407631	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214180	GGGAGTGCAGCGTGC[A/G]CAGCAGTGCCACCAC	8924
rs200377749	snp	A/C	0.000187073	0.00966962	intron-variant	HERC2	GRCh38.p7	15:28182368	CTGCTGCCGAGTGCC[A/C]CACCCTGCTGGGTCC	8924
rs200379545	snp	A/G	0.00415799	0.045406	intron-variant	HERC2	GRCh38.p7	15:28202658	TTGGGAAGTGCCCTC[A/G]GCTAGCTTACACAGT	8924
rs200380652	snp	A/G	0.000516628	0.0160638	intron-variant	HERC2	GRCh38.p7	15:28268456	CCTACAGGAATAAGC[A/G]ATACATACACAGTGT	8924
rs200386488	snp	A/G	0.0232847	0.105357	intron-variant	HERC2	GRCh38.p7	15:28250613	TCTACTCTGAAATAC[A/G]TTTCACGGCTTATTT	8924
rs200387417	snp	A/G	0.00187432	0.0305556	intron-variant	HERC2	GRCh38.p7	15:28198573	TCTCTAAGAAAAAAC[A/G]AAAGCACTGAACAAA	8924
rs200403368	snp	C/T	0.00199801	0.0315438	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213942	CCACTTCAGGGTTCT[C/T]GGAGTCGGGGAAGTA	8924
rs200412833	snp	A/G	0.0023933	0.0345097	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28234144	GGTCCCCCAGGGCCC[A/G]TCTGTGGGAGCAGAG	8924
rs200418044	snp	C/G	0.000463369	0.0152141	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229254	ATGTTCTGTACAGCC[C/G]AAGCGTACAGCTTGC	8924
rs200457382	snp	A/G	5.77062e-05	0.0053712	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28269252	AGAACACTCACCAGC[A/G]TGTCACTATTATAGG	8924
rs200464029	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28285820	AAAAAAAAAAAAAAA[C/T]ACATAAATTACCAAC	8924
rs200466569	snp	A/C/G	0.000344228	0.0131149	intron-variant	HERC2	GRCh38.p7	15:28124003	GTACTGAAGACACCA[A/C/G]TTTCCCCTAGAGCAA	8924
rs200469818	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28170661	AAAAACCTGATGAAT[C/T]AGACTTCATCAAAAT	8924
rs200485883	snp	A/C	0.000166903	0.00913366	intron-variant	HERC2	GRCh38.p7	15:28117003	GCTCCAGCACGTGGC[A/C]AGTTCTCACCCACAA	8924
rs200506884	snp	C/T	0.000116615	0.00763505	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202368	AGCTGGATGCATTCC[C/T]GGAAGCACCAGTGAG	8924
rs200515902	snp	C/G	0.000282756	0.0118869	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274926	GCCAGGCCCTGCGCA[C/G]GAAGGCAAAGGCAAA	8924
rs200516928	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28234697	CAACAGATGACTATG[A/G]GGGTACCAGGGAGAC	8924
rs200536152	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28270025	GCAGTGCAATGGCGC[A/G]ATCTTGGCTCACTGC	8924
rs200545514	snp	A/C/G	0.000153988	0.00877328	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28246023	ACCAGCATTTTTACT[A/C/G]AGCAGAAGCACTATA	8924
rs200562761	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28115744	TGCCTAAAAGCCTCT[A/T]ACTCTTCACATCCTT	8924
rs200571073	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28136118	ATATAAACCACAAGG[A/G]AAAAAACACCTTTTT	8924
rs200571641	snp	A/G	0.00161532	0.0283734	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28228291	GAGGTTGTTTGCGCC[A/G]TGCTGCAGGGTGAGC	8924
rs200587201	snp	A/C	1.64806e-05	0.00287054	intron-variant	HERC2	GRCh38.p7	15:28144668	GCCATAAGCCCCTTC[A/C]TTACCAGCAGCTGGC	8924
rs200589745	snp	A/G	0.000507934	0.0159282	intron-variant	HERC2	GRCh38.p7	15:28182558	AAAGAGAGGTTATTC[A/G]GCATAAAACATTTAA	8924
rs200591481	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28276656	AGAATTGCTTGAACC[A/T]GGGAGGCAGAGGTTG	8924
rs200593171	snp	A/G	0.000362671	0.0134612	intron-variant	HERC2	GRCh38.p7	15:28233619	CCTCAGGTTAGTCGA[A/G]GAATCTGCAGTGTAC	8924
rs200599434	snp	G/T	1.69619e-05	0.00291216	intron-variant	HERC2	GRCh38.p7	15:28113535	GGTCAGCAGGCAAAA[G/T]GCAGCTGCAGGGCAG	8924
rs200605180	snp	C/T	0.000232361	0.0107762	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213948	CAGGGTTCTCGGAGT[C/T]GGGGAAGTAGTCCTC	8924
rs200605638	in-del	-/T			intron-variant	HERC2	GRCh38.p7	15:28196667	ACTACATTGTAGTTA[-/T]TTTGTTTTTTACAAA	8924
rs200625252	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28121514	ATAGTTTTGTTTAAA[A/G]TCTGTGTTGAAGACC	8924
rs200632307	snp	G/T	0.00174594	0.0294944	intron-variant	HERC2	GRCh38.p7	15:28255999	TCATTGCCTGAAACT[G/T]AAATAGAAAGTGTGT	8924
rs200641367	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28294712	TTCTTACTACAAAAT[G/T]TGCCTCCCACAGCCC	8924
rs200646592	snp	C/T	0.00199792	0.0315431	intron-variant	HERC2	GRCh38.p7	15:28202318	GGGAACCCACACATA[C/T]ACAAGCAGAGGCCAG	8924
rs200651761	snp	A/G	0.000399281	0.0141238	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213750	CACCTACTGGTTTCA[A/G]CTGATTCAATGGGCA	8924
rs200659600	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28162307	CACCGCACTCCAGCC[C/T]GGGTGAAGGAGACTG	8924
rs200667217	snp	A/G	3.33e-05	0.00408031	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274949	AAGGCAAAAGACAGC[A/G]CCGCTCGGGATCCCA	8924
rs200697058	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28276773	ACAAAAAAAAACTAC[A/G]CAGCCATAATAAAAT	8924
rs200699030	snp	A/C			stop-gained	HERC2	GRCh38.p7	15:28141581	GATTATGTCCCCATC[A/C]ATAAATTGTTCCACT	8924
rs200702875	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28173381	TAAGATACTATTCAA[A/C]AATTTAAAAAGAATA	8924
rs200702908	snp	A/G	1.76393e-05	0.00296974	synonymous-codon	HERC2	GRCh38.p7	15:28132683	CTGGTCCTCACTGTC[A/G]CTGTGCCCCAGCCGG	8924
rs200703084	snp	A/C/G	0.000121224	0.00778453	intron-variant	HERC2	GRCh38.p7	15:28269209	GACAGACCCTGCCCC[A/C/G]CAAGGGAACACTGCA	8924
rs200709278	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28273295	CATTATCAAAAACAT[A/G]AGTAGAAGAATATCT	8924
rs200710093	snp	A/C	0.000247257	0.0111161	intron-variant	HERC2	GRCh38.p7	15:28233645	TGTACCTAAAGTACA[A/C]AGATATCGAGCTCCT	8924
rs200733599	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28165286	GTGCCCACCACGGAG[A/C]GGGGGACAGCCAAGA	8924
rs200741102	snp	C/T	0.000395289	0.0140531	missense	HERC2	GRCh38.p7	15:28114643	GCCGCACGTACTCCG[C/T]GCGGTTGTCCAGGGT	8924
rs200741773	snp	A/T	0.000209578	0.0102345	intron-variant	HERC2	GRCh38.p7	15:28117189	CAAGCGTGAGGCCGC[A/T]GCCGCAGCAGGAAGC	8924
rs200754559	snp	C/T	4.94336e-05	0.00497135	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28270747	CAGGGCGTAGCCAGA[C/T]GGTCTAAATGGGCCA	8924
rs200763932	snp	C/G	1.65433e-05	0.002876	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213930	CCATGAGGCCCCCCA[C/G]TTCAGGGTTCTCGGA	8924
rs200772464	snp	A/C	0.0381606	0.132756	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256152	TGGGCAGCAGCACGG[A/C]CCAGCCACTCTGCAG	8924
rs200787864	snp	C/G/T	0.000274468	0.0117116	intron-variant	HERC2	GRCh38.p7	15:28169445	AAAATGTGAAGCTCA[C/G/T]ATAATTGCAGAATTT	8924
rs200810082	in-del	-/ATC			intron-variant	HERC2	GRCh38.p7	15:28236271	ATTATTATTATTTTT[-/ATC]ATCATCATCAGCTGT	8924
rs200811930	snp	A/G	1.77852e-05	0.00298199	missense	HERC2	GRCh38.p7	15:28132254	CGGTGGCCCTGCAGC[A/G]CCTCCACCTTCAGAG	8924
rs200818684	snp	C/T			missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28245949	GCCAGATGGTTGAAC[C/T]GATCCAGATGTTCCA	8924
rs200823016	snp	G/T	0.0244777	0.107887	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202511	CGGATGTGCTGCACG[G/T]CGACAGGCGTGGTGG	8924
rs200836800	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28194386	CCATCCTGGCTAACA[C/T]GGTGAAACCCCATCT	8924
rs200844089	snp	A/G	0.00199803	0.031544	intron-variant	HERC2	GRCh38.p7	15:28196182	ATTTCATTAATATTT[A/G]GTGGAAGAGAGAATA	8924
rs200844152	in-del	-/G	0.270892	0.249126	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313474	CACCCAGCCCGTTAA[-/G]GCATTTATTAAAGTG	8924
rs200851435	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28163324	TTAACATGAGGAATG[A/G]TATGCTAAGAGATAA	8924
rs200851769	in-del	-/T	0.084364	0.187256	intron-variant	HERC2	GRCh38.p7	15:28155990	CACATGGTTAGCCAG[-/T]TTTTCCCAGCACCAT	8924
rs200859595	snp	A/C	0.324488	0.238645	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272966	TCCTGCAGGGGGATG[A/C]TTCCTGGCCCTTTGG	8924
rs200862122	in-del	-/AG			intron-variant	HERC2	GRCh38.p7	15:28298037	GTGTGTGTGTGTGTG[-/AG]TGAATATTTTCAAAC	8924
rs200862998	in-del	-/ACACACACACAC			intron-variant	HERC2	GRCh38.p7	15:28245567	AAAAAAAAAATATAT[-/ACACACACACAC]ACACACACACACACA	8924
rs200864382	snp	G/T	0.000875765	0.0209073	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233170	TCCTTCGTTCTCGAA[G/T]TATCTTTTGAGCTAT	8924
rs200866686	snp	C/T	0.000334272	0.0129238	intron-variant	HERC2	GRCh38.p7	15:28246102	GATTTAAATAAGTAT[C/T]TATCCTATAAAAGCT	8924
rs200909165	snp	A/G	3.42536e-05	0.00413831	missense	HERC2	GRCh38.p7	15:28113094	CGAAGTCTCGGCCCC[A/G]GAAGTCGGCGATGGT	8924
rs200911598	snp	A/G	3.29677e-05	0.00405989	intron-variant	HERC2	GRCh38.p7	15:28191061	GGAATTTCCACCTAG[A/G]AAAAAATGGGTAAAG	8924
rs200915075	snp	A/G	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28136451	TCTCTGGTGCACAGG[A/G]TGCAGGGTAATGCAG	8924
rs200922469	snp	C/T	0.000116081	0.00761756	missense, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28299408	GGCCCTTACCTTTTC[C/T]AGGAGGGAGCTCTCC	8924
rs200931637	snp	C/G	0.000115423	0.00759593	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28178976	CTGGAAATGCCCAGC[C/G]CCAGCCGGCCATTCG	8924
rs200971181	snp	C/T	1.65798e-05	0.00287917	intron-variant	HERC2	GRCh38.p7	15:28121449	AACACATCAAACAGA[C/T]AAAATTTAGAATCTG	8924
rs200980383	in-del	-/ACAG	0.00993419	0.0697739	intron-variant	HERC2	GRCh38.p7	15:28224181	CAGAGAGAGAGAGAA[-/ACAG]ACAGACAGACAGACA	8924
rs200987196	snp	A/G	9.89022e-05	0.00703145	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28182471	ACCTTGGTTCTTATC[A/G]TAGCTGCTGATTCCA	8924
rs200987238	snp	C/T			upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28323594	TTGGTTATGTTCTAT[C/T]TATATTTTCTAATTT	8924
rs200990708	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28294334	GACTGAAGAATCTGC[A/G]CAAAGCCCACACAAG	8924
rs200993824	snp	A/G	0.000399281	0.0141238	missense	HERC2	GRCh38.p7	15:28116715	CTGGCGGCCGGGCTG[A/G]GCAGGTAGCAGTCTC	8924
rs200997244	snp	A/T	0.00383081	0.0435973	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28222103	AGCCAGTTCTGGTCC[A/T]GAAACAGGGAGCTGC	8924
rs201000933	snp	A/G	0.000197925	0.00994602	intron-variant	HERC2	GRCh38.p7	15:28265614	TGGCGAGAGCTCTAC[A/G]TACCGTTCTCAGTGA	8924
rs201001609	snp	A/G	0.00395566	0.0442965	intron-variant	HERC2	GRCh38.p7	15:28254305	AAAAAAAGTAAATAA[A/G]TAACATATAATACAA	8924
rs201003752	snp	C/T	0.000115309	0.00759218	synonymous-codon	HERC2	GRCh38.p7	15:28114641	CAGCCGCACGTACTC[C/T]GCGCGGTTGTCCAGG	8924
rs201018425	snp	A/G			intron-variant, downstream-variant-500B	HERC2, LOC107987422	GRCh38.p7	15:28312460	CAACATGGTAAGACC[A/G]TGTCTCTACAGAAAT	8924
rs201029214	snp	A/G			intron-variant, upstream-variant-2KB, downstream-variant-500B	HERC2, LOC107987422	GRCh38.p7	15:28319542	GTGAGCCAAGATTGC[A/G]CCACTGCACGCCAGC	8924
rs201040636	in-del	-/A	0.159951	0.233219	intron-variant	HERC2	GRCh38.p7	15:28185203	ATAACCTGATTTATT[-/A]CCAGAACTACTACCC	8924
rs201047588	in-del	-/TAA	0.0310518	0.120672	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28320868	TCTGAGCACTCCTCT[-/TAA]TAAGGAGTTACAAAG	8924
rs201056429	snp	C/T			intron-variant, upstream-variant-2KB, downstream-variant-500B	HERC2, LOC107987422	GRCh38.p7	15:28319490	CTCGGAAGGCTGAGG[C/T]GGGAGAATCACTTGC	8924
rs201061030	snp	A/G	3.42841e-05	0.00414016	missense	HERC2	GRCh38.p7	15:28132828	CGAGGGCGGTCACAC[A/G]GACTGCAAAAAAGTC	8924
rs201066159	snp	C/T	0.000133595	0.00817187	intron-variant	HERC2	GRCh38.p7	15:28269227	AGGGAACACTGCAGG[C/T]ACAGTGCCCAGAACA	8924
rs201074469	snp	A/G	6.662e-05	0.0057711	intron-variant	HERC2	GRCh38.p7	15:28274901	GCCACACCAGGGACC[A/G]TACCTGATCGCCAGG	8924
rs201074808	snp	C/G	0.00199792	0.0315431	missense	HERC2	GRCh38.p7	15:28143970	CTCAGTCTCTGAAGG[C/G]CCCACATTCTGTGAC	8924
rs201078187	in-del	-/AAAAAAAAAAAAAAAAAAAAAAAAAAA	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28119400	ACAAGACTCCCTCTC[-/AAAAAAAAAAAAAAAAAAAAAAAAAAA]AAAAAAAAAAAGGCC	8924
rs201088586	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28280881	TGTCACTGCACTCCA[A/G]CCTGGGTGACAGAGT	8924
rs201095943	snp	A/G	0.000115553	0.00760019	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28192014	TGCCGTCAATGAGAC[A/G]GGATGCCTGGTTCAC	8924
rs201109183	snp	A/G	0.00104545	0.0228393	intron-variant	HERC2	GRCh38.p7	15:28262866	TGCTAACTTTAAAAC[A/G]TTACTAAAGAAACTG	8924
rs201122066	snp	C/T	1.64958e-05	0.00287187	missense	HERC2	GRCh38.p7	15:28141830	TCTGCCATTAATTCA[C/T]GAATTTTCTTAGCCA	8924
rs201135544	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28216147	CTTCTAAGTATGTGT[A/C]GTAAAAGTAGTTAGG	8924
rs201136198	snp	A/G	9.93361e-05	0.00704686	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28182511	CCTTCTTTCTAATGA[A/G]GCTAACCAAACGGAA	8924
rs201138762	in-del	-/TATGTGTATATATATATATA			intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28301730	CACACTAGTTGTATG[-/TATGTGTATATATATATATA]TATATATATATATAT	8924
rs201142266	snp	A/G/T	6.59897e-05	0.00574381	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265905	AGTGCTCCCGCAAGC[A/G/T]ATGTGCACCACGTGC	8924
rs201160319	snp	C/G	0.0115144	0.0749975	intron-variant	HERC2	GRCh38.p7	15:28207481	TTCAGTAACCCCTGA[C/G]ACAGACACATCCCAC	8924
rs201163450	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28217474	ACTAATACACGCATG[C/T]TCTCACACACACTGG	8924
rs201171990	snp	A/G/T	0.00114686	0.0239223	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202214	TGACCTGTATGTCGG[A/G/T]GTGGTCCAGCAGCCA	8924
rs201179213	snp	A/G	0.000166811	0.00913114	intron-variant	HERC2	GRCh38.p7	15:28198330	ACTAAGTACACATGC[A/G]TTAATGAAAAGTTAA	8924
rs201180561	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28206769	ACCTGGGAGGCGGAG[C/G]TTGCAGTGAGCTGAG	8924
rs201182375	snp	C/T	0.0573934	0.159382	synonymous-codon, downstream-variant-500B	HERC2	GRCh38.p7	15:28174420	AGCACCTAAAGGGTC[C/T]CTTGCAGTCTGGAAG	8924
rs201212138	in-del	-/AC			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321773	TCAAATCCAAGAAGT[-/AC]ACACACATAACAGGG	8924
rs201216024	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28294021	AATCGGTGAAAGACA[C/T]GATATCCCATCCAGA	8924
rs201221568	snp	A/C/G	6.64722e-05	0.00576477	intron-variant	HERC2	GRCh38.p7	15:28132083	AGAGCACTGGGCAGG[A/C/G]AAAGAATGGGAAATA	8924
rs201227964	snp	C/G	1.73039e-05	0.00294137	intron-variant	HERC2	GRCh38.p7	15:28293049	AAAATTTTTTAATCT[C/G]TCACCGCTTTTCAGA	8924
rs201229596	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28311875	CAGAGGTACCATTTT[-/A]TAAAAAAAAAAGCCA	8924
rs201248316	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28136127	ACAAGGGAAAAAACA[A/C]CTTTTTTTTTTTTAA	8924
rs201274498	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28207291	AGGCACACGCCACCA[C/G]GCCCGGCTAATTTTT	8924
rs201279264	in-del	-/GGAG			intron-variant	HERC2	GRCh38.p7	15:28173896	ATACGGCAGGAAGGA[-/GGAG]GGGAGTTAAAAGCAA	8924
rs201289740	in-del	-/G			intron-variant	HERC2	GRCh38.p7	15:28258640	CTATTACAAAAAAAA[-/G]ATAGGTCTAAATCAG	8924
rs201338972	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28173403	AAAAGAATAAACTAT[C/T]GATACATGCAACATA	8924
rs201341093	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28273301	CAAAAACATAAGTAG[A/G]AGAATATCTAGCTAT	8924
rs201357777	in-del	-/ATT			intron-variant	HERC2	GRCh38.p7	15:28287078	CAACTTTTCTGTATA[-/ATT]ATTTTTTTCATAATA	8924
rs201359352	snp	A/G	0.00121201	0.0245873	intron-variant	HERC2	GRCh38.p7	15:28265595	CTCGTGGGCCTGTCC[A/G]GGGTGGCGAGAGCTC	8924
rs201366353	in-del	-/TA	0.492087	0.0623997	intron-variant	HERC2	GRCh38.p7	15:28234868	ATCCTCAGGGTAGGC[-/TA]TGTATTCCTAGAGCA	8924
rs201405431	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28294170	GCTGTGTGTCCCACA[A/G]TGCAATTCAATTCTG	8924
rs201416277	snp	C/T	1.64822e-05	0.00287068	intron-variant	HERC2	GRCh38.p7	15:28144073	CTGTAATGGTGGCAT[C/T]TACCTAGGGCACTCA	8924
rs201421899	in-del	-/CAC			intron-variant	HERC2	GRCh38.p7	15:28221033	TCCTTCCATGGCTCC[-/CAC]CAGACCTGCCACACA	8924
rs201423371	snp	C/G/T	0.000149087	0.00863257	intron-variant	HERC2	GRCh38.p7	15:28144826	GAGGAAAGCGCACCC[C/G/T]GGGGTTAGCTTCACT	8924
rs201428003	snp	C/G	3.32679e-05	0.00407834	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229264	CAGCCCAAGCGTACA[C/G]CTTGCCAAAGGTGAC	8924
rs201428305	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28296079	CATTTATTGAATGTC[-/A]AAAATATCTCCCTAA	8924
rs201434128	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299556	TTACAGAGTGCTCAC[A/G]CTCACATTGCAATTT	8924
rs201482973	snp	A/C	0.00104261	0.0228082	intron-variant	HERC2	GRCh38.p7	15:28201586	CATTCAAACAAAAAA[A/C]CAGGAGAACATGATA	8924
rs201488556	snp	A/C/G	0.000165138	0.00908534	intron-variant	HERC2	GRCh38.p7	15:28141410	GCTCAATGACCTTGT[A/C/G]ACATAGAAAAAGAGC	8924
rs201500188	snp	A/C/T	1.65444e-05	0.00287609	intron-variant	HERC2	GRCh38.p7	15:28202316	GCGGGAACCCACACA[A/C/T]ACACAAGCAGAGGCC	8924
rs201503867	in-del	-/C	0.444	0.157683	intron-variant	HERC2	GRCh38.p7	15:28226392	ATGTTCAAAACAGGG[-/C]GGTACCTGCACAATT	8924
rs201509405	snp	C/T	0.00245207	0.0349288	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28230487	ATCATCCGTAGATTC[C/T]GGCTTCTTAGGAACT	8924
rs201520077	snp	A/G	3.30104e-05	0.00406252	synonymous-codon	HERC2	GRCh38.p7	15:28116789	CAGGGGCGTGAGTCC[A/G]TTCTGCAGCTCCTCA	8924
rs201523297	snp	C/G/T	0.000395652	0.0140604	intron-variant	HERC2	GRCh38.p7	15:28233652	AAAGTACACAGATAT[C/G/T]GAGCTCCTTACCTAA	8924
rs201523564	in-del	-/G	0.0456336	0.143994	intron-variant	HERC2	GRCh38.p7	15:28303837	GGAATTATTTTTCTT[-/G]ATTTTTCATATTGTT	8924
rs201526446	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28194398	ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA	8924
rs201533365	snp	C/T	0.00029678	0.0121779	intron-variant	HERC2	GRCh38.p7	15:28233616	GTACCTCAGGTTAGT[C/T]GAGGAATCTGCAGTG	8924
rs201542966	snp	A/G	3.29843e-05	0.00406092	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265844	GGCCGTAGTTCCCGC[A/G]GCCCCAGGTGTACAG	8924
rs201548184	snp	C/G	1.65157e-05	0.0028736	missense	HERC2	GRCh38.p7	15:28168514	CAGATGCGTCGGAAG[C/G]GGCCGCCGAGGAGAA	8924
rs201558992	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28250835	CACATGATCCATGCT[G/T]ATGAAGACAGCCTGG	8924
rs201559931	snp	C/T	0.0101399	0.0704779	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28255955	CCAGAAGATCAATCA[C/T]GAATCGACGACCTGG	8924
rs201573521	snp	A/G	0.000313948	0.012525	intron-variant	HERC2	GRCh38.p7	15:28130130	CTCTTAGATTCACAG[A/G]CCTCAGTCCTGCGGC	8924
rs201574348	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28294323	AAACCCAGGCAGACT[A/G]AAGAATCTGCACAAA	8924
rs201578529	snp	A/G	0.000399281	0.0141238	missense	HERC2	GRCh38.p7	15:28163203	TCTACCACCACACGA[A/G]TGTCATCCGCAATCA	8924
rs201580113	snp	A/G			intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318903	GATCGGTTAAATCCT[A/G]TGGCTAAGAAACATC	8924
rs201592426	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28144460	ACAACTCCTTCCACA[C/T]CAGGTGAGGAGGAGT	8924
rs201607926	in-del	-/T			downstream-variant-500B	HERC2	GRCh38.p7	15:28110823	GCAGACAGATGGGGC[-/T]GGGGAGGAAGTCGGA	8924
rs201624767	snp	A/G	4.11294e-05	0.00453465	intron-variant	HERC2	GRCh38.p7	15:28124282	GCACCAAAGGCACAC[A/G]GGGGCCAGTGTGGCA	8924
rs201635201	in-del	-/AC			intron-variant	HERC2	GRCh38.p7	15:28136320	TTCAAACGTGCTGCT[-/AC]GCACTGACATAATAT	8924
rs201644037	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28278713	AGCAAGACGATCAGG[C/G]TTTTGCTCTTGTTTC	8924
rs201645936	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28136125	CCACAAGGGAAAAAA[A/C]ACCTTTTTTTTTTTT	8924
rs201647023	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28294361	CAAGATAAATCCAAA[A/G]GAAGCCATGACGAGG	8924
rs201651092	in-del	-/T			intron-variant	HERC2	GRCh38.p7	15:28183218	GTTTATTTATTTTTT[-/T]GTTTGTTTTGAGACA	8924
rs201661507	snp	A/T	9.8894e-05	0.00703116	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28270767	TAAATGGGCCATGAC[A/T]ACAACCGCCGTTTGT	8924
rs201664852	in-del	-/AGG	0.158632	0.232706	intron-variant	HERC2	GRCh38.p7	15:28171981	TTGGGAGGCTGAGGC[-/AGG]AGAATGGCGTGAACC	8924
rs201681256	snp	A/C/T	0.00623532	0.0554868	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28206257	CAAGTTCCTGTTTAT[A/C/T]AAATATGGCCTTCAC	8924
rs201702215	snp	A/C/T	0.000231269	0.010751	missense, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28292939	ACTTGGCCCTATATA[A/C/T]AGGTGCAGGAGTTTC	8924
rs201704003	snp	C/G	0.00500476	0.0497728	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28212519	AGGTTCACCAACTGA[C/G]CCCAGACAGACAGCA	8924
rs201715294	snp	A/G/T	4.99441e-05	0.004997	missense	HERC2	GRCh38.p7	15:28168547	AGGGGCACTCCACCG[A/G/T]GGCGATCATGGCGGC	8924
rs201724547	snp	C/T	0.000302424	0.0122931	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28270843	CTCAGGAAACTCTCA[C/T]TGGGGCTCAGAGGGC	8924
rs201731031	in-del	-/G	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28278125	AAATTGGCCAGGTAT[-/G]GTGGCTCATGCTTGT	8924
rs201738217	snp	A/G	0.000162344	0.00900809	intron-variant	HERC2	GRCh38.p7	15:28132057	TGGGGGCCCGACTGC[A/G]GTGAGCTGGGAGAGC	8924
rs201759538	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28205285	CATCTCCCAGCATGA[C/G]TGCTCTCAAGTTGCT	8924
rs201763647	in-del	-/AGCT			intron-variant	HERC2	GRCh38.p7	15:28259251	AGGCGCACATCACCA[-/AGCT]CGACGAAATTTTTGT	8924
rs201767944	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28182881	ATGGCACTGTAGAGA[A/C]ACTGAGGAAACCTGC	8924
rs201774473	snp	A/G	0.00796806	0.0626142	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28186515	TAAATGTTTCCTTTC[A/G]AAAGTGAGGATCCAG	8924
rs201778487	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28226917	TAATTCTTCTTTAAA[G/T]GTTTGGTACACTTAT	8924
rs201780395	snp	A/C			missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28174502	ACACTGTGGGACGAC[A/C]CACAAGCCACGCGTG	8924
rs201784305	in-del	-/CTAC			intron-variant	HERC2	GRCh38.p7	15:28147595	TGAGCCACGATCGTG[-/CTAC]CATACTCCAACCTGG	8924
rs201798633	snp	C/T	0.000115318	0.00759249	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28201496	GCATAATCATCATTA[C/T]TCAAGAAATCAGCTC	8924
rs201799561	in-del	-/ATAATAATAACA	0.0225045	0.103662	intron-variant	HERC2	GRCh38.p7	15:28277085	CTGTCTCCAAAAATT[-/ATAATAATAACA]ATAATAAAAAATTTA	8924
rs201804668	in-del	-/ACACACACACACACACACACACAC					GRCh38.p7	15:28245567	AAAAAAAAAATATAT[-/ACACACACACACACACACACACAC]ACACACACACACACA	8924
rs201821203	snp	C/T	0.00151929	0.0275197	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28222134	ACAGGAGCCGTTTCC[C/T]TCCTTGTTTCTTCCA	8924
rs201824814	snp	A/G	8.20227e-05	0.00640348	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28215666	TGCGTGCCCTTCCAC[A/G]ACCTTCATGAGCAGC	8924
rs201840469	in-del	-/T	0.358303	0.225323	intron-variant	HERC2	GRCh38.p7	15:28216313	ATATTTTTTTTTTTT[-/T]GTATTTTTAGTAGAG	8924
rs201841081	snp	C/T	0.00199792	0.0315431	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28269311	CAGAATCAGGAAACG[C/T]TTCTCTGCACAGGCA	8924
rs201843422	snp	A/G	0.000108869	0.00737718	intron-variant	HERC2	GRCh38.p7	15:28248506	AAAGCCTAAAGTAAC[A/G]AGCCCCGATCACATA	8924
rs201857249	snp	A/G	4.94662e-05	0.00497299	synonymous-codon	HERC2	GRCh38.p7	15:28125174	TCCCTCATCATTGTC[A/G]CCCCATGTATAAACC	8924
rs201857604	snp	A/G	0.000131796	0.00811668	missense	HERC2	GRCh38.p7	15:28169520	GCTGTAAGAATATGT[A/G]ATAAGGCCTGCTGTT	8924
rs201866535	snp	A/G	3.30447e-05	0.00406464	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213921	CCAGGACTGCCATGA[A/G]GCCCCCCACTTCAGG	8924
rs201870985	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28298113	GACACTGAAACTGAA[A/G]AGGGAGACTAATACT	8924
rs201871469	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28180647	CATCTGAACAGTTCC[A/G]TAGTAGAAAGTGAAA	8924
rs201872070	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28135046	CTCCAATCTGGCTGG[C/T]AGTTCTCATTAATTT	8924
rs201872292	snp	A/G	0.226368	0.248881	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28230479	TTTTCTTCATCATCC[A/G]TAGATTCTGGCTTCT	8924
rs201872418	snp	C/T	1.7607e-05	0.00296702	intron-variant	HERC2	GRCh38.p7	15:28117192	GCGTGAGGCCGCTGC[C/T]GCAGCAGGAAGCACA	8924
rs201884786	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28296831	CCACTTACTTGGAAC[A/G]TTCAGCCCTCAAAAT	8924
rs201933251	snp	A/G	1.64746e-05	0.00287002	missense	HERC2	GRCh38.p7	15:28167784	GCTGAGGGGGCCGAC[A/G]GAGTCACTGCAGAGG	8924
rs201936190	snp	A/G	0.00276848	0.0371022	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28269413	TCCTATTAACCCCCA[A/G]CCTATGACCTCTTGC	8924
rs201962727	snp	A/G	0.000716577	0.0189149	intron-variant	HERC2	GRCh38.p7	15:28245877	CTCCTTTAAGACGCC[A/G]TACCCATTATGCCAG	8924
rs201971030	snp	A/G	0.000399281	0.0141238	missense	HERC2	GRCh38.p7	15:28113207	AACCACTGGATCAGC[A/G]ATGCGGAAGGCTCGA	8924
rs201973387	snp	C/T	1.64893e-05	0.0028713	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28178961	ATGGGCACCGTCCCG[C/T]TGGAAATGCCCAGCC	8924
rs201979656	snp	A/G	0.113908	0.209712	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272990	CCTTTGGTGGCTGGC[A/G]TTCCGTGAACATCCC	8924
rs201990459	snp	C/T	0.49597	0.0447095	missense, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28321402	GAGTCGAGGCGAGCC[C/T]GGGCAGCCAAACAGA	8924
rs201990967	in-del	-/CACACACC			intron-variant	HERC2	GRCh38.p7	15:28224142	AAAATTATACACACA[-/CACACACC]CACACACACACACAC	8924
rs201994128	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28163792	CTCTCCTTGGGTTCA[C/T]TGAAAACATCATACA	8924
rs201995643	snp	C/T	3.80047e-05	0.00435901	intron-variant	HERC2	GRCh38.p7	15:28257273	AGCTCTAAGAGGAAA[C/T]GCAACAATCTAAAAT	8924
rs202001850	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28294050	GATTACAAATAATGA[C/G]TATCTAAAAATCTCG	8924
rs202006712	snp	A/G	0.00300039	0.038616	intron-variant	HERC2	GRCh38.p7	15:28274872	GTTGATGTATTAGGG[A/G]AGCAGAACAACGCGC	8924
rs202015379	in-del	-/GCG			intron-variant	HERC2	GRCh38.p7	15:28121042	CCCAATGTAACAGCA[-/GCG]GTTATCATCATGCAG	8924
rs202020698	snp	C/G	0.00035022	0.0132283	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28237107	TGGTGACGATTTCTT[C/G]GTCAGGCTGGAAAAA	8924
rs202023086	in-del	-/T	0.0115144	0.0749975	intron-variant	HERC2	GRCh38.p7	15:28162385	TCACATAAGCAAGCA[-/T]TTTTTTTTTCAGCAT	8924
rs202041788	snp	C/G	0	0	intron-variant	HERC2	GRCh38.p7	15:28206801	TTGTGCCACTGCACT[C/G]CAGCCTGGGCGACAG	8924
rs202042236	snp	C/G	0.000462588	0.0152013	intron-variant	HERC2	GRCh38.p7	15:28202343	GGCCAGGAAAACGAA[C/G]TACCAGGCAAGCTGG	8924
rs202042453	in-del	-/T			intron-variant	HERC2	GRCh38.p7	15:28240055	AATGATATTGTAGGG[-/T]TTTTTTTTAAATCCT	8924
rs202043474	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28288663	CGAGCCTGGCAAACA[C/T]AGTGAAACCCTGTCT	8924
rs202046283	snp	A/C/T	3.40015e-05	0.00412305	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28215707	GCGGGGAGCTGAGGG[A/C/T]GCCGCATACCTGCGG	8924
rs202096057	in-del	-/CCAC	0.0456336	0.143994	intron-variant	HERC2	GRCh38.p7	15:28259336	CTGACCTCAGGTGAT[-/CCAC]CCATCTCGGCCTCCC	8924
rs202096321	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28195674	TACCAGGGTTGGGGT[-/A]AGGGGAAGTAGGGCA	8924
rs202102990	snp	A/G	3.32187e-05	0.00407532	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28229758	TGTACTGAGGAGTGG[A/G]GACTGCGGATAAAGA	8924
rs202106740	snp	G/T	1.89485e-05	0.00307797	intron-variant	HERC2	GRCh38.p7	15:28124250	CTAGAACACAGAAAT[G/T]GCCTTCAGCCCCTCA	8924
rs202114709	snp	C/G	0.000148342	0.00861099	intron-variant	HERC2	GRCh38.p7	15:28121324	AGGCTGTCAGACTTG[C/G]AGAGTAATCTCCATG	8924
rs202126440	snp	C/T	1.65201e-05	0.00287398	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28178914	CCACCTTCTTGACCA[C/T]GTAGCTGCTGAGAGC	8924
rs202127129	in-del	-/GGAG	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28288449	AATCGTTTGAACCCA[-/GGAG]GGAGGCAGAGGCTGC	8924
rs202128423	in-del	-/TGT			intron-variant	HERC2	GRCh38.p7	15:28145628	GGCATCCAGTCTGCA[-/TGT]TGTTATGACAGAGGC	8924
rs202135257	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28216651	ACTCTCACACCCTCA[C/T]ATGCATCCTCACACT	8924
rs202137397	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28298195	GTCTCACTCTGTCAC[C/T]CAGGCTGGAGTGCAG	8924
rs202137777	snp	A/T	0.000291804	0.0120755	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28196277	GTCTTGAAACACGTT[A/T]CACAAAAATCAAAGT	8924
rs202144042	in-del	-/ACCTTAAT	0.00716266	0.059414	intron-variant	HERC2	GRCh38.p7	15:28175848	AGCCAGCTGGGAAAA[-/ACCTTAAT]ACCTTAATACATATT	8924
rs202145733	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28136129	AAGGGAAAAAACACC[C/T]TTTTTTTTTTTAATC	8924
rs202149426	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28257034	GACACTTACAAAAGG[A/G]GGAAGAAGAAGGGAA	8924
rs202151932	in-del	-/CC			intron-variant	HERC2	GRCh38.p7	15:28132047	GAGGGGCCCTGGGGG[-/CC]CCCGACTGCGGTGAG	8924
rs202156908	snp	A/C/G/T	0.00247674	0.035116	synonymous-codon	HERC2	GRCh38.p7	15:28115486	CTTCCAGACAGGCTC[A/C/G/T]GCAAGGTTGAGGCTC	8924
rs202167023	snp	A/G	3.3413e-05	0.00408722	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28228227	ACCTACCAATCAGGC[A/G]CAGTGCCGTCTGCGT	8924
rs202178731	snp	C/T	1.65343e-05	0.00287521	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28238735	TATAAGTGTCACTTC[C/T]TCATTATTTCTACAG	8924
rs202194327	snp	C/T	0.00183324	0.0302202	intron-variant	HERC2	GRCh38.p7	15:28198517	GCCTACAGATGTCAA[C/T]AACAAATCATTATAA	8924
rs202195884	in-del	-/A	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28217781	GGACATGCAGAACAC[-/A]GGGGCAGGGGCCATG	8924
rs202200969	snp	A/C/T	8.23668e-05	0.00641696	intron-variant	HERC2	GRCh38.p7	15:28141661	AGTGAGCATTTGCCA[A/C/T]GGGCAAGAACAATGC	8924
rs202202192	snp	C/G	1.70098e-05	0.00291627	intron-variant	HERC2	GRCh38.p7	15:28228206	AAGGCGCTCAAGCGG[C/G]TGCAGACCTACCAAT	8924
rs202215092	snp	C/T	0.000247302	0.0111171	synonymous-codon	HERC2	GRCh38.p7	15:28142271	GGGCAACGGTGTTCT[C/T]TTGTCAAGGGCCACA	8924
rs202216879	snp	A/C/T	0.000371892	0.0136315	intron-variant	HERC2	GRCh38.p7	15:28132642	GGCCTCTGCACACGG[A/C/T]GCCTCCTCACCAGCT	8924
rs202223174	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28292868	CAACCTTTCCAAAGT[A/G]CCAAAATTCACAAGA	8924
rs202230749	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28210759	CTGACCCATGCAGCA[A/C]ACTTTAAATGGGAAG	8924
rs202233446	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28294179	CCCACAGTGCAATTC[A/G]ATTCTGAAACTAACT	8924
rs207475348	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28170620	AATATACTTAGACTT[A/G]ACACCAAAAGTATGA	8924
rs207475349	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28174879	TCCAATTCTGCTTTG[C/T]TGCAAGACACACAGA	8924
rs207475350	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28228892	AATCCAATCAACTCT[A/C]TGTAGATGCTCAAAC	8924
rs207475351	snp	A/C			intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28317971	CCACTTAAAAAAGAA[A/C]ACAAAAATAGAAACT	8924
rs267604146	snp	A/G			missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28178889	GCTTGGCTTGTACCT[A/G]AGTGAACAGCCACCT	8924
rs267604147	snp	A/G			synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214118	GTGGGTGATGGAGCG[A/G]AGCTGGGAGTTGATG	8924
rs267604148	snp	A/G			missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233720	CCGACCTCTTCCACG[A/G]GATGCTCGGGGGGAA	8924
rs267604149	snp	A/G			stop-gained, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272355	CGCTGTCCCACAGCT[A/G]AAGCAACAACAGGAT	8924
rs367562821	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28127571	GGAGGTCTGGGGAGC[A/G]GTGACGCCTCAATAG	8924
rs367570065	snp	A/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28303941	GAGGCCAAGGCAGGC[A/G]GATCACCTGAGGTCA	8924
rs367649289	snp	A/G	3.67451e-05	0.00428616	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202398	GAGACTTCAGGGCAA[A/G]CTCGATGTTCCTTCT	8924
rs367658561	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28228129	TTTACAAAAAGCTTT[-/A]AAAAAAAAAAAAAAA	8924
rs367662488	snp	A/C	8.54927e-05	0.00653751	intron-variant	HERC2	GRCh38.p7	15:28246694	GACACTTTAGCTTTC[A/C]TCTATCTCCTAAAAT	8924
rs367666269	snp	A/C	4.9708e-05	0.00498513	missense	HERC2	GRCh38.p7	15:28168537	GAGGAGAACGAGGGG[A/C]ACTCCACCGGGGCGA	8924
rs367671774	snp	A/G	0.000121613	0.00779691	intron-variant	HERC2	GRCh38.p7	15:28293055	TTTTAATCTGTCACC[A/G]CTTTTCAGAATGCCA	8924
rs367682083	snp	A/T	3.76882e-05	0.00434082	intron-variant	HERC2	GRCh38.p7	15:28132608	ATCTGACAGCAGCAG[A/T]GAGGAGCATGCAGCC	8924
rs367686298	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28310419	CACTGTACTCCAGCC[C/T]GGGCAATAGAGCAAG	8924
rs367693536	snp	C/T	6.86401e-05	0.00585793	intron-variant	HERC2	GRCh38.p7	15:28191935	CGGTGTGAAAGTGCC[C/T]GCTGCTGTGCCCTAT	8924
rs367693728	in-del	-/CG			intron-variant	HERC2	GRCh38.p7	15:28177180	TCCCTTCTTAGAGAT[-/CG]GAAGGAAAAAAGACA	8924
rs367704254	snp	A/C/T	3.31177e-05	0.00406914	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28186742	ATAGCAATTTCAATA[A/C/T]ACCTGTGATACTAGA	8924
rs367705049	snp	A/C/T	0.000100198	0.00707742	synonymous-codon, missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28255908	TGCGTGTAAGGCTGA[A/C/T]TCCAACCCTCCATCA	8924
rs367709939	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28271192	TGGAGAAAGGCAGAA[C/G]CACCTCTGTGGGAAC	8924
rs367713996	snp	A/G	8.27315e-05	0.00643109	intron-variant	HERC2	GRCh38.p7	15:28175671	CCTGAGAGAAGGCCC[A/G]TGGTGGAGAGTTACA	8924
rs367717965	snp	C/T	0.000505433	0.015889	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202124	TGACCATGGAGTAGG[C/T]GGCATCATCCACGTC	8924
rs367725568	snp	C/T	4.22181e-05	0.00459427	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28215665	GTGCGTGCCCTTCCA[C/T]GACCTTCATGAGCAG	8924
rs367728956	snp	C/T	0.0158469	0.0875917	intron-variant	HERC2	GRCh38.p7	15:28163359	TCACCAGTTTACCCA[C/T]AAACTCAGAGAACAC	8924
rs367731248	snp	C/T			missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214092	CCTTCGGAAGGCCTT[C/T]CCACAAAGCTGTGGG	8924
rs367735305	snp	A/G	0.289683	0.24683	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28215396	GTGAAGCAGATGAGT[A/G]AGTAGTTGCAGGATT	8924
rs367737539	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28290444	CATGTTGGCCAGGCT[A/G]GTCTCAAACTCCTGA	8924
rs367741852	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28192700	GAGGTGTCAAGATGA[C/T]GCACACCACGGATCA	8924
rs367758620	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28142117	TCACCTATGTGTTAT[C/T]TTCTTTGATATTCCT	8924
rs367765229	snp	C/G	0.000153988	0.00877328	missense	HERC2	GRCh38.p7	15:28121394	CTGACGATCGCGTAC[C/G]ATAGTTGCTTGTACT	8924
rs367765685	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28133271	ATATGAATGTCACTA[A/G]TCTATAACATAGTGA	8924
rs367790815	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28159499	ATCTTCAATCACTGA[C/T]ACCCCTTCCTCCAGG	8924
rs367797355	snp	C/T	0.0287284	0.116357	intron-variant	HERC2	GRCh38.p7	15:28236145	GAGACCACCACAGGG[C/T]AGACGGGTAGAGATT	8924
rs367800576	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28259711	TGTAATCCCAGCACT[C/T]TGGGATGCCAAGGAG	8924
rs367818144	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28285982	TCACCAAATATAAAA[C/T]AGATCATTTGAATAG	8924
rs367818214	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28194312	CCTCGTGATCCACCC[A/G]CCTCGCCTCCAAAAG	8924
rs367840349	snp	C/T	1.72142e-05	0.00293374	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28237081	TGAAGAGAGACTCCC[C/T]AGATCTGGTATGGTG	8924
rs367898172	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28288844	CAACAGCAAAACTCC[A/G]TCTCAAAAAAAAAAA	8924
rs367923183	snp	A/G	1.64947e-05	0.00287177	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265882	TCGGCAGTGATGGCC[A/G]CACTGTAAGTGCTCC	8924
rs367923319	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28306521	CATCTGGGATACTGG[C/T]CTGTTTTGTTTTTTT	8924
rs367928013	snp	A/G	0.000174672	0.00934375	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274383	AAAGAGCGAGGCCTC[A/G]GGAAGTGCTCGCAGG	8924
rs367936957	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28217408	AGCCACTTGCCCATC[A/G]ACCGCTAACACACTC	8924
rs367948781	in-del	-/AGAA	0.0640937	0.167149	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174373	ACAGAAAAATCTCAG[-/AGAA]GATACAAATCTGTGT	8924
rs367950391	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28263400	GTTTTCATTCCATGA[A/G]AAACAAAGTCCTGAC	8924
rs367958285	in-del	-/C	0.0372196	0.131242	intron-variant	HERC2	GRCh38.p7	15:28236140	TACGTGAGACCACCA[-/C]AGGGTAGACGGGTAG	8924
rs367968336	snp	A/C	1.65814e-05	0.00287931	missense, downstream-variant-500B, nc-transcript-variant	HERC2	GRCh38.p7	15:28186647	GAACTGCAGCCAAAT[A/C]TTCCTCTTCTGCACG	8924
rs367972505	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28128723	AAACAACACACACTT[A/C]GGATCCTTTCGCTCT	8924
rs367975220	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28244299	AAAATGAAAGAACTC[A/G]ATAACGGGGTGAAGC	8924
rs367976820	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28204614	ACAGAGCGAGACTCC[A/G]TCAAAAAAAAAAAAA	8924
rs368026802	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28117001	GTGCTCCAGCACGTG[G/T]CAAGTTCTCACCCAC	8924
rs368036371	in-del	-/AT	0.0123036	0.0774623	intron-variant	HERC2	GRCh38.p7	15:28219832	CATGTGAAGCTTCAC[-/AT]GTCTTTTAGGAACAG	8924
rs368037084	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28267321	GCACTCATCTCTCTT[C/G]CTTCCTTGAAGTCCT	8924
rs368043104	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28226246	TCCCTAGCAAAAATC[C/T]CAATGGTCTTTTTTG	8924
rs368053486	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28304599	AACTCCTGACCTCAA[-/A]GTGATCCACTCACCT	8924
rs368064138	snp	C/T	0.00835141	0.0640778	intron-variant	HERC2	GRCh38.p7	15:28152966	TTGGAGTTTGAGAAA[C/T]TGAGTTCAAATCAGG	8924
rs368092780	snp	A/C/T	0.000134028	0.00818513	intron-variant	HERC2	GRCh38.p7	15:28175483	CAAGTCAGGATGGCA[A/C/T]GCCACCCCCAGGCCA	8924
rs368100662	snp	A/G	5.12072e-05	0.00505974	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214825	AAGAAAATTTATAAC[A/G]ACAAGCATTAAAAAA	8924
rs368102167	snp	C/T	1.65285e-05	0.00287471	intron-variant	HERC2	GRCh38.p7	15:28292875	TCCAAAGTGCCAAAA[C/T]TCACAAGATTACCTG	8924
rs368128025	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28291797	GTAGTCCCAGCTACT[C/G]GGAAGGCTGAGGCAG	8924
rs368130974	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28282894	CCGAGAACGTCCACT[A/G]CACTCCAGCCTGGGA	8924
rs368136636	snp	C/T	0.0126979	0.078662	intron-variant	HERC2	GRCh38.p7	15:28239272	GCATGCTTGAGGGCA[C/T]TTATGCCTTTAAATG	8924
rs368137638	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28271955	GCAGGCCGCTATTTT[C/T]GTTGTTCTTTTCTGG	8924
rs368139152	multinucleotide-polymorphism	CA/GG			intron-variant	HERC2	GRCh38.p7	15:28227920	GCAAATCCATAGACA[CA/GG]GAAAGCAGATTTGTG	8924
rs368139355	snp	C/T	1.64735e-05	0.00286993	missense	HERC2	GRCh38.p7	15:28135568	AGGCAGTGCTTTCCT[C/T]CAGAGTTCACAGCTA	8924
rs368143278	snp	G/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28310695	CGTGCTCCAGGAGTT[G/T]CAGACTATCTTTAGG	8924
rs368164074	snp	A/G			intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28215169	GGCATGAGCCACTGC[A/G]CCCGGCCTCTCTTTA	8924
rs368166576	in-del	-/G			intron-variant	HERC2	GRCh38.p7	15:28170761	ACACATCTGCCAAAG[-/G]ACTAGAAACATCTAG	8924
rs368191569	snp	A/C	0.000153988	0.00877328	intron-variant	HERC2	GRCh38.p7	15:28124019	TTTCCCCTAGAGCAA[A/C]GATTGCCACTTGAAT	8924
rs368195142	snp	C/T	9.36286e-05	0.00684146	intron-variant	HERC2	GRCh38.p7	15:28152843	CACCTGGAGAGGAAG[C/T]AAGGACATGAATGAG	8924
rs368232924	snp	C/T	0.00199481	0.0315187	intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28315826	ACATGGAATGCCAGA[C/T]GCTGGGGATGCTGGT	8924
rs368249666	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28287872	GGGACTACAGGTGCC[C/T]ACCACCACGCCCAGC	8924
rs368264669	snp	G/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28256723	ACTCAGCCTCCCGAG[G/T]AGCTGGAACTACAGG	8924
rs368301983	in-del	-/TTTTT			intron-variant	HERC2	GRCh38.p7	15:28226876	CTAGTATACACGAAA[-/TTTTT]AAAGAGTCTGAGGAC	8924
rs368309643	snp	A/G	0.000153988	0.00877328	intron-variant	HERC2	GRCh38.p7	15:28274468	CGCACACACGCGTCA[A/G]AGGAGCCCCCCCACT	8924
rs368314210	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28136655	CATGTGCCAAATCAG[G/T]CCCATCATTTCTTTC	8924
rs368320379	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28182991	AAGAATAAAACGGAT[A/G]TGGCCACATGACCAT	8924
rs368323587	snp	C/G	6.66622e-05	0.00577293	intron-variant	HERC2	GRCh38.p7	15:28256011	ACTGAAATAGAAAGT[C/G]TGTGCCAATTTGAGT	8924
rs368325924	snp	C/T	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28294534	CCTCAAATAGCCTAA[C/T]CACAAGGTCTCCCCT	8924
rs368331622	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28117869	AGGACCTCGGCACAT[C/T]GGAGGGCAGGTGGCC	8924
rs368332334	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314344	ACTCTGCTCAGCAGA[C/T]GTCAGCTCGGAACAA	8924
rs368334109	snp	A/G	1.6784e-05	0.00289685	intron-variant	HERC2	GRCh38.p7	15:28135447	AAAACAAAGACAAAT[A/G]GAATGTTGAAATAAT	8924
rs368334259	snp	C/T	3.30022e-05	0.00406202	missense	HERC2	GRCh38.p7	15:28163156	CCCTGCCCCTGTCCC[C/T]GGCCCGGCTGCACAC	8924
rs368337348	snp	A/G	3.44952e-05	0.00415288	intron-variant	HERC2	GRCh38.p7	15:28272193	GTGCCACCTAAACAC[A/G]AAGTTCCATCATGAC	8924
rs368350480	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28277172	AGTGGTTGCCAGCAG[C/T]TAAGGTGGGGAGAGA	8924
rs368367299	snp	C/T	0.000296653	0.0121753	missense	HERC2	GRCh38.p7	15:28146264	AGACGATCCTGTTGA[C/T]GCCGTCCATGACTGT	8924
rs368370323	snp	C/T	4.97038e-05	0.00498492	intron-variant	HERC2	GRCh38.p7	15:28220413	CACCTGGACAGTTTG[C/T]GGGCTGCCTTGGACT	8924
rs368374484	snp	A/G/T			intron-variant	HERC2	GRCh38.p7	15:28242453	CCTCGACAAACTAAC[A/G/T]TTCTCTGGTGGATAG	8924
rs368376058	snp	A/G	1.64732e-05	0.0028699	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28263111	TGGGGTTTTGCAGCC[A/G]TCACTACCACCTCTG	8924
rs368380320	snp	C/G	0.000153988	0.00877328	intron-variant	HERC2	GRCh38.p7	15:28113546	AAAAGGCAGCTGCAG[C/G]GCAGCCCCACCTGGG	8924
rs368385519	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28112800	TGAATGAGTGCTTTA[C/T]GTGTGTTTGAAATCT	8924
rs368389927	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28201719	ATAGCAGTAGCATAG[C/T]AGGCAGAATGAATCT	8924
rs368409663	snp	A/G	9.89854e-05	0.00703441	synonymous-codon	HERC2	GRCh38.p7	15:28116756	AGACTCATCCCTCCC[A/G]TTGGGTGTCACGATC	8924
rs368419232	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28206954	AGTTGGAGGTTGCAG[C/T]GAGCCAATATCACAC	8924
rs368423503	in-del	-/TTT			intron-variant	HERC2	GRCh38.p7	15:28209353	ATTTTTATTTATTTA[-/TTT]TTTTTTTTGAGACAG	8924
rs368435276	snp	C/T	6.67434e-05	0.00577644	intron-variant	HERC2	GRCh38.p7	15:28176386	TTCCCTGCACACACC[C/T]GCACAAGCACACACA	8924
rs368436331	snp	A/T	2.28511e-05	0.0033801	intron-variant	HERC2	GRCh38.p7	15:28269221	CCCGCAAGGGAACAC[A/T]GCAGGCACAGTGCCC	8924
rs368437995	snp	A/G	1.65007e-05	0.00287229	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28246799	GCCGCCAGCTGGTAG[A/G]AGCAATGCTGGCGGC	8924
rs368440552	snp	C/T	0.00023384	0.0108104	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28220619	AGCTCACCAATCACG[C/T]GGCCTAGGCCTGGAG	8924
rs368452993	snp	A/T	1.6727e-05	0.00289193	intron-variant	HERC2	GRCh38.p7	15:28169660	TGAAGGCACGCCTAT[A/T]AGAGGAAAATAAAAT	8924
rs368460220	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28289831	TGCAGTGAGAGGACG[A/C]CACACCTCAGTGAGA	8924
rs368462023	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28309818	CAAATTTGTGTTTGG[C/T]AACTTGTTCTGTAGC	8924
rs368463146	snp	C/T	1.65072e-05	0.00287286	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28192013	CTGCCGTCAATGAGA[C/T]GGGATGCCTGGTTCA	8924
rs368464772	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28152137	GGGCCTCCGAATCGG[A/G]CAGCACCTTGCAGAA	8924
rs368469948	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28134865	TTTTGTAGAAATGGG[A/G]TTTCATCATATTGCC	8924
rs368497314	snp	A/C/T			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28320896	CAAAGACAAAACAAA[A/C/T]AGCTCAACTGAACTA	8924
rs368500253	snp	A/G	0.000150395	0.00867034	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28191242	CTCCAAACGAATCCA[A/G]TGCTTTAGAAAAACA	8924
rs368509178	in-del	-/C			intron-variant	HERC2	GRCh38.p7	15:28264039	AAAAAAAAAAAAAAA[-/C]AAACAAAAACAAAAA	8924
rs368523467	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28129668	GCACAGCCCAGTAAT[A/T]AGTAATAAATAGAAC	8924
rs368533682	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28255287	CTGCAGTGAGCCAAC[A/C]TCAGGTCACTGCATC	8924
rs368537466	snp	C/G/T	4.942e-05	0.00497071	intron-variant	HERC2	GRCh38.p7	15:28141634	TCATCTGGTCGCCTA[C/G/T]AATACACATCAAGTG	8924
rs368545305	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28153519	AGCTGGGTATGGTGG[C/T]CCGTGCCTGTAGTCC	8924
rs368568508	snp	A/G	0.000148907	0.00862735	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28229782	ATAAAGACCCTGCAC[A/G]TTCTGCTTCAACCAC	8924
rs368571271	snp	A/G	0.000133191	0.00815953	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274302	TCACCCCGTCACGAC[A/G]GACCTGAGGAACCTG	8924
rs368577104	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28139325	TTGCTGGTGCTCCCT[C/G]CTGCGCCTCCCTTGC	8924
rs368579697	in-del	-/A	0.189261	0.242509	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321287	CCCCTTACATACCCT[-/A]AAAAAAAAGCCTTAC	8924
rs368608833	in-del	-/CA	0.201418	0.245234	intron-variant	HERC2	GRCh38.p7	15:28279616	GCAAGACCCCATCTC[-/CA]CACACACACACACAC	8924
rs368609644	snp	A/T	0.0232847	0.105357	intron-variant	HERC2	GRCh38.p7	15:28162780	CCTGTAGTCCCAGCT[A/T]CTTGGAAGGCTGAGG	8924
rs368617361	snp	A/G	0.100588	0.200439	intron-variant	HERC2	GRCh38.p7	15:28195678	AGGGTTGGGGTAAGG[A/G]GAAGTAGGGCAGTTA	8924
rs368625231	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28288532	AAGACCAAAACTCCG[A/C]CTCAAAAAAAAAAAA	8924
rs368626459	snp	C/T			intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318666	ACTGTTTATATGTAA[C/T]AACCACATATATATG	8924
rs368627632	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28304130	GAGATTGCGCCATTG[C/T]TTTCCAGCCTGGGCC	8924
rs368633461	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28184843	CTCCAGCCTAGGTGA[C/T]GGAGCAAGACTCCGT	8924
rs368674139	snp	A/G	0.000116191	0.00762116	intron-variant	HERC2	GRCh38.p7	15:28292844	TTATTTAGAAAGGGA[A/G]CGTCAGATCAACCTT	8924
rs368721777	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28284845	ACTTGAACCCGGTGG[A/G]GTTGGAGGTTGCAGT	8924
rs368740750	snp	C/T	6.6084e-05	0.00574784	intron-variant	HERC2	GRCh38.p7	15:28202339	CAGAGGCCAGGAAAA[C/T]GAAGTACCAGGCAAG	8924
rs368747061	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28224773	AGGCCACAAAGTCTT[A/G]AATTTAAACAGACTA	8924
rs368750008	snp	A/G	0.000181212	0.00951698	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28262952	TTTTGGATAACGAAC[A/G]TGTTCCTCTGTTCCA	8924
rs368764420	snp	A/G	0.000153988	0.00877328	intron-variant	HERC2	GRCh38.p7	15:28125202	ACCTCACCTGAATGA[A/G]GTGAATTTAGAATCA	8924
rs368765832	snp	A/G			intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299960	CACGAAGCTGAGGCA[A/G]GAGAATTGCTTGAAC	8924
rs368797389	snp	C/T			intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299583	ATTTTTAAAGAATGA[C/T]ATGGGAAAAAAATCT	8924
rs368801535	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28140980	TGGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT	8924
rs368805162	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28175855	TGGGAAAAACCTTAA[A/T]ACCTTAATACATATT	8924
rs368812828	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28165520	ATGTAGGCCAAACAC[A/G]GTGGCTCATGCCTGT	8924
rs368816548	snp	A/G	0.000437674	0.0147867	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28275003	TTGCCCGCAGGCCGG[A/G]AACTGCAGACGACAC	8924
rs368825903	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28136928	GGAGAAGGAAATGAT[G/T]TTATAAGATCTGAGA	8924
rs368827903	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28125306	GCCCTTCAGCTGGTG[C/T]TGACCTAGTTGTCAA	8924
rs368836833	snp	A/G	0.000153988	0.00877328	intron-variant	HERC2	GRCh38.p7	15:28114811	TATCAACCTTTTAAG[A/G]AGAAAAAGAAAGCCC	8924
rs368850610	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28208925	AGAGAGCAATGATCA[C/T]AGAAAAGGACTTTCC	8924
rs368864433	snp	A/C	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28309498	CTCTTTTGTGATTTC[A/C]ATTTACCTCTCCCTT	8924
rs368866419	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28277241	CCAATTGCAGTGGTG[G/T]TCTCAGAAAATCCAC	8924
rs368888287	snp	A/G	7.05169e-05	0.00593746	synonymous-codon	HERC2	GRCh38.p7	15:28142340	CCACTTGTGCGTCTC[A/G]GCACAGCAAGGCAGA	8924
rs368900932	snp	C/G/T	0.00041469	0.0143937	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229846	AGCGGCTGCCATTTG[C/G/T]CCTAACAAAGGAAAA	8924
rs368908508	snp	A/G	0.000153988	0.00877328	intron-variant	HERC2	GRCh38.p7	15:28146207	GACACAGGTGGGTAG[A/G]TCATGCCCTGCTCAA	8924
rs368926031	snp	A/T	3.29772e-05	0.00406048	intron-variant	HERC2	GRCh38.p7	15:28144639	AATCCACAGCCAGTC[A/T]TCTAACCTTGATCGC	8924
rs368940794	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28241448	GCCACTCCGAAAAAC[A/G]CTATGGCAACCCCTC	8924
rs368968327	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28157529	TTTCTAGTTTATTTG[C/T]GTAGAGGTGTTTGTA	8924
rs368971293	snp	C/T	3.31923e-05	0.0040737	synonymous-codon	HERC2	GRCh38.p7	15:28113579	TCGGCATACCATCGT[C/T]TCCAGTTCGTAGCCG	8924
rs368975169	snp	C/T	0.000153988	0.00877328	intron-variant	HERC2	GRCh38.p7	15:28163075	GGAATCAGACGGCCC[C/T]GCCCTCCCTGAGACT	8924
rs368979634	snp	A/C			intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174354	ATAAGGTTGCTGTAA[A/C]CCTACAGAAAAATCT	8924
rs369008500	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28195763	AGACAGTTGTGATGG[C/T]TGTGCAACACTGTAC	8924
rs369009846	snp	C/T	0.000248315	0.0111398	missense	HERC2	GRCh38.p7	15:28124198	TCCTCAGCGCAATGA[C/T]GGGGATCTCCTGCAG	8924
rs369012761	snp	C/G	5.77151e-05	0.00537161	intron-variant	HERC2	GRCh38.p7	15:28115396	CCTGTTAACAAGACC[C/G]TAGAGGCCCCGCCTG	8924
rs369053697	snp	C/T	8.26726e-05	0.0064288	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28257090	GATTCAGCGTTGCCA[C/T]GGCCACACACTCTTT	8924
rs369055218	snp	G/T	3.33128e-05	0.00408109	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265973	TAGGCTCCTCCAAAG[G/T]CCTTGGGGAGAAAGG	8924
rs369055949	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28295888	AAGGTCCCATGGCTA[C/T]GACAGAGACCATAGG	8924
rs369057401	snp	C/T	5.00404e-05	0.00500177	intron-variant	HERC2	GRCh38.p7	15:28245862	CTTTCCTCAGTAAAA[C/T]TCCTTTAAGACGCCG	8924
rs369063952	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28202641	AGAGGGTCCTGGGAG[A/G]TTTGGGAAGTGCCCT	8924
rs369070867	snp	A/G/T	0.00115472	0.0240006	intron-variant	HERC2	GRCh38.p7	15:28198805	GAGATCCAGTCCATC[A/G/T]TGTACACAGGTGAAA	8924
rs369071614	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28272624	GAGCACATTTACATG[-/A]AAGTTCTAGGATCTT	8924
rs369072680	snp	A/G	0.000248841	0.0111516	intron-variant	HERC2	GRCh38.p7	15:28233839	TCAGAGCCACCCAGT[A/G]AGTCTTCACAAATCT	8924
rs369079040	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28262253	ATCCCTCCAACATCA[C/T]AGTTTTGATGGCCCC	8924
rs369084802	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28245510	TGAGATCATGACACC[A/G]CACTCCAGCCTGGGC	8924
rs369088101	snp	A/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28221256	TTGCAGCAAGTCCTG[A/T]CCCCACAATCCCTCA	8924
rs369102126	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28172353	ACAAAGCTAAAGAAC[C/T]CTTGCAACCTGAGTT	8924
rs369107923	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28148734	ACGGCTGCATGAACG[C/T]GCATTCTAGTAAAAC	8924
rs369119305	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28289406	GCATGCACCTTATAA[A/C]ATTCTCAAATACATG	8924
rs369123124	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28198602	AAGAATGTGCTCACC[C/T]ATAAGTTCCACATGA	8924
rs369134785	snp	C/T	0.000362617	0.0134602	intron-variant	HERC2	GRCh38.p7	15:28144652	TCATCTAACCTTGAT[C/T]GCCATAAGCCCCTTC	8924
rs369146967	snp	A/G	0.000183237	0.00957	synonymous-codon	HERC2	GRCh38.p7	15:28124103	CCCGAGTCCAGTTTC[A/G]TCGAGCGAGCCTTCC	8924
rs369147975	snp	C/T	0.000263648	0.0114784	intron-variant	HERC2	GRCh38.p7	15:28176651	TTCATATCATTCCTA[C/T]CCACCCAGAAGCACA	8924
rs369175176	snp	A/G	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28135105	TTTACAAATGGTGTC[A/G]ATTGTGCGTTCTTTC	8924
rs369187425	snp	A/G	0.000197655	0.00993922	synonymous-codon	HERC2	GRCh38.p7	15:28141552	GCCTTCAATGCCCCC[A/G]AGCTGGCCCCTGTGA	8924
rs369193421	snp	A/C	1.64838e-05	0.00287083	intron-variant	HERC2	GRCh38.p7	15:28191078	AAAAATGGGTAAAGA[A/C]TCAAACAAAGGCGTC	8924
rs369195382	snp	A/G	0.000149379	0.00864101	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28228241	CGCAGTGCCGTCTGC[A/G]TGAGGGCCAGCATGC	8924
rs369201629	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28289401	AAAGTGCATGCACCT[A/T]ATAACATTCTCAAAT	8924
rs369206764	snp	A/G	1.6607e-05	0.00288153	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299526	TGCAAGCTGGCAATG[A/G]TAAACGAGATAAGCT	8924
rs369215770	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28209441	CTCTGCCTCCCGAGT[C/T]CACACCATTCTCCTG	8924
rs369217187	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28149124	CGTATAATCTAGTAA[C/T]ATTACCAAAAAAACA	8924
rs369231643	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28157641	CTTCTCTCTTTTCTT[A/T]TTAGTCTTGCTAGAG	8924
rs369232963	snp	C/T	3.33589e-05	0.00408391	intron-variant	HERC2	GRCh38.p7	15:28274883	AGGGAAGCAGAACAA[C/T]GCGCCACACCAGGGA	8924
rs369235273	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28241688	AGCTGGGCATGGTGG[C/T]GCACGCCTGTAGTCC	8924
rs369242998	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28306278	GGGTTTTTATCATGA[A/G]AGGATGTTGAATTTT	8924
rs369266337	snp	A/G			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28320499	AAATTAGGAAGGGGC[A/G]ATAACACTTCAGTGT	8924
rs369283808	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28171642	AAGCTCACTTTTTTT[-/A]AAAAAAAAAGCAATT	8924
rs369334109	snp	C/T	1.65176e-05	0.00287376	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214665	CCCACCTCTGAGTAA[C/T]GGCACGTCAGAGGAG	8924
rs369344026	snp	A/G	0.00191339	0.0308713	intron-variant	HERC2	GRCh38.p7	15:28218439	CACCCAGACACAAGC[A/G]TGCGGCCCCCAGCGC	8924
rs369357164	snp	C/G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28137194	CAATGAAAAGAAACA[C/G/T]AATTCTCCTGAGAAT	8924
rs369362041	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28187206	TGACTCCATGACCCA[A/G]CTCAACAGTTACCAA	8924
rs369365275	snp	A/T	1.9017e-05	0.00308353	intron-variant	HERC2	GRCh38.p7	15:28115419	CCCGCCTGCCGCCCC[A/T]GGGAGTTACCTCACT	8924
rs369369143	snp	C/T			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28320919	CTGAACTAACTCTTG[C/T]CTCTCCAGAAACACA	8924
rs369369732	snp	C/T	0.000103128	0.00718007	intron-variant	HERC2	GRCh38.p7	15:28144262	CACTGTAAACATCCC[C/T]GGGTTTCACAAGCTA	8924
rs369376814	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28285388	AAGTCAACAAGAGAA[C/T]AATTACAGGAAAATT	8924
rs369393399	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28226792	CTATCAAAGGAAATA[C/G]AATCCAGAGAACAGG	8924
rs369428114	in-del	-/CTTAATAC			intron-variant	HERC2	GRCh38.p7	15:28175858	GAAAAACCTTAATAC[-/CTTAATAC]ATATTTTATGATATT	8924
rs369443373	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28143078	AAACTAAAAAAAAAA[-/A]GCTTATCAAAATTCT	8924
rs369447939	in-del	-/G			intron-variant	HERC2	GRCh38.p7	15:28287739	TTTTTTTTTTTTTTT[-/G]GTTTGAGATGGAGTC	8924
rs369498766	snp	C/G/T	0.00378306	0.0433274	intron-variant	HERC2	GRCh38.p7	15:28238591	CCAGGAAATAACAAG[C/G/T]GTAATCTTACCAAGA	8924
rs369514497	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28115861	CTCCAGGGAGCTACA[A/G]CCCTGCCCAGGAGGT	8924
rs369515209	snp	C/T			utr-variant-3-prime	HERC2	GRCh38.p7	15:28111709	CAGTCTACACAGCAG[C/T]GAGCGCTCTGCTGCC	8924
rs369523422	snp	C/G	0.000153988	0.00877328	intron-variant	HERC2	GRCh38.p7	15:28167681	TAAAGAAGAACGCCT[C/G]TTCACCTCTTTGGTT	8924
rs369531791	snp	A/G	3.32912e-05	0.00407976	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214604	ACCCACCTGAGTGAC[A/G]GCACTGCGCCGCTCT	8924
rs369534225	snp	A/G	0.000307953	0.0124049	synonymous-codon	HERC2	GRCh38.p7	15:28111841	TGAATCGTCGCTGCT[A/G]TCGTCGGCGGCTGGC	8924
rs369538662	snp	C/T	4.96307e-05	0.00498125	intron-variant	HERC2	GRCh38.p7	15:28190952	CAAATGGAACACTAG[C/T]ATAGCTACTTACCTC	8924
rs369539007	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28158122	GTTATAATTTCTGTT[A/C]TTTTACATTTGCTGA	8924
rs369539657	snp	A/C			missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28254403	GAAGACTCACAGATC[A/C]CCGTATTAATAAGGT	8924
rs369542337	snp	A/G	6.01703e-05	0.00548466	intron-variant	HERC2	GRCh38.p7	15:28114841	CATGTGTCGACTCAC[A/G]GCTCATCTCCATCCC	8924
rs369545106	snp	A/C	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28210202	GCAGTGGCGCCATCT[A/C]GGCTCACTGTAAGCT	8924
rs369550096	snp	A/G	4.95127e-05	0.00497533	synonymous-codon	HERC2	GRCh38.p7	15:28144779	TGGGATGCGCAGCTC[A/G]CTGGACCAGTCGGAC	8924
rs369550808	snp	C/T	1.73366e-05	0.00294415	intron-variant	HERC2	GRCh38.p7	15:28191923	AGGCAAAACCATCGG[C/T]GTGAAAGTGCCCGCT	8924
rs369558040	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28248270	ATTCCATAGCACATG[G/T]AACAAATCTGATAAA	8924
rs369585550	snp	C/G	0.000718326	0.018938	missense	HERC2	GRCh38.p7	15:28152818	CACAGAGCTCCAACA[C/G]CATATCTGCCACCTG	8924
rs369586446	snp	A/C	5.62161e-05	0.0053014	intron-variant	HERC2	GRCh38.p7	15:28132094	CAGGGAAAGAATGGG[A/C]AATACCTTCATAGGC	8924
rs369596282	in-del	-/CT	0.00557765	0.0525139	intron-variant	HERC2	GRCh38.p7	15:28161639	TAAAACCTTCAGTTC[-/CT]CAGGTGCACTAGCCA	8924
rs369612942	snp	A/G	3.36016e-05	0.00409874	intron-variant	HERC2	GRCh38.p7	15:28229372	AAGATAAAGAATTTG[A/G]CTTGGGACACTGCCA	8924
rs369621267	snp	C/T	3.33483e-05	0.00408327	intron-variant	HERC2	GRCh38.p7	15:28117010	CACGTGGCAAGTTCT[C/T]ACCCACAAACTTGAC	8924
rs369655304	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28227269	GACGGAGTGAGACTC[C/T]GTCTCAAAAAAAAGT	8924
rs369664002	snp	C/T	1.66299e-05	0.00288352	intron-variant	HERC2	GRCh38.p7	15:28179227	AGGAACCTTTATCTA[C/T]AACAGAATTTTTTTA	8924
rs369702521	snp	A/G	0.000153988	0.00877328	intron-variant	HERC2	GRCh38.p7	15:28176803	AAAACAGAATCACGC[A/G]CAGGCACGGAGAAAG	8924
rs369707470	snp	C/T	3.65417e-05	0.00427428	intron-variant	HERC2	GRCh38.p7	15:28196174	CAATAAGTATTTCAT[C/T]AATATTTGGTGGAAG	8924
rs369709331	snp	C/T	1.65899e-05	0.00288005	intron-variant	HERC2	GRCh38.p7	15:28228418	TGGATACCTAATGAG[C/T]ATTGGCACCTACTGA	8924
rs369711858	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28227617	TTACACATAGTTGTA[C/T]CATATGACCCTGTAA	8924
rs369722172	snp	A/G	1.648e-05	0.0028705	intron-variant	HERC2	GRCh38.p7	15:28265736	CTCACTGGAGCCTTC[A/G]AACAGATAGGACGGC	8924
rs369729288	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28239995	AAAATGTAACATGGA[C/T]TGCATGTTAGATTAA	8924
rs369730745	snp	A/G	3.42173e-05	0.00413612	intron-variant	HERC2	GRCh38.p7	15:28228204	CAAAGGCGCTCAAGC[A/G]GGTGCAGACCTACCA	8924
rs369735391	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28206955	GTTGGAGGTTGCAGC[A/G]AGCCAATATCACACC	8924
rs369737160	snp	A/G/T	3.30416e-05	0.00406447	intron-variant	HERC2	GRCh38.p7	15:28175659	ATCCCCCTTTCCCCT[A/G/T]AGAGAAGGCCCATGG	8924
rs369739861	snp	A/G	4.99131e-05	0.0049954	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28211099	ACCTGCTTTCAGGAT[A/G]TATAGCTTCAACTGC	8924
rs369744290	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28307176	TTCCCAATTTATTGA[C/T]ATATAGCTGTTCATA	8924
rs369747171	snp	A/G	9.95933e-05	0.00705597	intron-variant	HERC2	GRCh38.p7	15:28179105	TTTTTGGTGCCAAGC[A/G]TAATTTAAAAATTTT	8924
rs369750290	snp	C/T			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28320968	ATGAGTGAGTTTCTA[C/T]AGGCCATAATTACTG	8924
rs369771197	snp	A/G			synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28255950	GCCCACCAGAAGATC[A/G]ATCATGAATCGACGA	8924
rs369772498	snp	C/G	3.29717e-05	0.00406015	intron-variant	HERC2	GRCh38.p7	15:28233635	GAATCTGCAGTGTAC[C/G]TAAAGTACACAGATA	8924
rs369782972	snp	C/T	6.63845e-05	0.00576089	missense	HERC2	GRCh38.p7	15:28142240	TATCATGCAATACCT[C/T]ATCAAGAAACAGACG	8924
rs369787802	snp	C/T	0.000313374	0.0125135	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28178940	AGAGCTGTGATCTGC[C/T]GTGGGATGGGCACCG	8924
rs369801815	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28165012	TAATTAAAAATAAAG[C/T]GTTTGCCCTCAAGGT	8924
rs369801891	snp	C/T	1.65051e-05	0.00287267	intron-variant	HERC2	GRCh38.p7	15:28130345	TGGGGCAAGGTGATC[C/T]CACTGACCACCCTGA	8924
rs369820699	snp	A/T	0.000161324	0.00897974	intron-variant	HERC2	GRCh38.p7	15:28299383	TACCAAATAAAAAAC[A/T]CTAGTTAAAGGCCCT	8924
rs369833599	snp	C/G/T	0.00011327	0.00752487	intron-variant	HERC2	GRCh38.p7	15:28113703	AAAGCTCACTTTACA[C/G/T]TTCTGTCTTCAGTGA	8924
rs369859152	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28192376	CTACTAAAACCTCCC[A/C]GGGAACAACAGCAGA	8924
rs369891215	snp	C/T	3.30797e-05	0.00406679	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28299418	TTTTCTAGGAGGGAG[C/T]TCTCCGTTCTGGGTT	8924
rs369908971	snp	A/G	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28307665	TTTCCAAAATTCCTC[A/G]TTATCAATTTTTAGT	8924
rs369931176	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28265310	GAATCAAGAGTGGCC[A/G]AACGTTAAGAAATGT	8924
rs369969805	snp	C/T	0.000287582	0.0119878	intron-variant	HERC2	GRCh38.p7	15:28265574	AGGGAAGCTGCCATG[C/T]GTGTCCTCGTGGGCC	8924
rs369973177	in-del	-/G			intron-variant	HERC2	GRCh38.p7	15:28143066	CTCTTCTAAAAAAAC[-/G]TAAAAAAAAAAAGCT	8924
rs369988486	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28314994	TGTTATAAAAGAGCA[C/T]GTACGGCCCACATAA	8924
rs369992485	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28219911	TAGGATCTAGCTTTC[G/T]TGGTCCACCCCTAAA	8924
rs369997607	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28211058	AGGATCTGCCGCAGT[C/T]TATCCTGGTGGGAGA	8924
rs370007504	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28144942	CTCTCCCAAGCCGAA[C/G]TGCACAGTGACACAA	8924
rs370009597	snp	C/T	0.000165766	0.0091025	missense	HERC2	GRCh38.p7	15:28163129	TGCCGGAAAGCACCG[C/T]GGAGAGCACATCCCT	8924
rs370009672	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28195012	AGTGAGCCAGGATCG[C/T]GCCACTGCACTCCAG	8924
rs370016361	snp	A/G	4.98194e-05	0.00499071	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28248733	AGTCTGAGAAGCAAT[A/G]TTTCTATACAGGAAA	8924
rs370023023	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28253025	CAACCTGCCAGTGCT[C/T]TGCTTTCTCTATGTG	8924
rs370036274	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28231879	GAAACAACACACAAT[A/T]AATCTATAAACCCAC	8924
rs370060661	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28266462	GGAGGTTGCAGTGAG[A/G]TGAGATCGCCCCATT	8924
rs370071411	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28129957	ATTTTTGTATTTTTA[C/G]TAGAGATGATGTTTA	8924
rs370083809	in-del	-/T/TTC/TTT	0.441244	0.168505	intron-variant	HERC2	GRCh38.p7	15:28207146	GTCTGATTCTTTCTC[-/T/TTC/TTT]TTTTCTTGAGATGGA	8924
rs370089551	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28287175	AAACAAATTCTAAAT[A/T]CCTATGGCTCAAATT	8924
rs370107869	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28228522	TTGAAACCCACTGAC[A/G]TTTCTTCTGCATGGA	8924
rs370114769	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28170133	GTCAACTCATCCAAA[C/T]TGATACACAGATTTA	8924
rs370123331	in-del	-/G			intron-variant	HERC2	GRCh38.p7	15:28183570	TGCAACTTGAAAAGA[-/G]TACACAGGACAGTGT	8924
rs370123738	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28199039	GTGGTCCCAGCTACT[C/T]GGGAGACTGAGTTGA	8924
rs370127281	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28205146	ATTTCATGAAAAAGA[A/T]GAGAACAACAACTCT	8924
rs370127897	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28127849	ATACATTAGGATCCA[G/T]GATTCCCACTCAGAT	8924
rs370138558	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28207699	CATCTAGGTACTCAT[C/T]CAGGTACTCACAGCA	8924
rs370151922	snp	C/T	1.65452e-05	0.00287616	intron-variant	HERC2	GRCh38.p7	15:28146379	AAAACATAGCAACCA[C/T]TCCAGATCAGCACCC	8924
rs370153928	snp	A/G	5.07859e-05	0.00503889	intron-variant	HERC2	GRCh38.p7	15:28266001	AGGGAACAAACATGA[A/G]TGCCCTTCTTCTTGG	8924
rs370156748	snp	C/G	1.70481e-05	0.00291955	intron-variant	HERC2	GRCh38.p7	15:28115565	TCAGGACACAAGTGA[C/G]AGAGGACACTTCAAA	8924
rs370163199	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28315098	GCAAATACAACCAAT[G/T]GTTCAGCCAGCACAT	8924
rs370191977	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28155704	AAATTTTCTCCCATT[C/T]TGTAGGTTGCCTGTT	8924
rs370198534	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28243877	ACAGAAAGAATGATT[A/G]AAGAAACAGATGTAA	8924
rs370201193	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28120260	AGACCAGCTCCATCA[A/G]TGTGGTCACATGAGC	8924
rs370207454	in-del	-/AGAA			intron-variant	HERC2	GRCh38.p7	15:28169841	TCCATACTTCGATAA[-/AGAA]GCTATTTTCAGCATA	8924
rs370212036	snp	A/G	0.000102189	0.00714733	intron-variant	HERC2	GRCh38.p7	15:28175493	TGGCACGCCACCCCC[A/G]GGCCACCTGCAGCCT	8924
rs370230277	snp	A/G			intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28300608	AGGTAAATCACTTGA[A/G]GTCAGGAGTTCATGA	8924
rs370254658	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28116124	CGACGGTCCACCACC[A/G]TCAGGCCCTCAATGC	8924
rs370271904	in-del	-/TGCAGGGAGCACGTGCACCGCCCCACG			intron-variant	HERC2	GRCh38.p7	15:28205285	ATCTCCCAGCATGAC[-/TGCAGGGAGCACGTGCACCGCCCCACG]TGCTCTCAAGTTGCT	8924
rs370281932	in-del	-/G			intron-variant	HERC2	GRCh38.p7	15:28166742	CGGGTCCCAGTGACC[-/G]AGTCCACGGGAGTCC	8924
rs370282963	snp	C/T	4.94205e-05	0.0049707	missense	HERC2	GRCh38.p7	15:28141628	GTCCAGTCATCTGGT[C/T]GCCTACAATACACAT	8924
rs370286721	snp	A/G	0.000223446	0.0105676	intron-variant	HERC2	GRCh38.p7	15:28275023	GCAGACGACACACAC[A/G]GAACATACAACCAGT	8924
rs370292009	snp	C/T			intron-variant, utr-variant-5-prime	HERC2, LOC107987422	GRCh38.p7	15:28317771	AACTACGCACACACA[C/T]TGTACCAACTTCAAT	8924
rs370294484	snp	A/G	0.000153988	0.00877328	missense	HERC2	GRCh38.p7	15:28167823	GCGTCCTCAGAGGAA[A/G]CAATCTAGTCCAAGA	8924
rs370313854	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28282693	AATCCCAGCACTTTC[A/G]GAGGCCGAGGCAGGC	8924
rs370318976	snp	C/T	1.64958e-05	0.00287187	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214751	TGTCCCTCGCCCTTT[C/T]GGTCTTGTCCCATGA	8924
rs370319760	in-del	-/G			intron-variant	HERC2	GRCh38.p7	15:28272749	TGAAGAAAAGGTAAA[-/G]AGAGAGAGCCCTGGG	8924
rs370324175	snp	C/T	0.00716266	0.059414	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28312954	CAGGCTCACTTTTTG[C/T]TAGTTACTAAACTGA	8924
rs370326422	snp	C/T	1.7731e-05	0.00297744	synonymous-codon	HERC2	GRCh38.p7	15:28132253	ACGGTGGCCCTGCAG[C/T]GCCTCCACCTTCAGA	8924
rs370333055	snp	A/G	3.30852e-05	0.00406712	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28182509	AGCCTTCTTTCTAAT[A/G]AGGCTAACCAAACGG	8924
rs370336881	snp	A/G	6.5987e-05	0.00574362	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28177031	GGTGTACAGTTCTCC[A/G]CTGGATGTGAGGGCT	8924
rs370346800	snp	A/G	6.58989e-05	0.00573978	missense	HERC2	GRCh38.p7	15:28125083	AGCCACAGGCCACAC[A/G]GTTGACCTTCTTACC	8924
rs370349654	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28275358	ATGGGAGACCAGGCC[A/G]GAGAAGAGCTGGAAG	8924
rs370357911	snp	A/G	0.00020767	0.0101878	intron-variant	HERC2	GRCh38.p7	15:28191275	AAAACCACATTCTCA[A/G]TTAGCAAAATTCAGC	8924
rs370374006	snp	C/T	0.000220197	0.0104905	intron-variant	HERC2	GRCh38.p7	15:28269205	GTAGGACAGACCCTG[C/T]CCCGCAAGGGAACAC	8924
rs370383303	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28294109	TTCTGACACCAAATG[C/T]ATGGACTTTTGCACC	8924
rs370387464	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28267045	GTAGAGAAGTCTTAC[C/T]AGTTGAAGAAATTTC	8924
rs370389324	snp	C/G	1.64732e-05	0.0028699	intron-variant	HERC2	GRCh38.p7	15:28141644	GCCTACAATACACAT[C/G]AAGTGAGCATTTGCC	8924
rs370398827	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28133495	AATCATGCTTTTGGA[A/G]TTCAATCTAAAAATC	8924
rs370408128	snp	C/T	3.30333e-05	0.00406393	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28229507	CCATCCACAAAACAT[C/T]GCATACTGCACAGAT	8924
rs370408923	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28161059	CCTACAGCTTTTTAG[C/T]TCTTCATGAATAGCA	8924
rs370419286	snp	A/G	0.000153988	0.00877328	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28260845	ATGCTGCAGGTTCTG[A/G]CTTGGTCACGCGCAA	8924
rs370439317	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28295880	ACAGCTGCAAGGTCC[C/T]ATGGCTATGACAGAG	8924
rs370441161	snp	A/C/T	0.000379871	0.013777	intron-variant	HERC2	GRCh38.p7	15:28202291	GCCACTGTGAGTCAA[A/C/T]AGCCCTGAAGCGGGA	8924
rs370450514	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28112489	GGTGACCCTGAAAGA[C/T]GGCCACTTTTCTAAC	8924
rs370478704	snp	A/T	0.000153988	0.00877328	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229242	AAAACATTTCGAATG[A/T]TCTGTACAGCCCAAG	8924
rs370495387	snp	C/T	0.000100639	0.00709291	intron-variant	HERC2	GRCh38.p7	15:28176939	CAAGCAACAAAAATG[C/T]GTATAATCACCATTT	8924
rs370500858	snp	A/G	6.73367e-05	0.00580205	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28275001	CTTTGCCCGCAGGCC[A/G]GGAACTGCAGACGAC	8924
rs370502414	snp	A/G	0.000314687	0.0125397	intron-variant	HERC2	GRCh38.p7	15:28144827	AGGAAAGCGCACCCC[A/G]GGGTTAGCTTCACTC	8924
rs370522424	snp	C/T	1.68783e-05	0.00290498	intron-variant	HERC2	GRCh38.p7	15:28124986	CTTGCCCCCGACCCA[C/T]CCAACCTGCCCGGAC	8924
rs370522679	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28139792	TTGGCCGGGCACGGT[A/G]GCTCATGCCTGTAAT	8924
rs370532874	snp	C/T	1.66515e-05	0.00288539	intron-variant	HERC2	GRCh38.p7	15:28112039	TTTATCCAACACCTG[C/T]TGAGCAGAAACATGA	8924
rs370537096	snp	A/G	3.33472e-05	0.0040832	intron-variant	HERC2	GRCh38.p7	15:28146205	GAGACACAGGTGGGT[A/G]GATCATGCCCTGCTC	8924
rs370544367	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28120596	AATGGTCTACTTGTC[A/G]TTTCTTTGATTACTA	8924
rs370549650	snp	A/G	4.99555e-05	0.00499752	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28254474	ATTCGCTTCCTGTTC[A/G]TCAATTTCTTTTTCC	8924
rs370552396	snp	C/T	1.65277e-05	0.00287464	missense	HERC2	GRCh38.p7	15:28113187	AGGACTCCATCACCT[C/T]CCAGAACCACTGGAT	8924
rs370565203	snp	A/G	3.29717e-05	0.00406015	intron-variant	HERC2	GRCh38.p7	15:28191091	GAATCAAACAAAGGC[A/G]TCTTTATTATAGAAG	8924
rs370579166	snp	A/T	1.75786e-05	0.00296462	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28257258	ATGATGACCAAGCAA[A/T]GCTCTAAGAGGAAAC	8924
rs370581395	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28228220	GGTGCAGACCTACCA[A/G]TCAGGCGCAGTGCCG	8924
rs370594237	snp	C/T	9.97258e-05	0.00706066	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28220501	GGGCTGTGCAGCAGC[C/T]GGCAGCTCTGCCAGC	8924
rs370614232	snp	A/G	3.2994e-05	0.00406152	synonymous-codon	HERC2	GRCh38.p7	15:28116768	CCCGTTGGGTGTCAC[A/G]ATCAGCAGGGGCGTG	8924
rs370633840	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28189365	GATTTAATTACTTAG[C/T]TTCTGGTTTGGCTAA	8924
rs370644793	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28298668	GGGCGTGGTGGCGGG[C/T]GCCTGTAGTCCCACC	8924
rs370673493	in-del	-/ATAG			intron-variant	HERC2	GRCh38.p7	15:28270244	TCTTTTTATTTATTT[-/ATAG]ATAGATAGATAGATA	8924
rs370673678	snp	A/G	0.000347939	0.0131852	intron-variant	HERC2	GRCh38.p7	15:28196409	ATTAAACTTAATTCA[A/G]CAGAAAACCATTCGT	8924
rs370685397	snp	C/T	1.64814e-05	0.00287061	missense	HERC2	GRCh38.p7	15:28168448	GACTCAGTCTGTCTT[C/T]GATATCAACAGCCAG	8924
rs370718552	snp	A/G	1.6636e-05	0.00288405	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233498	ACTGACTTAGGCAAC[A/G]TTCTGTGCTTTACTT	8924
rs370720005	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28153294	GGAGGCAGAGGTTGC[A/G]GTGAGCCGAGATCAC	8924
rs370722254	snp	A/G	0.00270085	0.0366488	intron-variant	HERC2	GRCh38.p7	15:28212623	GAGTGTGGCCAATAC[A/G]ACTAACAAATGAAAC	8924
rs370726322	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28293194	CCAGTATAATTTTCA[C/T]AAAGAAACCAATATA	8924
rs370732893	snp	C/T	0.000153988	0.00877328	intron-variant	HERC2	GRCh38.p7	15:28198507	GTGGAGGATAGCCTA[C/T]AGATGTCAATAACAA	8924
rs370736294	snp	A/G/T	0.000121017	0.00777787	intron-variant	HERC2	GRCh38.p7	15:28116654	CAGTCTCAAGCGGCC[A/G/T]AGAAGCTCACCCAGG	8924
rs370737323	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28204597	TGCACTCCAGCCTGG[A/T]GACAGAGCGAGACTC	8924
rs370752460	snp	A/C	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28216860	CTCCCAATGCATACA[A/C]AAACTCACATATGCA	8924
rs370756778	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28145933	AGAAGCTCTGCAGTA[C/T]GCCAACCATGACCTT	8924
rs370759006	snp	C/T	0.000125631	0.00792462	intron-variant	HERC2	GRCh38.p7	15:28117253	ACGAGGAGGAGGCAC[C/T]GTGCATGGGCCCCTC	8924
rs370784039	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28203303	GCTATTTTGTTAAAC[A/G]GAGCATGTGAGGAAG	8924
rs370785670	snp	C/T	0.000181292	0.0095191	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28270773	GGCCATGACAACAAC[C/T]GCCGTTTGTCGCAGA	8924
rs370808155	in-del	-/G			intron-variant	HERC2	GRCh38.p7	15:28187334	CTGGTTTTTTTTTTT[-/G]TTTTTTTGTTTTTTT	8924
rs370818978	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28208044	ATTGGGCTGAGTGCA[A/G]AACAGAACAGCCAAT	8924
rs370832566	snp	C/T	1.64961e-05	0.00287189	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28269381	ATTGGACCAATCACA[C/T]TGGCATAGTATTTCC	8924
rs370836666	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28257968	GAATTACAAGCGTGA[A/G]CCACCGCACCTGGCC	8924
rs370845249	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28156243	ATTGACTTGGCAATG[C/T]GGGCTCTTTTTTGGT	8924
rs370861431	snp	C/T	6.63438e-05	0.00575912	synonymous-codon	HERC2	GRCh38.p7	15:28163262	AGGCTCCGGACCTGC[C/T]GCTTTATTTTGGCTT	8924
rs370915742	snp	A/G	3.34314e-05	0.00408835	synonymous-codon	HERC2	GRCh38.p7	15:28132752	TGCTGTGACACAGGC[A/G]CTGTGGGCTCCGCCA	8924
rs370920798	snp	C/T	0.000299274	0.012229	intron-variant	HERC2	GRCh38.p7	15:28233371	AGGAAAAGACAACTT[C/T]AACAACAAATATTTC	8924
rs370937651	snp	G/T	3.30017e-05	0.00406199	intron-variant	HERC2	GRCh38.p7	15:28143836	TTTTATTCCCCAAGG[G/T]TCACAAATCTAGAAA	8924
rs370942840	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28211660	TGGCTCAACTAACTG[C/G]CAGACAGGTTTATTC	8924
rs370944225	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28284085	CATGAAACAAAGTTC[A/G]TGCTAAGTACTTATG	8924
rs370946687	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28189864	ATGGTTAACTACATT[C/T]AATAATTAAAAAATA	8924
rs370950174	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28304036	CCAGGCCTGGTGGCA[C/G]GCGCCTGTAATGCCA	8924
rs370958552	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28190011	TTTTTTTCTTTCTTT[C/T]TTTTTTTTTTTTTTG	8924
rs370958937	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28140025	GTGAGCCGAGACTGT[A/G]CCACTGCACTCCAGC	8924
rs370967275	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28121622	ACAGGGACAGACGGC[C/T]AGGCAGGTAGTGCCA	8924
rs370972786	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28162199	GCCAGGCATCGTGGC[A/G]CATGCCTGTAATCCC	8924
rs370975575	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28168817	CAGAGTAATGGCAGG[G/T]GAAAAACTGCCAAAC	8924
rs370977252	snp	C/T	9.04302e-05	0.00672361	intron-variant	HERC2	GRCh38.p7	15:28113039	GTCGGCCGACATCAG[C/T]CCAGGGCCGGCAAGC	8924
rs370980764	in-del	-/C			intron-variant	HERC2	GRCh38.p7	15:28199141	ACAAAGTGAGACCCC[-/C]ATCTCAAAAAAAAAA	8924
rs371090595	snp	C/T	3.38369e-05	0.00411307	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28215723	GCCGCATACCTGCGG[C/T]GTGAGAGCGATGCTC	8924
rs371110090	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28172073	GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	8924
rs371111142	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28204481	AAAAATTAGCCAGGC[A/G]TGGTGGCAGGCACCT	8924
rs371118987	snp	A/G	0.00101089	0.0224593	intron-variant	HERC2	GRCh38.p7	15:28274261	AGGCCAGCTGTCTGC[A/G]TGCAGAAGGCAAGAA	8924
rs371120219	snp	C/T	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28294093	CCTCTGTTTACAACA[C/T]TTCTGACACCAAATG	8924
rs371121930	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28150263	TACCGAAGAAACACA[C/T]GCGGCTTCTAACCGA	8924
rs371129181	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28293524	AAAGAAACCAATATA[A/T]CAAATTATTTAAAGC	8924
rs371129792	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28179739	GAAAGAGAGCAACAC[C/T]ATGATCCTAGCTAGG	8924
rs371143360	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316269	GTCATCAAAGTCCTA[C/T]GGCTAAACCCTTTTC	8924
rs371151360	snp	C/T	3.29451e-05	0.00405851	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28263021	AACTTGGCCATCTTT[C/T]GTCAAAGCAATGGAA	8924
rs371182370	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28222580	TATCTAACAGTGGGA[A/G]ACTAACAAACTTTAA	8924
rs371209362	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28265411	TGCCCACACAGGAAC[A/G]GCGGCAGCTGCTAAC	8924
rs371214592	in-del	-/TATAA			intron-variant	HERC2	GRCh38.p7	15:28210828	CCCTCAGTCTTGTCT[-/TATAA]GATGACGATGACAAT	8924
rs371217177	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28131229	ACAATGGCATCGGGA[C/T]GTCCTGCTCCAGCCC	8924
rs371224834	snp	C/T	1.65031e-05	0.00287251	missense, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28292911	TTGCCCCATACCCAG[C/T]TGTCCAGAATTGACT	8924
rs371271684	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28209545	AGATGGAGTTTCACC[A/G]TGTTAGCCAGGATGG	8924
rs371279684	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28310114	GTTTAAAACCAATCT[A/C]GGCAACATAGCAAGA	8924
rs371287419	snp	A/G/T	4.94436e-05	0.0049719	missense, synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28280103	CAGAGAAATACCGCT[A/G/T]CTTTTCCACTTAACT	8924
rs371305671	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28270039	CGATCTTGGCTCACT[A/G]CAACCTCCGCCTCCC	8924
rs371325151	snp	A/C/G/T	0.000330883	0.0128587	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28198387	TATTACCTTTCACAA[A/C/G/T]CCCCACACTCTGATG	8924
rs371346550	snp	A/C			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317406	AGTGACAATATTTAT[A/C]TACAATAAGCTTAAC	8924
rs371353206	snp	C/T	0.000153988	0.00877328	intron-variant	HERC2	GRCh38.p7	15:28143865	AATTGTACTAGAATG[C/T]TCCATACCAAAGCTC	8924
rs371355282	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28284730	GACCAGCCTGGCCAA[C/T]ATGGCAAAACCCCAT	8924
rs371359891	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28209325	ATAACAACTATTTAC[A/T]TATCATTTATTTTAT	8924
rs371360766	snp	C/T	0.000127628	0.00798736	intron-variant	HERC2	GRCh38.p7	15:28274463	CTGGGCGCACACACG[C/T]GTCAGAGGAGCCCCC	8924
rs371375104	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28118315	CCTCTCCTCCATGAC[A/G]ACACCCACTAGTAGA	8924
rs371376960	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28157542	TGTGTAGAGGTGTTT[A/G]TAGTATTCTCTGATG	8924
rs371395759	snp	C/T	0.000153988	0.00877328	synonymous-codon	HERC2	GRCh38.p7	15:28163154	ATCCCTGCCCCTGTC[C/T]CCGGCCCGGCTGCAC	8924
rs371406398	snp	A/G	0.00078406	0.0197842	stop-gained, downstream-variant-500B	HERC2	GRCh38.p7	15:28174431	GGTCTCTTGCAGTCT[A/G]GAAGAGGACGGGCTC	8924
rs371415400	snp	C/T	3.36496e-05	0.00410167	intron-variant	HERC2	GRCh38.p7	15:28112067	TGAAGTGATTAGAAA[C/T]TGAGTACGGCTGCAG	8924
rs371465740	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28254541	TCATAAAAAGAAATT[C/G]TTTACAAGTGATCTC	8924
rs371475859	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28193514	TGAAAGAAGAGTCCC[A/C]CCAAAAAGATAGAAA	8924
rs371488415	snp	A/G	8.25362e-05	0.00642349	intron-variant	HERC2	GRCh38.p7	15:28130143	AGGCCTCAGTCCTGC[A/G]GCACTGAGCCCCTAC	8924
rs371488509	snp	A/G	8.95391e-05	0.00669041	intron-variant	HERC2	GRCh38.p7	15:28163058	CCCAACATGGAGGAG[A/G]TGGAATCAGACGGCC	8924
rs371500499	snp	C/G/T	0.000100154	0.00707588	intron-variant	HERC2	GRCh38.p7	15:28113565	GCCCCACCTGGGGGT[C/G/T]GGCATACCATCGTCT	8924
rs371506388	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28142141	TATTCCTTGGCAAGC[A/G]AAATTTTTCTGTGTC	8924
rs371520119	snp	C/T	1.6834e-05	0.00290116	intron-variant	HERC2	GRCh38.p7	15:28178854	CAGGAGCAAAGGCCG[C/T]CCCGCACAGGCCTCC	8924
rs371551387	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28271562	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	8924
rs371555107	in-del	-/CAAAAA			intron-variant	HERC2	GRCh38.p7	15:28225273	AGACAAAAACAAAAA[-/CAAAAA]AATACAAAGCAGAAA	8924
rs371555393	snp	A/C/T	4.96498e-05	0.00498225	synonymous-codon, missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229788	ACCCTGCACATTCTG[A/C/T]TTCAACCACTTGTAT	8924
rs371556289	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28288644	TAAGGTCAGGAGTTC[A/G]AGGCGAGCCTGGCAA	8924
rs371561750	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28304549	ATTTTTATATTTTTA[A/G]TAGAGACAGGGTATC	8924
rs371566980	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28248996	CCTATGGAGCTGCGC[A/G]CAGTGGTCCAAACTG	8924
rs371607163	snp	C/T	1.6651e-05	0.00288535	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28202366	CAAGCTGGATGCATT[C/T]CCGGAAGCACCAGTG	8924
rs371614775	snp	C/T	0.000307953	0.0124049	intron-variant	HERC2	GRCh38.p7	15:28177410	TGAGACTAAAAAAAG[C/T]ACCCTTACATTCTGC	8924
rs371618943	in-del	-/AT			intron-variant	HERC2	GRCh38.p7	15:28220217	GGGGCGGGTGCACAC[-/AT]GAGAGTAAAATGCAG	8924
rs371625368	snp	G/T	9.90769e-05	0.00703766	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233179	CTCGAATTATCTTTT[G/T]AGCTATCCTCCTCCA	8924
rs371633379	snp	A/G	0.000132762	0.00814639	intron-variant	HERC2	GRCh38.p7	15:28292846	ATTTAGAAAGGGAGC[A/G]TCAGATCAACCTTTC	8924
rs371646839	snp	A/G	4.96956e-05	0.00498451	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28198626	CACATGAATGTACCT[A/G]ACCCAGTAGGTGCCC	8924
rs371648894	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28293967	ATCACAGAAGGCTGT[A/G]ACTAAATGTCTAACA	8924
rs371659985	snp	C/T	1.68579e-05	0.00290321	intron-variant	HERC2	GRCh38.p7	15:28256071	CCATGCCCTCTCCTG[C/T]TCCTTCCCCAGGCCC	8924
rs371660205	snp	A/G	6.60033e-05	0.00574433	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28228288	GTCGAGGTTGTTTGC[A/G]CCGTGCTGCAGGGTG	8924
rs371670194	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28242135	ATTCAGACACAGAAA[A/G]TAGAATGGTAGTTGC	8924
rs371670305	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28217412	ACTTGCCCATCGACC[A/G]CTAACACACTCACTC	8924
rs371671987	in-del	-/A	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28175285	TCACGTGGACTTCAG[-/A]GTGGGAACGCCTCTT	8924
rs371672757	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28157842	GATGTTAGGGTGTCA[A/T]TTTTAGATCTTTCCT	8924
rs371675001	snp	C/T	3.31483e-05	0.004071	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233781	TACAGTACCTTTCTA[C/T]TTGACACAAAAAGTC	8924
rs371676185	snp	A/G	3.33189e-05	0.00408146	missense	HERC2	GRCh38.p7	15:28124110	CCAGTTTCGTCGAGC[A/G]AGCCTTCCAGGTCGA	8924
rs371681072	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28247553	CCTGCCTCAGCCTCC[A/G]GAGTAGCTGGGATTA	8924
rs371682256	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28276815	CAATGACCCCTTTGG[A/G]AAAATGTTAAGGGGA	8924
rs371683509	snp	C/G	5.45152e-05	0.0052206	intron-variant	HERC2	GRCh38.p7	15:28248501	GTCGAAAAGCCTAAA[C/G]TAACGAGCCCCGATC	8924
rs371684164	snp	A/G	0.00247377	0.0350823	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28202510	GCGGATGTGCTGCAC[A/G]GCGACAGGCGTGGTG	8924
rs371695472	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28201017	CACAAGTGGGGCTAG[G/T]AGAAAACAGCCATCC	8924
rs371697885	snp	C/T	1.65233e-05	0.00287426	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28192061	AGGCTCTTCACCATG[C/T]GGGACCAGCTGTCCA	8924
rs371701003	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28119162	GCACTTTGGGAGGCC[A/G]AGGCGAGTGGATCAC	8924
rs371718759	in-del	-/ACCT	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28181715	TGCATCATTTCTTAC[-/ACCT]ATTCTTTTCAAAATA	8924
rs371721852	snp	G/T			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28315099	CAAATACAACCAATT[G/T]TTCAGCCAGCACATT	8924
rs371751432	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28185178	AAAGCCAAGATCACA[A/G]AGCCCTAGAATAACC	8924
rs371753501	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28292130	GCTACTCGGGAGGAT[A/G]AGGCAGGAGAATCAC	8924
rs371771613	snp	A/G	8.23649e-05	0.00641683	missense	HERC2	GRCh38.p7	15:28114642	AGCCGCACGTACTCC[A/G]CGCGGTTGTCCAGGG	8924
rs371780167	snp	A/G	1.65776e-05	0.00287898	missense	HERC2	GRCh38.p7	15:28169496	TACCTGGCATACATG[A/G]TTTGCAATGCTGTAA	8924
rs371789163	snp	A/G	6.84474e-05	0.0058497	intron-variant	HERC2	GRCh38.p7	15:28191936	GGTGTGAAAGTGCCC[A/G]CTGCTGTGCCCTATT	8924
rs371797618	snp	G/T	3.36536e-05	0.00410191	intron-variant	HERC2	GRCh38.p7	15:28116973	GCTCAGGCGACCACT[G/T]CCGGGGACACAGGTG	8924
rs371804343	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28285165	AAAGCTGCCAAGATA[C/T]AGAATTCAACATCAC	8924
rs371818304	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299733	TAGTATAAATACTAT[G/T]CTACCTCTTATGTAA	8924
rs371826254	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28140531	AGTGGCAATCTTTTT[C/T]TGGGGGCGGAGACAG	8924
rs371831757	in-del	-/AAAT	0.00279162	0.0372561	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111329	GAGTAAAATTAATTG[-/AAAT]ATTTATAATACGATT	8924
rs371837932	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28291811	TCGGAAGGCTGAGGC[A/G]GGAGAATGGCATGAA	8924
rs371843516	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28310725	GCACTCAAGGGAATA[C/T]GACATTTGACCCGTG	8924
rs371858439	snp	C/T	0.000167059	0.00913793	intron-variant	HERC2	GRCh38.p7	15:28113287	GCTGCCACACACCTG[C/T]GGGAGGATGTCTGTC	8924
rs371864909	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28271975	TTCTTTTCTGGTATT[G/T]ATTTAAAAGTGAATG	8924
rs371870709	snp	A/C	1.70974e-05	0.00292376	intron-variant	HERC2	GRCh38.p7	15:28246700	TTAGCTTTCATCTAT[A/C]TCCTAAAATAAACAT	8924
rs371871549	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28162716	AACATGGTAAAACCC[C/T]GACTCTACTAAAAAT	8924
rs371875139	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28164500	TGAAACATATTAACA[A/T]GAATATCTTTAGTCT	8924
rs371882633	snp	C/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28222668	GTTGCTGCAGGCTGG[C/T]CCTCGGCTGGAGTCT	8924
rs371885632	snp	C/T	5.07524e-05	0.00503722	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28211048	TGGCTGAGACAGGAT[C/T]TGCCGCAGTTTATCC	8924
rs371898815	snp	C/G	5.2288e-05	0.00511285	intron-variant	HERC2	GRCh38.p7	15:28163081	AGACGGCCCCGCCCT[C/G]CCTGAGACTCACCTG	8924
rs371898983	snp	C/T	4.96561e-05	0.00498253	missense	HERC2	GRCh38.p7	15:28113628	GGAACAGGCACAACG[C/T]GGGCCATTCCTTCCC	8924
rs371952258	snp	A/G			intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318369	CGGTGGCTCACGCCT[A/G]TAATCCCAGCACTTC	8924
rs371960392	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28152130	AACTTATGGGCCTCC[A/G]AATCGGGCAGCACCT	8924
rs371994529	snp	C/T	0.084889	0.187719	intron-variant	HERC2	GRCh38.p7	15:28272870	TGCCGCAGACGGGAA[C/T]GCTTTGGGGAAGCGC	8924
rs372043440	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28145716	AAAGGTGCATACACA[C/T]ACCCCTGCACTGCCA	8924
rs372048055	snp	C/T	0.000326993	0.0127824	intron-variant	HERC2	GRCh38.p7	15:28152873	GGGGGCCAACAGCCC[C/T]ACACCTGGTCACCTG	8924
rs372052305	snp	C/T			intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314627	TTTGGGAGGCCAAGG[C/T]GGGCGGATCATGAGG	8924
rs372058356	snp	C/T	8.30944e-05	0.00644518	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299531	GCTGGCAATGATAAA[C/T]GAGATAAGCTTACAG	8924
rs372097994	snp	A/G	0.000107995	0.00734751	intron-variant	HERC2	GRCh38.p7	15:28124018	GTTTCCCCTAGAGCA[A/G]AGATTGCCACTTGAA	8924
rs372112231	snp	A/G			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28320902	CAAAACAAACAGCTC[A/G]ACTGAACTAACTCTT	8924
rs372133360	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28263927	ATCCAGCTGAGGCAT[A/G]AGAATTGCTTGACCC	8924
rs372150072	snp	A/G	1.65004e-05	0.00287227	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28186711	ACAATCGATTCCTGA[A/G]CTCCTGCACTGCTTT	8924
rs372152404	snp	A/G	0.00011113	0.00745335	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28202167	CTCGTCAGAATACTC[A/G]TCGGACACCGTGTCT	8924
rs372154743	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28209492	GGGACTACAGGCACC[C/T]GCCACCACGCCCAGC	8924
rs372157643	in-del	-/G			intron-variant	HERC2	GRCh38.p7	15:28228145	AAAAAAAAAAAAAAA[-/G]AAAAGAAAAGAAAAG	8924
rs372161177	snp	C/T	1.64735e-05	0.00286993	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28237010	GTGCTCATTGCCAAA[C/T]ACGAAGCGTGTAATC	8924
rs372164018	snp	C/G	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28270500	AGGTTGGGTCGCCAG[C/G]CCTGTGCGCCTCAGC	8924
rs372169108	snp	A/G	1.64768e-05	0.00287021	missense	HERC2	GRCh38.p7	15:28135619	TGAATGGATTCAAGC[A/G]ATGTTGGGGTGGACA	8924
rs372174613	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28129828	TGTCACCAGGCTGGA[C/G]TGCAATGGCACGATC	8924
rs372237272	snp	C/T	5.77818e-05	0.00537471	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274410	CAGGGCGTCCAGGGA[C/T]TCCTGCAACAGCTCA	8924
rs372264233	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28167217	GGCAGAGACCCTTAA[C/T]CAAGTGATAAGCTAT	8924
rs372267451	snp	A/G	3.37319e-05	0.00410668	intron-variant	HERC2	GRCh38.p7	15:28238106	TCACTCAAGGCATAC[A/G]GCCTCACCTCCAAAT	8924
rs372281156	snp	C/T	0.000652758	0.0180542	intron-variant	HERC2	GRCh38.p7	15:28186776	AAAAACCATGATCTA[C/T]AGACTCTGTAGAATC	8924
rs372293459	snp	A/C	0.000153988	0.00877328	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274314	GACGGACCTGAGGAA[A/C]CTGGTCGCTCTCTCC	8924
rs372295687	snp	A/G	0.000153988	0.00877328	intron-variant	HERC2	GRCh38.p7	15:28125224	TTAGAATCAGAACCT[A/G]TATACTAGGGCCAAC	8924
rs372311463	snp	C/G	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28240214	ACAAGGTCAGGAGAT[C/G]GAGACCATCCTGGCT	8924
rs372326425	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28285000	TGAGAACTTGGTCAA[A/T]CCACCATTAAGACGC	8924
rs372342093	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28270244	CTCTTTTTATTTATT[G/T]ATAGATAGATAGATA	8924
rs372358029	snp	A/G	5.64685e-05	0.00531329	intron-variant	HERC2	GRCh38.p7	15:28212632	CAATACGACTAACAA[A/G]TGAAACGTTCTGAAA	8924
rs372361554	snp	C/T	0.000168856	0.00918692	synonymous-codon	HERC2	GRCh38.p7	15:28168563	GGCGATCATGGCGGC[C/T]GGCATCAGGGCCCCG	8924
rs372376197	snp	A/G	3.39225e-05	0.00411826	intron-variant	HERC2	GRCh38.p7	15:28299393	AAAACACTAGTTAAA[A/G]GCCCTTACCTTTTCT	8924
rs372392061	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28141094	AATACAAAAGTTAGC[C/G]AGGTGTGGTGGCGGG	8924
rs372405120	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28252465	AGCACCTCTGGAAAA[C/T]GCTCACTTTAAAACT	8924
rs372412891	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28133995	TCCATATACATTTTA[C/T]GCTCCGCTTATCAAT	8924
rs372420106	snp	A/G	0.0229705	0.104679	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174380	AATCTCAGAGAAGAT[A/G]CAAATCTGTGTTACC	8924
rs372423168	snp	A/G	8.23716e-05	0.00641709	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265694	CAGTCCTTTAAGCCC[A/G]GCTACCAGCATCGGA	8924
rs372436249	snp	A/G	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28147744	TTATTGTTAGAAAAA[A/G]GGAATAGGCTGGGTA	8924
rs372441542	in-del	-/G			intron-variant	HERC2	GRCh38.p7	15:28272690	TGAAAGAAAAAAAAA[-/G]AAGAACAGTTCCCAG	8924
rs372441652	snp	C/G	3.31115e-05	0.00406874	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28192089	CCAGCAGCATGCCTG[C/G]CTGGCTGCTGTGGCA	8924
rs372474094	snp	A/G			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28320953	ACAAGACCTCATAAA[A/G]TGAGTGAGTTTCTAT	8924
rs372498859	snp	C/T	0.000215031	0.0103667	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28233743	GGGGGGAAACATGAT[C/T]GGTGTGGTCAAATGG	8924
rs372508650	in-del	-/CATTTC			intron-variant	HERC2	GRCh38.p7	15:28283295	AAACAAAAGACAAAA[-/CATTTC]AAAAGCCACTAAACA	8924
rs372510625	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28155119	TTTATGGCTGCATAG[C/T]ATTCCATGGTGTATA	8924
rs372545906	snp	C/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28260509	TTCACACTGCAAGTC[C/G]TGGCCAGGGCAATCA	8924
rs372548775	snp	C/G	1.64887e-05	0.00287125	intron-variant	HERC2	GRCh38.p7	15:28144636	AACAATCCACAGCCA[C/G]TCATCTAACCTTGAT	8924
rs372563718	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28208788	TTCAAAGGCTGCCCG[C/T]CCAGTGCTCAGCTGC	8924
rs372574331	snp	A/T	0.000380546	0.0137887	intron-variant	HERC2	GRCh38.p7	15:28198523	AGATGTCAATAACAA[A/T]TCATTATAATCAATA	8924
rs372578918	snp	A/G	4.94319e-05	0.00497127	missense	HERC2	GRCh38.p7	15:28141445	ACCTTCCCATCAGCC[A/G]TCACAGCAAAGAGGG	8924
rs372583299	snp	C/T	0.000210231	0.0102504	intron-variant	HERC2	GRCh38.p7	15:28114833	AGAAAGCCCATGTGT[C/T]GACTCACGGCTCATC	8924
rs372583563	snp	A/T	0.000198771	0.00996724	intron-variant	HERC2	GRCh38.p7	15:28175680	AGGCCCATGGTGGAG[A/T]GTTACAATACGGTTA	8924
rs372583657	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28230824	ACTCTGCTGCTGTAG[C/G]ACAAAAAGTAACCAC	8924
rs372593621	snp	A/G	1.67975e-05	0.00289802	intron-variant	HERC2	GRCh38.p7	15:28142963	AAACTCTAAGAAACA[A/G]CAGAACAGTATTCTA	8924
rs372604046	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28243562	CCAGATAGAAAAATG[C/T]GCACAAAACTTGAAT	8924
rs372605299	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28157062	CGTTTATTGATTTGC[A/G]TATGTTGAATCAGCC	8924
rs372606458	snp	A/G/T	0.000178135	0.00943608	intron-variant	HERC2	GRCh38.p7	15:28117193	CGTGAGGCCGCTGCC[A/G/T]CAGCAGGAAGCACAC	8924
rs372618851	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28117873	CCTCGGCACATCGGA[A/G]GGCAGGTGGCCGAGG	8924
rs372620320	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28143067	TCTTCTAAAAAAACT[-/A]AAAAAAAAAAAGCTT	8924
rs372640210	snp	C/T	8.2426e-05	0.0064192	synonymous-codon	HERC2	GRCh38.p7	15:28121424	TACTTTCCGGAAAGC[C/T]GCCTCCTAAAACACA	8924
rs372640455	in-del	-/C			intron-variant	HERC2	GRCh38.p7	15:28274749	ATGTGAAAAGCCAAA[-/C]CAGCCTCTGCAGCCT	8924
rs372662914	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28289407	CATGCACCTTATAAC[A/G]TTCTCAAATACATGA	8924
rs372733603	snp	A/G	3.29837e-05	0.00406088	intron-variant	HERC2	GRCh38.p7	15:28167646	CTGTGTACATTTAAG[A/G]TTATTTCACAATACA	8924
rs372777009	snp	A/G	9.88745e-05	0.00703047	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28246825	GCGGCCACAGGCAGT[A/G]TATCTCCAATGTGCG	8924
rs372777406	snp	G/T	0.000153988	0.00877328	intron-variant	HERC2	GRCh38.p7	15:28220678	AGATCAGTTAGGAGG[G/T]TGCGTAACCTGCCCT	8924
rs372781480	snp	A/C	0.000153988	0.00877328	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214098	GAAGGCCTTCCCACA[A/C]AGCTGTGGGTGATGG	8924
rs372793125	snp	G/T	3.36428e-05	0.00410125	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229339	TTAAACAATCAGTAA[G/T]AGGTTCCCTTTCAAA	8924
rs372800762	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28206592	TAATCCCTGCACTTC[A/G]GGAGGCCAAGGCGGG	8924
rs372809346	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28224979	AAAACTTCTGTGCTG[C/T]GCCAAAAGCAGGGAT	8924
rs372819431	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28134870	TAGAAATGGGGTTTC[A/G]TCATATTGCCCAGGC	8924
rs372831622	snp	A/G			intron-variant, downstream-variant-500B	HERC2, LOC107987422	GRCh38.p7	15:28312375	GTGGTGGCCCACGCC[A/G]TAATCCCAGAGCTTT	8924
rs372842046	snp	C/T	0.000153988	0.00877328	intron-variant	HERC2	GRCh38.p7	15:28141722	ACTGCTTGTTTCTAA[C/T]ATAATAACCTGTTCA	8924
rs372855047	snp	A/G	6.60404e-05	0.00574594	missense	HERC2	GRCh38.p7	15:28142255	CATCAAGAAACAGAC[A/G]GGGCAACGGTGTTCT	8924
rs372866109	snp	G/T	1.8124e-05	0.00301026	intron-variant	HERC2	GRCh38.p7	15:28132872	GAAACACATTTTTAT[G/T]CTTAAACATTTTTCA	8924
rs372876251	snp	A/G	4.95348e-05	0.00497644	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214671	TCTGAGTAATGGCAC[A/G]TCAGAGGAGCAGGTA	8924
rs372877584	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28163005	CAGCACAAGATCACC[A/G]GTGATCCATAGCAGC	8924
rs372902013	snp	C/G	8.80972e-05	0.00663633	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28218528	CCACTAACATTCGCA[C/G]CAGTCCGCATAAAGT	8924
rs372909169	snp	A/G	3.69324e-05	0.00429707	intron-variant	HERC2	GRCh38.p7	15:28115422	GCCTGCCGCCCCAGG[A/G]AGTTACCTCACTGAG	8924
rs372917602	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28149142	TACCAAAAAAACACA[C/T]GCGACTTCTAACCGA	8924
rs372929410	in-del	-/C			intron-variant	HERC2	GRCh38.p7	15:28136125	CCACAAGGGAAAAAA[-/C]ACCTTTTTTTTTTTT	8924
rs372974834	snp	C/T	3.37775e-05	0.00410945	intron-variant, utr-variant-5-prime, upstream-variant-2KB	HERC2	GRCh38.p7	15:28213691	GGTGCTCGGTTCTAG[C/T]GTAAAGTCAATTTCC	8924
rs372988719	snp	C/T	0.000153988	0.00877327	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214316	TGCACCGCTCTTCAC[C/T]AGGGCACAGGGAAAG	8924
rs372997296	snp	C/T	0.000115486	0.007598	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28248689	AGACATGATGAAATC[C/T]GACGGGCAACATCTT	8924
rs373050129	snp	C/T	0.000217085	0.0104161	intron-variant	HERC2	GRCh38.p7	15:28268455	CCCTACAGGAATAAG[C/T]GATACATACACAGTG	8924
rs373057870	snp	A/G	6.62998e-05	0.00575721	intron-variant	HERC2	GRCh38.p7	15:28176811	ATCACGCACAGGCAC[A/G]GAGAAAGCAATGGAT	8924
rs373062724	snp	C/T	0.000761577	0.0194989	intron-variant	HERC2	GRCh38.p7	15:28254568	TCTCATTACCAGGTG[C/T]GAAGACACACAGGCT	8924
rs373068460	snp	A/C	1.66255e-05	0.00288314	intron-variant	HERC2	GRCh38.p7	15:28228426	TAATGAGCATTGGCA[A/C]CTACTGACATTTCTT	8924
rs373072225	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28295408	ATGGTCTGAAAACAG[A/G]GAAAGTATTTTACTT	8924
rs373088790	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28115316	AGCCAACAGCCTCTG[C/T]GTCACCTGGGCACTG	8924
rs373090493	snp	C/T	0.0314385	0.121371	intron-variant	HERC2	GRCh38.p7	15:28206689	ATACAAAACATTAGC[C/T]GGGCATGGTGGCGGG	8924
rs373128205	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28220875	CTTCCATGGCTCCCA[C/G]CAGACCTCAGTTAGG	8924
rs373164909	snp	A/C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28292628	TAAGACCAGCCTGGG[A/C/T]AACACAGTGAGATTC	8924
rs373175587	snp	A/T	0.00398169	0.0444409	missense	HERC2	GRCh38.p7	15:28130164	GAGCCCCTACCTACC[A/T]TCCTCTGTGCAGCAC	8924
rs373175870	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28172270	GATTTTATAAAAACT[C/G]ACAAGCTCATTTTAA	8924
rs373185646	snp	G/T	6.61441e-05	0.00575045	missense, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28299419	TTTCTAGGAGGGAGC[G/T]CTCCGTTCTGGGTTG	8924
rs373201950	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28179479	TCTGTGGTGATGCTG[C/G]TGTCAACAAGCCTCT	8924
rs373222485	snp	C/T	4.97211e-05	0.00498579	synonymous-codon	HERC2	GRCh38.p7	15:28117068	GCTGTCGGGACCAAA[C/T]GAGCTCATCTTAGCA	8924
rs373231248	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28152492	TTTACTTTGTGTGAC[C/T]TTCTATATCATGATT	8924
rs373236994	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28307446	TTTCTAGTTCTTTAA[C/G]ATGTATCATTAGGTT	8924
rs373246500	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28280634	AGTTGGCCGGGCACA[G/T]TGGCTCACACCTGGA	8924
rs373254209	in-del	-/C			intron-variant	HERC2	GRCh38.p7	15:28251251	AGTTCAAGACCACCC[-/C]AGCCAACATGGGGAA	8924
rs373262181	snp	A/G	0.0103295	0.0711199	intron-variant	HERC2	GRCh38.p7	15:28222628	AGACAGCTAACAGCT[A/G]GCCCGAGATACAACC	8924
rs373265886	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28158206	GCTGAGAAGAATGTA[C/T]ATTCTATTGATTTGG	8924
rs373275902	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28188715	AGTGAAACATGACTG[A/G]CAAAATGTTGATAAA	8924
rs373291791	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28138157	TTAAGGAAAGACGCC[A/G]TCTTCATAACATAAA	8924
rs373338385	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28267135	TTTCTTGAAAATCTA[C/T]AGAAGCCAGGCCTCT	8924
rs373346726	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28308235	AATGTCTTTCATCAG[C/T]GTTTTAGAGTTTTCA	8924
rs373351931	snp	C/T	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28174573	CCTGTTAACCGTGGT[C/T]GTGCCATTGCCCTGC	8924
rs373353004	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28289403	AGTGCATGCACCTTA[C/T]AACATTCTCAAATAC	8924
rs373378644	snp	A/C/G	4.95842e-05	0.00497896	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28257118	TTTCTCCTGGGGCGG[A/C/G]GGCCAGTCCGCGGAA	8924
rs373380855	snp	A/G	1.66885e-05	0.00288859	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214795	TGCAACAAATGCACA[A/G]CTAAGATCTGATAAA	8924
rs373381932	snp	G/T	0.000494421	0.0157152	intron-variant	HERC2	GRCh38.p7	15:28191089	AAGAATCAAACAAAG[G/T]CGTCTTTATTATAGA	8924
rs373382807	snp	A/G	1.6793e-05	0.00289763	intron-variant	HERC2	GRCh38.p7	15:28265988	GCCTTGGGGAGAAAG[A/G]GAACAAACATGAATG	8924
rs373384975	snp	C/T	1.64789e-05	0.0028704	intron-variant	HERC2	GRCh38.p7	15:28191126	TTCTTTTTAGGTAAA[C/T]TAACTGAATTACCTG	8924
rs373394433	snp	C/T	4.95315e-05	0.00497627	intron-variant	HERC2	GRCh38.p7	15:28201427	GAATGAAAAACGGAT[C/T]GAGGCTCCAGCTTAA	8924
rs373396365	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28173267	ATACACAAACTTGTA[C/T]GGAAATGTCCATTAG	8924
rs373399401	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28130830	TGGGACCCAGCACAG[C/G]GCACCAGAAATGGGA	8924
rs373402686	snp	C/T	5.75506e-05	0.00536395	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28196345	AGGAAACATCTGACA[C/T]CCATCACACCTATTT	8924
rs373409681	snp	A/C/G	0.000197835	0.00994388	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28228333	CACCAGGAGGAAGCG[A/C/G]GCTTGCGGGATGGTC	8924
rs373416507	snp	C/G/T	8.2761e-05	0.00643233	intron-variant	HERC2	GRCh38.p7	15:28167840	AATCTAGTCCAAGAG[C/G/T]GCACAGTAGGGGAAG	8924
rs373418507	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28216280	TTAAATATCTCCACA[A/G]TCTTGCTTATATTTA	8924
rs373419625	snp	C/T	5.04325e-05	0.00502132	intron-variant	HERC2	GRCh38.p7	15:28141898	TTATCTCAAACAAAA[C/T]AGATAAATACTAAGG	8924
rs373422807	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28195926	CAATTCCACATGCCA[C/T]GCAACTAAACACTTA	8924
rs373425948	in-del	-/TGTG			intron-variant	HERC2	GRCh38.p7	15:28298006	ACGTCTGTCAGTTAT[-/TGTG]TGTGTGTGTGTGTGT	8924
rs373431974	snp	A/G	0.000320353	0.012652	intron-variant	HERC2	GRCh38.p7	15:28265575	GGGAAGCTGCCATGC[A/G]TGTCCTCGTGGGCCT	8924
rs373433092	snp	A/C	8.46389e-05	0.00650479	intron-variant, splice-acceptor-variant	HERC2	GRCh38.p7	15:28275009	GCAGGCCGGGAACTG[A/C]AGACGACACACACGG	8924
rs373433977	snp	A/G	0.000105446	0.00726031	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28233263	AAACAGCAGGTCTCA[A/G]TTCATTAAAGAGGAA	8924
rs373434837	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28169029	ATTTTCCTATGTAAG[C/G]ACACCTGTCAGGTCC	8924
rs373439273	snp	C/T	0.000181301	0.00951934	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28196499	TACCAACTCCATTTC[C/T]GATAGCAACCCAGTC	8924
rs373446905	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28227626	GTTGTACCATATGAC[C/T]CTGTAATTCCAGTCC	8924
rs373451213	snp	C/T	0.000117506	0.00766414	intron-variant	HERC2	GRCh38.p7	15:28256050	ATTCCCTCCCAACAC[C/T]CTGACCCATGCCCTC	8924
rs373456240	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28287094	ATTTTTTTCATAATA[A/C]AACGTTGGAAAAAAA	8924
rs373458273	snp	C/T	3.31499e-05	0.0040711	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272342	GTCTCCTGTGCCCCG[C/T]TGTCCCACAGCTGAA	8924
rs373458880	snp	A/G	0.000248305	0.0111396	intron-variant	HERC2	GRCh38.p7	15:28179078	TTTTCACAACATTAA[A/G]AACTTTTTTGTTTTT	8924
rs373465646	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28154889	TCATTTACATTAGGT[A/G]TATCTCCTAATGCTA	8924
rs373467503	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28207295	ACACGCCACCACGCC[C/T]GGCTAATTTTTGTAT	8924
rs373468882	snp	C/T	0.0486741	0.148216	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321239	TTACAGGAAATAAAC[C/T]TGCTCCTCTAATTCA	8924
rs373519401	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28253104	ACATAGAGGTACAAA[C/T]GTGTTTCACTTTCTA	8924
rs373561014	snp	A/T	0.302184	0.244493	intron-variant	HERC2	GRCh38.p7	15:28210653	AACCAGCTTAGGTTC[A/T]ACTTGTTACAATACA	8924
rs373567330	in-del	-/T			intron-variant	HERC2	GRCh38.p7	15:28192940	TTCCCTTTTTTTTTT[-/T]TCCAACAGATTGCAA	8924
rs373567574	snp	C/G/T	0.000247206	0.0111151	intron-variant	HERC2	GRCh38.p7	15:28201448	TCCAGCTTAAGACAA[C/G/T]TACTCACCTGAATAT	8924
rs373616417	snp	A/G	0.000153988	0.00877328	intron-variant	HERC2	GRCh38.p7	15:28132267	GCGCCTCCACCTTCA[A/G]AGAAAAGGGACTTGG	8924
rs373616441	snp	A/G			missense	HERC2	GRCh38.p7	15:28163135	AAAGCACCGCGGAGA[A/G]CACATCCCTGCCCCT	8924
rs373641062	snp	C/T	1.6517e-05	0.00287372	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233711	AACAAGCGACCGACC[C/T]CTTCCACGGGATGCT	8924
rs373651534	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28150458	GGCCACACGAACGTA[C/T]ATTCTAGTGAAATTA	8924
rs373663289	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28133121	GAGCTGAGAACAGGT[C/T]TTACATTTTAACGGG	8924
rs373672636	snp	A/C/G	8.25043e-05	0.00642235	missense, synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28270803	ATCAATGGCAAGCTC[A/C/G]TTGTCTTGTGGAAGG	8924
rs373675745	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28197648	TCCCAGCTACTCTGG[A/T]GGCTGAGACTGGAGA	8924
rs373696705	snp	A/G/T	0.000224779	0.0105992	synonymous-codon, missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214258	GGCGCACCCTGCGCC[A/G/T]CCTCAGCGTGGACTC	8924
rs373714671	snp	A/G	0.000153988	0.00877328	intron-variant	HERC2	GRCh38.p7	15:28212410	ACACGAGTTTAAGAC[A/G]GCAGCTATTTCATCA	8924
rs373719424	snp	C/T	0.00140482	0.0264658	intron-variant	HERC2	GRCh38.p7	15:28248511	CTAAAGTAACGAGCC[C/T]CGATCACATACAAGA	8924
rs373723349	snp	C/T	5.08699e-05	0.00504305	intron-variant	HERC2	GRCh38.p7	15:28115406	AGACCCTAGAGGCCC[C/T]GCCTGCCGCCCCAGG	8924
rs373729311	snp	A/G			intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28315718	AGTGGAGGAAGAAGC[A/G]AATGCGCAGGCTGAA	8924
rs373735312	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28297490	GTTAAAAAAACTTTA[C/T]ATTAACTGAGTAACA	8924
rs373764727	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28149925	CAAGAACAGCCACAC[A/G]AACGCACATTCTAGT	8924
rs373772565	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28247407	AAATCTTCAGTTTTT[C/G]TGTCTACATGGTTCT	8924
rs373775051	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28279267	AGTGCTGGGATTACA[A/G]GCGTGAGCCACCACA	8924
rs373807532	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28181901	CCACCCACAACAAGC[C/T]CTGCAGAGAATAAGG	8924
rs373811268	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28241629	GATCAAGACCATCCT[A/G]GCCAACATGGTGAAA	8924
rs373839310	snp	A/C	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28200317	GGAGAATGGCATGAA[A/C]CCGGGAGGCGGAGCT	8924
rs373850620	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28147220	GGACTAGATATAAAG[C/T]GAGAGAGAAACAGAA	8924
rs373882716	snp	C/T	0.00038193	0.0138137	intron-variant	HERC2	GRCh38.p7	15:28233843	AGCCACCCAGTGAGT[C/T]TTCACAAATCTTAAA	8924
rs373894422	snp	C/G			intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28300649	CAACATGGTGAAACC[C/G]CATCTCTACTAAAAA	8924
rs373910888	snp	C/G	3.90656e-05	0.00441942	intron-variant	HERC2	GRCh38.p7	15:28124270	TCAGCCCCTCAGGCA[C/G]CAAAGGCACACGGGG	8924
rs373911530	snp	C/T	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28217350	ACACACCCACACAAC[C/T]ACATGCTACCAACAC	8924
rs373912015	snp	C/T	1.65416e-05	0.00287586	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28254351	TTACCTAAGAAGCTG[C/T]TGTATGAGCTGAACC	8924
rs373920666	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28249468	AGAAGGTAAAGTTAG[A/G]AGAGCAGTGAATGTT	8924
rs373924138	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28272553	GAATTGACACCAAGA[C/T]TTTAGCACAAGACAT	8924
rs373933226	snp	C/T	1.64743e-05	0.00287	missense	HERC2	GRCh38.p7	15:28114625	ACCTATAGTTTATCG[C/T]CAGCCGCACGTACTC	8924
rs373942206	snp	C/T	1.65236e-05	0.00287429	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28198418	AGTCACAGATCCCCA[C/T]TTGTATTTTGGTGTG	8924
rs373947216	snp	C/T	1.6855e-05	0.00290297	missense, downstream-variant-500B, nc-transcript-variant	HERC2	GRCh38.p7	15:28186617	CCTCCTCTTCATTAT[C/T]CGAAGCTAAGAAAGG	8924
rs373953643	snp	C/G	1.66214e-05	0.00288278	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28213981	ACTGGGCCTAGTGCA[C/G]ACCAAACAGCGAGCT	8924
rs373954015	snp	C/T	0.00054402	0.0164838	intron-variant	HERC2	GRCh38.p7	15:28143853	CACAAATCTAGAAAT[C/T]GTACTAGAATGCTCC	8924
rs373959383	snp	A/G/T	3.29518e-05	0.00405894	intron-variant	HERC2	GRCh38.p7	15:28143999	ACTGGCAGCTGAAAT[A/G/T]AGCAGAGAGAAAGTA	8924
rs373974195	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28165082	CCTGGTGTGGGGAGC[A/G]CCTCAGCGGGCTGGG	8924
rs373981957	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28298428	CCAAAGTGCTGGAAT[C/T]ACAGGCATGATCCAC	8924
rs373987814	snp	A/C	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318649	AAGTATTGTACAATT[A/C]AACTGTTTATATGTA	8924
rs373996817	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28223509	TTAGCCTAGCCGCTA[C/T]TTTAGGGCCCCCAGG	8924
rs374002844	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28127340	ATGCAAGGGGAGGAG[C/T]CACACAGGGGAGGAT	8924
rs374011266	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28250020	GGAACACGGAGGGGA[C/G]GAGAGCCCAACCAGA	8924
rs374056451	snp	C/G/T	3.35132e-05	0.00409334	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28238613	TTACCAAGAATACTA[C/G/T]TTCCTGTTAACGACT	8924
rs374062477	snp	G/T	8.29566e-05	0.00643983	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214628	CCGCTCTTCACCAGG[G/T]CACAGGGAAGGTAGA	8924
rs374064411	snp	A/C/G			intron-variant	HERC2	GRCh38.p7	15:28197216	CTGATGAAAAGAGAG[A/C/G]CTTCCACAAGGTTCA	8924
rs374075870	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28121508	CATCACATAGTTTTG[C/T]TTAAAATCTGTGTTG	8924
rs374114550	snp	C/T			intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174318	CAACCTCTAATTGTG[C/T]TGGCACAATTAAATA	8924
rs374123392	snp	C/T	1.64773e-05	0.00287026	missense	HERC2	GRCh38.p7	15:28168480	ATGCATTCTTCTCCA[C/T]TCATGGGACTAGCCA	8924
rs374126684	snp	A/T	0.000310484	0.0124557	intron-variant	HERC2	GRCh38.p7	15:28293044	AATTAAAAATTTTTT[A/T]ATCTGTCACCGCTTT	8924
rs374134608	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28264724	CTAACACAGCTTAGA[C/T]CTTACAAAACTTTTA	8924
rs374140989	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28237808	AAAATACTACCTCAA[C/G]ATTATAAGCCATTCC	8924
rs374146885	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314152	TGCTACAATATTGCA[C/T]ATACAATATCTGAAA	8924
rs374152423	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316538	AATGTCACATACAGG[A/G]TTACTACATCTTTTT	8924
rs374173895	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28277030	CAGTGAGCTATGATT[A/G]TATCACTGCACTCCA	8924
rs374182450	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28294102	ACAACATTTCTGACA[C/T]CAAATGCATGGACTT	8924
rs374186274	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28258254	GCGGCGGGGATCACC[G/T]GAGGTCAGGATTTCA	8924
rs374187501	snp	A/G	0.000307953	0.0124049	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28246025	CAGCATTTTTACTGA[A/G]CAGAAGCACTATAGA	8924
rs374187522	snp	C/T	0.000140521	0.00838098	intron-variant	HERC2	GRCh38.p7	15:28238554	ATACTCTGCTTAAAA[C/T]GATATAGGTTGTAAC	8924
rs374189356	snp	A/G	1.65321e-05	0.00287502	missense, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28292947	CTATATATAGGTGCA[A/G]GAGTTTCTTCTTCAT	8924
rs374191134	snp	C/T	1.65899e-05	0.00288005	intron-variant	HERC2	GRCh38.p7	15:28146220	AGATCATGCCCTGCT[C/T]AACCTCCTGTCCTTA	8924
rs374196761	snp	C/T	6.79613e-05	0.0058289	intron-variant	HERC2	GRCh38.p7	15:28113308	GATGTCTGTCAGGGC[C/T]GCGTGATGCTTCCCA	8924
rs374197569	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28281381	TCCCAGTGGCGAGGT[A/G]AGAGCTGGTCTCTTT	8924
rs374204285	snp	A/G	0.000360215	0.0134156	intron-variant	HERC2	GRCh38.p7	15:28222226	GGGGCCTGATGGAGC[A/G]TCAAAAACAATAGCT	8924
rs374206487	snp	C/T	3.33478e-05	0.00408323	intron-variant	HERC2	GRCh38.p7	15:28196418	AATTCAACAGAAAAC[C/T]ATTCGTCCCAAAGCA	8924
rs374209324	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28279153	TGAGCCACCAAGCCC[C/T]GGCTAATTTTTTTAT	8924
rs374217998	snp	A/T	0.000153988	0.00877328	intron-variant	HERC2	GRCh38.p7	15:28124957	GATGCAGCATGTGAC[A/T]GGAGCACACTTTGCT	8924
rs374218320	snp	A/G	3.45614e-05	0.00415686	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28215767	GCGTGCACCAGCTCC[A/G]GTGTTGCTCCCTGTA	8924
rs374219499	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28126384	ATCCCACCACTAGGT[A/G]CCTACCCAGAAGAAA	8924
rs374228133	snp	A/G	3.29478e-05	0.00405867	synonymous-codon	HERC2	GRCh38.p7	15:28111850	GCTGCTGTCGTCGGC[A/G]GCTGGCTCTCCTGTA	8924
rs374245104	snp	C/T	6.58924e-05	0.0057395	missense	HERC2	GRCh38.p7	15:28141485	CTCCGATTAACTGCA[C/T]GGGTCTGAGAGTTGC	8924
rs374283061	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28115262	GAAAATAGATGGTCT[A/T]TTTTTTTTTTTTTTT	8924
rs374298770	in-del	-/G			intron-variant	HERC2	GRCh38.p7	15:28293512	AAAAAAAAAAAAAAA[-/G]AAACCAATATAACAA	8924
rs374304067	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28250293	GGCCCTCATCACACA[C/T]GGCAAGGATGCGCCC	8924
rs374343039	snp	A/G			intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28319082	AATTCCTGTCTGCAG[A/G]GAAGCTCCCCAAAGA	8924
rs374349897	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28224202	AGACAGACAGACAGA[C/T]AGATAGAAAGATTCC	8924
rs374364040	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28204606	GCCTGGAGACAGAGC[A/G]AGACTCCGTCAAAAA	8924
rs374385629	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28140442	AGAAATCTTCACATA[C/T]ACTAGAATGGAGACA	8924
rs374429697	snp	A/G	0.000114712	0.0075725	intron-variant	HERC2	GRCh38.p7	15:28152638	ATCATTCTGAAGGTG[A/G]GAAAGGCTGCAGCTC	8924
rs374453464	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28272115	AGTGTTTTTCTCTGG[C/T]GTGTGTGTGTTTGGT	8924
rs374479623	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28254687	AACCCTAACTCAGTT[A/G]TGCAGTTTCAAACAG	8924
rs374481612	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28155769	CTCTTTAGTTTAATT[A/G]GATCCCATTTGTCAA	8924
rs374505560	snp	A/G	0.000248478	0.0111435	synonymous-codon	HERC2	GRCh38.p7	15:28163130	GCCGGAAAGCACCGC[A/G]GAGAGCACATCCCTG	8924
rs374508718	snp	A/G	0.000220588	0.0104998	missense	HERC2	GRCh38.p7	15:28116674	GCTCACCCAGGAAGC[A/G]GAACATGCTGCTGTG	8924
rs374512336	snp	G/T	8.26016e-05	0.00642604	intron-variant	HERC2	GRCh38.p7	15:28202333	CACAAGCAGAGGCCA[G/T]GAAAACGAAGTACCA	8924
rs374519281	snp	A/G	0.000724888	0.0190242	intron-variant	HERC2	GRCh38.p7	15:28130487	AGTGGGTTTAAACAA[A/G]CAGAATCTTGCGTAC	8924
rs374528497	snp	A/G	0.000216849	0.0104105	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28212575	CACATTAAAGGCCAC[A/G]GCAGGGAGCTGGAGA	8924
rs374531907	snp	A/G	1.9187e-05	0.00309728	intron-variant	HERC2	GRCh38.p7	15:28113708	TCACTTTACACTTCT[A/G]TCTTCAGTGACACTG	8924
rs374534381	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28288848	GCAAAACTCCATCTC[-/A]AAAAAAAAAAAAAAA	8924
rs374543627	snp	A/C	0.000904112	0.0212424	intron-variant	HERC2	GRCh38.p7	15:28254294	TCACACACACAAAAA[A/C]AAGTAAATAAATAAC	8924
rs374548424	snp	C/T	0.00014843	0.00861354	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214743	GCATTTCATGTCCCT[C/T]GCCCTTTCGGTCTTG	8924
rs374549481	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28199006	ACAAAAATTAGCCAG[A/G]CGTGGCGGTGCATGC	8924
rs374551104	snp	A/C	0.000153988	0.00877328	missense	HERC2	GRCh38.p7	15:28113197	CACCTCCCAGAACCA[A/C]TGGATCAGCGATGCG	8924
rs374553780	snp	A/G	9.05756e-05	0.00672901	intron-variant	HERC2	GRCh38.p7	15:28152834	CATATCTGCCACCTG[A/G]AGAGGAAGCAAGGAC	8924
rs374557988	in-del	-/AGGT			intron-variant	HERC2	GRCh38.p7	15:28266761	GTTGTCAGGAACTGG[-/AGGT]AGGAAGGGGGCATCA	8924
rs374594037	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28171814	GTGCGGTGACTCACG[C/G]CTGTAATCCCAGCAC	8924
rs374595044	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28198366	GGAATTTTATTACCC[A/G]GATAATATTACCTTT	8924
rs374602622	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28118036	GTTGAGTTTAAACAG[C/G]TTACAGAGCAGGCTG	8924
rs374607699	in-del	-/AC			intron-variant	HERC2	GRCh38.p7	15:28217066	ACACAAGGCACTCAT[-/AC]ACATTTACACAAATG	8924
rs374623112	in-del	-/TGGGA			intron-variant	HERC2	GRCh38.p7	15:28282975	CAGGAAGGGATGGGA[-/TGGGA]CGGGACGGGACTGGA	8924
rs374629722	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28146968	CGGTTACAGGGTTGA[C/G]AGGCTTGGACTGGTT	8924
rs374641673	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28198706	TGTCCAGCTTGATGA[C/T]TTTGCCAACATCACC	8924
rs374660504	snp	C/G	9.94843e-05	0.00705211	intron-variant	HERC2	GRCh38.p7	15:28233815	CAACAGAAACAGCTG[C/G]AAGTAACTTCAGAGC	8924
rs374662027	snp	A/G	8.48875e-05	0.00651433	synonymous-codon	HERC2	GRCh38.p7	15:28124154	GGGGCAGAAGAGCTC[A/G]GAGAGGTGGTGCAGC	8924
rs374665280	snp	A/G	0.000161987	0.00899818	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28202513	GATGTGCTGCACGGC[A/G]ACAGGCGTGGTGGCC	8924
rs374665784	snp	C/T	6.99044e-05	0.00591163	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233459	GAACATTTTGCTTGG[C/T]AGACAACTCTACAAA	8924
rs374669340	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28310316	GCCAGAGGTGGTGGC[A/G]CGCCTGTACTCCCAG	8924
rs374685260	in-del	-/TG			intron-variant	HERC2	GRCh38.p7	15:28298006	ACGTCTGTCAGTTAT[-/TG]TGTGTGTGTGTGTGT	8924
rs374693604	snp	A/G	1.66893e-05	0.00288867	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28254477	CGCTTCCTGTTCATC[A/G]ATTTCTTTTTCCTTC	8924
rs374694832	snp	C/T	1.6473e-05	0.00286988	synonymous-codon	HERC2	GRCh38.p7	15:28135546	TTCTCCTTCTGAAGA[C/T]AGGGCAAGGCAGTGC	8924
rs374708859	snp	A/G	6.61135e-05	0.00574912	intron-variant	HERC2	GRCh38.p7	15:28175664	CCTTTCCCCTGAGAG[A/G]AGGCCCATGGTGGAG	8924
rs374709094	snp	C/T	3.5417e-05	0.004208	missense	HERC2	GRCh38.p7	15:28132682	GCTGGTCCTCACTGT[C/T]GCTGTGCCCCAGCCG	8924
rs374716999	snp	A/G	0.000159987	0.00894248	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202121	CACTGACCATGGAGT[A/G]GGCGGCATCATCCAC	8924
rs374732640	snp	C/G	1.67097e-05	0.00289043	intron-variant	HERC2	GRCh38.p7	15:28257055	AAGAAGGGAAATCAT[C/G]AATACCTGAAGTCGT	8924
rs374737165	snp	A/G	1.64743e-05	0.00287	missense	HERC2	GRCh38.p7	15:28121390	CATGCTGACGATCGC[A/G]TACCATAGTTGCTTG	8924
rs374743507	snp	A/G	3.25696e-05	0.00403531	intron-variant	HERC2	GRCh38.p7	15:28274464	TGGGCGCACACACGC[A/G]TCAGAGGAGCCCCCC	8924
rs374751438	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28210862	TTTTATTCACAGTTG[C/G]TGGTTGCTGGGCAGG	8924
rs374764227	snp	A/G	0.00107679	0.0231784	intron-variant	HERC2	GRCh38.p7	15:28175684	CCATGGTGGAGAGTT[A/G]CAATACGGTTATGGT	8924
rs374768997	snp	A/G	4.95741e-05	0.00497841	missense, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28292942	TGGCCCTATATATAG[A/G]TGCAGGAGTTTCTTC	8924
rs374769838	snp	C/T	1.66754e-05	0.00288746	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28237048	CAGGCCCAGATTCCT[C/T]TCTGTGTCTATCAGA	8924
rs374773302	snp	C/G			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28320955	AAGACCTCATAAAAT[C/G]AGTGAGTTTCTATAG	8924
rs374773542	snp	C/T	0.000153988	0.00877328	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28196554	ACAATGATATCTTTT[C/T]CATTGGCACTGAAAG	8924
rs374790779	snp	A/T	6.28174e-05	0.00560399	intron-variant	HERC2	GRCh38.p7	15:28254524	CTTCAATATCCTGTA[A/T]TTCATAAAAAGAAAT	8924
rs374792928	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28283027	GAGAGAAAGAAATGT[A/C]CCAGCAAAAAAAAAA	8924
rs374813577	snp	C/T	9.08785e-05	0.00674025	intron-variant	HERC2	GRCh38.p7	15:28135712	GAAAAGAAAAAGCAA[C/T]AGTAACATCAGTTTT	8924
rs374833090	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28194146	TCTCGGCTCACTGCA[-/A]GCTCCACATCCTGGG	8924
rs374833379	snp	A/G			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317433	TAACTCTAAGAGCTT[A/G]CATTTATGCGTAGTC	8924
rs374859136	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28125743	AAACTGGCATGATCA[C/T]GGTTCACTGCAGCCT	8924
rs374898463	snp	A/C/T	0.000313206	0.0125103	intron-variant	HERC2	GRCh38.p7	15:28144645	CAGCCAGTCATCTAA[A/C/T]CTTGATCGCCATAAG	8924
rs374899950	snp	A/G	0.000215184	0.0103704	intron-variant	HERC2	GRCh38.p7	15:28292863	CAGATCAACCTTTCC[A/G]AAGTGCCAAAATTCA	8924
rs374904521	snp	A/G	1.69686e-05	0.00291273	missense	HERC2	GRCh38.p7	15:28124068	AGAATTCCTCGGAGA[A/G]TGTCGAACCCAACAG	8924
rs374923685	snp	A/G	0.000132628	0.00814227	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28246743	GAAACAAAAGGTACC[A/G]GTAAAGTCCCCTTCC	8924
rs374925472	snp	G/T	4.66875e-05	0.00483131	intron-variant	HERC2	GRCh38.p7	15:28269215	CCCTGCCCCGCAAGG[G/T]AACACTGCAGGCACA	8924
rs374932596	snp	A/T	0.000153988	0.00877328	intron-variant	HERC2	GRCh38.p7	15:28280039	TATATTTAACTGGCA[A/T]CAGGATTCTTTCTTC	8924
rs374943373	snp	C/G			intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28215051	GGCTCATTTTTTTTT[C/G]GATTTTTGGTAGAGA	8924
rs374946389	snp	C/T	1.97178e-05	0.00313983	intron-variant	HERC2	GRCh38.p7	15:28246081	CCTACATTTAAGAAA[C/T]AATAAGATTTAAATA	8924
rs374958990	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28142462	GCCAAGGTTTCTGTG[G/T]CTCCTTCCGCAGGAC	8924
rs374966794	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28315274	GGAATTCACACCCAC[A/G]CTCGCCACACCTTCC	8924
rs374989572	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28255522	CATACTATATAGTTA[C/T]ATTGCTGCGACACTC	8924
rs374990078	snp	C/T	0.000236666	0.0108755	intron-variant	HERC2	GRCh38.p7	15:28263216	AACTCTGCATTTTAA[C/T]GAAAAATTTTAAATG	8924
rs375002955	snp	C/T			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28315508	AGCAATTAAAAGATC[C/T]TATTAACAGCCGGGC	8924
rs375020268	snp	C/T	3.37798e-05	0.00410959	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28211052	TGAGACAGGATCTGC[C/T]GCAGTTTATCCTGGT	8924
rs375028808	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28287572	GATTTTTAAAATCAC[A/C]ACAAATCTTTATCAA	8924
rs375031915	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28185796	CAGACTCTCAAGGCT[A/G]TATGCACTTCTTCCT	8924
rs375033319	snp	C/T	5.21671e-05	0.00510694	intron-variant	HERC2	GRCh38.p7	15:28238802	ACCAGAATCAGTCCA[C/T]TGATCAATCAACAGG	8924
rs375034743	snp	C/G	0.000182091	0.00954003	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28233198	TATCCTCCTCCAACG[C/G]GGCAAAGAACTTAAC	8924
rs375037938	snp	C/T	0.000247062	0.0111117	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28263086	AGTCTTGAAGCTTTT[C/T]AATCAGCTTTGGGGT	8924
rs375039081	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28232269	GATCAGAGGCCAGGC[G/T]CGGTGGCTCACGCCT	8924
rs375047461	snp	A/G	1.72806e-05	0.00293938	intron-variant	HERC2	GRCh38.p7	15:28117183	AGCAAGCAAGCGTGA[A/G]GCCGCTGCCGCAGCA	8924
rs375051583	snp	C/T	0.000800377	0.0199887	intron-variant	HERC2	GRCh38.p7	15:28163069	GGAGGTGGAATCAGA[C/T]GGCCCCGCCCTCCCT	8924
rs375052633	snp	A/G	1.65004e-05	0.00287227	intron-variant	HERC2	GRCh38.p7	15:28130149	CAGTCCTGCGGCACT[A/G]AGCCCCTACCTACCA	8924
rs375066309	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28137236	GGCTATATTTCAAAC[C/T]TTTTTATGAGGCTAG	8924
rs375070470	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28188140	AAAAACCAAGAGTGA[C/G]TTAAGTGTAGTGTAG	8924
rs375075181	snp	C/T	0.0154538	0.0865337	intron-variant	HERC2	GRCh38.p7	15:28217441	TCTCATCAATATGTG[C/T]GGACGCTCCAGCACA	8924
rs375076029	snp	C/T	1.68607e-05	0.00290346	missense	HERC2	GRCh38.p7	15:28116682	AGGAAGCGGAACATG[C/T]TGCTGTGCACGGGTG	8924
rs375076595	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28158023	AGGAGCAGGTTGTTC[A/G]GTTTCCATGTAGTTG	8924
rs375117013	in-del	-/GGGAG			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321787	TACACACACATAACA[-/GGGAG]CCCATCGTTTTAACG	8924
rs375125401	snp	G/T	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28138535	GTCAGCACATTTGTT[G/T]ACAGCATGGTTCACT	8924
rs375127960	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28264666	ATCATCGCAAACTTT[A/T]ACTAAAGTAGCAACT	8924
rs375167274	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28254219	ACCTGGGAGGCGGAG[C/G]TTGCAGTGAGCCAAG	8924
rs375179806	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28161515	CCCACGGCCTTTACG[A/G]CTGATCAGTCCTATT	8924
rs375192636	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28291837	ATGAACCCGGGAAGC[A/G]GAGGTTGCAGTGAGC	8924
rs375197756	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28310801	AGCTATTACTGGCCA[C/G]GCACGGTGGCTGACG	8924
rs375200282	snp	A/G	0.000153988	0.00877328	intron-variant	HERC2	GRCh38.p7	15:28115407	GACCCTAGAGGCCCC[A/G]CCTGCCGCCCCAGGG	8924
rs375217937	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28272061	CTCCACAAACAAGTG[A/G]CCTCCCACACCTGTC	8924
rs375231545	snp	A/G	0.00993419	0.0697739	intron-variant	HERC2	GRCh38.p7	15:28206650	CATCCTGGGTAACAC[A/G]GTGAAACCCCATCTC	8924
rs375233485	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28194765	TTTATATAAAATGTA[C/T]AAAATTTTGGCTGGA	8924
rs375249825	snp	C/T	8.13041e-05	0.00637538	intron-variant	HERC2	GRCh38.p7	15:28175478	TCCCCCAAGTCAGGA[C/T]GGCACGCCACCCCCA	8924
rs375257482	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28261055	GGCCATTCAGGTCAG[A/G]CAGCTTTTAACATTA	8924
rs375262770	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28298797	CAAGACTCCTTCCCC[C/G]CCAAAAAAAAGAAGA	8924
rs375265161	snp	G/T	6.69781e-05	0.00578659	intron-variant	HERC2	GRCh38.p7	15:28113558	CAGGGCAGCCCCACC[G/T]GGGGGTCGGCATACC	8924
rs375282758	snp	A/G	1.64977e-05	0.00287203	intron-variant	HERC2	GRCh38.p7	15:28201563	CAGTAGACTGCAAGA[A/G]ATAAATACATTCAAA	8924
rs375283163	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28206562	CTCTAGGTTGGGTGC[A/G]GTGGCTCACGCGTGT	8924
rs375294632	snp	C/G/T	5.022e-05	0.00501078	intron-variant	HERC2	GRCh38.p7	15:28124997	CCCACCCAACCTGCC[C/G/T]GGACTCACCTGTGCA	8924
rs375305957	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28161546	TCTAAGACATACTAG[A/T]AAGACGCTCACTTTA	8924
rs375306215	snp	A/G	1.69766e-05	0.00291342	synonymous-codon	HERC2	GRCh38.p7	15:28113101	TCGGCCCCGGAAGTC[A/G]GCGATGGTCCTGGGC	8924
rs375308006	snp	A/G	0.00113211	0.0237649	intron-variant	HERC2	GRCh38.p7	15:28274897	ACGCGCCACACCAGG[A/G]ACCGTACCTGATCGC	8924
rs375385698	snp	C/G/T	6.31377e-05	0.00561832	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28175524	TACCTGCCCCGAGTC[C/G/T]GTGACCGCCAGGCAG	8924
rs375431949	snp	A/G	1.65288e-05	0.00287474	missense	HERC2	GRCh38.p7	15:28141842	TCACGAATTTTCTTA[A/G]CCACCTAAACAAAAT	8924
rs375432885	snp	A/G	8.29029e-05	0.00643775	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28229259	CTGTACAGCCCAAGC[A/G]TACAGCTTGCCAAAG	8924
rs375437791	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28280959	GTCAATATTAGTCAA[C/T]ATTTATCAGCAGCAC	8924
rs375450605	snp	C/T	0.000281152	0.0118531	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28229594	AACCTCTGCTCTCTC[C/T]AACTGCAAAATATCA	8924
rs375462789	snp	C/T			intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28301742	ATGTATGTGTATATA[C/T]ATATATATATATATA	8924
rs375465519	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28129624	GTCTGTCTAAGGACA[C/T]GTCTCAGGCTGGCTG	8924
rs375479207	snp	C/G	3.30202e-05	0.00406313	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28177067	GTGCGAGCTCCCACA[C/G]GCGATATCCCGGATA	8924
rs375491831	snp	A/G	1.64746e-05	0.00287002	synonymous-codon	HERC2	GRCh38.p7	15:28125141	CTGGATGGCATTGGT[A/G]GTTCCGTCTCCCAGT	8924
rs375504970	in-del	C/GGCAGTGTTTGTAA			intron-variant	HERC2	GRCh38.p7	15:28262670	CCTGCCACAGAAAGT[C/GGCAGTGTTTGTAA]AACTCAACAGGTTTA	8924
rs375509794	snp	C/T	0.000153988	0.00877328	intron-variant	HERC2	GRCh38.p7	15:28265998	GAAAGGGAACAAACA[C/T]GAATGCCCTTCTTCT	8924
rs375512906	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28274845	GGCTGAACCGAGTTC[A/G]AAACCCAGTCTGTTG	8924
rs375534446	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28169007	GACTGTTTTTGTTCT[G/T]AAACTAATTTTCCTA	8924
rs375534803	snp	C/T	0.0115144	0.0749975	intron-variant	HERC2	GRCh38.p7	15:28217038	CACAATAACATCACT[C/T]GTGCTCACACTGACA	8924
rs375563185	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28156641	GCTGATCAGCTTAAG[A/G]AGATTTTAGGCTGAG	8924
rs375586875	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28181368	AGACACTCACAGCTC[A/G]CTGCCCACTGTCCAC	8924
rs375601111	snp	C/T	1.74084e-05	0.00295024	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28215778	CTCCGGTGTTGCTCC[C/T]TGTACACCAGCCTGT	8924
rs375601172	in-del	-/CATC	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28113989	GGGGAAACACATGTG[-/CATC]CATCCGCCCCAGGCC	8924
rs375617077	snp	C/G	3.34024e-05	0.00408657	intron-variant	HERC2	GRCh38.p7	15:28256023	AGTGTGTGCCAATTT[C/G]AGTGAAACGCCATTC	8924
rs375619761	snp	A/G	1.64762e-05	0.00287016	missense, utr-variant-5-prime, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28280215	GCTGAGAGGGTGGTG[A/G]TGGCTGACTGGACGG	8924
rs375653136	in-del	-/G			intron-variant	HERC2	GRCh38.p7	15:28295309	GTCCTACATGTGTGT[-/G]GGGGGGGGGGAGTGG	8924
rs375677686	snp	A/C	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28184636	GGAGGCTGAGGCAGG[A/C]GGATTACGAGGTCAG	8924
rs375681842	snp	A/G	3.30355e-05	0.00406407	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28202170	GTCAGAATACTCGTC[A/G]GACACCGTGTCTGCA	8924
rs375690998	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28253021	GACCCAACCTGCCAG[G/T]GCTTTGCTTTCTCTA	8924
rs375693734	snp	C/T	0.000909925	0.0213104	intron-variant	HERC2	GRCh38.p7	15:28198527	GTCAATAACAAATCA[C/T]TATAATCAATATTCA	8924
rs375713638	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28249934	TGCTGGGATTACAGG[C/T]GTGAGCCACCACGCC	8924
rs375724472	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28281576	AGGAGGGCCTTAGAA[A/G]GCAGTAGAGAGAAAC	8924
rs375731015	snp	C/G	6.34337e-05	0.00563141	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28215596	GCCTCTCTCAGGGAA[C/G]TGGTTTTGCCTGGCA	8924
rs375731096	snp	C/T	1.67649e-05	0.0028952	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28192141	ACGGCCACAAAATAC[C/T]GCAGACTGACCTATT	8924
rs375734016	snp	G/T	0.000183693	0.0095819	intron-variant	HERC2	GRCh38.p7	15:28254327	ATAATACAATACAGC[G/T]ACTACGATTTACCTA	8924
rs375746566	snp	A/G	3.29788e-05	0.00406058	intron-variant	HERC2	GRCh38.p7	15:28121297	CAGGTACCCACGAAA[A/G]CATCACTTCTAAGGC	8924
rs375746833	snp	A/G	4.95381e-05	0.0049766	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28175626	GTGCACGTCAGAGCC[A/G]TGGCCCAATCTGAAG	8924
rs375750342	snp	A/G	6.71513e-05	0.00579406	intron-variant	HERC2	GRCh38.p7	15:28142966	CTCTAAGAAACAACA[A/G]AACAGTATTCTATCG	8924
rs375754511	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28268845	GCCGATGCAGGGGCA[A/G]GGCAGGCTAGCCCCA	8924
rs375761052	snp	C/T	1.64735e-05	0.00286993	missense	HERC2	GRCh38.p7	15:28114661	GGTTGTCCAGGGTGA[C/T]GTGTGTGTGCTTGGA	8924
rs375770749	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28113497	GGCAAGGTTCTGACT[C/G]TAACTGCTGTCACTG	8924
rs375774175	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28289766	TTCCCTAAGGTGTAT[A/G]AACTATCTGACTACA	8924
rs375785674	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28148311	AAATAAACACAGCAG[A/G]TGCTACCTTAAGACA	8924
rs375790790	in-del	-/G			intron-variant	HERC2	GRCh38.p7	15:28284950	AAAAAAAAAAAAAAA[-/G]ATAATTACCAGGAAC	8924
rs375795824	snp	C/G	0.000397418	0.0140908	intron-variant	HERC2	GRCh38.p7	15:28163087	CCCCGCCCTCCCTGA[C/G]ACTCACCTGTGGGTA	8924
rs375796516	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28190583	TGCCAACAGGTGTGA[C/T]GACAAAAAAGCAACT	8924
rs375797517	snp	C/T	1.87054e-05	0.00305816	intron-variant	HERC2	GRCh38.p7	15:28113701	AAAAAGCTCACTTTA[C/T]ACTTCTGTCTTCAGT	8924
rs375799955	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28134952	TGCTGGGATTACAGG[C/T]GTGAGCCACCACGCC	8924
rs375805083	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28112319	GGCGGCCTGGCTGGC[A/G]GAGGACCAGGCACGT	8924
rs375810275	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28294799	CCCCCAGGGCTGTGA[A/G]CATGCGTGACTAATA	8924
rs375864233	snp	A/G	8.43064e-05	0.006492	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28293012	TGTTCCACTTGGTTC[A/G]ACACTATCATCTGCA	8924
rs375892848	snp	A/T			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321265	ATTCAGCAAGATACA[A/T]CTGACTTCCCCTTAC	8924
rs375894135	snp	C/T	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28295670	CCAAAAGTGCTGGGA[C/T]TACAGGTGTGAGCCA	8924
rs375901514	in-del	-/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28223670	TGGGGGAATTTTTCA[-/T]TTTGCATAGCTTTAT	8924
rs375902946	snp	G/T	1.68525e-05	0.00290275	intron-variant	HERC2	GRCh38.p7	15:28178842	TTAACAACGGAGCAG[G/T]AGCAAAGGCCGCCCC	8924
rs375906595	snp	C/T	1.64727e-05	0.00286986	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28263058	CTTCCACAGCGGACT[C/T]TGACCACATCCAAGT	8924
rs375908643	in-del	-/T	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28187052	CTGCAAACTCTTCCG[-/T]CTTAGAGCTTTCTTG	8924
rs375918078	in-del	CCAGAAGGC/T			intron-variant	HERC2	GRCh38.p7	15:28278841	CATCTGGCAGTCTTG[CCAGAAGGC/T]AGTTTAACCTTCTGA	8924
rs375928997	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28209436	GCAAGCTCTGCCTCC[C/T]GAGTTCACACCATTC	8924
rs375955574	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28209726	TTTATAGAAGGGCCT[C/T]AAGCATTAGTGAATT	8924
rs376002281	in-del	-/T			intron-variant	HERC2	GRCh38.p7	15:28272745	GAAGTGAAGAAAAGG[-/T]AAAGAGAGAGAGCCC	8924
rs376016673	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28180606	GGGACATGAGGGTTC[A/C]TGAAGCTATTCACTC	8924
rs376018767	snp	A/G	1.65386e-05	0.00287559	synonymous-codon	HERC2	GRCh38.p7	15:28113167	AGAGCGCTCTGTGTT[A/G]GAGAAGGACTCCATC	8924
rs376020684	snp	A/G	0.000153988	0.00877328	synonymous-codon	HERC2	GRCh38.p7	15:28141612	GCCACCAGCAGAGAG[A/G]GTCCAGTCATCTGGT	8924
rs376023743	snp	A/G	5.28686e-05	0.00514116	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28218556	AGTCTTGGTGGCTTC[A/G]CTCTGCATGATCTCA	8924
rs376031242	snp	A/C/G	1.70012e-05	0.00291553	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28260936	CAGAGCCAGGCAGTG[A/C/G]GTGGAGCCTGCAGCC	8924
rs376031823	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28249796	GGAATTACAGGCACA[C/T]GCCACCACGCCAAGC	8924
rs376036619	snp	A/G	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28298665	GCCGGGCGTGGTGGC[A/G]GGCGCCTGTAGTCCC	8924
rs376040279	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28289405	TGCATGCACCTTATA[A/T]CATTCTCAAATACAT	8924
rs376067047	snp	A/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28310634	CCTACCACAATGCAC[A/T]TGATAAGAGGCTAAC	8924
rs376071931	in-del	-/T			intron-variant	HERC2	GRCh38.p7	15:28275130	CTTCAAGTGACAGGA[-/T]CACAAGTGGATTTTT	8924
rs376081134	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28288482	CAGTGAGCCAAGATC[A/G]TGCCATTGCACTCCA	8924
rs376094729	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28226107	CTGATAACTGTAAAA[C/T]AATAAAATACTGCTG	8924
rs376099384	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28271905	TCAGGTGACGTGCCC[C/T]GCACAGAGCCCAGTA	8924
rs376114341	snp	A/G			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28320918	ACTGAACTAACTCTT[A/G]TCTCTCCAGAAACAC	8924
rs376124795	snp	C/T	3.4293e-05	0.00414069	intron-variant	HERC2	GRCh38.p7	15:28275022	TGCAGACGACACACA[C/T]GGAACATACAACCAG	8924
rs376129407	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28128473	TAAAAGAATTAAATA[A/G]GTCAAATAAAAAGTT	8924
rs376135972	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28157443	TACTGGTCTATTCAG[A/G]GATTCAACTTCTTCC	8924
rs376167368	snp	A/G/T	8.45739e-05	0.00650239	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28269292	ACACGCGGCCATTGC[A/G/T]TGACAGAATCAGGAA	8924
rs376200931	snp	C/T	0.000153988	0.00877328	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213779	CAAACGCGACACGTC[C/T]GCATGTCAGAGAACT	8924
rs376212338	snp	C/T	0.000347939	0.0131852	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214603	CACCCACCTGAGTGA[C/T]GGCACTGCGCCGCTC	8924
rs376242930	snp	C/T	0.00091844	0.0214097	intron-variant	HERC2	GRCh38.p7	15:28261017	CAAGCCTATGACTTC[C/T]GCTGCAAGAAAGATA	8924
rs376246377	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28189287	GTATCACAGGATGAA[C/T]GGTTTTGAATTGAAA	8924
rs376263469	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28177830	GAAAAAAGTAAAAAT[A/G]ATTTGTGATTAGACA	8924
rs376280253	snp	C/T	3.41804e-05	0.00413389	intron-variant	HERC2	GRCh38.p7	15:28274264	CCAGCTGTCTGCGTG[C/T]AGAAGGCAAGAAAGG	8924
rs376281034	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28167520	TAAGCAGTGACAGGG[A/G]CCGTGTCCTGCGGCA	8924
rs376282787	in-del	-/T/TT/TTT/TTTT/TTTTT			intron-variant	HERC2	GRCh38.p7	15:28272428	TAAAAACAGATTAAC[-/T/TT/TTT/TTTT/TTTTT]TTCTTTTCTTCACAG	8924
rs376290379	snp	A/C/G	6.64467e-05	0.00576364	synonymous-codon	HERC2	GRCh38.p7	15:28113576	GGGTCGGCATACCAT[A/C/G]GTCTCCAGTTCGTAG	8924
rs376308925	snp	C/G	1.66545e-05	0.00288565	intron-variant	HERC2	GRCh38.p7	15:28256005	CCTGAAACTGAAATA[C/G]AAAGTGTGTGCCAAT	8924
rs376309745	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28235117	CTGCTCCAAATCCAA[A/G]CAATCAAAGCGGGAT	8924
rs376318971	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28295693	GTGAGCCACCACGCC[C/T]GGCCACCGTATTTTA	8924
rs376345125	snp	A/C/G	0.00010428	0.00722018	synonymous-codon	HERC2	GRCh38.p7	15:28168578	CGGCATCAGGGCCCC[A/C/G]ACAACAGCATCTCTG	8924
rs376347029	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28147367	GATGTAGTGGTACAC[G/T]CCTGTAATCTTAGCA	8924
rs376350858	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28164843	GTTCTGCATTAAACC[C/G]TCAAACCAGGAGACT	8924
rs376363410	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28253807	TCTCTACTAAAAATA[C/T]AAAAATCAGCCAGGT	8924
rs376369212	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28285014	ATCCACCATTAAGAC[A/G]CAGCAATTCAAAACG	8924
rs376403165	snp	A/G	0.000798403	0.0199641	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174093	GTTAAAAAATACAAA[A/G]GAGCCCAGTACAGTG	8924
rs376424605	snp	C/G	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28189062	ACTGCACTCCAGCCT[C/G]GGCGACAGAGTGAGA	8924
rs376426215	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28208004	CAGACTTGATCATCC[A/T]GATTCAGGTCTGCTG	8924
rs376433470	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28175835	AATTAACTTATTAAG[C/G]CAGCTGGGAAAAACC	8924
rs376434068	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28293164	TAAAATACATCAATC[A/G]TACCTGTAACAGACC	8924
rs376442760	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28152285	TTTGTTGAGTTGTTA[A/G]AAACAAAAGATATAC	8924
rs376492281	snp	A/G	1.76204e-05	0.00296814	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256135	GGCCCGCTCCTCCGC[A/G]GTGGGCAGCAGCACG	8924
rs376504565	snp	C/T	0.000580322	0.0170242	intron-variant	HERC2	GRCh38.p7	15:28196367	CACCTATTTGTAAAA[C/T]AGCAACTGAGTTAAG	8924
rs376514334	snp	A/G	1.73691e-05	0.00294691	intron-variant	HERC2	GRCh38.p7	15:28116650	GACACAGTCTCAAGC[A/G]GCCGAGAAGCTCACC	8924
rs376516190	snp	G/T	1.72585e-05	0.00293751	intron-variant	HERC2	GRCh38.p7	15:28168367	ACAAAGTAGCCACCT[G/T]TTCCTTTCTGATCTA	8924
rs376523091	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28199008	AAAAATTAGCCAGAC[A/G]TGGCGGTGCATGCCT	8924
rs376524441	snp	C/T	3.29875e-05	0.00406112	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265843	CGGCCGTAGTTCCCG[C/T]GGCCCCAGGTGTACA	8924
rs376542302	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28228045	ATGACTCTAGAAAAT[C/T]GTAAATGTATTTGAT	8924
rs376550266	snp	C/G	3.29457e-05	0.00405854	missense	HERC2	GRCh38.p7	15:28141524	CACAGGGAGTGGGAA[C/G]TTTGACTTTTGCGCC	8924
rs376557986	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28164900	CACCTAATTCATAAA[C/T]AGAGGCTTTCTTACT	8924
rs376611895	snp	A/G	2.45336e-05	0.00350231	missense	HERC2	GRCh38.p7	15:28132104	ATGGGAAATACCTTC[A/G]TAGGCACTTTACAGC	8924
rs376616288	snp	A/G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28278790	TCACTATCACAGTCA[A/G/T]ATAAAGCCAGCACTC	8924
rs376634914	snp	C/T			missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202614	CGGCCAGTGCAGCAG[C/T]CTGGGCAGACAAGAG	8924
rs376640979	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28221063	ACAGATGTCGCCATA[C/T]GCCACCCTGTCTGTC	8924
rs376644217	snp	C/T	0.000153988	0.00877328	intron-variant	HERC2	GRCh38.p7	15:28143857	AATCTAGAAATTGTA[C/T]TAGAATGCTCCATAC	8924
rs376646045	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28131207	GGCTCTAGTGTCTGG[C/G]CCTACCACAATGGCA	8924
rs376655182	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28130351	AAGGTGATCTCACTG[A/G]CCACCCTGACCAGCC	8924
rs376656479	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28172351	GAACAAAGCTAAAGA[A/C]CTCTTGCAACCTGAG	8924
rs376659586	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28148391	ACTTGAAAGAGAAAG[C/T]AACCAACATTAACTC	8924
rs376670151	snp	C/T	8.40597e-05	0.0064825	intron-variant	HERC2	GRCh38.p7	15:28178857	GAGCAAAGGCCGCCC[C/T]GCACAGGCCTCCTGG	8924
rs376723119	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28171935	AAAAAATTAGCCGGG[C/T]GTGGTGGCAGGTGCC	8924
rs376732842	snp	A/G	0.000165681	0.00910016	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28196565	TTTTCCATTGGCACT[A/G]AAAGCTAGGACAGAA	8924
rs376770051	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28220139	AGACACAGGCTCAGC[A/G]CCAACCACATGAGAC	8924
rs376770308	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28197251	AACAAATAATCTCTT[C/T]ATGGCATCAAGAGTT	8924
rs376779558	snp	A/C			intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28320357	GACCTCAGGGCATCC[A/C]CCCGCCTCGGCCTCC	8924
rs376794170	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28146525	CCCCACTGAAGATCA[C/T]GTCTGTGGACTGGAA	8924
rs376808431	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299833	GAGCGGGGCACATCA[C/T]GGGGGATCAGGAATT	8924
rs376812484	snp	C/T	1.68046e-05	0.00289862	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28238117	ATACAGCCTCACCTC[C/T]AAATACTGGCCAACA	8924
rs376870436	snp	A/G	3.52417e-05	0.00419757	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28218535	CATTCGCAGCAGTCC[A/G]CATAAAGTCTTGGTG	8924
rs376877594	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28145260	TGTGTGGTTCAGCAC[A/G]GCCCAGAGTAGGCCG	8924
rs376878592	snp	A/G	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28270522	CGCCTCAGCTTGCTC[A/G]TCACTCACTCTCAAC	8924
rs376927575	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28204395	GGGAGCCCGAGGAGG[A/G]CGGATCATGAGGTCA	8924
rs376964622	snp	A/G	0.000307953	0.0124049	intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28179051	AGGAACGACAGCCAG[A/G]AGAGGACTCTCTTTT	8924
rs376964632	snp	C/G			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28320885	ATAAGGAGTTACAAA[C/G]ACAAAACAAACAGCT	8924
rs376968942	snp	A/G	3.29826e-05	0.00406082	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214704	GAGCAAGCTTCCCAA[A/G]AAGTCAAACAGCTTC	8924
rs376970711	snp	C/G	8.60933e-05	0.00656043	intron-variant	HERC2	GRCh38.p7	15:28220681	TCAGTTAGGAGGGTG[C/G]GTAACCTGCCCTGGT	8924
rs376972283	snp	A/G	3.32751e-05	0.00407878	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28211083	GGGAGAGCAGCGCCC[A/G]ACCTGCTTTCAGGAT	8924
rs376972479	snp	A/G	1.67175e-05	0.0028911	intron-variant	HERC2	GRCh38.p7	15:28265979	CCTCCAAAGGCCTTG[A/G]GGAGAAAGGGAACAA	8924
rs376975329	snp	A/G	0.000153988	0.00877328	intron-variant	HERC2	GRCh38.p7	15:28246905	CTCTGGACCTTGAAG[A/G]AGGATTGAGAAATTT	8924
rs376978108	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28144290	CTAGGTACCACCCCA[C/T]AAGAAGCCGCCAACG	8924
rs376992464	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28176289	ATCCCAACTCAATAT[C/T]CTTTAAAGGACAAAG	8924
rs377000104	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28277146	CACATAATAGGCACA[A/C]AGAACAGATGAGTGG	8924
rs377009957	snp	C/T	4.97014e-05	0.0049848	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28233764	GGTCAAATGGCACTG[C/T]CTACAGTACCTTTCT	8924
rs377021578	snp	C/T	1.68001e-05	0.00289823	missense	HERC2	GRCh38.p7	15:28132723	CCTTTGCCCCATGTG[C/T]AGAGGTCCCCGGCTG	8924
rs377022909	snp	A/C	1.96408e-05	0.00313369	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28186565	TGAGCACCTGTAACA[A/C]ATGGTTCTCACCTTC	8924
rs377028850	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28160260	TACTCTCTTCAAAGC[C/T]GTCAGACAGGGACAT	8924
rs377030339	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28173791	GTGAGACCCTGTCTA[A/C]AAAAAAAAAAAAAAA	8924
rs377036417	snp	C/T	1.66037e-05	0.00288125	intron-variant	HERC2	GRCh38.p7	15:28233844	GCCACCCAGTGAGTC[C/T]TCACAAATCTTAAAC	8924
rs377042626	snp	C/G/T	9.89718e-05	0.00703404	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28228366	CAGGCTCGGTCCTGA[C/G/T]GGGTTCTCATTGGTG	8924
rs377054106	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28272005	GTTTCAAGCTTGGTT[C/T]TGTGCTGACAAGGAA	8924
rs377062883	snp	C/T	6.11129e-05	0.00552745	intron-variant	HERC2	GRCh38.p7	15:28124281	GGCACCAAAGGCACA[C/T]GGGGGCCAGTGTGGC	8924
rs377085389	snp	A/G	0.000153988	0.00877328	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274348	ACCTCCAGCCACACA[A/G]AGGACACGGTGCTCT	8924
rs377103198	snp	C/T	3.33456e-05	0.0040831	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28238624	ACTATTTCCTGTTAA[C/T]GACTGTGTCTGGAAG	8924
rs377109332	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28270270	AGATAGATAGATAGA[C/T]AGACAGACAGACATG	8924
rs377119782	snp	A/G	0.000153988	0.00877328	intron-variant	HERC2	GRCh38.p7	15:28191073	TAGGAAAAAATGGGT[A/G]AAGAATCAAACAAAG	8924
rs377126589	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28287303	CAGTTTGATTAAAGA[C/T]GGAGTGGCTCAAGAA	8924
rs377126782	snp	C/T	0.000153988	0.00877328	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28254452	TGCTTCTATGAAATG[C/T]TGAGGCATTCGCTTC	8924
rs377135355	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28134517	AGAGAAGTGGTGATA[C/G]CAGACATCCTTGCCT	8924
rs377143417	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28112197	AACGAGGAGCAATTA[A/C]TTCCTAGAACTTGGA	8924
rs377201728	snp	C/T	0.000153988	0.00877328	missense	HERC2	GRCh38.p7	15:28169527	GAATATGTGATAAGG[C/T]CTGCTGTTTGGCCAG	8924
rs377205872	snp	A/G	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28257931	CCTCATGATCTGCCC[A/G]CCTCAGCCTCCCAAA	8924
rs377209975	snp	A/G	1.67699e-05	0.00289563	intron-variant	HERC2	GRCh38.p7	15:28116986	CTGCCGGGGACACAG[A/G]TGCTCCAGCACGTGG	8924
rs377214876	snp	C/T	8.35108e-05	0.0064613	intron-variant	HERC2	GRCh38.p7	15:28198329	TACTAAGTACACATG[C/T]GTTAATGAAAAGTTA	8924
rs377215913	snp	C/T	0.000309952	0.0124451	intron-variant	HERC2	GRCh38.p7	15:28132639	TCCGGCCTCTGCACA[C/T]GGCGCCTCCTCACCA	8924
rs377223915	snp	A/T	0.000362976	0.0134669	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28198481	AATCTTGATGTGAGA[A/T]GAAGAACTTGGTGGA	8924
rs377229245	snp	C/T	3.61781e-05	0.00425297	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214305	GGAGAAGCTGCTGCA[C/T]CGCTCTTCACCAGGG	8924
rs377237258	snp	A/G	0.000422914	0.0145354	intron-variant	HERC2	GRCh38.p7	15:28230530	ATCATTCACTATAAA[A/G]ATCATACACTTAAAT	8924
rs377237386	snp	A/G	1.64765e-05	0.00287019	intron-variant	HERC2	GRCh38.p7	15:28114603	CAACAGAGACGGATG[A/G]CCACCAACCTATAGT	8924
rs377239649	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28289541	CCTCCCCAGCACGAT[A/G]GAGATACTCCTGGGA	8924
rs377243338	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28129870	CAACCTCCACCTCCC[A/G]GGTTCAAGTGATTCT	8924
rs377258956	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28202748	CCGCATTCACATGTG[C/T]GTTTTTCAATGAGTT	8924
rs377265260	snp	C/T	8.23974e-05	0.00641809	intron-variant	HERC2	GRCh38.p7	15:28121338	GGAGAGTAATCTCCA[C/T]GTGCTACCTGGATGC	8924
rs377274604	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28149248	AAACATCACCGAAAA[C/T]GGCCACACGAACACG	8924
rs377301345	snp	C/T	0.000214191	0.0103465	intron-variant	HERC2	GRCh38.p7	15:28167676	AAAGTTAAAGAAGAA[C/T]GCCTCTTCACCTCTT	8924
rs377314955	snp	A/G	0.000104244	0.00721882	intron-variant	HERC2	GRCh38.p7	15:28191921	CAAGGCAAAACCATC[A/G]GTGTGAAAGTGCCCG	8924
rs377317962	snp	A/G	0.000268297	0.0115791	intron-variant	HERC2	GRCh38.p7	15:28114834	GAAAGCCCATGTGTC[A/G]ACTCACGGCTCATCT	8924
rs377331698	snp	C/T	0.000157988	0.00888644	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28233264	AACAGCAGGTCTCAA[C/T]TCATTAAAGAGGAAT	8924
rs377342868	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28294107	ATTTCTGACACCAAA[C/T]GCATGGACTTTTGCA	8924
rs377349903	snp	A/G	1.65307e-05	0.0028749	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28229241	CAAAACATTTCGAAT[A/G]TTCTGTACAGCCCAA	8924
rs377382723	snp	A/C/T	6.62815e-05	0.00575647	intron-variant	HERC2	GRCh38.p7	15:28229426	TTGTTGCCATAGCTA[A/C/T]CTTAATTAAGAAAAA	8924
rs377384709	snp	C/T	3.30071e-05	0.00406232	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28260811	ATTCCCACTATGTGT[C/T]TGGTGTCCAGTCCTG	8924
rs377390750	snp	G/T	3.3399e-05	0.00408637	intron-variant	HERC2	GRCh38.p7	15:28146199	TCTACGGAGACACAG[G/T]TGGGTAGATCATGCC	8924
rs377395181	snp	C/T	0.000132133	0.00812706	intron-variant	HERC2	GRCh38.p7	15:28201571	TGCAAGAAATAAATA[C/T]ATTCAAACAAAAAAA	8924
rs377396895	snp	A/G	1.65326e-05	0.00287507	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28176983	TGTCGTATTATCCCC[A/G]TGTCCCAGCCGGCCG	8924
rs377405907	snp	A/G	8.31469e-05	0.00644721	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274936	GCGCAGGAAGGCAAA[A/G]GCAAAAGACAGCGCC	8924
rs377429184	snp	A/C	4.96726e-05	0.00498335	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28248724	TCTGGCTACAGTCTG[A/C]GAAGCAATGTTTCTA	8924
rs377451312	snp	C/T			intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28315983	TCTGCCCTGGACCTG[C/T]GACATTCTGGACTAT	8924
rs377454218	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28134235	TCTGGGAGAGGGTAT[A/T]CTAAGTGGTATTTTA	8924
rs377463561	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28281069	AAATTACCCAGCATG[C/T]ATGACTCATGAAGCA	8924
rs377475401	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28222691	TGGAGTCTGGATCTC[A/G]GGAGGGCTCTCCCAT	8924
rs377493236	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28161719	TGGCTCCGGTCCAGA[-/A]CATTTCCACAATGAC	8924
rs377528780	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28216364	CAATCCAAGTTTAAT[A/G]CATCTGCATTAACAA	8924
rs377528939	snp	A/G	6.65259e-05	0.00576702	intron-variant	HERC2	GRCh38.p7	15:28196428	AAAACCATTCGTCCC[A/G]AAGCAAATCTAGCAA	8924
rs377536344	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28240194	GAGGCCAAGGTGGGC[A/G]GATCACAAGGTCAGG	8924
rs377543692	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28166252	CCTTATGAATACAGA[C/T]GTAAAAATCTTCAAC	8924
rs377556840	snp	A/G	9.9005e-05	0.0070351	intron-variant	HERC2	GRCh38.p7	15:28201428	AATGAAAAACGGATC[A/G]AGGCTCCAGCTTAAG	8924
rs377563287	snp	A/G	3.31472e-05	0.00407093	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111752	TCATCTCACGAGGAC[A/G]TTTCCCCATCTTAGT	8924
rs377564364	snp	A/G	5.72328e-05	0.00534912	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28211006	TAAAAAGACACCTGT[A/G]TGAACAGTTCCAGTC	8924
rs377567998	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28293759	CTGCCAACTGGGAAG[C/T]ACTGCTATGCAGAGG	8924
rs377587657	snp	A/G	6.61244e-05	0.0057496	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28233719	ACCGACCTCTTCCAC[A/G]GGATGCTCGGGGGGA	8924
rs377588145	snp	A/G	1.69163e-05	0.00290824	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28233476	GACAACTCTACAAAC[A/G]TCCACCACTGACTTA	8924
rs377595702	snp	A/G	3.37012e-05	0.00410481	intron-variant	HERC2	GRCh38.p7	15:28212426	GCAGCTATTTCATCA[A/G]GAAGCACCATGTACT	8924
rs377596158	snp	A/G	0.000171736	0.0092649	intron-variant	HERC2	GRCh38.p7	15:28182361	GGTGTGGCTGCTGCC[A/G]AGTGCCCCACCCTGC	8924
rs377603097	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28247962	GATGGAGGGCCAGCC[A/G]CTGCCCTGGATGCTG	8924
rs377604195	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28189744	ATTTGATCATTCCAC[A/G]AAGTATACATGTAAC	8924
rs377604299	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28279417	AAAACAAAATAAAAC[A/G]TATACAACGTTCAGA	8924
rs377605106	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28236416	CTACCTCAGCCTCCC[A/G]AGTAACTGGGATTAC	8924
rs377609546	snp	C/T	0.00102315	0.0225949	synonymous-codon	HERC2	GRCh38.p7	15:28163148	GAGCACATCCCTGCC[C/T]CTGTCCCCGGCCCGG	8924
rs377611083	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28161795	AAGCTGTAATAGTTA[A/G]AATACCATAGTATCA	8924
rs377613646	snp	A/G	0.000214195	0.0103466	intron-variant	HERC2	GRCh38.p7	15:28130499	CAAACAGAATCTTGC[A/G]TACCAGGTATAAACA	8924
rs377614550	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28121284	TCTCGTCCCAGCCCA[C/G]GTACCCACGAAAGCA	8924
rs377636465	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28143594	TGGGACTACAGGTGC[C/T]CACCACCACGCCCAT	8924
rs377647927	snp	C/T			intron-variant, downstream-variant-500B	HERC2, LOC107987422	GRCh38.p7	15:28312373	GCGTGGTGGCCCACG[C/T]CGTAATCCCAGAGCT	8924
rs377653565	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28240412	GAAAGAGCGAGACTC[C/T]GTCTAAAAACAAAAA	8924
rs377654679	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28273962	ACCAAGCACCACTCC[A/G]CACTCAGAACAGCAG	8924
rs377658258	in-del	-/TT			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28320916	CAACTGAACTAACTC[-/TT]GTCTCTCCAGAAACA	8924
rs377658274	snp	C/T	0.000335396	0.0129455	intron-variant	HERC2	GRCh38.p7	15:28176937	TGCAAGCAACAAAAA[C/T]GCGTATAATCACCAT	8924
rs377661664	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28216940	TTTACCCACACACTT[G/T]CTCACTTTGCACTCA	8924
rs377663104	snp	A/C/G	0.000999794	0.022339	intron-variant	HERC2	GRCh38.p7	15:28124980	ACTTTGCTTGCCCCC[A/C/G]ACCCACCCAACCTGC	8924
rs377666529	snp	A/C	0.000253846	0.0112632	missense	HERC2	GRCh38.p7	15:28142830	GTGAAACATTACCTT[A/C]AAGAATGGGCTGTGG	8924
rs377680353	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28149263	TGGCCACACGAACAC[A/G]TGTTCTAGTAAAATT	8924
rs377685479	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28200053	GTCATTAAGGTAAAA[G/T]CAGGTCATAAGAGTG	8924
rs377689868	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28145135	GCCTCCAGGTGTCCA[C/G]CACACACCAGGCCAG	8924
rs377718130	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28259155	GCTGGAGTGCAATGG[A/C]GCCATCCCGGCTCAC	8924
rs377723464	in-del	-/C			intron-variant	HERC2	GRCh38.p7	15:28287719	ATTATACTTATTCCT[-/C]TTTTTTTTTTTTTTT	8924
rs377739906	in-del	-/T			intron-variant	HERC2	GRCh38.p7	15:28141241	AAAACTGTCTTAAAC[-/T]TTTTTTTTTTTTAAT	8924
rs386382557	in-del	-/TT			intron-variant	HERC2	GRCh38.p7	15:28129796	TTTTTTTTTTTTTTT[-/TT]TGAGACAGTCTTGCT	8924
rs386782468	multinucleotide-polymorphism	AT/GC			intron-variant	HERC2	GRCh38.p7	15:28122405	GGTCCCTCAGTGGAG[AT/GC]TGAGCCCTTGCCCAG	8924
rs386782469	multinucleotide-polymorphism	ACG/GCA			intron-variant	HERC2	GRCh38.p7	15:28136321	TTCAAACGTGCTGCT[ACG/GCA]CTGACATAATATAAG	8924
rs386782470	multinucleotide-polymorphism	CA/TG			intron-variant	HERC2	GRCh38.p7	15:28136390	ACTCAGGTGGATAAA[CA/TG]AGCCCCACCCCCAAA	8924
rs386782471	multinucleotide-polymorphism	AAC/GAT			intron-variant	HERC2	GRCh38.p7	15:28146411	AAGTAGAAACAGTGA[AAC/GAT]TAAAACCACATTTAA	8924
rs386782472	multinucleotide-polymorphism	CA/TC			intron-variant	HERC2	GRCh38.p7	15:28146612	CTTTCCTACTGCAAC[CA/TC]CACTCCCCTGATCAA	8924
rs386782473	multinucleotide-polymorphism	CT/TC			intron-variant	HERC2	GRCh38.p7	15:28147814	GCCCAGCTGGGAGGA[CT/TC]GCTTGAGCCCAGGAG	8924
rs386782474	multinucleotide-polymorphism	GC/TT			intron-variant	HERC2	GRCh38.p7	15:28160489	ATCTCAGGCTGCTGT[GC/TT]TAGCAATGAGCGAGG	8924
rs386782475	multinucleotide-polymorphism	AGT/GGC			intron-variant	HERC2	GRCh38.p7	15:28171057	GCCATTCTGGAAAAC[AGT/GGC]TTGGCAGTTTCTTAT	8924
rs386782476	in-del	AC/T			intron-variant	HERC2	GRCh38.p7	15:28185203	ATAACCTGATTTATT[AC/T]CAGAACTACTACCCC	8924
rs386782477	multinucleotide-polymorphism	GC/TT			intron-variant	HERC2	GRCh38.p7	15:28185292	CTCATGTCACACGCT[GC/TT]AGAGTACTTAGAGCA	8924
rs386782478	multinucleotide-polymorphism	ATC/TTT			intron-variant	HERC2	GRCh38.p7	15:28236269	CTTATTATTATTATT[ATC/TTT]ATCATCATCAGCTGT	8924
rs386782479	multinucleotide-polymorphism	CT/GC			intron-variant	HERC2	GRCh38.p7	15:28269134	ATACAATAAACAGAA[CT/GC]TTGTCAATCTTCAGA	8924
rs386782480	multinucleotide-polymorphism	CA/TG			intron-variant	HERC2	GRCh38.p7	15:28272548	TCACTGAATTGACAC[CA/TG]AGACTTTAGCACAAG	8924
rs386782481	in-del	AGT/GA			intron-variant	HERC2	GRCh38.p7	15:28272626	GCACATTTACATGAA[AGT/GA]TCTAGGATCTTAAAT	8924
rs386782482	multinucleotide-polymorphism	AAC/GAG			intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314769	CGGAGTCTGAGGCAG[AAC/GAG]AATTGCTTAAACCCA	8924
rs386782483	multinucleotide-polymorphism	AA/TC			intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318590	ATGGCACCACTGCAC[AA/TC]CAGCCTGGGAGACAG	8924
rs397518474	snp	C/T			missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265707	AGGACGAGGCCATTC[C/T]GATGCTGGTAGCCGG	8924
rs397779106	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28136124	CCACAAGGGAAAAAA[-/A]CACCTTTTTTTTTTT	8924
rs397783208	in-del	-/T	0	0	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174354	AGATTTTTCTGTAGG[-/T]TTACAGCAACCTTAT	8924
rs397854007	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28225697	GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	8924
rs397938411	in-del	-/C			intron-variant	HERC2	GRCh38.p7	15:28257458	CCATTTCACTAGCCC[-/C]ATCTCATTTGGCCAT	8924
rs397961726	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28232565	GAAAAAAAAAAAAAA[-/A]GAATATAATCAGAAA	8924
rs398026680	in-del	-/A	0	0	intron-variant	HERC2	GRCh38.p7	15:28115280	CCACCTTTGAGTAGC[-/A]AAAAAAAAAAAAAAA	8924
rs398026683	in-del	-/T	0	0	intron-variant	HERC2	GRCh38.p7	15:28292253	AAATACTTTGCCTGG[-/T]TTTTTTTTTTTTTTT	8924
rs398026684	in-del	-/T	0	0	intron-variant	HERC2	GRCh38.p7	15:28293511	TGTTATATTGGTTTC[-/T]TTTTTTTTTTTTTTT	8924
rs398026685	in-del	-/A	0	0	intron-variant	HERC2	GRCh38.p7	15:28296084	GGGTGTTAGGGAGAT[-/A]ATTTTGACATTCAAT	8924
rs398099693	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28227282	TCCGTCTCAAAAAAA[-/A]GTAAAATAAACAATA	8924
rs527242204	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28131023	GGATGGCCAAAAGCA[C/T]TGGGCCCCACCCACC	8924
rs527257387	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28260528	CCAGGGCAATCAGGC[C/T]GGGAAAAGACATAAA	8924
rs527290788	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28254023	GAGTGGTGGGTGATG[C/T]CTGTAATCCCAACAC	8924
rs527308646	snp	A/G	3.54051e-05	0.00420729	synonymous-codon	HERC2	GRCh38.p7	15:28113080	GCCTACCTGGATGAC[A/G]AAGTCTCGGCCCCGG	8924
rs527310472	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28131602	GAGTGGAGCAGAGCC[A/G]CCGACCCCACCAGGA	8924
rs527311057	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28253049	CTATGTGTAGAAACT[A/G]AAACCAGGAGCCCAA	8924
rs527341879	snp	A/G	0.0154538	0.0865337	intron-variant	HERC2	GRCh38.p7	15:28173967	GTGTATGAGTTCATT[A/G]TCTTTGATTGTGCTG	8924
rs527355954	snp	C/G	1.66172e-05	0.00288242	intron-variant	HERC2	GRCh38.p7	15:28167855	TGCACAGTAGGGGAA[C/G]TTTAAGTGGAAAAAC	8924
rs527374113	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28254578	AGGTGTGAAGACACA[C/T]AGGCTGGCTGAGCCC	8924
rs527378149	snp	C/T	1.66651e-05	0.00288657	intron-variant	HERC2	GRCh38.p7	15:28248740	GAAGCAATGTTTCTA[C/T]ACAGGAAAGAAGAGG	8924
rs527383549	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28287898	CCAGCTAATTTTTTT[C/G]TATCTTTAGTAGAGA	8924
rs527384826	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28293362	GCCAGCCGTGGTGGC[A/G]GGCGCCTGTAGTCCC	8924
rs527403760	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28161606	CTACTAGCCACATGT[A/G]CCTCAAGTTGAGTGT	8924
rs527409855	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28249307	GGTGCCGAGGGCTCA[C/G]GGAGTCCAGGAAGGA	8924
rs527412710	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28241563	GCAGTGGCTCCCTCC[C/T]GTAATCCCATCACTT	8924
rs527415945	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28132349	CTGCCATTCTTTTTT[A/T]ATGGGGGTACCTGTT	8924
rs527416867	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28212201	GATAAAGGGTGACAC[A/G]GAGAAGAGGGTGTGA	8924
rs527475683	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28118249	TGCCCTATGTCACGG[C/T]GGCTGTGTGAGAGGA	8924
rs527491287	in-del	-/T	0.491732	0.0637633	intron-variant	HERC2	GRCh38.p7	15:28115262	AAAATAGATGGTCTA[-/T]TTTTTTTTTTTTTTT	8924
rs527491524	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28200825	TACTCACTGACATAT[A/G]TACAGGTGAAATGAG	8924
rs527499433	snp	A/C/G/T	6.60913e-05	0.00574824	synonymous-codon, missense	HERC2	GRCh38.p7	15:28113200	CTCCCAGAACCACTG[A/C/G/T]ATCAGCGATGCGGAA	8924
rs527515162	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28162166	GAAACCCCATCTCAA[C/G]TAAAAATACAAAAAT	8924
rs527515209	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28155452	GACTTTTTAACGATC[A/G]CCATTCTAACTGGTG	8924
rs527561706	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28194814	TAACCCCAGCACTTT[A/G]GGAGACTGAGGTGGG	8924
rs527573367	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318238	AAAAATAAAAAGTGA[C/T]GTGACTGACACCTCT	8924
rs527574482	snp	A/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28156004	AGTTTTCCCAGCACC[A/G]TTTGTTGAATAGGGA	8924
rs527584008	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28142614	CAAGTGACAAGAACA[C/G]CTGTGCATCTCAAGG	8924
rs527592753	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28156384	ACGATTTCCTATCCA[C/T]GAGCATGGAATGTTA	8924
rs527604154	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28150045	AACACACGTGACTTC[C/T]AACCAAGAACATCAC	8924
rs527607486	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28282681	GCTCACAGCTGTAAT[A/C]CCAGCACTTTCGGAG	8924
rs527612728	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318469	CTGTCTCTACTAAAA[G/T]TACACAAAATTAGCC	8924
rs527615381	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28139541	GAGGACGGAGCTATG[C/T]TGCATCCAGAGTCCT	8924
rs527619883	in-del	-/TTCACTCACCAC			intron-variant	HERC2	GRCh38.p7	15:28180055	GTCCTGGCCTTCACG[-/TTCACTCACCAC]TCTCTCACTGACTCG	8924
rs527622847	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28236849	TGCCACAACCTCCCA[A/C]ACTGCTGGGATTACA	8924
rs527625588	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28229911	AAACTGTGCTCTAAA[A/G]GTTATTCAAGTAAAA	8924
rs527648604	snp	A/C			missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28263029	CATCTTTCGTCAAAG[A/C]AATGGAAAACTGACT	8924
rs527693265	snp	G/T	8.88297e-05	0.00666385	intron-variant	HERC2	GRCh38.p7	15:28206228	AAAACTGTCAAGGCT[G/T]CATGGCTGTACCTCA	8924
rs527702609	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28175088	AAAATTGAATATCCA[C/T]AAGCCAGTCATAGCG	8924
rs527721933	snp	C/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28287141	GAAGCTTTAGTCAAA[C/T]ATATCTAAGCAAAAG	8924
rs527736761	snp	A/G	0.000597312	0.0172713	intron-variant	HERC2	GRCh38.p7	15:28117296	CCTGCTTGTGTGGAC[A/G]CCAGGCAGACCCTGC	8924
rs527737694	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28235162	TTTACTGGACATTTA[G/T]ATTTTAGAGCACTCA	8924
rs527738539	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28112069	AAGTGATTAGAAATT[C/G]AGTACGGCTGCAGTT	8924
rs527741176	snp	A/G	0.000115307	0.00759211	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213832	GGTGATGCGAGTCAC[A/G]GTGCCTTCTCCAAAC	8924
rs527786706	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28153787	TTACTTCCTAGTGAG[A/G]AAAGTTGGCCTCGGA	8924
rs527797268	snp	G/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28154447	GCCGTATCCTTATTC[G/T]TGTCTCTCCTGGAAC	8924
rs527809807	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317350	CTCCTCGGCCTCCCA[A/G]AGTGCTGTGATTACA	8924
rs527811202	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28280732	CAACATGGTGAAACC[C/G]CTTCTCTACTAAAAA	8924
rs527812191	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28199623	AGGTCTAGATGATGA[C/T]GCTAATGCCTACTGG	8924
rs527835368	in-del	-/AGTT	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28220830	CTCCCACCAGACCTC[-/AGTT]AGGAGGGTGCGTGCC	8924
rs527838569	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28273624	ATGCCTTCACCAGCC[A/G]GCTCAGGAAGTGGAC	8924
rs527859388	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28284904	CCTGGGCAAAAGGAG[A/C]GAAACTCCGTCTCGG	8924
rs527896936	snp	A/G	0.00119737	0.0244387	intron-variant, utr-variant-5-prime	HERC2, LOC107987422	GRCh38.p7	15:28317707	AACAGTTCTGCATAG[A/G]AAATTGTAGTAGTAG	8924
rs527910284	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28240335	AGGCAGGAGAATGGC[A/G]TGAACCTGGGAGACA	8924
rs527935950	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28312009	AGGAAGAGGATAGGC[C/G]AGACCTTGTCTTTCT	8924
rs527942699	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28228879	CCTCCACAAAACCAA[A/T]CCAATCAACTCTCTG	8924
rs527942950	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28306444	TCATGATGAATGATG[C/T]TTTTAATGTGTTGTT	8924
rs527947101	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28282004	CCTGCTTATTCCGTC[A/G]CAATCCTGACTGCCC	8924
rs527960090	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28143712	CAGCCTCCCAAAGTG[C/G]TGGCATTACACGCAT	8924
rs527963671	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28259877	GGAGGCTGACGCAGG[A/C]GAATTGCGTGAACCC	8924
rs527964692	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28222816	TATGCGCCAGGAAGG[G/T]GGTGCCCGTGTGATC	8924
rs528026178	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28223112	GGAGACCCCTGACAA[C/T]TGGTGCCCTGGGTGG	8924
rs528035863	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28216991	CCCATTCACTGACAC[A/C]AGCAAAATGCTCACA	8924
rs528037539	snp	A/G			intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313401	AGCCTGGATGGTCTC[A/G]ACCTCCTGACCTTGT	8924
rs528042076	snp	C/G	5.11409e-05	0.00505646	intron-variant	HERC2	GRCh38.p7	15:28270648	TGAGAACCTACAAGT[C/G]GTACTAGCTACAAAA	8924
rs528050438	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28189081	GACAGAGTGAGACTC[A/G]GTCTCAAAAAAAAGA	8924
rs528059866	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28308464	GTGGAGTCTTTAGGT[C/T]TTTCCAAATATAAGA	8924
rs528064744	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28283717	TATAACATTGTCATA[C/T]GTGGTTATCAATGTA	8924
rs528066524	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28289872	CCGCAGTGAAAGGAC[A/G]ACACATCTGAGAGGA	8924
rs528072742	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28209102	GGTCACTATTTCACT[A/C]AACAGATAACTATGG	8924
rs528075333	snp	C/T	4.06793e-05	0.00450977	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28202197	TGCATCTGAGAGCTC[C/T]GTGACCTGTATGTCG	8924
rs528077280	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28136449	GCTCTCTGGTGCACA[C/G]GGTGCAGGGTAATGC	8924
rs528077459	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28319147	CACCATTCATTCCTT[A/G]TGTTTAACAACCAAT	8924
rs528081351	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28196008	AGCCTAGTTATTCTA[A/C]TTCTTCCCCGACACC	8924
rs528085835	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28202784	AACATGTTAGAAAAT[C/G]ACAAAGCCAAGTTTC	8924
rs528092918	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28120767	GACCCACTCCACTTC[G/T]CAGAACTTAACAAAA	8924
rs528094088	snp	C/T	0.000115318	0.00759249	synonymous-codon	HERC2	GRCh38.p7	15:28114623	CAACCTATAGTTTAT[C/T]GCCAGCCGCACGTAC	8924
rs528115265	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28284432	ATGTAAACAGTCTAA[A/G]TGCATCAATTAAAAG	8924
rs528120031	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28276221	AAAAAAAAAAAAGAG[C/G]GTTGTTATAGAAGGA	8924
rs528130997	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28231498	TGCGTATGTGACTGG[C/T]CCCCAACAAAATCTC	8924
rs528143562	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28190255	CGATCTCCTGAGCTC[A/G]TGATCTGCCCGCCTC	8924
rs528144828	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28238439	TCAAAGGAAATTCTT[C/T]AAATGTGCTGAATTT	8924
rs528201919	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28151690	TGTCTAGAAACAGGA[A/T]AATCTCAGCTTCAAC	8924
rs528249987	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28225987	AAGCTTAGCTGGTCA[A/G]CTCTACCAAAGATTT	8924
rs528263566	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28146954	CAGGTCCTCTCTTAC[A/G]GTTACAGGGTTGACA	8924
rs528273761	snp	A/T	0.000369104	0.01358	intron-variant	HERC2	GRCh38.p7	15:28190919	CCAAGTCACCTCCCT[A/T]GTCATCTGTAAATCA	8924
rs528285477	snp	C/G	0.000399281	0.0141238	intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28315585	GGATCACGAGCTCAG[C/G]AGTTCAAGACCAGCC	8924
rs528324523	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28237741	TTCGTGAATACATAG[G/T]AAGGACATATTTCTA	8924
rs528336403	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28226698	TGTATTTGGAAATGG[C/T]TTTTTGGATACGATA	8924
rs528337899	snp	A/G	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28184811	AGCTTGCAGTGAGCC[A/G]AGATTGCACCACTGC	8924
rs528345596	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28271427	CAGCACTTTGGGAGG[C/G]CCAGGCAGGCGCAGG	8924
rs528349178	in-del	-/G	0.000481548	0.0155094	intron-variant, utr-variant-5-prime, upstream-variant-2KB	HERC2	GRCh38.p7	15:28213726	TCATGCAGTAACTAA[-/G]CACAAGTTCACCTAC	8924
rs528352060	snp	G/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28176347	GTCACAATCACGCCG[G/T]GTGAGCCTGGGGCGA	8924
rs528374043	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28140405	TCATTTAGAGACTAC[A/G]GCACTCTATAAAGAA	8924
rs528413378	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28273673	ACGCCAAAGGCCTCC[C/T]GCTGGCTGCAAGAAG	8924
rs528413944	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28177223	CACATGTAGTCAACA[A/C]AGGATCCACAGATCA	8924
rs528416260	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28220343	GACAGAGCGCCAGCT[A/G]CAGGTGCGTCCTGAC	8924
rs528423773	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28303691	CATGAACACGGAGTA[C/T]CTTTTCCTTTTTTGT	8924
rs528430301	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28268792	CCAGCAGCAACAGAA[C/T]AGCGGGCAGCCTCCA	8924
rs528455757	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28150294	GAACATCACTGAGGA[C/T]GGCCACACGAATGTA	8924
rs528471191	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28230621	AACATCTGAACAACA[C/T]TATAAATTGCAATGC	8924
rs528478599	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28195322	AAAAGTTAGCTGAGC[A/G]TGGTGGCTCAGGCCT	8924
rs528489578	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28113985	CAAGAGGGGAAACAC[A/T]TGTGCATCCGCCCCA	8924
rs528493895	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313975	GCTGGAACCTCAAAG[C/G]GCCACACACCAGAAA	8924
rs528510442	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28182267	GACGCTTCTGAGGGG[C/T]AATTTGATAATGTCT	8924
rs528531913	snp	A/G	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28307902	TCTCTATTCTGTTCC[A/G]TTGGTCTGTGTCTGT	8924
rs528534281	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28182804	TCTTTCATCTTAAAT[A/G]CCAACGTGAACATGG	8924
rs528554281	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28262489	TCACCCACCAAGGAT[G/T]AGTTCACATGAGGGT	8924
rs528560595	snp	A/C	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28224702	AAAAGAGCAGAATAC[A/C]CATTCTTCTCAAGTA	8924
rs528568240	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28145314	GCTGCTGTGGACAGG[A/G]GCGGTGGTGTACTAC	8924
rs528569835	in-del	-/C	0.00159617	0.0282053	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321154	AGTTTCGTGCACTTG[-/C]CAAGAAACTAATTAA	8924
rs528606423	snp	A/G	0.00993419	0.0697739	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28300064	TGTTAAAAAAAAAAA[A/G]AAAAGAAAAGAAAAG	8924
rs528625234	snp	A/T	0.000459794	0.0151554	intron-variant	HERC2	GRCh38.p7	15:28218682	GGCTTCTAAAAAAAA[A/T]AATCAAAATTACAAA	8924
rs528637315	snp	C/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28212939	TAGTCAGGCCAGGCA[C/T]GGTGGCTCACGCCTG	8924
rs528641377	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28255330	CAGAGCAAGACGCTG[A/T]CTCAAAAAAAAAGAA	8924
rs528641967	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28232754	ATTCTCCATGTATCA[A/G]AATACTCAATATTTC	8924
rs528642321	snp	C/T	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28139245	AGAATAGGGCAAGAA[C/T]TGGAGTGTGGTCACT	8924
rs528644618	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28175177	AATGAGGCATGGATC[C/G]CTCCTCGCCAGTTAC	8924
rs528656290	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28139760	TCCAACTGGCTATAC[C/T]AATCCATTAGAAAAC	8924
rs528656305	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28133199	CATCTGGCCCTATAA[A/G]GAAAGTTTGCACCTC	8924
rs528682119	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28126187	AGGGAACACTTATAC[C/T]GCTGGTGGGAACAGA	8924
rs528716484	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28134036	ATCTTGATTGGGAAG[A/G]TGTTGAATCTATAGA	8924
rs528723200	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28227418	AAATCAAAATCACAA[C/T]GAGACACCACTTCAC	8924
rs528723510	snp	A/C	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28294516	TTGGTAAAATCAAGA[A/C]GGCCTCAAATAGCCT	8924
rs528739135	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28162878	CCTGGGCGACAGAGC[A/G]AGACTCCGTCTCAAA	8924
rs528740459	snp	C/T	0.00113343	0.0237788	intron-variant	HERC2	GRCh38.p7	15:28169679	GGAAAATAAAATTTG[C/T]ATTGTTTTTAAAATC	8924
rs528772813	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28157990	TTTCTGCCTTCGTTA[C/T]GTACCCACTAGTCAT	8924
rs528782041	snp	A/G	0.0115144	0.0749975	intron-variant	HERC2	GRCh38.p7	15:28289611	GAGACTGGCTTCTCT[A/G]TAAATAAATGACTGG	8924
rs528783861	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28250498	GCCATAATCAAAACG[G/T]GTAATTCTGATGGGG	8924
rs528796946	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28208738	GGTCCACCACCAGCA[A/G]AGTGCTTGTCTGCTG	8924
rs528807801	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28200104	TAGGGTCTTTATAAG[A/C]AGAGACTCCAGGATG	8924
rs528812675	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28154180	ACATTTTTAATCCAG[-/A]AAAAAATAAAACTCT	8924
rs528819609	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28272809	TGCTGCGGTCACAAA[C/T]GATTCAGTGAAACAC	8924
rs528831757	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28149033	GAACGGCCGCACAAA[C/T]GTACATTCTAGTAAA	8924
rs528854635	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28142470	TTCTGTGGCTCCTTC[C/T]GCAGGACCTCCTATT	8924
rs528864870	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28186452	AACAACTGTAATTTA[C/T]CAATCGTGTGGACAT	8924
rs528865373	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28192734	GCTGCTGTTCCCTGA[C/T]GGCATCACCAGGTTC	8924
rs528913711	snp	A/C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28178556	TCAGAGGCCTAGCAC[A/C/G]GTGCCTCCAAAATAA	8924
rs528929209	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28186929	ACATCTGAGTAATGT[C/T]TACTTCAAAAGAAGT	8924
rs528934685	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28305958	GCCATCAGAGAAATG[C/G]AAATCAAAACCACTA	8924
rs528942423	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28266942	ACCGACATTTATATG[C/T]ATTTGTTAAATGAAT	8924
rs528969974	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28259048	ACAGGTCACCTGAAT[A/G]CTTCTATATCTGTTA	8924
rs528972218	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28172887	ACTTGTAACCCAGAA[C/T]ATATAAGAAACTCTC	8924
rs528974619	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28179521	TACATATCAACAATC[C/T]CTAATACCTCACCAT	8924
rs529017261	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28306321	TTCAGCATGAATTTA[A/T]ATGATCATATGGTTT	8924
rs529020183	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28184727	ATTAGCCGGGCATGG[C/T]GGCGTGCACCTGTAG	8924
rs529045200	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28222684	CCTCGGCTGGAGTCT[A/G]GATCTCAGGAGGGCT	8924
rs529054962	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28298447	GGCATGATCCACCAC[A/G]CCCGATCCCCATGTA	8924
rs529058295	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28216919	GATTACTCACCCACT[C/T]ACACCTTTACCCACA	8924
rs529059600	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28252953	TCCCATGAATAGGCC[A/G]GCTGAGAGCTGTGGC	8924
rs529060283	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28130051	GTGCTGGGGCAACAG[A/G]AGTGAGCCACCACAC	8924
rs529062667	snp	A/G	0.00716266	0.059414	intron-variant	HERC2	GRCh38.p7	15:28173704	GCTATTTGGGAGGCT[A/G]AGGTGGAAGGATCAC	8924
rs529116129	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28166477	TGAGAGGGCCTAACC[A/G]AAGACACTCAGTAAC	8924
rs529119933	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28292015	GGTGGATCACCTGAG[G/T]TCAGGAGTTCAAGAC	8924
rs529123723	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28130790	CCGTGACTGACAGCA[C/T]ACCCGTTGGCACACT	8924
rs529145744	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28210424	TACAGGCATGAGCCA[C/T]TGTGCCCGGCTGGTG	8924
rs529147368	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28171797	CCTATACAATAGACC[A/G]GGTGCGGTGACTCAC	8924
rs529160483	in-del	-/TC	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28268002	CATTTATAACAACTT[-/TC]TGTTTCATTTGTTCT	8924
rs529168961	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28167299	GAAAAGAATTCTGCA[C/T]CGTTCCTGTGGTGTC	8924
rs529205462	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28240211	ATCACAAGGTCAGGA[A/G]ATGGAGACCATCCTG	8924
rs529205569	snp	C/T	0.000798403	0.0199641	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28206330	GATCATGGGGGGCTG[C/T]GGCCCTTCAGGAGAC	8924
rs529242248	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28179689	CAGAAGGCACTGCTG[C/T]CACAGGAAAGGACAG	8924
rs529243703	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28123976	CAGTATAGGAATTCT[A/G]TTGGGTTACATGTAC	8924
rs529245248	snp	A/G	1.71202e-05	0.00292572	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214828	AAAATTTATAACGAC[A/G]AGCATTAAAAAAAAT	8924
rs529259854	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28275224	ATCAAAGAAATGTAT[A/G]AGGAATTTTAAATGT	8924
rs529271674	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28128305	AGTGTGAACTGGCTG[A/G]CAGGACGAGCCTCCC	8924
rs529279718	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28175756	TTCACAGCCAGCTCA[A/G]TGACATCACACACAG	8924
rs529286148	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28295866	GCTACTCTGGCACTA[C/T]AGCTGCAAGGTCCCA	8924
rs529292974	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28215227	AAGTGAAAATTTTGA[A/G]ATTCATTATTTTACA	8924
rs529308048	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28209638	ATGAGCCACCGCGCC[A/C]GGCCTATATATCATT	8924
rs529312329	snp	C/T	0.00835141	0.0640778	intron-variant	HERC2	GRCh38.p7	15:28238040	CAGTACTTCTAGATC[C/T]AAATATTCCTATCAC	8924
rs529318307	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28171614	AAAAACAAAATATTT[A/G]TATGACAAGATGAAG	8924
rs529343372	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28245684	ACACATACATAAACA[C/T]ACATATATTTGGTTA	8924
rs529344035	in-del	-/TTC	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28115797	CCACACAGTGGCCAA[-/TTC]TTCTTCTTATGACAG	8924
rs529345766	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28275739	AGTGAGCCAAGATCG[C/T]GCCACTGCACTCCAG	8924
rs529362813	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28172052	TGCACTCCAGCCTGG[C/T]GACAGAGCGAGACTC	8924
rs529374818	snp	A/C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28290411	ATTTTTGTATGTTTC[A/C/G]TAGAGACAGGGTTTC	8924
rs529375922	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28246350	TTGATATGTTTATCA[C/T]CAGGGAAAAAACACT	8924
rs529387911	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28165684	TGGTGGTGCATGCTT[A/G]TAGTTCCAGCTACTT	8924
rs529400388	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28224748	TCTTAGACTGACCAG[A/G]CCATATGTTAGGCCA	8924
rs529404162	snp	A/G	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28210107	GCTGGGATTACAGGC[A/G]GCCACCACTATGCCC	8924
rs529407730	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28290856	TTTGAACACTTGTTA[C/G]AAAAGACAAAAAATC	8924
rs529439766	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28203965	GTGACGCCCAGAAGA[G/T]ATTCTAAATCCTTGA	8924
rs529453407	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28307845	TCTTGGTACCTTTGT[C/T]GAAAATGAGTTCACC	8924
rs529462070	snp	A/C	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28239810	CTCCAAAATAACCAA[A/C]CTGCTTCTTTGAAAA	8924
rs529466987	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28115916	CGAGGACACCCTGCA[C/T]ACCCTCAGTGGGACA	8924
rs529479316	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28285853	TAGTGATGAAACGGA[C/T]TCTAAAGATACCAAA	8924
rs529480306	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28116265	GTTGCCCAGGCTGGA[C/G]TGCAATGGTACGATC	8924
rs529490700	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28286329	AGACAGTACAAAGTA[C/G]AGAACAATATATATA	8924
rs529491724	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28306133	GGTGACAGTGGGCAT[A/C]CGTGTCTTGTTCCAG	8924
rs529516745	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28198210	ATTGTTTCACTGCAG[G/T]TGAGTTCCTCTGTGG	8924
rs529561397	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28192231	GAATATTACATAGTA[A/C]GGAGCTTCTTAAAGA	8924
rs529573956	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28279947	ATACAAAAAGGGAAA[A/G]CAAGAATAAATTTCA	8924
rs529574107	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28125459	CCAGGCCTCTTCTAG[C/T]GAGAGACACACAACT	8924
rs529582799	snp	A/G	1.66012e-05	0.00288103	intron-variant	HERC2	GRCh38.p7	15:28198595	CTGAACAAAGAATGT[A/G]CTCACCTATAAGTTC	8924
rs529594488	in-del	-/AAAAAG	0.046775	0.145601	intron-variant	HERC2	GRCh38.p7	15:28228140	GCTTTAAAAAAAAAA[-/AAAAAG]AAAAGAAAAGAAAAG	8924
rs529600779	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28148721	AACATCACCGAGAAC[A/G]GCTGCATGAACGCGC	8924
rs529602580	snp	C/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28235050	ACTGCTTATGGCAAC[C/T]TGAGGGAGTGCACCA	8924
rs529605361	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28132442	CTATTTGAACTACAT[A/G]CATCTAAACCGCAGG	8924
rs529618006	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28212243	CTTCAAGTGTGGCTC[C/T]GAACATGGCGACAAA	8924
rs529628117	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28121443	TCCTAAAACACATCA[A/G]ACAGACAAAATTTAG	8924
rs529631889	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28254645	AATGCACACACCTAC[A/C]CACAGGCCCCCATCT	8924
rs529635315	snp	A/C	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28227461	GGCCTTCATCCAAAA[A/C]AAAAAAGAAAAAAAA	8924
rs529636806	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28159702	TTAGCTCGGAGAAGT[C/T]TGATCGTCTGAAGCC	8924
rs529641658	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28310262	ACCAGCCTGAACAAC[A/G]TGGCAAAACCACATT	8924
rs529668857	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28249350	GTGCCCAAAGAGCAC[A/G]GCAGCGAAGAAAGTA	8924
rs529669637	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299926	GGCGTGGTGGCGGGC[A/G]CCTGTAATCCCAGCT	8924
rs529673642	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28151883	CAAACAGCACCTTGA[A/G]CAACTAACTACAGGA	8924
rs529677095	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28207443	GCCTGACCTACACAC[A/T]CTCTTTCGTGTTCAC	8924
rs529682767	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28164898	GGCACCTAATTCATA[A/G]ATAGAGGCTTTCTTA	8924
rs529704684	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28255123	GGGGGATCACTGGAG[C/T]CCAGGAGTTCGAGAC	8924
rs529710964	snp	A/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28212704	CCCGTAAGCCTTTTA[A/T]AGCTGAGAATAATCA	8924
rs529722206	snp	C/T	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28206561	ACTCTAGGTTGGGTG[C/T]GGTGGCTCACGCGTG	8924
rs529746775	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28162216	ATGCCTGTAATCCCA[A/G]CTACTCAGGAAGCTG	8924
rs529756781	snp	A/G	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28156120	CTGTTCCATTGGTCT[A/G]TATCTCTGTTTTGGT	8924
rs529771447	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28242974	GAAATCTGGAAAGCT[C/T]TTTCTCTGCTACTAA	8924
rs529780777	snp	C/T	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28288441	TGAGCCAGAATCGTT[C/T]GAACCCAGGAGGGAG	8924
rs529794639	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28249805	GGCACACGCCACCAC[A/G]CCAAGCTAACTTTTT	8924
rs529802652	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28162833	GAGGCAGAGCTTGCA[C/G]TGAGTCGAGATGGCG	8924
rs529807535	snp	C/T	1.65127e-05	0.00287334	intron-variant	HERC2	GRCh38.p7	15:28202312	TGAAGCGGGAACCCA[C/T]ACATACACAAGCAGA	8924
rs529820193	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28191589	CGAGGTGCCTCCACG[C/T]GTTGGTGTAATCACA	8924
rs529827144	snp	A/G			missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28246058	CTACTAGTTCTGGAA[A/G]GAGAACACCTACATT	8924
rs529828148	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28113741	TTTATGCTGCTCACA[C/T]CAAGCCTTGGCATGC	8924
rs529829188	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28232824	TAAATGTTCCCATTA[C/T]ATCTCATTACCAGGA	8924
rs529847113	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28195878	AAATACAATAAAAGG[C/T]ATATAAATTAAAAAA	8924
rs529851004	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28201066	GGACAGGCCACTTGT[A/G]CTCTCCGGCTGCCCC	8924
rs529858715	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28236898	TGGCCCTCTCCCACT[C/T]TTAATGGCACTTACA	8924
rs529866403	snp	A/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28156400	GAGCATGGAATGTTA[A/T]TCCATTTGTTTGTAT	8924
rs529872107	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318505	TGGTGGTGGACACCC[A/G]TAGTCCCAGCTACTC	8924
rs529878092	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28275464	CGCGGGTGAAGCCCT[A/G]CGTGCTTGACCCACC	8924
rs529903121	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28230680	GGCAGAACAAAAAGA[C/G]AAAGTGAGAGTGCGA	8924
rs529908992	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28260722	TACATACTGGTAATG[A/C]ACAACTGGAAACCAA	8924
rs529910500	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28201733	GTAGGCAGAATGAAT[A/C]TCAAAAGCTACAAGT	8924
rs529914334	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28114071	CAGGACACCTGCCAG[G/T]ACTACCCCCACCAGA	8924
rs529924866	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28195412	GTTGCACTGAGCCAA[C/G]ATCGTGCCACTGCAG	8924
rs529943698	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28283292	AAAAAACAAAAGACA[A/G]AACATTTCAAAAGCC	8924
rs529961744	snp	A/C	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318989	AGTCTCAAGCAGTGA[A/C]GCGCTTCCCACTCCA	8924
rs530019218	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28276015	AATATGACGAAACCC[C/T]GTCTCCACTAAAAAT	8924
rs530020131	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28117337	GCTCGACTGTGGACA[A/C]CCGAGACCGCTGCCT	8924
rs530028806	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28287797	GGTGCAATCTTGGCT[C/T]ACTGCAAGCTCCGCC	8924
rs530036559	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28199706	ACAAGACCTAACCCA[C/T]CCAACCCTGCTTGCC	8924
rs530046661	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28193661	ATGCACATGTAAAAC[C/T]TGTGCAAGATGAAAA	8924
rs530047139	snp	A/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28231171	TAAATCTCCTCAGCA[A/T]ATAATATAAAAAATA	8924
rs530053591	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28112591	CAGGCACTGCTGTTA[C/T]GGTCCCAACAGAGAG	8924
rs530066310	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314425	TATGCAGTATATGAC[C/T]TCACAGTCAGCTAAG	8924
rs530072114	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28161264	AATGATTTTTTTTTT[A/G]AATATAATTCTACTT	8924
rs530082855	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28154712	AAGGTAACCCCTACC[A/C]TCTCTACTGAGAATG	8924
rs530088235	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28292054	CTAACATAGTGAAAC[C/T]TCGTCTCTACTAAAA	8924
rs530100928	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28206649	CCATCCTGGGTAACA[C/T]GGTGAAACCCCATCT	8924
rs530108787	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28194222	AGGCGCCCGCCACCA[C/T]GCCCGGCTAATTTTT	8924
rs530121833	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28117926	AAGCCCAGTCTGGAA[A/G]GATGTCAAAAAGAAA	8924
rs530138737	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28241207	CCCAATTAAAACACG[A/G]GCAAAAGACTTGAAT	8924
rs530159054	snp	A/G	4.71631e-05	0.00485586	intron-variant	HERC2	GRCh38.p7	15:28113027	CAGCCACCCACCGTC[A/G]GCCGACATCAGCCCA	8924
rs530181494	snp	A/T	0.124144	0.21601	intron-variant, downstream-variant-500B	HERC2, LOC107987422	GRCh38.p7	15:28312141	CACCATTCAAAAAAC[A/T]ATTTGGGCACCTTAA	8924
rs530200810	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28223182	CTGTCACCTGAGAGC[A/C]GTAAAACTTCCCAAT	8924
rs530238342	snp	A/C	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318129	AAAAGCTTTTAAGGT[A/C]TCATATATTGTTTTT	8924
rs530239648	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28191553	GAAAGGCCCTGTCCT[A/G]AAGTCTGACCTGTGT	8924
rs530245023	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313024	ACTGAGGCTGTGAGA[A/G]GTGGGATTTGGGAAG	8924
rs530258030	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28149606	CACGCGGCTCCTAAC[C/T]GAGAACATCACCGAG	8924
rs530267476	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28274833	AGGGCACATGGTGGC[G/T]GAACCGAGTTCGAAA	8924
rs530278742	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28180749	TATTTTTTATTGCAC[A/G]TGTACTAAATATGTA	8924
rs530282882	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28307269	TTTGGGTCTTCTTTT[C/T]CTCTTAGCCTGCCTG	8924
rs530309501	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28144859	ATCATCCAATCAACA[C/T]AAACCTTCTTAGACG	8924
rs530312064	snp	A/C	0.0119091	0.0762411	intron-variant	HERC2	GRCh38.p7	15:28217416	GCCCATCGACCGCTA[A/C]CACACTCACTCTCAT	8924
rs530314781	snp	G/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28137807	ATTTCTCACTTTAAG[G/T]CAAAAGCTAGAAATG	8924
rs530331894	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28306944	GGCTCAAGTGATTCT[C/T]GTGCCTCAGCCTTCC	8924
rs530345050	in-del	-/T			intron-variant	HERC2	GRCh38.p7	15:28231138	CCTATACTTTATCTC[-/T]TTTTAAAATTTTTGG	8924
rs530358519	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28128912	AGCCCTGTTCCTCCA[C/T]GAAAGCCAGCAACAG	8924
rs530363957	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28188673	ACTAGGACTTGCTGA[A/G]GCAGGGAAGTAAGGT	8924
rs530364448	snp	A/G	1.64784e-05	0.00287035	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28268512	CCCACAGCCCCAGGA[A/G]TACACCTCTCCAGTA	8924
rs530366287	snp	C/T	1.65053e-05	0.0028727	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28260810	AATTCCCACTATGTG[C/T]TTGGTGTCCAGTCCT	8924
rs530366833	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299621	CCTTATGTATTCGAT[C/T]ATTTGGTAATAAAAT	8924
rs530371377	snp	C/T	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28218042	AGCCCTAACCCCTAT[C/T]GTACCTCGGCAGGTG	8924
rs530375540	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28131758	GCAACTCCACACCAC[C/T]GTAAACTGAGAGAGT	8924
rs530402329	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28261523	TCAGCTGAAAAACCA[C/T]ACTGCAGTAAGGGGA	8924
rs530413129	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28163547	AAGCTATAAAGAAAT[G/T]ACAATTTATTACTGG	8924
rs530417987	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28284917	AGCGAAACTCCGTCT[C/T]GGAAAAAAAAAAAAA	8924
rs530420618	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28203702	GGTCCCGGCCTGGCA[A/G]AGTAACCAGAATGCG	8924
rs530423834	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28196806	CCTGAGGCGACAATC[C/G]TTAAAGCCAGGTAAT	8924
rs530435799	snp	G/T	0.000955456	0.0218361	intron-variant	HERC2	GRCh38.p7	15:28191071	CCTAGGAAAAAATGG[G/T]TAAAGAATCAAACAA	8924
rs530437099	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28115816	TCTTCTTATGACAGC[A/C]AAGAGCTGGAACTTC	8924
rs530487730	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28151786	AAAAAAAAAACAGGT[C/T]ACCTTCAAGAAATAA	8924
rs530492096	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28133134	GTTTTACATTTTAAC[A/G]GGTTTAAAAAAAAAA	8924
rs530495007	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28191626	CTCCAATGTGCAACA[C/T]AAATTTGCTAGACTA	8924
rs530502469	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28115177	CCCAGCTGCCCAAAA[A/G]CTCAGCTTCTTCACA	8924
rs530531049	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28170633	TTGACACCAAAAGTA[C/T]GATCTATAAAAGAAA	8924
rs530539793	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28238947	CTGTTAAATATAGAA[C/T]GCTTTAAAAAAAAAT	8924
rs530542657	in-del	-/C	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28154446	GGCCGTATCCTTATT[-/C]TTGTCTCTCCTGGAA	8924
rs530550694	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28320616	ACCTTAGGGAGTAGG[A/C]AAATACAGACACACA	8924
rs530557988	in-del	-/GTGGA	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28160331	GGCCTGCCCCCAGAG[-/GTGGA]GTCTATAGAGGCAGG	8924
rs530558901	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28278007	ACACCTATAATCCCA[A/G]CCCTTTGGGAGGTCA	8924
rs530560180	in-del	-/GATG	0.0126979	0.078662	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28213493	TAGAACTACCTCATA[-/GATG]CACGGTACCTTCTAG	8924
rs530567683	snp	A/C	0.000798403	0.0199641	intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28316076	AAAAAAAAAAAAATT[A/C]TCTGGGTGTGGTGGT	8924
rs530568271	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28309540	CCGCACCGTCCTGAA[C/G]GGATGGTCTTCAATT	8924
rs530570254	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28247100	TGTCAAGTTTTATAC[C/T]CTGCACTACAGAGTA	8924
rs530577783	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28271948	CAACAAAGCAGGCCG[C/T]TATTTTCGTTGTTCT	8924
rs530578972	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28232951	ACTCAATTCCTAAAC[C/T]GTCTCATTGTCTGAT	8924
rs530586460	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28220375	TCCCATTCTAAGGCC[A/C]AGATGACAGTGGTGG	8924
rs530597221	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28147043	GGGGCCGCAGGAGGT[A/G]GGGAGTGGAAGCAGG	8924
rs530602093	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28152320	GGGTAACAGAAGCTG[C/T]CCAGAAATGCAAGTC	8924
rs530606976	snp	C/T	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28310019	CTTCCAAAAAGTGAG[C/T]CCTAGCCAGGTAGAG	8924
rs530620507	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28165340	ACTGAACTGTAAGTA[A/C]ATAGCCTGCTGATGA	8924
rs530633407	snp	C/T	0.0429648	0.14013	intron-variant	HERC2	GRCh38.p7	15:28203604	CAGCAATAAAACGAG[C/T]ACAACCCCTGACCCC	8924
rs530665894	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28206593	AATCCCTGCACTTCG[A/G]GAGGCCAAGGCGGGT	8924
rs530667111	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28186429	TTTTAAAAAATACAA[A/T]TTTTGGAAACAACTG	8924
rs530669539	snp	G/T	4.98724e-05	0.00499337	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233210	ACGGGGCAAAGAACT[G/T]AACAATTTAAACTTA	8924
rs530670950	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28268693	GCTCTCCGTTATCAT[A/G]TATCCCCAAGCAAAG	8924
rs530693988	snp	A/G	0.00354894	0.0419747	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214849	TAAAAAAAATCTGAT[A/G]AGGAAACTACAGATT	8924
rs530694998	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28220843	TCAGTTAGGAGGGTG[C/T]GTGCCCTGCCCTGGT	8924
rs530696539	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28266034	TTATTTCTTATTAAT[G/T]TTAACAAAGGAAATT	8924
rs530731202	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28249492	GAATGTTTCTGGTTC[C/T]TCAGCAGAACACCAA	8924
rs530736479	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28249300	TGCAGCAGGTGCCGA[A/G]GGCTCAGGGAGTCCA	8924
rs530738222	snp	C/T	4.94858e-05	0.00497398	synonymous-codon	HERC2	GRCh38.p7	15:28142262	AAACAGACGGGGCAA[C/T]GGTGTTCTTTTGTCA	8924
rs530755563	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28265005	TTACCAATCTGCCAT[G/T]CAACTTCTGCAGGAG	8924
rs530757618	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28215305	CTTTAAAAAAAGCAA[C/T]ATTACAGATGCATGT	8924
rs530766626	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28146029	TCCGACAGGGATGTG[A/G]TACATACATCACAGA	8924
rs530772585	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28269942	AGGTCAGGCCTTGCA[A/G]CACTATTTGTGTTTG	8924
rs530777608	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28171730	GATATTTTTAAAAGA[C/G]CATTTAATAATCTGA	8924
rs530793191	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28299249	AGCAGCTTGTATTAA[C/T]TACCATTTTAGACAA	8924
rs530802991	in-del	-/T	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28303659	CAGACATTTTAACAA[-/T]ATTGATTCTTCCAAT	8924
rs530840248	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28172159	AAATAAAGAGAAACA[C/T]TATGTTCATGGGTTA	8924
rs530879459	snp	A/C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28294738	AGCCCCTCGTGGTTC[A/C/G]CTCTGTTCCCAAGTG	8924
rs530882225	snp	A/G	0.00636936	0.0560724	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28301131	GCTGTTTCCTCAAAC[A/G]TGGCCAGGTGCGGTG	8924
rs530912954	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28308366	TATTGTTTACTGTTG[A/G]CACACAGAAATGCTA	8924
rs530918522	snp	A/C	0.0418186	0.138422	intron-variant	HERC2	GRCh38.p7	15:28294632	CCTGCTCATCCCTGC[A/C]GGCCCAGAGTTATTC	8924
rs530927467	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28169830	AAAACCACTTATCCA[C/T]ACTTCGATAAAGAAG	8924
rs530933665	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28176264	ATTTCTTCTTGTACT[A/G]TTGTCACTAATCCCA	8924
rs530947455	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28139809	CTCATGCCTGTAATC[A/C]CAGCACTTTGGGAGG	8924
rs530963031	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28208745	CACCAGCAAAGTGCT[C/T]GTCTGCTGGCATCTG	8924
rs530981473	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28183896	ATTTTTACTTAAAAA[C/T]ATGTATGGGGACCAG	8924
rs530999546	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28308810	ATTGAAATAATCACA[C/T]GGTTTTTATCCTTCT	8924
rs531007612	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28219331	CCGTGGGGCCACCCC[A/T]GCCCAGGCTCTGATG	8924
rs531038692	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28180804	CCTAAACAATGTAAT[A/G]TAACAACTATTGACA	8924
rs531038925	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28163617	TTTGGAATGAAGCTG[C/T]ATCCTGTATAATCTA	8924
rs531044031	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28302087	ACAGGCGTAAGCCAC[C/T]GTGCCCAGCCCTATC	8924
rs531058487	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28134270	TTCACTTTCTGGTTA[C/T]GTATATGTATACGTA	8924
rs531068689	in-del	-/G	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28137124	ATTGGGAGGAGGGGA[-/G]AAATACTAATTAACT	8924
rs531069148	snp	C/T	3.30518e-05	0.00406507	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214017	GAGACACTCACGGAG[C/T]TGCCCAATCCCTACA	8924
rs531076319	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28289919	GAGGACTACACACCT[A/C]AGTGAGAGGATTACA	8924
rs531078026	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28126296	TGATGGAAAGCATTT[-/A]TCCACGCTCCACTAT	8924
rs531113888	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28126805	CCTCTCAGACATCAC[C/T]TCTAAAGAGCTTATT	8924
rs531115100	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28284452	TCAATTAAAAGACAC[C/T]AGGAGAGCAGACTAG	8924
rs531117168	in-del	-/CA	0.00279608	0.0372857	intron-variant	HERC2	GRCh38.p7	15:28217097	GCTCGCACTCAATCG[-/CA]CACTTACACACTTGT	8924
rs531130837	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28295069	AAACCACAATGAGAT[A/C]CCACTAGACTTGTTA	8924
rs531142158	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28187425	CAACCCCTGCCTCCC[A/G]GGTTCAAGCGATTCT	8924
rs531152634	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28120340	GTATAACTCTGAAAA[A/C]ATTTCTAGTCTTGTA	8924
rs531152986	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28127400	CCAAATCGCCAGAAA[A/C]GAAAGGATCTGCAAG	8924
rs531157048	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28240834	GTACTGGGAAATCCA[A/G]ACATGCACATGTAAA	8924
rs531160427	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28143693	CCTCGTGATCCGCCC[A/G]CCTCAGCCTCCCAAA	8924
rs531181674	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28167221	GAGACCCTTAACCAA[C/G]TGATAAGCTATCTCA	8924
rs531222293	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28137279	CCTGTGCTAGCAGTC[C/T]GCCTCTGATACGGTT	8924
rs531225751	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28164101	CCCAGCATGGGAACC[A/G]CTGTGACCCTGTGCA	8924
rs531242032	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28158040	TTTCCATGTAGTTGA[A/G]CAGTTTTGAGTGAGT	8924
rs531267290	snp	A/T			missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28255897	GCAGTAATGGCTGCG[A/T]GTAAGGCTGACTCCA	8924
rs531270647	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28203252	TGTCTGTAACTCCCT[G/T]GTCCTCCTCCCCAGC	8924
rs531270931	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28228076	ACCGCTGAATTGTGA[C/T]GTTAAAATGGTACAC	8924
rs531272486	in-del	-/A	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28189086	GTGAGACTCAGTCTC[-/A]AAAAAAAAGAAAAGA	8924
rs531290976	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28136984	TAGTAAGCAAAGATG[C/T]GCAACATTTAGCTAA	8924
rs531311330	snp	C/T	1.68508e-05	0.0029026	intron-variant	HERC2	GRCh38.p7	15:28178852	AGCAGGAGCAAAGGC[C/T]GCCCCGCACAGGCCT	8924
rs531318501	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28167324	GGTGTCTGTCAAAAC[A/G]AAGAACTGAAGGACT	8924
rs531373441	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28253949	CCTGGGCAATAGAGC[A/G]AGATTCCGTCTTAAA	8924
rs531399429	snp	A/C/G			intron-variant	HERC2	GRCh38.p7	15:28164320	ATGACCCAACCAGTG[A/C/G]ACCCTGGAAACCACA	8924
rs531403228	in-del	-/A	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28280441	CACATGAGCTCAGGC[-/A]ACCCTCACACCCAGC	8924
rs531408677	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28306675	AAATGTTTGGTAAAA[C/T]TCAGCAGTGAAGTCA	8924
rs531423964	snp	A/G	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28206661	ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA	8924
rs531434815	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28287825	GCCTCCTGGGTTCAC[A/G]CCATTCTCCTGCCTG	8924
rs531476264	snp	C/T	0.0126979	0.078662	intron-variant	HERC2	GRCh38.p7	15:28217213	ACACCCAGTAATCCC[C/T]TCACACTCACTCATG	8924
rs531490005	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28206533	CAAGGTTCAGACATC[C/G]AACAAAAACTAGACT	8924
rs531490370	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28211839	AGGTCTGTGGGAGCA[A/C]GAGGGGAGAAAACTC	8924
rs531506284	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28248152	CTGTAACTGAAACCC[A/G]GGCTTTCTCCAACAG	8924
rs531509335	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28155351	GCCACACTGTGTTCC[A/G]CAGTGGTTGAACTAG	8924
rs531512113	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28123096	CTTCTGCCTCTCTCA[A/T]CAGAGAGATGGTCTT	8924
rs531522738	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28131587	GCAGCCACCGGGCTT[C/G]AGTGGAGCAGAGCCG	8924
rs531523135	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28281540	TGGCTACCCACTACC[C/T]GGATATGCTCTCCAC	8924
rs531551915	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28210174	AGTCTTGCTCTGTCG[C/T]CCAGGCTGGAGTGCA	8924
rs531560438	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28117432	ACACACCTTCCAACA[C/T]GACACACACCACCAC	8924
rs531563167	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28161750	AAAGTCCTACAGACC[C/T]AGTGCTACCAAATAT	8924
rs531586247	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28129010	TTCTGCCTCCTTTTC[C/T]GATCAAAGGGTCTGT	8924
rs531589788	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28144619	GTCCCTGTTGCTCCA[A/G]AAACAATCCACAGCC	8924
rs531595520	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28118104	AGCCACAGTTGCCTG[C/T]AGAATGAACTTGTCT	8924
rs531604507	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28297226	AGAATCCTAGGAAAT[C/T]GCCACTGTTCAGTCG	8924
rs531612369	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28210422	ATTACAGGCATGAGC[C/T]ATTGTGCCCGGCTGG	8924
rs531616755	snp	G/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28252844	CTTCCTGTTTCAAAA[G/T]TTCACTGTGCGTCTA	8924
rs531619509	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28122199	GTGGCCAAACATCAG[A/C]ACCACGGTGAGGACC	8924
rs531642526	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28291418	TTATATATGTACATT[C/T]ACATATGTATGTCCA	8924
rs531654682	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28122765	AGGTACCTTTCAGAC[A/G]CCCTCAGCACTCCCC	8924
rs531668467	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28241876	ATATACACACCCACA[C/T]TCATAGCAGCATTAT	8924
rs531713743	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28160132	GCCGTGTGAGGTGTC[A/G]GTCTGCTCCTACTGG	8924
rs531741688	snp	A/C/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28246589	CTTAACAACAGAACT[A/C/G]TCAGTAACTAAAAAA	8924
rs531742375	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28205028	CAAGGAGGACGGTGG[A/G]GTGGGCGGGGTGTGC	8924
rs531747731	snp	C/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28204451	ATGGTAAAACCCCAT[C/G]TCTACTAAATATACA	8924
rs531747882	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28143068	TCTTCTAAAAAAACT[-/A]AAAAAAAAAAGCTTA	8924
rs531750547	snp	C/T	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28217125	TTGTGCTGCCACCCA[C/T]TCATACTTCCTCACA	8924
rs531766217	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28165730	GCTTGAGACCAGGAG[A/G]TTGAGGCTGCAGTGA	8924
rs531770742	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28285980	ACTCACCAAATATAA[A/G]ATAGATCATTTGAAT	8924
rs531793865	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28116389	CAGCTAATTTTTTTT[A/G]TATTTTTACTAGAGA	8924
rs531802613	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28198902	TCTGTAATCCTAGCA[C/T]TTTGGGAGGCTGAGG	8924
rs531810114	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28235104	GTGTTATCAAATACT[C/G]CTCCAAATCCAAGCA	8924
rs531820153	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28159783	CTGGTGAGGAGCTGC[A/G]TTCCTTTGGAGGAGG	8924
rs531833675	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28153302	AGGTTGCGGTGAGCC[A/G]AGATCACACCGTTGC	8924
rs531835830	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28249967	GCCTAAGGAAACTAA[C/T]TCTTATGTCAATGTG	8924
rs531839182	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28181166	GCCCTTTGTCTAAAA[A/C]ACCTTTATGATTCCC	8924
rs531842739	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28287810	CTTACTGCAAGCTCC[A/G]CCTCCTGGGTTCACG	8924
rs531869293	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317301	ACCATGGGCGCCAGG[C/T]TGGTTTTGAACTCCT	8924
rs531931799	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28273451	ATCTCTGATCAATGA[A/C]ATATTTTTAACTTTT	8924
rs531932665	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28208091	AATCTTCCAATCTCT[A/G]CAACTGGGAAATCTT	8924
rs531956315	snp	C/T	0.0257252	0.110457	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214037	CAATCCCTACAGGTT[C/T]ACCGTTGAACTAAAT	8924
rs531957823	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28228468	AAGAATAAACGTAAC[A/G]CAGAAAGCACGGGCG	8924
rs531993398	in-del	-/G			intron-variant	HERC2	GRCh38.p7	15:28247183	TTTTTTTTAACAGAC[-/G]GGGGGTCTCACCATG	8924
rs531997122	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28208679	GCAATGCAGAGCTGC[G/T]CAACACGCTTCCAAA	8924
rs532000466	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28310790	GTGAACTAAGAAGCT[A/G]TTACTGGCCACGCAC	8924
rs532000898	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28119546	ACAACCTCTGCCTCC[C/T]GGGCTCAAGCAATCC	8924
rs532006612	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28187035	ACAGCCTTACTGAAT[C/G]ACTGCAAACTCTTCC	8924
rs532010369	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28289281	CACACCACGCAAACA[A/C]CAAATCAGAAGAAAG	8924
rs532011823	snp	A/C	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28266616	TACCCATACACCCAA[A/C]CCAACATGGCTGGAT	8924
rs532024080	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28201825	TGATGTGTCAAAACA[C/T]GGTATTTTAATAAAA	8924
rs532028349	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28195143	AAGGTTTTTGCATTG[C/T]TTAGGTGGAGAATAT	8924
rs532035082	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28222296	AAACATTCACAAAGT[A/G]CTAATGAAGATCGTA	8924
rs532038907	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28120155	AGGTAGGGAAATAAA[A/T]GCTTTTTTATGAACC	8924
rs532092955	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28311262	TTGAGCCCAGGAGTT[C/T]GAGACCAGCCAAAGC	8924
rs532105389	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28156611	GATTTTGTATCCTGA[C/G]ACTTTGCTGAAGTTG	8924
rs532107749	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28319087	CTGTCTGCAGGGAAG[C/T]TCCCCAAAGAGGGAA	8924
rs532111926	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28237728	TAAATTCTATGTGTT[C/T]GTGAATACATAGGAA	8924
rs532117936	snp	A/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28126060	GGTGATCCACCTGAA[A/T]ATCTATGTTTTTAAA	8924
rs532128191	snp	C/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28294465	ATTTCTCGTGTGGCC[C/T]GAAATTAAGACTAAA	8924
rs532135572	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28171803	CAATAGACCGGGTGC[A/G]GTGACTCACGCCTGT	8924
rs532139350	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28195454	CGACAGACTGAGACT[C/G]TGTCTCACAAAGAAA	8924
rs532153558	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28250462	AATGAAATTTTTAGT[G/T]TATTTAATATAAAAT	8924
rs532165262	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28289586	CTGGAGCTGATCTCC[C/T]CAGAACGCTGAGACT	8924
rs532166190	snp	A/C/T			intron-variant	HERC2	GRCh38.p7	15:28201977	TGCCCGGCAATACCA[A/C/T]AGGTTGGTTTTATGG	8924
rs532179984	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28162869	GCACTCTAGCCTGGG[C/T]GACAGAGCGAGACTC	8924
rs532180078	snp	C/T	0	0	intron-variant	HERC2	GRCh38.p7	15:28282800	AGCTGGGCATGGTGG[C/T]GGGCACCTATAATCC	8924
rs532195182	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28320008	CTAAATCAAAGGAAA[C/T]GTTTAAAGAGAAACA	8924
rs532199318	snp	A/T	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28231483	CACATGGGCACTGCC[A/T]GCGTATGTGACTGGC	8924
rs532225136	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28190408	AAGGTTTACTAAAAA[C/T]TTGAGAGAGAGAGAT	8924
rs532234145	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28163371	CCATAAACTCAGAGA[A/G]CACATGAATACCAAC	8924
rs532237400	snp	A/T	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28157262	TGCTGGCCTCATAAA[A/T]TGAGTTAGGGAGGAT	8924
rs532248715	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28270276	ATAGATAGACAGACA[G/T]ACAGACATGTAATAT	8924
rs532264412	snp	C/T	0.000399281	0.0141238	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202148	CCACGTCCTCCACCA[C/T]CTCCTCGTCAGAATA	8924
rs532269409	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28291503	CTTAGAGGAAAGCTG[A/C]AACTGGGGTGGGCAG	8924
rs532283615	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28259613	CTCTAATGAGCATCA[A/T]CAGAAAAATCCTCAA	8924
rs532299564	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28150850	ACAGAGGAAAAAGAC[A/G]TGATCCAAGGCTTTA	8924
rs532310360	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28293606	GAAACTTAAGTCTTT[C/G]ATATTTACCTACTTC	8924
rs532315580	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28146819	TGGTGTGAGAGGTGT[A/G]CGAGCAGAGGCACAA	8924
rs532315696	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28139831	TTTGGGAGGCCAAGG[C/T]GGTCGGATCACAAGG	8924
rs532321897	snp	G/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28225915	AATAGAAAATCTGAA[G/T]AGACCCGTAACAAGT	8924
rs532322540	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28195881	TACAATAAAAGGTAT[A/G]TAAATTAAAAAACTC	8924
rs532330067	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28282035	AGTCCATCAGTCATG[C/T]ACACTCTGAAACAGT	8924
rs532348884	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28190135	CGCCTCAGCCTCCCA[A/G]GTAGCTGGGACTACA	8924
rs532359916	snp	A/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28194336	CCAAAAGTGCTGGGA[A/T]TACAGGTGTGGATCA	8924
rs532373224	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28194628	CCACTGTGCCTGGCC[A/G]ATCCTTTGACATTTT	8924
rs532373265	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28188308	AGCACTTTGGGAGGC[C/T]GAGGCAGGTGGATCA	8924
rs532393534	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28276870	ATTGCTTGAGGCCAG[A/G]AGTTCCAGACAAGCC	8924
rs532405988	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28308420	TATACTGCAATTGTA[C/T]TGAATTTATCGGCTC	8924
rs532411736	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28190864	AAGAACCAATTATTT[A/T]AACGGGGAAAAACTG	8924
rs532412076	snp	G/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28183972	GTGGGCAGATTCCTT[G/T]AGCCCAGGAGTTGGA	8924
rs532422436	snp	C/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318207	AATCACATCAGATTA[C/G]AAGTACTTTCACTGT	8924
rs532460763	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313326	GGGACTACAGGCGCA[C/T]GCCACCACGCCCGGC	8924
rs532483415	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28308933	TTCTAACGTATTGCT[C/G]AATTTGGTTTGCTAG	8924
rs532513500	snp	A/G			utr-variant-3-prime	HERC2	GRCh38.p7	15:28111238	CTGGTTTTTCATTTT[A/G]GTTTAAATATCCTCT	8924
rs532514095	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28307364	TCTTCATTTCAACTC[C/T]ATTTTATTTCTGCTC	8924
rs532546649	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28223978	GGCCATTTCTCGATG[C/G]AGATATGCTTTTGTA	8924
rs532550626	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28307815	TGAAGAGATTGTCTT[C/T]TCCCCAGTGTATGTT	8924
rs532550682	snp	A/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299688	ATTTCAGGAAAGTCA[A/T]CCAAGAAATATAAAT	8924
rs532551809	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28149460	GCTCCTAACCGAGAA[C/T]GTCACCGAGAACGGC	8924
rs532613235	snp	A/G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28132576	ATTTTTCATAACAAC[A/G/T]GTGGCAAACCGCCCC	8924
rs532623182	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28252543	TCTCATTGATTCTTA[A/C]TTAACTCCATGAAAG	8924
rs532630471	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28144310	AGCCGCCAACGAACA[A/G]GGGTGGCTCCACCCA	8924
rs532635877	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299990	CCCAGGAGGCAGAGG[C/T]TGCAGTGAGCCAAGA	8924
rs532642019	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28212279	ACTCGAAAATACTCA[C/T]TACCACGAACACAGG	8924
rs532645243	snp	C/G/T	4.9728e-05	0.00498618	synonymous-codon, downstream-variant-500B	HERC2	GRCh38.p7	15:28174483	ATCCACAGTTGTCCA[C/G/T]GCCACACTGTGGGAC	8924
rs532686040	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313871	AACCTAAGCAAGCAG[G/T]GATGAGACTGAGAAG	8924
rs532704319	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28250109	GCACAACACCAAGAG[C/T]GAGGACATGCTTTCA	8924
rs532704507	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28120481	CATTAAATGTCAAGT[C/T]CTGCACGCTATCATC	8924
rs532706367	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28212747	ACATTAAAGGCAGGA[C/T]AGAGATTTACACATA	8924
rs532709071	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28269158	TCTTCAGAAATCAAA[C/T]GCCTTAAAGAAACAC	8924
rs532722247	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28249950	GTGAGCCACCACGCC[C/T]GGCCTAAGGAAACTA	8924
rs532725391	snp	C/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28224579	CTTGGGAAAACCTTG[C/T]TTTTTCACTGTGACT	8924
rs532747255	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28288299	GGGAGGCCGAGGTGG[A/G]TGGATCACCTGAGGT	8924
rs532756441	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28254685	GAAACCCTAACTCAG[C/T]TGTGCAGTTTCAAAC	8924
rs532758506	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28191683	AAATCTGAATTCATA[C/T]ATTCTATGCAGGAGA	8924
rs532758900	snp	A/C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28262402	GGCACTCTTATCTAC[A/C/T]TACCTTGGCTTCCAT	8924
rs532768153	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28185892	ATCACAGTGTTCCCA[C/G]TACACATAACTGGGA	8924
rs532769304	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28139177	CTCCAAGCATGCCTA[C/G]AGCTCCCTCTCCCTG	8924
rs532778750	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28182683	ATGTACAGGAGTAAG[C/T]CCTCTGGAGGGTCAA	8924
rs532783995	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28197993	CCTTACCAATCATGA[C/T]GTTAGCATGGCTCCA	8924
rs532791230	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28218075	CTTGTTTGGAAATAG[A/G]GTCGCTGCAGCTGTA	8924
rs532795517	snp	C/T	1.70351e-05	0.00291843	intron-variant	HERC2	GRCh38.p7	15:28192158	CAGACTGACCTATTT[C/T]GTGATAGTCAAAAAG	8924
rs532803074	snp	A/T	0	0	intron-variant	HERC2	GRCh38.p7	15:28175036	TCATTCTGACTAAAA[A/T]ACAGTAATGGTAATT	8924
rs532818755	snp	C/T	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28218607	ACAAAGAGTCTGCAG[C/T]AAGTTAATAGTGCTG	8924
rs532826376	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28285924	AACTTTGACAACTTG[A/G]GCAAAATGGACTTAT	8924
rs532830565	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28186441	CAATTTTTGGAAACA[A/T]CTGTAATTTACCAAT	8924
rs532847626	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28255280	GACAAGGCTGCAGTG[A/G]GCCAACATCAGGTCA	8924
rs532867878	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28133058	GCTGGAAAGTGACCA[C/T]ACATACTGGGTCAAG	8924
rs532871531	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28148589	CGAGAACGGCCGCAT[A/G]AACGTACATTCTGGT	8924
rs532904142	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28304425	CAGGCTGGAATATAG[C/T]GGCACAATCTCAGCT	8924
rs532930365	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28310539	CCCCTGAAGTTTAAC[G/T]AGTGAATGGAAAGGT	8924
rs532939225	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28296625	TAATTTATAAACAAA[C/T]ACTGGAGGGCTAGGA	8924
rs532945314	snp	A/G	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28305739	CATCAGAGTGAACAG[A/G]CAACCTACAACATGG	8924
rs532946777	snp	A/T	5.68295e-05	0.00533025	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28222130	CTGCACAGGAGCCGT[A/T]TCCTTCCTTGTTTCT	8924
rs532950768	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28266360	GTCTCTACTAAAAAT[A/T]CAAAATTAGGTGGGC	8924
rs532959858	snp	A/G	0.000399281	0.0141238	intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28316126	CACTTAGGAGGCTGA[A/G]GCATGAGAATGGCTT	8924
rs532987255	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28258974	GTAAAAATCAGACAA[C/T]GTAGATGAAGTAAAG	8924
rs532990591	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111230	ATGGCCTTCTGGTTT[G/T]TCATTTTGGTTTAAA	8924
rs533000198	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28178434	GTAAAACTCTATATT[A/G]CTTAAGCCACCATCA	8924
rs533028909	in-del	-/C	0.00755907	0.0610114	intron-variant	HERC2	GRCh38.p7	15:28298792	AGAGCAAGACTCCTT[-/C]CCCCCCCAAAAAAAA	8924
rs533030542	snp	A/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28297554	CCCATTATGTTGTTT[A/T]AAAAAAAAAACATGA	8924
rs533038400	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28172788	AAATTAAAAACTTCT[A/G]ATCTTTAAGATTCAC	8924
rs533043936	snp	A/G	1.64738e-05	0.00286995	intron-variant	HERC2	GRCh38.p7	15:28141660	AAGTGAGCATTTGCC[A/G]TGGGCAAGAACAATG	8924
rs533045210	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28137173	ATGTTAAAATAACCA[C/G]AGAAACAATGAAAAG	8924
rs533047709	snp	C/T			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317442	GAGCTTACATTTATG[C/T]GTAGTCATTCTTAAT	8924
rs533065656	in-del	-/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28284156	AAAGTTTCAAATTTT[-/G]GGGGCATTTCAGATT	8924
rs533066248	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28174708	CAAAATGCTTAACGC[A/G]TATGCCACGGTAGTT	8924
rs533098438	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28220897	TCAGTTAGGAGGGTG[C/T]ATGCCCTGCCCTGGT	8924
rs533099327	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28166397	GATTTGGGCTGTTAA[G/T]GGTTTTTATTATATA	8924
rs533102717	snp	C/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28212177	GGTGAACACAGACTT[C/G]TCTTCCGGGATAAAG	8924
rs533106317	snp	A/G	6.87592e-05	0.00586301	missense	HERC2	GRCh38.p7	15:28142335	CAGGCCCACTTGTGC[A/G]TCTCGGCACAGCAAG	8924
rs533106836	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28129925	GAGATGCAGGCGCGC[A/G]CCACCATGCCCAGCT	8924
rs533111188	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28140307	GAATCACACCGCAAC[C/T]CCAGCCTGCACCATG	8924
rs533118396	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28136417	CCAAAGCCAGCTTCT[A/G]GCGGGGAGGGTGTGA	8924
rs533151020	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28175790	CCAAGGTCTTCAAAC[G/T]TGTATTCAAAATCAT	8924
rs533161539	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28256720	CTGACTCAGCCTCCC[A/G]AGTAGCTGGAACTAC	8924
rs533170455	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28129147	GGGGTTCCCCGGACC[A/G]CCCCACGCTCCTGAT	8924
rs533179515	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28136742	GGCTGCTTTTGTAGT[C/T]GCAACAGAGACTATA	8924
rs533198171	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28131652	TGCAGGCCTTGCTCT[A/C]GCTCCTCACAGGACA	8924
rs533221216	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28165786	GCCTGGGCAACAGAA[A/C]AAGACCCTGTCTAAA	8924
rs533244828	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28251122	ACCAATGGAGCTACA[C/G]GTGCAATTCAAAATG	8924
rs533276125	snp	C/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28289951	ACCTAAGTGAGAGGA[C/T]CACACACCTCAGTGA	8924
rs533280358	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28251569	ACTTTGGGAGGCCAA[A/G]GCGGGCAGATTACTT	8924
rs533290273	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28171379	GACATGAAAAGAGCT[A/G]TACGTTAAGAAGATA	8924
rs533292230	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28244489	AATGAGTCCGAGTTT[A/G]GGAGGGTCCTGCCAC	8924
rs533300747	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28122252	AGGTCGGCCATGCCC[A/G]TGGGGAAAGGGCAGA	8924
rs533376895	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28210534	CATACATCTATGCAT[G/T]TCAAAGACCAACTCA	8924
rs533380870	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28135057	CTGGTAGTTCTCATT[A/C]ATTTTTTAATACTTG	8924
rs533385754	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28158101	CTATGGTCTGAGAGA[C/T]AGTTTGTTATAATTT	8924
rs533403633	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28176344	CACGTCACAATCACG[C/G]CGGGTGAGCCTGGGG	8924
rs533417482	snp	A/C/G			intron-variant	HERC2	GRCh38.p7	15:28240240	TGGCTAACACGGTGA[A/C/G]ACCCCATCTCTACTA	8924
rs533435786	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28303632	TGAACCTGTAGATTG[C/T]TTTGGGTAGTACAGA	8924
rs533443154	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28158919	CTTCAGGAGTTCTTT[C/T]AGGGCAGGCCTGGTG	8924
rs533479398	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28285759	AAAAAGCTGGTTCTT[C/T]GATAAGATCAATAAA	8924
rs533487508	snp	A/G	0.000399281	0.0141238	intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28315724	GGAAGAAGCGAATGC[A/G]CAGGCTGAAGCGCAA	8924
rs533495098	snp	A/G	0.00517822	0.0506191	intron-variant	HERC2	GRCh38.p7	15:28239665	CCCAGACATAACACC[A/G]CCCCAACGAGACTGA	8924
rs533505779	snp	A/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28209353	TATTTTTATTTATTT[A/T]TTTTTTTTGAGACAG	8924
rs533510379	snp	A/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28253641	AGATTTCACTATCTT[A/T]ATATGAAAACCAATA	8924
rs533512355	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28247587	GCACCTGCCACTATG[A/C]CCAGCTAATTTTTTG	8924
rs533516106	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28209595	TGATCTGCCCGCCTT[A/G]GCCTCCCAAAGTGCT	8924
rs533545324	snp	A/C	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28276502	AAGTGTGGTCAGAGG[A/C]GGTGGGCCAGTCACT	8924
rs533548383	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28248261	GTCTCCAGCATTCCA[C/T]AGCACATGGAACAAA	8924
rs533561707	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28219219	CTAGATGAGGACAAA[A/G]CACCGGCATCTGTGG	8924
rs533563728	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28177795	ATTATGTTAAATACA[C/T]GAAAAATCAAAATTT	8924
rs533572137	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28290363	TGCAGGGGTGCAATC[A/G]AGATTACAGGCACCC	8924
rs533580824	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28203729	TGCGAGGGAAAGCCC[A/G]CCTGAGAAAGAAACC	8924
rs533586793	snp	G/T	0.0991586	0.199366	intron-variant	HERC2	GRCh38.p7	15:28245606	ACACACACACACACA[G/T]ATATATATATACACA	8924
rs533587640	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28121643	GGTAGTGCCAATGGC[A/C]GGGCAAGAGGCAGGT	8924
rs533587865	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28115350	TTAGGCCAGAGTTCA[C/T]AGCCTGACCGGACCC	8924
rs533590028	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28160395	CCCAGTTTCAGCTTC[C/T]GGGCCGCTTTGTTTA	8924
rs533600707	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28153968	CCGACCCCAACACAG[C/T]TGCCCCTGCTGACCC	8924
rs533626385	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28115885	AGGAGGTGCTGGCTG[C/T]GGTGGGACGCACAGC	8924
rs533644683	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28240780	TGACATGGGAGCCAA[A/G]ACCACTCAATGGGGA	8924
rs533645305	snp	C/T	0.00993419	0.0697739	intron-variant	HERC2	GRCh38.p7	15:28308066	ATGAATTTTAGGATT[C/T]TTTTTTTTTCTGTTT	8924
rs533651142	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28280869	GAGCTGAGATTTTGT[A/C]ACTGCACTCCAGCCT	8924
rs533679475	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28235699	ACCACGTATGAACGT[C/T]TCCATTTCACCATTC	8924
rs533695804	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28247889	TTGGGAAAAAAACAG[C/T]TACAAAATTACTAAT	8924
rs533710399	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28197652	AGCTACTCTGGAGGC[C/T]GAGACTGGAGAATTC	8924
rs533719678	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28242968	GTGTGTGAAATCTGG[A/G]AAGCTTTTTCTCTGC	8924
rs533734646	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28286580	TGAATGATAAAAATT[A/C]TCAGAAAATAGCAAC	8924
rs533744135	snp	C/T	0.0193772	0.0965046	intron-variant	HERC2	GRCh38.p7	15:28211236	CATGGCGACGAGTAA[C/T]GCTCTGCCCTTCAGG	8924
rs533744720	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28292197	TTGCACCACTGCACT[C/T]CAGCCTGGGCAACAA	8924
rs533745015	snp	C/T	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28193862	AGACATTTTCAGACA[C/T]ACAAAAATAGACAAT	8924
rs533745376	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28187842	TGGAGTTGGTCTACT[C/T]GTCCTGCAAATGTCC	8924
rs533763585	snp	A/C	2.18176e-05	0.00330278	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274432	AACAGCTCACTGCAG[A/C]GGTCCGCATCCTCGC	8924
rs533775511	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28267668	ATACGCATTACTCTG[C/T]TTTTCTCCCAGTTTG	8924
rs533783017	snp	C/T	0.00755907	0.0610114	intron-variant	HERC2	GRCh38.p7	15:28149384	GCTCCTAACCGAGAA[C/T]GTCACCGAGAACGGC	8924
rs533787814	snp	A/G	1.80218e-05	0.00300176	synonymous-codon	HERC2	GRCh38.p7	15:28124213	TGGGGATCTCCTGCA[A/G]GTGATTGTACTCCAT	8924
rs533802467	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28199361	TCATCAAAAACATAA[C/T]AGTGGAAACATCACA	8924
rs533828091	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28167522	AGCAGTGACAGGGAC[C/T]GTGTCCTGCGGCATT	8924
rs533834668	snp	A/C	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28312619	CTGGGTGACAGAGAC[A/C]CTATTCATAAAAAAA	8924
rs533844255	snp	G/T	8.23703e-05	0.00641704	synonymous-codon	HERC2	GRCh38.p7	15:28143980	GAAGGGCCCACATTC[G/T]GTGACTGGCAGCTGA	8924
rs533860840	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28268244	CCAAGGCTGCACGGG[G/T]TCAAGAAGAACAGAA	8924
rs533868076	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28224991	CTGCGCCAAAAGCAG[A/G]GATGAAGGGGCAATT	8924
rs533869867	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28307082	TCAAGTGACCCACCC[C/G]CCTCAGCCTCCCAAA	8924
rs533898009	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321788	ACACACACATAACAG[A/G]GAGCCCATCGTTTTA	8924
rs533912288	snp	C/T	0.00119737	0.0244387	downstream-variant-500B	HERC2	GRCh38.p7	15:28110723	GCAGAGTGCGTGCCA[C/T]ACACAAGCAGCCCAA	8924
rs533912321	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28116457	CCTGACCTCAGGCAA[C/T]CTGCCTGCCTCAGCC	8924
rs533915686	snp	C/T	0.000157741	0.00887951	intron-variant	HERC2	GRCh38.p7	15:28117494	CCTGGCACGGACCAT[C/T]CTCACACCCTAAGCA	8924
rs533935790	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316465	GACAACAAAGAAAGA[C/T]CCTGCCTCTACAAAA	8924
rs533937184	snp	A/G	0.000132096	0.00812592	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28198453	CAGAGGCTTTGACCC[A/G]CACTTTATCACCAAT	8924
rs533940540	snp	C/G	0.00318978	0.0398085	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317489	AGACAAATAAATGGT[C/G]CCAGTTTAGCTACTG	8924
rs533948134	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111526	AGTCCTACATGTAAT[A/G]CAGCATTACGGGTGA	8924
rs533949350	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28192327	TAGTTACACCAATTT[A/G]TGAGATGAAGTCCAC	8924
rs533949762	snp	C/G	8.29304e-05	0.00643882	intron-variant	HERC2	GRCh38.p7	15:28233833	GTAACTTCAGAGCCA[C/G]CCAGTGAGTCTTCAC	8924
rs533954152	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28112817	TGTGTTTGAAATCTA[C/G]AGCAGGCTGACACAG	8924
rs533970399	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28153358	GACTGCGTCTCAAAC[A/G]AAAAAAGTCATTGGG	8924
rs533978406	snp	A/C	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28281614	CACTCCCTGGAAAGG[A/C]ACAGGGTGGCGCACA	8924
rs533982816	snp	A/G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28227672	AAGAACTAGAAACAA[A/G/T]CATTCAAACAAGTAT	8924
rs533994436	snp	C/G	0.0142736	0.0832652	intron-variant	HERC2	GRCh38.p7	15:28311713	AACAAATGGACTGTA[C/G]GTGATGTCCTGGAGA	8924
rs534030524	in-del	-/GA			intron-variant	HERC2	GRCh38.p7	15:28298036	TGTGTGTGTGTGTGT[-/GA]GTGAATATTTTCAAA	8924
rs534034271	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28148805	CGAGAACGGCCACAC[A/G]AACGTACATTCTAGT	8924
rs534034988	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28142680	TAGATTACACGATCA[C/T]TTCTTGAGATTTTTT	8924
rs534055087	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28317939	AAAATTGCTTCATGC[A/C]TATCTAATTTCATGT	8924
rs534061986	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28310849	TTGGGAGGCCGAAGC[A/G]GGTGGATCATGAAGT	8924
rs534063105	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28188367	CTAACGGTGAAACCC[C/T]GTCTCTACTAAAAAT	8924
rs534066690	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28228093	TTAAAATGGTACACT[C/T]CCTATTTGTGTCTTA	8924
rs534089933	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28137531	TTTCATTATTTTATC[A/T]GTTATGATGATCTGT	8924
rs534093425	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28149716	GGCCACATGAACGCA[C/T]GTTCTAGTAAAATTA	8924
rs534097289	snp	A/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28136649	ATGGCCCATGTGCCA[A/T]ATCAGGCCCATCATT	8924
rs534099230	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28222372	AATATTTTACTGATA[C/T]AGGATAAAAAGAAGA	8924
rs534102890	snp	A/G	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28253684	AATACAATACAGGCC[A/G]GGAACAGTGGCTTAC	8924
rs534105653	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28144464	CTCCTTCCACACCAG[A/G]TGAGGAGGAGTGTGA	8924
rs534172406	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28279462	TTATACTTGAGCTGA[C/T]CTAAAGCTGTGGCTG	8924
rs534196033	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28173182	CTTAAGAAGCTAGAC[A/G]TACACCTGCCATATG	8924
rs534198865	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28253186	TACACAACACTGACC[A/G]TTTTGGCTTCTGCCA	8924
rs534204547	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28136994	AGATGTGCAACATTT[A/G]GCTAACTCAAAAAAA	8924
rs534209639	snp	A/C	1.6651e-05	0.00288535	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272376	ACAACAGGATGGCAG[A/C]CAACATTTGGCTAAA	8924
rs534212162	snp	C/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28216338	TTTGTATTTTTAGTA[C/G]AGACAGTTTCCAATC	8924
rs534236153	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28148329	CTACCTTAAGACAAA[C/T]AGGAAAAAAGGAGGA	8924
rs534248352	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28209055	AGAAATATAAAGAAA[G/T]AAAGACAGCCAAATT	8924
rs534291587	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28310396	GCTGCAGTGAGTTGA[A/G]ATCACTCCACTGTAC	8924
rs534299968	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28114239	GCACAGTCACACCTG[C/G]GCGCCTGGCAAAGGC	8924
rs534310226	snp	A/G	0.166832	0.235761	intron-variant	HERC2	GRCh38.p7	15:28221807	CCAGTGAGTTTCCTG[A/G]AAAGAGCTGCCTCTC	8924
rs534318160	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314240	AAAAATAGAAGTCAA[C/T]AGAACAGACCAAGAG	8924
rs534319439	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28189164	GCAGTGGCTCCACAG[A/G]AATGGTACAGTCTAG	8924
rs534334303	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28172927	AAGAAAACAATCAAC[C/G]TATTTAAATATAGGA	8924
rs534335049	in-del	-/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28158389	CTCTTTGTGGGTCTC[-/T]TAAGGACTTGCTTTA	8924
rs534355550	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28258584	TGTAGGTTTAATTAA[A/C]GCACTGCTAAACAGG	8924
rs534357061	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28145094	CCAGTGGGGAAATGA[A/C]CCCACCAGCCAGGAT	8924
rs534384525	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28187145	TTTAAAACATAAAAC[A/G]TATTTGAATATACAC	8924
rs534398599	snp	A/T	0.00046181	0.0151885	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28178937	CTGAGAGCTGTGATC[A/T]GCCGTGGGATGGGCA	8924
rs534401737	snp	C/G	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314577	AAGAATCATATGTCA[C/G]CCAAGCACGGTGGCT	8924
rs534442514	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28262688	CTCAACAGGTTTAAA[C/T]TACATTTCAGTCATT	8924
rs534453656	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28207496	CACAGACACATCCCA[C/T]GTGCATATTTCTAGC	8924
rs534480609	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28219481	AGCACCACATCCGCC[C/T]TCAGGGACAGGGTTC	8924
rs534480847	in-del	-/AT	0.0314385	0.121371	intron-variant	HERC2	GRCh38.p7	15:28216833	CCCATGCACTCTCAC[-/AT]ACACTTACCCCTCCC	8924
rs534481280	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28255703	TATCACAATTAAATC[A/G]TATCTCAATAATTTT	8924
rs534534626	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28291761	AAAAATGGAATTAGC[C/T]GGGTGTGGTGGTGCA	8924
rs534539896	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28298576	TGAGGCGGGCGGATC[A/C]CGAGGTCAGGAGCTC	8924
rs534548237	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28210695	tttggtctggggtgc[A/G]gcctgggagtctgca	8924
rs534551613	snp	A/G	0.00398564	0.0444627	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317019	TGACCTCAGCCTCCC[A/G]AACTGCTAGGATTAC	8924
rs534558989	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28140847	CATTTTTTAAAAGAT[A/G]GTATTTACAATAGCA	8924
rs534564265	in-del	-/A	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28161945	GGTTTACCATCTAGG[-/A]AAAAAAGTAAAGTTG	8924
rs534564324	in-del	-/C	0.000856869	0.0206809	intron-variant	HERC2	GRCh38.p7	15:28144259	GAACACTGTAAACAT[-/C]CCCGGGTTTCACAAG	8924
rs534589936	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28134471	TTTGCACTGCTGTAC[C/T]GCACTTACTAAACCT	8924
rs534591605	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28250716	TTACGATCTTTAGAT[A/T]AACTACTGTTCAACA	8924
rs534602056	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28126558	ACTAGCCATAAAAAG[G/T]AATGAAATGATTGCA	8924
rs534628796	snp	G/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28127034	GTCCCTGGTGACCAG[G/T]ATGGAAACAAGGCTC	8924
rs534629224	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28170807	CTCTAAACTCAACAG[A/G]AAAAAAAAAAGCCAA	8924
rs534631576	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28230792	TTTCAGGCCATGCAG[C/T]CTGTCGCAAATACTC	8924
rs534677117	snp	C/T	0.00874735	0.0655527	intron-variant	HERC2	GRCh38.p7	15:28252623	TCTATGTGAACAAGC[C/T]GTTGCAACTGAAATT	8924
rs534688924	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28198133	ACTCCCTCTGATGGA[A/G]ACACCCATTCCCCAA	8924
rs534726935	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28139432	CTGCCAACAGCTCAT[A/G]AGGGACTGAGGCCTC	8924
rs534731236	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28270402	GGCTGTGGAACCCCC[C/T]GCAGAAGGTGGGAGG	8924
rs534738661	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28127577	CTGGGGAGCGGTGAC[A/G]CCTCAATAGCAATGA	8924
rs534741504	snp	A/G	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28308462	TTGTGGAGTCTTTAG[A/G]TTTTTCCAAATATAA	8924
rs534745245	snp	A/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB, utr-variant-5-prime	HERC2	GRCh38.p7	15:28299761	TAACATACAAGAAAA[A/T]TGACACGTGGTCGGG	8924
rs534751272	snp	A/G	0.000428689	0.0146342	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28174550	AAGCCTTGCACGAGT[A/G]TGGGCTTCCTGTTAA	8924
rs534764330	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28168155	AAATTCTTGACTGTC[A/G]GAACTTTAAGGTTTC	8924
rs534773454	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28271093	CAACATTGACTGCGC[A/G]TGTATACATTTATGA	8924
rs534782008	in-del	-/AAG	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28193454	TTTAGAAAACATAAC[-/AAG]AAGGTAAAAGATCTG	8924
rs534788503	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28238336	TGAGGGTTACCAGAG[C/T]ATAATGACCTTCTAC	8924
rs534789232	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28175422	GATTTCATCAACAGC[C/T]GTGATTTCAACAGGA	8924
rs534791350	snp	A/C	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28212085	GGCCCCTGGATCCGG[A/C]AGAGAACAGGCTGTG	8924
rs534792925	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28184003	GACCAGCCTGGGCAA[A/C]ACGGTGAAACCTCAT	8924
rs534828846	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28293632	ACTTCAATTTCACAC[C/T]AATTGCTTTTATCCA	8924
rs534831379	snp	C/T	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28301510	TCAAAATCAAAAACG[C/T]CTTTGCTTGTCAACA	8924
rs534834941	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28206937	AATTGCTTGAACCAG[G/T]GAGTTGGAGGTTGCA	8924
rs534837258	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28262115	ACCTCTCACACTGCC[C/T]TTTCCCTTCTTCCTA	8924
rs534850615	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28207666	AGGGAGATCCACTGC[C/G]CTCAAGCCCACTTCA	8924
rs534860478	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28175897	AAGTTACTGTTGTAG[A/G]TTTTCATATAAAGAG	8924
rs534865714	snp	A/C/G	0.00017358	0.00931473	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256286	AAACCAAGGAATTCC[A/C/G]GGTCAACCTGGTGAC	8924
rs534874161	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28160697	AGGTGAGGCGATGCC[C/T]CGCCCTGCTTCAGCT	8924
rs534874252	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28169982	TTTCTTACCCCGGTA[A/C]GACAAGACAAAAAAG	8924
rs534903278	snp	C/T	1.66183e-05	0.00288251	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214181	GGAGTGCAGCGTGCG[C/T]AGCAGTGCCACCACC	8924
rs534906273	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28201287	TTCCAGGGTACACAG[A/C]ACCTTCTAGCGTACC	8924
rs534936507	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28163779	ATCCAGTCTCTCTCT[C/G]TCCTTGGGTTCATTG	8924
rs534958950	snp	A/G	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28289788	CTGACTACAAAAGGG[A/G]AACACTGCACATCCT	8924
rs534960535	snp	A/C	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28295181	GGAATGCAAACTAAA[A/C]CAGCCTCCAGTTTAC	8924
rs534962178	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28208849	ACATGCCTCACCGCC[C/T]CCTGACCCCAGAGGA	8924
rs534989777	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28138168	CGCCGTCTTCATAAC[A/G]TAAAAGTGCAAGGGA	8924
rs535006102	in-del	-/AA			intron-variant	HERC2	GRCh38.p7	15:28264037	AAAAAAAAAAAAAAA[-/AA]CAAACAAAAACAAAA	8924
rs535020661	snp	A/G	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28209633	CAGGCATGAGCCACC[A/G]CGCCAGGCCTATATA	8924
rs535021960	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28201881	ATGAGATGTTTGAAC[A/G]AGGGTCTGTTCTGAA	8924
rs535037432	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28230288	CCTCCCTCCAGATGC[C/T]CAGGACAAGACTGTG	8924
rs535065576	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28282536	TACAATAACCAAAAT[A/T]AAAAGCTCAGTGAAT	8924
rs535095945	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28254721	CTTCTTTTTACAGAA[C/T]CAAGGTCCAGGCTGC	8924
rs535096758	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28296192	AAAATTCATCAAATG[A/T]GGGCCGGGCATGGTG	8924
rs535106074	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28131973	AAAGAGGAGGTTAAA[A/G]TGCTCCTAAGGAGCA	8924
rs535106120	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28249063	CCCAATGTTTAAGGA[A/G]TGTAAACATTAAGAC	8924
rs535120085	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28304459	TGCAATCTCCACCTC[C/T]GGGGTTCAAGTGATT	8924
rs535121057	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28171841	GCACTTTGGGAGGCC[C/G]AGGTGGGCGGATCAC	8924
rs535135265	in-del	-/A	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28304597	CAAACTCCTGACCTC[-/A]AAGTGATCCACTCAC	8924
rs535154448	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28258291	CCTGGCCAACATGGA[A/G]AAACCCCATCTCTAC	8924
rs535157614	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28296749	CACTGTCATATGGAC[A/G]CTCTTAGCCTCAGCA	8924
rs535169061	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28212323	CCGCAACTCAACAAA[C/T]GGTGAGCCCACGTGA	8924
rs535185038	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28125370	TAGGTATGACCTAAA[C/T]ATGAATACATGCTAA	8924
rs535186721	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28252542	TTCTCATTGATTCTT[A/C]ATTAACTCCATGAAA	8924
rs535195669	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28249451	AAGAAACATATGTTC[C/G]CAGAAGGTAAAGTTA	8924
rs535202811	snp	A/C	1.74054e-05	0.00294998	missense	HERC2	GRCh38.p7	15:28168579	GGCATCAGGGCCCCG[A/C]CAACAGCATCTCTGT	8924
rs535205664	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28294851	GTGTCAGTGTCCTAC[A/G]TTCAGCCATCCCATA	8924
rs535230284	snp	C/T	0.089084	0.191327	intron-variant	HERC2	GRCh38.p7	15:28204746	AAAGTATGTCTTGGA[C/T]GGATATAACAACAGA	8924
rs535234383	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28242262	ATGTGAATGTATTAA[C/T]GCCACTAAATGGTAC	8924
rs535301656	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28266741	CAACAGAGGGCAGAT[C/G]AGAGGTTGTCAGGAA	8924
rs535325847	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28243209	ATGGACAAAATGCCC[A/T]TGGAAAAAAAGTGAC	8924
rs535339094	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28275201	AAGGAAAAGTTTTCT[C/G]TTTAAGAATCAAAGA	8924
rs535356866	snp	A/G	1.77827e-05	0.00298178	intron-variant	HERC2	GRCh38.p7	15:28237138	TAAATTTCATCATCA[A/G]TCTGAGGAAACAGAA	8924
rs535390266	snp	A/C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28280345	GGCCACAGTTTGTTG[A/C/T]AATGTTGAGAAAATG	8924
rs535390804	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28257589	TAATAGCAACTCTAA[C/G]TAGACAACGAATTGT	8924
rs535396899	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316923	CTGGGACTACAGGCA[C/T]GTGCCACCACACCCA	8924
rs535399793	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214956	CGGCTCACTACAAAC[C/T]CCCACCTCCCAGGTT	8924
rs535411436	snp	C/G	0.0618563	0.164627	intron-variant	HERC2	GRCh38.p7	15:28220979	TCCTTCCATGGCTCC[C/G]ACCAGACCTCAGTTA	8924
rs535415531	snp	A/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28135997	TAACACCAAGAAAAA[A/T]AAAAAACAATTTAAT	8924
rs535415881	snp	A/G	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28235212	CACATTCGTTCTTCT[A/G]AAACACTAATCCAAT	8924
rs535439278	snp	C/G	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28209389	CGCTCTGTCACCCAG[C/G]CTGGAGTGCAGTGAC	8924
rs535465713	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28244687	GAGAGACAAAATAAC[A/G]CAGGACTAAGCTCAC	8924
rs535478105	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28161930	GATGTTAGGGCAACC[A/G]GTTTACCATCTAGGA	8924
rs535480123	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28206714	GGCGGGCGCCTGTAG[C/T]CCCAGCTACTTGGGA	8924
rs535482584	snp	A/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28252062	TCACATGGCCAAGTG[A/T]TTCTAAACATACTTA	8924
rs535485885	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28157765	CTCTGATCTTAGTTA[A/T]TTTTTGCCTTCTGCT	8924
rs535491221	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28236320	TTTGAGACGGAGTCT[C/G]GCTCTTGTCACCAAG	8924
rs535517727	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28209814	AAGTACCATCATTTT[C/G]AATGGCACCATGGTA	8924
rs535518895	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28204870	GTAAAAGGAAACTCA[C/G]TAACAGTGTAACAGA	8924
rs535557262	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28152125	GGCGGAACTTATGGG[C/T]CTCCGAATCGGGCAG	8924
rs535561917	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28122056	AGCAGCCACGGGGCC[A/G]GGGAGCACCGTGCAG	8924
rs535594453	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28129351	TTAACTGCCCCGGCA[C/T]TGAGCTGTGTCAGGT	8924
rs535599285	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28256415	AATTTCAAGTATTAT[G/T]TAAATAGACAATTTC	8924
rs535613400	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28115366	AGCCTGACCGGACCC[A/G]CAGAACAGACTGTGC	8924
rs535618573	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28286120	GAATTAACACGGACT[C/G]AAAACAATCTCTTCT	8924
rs535636850	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28320783	TCCTGACAAGCTTGC[A/G]GTTATCTCATTAAAT	8924
rs535655256	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28210376	CTGACCTCGTGATCC[A/G]CCGCCCGCCTCGGCC	8924
rs535655485	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28247281	ATCTACAGGCATGCA[C/T]TACCACACCCAGCTC	8924
rs535679180	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28191749	TGGTCAGTTAGATAA[A/G]ATCTATTACTCGTAT	8924
rs535691880	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28216272	TTCGTGTTTTAAATA[C/T]CTCCACAATCTTGCT	8924
rs535692625	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28309225	TCGTTAATTTTGTCT[A/G]GATGATCTGATCTGT	8924
rs535709120	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28279610	CCAGGAGCAAGACCC[C/T]ATCTCCACACACACA	8924
rs535736764	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28234043	AAACAGAGCACTGAG[A/G]TGGCAGTGGGGGCAG	8924
rs535745528	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28262796	TTCATGGAATGTCAG[G/T]TTAAGAACATAAAAC	8924
rs535753254	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28153873	AAGGCAACGGAGCCC[A/G]GTGGGAGGGGCGGGA	8924
rs535762344	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28171706	TGAATATTCCCATAC[A/G]GAAGAAATGATATTT	8924
rs535768603	snp	C/T	3.37878e-05	0.00411008	intron-variant	HERC2	GRCh38.p7	15:28265570	CTCCAGGGAAGCTGC[C/T]ATGCGTGTCCTCGTG	8924
rs535772027	snp	C/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28148103	AGGCAATAAAAGCAG[C/G]CCAGAAAGATACACC	8924
rs535784507	snp	A/G	9.8868e-05	0.00703024	intron-variant	HERC2	GRCh38.p7	15:28141701	CTCACACTCACGATC[A/G]ACATTACTGCTTGTT	8924
rs535806844	snp	C/T	0.000250228	0.0111826	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28202447	GAGCTGCACCACGAT[C/T]GGCAGAGCGGGAACG	8924
rs535841926	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28114887	CAGCACACTCTGTCA[A/G]GCAGGAACCAGGGTC	8924
rs535851631	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28241671	CTAAAATACAAAAAA[A/T]TAGCTGGGCATGGTG	8924
rs535857864	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28117623	CAAAGATTCAACCCA[A/G]TGCCCCTGAGACTGA	8924
rs535869846	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28203591	CAGCTGACGCAATCA[A/G]CAATAAAACGAGTAC	8924
rs535874157	snp	A/C/G	8.32433e-05	0.00645104	intron-variant	HERC2	GRCh38.p7	15:28196423	AACAGAAAACCATTC[A/C/G]TCCCAAAGCAAATCT	8924
rs535891828	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28112860	CTGGGGATGGCCAGA[C/T]ACATTTTTAAAAAAT	8924
rs535911087	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28284656	GGCCGGGCACAGTGG[C/T]TCACGCCTGTAATCC	8924
rs535934372	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28281668	ATGTGAGACCTGGAG[C/T]TTTGCAGCTAAGAGC	8924
rs535939941	snp	A/G	4.99879e-05	0.00499915	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28238625	CTATTTCCTGTTAAC[A/G]ACTGTGTCTGGAAGT	8924
rs535948380	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28277623	CTGAGGGAATTCAGT[A/T]TGATTCGACAAACAC	8924
rs535952241	snp	A/G	0.00676609	0.0577691	intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28320240	CTGCCTCAGCCTCCC[A/G]AGTGGCTGGGATTAC	8924
rs535961852	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28114039	ACAGCAGACACGATA[C/T]GGGGGACAGCACCGC	8924
rs535963584	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318000	CTGTAGGAAATTCAT[C/T]TGAGTGCAGCTTATG	8924
rs535970207	snp	A/G	8.504e-05	0.00652018	intron-variant	HERC2	GRCh38.p7	15:28274454	CATCCTCGCCTGGGC[A/G]CACACACGCGTCAGA	8924
rs535973292	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28236369	GATCTCGGCTCACTG[A/C]AACCTCCGTCTCCTG	8924
rs535977550	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28232376	TGAAACTCCGTCTCT[A/C]CTAAAATACAAAAAT	8924
rs535990934	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28197082	TTAACAATCTCTTAA[C/G]CAAAGAAAAATGTTT	8924
rs535997950	snp	A/G	3.36502e-05	0.0041017	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229341	AAACAATCAGTAAGA[A/G]GTTCCCTTTCAAATA	8924
rs536005670	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28150080	AACGGCCACACAAAC[A/G]CACATTCTAGTAAAA	8924
rs536024176	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28144524	TGTGTTCTGTTCCAC[A/G]CCTCAGCAGGGCCTG	8924
rs536029210	snp	A/C	8.2648e-05	0.00642784	intron-variant	HERC2	GRCh38.p7	15:28265604	CTGTCCAGGGTGGCG[A/C]GAGCTCTACGTACCG	8924
rs536047047	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28191382	GAGAGAATTTTCCCT[C/T]AACCTGGCAGCAACA	8924
rs536049796	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28197665	GCTGAGACTGGAGAA[C/T]TCCTTAAACCTGGGG	8924
rs536075056	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28268853	AGGGGCAGGGCAGGC[C/T]AGCCCCATGCCACAG	8924
rs536076072	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28226272	TTTTGCAGATATGGA[A/G]AAGCCAGCCTTGAAG	8924
rs536112822	snp	A/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28227055	CAAGGCAGGCAGATC[A/T]CCTGAGGTCAGGAGT	8924
rs536115809	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28144873	ACAAACCTTCTTAGA[C/T]GCAAAGCAGAATGAT	8924
rs536124208	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28140884	AAATACATCTAACGA[A/G]TGATGTGCAAATAAA	8924
rs536125373	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28300686	AAATTAGCCGGGTGT[A/G]CTGGTGCATGCCTGT	8924
rs536133209	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28138295	ACGTAGATGGAACAA[C/T]CGTCTATTGGAAGAA	8924
rs536136394	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28309732	CTGAAGTAGAGGATA[A/G]AACTAAGCTATGGCC	8924
rs536162275	snp	A/G	0.000267366	0.0115591	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28220635	GGCCTAGGCCTGGAG[A/G]AGGCCCATCCTGAGA	8924
rs536175159	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28303953	GGCGGATCACCTGAG[A/G]TCAGGAGTTCAAGAC	8924
rs536199006	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28149052	CATTCTAGTAAAATT[A/G]CCGAAAAAACAAACG	8924
rs536207541	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28199974	TGTTTGTGTCCCCCC[C/T]ACCAAAATTCATGAA	8924
rs536218534	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28248927	CAAAACGGAGCAGAA[C/G]GGCACGGAAGGCTCA	8924
rs536221000	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28112082	TTGAGTACGGCTGCA[A/G]TTTACTTTACTGTGC	8924
rs536247238	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28273235	AGATACTATATTACA[A/G]TAGATGACATACTCC	8924
rs536259825	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28187305	TTCAGTATATATCAC[C/T]GAATTAAGGAGGTCT	8924
rs536271134	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28310902	CTAACACAGCGAAAC[C/G]CCATCTCTACTAAAA	8924
rs536271174	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317392	CCGCGCCCAGCCGAA[A/G]TGACAATATTTATAT	8924
rs536276359	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28200360	AGATCACGCCACTGC[A/G]CTCCAGCCTGGGTGA	8924
rs536307953	snp	A/G	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28311516	GTTAAATCAAATGTG[A/G]AAGGGAAAATAAGGG	8924
rs536327152	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28143191	GATTTCAGTACATCC[A/G]CTTCCAGAGAAATAG	8924
rs536328299	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28187434	CCTCCCGGGTTCAAG[C/T]GATTCTCCAACCTCA	8924
rs536335512	snp	A/G	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28247184	TTTTTTTTAACAGAC[A/G]GGGGTCTCACCATGT	8924
rs536338946	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28155593	CTGTTCATATCCTTC[A/G]CCCACTTGTTGATGG	8924
rs536351916	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28282259	TAAGTAAGACCTAGA[A/G]TCGCCTAACAACATG	8924
rs536352750	snp	A/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28216620	CACACTCACATGCGC[A/T]CACACACACACACTC	8924
rs536385207	snp	A/C	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28137012	TAACTCAAAAAAAAA[A/C]ACCACAGTCCATATA	8924
rs536386289	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28113336	CCACCCTGGCATTTC[C/T]GCAAGACTCCGTCAC	8924
rs536388785	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28312682	ATGGGACTTTCCATT[G/T]GTAAAGTGAGAGTAT	8924
rs536399207	snp	C/G	0.00136737	0.0261116	intron-variant	HERC2	GRCh38.p7	15:28130453	GGTGGTGCACATACC[C/G]CAATAAAAATCTGGT	8924
rs536430313	snp	C/G/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28298648	AAAAATACAAAAAAT[C/G/T]AGCCGGGCGTGGTGG	8924
rs536432632	in-del	-/TAAAG			intron-variant	HERC2	GRCh38.p7	15:28136885	ACGAAAGAATTTCAC[-/TAAAG]TAAATTGAGAAAGAT	8924
rs536439156	snp	A/T	3.3857e-05	0.00411429	intron-variant	HERC2	GRCh38.p7	15:28275010	CAGGCCGGGAACTGC[A/T]GACGACACACACGGA	8924
rs536453427	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28175906	TTGTAGGTTTTCATA[C/T]AAAGAGACTGAAAAT	8924
rs536461176	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28131105	TCATGACCTCTGTGA[C/T]TGCTCTCATATGTAA	8924
rs536467875	snp	A/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28229998	ACTATGCTATAAATA[A/T]ACTTATAAGTGATTT	8924
rs536474133	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313635	AAATATTTGCAGATG[A/G]GTAAAGGTATATGGC	8924
rs536497284	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28167533	GGACCGTGTCCTGCG[A/G]CATTCCCACAAACGC	8924
rs536507233	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28226437	TGTGATAATGTAATT[C/G]AGAGTCCAGAAATAA	8924
rs536512935	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28189065	GCACTCCAGCCTGGG[C/T]GACAGAGTGAGACTC	8924
rs536513179	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28307546	CGTATGCTGTGTTGC[C/T]ATTGCCATTTGTTTC	8924
rs536520474	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28182291	AATGTCTTTTAGTTC[A/G]TGTAAAGAAACAATA	8924
rs536532110	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28248309	AAGACTAAACTGAAC[A/G]TACAGGATGCTATTA	8924
rs536540110	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28143797	CCTCTCAACGATTTA[G/T]AGGTTTAGACTACTA	8924
rs536579182	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28182097	TTATTTTGTTCATGA[C/T]AGTCAAAAATGTTTA	8924
rs536584642	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28206574	TGCGGTGGCTCACGC[C/G]TGTAATCCCTGCACT	8924
rs536588388	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28138832	GTGGACAAACTAAAT[G/T]GAAAACCTTCTGGAA	8924
rs536593054	in-del	-/AG	0.136166	0.22258	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314523	AACATATATTTAAAA[-/AG]AGTGATTTTATATTT	8924
rs536597371	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28307960	TACTATAGCTCTGTA[A/G]TATAATTTGAAGTCA	8924
rs536668846	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28308539	ATGTGGAGGCCTTTT[A/C]TTTCTTTCTCTTGTC	8924
rs536671009	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28315168	AGAAACTACACCATA[A/G]AATAGTCCAAGGAGG	8924
rs536705094	snp	G/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28301673	ATTAAAAGAGACACA[G/T]ATGTTTGCCCATCTT	8924
rs536707695	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28228567	TAACGCAGAAAGCAC[A/G]GGCGATTACTCTAAA	8924
rs536709110	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28309073	GACTTATTTTGTGGC[C/T]TAACATACGGTCTAA	8924
rs536710096	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28306210	AGCTGTGTGTCAGCT[C/G]TATATGGCTTTTATT	8924
rs536721594	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28185184	AAGATCACAGAGCCC[C/T]AGAATAACCTGATTT	8924
rs536724214	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28187688	TTATCATAGCACAAA[C/T]AATAACTCCCATATC	8924
rs536743364	in-del	-/C	0.0146363	0.0842849	intron-variant	HERC2	GRCh38.p7	15:28216319	ACTTAAATATTTTTT[-/C]TTTTTTGTATTTTTA	8924
rs536745264	in-del	-/G	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28170760	CACACATCTGCCAAA[-/G]GACTAGAAACATCTA	8924
rs536763288	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28267531	CAATCCAGTGTGAGA[A/G]TAACAGCTATAAATT	8924
rs536784212	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28140615	CAACCTCCATCTCCC[A/G]GGTTCCAGTGATTCT	8924
rs536791846	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28143737	ACGCATGAGCCACCG[C/T]GCCCGGTCCAAGGCC	8924
rs536798243	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28135125	TGCGTTCTTTCTTCC[A/T]CACCCCTGCTATTTC	8924
rs536799635	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28297920	GACAAACGGTGGATG[A/G]ACAGACAGCAGGATG	8924
rs536804090	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28137377	GCTTTACTGTACCTC[A/G]CAGATACTGTTTTTT	8924
rs536810818	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28253260	ACCTCCTCCTAGTCT[A/G]GCCTTCCAAAATAAT	8924
rs536817594	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214555	TGACGGCACTGCGCC[A/G]CTCTTCACCAGGGCA	8924
rs536837261	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28179786	GGTCTTAGTTTTTAA[A/C]AAACACGTTAAAAAG	8924
rs536917371	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28296019	TGAGACCCTGTCTCA[A/G]AAAATAAAATAAAAT	8924
rs536948943	in-del	-/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28192666	AAGGTCAGAACCGCA[-/G]GAAGACCCGAGGCGA	8924
rs536983778	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28193657	CTCCATGCACATGTA[A/G]AACCTGTGCAAGATG	8924
rs536986611	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28140723	GACAGGGTTTTCCTA[C/T]GTTGGCCAGGCTGGT	8924
rs536998935	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28211962	ACATGGAAACAAACT[C/G]AGGAGAGCCGCATTC	8924
rs537007029	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28262572	CACTCATGGTCTCAG[C/T]GTGCCTGCAGTACAA	8924
rs537007642	snp	C/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28270438	GGGCTGTGGATAAAG[C/G]GGAGCTCTCTGGGGC	8924
rs537013799	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28276626	TATAGTCCCAGCTAT[A/G]TGGGAGGCTGAGGCA	8924
rs537027564	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28226769	CTTCATCAAAATAAA[A/G]AACTTCTCTATCAAA	8924
rs537028069	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28261741	GTAAACTTCTTACTC[G/T]GCAACTTATCTCAGA	8924
rs537033640	snp	C/G/T	0.00677024	0.0578401	intron-variant	HERC2	GRCh38.p7	15:28293706	AGAACAGGAGTATGA[C/G/T]TCAAAAATCTTTTAA	8924
rs537036546	in-del	-/TTTA	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28250461	CAATGAAATTTTTAG[-/TTTA]TTTAATATAAAATTT	8924
rs537064481	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28133361	TTGGCTATCAGACCT[C/T]AGTCAGATTATATGA	8924
rs537084650	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28116940	TCCCACACCATGTGG[C/T]CTCTGTGCTCCCTGT	8924
rs537095386	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28249552	AGCAAGGGAGAGACA[A/G]TGCAGGTAATGGAAT	8924
rs537103255	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28162594	TGCACAAATCAGTTA[C/T]AAAACAGGTAAAGGG	8924
rs537112862	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28175989	CTCAAGCTGCCTCGG[A/G]TCATGACATTGGCAC	8924
rs537122980	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28280346	GCCACAGTTTGTTGC[A/G]ATGTTGAGAAAATGG	8924
rs537129793	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28139997	CGCTTGAACCCAGGA[A/G]GCAGAGGTTGTAGTG	8924
rs537130608	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28121693	ACCCAGCAGCGTTCC[A/G]GAGGCTGGAAGAGCC	8924
rs537157566	snp	C/T	0.0256215	0.110247	intron-variant	HERC2	GRCh38.p7	15:28289373	AATTTACAAATATGA[C/T]GTAAAAATCCTAAAA	8924
rs537163159	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28264782	TCACTCAATAATAGA[A/T]ATTTTAAAATGACGA	8924
rs537164262	in-del	-/C	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28275775	AGACAGAGCAAGACT[-/C]CCATCTCAAAAAAAA	8924
rs537169244	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28118873	GCTACCCTGAACGGG[A/G]AGGAGCCACCTCTGG	8924
rs537169404	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28159666	TTTTAACTTCTTTGC[A/C]ATGGGTTCGAACTTC	8924
rs537189119	in-del	-/C	0.00755907	0.0610114	intron-variant	HERC2	GRCh38.p7	15:28143313	AGTTAGCCTCATTGT[-/C]AAAGTCCAATCAACA	8924
rs537196728	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28119212	ACCAGCCTGGCCAAC[A/G]TGGTGAAATTGTCTC	8924
rs537199355	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28303174	TCCATTTTGATGTGA[C/T]TTTCGTATATGGTGA	8924
rs537202002	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28256810	CATGTTAGCCGGGAT[G/T]GTCTCGATCTCCTGA	8924
rs537230064	snp	A/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28170043	ACCAATAAAGTCTCA[A/T]CAGGCTCACTTCGTT	8924
rs537241040	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28282926	ACAGGGAGAGACTCC[A/G]AAGATGGGAAGGGAC	8924
rs537243027	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28289720	ATACCTAAAATCCAT[C/G]GACTTACGGGACATG	8924
rs537256197	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318734	ATGTAGGGCCCTAGG[A/C]CTGACGTATCCAAAT	8924
rs537256478	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28155014	AGTGAGAACATGCAG[C/T]GTTTGGTTTTTTTGT	8924
rs537264227	snp	C/G	0.000280757	0.0118448	intron-variant	HERC2	GRCh38.p7	15:28202324	CCACACATACACAAG[C/G]AGAGGCCAGGAAAAC	8924
rs537279471	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28275681	GCATATATAGGGGAG[G/T]CTGAGGCAGGAGAAT	8924
rs537281101	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28170920	TAGCCATAAGGAAAA[C/T]ATTAAAACCACAATG	8924
rs537297639	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28251209	ACACTTTTGGAGGCC[A/G]AGGCGGGCAGATTAC	8924
rs537303792	snp	C/T	0.000474651	0.0153981	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28196325	TTGAATCTGGATCCA[C/T]TGATAGGAAACATCT	8924
rs537311589	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28290098	GTGAGGATATAACTT[G/T]TATCTTTAAAGTTAC	8924
rs537336840	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28244860	AAAACACGAGAAGAA[A/G]AAAAGCCCATCCAGC	8924
rs537341573	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28230878	TGCTCCTGTAAAACT[G/T]TATTTATGGTGCTAC	8924
rs537348856	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28290474	ACCTCAAGTAATCCA[C/T]CCACCTCAGCCTCCC	8924
rs537350896	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28284690	CACTTTGGGAGGCCA[A/G]GGTGGGTGGATCTCA	8924
rs537356727	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28165297	GGAGTGGGGGACAGC[C/G]AAGATCGGAGGTTGG	8924
rs537365709	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28158375	TGTGGGAGTCGAAGT[C/T]TCTTTGTGGGTCTCT	8924
rs537376527	snp	A/C	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28189600	AAATAGTTCCATGAC[A/C]TTCCAGAATAAATGG	8924
rs537382251	in-del	-/C	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28118288	CCCAGCTCCCCGAAG[-/C]CCACGGGGCTGCCTC	8924
rs537382662	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314614	TGTCATCTCAGACTT[C/T]GGGAGGCCAAGGCGG	8924
rs537384905	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28146638	GATCAAGCTTTACAG[C/T]GAACATCACACTGAC	8924
rs537391666	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28194599	ACAAAACAAAACAAA[A/G]AAACAGGCATGAGCC	8924
rs537391881	snp	C/T	3.57136e-05	0.00422558	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28230444	AAGCTTCTTCTAAAT[C/T]ACTCTCTTCGTTTCC	8924
rs537408763	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28212360	GGACTTTAGTACGTC[C/T]GTGAATTCACTCATA	8924
rs537410788	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28218748	ATATAATTCAACAGC[A/T]TTAATATTACATTCT	8924
rs537415931	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28259163	GCAATGGCGCCATCC[C/T]GGCTCACTGCAATTT	8924
rs537429307	snp	C/T	0.000214931	0.0103643	intron-variant	HERC2	GRCh38.p7	15:28177387	AGAAACAGTTTCTTA[C/T]TAGCAAATGAGACTA	8924
rs537439123	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28300134	GCTCTGAAAAGATAA[A/G]CCAAAAGCAAGTACC	8924
rs537452259	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28253134	AATCTCTTTCACAAA[C/T]CACCTTGCTTTTTCG	8924
rs537453776	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28125641	AATTGCTCTTGCATG[C/T]GAAACAGAAAAGAAA	8924
rs537458268	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28134515	GAAGAGAAGTGGTGA[G/T]AGCAGACATCCTTGC	8924
rs537470911	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28187172	ACACAAATCAGAACA[A/G]ATAGTACAAAGAACT	8924
rs537479999	in-del	-/AT	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28285985	CCAAATATAAAATAG[-/AT]CATTTGAATAGCCCT	8924
rs537496949	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28165984	TGATTCCTATGTTGG[A/G]GCATAAAACATCTTA	8924
rs537498162	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28255403	GAACAAACAGTACTA[C/T]ACCTATAAAATGGAA	8924
rs537509026	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28166676	GGACACATCAGACAA[C/T]GGAACCAGTCCACAG	8924
rs537523127	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28294080	GAAGGAAACAGTTCC[A/T]CTGTTTACAACATTT	8924
rs537523889	snp	A/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28213449	GTTGAATAAAAAGTA[A/T]ACTTCATAAATTCAC	8924
rs537558778	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28286755	AGTTTACTCCCCTAA[A/T]AGATTACAACACCCA	8924
rs537567225	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28160310	TGCTGCCTTTTGTTC[A/G]GCTATGGCCTGCCCC	8924
rs537581321	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28205190	TGGAGACAAAACAGC[A/G]GAAGGTCTCTTTTTG	8924
rs537590907	snp	A/G	0	0	intron-variant	HERC2	GRCh38.p7	15:28126283	GTGAAAACGCGTTGT[A/G]ATGGAAAGCATTTTC	8924
rs537592113	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28208383	ACCATCACAGTGGAT[A/G]GCACCTTCCTTCCAC	8924
rs537599672	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28199248	TGTCTGGCTTTGTGT[C/T]TCAGGCAGGAAATAT	8924
rs537606206	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28201923	TTATGATATAGAAAC[C/T]CAATCATCCCTTCAG	8924
rs537621996	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28251077	CAGGAGACAACCTGT[A/G]TGGACAGCACAGAGC	8924
rs537645842	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28287311	TTAAAGATGGAGTGG[C/T]TCAAGAATATGCTTT	8924
rs537663380	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28112639	CCCCTCTCAGTGACC[C/T]GGCAGGTCCACTGAG	8924
rs537664910	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28112148	TTGCTAAGAACAAAA[A/C]AGCAGAAAACATAAT	8924
rs537668308	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28193160	AAGGCAAGAAAATAT[G/T]ACTAAAAATTACCAG	8924
rs537677748	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28156733	CTTGTTCTAATTGAA[C/T]ACCCTTTATTTCTTT	8924
rs537679305	snp	A/G	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28153907	AGGAACCATCAAGCC[A/G]CTCAGGCCAGACAGA	8924
rs537682836	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28280856	AGGAGGTTGCAGTGA[G/T]CTGAGATTTTGTCAC	8924
rs537740032	snp	C/T	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28237964	ATGTAAATTCATTTA[C/T]GACAAAACTTCTAAA	8924
rs537744502	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317443	AGCTTACATTTATGC[G/T]TAGTCATTCTTAATT	8924
rs537745657	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, downstream-variant-500B	HERC2, LOC107987422	GRCh38.p7	15:28319366	CGAGGCAGGCAGATC[A/G]CTTTGAGGTCAGGAG	8924
rs537746287	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28151036	ATGTAACAGCTATTA[G/T]GCTCTTGTAGATGCA	8924
rs537767066	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28273874	AATTTTTTACACTAA[A/G]AAGATCAGCTACAGG	8924
rs537775672	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28193760	TCAGGAGAAATAATA[C/T]AAACCAAATTGCAAT	8924
rs537777920	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28187331	GGTCTGGTTTTTTTT[G/T]TTGTTTTTTTGTTTT	8924
rs537783413	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28311577	CGTTTTAACCACTAA[G/T]ATTTGCACTAACTAC	8924
rs537784518	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28231641	CGTGTGCCTAGTTTC[C/G]TCTGGACTTCCCTCC	8924
rs537815209	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28252608	TGTGTTGGAAGTTCA[A/T]CTATGTGAACAAGCT	8924
rs537824299	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28245747	TTTGGATTATCTCCA[C/T]TTTTTACTTATACTA	8924
rs537835630	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28291209	ATAACCTACGAGGTA[A/G]GTACTACTATTAACC	8924
rs537847602	snp	C/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28122487	GCGCCAGAGGAGACC[C/T]AGAAAGGGTATCCTG	8924
rs537879815	snp	A/G	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28159330	AATATCCTGCAGAGT[A/G]TTTTCCAACTTGGTT	8924
rs537906984	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28159952	TTTTCCTTCTAACAG[A/T]CAGGACCCTCAGCTG	8924
rs537914498	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	HERC2	GRCh38.p7	15:28110674	GTTAGACCTGCCAGC[C/G]AGTTTTCCTAGCCTG	8924
rs537923284	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28204796	GCATCTTGACCTTTC[A/G]AACAGATCAAGACAA	8924
rs537942903	snp	G/T	9.49172e-05	0.00688837	missense	HERC2	GRCh38.p7	15:28152761	GCTGAGAAGAGAGGC[G/T]GCCGCTCTGCGAGTC	8924
rs537948579	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321709	CGCTGACGAGACCTT[C/G]AGAATGGACGGTCAC	8924
rs537949137	snp	A/C	1.65302e-05	0.00287486	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233186	TATCTTTTGAGCTAT[A/C]CTCCTCCAACGGGGC	8924
rs537953217	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28148237	AACATTTTATAAAGC[A/T]GAAGACAGAATTACA	8924
rs537986260	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28116562	AAAAACTAAAAGCAG[A/G]TATTCAAGATATCTA	8924
rs537986275	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28123291	AATCACTAAGAATGG[A/G]CCATAATATTCGACA	8924
rs537987604	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316373	GGCCAGGCACAGTGG[A/C]TCATACATGTAATCA	8924
rs538022409	snp	C/T	1.65765e-05	0.00287888	missense	HERC2	GRCh38.p7	15:28117082	ACGAGCTCATCTTAG[C/T]ACACATCTGCCCAAA	8924
rs538050766	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316977	AGATGGGGTTTCACC[A/G]TGTTGGCCAGGATGA	8924
rs538053107	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28235309	CTCTGATCCTCCTGT[A/G]GATTGGACCCACCTG	8924
rs538057040	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28199822	TCCTATTGTATTGGA[C/G]AAACAGGGAGAGAGG	8924
rs538073038	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28273351	GTATAAGACTATACC[A/T]GTATCAGCATTTATC	8924
rs538092151	in-del	-/AGA			intron-variant	HERC2	GRCh38.p7	15:28166066	TGATGGGAATATGCC[-/AGA]AGAACACATAAAATT	8924
rs538105704	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28112677	CTGACCACCGGCCCA[C/T]AGAGTTGGAACCCAA	8924
rs538108149	in-del	-/C	3.61448e-05	0.00425101	intron-variant	HERC2	GRCh38.p7	15:28248509	GCCTAAAGTAACGAG[-/C]CCCGATCACATACAA	8924
rs538115845	in-del	-/CA	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28220989	GCTCCCACCAGACCT[-/CA]GTTAGGAGGGTGCGT	8924
rs538128004	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28258479	CTCCATCTCAAAATA[A/G]TAATAATAATAATCA	8924
rs538129978	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28142518	GGCACAGCAAGGATA[C/T]GGCCACCATCAGTGA	8924
rs538141426	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28286725	TCATTAAGAATGATT[C/T]AGATAGTTACTAAGA	8924
rs538145487	snp	A/C/G	0.00755907	0.0610114	intron-variant	HERC2	GRCh38.p7	15:28143314	AGTTAGCCTCATTGT[A/C/G]AAGTCCAATCAACAC	8924
rs538178721	snp	A/T	0	0	intron-variant	HERC2	GRCh38.p7	15:28228658	CGTAATGCAGAAAGC[A/T]CGGGCAATTACTTTA	8924
rs538193239	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28197226	GAGAGCCTTCCACAA[G/T]GTTCAAACAAACAAA	8924
rs538214208	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28292556	TGCGATGGCTCACAC[C/T]TGAAATCTCAGCAAC	8924
rs538232440	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28119006	CGCACGGTGGCTCAC[A/G]CCTATAATACCAGCA	8924
rs538234232	in-del	-/C	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28289584	CGCTGGAGCTGATCT[-/C]CCCAGAACGCTGAGA	8924
rs538240188	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28285269	AGCATCCACAAAACA[A/C]ATACTAAGTTAGAAC	8924
rs538246012	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28320813	TCAAAAAATTAGGAT[C/T]TAAGGCCAACATTGT	8924
rs538256605	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28197682	CCTTAAACCTGGGGG[C/T]GGAGGTTGCAGTGAG	8924
rs538266174	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28152156	CACCTTGCAGAAGGA[C/T]GGGCCTGAGGAACAC	8924
rs538267239	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28113802	AGAACAGAGGGAGCA[A/G]CTCCAGATGGCATGA	8924
rs538270732	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28278650	CACAAAAATTAAAAC[A/G]TAAGAAAACAAGGAA	8924
rs538283018	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28194402	GGTGAAACCCCATCT[A/C]TACTAAAAATACAAA	8924
rs538297937	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28230132	AAAGAATATATTTAA[C/G]GAATGAATGGTGAAT	8924
rs538326668	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28253767	AGGAGTTTGAGACCA[G/T]CCTGACCAATATTTT	8924
rs538340512	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28139879	GCCTGGCCAATATGG[C/T]GAAACCCCATCTCTA	8924
rs538355516	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28145012	GCAAACACGCATTCA[G/T]CCCCTGTACCAGGTA	8924
rs538369930	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28268919	AATGAAAACATGCCA[C/T]GTCCCAATTTGCCAC	8924
rs538372741	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28138092	GGCTAACAGAGGTGA[G/T]AAGGCTGCTGAAGGA	8924
rs538377102	snp	C/T	0.0103295	0.0711199	intron-variant	HERC2	GRCh38.p7	15:28309856	ACCAAGCCAGCATCC[C/T]TCAGTTTTTGTAGAA	8924
rs538407524	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28262091	AACCCTAAAGAGTCC[A/G]TCTGATGTACCTCTC	8924
rs538410663	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28145309	GCCTGGCTGCTGTGG[A/G]CAGGAGCGGTGGTGT	8924
rs538416456	snp	A/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28138945	AAGAAGTGGATTCCA[A/T]CCCTCACAGATGACC	8924
rs538430069	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28218294	AGCCCCAGAAGGAAC[C/T]ACCCTTGATCTCAGC	8924
rs538435210	snp	A/C			downstream-variant-500B	HERC2	GRCh38.p7	15:28110665	CTCTAATGCGTTAGA[A/C]CTGCCAGCCAGTTTT	8924
rs538449553	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28112270	GTCATCCCGGGAAGA[C/G]GGCCCGAGGACCACA	8924
rs538458250	snp	A/G	1.7297e-05	0.00294078	intron-variant	HERC2	GRCh38.p7	15:28220684	GTTAGGAGGGTGCGT[A/G]ACCTGCCCTGGTCCT	8924
rs538460931	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28310280	GCAAAACCACATTTC[C/T]ACCAAAAATACAAAA	8924
rs538464536	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28174787	CAAAATGGCATCAGC[A/G]TACTACAATTCTGAA	8924
rs538497568	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28304492	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACAA	8924
rs538517803	in-del	-/ATCA	0.150333	0.229274	intron-variant	HERC2	GRCh38.p7	15:28155609	CCACTTGTTGATGGG[-/ATCA]GTTGTTTTTTTCTTG	8924
rs538522182	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28255519	GTGCATACTATATAG[C/T]TATATTGCTGCGACA	8924
rs538528415	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28139368	AGTCAGCTGCCACCC[G/T]GTGAGACGCTCTATG	8924
rs538578642	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28297016	TGCGGGCATACGCAC[A/G]AAAGATAAAAATGAA	8924
rs538583534	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28306069	ATAGGAACACTTTTA[C/T]ACTGTTGGTGGGACT	8924
rs538587583	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28209972	TTTTTTTTTTGAGAC[A/G]AAGTCTCACTCTGTC	8924
rs538592035	snp	A/C	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28194492	GGAGAATGGCATGAA[A/C]CCGGGAAGCGGAGCT	8924
rs538595667	in-del	-/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28149723	TGAACGCACGTTCTA[-/G]TAAAATTACCGAAAA	8924
rs538596861	snp	A/C	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28294192	TCAATTCTGAAACTA[A/C]CTACCTAGAATTAGC	8924
rs538601327	in-del	-/A	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28177623	AATGAGCGTGAGCTG[-/A]ATAAATGAGTAACTC	8924
rs538646358	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28288785	CCCACGTGGGGGAGG[C/T]TGCAGTGAGCTGAGA	8924
rs538647487	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28194986	GCTTGAGCCCGGGAG[A/G]TGTCAGTTACAGTGA	8924
rs538658881	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28179895	TGTGTTTTAAGCTAA[A/G]TATTATTACAAGAGT	8924
rs538668546	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28306498	TTGGGTATTTCCGCA[C/T]CAATGTTCATCTGGG	8924
rs538673077	snp	A/C	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28275119	CCAATGGTTTTCTTC[A/C]AGTGACAGGATCACA	8924
rs538682884	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28222866	GGCCTGGAGTCTCTA[C/T]CCAGCTTCCCGGCAG	8924
rs538683762	snp	A/G	0.000165066	0.00908326	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28192003	GCAGGGCTCGCTGCC[A/G]TCAATGAGACGGGAT	8924
rs538706698	snp	A/T	0.00874735	0.0655527	intron-variant	HERC2	GRCh38.p7	15:28306974	CAAGTGGCTGGAATT[A/T]CAGGCACACAAAACC	8924
rs538720545	snp	A/T	0.0023933	0.0345097	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318590	ATGGCACCACTGCAC[A/T]CCAGCCTGGGAGACA	8924
rs538722836	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28150175	TTCTAGTGAAATCAC[A/G]AAAAAAACGCACGCG	8924
rs538735681	snp	C/T	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28217073	GCACTCATACACATT[C/T]ACACAAATGCTCGCA	8924
rs538772405	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28194040	TAAAATCATCACATG[C/T]CCCACATGTATTGTT	8924
rs538779282	snp	C/G	3.79939e-05	0.00435838	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28269254	AACACTCACCAGCGT[C/G]TCACTATTATAGGCC	8924
rs538793257	snp	C/T	0.0134861	0.0810011	intron-variant	HERC2	GRCh38.p7	15:28299311	GAGTTAAGCTCAAAG[C/T]TCCTGTTCCTATAGC	8924
rs538799050	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28131141	TATATTTAATTCTGA[A/C]CTCAAATTAATTAAA	8924
rs538802428	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28224894	ACACACAGTAAACAA[C/T]CAGTGGGTCAAAGAA	8924
rs538814021	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28211985	CCGCATTCTACAACC[A/G]AAGGAAGGCAAAGCC	8924
rs538815397	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28223212	TGGATTTGAAAATAG[A/G]AGCGCTAACCCCAGG	8924
rs538829323	snp	A/G	0.0012075	0.0245416	intron-variant	HERC2	GRCh38.p7	15:28182397	CCCAGGGAGCAGGCC[A/G]TACCTTGGAGCCTTT	8924
rs538829421	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28189465	TTACCAGTAAAATGC[A/G]TTAAAACTCAAGATT	8924
rs538839844	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28183104	AGGAACCTGATCATC[G/T]GCCAGCTAAGCTGAA	8924
rs538854709	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28124951	CGACAGGATGCAGCA[G/T]GTGACAGGAGCACAC	8924
rs538889277	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28300260	CTTCTGAAACATACA[C/T]GACTTTCATCCTCAA	8924
rs538896658	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28175396	GGTTCTCCAAGCAGT[A/G]AGACTCAGCTGATTT	8924
rs538899624	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28254011	TAAATAGACCGGGAG[G/T]GGTGGGTGATGCCTG	8924
rs538918408	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28177286	CAAAACACAAACAAC[C/T]GTGTTAAAAAAATTT	8924
rs538926313	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28289518	AAGCAGTGAAACTGC[A/T]CTTCATGCCTCCCCA	8924
rs538934974	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28288133	AAAACTTCTCTGTCA[A/G]AAGATCTAGAAACGG	8924
rs538939151	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28251538	AGGCGCGGTGGCTCA[C/T]GCCTGCAATCCCAGC	8924
rs538977332	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28190822	AAAATAAGTTGTATC[C/T]TTTAAAGTGTCAAAA	8924
rs538987858	snp	G/T	0.150333	0.229274	intron-variant	HERC2	GRCh38.p7	15:28155610	CCACTTGTTGATGGG[G/T]TTGTTTTTTTCTTGT	8924
rs538991086	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28118524	TATAAAAAAGTTTTT[A/G]TGTAGTGATGTTCAG	8924
rs539002503	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28143821	ACTACTAAAGCAACA[C/T]TTTATTCCCCAAGGG	8924
rs539006185	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28200417	AAACAAAAAAAAAAG[G/T]TAGCCACCTACAAGC	8924
rs539042678	snp	C/T	0.144296	0.226554	intron-variant, downstream-variant-500B	HERC2, LOC107987422	GRCh38.p7	15:28312324	CAACTGGAAGACAGC[C/T]GTGGCACTGAGAAGA	8924
rs539057001	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28148038	AAGACTGTGTCTCCA[-/A]AAAAAAAAAAAAAGA	8924
rs539077961	snp	C/G	0.0391387	0.134304	intron-variant	HERC2	GRCh38.p7	15:28309600	GTGGGGAGGGGCAGC[C/G]TCCAAGAGCCCAGGG	8924
rs539078786	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28287623	CTTAGGAGCTTCAAA[C/T]GCATTACTTCATGTC	8924
rs539078811	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28260157	CCAGCCTGGGCAACA[C/T]AGTGAAACCGTATCT	8924
rs539100933	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28303888	GCTACTGATTTGGCC[A/G]GGCACAGTGGCTCAT	8924
rs539102355	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28265452	GCCTCAGGCAAACAA[G/T]CCCAGTAACCACCCG	8924
rs539113745	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28261033	GCTGCAAGAAAGATA[G/T]TTCCTAGGCCATTCA	8924
rs539114994	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28242298	AATGGCAAATTTTAC[C/T]AATCTTATACACACC	8924
rs539115935	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28253769	GAGTTTGAGACCAGC[C/T]TGACCAATATTTTGA	8924
rs539122573	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28217510	GCCCACATACCCACC[C/T]ACACTCACATGTGCT	8924
rs539137204	snp	C/T			intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28320273	GCATACACCACCACG[C/T]CTGGCTAATTTTGTA	8924
rs539143573	in-del	-/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28260201	AAAAAAAATGTTTAA[-/G]AAAAAGAAAAGTAAA	8924
rs539148320	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28283358	CAAGTCAAATGACAG[A/C]GAATTTCTCATCAGA	8924
rs539187572	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28296135	TAAAAAACAATTATG[C/T]TCTGCTTTCCAATCA	8924
rs539194063	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28209449	CCCGAGTTCACACCA[C/T]TCTCCTGCCTCAGCC	8924
rs539203255	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28254239	AGTGAGCCAAGATGG[C/T]GCCATAGCACTCCGG	8924
rs539206353	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28209738	CCTTAAGCATTAGTG[A/T]ATTCTGGTATAACTG	8924
rs539221417	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28167560	ACGCTTCGAAGATGC[C/T]AACAAGTGGACAGCC	8924
rs539238815	in-del	-/T			intron-variant	HERC2	GRCh38.p7	15:28279000	GCCCAAAAGCATCTC[-/T]TTTTTTTTGCTTCTT	8924
rs539245332	in-del	-/T			intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314045	CAGCCCAGTTTCGCA[-/T]TCTCTCAATTTCCAA	8924
rs539252067	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28140357	AAACGGGAAAAATAA[A/C]AGAGAGGTAGGCTAG	8924
rs539261821	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28122011	CACCGCGGAGCCAGC[C/T]GGACCTTGGATCGCC	8924
rs539271496	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28204125	CCAGAGGCGGCAGAA[C/T]CCAGAGCCAATACAA	8924
rs539286544	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28168030	TTTTGCAAAGTCAAG[C/T]ACATTCATATTTTCA	8924
rs539292232	snp	C/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28293584	TCCTAGTACATTTCT[C/T]AACTGAGAAACTTAA	8924
rs539310566	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28249365	GGCAGCGAAGAAAGT[A/G]GAAGAGGCTCCAGTT	8924
rs539318253	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28291060	ACTTCTGGGAAGACT[A/G]ATCCAAACGGAAAGA	8924
rs539325726	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321216	CATAAAGACTGTTAC[A/G]TTTTAAGTTACAGGA	8924
rs539382976	snp	C/T	0.0138799	0.0821421	intron-variant	HERC2	GRCh38.p7	15:28204613	GACAGAGCGAGACTC[C/T]GTCAAAAAAAAAAAA	8924
rs539391126	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28116096	CAGTGCCTGCAGCTG[C/T]GCACAGAGCTTCCGA	8924
rs539395410	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28228046	TGACTCTAGAAAATC[A/G]TAAATGTATTTGATA	8924
rs539400361	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28210877	GTGGTTGCTGGGCAG[G/T]CCACATGTCTGTCTT	8924
rs539407711	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28140812	CAGGCATGAGCCACC[A/G]CACCGGGTCAGCAGC	8924
rs539442129	in-del	-/ATAG	0.0513888	0.151834	intron-variant	HERC2	GRCh38.p7	15:28270249	TTTATTTATTTATAG[-/ATAG]ATAGATAGATAGATA	8924
rs539450058	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28243384	CCATTAAAACAGAAA[C/G]AAACTGGATTTCACG	8924
rs539454251	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28250620	TGAAATACGTTTCAC[A/G]GCTTATTTTTGGCAA	8924
rs539462770	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28129289	CAGTGGGGGAACCAG[A/G]AGCAAGCTTCCAGAG	8924
rs539462890	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28172023	GAGCTTGCAGTGAGC[C/T]GAGATTGCGCCACTG	8924
rs539463337	in-del	-/A	0.00279832	0.0373005	intron-variant	HERC2	GRCh38.p7	15:28138107	GAAGGCTGCTGAAGG[-/A]AAGTCTGAAGGTAAC	8924
rs539477545	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28256918	GTTTTTTAAGACTCG[C/T]GTCCATTATTAGTGC	8924
rs539477559	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28225366	CAAAAGTTTGGTTTC[C/T]GACAAGAACAAAAAA	8924
rs539496753	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28169958	AAATGCTACAATAAC[C/T]ACCTGTATTTTCTTA	8924
rs539499563	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28167524	CAGTGACAGGGACCG[G/T]GTCCTGCGGCATTCC	8924
rs539506316	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214582	GGCACAGGGAAGGGA[A/G]ACGGCCACCCACCTG	8924
rs539507737	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28163644	TCTACCCATAAGATA[C/T]GCTAGGGAATCGTTT	8924
rs539509607	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28156826	GGCATCCCTGTCTTG[C/T]GCCAGTTTTCAAAGG	8924
rs539516625	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28257343	CACCAGCGTGTGTGA[C/T]GGAGCTGCCTTATAC	8924
rs539566197	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28127965	TTATAAAGAATGTTC[A/G]CAGTGAAAAGCATGG	8924
rs539585828	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28135933	ATTGTGAAAATAAGG[A/T]CTTCTTGCTGGAAGC	8924
rs539598405	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28290602	CAGACAAGCCTCAAC[A/G]TTGAAATCACAGAAT	8924
rs539601460	snp	C/T	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28209840	TGGTATCACACTGTA[C/T]GGATACACAACATAA	8924
rs539607469	snp	C/T	0.00874735	0.0655527	intron-variant	HERC2	GRCh38.p7	15:28289855	AGTGAGAGGATGACA[C/T]GCCGCAGTGAAAGGA	8924
rs539608094	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28251880	CAACATGATATCACT[A/G]TAAGAAAAATTATTG	8924
rs539645296	snp	A/G	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28258208	GGCGCAGTGGCTCAC[A/G]CCTGTAATCCAAACA	8924
rs539657558	snp	C/T	5.26561e-05	0.00513081	intron-variant	HERC2	GRCh38.p7	15:28238557	CTCTGCTTAAAATGA[C/T]ATAGGTTGTAACTTT	8924
rs539661013	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28190487	ATTCTTTCAAACTTT[G/T]CCAGAGATAAACTTA	8924
rs539664889	in-del	-/C	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28116225	CTTTTCTTTTTCTTT[-/C]TTTTTTTTTTTTTTG	8924
rs539691090	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28165342	TGAACTGTAAGTAAA[C/T]AGCCTGCTGATGACA	8924
rs539701520	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28159444	TTCATTTCTTTTTAT[C/T]CTTTTTTCTCTAAAC	8924
rs539739338	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28152890	CACCTGGTCACCTGC[A/C]TGCCACCTCTGCCCG	8924
rs539744463	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28278744	TTTCTGCCTCCCGTA[C/T]CTTCTATGTGCTCTC	8924
rs539752250	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28147259	GGGTCACAAGATTTT[C/T]GTCTAGGAAAAGGCT	8924
rs539755315	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28197765	CAGTCCTGACAGTCA[A/G]GAGCTGGCCTGTTAA	8924
rs539764126	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28159869	TTTGTGGTTTTATCT[A/G]CCTTTGGTCTTTGAT	8924
rs539773127	snp	C/T	0.000263683	0.0114792	intron-variant	HERC2	GRCh38.p7	15:28191101	AAGGCGTCTTTATTA[C/T]AGAAGGTACTTCTTT	8924
rs539803743	snp	C/T	1.70618e-05	0.00292072	intron-variant	HERC2	GRCh38.p7	15:28169458	CACATAATTGCAGAA[C/T]TTCAAAAATTAGCAC	8924
rs539804367	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28208461	AGGAGCAATTCTCCA[C/T]CTCTGTCATCTCCTG	8924
rs539805640	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28294713	TCTTACTACAAAATG[G/T]GCCTCCCACAGCCCC	8924
rs539806708	snp	A/G	0.000198121	0.00995095	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214117	TGTGGGTGATGGAGC[A/G]GAGCTGGGAGTTGAT	8924
rs539813803	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28240189	TTTGGGAGGCCAAGG[C/T]GGGCAGATCACAAGG	8924
rs539820679	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28279865	TAAAATAATGGCACA[A/G]ATTACACAGCATGGT	8924
rs539848629	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28120010	GCCCAAAAAGTCTGC[A/G]TGCGGTTTTGAGGGA	8924
rs539853020	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28235005	GCGTGGTGCAAGGCA[C/T]GGGATCAACCAGTGC	8924
rs539866856	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28120300	AAGGACAAGAGTTTC[A/G]TGTCTTAATTCAAAA	8924
rs539867536	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28192721	CCACGGATCAGAGGC[A/T]GCTGTTCCCTGATGG	8924
rs539888144	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28153642	AGCGACAGAGAGAGA[C/G]TCTGTCTCGAAAAAA	8924
rs539904889	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28280549	CCACACAGAGGAGTG[C/T]GGCACATGACAGAGA	8924
rs539909572	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28149021	GAACATCACCGAGAA[C/T]GGCCGCACAAACGTA	8924
rs539910270	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28244063	TGCTTGCAGTCCCAC[A/G]CAGGTGGAAGGATCT	8924
rs539912983	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28272699	AAAAAAAAAGAACAG[C/T]TCCCAGGCTAGAACA	8924
rs539917597	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28208787	CTTCAAAGGCTGCCC[A/G]TCCAGTGCTCAGCTG	8924
rs539950607	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28273391	AAAGAACCAATTTCT[A/G]AAACCACCTTAGAAT	8924
rs539960594	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28206962	GTTGCAGCGAGCCAA[G/T]ATCACACCACCATAC	8924
rs539975902	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28143006	AGGTGCCGGGGAGGC[C/T]GACCATTTGTTTCTA	8924
rs539983543	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28120383	GTAAAAATCATGTGT[G/T]AATACAAAGGTACAG	8924
rs539984218	snp	C/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28211598	CAGAAGCAGCACAGA[C/G]AGCATGGGGTGGGAA	8924
rs540016556	snp	A/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28311044	ATCGCACCACAGCAC[A/T]CCAGCCTGGGTGACA	8924
rs540035380	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28178483	CAAGTTACACTGAGC[A/C]CCGTTCAGCATAGGC	8924
rs540042719	snp	A/C	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28320217	CCTCCCGGGTTCAAG[A/C]GATTCTCCTGCCTCA	8924
rs540047081	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28179507	TCTGTGCTGCCAGCT[A/T]CATATCAACAATCCC	8924
rs540054284	in-del	-/AAAAG	0.00688083	0.05825	intron-variant	HERC2	GRCh38.p7	15:28179251	TTTTTTAACAAAAAA[-/AAAAG]AAAAGAAAATTTTAC	8924
rs540061943	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28151190	GGTTATGTAAAGCAA[A/G]TGAAAAATCATGAGA	8924
rs540120090	snp	C/T	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28146523	ATCCCCACTGAAGAT[C/T]ATGTCTGTGGACTGG	8924
rs540125438	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28298340	TGTATTTTTTAGTAG[A/G]GACGGGGTTTCACCA	8924
rs540140502	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28271018	ATACTATACATCTAT[A/G]TATTTATGCAGCATA	8924
rs540146244	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28140120	GAACATTTCAAAACA[C/T]GTAGAAAGAGTGTTG	8924
rs540151283	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28216900	CTCAACACTAGTAAC[C/G]ACCGATTACTCACCC	8924
rs540162408	snp	A/C	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28298800	GACTCCTTCCCCCCC[A/C]AAAAAAAGAAGAAGA	8924
rs540167244	snp	C/T	0.000150342	0.00866882	intron-variant	HERC2	GRCh38.p7	15:28210972	CTACTGCCCTTCTTA[C/T]AAAGATTTAAGAACT	8924
rs540174672	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28226226	AAAACAATCTACAGA[G/T]TCAATCCCTAGCAAA	8924
rs540232178	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28210413	AGTGCAGGGATTACA[A/G]GCATGAGCCATTGTG	8924
rs540237936	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111665	GGCTCGAGGACGGAC[A/G]CTTCTCATCAGACAC	8924
rs540263235	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28311335	CCAGGCGTGGTGGTA[C/T]GCACCTGTAGTCCCA	8924
rs540267950	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28141330	ATTAATCCTGAGAAA[C/T]GTTTTAGTACAGATC	8924
rs540270416	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316684	TTACAAATTCTTTTA[G/T]TTCTACATGTCATCT	8924
rs540283258	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28136508	AGTGGGGCTCCAAAG[C/G]GTTGCCCCTCAGTGA	8924
rs540316143	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28235356	CCTCTGCCCTGGAAC[C/T]CGCCAGCCCTGCCCT	8924
rs540317226	snp	C/T	0.00199481	0.0315187	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111580	CCACAGTGTTCCACG[C/T]GCACAGGCGGACCTT	8924
rs540323857	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28227985	CTGATGGCTAAATGG[G/T]GTGCATTTATAGTGA	8924
rs540334340	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28266429	CTGAGGCAGGAGAAT[A/C]GCTTGAACCTGGGAG	8924
rs540346071	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28149245	TGAAAACATCACCGA[A/G]AATGGCCACACGAAC	8924
rs540354780	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28193266	TATGCTTACTGTGTT[A/C]AAAAAGATAATATTT	8924
rs540366800	snp	A/C	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28220709	GGTCCTTCCATGGCT[A/C]CCAGCAGACCTCAGT	8924
rs540371265	snp	A/C	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28173626	CAACATGGCAAAACC[A/C]TCTCTCCACCAAACA	8924
rs540379036	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28215168	AGGCATGAGCCACTG[C/T]GCCCGGCCTCTCTTT	8924
rs540393335	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28258006	TACTTTTTAAGCACA[G/T]ACAGAATGTTCACTA	8924
rs540444645	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28128754	GCAGGTGAGAAGCCC[C/T]GCATGGGTCTGTCTC	8924
rs540472657	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28246198	CATATTTCTAAAGAA[C/T]TATCTTATATTTTAT	8924
rs540479076	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28159681	AATGGGTTCGAACTT[C/G]CTCCTTTAGCTCGGA	8924
rs540488488	snp	A/C/G	5.15427e-05	0.00507633	intron-variant	HERC2	GRCh38.p7	15:28168380	CTTTTCCTTTCTGAT[A/C/G]TAACATTGCTTTAGA	8924
rs540512744	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28165659	AAAAAATACAAAAAT[C/T]AGCCAGGTATGGTGG	8924
rs540521092	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28291277	TCACCCAGGCTGGAG[C/T]GTAGAGGCACAATCA	8924
rs540530437	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28217159	ACCAACCCTCACTGA[C/T]TTACACTGACTTACA	8924
rs540533496	snp	G/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28137068	GTCTATGGCAGAGGG[G/T]AATAGGTTAGAACCC	8924
rs540540468	snp	A/C	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28153119	AGCACTTTGGAAGGC[A/C]GAGGCAAGCGGATCA	8924
rs540625258	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28185463	ACTTAGCAATTTCAC[C/T]TTCAGCAATTTATCT	8924
rs540631211	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28271910	TGACGTGCCCTGCAC[A/C]GAGCCCAGTACATAG	8924
rs540639266	snp	A/C	1.64961e-05	0.00287189	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28177032	GTGTACAGTTCTCCG[A/C]TGGATGTGAGGGCTG	8924
rs540652633	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28260487	ACTGTCACCTCTCCT[A/G]TTCAGCTTCACACTG	8924
rs540654314	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28307739	AACTTTTATATGGCA[A/G]AAGAGGAATCTAGCT	8924
rs540656101	snp	C/T	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28220321	TATTTAAATTGCAGG[C/T]TCCGAGGACAGAGCG	8924
rs540699974	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28218018	AGAATTGCAAAATTC[A/G]TATGTTGAAGCCCTA	8924
rs540700358	snp	A/G	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28177615	ACACACTCAATGAGC[A/G]TGAGCTGAATAAATG	8924
rs540700757	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28132407	AAAATCCTATAAGAC[A/C]AAAGAGAAAGCACCT	8924
rs540701978	snp	G/T	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28254583	TGAAGACACACAGGC[G/T]GGCTGAGCCCTAACC	8924
rs540717296	snp	A/C	3.31186e-05	0.00406918	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214782	TGGAAGGACTGCTTG[A/C]AACAAATGCACAGCT	8924
rs540718252	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28304261	GAATTTATCAGTTCT[A/G]ATCATTTTTTGGTGG	8924
rs540721781	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28218360	GTAAGCCCCCAAGTT[C/T]GTATACTTTGTTACA	8924
rs540726003	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28139102	AACCAAGAAATTTGT[A/G]TGACATGCTTTGCGA	8924
rs540733711	snp	A/C/G	6.7258e-05	0.00579873	intron-variant	HERC2	GRCh38.p7	15:28168399	CATTGCTTTAGATTC[A/C/G]CTTTTACCTCTCTCT	8924
rs540743710	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28267576	CTTTTCTTTTTCACT[C/T]GTCTTAGATTTGTCT	8924
rs540761221	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28296402	TGCTTGAACCGGGGA[A/G]GCAGTGGTTGCAGTG	8924
rs540761948	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28212209	GTGACACGGAGAAGA[A/G]GGTGTGAGCCATGGG	8924
rs540784953	in-del	-/C	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28297562	TTGTTTAAAAAAAAA[-/C]AACATGAAAATCAAA	8924
rs540839346	snp	A/G	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28290831	CTTAGAGGGAAATTT[A/G]TATTATAGTTTTGAA	8924
rs540841579	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28125231	CAGAACCTGTATACT[A/T]GGGCCAACAAACGCA	8924
rs540842772	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28297107	GAAACTAAATGTAAG[A/C]TTTGGTGTCTGAAAG	8924
rs540871035	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28242952	ACAAACATCATACTT[G/T]GTGTGTGAAATCTGG	8924
rs540876044	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28285763	AGCTGGTTCTTTGAT[A/G]AGATCAATAAAACTG	8924
rs540880168	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28164692	TTGCCTTAAATTCAT[A/G]AGTCAAGCCAAAACT	8924
rs540898015	in-del	-/A	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28172504	AATTCTCACAAAGGC[-/A]AAAGGCAATTCAGTA	8924
rs540900943	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28293984	CTAAATGTCTAACAA[C/G]ATAATTAGAAAAATG	8924
rs540904764	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28239673	TAACACCGCCCCAAC[A/G]AGACTGAATTCAAAT	8924
rs540910215	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28204401	CCGAGGAGGGCGGAT[C/T]ATGAGGTCAGGAGTT	8924
rs540914435	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28210369	CTAGCTCCTGACCTC[A/G]TGATCCGCCGCCCGC	8924
rs540923548	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28282692	TAATCCCAGCACTTT[C/T]GGAGGCCGAGGCAGG	8924
rs540923767	snp	C/T	8.24069e-05	0.00641846	synonymous-codon	HERC2	GRCh38.p7	15:28163193	CTTGAGCAGGTCTAC[C/T]ACCACACGAGTGTCA	8924
rs540944676	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28156951	TTTGTTGAGTTTTTA[A/G]CATGAAGGGCTGTTG	8924
rs540949853	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28122578	GCCTGGACCTCAGGG[C/T]GGCTCCCCCTCCACA	8924
rs540952102	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28208508	ACCTTCCTAGCAGGT[A/G]TATCACCCGAAGGTC	8924
rs540955122	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28116241	TTTTTTTTTTTTTTG[A/C]TACAGAGTGTTGCCC	8924
rs540970359	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28198001	ATCATGACGTTAGCA[C/T]GGCTCCATTCTTTCT	8924
rs540993571	snp	A/C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28266852	TGGTGACCCAACTGC[A/C/G]TGCACTTGTCAAAAC	8924
rs541010417	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28235548	CCGCAAGCCTTCTGC[A/G]ACACCCACTCTCGAA	8924
rs541017751	snp	A/G	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28123932	CGTGAACATTTGCTG[A/G]ATGAGCTGTATTCTA	8924
rs541024868	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28181873	GACAAGGTGAATGAG[A/G]TCATGGCGCTCTCCA	8924
rs541030907	snp	A/G	2.0325e-05	0.0031878	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174362	GCTGTAAACCTACAG[A/G]AAAATCTCAGAGAAG	8924
rs541041537	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28244332	AGAAACCAAAAGGTA[C/T]GTACCGTCTAGTTCC	8924
rs541049423	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299585	TTTTAAAGAATGATA[C/T]GGGAAAAAAATCTCA	8924
rs541056168	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28262210	CTAGGCCAGGTGGTA[C/T]GGAAAAGTCCTGTTT	8924
rs541096372	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28232510	GCTGAGATCGCACCA[C/T]TGCACTCCAGCCTGG	8924
rs541111046	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299923	CCAGGCGTGGTGGCG[A/G]GCGCCTGTAATCCCA	8924
rs541121951	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28287691	TATATATAATTTTAA[G/T]TATTTACATTATATT	8924
rs541133418	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28263605	TGTTCCCAACTGCAT[A/T]TCAGCATAATTATGT	8924
rs541155643	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28293787	AGGCACTGTGACTGA[C/T]AGCATAATTCAAGAG	8924
rs541170595	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28125842	CTGTGATGAAGTCTC[A/C]CTTTGTCGCCCAGGC	8924
rs541189798	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28200539	TTGAAGCTGCCAGTC[C/T]ATGGTACTGTGTTAT	8924
rs541189988	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28112967	ATTTCTGTAAAGACT[C/G]AAGAGGCTCGTTTTC	8924
rs541199242	snp	C/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28168810	GAAAAACCAGAGTAA[C/T]GGCAGGTGAAAAACT	8924
rs541209862	snp	C/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28224216	ATAGATAGAAAGATT[C/T]CCCCCACCCCCAAGA	8924
rs541210229	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28180293	TATAGCCTGAGTGTG[C/T]AGTAGGCTACACCAT	8924
rs541212527	snp	C/T	1.66192e-05	0.00288259	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28191234	GGGAAAATCTCCAAA[C/T]GAATCCAGTGCTTTA	8924
rs541220413	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28298052	GTGAATATTTTCAAA[A/C]AAATATAAAAAATAA	8924
rs541228279	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28194194	CTTCAGCCTCCCGAG[C/T]AGCTGGGACTACAGG	8924
rs541233735	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28228939	ATTAATATAGGACAC[A/G]GACACTTTAGGATAT	8924
rs541237909	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318089	TTACAACAAAACTGG[C/T]GAACAGGCATGTGTT	8924
rs541245391	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28294303	CTAGGTTCAGCAAAT[A/G]ACATAAACCCAGGCA	8924
rs541262976	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28162806	TGAGGCAGGAGAATG[A/G]TGTGAACCCAGGAGG	8924
rs541267965	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28174998	AAGTTGCTTCTTGGC[C/T]TTATAGAATTATAAA	8924
rs541284251	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28119348	GAGGTTGCAGTGAGC[C/T]AAGATTGCACCACTG	8924
rs541287108	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28188224	AGGAAAATCTGGACA[C/T]TGACTGAATATTATA	8924
rs541295213	in-del	-/G	0.000506256	0.0159019	intron-variant	HERC2	GRCh38.p7	15:28238067	TCACAAACACACAGA[-/G]GGTATCCCCTGCCAT	8924
rs541298781	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28255068	AGCCTGGGCGTGGTC[A/G]CTCATGCTTGTAATC	8924
rs541306558	snp	C/T	0.0123036	0.0774623	intron-variant	HERC2	GRCh38.p7	15:28119378	GTACTCCAGGCTGGG[C/T]GACAGAACAAGACTC	8924
rs541319356	snp	C/T	0.000399281	0.0141238	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229560	CCAGTTTTAAAATTG[C/T]ATCTATCCCTTCCAG	8924
rs541325037	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313003	CTTGACCAAAGGCCA[C/T]ACAACACTGAGGCTG	8924
rs541337412	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28252546	CATTGATTCTTAATT[A/G]ACTCCATGAAAGTAA	8924
rs541343841	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28223715	ACATGTGGATGTATA[C/T]ATTAAGCTGGTATAA	8924
rs541383377	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28202063	TAAGACTGTTAGAGC[A/G]CTAGACGGACAGCGG	8924
rs541384732	snp	G/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28211668	CTAACTGGCAGACAG[G/T]TTTATTCACCACGAT	8924
rs541391975	snp	C/T	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28203141	TAAAAGAGTATTAGT[C/T]GGGAAACACACTGCA	8924
rs541395544	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28247822	CCTACTGAAACCTGA[A/C]AGTTTCCATTACTGA	8924
rs541397094	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28307166	TCTTCCACGTTTCCC[A/T]ATTTATTGACATATA	8924
rs541408483	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28290280	CTTGATCTCATTAAG[C/G]TTTACAGAGCAGCAA	8924
rs541417818	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28251440	AGAGTGAGGCTCCAT[C/T]TCGGGGGAAAAAAAT	8924
rs541427843	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28209550	GAGTTTCACCGTGTT[A/C]GCCAGGATGGTCTCG	8924
rs541474283	snp	A/C/T	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28194219	TACAGGCGCCCGCCA[A/C/T]CACGCCCGGCTAATT	8924
rs541481485	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28160607	TTAGGGTGGGAGTGA[C/T]CCAATTTTCCAGGTG	8924
rs541493059	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28225820	AACACTGTGAACTAC[C/T]GTATGCCAACAAATA	8924
rs541499754	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28164572	CTTAAAACATGCACA[C/T]ACACAAACACAGAAA	8924
rs541504913	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28124501	GTGGAAGAGTTTGGT[A/G]TGGGTTATAAGATAT	8924
rs541527564	in-del	-/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28187334	TGGTTTTTTTTTTTG[-/T]TTTTTTTGTTTTTTT	8924
rs541541485	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28117848	GCCCTAGGGCCCCGC[C/T]GCAGCAGGACCTCGG	8924
rs541555153	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28155165	TAATCCAGTCTATCA[C/T]TGTTGGACATTTGGG	8924
rs541593070	snp	A/G	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28162848	GTGAGTCGAGATGGC[A/G]CCACTGCACTCTAGC	8924
rs541603635	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28285493	TAAAATATATTCTGA[A/T]CTGAGAGAAAATGCA	8924
rs541608071	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28115734	TATCCTTTTGTGCCT[A/G]AAAGCCTCTAACTCT	8924
rs541620298	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28265793	CTCCTGCTGCATGCT[A/C]CCACTCATGCAGAGC	8924
rs541631522	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321297	TACCCTAAAAAAAAG[C/T]CTTACACGAGAAATT	8924
rs541634121	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28194559	CCTGGGCGACAGAGC[A/G]AGACTCCGTCTCAAA	8924
rs541651604	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28303677	TGATTCTTCCAATCC[A/G]TGAACACGGAGTATC	8924
rs541667217	snp	C/T	1.68735e-05	0.00290456	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28233479	AACTCTACAAACATC[C/T]ACCACTGACTTAGGC	8924
rs541674167	snp	A/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28155760	GTGCAGAAGCTCTTT[A/G]GTTTAATTGGATCCC	8924
rs541680935	snp	G/T	0.000214576	0.0103558	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28192016	CCGTCAATGAGACGG[G/T]ATGCCTGGTTCACGG	8924
rs541687216	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28264539	TAACAGTCGCCTCAG[-/A]AAAATATATAGCAGC	8924
rs541711239	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28274729	TTTTTTTTCTTTAAA[A/G]CACAGATGTGAAAAG	8924
rs541712773	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28144611	GTGCACGTGTCCCTG[C/T]TGCTCCAGAAACAAT	8924
rs541738451	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28220734	CTCAGTTAGGAGGGT[C/G]CATGCCCTGCCCTGG	8924
rs541738458	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28298751	CAGTGAGCTGAGATC[A/G]CGCCACTGTACTCCA	8924
rs541745346	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28188639	ATATTGAAGCAAGTG[C/G]TCCTGAAATAAGACC	8924
rs541758758	snp	C/T	1.67156e-05	0.00289093	intron-variant	HERC2	GRCh38.p7	15:28142230	GATTCCAAAATATCA[C/T]GCAATACCTCATCAA	8924
rs541784228	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28120839	CAGAAAAGTGGGCAC[A/G]GCCCCCCAGCACCAT	8924
rs541795201	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28186147	ACTGTACACTTAAAA[C/T]GGTAAACAATATATA	8924
rs541796811	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28128044	AAACTGCATGTCACC[C/T]GCAAGGATGAACTGT	8924
rs541819024	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28115120	TGAGCTGGCTGTGGT[C/T]GCCCCAGGACAGAGC	8924
rs541823342	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28165139	AGAGACACAGCCAGG[C/T]CAAGTGAGGAAGGTG	8924
rs541823522	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28207947	GTGCACGGCAGTTTT[G/T]TCAATCTAGCTCTGT	8924
rs541853748	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28129526	GTTCAGGCACAGTGA[A/G]CCACACCTACCACCT	8924
rs541879959	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28284881	GAGATCGTGCCACTT[C/T]ACTCCTGCCTGGGCA	8924
rs541883641	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28156146	TTGGTACCAGTACCA[C/T]GCTGTTTTGGTTACT	8924
rs541890152	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28269762	TTTAGCAGGCAAAAT[A/C]CCAAAAGCCCACACA	8924
rs541892670	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28320481	TGTTTAAAAAGAAAA[A/C]AAAAATTAGGAAGGG	8924
rs541896876	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28245424	TGGTGGTGTGCACCT[C/G]TGGTGCCAGCTACTC	8924
rs541909364	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28264317	CCAATACAACTCTAC[C/G]TGCAAAAACAGGCCA	8924
rs541911381	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28206571	GGGTGCGGTGGCTCA[C/T]GCGTGTAATCCCTGC	8924
rs541915104	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28277938	AGTATTTGCATATAA[A/C]CTGTGCACATCCTCC	8924
rs541925416	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28159520	TTCCTCCAGGTGATC[A/G]AATTGGCTACTGAAG	8924
rs541957079	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28308259	GTTTTCATTACAGAG[A/G]TCTTTGTAATTATCT	8924
rs541995569	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28190579	TTGATGCCAACAGGT[A/G]TGACGACAAAAAAGC	8924
rs542004369	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28194596	AAAACAAAACAAAAC[-/A]AAAAAACAGGCATGA	8924
rs542014741	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28264224	CCTCTGTGGGCTTTC[C/T]GTCCCAACTACCCAG	8924
rs542015724	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28239417	TAGGATACCAACTCA[A/G]TATTATGAAAAATAG	8924
rs542027719	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28271456	GGCGGATCACAAGGT[C/G]GAGAGATCGAGACCA	8924
rs542031583	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28185746	TATGGCCTGGGGGGA[A/T]GTTTTCCTTGTCCTG	8924
rs542037758	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28147805	CTTTGGGAGGCCCAG[C/G]TGGGAGGACTGCTTG	8924
rs542058503	snp	C/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28222833	GTGCCCGTGTGATCA[C/G]CCCTAATGGAAACCC	8924
rs542076044	snp	A/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28295007	ACAAGAGTGGCAAAA[A/T]AGAACATGATATTCA	8924
rs542076799	snp	C/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28152940	AAGGACAGCGTGGCA[C/G]AGTGGAGGGCTTGGA	8924
rs542113965	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28271945	GACCAACAAAGCAGG[C/T]CGCTATTTTCGTTGT	8924
rs542118225	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28163769	TTAACACACTATCCA[C/G]TCTCTCTCTCTCCTT	8924
rs542118308	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28303246	CATTTTCCCAGCACC[A/G]TTTATCAATGAGGCT	8924
rs542132331	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28148371	AAGAAACAGAGGTAG[A/C]AAGTACTTGAAAGAG	8924
rs542144038	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28304369	CCTTTATTTCTTCTT[C/T]TTTTTTTTTTTTTCC	8924
rs542163867	snp	A/C/G	1.65023e-05	0.00287244	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214678	AATGGCACGTCAGAG[A/C/G]AGCAGGTAGTGAGCA	8924
rs542168156	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28195794	TTAAGGTACTTAATA[C/G]CCTGAATTATAAACT	8924
rs542176462	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28237526	CTGTGACCACACATG[C/T]AGAGGAAATGAAATT	8924
rs542186829	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28275922	AAACTATATTCTCCA[A/T]ATTTACTAAAATTTG	8924
rs542215531	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28231168	GTCTAAATCTCCTCA[A/G]CATATAATATAAAAA	8924
rs542217998	snp	A/G	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318924	AAGAAACATCTTCCT[A/G]TCCCATGTATTATTC	8924
rs542230565	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28189856	AAAAATGAATGGTTA[A/C]CTACATTTAATAATT	8924
rs542232575	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28120052	AGGTGCACTCAATCG[C/T]GGGGGTTAGACAACG	8924
rs542256130	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, downstream-variant-500B	HERC2, LOC107987422	GRCh38.p7	15:28319715	TGGTGCTTCACTGTA[C/T]GTTTATCTGCCCAAC	8924
rs542332322	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28267781	CTCAAGGGACACAAG[G/T]GCAGTCATGACTTCA	8924
rs542338166	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28225314	ATAGAGATTAGAGCA[C/G]CCATAAATTAAATAG	8924
rs542342373	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314817	AGTGAGCCAAGATCG[C/T]GCCACTGCACTCCAG	8924
rs542374787	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28225722	AAAAAAAAAGAAAGA[A/G]AAAAAAGAAGATGCA	8924
rs542382674	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28179528	CAACAATCCCTAATA[C/T]CTCACCATGATAACA	8924
rs542388823	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28286486	ATGTAACCCACCCTA[C/T]TAATAGGCTAAAGAA	8924
rs542390534	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28306648	CACTAGGATTGGTAA[C/T]AGTTCTTCTTTAAAT	8924
rs542426305	snp	G/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28173887	AAATTGGTGCATACG[G/T]CAGGAAGGAGGGAGT	8924
rs542432881	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28184626	CAGCACTTTGGGAGG[C/G]TGAGGCAGGCGGATT	8924
rs542432901	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28301903	CTTTTGGGTTCAAGG[G/T]TTTCTCCTGCCTCAG	8924
rs542441193	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28256480	AACTCTTACCCACAA[A/T]AGTTGAGGTATTTGC	8924
rs542446669	snp	A/C/G	0.00358891	0.0422285	intron-variant	HERC2	GRCh38.p7	15:28261167	TGTCAGCTACAATTC[A/C/G]TTAGGACCCACAGTC	8924
rs542471215	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28292662	CTCTAATTAGTCAAG[C/T]GTGATGGCTGGGCAA	8924
rs542473908	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28170328	GTACTGGCATAAGAA[G/T]CAATGGAATAAACAG	8924
rs542482472	snp	G/T	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28298936	GGGGACCAACGAACT[G/T]CAACAGTGGTTCTCA	8924
rs542490769	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28253887	GAATTGCTAGAACCC[A/G]GGAGGCAGAGGTTGC	8924
rs542502654	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214351	CGGCTACCCACCTCT[A/G]AGTGACGGCACTGCG	8924
rs542518886	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28258646	CAAAAAAAAGATAGG[C/T]CTAAATCAGCAATCT	8924
rs542529370	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28250989	ATTACAAATCTGCTG[C/T]AGAACCAATGTCCCA	8924
rs542583779	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28135338	AAAACTATTTCTGCC[A/G]AATGAGTCATTAACA	8924
rs542592958	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28112289	CCGAGGACCACACCA[C/T]CTGTGTGGATGCGGG	8924
rs542617418	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	HERC2, LOC107987422	GRCh38.p7	15:28317565	AAAGAAAATCATTTC[C/T]GAAGGTCACATATCA	8924
rs542619379	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28235795	CGTGTCCTACCCATC[A/G]CTGCATCCTGAACAC	8924
rs542620166	snp	C/T	0.00755907	0.0610114	intron-variant	HERC2	GRCh38.p7	15:28136356	AGCCACAAGGGCCAA[C/T]GCAGGAAGTGAAACC	8924
rs542641416	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28215278	TTGATTAGTGATTAG[G/T]ATTGTCAGGAACTTT	8924
rs542653298	snp	C/G	0.0107246	0.0724382	intron-variant	HERC2	GRCh38.p7	15:28311237	TGGGAGGCCGAGGTG[C/G]GCAGACTGCTTGAGC	8924
rs542659477	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28193931	GGTATCTTCAGGCAG[C/G]AGAAAAACAGTATAG	8924
rs542662881	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28240162	AGTGGCTCACGCCTG[C/T]AATCCCAGCACTTTG	8924
rs542673752	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28290617	ATTGAAATCACAGAA[A/T]ATGTTCTCTGACTAC	8924
rs542679545	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28305354	AATGGAACAGAACAG[A/G]GCCCTCAGAAATAAC	8924
rs542689766	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28258732	AGGGACAAATGACAA[C/G]ACAAAAGCAGAAATC	8924
rs542703073	snp	A/G	0.000181045	0.0095126	intron-variant	HERC2	GRCh38.p7	15:28215808	TTTGGAGAAGCTGCA[A/G]GAGGGAAAATAGACA	8924
rs542703212	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28306322	TCAGCATGAATTTAA[A/G]TGATCATATGGTTTT	8924
rs542713900	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28297208	CATAAATGGATTTTG[C/T]CCAGAATCCTAGGAA	8924
rs542733923	snp	A/G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28187944	AACGAAGAGAGATGC[A/G/T]TCTGGAAGCACACAC	8924
rs542757832	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28216935	ACACCTTTACCCACA[C/T]ACTTTCTCACTTTGC	8924
rs542761170	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28210382	TCGTGATCCGCCGCC[C/T]GCCTCGGCCTCCCAA	8924
rs542765377	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28249885	TGGTCTCGATTTCCC[A/G]ACCTCGTGATTCACC	8924
rs542774754	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28137602	GCACCACAAACCACA[C/G]CCATAGAAGACGGTG	8924
rs542775473	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28252710	CTCTTTATTTCCATT[G/T]GTTAAAGACCAGAAT	8924
rs542786472	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28122729	ACCAGAACCGAGGCT[A/G]CCTACACATTCCCTG	8924
rs542795371	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28180394	AATATATCCCCATCA[C/T]TAAGTAATGCATGAC	8924
rs542820671	snp	A/C	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28204934	AGCAAGGCAGGGGGA[A/C]AAAACAATAGTCAAA	8924
rs542828702	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28166123	AACCCGAATGCTTCA[C/G]CAACTCTTCTAAAAA	8924
rs542830245	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28148715	ACCGAGAACATCACC[A/G]AGAACGGCTGCATGA	8924
rs542847828	snp	C/G			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28320710	CATTTCCAAATAAAA[C/G]TAGATTGGGTGTAAA	8924
rs542848981	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28287640	CATTACTTCATGTCA[G/T]TTGCACAGCAACTCT	8924
rs542862364	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28247670	CCTGACCTTGTGATC[C/T]GCCCACCTTGGCCTC	8924
rs542862489	snp	A/G	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28240201	AGGTGGGCAGATCAC[A/G]AGGTCAGGAGATGGA	8924
rs542869033	snp	C/T	1.6522e-05	0.00287414	missense, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28299443	TGGGTTGATTCTGTT[C/T]CAGTGTATACAATTT	8924
rs542892096	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28160115	TCTCAGAGGGGTACC[C/T]GGCCGTGTGAGGTGT	8924
rs542913782	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28212127	AACAGGGTGACTGGG[C/T]CACAGGGCCCTGGGA	8924
rs542921335	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28131550	GAGCAAAAGACATTC[C/T]GGCAAAGATAAGAAA	8924
rs542935340	snp	A/G	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28217871	CAGAAGCTGGACAAA[A/G]TAAGGAAGGACCTTC	8924
rs542947077	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28277275	TGAAAAAATTGCAAA[A/G]AAATACACACACAAT	8924
rs542978344	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28124697	CCCAGGTAGCTGGGA[C/T]TACAGGTGCATGCCA	8924
rs542991136	snp	C/T	0.0115144	0.0749975	intron-variant	HERC2	GRCh38.p7	15:28187521	TATTTTTAGTAGAGA[C/T]AAGGTTTCACCATGT	8924
rs542991472	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28117849	CCCTAGGGCCCCGCC[G/T]CAGCAGGACCTCGGC	8924
rs543007816	snp	A/T	3.31488e-05	0.00407103	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28186748	ATTTCAATATACCTG[A/T]GATACTAGACACAAA	8924
rs543016847	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28139546	CGGAGCTATGCTGCA[C/T]CCAGAGTCCTGACCC	8924
rs543028171	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28296458	AGCCTGAGCGACAGA[A/G]CAAGACTCCCTCTCG	8924
rs543031343	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28180598	CTGTACCAGGGACAT[A/G]AGGGTTCATGAAGCT	8924
rs543040357	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28219192	GCTGGTTTCTGATGA[C/G]CTGGCTGTGTCCTAG	8924
rs543040777	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28252319	CAAGCAGGAGACGGG[G/T]AAAACGGGCACTGCC	8924
rs543042209	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28212706	CGTAAGCCTTTTATA[G/T]CTGAGAATAATCATT	8924
rs543045579	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28172053	GCACTCCAGCCTGGC[A/G]ACAGAGCGAGACTCC	8924
rs543051473	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28175446	AACAGGACGAAGGCC[A/G]TGTCATGACCCCCAC	8924
rs543054183	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28178208	AATGAGTGGGGCTTC[C/T]GAGGGGCTCTGGAGA	8924
rs543071246	snp	C/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28165687	TGGTGCATGCTTGTA[C/G]TTCCAGCTACTTGGG	8924
rs543075766	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28293847	AATCACTTTAGGCCA[C/T]TGACAATGTCAAGTT	8924
rs543103599	snp	A/G	0.000510704	0.0159716	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213868	GTGCATAACTTGACC[A/G]CCCAGGCGCAGGCGA	8924
rs543111974	in-del	-/GTA	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28147575	CCAGAGTTTGGGGCT[-/GTA]GTAGTGAGCCACGAT	8924
rs543117181	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28216677	ACACTCACACTGATA[C/G]TAAGTTATTCAGACA	8924
rs543143033	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28122186	AAGACAGCAGGGCGT[A/G]GCCAAACATCAGCAC	8924
rs543172589	snp	A/C	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28210804	TTTTCCCTCCCCACC[A/C]ACCAGATGCCCTCAG	8924
rs543177922	in-del	-/AGTG	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28281144	ATACACATTCTAACT[-/AGTG]AGTAAGTGATATTTC	8924
rs543187960	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28291367	AGTGCTGGGATTACA[A/G]GCGTGAGATACCATG	8924
rs543202680	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28294816	ATGCGTGACTAATAA[A/G]CTGCTATTTCATCTG	8924
rs543215131	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28208948	GACTTTCCCCGAAAA[C/G]ACTTAGCATAATGTC	8924
rs543218903	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28250855	AGACAGCCTGGATAT[C/T]GGCTACTGGAAAGCT	8924
rs543224743	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28286372	AATATACAGCGAATT[A/G]TTAGCAAGTAGAATT	8924
rs543239964	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28284977	GAACAGATGGCAACA[G/T]TACAAAATGAGAACT	8924
rs543246199	snp	A/C	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28166934	TACAATATAAAAAGA[A/C]AGGTAGGTAGGTAGG	8924
rs543274865	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28279948	TACAAAAAGGGAAAG[C/T]AAGAATAAATTTCAG	8924
rs543285501	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28205936	CTCTTTGAATAATTC[C/T]ACTTCCTGGAAAAAG	8924
rs543291353	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28235059	GGCAACTTGAGGGAG[C/T]GCACCACTACAGATC	8924
rs543294873	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28319066	CAAGGCTTCCATCTG[C/T]AATTCCTGTCTGCAG	8924
rs543299069	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28238364	TACTGTCTCCCAGGG[A/T]TGCCTGGGCCAACTC	8924
rs543301667	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28231973	TCTCTCTCCCTCATG[C/T]CGAGGCAGCCTGTCT	8924
rs543312947	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28157835	TAATTGTGATGTTAG[C/G]GTGTCAATTTTAGAT	8924
rs543327313	snp	G/T	0.000808734	0.0200926	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202574	CTCGAAGGGTGAGTG[G/T]ACTCCACAGCCAAGC	8924
rs543355525	snp	A/G	6.9913e-05	0.00591199	intron-variant	HERC2	GRCh38.p7	15:28117223	CAGTCGGGGATATGC[A/G]GCACTGGCGAATGCA	8924
rs543358860	in-del	-/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28194232	ACCACGCCCGGCTAA[-/T]TTTTTTGTATTTTTA	8924
rs543368127	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28151447	GCACTCCAGCCTGGA[G/T]GACAGAGCAAGATCC	8924
rs543373600	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28133019	AAGGCCAGAGGACAC[A/G]GCTTCCCCAGCTCTG	8924
rs543381645	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28199493	ATAAAGTCTCCCTGT[A/G]TTATCAAGAGCAACC	8924
rs543389017	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28168253	TTAAGCACTTTAAAA[C/G]CTCCTTTACAGAGAA	8924
rs543393483	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28288235	CCCATAATGGTAAAA[C/T]GTAAGTTAACATAAA	8924
rs543397054	snp	A/G	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28114923	CAAGTGCATCTCGAG[A/G]CTGCAAGTGCATGGC	8924
rs543398080	snp	A/C	0.000533778	0.016328	intron-variant	HERC2	GRCh38.p7	15:28263201	CATTTAAATAACAAC[A/C]ACTCTGCATTTTAAC	8924
rs543413841	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28271385	GCCAAATAATAGGCT[A/G]GGCATGGTGGCTCAC	8924
rs543430505	in-del	-/AAC	4.99538e-05	0.00499744	intron-variant	HERC2	GRCh38.p7	15:28263195	CAAATGCATTTAAAT[-/AAC]AACAACTCTGCATTT	8924
rs543440825	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28174996	GTAAGTTGCTTCTTG[A/G]CCTTATAGAATTATA	8924
rs543453281	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28168862	AGAATGAGACTCTGG[C/T]TCTCCCTGAGAAAGA	8924
rs543467750	snp	C/T	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28294425	AAACCTTTTGAAAAG[C/T]GCCACGGAAAGTAGA	8924
rs543469256	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28259501	AAAATGAAAAAGGAC[A/G]GAACACATGCCAATA	8924
rs543483656	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28250378	ATAACACCACTGTAA[C/T]ACAAGAAACAGGTCT	8924
rs543484597	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28255807	TCAGTTATTCTTCAC[A/G]TGTGTGAGTGTGGTA	8924
rs543506104	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28208645	GCCCCACCACTCATC[A/G]ACAAACCCTGAGCTC	8924
rs543515537	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28254573	TTACCAGGTGTGAAG[A/G]CACACAGGCTGGCTG	8924
rs543518093	snp	C/T	3.29554e-05	0.00405914	missense	HERC2	GRCh38.p7	15:28169605	GCTTAGAATTACTTG[C/T]ACCACTTATTTTATT	8924
rs543519363	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28282453	AAATAAATGAAAAAA[C/T]AGAAAGCCTAAGACA	8924
rs543523292	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28281974	GCACCCACGTGCCCT[C/T]CTCCCTGACACCCTC	8924
rs543535097	snp	C/G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318140	AGGTATCATATATTG[C/G/T]TTTTTATAGTTCCTT	8924
rs543553558	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28221461	GCCGGGGCTTACCAG[C/T]GTGGCTGAGAAAAGC	8924
rs543560825	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28195101	ACATATAAATCAGAA[C/T]GAAGATAAATGATCT	8924
rs543567383	snp	A/G	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28202125	GACCATGGAGTAGGC[A/G]GCATCATCCACGTCC	8924
rs543567822	snp	A/T	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28156290	AGTAGTTTTTTCCAA[A/T]TCTGTGAAGAAAGTC	8924
rs543569436	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28243563	CAGATAGAAAAATGC[A/G]CACAAAACTTGAATT	8924
rs543579217	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313063	CTCCAAGGCTTATTC[C/G]CTTCCCACCAACACC	8924
rs543595217	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28290835	GAGGGAAATTTATAT[C/T]ATAGTTTTGAACACT	8924
rs543610417	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28114546	GAAAAACACACATGT[C/T]CACACAACCACGTTC	8924
rs543616029	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313787	CGATTTGAAGACATC[C/G]TAGAAGCAGTAAGAT	8924
rs543627446	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28283302	AGACAAAACATTTCA[A/G]AAGCCACTAAACAAA	8924
rs543641300	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28113889	CAGCCGACAGGGTAC[A/G]GCCTAATGACCACCT	8924
rs543648835	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28157227	TGTTGTGTCTCTGCC[A/C]GGCTTTGGTATCAGG	8924
rs543656017	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28114280	CACTCAAGCAGCCTG[C/G]AGGGGGTTGAGACAG	8924
rs543683518	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28319990	CAAAACAGATCATTA[C/T]AGCTAAATCAAAGGA	8924
rs543694684	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28151005	CTAAGACTTGAAGAC[C/T]GAAAGAAAGTATAGT	8924
rs543709691	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28276776	AAAAAAAACTACTCA[C/G]CCATAATAAAATAAT	8924
rs543768396	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28207019	CATCTCAAAACAAAA[A/C]AAAAAAAACTAGACT	8924
rs543777261	snp	C/T	0.000198883	0.00997005	intron-variant	HERC2	GRCh38.p7	15:28196444	AAGCAAATCTAGCAA[C/T]CATAAAAATAACTCA	8924
rs543780915	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28149050	TACATTCTAGTAAAA[G/T]TACCGAAAAAACAAA	8924
rs543793175	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28165498	ATATATAACAACACA[A/G]ATACTGATGTAGGCC	8924
rs543799155	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28241245	TCTCCAAAAAAGGTA[G/T]GCAAATGGTCAATAA	8924
rs543810511	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28118836	ACATCTGTAGAAAAT[G/T]TCCTCGCTTTGGGAG	8924
rs543815919	snp	A/C/T	0.00557901	0.0525714	intron-variant	HERC2	GRCh38.p7	15:28195842	GCTAATTTTAAGTTA[A/C/T]ATATATTTTGCCACA	8924
rs543817240	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28145923	AACCTTTTGAAGAAG[C/T]TCTGCAGTATGCCAA	8924
rs543825674	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28204293	AACAAGAAATTCAAC[A/G]TAACTATCAGAAATA	8924
rs543825829	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28246174	AAATAAGAAATGTTT[A/G]TCCTTTAGCATATTT	8924
rs543839423	snp	A/C	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28154837	TTGTTACATATGTAC[A/C]CATGTGCCATGTTGT	8924
rs543850528	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28155805	GCTTTTGTTGCCATT[A/G]CTTTTGGTGTTTGAG	8924
rs543856129	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28141192	GCAGTGAGCCGAGAC[C/G]ACGCCATTGCACTCC	8924
rs543860942	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28223911	ACTTAATGATTTGTG[C/T]TGTGATTGTTACTTA	8924
rs543884024	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28241798	GCACTCCAACCTGGG[C/T]GACAGAGCAAGACTC	8924
rs543900999	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28184857	ACGGAGCAAGACTCC[A/G]TCTCAAAAAATAAAT	8924
rs543918740	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28159563	TCACGTAGTTCTCAT[A/G]CCATGGTTTTCAGCT	8924
rs543933246	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28153050	TGAAGCTTAGGGATG[A/C]TCTATGTTAAAAAGT	8924
rs543941865	snp	C/T	4.94654e-05	0.00497295	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28179013	CTCCACAGGCATACA[C/T]CTTCCCTTCCACAGT	8924
rs543941960	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28138893	CATTTGTGATTCATG[G/T]GAGGAGGTGAAAATA	8924
rs543946257	snp	A/C/G	8.32555e-05	0.00645148	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28192128	GCTGTTTTCCAGAAC[A/C/G]GCCACAAAATACCGC	8924
rs543950704	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28149960	TTACCAAAAAACACA[C/T]ACGGCTCCTAACCGA	8924
rs543952012	snp	A/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28197974	GTGATATGAATGACT[A/G]CTTCCTTACCAATCA	8924
rs543955766	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28157678	CAATTTTGTTGATCT[C/T]TTCAAAAAACCAGCT	8924
rs543956513	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28186439	TACAATTTTTGGAAA[C/T]AACTGTAATTTACCA	8924
rs543958360	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28192688	CCGAGGCGAATGGAG[A/G]TGTCAAGATGACGCA	8924
rs543965710	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318392	AGCACTTCCGGAGGC[C/T]GAGACGGGTGGATCA	8924
rs543971307	snp	C/T	0.00755907	0.0610114	intron-variant	HERC2	GRCh38.p7	15:28119705	GCAATCCATCCACGT[C/T]AGCCTCCCAAAGTGC	8924
rs543991996	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28275300	TGGGAGGAAGCAGAC[A/G]ATAAGGAGATAAATA	8924
rs544004777	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28236556	TCAGCCTCCCAAAGT[G/T]CTGGGATTACAGGCA	8924
rs544006449	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28310532	TTCAGGGCCCCTGAA[A/G]TTTAACTAGTGAATG	8924
rs544019497	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111121	TATAGTACACTTTCC[A/G]TGATAGAAGTTATGA	8924
rs544022520	snp	C/T	1.64781e-05	0.00287033	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28268515	ACAGCCCCAGGAGTA[C/T]ACCTCTCCAGTAGCA	8924
rs544044655	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316586	AACAAAAATTGTTCT[A/C]TTGAGGCACCAGTAT	8924
rs544091862	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28305475	AAACTGGCTAGCCAT[A/G]TGTAGAAAGCTGAAA	8924
rs544094310	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28224478	CCACCCGCCTCAGCC[A/G]CCCAAAGTGCTAGGA	8924
rs544098632	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28139148	TGTGTTGATTTAGAA[C/T]CAAGCCTGCATATCT	8924
rs544100149	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28252424	AGCCTCCTCAGAAAA[G/T]GGAGGGGCATTCAAG	8924
rs544118975	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28145261	GTGTGGTTCAGCACG[A/G]CCCAGAGTAGGCCGC	8924
rs544142641	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28212005	AAGGCAAAGCCAAGC[C/T]AGGCTACAGTCACAG	8924
rs544147274	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28262357	CTCCCATCCTCTCTG[C/T]CTGCACCGGCAGCCC	8924
rs544164772	snp	C/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28115822	TATGACAGCAAAGAG[C/G]TGGAACTTCCCCACG	8924
rs544179932	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28244355	CTAGTTCCACTTATA[C/T]GAAGTCCGAGAACAG	8924
rs544183173	snp	A/G	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28158876	GCAGTGGTTGGTACC[A/G]GTTGTTCCTTTCCAT	8924
rs544186080	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28136731	AATATGTCCAGGGCT[A/G]CTTTTGTAGTCGCAA	8924
rs544198637	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28122089	AGCCAGACCTTGGAT[C/T]GGGACAGAAAAGACA	8924
rs544210844	snp	G/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28232486	CCTGGGAGGCGGAGG[G/T]TGCAGTGAGCTGAGA	8924
rs544227410	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28146777	CAGAGAACTGGAGAA[A/C]CGCTTGGTGTGGAGA	8924
rs544228991	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28239649	AAGCATGCAGCATGA[A/C]CCCAGACATAACACC	8924
rs544237122	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321534	CACTCCCGAAAGCCA[A/G]AAAAGAAAAAAGAGA	8924
rs544250507	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28320360	CTCAGGGCATCCACC[C/T]GCCTCGGCCTCCCAA	8924
rs544275892	snp	G/T	0.00993419	0.0697739	intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28316085	AAAATTATCTGGGTG[G/T]GGTGGTGCACACTTG	8924
rs544287652	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28315422	GGGACAGAGAGAGGC[A/G]GCTAAGGAATCTATG	8924
rs544290986	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28147553	TAAGGAAGGGGGATC[A/G]CTTGAGCCCAGAGTT	8924
rs544308094	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28271294	TCTGGAGAACACCTA[C/T]TTTCATTTGCAAATT	8924
rs544311276	snp	A/G	3.31598e-05	0.00407171	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233528	TGCTCAATACCAAGT[A/G]CACCTGCATGAACTA	8924
rs544318010	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28153483	GTACGGTGAAACCCC[A/G]TCTCTACTAAAAATA	8924
rs544320255	snp	A/C	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28227293	AAAAAGTAAAATAAA[A/C]AATAAAGAGAAAGGG	8924
rs544336629	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28198528	TCAATAACAAATCAT[C/T]ATAATCAATATTCAT	8924
rs544349943	snp	A/G	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28234202	TGGGGAGCTGCAGTG[A/G]TCCTCGTCTTTCTCC	8924
rs544356270	snp	C/T	9.94233e-05	0.00704995	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28257070	GAATACCTGAAGTCG[C/T]AGAAGATTCAGCGTT	8924
rs544376555	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111581	CACAGTGTTCCACGC[A/G]CACAGGCGGACCTTC	8924
rs544379939	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28226326	CAAAGTAGCCAAAAT[C/T]ATCTTGAGAAAGAAA	8924
rs544393670	snp	A/C	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28220265	AGATCGCCGGATCCC[A/C]CAGCCACTCCACACA	8924
rs544406052	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28185388	GGCCCCGGTCACACT[A/G]GCAATCCAAAGCGCC	8924
rs544446961	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28257673	CAAGGATCTAAGAGA[A/G]CGGTGGAACACTATG	8924
rs544447636	snp	C/T	1.6522e-05	0.00287414	intron-variant	HERC2	GRCh38.p7	15:28135472	AATAATTTTTTCACA[C/T]CATACCTTCTGTTGC	8924
rs544448681	in-del	-/A	0.0115144	0.0749975	intron-variant	HERC2	GRCh38.p7	15:28225193	GGAGGTTGAGGCTGC[-/A]AGTGAGCCATGACTG	8924
rs544452707	snp	C/G/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28148992	CCAAAAAAACACACA[C/G/T]GGCTCCTAACCGAGA	8924
rs544495098	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28210483	GTGATAAAGTCCCAC[A/G]GAATGACTTGCTGGG	8924
rs544509434	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28266838	CCATGTCTTGATGGT[A/G]GTGACCCAACTGCGT	8924
rs544523382	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28297353	GGAAACTTTTATCTC[C/T]GGAAAGAAAAAAAAT	8924
rs544532122	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28258851	GAAAACTGACAAAGA[A/C]AAAAACAGAAAAGAT	8924
rs544558084	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28252206	AGCAAACGGTGTTGA[A/G]TGTAGCCAGACGGGC	8924
rs544559641	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28128100	TCTACGCAGAAACAT[C/T]GCAAAAAATCCAAAC	8924
rs544582895	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28240220	TCAGGAGATGGAGAC[C/T]ATCCTGGCTAACACG	8924
rs544585070	snp	C/T	0.000399281	0.0141238	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28270717	GATGTCGGAGAGCTA[C/T]ACAGCGGAGGCATAC	8924
rs544609334	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28184718	TACAAAAAAATTAGC[C/T]GGGCATGGCGGCGTG	8924
rs544610100	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28284157	AAAGTTTCAAATTTT[A/G]GGGCATTTCAGATTT	8924
rs544618464	snp	C/G/T	3.30689e-05	0.00406615	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229470	TTTACCCTATATCGA[C/G/T]TCCCTCAGGAATAAG	8924
rs544626068	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28308884	CATCCTTGTACCCCA[A/G]GGATAAACCCCACTT	8924
rs544627510	snp	A/C	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28290776	ATGAAGATGAAAATG[A/C]ATAAACATTTCCAAA	8924
rs544630715	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28260441	AGACTGAACTGCCTT[C/T]CCCTACAGTCAGGAT	8924
rs544644395	snp	A/G	0.00517822	0.0506191	intron-variant	HERC2	GRCh38.p7	15:28219825	ACCCAGCCATGTGAA[A/G]CTTCACATGTCTTTT	8924
rs544645536	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28311882	TACCATTTTTAAAAA[A/G]AAAAGCCAAAAGATG	8924
rs544646913	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28279511	AGAAAAATGTCTTTA[A/C]AATAATGACACAGAG	8924
rs544667989	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28267913	AATGCCAAAGTTCCA[C/T]GCACAACAGCAAAGT	8924
rs544685082	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28140235	AAGCCTGGGAACGCT[C/T]CATCTGCACCCGCTC	8924
rs544696607	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28180502	AATGAAATGATACAC[C/T]GTGATTGACTTTAAA	8924
rs544699159	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28134992	TAATATATTTTATAT[A/G]GTGGTTTAGTTATTC	8924
rs544700407	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28144539	GCCTCAGCAGGGCCT[A/G]TGAGAGCACTCACTC	8924
rs544710577	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28138336	AGGACTTTCATAGCT[A/G]GAGAGAAGTCAATGT	8924
rs544713415	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28223054	ACTACATGCTGAGTC[C/T]TGTGAGTCCTCCTGG	8924
rs544718950	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28261242	TTCTCCTCCTCATTC[A/T]GATTTTCAGTCAGAA	8924
rs544750972	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28303514	GTTTTTTGCTCAGGA[C/T]GGCTTTGGCTATTCT	8924
rs544772290	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28307861	GAAAATGAGTTCACC[A/G]TAGATGTGCGGATTT	8924
rs544785440	snp	A/G	0.000115772	0.00760741	missense	HERC2	GRCh38.p7	15:28142248	AATACCTCATCAAGA[A/G]ACAGACGGGGCAACG	8924
rs544786125	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28131594	CCGGGCTTGAGTGGA[A/G]CAGAGCCGCCGACCC	8924
rs544812790	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28168333	CTAAACTAAATGACA[C/G]AATGAGACTTTCCTA	8924
rs544813381	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28295694	TGAGCCACCACGCCC[A/G]GCCACCGTATTTTAT	8924
rs544830043	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28244700	ACACAGGACTAAGCT[C/T]ACTCCTTAACAAAAG	8924
rs544843276	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28254948	CACCTGCCCCAGGAC[C/T]TAACAAATTCCACTC	8924
rs544844709	snp	A/C/T	3.298e-05	0.00406068	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214724	CAAACAGCTTCTCCA[A/C/T]GAGGCATTTCATGTC	8924
rs544866331	snp	A/T	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28245558	TGTCAAAAAAAAAAA[A/T]AAATATATACACACA	8924
rs544874097	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28168675	CAGGGCTAGCACGCA[C/G]TGAGGCGTTTCCTCA	8924
rs544889626	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28293291	AAGGTCAGGAGATCG[A/G]GACCATCCTGGCTAA	8924
rs544898719	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28191474	ATGTATCTATATACT[C/T]CTGGCCTAGGGTGGT	8924
rs544911048	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28209578	TCGATCTCCTGACCT[C/T]GTGATCTGCCCGCCT	8924
rs544913552	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28249285	CACTGGGGTGGGCCA[C/T]GCAGCAGGTGCCGAG	8924
rs544921302	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28209860	ACACAACATAAGAAT[A/G]GGTATTTTGGTGTCT	8924
rs544942203	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28179412	AAAAATCCTTACTGC[C/T]TAGTGGTGTCCTGGC	8924
rs544953843	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28121606	GCTGGCCCCGAAGCA[C/T]ACAGGGACAGACGGC	8924
rs544975601	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28210473	GCCTTTTCGTGTGAT[A/G]AAGTCCCACGGAATG	8924
rs544976442	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28187985	TTTTTATTGCCTAAA[C/T]GACCTGCTCAAACCT	8924
rs544978978	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28215892	TTATCAACTTATTTT[A/G]TTTTTCTAAAATAAG	8924
rs544979748	in-del	-/AG	0.00716266	0.059414	intron-variant	HERC2	GRCh38.p7	15:28147232	AAGCGAGAGAGAAAC[-/AG]AAGAGAAAAAGGGTC	8924
rs544981632	in-del	-/T	0.00318978	0.0398085	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174313	CACTACAACCTCTAA[-/T]TGTGTTGGCACAATT	8924
rs545019513	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28200658	CTTGGTTGTATCCAA[A/G]TTCAAAAACTAACCA	8924
rs545026483	snp	A/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28216815	TGCAAGCTGACACAC[A/G]CTCCCATGCACTCTC	8924
rs545028771	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28306692	CAGCAGTGAAGTCAC[C/T]AGGTCCTGGGGTTTT	8924
rs545043381	snp	G/T	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28129809	TTTTGAGACAGTCTT[G/T]CTCTGTCACCAGGCT	8924
rs545071145	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28172654	ATATCTAAAACTACA[A/G]AACTTCTATAACAGA	8924
rs545088620	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28210911	CATTTATAAGCCACC[C/T]ATGTCCATTTTTATG	8924
rs545094855	snp	A/C	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28298133	AGACTAATACTTTTT[A/C]CCATGGTTTGTTTTG	8924
rs545100823	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28217945	TTTGGGACTTCTGGT[C/G]TCCAGAACTCTGAGA	8924
rs545110993	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28187941	GTGAACGAAGAGAGA[A/T]GCGTCTGGAAGCACA	8924
rs545111988	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28148015	GCACTTCAGCCTGGG[C/T]GACAGAGCAAGACTG	8924
rs545116274	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28307149	CTGCAAACTTATCTA[C/T]TTCTTCCACGTTTCC	8924
rs545158197	snp	A/C	1.83085e-05	0.00302554	intron-variant	HERC2	GRCh38.p7	15:28132266	AGCGCCTCCACCTTC[A/C]GAGAAAAGGGACTTG	8924
rs545168564	in-del	-/T			intron-variant	HERC2	GRCh38.p7	15:28183384	CAGCTAATTTTTGCA[-/T]TTTTTTTTTGTAGAG	8924
rs545174136	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28206129	ATTAGAATTATTTGC[A/G]TACTATCATTTAACA	8924
rs545184626	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174300	GCAGTTAACATGGCA[C/T]TACAACCTCTAATTG	8924
rs545199434	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28235500	AAAGGTCCACCCAAC[A/G]GGGGGCTGTATGGAC	8924
rs545203740	snp	A/C	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28117761	CAGTCACTCCCTGCC[A/C]ATCCTTCTCATCCTA	8924
rs545229795	in-del	-/A	0.00159617	0.0282053	intron-variant, utr-variant-5-prime	HERC2, LOC107987422	GRCh38.p7	15:28317643	TGGTTGTCAGGAGTT[-/A]AGAGATGGTGGCAGA	8924
rs545235380	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28240494	CAGAGAAGTATGAGA[A/G]GGGAACATACTCACC	8924
rs545237442	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28199538	AGCTTTTTTTCCCAG[A/G]AGAGAATTCCAGCTA	8924
rs545270170	snp	A/G			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28315521	TCCTATTAACAGCCG[A/G]GCACGGTTCATGCTT	8924
rs545280792	snp	C/T	4.94189e-05	0.00497062	missense	HERC2	GRCh38.p7	15:28125118	AGGGCAGCTACCAAC[C/T]GAGGCCTCTGGATGG	8924
rs545308690	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28207207	GTGGCACAATCTTGG[A/C]AAACTGCAACCTCTG	8924
rs545310504	snp	C/T	1.70912e-05	0.00292324	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28212468	GCCTGTTTAGTCGAT[C/T]TCTTTATTTTGTGCT	8924
rs545326398	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28289038	TCAGAGCACTGCCCC[A/G]CAGCTCAGGCAGTGT	8924
rs545334122	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28149300	AAAACACACGCAGCT[C/T]CTGAGAACATCACCG	8924
rs545349317	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28125888	CGATCTCAAGCTCAC[C/T]GCAACCTCCGCCTCC	8924
rs545367722	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28208699	ACGCTTCCAAAGACT[C/T]GCCACTTTCACTCCT	8924
rs545370251	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28207939	AAAAACAGGTGCACG[A/G]CAGTTTTGTCAATCT	8924
rs545376486	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28259331	AACTCCTGACCTCAG[A/G]TGATCCACCCATCTC	8924
rs545389587	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28274184	CCGCTGAAAACAGGT[A/G]AAAAACCAACCTACT	8924
rs545407880	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28294896	ATCTTCTAGGGTTAT[A/C]AACAGAACTTTAATC	8924
rs545410826	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28248980	GCTTCACTAATGTGC[C/G]CCTATGGAGCTGCGC	8924
rs545428975	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28166335	AAATATGGAAAAAGG[A/G]AGAGTAGGAATAAGC	8924
rs545453866	snp	C/T	3.61795e-05	0.00425305	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214303	GGGGAGAAGCTGCTG[C/T]ACCGCTCTTCACCAG	8924
rs545459911	snp	C/G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28173509	GTAAGCTGTACAACA[C/G/T]GCAAACTGGTCTGCC	8924
rs545462176	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28253294	CACCATTCTTTCACA[C/T]TGACTTTAGTTTTGA	8924
rs545465333	snp	C/T	0.00013182	0.00811742	missense	HERC2	GRCh38.p7	15:28130513	CGTACCAGGTATAAA[C/T]AGCTCCAGATTTGGT	8924
rs545479401	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28209037	CTAGAAAACTAAATA[C/T]AGAGAAATATAAAGA	8924
rs545486154	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28120178	TATGAACCTAGTTAA[A/C]CAACCTATTTATGTG	8924
rs545489128	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28245117	ACTCTGGAGAGTCTT[C/G]CCATTATCAATCTCT	8924
rs545498677	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28239289	TATGCCTTTAAATGT[A/G]TATATTAGAGGGAAA	8924
rs545522947	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28120698	GAGGATGGTGGGAAC[A/G]TGAACTGTTATAACC	8924
rs545527843	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28284472	GAGCAGACTAGAGAA[C/T]ATGATCCAACTATAT	8924
rs545538805	in-del	-/T			intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28320121	ATCATCCACAACAGC[-/T]TTTTTTTTTTTTGAA	8924
rs545543410	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28202735	AAGTCTAGAAAGCCC[A/G]CATTCACATGTGTGT	8924
rs545545522	snp	A/C	0.000798403	0.0199641	intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28320057	ACCAATTCTTGACCC[A/C]ATTCTCTGTACTCTG	8924
rs545549094	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28210133	TGCCCCACTATTTTT[A/T]TTTATTTATTTATTT	8924
rs545571820	snp	A/G	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28127203	CACGAGGCGGGTGTC[A/G]CACACACAAGGTGAG	8924
rs545575101	in-del	-/AT	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28193756	ACTTCAGGAGAAATA[-/AT]ATATAAACCAAATTG	8924
rs545584604	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28237536	ACATGTAGAGGAAAT[A/G]AAATTTATTCTAACA	8924
rs545594178	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28128613	CACCAAAGGCTTTAA[C/T]GAGGAGCACAGTTTG	8924
rs545598938	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28115622	ACACACGCCACTGAC[A/G]GCAGCTCCACACTCA	8924
rs545603316	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28287457	TAAGCTGGGCTTTAA[C/T]CTGAGCAAGAAAGGT	8924
rs545603543	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28160527	GGGCGTGGGACCCTC[C/T]GAGCCAGGCGCGAGA	8924
rs545605324	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28280702	TTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC	8924
rs545620609	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28290169	AAACTAATGCAGTAA[A/G]CCAACCTTGTGTGTT	8924
rs545623699	snp	A/C	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28277727	GTTAGGAAGGAAGAA[A/C]GAACCATGGCACTCC	8924
rs545644688	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28155098	AAGCACATGAACTCA[C/T]CCTTTTTTATGGCTG	8924
rs545647376	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28245319	TGGGAGGCAGAGGCG[A/G]GTGGATCACTTGAGG	8924
rs545655310	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28284823	AGGAGGCTGAGGCAG[A/G]AGAATCACTTGAACC	8924
rs545659186	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28183038	AGACACATGTCCCAA[C/T]GTAAAATGCTTCTCT	8924
rs545670739	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28138296	CGTAGATGGAACAAC[C/T]GTCTATTGGAAGAAG	8924
rs545684444	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28232704	TTTACACAGCTACTT[A/C]CAGGAAAATGTAACT	8924
rs545686064	snp	A/G	0.000148683	0.00862087	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28238721	AAATCAGCTTTGCGT[A/G]TAAGTGTCACTTCCT	8924
rs545695364	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28193524	GTCCCCCCAAAAAGA[C/T]AGAAAAGAGAATAGA	8924
rs545700467	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28197288	ACTATACACATACTT[A/G]TTTCTCATGCAACTG	8924
rs545721367	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28226600	GTAAAAGAAATTACC[C/T]AAAAATGGACCAAAG	8924
rs545730574	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28112937	CATCAGAGAAGTTCG[A/G]TGTTTTCCATTTTCA	8924
rs545734304	in-del	-/TC	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28289541	CTCCCCAGCACGATG[-/TC]GAGATACTCCTGGGA	8924
rs545736907	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28126677	GAGGATGCAACGGCA[C/T]AAGAATGACACAATG	8924
rs545756761	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28194152	CTCACTGCAAGCTCC[A/G]CATCCTGGGTTCACG	8924
rs545756880	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28136425	AGCTTCTGGCGGGGA[A/G]GGTGTGAGGCTCTCT	8924
rs545759741	snp	A/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28164253	CAACTCTTTCCACAA[A/T]CATAAACAGGCTGGG	8924
rs545768504	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28282619	ATAGAAGTTATCCAA[C/T]GTGAATAACACAGAA	8924
rs545768793	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28250472	TTAGTTTATTTAATA[C/T]AAAATTTAGAGCCAT	8924
rs545768938	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28256464	AAAACTGGACTAAAA[A/G]AACTCTTACCCACAA	8924
rs545774573	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28162726	AACCCCGACTCTACT[A/G]AAAATACAAAAAAAA	8924
rs545777717	snp	A/C	3.30017e-05	0.00406199	missense	HERC2	GRCh38.p7	15:28169638	TGGCAGCAGAAGAAT[A/C]AGCATCTGAAGGCAC	8924
rs545800321	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28207014	ACTCCATCTCAAAAC[-/A]AAAAAAAAAAAAACT	8924
rs545833005	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28289868	CACGCCGCAGTGAAA[C/G]GACGACACATCTGAG	8924
rs545854323	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28250892	GCATTTTTCTTTTTC[A/T]ACTTTCCAAAATTTT	8924
rs545856631	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28275391	GAGCAGCAGAGCCGC[A/G]GAGGGTAGCCTGGCT	8924
rs545860040	snp	C/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28155879	TAGGTCTTCTTCTAG[C/G]GTTTTTATGGTTTTA	8924
rs545866996	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28283092	TGGGACTATAACAAC[G/T]CCAGTCACTGAACTC	8924
rs545884683	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28164025	GGAGGGCAGCACTGG[G/T]GCTGAGCTTGTGGAA	8924
rs545886112	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28208135	ACCTCTACTATTAAT[G/T]GATTCTATACTTTCA	8924
rs545924657	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28284331	AGGAAGAACCAAACC[A/G]AAAAAATGAAAAACA	8924
rs545934454	snp	A/C/G			intron-variant	HERC2	GRCh38.p7	15:28120450	GATCCAAGAGGCGAG[A/C/G]CCAGTTTCATTTGAG	8924
rs545941011	snp	C/T	1.6504e-05	0.00287258	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28196549	AGTCGACAATGATAT[C/T]TTTTCCATTGGCACT	8924
rs545948295	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28238400	TTGAAATGAGTTCCA[A/G]GTATTAAAACAAAAA	8924
rs545970239	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28237343	TGCACAGCCCTACTG[C/T]AGAAAAACTAAACCA	8924
rs545981913	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28182740	TTTAATACTAGCACT[C/T]AATTTCAGCCTTTAT	8924
rs545992875	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28269159	CTTCAGAAATCAAAC[A/G]CCTTAAAGAAACACC	8924
rs545997516	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28277048	TCACTGCACTCCAGC[C/T]TGTGGGCATCAGGGT	8924
rs546000752	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28150722	ACACACGCGGCTTCT[A/C]ACTAACCGAGAACAT	8924
rs546004647	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28183417	GGGGTCTCACTATAT[C/T]GTCAAGGCTGGTCTT	8924
rs546038838	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28146915	GAGGAAGGAGGGAAG[A/G]AGGAGGGACGTGGGG	8924
rs546040131	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28190868	ACCAATTATTTAAAC[A/G]GGGAAAAACTGGGCT	8924
rs546056880	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28315519	GATCCTATTAACAGC[C/T]GGGCACGGTTCATGC	8924
rs546113011	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28294476	GGCCTGAAATTAAGA[A/C]TAAATATTACGTGCT	8924
rs546118780	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28301753	TATATATATATATAT[A/G]TATATATATATATAT	8924
rs546127335	snp	C/G	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28240157	GGCGCAGTGGCTCAC[C/G]CCTGTAATCCCAGCA	8924
rs546129886	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28271383	CTGCCAAATAATAGG[C/T]TGGGCATGGTGGCTC	8924
rs546146152	snp	C/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313421	CCTGACCTTGTGATC[C/T]ACCCGCCTCGGCCTG	8924
rs546149879	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28185895	ACAGTGTTCCCAGTA[A/C]ACATAACTGGGAATG	8924
rs546191251	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28219667	CCTCTTCCAGCCCCC[A/C]TACCACCTGCTCTCT	8924
rs546193404	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28264013	GACAGAGCAAAACTT[C/T]GTCTTACAAAAAAAA	8924
rs546211477	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28186442	AATTTTTGGAAACAA[C/T]TGTAATTTACCAATC	8924
rs546240683	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28150270	GAAACACACGCGGCT[C/T]CTAACCGAGAACATC	8924
rs546298572	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318758	TCCAAATAATGTCTA[C/T]GATAAAGAAGTCAAT	8924
rs546310835	snp	G/T	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318351	TGTTGAACAGGCCGG[G/T]CGCGGTGGCTCACGC	8924
rs546311210	snp	C/T	1.96284e-05	0.0031327	intron-variant	HERC2	GRCh38.p7	15:28230519	TGTTTTAAAACATCA[C/T]TCACTATAAAAATCA	8924
rs546330277	snp	A/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28154773	ATTTTATATATATAT[A/T]TTTTTATTATACTTT	8924
rs546343757	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28145305	GAGGGCCTGGCTGCT[A/G]TGGACAGGAGCGGTG	8924
rs546344828	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314316	AGCCTGAGGAATGAA[A/C]TAAAGTGTTAACACT	8924
rs546347630	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28231059	GTCCACCCTGGTCCA[G/T]TTCAGTGGTTCTGTT	8924
rs546353582	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28149745	TACCGAAAAAACACA[C/T]GCGACTTCCAACCAA	8924
rs546367158	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28269700	TGGCCCTTAAATACT[A/G]ATATATTTTTAAATG	8924
rs546394180	snp	A/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28297561	TGTTGTTTAAAAAAA[A/T]AAACATGAAAATCAA	8924
rs546397568	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28215402	CAGATGAGTGAGTAG[C/T]TGCAGGATTTACCAC	8924
rs546404062	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28263318	GGCTACTGAGCAAAC[A/G]AAATCTAGGTGACAC	8924
rs546425844	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28134172	GTAGTCTTCTGTCTA[A/C]AGGGTCATTCACATT	8924
rs546444819	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28199191	CAGAGTGCATTCTAA[C/G]TATTATTTAATGATA	8924
rs546452079	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28145803	TGTCCCAGCTGGCCT[C/T]ATGGAGCCCAGCAGC	8924
rs546456003	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28139184	CATGCCTACAGCTCC[C/T]TCTCCCTGAGTGTGG	8924
rs546463048	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28171306	AACAACTTGGATGAA[C/T]AGCCAGAGGATTAGG	8924
rs546463998	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28208913	CATCCAAACCCTAGA[G/T]AGCAATGATCACAGA	8924
rs546469043	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28172235	AATTAATGCAATCCA[C/T]ATCAAAATCCCAAGC	8924
rs546481488	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28165839	ATGTATGTACCTATT[A/G]TGTTACACACACACA	8924
rs546485666	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28134008	TATGCTCCGCTTATC[A/G]ATTTCTATACAAATC	8924
rs546486293	snp	C/T	0.00993419	0.0697739	intron-variant	HERC2	GRCh38.p7	15:28204643	AAAAAAAGATAGACT[C/T]AAAGGATGAAGAAAG	8924
rs546502532	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28206703	CTGGGCATGGTGGCG[A/G]GCGCCTGTAGTCCCA	8924
rs546502917	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28116467	GGCAATCTGCCTGCC[A/T]CAGCCTCCCAAAGTG	8924
rs546504846	in-del	-/CT	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28162320	CCCGGGTGAAGGAGA[-/CT]GTCTCAAAAACCTTA	8924
rs546511844	in-del	-/ACATCACAC	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28175759	ACAGCCAGCTCAATG[-/ACATCACAC]ACAGCACCCAAGGTC	8924
rs546515387	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28139653	CAAAAATCTAAAACA[A/G]AACTATCACAAACAC	8924
rs546515763	snp	G/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28129278	CTGTGGCAAAGCAGT[G/T]GGGGAACCAGGAGCA	8924
rs546533883	snp	C/T	0.000399281	0.0141238	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28255976	GACGACCTGGACTTA[C/T]GTTCACTTCATTGCC	8924
rs546536987	snp	A/G	3.40959e-05	0.00412878	intron-variant	HERC2	GRCh38.p7	15:28192159	AGACTGACCTATTTC[A/G]TGATAGTCAAAAAGA	8924
rs546548955	snp	C/T	0.00517822	0.0506191	intron-variant	HERC2	GRCh38.p7	15:28309679	AGCTCCAGATGACAG[C/T]GTGCCCTAGCCAACA	8924
rs546554666	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28122278	GCAGAGGATGCGGCA[C/T]GCAGCCGTGCCAATG	8924
rs546588984	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28226973	AAGGTGATGACAACC[C/T]TATTTAAAAAGGAGA	8924
rs546608129	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28286599	GAAAATAGCAACAAA[C/T]GGGAACTTCATCATC	8924
rs546625245	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28251146	CAAAATGTTCTTGGT[G/T]GTATTAATAAATGTG	8924
rs546625553	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28135101	TTCTTTTACAAATGG[C/T]GTCAATTGTGCGTTC	8924
rs546658003	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28164197	GAGCCAGGGAAGTGC[C/T]GCTTTTCTCTCCTGC	8924
rs546673327	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28274527	CCCTCAGCGAGAGAT[A/G]ACGCCACTGTCACCT	8924
rs546673334	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28176345	ACGTCACAATCACGC[C/T]GGGTGAGCCTGGGGC	8924
rs546674918	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28220922	CCTGGTCCTTCCATG[A/G]CTCCCACCAGACCTG	8924
rs546707505	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28135953	TTGCTGGAAGCTCTT[A/C]CATTTTTGTGTAGAA	8924
rs546707634	snp	C/T	9.34012e-05	0.00683315	synonymous-codon	HERC2	GRCh38.p7	15:28142367	CAGAGTGTCCAGCTC[C/T]AGGTCACAAGCAAGA	8924
rs546709968	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214441	GCGCCGCTCTTCACC[A/G]GGGCACAGGGAAGGG	8924
rs546713083	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28251582	AAGGCGGGCAGATTA[C/G]TTGAGGTCAGGAGTT	8924
rs546740576	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28305747	TGAACAGGCAACCTA[C/T]AACATGGGAGAAAAT	8924
rs546749393	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28245614	ACACACAGATATATA[C/T]ATACACACACATATA	8924
rs546758969	in-del	-/CATGGCGGGAA			intron-variant	HERC2	GRCh38.p7	15:28127686	GGTCGAGGCGTGGGG[-/CATGGCGGGAA]CAAGTGGAGGCTAAT	8924
rs546769825	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28158109	TGAGAGACAGTTTGT[C/T]ATAATTTCTGTTATT	8924
rs546771845	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28165059	GAGTACACATGAGCA[A/G]GGGCTGGCCTGGTGT	8924
rs546773025	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28258991	TAGATGAAGTAAAGC[A/C]CATCTGAGGGCCAAA	8924
rs546777157	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28172799	TTCTAATCTTTAAGA[C/T]TCACCTGTGAAGAGA	8924
rs546778986	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28252901	AGCAGGCCCACCCCA[C/T]GCCACAGGCCCAACC	8924
rs546793944	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28121232	GTGGCACCTGCTCTT[C/T]AAAGTTGGGGTGCAC	8924
rs546800229	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28305910	AGACATTTATGCAGC[C/T]AAAAAATACATGAAA	8924
rs546805752	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28216072	TCTAAAACTCCTGGG[C/T]TCAAGTGATTCTCCT	8924
rs546810149	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28290374	AATCAAGATTACAGG[C/T]ACCCACCACCACACC	8924
rs546831254	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28159203	CTTTGGTGAATCTGA[C/G]AATTATGTGTCTTGG	8924
rs546840390	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28166411	ATGGTTTTTATTATA[C/T]AGATAAATGCAGAAG	8924
rs546846408	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28166680	ACATCAGACAATGGA[A/G]CCAGTCCACAGGGAT	8924
rs546863265	in-del	-/T	0.0123036	0.0774623	intron-variant	HERC2	GRCh38.p7	15:28239180	ATTCTAAGAAAAAAA[-/T]GACTATGAAAATTAG	8924
rs546869084	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28210565	TTTCCTCAGACGCCC[A/G]TTAGATGGCTACACC	8924
rs546884794	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28159891	GTCTTTGATGATGGT[G/T]ATGTACAGATGGGGT	8924
rs546885586	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28122860	CTCCCACCCATGCCC[C/T]GCTCACAGCCTGCAC	8924
rs546894233	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28285124	CTCAAAGTCTCTCTC[C/T]ACAGCTGATAAAATT	8924
rs546924701	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28238998	ATTGGGCCATGCCAG[A/G]CCACAGAGCAAATCT	8924
rs546931171	snp	A/G	0.000217628	0.0104291	intron-variant	HERC2	GRCh38.p7	15:28152657	AGGCTGCAGCTCCCC[A/G]CTGGGGCCAGCCCCT	8924
rs546935582	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28271794	AAAGACCAGCAGTCC[C/T]GGAGGTTTAGGCCCA	8924
rs546935647	snp	A/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28118375	CAGCAGCCATAAGGC[A/T]GGAGGCAGACAGGCT	8924
rs546951854	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28131701	GGCTAACCCAGATGC[A/G]GTCCCTTTAGCAAGC	8924
rs546980982	snp	C/T	0.040671	0.13668	intron-variant	HERC2	GRCh38.p7	15:28302591	GAACCTCCAAGCTAA[C/T]CTCCATAATGGCTGT	8924
rs546994117	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28148025	CTGGGTGACAGAGCA[A/G]GACTGTGTCTCCAAA	8924
rs547007500	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28252998	CCCTGCTCTGTGCTC[A/G]GCTGCCTGACCCAAC	8924
rs547009795	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28126904	AAAAAAGAACATGCC[A/G]TTTCTGTTCATATCC	8924
rs547020541	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28295116	AAACACTGATAACAC[C/T]AAGTGCTAACAAAGA	8924
rs547024753	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28158008	ACCCACTAGTCATTC[A/G]GGAGCAGGTTGTTCG	8924
rs547027130	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28191711	AGAGGAGGAAAAAAA[A/G]CCTGACCACATCCTC	8924
rs547092733	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28244504	GGGAGGGTCCTGCCA[C/T]CATCCAGGCTAAGGT	8924
rs547092746	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28265513	ACCCACTGGGCGACA[A/G]GGTGGGTGGCCTCGT	8924
rs547107930	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28295701	CCACGCCCGGCCACC[A/G]TATTTTATAGTTTTT	8924
rs547108424	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28249313	GAGGGCTCAGGGAGT[C/T]CAGGAAGGAAGACCA	8924
rs547108981	in-del	-/AT	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28197282	TATAAAACTATACAC[-/AT]ACTTATTTCTCATGC	8924
rs547135382	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28287924	AGAGACGCTGTTTCA[C/G]CGTGTTAGCCAGCAT	8924
rs547145944	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28196940	TACCTTCGGTATCTC[A/C]GGGAATAAAAACCAC	8924
rs547147050	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28241976	ACTCATATAACAGAA[C/T]ATGATTTCACCTTAA	8924
rs547185464	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28203761	CAGAGGGAAAACCAC[A/G]AAATATGCGGACGGA	8924
rs547186651	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28192651	AAAATAAAGAATTAC[A/T]AGGTCAGAACCGCAG	8924
rs547213217	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28151950	CTAACAAATAAGCAA[C/G]AAATGATTCCACTAG	8924
rs547224437	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28145396	GCTTCAGAAGGACCA[C/T]CTGCCAGCAGCTCAG	8924
rs547232821	snp	C/T	0.00755907	0.0610114	intron-variant	HERC2	GRCh38.p7	15:28156037	CCTTTCCCCATTTCT[C/T]GTTTTTGTCAGGTTT	8924
rs547232833	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28149717	GCCACATGAACGCAC[A/G]TTCTAGTAAAATTAC	8924
rs547233021	in-del	-/C	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28283236	CCTAAACAGGATGAA[-/C]CCAAAGAAATCCAAA	8924
rs547239196	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28150062	ACCAAGAACATCACC[C/T]AGAACGGCCACACAA	8924
rs547240015	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28194461	TGTAGTCGCAGCTAC[A/T]CGGGAGGCTGAAGCG	8924
rs547247778	snp	A/G			synonymous-codon	HERC2	GRCh38.p7	15:28144219	GACGCAGCGGTCAGA[A/G]AGGAGTTCTTTAGGG	8924
rs547264972	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28320751	TCGAAATATTAGTTA[G/T]TATTTATTTAATAAT	8924
rs547272647	in-del	-/ATAG	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28270203	TCTTTTTATTTATTT[-/ATAG]ATAGATAGATAGATA	8924
rs547297634	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28233018	GTAACTGTAATAAAA[A/G]TGATGGCAGCAGGTA	8924
rs547301388	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321581	GGGAGAGAAGAGCTG[A/G]TGGAGGGGAGAGAAG	8924
rs547330107	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28275460	TGGCCGCGGGTGAAG[C/G]CCTGCGTGCTTGACC	8924
rs547332001	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28268796	CAGCAACAGAACAGC[A/G]GGCAGCCTCCAAGTG	8924
rs547338142	snp	C/T	1.73387e-05	0.00294432	intron-variant	HERC2	GRCh38.p7	15:28116890	AGCCACTCGAAGTCC[C/T]CTCACACAGTCCTGT	8924
rs547352964	snp	A/C/T	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28154309	ATTAACAAACTAATA[A/C/T]CATTGTCACATAGGC	8924
rs547365114	snp	C/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28254032	GTGATGCCTGTAATC[C/G]CAACACTTTGGGAGG	8924
rs547371401	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28167901	ATTTCCTATGCAAGT[C/T]CCAAATGCTTTACCT	8924
rs547398041	snp	C/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28211862	GAAAACTCAAGAAGA[C/G]TGGGCAGAATACGCC	8924
rs547431547	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28240274	ATACAAAAAATTAGC[C/T]GGGCGTGGTGGCAGG	8924
rs547432810	snp	C/T	0.00080064	0.019992	intron-variant	HERC2	GRCh38.p7	15:28161638	TTAAAACCTTCAGTT[C/T]CTCAGGTGCACTAGC	8924
rs547434461	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316886	GGTTCAAGCGATTCT[C/T]CTGCCTCAGCCTCCT	8924
rs547437437	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28292790	TTTATTTACTTTTTT[A/T]AAAATTGTTACCAAA	8924
rs547443001	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28195156	TGTTTAGGTGGAGAA[C/T]ATACTAATAATAGAT	8924
rs547468617	snp	A/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28228112	ATTTGTGTCTTACCA[A/T]AATTTACAAAAAGCT	8924
rs547472607	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317377	TACAGGCGTGAGCCA[C/G]CGCGCCCAGCCGAAG	8924
rs547492310	snp	A/C/T	3.29632e-05	0.00405964	missense, utr-variant-5-prime, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28280228	TGGTGGCTGACTGGA[A/C/T]GGCCAGGGCCTGCTG	8924
rs547505823	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28118278	GAGAGGTGCACCCAG[C/T]TCCCCGAAGCCCACG	8924
rs547506255	snp	C/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28206701	AGCTGGGCATGGTGG[C/T]GGGCGCCTGTAGTCC	8924
rs547512916	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28112464	ATAGAAAACTATGCA[C/T]GCTCTCCAAGGTGAC	8924
rs547518442	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28200324	GGCATGAACCCGGGA[A/G]GCGGAGCTTGTAGTG	8924
rs547526376	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28228717	ACAGAGTGGGCAGCT[C/T]TGTCATGCTGCACGA	8924
rs547566498	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28171850	GAGGCCGAGGTGGGC[A/G]GATCACGAGGTCAGG	8924
rs547586755	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28282202	GCCCTATCCCTGCCA[G/T]AGCAGGGTCACAGAA	8924
rs547587372	snp	C/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28200849	AAATGAGATGATTTG[C/G]GGGATTTTCTCTAAA	8924
rs547607172	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28259838	CCAGGCATGGTAGTG[A/C]ACACCTATAATCCCA	8924
rs547613280	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28226224	CCAAAACAATCTACA[G/T]ATTCAATCCCTAGCA	8924
rs547626985	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28222817	ATGCGCCAGGAAGGG[G/T]GTGCCCGTGTGATCA	8924
rs547640991	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28223125	AATTGGTGCCCTGGG[C/T]GGCTACAGAGTCATC	8924
rs547644238	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28256841	CCTCGTGATCCACCC[A/G]CCCAGGCCTCCCAAA	8924
rs547650823	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28311414	AGGCTGCAGTGAGCC[A/G]TGACGGTGCCACTGC	8924
rs547660423	snp	A/G	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318241	AATAAAAAGTGATGT[A/G]ACTGACACCTCTTAG	8924
rs547672770	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28137362	ATTTGACTGTGCCTT[A/G]CTTTACTGTACCTCG	8924
rs547683941	snp	G/T	1.65712e-05	0.00287843	intron-variant	HERC2	GRCh38.p7	15:28144834	CGCACCCCGGGGTTA[G/T]CTTCACTCCATCATC	8924
rs547684475	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28306455	GATGTTTTTAATGTG[C/T]TGTTGAATTCGGTTT	8924
rs547685881	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28131068	CCTGCCAGCCAACTT[G/T]CCCTATCCCACAAGC	8924
rs547690962	snp	A/C	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28121599	GGAACAGGCTGGCCC[A/C]GAAGCACACAGGGAC	8924
rs547699411	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318489	CAAAATTAGCCAGGC[A/G]TGGTGGTGGACACCC	8924
rs547700751	snp	A/G	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313426	CCTTGTGATCCACCC[A/G]CCTCGGCCTGGGATT	8924
rs547718343	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28189028	AGGATGTGGTGGTTG[C/T]GGTAAGCTGAGATCT	8924
rs547742191	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28319250	CTGGTGCACACTATC[C/T]AAAACCTAGTCATTT	8924
rs547743202	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28259889	AGGAGAATTGCGTGA[A/T]CCCAGGAGGCACAGG	8924
rs547745279	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28181804	TAGGGGATGAAGGAC[A/G]TTGTGAACACAGAGG	8924
rs547765924	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28209129	ATGGCATATCTATAA[A/G]CGGATATACATAGCA	8924
rs547790982	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28211281	ACACACTGTCCGTGA[C/T]GAAGGGCTTGCCTTT	8924
rs547793864	snp	C/T	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28160225	TTCTCAGGTCTCAAA[C/T]TCCGTTCTGGGAGAA	8924
rs547825634	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28280742	AAACCCCTTCTCTAC[A/T]AAAAAAAAAATACAA	8924
rs547828551	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314585	TATGTCAGCCAAGCA[C/T]GGTGGCTCACACCTG	8924
rs547832290	snp	A/T			utr-variant-3-prime	HERC2	GRCh38.p7	15:28111367	ACACAGTTATTTCCA[A/T]TATACAATCAAGACG	8924
rs547839388	in-del	-/AG	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28126001	ATTTTTAGCAGAGAC[-/AG]GGTTTCACCATGTGG	8924
rs547854322	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28153788	TACTTCCTAGTGAGG[A/G]AAGTTGGCCTCGGAA	8924
rs547859384	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28284433	TGTAAACAGTCTAAA[G/T]GCATCAATTAAAAGA	8924
rs547864830	snp	A/T	0.00318978	0.0398085	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28315125	ACATTCACTAGGCAC[A/T]TGTGGCTTTTCCAGA	8924
rs547866626	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28154575	CATCATCTGCAGAGG[G/T]GTCATGATGGAGCTG	8924
rs547919394	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28193616	CATGCCCCAGAAGCC[C/G]TACCAACCCCAAGAA	8924
rs547922956	snp	G/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28320154	AGTTTTGCTCTCATT[G/T]TCCAGGCTGGAGTGC	8924
rs547929638	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28187678	CGCATTGCTATTATC[A/G]TAGCACAAACAATAA	8924
rs547951625	snp	C/T			intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28186398	TATAATGTGTTTCTA[C/T]ATTAAACACTTTATT	8924
rs547960219	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28187163	TTTGAATATACACAA[A/G]TCAGAACAAATAGTA	8924
rs547962668	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28232198	TCGGAAACTCAGTAA[C/T]CAATACTGGTCAATA	8924
rs547993193	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28309526	CTTTTTCCATCCCCC[C/T]GCACCGTCCTGAAGG	8924
rs547997043	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28143721	AAAGTGGTGGCATTA[C/T]ACGCATGAGCCACCG	8924
rs547998550	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28146990	GGACTGGTTTTAAGA[C/T]ACTATCTCTGCATGC	8924
rs548021877	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28219954	CTTCCCTAGAAGCGA[G/T]AAAGTGCTGACTAAC	8924
rs548034398	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28220351	GCCAGCTGCAGGTGC[A/G]TCCTGACATCCCATT	8924
rs548067485	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28306798	CTTCATGGTTCAAAC[C/T]TGGAAGGCTGTATGT	8924
rs548070139	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28232983	ACTTGGAAAAACAAG[C/T]GAGATTTCTGTATTT	8924
rs548077791	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28260608	AGCATTTAATTGTCC[A/C]TGAAGAAAACCCAAG	8924
rs548081273	snp	C/T	0.00114656	0.0239158	synonymous-codon	HERC2	GRCh38.p7	15:28135690	ATACCCAGTGGCATA[C/T]AGCTAAGAAAAGAAA	8924
rs548083116	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28127706	CGGGAACAAGTGGAG[A/G]CTAATCATCTTCTTC	8924
rs548106965	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28298578	AGGCGGGCGGATCAC[A/G]AGGTCAGGAGCTCGA	8924
rs548131690	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28237907	GATCATTTAAAAAAC[A/T]ATTTTTCAAGACCAG	8924
rs548134431	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28294722	AAAATGTGCCTCCCA[C/T]AGCCCCTCGTGGTTC	8924
rs548140483	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28182280	GGTAATTTGATAATG[C/T]CTTTTAGTTCGTGTA	8924
rs548143252	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28299202	GTTTTGCAATAAAAA[C/T]GCCTTCAATTAACGT	8924
rs548185219	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28157472	CCTGGTTTAGTCTTG[C/G]GTGGGTGTATGTGTC	8924
rs548190535	snp	A/G	1.6713e-05	0.00289072	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28174603	CTGGCCGTGGTCGTT[A/G]TCACCCCAAGCATAC	8924
rs548200884	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28182820	CCAACGTGAACATGG[A/G]TGGGAATCATTCCAA	8924
rs548216423	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28231503	ATGTGACTGGCCCCC[A/G]ACAAAATCTCTAGAC	8924
rs548224682	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28146184	ATGTGAAGGGTTGTG[C/T]CTACGGAGACACAGG	8924
rs548244922	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28190312	GCGTGAGCCACCGCG[C/T]CCGGCCAACAAAAGT	8924
rs548256026	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28238457	ATGTGCTGAATTTGT[G/T]GATAAGACAGACATC	8924
rs548258019	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28151692	TCTAGAAACAGGATA[A/C]TCTCAGCTTCAACAA	8924
rs548260659	snp	C/G	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28230644	TGCAATGCTCAACAA[C/G]AAGAGTGAAATGATC	8924
rs548270331	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28159397	CATAGATTTGGTCTT[G/T]TCACATAGTCCCATA	8924
rs548270930	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28261919	ACACACAAAGAATGT[A/G]TGTAGTACCAGGACC	8924
rs548301574	snp	A/G	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28175253	TCTTCAAGAATAACA[A/G]TCTTTCCACACACTT	8924
rs548308320	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28203435	GTTTCATTCTAAAAG[C/T]TTAAAATTCAGAGCC	8924
rs548309380	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28294053	TACAAATAATGACTA[C/T]CTAAAAATCTCGAAG	8924
rs548312033	snp	C/T	0.000296878	0.0121799	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28270783	ACAACCGCCGTTTGT[C/T]GCAGATCAATGGCAA	8924
rs548371366	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28303118	CCCAATGTTTTCTTT[C/T]AGCACTTTCATAGTC	8924
rs548391736	snp	C/G/T	1.65116e-05	0.00287324	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229550	TTCTTGCTCGCCAGT[C/G/T]TTAAAATTGTATCTA	8924
rs548397580	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28264710	GCAAGGCTAATCTCC[A/T]AACACAGCTTAGACC	8924
rs548417939	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28176360	CGGGTGAGCCTGGGG[C/G]GAGGCCCAGGTTCCC	8924
rs548418055	snp	A/G	0.000736217	0.019172	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28192139	GAACGGCCACAAAAT[A/G]CCGCAGACTGACCTA	8924
rs548465884	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28201883	GAGATGTTTGAACAA[A/G]GGTCTGTTCTGAAGC	8924
rs548474516	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28265366	GAGTGTCAATCATCC[C/T]ATTTCAACTCTCATT	8924
rs548477393	snp	C/G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28209410	GTGCAGTGACACGAT[C/G/T]TCGCCTCACTGCAAG	8924
rs548479494	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28251176	GGCCAGGTGCAGTGG[C/T]TCACACCTGTAATCC	8924
rs548483155	snp	A/G	4.94817e-05	0.00497377	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28260855	TTCTGGCTTGGTCAC[A/G]CGCAAGGTGTCAAAG	8924
rs548490482	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28168384	TCCTTTCTGATCTAA[C/T]ATTGCTTTAGATTCG	8924
rs548500520	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28169754	CCAAAACACACTGCA[A/G]TCTGCATTTTGCTAT	8924
rs548502499	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28295264	CAGCTCAGGTGAGAA[C/T]ACAGGTGCTGCTTCT	8924
rs548522225	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28177867	AAAAATAGTGTCAAT[C/T]TAAGTTTTTGAGAAC	8924
rs548531154	snp	A/C/G	0.000762808	0.0195149	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28213998	CCAAACAGCGAGCTC[A/C/G]ACAGAGACACTCACG	8924
rs548562186	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28266582	AAACCATGGTCCATC[G/T]GCAACAGAAGGAATG	8924
rs548564922	snp	A/C/T	1.64779e-05	0.00287031	missense	HERC2	GRCh38.p7	15:28146279	CGCCGTCCATGACTG[A/C/T]GAGAGGGTCGTGGCG	8924
rs548574851	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313985	CAAAGGGCCACACAC[C/G]AGAAATACAGGTGAG	8924
rs548576332	snp	A/T	0.0486741	0.148216	intron-variant	HERC2	GRCh38.p7	15:28307933	TTTATGCTAGTACTA[A/T]GCTGTTTTGGTTACT	8924
rs548596386	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28219224	TGAGGACAAAGCACC[A/G]GCATCTGTGGAGTGG	8924
rs548598080	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28259131	CGGAGTTTCGCTCTT[A/G]TTGCCCAAGCTGGAG	8924
rs548611499	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28224729	AGTATACCACAGAAC[A/T]CTCTCTTAGACTGAC	8924
rs548633417	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28262551	GTGGCTCCACAGCAC[A/G]ATGCACACTCATGGT	8924
rs548644132	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28218217	CTACAAGCCGAGGAA[C/T]GCTAAAGAGACCAGT	8924
rs548656617	snp	A/G	3.53807e-05	0.00420584	intron-variant	HERC2	GRCh38.p7	15:28218695	AATAATCAAAATTAC[A/G]AATTATATTCCCAAG	8924
rs548671888	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28255335	CAAGACGCTGTCTCA[A/G]AAAAAAAGAAAACAA	8924
rs548678272	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28213237	AAAGAAAAAGAATAT[A/G]TAGTAAGATTGCACT	8924
rs548701515	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28161815	CCATAGTATCAGAAC[A/C]TAAGAAGTTTTGTAA	8924
rs548703462	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28133259	AGGAGTTTTAACATA[C/T]GAATGTCACTAGTCT	8924
rs548706079	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28291635	AATTACACAAAAAAA[A/G]GTAAGCAAAGAATAA	8924
rs548708799	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28306006	CCAGTTAGAATGGCA[A/G]TCATTAAAAAGTCAG	8924
rs548731316	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28208939	ACAGAAAAGGACTTT[C/G]CCCGAAAAGACTTAG	8924
rs548750073	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28149746	ACCGAAAAAACACAC[A/G]CGACTTCCAACCAAG	8924
rs548751888	snp	A/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28169357	GAACTTGTGACTTAC[A/T]ACATACAGCATTTAA	8924
rs548760005	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28126192	ACACTTATACTGCTG[A/G]TGGGAACAGAAACCA	8924
rs548766879	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28162882	GGCGACAGAGCGAGA[C/T]TCCGTCTCAAAAAAA	8924
rs548790411	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28292020	ATCACCTGAGGTCAG[A/G]AGTTCAAGACCAGCC	8924
rs548796919	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28250016	CATGGGAACACGGAG[A/G]GGAGGAGAGCCCAAC	8924
rs548804109	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28297630	ACCCGACTACGTGAT[C/T]CCATGTATGGAGTTC	8924
rs548818499	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28210625	TGGAGTGCGGCTTTA[C/T]GCGCATTTGAAGAAC	8924
rs548822405	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28252988	GCCCAGGGCTCCCTG[C/G]TCTGTGCTCGGCTGC	8924
rs548832053	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28250506	CAAAACGTGTAATTC[C/T]GATGGGGTTCACTAC	8924
rs548857332	snp	A/G	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28247449	TTTTTTTTTTTTGAG[A/G]CCGAGTTTCACTCTT	8924
rs548858046	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28199216	ATGATAAAGGGAAGA[A/G]AAACTCTTTAGAACA	8924
rs548864629	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28156699	ATGTCATCTGCAAAC[A/C]GGGACAATTTGACTT	8924
rs548901699	snp	A/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28114245	TCACACCTGGGCGCC[A/T]GGCAAAGGCTGCTCT	8924
rs548931890	snp	A/C	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28128306	GTGTGAACTGGCTGG[A/C]AGGACGAGCCTCCCT	8924
rs548934571	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28304460	GCAATCTCCACCTCC[A/G]GGGTTCAAGTGATTT	8924
rs548936667	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28228048	ACTCTAGAAAATCGT[A/C]AATGTATTTGATACC	8924
rs548957133	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28258422	GGTTGCCGTGAGCTG[A/C]GATCATGTCATTGCA	8924
rs548963119	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28129749	GCTGACTGCAGATAG[A/G]TTCTCAGGACACAGT	8924
rs548976312	snp	C/T	0.0142736	0.0832652	intron-variant	HERC2	GRCh38.p7	15:28221003	TCAGTTAGGAGGGTG[C/T]GTGCCCTGCCCTGGT	8924
rs548993895	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28143040	TCAAATGTTTTATTA[C/T]GTTGGTACTAACTCT	8924
rs549052042	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28216192	CATTGTTTCTAGGCA[A/G]TAGGAAAACCATCTA	8924
rs549055084	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28280817	CAGGAGGCTGAGGCA[A/C]GAGAATTGCCTGAAC	8924
rs549067620	in-del	-/TTA	0.00159617	0.0282053	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28320748	CTATCGAAATATTAG[-/TTA]TTATTTATTTAATAA	8924
rs549089202	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28246414	CATACCAGGTAATAT[C/G]AGAATTTTTAAGATC	8924
rs549092775	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28129377	CAGGTGCTGTCTGCC[G/T]GGAAGCTGGGTAGAG	8924
rs549094199	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28139565	GAGTCCTGACCCAGA[A/G]AAACTATGAAATAAT	8924
rs549094335	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28298451	TGATCCACCACGCCC[A/G]ATCCCCATGTACTTT	8924
rs549097109	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28188483	CGGGAGATAGAGCTT[A/G]CAGTGAGCCGGGATC	8924
rs549103407	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28130093	CCCCTTTTAAGGCTG[C/T]GCATGTCCTTCATGC	8924
rs549104353	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28251673	GGCGTGGTGGTGTAC[A/G]CCTGTGGTCCCAGCT	8924
rs549110264	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28165271	TACAGAGGAAGAAAG[A/G]TGCCCACCACGGAGT	8924
rs549126056	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28239851	ATGATCACAGGGAGA[A/G]GAGGGCCTGGAGCCA	8924
rs549139094	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28209639	TGAGCCACCGCGCCA[A/G]GCCTATATATCATTT	8924
rs549144322	snp	A/G	0.000286246	0.01196	synonymous-codon	HERC2	GRCh38.p7	15:28152714	GGTGGAGGTGTCGTC[A/G]GTGTAAGGGTGGCTA	8924
rs549158119	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28123153	CCACCCTCAGGCACA[C/T]GTGAAAGTAAAATGA	8924
rs549186409	snp	C/G	1.66374e-05	0.00288417	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28211075	ATCCTGGTGGGAGAG[C/G]AGCGCCCGACCTGCT	8924
rs549200705	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28247898	AAACAGCTACAAAAT[C/T]ACTAATGGAAGCAGC	8924
rs549205739	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28153290	CCTGGGAGGCAGAGG[C/T]TGCGGTGAGCCGAGA	8924
rs549205981	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28148155	ACATTTCAAAACAAA[C/T]TGAGTGAAATTAGAA	8924
rs549206583	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28121869	CGGGCCAGGGAGCAC[C/T]GCGGAGCCAGCCGGA	8924
rs549239933	snp	A/G	0.0130921	0.0798413	intron-variant	HERC2	GRCh38.p7	15:28240291	GGCGTGGTGGCAGGC[A/G]CCTGTAGTCCCAGCT	8924
rs549247751	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28206400	GAATTTAAAAACAAA[A/G]TATGTGTAAGATTCT	8924
rs549267831	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321614	GAGAGAGGGAAAGAG[A/G]GAAGAGATGGAGGGA	8924
rs549276685	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28240711	ACATACAGAAAAATG[C/G]AATAGAATGGAGACC	8924
rs549279162	snp	A/C			intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28317941	AATTGCTTCATGCCT[A/C]TCTAATTTCATGTGC	8924
rs549317335	snp	C/T	6.59217e-05	0.00574078	intron-variant	HERC2	GRCh38.p7	15:28121336	TTGGAGAGTAATCTC[C/T]ATGTGCTACCTGGAT	8924
rs549322643	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28125283	CACACACAGCACCAA[C/T]GCTCCCTGCCCTTCA	8924
rs549357999	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28164267	AACATAAACAGGCTG[A/G]GGGAAGGACAGCCCC	8924
rs549380960	snp	C/T	0.00716266	0.059414	intron-variant	HERC2	GRCh38.p7	15:28168262	TTAAAAGCTCCTTTA[C/T]AGAGAATATTCTTCT	8924
rs549388138	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28192235	ATTACATAGTAAGGA[A/G]CTTCTTAAAGAAAAA	8924
rs549398395	snp	A/G	0.0130921	0.0798413	intron-variant	HERC2	GRCh38.p7	15:28227467	CATCCAAAAAAAAAA[A/G]GAAAAAAAAAAAAAA	8924
rs549418381	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28290421	GTTTCATAGAGACAG[G/T]GTTTCACCATGTTGG	8924
rs549420062	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28135113	TGGTGTCAATTGTGC[A/G]TTCTTTCTTCCTCAC	8924
rs549427388	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28142474	GTGGCTCCTTCCGCA[A/G]GACCTCCTATTCCAG	8924
rs549432795	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28282033	CCAGTCCATCAGTCA[C/T]GTACACTCTGAAACA	8924
rs549451407	snp	A/C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28186458	TGTAATTTACCAATC[A/C/G]TGTGGACATAAAATG	8924
rs549460628	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28118926	AGAGCAGCCCCCAGA[A/C]GTCAATCCACATTGC	8924
rs549462302	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28204434	AGACCAGCCTGGCCA[A/C]CATGGTAAAACCCCA	8924
rs549473928	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28175094	GAATATCCATAAGCC[A/G]GTCATAGCGTATGCT	8924
rs549498779	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28197667	TGAGACTGGAGAATT[C/G]CTTAAACCTGGGGGC	8924
rs549499545	snp	A/G	0	0	intron-variant	HERC2	GRCh38.p7	15:28119518	GAGTACGCTGGTATG[A/G]TCTCGGCTCACTACA	8924
rs549510409	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28161693	ATGTGGCTGGTGCCA[A/G]TGGTCCCAGATGGCT	8924
rs549519432	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28191760	ATAAAATCTATTACT[A/C]GTATTGTTTAAAATC	8924
rs549530398	snp	G/T	1.71965e-05	0.00293222	intron-variant	HERC2	GRCh38.p7	15:28236956	CAAAAAGCAAAGATT[G/T]TCTTACTGGCACATT	8924
rs549532089	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28159708	CGGAGAAGTTTGATC[A/G]TCTGAAGCCTTCCTC	8924
rs549540981	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28187536	CAAGGTTTCACCATG[C/T]TGGCTAGGCTGGTCT	8924
rs549547261	in-del	-/T	0.252983	0.249982	intron-variant	HERC2	GRCh38.p7	15:28249816	CCACGCCAAGCTAAC[-/T]TTTTTTTTTTTTTTT	8924
rs549553331	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28249891	CGATTTCCCGACCTC[A/G]TGATTCACCCGCCTC	8924
rs549563869	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28198223	AGGTGAGTTCCTCTG[C/T]GGCCTTTGGCAGAAG	8924
rs549610219	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28150443	AACATCACCGACAAC[A/G]GCCACACGAACGTAC	8924
rs549612490	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28201744	GAATCTCAAAAGCTA[C/T]AAGTATACAAAATTT	8924
rs549641993	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316296	TTTCCTTTTTTTTTA[A/G]TAACTAGTATTACTA	8924
rs549667245	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28262598	TACAAGTACAGGTGA[C/T]CTCACCACACAGAGG	8924
rs549675808	snp	A/T	0	0	intron-variant	HERC2	GRCh38.p7	15:28230084	GTTATGGTTCATATT[A/T]ATAGCCACAGGGCCC	8924
rs549696223	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28156546	TTCACTCATTATTTT[G/T]CTGTTTGTCTGTTAT	8924
rs549705575	snp	A/G	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28249356	AAAGAGCACGGCAGC[A/G]AAGAAAGTAGAAGAG	8924
rs549762741	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28162261	CCTGATCCCGGGAGG[C/T]AGAGGTGATCCTGGG	8924
rs549775152	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28207462	TTTCGTGTTCACTCA[C/T]GGCTTCAGTAACCCC	8924
rs549780580	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28276069	ACGGGTGCCTGTAGT[C/T]CCAGCTACTCGGAGG	8924
rs549786926	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314467	CCTACTCTGCCTATG[G/T]AGGAGCCATTCTTAT	8924
rs549796900	snp	C/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28231354	AGTTTTTTGGTATAC[C/G]TGACACCCAGGACCT	8924
rs549800096	snp	C/T	1.65002e-05	0.00287225	missense	HERC2	GRCh38.p7	15:28168505	TAGCCATCGCAGATG[C/T]GTCGGAAGGGGCCGC	8924
rs549805035	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28311527	TGTGAAAGGGAAAAT[A/G]AGGGAGGGAACAGAA	8924
rs549822062	snp	C/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28156121	TGTTCCATTGGTCTA[C/T]ATCTCTGTTTTGGTA	8924
rs549832070	snp	C/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28225361	AAAACCAAAAGTTTG[C/G]TTTCTGACAAGAACA	8924
rs549840416	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28201116	GTCCTCTGGCTACAC[C/T]GGGGCAGCCACAGCA	8924
rs549845738	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HERC2, LOC107987422	GRCh38.p7	15:28312176	GGAACATTACTAAGG[C/T]AATAAAGCAAGCCTC	8924
rs549862638	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317425	AATAAGCTTAACTCT[A/G]AGAGCTTACATTTAT	8924
rs549863735	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28282272	GAGTCGCCTAACAAC[A/G]TGTTCTATTGAGAAA	8924
rs549865387	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28289209	ATATGATACCTGAAA[A/G]AAATGCACTTTACAC	8924
rs549881645	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28113769	TGCAGCACTGTGGCC[A/G]CACACGTCCCAGCTG	8924
rs549900419	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28240990	ACTGAATTTGGTGAC[A/G]TGTCTTGAATAGGAC	8924
rs549906461	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28194970	CTGATGCAGGAGAAT[C/T]GCTTGAGCCCGGGAG	8924
rs549910144	in-del	-/ATA	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28264151	CCCACACTCTATTTT[-/ATA]ATAACTAAAGATAGG	8924
rs549933408	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28306945	GCTCAAGTGATTCTC[A/G]TGCCTCAGCCTTCCA	8924
rs549948139	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28155306	TGGCTGGGTCAAATG[G/T]TATTTCTAGTTCTAG	8924
rs549955351	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28253442	CTTATTAGTAAGAAT[A/C]TTTTTACATGTTTAC	8924
rs549964983	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28143742	TGAGCCACCGCGCCC[A/G]GTCCAAGGCCTCCTT	8924
rs549968936	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28222847	AGCCCTAATGGAAAC[A/C]CTGGGCCTGGAGTCT	8924
rs549969815	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28195416	CACTGAGCCAAGATC[A/G]TGCCACTGCAGTCCA	8924
rs549987096	snp	G/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28187720	CCCAATATGCTACAG[G/T]GATCAAACTTTTCTG	8924
rs550012533	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28218046	CTAACCCCTATCGTA[C/T]CTCGGCAGGTGACCT	8924
rs550013373	snp	C/T	3.88041e-05	0.0044046	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28269251	CAGAACACTCACCAG[C/T]GTGTCACTATTATAG	8924
rs550026141	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28137420	TCTGTGGCAACCCTA[C/T]ACTGATCAAGTCTAT	8924
rs550037873	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28224839	ATGAGAAATAAAAAA[A/C]AGAAAAGTGGAAAAT	8924
rs550048423	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28179793	GTTTTTAACAAACAC[G/T]TTAAAAAGTAAAAGA	8924
rs550076352	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28212253	GGCTCCGAACATGGC[G/T]ACAAAAGCTGACTCG	8924
rs550077823	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28308023	AATTATGAGAGCTTC[A/G]GCTATTCTGGGTCTT	8924
rs550080407	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28124831	TTGGGATTACAGGTG[G/T]GAGCCACCACAACCA	8924
rs550112673	in-del	-/CTCT	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28285785	ATAAAACTGACAAAC[-/CTCT]CTAAGCATGACTGAC	8924
rs550116472	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28299233	AAAACAATAAAATCC[A/G]AGCAGCTTGTATTAA	8924
rs550122091	snp	C/G/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28288774	ACTCGCTTGAACCCA[C/G/T]GTGGGGGAGGTTGCA	8924
rs550131902	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28281376	ACAGCTCCCAGTGGC[A/G]AGGTGAGAGCTGGTC	8924
rs550138846	snp	C/T	0.0260695	0.111154	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214040	TCCCTACAGGTTCAC[C/T]GTTGAACTAAATTAA	8924
rs550142400	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28190047	AGAGTCTGGCTCTGT[A/C]GCCCAGGCTGGAGTG	8924
rs550145333	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28223877	ACACATGAATACTAT[A/C]AACAGAACAAGTCCC	8924
rs550163008	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28235592	CCCTGCTCCTCTCAG[C/T]ATTGCCCTTGACACT	8924
rs550200249	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28138639	ACAATGTACCTGGTC[A/G]CCCAAGAGCTCTGAT	8924
rs550203080	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28309110	GGACGATCCATGTGC[C/T]AAAGAGAACAATGTA	8924
rs550204397	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28292876	CCAAAGTGCCAAAAT[A/T]CACAAGATTACCTGG	8924
rs550212454	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28132471	GGAGGAGGTATCAGC[A/G]TCTTTGATGAGCCAA	8924
rs550224849	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28247643	CTATGTTGGTCAGGC[G/T]GGTCTTGAACTCCTG	8924
rs550224972	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28248928	AAAACGGAGCAGAAG[A/G]GCACGGAAGGCTCAA	8924
rs550239671	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28191628	CCAATGTGCAACACA[A/G]ATTTGCTAGACTATA	8924
rs550241870	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28309553	AAGGGATGGTCTTCA[A/G]TTTGAAGAAGCAAGC	8924
rs550261632	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28320689	CCAAAAGTAGTTTTT[C/T]CAAGCCATTTCCAAA	8924
rs550263218	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28267583	TTTTCACTCGTCTTA[C/G]ATTTGTCTGAATCCC	8924
rs550265077	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28143309	CAATCAGTTAGCCTC[A/G]TTGTAAAGTCCAATC	8924
rs550301720	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28181631	AAATTTAGAGGAATT[C/T]GCTTTGTGGCTCCTC	8924
rs550313929	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28144299	ACCCCATAAGAAGCC[G/T]CCAACGAACAAGGGT	8924
rs550329386	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28303791	TAGTTTTATTCCTAC[A/G]TATTTTACTTTATTT	8924
rs550341553	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28217729	CATGTTGGATTAGAG[G/T]CAAAGAAACTCAAAG	8924
rs550346765	snp	A/G	0.000798403	0.0199641	intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28315658	AATTATCTGGCTCTC[A/G]GCGTTAGCGCCATTT	8924
rs550369229	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28271617	CAGCTTGCAGTGAGC[C/T]GAGATCACGCCACTG	8924
rs550384861	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28247147	GTATGAACACTAAAG[C/T]CATAATTTAATTTAA	8924
rs550393769	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28226804	ATACAATCCAGAGAA[A/C]AGGAGAAAATACCCT	8924
rs550395129	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214868	AAACTACAGATTGTT[A/T]TTTTTTTATTTTTTA	8924
rs550404286	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28265414	CCACACAGGAACGGC[A/G]GCAGCTGCTAACCAG	8924
rs550426642	snp	G/T	1.65759e-05	0.00287883	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28220465	ACCAGAGTCATCCTC[G/T]GTGTCCGAATCCTCT	8924
rs550445531	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299649	AATCAATGATTTACT[A/G]AATTAGTGATTTAAT	8924
rs550452997	snp	A/G	0.00015659	0.00884706	intron-variant	HERC2	GRCh38.p7	15:28274462	CCTGGGCGCACACAC[A/G]CGTCAGAGGAGCCCC	8924
rs550460884	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28193046	CTCACAGAACAACCT[C/T]CTCTCCTCCATTCCT	8924
rs550460968	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28209656	CCTATATATCATTTA[C/T]ATTTTTAAAGTATTT	8924
rs550461065	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28215356	TTTTTAGTTTAATTC[G/T]TAAGACAATTACACT	8924
rs550463144	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28171958	CAGGTGCCTGTGGTC[C/T]CAGCAACTTGGGAGG	8924
rs550468589	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28254658	ACCCACAGGCCCCCA[C/T]CTGCCTTGTTGGAAA	8924
rs550477420	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28121985	CCATACAGCAGCCAC[A/G]GGCCAGGGAGCACCG	8924
rs550485067	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28293451	TGAGCTGAGATCACA[C/T]CACTGCACTCCAGCC	8924
rs550497661	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28249539	AACAACACAAGGAAG[A/C]AAGGGAGAGACAGTG	8924
rs550505181	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28242097	GTATGGTTCCATGTA[A/T]ATGAAGTACCTGGAG	8924
rs550505198	snp	C/T	0.0134861	0.0810011	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28315231	TCCCTCATCTCTCCT[C/T]GTAAAGTGGTGAACG	8924
rs550517664	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28197590	AACCCCATCTCTACT[A/G]AAAATACAAAAATTA	8924
rs550525910	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28270970	GGTATTGACTCATTT[A/G]ACCCATCAAATGACA	8924
rs550548914	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28255406	CAAACAGTACTACAC[C/T]TATAAAATGGAATAC	8924
rs550550781	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28263517	ATTGCAGATGCTTGC[A/G]GACCACCCTCCCGTT	8924
rs550558057	snp	A/G	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28238961	ATGCTTTAAAAAAAA[A/G]TCTAGGCAGCATGAA	8924
rs550587588	snp	C/T	1.69438e-05	0.00291061	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256092	CCCCAGGCCCACCTG[C/T]GCAGGGCAGGAGAGC	8924
rs550591596	snp	A/G	0.0111196	0.0737302	intron-variant	HERC2	GRCh38.p7	15:28206812	CACTCCAGCCTGGGC[A/G]ACAGACCAAGACTCG	8924
rs550596340	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28128315	GGCTGGCAGGACGAG[C/G]CTCCCTGTTTGTGGG	8924
rs550597016	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28232958	TCCTAAACTGTCTCA[C/T]TGTCTGATTACTTGG	8924
rs550611953	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28279538	AGAGCCAGGCGCAGT[A/G]TCTCATGCCTGTAAT	8924
rs550628987	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28291018	ATAAAACCAACAACT[G/T]GTTCTTTGAAAAAAC	8924
rs550631340	snp	C/T	0.159951	0.233219	intron-variant	HERC2	GRCh38.p7	15:28185204	TAACCTGATTTATTA[C/T]CAGAACTACTACCCC	8924
rs550694932	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28169891	AAAAAGATGTAGGTG[C/T]TTTTATAAAATGCAC	8924
rs550715653	snp	A/C/T	0.00283567	0.0375486	intron-variant	HERC2	GRCh38.p7	15:28175690	TGGAGAGTTACAATA[A/C/T]GGTTATGGTCTGACA	8924
rs550730427	snp	A/C	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28139813	TGCCTGTAATCCCAG[A/C]ACTTTGGGAGGCCAA	8924
rs550753490	snp	C/T	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28296090	ATGTCAAAATATCTC[C/T]CTAACACCCCGAATC	8924
rs550759406	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28170605	CTAGCACTAGGCAAA[A/G]ATATACTTAGACTTG	8924
rs550763456	in-del	-/T			intron-variant	HERC2	GRCh38.p7	15:28134709	TTTTTTCCTCTTTTT[-/T]TTTTTTTTTTTGAGA	8924
rs550768216	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28177681	AAAGCTTCCTGGGAC[A/G]TATGTGCCAAATAGG	8924
rs550773422	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28164159	TTCCCCAGGCAGAGT[A/C]TGGCTCCCCAGAGGA	8924
rs550778389	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28251777	CGCACTCCAGCCTGG[A/G]CAACAGAGCAAGACT	8924
rs550788264	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28220892	AGACCTCAGTTAGGA[A/G]GGTGCATGCCCTGCC	8924
rs550791365	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28134286	GTATATGTATACGTA[C/T]AGATGTACAAGTAAC	8924
rs550824564	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28284460	AAGACACCAGGAGAG[C/T]AGACTAGAGAACATG	8924
rs550830291	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28295079	GAGATCCCACTAGAC[G/T]TGTTAGAATGGCTCA	8924
rs550846254	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28136397	TGGATAAATGAGCCC[C/T]ACCCCCAAAGCCAGC	8924
rs550858689	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28129016	CTCCTTTTCTGATCA[A/G]AGGGTCTGTGTGATT	8924
rs550884996	snp	C/T	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28172162	TAAAGAGAAACACTA[C/T]GTTCATGGGTTAGAA	8924
rs550900361	in-del	-/CCA	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28220184	GCTGCCCCGGCCTGG[-/CCA]CCACATTCTCAAAGA	8924
rs550903570	in-del	-/AAA	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28177626	GAGCGTGAGCTGAAT[-/AAA]TGAGTAACTCAACAG	8924
rs550908816	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28252386	ACTCACCCCCTGCCA[A/G]AGACACCAATAGCCC	8924
rs550911388	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28175370	GCAAAAGGAACAGGA[A/C]CCGCCCTCATGGTTC	8924
rs550916412	snp	A/C	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28289940	GAGGATTACACACCT[A/C]AGTGAGAGGACCACA	8924
rs550925499	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28165304	GGGACAGCCAAGATC[A/G]GAGGTTGGTTATCTA	8924
rs550930639	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28244473	GGGCACTTTTCAGAG[A/G]AATGAGTCCGAGTTT	8924
rs550943953	in-del	-/AACCACAT	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28217347	GACACACACCCACAC[-/AACCACAT]GCTACCAACACACCA	8924
rs550951542	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28259836	AGCCAGGCATGGTAG[C/T]GCACACCTATAATCC	8924
rs550956536	snp	A/C	0.040671	0.13668	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28301265	TCTAAAAATACAAAA[A/C]TTAGCTGGGCATGGT	8924
rs550957355	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28250135	TTTCAGCTCCACTTT[A/G]ACTCAGGTTCCTAAT	8924
rs550960302	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28308384	CACAGAAATGCTACT[G/T]ATTTTTGTATGTTGA	8924
rs550965479	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28158075	TAATCCTGAGTTCTA[A/G]TTTGATGGCACTATG	8924
rs550981681	snp	A/G	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28203288	TCATAGCACTGACTT[A/G]CTATTTTGTTAAACG	8924
rs550985345	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28133388	ATGATTGTGAATATC[C/G]TTTCCCAGCTTGTGG	8924
rs551028652	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28125994	TTTTTGTATTTTTAG[C/G]AGAGACAGGGTTTCA	8924
rs551031669	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28213453	AATAAAAAGTAAACT[C/T]CATAAATTCACATTT	8924
rs551076125	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28253955	CAATAGAGCGAGATT[C/T]CGTCTTAAAAAATAA	8924
rs551079526	in-del	-/AAAAAAA	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28148038	CAAGACTGTGTCTCC[-/AAAAAAA]AAAAAAAGAAAAGTG	8924
rs551083741	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28173163	CAAAACAGTATGTAG[C/T]GATCTTAAGAAGCTA	8924
rs551091032	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28302142	CCATCCGCACTTCAC[C/G]CCCACTTTATCCTTC	8924
rs551103991	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28271812	AGGTTTAGGCCCAGG[A/G]CCCCGCACGCCTGCT	8924
rs551109252	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214365	TAAGTGACGGCACTG[C/T]GCCGCTCTTCACCAG	8924
rs551124716	snp	A/G	8.24029e-05	0.00641831	missense	HERC2	GRCh38.p7	15:28130171	TACCTACCATCCTCT[A/G]TGCAGCACACACAGT	8924
rs551126207	snp	A/G	1.6516e-05	0.00287362	intron-variant	HERC2	GRCh38.p7	15:28202328	ACATACACAAGCAGA[A/G]GCCAGGAAAACGAAG	8924
rs551152198	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28127401	CAAATCGCCAGAAAA[C/G]AAAGGATCTGCAAGG	8924
rs551157691	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28160732	CTCGGTGCACTGCAC[C/T]CACTGTCCTGCACCC	8924
rs551161141	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28157574	TAGTTTGTACTTCTA[A/T]GGAATCAGTGGTGAT	8924
rs551170313	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28161514	GCCCACGGCCTTTAC[A/G]ACTGATCAGTCCTAT	8924
rs551176253	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28292136	CGGGAGGATGAGGCA[A/G]GAGAATCACTTGAAC	8924
rs551212809	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28287331	GAATATGCTTTGAAT[A/C]CAAGCCCCTTCAAGG	8924
rs551217952	snp	A/C	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28139387	AGACGCTCTATGGAC[A/C]CGTGGCAAAGGGCTG	8924
rs551234554	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28306228	TATGGCTTTTATTGC[A/G]TTGAGGTGTGTTCCT	8924
rs551241448	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28240745	AAAACAATCCATCAC[A/G]TATTTGGTCATACGA	8924
rs551241456	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28124741	ATTTTGTAGAGACAG[G/T]GTTTTGCTATGTTGT	8924
rs551245292	snp	A/G			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317462	TCATTCTTAATTGAT[A/G]ATTAGAGGAAGAGAC	8924
rs551271260	snp	C/G			intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28300949	TTTTTGAATATATTT[C/G]CTTACTCTGTTTTTT	8924
rs551301503	snp	A/G	1.72347e-05	0.00293548	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274375	CTCTCGTCAAAGAGC[A/G]AGGCCTCGGGAAGTG	8924
rs551307585	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28137328	TAAATATGTGTGCTC[C/T]TGTATACAGGCACAC	8924
rs551313189	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28179709	GGAAAGGACAGCTAG[C/T]TCCTTTGTGGGGGTG	8924
rs551327935	in-del	-/AAAAAAAAAAAA	0.118584	0.212673	intron-variant	HERC2	GRCh38.p7	15:28284920	GAAACTCCGTCTCGG[-/AAAAAAAAAAAA]AAAAAAAAAAAAAAA	8924
rs551393196	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28288323	CTGAGGTCAGGAGTT[C/T]GAAACCAGCCTGACC	8924
rs551400526	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28317871	GTGACCTCTCTAGTT[C/T]CTTTACAACTTCCTG	8924
rs551402174	snp	C/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28298566	TTTGGGAGGCTGAGG[C/T]GGGCGGATCACGAGG	8924
rs551441683	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28246594	CAACAGAACTGTCAG[C/T]AACTAAAAAAAAAAA	8924
rs551452372	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28130936	AACTCCAGCAATCCC[C/T]GTGTCTCTCCTCACC	8924
rs551454712	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28116406	ATTTTTACTAGAGAC[A/G]AGGTTTCACCACATT	8924
rs551480720	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28292719	AACTCTACACATAAA[A/G]ATGGTTAAAACGGTA	8924
rs551490745	snp	A/C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28159792	AGCTGCGTTCCTTTG[A/C/G]AGGAGGAGAGATGCT	8924
rs551505149	in-del	-/A	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28199977	TGTGTCCCCCCCACC[-/A]AAAATTCATGAAGTC	8924
rs551507679	snp	A/G	6.60055e-05	0.00574442	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28248693	ATGATGAAATCCGAC[A/G]GGCAACATCTTTCAA	8924
rs551513939	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28211850	AGCAAGAGGGGAGAA[A/G]ACTCAAGAAGAGTGG	8924
rs551526850	snp	A/C	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28235127	TCCAAGCAATCAAAG[A/C]GGGATGCACTTAGTG	8924
rs551545871	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28148790	AACCGAGAGCATCAC[C/T]GAGAACGGCCACACG	8924
rs551547913	in-del	-/A	0.0452528	0.143452	intron-variant	HERC2	GRCh38.p7	15:28126136	TAATAAAATAAGAAT[-/A]AAAAAAAAATAGATG	8924
rs551555052	snp	C/T	0.000314812	0.0125422	intron-variant	HERC2	GRCh38.p7	15:28117467	TCCACAGCTGCGGCC[C/T]GGCAGCACCACCCTG	8924
rs551555233	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28153337	CAGCCTGGGTGACCC[A/G]AGCGAGACTGCGTCT	8924
rs551555649	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28210541	CTATGCATGTCAAAG[A/T]CCAACTCATTTCCTC	8924
rs551576742	snp	C/T	0.0232847	0.105357	intron-variant	HERC2	GRCh38.p7	15:28206665	GGTGAAACCCCATCT[C/T]TACTAAAAATACAAA	8924
rs551612252	snp	G/T	0.00199481	0.0315187	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111422	GAAAGAAAAAAAATC[G/T]ATTGCACCCACAAGT	8924
rs551623963	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28155358	TGTGTTCCGCAGTGG[C/T]TGAACTAGTTTACAC	8924
rs551635078	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28136696	GCTTTACGGGAACAC[A/G]GCCACACCCACTCAT	8924
rs551636174	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28200308	GCTGAGGCAGGAGAA[C/T]GGCATGAACCCGGGA	8924
rs551649282	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28228498	GATTACTCTAAACAT[C/G]TGACTATTTTGAAAC	8924
rs551677459	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28143698	TGATCCGCCCACCTC[A/G]GCCTCCCAAAGTGGT	8924
rs551683059	snp	A/C	0	0	intron-variant	HERC2	GRCh38.p7	15:28236045	TGTTCCCTGAGAGGA[A/C]AGCTGATCCACATTC	8924
rs551698530	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28194390	CCTGGCTAACACGGT[A/G]AAACCCCATCTCTAC	8924
rs551726229	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28310816	CGCACGGTGGCTGAC[A/G]CCTGTAATCCCAGCA	8924
rs551730725	snp	A/G	4.97022e-05	0.00498484	synonymous-codon	HERC2	GRCh38.p7	15:28113149	GACGAAGCGAAGGAA[A/G]AGAGAGCGCTCTGTG	8924
rs551746603	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28222301	TTCACAAAGTACTAA[C/T]GAAGATCGTAATTTT	8924
rs551761101	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28266636	CATGGCTGGATCTCA[A/T]GACATCTGCTAAGTC	8924
rs551780484	snp	A/C	0.00279162	0.0372561	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318591	TGGCACCACTGCACT[A/C]CAGCCTGGGAGACAG	8924
rs551795279	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28247071	ATCATGTGACTGGAG[A/G]GACAGGGTTTTTATG	8924
rs551798719	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28122362	ATCGTGCCTTCTTTC[A/G]GTTAGGGGTGGGCTG	8924
rs551807964	snp	A/T	0.0310518	0.120672	intron-variant	HERC2	GRCh38.p7	15:28216313	CTGCACCACTTAAAT[A/T]TTTTTTTTTTTTGTA	8924
rs551810009	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28136989	AGCAAAGATGTGCAA[C/T]ATTTAGCTAACTCAA	8924
rs551812078	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28308189	CCAATCCATGAAGAT[G/T]AAATATTTTTCCATC	8924
rs551812515	snp	A/G	0.00716266	0.059414	intron-variant	HERC2	GRCh38.p7	15:28286042	TAATTCAAAGAATCC[A/G]AAAAAAAAGAAATTA	8924
rs551818335	snp	A/G	5.05131e-05	0.00502534	intron-variant	HERC2	GRCh38.p7	15:28178853	GCAGGAGCAAAGGCC[A/G]CCCCGCACAGGCCTC	8924
rs551833761	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28240222	AGGAGATGGAGACCA[C/T]CCTGGCTAACACGGT	8924
rs551835651	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28230772	AGAGAGTGAACATTT[A/G]AGTCTTTCAGGCCAT	8924
rs551838026	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28205029	AAGGAGGACGGTGGG[A/G]TGGGCGGGGTGTGCC	8924
rs551845467	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28114211	GCCTGAATCACGGCA[C/T]CCAAAGGACCGTGCA	8924
rs551868334	snp	C/T	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28319121	ATGTCTTATTCCTTA[C/T]GGTAAAACACCACCA	8924
rs551897899	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28198921	GGGAGGCTGAGGTGG[A/G]AGGATCACTTGAGCT	8924
rs551920836	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28231485	CATGGGCACTGCCTG[C/T]GTATGTGACTGGCCC	8924
rs551926118	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28243728	GGGAGTGCTAGCAAT[G/T]CTAGGTCTTGGCATG	8924
rs551942014	snp	A/T	0.000399281	0.0141238	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28280089	TTGTCCACAGGAGGC[A/T]GAGAAATACCGCTGC	8924
rs551962449	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28192960	ACAGATTGCAACTCA[A/G]CATAAAATCATCTCA	8924
rs551973035	snp	C/T	0.00020591	0.0101446	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202154	CCTCCACCACCTCCT[C/T]GTCAGAATACTCGTC	8924
rs551991866	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317331	TGACCTCAAGTGATC[C/T]GCCCTCCTCGGCCTC	8924
rs552000133	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28149055	TCTAGTAAAATTACC[A/G]AAAAAACAAACGAGA	8924
rs552014319	snp	A/C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28273596	GGGCCTCCAGCGTTA[A/C/G]AACTCTGTGGTGATG	8924
rs552014887	snp	G/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28139834	GGGAGGCCAAGGTGG[G/T]CGGATCACAAGGTCA	8924
rs552023626	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28187092	GCTTTAACTAAGGAA[A/G]ATATTAAATGTCAGG	8924
rs552039926	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28276627	ATAGTCCCAGCTATA[C/T]GGGAGGCTGAGGCAG	8924
rs552053011	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28267190	AGTTTGCAAAATACA[C/T]ACAGTGGCACAGGTG	8924
rs552076047	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28140395	GGAACAGCATTCATT[C/T]AGAGACTACGGCACT	8924
rs552078772	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28306135	TGACAGTGGGCATCC[A/G]TGTCTTGTTCCAGAT	8924
rs552110705	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28243185	CAAAGGTGCTGGCAC[A/C]AAGACACTATGGACA	8924
rs552119280	snp	A/G	0.0138799	0.0821421	intron-variant	HERC2	GRCh38.p7	15:28201859	CTTCTAATGGCTACC[A/G]AAGATCATGAGATGT	8924
rs552136317	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28146089	AGGCAAGCAAACCCA[C/G]TGTGTTTCACAGCTG	8924
rs552146034	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28187550	GTTGGCTAGGCTGGT[A/C]TTGAACTTCTGACCT	8924
rs552165251	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28308955	GTTTGCTAGTATTTT[A/G]TTGAGGATATTTGCA	8924
rs552173600	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28181083	TCTCTGATTCTGACT[A/C]TGACATCTCTAAGAA	8924
rs552182472	in-del	-/AA			intron-variant	HERC2	GRCh38.p7	15:28245560	TCAAAAAAAAAAAAA[-/AA]TATATACACACACAC	8924
rs552182743	snp	C/T	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28162872	CTCTAGCCTGGGCGA[C/T]AGAGCGAGACTCCGT	8924
rs552197798	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28264615	GTGTGAGGAAGACAA[C/T]GTCTGCAGCCCTACT	8924
rs552228863	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28307423	TATGGGTTTGGTTAG[C/T]TCCTTCTTTTCTAGT	8924
rs552242516	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HERC2, LOC107987422	GRCh38.p7	15:28312435	GCCAAGAGTTCAAGA[G/T]CAGCCTGGGCAACAT	8924
rs552248726	snp	A/C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28194747	AGTTCTGTTAGATAT[A/C/G]TATTTATATAAAATG	8924
rs552254421	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28283551	CAAAAGAAAGGCTAA[C/T]GGAAGTTCTCTAAGC	8924
rs552254686	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28275588	CACAGTTTCATTCTG[A/C]ATGTTCTAAAAGGTT	8924
rs552270713	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28126405	CCAGAAGAAAAGACG[C/T]CATTATTTGAAAAAA	8924
rs552273130	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28157264	CTGGCCTCATAAAAT[A/G]AGTTAGGGAGGATTC	8924
rs552275900	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28294805	GGGCTGTGAGCATGC[A/G]TGACTAATAAACTGC	8924
rs552286135	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28182173	TTTATGCACTTGTCA[A/G]ATCTTTTCAAAAGTT	8924
rs552299735	snp	C/T	0.140581	0.224783	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314511	CTAAAAAAAGAAAAA[C/T]ATATATTTAAAAAGT	8924
rs552324498	snp	C/T	6.61255e-05	0.00574964	missense, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28299423	TAGGAGGGAGCTCTC[C/T]GTTCTGGGTTGATTC	8924
rs552334215	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28145550	ATTTCATGCAAAGCT[C/T]TACTTAACTAAGTAA	8924
rs552334721	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28223260	TAACCCCCCTTTTCC[C/T]ACTTGCTAAACTGAG	8924
rs552341750	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28276121	AACCTGGGAGACAAA[G/T]GTTGCAGTGAGCCAA	8924
rs552350646	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28204140	CCCAGAGCCAATACA[A/G]TGTAACGTCCAAAGA	8924
rs552382871	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28159914	GATGGGGTTTTGGTG[G/T]AGATGTCCTTTCTGT	8924
rs552386257	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28212285	AAATACTCATTACCA[C/T]GAACACAGGGTTACA	8924
rs552389332	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28308430	TTGTATTGAATTTAT[C/T]GGCTCTAATCATTTT	8924
rs552405830	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28219423	GAGGGAGGAAGCAGC[A/G]ACTGGTGTCAGGCAG	8924
rs552417727	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28203662	TAACCACAGACGGCG[C/T]ACCTTCCTGCACTGC	8924
rs552418087	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28266379	AATTAGGTGGGCATA[C/G]TGGAGGGTGTCTGTA	8924
rs552419648	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28263711	AAGCTGAAAACTTTG[C/T]AAAAACTTAAAGTGA	8924
rs552446016	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28207501	ACACATCCCACGTGC[A/C]TATTTCTAGCTGTAG	8924
rs552447940	snp	A/G	0.0433465	0.140692	intron-variant, utr-variant-5-prime	HERC2	GRCh38.p7	15:28212809	ACAAACCTGTCAACA[A/G]TAATTACATCAGTGT	8924
rs552453452	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28252333	GGAAAACGGGCACTG[C/T]CCTCGTGAGAACAAA	8924
rs552458167	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28150174	ATTCTAGTGAAATCA[C/T]GAAAAAAACGCACGC	8924
rs552464918	snp	A/G	4.97022e-05	0.00498484	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214160	GAGCCCATTCCACTG[A/G]GTCAGGGAGTGCAGC	8924
rs552473618	snp	A/C	1.6483e-05	0.00287076	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28270728	GCTACACAGCGGAGG[A/C]ATACAGGGCGTAGCC	8924
rs552479127	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28175816	ATCATACACCATTAA[C/T]TCAAATTAACTTATT	8924
rs552494745	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28262417	ATACCTTGGCTTCCA[A/T]CTCTTGCCTCCAACT	8924
rs552495800	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318219	TTACAAGTACTTTCA[C/T]TGTAAAAATAAAAAG	8924
rs552502782	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28175073	CCATAAATAAAATTT[A/T]AAATTGAATATCCAT	8924
rs552525644	snp	A/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28303213	GGTCTAGTTTCATTT[A/T]TCTGCATATGGGTGT	8924
rs552530209	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28149700	GAACATCACTTAGAA[C/T]GGCCACATGAACGCA	8924
rs552531283	snp	A/G	0.000123613	0.00786073	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28218614	GTCTGCAGTAAGTTA[A/G]TAGTGCTGGTAAACA	8924
rs552533042	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28184785	GAGAATGGCGTGAAC[C/T]CAGGAAGCGGAGCTT	8924
rs552558669	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28303940	GGAGGCCAAGGCAGG[C/T]GGATCACCTGAGGTC	8924
rs552562272	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28169272	TAGTGAAAATGTTCA[A/G]GTTAGTTTTCTAATT	8924
rs552573275	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28229120	TCTCAAAAGCAAAAA[C/T]TGGCATTTGCAAGTT	8924
rs552581885	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313411	GTCTCGACCTCCTGA[A/C]CTTGTGATCCACCCG	8924
rs552598107	snp	C/G	0.00716266	0.059414	intron-variant	HERC2	GRCh38.p7	15:28194847	GATCACCTGAGGTCA[C/G]GAGTTCAAGAGCAGC	8924
rs552601055	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28195043	CCTGGGCAACAGAGT[A/G]AGACTCCGTCTCAAA	8924
rs552609550	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28246598	GAACTGTCAGTAACT[-/A]AAAAAAAAAAAACAA	8924
rs552632180	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28223986	CTCGATGGAGATATG[C/T]TTTTGTAATTTTTAA	8924
rs552646895	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28296139	AAACAATTATGCTCT[A/G]CTTTCCAATCATGAT	8924
rs552674130	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28220164	TGAGACTCACTGGTG[A/G]TGCAGCTGCCCCGGC	8924
rs552708775	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28171071	CGGCTTGGCAGTTTC[C/T]TATCAAACTAAACAT	8924
rs552712238	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28115669	GAAGCAGCAACACCC[A/G]CATCATAGGTCTAGG	8924
rs552727547	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28138690	AAGTTGTTTTCATGC[C/T]GGCTAACACATCATT	8924
rs552730343	snp	A/G	0.000329522	0.0128317	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28174515	ACCCACAAGCCACGC[A/G]TGTGATCTTCTGGCC	8924
rs552731655	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28253370	GTAAAGTGAGGCAAT[A/G]ATAGAACCAGTTTTA	8924
rs552737206	snp	C/G	0.000232219	0.0107729	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214627	GCCGCTCTTCACCAG[C/G]GCACAGGGAAGGTAG	8924
rs552743016	snp	C/T	6.67167e-05	0.00577528	missense	HERC2	GRCh38.p7	15:28168550	GGCACTCCACCGGGG[C/T]GATCATGGCGGCCGG	8924
rs552745443	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28252198	TGCTGATCAGCAAAC[A/G]GTGTTGAGTGTAGCC	8924
rs552773453	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28132580	TTCATAACAACGGTG[C/G]CAAACCGCCCCCATC	8924
rs552783288	snp	A/T	0.0023933	0.0345097	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321219	AAAGACTGTTACATT[A/T]TAAGTTACAGGAAAT	8924
rs552801309	snp	G/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28254710	TCAAACAGTGTCTTC[G/T]TTTTACAGAATCAAG	8924
rs552828795	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28293945	CCTTGAAGTGTAAAC[A/G]CGTTCCATCACAGAA	8924
rs552839928	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28249377	AGTAGAAGAGGCTCC[A/G]GTTCCAACACTGTGA	8924
rs552871735	snp	C/G	0.00159617	0.0282053	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321792	ACACATAACAGGGAG[C/G]CCATCGTTTTAACGA	8924
rs552884249	snp	C/T	0.00159617	0.0282053	downstream-variant-500B	HERC2	GRCh38.p7	15:28110740	CACAAGCAGCCCAAA[C/T]CGTGTACCATGGCTG	8924
rs552912947	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28285453	AATAATCCATGGATC[A/G]AAGAGGAAGTCTCAA	8924
rs552941509	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28163083	ACGGCCCCGCCCTCC[C/T]TGAGACTCACCTGTG	8924
rs552947677	snp	A/G	0.0471551	0.14613	intron-variant	HERC2	GRCh38.p7	15:28250679	AAGGGAAAAAAGGAC[A/G]TGAAATGTCTCCAAA	8924
rs552955567	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28156882	AGTATGATATTGGCT[A/G]TGGGTTTGTCATAAA	8924
rs552966248	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28122512	ATCCTGGCGGCACCC[A/C]AGCCCCATGCCTCTC	8924
rs553012467	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28268021	TTTCATTTGTTCTTT[C/T]ACAATAAAAGGTTCC	8924
rs553015448	snp	C/T	0.000252198	0.0112266	intron-variant	HERC2	GRCh38.p7	15:28233396	TATTTCAGCAACTGT[C/T]TGCAAAGCACAGAAT	8924
rs553018804	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28157629	ATCCACTTGATTCTT[C/T]TCTCTTTTCTTATTA	8924
rs553028928	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28290210	CTCTCCTAACAGTGA[A/C]TAGAACAAGTAGGCA	8924
rs553032932	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28128520	AATGTCCTTCCACTA[A/C]AGGCCACAGAAGTTG	8924
rs553076280	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28187613	ACTGGGATTACAGGA[A/G]TGAGCCACCGCGCCT	8924
rs553080333	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28276537	GTCAGGAGTTTGAGA[C/T]CAGCTTGGCCAACAT	8924
rs553094249	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28122012	ACCGCGGAGCCAGCC[A/G]GACCTTGGATCGCCA	8924
rs553100350	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28303198	ATGGTGAGAGATAGC[A/G]GTCTAGTTTCATTTT	8924
rs553109970	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28251992	ACAGTGATATTTGCA[C/T]TGAAAATATCTGATC	8924
rs553111394	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28243925	CAGGAGCGCTGGCTC[A/G]TGCCTCTTATGTCAG	8924
rs553115880	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28245355	AGTTCGAGACCATCC[C/T]GGACAACATGGTGAA	8924
rs553125679	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28244129	TGATTGCACCATTGC[A/C]TTCCAGCCTGGATGA	8924
rs553131786	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28120022	TGCGTGCGGTTTTGA[A/G]GGAGGTGCAAGTCAA	8924
rs553134131	in-del	-/A	0.0166325	0.0896639	intron-variant	HERC2	GRCh38.p7	15:28201692	TAAAAATCTTCATTT[-/A]AAAAAAGACTAATAG	8924
rs553164838	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28210175	GTCTTGCTCTGTCGT[C/T]CAGGCTGGAGTGCAG	8924
rs553201610	snp	C/T	2.97137e-05	0.00385434	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28196329	ATCTGGATCCATTGA[C/T]AGGAAACATCTGACA	8924
rs553205819	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28159446	CATTTCTTTTTATTC[C/T]TTTTTCTCTAAACTT	8924
rs553209055	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28271027	ATCTATATATTTATG[A/C]AGCATATAAACTGAC	8924
rs553211421	snp	A/G/T	9.97878e-05	0.00706293	missense, synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28238159	CATGGATTCCCGGGT[A/G/T]TCTTCAAACTGCAAA	8924
rs553224913	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28286105	TCAAACATTAAAAAA[C/G]AATTAACACGGACTC	8924
rs553243132	snp	A/G	0.000399281	0.0141238	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28198477	CACCAATCTTGATGT[A/G]AGAAGAAGAACTTGG	8924
rs553262891	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28190566	ACAAGTTCAGCACTT[G/T]ATGCCAACAGGTGTG	8924
rs553267254	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28152923	CTGCTCAGGAGCTCC[A/T]CAAGGACAGCGTGGC	8924
rs553271037	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28151237	CTTGGAACCAGGATT[C/T]GATATGGAAGAAAGG	8924
rs553300952	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28176126	ATTCAGAAGGCTATT[C/T]TGCTCCATTTTATCC	8924
rs553325256	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28243449	GTGACTACACAGGCC[C/T]GAGTGAGAGAAAAAG	8924
rs553337258	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28283110	AGTCACTGAACTCAC[A/G]AAGGGACAGGAGAAA	8924
rs553341974	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28160400	TTTCAGCTTCCGGGC[C/T]GCTTTGTTTACCTAC	8924
rs553347157	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28271923	ACAGAGCCCAGTACA[C/T]AGGAAGGACCAACAA	8924
rs553352163	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28160819	TCACCCATCTTCTGC[A/G]TTGCTCACACTGGGA	8924
rs553354112	snp	A/C	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28154009	GGGTCAGACCCATAC[A/C]ACATTCTCAACAATC	8924
rs553364042	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28237412	GTTTCCAAAGTGACT[A/G]TACACCATGCTTCAG	8924
rs553388879	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28240783	CATGGGAGCCAAGAC[C/T]ACTCAATGGGGAAAG	8924
rs553429331	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28195686	GGTAAGGGGAAGTAG[A/G]GCAGTTAAATTGCTT	8924
rs553438326	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28202001	TTTATGGAACAGTCC[A/G]CAGTAGATATAGTTA	8924
rs553438339	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28208817	GCCACTGGCTCCAGA[C/T]GCCTGTGGAACCACT	8924
rs553441699	snp	C/G	0.00874735	0.0655527	intron-variant	HERC2	GRCh38.p7	15:28183501	TACAGGTGGGAGCCA[C/G]CACACCCAGCAGGTT	8924
rs553463807	snp	C/T	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28247812	TATCAGCTCACCTAC[C/T]GAAACCTGAAAGTTT	8924
rs553476225	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28137002	ACATTTAGCTAACTC[-/A]AAAAAAAAAAACCAC	8924
rs553486104	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28240393	ACTACACTCCCGCCT[A/G]GGCGAAAGAGCGAGA	8924
rs553495370	snp	A/C	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28273978	CACTCAGAACAGCAG[A/C]TCCTAATCATCACAG	8924
rs553499822	snp	C/T	0.000399281	0.0141238	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202429	GGAAAATCCCATCTC[C/T]ATGAGCTGCACCACG	8924
rs553500786	in-del	-/A	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28251447	GCTCCATCTCGGGGG[-/A]AAAAAAATTGTCCTT	8924
rs553508647	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28280566	GCACATGACAGAGAC[G/T]CTTGAGCCACCATGG	8924
rs553524906	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28235386	TCCTTGCCAATTTAA[A/G]CAAAGCCCATCTTCT	8924
rs553526491	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, downstream-variant-500B	HERC2, LOC107987422	GRCh38.p7	15:28319564	CACGCCAGCCTGGGC[A/G]ACAGAGCAAGACTGC	8924
rs553532033	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28267697	TGGGATCTTCCCAGC[A/G]GATGCTGTCGGCAAT	8924
rs553559612	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28150531	AACAGCCACATGAAC[G/T]TATACTCTAGTGAAA	8924
rs553565303	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28320218	CTCCCGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG	8924
rs553574020	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28193269	GCTTACTGTGTTCAA[A/G]AAGATAATATTTCAG	8924
rs553580683	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28308696	TGGGTCTGTCATATA[C/T]GGCTTTTATTATGTT	8924
rs553586140	snp	A/G	0.00015685	0.00885441	intron-variant	HERC2	GRCh38.p7	15:28117536	TCACCATCTTGCCAC[A/G]ACCTCATGAAATAAG	8924
rs553608194	in-del	-/A	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28289238	CATACACAAAGGTTG[-/A]AAAGTGAAAAAAGCT	8924
rs553609324	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28292615	GAAGCCAGGAGTATA[A/G]GACCAGCCTGGGCAA	8924
rs553618039	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28268326	CAAGGAGGAGGCATA[G/T]CGTAGTGTCCTGCTC	8924
rs553647890	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28232349	AGATCAAGACCATCT[A/T]GGCCAACATGGTGAA	8924
rs553654442	in-del	-/A	0.211819	0.247067	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28301635	GCTCCCTTGTCTGGC[-/A]AAAAAAAAAAAAGCC	8924
rs553671806	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28277313	ATGTAAAACTGGGAA[A/G]ATCTGAATAAGATAG	8924
rs553688041	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28181240	CACAACCGTGGAACA[C/T]CGACTCTGTCCTTGA	8924
rs553688345	snp	G/T	1.82887e-05	0.00302391	intron-variant	HERC2	GRCh38.p7	15:28117200	CCGCTGCCGCAGCAG[G/T]AAGCACACAGTCGGG	8924
rs553702302	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111560	GACCCTTGGAAGTCG[A/G]GCGTCCACAGTGTTC	8924
rs553710390	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28227219	GGCGGAGGTTGCAGT[A/G]AGCTGAGATCGTGCC	8924
rs553710543	snp	G/T	0.00119737	0.0244387	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316487	TCTACAAAAAAAAAT[G/T]TTTTTGCTGCAAAAT	8924
rs553717472	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28134904	TCTTGAACTCCTGAG[C/T]TCAAGCAATCTGCCC	8924
rs553717664	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28140878	AACAAGAAATACATC[A/T]AACGAGTGATGTGCA	8924
rs553717825	snp	C/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28148667	CGAACGCACATTCTA[C/G]TAACACTACCGAAGA	8924
rs553721961	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28183385	CAGCTAATTTTTGCA[C/T]TTTTTTTTGTAGAGA	8924
rs553730464	snp	C/T	8.34383e-05	0.0064585	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28229280	CTTGCCAAAGGTGAC[C/T]TCCAGCAGCATCCGA	8924
rs553748765	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28217165	CCTCACTGACTTACA[C/T]TGACTTACACTTACA	8924
rs553758973	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28188399	CAAAAACAAAATTAG[C/T]CAGGCATGGTGGCAG	8924
rs553786639	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28280977	TTATCAGCAGCACAT[C/T]TCCTAAACAGAGAAA	8924
rs553796287	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28227687	GCATTCAAACAAGTA[C/T]TTGTATATAAATGTT	8924
rs553816444	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28221837	CTTTCCAGACTTGAT[G/T]CTGCTCAGATGCCCT	8924
rs553832091	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28206563	TCTAGGTTGGGTGCG[A/G]TGGCTCACGCGTGTA	8924
rs553841627	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28148593	AACGGCCGCATGAAC[A/G]TACATTCTGGTGAAA	8924
rs553861151	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28148339	ACAAATAGGAAAAAA[A/G]GAGGAAATTTTAAAA	8924
rs553894726	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28199921	CTACAAATAAACAGC[A/G]TGAAAGGAGAGGACG	8924
rs553896154	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28187867	ATGTCCCACACCCCA[C/T]GTGGCCGACTGCATG	8924
rs553925881	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317504	CCCAGTTTAGCTACT[A/G]ATATACTCAACAAAC	8924
rs553926884	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28310404	GAGTTGAGATCACTC[C/T]ACTGTACTCCAGCCT	8924
rs553929826	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28252631	AACAAGCTGTTGCAA[C/T]TGAAATTTTATGAGA	8924
rs553932487	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28188539	ACAGAGTGAGACTCC[A/G]TCTTAAAAAAAAAAA	8924
rs553933586	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28266192	CAAACATGGTACCCA[A/G]TAGAAATATAAAAAT	8924
rs553962242	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28304859	ATGCTACCCCTCCCC[C/G]CTCCCCCCACCCCAC	8924
rs553968767	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28311717	AATGGACTGTAGGTG[A/G]TGTCCTGGAGAAGAT	8924
rs553970766	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28228734	GTCATGCTGCACGAT[C/G]GGCCTACCCCCTGCA	8924
rs553973941	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28137000	GCAACATTTAGCTAA[C/T]TCAAAAAAAAAAACC	8924
rs554004866	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28113863	TCTCCTGACACTGGG[A/C]TCATCTCGTCCAGCC	8924
rs554014660	in-del	-/CT	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28236298	CTGTGTTGAATCCGC[-/CT]CTCCTTTTGAGACGG	8924
rs554016897	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28307117	TGGGATTACAGGCAT[A/G]AGCCACCACGCCCGG	8924
rs554032899	snp	C/T	1.64978e-05	0.00287205	intron-variant	HERC2	GRCh38.p7	15:28130330	GAAGCATGGAAATTA[C/T]GGGGCAAGGTGATCT	8924
rs554046405	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28223335	TCTCCTCCAGGTGGG[A/C]GGGAAAAAGACCCAA	8924
rs554055109	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28247616	TGTATTTTTAGTAGA[C/G]ACGGGGTTTCACTAT	8924
rs554062423	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28137552	GATGATCTGTGATCA[C/G]TAATGTTTGATGTTA	8924
rs554074498	snp	C/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28223477	TAGATAAACTAGCAG[C/G]GGAAACAGCCTTTCC	8924
rs554085463	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28166075	TATGCCAGAAGAACA[C/T]ATAAAATTCTACCAA	8924
rs554106275	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28224409	GTATTTTTTGTAGAG[A/G]CAGGGTTTCTCTATG	8924
rs554125713	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28131354	CTCCAGAAGCACCTG[C/T]GCCACACCTGCAACC	8924
rs554125803	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28138177	CATAACATAAAAGTG[C/T]AAGGGAAAGTAGCAA	8924
rs554130143	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28219876	ACGAAACCTCCTCCC[A/G]CAACCTGGATCTCCA	8924
rs554154818	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28122666	TTGGTGCTCTGGACC[A/G]GGAGTAGTAACACCC	8924
rs554168885	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28251573	TGGGAGGCCAAGGCG[C/G]GCAGATTACTTGAGG	8924
rs554172676	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28120050	CAAGGTGCACTCAAT[A/C]GCGGGGGTTAGACAA	8924
rs554192310	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28225052	GATCTCAAATCAATA[A/G]CTTAACTCTACATCT	8924
rs554202092	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28287005	ATAAAGCACGTGGGA[C/T]AATGCCAGCGGCACA	8924
rs554223629	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28310885	GATAAAGACCATCCC[A/G]GCTAACACAGCGAAA	8924
rs554230390	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28230859	AAAGCAACAGGTGTG[A/G]CTGTGCTCCTGTAAA	8924
rs554261774	snp	C/T	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28133835	CCCTATTCTGCTCCA[C/T]TGATGTATCTGTCTC	8924
rs554272152	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28210282	AGAACTACAGGCGTC[C/T]GCCACCGTGCCCAGC	8924
rs554293555	snp	C/T	4.9507e-05	0.00497504	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28186680	TCCGTCCCAGCAGGA[C/T]GAGACCATGGATTTT	8924
rs554327530	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28259239	AGCTGGGATTACAGG[A/C]GCACATCACCAAGCT	8924
rs554345232	snp	C/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28183173	TCCACCTTGCTCATC[C/T]ATCTCCTGACCTGCC	8924
rs554372262	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28134547	TTGATCCTCAACTCA[A/G]GGGGAAAGCTTTTGG	8924
rs554377006	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28297129	GTCTGAAAGTTTCCA[A/G]GAATTACTAAGTAGG	8924
rs554386725	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28216351	TAGAGACAGTTTCCA[A/T]TCCAAGTTTAATACA	8924
rs554417588	in-del	-/C			intron-variant	HERC2	GRCh38.p7	15:28140455	ATACTAGAATGGAGA[-/C]CAGTCAAGTAGGTCA	8924
rs554438807	snp	C/T	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28301544	GTGAGTCAGAAAAGG[C/T]TTCCCAGAACAGGAA	8924
rs554457672	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28256333	CTGAAAGGAGAAAAA[C/T]AATTTTCACTTAGAA	8924
rs554470787	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28123601	GCACGGACCTTCGAG[A/G]TGATATATCTGTGAC	8924
rs554472999	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28199987	CCCACCAAAATTCAT[G/T]AAGTCCCAACTCCTA	8924
rs554474648	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28166789	GTGACCAGTCCACGG[C/G]AGTCCCAGTGACCGA	8924
rs554493744	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28153901	GGAATCAGGAACCAT[C/T]AAGCCGCTCAGGCCA	8924
rs554505073	snp	C/T	0.00517822	0.0506191	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174232	TTTCATTCCAGCATG[C/T]ATAAATCGCATGAGA	8924
rs554508398	snp	A/C/T	0.00030507	0.0123474	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214232	GTGGGTGGCAGTCAG[A/C/T]GAGGCCTGCGGGCGC	8924
rs554515996	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28138398	GGCTAATGCAGCTGA[A/T]GACTATATTAGTTGA	8924
rs554518507	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28208854	CCTCACCGCCTCCTG[A/G]CCCCAGAGGACAAAG	8924
rs554555919	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28293098	CTGCAAATGTCCCTC[A/C]CCGAAAAGTTACAAC	8924
rs554580166	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28226542	TGGTATTGAAACAAT[C/G]AGATCATCAAAAAAA	8924
rs554590054	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28120509	ATCATCAGGGGCCGA[C/G]GCTTCTCTTTGTTTT	8924
rs554595502	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28308158	TAGTATGGACATTTT[A/G]ACAATATTGATTCTT	8924
rs554604561	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28163783	AGTCTCTCTCTCTCC[G/T]TGGGTTCATTGAAAA	8924
rs554632231	snp	G/T	0.0107246	0.0724382	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28300555	AGGCCGGCCACGGTG[G/T]CTCACACCCGTAATC	8924
rs554637748	snp	A/G	0.0456336	0.143994	intron-variant	HERC2	GRCh38.p7	15:28293634	TTCAATTTCACACCA[A/G]TTGCTTTTATCCAGT	8924
rs554642018	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28288227	CTTAAGGGCCCATAA[A/T]GGTAAAATGTAAGTT	8924
rs554652401	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28114044	AGACACGATACGGGG[A/G]ACAGCACCGCCCAGG	8924
rs554654767	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28255717	CATATCTCAATAATT[G/T]TGTAAATTGGCACAT	8924
rs554662329	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28200551	GTCTATGGTACTGTG[C/T]TATAGCCAACTGAGC	8924
rs554674802	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28288800	TTGCAGTGAGCTGAG[A/C]TTGTGCCATTACACT	8924
rs554677760	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	HERC2	GRCh38.p7	15:28299802	CATGCTTGTCATCCC[A/G]GCACTTTGGGAGGCC	8924
rs554688134	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28150231	AATGGCCACATGAAC[A/G]TACGTTCTAGTAAAA	8924
rs554701073	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28113462	GCGCTCAGAGTGCAC[G/T]CCCTTCAGTCAACAC	8924
rs554705460	in-del	-/CACACACACACA			intron-variant	HERC2	GRCh38.p7	15:28245594	ACACACACACACACA[-/CACACACACACA]GATATATATATACAC	8924
rs554720684	snp	A/G	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28212335	AAATGGTGAGCCCAC[A/G]TGAACCCCAGGACTT	8924
rs554740788	snp	A/C	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28250347	CATCACCTTCACTAC[A/C]TGATACCCTGCCTGG	8924
rs554753694	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28175424	TTTCATCAACAGCTG[C/T]GATTTCAACAGGACG	8924
rs554768482	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28201297	CACAGCACCTTCTAG[C/T]GTACCATGAGCTCAC	8924
rs554778447	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28294372	CAAAGGAAGCCATGA[C/G]GAGGCACATCATAAT	8924
rs554783465	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28207721	CTCACAGCATTTGCA[C/T]GTGCTGGTTTTCTTC	8924
rs554792091	snp	C/T	2.16378e-05	0.00328914	intron-variant	HERC2	GRCh38.p7	15:28168632	GGTGAGCTGCCCCTT[C/T]TCCACTGCAGCACAG	8924
rs554813323	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28170806	CTCTAAACTCAACAG[-/A]AAAAAAAAAAAGCCA	8924
rs554829522	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28193530	CCAAAAAGATAGAAA[A/C]GAGAATAGAGCAGAG	8924
rs554831413	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28148778	CATGCGGCTTCTAAC[C/T]GAGAGCATCACCGAG	8924
rs554842067	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28113881	ATCTCGTCCAGCCGA[C/G]AGGGTACGGCCTAAT	8924
rs554853613	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28162335	CTGTCTCAAAAACCT[C/T]AGACGAAAACTTGGA	8924
rs554856006	snp	C/T	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28176342	GACACGTCACAATCA[C/T]GCCGGGTGAGCCTGG	8924
rs554862705	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313770	AGGAACATTAAGTAC[A/G]TCGATTTGAAGACAT	8924
rs554902183	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28289798	AAGGGAAACACTGCA[A/C]ATCCTTAATGCTCCT	8924
rs554902846	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28171857	AGGTGGGCGGATCAC[A/G]AGGTCAGGAGATCGA	8924
rs554937540	snp	C/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28151561	AGAATCCAGGGCAGA[C/G]CCCAGGTGAAGAGTG	8924
rs554939012	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28290006	GTCTCATCTCTCAGG[C/T]GGGGTTCAAAGAGGA	8924
rs554947703	in-del	-/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28261219	TACAAAAAGGATCTG[-/T]TTTTTTTTTCTCCTC	8924
rs554950834	in-del	-/T			intron-variant	HERC2	GRCh38.p7	15:28296689	TGAATTACTGATACA[-/T]AAAAAAAAAAAAAAA	8924
rs554951229	snp	A/G	3.48147e-05	0.00417207	intron-variant	HERC2	GRCh38.p7	15:28116648	GCGACACAGTCTCAA[A/G]CGGCCGAGAAGCTCA	8924
rs554971935	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28168180	GGTTTCAGAATTGCA[C/G]ATAAAGGACTGTGAA	8924
rs554972627	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28177983	CCCCAGCATGGAATA[C/T]TCTCAAAGTCCATAC	8924
rs554979300	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28217686	GAGGTCTCTGTAGAC[A/G]TCATTAAGGTAAGAA	8924
rs554985832	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28237178	AACATAAAACCAAAA[A/G]GACAGCTCTCTCCTG	8924
rs554986889	snp	G/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28212123	GTCCAACAGGGTGAC[G/T]GGGCCACAGGGCCCT	8924
rs555030478	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28249081	TAAACATTAAGACAA[C/T]GAAATTTAAAATACT	8924
rs555032147	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28131991	CTCCTAAGGAGCACA[A/C]ACGGGGGACAGTAAT	8924
rs555042046	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28291198	CTGATCCTATAATAA[C/T]CTACGAGGTAGGTAC	8924
rs555044066	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28285546	GGGAAAGAGCTACAG[G/T]GGGTGATGAGAAATT	8924
rs555057876	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28140742	GGCCAGGCTGGTCTC[C/G]AACTCCTGACATCAG	8924
rs555059618	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28197891	ACAACCAAAACCCCT[A/C]CTTAACCATGTGTGA	8924
rs555079949	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28286124	TAACACGGACTCAAA[A/C]CAATCTCTTCTGGAA	8924
rs555080994	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28161882	AAAACTGGTTTTTAA[A/G]TCACCAGGGAAAAGA	8924
rs555116066	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28241769	AGGTTGCAGTGAGCC[A/G]AGATCACACCACTGC	8924
rs555120221	in-del	-/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28179718	AGCTAGCTCCTTTGT[-/G]GGGGTGAAAGAGAGC	8924
rs555121329	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28204255	GCAGCAGACCAACAG[A/G]TGGGCAGATGTTAGA	8924
rs555158849	in-del	-/AGA	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28171418	TTTGAACCAGAAAGG[-/AGA]AGATGAGAGTCAAGC	8924
rs555173696	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316566	TTTTATCATGGAATT[C/T]TGAAAACAAAAATTG	8924
rs555190564	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28116159	CACGGAAGTCAACAG[C/T]ACCTCGTTCGCTTCC	8924
rs555198123	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28155767	AGCTCTTTAGTTTAA[C/T]TGGATCCCATTTGTC	8924
rs555204064	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28156246	GACTTGGCAATGCGG[A/G]CTCTTTTTTGGTTCC	8924
rs555231372	snp	C/T	0.00119737	0.0244387	downstream-variant-500B	HERC2	GRCh38.p7	15:28110915	CCATTCTCCTAATCA[C/T]TTCTTTGTGACTTGA	8924
rs555235385	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28192609	CAAAAATAAATAAAT[C/T]CTCTTCGAACTATCA	8924
rs555246756	in-del	-/GT	0.0295035	0.117819	intron-variant, utr-variant-5-prime	HERC2	GRCh38.p7	15:28212821	ACAATAATTACATCA[-/GT]GTGGTGGTTACTATC	8924
rs555249262	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28193118	TAACTTTTTAAATAC[A/G]ATGTCCAGTACATAA	8924
rs555257787	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28310426	CTCCAGCCTGGGCAA[C/T]AGAGCAAGACCCTAT	8924
rs555264305	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321931	CTTAAGAGATGGAGA[A/G]AGGCCCGAGGCTGCC	8924
rs555266904	snp	C/T	7.05355e-05	0.00593825	intron-variant	HERC2	GRCh38.p7	15:28230321	TTCCTGTGCTACATG[C/T]TATGATTCTATTCAG	8924
rs555267547	snp	A/G	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28150213	ACCGAGAACATCACC[A/G]AGAATGGCCACATGA	8924
rs555348720	in-del	-/C	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314597	GCACGGTGGCTCACA[-/C]CTGTCATCTCAGACT	8924
rs555349670	snp	G/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28227871	CAAAGGCCACAAATG[G/T]TATGATTCCATTTAT	8924
rs555352065	snp	C/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28151341	AGGCAAGGTGGCATG[C/T]GTCTGTACTCCTAGC	8924
rs555352736	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28296906	TATGTCACTGCTTTT[C/G]GTGCTGCCTGCTGTC	8924
rs555355614	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28284021	TTTATATATAACTTA[C/T]ACACAGAGCCTGAAG	8924
rs555371292	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28252586	TTATTCTTATTCCTA[C/T]AGTTACTGTGTTGGA	8924
rs555393739	snp	A/C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28210248	ATGCCATTCTCCTGC[A/C/G]TCAGCCTCCCAAGTA	8924
rs555413465	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28146693	TGCAGCCAAGTCAGA[C/T]GGCAGCTGTGGGTCA	8924
rs555428725	snp	A/G	1.66222e-05	0.00288285	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28245920	CTTCATGATCATCCC[A/G]TTCCTTTCCTGGTGC	8924
rs555433226	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28114888	AGCACACTCTGTCAA[A/G]CAGGAACCAGGGTCA	8924
rs555454850	snp	C/T	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28204755	CTTGGATGGATATAA[C/T]AACAGATTAGGCCCA	8924
rs555474303	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28157808	TGTTTGCTCTTGCTT[C/T]TCTAGTTCTTTTAAT	8924
rs555484244	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28122057	GCAGCCACGGGGCCA[A/G]GGAGCACCGTGCAGC	8924
rs555489315	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28248167	AGGCTTTCTCCAACA[C/G]TTCTTCCCATTCCAC	8924
rs555495155	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28116501	GGGTTATAGGCGTGA[A/G]CCACCGCGCCTCACC	8924
rs555508997	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28320287	GCCTGGCTAATTTTG[C/T]ATTTTTAGTAGAGAC	8924
rs555514888	snp	A/G	0.000231397	0.0107538	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28246784	CCACCTCCGCGAAGT[A/G]CCGCCAGCTGGTAGA	8924
rs555520662	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28271817	TAGGCCCAGGGCCCC[A/G]CACGCCTGCTCCTCC	8924
rs555520758	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28265064	GATTATAACGGAAAG[A/G]CTCCACAACGCCAGA	8924
rs555524930	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28147434	AGGAGTTAAAGACAG[A/G]CCTGGACAACAGGCT	8924
rs555539508	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28277673	CTTAGCACCTACCGC[C/T]GACCCGTACATAACA	8924
rs555564450	in-del	-/A	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28286226	TAAGAAGCTAATATT[-/A]AGAAGCTAATAGAAG	8924
rs555579189	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28286660	TAAAACCTATGCCAA[A/C]AACAATGTCAGAAAG	8924
rs555584761	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28191409	AACAAGAATATTCTA[C/T]GCCATTCTTTGATTG	8924
rs555597449	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28280359	GCAATGTTGAGAAAA[C/T]GGATGATGACGACAG	8924
rs555611683	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28235246	GACTCTCTCTGGCCC[A/C]CTCTCTTTAAGCACA	8924
rs555632084	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111578	GTCCACAGTGTTCCA[C/T]GCGCACAGGCGGACC	8924
rs555643978	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28226291	CCAGCCTTGAAGTTC[A/G]TGTGAAAATGCAAGG	8924
rs555652431	snp	G/T	0.00478085	0.0486577	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316924	TGGGACTACAGGCAC[G/T]TGCCACCACACCCAG	8924
rs555673175	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28273281	AAAATAATTTATCTC[A/G]TTATCAAAAACATAA	8924
rs555687105	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28171254	TCCTTCGATGGTTGA[A/G]TATTCGATGGAATAC	8924
rs555691109	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28241674	AAATACAAAAAATTA[A/G]CTGGGCATGGTGGCG	8924
rs555691180	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28235799	TCCTACCCATCACTG[C/T]ATCCTGAACACCTCG	8924
rs555733909	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28146658	ATCACACTGACCAGG[A/G]GCTGTGGGAATGCCC	8924
rs555746295	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28149467	ACCGAGAACGTCACC[A/G]AGAACGGCCACACCA	8924
rs555755146	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28276715	CCAGCCTGGCCTGGG[C/T]GACAAAGCGAGACTC	8924
rs555769912	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28231933	TGGGCTCAGAACCCA[C/T]GGATATGAGATGGCA	8924
rs555780727	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28236198	CTGCAGCAACAGACC[A/G]TGAGGGCAAATGACA	8924
rs555782528	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28127802	AGAGCACAACTAGAG[C/T]ATCAAAATAAATAGA	8924
rs555787937	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28266783	AAGGGGGCATCAACT[C/G]AAAGGGTACAAAGAG	8924
rs555792931	in-del	-/C	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28129435	CTGATCACACAGGCA[-/C]CCCCTGCCTGGCGCG	8924
rs555799719	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28311336	CAGGCGTGGTGGTAC[A/G]CACCTGTAGTCCCAC	8924
rs555806322	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28138053	GCTAATCCAGAGCTT[A/G]CTAACTGTCTTCAAT	8924
rs555809579	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28149798	TCTAGTAAAATCACC[A/G]AAAAAACACACGTGA	8924
rs555809688	snp	A/C/T	3.29882e-05	0.00406118	synonymous-codon	HERC2	GRCh38.p7	15:28144114	AGCTGCCAGCGAGGC[A/C/T]GCAAGGCGAGGGACG	8924
rs555822967	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28190613	TTCAGCGTCACATAT[A/G]TGGTCAGGAAAACCA	8924
rs555825051	snp	A/C	1.99047e-05	0.00315467	intron-variant	HERC2	GRCh38.p7	15:28115416	GGCCCCGCCTGCCGC[A/C]CCAGGGAGTTACCTC	8924
rs555877900	snp	A/G	0.00597247	0.0543191	intron-variant, utr-variant-5-prime	HERC2, LOC107987422	GRCh38.p7	15:28317595	ACTTGGTAATCTCAC[A/G]GTAACAAAATTATAG	8924
rs555891633	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28197084	AACAATCTCTTAAGC[A/C]AAGAAAAATGTTTAA	8924
rs555914473	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28315395	CGGCTCACAGGCATG[A/G]GTCAACCAAGAGGGA	8924
rs555914927	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28200381	GCCTGGGTGACAGAG[A/C]GAGACTCTGCCTCAA	8924
rs555952333	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28168664	AAGTGGAGAGGCAGG[A/G]CTAGCACGCACTGAG	8924
rs555955033	snp	C/T	0.00159617	0.0282053	intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28315847	GGATGCTGGTACAAG[C/T]TGTGGGACTGCATGC	8924
rs555972679	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28303329	TAGATGTATAGATCT[A/G]TTTCTGGGTTCTCTA	8924
rs555976508	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28227106	ATGGCTAAACCCCAT[C/T]TCTACTAAAAATATA	8924
rs555980074	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28134374	AGCTTTTTGTAAATA[A/C]CACCAGGTTCTCTGC	8924
rs555985112	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28144886	GACGCAAAGCAGAAT[A/G]ATTTCCGTCACGTGT	8924
rs555993119	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28256968	ATATTTCACCGAACA[C/G]GCTAAAACCCATGCC	8924
rs555997899	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28220223	GGTGCACACATGAGA[C/G]TAAAATGCAGAAAGT	8924
rs556003045	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28185963	ATACAACAACAGTCA[C/T]CATCACAGTGCTCAG	8924
rs556040470	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28254932	GGAAACTATGAACAC[A/G]CACCTGCCCCAGGAC	8924
rs556042913	snp	C/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28309779	GAAACTGTGAGAGTG[C/T]AAATGCTTGTTGTTA	8924
rs556059299	snp	C/T	1.69594e-05	0.00291194	intron-variant	HERC2	GRCh38.p7	15:28220670	CAAAGTAGAGATCAG[C/T]TAGGAGGGTGCGTAA	8924
rs556059600	snp	C/G	0.000399281	0.0141238	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214683	CACGTCAGAGGAGCA[C/G]GTAGTGAGCAAGCTT	8924
rs556061778	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28268898	CAGGGAGGAACACCT[C/T]GCTTTAATGAAAACA	8924
rs556083367	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28112869	GCCAGATACATTTTT[A/T]AAAAATAGGTAATGG	8924
rs556086491	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28224218	AGATAGAAAGATTCC[A/C]CCCACCCCCAAGACA	8924
rs556093391	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28310947	CCAGGTGAGGTGGCA[C/T]GCACCTATAGTCCCA	8924
rs556110554	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28238870	GCAGAAATAAACAAA[C/T]CCACAATCACAATGG	8924
rs556110655	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28207720	ACTCACAGCATTTGC[A/G]TGTGCTGGTTTTCTT	8924
rs556125602	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28221963	TCCACCCACCAATAT[C/T]GTACAGAACTGTGCA	8924
rs556153040	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318001	TGTAGGAAATTCATC[C/T]GAGTGCAGCTTATGC	8924
rs556187311	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28222578	AATATCTAACAGTGG[A/G]AAACTAACAAACTTT	8924
rs556199640	snp	A/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28216650	CACTCTCACACCCTC[A/T]TATGCATCCTCACAC	8924
rs556200166	snp	C/T	8.4047e-05	0.00648201	intron-variant	HERC2	GRCh38.p7	15:28229368	AATAAAGATAAAGAA[C/T]TTGACTTGGGACACT	8924
rs556204835	snp	A/G	0.00122568	0.0247252	synonymous-codon	HERC2	GRCh38.p7	15:28132701	GTGCCCCAGCCGGCC[A/G]TAGCGGCCTTTGCCC	8924
rs556218006	snp	C/T	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28306494	TTTGTTGGGTATTTC[C/T]GCATCAATGTTCATC	8924
rs556229691	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28174705	CTTCAAAATGCTTAA[C/T]GCGTATGCCACGGTA	8924
rs556230374	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28188463	GCAGGAGAATGGAGT[A/G]AACCCGGGAGATAGA	8924
rs556262883	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28217040	CAATAACATCACTCG[C/T]GCTCACACTGACACA	8924
rs556263663	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28268376	AGGGCAATTGGAAAA[C/T]ACCTGGACACACTTC	8924
rs556268331	snp	A/C	0.004237	0.0458317	intron-variant	HERC2	GRCh38.p7	15:28142801	AATAGCTCTATTGTC[A/C]CTTTAAAAAAGAAGT	8924
rs556278186	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28219695	TCTAGTGAGTACACC[A/T]TCTAAGATCTCGTGC	8924
rs556310220	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28312752	GCTGACTTACCTAAA[C/T]GTGCCCAGTAGATTT	8924
rs556347296	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313664	GCTTTTTTTCTTAAA[A/C]CTACAGAAAAATACT	8924
rs556360317	snp	A/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28297991	AGCCACTCACTGTAC[A/T]CGTCTGTCAGTTATT	8924
rs556370034	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28138320	GAAGAAGATGCCAGC[C/T]AGGACTTTCATAGCT	8924
rs556370972	snp	C/T	0	0	intron-variant	HERC2	GRCh38.p7	15:28131114	CTGTGATTGCTCTCA[C/T]ATGTAAGTTCTTATA	8924
rs556405364	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28210829	CCTCAGTCTTGTCTT[A/G]TAAGATGACGATGAC	8924
rs556432239	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28251263	CCCCAGCCAACATGG[G/T]GAAACCCCATCTCTA	8924
rs556444560	snp	A/G	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28217875	AGCTGGACAAAGTAA[A/G]GAAGGACCTTCCCCT	8924
rs556452413	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28240989	CACTGAATTTGGTGA[C/T]GTGTCTTGAATAGGA	8924
rs556459027	snp	G/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28225473	GGAGCTGAGGTGGGC[G/T]GATCGCGAGGTCAAG	8924
rs556473773	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28247671	CTGACCTTGTGATCC[A/G]CCCACCTTGGCCTCC	8924
rs556514702	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28205956	CCTGGAAAAAGATCC[C/T]TTCATGAAGATGTGA	8924
rs556522385	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28212374	CCGTGAATTCACTCA[C/T]AAAAGAACACTGTAC	8924
rs556566567	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28143238	AAACGCTGCCTGTCT[C/T]GTCCCATGGGTAGGA	8924
rs556576005	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28166636	AGTTGTGCCAGAAAT[G/T]AAGGAAGAGCCCTAA	8924
rs556576749	snp	A/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28137024	AAAAACCACAGTCCA[A/T]ATAAAACAACCAAAA	8924
rs556581419	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28149185	GAATGGCCACACGAA[C/T]GCACATTCTAGAAAA	8924
rs556582966	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28301698	CATCTTTTTTTTTTT[A/T]TAAACTTCTGTGGAT	8924
rs556617202	snp	C/G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28278426	CTATAACACCCAATA[C/G/T]AAGGTAAATGCTCTG	8924
rs556620594	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28281028	TGTTACAAAACCAAA[C/T]TCAATATAAAAACGA	8924
rs556637029	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28209988	AAGTCTCACTCTGTC[A/G]CCCAGGCTGGAGTGC	8924
rs556651287	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28184156	AGATCATACCATTGC[A/G]ATCCAGCCTGGGCAA	8924
rs556658708	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28259302	GTTTCACCATGTTAG[C/T]CAGGCTGGTCTCAAA	8924
rs556659969	snp	A/C	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214563	CTGCGCCGCTCTTCA[A/C]CAGGGCACAGGGAAG	8924
rs556695806	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28260120	CAAGGCAGGCAGATC[G/T]CTAGAGCTCAGGAGT	8924
rs556722954	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28239187	GAAAAAAATGACTAT[A/G]AAAATTAGAAAATGT	8924
rs556728903	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28219636	CCCCGAGCCCAGACG[A/G]TGCGCTATGGCATAG	8924
rs556739582	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28307482	TTTGAAGTTTTTCTA[C/T]TTTTTTGATTTTCCT	8924
rs556740772	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28173463	GAAAAAGATTTTTAA[A/G]AAGAGTATATGCTGT	8924
rs556740889	snp	A/C	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28134766	GGAGTGCAGTGGCGC[A/C]ATCTCGGCTCACTGC	8924
rs556748192	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28248320	GAACATACAGGATGC[C/T]ATTACTGATGTCTAA	8924
rs556752406	snp	C/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28211481	TTTCAGCCGCTTTCA[C/G]TCTTCTTCTAAGACT	8924
rs556754732	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28173723	TGGAAGGATCACTTG[A/C]GCCCAGGAGGTGGAA	8924
rs556759096	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28291823	GGCAGGAGAATGGCA[C/T]GAACCCGGGAAGCGG	8924
rs556761688	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28176020	TAAGGCCTGACACAC[C/T]ATCCACAGCCAGTCC	8924
rs556774489	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28209438	AAGCTCTGCCTCCCG[A/G]GTTCACACCATTCTC	8924
rs556778645	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28120595	AAATGGTCTACTTGT[C/T]GTTTCTTTGATTACT	8924
rs556816408	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28167548	GCATTCCCACAAACG[C/T]TTCGAAGATGCTAAC	8924
rs556836141	snp	A/G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28117653	AAGCAGACACAGTGA[A/G/T]TGAGTGCCTCAGCCA	8924
rs556872882	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28175454	GAAGGCCGTGTCATG[A/G]CCCCCACGTCCCCCA	8924
rs556895108	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28168671	GAGGCAGGGCTAGCA[C/T]GCACTGAGGCGTTTC	8924
rs556901365	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28219199	TCTGATGAGCTGGCT[A/G]TGTCCTAGATGAGGA	8924
rs556901715	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28139571	TGACCCAGAGAAACT[A/G]TGAAATAATAAATGT	8924
rs556914391	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28173488	TGCTGTATGATTCTA[C/T]TTATAGTAAGCTGTA	8924
rs556927799	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28166786	CCAGTGACCAGTCCA[C/T]GGGAGTCCCAGTGAC	8924
rs556972987	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28263806	GGAGGCCAAGGCGGG[C/T]GGATCACTTGAGCCC	8924
rs556974239	snp	G/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28203632	CCCGAGAAGCCTGCA[G/T]GCAAGACGCGCATTT	8924
rs556978390	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28129090	AAGTCAGCTGACTCA[C/T]AAACTTCATTTGACC	8924
rs556982482	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28197271	CATCAAGAGTTTATA[A/G]AACTATACACATACT	8924
rs556996266	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28237293	TAACAGCAGATACCA[C/T]ATAAACCCACATGCC	8924
rs556997130	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28182714	ATTTTCTAGATACAA[C/T]CATGCCACCTTTTAA	8924
rs557010852	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28142158	AATTTTTCTGTGTCT[C/T]GTAATATTGGCATCT	8924
rs557022541	snp	A/G	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28250856	GACAGCCTGGATATC[A/G]GCTACTGGAAAGCTG	8924
rs557023664	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28282467	ATAGAAAGCCTAAGA[C/T]AAGAAAAGGAAGACA	8924
rs557040658	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28140008	AGGAGGCAGAGGTTG[C/T]AGTGAGCCGAGACTG	8924
rs557044212	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28195121	ATAAATGATCTTAAA[A/G]AGAACTAAGGTTTTT	8924
rs557056963	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28264846	CCTTTCAGATGAGGC[C/T]ATCTTTGCTCTAGGA	8924
rs557058706	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28256439	CAATTTCTCAGTTTA[C/T]GTATTTTTAAAAACT	8924
rs557061893	snp	A/C	1.64811e-05	0.00287059	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28176594	CACCCCAGGAAAATA[A/C]CAAACCTAGGTTTAA	8924
rs557078617	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28239076	AATGCAGTTAAATTA[C/G]AAATAGGTTTTCAAA	8924
rs557110933	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28244353	GTCTAGTTCCACTTA[C/T]ATGAAGTCCGAGAAC	8924
rs557123688	snp	C/G	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28257364	TGCCTTATACTATTA[C/G]CTATCATCCCTCGAA	8924
rs557136833	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28170107	CAAGTAGAGCTGGGA[C/T]ATGTGTCTATGTCAA	8924
rs557150934	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28170959	TGACCTATCTATCAG[C/T]ATGGCTACATTTTAA	8924
rs557153899	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28127759	CAGACAACGGGGACA[C/T]ACAAAAAGGGGGCAG	8924
rs557157916	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28202636	AGACAAGAGGGTCCT[A/G]GGAGATTTGGGAAGT	8924
rs557158758	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28210403	GGCCTCCCAAAGTGC[A/T]GGGATTACAGGCATG	8924
rs557171931	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28208406	CCTTCCACCAGAACC[C/T]TCTTTCCCTTTTCAT	8924
rs557184301	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28201924	TATGATATAGAAACC[C/G]AATCATCCCTTCAGT	8924
rs557215723	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28189636	ACTGTGAATGTACTA[C/T]GTATTTCAAAATAGC	8924
rs557215827	snp	C/T	0.000924878	0.0214845	intron-variant	HERC2	GRCh38.p7	15:28196202	AAGAGAGAATATAAA[C/T]ATTCTGCCATACCTG	8924
rs557223259	snp	A/G	0.0023933	0.0345097	intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28320366	GCATCCACCCGCCTC[A/G]GCCTCCCAAACTGCC	8924
rs557227264	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28114318	CACAGCCCTGTCCCA[A/G]GGAAGCCAACAAAGA	8924
rs557233591	snp	A/T	0.0126979	0.078662	intron-variant	HERC2	GRCh38.p7	15:28204105	AGAAGAAAACTCCCC[A/T]TTCTCCAGAGGCGGC	8924
rs557284262	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28150672	AACATCACCAACAAC[A/G]GCCACACAGACATTC	8924
rs557300396	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, downstream-variant-500B	HERC2, LOC107987422	GRCh38.p7	15:28319478	TAATCCCAGCTACTC[A/G]GAAGGCTGAGGCGGG	8924
rs557312928	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28249581	ATGTCAGGCTGTGGG[A/C]CCAGAGTCTGCAATG	8924
rs557318378	snp	G/T	0	0	intron-variant	HERC2	GRCh38.p7	15:28285339	AATTAAAATCACACA[G/T]CATATGTTCCCTCAA	8924
rs557318759	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28277734	AGGAAGAAAGAACCA[C/T]GGCACTCCTATTACC	8924
rs557324063	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28165996	TGGAGCATAAAACAT[C/T]TTATTGAGCCTGGAA	8924
rs557336302	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28159966	GTCAGGACCCTCAGC[C/T]GCAGGTCTGTTGGAG	8924
rs557407000	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28270476	CCTGAACCTGGAACC[C/T]GGGCCCCCAGGTTGG	8924
rs557422727	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28279806	TGACAGAGCAAGACA[C/T]TGTCTCTCCAAAAAA	8924
rs557434300	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28125654	TGCGAAACAGAAAAG[A/G]AAAAGTCTGTTTTAT	8924
rs557444120	snp	C/T	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28113902	ACGGCCTAATGACCA[C/T]CTACAGCTATGCACA	8924
rs557457700	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28280515	TGAGGCACCAAGTGG[C/T]TAAGCAACTTGTCCG	8924
rs557460694	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28156298	TTTCCAATTCTGTGA[A/G]GAAAGTCATTGGTAG	8924
rs557463711	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28160358	GAGGCAGGCAGGCCT[C/T]CTTGAGCTGCGGTGG	8924
rs557464251	snp	A/G	1.64827e-05	0.00287073	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28246868	CTGTGTACTTCTTCA[A/G]CAAGGAACCAACACC	8924
rs557469220	in-del	-/TTTAT	0.0134861	0.0810011	intron-variant	HERC2	GRCh38.p7	15:28210138	CACTATTTTTTTTTA[-/TTTAT]TTATTTTTTGAGACA	8924
rs557471279	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28126285	GAAAACGCGTTGTGA[C/T]GGAAAGCATTTTCCA	8924
rs557499143	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28204829	TAACCAAGCTACTAA[C/T]AAGGAGAAGACTTTC	8924
rs557509900	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28119849	CAAGATGAGTAAGAA[A/G]GAGGTGCTCAGCATG	8924
rs557521735	snp	C/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318741	GCCCTAGGCCTGACG[C/T]ATCCAAATAATGTCT	8924
rs557535472	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28153546	GTCCCACCTACCCAG[A/G]AGGCTGAGGCAGGAG	8924
rs557544569	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28237205	CCTGCAGCTGTAACC[A/G]CACGTGAGCCCAGGG	8924
rs557547471	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28280857	GGAGGTTGCAGTGAG[A/C]TGAGATTTTGTCACT	8924
rs557558395	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314255	CAGAACAGACCAAGA[G/T]TAGATCCTGAAAACA	8924
rs557582036	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111655	CCTCCCGCCTGGCTC[A/G]AGGACGGACGCTTCT	8924
rs557591778	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28273899	TACAGGACTAAAGAA[C/T]TTGATCTTGAGTAGT	8924
rs557595034	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28269583	TAGCTCATACCAGCC[G/T]GTATTACCTCATTTA	8924
rs557609399	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28262829	GCTAACTCATGGAAT[C/G]TCAGGTTAAGAACAT	8924
rs557655869	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316986	TTCACCATGTTGGCC[A/G]GGATGACCTCGATCT	8924
rs557680810	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28183315	CCCAGGCTCAAGCAA[C/T]CCTTCCACCTCAGCC	8924
rs557686145	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28232503	GCAGTGAGCTGAGAT[C/T]GCACCACTGCACTCC	8924
rs557690454	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28273371	CAGCATTTATCTACA[A/G]AATTAAAGAACCAAT	8924
rs557694538	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28311008	TTTGAACCTGGGAGG[C/T]GGACGTTGCAGTGAG	8924
rs557712650	snp	C/T	1.68318e-05	0.00290096	intron-variant	HERC2	GRCh38.p7	15:28135442	AAACAAAAACAAAGA[C/T]AAATAGAATGTTGAA	8924
rs557730884	in-del	-/ATAG	0.272522	0.248983	intron-variant	HERC2	GRCh38.p7	15:28270252	TTTATTTATAGATAG[-/ATAG]ATAGATAGATAGATA	8924
rs557748827	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28297655	GAGTTCTAGAACAGG[C/T]GCAATTTGTCAAATG	8924
rs557763896	snp	A/G	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28247498	CAATGGTCTGATCTC[A/G]GCTCACTGCAACCTC	8924
rs557791953	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28141071	GGTGAAAACCTGTCT[C/T]TACTAAAAATACAAA	8924
rs557797091	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28182221	GACCGCAATAAGACA[A/G]TTATACCTAAAGTGA	8924
rs557804472	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28148269	TAAAACTACATTCCA[A/G]TGGAGACTAAAACAG	8924
rs557823453	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28286848	AGGTTCACTGTGAAA[C/T]GTGCACTTCTGAACT	8924
rs557826641	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28122495	GGAGACCCAGAAAGG[C/G]TATCCTGGCGGCACC	8924
rs557833745	snp	G/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28205225	ACAGTCCTTCTCAGT[G/T]CCTGAAGGACAACTC	8924
rs557856550	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28320874	CACTCCTCTTAATAA[A/G]GAGTTACAAAGACAA	8924
rs557862829	snp	A/C	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28152173	GGCCTGAGGAACACA[A/C]TGAACAGCAGCACAC	8924
rs557890617	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28112149	TGCTAAGAACAAAAC[A/G]GCAGAAAACATAATC	8924
rs557890840	in-del	-/C	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28283433	GAAAAGAACCATTAA[-/C]CCAGAATTCTTATAT	8924
rs557895195	snp	C/T	0.000399281	0.0141238	intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28315880	CTGTCTAGAGCTTGT[C/T]TCAATGGATCTAGAA	8924
rs557904011	snp	C/T	1.67144e-05	0.00289084	synonymous-codon	HERC2	GRCh38.p7	15:28117140	CAGCCCGCCTTTGCT[C/T]CTTGATCGTTTGACC	8924
rs557928349	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28153952	GTGACAGGAGGGACC[A/G]CCGACCCCAACACAG	8924
rs557933121	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28271899	GACAGCTCAGGTGAC[A/G]TGCCCTGCACAGAGC	8924
rs557940703	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28235312	TGATCCTCCTGTGGA[C/T]TGGACCCACCTGCCA	8924
rs557942435	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28149221	CGAAAAATACACGCA[G/T]CTCCTAACTGAAAAC	8924
rs557949741	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28227168	TAATCCCAGCTACTC[A/G]GGAGGCTGAGGCATG	8924
rs557958858	snp	A/C	0.00199481	0.0315187	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317455	TGCGTAGTCATTCTT[A/C]ATTGATGATTAGAGG	8924
rs557977123	snp	A/G			intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314556	CAATGGTTGCAACAT[A/G]ATCAAAAGAATCATA	8924
rs557978730	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28142552	GGCGACCTCTGACAG[C/T]TCCTAGCCACGTGCC	8924
rs558003099	snp	A/C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28258490	AATAATAATAATAAT[A/C/T]ATCATCCATGGGTCA	8924
rs558003179	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28252209	AAACGGTGTTGAGTG[C/T]AGCCAGACGGGCCAG	8924
rs558018150	snp	C/G	0.000399281	0.0141238	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265645	CAGCCAGGGTTTGAG[C/G]ATCCCCACTCCCACA	8924
rs558039892	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28252609	GTGTTGGAAGTTCAT[C/T]TATGTGAACAAGCTG	8924
rs558045339	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28311652	AAATATAGATCCAGA[C/T]CTTAGCAGAGTGTTC	8924
rs558052735	snp	A/C	1.73222e-05	0.00294292	intron-variant	HERC2	GRCh38.p7	15:28220685	TTAGGAGGGTGCGTA[A/C]CCTGCCCTGGTCCTT	8924
rs558057887	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28143318	AGCCTCATTGTAAAG[A/T]CCAATCAACACAATC	8924
rs558074398	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28137671	CAACCAGCTGTTCTC[C/T]CATCTCTCTCCCTCT	8924
rs558081088	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28113810	GGGAGCAGCTCCAGA[C/T]GGCATGAGCATGCTT	8924
rs558087264	snp	A/G	1.65151e-05	0.00287355	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229508	CATCCACAAAACATC[A/G]CATACTGCACAGATG	8924
rs558093078	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318339	CAAGCAGAAAAGTGT[C/T]GAACAGGCCGGGCGC	8924
rs558116059	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28136164	TGGGAATGTTTTAGG[A/T]CACAAAACATCTATG	8924
rs558120710	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28315437	GGCTAAGGAATCTAT[C/G]GGGTCGGACAAGGTT	8924
rs558128477	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28128734	ACTTAGGATCCTTTC[A/G]CTCTGCAGGTGAGAA	8924
rs558136706	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28259318	CAGGCTGGTCTCAAA[A/C]TCCTGACCTCAGGTG	8924
rs558141062	snp	A/G	0.000825499	0.0202995	synonymous-codon	HERC2	GRCh38.p7	15:28152798	CACATCCTCCAACTC[A/G]GTGACACAGAGCTCC	8924
rs558148830	snp	C/T	0.00716266	0.059414	intron-variant	HERC2	GRCh38.p7	15:28297032	AAAGATAAAAATGAA[C/T]AGATGTGACTTTGAA	8924
rs558153872	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28191492	GGCCTAGGGTGGTCC[C/T]TTTACCCACCAAGTG	8924
rs558175079	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28230144	TAAGGAATGAATGGT[A/G]AATAATTAATGATAC	8924
rs558175787	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28226431	ATAGAATGTGATAAT[A/G]TAATTGAGAGTCCAG	8924
rs558211842	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28224297	CTTTATCTCCGCTCA[C/T]TGCAACCTCTGCCTC	8924
rs558223183	snp	C/G	0.00119737	0.0244387	downstream-variant-500B	HERC2	GRCh38.p7	15:28110708	TCAGTTCTACCCTTT[C/G]CAGAGTGCGTGCCAT	8924
rs558244323	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28139000	GAAGTGACCTCAGAT[A/G]TGGTGGAAACAGCAA	8924
rs558247564	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316414	GGAGGCCAAGGCAGG[A/G]GGATCACTTGAATGC	8924
rs558268245	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28191848	AACATAACGTGAGTA[C/T]TGACAGGTGCTATCA	8924
rs558280248	snp	A/G	1.65427e-05	0.00287595	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272292	GCAAGGGCAAAAGTG[A/G]GGCGCTGGTGCCCTG	8924
rs558296711	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28227647	ATTCCAGTCCTAGGT[A/G]TATAATCAAAAGAAC	8924
rs558296876	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28309885	AAGGAACAGCTTTCT[C/G]TCAGCACTCTTATTT	8924
rs558308521	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28150188	ACGAAAAAAACGCAC[A/G]CGGCTGCTAACCGAG	8924
rs558312130	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28255027	ACAGCACAACCGTGG[C/T]AGCTCTACATGGCCA	8924
rs558317005	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28266120	TTGTGAAAGAAGGAA[G/T]AGAGAATTCCAACAC	8924
rs558318405	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28302867	TATTAGATTTTTTTC[C/T]TATAGAGGTGCTTAA	8924
rs558325382	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28164077	GCCAGGGACTCCCAC[C/T]GCTTCCGACCCAGCA	8924
rs558327905	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28186016	TAAATGAGAACAGTC[A/G]TAAGATGAAATACTG	8924
rs558341357	snp	A/C	1.67609e-05	0.00289486	missense, downstream-variant-500B, nc-transcript-variant	HERC2	GRCh38.p7	15:28186623	CTTCATTATCCGAAG[A/C]TAAGAAAGGAACTGC	8924
rs558362637	snp	A/C	0.00716266	0.059414	intron-variant	HERC2	GRCh38.p7	15:28291715	ATCCATGATAAAGAA[A/C]TCCTATAACCCAAAA	8924
rs558372690	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28296346	GGGCATGGTGGAGGG[C/T]GCCTGTAATCCTAGC	8924
rs558376773	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28221313	AACAAGCACCAGCAC[C/T]TCCACATTCCCTTTG	8924
rs558383327	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314177	CTGAAAGTCAAGCAA[A/C]TATAATAATGACAAA	8924
rs558392345	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28133508	GAGTTCAATCTAAAA[A/G]TCTTTTCTGACCTAA	8924
rs558415243	snp	C/G	0.000269378	0.0116024	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28269296	GCGGCCATTGCGTGA[C/G]AGAATCAGGAAACGC	8924
rs558420089	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28308115	GTATTTTGCTAGGGA[C/T]TGCACTGAATCGGTA	8924
rs558427029	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28304550	TTTTTATATTTTTAG[C/T]AGAGACAGGGTATCA	8924
rs558441082	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28250294	GCCCTCATCACACAC[A/G]GCAAGGATGCGCCCT	8924
rs558447610	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28129536	AGTGAACCACACCTA[C/T]CACCTAGGGAACAGG	8924
rs558450056	snp	A/C	0.000399281	0.0141238	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28215653	TGGCAGTGAAGGGTG[A/C]GTGCCCTTCCACGAC	8924
rs558458867	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28262668	TGCCTGCCACAGAAA[A/G]TCAACTCAACAGGTT	8924
rs558460581	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28172354	CAAAGCTAAAGAACT[C/G]TTGCAACCTGAGTTC	8924
rs558489526	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28175403	CAAGCAGTAAGACTC[A/G]GCTGATTTCATCAAC	8924
rs558506821	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28210335	AAATGGGGTTTCACC[A/G]TGTTAGCCAGGATGG	8924
rs558514500	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28218909	ATCATAGCTCACTGC[A/G]GCTTTGACCTCGCAG	8924
rs558529201	snp	C/T	8.23757e-05	0.00641725	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213775	TGGGCAAACGCGACA[C/T]GTCCGCATGTCAGAG	8924
rs558566329	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28307010	TGGTTAATTTTTGTA[C/T]TTTTAGTAGAGTTGG	8924
rs558568189	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28298793	AGAGCAAGACTCCTT[C/T]CCCCCCAAAAAAAAG	8924
rs558575498	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28126535	GTATATATACACCAT[A/G]GAATACTACTAGCCA	8924
rs558586210	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28211603	GCAGCACAGAGAGCA[C/T]GGGGTGGGAAGGAAG	8924
rs558601794	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28275135	AGTGACAGGATCACA[A/G]GTGGATTTTTCGTTT	8924
rs558602818	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28297050	ATGTGACTTTGAAGG[C/G]CCTAATGAATGAAAC	8924
rs558603998	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28299339	AGCACATTACAAAAT[C/T]TCTATAAAATGCATT	8924
rs558607445	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28169470	GAATTTCAAAAATTA[C/G]CACAGAAGCCTACCT	8924
rs558644097	in-del	-/AC	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28150707	GAAATTACAGAAAAA[-/AC]ACACGCGGCTTCTAA	8924
rs558645142	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28212036	TCTTAGCCATCCTGA[A/G]TGTCACAGGCAAGCC	8924
rs558661133	in-del	-/AAGTACA	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28229074	CAGCATAGATTATAC[-/AAGTACA]AAGTACAAACTTTAA	8924
rs558671148	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28189123	CCATAACAAACTATT[G/T]GTACAGCAAAGGCCA	8924
rs558685965	snp	C/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28292529	CCTCAAACAGTTACA[C/T]GTAGTGCCAGGTGCG	8924
rs558691614	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28121980	GCCTGCCATACAGCA[C/G]CCACGGGCCAGGGAG	8924
rs558731046	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28168691	TGAGGCGTTTCCTCA[C/T]TTTTACTGAATACAT	8924
rs558758595	snp	A/G	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28206912	GCTACTCGCAAGGCT[A/G]AGGCAGGAGAATTGC	8924
rs558764475	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28117794	CTACAATTGCTAAAG[A/G]CTCAGGGGCCTCCAA	8924
rs558767161	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28118893	GCCACCTCTGGCACC[C/T]GGGGCCGTGGCTGAG	8924
rs558775104	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28289728	AATCCATGGACTTAC[A/G]GGACATGGCTCCCTG	8924
rs558802129	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28125767	GCAGCCTCAACCTCC[A/C]CAGCTCAAGTGATCC	8924
rs558802873	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28118576	AAATTCCCAACAAAC[A/C]AAACCTTCCAGTAAG	8924
rs558813339	snp	A/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174094	TTAAAAAATACAAAA[A/G]AGCCCAGTACAGTGC	8924
rs558845994	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318064	ATGCTCAAAGACATG[C/T]GCCTTTACCTTACAA	8924
rs558869648	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28294200	GAAACTAACTACCTA[C/G]AATTAGCACAGACCC	8924
rs558878438	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28168124	CGAGTTGGTTCTTTC[A/C]CCCAAAATGTTACTA	8924
rs558893443	snp	G/T	0.00716266	0.059414	intron-variant	HERC2	GRCh38.p7	15:28294934	CCTTGGTTATTTTAC[G/T]GGTTCCATGATACAG	8924
rs558894323	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28222889	CCCGGCAGACAGCAC[C/T]TGACACAGCTCAGTG	8924
rs558898030	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28151006	TAAGACTTGAAGACT[A/G]AAAGAAAGTATAGTA	8924
rs558901572	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28286488	GTAACCCACCCTATT[A/T]ATAGGCTAAAGAACA	8924
rs558943576	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28226791	TCTATCAAAGGAAAT[A/T]CAATCCAGAGAACAG	8924
rs558966882	snp	C/T	0.000166938	0.00913461	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202162	ACCTCCTCGTCAGAA[C/T]ACTCGTCGGACACCG	8924
rs558966930	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28209096	TTACTGGGTCACTAT[A/T]TCACTAAACAGATAA	8924
rs558972397	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28131217	TCTGGCCCTACCACA[A/G]TGGCATCGGGACGTC	8924
rs558978207	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28137059	AACAATAATGTCTAT[A/G]GCAGAGGGGAATAGG	8924
rs558979767	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28288710	AACATTAGCCAGGCA[C/T]GGTGGTGCCTGCCTG	8924
rs559009703	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28242224	AAGCTCTAGAGATGA[C/G]TGGCGGTGATGGCTA	8924
rs559010562	snp	C/T	1.64754e-05	0.00287009	missense	HERC2	GRCh38.p7	15:28114615	ATGACCACCAACCTA[C/T]AGTTTATCGCCAGCC	8924
rs559011348	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28124365	GTCTGAGTTTGGTTT[C/G]CACAACCTCACTGTG	8924
rs559021393	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28177389	AAACAGTTTCTTATT[A/C]GCAAATGAGACTAAA	8924
rs559030097	snp	A/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28320111	ATAACAATCCCATCA[A/T]CCACAACAGCTTTTT	8924
rs559062695	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28245660	ATACACACTCATATA[C/T]ACACACACACACATA	8924
rs559064901	snp	A/G	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28160755	CTGCACCCGCTGTCC[A/G]ACAAGCCCCAGTGAG	8924
rs559093590	snp	A/C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28289871	GCCGCAGTGAAAGGA[A/C/T]GACACATCTGAGAGG	8924
rs559103581	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28254244	GCCAAGATGGCGCCA[C/T]AGCACTCCGGCCTGG	8924
rs559112159	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28288146	CAGAAGATCTAGAAA[C/T]GGTAAAGGGAGATCT	8924
rs559138054	in-del	-/A	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28298131	GAGACTAATACTTTT[-/A]TCCCATGGTTTGTTT	8924
rs559139329	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28241735	TGAGGCAGGGGAATT[A/G]CTTGAACCTGGGAGA	8924
rs559147402	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28245509	CTGAGATCATGACAC[C/T]GCACTCCAGCCTGGG	8924
rs559177595	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28284387	ATGGCAGTGTTAAGC[C/T]TCAGTTTACTAATAA	8924
rs559180172	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28281966	GCCCTTGAGCACCCA[C/T]GTGCCCTTCTCCCTG	8924
rs559188509	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28161167	CTTTATCGTTTTGGT[A/G]ATCATGTAAGTTACT	8924
rs559198540	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28161769	GCTACCAAATATTAA[A/G]AGACATTTTAAAGCT	8924
rs559215320	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28194502	ATGAACCCGGGAAGC[A/G]GAGCTTGCAGTGAGC	8924
rs559244986	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28226625	CCAAAGATCTAAATA[C/T]AAGAGCTGAAACTAT	8924
rs559250671	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28263832	AGCCCAGGAGTTCGA[C/G]ACCAGCCTGGGCAAC	8924
rs559252334	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28170286	ACCCAATTTCAAAAG[C/T]TGTAATACCATAACC	8924
rs559254428	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28158022	CAGGAGCAGGTTGTT[C/T]GGTTTCCATGTAGTT	8924
rs559270639	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28289596	TCTCCCCAGAACGCT[A/G]AGACTGGCTTCTCTA	8924
rs559271279	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28151649	TACCAGAATCACTTC[A/G]GGAGCTACACTGAAG	8924
rs559280517	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214337	ACAGGGAAAGGAGAC[A/G]GCTACCCACCTCTAA	8924
rs559281048	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28232069	CTTCCGGATCCAGAG[C/T]ACCCCTCGCATTCAG	8924
rs559289219	snp	C/G	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28146942	GGGGCAGGGGCTCAG[C/G]TCCTCTCTTACGGTT	8924
rs559309989	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28156371	TATGGCCATTTTCAC[A/G]ATTTCCTATCCATGA	8924
rs559312793	snp	A/T	0.000370629	0.013608	intron-variant	HERC2	GRCh38.p7	15:28190918	GCCAAGTCACCTCCC[A/T]TGTCATCTGTAAATC	8924
rs559322465	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28274618	TCACGGCTGTCACAT[C/G]AGCAATACACTAACT	8924
rs559347950	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28127236	GGGTGTCTCTGCAGA[C/T]GCAGCTGGGCATAGG	8924
rs559349675	snp	A/C	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28261140	GGGTGTGTTATTAAA[A/C]CTGCTGTATTTTGTC	8924
rs559358164	in-del	-/A	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28134407	AACAATGTTTTCTGC[-/A]AAAAAAGACAGTTTT	8924
rs559374661	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28250964	GTATTTTTTAAGTAC[A/G]TACATCCTTATTACA	8924
rs559405380	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28157347	TTTGTACCTCTGACA[A/G]AATTCAGCTGTGATT	8924
rs559418959	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28189330	AAAGATATCTTTTAC[A/G]AATGATAATCTCCAT	8924
rs559429770	snp	A/G	4.95438e-05	0.00497689	intron-variant	HERC2	GRCh38.p7	15:28202303	CAACAGCCCTGAAGC[A/G]GGAACCCACACATAC	8924
rs559429879	snp	A/C	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28235761	TGGCTCATCAACAAG[A/C]AGCAGCTGAAAGCAG	8924
rs559430572	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28284839	AGAATCACTTGAACC[C/T]GGTGGGGTTGGAGGT	8924
rs559431345	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28265273	ACAGAACACAGAAAG[A/G]CTTAGCAGGAATTAC	8924
rs559435043	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28194227	CCCGCCACCACGCCC[A/G]GCTAATTTTTTGTAT	8924
rs559466844	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28232720	CAGGAAAATGTAACT[A/C]TTTTAGCTTGCCTTT	8924
rs559486697	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28236819	TCTCAAACTCTTGAC[C/T]TCAAGCAATCCACGT	8924
rs559488539	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28115786	ACTAGTTTAAGCCAC[A/G]CAGTGGCCAATTCTT	8924
rs559494690	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28150291	CGAGAACATCACTGA[C/G]GACGGCCACACGAAT	8924
rs559498148	snp	A/G	5.14858e-05	0.00507348	intron-variant	HERC2	GRCh38.p7	15:28238790	GTATATACAGAAACC[A/G]GAATCAGTCCATTGA	8924
rs559505986	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28260006	GAGTAGTAAATTGTG[A/G]CCAAGTGATGCCTAT	8924
rs559515338	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28195290	TCTCAAAAAAATAAT[A/C]ATTAAAAAACAAATA	8924
rs559515925	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28158003	TATGTACCCACTAGT[C/T]ATTCAGGAGCAGGTT	8924
rs559522085	snp	A/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28277056	CTCCAGCTTGTGGGC[A/T]TCAGGGTGAGACCCT	8924
rs559534551	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28232761	ATGTATCAGAATACT[A/C]AATATTTCCAAACAA	8924
rs559561730	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28224226	AGATTCCCCCCACCC[C/G]CAAGACAGGATTTCA	8924
rs559565741	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28147691	TTTCACAAAAAAAGT[A/G]AGTGAGATAAAAGTA	8924
rs559568460	snp	A/C	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28301023	TTGGTCTCTCAGAAC[A/C]ATTTCCCAATAAAAG	8924
rs559574157	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28180053	ATGTCCTGGCCTTCA[C/T]GTTCACTCACCACTC	8924
rs559588625	snp	C/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28152245	ATCAAAGGCCGGGGC[C/G]TCAACAATTTTCTTC	8924
rs559590983	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28294124	CATGGACTTTTGCAC[C/G]AAGTAATTCTCCAGT	8924
rs559595907	snp	C/T	2.90272e-05	0.00380956	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28222126	GGAGCTGCACAGGAG[C/T]CGTTTCCTTCCTTGT	8924
rs559600814	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28294515	ATTGGTAAAATCAAG[A/G]AGGCCTCAAATAGCC	8924
rs559604873	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28301755	TATATATATATATAT[A/G]TATATATATATATAT	8924
rs559674154	snp	A/G	0.00517822	0.0506191	intron-variant	HERC2	GRCh38.p7	15:28184794	GTGAACCCAGGAAGC[A/G]GAGCTTGCAGTGAGC	8924
rs559686709	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28185513	GAGGACACTGATTAT[C/T]CTCCATTGTTATTAT	8924
rs559686854	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28252849	TGTTTCAAAATTTCA[C/T]TGTGCGTCTACTAAG	8924
rs559707764	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28153643	GCGACAGAGAGAGAC[A/T]CTGTCTCGAAAAAAG	8924
rs559732950	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313963	CCCATGCTCTGAGCT[A/G]GAACCTCAAAGGGCC	8924
rs559734022	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28117885	GGAGGGCAGGTGGCC[A/G]AGGCTGTGCATCAGA	8924
rs559744822	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28113979	CAGCACCAAGAGGGG[A/G]AACACATGTGCATCC	8924
rs559745379	snp	A/G			missense	HERC2	GRCh38.p7	15:28163201	GGTCTACCACCACAC[A/G]AGTGTCATCCGCAAT	8924
rs559761830	snp	A/G	0.000166234	0.00911535	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213970	GTAGTCCTCTAACTG[A/G]GCCTAGTGCAGACCA	8924
rs559770461	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28273405	TAAAACCACCTTAGA[A/T]TCTGGAGGCAAAATG	8924
rs559775690	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28255095	AATCCCAACACTTTG[G/T]GAGGACAAGGTGGGG	8924
rs559806020	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28126707	GGACTTTGGAGACTC[A/G]GGGGAAAGGGTAGGA	8924
rs559819080	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318785	CAATAAGTGCTCTCT[A/G]TAACACACAAGCATT	8924
rs559819118	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28178486	GTTACACTGAGCCCC[A/G]TTCAGCATAGGCATG	8924
rs559830161	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28262437	TGCCTCCAACTACAA[G/T]GCATGCTGGACACCT	8924
rs559857861	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28266909	GTCATCTGGTTGTAT[C/G]GAAGCCTCATAAAGC	8924
rs559873649	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28145830	CAGCAGAGATAAGCC[A/G]GACATGTGGCTGCCT	8924
rs559879932	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28179509	TGTGCTGCCAGCTAC[A/G]TATCAACAATCCCTA	8924
rs559884706	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28148707	GGCTTCTAACCGAGA[A/G]CATCACCGAGAACGG	8924
rs559905953	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28231110	GAATTCACTGCGATA[C/T]GTGGAATTTCCTCCC	8924
rs559907890	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28224665	AATCAGATCTAATAG[A/C]CATATACAGAACATC	8924
rs559923953	snp	C/T			missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28215710	GGGAGCTGAGGGCGC[C/T]GCATACCTGCGGCGT	8924
rs559944783	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28225246	GGAAAAGTAAGACCC[C/T]GTCTCAAAACAAAGA	8924
rs559960099	snp	C/G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28298401	CTCAAATGATCTGCC[C/G/T]GCCTCAGCCTCCCAA	8924
rs559981541	snp	A/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28126149	AATAAAAAAAAATAG[A/T]TGTTGGTATGGATGT	8924
rs559994541	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28187426	AACCCCTGCCTCCCG[A/G]GTTCAAGCGATTCTC	8924
rs560002118	snp	G/T	0.0197687	0.0974348	intron-variant	HERC2	GRCh38.p7	15:28291939	AAAAAAAAAAAAGAG[G/T]CAAAAGGGCCAGGTG	8924
rs560033052	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28259038	CTAGAAACAAACAGG[C/T]CACCTGAATACTTCT	8924
rs560040754	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28134029	TATACAAATCTTGAT[C/T]GGGAAGGTGTTGAAT	8924
rs560067437	snp	A/G	0.00517822	0.0506191	intron-variant	HERC2	GRCh38.p7	15:28143572	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	8924
rs560077381	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28216116	AAATAGCTGGGACTA[C/T]GGGCATTTTTAAAAC	8924
rs560094936	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28141407	CAGGCTCAATGACCT[C/T]GTGACATAGAAAAAG	8924
rs560117286	snp	C/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28220714	TTCCATGGCTCCCAG[C/G]AGACCTCAGTTAGGA	8924
rs560118548	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28192730	AGAGGCTGCTGTTCC[C/T]TGATGGCATCACCAG	8924
rs560151766	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111706	CTACAGTCTACACAG[C/G]AGCGAGCGCTCTGCT	8924
rs560156561	snp	C/T	1.6477e-05	0.00287024	missense	HERC2	GRCh38.p7	15:28135623	TGGATTCAAGCAATG[C/T]TGGGGTGGACACCGA	8924
rs560178844	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28251598	TTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC	8924
rs560183992	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28186923	GCAGCCACATCTGAG[G/T]AATGTTTACTTCAAA	8924
rs560214516	snp	A/C	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28311229	CAGCAGTCTGGGAGG[A/C]CGAGGTGGGCAGACT	8924
rs560222237	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317024	TCAGCCTCCCAAACT[A/G]CTAGGATTACAGGCT	8924
rs560224449	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28188544	TGAGACTCCGTCTTA[-/A]AAAAAAAAAAAAAAG	8924
rs560226359	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28227988	ATGGCTAAATGGTGT[A/G]CATTTATAGTGATGA	8924
rs560229049	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28128761	AGAAGCCCCGCATGG[C/G]TCTGTCTCCCTTCCC	8924
rs560245511	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28303684	TCCAATCCATGAACA[C/T]GGAGTATCTTTTCCT	8924
rs560251129	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28306295	GGATGTTGAATTTTA[A/T]CAAATGCCTTTTCAG	8924
rs560271694	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28254753	TCTGCTGATGCTCTC[C/T]AGCATCCTTCTGTGA	8924
rs560273491	snp	C/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28259500	GAAAATGAAAAAGGA[C/T]GGAACACATGCCAAT	8924
rs560297829	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28246329	ATTCAGAAAATTAAA[C/T]GTTTATTGATATGTT	8924
rs560298080	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28216909	AGTAACGACCGATTA[C/T]TCACCCACTCACACC	8924
rs560315083	snp	A/G	0.000154923	0.00879985	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28222199	CATATCTTCCTCAAC[A/G]TTGTCACAACTGGGG	8924
rs560331087	snp	C/T			missense	HERC2	GRCh38.p7	15:28142314	GCCATGCAGTACCTC[C/T]GGAACCAGGCCCACT	8924
rs560348232	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28209637	CATGAGCCACCGCGC[A/C]AGGCCTATATATCAT	8924
rs560356535	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28253023	CCCAACCTGCCAGTG[C/T]TTTGCTTTCTCTATG	8924
rs560358810	snp	A/C	0.000467399	0.0152801	intron-variant	HERC2	GRCh38.p7	15:28210986	ATAAAGATTTAAGAA[A/C]TTTTTAAAAAGACAC	8924
rs560370276	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28136840	AGGACAAAATGAAGA[C/T]ATTTTGAAACAAACA	8924
rs560370756	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28171472	AAAGAAGACAGCACA[A/G]GAAGGTGAAGCCACT	8924
rs560378441	snp	A/C	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28222675	CAGGCTGGCCCTCGG[A/C]TGGAGTCTGGATCTC	8924
rs560386150	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28246970	AACTAACTGCTCCAT[A/G]ATGCTATTCTCATCT	8924
rs560404195	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28123943	GCTGAATGAGCTGTA[C/T]TCTATGTGTTCTATT	8924
rs560420434	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28179429	AGTGGTGTCCTGGCC[A/G]TGACAACGTCACAGC	8924
rs560429599	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28137120	CACTGATTGGGAGGA[A/G]GGGAAAATACTAATT	8924
rs560431550	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28129975	GAGATGATGTTTACC[A/G]TGTAGGCCAGGCTGG	8924
rs560441001	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28160109	GTTTTGTCTCAGAGG[G/T]GTACCCGGCCGTGTG	8924
rs560441307	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28153128	GAAGGCCGAGGCAAG[C/T]GGATCACCTGAGGTC	8924
rs560446890	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28167204	AGTGGAGAAACTTGG[C/T]AGAGACCCTTAACCA	8924
rs560455163	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28309959	TGGAACCAAAACATA[C/T]GACTTTTGGTAAAAA	8924
rs560480692	in-del	-/CCTGCCTTGC			intron-variant	HERC2	GRCh38.p7	15:28216085	GGTTCAAGTGATTCT[-/CCTGCCTTGC]CCTGCCAAATAGCTG	8924
rs560523208	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28281706	TATTTAAAACGACAT[A/G]AAGAATACTGAATTG	8924
rs560527348	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28285848	AACATTAGTGATGAA[A/T]CGGACTCTAAAGATA	8924
rs560545759	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28177644	TGAGTAACTCAACAG[A/G]ATCAACAGCGGAGTT	8924
rs560549845	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28296407	GAACCGGGGAGGCAG[C/T]GGTTGCAGTGAGCCA	8924
rs560567815	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28200315	CAGGAGAATGGCATG[A/T]ACCCGGGAGGCGGAG	8924
rs560593358	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28132413	CTATAAGACAAAAGA[C/G]AAAGCACCTTCATCT	8924
rs560596941	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28239678	CCGCCCCAACGAGAC[C/T]GAATTCAAATCCAAC	8924
rs560618229	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28125274	TCTTCCCACCACACA[C/T]AGCACCAACGCTCCC	8924
rs560635555	snp	A/C	6.99704e-05	0.00591442	intron-variant	HERC2	GRCh38.p7	15:28192188	GAGAATTAACCCTTG[A/C]TGAACTGGGGAGAAA	8924
rs560638205	snp	A/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28290851	ATAGTTTTGAACACT[A/T]GTTAGAAAAGACAAA	8924
rs560645406	snp	C/T	0.000365838	0.0135198	intron-variant	HERC2	GRCh38.p7	15:28116649	CGACACAGTCTCAAG[C/T]GGCCGAGAAGCTCAC	8924
rs560656973	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28125904	GCAACCTCCGCCTCC[C/T]GGGTTCGAGCGATTC	8924
rs560686936	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28258790	AAAAATTAATGAAAC[A/G]AAAAGATTGTTCTTT	8924
rs560701414	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28138490	TAACTCCACTCTGAC[C/T]GTGCTCCAGAAATAG	8924
rs560702462	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28284806	TATAATCCCAGCTAC[C/T]CAGGAGGCTGAGGCA	8924
rs560711052	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28204411	CGGATCATGAGGTCA[A/G]GAGTTCGAGACCAGC	8924
rs560716769	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28210071	GGTTCAAGTGATTCT[C/T]CTGCCTCAGCCTTCC	8924
rs560719018	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28198194	AATATTAATAAATCT[A/G]ATTGTTTCACTGCAG	8924
rs560723376	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28204925	AACAAAAAGAGCAAG[A/G]CAGGGGGAAAAAACA	8924
rs560753818	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28116252	TTTGATACAGAGTGT[G/T]GCCCAGGCTGGAGTG	8924
rs560772741	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28156399	TGAGCATGGAATGTT[A/C]TTCCATTTGTTTGTA	8924
rs560775143	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28243559	CAACCAGATAGAAAA[A/G]TGCGCACAAAACTTG	8924
rs560834955	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28286328	AAGACAGTACAAAGT[A/G]CAGAACAATATATAT	8924
rs560840236	snp	C/T	0.000100201	0.00707748	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174369	ACCTACAGAAAAATC[C/T]CAGAGAAGATACAAA	8924
rs560849160	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28240193	GGAGGCCAAGGTGGG[C/T]AGATCACAAGGTCAG	8924
rs560863981	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28237627	CAAAGTTAATTCTCC[C/T]CTTCATAAACTGTTT	8924
rs560866433	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28168825	TGGCAGGTGAAAAAC[C/T]GCCAAACATAAAAAC	8924
rs560873599	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28279873	TGGCACAGATTACAC[A/C]GCATGGTCTATTACT	8924
rs560880395	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28150402	TCTAGTAAAATTACC[A/G]AAAAACACACACTGG	8924
rs560882538	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28162807	GAGGCAGGAGAATGG[C/T]GTGAACCCAGGAGGC	8924
rs560884171	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28156955	TTGAGTTTTTAGCAT[A/G]AAGGGCTGTTGAATT	8924
rs560900186	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299618	CCCCCTTATGTATTC[A/G]ATCATTTGGTAATAA	8924
rs560904915	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28224978	CAAAACTTCTGTGCT[A/G]CGCCAAAAGCAGGGA	8924
rs560913683	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28293411	GGCAGGAGAATGGCG[G/T]GAACCCGGGAGGCAG	8924
rs560950647	snp	A/C	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28174882	AATTCTGCTTTGTTG[A/C]AAGACACACAGAAGG	8924
rs560950761	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28293788	GGCACTGTGACTGAT[A/G]GCATAATTCAAGAGC	8924
rs560954780	snp	A/G	0.0162398	0.0886349	intron-variant	HERC2	GRCh38.p7	15:28290703	AAATAACAATTTCCA[A/G]ATAATAAGCGGGTAA	8924
rs560978853	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28254253	GCGCCATAGCACTCC[A/G]GCCTGGGCAACAAGA	8924
rs560989178	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28199641	TAATGCCTACTGGAG[C/T]TATGAGATGGATAAT	8924
rs561004229	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28207328	TTAGTATAGATGGGG[A/G]TTTCACCATGTTGGC	8924
rs561023140	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28283269	AAGACATACAATAAT[A/C]AAACTCCAAAAAACA	8924
rs561030617	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318926	GAAACATCTTCCTAT[C/T]CCATGTATTATTCAT	8924
rs561045948	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28118912	GCCGTGGCTGAGCCA[A/G]AGCAGCCCCCAGACG	8924
rs561052554	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	HERC2, LOC107987422	GRCh38.p7	15:28317723	AAATTGTAGTAGTAG[C/T]TACATTTACAGACCC	8924
rs561075365	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28289548	AGCACGATGGAGATA[C/T]TCCTGGGAAATAAAG	8924
rs561098025	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28287225	GCTGAGATGGAAGAG[C/T]AAAAAAACAGAAAAA	8924
rs561119970	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28195385	AGAATTGCTTGAACC[C/T]AGGAGGCGGAGGTTG	8924
rs561133927	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318504	GTGGTGGTGGACACC[C/T]GTAGTCCCAGCTACT	8924
rs561139179	snp	A/C	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HERC2, LOC107987422	GRCh38.p7	15:28312133	ATGGTAAGCACCATT[A/C]AAAAAACTATTTGGG	8924
rs561141129	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318103	GCGAACAGGCATGTG[C/T]TTTAAGAATAAAAAG	8924
rs561148940	snp	A/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28161263	TAATGATTTTTTTTT[A/T]AAATATAATTCTACT	8924
rs561149814	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28282709	GAGGCCGAGGCAGGC[A/G]GATCACAAGGTCAGG	8924
rs561153009	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28117944	TGTCAAAAAGAAAAA[C/T]TGAAGAAAAAATGGT	8924
rs561157830	snp	A/C	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28223181	GCTGTCACCTGAGAG[A/C]AGTAAAACTTCCCAA	8924
rs561162292	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28236873	GATTACAGGCATGAA[C/G]CACTGTGCCTGGCCC	8924
rs561208463	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28117895	TGGCCGAGGCTGTGC[A/G]TCAGAATCATCTGGG	8924
rs561221818	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28184658	CGAGGTCAGGAGATC[A/G]AGATCATCCTGGCTA	8924
rs561240043	in-del	-/AAAAG			intron-variant	HERC2	GRCh38.p7	15:28228141	CTTTAAAAAAAAAAA[-/AAAAG]AAAAGAAAAGAAAAG	8924
rs561251655	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28230655	ACAACAAGAGTGAAA[C/T]GATCACCCTGGCAGA	8924
rs561255532	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28189354	TCTCCATTGTTGATT[C/T]AATTACTTAGTTTCT	8924
rs561255630	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28114503	TAGTTGGAGCCAAAT[A/C]CATTACTTTACTGTG	8924
rs561256735	snp	A/G	3.59454e-05	0.00423927	intron-variant	HERC2	GRCh38.p7	15:28248513	AAAGTAACGAGCCCC[A/G]ATCACATACAAGACA	8924
rs561259246	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28281961	GCTCTGCCCTTGAGC[A/C]CCCACGTGCCCTTCT	8924
rs561274589	snp	C/T			intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28315860	AGTTGTGGGACTGCA[C/T]GCCACTGTCTAGAGC	8924
rs561293544	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28241206	ACCCAATTAAAACAC[A/G]GGCAAAAGACTTGAA	8924
rs561294835	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28160691	CTTCCCAGGTGAGGC[A/G]ATGCCTCGCCCTGCT	8924
rs561307294	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28180690	TTGGTCCTCTGTATC[C/T]ATAGGTTCCACGTCC	8924
rs561307627	snp	A/G	0.00755907	0.0610114	intron-variant	HERC2	GRCh38.p7	15:28220082	AGGAGGCAATGGACC[A/G]AGACCACAGGGCAAT	8924
rs561311199	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28284447	ATGCATCAATTAAAA[A/G]ACACCAGGAGAGCAG	8924
rs561327908	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28245710	GGTTAATATATACAT[A/G]TATGACCCAAATTTC	8924
rs561346586	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28287775	CTGTCACCCAGGCTA[C/G]AGTGGTGGTGCAATC	8924
rs561349594	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28194566	GACAGAGCGAGACTC[C/T]GTCTCAAAAAAAACA	8924
rs561357550	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28284913	AAGGAGCGAAACTCC[A/G]TCTCGGAAAAAAAAA	8924
rs561380062	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28196707	TTTTAGAGATAGGTA[C/T]TAAAATGCTTATGGA	8924
rs561390515	snp	A/G	0.000181325	0.00951996	intron-variant	HERC2	GRCh38.p7	15:28144653	CATCTAACCTTGATC[A/G]CCATAAGCCCCTTCC	8924
rs561400837	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28197566	AGACCAGCCTGGCCA[A/T]CATGGTGAAACCCCA	8924
rs561402739	snp	C/T	0.00874735	0.0655527	intron-variant	HERC2	GRCh38.p7	15:28155214	TATTGTGAATAGTGC[C/T]ACAATAAACATATGT	8924
rs561432491	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28281176	TCATTATATTATTCT[C/T]TCTTCTTCTATGTAT	8924
rs561481718	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28268130	CAACCTTATCTATGA[C/G]AGACAGGGTGAACTG	8924
rs561482773	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28228944	TATAGGACACAGACA[A/C]TTTAGGATATGTGGT	8924
rs561483233	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28158038	GGTTTCCATGTAGTT[C/G]AGCAGTTTTGAGTGA	8924
rs561487926	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28274827	AGCCAAAGGGCACAT[A/G]GTGGCTGAACCGAGT	8924
rs561498326	snp	C/G	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28173628	ACATGGCAAAACCCT[C/G]TCTCCACCAAACAAA	8924
rs561500908	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28249945	CAGGCGTGAGCCACC[A/G]CGCCCGGCCTAAGGA	8924
rs561536828	snp	A/G	0.000399281	0.0141238	intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28316019	TGTTTATTTGTGGCC[A/G]AGTGTAACAACCATA	8924
rs561538348	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28309531	TCCATCCCCCCGCAC[C/T]GTCCTGAAGGGATGG	8924
rs561539431	snp	A/G	5.00046e-05	0.00499998	synonymous-codon	HERC2	GRCh38.p7	15:28144207	TGGACAGGAGAGGAC[A/G]CAGCGGTCAGAGAGG	8924
rs561558423	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28188230	ATCTGGACACTGACT[A/G]AATATTATATGACAT	8924
rs561570623	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28115171	ACGGCCCCCAGCTGC[C/T]CAAAAGCTCAGCTTC	8924
rs561578489	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28310002	GGGGGAGAGGTAAAC[G/T]CCTTCCAAAAAGTGA	8924
rs561594583	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28320561	CTACACGACTTTTGA[C/T]GAACAGTCAAGGCAC	8924
rs561621696	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28220812	GCCCTGGTCCTTCCA[C/T]AGCTCCCACCAGACC	8924
rs561627999	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28208982	CAATAGCAGGAGATC[A/G]AAAAATGTTTTTTTC	8924
rs561643268	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28232868	AAAAATACTTCCTTG[C/T]TCCCATCAATTTAGT	8924
rs561647620	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28307212	TAATGACCCTTTGAA[C/T]TTCTGCAATATCAGT	8924
rs561656288	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28271498	ATGGTGAAACCCCAT[A/C]TTTACTAAAAATACA	8924
rs561656732	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28245450	TACTCAGGAGGCTGA[C/G]GCAAGAGAATCACTT	8924
rs561660845	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28238464	GAATTTGTTGATAAG[A/G]CAGACATCGAAGCCA	8924
rs561684493	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28226735	GCATAGACGACAAAA[A/G]AGAAACAGATAAATT	8924
rs561693207	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28238904	AAATACATACCTAGC[C/T]CTGAAACTAATACCA	8924
rs561750896	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28138438	AGTCAATGCTCATTG[A/G]CCATTCTGAAAATCT	8924
rs561804210	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28115767	ACATCCTTTCTGCAC[A/G]CACACTAGTTTAAGC	8924
rs561805511	snp	G/T	0.000960532	0.0218939	intron-variant	HERC2	GRCh38.p7	15:28135697	GTGGCATACAGCTAA[G/T]AAAAGAAAAAGCAAT	8924
rs561826318	snp	C/T	0.02016	0.0983543	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321493	CATACGCTGAAGACC[C/T]AACGCTTTTTAATAG	8924
rs561852564	snp	C/T	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28304382	TTTTTTTTTTTTTTT[C/T]CCTGAGATGGAGTCT	8924
rs561857762	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28278906	ACAAATTTACATAAG[C/T]CTTAAACATTCTAGT	8924
rs561858190	in-del	-/G	0.00243734	0.0348243	intron-variant	HERC2	GRCh38.p7	15:28132640	CCGGCCTCTGCACAC[-/G]GCGCCTCCTCACCAG	8924
rs561874529	snp	A/G	1.66832e-05	0.00288814	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233493	CCACCACTGACTTAG[A/G]CAACGTTCTGTGCTT	8924
rs561877894	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28265399	TAAAAAATAAAATGC[C/T]CACACAGGAACGGCG	8924
rs561884330	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28231170	CTAAATCTCCTCAGC[A/G]TATAATATAAAAAAT	8924
rs561902662	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28237877	GTGGAACACTGTCTA[C/T]ATTTCTCACAAATTG	8924
rs561912095	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28176259	GGGAAATTTCTTCTT[A/G]TACTATTGTCACTAA	8924
rs561917831	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28169808	ATTAATAGGCCTTCA[A/G]AATAAGAAAACCACT	8924
rs561933323	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28271946	ACCAACAAAGCAGGC[C/T]GCTATTTTCGTTGTT	8924
rs561936385	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28275373	GGAGAAGAGCTGGAA[A/G]AAGAGCAGCAGAGCC	8924
rs561956427	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28177339	TCTATTCTATTCTAA[C/T]TTTCTGCAAAATAAT	8924
rs561957077	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28227257	TCCAGCCTAGGCGAC[A/G]GAGTGAGACTCCGTC	8924
rs561970775	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28189930	ATCAACTATTTGATA[C/T]TTTTATCTGCTATCA	8924
rs562009531	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28186167	AACAATATATATATT[A/T]CACCATAATAAAAAA	8924
rs562010117	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28139786	AAAACATTGGCCGGG[C/G]ACGGTAGCTCATGCC	8924
rs562021647	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28177654	AACAGGATCAACAGC[A/G]GAGTTAGCAGGAAAG	8924
rs562022605	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28289909	ACCTCAGTGAGAGGA[C/T]TACACACCTCAGTGA	8924
rs562028924	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28170452	GTGGTGGAGCAACTG[A/G]ACGTCTGTGGGCAAA	8924
rs562032641	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28183808	TTTGGAATAAAAGTG[C/G]AAAACTCTTTCATCC	8924
rs562040385	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28126706	TGGACTTTGGAGACT[C/T]GGGGGAAAGGGTAGG	8924
rs562066369	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28203208	GCTGGGAACTCCCCA[C/T]CTACAGCACAAATAG	8924
rs562093249	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28308296	GTTACTTCCCAGGTA[C/T]TTAATTTCATGTGTG	8924
rs562095196	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28314955	CATCTGGCAGCTTCT[C/T]GCAGGACAATAGCCA	8924
rs562112936	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28287900	AGCTAATTTTTTTGT[A/C]TCTTTAGTAGAGACG	8924
rs562118418	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28256542	TGTTTATGGAAAGCT[C/G]AAGATCAGCAGAAGA	8924
rs562138233	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28219299	AGGAGATGTGTGGCA[A/G]ATGAGGCCACCCTCT	8924
rs562144023	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28149282	TCTAGTAAAATTACC[A/G]AAAAAACACACGCAG	8924
rs562156039	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28143648	AGTCAGGATTTCACC[A/G]TGTTAGCCAGGATGG	8924
rs562168467	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28266981	AATGAAGCCAGCACT[A/C]TGCAATCTATACTTT	8924
rs562183895	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28295014	TGGCAAAAAAGAACA[C/T]GATATTCAGCATTGT	8924
rs562186548	snp	A/C	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28225728	AAAGAAAGAAAAAAA[A/C]GAAGATGCAAATAAC	8924
rs562189213	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28306032	GTCAGGAAACAACAG[A/G]TGCTGGAGAGGATGT	8924
rs562205196	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28259534	TTGTATAAGGTCAGC[C/T]TTCCCCTGATAGAAA	8924
rs562208177	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28251005	AGAACCAATGTCCCA[C/T]ACAGGACCCCACGTG	8924
rs562249340	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28141267	TTAATTTAAAGATTA[C/T]ACAAAAATATCTTAG	8924
rs562249493	snp	A/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28120861	CAGCACCATCAGAGA[A/T]ATCTGACAGAGTAAA	8924
rs562250019	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28134132	ACGACTTTAGGTTTT[C/T]TAAAAATTATCTCAG	8924
rs562254369	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28219775	CACTGCGGTGCTTCC[A/G]GAGGCAGCCCCAGCC	8924
rs562257765	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28164824	GTTGCCTTCCTCAGA[A/G]TAAGTTCTGCATTAA	8924
rs562282072	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28260350	CTTCTAAAACGGGGA[A/T]TTAAAGACACTCCCT	8924
rs562290677	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28164084	ACTCCCACCGCTTCC[A/G]ACCCAGCATGGGAAC	8924
rs562290967	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28140231	CTGGAAGCCTGGGAA[C/T]GCTCCATCTGCACCC	8924
rs562297088	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28131204	TAGGGCTCTAGTGTC[C/T]GGCCCTACCACAATG	8924
rs562297737	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28167316	GTTCCTGTGGTGTCT[A/G]TCAAAACGAAGAACT	8924
rs562298280	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28126790	TGATGGGAGCACCCA[C/T]CTCTCAGACATCACC	8924
rs562311860	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28173899	ACGGCAGGAAGGAGG[C/G]AGTTAAAAGCAAAAG	8924
rs562313034	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28134981	CCGGACCTGTTTAAT[A/G]TATTTTATATGGTGG	8924
rs562317354	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214352	GGCTACCCACCTCTA[A/C]GTGACGGCACTGCGC	8924
rs562338968	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28138899	TGATTCATGGGAGGA[C/G]GTGAAAATATCAACA	8924
rs562373847	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28244430	GATGATCAGAAGTAA[A/G]GTGGCGATGACCACA	8924
rs562391170	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28295582	TTTTTGTTTTTAGTA[A/G]AGATGGGGTTTCACC	8924
rs562416157	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28223036	ACTATAGCCCTGAGT[A/T]CAACTACATGCTGAG	8924
rs562457674	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28311256	GACTGCTTGAGCCCA[A/G]GAGTTCGAGACCAGC	8924
rs562464267	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28173752	AAGCTGCAGTGAGCC[-/A]AAATCGTGCCACTGC	8924
rs562492192	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28253456	TCTTTTTACATGTTT[A/C]CTGCACACCGCAATT	8924
rs562493920	snp	C/G	0.0107246	0.0724382	intron-variant	HERC2	GRCh38.p7	15:28306343	ATATGGTTTTTTATC[C/G]TTCATTCTATTGATA	8924
rs562497845	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28311807	CCCCAGACTGGCTGG[C/G]CTCCACACATCAGTG	8924
rs562511516	in-del	-/A			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28320799	TTATCTCATTAAATC[-/A]AAAAAATTAGGATCT	8924
rs562513405	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28222766	CAAACAATGTGGTCT[G/T]TGCTGAAACCTGCTT	8924
rs562528272	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28215283	TAGTGATTAGGATTG[C/T]CAGGAACTTTAAAAA	8924
rs562540872	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28216936	CACCTTTACCCACAC[A/G]CTTTCTCACTTTGCA	8924
rs562576317	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28137233	AGGGGCTATATTTCA[A/T]ACCTTTTTATGAGGC	8924
rs562586290	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28179571	TGGGCTATATATTCA[C/T]TCTCCTGTACTTTCT	8924
rs562587482	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28131578	AAATCGCCTGCAGCC[A/G]CCGGGCTTGAGTGGA	8924
rs562588878	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28128950	AGAGCTCTCAGACTT[C/T]GAAAATCTTTCTACT	8924
rs562589818	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28306666	TTCTTCTTTAAATGT[C/T]TGGTAAAATTCAGCA	8924
rs562592943	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28215888	TTTTTTATCAACTTA[C/T]TTTATTTTTCTAAAA	8924
rs562601203	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28129769	CAGGACACAGTATAA[A/G]CCTCTGCCTCCTTTT	8924
rs562609081	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28122195	GGGCGTGGCCAAACA[C/T]CAGCACCACGGTGAG	8924
rs562617474	snp	C/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28293234	CGTGGTGGCTCACGC[C/G]TGTAATCCCAGCACT	8924
rs562647758	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28122749	CACATTCCCTGACCA[A/G]AGGTACCTTTCAGAC	8924
rs562655048	snp	C/T	0.000258231	0.01136	intron-variant	HERC2	GRCh38.p7	15:28211149	GGTCCACTTGTCCTG[C/T]GGAAGGAAAGACTCA	8924
rs562658824	snp	C/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28217184	CTTACACTTACACTG[C/G]GTGTCTCATTCGCAC	8924
rs562664510	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28207103	TCTCTTAGAGCCAGC[A/G]AATGCTCCTTCCCAG	8924
rs562688501	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28130794	GACTGACAGCACACC[C/T]GTTGGCACACTGTGG	8924
rs562691284	snp	A/C	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28296487	CGAGAGGAAAAAACA[A/C]ACAAAAAATATTCAT	8924
rs562696696	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28210533	ACATACATCTATGCA[C/T]GTCAAAGACCAACTC	8924
rs562699983	snp	A/C/G	6.67561e-05	0.00577704	synonymous-codon	HERC2	GRCh38.p7	15:28124091	CCCAACAGAAGGCCC[A/C/G]AGTCCAGTTTCGTCG	8924
rs562735836	snp	A/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28240213	CACAAGGTCAGGAGA[A/T]GGAGACCATCCTGGC	8924
rs562738648	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28124705	GCTGGGACTACAGGT[A/G]CATGCCACTATGCCT	8924
rs562741175	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28292663	TCTAATTAGTCAAGC[A/G]TGATGGCTGGGCAAC	8924
rs562768709	snp	C/T	0.000399281	0.0141238	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28248613	ACTAATAAGCAAACG[C/T]TGAAAACGCAGTAAC	8924
rs562771201	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28235103	TGTGTTATCAAATAC[C/T]GCTCCAAATCCAAGC	8924
rs562776305	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28241382	GTGTTGGTGAGGATG[G/T]GGAGAAACTGGAACT	8924
rs562791701	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28210172	AGAGTCTTGCTCTGT[C/T]GTCCAGGCTGGAGTG	8924
rs562802246	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28204436	ACCAGCCTGGCCAAC[A/G]TGGTAAAACCCCATC	8924
rs562808335	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28246579	TACCAGCTGGCTTAA[C/T]AACAGAACTGTCAGT	8924
rs562840073	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28172154	CTAAAAAATAAAGAG[A/G]AACACTATGTTCATG	8924
rs562845084	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28116381	ACCACAGCCAGCTAA[A/T]TTTTTTTGTATTTTT	8924
rs562851014	snp	C/T	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318352	GTTGAACAGGCCGGG[C/T]GCGGTGGCTCACGCC	8924
rs562879719	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28149046	AACGTACATTCTAGT[A/G]AAATTACCGAAAAAA	8924
rs562887395	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28159715	GTTTGATCGTCTGAA[C/G]CCTTCCTCTCTCAGC	8924
rs562895456	snp	C/G	0.0130921	0.0798413	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299878	CCAACACGGTGAAAC[C/G]CCGTCCCAACTAAAA	8924
rs562929131	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28212745	TGACATTAAAGGCAG[G/T]ATAGAGATTTACACA	8924
rs562940493	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28297220	TTGCCCAGAATCCTA[C/G]GAAATCGCCACTGTT	8924
rs562940907	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28207322	GTATTTTTAGTATAG[A/G]TGGGGGTTTCACCAT	8924
rs562942009	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28279967	AATAAATTTCAGAAG[A/G]TGAAGACAGCCTATA	8924
rs562951482	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28165702	GTTCCAGCTACTTGG[A/G]AGGCTGAGGATGGCT	8924
rs562957418	snp	C/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28280656	ACACCTGGAATCCCA[C/G]CACTTTGGGAGGCCA	8924
rs562960797	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28210406	CTCCCAAAGTGCAGG[A/G]ATTACAGGCATGAGC	8924
rs562963284	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28252811	TACTAAAATCTATGA[C/T]AGAAACTAGCTCTAA	8924
rs562972104	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28126031	GGGTCAGGCTGGTCT[C/T]GAACTCCTGACTTGG	8924
rs562990557	snp	C/T	0.00033123	0.0128649	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213900	CATCGATGCCTCCAA[C/T]CACAGCCAGGACTGC	8924
rs563005945	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316757	TCAAGATACTCATGT[G/T]TATACTTTTTTTATC	8924
rs563010820	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28119537	CGGCTCACTACAACC[G/T]CTGCCTCCCGGGCTC	8924
rs563019516	snp	A/C	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28166220	AAGACATCACAAGAA[A/C]ACTACAGAGCCGTAT	8924
rs563033774	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28286411	TATAAAAAGAATTCC[A/G]CATCATTGCCAAGTA	8924
rs563038787	snp	C/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28272832	TGAAACACACACAAT[C/G]CAACAGGTATTTCCA	8924
rs563046272	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28311471	CCTGACTTAAAAAAC[-/A]AAAAAAAGAAACTAT	8924
rs563046361	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28276345	TGCACCGGGAGCTCA[A/G]AGAGGAAACACAAGA	8924
rs563055955	snp	A/G	0.0648419	0.167978	intron-variant	HERC2	GRCh38.p7	15:28160116	CTCAGAGGGGTACCC[A/G]GCCGTGTGAGGTGTC	8924
rs563056575	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28112301	CCACCTGTGTGGATG[C/G]GGGGCGGCCTGGCTG	8924
rs563070941	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28154323	ATCATTGTCACATAG[G/T]CATGATTTTAAATCT	8924
rs563074942	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28287048	GAATATGTGCGTGCG[C/T]GCTGTAAAATTCTTT	8924
rs563109069	snp	C/G/T	5.34786e-05	0.00517078	intron-variant	HERC2	GRCh38.p7	15:28198806	AGATCCAGTCCATCA[C/G/T]GTACACAGGTGAAAT	8924
rs563116465	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28153680	AAAAAAAAGTAGTTG[A/G]AAGGCTCCCAACACA	8924
rs563117957	in-del	-/TTAAGA	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28208207	TAACATCCTCTCCTC[-/TTAAGA]TTAAGAAACAAACCC	8924
rs563123000	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28133026	GAGGACACGGCTTCC[C/T]CAGCTCTGACTCAGA	8924
rs563171154	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28199532	TAACAAAGCTTTTTT[C/T]CCCAGAAGAGAATTC	8924
rs563172840	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28192793	CATTTTGACAGCCTC[A/G]TGAAGGGAAGGGAAA	8924
rs563175513	snp	A/G	3.29468e-05	0.00405861	synonymous-codon	HERC2	GRCh38.p7	15:28111871	CTCTCCTGTAAGTGC[A/G]ATGCGAGCGTAGTCA	8924
rs563180074	snp	A/C	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28294449	AAGTAGATACAGAAG[A/C]ATTTCTCGTGTGGCC	8924
rs563190895	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28268368	TACATGTCAGGGCAA[C/T]TGGAAAACACCTGGA	8924
rs563199964	snp	C/G	0.0023933	0.0345097	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317294	GGGTTTCACCATGGG[C/G]GCCAGGCTGGTTTTG	8924
rs563209749	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28250389	GTAACACAAGAAACA[G/T]GTCTAGAATCTAACA	8924
rs563227322	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28264923	AATGGCAGCAGGACC[A/G]ACATACAGGGAAGTA	8924
rs563227424	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28303784	CTTGGGTTAGTTTTA[A/T]TCCTACGTATTTTAC	8924
rs563231630	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28169120	ATACTGCAAAATGCC[A/G]CACTGGCAAAACTCA	8924
rs563233035	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28273426	AGGCAAAATGTCAAC[A/G]CTAATTTCTATCTCT	8924
rs563246760	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28243565	GATAGAAAAATGCGC[A/C]CAAAACTTGAATTGG	8924
rs563259102	snp	A/G	1.68539e-05	0.00290287	intron-variant	HERC2	GRCh38.p7	15:28255847	TCAGTGCACCACCAG[A/G]TCACGTGTGCCTCCA	8924
rs563259275	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28232008	GGCCCAGGCTGAGTT[C/G]CTGCATGCCTGGGTT	8924
rs563266790	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28126266	CTAACAACAAGCTAT[C/G]TGTGAAAACGCGTTG	8924
rs563288640	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28162854	CGAGATGGCGCCACT[A/G]CACTCTAGCCTGGGC	8924
rs563330285	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28157245	CTTTGGTATCAGGAT[A/G]GTGCTGGCCTCATAA	8924
rs563337174	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28208059	GAACAGAACAGCCAA[A/T]CCAATTCCCAGGCTC	8924
rs563340774	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28150811	ACTTCTAAGGGGAAA[A/G]GATGTTATCATTATC	8924
rs563374890	snp	C/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28194293	GATGGTCTCGATCTC[C/T]TGACCTCGTGATCCA	8924
rs563375595	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28114551	ACACACATGTCCACA[A/C]AACCACGTTCTGCTA	8924
rs563378398	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28264566	CAGCACAGCAGGGAC[A/G]CTTCCCTACAAGATC	8924
rs563398180	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28114111	GCCCACCTGCCACAC[G/T]GGGCCTCACCCAGAC	8924
rs563399483	snp	A/C	0.00597247	0.0543191	intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28319996	AGATCATTATAGCTA[A/C]ATCAAAGGAAATGTT	8924
rs563439366	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28282261	AGTAAGACCTAGAGT[A/C]GCCTAACAACATGTT	8924
rs563442640	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313308	TCAGCCTCCCGAGTA[G/T]CTGGGACTACAGGCG	8924
rs563470218	snp	C/T	0.000399281	0.0141238	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28270719	TGTCGGAGAGCTACA[C/T]AGCGGAGGCATACAG	8924
rs563496910	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28152905	ATGCCACCTCTGCCC[A/G]TCCTGCTCAGGAGCT	8924
rs563498451	snp	G/T	0.0170251	0.090679	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28319070	GCTTCCATCTGCAAT[G/T]CCTGTCTGCAGGGAA	8924
rs563501927	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28276073	GTGCCTGTAGTCCCA[A/G]CTACTCGGAGGCTGA	8924
rs563517577	snp	C/T	0.000165637	0.00909896	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28248583	CTGACCAATACTTTC[C/T]CCTGGATAAAGTTTA	8924
rs563518607	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28157847	TAGGGTGTCAATTTT[A/G]GATCTTTCCTGCTTT	8924
rs563547881	snp	A/G	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28218050	CCCCTATCGTACCTC[A/G]GCAGGTGACCTTGTT	8924
rs563564645	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28307805	CACCATTTATTGAAG[A/G]GATTGTCTTTTCCCC	8924
rs563565789	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28200621	AAAGATCCATCAACC[A/G]AATGTAGATAAGGCA	8924
rs563573285	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28190065	CCAGGCTGGAGTGCA[C/G]TGGCACGATCTCGGC	8924
rs563580934	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28194786	TTTGGCTGGATGCAG[C/T]GGCTCATGCATGTAA	8924
rs563583157	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28190816	TTGTACAAAATAAGT[G/T]GTATCTTTTAAAGTG	8924
rs563596094	snp	C/T	0.0111196	0.0737302	intron-variant	HERC2	GRCh38.p7	15:28270266	AGATAGATAGATAGA[C/T]AGACAGACAGACAGA	8924
rs563605504	snp	C/T	3.36865e-05	0.00410391	synonymous-codon, downstream-variant-500B, nc-transcript-variant	HERC2	GRCh38.p7	15:28186618	CTCCTCTTCATTATC[C/T]GAAGCTAAGAAAGGA	8924
rs563609623	snp	C/T	1.78694e-05	0.00298905	intron-variant	HERC2	GRCh38.p7	15:28218478	TGGGCCCTCGATCTC[C/T]CATTCCATACATGTC	8924
rs563610355	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28183937	TCACACCTGTAATCC[C/T]AGCACTTTGGGAGGC	8924
rs563633411	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318393	GCACTTCCGGAGGCC[A/G]AGACGGGTGGATCAC	8924
rs563644026	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28163876	AAACATACCACATCT[C/T]GATCCTTCAACTCCT	8924
rs563664291	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28241856	AAAAGAAGGGACGCA[A/G]ATGGATATACACACC	8924
rs563666068	snp	A/T	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28236025	ACAGTCCTCAAGTAG[A/T]ATGCTGTTCCCTGAG	8924
rs563685725	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28175728	ACAAGAAGACACTCA[C/T]TGTCTCACATCTTTC	8924
rs563694969	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28149645	CACGAACGTACATTC[C/T]AGTAAAATTACCGAA	8924
rs563701103	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28236312	CCTCTCCTTTTGAGA[C/T]GGAGTCTCGCTCTTG	8924
rs563705405	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28285670	AAATCAACCCAAAAG[C/T]AAGCAGAAAAGAAGA	8924
rs563713295	snp	C/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28118848	AATTTCCTCGCTTTG[C/G]GAGGGGCATGCTACC	8924
rs563720824	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313848	GAGAGGAAGAAAGAG[A/G]CCCAGAGAACCTAAG	8924
rs563729944	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28159630	TTCTAGTTAGCCATT[C/T]GTCTAATCTTTTTTC	8924
rs563744102	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28279085	CAACCTCCACCTCCC[A/G]GGATCAAGCAATTCT	8924
rs563771785	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28224561	CTGATGTGATTAAAA[G/T]AGCTTGGGAAAACCT	8924
rs563800808	snp	A/G	0.0146672	0.084371	intron-variant	HERC2	GRCh38.p7	15:28139158	TAGAACCAAGCCTGC[A/G]TATCTCCAAGCATGC	8924
rs563808156	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28227777	ATAAATGAACAAAAT[A/G]TTATATATTCATACA	8924
rs563822823	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28116505	TATAGGCGTGAGCCA[C/T]CGCGCCTCACCCTAA	8924
rs563823025	snp	A/G	6.6324e-05	0.00575826	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229765	AGGAGTGGAGACTGC[A/G]GATAAAGACCCTGCA	8924
rs563848205	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28186440	ACAATTTTTGGAAAC[A/T]ACTGTAATTTACCAA	8924
rs563877577	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28182140	CAAGATACACCTATT[G/T]ACAGTCTATAATTTT	8924
rs563897371	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28304416	TCTGTAGCCCAGGCT[A/G]GAATATAGCGGCACA	8924
rs563902169	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28223974	AAAAGGCCATTTCTC[A/G]ATGGAGATATGCTTT	8924
rs563911967	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28186845	GAGACACGAACATGT[A/G]CACACGGTTAGAGCT	8924
rs563917787	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28152579	TGTAACTTCTTTTTA[G/T]AAAATGGAGATGGTT	8924
rs563933565	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28262374	TGCACCGGCAGCCCA[C/T]ACTGAAGGCGCCGGC	8924
rs563938019	in-del	-/A	0.0356815	0.128715	intron-variant	HERC2	GRCh38.p7	15:28279816	AGACATTGTCTCTCC[-/A]AAAAAAAGAAAAGAA	8924
rs563962721	snp	A/G	0.000399281	0.0141238	intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28316120	TCCAGCCACTTAGGA[A/G]GCTGAGGCATGAGAA	8924
rs563979471	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28271522	AAATACAAATATATT[A/G]GCTGGGCTTGGTGGT	8924
rs563981651	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28132512	CCATGAAGGCTGTTT[A/G]TTCACTTCTTGCACC	8924
rs563986304	snp	A/C	0.00517822	0.0506191	intron-variant	HERC2	GRCh38.p7	15:28305587	ACCCTAGAAGAAAAC[A/C]TAGGCATTACCATTC	8924
rs564019045	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28255225	CTGTGGTCCCTGCAA[A/C]ACAGGAGGCTGAGGT	8924
rs564021813	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28272038	CAGTGCTCACTGATC[C/T]GAGTCTTCTCCACAA	8924
rs564022916	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28275239	AAGGAATTTTAAATG[C/T]CTTGGGAAAATGCTC	8924
rs564048516	snp	A/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28310146	CGTCTCTACAAAAAA[A/T]TTGTAAAATTAGCCA	8924
rs564053651	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28306259	TCTATAACCAGTTTT[C/T]TGGGGGTTTTTATCA	8924
rs564060683	snp	A/C	8.2464e-05	0.00642069	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265871	ACAGCTCCCCCTCGG[A/C]AGTGATGGCCGCACT	8924
rs564066094	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28232971	CATTGTCTGATTACT[C/T]GGAAAAACAAGCGAG	8924
rs564105317	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28133494	GAATCATGCTTTTGG[A/T]GTTCAATCTAAAAAT	8924
rs564105686	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28239653	ATGCAGCATGACCCC[A/C]GACATAACACCGCCC	8924
rs564110884	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28269600	TATTACCTCATTTAA[C/T]AGGTAAGATGAAGCA	8924
rs564111092	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28116168	CAACAGCACCTCGTT[C/T]GCTTCCACAATGTTG	8924
rs564113614	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28153067	CTATGTTAAAAAGTC[A/G]TTGGGGCCAGGCACG	8924
rs564118599	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28220893	GACCTCAGTTAGGAG[A/G]GTGCATGCCCTGCCC	8924
rs564125065	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28267651	CATACATGTACCACA[C/T]GATACGCATTACTCT	8924
rs564137247	snp	A/G	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28146797	TGGTGTGGAGAACCC[A/G]CACATCTGGTGTGAG	8924
rs564144545	snp	A/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28197977	ATATGAATGACTACT[A/T]CCTTACCAATCATGA	8924
rs564172584	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28148575	CCCGAGAACATCACC[A/G]AGAACGGCCGCATGA	8924
rs564190311	snp	C/T	0.000823624	0.0202764	intron-variant	HERC2	GRCh38.p7	15:28234293	AGCCATTCTGGAAAA[C/T]GCACACGCAAACATG	8924
rs564202289	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28256593	AACCTCCACCCCGCG[C/T]CAACAATCTGCACCA	8924
rs564209970	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28267271	CAGCTTAAGTTTCAA[C/T]TTCCCCAAAAGGTTA	8924
rs564230518	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316614	TATTTGGATATTAGA[C/G]GTAAAAACCACCCTT	8924
rs564251604	snp	A/G	0.000399281	0.0141238	missense	HERC2	GRCh38.p7	15:28142299	ACAGCAACACGGGAG[A/G]CCATGCAGTACCTCC	8924
rs564291000	snp	G/T	0.000399281	0.0141238	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28257117	CTTTCTCCTGGGGCG[G/T]GGGCCAGTCCGCGGA	8924
rs564295004	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28164179	TCCCCAGAGGAAGAT[C/T]GAGAGCCAGGGAAGT	8924
rs564312885	snp	A/T	1.71258e-05	0.00292619	synonymous-codon	HERC2	GRCh38.p7	15:28142932	TTTCACCAAAGCAGC[A/T]AGAGCACTACCTGTA	8924
rs564323548	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28136738	CCAGGGCTGCTTTTG[C/T]AGTCGCAACAGAGAC	8924
rs564326055	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28251539	GGCGCGGTGGCTCAC[A/G]CCTGCAATCCCAGCA	8924
rs564326472	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28266345	ACATGGTGAAATCCC[A/G]TCTCTACTAAAAATA	8924
rs564331340	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28258861	AAAGAAAAAAACAGA[A/G]AAGATACAAATTATC	8924
rs564337950	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28120469	GTTTCATTTGAGCAT[C/T]AAATGTCAAGTTCTG	8924
rs564347161	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28264520	AGGGTAGGATACTTC[C/T]ACTGTAACAGTCGCC	8924
rs564356394	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28164953	TTCTGTAGGACATAT[G/T]TTCTGCCAGCAGTAA	8924
rs564373467	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28215970	AAAGTGAGAAGTGGA[A/G]GGCAGCTTTTAAGTT	8924
rs564384931	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28175324	ACCCCGCCCCCAACC[C/G]CTGCTGCAAAGCAGG	8924
rs564389980	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28178426	GGAGAAAAGTAAAAC[A/T]CTATATTGCTTAAGC	8924
rs564398969	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28135001	TTATATGGTGGTTTA[A/G]TTATTCCTAGGATAA	8924
rs564412596	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28263805	GGGAGGCCAAGGCGG[A/G]CGGATCACTTGAGCC	8924
rs564418458	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28129840	GGAGTGCAATGGCAC[A/G]ATCTTGGCTCACTGC	8924
rs564446156	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28241737	AGGCAGGGGAATTGC[C/T]TGAACCTGGGAGACA	8924
rs564446226	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28172718	AAGGTTTTGTAGACA[C/T]AACATCAAAAGTACA	8924
rs564462491	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28153701	TCCCAACACACACAA[C/T]ACTTAATATGTGCCA	8924
rs564463290	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28308908	CCCACTTGGTCACAA[C/T]GAACGATCTTTCTAA	8924
rs564470124	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28225882	AAAACATAAATTACC[C/T]GAACTGACTCAAGAA	8924
rs564470977	snp	A/G	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28165634	TATCTCTGAAAAAAA[A/G]AGAGAAAAAAAAAAA	8924
rs564477990	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28295696	AGCCACCACGCCCGG[C/G]CACCGTATTTTATAG	8924
rs564500978	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28309428	ATAATGACTTTTTTG[C/G]TCTCCTTTTATAGTT	8924
rs564510803	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28127476	CCTGGGGATACTGGT[A/G]TGAACTCACAGTTTT	8924
rs564524792	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28252261	TCAAACAGCATAGTT[C/G]CAGGTCAAACAGGCC	8924
rs564541576	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214396	GGCACAGGGAAGGGA[A/G]ACGGCCATGCACCTC	8924
rs564560757	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28157770	ATCTTAGTTATTTTT[G/T]GCCTTCTGCTAGCTT	8924
rs564564555	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28265184	TCAGGTACCCTTGAA[A/G]AAAGGATGATCTCAC	8924
rs564585285	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28187664	TTGAAAAACATATCC[A/G]CATTGCTATTATCAT	8924
rs564594214	snp	C/G	0.102726	0.202016	intron-variant	HERC2	GRCh38.p7	15:28245604	ACACACACACACACA[C/G]AGATATATATATACA	8924
rs564601099	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299880	AACACGGTGAAACCC[C/T]GTCCCAACTAAAAAT	8924
rs564621488	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28295086	CACTAGACTTGTTAG[A/G]ATGGCTCAACTAAAA	8924
rs564631490	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28238965	TTTAAAAAAAAATCT[A/C]GGCAGCATGAATACC	8924
rs564648329	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28197608	AATACAAAAATTATC[C/T]AGGCATGGTGGTGGG	8924
rs564648492	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28199843	GGGAGAGAGGAAGAT[A/G]TTAGCCACAAGGAAG	8924
rs564651634	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28251106	GCCACCTGCCGAGGA[C/T]ACCAATGGAGCTACA	8924
rs564653026	snp	G/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28209278	TTCAGAATAAAACAA[G/T]TTTTTAAAATATAAT	8924
rs564657447	snp	C/T	0.246485	0.249975	intron-variant	HERC2	GRCh38.p7	15:28158913	TGCTTCCTTCAGGAG[C/T]TCTTTTAGGGCAGGC	8924
rs564690065	snp	C/T	0.000399281	0.0141238	missense	HERC2	GRCh38.p7	15:28135518	CATCTTCTGCCTCAC[C/T]CCAAGAGTAAACTTC	8924
rs564726077	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28209909	AACAATACCAAAAAG[A/G]AGGCCATAACGACAC	8924
rs564733949	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28121618	GCACACAGGGACAGA[C/T]GGCCAGGCAGGTAGT	8924
rs564751399	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28162157	CAACATGGTGAAACC[C/T]CATCTCAACTAAAAA	8924
rs564771114	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28122108	ACAGAAAAGACAGAC[C/T]GGGGAGGGGAAACAA	8924
rs564774653	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28307158	TATCTATTTCTTCCA[C/T]GTTTCCCAATTTATT	8924
rs564781016	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28320712	TTTCCAAATAAAAGT[A/T]GATTGGGTGTAAATA	8924
rs564781905	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28290819	GGCTAAACAATGCTT[A/G]GAGGGAAATTTATAT	8924
rs564810269	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28246177	TAAGAAATGTTTGTC[C/T]TTTAGCATATTTCTA	8924
rs564861994	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28162772	GGTGGGCACCTGTAG[C/T]CCCAGCTACTTGGAA	8924
rs564883879	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28168334	TAAACTAAATGACAC[A/G]ATGAGACTTTCCTAG	8924
rs564888552	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28298150	CATGGTTTGTTTTGT[A/G]TTTTTTGTTTTTTTT	8924
rs564903094	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28217275	GGCTCAATGCACTGA[C/T]GCTTTCACTCCCACT	8924
rs564916153	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28210497	CGGAATGACTTGCTG[A/G]GCCAAAGTATATAAA	8924
rs564921753	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28299072	ATGATAGTCTTACTG[A/C]GCATGCAAAACTACA	8924
rs564969447	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28173953	GGAACGCTGGGGTAG[C/T]GTATGAGTTCATTAT	8924
rs564984948	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28205064	TTGTATACATGAGCC[C/T]AGCTTAGGGAAACTG	8924
rs564997886	snp	A/G	0.0185938	0.0946107	intron-variant	HERC2	GRCh38.p7	15:28206137	TATTTGCGTACTATC[A/G]TTTAACATTCAGAAT	8924
rs565002151	snp	C/G	1.65847e-05	0.0028796	synonymous-codon	HERC2	GRCh38.p7	15:28116819	ACAGATCTCAGCTAT[C/G]GACTCGCTGTAGCCG	8924
rs565043768	snp	C/T			missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256118	AGAGCAGAGAGTGCC[C/T]GGGCCCGCTCCTCCG	8924
rs565049254	snp	C/T	1.6486e-05	0.00287102	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28201548	CCGTCACAACAGCAC[C/T]AGTAGACTGCAAGAA	8924
rs565052062	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28212200	GGATAAAGGGTGACA[A/C]GGAGAAGAGGGTGTG	8924
rs565060933	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28293328	GAAACCCCATCTCTA[C/T]TAAAAATACAAAAAA	8924
rs565065694	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28282662	CCCAAGGCAGGGCAC[A/G]GTGGCTCACAGCTGT	8924
rs565083645	snp	C/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28293781	ATGCAGAGGCACTGT[C/G]ACTGATAGCATAATT	8924
rs565097870	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28288371	TCTCTACTCAAAAAT[A/G]CAAAATTAGCCAGGT	8924
rs565104849	snp	A/C	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28291448	ATGCAAGGAAAAAAA[A/C]CCCTGAATATCCACA	8924
rs565116781	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28247109	TTATACCCTGCACTA[C/T]AGAGTACCTAGAAAT	8924
rs565130787	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28207977	TTAGGAGTCCCTGCT[C/G]GGCCCAAAGCACAGA	8924
rs565139867	snp	A/T	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28200696	CATTTCTGAGAAAAC[A/T]GGAAAACTACAAGCA	8924
rs565162277	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28241930	CAACCCAAATGTCAT[C/T]AACTGATGGATGGAC	8924
rs565167372	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28189587	TCAGTGTATTATGAA[A/G]TAGTTCCATGACATT	8924
rs565176221	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28286543	TGATTTAGAAAAAGC[A/T]AATGACAAAATTCAA	8924
rs565176936	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28112317	GGGGCGGCCTGGCTG[A/G]CGGAGGACCAGGCAC	8924
rs565187166	snp	C/T			downstream-variant-500B	HERC2	GRCh38.p7	15:28110908	GAATCTTCCATTCTC[C/T]TAATCACTTCTTTGT	8924
rs565187411	snp	G/T	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318220	TACAAGTACTTTCAC[G/T]GTAAAAATAAAAAGT	8924
rs565188725	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28252481	GCTCACTTTAAAACT[C/T]TGCGTGGAACTTTAC	8924
rs565196320	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28236338	TCTTGTCACCAAGGC[G/T]GGAGTGCAGTGGCGC	8924
rs565201843	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28119346	TGGAGGTTGCAGTGA[A/G]CCAAGATTGCACCAC	8924
rs565215554	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28112946	AGTTCGATGTTTTCC[A/G]TTTTCATTTCTGTAA	8924
rs565225701	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28250102	GCTCTCTGCACAACA[C/T]CAAGAGTGAGGACAT	8924
rs565266577	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28253301	CTTTCACATTGACTT[C/T]AGTTTTGAAAAGAAA	8924
rs565314007	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28145972	TCTGGCACCTCACAC[A/G]TCTCCAGCACCTTCT	8924
rs565319009	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318612	TGGGAGACAGAGTCA[A/G]ACTCCATCTCAAAAA	8924
rs565321954	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28291862	GTGAGCCAAGATCAC[A/G]CCACTGTACTCCAGC	8924
rs565329962	snp	A/C	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28122842	TCCCCTACCACACAC[A/C]AGCTCCCACCCATGC	8924
rs565331229	snp	C/T	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28241048	AAAAAAATAGGTAAG[C/T]TGGACTTGATCAAAA	8924
rs565335317	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317341	TGATCCGCCCTCCTC[A/G]GCCTCCCAAAGTGCT	8924
rs565360598	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28287135	AAAAAGGAAGCTTTA[C/G]TCAAACATATCTAAG	8924
rs565373909	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28311308	GGTCTCTACAAAAAA[C/T]ACAAAAATTAACCAG	8924
rs565384905	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28114222	GGCACCCAAAGGACC[A/G]TGCACAGTCACACCT	8924
rs565385845	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28120198	CTATTTATGTGAGGA[C/T]GTGACTGACGTACAG	8924
rs565387129	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28240525	TGTTAAAACTAGATT[C/T]ATTTTACTATTTTTC	8924
rs565388246	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28217791	AACACAGGGGCAGGG[G/T]CCATGTGAAGACGCA	8924
rs565399567	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28185288	TCTCCTCATGTCACA[C/T]GCTGCAGAGTACTTA	8924
rs565407483	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28319144	CACCACCATTCATTC[C/T]TTGTGTTTAACAACC	8924
rs565408288	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28160538	CCTCCGAGCCAGGCG[C/T]GAGATATAATCTCCT	8924
rs565432881	snp	A/C	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28267240	GACTCTACTCCAGTA[A/C]AAACTATCCCTTATT	8924
rs565436941	snp	C/T	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28194177	TTCACGCCATTCTCC[C/T]GCTTCAGCCTCCCGA	8924
rs565447525	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28280703	TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA	8924
rs565449204	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28224999	AAAGCAGGGATGAAG[A/G]GGCAATTATACTATG	8924
rs565470274	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28154410	GCCATCTTGCCAACC[G/T]GGCAAGGGCAGTTTG	8924
rs565476022	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28149303	ACACACGCAGCTCCT[C/G]AGAACATCACCGAAA	8924
rs565487126	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28273612	AACTCTGTGGTGATG[C/T]CTTCACCAGCCGGCT	8924
rs565492890	snp	A/G	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28118715	TGGCGGGTTGGAGGC[A/G]CCTGTGCAGCCTTCC	8924
rs565510633	snp	C/T	0.0023933	0.0345097	intron-variant, utr-variant-5-prime	HERC2, LOC107987422	GRCh38.p7	15:28317704	TGAAACAGTTCTGCA[C/T]AGGAAATTGTAGTAG	8924
rs565510753	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28193539	TAGAAAAGAGAATAG[A/G]GCAGAGGCAACATGT	8924
rs565511144	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28282884	TTGCAGTGAGCCGAG[A/G]ACGTCCACTGCACTC	8924
rs565537501	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28225509	GAGACCATCCTGGTC[A/G]ACACGGTGAAACCCC	8924
rs565555077	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28150518	GAATATCACCGAGAA[C/G]AGCCACATGAACGTA	8924
rs565579266	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28154725	CCCTCTCTACTGAGA[A/G]TGTGGGGATGTGCAT	8924
rs565589220	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28187993	GCCTAAACGACCTGC[C/T]CAAACCTCAAGATCT	8924
rs565604301	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28267956	CCATCACTCCATGGG[G/T]CTGGCAGACCTCCCA	8924
rs565606829	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28134462	TTTTATTTCTTTGCA[C/T]TGCTGTACCGCACTT	8924
rs565632446	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28156661	TTTAGGCTGAGACGA[C/T]GGGGTTTTCTAGATA	8924
rs565643977	snp	A/T	0.140242	0.224618	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314519	AGAAAAACATATATT[A/T]AAAAAGTGATTTTAT	8924
rs565667516	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28145602	CTGGGACACAGCCAC[A/G]CCCATTCTCTGGCAT	8924
rs565676452	in-del	-/ATAGATAG	0.00292183	0.0381101	intron-variant	HERC2	GRCh38.p7	15:28270245	TCTTTTTATTTATTT[-/ATAGATAG]ATAGATAGATAGATA	8924
rs565687813	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28275597	ATTCTGCATGTTCTA[A/G]AAGGTTATGCATATG	8924
rs565734767	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28275220	AAGAATCAAAGAAAT[C/G]TATAAGGAATTTTAA	8924
rs565738317	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314230	AAATGAAAAAAAAAA[C/T]AGAAGTCAACAGAAC	8924
rs565747775	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28150585	TTCTAACCAAGAACA[A/T]CACCGAGAATGGCCA	8924
rs565752896	in-del	-/CTC	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28250329	GGCTCACCACCACCA[-/CTC]GACATCACCTTCACT	8924
rs565752924	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28263733	TTAAAGTGAATTGCT[A/G]AAAAACAGAATTGTT	8924
rs565756743	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28195726	AGAGTTTCTGATCGG[A/C]GTGGTGAAAAGTTTT	8924
rs565762361	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28188886	TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA	8924
rs565762467	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28181219	AGCGGAAGAAAGGAT[G/T]TTCATCACAACCGTG	8924
rs565767910	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28191384	GAGAATTTTCCCTCA[A/T]CCTGGCAGCAACAAG	8924
rs565768562	snp	G/T	1.69132e-05	0.00290797	intron-variant	HERC2	GRCh38.p7	15:28299394	AAACACTAGTTAAAG[G/T]CCCTTACCTTTTCTA	8924
rs565771108	snp	C/T	1.65482e-05	0.00287643	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28269337	AGGCAATCTGTGTGA[C/T]TCCCAGGTTGGCCAG	8924
rs565775419	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28171882	GATCGATTCTGTCCT[A/G]GCTAACACGGTGAAA	8924
rs565791891	snp	A/T	4.12218e-05	0.00453974	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256280	AGACCTAAACCAAGG[A/T]ATTCCGGGTCAACCT	8924
rs565809885	snp	A/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28270305	ATAGATATATAATAT[A/T]TAATATATAACATAT	8924
rs565823617	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28182254	TTTTTCAAGGAGAGA[C/T]GCTTCTGAGGGGTAA	8924
rs565824509	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28256885	CAGGCGTGAGCCACC[A/G]CGCCCAGCCCAGATC	8924
rs565846266	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28192674	AACCGCAGGAAGACC[C/T]GAGGCGAATGGAGGT	8924
rs565846517	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28169977	TGTATTTTCTTACCC[C/T]GGTAAGACAAGACAA	8924
rs565855481	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, utr-variant-5-prime	HERC2	GRCh38.p7	15:28299744	CTATGCTACCTCTTA[C/T]GTAACATACAAGAAA	8924
rs565858049	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28146122	TAGCATATTGTCCCT[C/T]CCTTAAGACTTCCAT	8924
rs565860013	snp	C/T	0.000680266	0.0184301	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214175	AGTCAGGGAGTGCAG[C/T]GTGCGCAGCAGTGCC	8924
rs565861810	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28291884	TACTCCAGCCTGGGC[A/G]ACAGAACAAGACTCC	8924
rs565897192	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28293607	AAACTTAAGTCTTTG[A/G]TATTTACCTACTTCA	8924
rs565897271	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28300040	CTGAGTGACAAGAGC[A/G]AGACTCGGTGTTAAA	8924
rs565910396	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28183983	CCTTGAGCCCAGGAG[C/T]TGGAGACCAGCCTGG	8924
rs565916438	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28301470	CTCCTGACCAAATTT[A/G]TAATAATTATAATAA	8924
rs565934414	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28207604	GCTTTTTGTCTGTTA[C/T]GAGTAGCTTTAGGTG	8924
rs565941829	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28116615	TACATTTTAACTCAA[G/T]AGCAGGCACAGGCCA	8924
rs565943048	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28148907	CTAGTAAAATTACTG[A/G]AAAAACACACAACTC	8924
rs565945868	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28182018	AAGAATCTCAGGCGC[A/G]AAGCACCTGGAGGAC	8924
rs565958558	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28268789	CACCCAGCAGCAACA[C/G]AACAGCGGGCAGCCT	8924
rs565970057	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28175844	ATTAAGCCAGCTGGG[A/G]AAAACCTTAATACCT	8924
rs565972299	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28223428	CCAAGAGAGCAACAA[A/C]GGATATTCAATTCCC	8924
rs565977457	snp	A/G	0.0429648	0.14013	intron-variant	HERC2	GRCh38.p7	15:28293947	TTGAAGTGTAAACAC[A/G]TTCCATCACAGAAGG	8924
rs565981795	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28176346	CGTCACAATCACGCC[A/G]GGTGAGCCTGGGGCG	8924
rs565984624	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28302788	GTTCGTACTGCCTGT[C/T]TGTCATTTGTATATC	8924
rs565989554	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28133423	AATCTCTTCATAGTG[C/T]CTTTTGAAGAACAGT	8924
rs565992621	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28219885	CCTCCCGCAACCTGG[A/G]TCTCCACAGATAGGA	8924
rs565995364	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28261776	TAGAAAACAATAAAC[A/G]CCATATGGGCGCACA	8924
rs566001853	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28201269	GTAGTCTGTTCTTTC[C/T]CATTCCAGGGTACAC	8924
rs566006850	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28256728	GCCTCCCGAGTAGCT[A/G]GAACTACAGGCGCCC	8924
rs566041114	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28113831	GAGCATGCTTAGCAG[C/T]TCGGCACTGCAGAGC	8924
rs566059982	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28307081	CTCAAGTGACCCACC[C/T]GCCTCAGCCTCCCAA	8924
rs566067550	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28218188	AGATGACGGCAGAGA[C/T]AGGGGTGACACCTCT	8924
rs566070338	snp	A/G	0.000132437	0.0081364	intron-variant	HERC2	GRCh38.p7	15:28144820	CTGCGGGAGGAAAGC[A/G]CACCCCGGGGTTAGC	8924
rs566077306	snp	A/G	1.86827e-05	0.0030563	intron-variant	HERC2	GRCh38.p7	15:28229876	ACAATTTTCATCATT[A/G]GTCTACCCTATTTAA	8924
rs566080627	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28217643	ACTTCACATACATTC[A/G]GAACCTCAGAATATG	8924
rs566082863	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28261069	GACAGCTTTTAACAT[G/T]AACTTCTTGAGGATA	8924
rs566083262	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28138154	GGTTTAAGGAAAGAC[A/G]CCGTCTTCATAACAT	8924
rs566092003	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28146164	GGCAGCATTCTGTCC[C/T]ACAAATGTGAAGGGT	8924
rs566094382	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28219120	CATATAACTCAGAAG[C/T]AATAAATGATTCCAA	8924
rs566131135	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28212314	CATTCCCAACCGCAA[C/T]TCAACAAATGGTGAG	8924
rs566132709	snp	A/G			synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214169	CCACTGAGTCAGGGA[A/G]TGCAGCGTGCGCAGC	8924
rs566144759	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28138691	AGTTGTTTTCATGCC[A/G]GCTAACACATCATTT	8924
rs566164358	snp	A/C	0.00795532	0.062565	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174210	GCAACATACTTTCTT[A/C]TAAAATTTTCATTCC	8924
rs566182373	snp	A/C/T	9.92326e-05	0.00704318	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28186661	TCTTCCTCTTCTGCA[A/C/T]GGATCCGTCCCAGCA	8924
rs566213110	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28119130	AAAAAGGCTGGGTGC[A/G]GTGGCTCATGCCTAC	8924
rs566218459	in-del	-/CA	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28247782	TGTCTTTAAGATGGT[-/CA]CACCTCTTTCAAACT	8924
rs566220096	snp	A/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28254720	TCTTCTTTTTACAGA[A/T]TCAAGGTCCAGGCTG	8924
rs566220418	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28177813	AAAATCAAAATTTAG[A/G]TGAAAAAAGTAAAAA	8924
rs566251508	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28296742	TGGAAGACACTGTCA[C/T]ATGGACACTCTTAGC	8924
rs566256255	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28249387	GCTCCAGTTCCAACA[C/G]TGTGATGTGACTTGA	8924
rs566267700	snp	C/T	0.00199481	0.0315187	intron-variant, utr-variant-5-prime	HERC2	GRCh38.p7	15:28212913	TAAAAAAGAGTACTT[C/T]ATAGAAAATATAGTC	8924
rs566290814	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28297569	AAAAAAAAAAACATG[A/G]AAATCAAAAGCACTA	8924
rs566292140	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28243206	ACTATGGACAAAATG[C/T]CCATGGAAAAAAAGT	8924
rs566302123	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28143790	CCCAACTCCTCTCAA[C/T]GATTTAGAGGTTTAG	8924
rs566311994	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28288763	TGAGGCAGGAGACTC[A/G]CTTGAACCCACGTGG	8924
rs566333487	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28204649	AGATAGACTTAAAGG[A/T]TGAAGAAAGGAACTG	8924
rs566334831	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28126184	AAAAGGGAACACTTA[C/T]ACTGCTGGTGGGAAC	8924
rs566336124	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28249980	AACTCTTATGTCAAT[A/G]TGAAAGCAAATCAGA	8924
rs566338833	snp	C/G	0	0	intron-variant	HERC2	GRCh38.p7	15:28169345	ATCACCATCAAAGAA[C/G]TTGTGACTTACAACA	8924
rs566340803	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28181887	GATCATGGCGCTCTC[C/T]ACCCACAACAAGCCC	8924
rs566348786	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28282354	TTATAGAAATACCAC[A/G]ATGAAAGATGTTGGA	8924
rs566349764	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28142443	TCAGAAATGCAGTGA[A/G]CAGGCCAAGGTTTCT	8924
rs566358210	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28257565	GATCTCCATCCACTT[A/G]AAGTGGTATAATAGC	8924
rs566372357	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28186443	ATTTTTGGAAACAAC[G/T]GTAATTTACCAATCG	8924
rs566394643	snp	C/T	1.65059e-05	0.00287275	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28198500	GAACTTGGTGGAGGA[C/T]AGCCTACAGATGTCA	8924
rs566415804	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28162874	CTAGCCTGGGCGACA[C/G]AGCGAGACTCCGTCT	8924
rs566423816	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28156239	TAGGATTGACTTGGC[A/G]ATGCGGGCTCTTTTT	8924
rs566437427	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111562	CCCTTGGAAGTCGAG[C/T]GTCCACAGTGTTCCA	8924
rs566441685	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28171813	GGTGCGGTGACTCAC[A/G]CCTGTAATCCCAGCA	8924
rs566459121	snp	A/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28310259	AAGACCAGCCTGAAC[A/T]ACATGGCAAAACCAC	8924
rs566459129	snp	A/C	1.64773e-05	0.00287026	intron-variant	HERC2	GRCh38.p7	15:28141692	ACACAGCCTCTCACA[A/C]TCACGATCGACATTA	8924
rs566474566	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28227458	GATGGCCTTCATCCA[A/G]AAAAAAAAAGAAAAA	8924
rs566474624	snp	C/T	1.67027e-05	0.00288982	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28220617	CCAGCTCACCAATCA[C/T]GCGGCCTAGGCCTGG	8924
rs566482109	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28135991	TACAATTAACACCAA[A/G]AAAAATAAAAAACAA	8924
rs566488244	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28220934	ATGGCTCCCACCAGA[C/T]CTGTTAGGAGGGTGC	8924
rs566497017	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28304433	AATATAGCGGCACAA[C/T]CTCAGCTCACTGCAA	8924
rs566507274	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28135102	TCTTTTACAAATGGT[A/G]TCAATTGTGCGTTCT	8924
rs566507355	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28251152	GTTCTTGGTTGTATT[A/C]ATAAATGTGGCCAGG	8924
rs566517109	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28258241	TTGGGAGGCCAAGGC[A/G]GCGGGGATCACCTGA	8924
rs566552120	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28210583	AGATGGCTACACCAA[C/G]TGAAATTCCCAGCAG	8924
rs566561959	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28283787	AGAACATAAAGGAAC[A/G]TCAAGGGAGGTAGTT	8924
rs566565695	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28135771	TTCATAAACCTAATC[C/T]ATGCTTTAGACATTT	8924
rs566572086	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28172237	TTAATGCAATCCACA[A/T]CAAAATCCCAAGCAA	8924
rs566591428	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28244548	ACACAGTTCTCTCTA[C/T]GATCAATTACAGGTA	8924
rs566592658	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28286532	TACATATCAATTGAT[A/T]TAGAAAAAGCAAATG	8924
rs566614445	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28240064	GTAGGGTTTTTTTTT[A/T]AATCCTTATCATTAA	8924
rs566623581	snp	A/G	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28123011	AAGGTAAAATTAATC[A/G]TTTGCTACTTTTTAT	8924
rs566626647	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28245638	ACATATATGTACACA[C/T]ATATATATACACACT	8924
rs566639184	snp	A/G	0	0	intron-variant	HERC2	GRCh38.p7	15:28166456	CATGTGTATAGGTCT[A/G]TTTGCTGAGAGGGCC	8924
rs566659841	snp	C/G	3.47494e-05	0.00416815	intron-variant	HERC2	GRCh38.p7	15:28116891	GCCACTCGAAGTCCC[C/G]TCACACAGTCCTGTG	8924
rs566670920	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28158183	TTTTGGAGTAAGTGC[A/G]GTGTGGTGCTGAGAA	8924
rs566685065	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28152068	GCAGGCAGGAGGTGC[C/T]TGCTGAGGCTGAGTC	8924
rs566690359	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28122284	GATGCGGCACGCAGC[C/T]GTGCCAATGGAAAGG	8924
rs566729506	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28116495	GTGCTAGGGTTATAG[C/G]CGTGAGCCACCGCGC	8924
rs566736427	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28247262	CAGCCTCCTGAGTAG[C/T]TAGATCTACAGGCAT	8924
rs566747163	snp	A/C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28126999	CCAAGAAATACCACC[A/C/G]GAAAATATTCTCAGG	8924
rs566773141	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28240275	TACAAAAAATTAGCC[A/G]GGCGTGGTGGCAGGC	8924
rs566815217	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28271802	GCAGTCCTGGAGGTT[C/T]AGGCCCAGGGCCCCG	8924
rs566822070	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28153391	GAGCGCAGTGGCTCA[C/T]ACTTGTAATACAAGC	8924
rs566827349	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28172255	AAATCCCAAGCAAAC[G/T]ATTTTATAAAAACTG	8924
rs566837420	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28284645	ATTACCAGGAAGGCC[A/G]GGCACAGTGGCTCAC	8924
rs566840010	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28185912	CATAACTGGGAATGG[C/T]CCACAGTAGGCATTC	8924
rs566849106	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214489	TGAGTGACGGCAGTA[C/T]ACCGCTCTTCACCAG	8924
rs566853515	snp	C/T	5.01811e-05	0.00500879	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28238616	CCAAGAATACTATTT[C/T]CTGTTAACGACTGTG	8924
rs566861186	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28208845	ACTCACATGCCTCAC[C/T]GCCTCCTGACCCCAG	8924
rs566890753	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28127650	CTCCACAGATGCCAG[C/G]GCTCCTTGGAGAAAT	8924
rs566917529	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28209489	GCTGGGACTACAGGC[A/G]CCTGCCACCACGCCC	8924
rs566934177	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28203483	CTGGTTCTGATAATT[A/G]AGAGTTAGGATGCAC	8924
rs566939351	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28232357	ACCATCTTGGCCAAC[A/G]TGGTGAAACTCCGTC	8924
rs566954105	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28124827	AGTGTTGGGATTACA[A/G]GTGTGAGCCACCACA	8924
rs566956633	snp	A/C	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28290375	ATCAAGATTACAGGC[A/C]CCCACCACCACACCC	8924
rs566964289	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28130891	CCAGAATGGCCTCCC[A/G]CAACCATGCTTCTCT	8924
rs566971163	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28245548	CAAGATGTAGTGTCA[-/A]AAAAAAAAAAAAATA	8924
rs566972005	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28147385	TGTAATCTTAGCACT[C/T]CGGGAGGCCGAGGCA	8924
rs566977138	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28115365	CAGCCTGACCGGACC[C/G]GCAGAACAGACTGTG	8924
rs566984688	in-del	-/AA	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28217741	GAGTCAAAGAAACTC[-/AA]AGAGTCCTTTCAGAG	8924
rs567013703	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28320239	CCTGCCTCAGCCTCC[C/T]GAGTGGCTGGGATTA	8924
rs567022520	snp	A/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28242078	TCCCAAAAGGATAAA[A/T]ACTGTATGGTTCCAT	8924
rs567027582	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28285126	CAAAGTCTCTCTCTA[A/C]AGCTGATAAAATTAG	8924
rs567043853	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28239050	ACTTATAGAGCATGT[A/G]TGCTGACTACAATGC	8924
rs567046430	snp	C/T	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28203850	GCACAAAGGGACCGC[C/T]GGAAGGCTGCAGGGG	8924
rs567050994	snp	A/C			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28314983	CCAAGGTGAGTTGTT[A/C]TAAAAGAGCACGTAC	8924
rs567052346	snp	C/T	0.00636936	0.0560724	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28320778	TAATGTCCTGACAAG[C/T]TTGCAGTTATCTCAT	8924
rs567057027	snp	C/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28309728	ACACCTGAAGTAGAG[C/G]ATAGAACTAAGCTAT	8924
rs567064373	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28278425	ACTATAACACCCAAT[A/G]CAAGGTAAATGCTCT	8924
rs567066104	snp	C/T	0.143959	0.226396	intron-variant	HERC2	GRCh38.p7	15:28155592	TCTGTTCATATCCTT[C/T]GCCCACTTGTTGATG	8924
rs567072767	snp	C/T	0.000801456	0.0200021	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28238657	CTTTATATCATACAC[C/T]TTCCCGTCAATCACA	8924
rs567079533	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28265509	CCACACCCACTGGGC[A/G]ACAGGGTGGGTGGCC	8924
rs567080554	snp	A/C	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28233035	GATGGCAGCAGGTAG[A/C]AATGTCACATGGAAT	8924
rs567085413	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28156077	CAGATAGTTGTAGAT[A/G]TGTGGTATTATTTCT	8924
rs567098321	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28197659	CTGGAGGCTGAGACT[A/G]GAGAATTCCTTAAAC	8924
rs567115551	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28115901	GGTGGGACGCACAGC[C/T]GAGGACACCCTGCAC	8924
rs567145515	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28277069	GCATCAGGGTGAGAC[A/C]CTGTCTCCAAAAATT	8924
rs567179620	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316253	AAAAAAAAAAGGAAT[C/T]GTCATCAAAGTCCTA	8924
rs567182252	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28308331	CTATAAATGGGATTA[C/G]TTTTCTAATTTCTTT	8924
rs567183965	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28227048	GGGAGGCCAAGGCAG[A/G]CAGATCACCTGAGGT	8924
rs567188269	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28148087	AAAATAACATCCCCA[C/T]AGGCAATAAAAGCAG	8924
rs567197282	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28206752	ACAGGAGAATGGCAT[C/G]AACCTGGGAGGCGGA	8924
rs567217674	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28118284	TGCACCCAGCTCCCC[A/G]AAGCCCACGGGGCTG	8924
rs567223180	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28160875	CAGCCATCTTGGCAC[C/T]GCCCCCCGCTCAGCA	8924
rs567232037	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28161656	CAGGTGCACTAGCCA[C/T]ATTTCAGTGTGCAGT	8924
rs567234080	snp	G/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28253284	AAATAATGCTCACCA[G/T]TCTTTCACATTGACT	8924
rs567245861	snp	A/C	3.75115e-05	0.00433063	intron-variant	HERC2	GRCh38.p7	15:28124243	TGGGGACCTAGAACA[A/C]AGAAATGGCCTTCAG	8924
rs567248821	snp	C/G	0.0011441	0.0238902	intron-variant	HERC2	GRCh38.p7	15:28269225	CAAGGGAACACTGCA[C/G]GCACAGTGCCCAGAA	8924
rs567308818	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28287971	CATCATGATCCACCC[A/G]CCTCAGCCTCCCAAA	8924
rs567323198	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28282219	GCAGGGTCACAGAAA[A/G]ATTTAACCACTTACA	8924
rs567328711	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28200327	ATGAACCCGGGAGGC[A/G]GAGCTTGTAGTGAGC	8924
rs567329651	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28249603	TCTGCAATGCCAACC[C/T]ACCAAGGTTATGATA	8924
rs567338095	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28219256	GCGACCAGACGCTCA[G/T]GCAGCCCGCTTGGCT	8924
rs567373505	snp	A/G	0.000798403	0.0199641	missense	HERC2	GRCh38.p7	15:28113234	TCGATGCCTTTATAG[A/G]TGGCCACCGACTTGA	8924
rs567376353	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28229971	TTAAATTTAGTAATA[C/G]ATGGTTTTAAAACTA	8924
rs567389904	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28194465	GTCGCAGCTACTCGG[A/G]AGGCTGAAGCGGGAG	8924
rs567390227	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28247183	TTTTTTTTTAACAGA[C/T]GGGGGTCTCACCATG	8924
rs567403333	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28189040	TTGCGGTAAGCTGAG[A/C]TCTGCCACTGCACTC	8924
rs567427089	snp	C/T	0.137527	0.223271	intron-variant	HERC2	GRCh38.p7	15:28311418	TGCAGTGAGCCGTGA[C/T]GGTGCCACTGCATTC	8924
rs567444544	snp	A/G	1.67638e-05	0.0028951	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28229307	CCGATTAAAAGGCGG[A/G]ATCAAATCAACATCC	8924
rs567447000	snp	A/T	0.00398564	0.0444627	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318242	ATAAAAAGTGATGTG[A/T]CTGACACCTCTTAGC	8924
rs567447089	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28201048	CTGCGCCATGTCCAC[C/G]GTGGACAGGCCACTT	8924
rs567455991	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28222505	AAAAGCAAAATAACT[A/G]AGTTAGAAAGATATT	8924
rs567472809	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28144523	CTGTGTTCTGTTCCA[C/T]GCCTCAGCAGGGCCT	8924
rs567477805	in-del	-/C	3.3676e-05	0.00410327	intron-variant	HERC2	GRCh38.p7	15:28135436	TAAAACAAACAAAAA[-/C]AAAGACAAATAGAAT	8924
rs567495301	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28188421	TGGTGGCAGGCGCCT[A/G]TAGTCCCAGCTACTC	8924
rs567499251	snp	G/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28113733	ACACTGACTTTATGC[G/T]GCTCACACCAAGCCT	8924
rs567509401	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28194875	AGCCTGGCCAACATG[G/T]TGAAATCTCACCTCT	8924
rs567516609	snp	A/C	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28137002	AACATTTAGCTAACT[A/C]AAAAAAAAAAACCAC	8924
rs567532738	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28217015	GCTCACATTCACTCA[C/T]ACGCATTCACAATAA	8924
rs567533587	snp	C/T	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313604	GTCCTTACAATTTGA[C/T]AGAAAAGTAATCTTC	8924
rs567563776	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28286663	AACCTATGCCAAAAA[C/G]AATGTCAGAAAGGGT	8924
rs567569798	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314001	AGAAATACAGGTGAG[C/T]TAGAAGTAGACCAGC	8924
rs567579705	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28235560	TGCGACACCCACTCT[C/T]GAAAGCAGCAGGAGA	8924
rs567581362	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28224214	AGATAGATAGAAAGA[C/T]TCCCCCCACCCCCAA	8924
rs567582750	in-del	-/C	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28259416	CTTTTAGAAAGCAAT[-/C]TCCAGACTCAGATGG	8924
rs567603856	snp	C/T			intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318054	TTCTGGACTTATGCT[C/T]AAAGACATGCGCCTT	8924
rs567606595	in-del	-/T	0.093417	0.194889	intron-variant	HERC2	GRCh38.p7	15:28304367	GCCCTTTATTTCTTC[-/T]TTTTTTTTTTTTTTT	8924
rs567624612	snp	C/T	1.79757e-05	0.00299792	intron-variant	HERC2	GRCh38.p7	15:28280316	CAAGAAAACATCTCA[C/T]CTGTGGACAATGTGG	8924
rs567634153	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28138078	TTCAATTCCACGAAG[C/G]CTAACAGAGGTGAGA	8924
rs567642520	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28235204	CAACCCACCACATTC[C/G]TTCTTCTGAAACACT	8924
rs567661694	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28248296	ATAAATCTTCTGTAA[C/G]ACTAAACTGAACATA	8924
rs567665755	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28273185	TAAGTGTACAATTAG[C/T]TTACACAACTATATT	8924
rs567668692	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28228566	GTAACGCAGAAAGCA[C/T]GGGCGATTACTCTAA	8924
rs567670827	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28187686	TATTATCATAGCACA[A/G]ACAATAACTCCCATA	8924
rs567694512	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28139869	TTCAAGACCAGCCTG[A/G]CCAATATGGCGAAAC	8924
rs567694992	snp	C/G	0.00636936	0.0560724	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314589	TCAGCCAAGCACGGT[C/G]GCTCACACCTGTCAT	8924
rs567708534	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28187296	TTTCAAAACTTCAGT[A/G]TATATCACTGAATTA	8924
rs567750626	snp	C/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28266753	GATCAGAGGTTGTCA[C/G]GAACTGGAGGTAGGA	8924
rs567755132	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28143724	GTGGTGGCATTACAC[A/G]CATGAGCCACCGCGC	8924
rs567779097	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28143152	AAGAGGAGTTTGAAG[A/G]CTCATCTCAGAATGT	8924
rs567788430	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28267347	GTCCTAGAATAAGGC[A/G]TAAGTTACTCATCCC	8924
rs567789531	in-del	-/TCTTT	0.0360663	0.129354	intron-variant	HERC2	GRCh38.p7	15:28287718	TATTATACTTATTCC[-/TCTTT]TTTTTTTTTTTTTTT	8924
rs567792106	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28306873	ACAGTCTCACTCTGT[C/G]ACCCAGGCTGGAGTG	8924
rs567794473	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28149326	CACCGAAAATGGCCA[C/T]ACCAACATACATTCT	8924
rs567814653	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28260687	CACAAGAACAACAAA[A/C]AAAACTCAGTGGTAT	8924
rs567838592	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28306465	ATGTGTTGTTGAATT[C/T]GGTTTGCTGGTATTT	8924
rs567849271	in-del	-/AATTT	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28136005	AGAAAAATAAAAAAC[-/AATTT]AATTATCTACTATAT	8924
rs567864057	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28210663	GGTTCTACTTGTTAC[A/G]ATACAGGCTCTATTT	8924
rs567877384	snp	A/C	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28298600	GGAGCTCGAGACCAT[A/C]CTGGCTAACACGGTG	8924
rs567880769	snp	C/G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28299204	TTTGCAATAAAAATG[C/G/T]CTTCAATTAACGTAA	8924
rs567921984	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214551	TGAGTGACGGCACTG[C/T]GCCGCTCTTCACCAG	8924
rs567927034	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28276281	TGGCAATGAAGAACA[C/T]GGCTGGCCAGGGGCA	8924
rs567935126	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28238924	AACTAATACCACACA[C/T]ACAAATTCTGTTAAA	8924
rs567953651	snp	C/T	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28231520	CAAAATCTCTAGACT[C/T]GCTCAGGTGCGCTGG	8924
rs567958371	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28167532	GGGACCGTGTCCTGC[A/G]GCATTCCCACAAACG	8924
rs567986805	snp	C/G	1.72847e-05	0.00293974	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214846	CATTAAAAAAAATCT[C/G]ATGAGGAAACTACAG	8924
rs567992402	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28225537	CCCGTCTCCACTAAA[A/C]ATACAAAAAAATTAG	8924
rs567998254	snp	A/C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28190314	GTGAGCCACCGCGCC[A/C/T]GGCCAACAAAAGTAT	8924
rs568020657	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28151010	ACTTGAAGACTGAAA[G/T]AAAGTATAGTATGTA	8924
rs568026184	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28320166	ATTGTCCAGGCTGGA[A/G]TGCAATGGCATGATC	8924
rs568028449	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28224913	TGGGTCAAAGAAGAA[A/G]TCACAAGGGAAATTA	8924
rs568055098	snp	A/C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28244851	TGATGGTCTAAAACA[A/C/T]GAGAAGAAAAAAAGC	8924
rs568081801	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28206705	GGGCATGGTGGCGGG[C/T]GCCTGTAGTCCCAGC	8924
rs568088622	snp	C/T	8.27397e-05	0.00643141	intron-variant	HERC2	GRCh38.p7	15:28146228	CCCTGCTCAACCTCC[C/T]GTCCTTACCTGACCG	8924
rs568097711	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28139961	TTGTCCCAGCTACTC[A/G]GGAGGCTGAGGTAGG	8924
rs568118345	snp	A/G	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28204851	AAGACTTTCTATTAA[A/G]ATCGTAAAAGGAAAC	8924
rs568148486	snp	A/G	5.70521e-05	0.00534067	intron-variant	HERC2	GRCh38.p7	15:28174645	AGGAGAAAAAAGCTT[A/G]TAATTTTTCAACATT	8924
rs568150220	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28303126	TTTCTTTTAGCACTT[C/T]CATAGTCTGAAGTCT	8924
rs568160067	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28263802	TTTGGGAGGCCAAGG[C/T]GGGCGGATCACTTGA	8924
rs568161836	snp	C/T	0.000282006	0.0118711	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28270829	GAAGGGTGAGGTACC[C/T]CAGGAAACTCTCATT	8924
rs568163538	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28226016	TTAAAGCAGAATTGA[C/T]ACCAATCCTCAAACT	8924
rs568179378	in-del	-/AC	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28267187	ACTAGTTTGCAAAAT[-/AC]ACACAGTGGCACAGG	8924
rs568185444	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28256805	TTCACCATGTTAGCC[A/G]GGATGGTCTCGATCT	8924
rs568187530	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28295338	GGGGGGGAGGCGGTG[G/T]GGGGGTCACTAACCA	8924
rs568198643	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28147010	TCTCTGCATGCTCTG[C/T]TGGGAGCTGATTCTG	8924
rs568206909	snp	A/G	1.65759e-05	0.00287883	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233780	CTACAGTACCTTTCT[A/G]TTTGACACAAAAAGT	8924
rs568209015	snp	C/G/T	0.000496261	0.0157446	intron-variant	HERC2	GRCh38.p7	15:28168642	CCCTTCTCCACTGCA[C/G/T]CACAGGAAGTGGAGA	8924
rs568210841	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28175293	ACTTCAGAGTGGGAA[C/T]GCCTCTTTTCTGAGG	8924
rs568230801	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28176370	TGGGGCGAGGCCCAG[C/G]TTCCCTGCACACACC	8924
rs568242771	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28166750	CAGTGACCAGTCCAC[A/G]GGAGTCCCAGTGACC	8924
rs568244307	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28140558	ACAGAATCTCACTCC[A/G]TCACCCAGGCTGGAG	8924
rs568265944	snp	A/G	0.0256215	0.110247	intron-variant	HERC2	GRCh38.p7	15:28289372	AAATTTACAAATATG[A/G]TGTAAAAATCCTAAA	8924
rs568271457	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28164288	GGACAGCCCCACATG[C/T]TCCCCTTAAGGGGAA	8924
rs568277017	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28303748	TGTTTTACAGTTTTC[A/G]TGGTAGAGATCTTTT	8924
rs568314520	snp	C/T	3.39115e-05	0.0041176	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28257247	CCACTCAGAACATGA[C/T]GACCAAGCAAAGCTC	8924
rs568356296	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28170855	GACATATTTTACCAA[A/C]GAGGAGATATGGACA	8924
rs568356573	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28307957	GGTTACTATAGCTCT[A/G]TAGTATAATTTGAAG	8924
rs568357477	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28295909	AGACCATAGGGTCCA[C/G]TGAGACCTTAAAATA	8924
rs568358804	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28138812	CAGTGATTCCTCTAA[C/T]GGATGTGGACAAACT	8924
rs568362864	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28201891	TGAACAAGGGTCTGT[G/T]CTGAAGCTAAAAGTA	8924
rs568369564	snp	A/T	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28171642	AAGCTCACTTTTTTT[A/T]AAAAAAAAAGCAATT	8924
rs568373032	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28195608	ATGGTTTCACCTAGA[C/T]GAGATGTCTGGAGTG	8924
rs568434672	snp	A/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28213421	ACATGTTTGTTTTTT[A/T]AAAACTTGAGTTGTT	8924
rs568435248	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299822	TTTGGGAGGCCGAGC[A/G]GGGCACATCACGGGG	8924
rs568439015	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28254941	GAACACGCACCTGCC[C/G]CAGGACCTAACAAAT	8924
rs568439844	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28209012	CTATTAAAAGTGACA[C/G]AAGCTCATTCTAGAA	8924
rs568447391	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28236326	ACGGAGTCTCGCTCT[G/T]GTCACCAAGGCTGGA	8924
rs568453699	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28212357	CCAGGACTTTAGTAC[A/G]TCCGTGAATTCACTC	8924
rs568462338	snp	C/T	0.0154538	0.0865337	intron-variant	HERC2	GRCh38.p7	15:28218232	CGCTAAAGAGACCAG[C/T]AAACTCCAGAAGCTG	8924
rs568475976	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28218744	CTGCATATAATTCAA[A/C]AGCTTTAATATTACA	8924
rs568480508	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28172324	TACAACAGCCAACAT[A/G]TATTTGAAAAAGAAC	8924
rs568482757	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28274849	GAACCGAGTTCGAAA[C/T]CCAGTCTGTTGATGT	8924
rs568487865	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28247648	TTGGTCAGGCTGGTC[C/T]TGAACTCCTGACCTT	8924
rs568520633	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28285890	AATTAGGAATTACTA[C/G]GAACAACTCTACACA	8924
rs568521537	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28125585	CGAACATCCCAAATC[C/T]ATCTAATATTAAAAC	8924
rs568532572	snp	A/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28162904	TCAAAAAAACAAAAA[A/T]CAGGTAAAGGATGTC	8924
rs568535026	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28259147	TTGCCCAAGCTGGAG[C/T]GCAATGGCGCCATCC	8924
rs568589244	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28119797	TTTGTTTTTTCAATT[A/G]CATACTGAACGTTTT	8924
rs568606114	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28283095	GACTATAACAACTCC[A/G]GTCACTGAACTCACG	8924
rs568614830	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28250582	CTGTGGCTCCTCGCC[A/G]GCATGTAAATAACGA	8924
rs568654817	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28166606	GAGGGTAGGTGAAAG[A/G]TAAGTCTAGAGCACA	8924
rs568683925	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28208743	ACCACCAGCAAAGTG[C/T]TTGTCTGCTGGCATC	8924
rs568689725	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28295640	TGACCTCAGGTGATC[C/T]GCCTGCCTCGGCCTC	8924
rs568699065	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28319276	CATTTCCCTTACTCC[C/T]AGGAGGAATTTAGAT	8924
rs568720568	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28163584	GTTTGGATCATAAGC[A/G]GATACTACAGGGGGA	8924
rs568733881	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28210749	ACCAATCTTGCTGAC[C/T]CATGCAGCACACTTT	8924
rs568738590	snp	A/G	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28237182	TAAAACCAAAAGGAC[A/G]GCTCTCTCCTGCAGC	8924
rs568750632	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28121035	CACACCTCCCAATGT[A/G]ACAGCAGCGGTTATC	8924
rs568751894	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28280369	GAAAATGGATGATGA[C/T]GACAGGTAGTACTCG	8924
rs568769698	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28136907	AATTGAGAAAGATAT[A/G]CTAAAGGAGAAGGAA	8924
rs568776518	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28237925	TTTTCAAGACCAGTA[C/T]ATCACAGATCTTAAC	8924
rs568781126	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28157475	GGTTTAGTCTTGGGT[A/G]GGTGTATGTGTCCAG	8924
rs568783663	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28252592	TTATTCCTATAGTTA[C/T]TGTGTTGGAAGTTCA	8924
rs568788572	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28280854	GGAGGAGGTTGCAGT[A/G]AGCTGAGATTTTGTC	8924
rs568828275	snp	G/T			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316686	ACAAATTCTTTTATT[G/T]CTACATGTCATCTAT	8924
rs568831410	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28193757	ACTTCAGGAGAAATA[A/G]TATAAACCAAATTGC	8924
rs568832409	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28136465	GGTGCAGGGTAATGC[A/C]GCATGCCTCCCAGGA	8924
rs568859866	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28306055	GAGGATGTGGAGAAA[C/T]AGGAACACTTTTACA	8924
rs568865139	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28297637	TACGTGATTCCATGT[A/G]TGGAGTTCTAGAACA	8924
rs568880566	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28129389	GCCGGGAAGCTGGGT[A/G]GAGACTCCAGGCCCA	8924
rs568893942	snp	C/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28253000	CTGCTCTGTGCTCGG[C/G]TGCCTGACCCAACCT	8924
rs568894816	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28128308	GTGAACTGGCTGGCA[A/G]GACGAGCCTCCCTGT	8924
rs568902912	snp	C/G	8.23703e-05	0.00641704	synonymous-codon	HERC2	GRCh38.p7	15:28121364	GATGCGGTTCAGCTC[C/G]ACGACGGGGCCATGC	8924
rs568914765	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28292048	GCCTGGCTAACATAG[C/T]GAAACTTCGTCTCTA	8924
rs568939147	snp	A/G	0.0437281	0.141251	intron-variant	HERC2	GRCh38.p7	15:28121955	GCCAGCCGGACCTTG[A/G]ATCGCCACTGCCTGC	8924
rs568942815	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28248064	AGGCTGCCTCAGGGA[G/T]TATCCCAAGTCTGCA	8924
rs568944849	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28161551	GACATACTAGTAAGA[C/T]GCTCACTTTATACTG	8924
rs568950133	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28291637	TTACACAAAAAAAAG[C/T]AAGCAAAGAATAAAT	8924
rs568974773	snp	A/G	0	0	intron-variant	HERC2	GRCh38.p7	15:28160699	GTGAGGCGATGCCTC[A/G]CCCTGCTTCAGCTCA	8924
rs568976067	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28239194	ATGACTATGAAAATT[A/G]GAAAATGTGTTCAAT	8924
rs568980404	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28247452	TTTTTTTTTGAGACC[A/G]AGTTTCACTCTTGTC	8924
rs569001496	snp	A/T	0.00598797	0.0543887	intron-variant	HERC2	GRCh38.p7	15:28206415	ATATGTGTAAGATTC[A/T]ATTTTCAACTGCGAA	8924
rs569029189	snp	G/T	0.000371045	0.0136156	intron-variant	HERC2	GRCh38.p7	15:28280058	GATTCTTTCTTCGCT[G/T]TATTGTTACCTTTTT	8924
rs569049995	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28153902	GAATCAGGAACCATC[A/G]AGCCGCTCAGGCCAG	8924
rs569055694	snp	C/T	9.52064e-05	0.00689885	synonymous-codon	HERC2	GRCh38.p7	15:28152732	GTAAGGGTGGCTACT[C/T]TCCACCACCACAGGC	8924
rs569062735	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28112666	TGAGCTTGTTTCTGA[C/G]CACCGGCCCACAGAG	8924
rs569069692	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28148227	CAAAAACCAAAACAT[C/T]TTATAAAGCTGAAGA	8924
rs569085388	snp	A/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28154766	CAGCATTATTTTATA[A/T]ATATATTTTTTTATT	8924
rs569097137	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28112124	TTCGTGCTCACAAAA[A/C]CATATTTTTTGCTAA	8924
rs569128336	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28158373	TGTGTGGGAGTCGAA[A/G]TCTCTTTGTGGGTCT	8924
rs569130939	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28148732	GAACGGCTGCATGAA[C/T]GCGCATTCTAGTAAA	8924
rs569137590	snp	A/G	0.000156728	0.00885094	intron-variant	HERC2	GRCh38.p7	15:28117340	CGACTGTGGACACCC[A/G]AGACCGCTGCCTCAC	8924
rs569143431	snp	A/G	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28235257	GCCCCCTCTCTTTAA[A/G]CACAGGACAGCCCCT	8924
rs569170283	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317429	AGCTTAACTCTAAGA[G/T]CTTACATTTATGCGT	8924
rs569187104	snp	C/T	4.99513e-05	0.00499731	synonymous-codon	HERC2	GRCh38.p7	15:28115483	CTGCTTCCAGACAGG[C/T]TCGGCAAGGTTGAGG	8924
rs569203380	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28149206	TTCTAGAAAAATTAC[C/T]GAAAAATACACGCAG	8924
rs569203792	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28165278	GAAGAAAGGTGCCCA[A/C]CACGGAGTGGGGGAC	8924
rs569207680	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28265986	AGGCCTTGGGGAGAA[A/C]GGGAACAAACATGAA	8924
rs569225072	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28290452	CCAGGCTGGTCTCAA[A/G]CTCCTGACCTCAAGT	8924
rs569235124	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28206872	AAAAATTAACTGGGC[A/G]TGGTGGTGCGTGCCT	8924
rs569271000	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28253395	GTTTTAAAAATAACC[A/T]TTCCATGATGATTTT	8924
rs569279837	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28209222	CCTCCATATCCATGG[G/T]TTCTGCATCCAAAGA	8924
rs569284067	snp	A/C	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28204017	GGCTAAGGGCAAATA[A/C]AAAATCATTAGAAAG	8924
rs569299276	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28125284	ACACACAGCACCAAC[A/G]CTCCCTGCCCTTCAG	8924
rs569300577	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28116015	AGATGCAGAAACAGA[A/G]TCTCCCATCTTCTGA	8924
rs569317007	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28159269	TCTGTACTTCCTGAA[C/T]TTTAATGTTGGCCTG	8924
rs569331541	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28197676	AGAATTCCTTAAACC[C/T]GGGGGCGGAGGTTGC	8924
rs569343983	snp	C/T	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28227159	GTGTGACTGTAATCC[C/T]AGCTACTCGGGAGGC	8924
rs569352467	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28285966	TACAAATTACCACAA[C/T]TCACCAAATATAAAA	8924
rs569373359	snp	A/G	0.0429648	0.14013	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321645	GAGGGAGGTGGGGAA[A/G]GGAAAGCCTCCTTCC	8924
rs569374388	snp	C/T	1.64751e-05	0.00287007	missense	HERC2	GRCh38.p7	15:28141785	TTAAAAATGTCATGG[C/T]TCTCATGCAGAACAT	8924
rs569393915	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111389	ATCAAGACGACTCAC[A/G]ACACTTGAAAGAAAG	8924
rs569410080	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316362	TTAAAACACCAGGCC[A/G]GGCACAGTGGCTCAT	8924
rs569412665	snp	C/T	0.000798403	0.0199641	intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28315850	TGCTGGTACAAGTTG[C/T]GGGACTGCATGCCAC	8924
rs569503924	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28192251	CTTCTTAAAGAAAAA[C/T]AGAAAGTTTCAAACT	8924
rs569504454	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28144997	ACATACCATTCTTCA[A/G]CAAACACGCATTCAG	8924
rs569514695	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28138915	GTGAAAATATCAACA[G/T]TAACAGGGATTTGGA	8924
rs569529592	snp	C/T	2.24027e-05	0.00334677	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28186539	GATCCAGGAATGTAG[C/T]GGGAGGTAAGTGAGC	8924
rs569530090	snp	A/G	4.95585e-05	0.00497763	synonymous-codon	HERC2	GRCh38.p7	15:28116719	CGGCCGGGCTGAGCA[A/G]GTAGCAGTCTCGGTT	8924
rs569532088	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28207463	TTCGTGTTCACTCAC[A/G]GCTTCAGTAACCCCT	8924
rs569533981	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28242167	AGGTGCTAGGGAAAA[C/T]TGGTGTTTAATAGAT	8924
rs569565317	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28266475	AGGTGAGATCGCCCC[A/C]TTGCACTCCACCTTG	8924
rs569566769	snp	C/G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28156143	GTTTTGGTACCAGTA[C/G/T]CATGCTGTTTTGGTT	8924
rs569566970	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28306246	GAGGTGTGTTCCTTC[C/T]ATAACCAGTTTTTTG	8924
rs569571455	snp	A/G	0.0103295	0.0711199	intron-variant	HERC2	GRCh38.p7	15:28310738	TACGACATTTGACCC[A/G]TGTCTTAAAGTGTTT	8924
rs569571491	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28304461	CAATCTCCACCTCCG[A/G]GGTTCAAGTGATTTC	8924
rs569572068	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28142492	CCTCCTATTCCAGGA[C/T]GACGGCCATGGGCAC	8924
rs569577896	snp	C/G	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28139354	GCTCTCGCTGACAGA[C/G]TCAGCTGCCACCCTG	8924
rs569582796	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28121604	AGGCTGGCCCCGAAG[A/C]ACACAGGGACAGACG	8924
rs569588825	snp	G/T	0.143959	0.226396	intron-variant	HERC2	GRCh38.p7	15:28155601	ATCCTTCGCCCACTT[G/T]TTGATGGGGTTGTTT	8924
rs569599317	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28201189	CCTGTAGGCTTTGCA[C/G]CCATGTCACCTTCTC	8924
rs569604049	snp	A/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28221062	CACAGATGTCGCCAT[A/T]TGCCACCCTGTCTGT	8924
rs569624303	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28162289	GGGAGGCTGAGATTG[C/T]GCCACCGCACTCCAG	8924
rs569626552	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28288653	GAGTTCAAGGCGAGC[A/C]TGGCAAACACAGTGA	8924
rs569650572	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28263528	TTGCGGACCACCCTC[C/T]CGTTTGCCTGCCTGC	8924
rs569661482	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28113343	GGCATTTCCGCAAGA[C/T]TCCGTCACGCTCCCT	8924
rs569663279	snp	C/T	0.00795532	0.062565	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318550	GGAGAATGGCATGAA[C/T]CCAGGAGGCTTGCAG	8924
rs569691431	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28311560	GGAATGAGAATTAGT[C/T]CCGTTTTAACCACTA	8924
rs569712323	snp	C/G	1.75075e-05	0.00295862	intron-variant	HERC2	GRCh38.p7	15:28275039	GAACATACAACCAGT[C/G]AGCAGCAGAGGGTGC	8924
rs569717497	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28275505	TTGCCCTCTTCTGAC[A/G]GTGGTGCTCATCACC	8924
rs569726339	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28294731	CTCCCACAGCCCCTC[A/G]TGGTTCACTCTGTTC	8924
rs569746219	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28282789	ATACAAAACTGAGCT[A/G]GGCATGGTGGCGGGC	8924
rs569749586	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314047	GCCCAGTTTCGCATT[C/G]TCTCAATTTCCAAAG	8924
rs569753144	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28118862	GGGAGGGGCATGCTA[C/G]CCTGAACGGGAAGGA	8924
rs569778550	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HERC2, LOC107987422	GRCh38.p7	15:28312309	GCAGCAGCCTGGGAA[C/T]AACTGGAAGACAGCC	8924
rs569778840	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28306495	TTGTTGGGTATTTCC[A/G]CATCAATGTTCATCT	8924
rs569786447	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28159596	ATCAGCTCCTTTAAG[G/T]ACTTCTCTGCATTGG	8924
rs569804107	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28268899	AGGGAGGAACACCTC[A/G]CTTTAATGAAAACAT	8924
rs569814197	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28292297	TCCAGTGAATGTATA[C/T]AAATGGTCAATAAGC	8924
rs569818127	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28306947	TCAAGTGATTCTCGT[A/G]CCTCAGCCTTCCAAG	8924
rs569832150	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28230265	CATGTTTCTAACAAC[C/T]GCCCGTCCCTCCCTC	8924
rs569846418	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28217041	AATAACATCACTCGT[G/T]CTCACACTGACACAA	8924
rs569849638	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28182850	AGCCATGGAAACAGA[C/T]GCACAGCTGCTACAA	8924
rs569854055	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28175372	AAAAGGAACAGGACC[C/T]GCCCTCATGGTTCTC	8924
rs569857977	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28270590	CACAGGCCAGCTCCC[C/G]CTACCAATACCAGAA	8924
rs569901352	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28189462	AAGTTACCAGTAAAA[C/T]GCATTAAAACTCAAG	8924
rs569909873	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28217492	TCACACACACTGGAG[A/G]ACGCCCACATACCCA	8924
rs569912986	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28196144	AAATAACAAATTCCA[A/G]TACACTGTGGTCCAC	8924
rs569924371	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28211983	AGCCGCATTCTACAA[C/G]CGAAGGAAGGCAAAG	8924
rs569925118	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	HERC2, LOC107987422	GRCh38.p7	15:28317773	CTACGCACACACATT[A/G]TACCAACTTCAATTT	8924
rs569933693	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28228529	CCACTGACATTTCTT[C/G]TGCATGGATGCAAGA	8924
rs569945936	snp	C/T	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28194475	CTCGGGAGGCTGAAG[C/T]GGGAGAATGGCATGA	8924
rs569966705	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28124902	TTTACTGAGCCTGAA[C/T]TATTTTCACCAAGAA	8924
rs569968243	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28308403	TTTGTATGTTGATTT[C/T]GTATACTGCAATTGT	8924
rs569986754	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28212265	GGCGACAAAAGCTGA[C/T]TCGAAAATACTCATT	8924
rs569987062	snp	A/G	0.00242472	0.0347344	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28176998	ATGTCCCAGCCGGCC[A/G]TACTCGCCGAGGCCC	8924
rs569988698	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28300162	ACCAATGACTACCTA[C/T]GGGGAAATGGGGAGG	8924
rs570022590	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28224726	TCAAGTATACCACAG[A/G]ACACTCTCTTAGACT	8924
rs570106649	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28112490	GTGACCCTGAAAGAC[A/G]GCCACTTTTCTAACC	8924
rs570117067	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174078	TAACTGAATAAAGCT[C/G]TTAAAAAATACAAAA	8924
rs570150673	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28303201	GTGAGAGATAGCGGT[A/C]TAGTTTCATTTTTCT	8924
rs570165303	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28131834	AACCAGGAGGCTCCA[C/T]GGTGCCCGGATGATC	8924
rs570166195	snp	G/T	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28173747	GGTGGAAGCTGCAGT[G/T]AGCCAAAATCGTGCC	8924
rs570168686	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28137437	CTGATCAAGTCTATC[A/G]GCGCCATTTTCCCAA	8924
rs570198691	snp	A/G	0.000149037	0.00863114	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28260900	GTTGCTCCCCCAGCT[A/G]TGGACCTCGCTGTCC	8924
rs570198849	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28144308	GAAGCCGCCAACGAA[C/G]AAGGGTGGCTCCACC	8924
rs570210412	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28185813	ATGCACTTCTTCCTG[A/C]CTCTTACCAAAGGCC	8924
rs570221669	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28299239	ATAAAATCCGAGCAG[A/C]TTGTATTAACTACCA	8924
rs570226182	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28171282	TACTGAACATACTAT[A/G]TAATATGTAACAACT	8924
rs570235592	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28303849	CTTGATTTTTCATAT[A/T]GTTCACTGTTGACAT	8924
rs570241620	snp	G/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214580	AGGGCACAGGGAAGG[G/T]AAACGGCCACCCACC	8924
rs570260553	snp	A/G	0.000274843	0.0117195	intron-variant	HERC2	GRCh38.p7	15:28293034	TCATCTGCAGAATTA[A/G]AAATTTTTTAATCTG	8924
rs570287569	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28254140	ACTACAAGATTAGTC[A/G]GGTGTGGTGGCACAC	8924
rs570291369	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28248975	CTCGTGCTTCACTAA[C/T]GTGCGCCTATGGAGC	8924
rs570300733	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28249359	GAGCACGGCAGCGAA[C/G]AAAGTAGAAGAGGCT	8924
rs570317648	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28209707	TATGCAAATACTACA[C/G]CATTTTATAGAAGGG	8924
rs570324736	in-del	-/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28183219	GTTTATTTATTTTTT[-/G]TTTGTTTTGAGACAG	8924
rs570326058	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28254677	CCTTGTTGGAAACCC[C/T]AACTCAGTTGTGCAG	8924
rs570349424	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28226165	TGGAAAGACATTCCA[C/T]ATTCAGAGAATGGAT	8924
rs570369970	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28220091	TGGACCGAGACCACA[C/G]GGCAATTCCACCAGG	8924
rs570370184	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28306693	AGCAGTGAAGTCACC[A/G]GGTCCTGGGGTTTTT	8924
rs570379449	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28288051	TATACATGAGAGGCC[A/C]AAGGTGAGACAAAGT	8924
rs570387657	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28121999	CGGGCCAGGGAGCAC[C/T]GCGGAGCCAGCCGGA	8924
rs570425796	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28116083	GGGCTGGCTCTGCCA[A/G]TGCCTGCAGCTGTGC	8924
rs570425905	snp	A/C	0.0107246	0.0724382	intron-variant	HERC2	GRCh38.p7	15:28122212	AGCACCACGGTGAGG[A/C]CCCAGCCGTTCCCCA	8924
rs570426433	snp	A/G	0.000399281	0.0141238	intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28315693	GGAAACCTCTGCGCC[A/G]TGAGAGCCAAGTGGA	8924
rs570450840	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28147169	TGGTTGAATTTGGAA[C/T]ATATTTTAAAAGCAG	8924
rs570460277	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28226808	AATCCAGAGAACAGG[A/G]GAAAATACCCTCAAA	8924
rs570462318	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28309575	GAAGCAAGCAGCCAA[A/T]GAACTGCCTGTGGGG	8924
rs570462923	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28140767	CATCAGGTGATCCAC[C/T]CACCTTGGGCTCCCA	8924
rs570515095	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28230694	ACAAAGTGAGAGTGC[A/G]ACGAGGGGAGAAGCC	8924
rs570531775	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28127799	AATAGAGCACAACTA[A/G]AGCATCAAAATAAAT	8924
rs570557892	snp	A/G	0.000399281	0.0141238	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28220488	AATCCTCTGCTGAGG[A/G]CTGTGCAGCAGCCGG	8924
rs570585703	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28127190	TTGGTCCTAAAGCCA[C/T]GAGGCGGGTGTCGCA	8924
rs570590710	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28169940	TATACATATAAACTA[C/T]GAAAATGCTACAATA	8924
rs570593114	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28257334	CACAGGAGTCACCAG[A/C]GTGTGTGATGGAGCT	8924
rs570600669	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28290565	TGAAACATTCCACAG[A/C]ATACACCATATTCTG	8924
rs570601926	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28135920	ATTCAGAAAACATAT[C/T]GTGAAAATAAGGTCT	8924
rs570606341	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28129146	TGGGGTTCCCCGGAC[C/T]GCCCCACGCTCCTGA	8924
rs570616649	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28245758	TCCATTTTTTACTTA[C/T]ACTACCATCAGTAGA	8924
rs570622745	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28204118	CCTTTCTCCAGAGGC[A/G]GCAGAACCCAGAGCC	8924
rs570634139	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28172167	AGAAACACTATGTTC[A/G]TGGGTTAGAAGACTG	8924
rs570642236	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28203693	AGGGGCTGGGGTCCC[A/G]GCCTGGCAGAGTAAC	8924
rs570665129	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28128356	AAAAGCTCAGGACGC[A/G]GCAGCAGGACAGCAA	8924
rs570668162	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28283950	TAGGAATATCTGCAT[A/G]TAAATAATGAGATAT	8924
rs570679945	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28251872	TACCATTTCAACATG[A/G]TATCACTATAAGAAA	8924
rs570706692	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28239265	ACTAAATGCATGCTT[C/G]AGGGCATTTATGCCT	8924
rs570718941	snp	A/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28209135	TATCTATAAACGGAT[A/T]TACATAGCAATGTGC	8924
rs570741042	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28285351	ACAGCATATGTTCCC[G/T]CAAACAATGGAAACA	8924
rs570746139	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28252429	CCTCAGAAAAGGGAG[A/G]GGCATTCAAGAACTT	8924
rs570754591	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28284485	AACATGATCCAACTA[C/T]ATGTTGTCCATAAGA	8924
rs570754696	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28276394	GGGTACCTGGAAGAT[A/G]GAAATCTTTGCTCCT	8924
rs570770594	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28190460	GGGTACTGTTTAAAA[C/G]AACCTTCACTGATTC	8924
rs570785204	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28294136	CACCAAGTAATTCTC[A/C]AGTTCTCTGCGACAT	8924
rs570789196	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28277404	TGAGGGCAACGGGAC[C/G]AACAGTACAAGGAAT	8924
rs570789470	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28197721	GCGCCACTGCACTCC[A/G]GCCTGGTCAGGGGAG	8924
rs570794483	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28126354	CTAAAAGTAGATCTA[C/T]CATTTGATCCAGCAA	8924
rs570797530	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28175718	ACAATGCTATACAAG[A/T]AGACACTCATTGTCT	8924
rs570800071	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28165755	CAGTGAGCCAAGATC[A/G]TGCCACTCTACTGCA	8924
rs570819216	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28250619	CTGAAATACGTTTCA[C/T]GGCTTATTTTTGGCA	8924
rs570820016	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28219388	GGAGCCAGGCCTGCT[C/T]CCTGCAGGCAAGGGA	8924
rs570833725	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28112977	AGACTCAAGAGGCTC[A/G]TTTTCCATGTGCTGC	8924
rs570853149	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	HERC2	GRCh38.p7	15:28213676	TCAAGTGCTGATGCT[C/G]GTGCTCGGTTCTAGT	8924
rs570863125	snp	A/C	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28208443	CCCCTCATCACCTGA[A/C]GCAGGAGCAATTCTC	8924
rs570866992	snp	A/G	0.00102371	0.022601	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214095	TCGGAAGGCCTTCCC[A/G]CAAAGCTGTGGGTGA	8924
rs570873806	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28166749	CCAGTGACCAGTCCA[C/T]GGGAGTCCCAGTGAC	8924
rs570874187	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28289750	GGCTCCCTGGAAAAC[A/G]TTCCCTAAGGTGTAT	8924
rs570874855	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28126837	ATGTAACCAAACACC[A/G]CCTGTTCGCCAAAAA	8924
rs570888207	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28137335	GTGTGCTCCTGTATA[C/G]AGGCACACCCCATTT	8924
rs570900930	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28243988	TGAGACCAGCCTGGG[C/T]AACAGAGGGAGACCG	8924
rs570911350	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28157584	TTCTATGGAATCAGT[A/G]GTGATATCCCCTTTA	8924
rs570928709	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28208786	CCTTCAAAGGCTGCC[C/G]GTCCAGTGCTCAGCT	8924
rs570970264	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28151147	GCAGTATTGAAATTA[C/T]ATCCTAAGTCTGTCG	8924
rs570992506	snp	A/C/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28170000	CAAGACAAAAAAGAA[A/C/T]ACAAAACAACAAAGA	8924
rs571031539	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28215173	TGAGCCACTGCGCCC[A/G]GCCTCTCTTTATTTT	8924
rs571033047	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28139827	GCACTTTGGGAGGCC[A/G]AGGTGGTCGGATCAC	8924
rs571040714	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28238043	TACTTCTAGATCCAA[A/G]TATTCCTATCACAAA	8924
rs571050043	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28160748	CACTGTCCTGCACCC[A/G]CTGTCCGACAAGCCC	8924
rs571060239	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28161578	ACTGCAGACCTACAG[A/G]CCAATTCAGCAGCTA	8924
rs571071511	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28203335	AATCAGGAAGAAACC[A/G]AGGACACTGTGGAGC	8924
rs571080389	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28280868	TGAGCTGAGATTTTG[A/T]CACTGCACTCCAGCC	8924
rs571080918	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28121058	CGGTTATCATCATGC[A/G]GTGGGAAGAGGGCTG	8924
rs571096072	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28162399	CATTTTTTTTTCAGC[A/G]TAATACAAAACTCAG	8924
rs571113663	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28273932	TTTACTCCCACATTA[G/T]CTATAAGACTTCAAA	8924
rs571116809	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28281565	CTCCACGGGACAGGA[A/G]GGCCTTAGAAGGCAG	8924
rs571123054	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28155447	TTCCTGACTTTTTAA[C/T]GATCGCCATTCTAAC	8924
rs571130072	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28231775	GCCTGAGAGAAGGCT[C/T]GGGGATCCCTGACAC	8924
rs571146702	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28216974	CTATACTGTTATAAC[C/T]TCCCATTCACTGACA	8924
rs571170336	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28232336	TCACGAGGTCAGGAG[A/G]TCAAGACCATCTTGG	8924
rs571187796	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28146494	TCTCAGACTGACCAC[C/T]CTTTCCCCAGCTCAT	8924
rs571194740	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28130980	TCAGAGCAGAGGCCC[A/G]CGGGGGAGGAGCAGC	8924
rs571199554	snp	C/G	1.64803e-05	0.00287052	missense	HERC2	GRCh38.p7	15:28130177	CCATCCTCTGTGCAG[C/G]ACACACAGTGCAGGG	8924
rs571202601	snp	A/G	9.29256e-05	0.00681573	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274401	AAGTGCTCGCAGGGC[A/G]TCCAGGGACTCCTGC	8924
rs571204932	snp	C/T			missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28192002	AGCAGGGCTCGCTGC[C/T]GTCAATGAGACGGGA	8924
rs571220374	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28188356	GACCATCCTCGCTAA[C/T]GGTGAAACCCCGTCT	8924
rs571225163	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28298567	TTGGGAGGCTGAGGC[A/G]GGCGGATCACGAGGT	8924
rs571229189	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28167521	AAGCAGTGACAGGGA[C/T]CGTGTCCTGCGGCAT	8924
rs571241243	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28225598	AGCTACTCGGGAGGC[C/T]GAGGCAGGAGAATCA	8924
rs571268397	snp	A/G	0.005231	0.0508737	intron-variant	HERC2	GRCh38.p7	15:28211172	AAGACTCAGTGAGAA[A/G]GGCGTGCCCTGCTCA	8924
rs571292094	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321748	AAGTCACAATGTCAT[C/T]CCCCTGCCCTCAAAT	8924
rs571326009	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28287888	ACCACCACGCCCAGC[C/T]AATTTTTTTGTATCT	8924
rs571331875	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28206560	GACTCTAGGTTGGGT[A/G]CGGTGGCTCACGCGT	8924
rs571340546	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28241522	CCTCTGGCTATATAC[C/G]CAAAAGAAGTAAAAG	8924
rs571375140	snp	C/T	0.00031511	0.0125481	intron-variant	HERC2	GRCh38.p7	15:28117486	AGCACCACCCTGGCA[C/T]GGACCATCCTCACAC	8924
rs571396997	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28199865	ACAAGGAAGCCACCT[C/G]CAAATGCAGACTGTA	8924
rs571403969	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28194427	TACAAAAAATTAGCC[A/G]GGCGTGGTGGCGGGC	8924
rs571407404	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28235696	AAAACCACGTATGAA[C/T]GTCTCCATTTCACCA	8924
rs571416409	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28235157	GTTCTTTTACTGGAC[A/G]TTTAGATTTTAGAGC	8924
rs571446969	snp	C/T	0.0228947	0.104514	intron-variant	HERC2	GRCh38.p7	15:28206675	CATCTCTACTAAAAA[C/T]ACAAAACATTAGCTG	8924
rs571449349	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317458	GTAGTCATTCTTAAT[G/T]GATGATTAGAGGAAG	8924
rs571480925	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28149713	AATGGCCACATGAAC[A/G]CACGTTCTAGTAAAA	8924
rs571490146	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28134241	AGAGGGTATTCTAAG[C/T]GGTATTTTAAAATTT	8924
rs571500299	snp	C/T	0.00755907	0.0610114	intron-variant	HERC2	GRCh38.p7	15:28142585	ACAACTGCTGCAACA[C/T]TTGTTGCCTGCATCA	8924
rs571508179	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28143108	TCAAGTAGGAAAAAA[A/G]CTAAAAGAACATAAA	8924
rs571516583	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28112719	TGTTCTCAATCCAAC[A/G]AGCGGCCTCATTTTT	8924
rs571516619	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28118137	GTGCCACACACACGG[C/G]TAGTGTTCACAGACG	8924
rs571527288	snp	C/T	0.0111196	0.0737302	intron-variant, downstream-variant-500B	HERC2, LOC107987422	GRCh38.p7	15:28312459	GCAACATGGTAAGAC[C/T]GTGTCTCTACAGAAA	8924
rs571527843	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28197708	GTGAGTCAAGATGGC[A/G]CCACTGCACTCCAGC	8924
rs571540592	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28228686	TTAAACATCTAACTA[C/T]TTTCCAGGGGTTTCC	8924
rs571567100	in-del	-/TA	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28209352	TTATTTTTATTTATT[-/TA]TTTTTTTTGAGACAG	8924
rs571572585	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28136992	AAAGATGTGCAACAT[C/T]TAGCTAACTCAAAAA	8924
rs571586359	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28286061	AAAAAGAAATTACCA[G/T]ACCCAAATGAACTCA	8924
rs571596218	snp	G/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28204594	CACTGCACTCCAGCC[G/T]GGAGACAGAGCGAGA	8924
rs571599241	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	HERC2	GRCh38.p7	15:28110717	CCCTTTGCAGAGTGC[A/G]TGCCATACACAAGCA	8924
rs571601595	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28239932	GAACATGCTCAGGTC[C/T]TAATTCAAAATTACC	8924
rs571620725	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28159813	GAGAGATGCTCTGAT[C/T]TTTAGAATTTTCAGT	8924
rs571644746	in-del	-/T			intron-variant	HERC2	GRCh38.p7	15:28125680	TTATTTATTTTATAC[-/T]TTTTTTTTTTGAGAC	8924
rs571658129	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28310318	CAGAGGTGGTGGCGC[A/G]CCTGTACTCCCAGCT	8924
rs571669413	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28223691	ATAGCTTTATGTTTT[C/G]TGGCTGTTACATGTG	8924
rs571680749	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28153778	AAGACAAGATTACTT[C/T]CTAGTGAGGAAAGTT	8924
rs571699749	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111505	TTTACACACTTTAGT[A/G]AACACAGTCCTACAT	8924
rs571702618	snp	A/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28221496	CAGACCATGGGAAGG[A/T]GAACACTGCCCTAAC	8924
rs571733429	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28224315	CAACCTCTGCCTCCC[G/T]GGCTCAAGCAATCCT	8924
rs571736431	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28149067	ACCGAAAAAACAAAC[A/G]AGACTCCTAACCGAG	8924
rs571790115	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28143548	ACGTCCCAGGTTCAA[C/G]CGATTCTCCTGCCTC	8924
rs571806384	in-del	-/A	0.02016	0.0983543	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321865	GCGCGTGCGTGAAAC[-/A]AAAAAATTACTCAAA	8924
rs571827670	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28222307	AAGTACTAATGAAGA[C/T]CGTAATTTTGAACAA	8924
rs571829048	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28139932	GATTAGCCAGGCGTG[A/G]TGGCGGGCGCCTGTT	8924
rs571858075	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28176074	AATAAAATAAGCTTT[C/T]ACAAGAAACACATGT	8924
rs571876707	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28222815	GTATGCGCCAGGAAG[G/T]GGGTGCCCGTGTGAT	8924
rs571893621	in-del	-/AC	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28311162	TCAAGACAGGGAAGT[-/AC]AGTCTTTAAGATTAT	8924
rs571894944	snp	C/G	0.0251858	0.109355	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214044	TACAGGTTCACCGTT[C/G]AACTAAATTAATTCT	8924
rs571904932	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28259181	CTCACTGCAATTTCT[A/G]CCTCCCAGATTCAAG	8924
rs571909058	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28173164	AAAACAGTATGTAGC[A/G]ATCTTAAGAAGCTAG	8924
rs571926212	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313727	AAATGTTAAGAACAG[A/G]TTCCTAGAACAATTA	8924
rs571928885	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28249731	AGCTCACTGCAACCT[C/T]CGCCTCCCGGGTTAA	8924
rs571965714	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28250305	ACACGGCAAGGATGC[A/G]CCCTCACTGGGCTCA	8924
rs571972603	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28268410	GCTCCATCCTGTTTA[A/G]GATATGGCAACATAA	8924
rs571986891	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28307159	ATCTATTTCTTCCAC[A/G]TTTCCCAATTTATTG	8924
rs571989721	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28297656	AGTTCTAGAACAGGC[A/G]CAATTTGTCAAATGC	8924
rs571995782	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28306388	GATTGATTTGGATAC[A/G]GTGAACCATCCTGGC	8924
rs572009801	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28261305	CATATTCTCCCATCC[A/G]AGATTTAACAATGCA	8924
rs572027816	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28145040	GTACCCAGGAAACTG[C/T]GGCAGGCGGGCAGAC	8924
rs572029790	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28290463	TCAAACTCCTGACCT[C/T]AAGTAATCCACCCAC	8924
rs572043027	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28275175	ACAACTTTCATCAAA[C/T]GTCTTTTGTAAAGGA	8924
rs572047575	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28243508	TATCCCAAATACACA[A/G]TAACACTCACATGAA	8924
rs572048074	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28113775	ACTGTGGCCGCACAC[A/G]TCCCAGCTGGGAGAA	8924
rs572049373	snp	A/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28188598	TGGTACCAAGGTTAT[A/T]TTTTGTTAAGCCCTG	8924
rs572061785	snp	C/T	0.000290909	0.0120569	intron-variant	HERC2	GRCh38.p7	15:28210954	ACTTCCTTTGTCTAC[C/T]TTCTACTGCCCTTCT	8924
rs572066378	snp	A/T	2.02846e-05	0.00318463	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174360	TTGCTGTAAACCTAC[A/T]GAAAAATCTCAGAGA	8924
rs572068854	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28174837	TGCTTGCTAATACCT[A/G]TAAAAGGAGTATTTT	8924
rs572097188	snp	C/T	0.000154349	0.00878354	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28212539	GACAGACAGCATGGG[C/T]TCTGTGAAGGGCAGG	8924
rs572104143	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28298798	AAGACTCCTTCCCCC[A/C]CAAAAAAAAGAAGAA	8924
rs572114373	in-del	-/ACCGAGAACATC	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28148700	CACATGCGGCTTCTA[-/ACCGAGAACATC]ACCGAGAACGGCTGC	8924
rs572124059	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28211630	GAAGGAGGGCCGCAG[A/G]TGCCGCTCGGACACT	8924
rs572166574	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28125819	GTTGGGATTACATGC[A/G]TGAACCACTGTGATG	8924
rs572180097	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299922	GCCAGGCGTGGTGGC[A/G]GGCGCCTGTAATCCC	8924
rs572203612	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28119358	TGAGCCAAGATTGCA[A/C]CACTGTACTCCAGGC	8924
rs572230650	snp	A/G	3.48159e-05	0.00417214	intron-variant	HERC2	GRCh38.p7	15:28293063	TGTCACCGCTTTTCA[A/G]AATGCCATACCATTA	8924
rs572240583	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28271071	AAATTTGCTGTACAC[A/G]CATACACAACATTGA	8924
rs572261286	snp	C/T	0.0103295	0.0711199	intron-variant	HERC2	GRCh38.p7	15:28126544	CACCATGGAATACTA[C/T]TAGCCATAAAAAGGA	8924
rs572266495	snp	A/C	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28293786	GAGGCACTGTGACTG[A/C]TAGCATAATTCAAGA	8924
rs572266605	snp	A/G			synonymous-codon	HERC2	GRCh38.p7	15:28116711	TGCTCTGGCGGCCGG[A/G]CTGAGCAGGTAGCAG	8924
rs572274708	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28189021	TGAACCCAGGATGTG[A/G]TGGTTGCGGTAAGCT	8924
rs572295825	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28183609	CTTGGCTGATGGTCT[A/G]ATGCCAGGTGCTAAG	8924
rs572302463	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28117845	GGAGCCCTAGGGCCC[C/T]GCCGCAGCAGGACCT	8924
rs572305091	snp	A/G	0.0111196	0.0737302	intron-variant	HERC2	GRCh38.p7	15:28294257	GTGAATGCTGAAAAA[A/G]ATATCCAAAGAACTA	8924
rs572305153	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28175409	GTAAGACTCAGCTGA[G/T]TTCATCAACAGCTGT	8924
rs572354212	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28131225	TACCACAATGGCATC[A/G]GGACGTCCTGCTCCA	8924
rs572359455	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318065	TGCTCAAAGACATGC[A/G]CCTTTACCTTACAAC	8924
rs572366405	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28251672	AGGCGTGGTGGTGTA[C/T]GCCTGTGGTCCCAGC	8924
rs572397581	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28130706	GAAAACTTGTACCCA[C/T]GATGAATAATTAGTG	8924
rs572398436	snp	C/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28208494	TCAGATACTCCTATA[C/T]CTTCCTAGCAGGTGT	8924
rs572400602	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28219904	CCACAGATAGGATCT[A/G]GCTTTCTTGGTCCAC	8924
rs572401343	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28288947	ACATCATATTGTGGG[A/G]TTTATACCATGTTTC	8924
rs572424313	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28123889	ATATAAAGTACCCAG[A/C]ACAGAGCCTGGCATG	8924
rs572437664	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28167193	TACTGACTTCCAGTG[C/G]AGAAACTTGGCAGAG	8924
rs572439706	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28292618	GCCAGGAGTATAAGA[C/T]CAGCCTGGGCAACAC	8924
rs572444849	snp	A/G	1.64871e-05	0.00287111	intron-variant	HERC2	GRCh38.p7	15:28167656	TTAAGATTATTTCAC[A/G]ATACAAAGTTAAAGA	8924
rs572448460	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318349	AGTGTTGAACAGGCC[A/G]GGCGCGGTGGCTCAC	8924
rs572464299	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28137517	AATATTTTAAACTTT[C/T]TCATTATTTTATCTG	8924
rs572494939	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28295555	AGGCGTGCATCACCA[C/T]GCCCAGCTAATTTTT	8924
rs572509535	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28288157	GAAACGGTAAAGGGA[A/G]ATCTTCAAACTGAAG	8924
rs572514266	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28168153	TAAAATTCTTGACTG[C/T]CAGAACTTTAAGGTT	8924
rs572528358	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28212062	AAGCCAGGCGCTTCC[A/G]GGACAGAGGCCCCTG	8924
rs572533305	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28290216	TAACAGTGAATAGAA[C/T]AAGTAGGCAGAAAAT	8924
rs572542498	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28287630	GCTTCAAATGCATTA[C/T]TTCATGTCAGTTGCA	8924
rs572542687	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28241083	ATACTTCTGTGCATC[A/G]AAGGAGGCTATCAAG	8924
rs572557304	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28200496	TGGATTTCCAGCCTC[C/T]AGAACCATGAGAAAT	8924
rs572575420	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28235886	CAGACAGATGGGAAA[A/T]GCACAACTATATGAA	8924
rs572576381	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28203668	CAGACGGCGCACCTT[C/T]CTGCACTGCAGGGGC	8924
rs572591971	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28200088	TCTGACACAACAGGA[C/T]TAGGGTCTTTATAAG	8924
rs572595931	snp	A/G	3.41606e-05	0.00413269	intron-variant	HERC2	GRCh38.p7	15:28124960	GCAGCATGTGACAGG[A/G]GCACACTTTGCTTGC	8924
rs572597315	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28211564	GCAATGCCCAAGGCT[C/T]ATCTGATAGCAGAGG	8924
rs572606489	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28194184	CATTCTCCCGCTTCA[A/G]CCTCCCGAGTAGCTG	8924
rs572613419	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28249062	TCCCAATGTTTAAGG[A/C]ATGTAAACATTAAGA	8924
rs572616130	snp	C/T			intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28315657	AAATTATCTGGCTCT[C/T]GGCGTTAGCGCCATT	8924
rs572618417	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28194535	AGATCACGCGCCACT[A/G]CACTCCAGCCTGGGC	8924
rs572626161	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28290637	TCTCTGACTACAACT[A/G]ATTTAGAAATTAACA	8924
rs572628817	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28140703	ATTTTTGTATTTTTC[A/G]TAGAGACAGGGTTTT	8924
rs572649122	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28161787	ACATTTTAAAGCTGT[A/C]ATAGTTAAAATACCA	8924
rs572649261	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28155126	CTGCATAGTATTCCA[C/T]GGTGTATATATGCCA	8924
rs572682222	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28149594	ACCAAAAAAACACAC[A/G]CGGCTCCTAACCGAG	8924
rs572695677	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28149922	CACCAAGAACAGCCA[C/T]ACGAACGCACATTCT	8924
rs572700666	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28236440	GGATTACAGGCACCC[A/G]TCACCACGCCCAGCT	8924
rs572705132	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28197814	TCACAGAATAACTGA[C/T]AGGACAAGTTTACAG	8924
rs572719446	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28239542	TGGTAGGGGATTTTA[C/T]AGAGGATACGCAACA	8924
rs572755044	snp	C/G	0.000798403	0.0199641	intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28315940	CTGAGACCCACCTTG[C/G]TCATAAACAAAATGC	8924
rs572763778	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28138403	ATGCAGCTGATGACT[A/G]TATTAGTTGAATTCA	8924
rs572803879	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28227246	TGCCACTGTGCTCCA[A/G]CCTAGGCGACGGAGT	8924
rs572842605	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316516	ATGCTCTCAATTAAC[C/G]TGACAAAATGTCACA	8924
rs572851492	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28121583	GTTGTGAGGGTGCAG[A/G]GGAACAGGCTGGCCC	8924
rs572859993	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28165399	AGGAAGTTATAAATA[C/T]AGAAAGGGTGAAAAC	8924
rs572864411	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28284840	GAATCACTTGAACCC[A/G]GTGGGGTTGGAGGTT	8924
rs572875447	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28156892	TGGCTGTGGGTTTGT[C/T]ATAAATAGCTCATTA	8924
rs572883178	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28128014	AACTGTAGTGAGCAT[C/T]ATCAGCAAGCAGACA	8924
rs572889265	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28251285	CCATCTCTACTAAAA[A/G]TACAAAAATTAGTCA	8924
rs572890282	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28164539	AAATGTACCTACCAT[C/T]TTTTTTTATGAGGGT	8924
rs572931547	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28245421	GCATGGTGGTGTGCA[C/G]CTGTGGTGCCAGCTA	8924
rs572934973	in-del	-/AAG	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28218998	GAAACAGATCTTTAC[-/AAG]AAGAAAAGATGGAAC	8924
rs572950997	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28275857	AGCAAGTAATTGTAT[A/G]TTATACTTTATACTA	8924
rs572969898	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28239384	GAAAACCTGAGTGGT[C/G]GTCACCTATGCAAGT	8924
rs572985951	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28116112	GCACAGAGCTTCCGA[C/T]GGTCCACCACCGTCA	8924
rs573008186	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321817	TAACGACAAATGACA[A/G]CAGCATGAATCTGCC	8924
rs573042617	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28278787	AAGTCACTATCACAG[C/T]CAAATAAAGCCAGCA	8924
rs573043671	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28152302	AACAAAAGATATACA[C/T]GTGGGTAACAGAAGC	8924
rs573049443	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28159478	TCGCTTCATTTCATT[A/C]ATTTGATCTTCAATC	8924
rs573050017	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28151274	AGATGTAACAGAAGA[A/C]GTACAGACCCCATAC	8924
rs573056894	snp	A/C/T	7.44733e-05	0.00610182	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28233443	TATCACCTTAATGAG[A/C/T]GAACATTTTGCTTGG	8924
rs573057091	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28233861	CACAAATCTTAAACA[C/T]GCCACAGCTTCTGAC	8924
rs573066362	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28270555	GGATAACACCTTCAA[C/T]TGCAAACGCGTTTAA	8924
rs573130808	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28307736	TTTAACTTTTATATG[C/G]CAAAAGAGGAATCTA	8924
rs573130965	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28237456	TTGTTACATGCATAA[A/G]GAACCCACTGGGCAA	8924
rs573150544	snp	C/G	0.00557542	0.0525036	intron-variant	HERC2	GRCh38.p7	15:28289785	TATCTGACTACAAAA[C/G]GGAAACACTGCACAT	8924
rs573162874	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28152935	TCCACAAGGACAGCG[C/T]GGCAGAGTGGAGGGC	8924
rs573202503	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28294977	AAAAGATCTGAACAG[A/G]AACTCACAGAGGATA	8924
rs573221538	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28231146	TTTATCTCTTTTAAA[A/G]TTTTTGGTCTAAATC	8924
rs573223289	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28189854	TAAAAAATGAATGGT[C/T]AACTACATTTAATAA	8924
rs573257675	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28144378	GCATGCCACTGCGAG[A/T]CGGTGAGACTCGCTC	8924
rs573263512	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28202047	AGAGAAAGCCAAGGT[G/T]TAAGACTGTTAGAGC	8924
rs573268164	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28190454	GTATGTGGGTACTGT[G/T]TAAAAGAACCTTCAC	8924
rs573272355	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28154127	TTTTTAAAAATAAAT[A/G]AGAGAATACATCATA	8924
rs573275628	snp	A/G	0.000666538	0.0182435	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28202444	CATGAGCTGCACCAC[A/G]ATCGGCAGAGCGGGA	8924
rs573287440	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28231896	ATCTATAAACCCACA[A/G]GAAACTCTAAAAGTG	8924
rs573291637	snp	A/C	0.0437281	0.141251	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318876	TTCAAACAAAAACAG[A/C]TGTGGAAAACAGATC	8924
rs573330473	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB, downstream-variant-500B	HERC2, LOC107987422	GRCh38.p7	15:28319617	AAAAAAGACTTTCTA[A/G]TCATATTGGAAATGT	8924
rs573350202	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28273414	CTTAGAATCTGGAGG[C/T]AAAATGTCAACACTA	8924
rs573359443	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28264068	AAAAAGTGAAATTAC[A/G]TAAAGGTGAAAACTG	8924
rs573366933	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28190577	ACTTGATGCCAACAG[A/G]TGTGACGACAAAAAA	8924
rs573384168	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28178585	AAACACTCCCTACAC[C/T]GAAAGAGTGGTTTCA	8924
rs573385480	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28207346	TCACCATGTTGGCCA[A/G]GCTGGTCTCGAACTC	8924
rs573399310	in-del	-/TATTCATGG	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28180114	TCCTGCAAACTCCAT[-/TATTCATGG]TAAGTGCCCTATGCA	8924
rs573402569	in-del	-/A	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28297554	CCCATTATGTTGTTT[-/A]AAAAAAAAAACATGA	8924
rs573403760	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28140207	TCAAGGGCTTCTACT[C/G]AAACCCCACTGGAAG	8924
rs573417737	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314754	TAATCCCAGCTACTC[C/T]GGAGTCTGAGGCAGG	8924
rs573424785	snp	C/G	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28301856	CTAAGCTGGAGTGCA[C/G]TTGTGCGATCTCAGC	8924
rs573447063	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28256478	AAAACTCTTACCCAC[A/G]ATAGTTGAGGTATTT	8924
rs573448970	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28309212	GTTTGATGTTTCTTC[A/G]TTAATTTTGTCTGGA	8924
rs573456322	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28315276	AATTCACACCCACAC[C/T]CGCCACACCTTCCAG	8924
rs573464426	snp	A/C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28225691	AAGAGAGCAAGACTC[A/C/T]GTCTCAAAAAAAAAA	8924
rs573473135	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28264940	CATACAGGGAAGTAT[C/T]TAAAATGATTTTTCA	8924
rs573479807	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28170305	AATACCATAACCAAA[A/G]CTGTGTGGTACTGGC	8924
rs573483337	snp	A/C/T			intron-variant	HERC2	GRCh38.p7	15:28240396	ACACTCCCGCCTGGG[A/C/T]GAAAGAGCGAGACTC	8924
rs573495250	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28259840	AGGCATGGTAGTGCA[C/T]ACCTATAATCCCAGC	8924
rs573500911	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28219759	CTGTAGCCATGGGGG[A/G]CACTGCGGTGCTTCC	8924
rs573503040	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28226271	TTTTTGCAGATATGG[A/G]AAAGCCAGCCTTGAA	8924
rs573531175	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28180363	TGACAAAATCACCCA[A/G]CCAAAACTTTCTCAG	8924
rs573531710	in-del	-/AAT	0.0111196	0.0737302	intron-variant	HERC2	GRCh38.p7	15:28258474	AAAACTCCATCTCAA[-/AAT]AATAATAATAATAAT	8924
rs573532374	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28280593	ATGGCACACTGCCTC[A/T]CTCTATGGAAACATC	8924
rs573555021	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28181260	TCTGTCCTTGAAGTG[A/G]AAACTCCATGTAAGG	8924
rs573587298	snp	A/C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28261147	TTATTAAAACTGCTG[A/C/T]ATTTTGTCAGCTACA	8924
rs573615451	snp	A/G/T	0.00518141	0.0506816	intron-variant	HERC2	GRCh38.p7	15:28220177	TGGTGCAGCTGCCCC[A/G/T]GCCTGGCCACCACAT	8924
rs573627226	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28193287	GATAATATTTCAGCA[A/G]AGAACCAAAAACTAC	8924
rs573631798	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28287371	AGAGAGTCGGTTCTG[C/T]GAAAGCTCTGTACCT	8924
rs573637389	snp	A/C	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28187445	CAAGCGATTCTCCAA[A/C]CTCAGCCTCCTGAGT	8924
rs573647501	snp	A/G	1.64901e-05	0.00287137	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28228353	GCGGGATGGTCCCCA[A/G]GCTCGGTCCTGACGG	8924
rs573658522	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28228744	ACGATGGGCCTACCC[A/C]CTGCATTCTATGCAC	8924
rs573659032	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28220723	TCCCAGCAGACCTCA[A/G]TTAGGAGGGTGCATG	8924
rs573662362	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28199480	ATTCTGAAAACTGAT[A/G]AAGTCTCCCTGTATT	8924
rs573687795	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28227705	GTATATAAATGTTCC[C/T]AGCAGCACTATTCAC	8924
rs573693228	snp	A/C	0.00159617	0.0282053	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317038	TGCTAGGATTACAGG[A/C]TGAGCCACCACACCC	8924
rs573694321	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28286478	AAAAATCAATGTAAC[C/T]CACCCTATTAATAGG	8924
rs573709136	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28112253	GATGATGGCTCTCTA[C/T]TGTCATCCCGGGAAG	8924
rs573718446	snp	C/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28136351	AAGGAAGCCACAAGG[C/G]CCAATGCAGGAAGTG	8924
rs573725697	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28199964	TTATCATGAATGTTT[C/G]TGTCCCCCCCACCAA	8924
rs573731870	snp	G/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	HERC2, LOC107987422	GRCh38.p7	15:28317545	CTGAGGGCATTATGC[G/T]GAGTAAAGAAAATCA	8924
rs573745581	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28112858	TTCTGGGGATGGCCA[A/G]ATACATTTTTAAAAA	8924
rs573755878	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28142159	ATTTTTCTGTGTCTC[A/G]TAATATTGGCATCTT	8924
rs573756006	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28306646	TTCACTAGGATTGGT[A/G]ACAGTTCTTCTTTAA	8924
rs573762412	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28248378	TAAAAATATTAACGA[A/G]GCTATTATAGAAAGG	8924
rs573765746	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28187415	TGGTTCATTGCAACC[C/T]CTGCCTCCCGGGTTC	8924
rs573776832	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28137570	ATGTTTGATGTTACT[A/G]TTGTACTTGTTTTGA	8924
rs573790527	snp	C/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28260345	AGAAGCTTCTAAAAC[C/G]GGGAATTAAAGACAC	8924
rs573820562	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28311764	AGAGGGGAGACCCCT[A/G]CCCAGACCTGAAAGC	8924
rs573821773	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28307121	ATTACAGGCATGAGC[C/T]ACCACGCCCGGCCTG	8924
rs573839301	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28222992	GTCCTTTTTTCATGA[A/T]TTTGCTCTGTGTGCC	8924
rs573841934	snp	C/T	0.046775	0.145601	intron-variant	HERC2	GRCh38.p7	15:28298889	TACTTTCTAAAGTGG[C/T]AGCTTTATCCACGTT	8924
rs573859626	snp	A/C	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28312638	TTCATAAAAAAAATA[A/C]AATAAAATAAAGAAA	8924
rs573891854	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28129666	CTGCACAGCCCAGTA[A/G]TAAGTAATAAATAGA	8924
rs573901102	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28217172	GACTTACACTGACTT[A/G]CACTTACACTGGGTG	8924
rs573903018	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28223478	AGATAAACTAGCAGG[A/G]GAAACAGCCTTTCCT	8924
rs573904501	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28130441	CATCCATGAAAAGGT[A/G]GTGCACATACCCCAA	8924
rs573911635	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28211741	ATGTGGTGATTTGCA[C/T]GCACTGCACCTCCAA	8924
rs573912820	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28247032	ACAGAAGCCTGTTAA[C/T]CCTTGTCCTTGCGCT	8924
rs573915643	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28284145	CTGGAGTGCCAAAAA[A/G]TTTCAAATTTTGGGG	8924
rs573930248	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28192397	CAACAGCAGATTAAT[A/G]TATTTCCAAAGAAAA	8924
rs573950915	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28247642	ACTATGTTGGTCAGG[A/C]TGGTCTTGAACTCCT	8924
rs573957950	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28186094	GATGGACAATAGTGA[C/T]GGTTGCACAAAAATA	8924
rs573959529	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28310413	TCACTCCACTGTACT[C/G]CAGCCTGGGCAATAG	8924
rs573970457	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28142745	CAGAGGCCTAAAACA[C/T]ACACACTGCACATGA	8924
rs574018456	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28131461	TGGGCTACACGGCAG[C/T]GTGGTGTGCATGCAC	8924
rs574018664	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28217864	GAGCTCCCAGAAGCT[A/G]GACAAAGTAAGGAAG	8924
rs574046292	snp	C/T	0.084364	0.187256	intron-variant	HERC2	GRCh38.p7	15:28305210	TAGCAGCATGATTTA[C/T]AGTCATTTGGGTATA	8924
rs574070430	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28258726	AGCCAAAGGGACAAA[C/T]GACAAGACAAAAGCA	8924
rs574083291	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28266207	GTAGAAATATAAAAA[C/T]AGTGTTTGTTAAAGA	8924
rs574092724	in-del	-/CATATATA	0.0364509	0.129988	intron-variant	HERC2	GRCh38.p7	15:28245653	ATATATATACACACT[-/CATATATA]CATATATACACACAC	8924
rs574105519	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28252674	CTCTTTCCATTAACA[C/G]AAACTATATGAAGTT	8924
rs574113050	snp	C/G	1.70397e-05	0.00291883	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28215743	GAGCGATGCTCCGCA[C/G]AAACCCCAGCGTGCA	8924
rs574125940	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28177649	AACTCAACAGGATCA[A/G]CAGCGGAGTTAGCAG	8924
rs574138070	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28178194	GAGATGGTGACTGAA[A/G]TGAGTGGGGCTTCCG	8924
rs574140848	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28297839	ATATACAAATTTTAC[C/T]TGAAAGTCAAAAACA	8924
rs574144071	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28311371	CAGGGGGCTGAGGTG[C/G]GAGGATCACCTGAGC	8924
rs574151118	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28216442	GCCCACCTCTGCTCC[A/G]CCTGGCTCCAGGACT	8924
rs574161253	snp	A/T	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28210745	TGCCACCAATCTTGC[A/T]GACCCATGCAGCACA	8924
rs574162045	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28167495	ACTCAAGGAATACAC[A/G]TGGAAGCAGTAAGCA	8924
rs574182500	snp	C/T	0.0103295	0.0711199	intron-variant	HERC2	GRCh38.p7	15:28297187	TGAAATGGGAACAAA[C/T]TGGTACATAAATGGA	8924
rs574194288	snp	G/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28122670	TGCTCTGGACCGGGA[G/T]TAGTAACACCCACTC	8924
rs574195919	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28132019	AATGGTGGCTCTGAG[G/T]CTGTGTTTTCCCAGA	8924
rs574198793	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28163896	CTTCAACTCCTCTCC[C/T]TGTTTGCTATGAGCC	8924
rs574201673	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28172532	GTAGGAAAAGCGTAG[C/T]TTTTCAACAAATACA	8924
rs574228980	snp	C/T	0.00011601	0.00761523	synonymous-codon	HERC2	GRCh38.p7	15:28116708	GGGTGCTCTGGCGGC[C/T]GGGCTGAGCAGGTAG	8924
rs574247848	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28166910	CTAAAACAGGAACTC[C/T]TGATTCTATACAATA	8924
rs574269543	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28126591	TGCCACAACCTGGAT[G/T]GGACTAGAGACCATT	8924
rs574272053	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28160110	TTTTGTCTCAGAGGG[C/G]TACCCGGCCGTGTGA	8924
rs574272509	snp	A/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28291328	CTGCTGGCCTCAAGC[A/T]ATTCTCTCACCTCAG	8924
rs574288995	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28173149	GAACATCCACTTTGC[A/G]AAACAGTATGTAGCG	8924
rs574295150	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28204933	GAGCAAGGCAGGGGG[A/T]AAAAACAATAGTCAA	8924
rs574343245	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28120578	AAGCAGTATACATTT[A/T]GAAATGGTCTACTTG	8924
rs574360555	snp	G/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28205405	AGAAGAAGCTGGAGT[G/T]CAGAAGAGCTCATGG	8924
rs574366785	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28225061	TCAATAACTTAACTC[C/T]ACATCTGGAAGAACT	8924
rs574370422	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28168773	TAATAGCTAAAATGT[C/T]TACTCTGGATCCTAT	8924
rs574378909	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28209700	TAGGTTATATGCAAA[C/T]ACTACACCATTTTAT	8924
rs574413134	snp	A/G	0.0402882	0.136092	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28300565	CGGTGGCTCACACCC[A/G]TAATCCCAGCATTTG	8924
rs574437731	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28238335	GTGAGGGTTACCAGA[A/G]TATAATGACCTTCTA	8924
rs574441147	snp	C/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28261722	TACCATTCAATGACA[C/G]AGAGTAAACTTCTTA	8924
rs574445076	snp	C/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28235813	GCATCCTGAACACCT[C/G]GCATGGTAACTGCAC	8924
rs574453319	snp	C/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28294401	ATCAACTGCTAAACA[C/G]TAAGGACAAAACCTT	8924
rs574459219	snp	C/T	1.65529e-05	0.00287683	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28269434	GACCTCTTGCAATGA[C/T]CCCTGTAAGATAAGA	8924
rs574473075	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28273654	CTCAGAGCCGGGGAC[A/G]CAAACGCCAAAGGCC	8924
rs574475383	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28301562	CCCAGAACAGGAAAA[A/G]GGAGCATTTCAGACA	8924
rs574480462	snp	G/T	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28293185	GTAACAGACCCAGTA[G/T]AATTTTCATAAAGAA	8924
rs574483887	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28250355	TCACTACCTGATACC[C/T]TGCCTGGATAACACC	8924
rs574513853	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28174929	GTGTAATAATTTTTT[C/T]CCTTTTATTTTGCAA	8924
rs574519212	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28288228	TTAAGGGCCCATAAT[G/T]GTAAAATGTAAGTTA	8924
rs574519217	snp	A/G	0.0103295	0.0711199	intron-variant	HERC2	GRCh38.p7	15:28293658	ATCCAGTGAGTCCCA[A/G]TGCTTGTGTATCCAT	8924
rs574536715	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28295998	TTTTACATATTTGAC[A/G]AATTCTGAGACCCTG	8924
rs574541167	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28208642	TCAGCCCCACCACTC[A/G]TCGACAAACCCTGAG	8924
rs574561697	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28120077	ACAACGCAGAAGCCA[C/T]CAGCTGGCCTTGCCT	8924
rs574562524	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28200584	AGACAAGGGGGAACC[A/G]CTCTAGCTTGGAATA	8924
rs574583513	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28208866	CTGACCCCAGAGGAC[A/G]AAGAGAGCCATCTGC	8924
rs574591729	snp	A/T	0.000399281	0.0141238	missense	HERC2	GRCh38.p7	15:28169568	AATGACAAGAGAATC[A/T]TGGCAAGAGAAGGGC	8924
rs574596314	snp	A/G	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28114538	ACACTCCTGAAAAAC[A/G]CACATGTCCACACAA	8924
rs574597439	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28250843	CCATGCTTATGAAGA[C/T]AGCCTGGATATCGGC	8924
rs574600688	in-del	-/TACAGAGGT	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28230292	CTCCAGATGCTCAGG[-/TACAGAGGT]ACAAGACTGTGGATT	8924
rs574621604	snp	A/C/G			intron-variant	HERC2	GRCh38.p7	15:28194453	CGGGCGCCTGTAGTC[A/C/G]CAGCTACTCGGGAGG	8924
rs574621618	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28231185	ATATAATATAAAAAA[C/T]AAGCAACATGATAAT	8924
rs574644982	snp	A/C	0.000318962	0.0126246	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202515	TGTGCTGCACGGCGA[A/C]AGGCGTGGTGGCCTC	8924
rs574655734	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28123881	TCTCATTGATATAAA[C/G]TACCCAGAACAGAGC	8924
rs574674631	snp	A/G	0.00016515	0.00908558	intron-variant	HERC2	GRCh38.p7	15:28201423	TGCTGAATGAAAAAC[A/G]GATCGAGGCTCCAGC	8924
rs574674725	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28194567	ACAGAGCGAGACTCC[A/G]TCTCAAAAAAAACAA	8924
rs574677379	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28289555	TGGAGATACTCCTGG[G/T]AAATAAAGCCAGTCG	8924
rs574693836	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28319911	ATTAAAACTTTGCCT[C/G]AATCTCAGGATTTCA	8924
rs574714537	snp	G/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28289826	CCTTGTGCAGTGAGA[G/T]GACGACACACCTCAG	8924
rs574718930	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28157834	TTAATTGTGATGTTA[A/G]GGTGTCAATTTTAGA	8924
rs574725991	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28173831	AACAACAACAATAAC[-/A]AAAAAGAAAACATGC	8924
rs574735462	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28195091	TATGTTAAGAACATA[C/T]AAATCAGAATGAAGA	8924
rs574740440	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28212125	CCAACAGGGTGACTG[A/G]GCCACAGGGCCCTGG	8924
rs574741750	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313773	AACATTAAGTACGTC[A/G]ATTTGAAGACATCCT	8924
rs574742866	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28161393	CTTTCCTCCACACAA[A/G]GTAGGCACCCAGAGA	8924
rs574746789	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28156039	TTTCCCCATTTCTCG[A/T]TTTTGTCAGGTTTGT	8924
rs574752833	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28206969	CGAGCCAATATCACA[A/C]CACCATACTCCAGCC	8924
rs574801112	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28284261	AAAAGATACACTCTA[A/T]AACACTACAGATAAA	8924
rs574833614	snp	A/C	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314246	AGAAGTCAACAGAAC[A/C]GACCAAGAGTAGATC	8924
rs574850283	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28207883	GCATCCAGAGACGAT[C/G]TGTAAACAAGTGGTG	8924
rs574860041	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28165488	ATGTACGTAAATATA[C/T]AACAACACAAATACT	8924
rs574863246	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28124637	CAATCACTGCAGCTT[A/G]GACCTTTCAGACTCA	8924
rs574883435	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28131993	CCTAAGGAGCACACA[C/G]GGGGGACAGTAATGG	8924
rs574884765	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28290712	TTTCCAAATAATAAG[C/T]GGGTAAAAGAAGAAA	8924
rs574888371	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28282425	CTTCAACAAGCAATT[A/G]CAAACACATGTGAAA	8924
rs574888396	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28184299	TAATGTCTGGCACCA[C/T]GTAAGTATCAATCAG	8924
rs574893249	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28210357	CCAGGATGGTCTCTA[G/T]CTCCTGACCTCGTGA	8924
rs574901938	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28249082	AAACATTAAGACAAC[A/G]AAATTTAAAATACTG	8924
rs574902055	snp	G/T	1.66145e-05	0.00288218	synonymous-codon	HERC2	GRCh38.p7	15:28125009	GCCCGGACTCACCTG[G/T]GCAGGGAGTTTGCCA	8924
rs574911008	in-del	-/ACG	0.106987	0.205054	intron-variant	HERC2	GRCh38.p7	15:28218432	CATGAACACCCAGAC[-/ACG]ACAAGCGTGCGGCCC	8924
rs574925804	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28291202	TCCTATAATAACCTA[C/T]GAGGTAGGTACTACT	8924
rs574927195	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28113521	GTCACTGATTTGTGG[C/G]TCAGCAGGCAAAAGG	8924
rs574966952	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28197940	CAAACCACAAACAAC[C/G]ACACAGTCCCCTATC	8924
rs574968299	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28119202	GGAGTTTGGGACCAG[C/T]CTGGCCAACATGGTG	8924
rs574995496	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28155774	TAGTTTAATTGGATC[A/C]CATTTGTCAATTTTG	8924
rs575000351	snp	C/G	1.7648e-05	0.00297047	intron-variant	HERC2	GRCh38.p7	15:28230364	TCACAGAAAATACTG[C/G]ACCTTGGGTGATTTA	8924
rs575007455	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28113888	CCAGCCGACAGGGTA[C/T]GGCCTAATGACCACC	8924
rs575010918	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28286233	GCTAATATTAGAAGC[A/T]AATAGAAGCTAATAT	8924
rs575027975	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28278918	AAGCCTTAAACATTC[C/T]AGTGGCTGTTAGCAA	8924
rs575053713	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28275655	GAGAGAAAAGGCTAG[A/C]ATACAAAAATGCATA	8924
rs575057043	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28156270	TGGTTCCAAATGAAC[C/T]TTAAAGTAGTTTTTT	8924
rs575059262	in-del	-/TCGAACTTCC	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28159673	TTCTTTGCAATGGGT[-/TCGAACTTCC]TCCTTTAGCTCGGAG	8924
rs575064674	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28236538	TCAGGTGATCCACCC[A/G]CCTCAGCCTCCCAAA	8924
rs575069742	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28292745	CGGTAAGTTTTATGG[C/T]ATGTATATTTTACCA	8924
rs575076549	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28191879	GCAAAACTTTGCAGG[C/T]TGCTCAAAGTTCATT	8924
rs575077771	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28145231	ACCCTAGCTCTCCCA[A/T]CAAAAGGCCTATGTG	8924
rs575082208	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28230868	GGTGTGGCTGTGCTC[A/C]TGTAAAACTTTATTT	8924
rs575145271	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28192610	AAAAATAAATAAATT[A/C]TCTTCGAACTATCAG	8924
rs575160436	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28293141	CTGAATGTTGGACAA[C/T]GTAAAAATAAAATAC	8924
rs575172250	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28269096	ATCTTGACAATATTA[C/T]AACTGAGATCATTAA	8924
rs575183648	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28305373	CTCAGAAATAACGCC[A/G]CATACCTACAACTAT	8924
rs575183785	snp	A/G	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28310963	GCACCTATAGTCCCA[A/G]CTACTCGGGAGGCTG	8924
rs575191353	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28303829	TTATAAATGGAATTA[C/T]TTTTCTTGATTTTTC	8924
rs575195658	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28129114	TTTGACCTGAAAAGT[C/T]CCTTTTGCCATTGTG	8924
rs575202221	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28204275	CAGATGTTAGAATTA[A/G]CAAACAAGAAATTCA	8924
rs575206005	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28210048	ACACACTGCAACCTC[C/T]GCCCCCCGGTTCAAG	8924
rs575210913	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28194499	GGCATGAACCCGGGA[A/T]GCGGAGCTTGCAGTG	8924
rs575211462	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321496	ACGCTGAAGACCTAA[C/T]GCTTTTTAATAGTTT	8924
rs575214532	snp	C/T	3.3151e-05	0.00407117	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28238649	TGGAAGTCCTTTATA[C/T]CATACACCTTCCCGT	8924
rs575215179	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28149035	ACGGCCGCACAAACG[C/T]ACATTCTAGTAAAAT	8924
rs575219746	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28204777	TTAGGCCCAACAAAG[A/C]AAAGCATCTTGACCT	8924
rs575252473	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28146709	GGCAGCTGTGGGTCA[C/T]CTGGGGAGTGAGCGG	8924
rs575263041	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28157450	CTATTCAGAGATTCA[A/G]CTTCTTCCTGGTTTA	8924
rs575278788	snp	A/G	0.00636936	0.0560724	intron-variant	HERC2	GRCh38.p7	15:28159552	GTGTGCATTTGTCAC[A/G]TAGTTCTCATGCCAT	8924
rs575279936	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28237303	TACCACATAAACCCA[C/T]ATGCCCAGTAAAGCA	8924
rs575286125	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28159951	GTTTTCCTTCTAACA[A/G]TCAGGACCCTCAGCT	8924
rs575287822	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28121603	CAGGCTGGCCCCGAA[A/G]CACACAGGGACAGAC	8924
rs575296457	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28239198	CTATGAAAATTAGAA[A/C]ATGTGTTCAATTAAT	8924
rs575307740	snp	C/T			downstream-variant-500B	HERC2	GRCh38.p7	15:28110953	TTAACAAAAAAATAA[C/T]CTCAACTTGGCTGAA	8924
rs575311138	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28128657	TTAATGAAAGATGGC[A/G]CCCACGTTTTTCACT	8924
rs575319969	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28163732	TCTTTCCTGGAATCT[A/T]ATTTCAAGCAACTCA	8924
rs575325634	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28122065	GGGGCCAGGGAGCAC[C/T]GTGCAGCCAGCCAGA	8924
rs575336788	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28116509	GGCGTGAGCCACCGC[A/G]CCTCACCCTAAAAGT	8924
rs575339532	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28153011	CACATAAAACAGAGA[C/G]AGCACAGAGCCTGTA	8924
rs575350678	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28279654	ACACACACACACAAA[C/T]TGTTTTTATTTAGCC	8924
rs575367579	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28239551	ATTTTATAGAGGATA[C/T]GCAACACATGAATTC	8924
rs575392562	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28257714	ATCTAATTTATAGAA[A/C]ATTTCACCCAACAAC	8924
rs575406724	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28156593	TTGTGATTTTTGCAC[A/T]TTGATTTTGTATCCT	8924
rs575433742	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28273293	CTCATTATCAAAAAC[A/G]TAAGTAGAAGAATAT	8924
rs575440883	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28272570	TTAGCACAAGACATC[A/G]CCTTCTGCTCATAAG	8924
rs575445107	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28256990	ACCCATGCCCTTCAA[A/G]ATACATAAACCTTCT	8924
rs575456303	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28228210	CGCTCAAGCGGGTGC[A/C]GACCTACCAATCAGG	8924
rs575457944	snp	C/T	4.97492e-05	0.0049872	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233522	TTTACTTGCTCAATA[C/T]CAAGTGCACCTGCAT	8924
rs575462053	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28148400	AGAAAGTAACCAACA[C/T]TAACTCTAAAAGGCA	8924
rs575472623	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28187324	TTAAGGAGGTCTGGT[G/T]TTTTTTTTTGTTTTT	8924
rs575492335	snp	A/G	0.000798403	0.0199641	stop-gained, nc-transcript-variant	HERC2	GRCh38.p7	15:28234162	TGTGGGAGCAGAGTC[A/G]AGATTTGCTGGCAGG	8924
rs575502585	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28276730	CGACAAAGCGAGACT[C/T]TGTCTCAAAAAAAAA	8924
rs575511596	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28289937	TGAGAGGATTACACA[A/C]CTAAGTGAGAGGACC	8924
rs575517842	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28178304	ACTCTGGGGGCGAGA[G/T]CTAGTCTAAGACCAT	8924
rs575523004	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28171260	GATGGTTGAGTATTC[A/G]ATGGAATACTGAACA	8924
rs575524373	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28148963	CCACACCAACATACA[C/T]TCTAGTAAAATTACC	8924
rs575529528	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28218785	ATTGAAGACTTGAAT[C/T]TTAGTGCAGTTTTAG	8924
rs575531701	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28257650	ACAGTGAAATAACAA[G/T]TAATCGGCAAGGATC	8924
rs575537569	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28164627	AAGAAAATCACTAGC[A/G]GCATATCCTTAAATA	8924
rs575537647	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28171869	CACGAGGTCAGGAGA[C/T]CGATTCTGTCCTGGC	8924
rs575538112	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28221975	TATCGTACAGAACTG[C/T]GCAGAAGATAACTAA	8924
rs575582815	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28149519	CCAAAAAAACACACG[C/T]GGCTCCTAACCGAGA	8924
rs575596361	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28270633	CACACGGGCCCAGGA[G/T]GAGAACCTACAAGTG	8924
rs575607620	snp	A/G	0.00199481	0.0315187	intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28320325	CACCATGTTGGTCAG[A/G]CTGGTCTCCAACTCC	8924
rs575610570	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28184689	ACACGGTGAAAGCCC[A/G]TCTCTACTAAAAATA	8924
rs575618862	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28225756	AACTAACATCAGAAA[C/T]GTAAGTGGAGACAGT	8924
rs575632871	in-del	-/C	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28153519	AGCTGGGTATGGTGG[-/C]CCGTGCCTGTAGTCC	8924
rs575636986	snp	A/G	9.0592e-05	0.00672962	intron-variant	HERC2	GRCh38.p7	15:28142819	TTAAAAAAGAAGTGA[A/G]ACATTACCTTAAAGA	8924
rs575645982	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28149800	TAGTAAAATCACCGA[A/G]AAAACACACGTGACT	8924
rs575646071	snp	A/G	3.29913e-05	0.00406135	missense	HERC2	GRCh38.p7	15:28144115	GCTGCCAGCGAGGCC[A/G]CAAGGCGAGGGACGA	8924
rs575661062	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28232464	TGAGGCAGGGGAATC[A/G]TTTGAACCTGGGAGG	8924
rs575661491	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28284674	ACGCCTGTAATCCTA[A/G]CACTTTGGGAGGCCA	8924
rs575676002	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28140232	TGGAAGCCTGGGAAC[A/G]CTCCATCTGCACCCG	8924
rs575678604	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28271123	ATACCACAGGTAAGA[C/T]GGATCCACACAGATT	8924
rs575688963	in-del	-/AAAG	0.00914312	0.0669923	intron-variant	HERC2	GRCh38.p7	15:28169839	TATCCATACTTCGAT[-/AAAG]AAGCTATTTTCAGCA	8924
rs575696212	snp	C/T	1.65999e-05	0.00288091	intron-variant	HERC2	GRCh38.p7	15:28196438	GTCCCAAAGCAAATC[C/T]AGCAACCATAAAAAT	8924
rs575713639	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28185372	CTGTGCCTGTCTGGA[A/G]GGCCCCGGTCACACT	8924
rs575727276	snp	A/G	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28303420	TTTCTAGTAAACTTT[A/G]CACTTGATCTAAGCC	8924
rs575754897	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28140960	AAAAATAAATTGGCC[A/G]GGCGTGGTGGCTCAT	8924
rs575758707	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28315420	GAGGGACAGAGAGAG[G/T]CGGCTAAGGAATCTA	8924
rs575766586	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28191441	TAGAGAAAAGTCTCA[C/T]TCTAAGACTCAGAAA	8924
rs575768971	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28205052	GGTGTGCCACCATTG[C/T]ATACATGAGCCCAGC	8924
rs575801053	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28261212	TACTAGGATACAAAA[A/C]GGATCTGTTTTTTTT	8924
rs575828936	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28176875	TTTATGAACTTTCCT[A/G]GACTTGAAGCTTATT	8924
rs575846805	snp	C/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28231660	GGACTTCCCTCCATG[C/T]ACCCTTCCCTCTGCT	8924
rs575847127	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28251457	CGGGGGAAAAAAATT[A/G]TCCTTAGTCACATTA	8924
rs575848238	snp	A/G	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28309282	CCTCCATCTATTAAT[A/G]TGTTAAGGCCTATCT	8924
rs575859492	snp	C/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28303999	GGTGAAACCCTGTCT[C/G]TACTAAAAATACAAA	8924
rs575884709	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28309803	GTTGTTACAAGCTGC[C/G]AAATTTGTGTTTGGT	8924
rs575885644	snp	A/G	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28136103	TTTCAGCAGGGCAGC[A/G]TATAAACCACAAGGG	8924
rs575901064	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28244436	CAGAAGTAAGGTGGC[A/G]ATGACCACACAGCCT	8924
rs575923446	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28128991	TCACATCTCTGACTG[A/G]CTCTTCTGCCTCCTT	8924
rs575925133	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28254935	AACTATGAACACGCA[C/T]CTGCCCCAGGACCTA	8924
rs575930429	snp	A/G	0.000399281	0.0141238	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214684	ACGTCAGAGGAGCAG[A/G]TAGTGAGCAAGCTTC	8924
rs575930574	snp	A/G	0.000103277	0.00718526	intron-variant	HERC2	GRCh38.p7	15:28220682	CAGTTAGGAGGGTGC[A/G]TAACCTGCCCTGGTC	8924
rs575933651	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318040	GCAGGATAACTCCAT[C/T]CTGGACTTATGCTCA	8924
rs575935064	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28162112	AGGTGGGTAGATCAC[C/T]TGAGGTCAGCAGTTC	8924
rs575935071	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28168672	AGGCAGGGCTAGCAC[A/G]CACTGAGGCGTTTCC	8924
rs575938325	in-del	-/AG	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313503	TGACTTCAGAACTAT[-/AG]AGTCAGGCAATAAAA	8924
rs575963976	in-del	-/T	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28185262	AGCGGCACAGGGCAG[-/T]TGCTCTGTTGTCTCC	8924
rs576038961	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28268381	AATTGGAAAACACCT[A/G]GACACACTTCTGCGC	8924
rs576039891	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28215036	CCCACCACCAAGCCC[A/G]GCTCATTTTTTTTTG	8924
rs576039939	snp	C/T			missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28262983	TGTCCAAGTCTCTGG[C/T]TGTCACCTTTTCCCC	8924
rs576049890	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28180493	TATTTTAAGAATGAA[A/G]TGATACACTGTGATT	8924
rs576066236	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28223045	CTGAGTTCAACTACA[C/T]GCTGAGTCTTGTGAG	8924
rs576087493	in-del	-/T	0.0138799	0.0821421	intron-variant	HERC2	GRCh38.p7	15:28236598	CTGGCTATCTCCTAC[-/T]TTTTTTAAAGAGAGA	8924
rs576093087	snp	A/G	0.0197687	0.0974348	intron-variant	HERC2	GRCh38.p7	15:28311829	ACATCAGTGTTCTGC[A/G]GTACAGCCTAGATTG	8924
rs576097936	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28223537	AGGAAGGGGCCCCAA[A/G]GAAGGGACAGGAGTT	8924
rs576125314	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28134827	AGGTGTGTGTCACCA[C/T]ATCTGGCTAATTTTT	8924
rs576148627	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28138326	GATGCCAGCTAGGAC[C/T]TTCATAGCTAGAGAG	8924
rs576158259	snp	A/C	0.00597247	0.0543191	intron-variant	HERC2	GRCh38.p7	15:28210857	GACAATTTTATTCAC[A/C]GTTGGTGGTTGCTGG	8924
rs576159283	snp	A/G/T	3.38663e-05	0.00411488	synonymous-codon	HERC2	GRCh38.p7	15:28132175	CCCCCAGGACCAGAC[A/G/T]GTGTCGTCATCTGTG	8924
rs576159771	in-del	-/TA	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28136221	AAAACATACACACAC[-/TA]AATCAGACTGCCGTT	8924
rs576164830	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28293388	GTCCCAGCTACTCAG[A/G]AGGCTGAGGCAGGAG	8924
rs576168752	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28188473	GGAGTGAACCCGGGA[A/G]ATAGAGCTTGCAGTG	8924
rs576183759	snp	A/G	0.0240643	0.107019	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174296	TAATGCAGTTAACAT[A/G]GCACTACAACCTCTA	8924
rs576227788	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28123761	ATGAAGGCCCCACCT[C/T]ATCCTTCTGGAGCAG	8924
rs576249874	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28289063	CAGTGTAATACCATT[G/T]GAGAGTGGACAGTGA	8924
rs576250950	snp	C/T	0.000399281	0.0141238	missense	HERC2	GRCh38.p7	15:28132778	CGCCAGCAGCAACAT[C/T]GACCACTTCAATTCC	8924
rs576257916	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28217908	AGCCTGTGGAAGAAG[C/T]ATGGCCCTGCCCGCA	8924
rs576264608	snp	A/C	0.00017473	0.0093453	intron-variant	HERC2	GRCh38.p7	15:28117247	GAATGCACGAGGAGG[A/C]GGCACCGTGCATGGG	8924
rs576275650	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28174717	TAACGCGTATGCCAC[A/G]GTAGTTGAAAGAATT	8924
rs576279086	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28293748	GCCCTACTCCACTGC[C/T]AACTGGGAAGCACTG	8924
rs576316474	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28207110	GAGCCAGCAAATGCT[C/T]CTTCCCAGATTTCTG	8924
rs576340443	snp	C/T	0.00597247	0.0543191	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299860	AATTTGAGACCAGCC[C/T]GGCCAACACGGTGAA	8924
rs576350942	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28150970	TCCACTTCAGACCCC[A/G]CGAGGACCAGTCAGT	8924
rs576366377	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28223761	TGATTTCTTAAATGA[C/T]AAGAAGGATACCCTG	8924
rs576373488	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28136720	CACTCATTTATAATA[C/T]GTCCAGGGCTGCTTT	8924
rs576387353	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28193640	CCAAGAAAGATAAAC[A/G]TCTCCATGCACATGT	8924
rs576392808	snp	C/T	3.31208e-05	0.00406931	intron-variant	HERC2	GRCh38.p7	15:28179081	TCACAACATTAAAAA[C/T]TTTTTTGTTTTTTGG	8924
rs576418052	snp	A/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28298132	GAGACTAATACTTTT[A/T]CCCATGGTTTGTTTT	8924
rs576435292	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28212393	AGAACACTGTACAAA[C/T]GACACGAGTTTAAGA	8924
rs576461625	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28151621	TGTAGACTGCCTGGA[C/T]GCTACTGAAGACTAC	8924
rs576462219	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28298718	GGAGAATGGCATGAA[C/T]CCGGGAGGTGGAGCG	8924
rs576475701	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28258770	TTGAAAGCAAAACAA[A/G]AGGGAAAAATTAATG	8924
rs576475779	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28189224	AGGTCAGGAGTTTTC[A/C]ATTTACCTGCAATGC	8924
rs576494521	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28143239	AACGCTGCCTGTCTC[C/G]TCCCATGGGTAGGAT	8924
rs576501629	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28291830	GAATGGCATGAACCC[A/G]GGAAGCGGAGGTTGC	8924
rs576511901	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28252317	GGCAAGCAGGAGACG[A/G]GGAAAACGGGCACTG	8924
rs576517857	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28247717	ACAGGCGTGAGCCAC[C/T]ACACCCAGCCTCCTA	8924
rs576533553	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28172587	CAAAAAAAGCCTTTC[A/C]ATCTGAACCTCCCAC	8924
rs576544291	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28160516	CGAGGCTCCGTGGGC[A/G]TGGGACCCTCCGAGC	8924
rs576559323	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28209031	CTCATTCTAGAAAAC[A/T]AAATATAGAGAAATA	8924
rs576570417	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28206604	TTCGGGAGGCCAAGG[C/T]GGGTGGATCACAAGG	8924
rs576570815	snp	C/T	0.24932	0.249999	intron-variant	HERC2	GRCh38.p7	15:28206015	TATTTTTTCACAATT[C/T]ACACAAACCCAAAAT	8924
rs576606135	snp	A/G	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28119010	CGGTGGCTCACGCCT[A/G]TAATACCAGCACTTT	8924
rs576612603	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28167035	AACAATAAATGTGAA[A/C]AATGAAAATGTGACA	8924
rs576626612	snp	A/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28120628	CCATGAGACAGTATT[A/T]GTAATTCTGGCCTAT	8924
rs576641728	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28161120	TACCAAACTCTGCTG[A/C]GCTTTCAAGACTGCT	8924
rs576647981	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28253759	CTGAGGTCAGGAGTT[G/T]GAGACCAGCCTGACC	8924
rs576649087	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28112302	CACCTGTGTGGATGC[A/G]GGGCGGCCTGGCTGG	8924
rs576663174	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28114948	CATGGCACACACCAA[A/G]ATATAAGAGGAGCAA	8924
rs576676324	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28167552	TCCCACAAACGCTTC[A/G]AAGATGCTAACAAGT	8924
rs576683564	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28320405	AGGCGTGAGCCACTG[C/T]GCCCGGCCACGCAAC	8924
rs576704357	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28120488	TGTCAAGTTCTGCAC[A/G]CTATCATCATCAGGG	8924
rs576708286	snp	A/G	0.0023933	0.0345097	intron-variant	HERC2	GRCh38.p7	15:28155063	AGAATGATGGTTTCC[A/G]GCTCATCCATATCCC	8924
rs576714447	snp	C/T	0.00676609	0.0577691	intron-variant	HERC2	GRCh38.p7	15:28243228	AAAAAAAGTGACATG[C/T]GACCCCTTTCTCATA	8924
rs576739561	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28287416	CTTCCAAGTAAACCC[A/T]CTTCATTAAAGCCAC	8924
rs576742264	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28263837	AGGAGTTCGAGACCA[C/G]CCTGGGCAACATGGC	8924
rs576773592	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321035	TCAACAGCTCAAAAA[C/T]GATCAGTAACAAACA	8924
rs576776094	snp	A/T	0.00358779	0.0422022	intron-variant	HERC2	GRCh38.p7	15:28232624	GACTAAATTCTAAAC[A/T]ATTTTATAATTTCTA	8924
rs576785880	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28126672	GCGATGAGGATGCAA[C/T]GGCATAAGAATGACA	8924
rs576789661	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28162705	CCATCCTGGCTAACA[C/T]GGTAAAACCCCGACT	8924
rs576809530	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28176021	AAGGCCTGACACACC[A/C]TCCACAGCCAGTCCA	8924
rs576826388	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28281041	AATTCAATATAAAAA[C/T]GATGTCTTGATAAAA	8924
rs576827806	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28303153	GTCTTAGGTTTAAGT[C/G]TTTACTCCATTTTGA	8924
rs576850677	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28200405	CCTCAAAAAACAAAC[-/A]AAAAAAAAAAGGTAG	8924
rs576860037	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28170243	GAGCAAGAATAGAAA[C/T]AGAAAAATAAGGAGG	8924
rs576870029	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28282568	GACACAGCAGTAGAA[C/T]GGAGGAAAAAGGGCA	8924
rs576894643	in-del	-/T			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316285	GCTAAACCCTTTTCC[-/T]TTTTTTTTTAATAAC	8924
rs576897504	snp	A/C	0.00398564	0.0444627	intron-variant	HERC2	GRCh38.p7	15:28140038	GTGCCACTGCACTCC[A/C]GCCTGGGCGACAGAG	8924
rs576915581	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28227200	GAAGCGCTTGAACCC[A/G]GGAGGCGGAGGTTGC	8924
rs576926755	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28232385	GTCTCTACTAAAATA[C/G]AAAAATTAGCCAGGA	8924
rs576939131	snp	A/G	3.29783e-05	0.00406055	missense	HERC2	GRCh38.p7	15:28169631	TTATTACTGGCAGCA[A/G]AAGAATCAGCATCTG	8924
rs576949787	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28224198	AGACAGACAGACAGA[C/T]AGATAGATAGAAAGA	8924
rs576956439	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28202696	CACAGGGGTGATGGC[A/C]TTCTACTGTGAACTG	8924
rs576972977	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28203633	CCGAGAAGCCTGCAT[A/G]CAAGACGCGCATTTA	8924
rs576998833	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28189259	TATTTCTCATGTACA[C/T]GACATACACTAAGTA	8924
rs577009333	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28250866	ATATCGGCTACTGGA[A/C]AGCTGCGAATGCATT	8924
rs577013516	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28164014	AGAAGCCTCCTGGAG[A/G]GCAGCACTGGGGCTG	8924
rs577039760	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28151578	CCAGGTGAAGAGTGG[A/C]AACCTACAAAAAACC	8924
rs577040171	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28254965	AACAAATTCCACTCC[A/T]AGTGTTTACCCAAAA	8924
rs577062487	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28189697	CAAAAAAGTGATAAA[C/T]ATTTGAGGTGATGGA	8924
rs577074589	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28183384	CCAGCTAATTTTTGC[A/T]TTTTTTTTTGTAGAG	8924
rs577075354	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28164452	GATGACATTCCAGAA[C/T]ATAACTCACTGAAGG	8924
rs577077199	snp	A/G	0.00795532	0.062565	intron-variant	HERC2	GRCh38.p7	15:28157910	TCTACACACTGCTTT[A/G]AATGTGTCCCAGAGA	8924
rs577092975	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28308214	TCCATCTTTTGTGTC[C/T]TCTTTAATGTCTTTC	8924
rs577121985	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28288985	CATGACACAGCAACA[C/T]TGCCAACCAAGAACA	8924
rs577131884	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28308596	ACTATGTTGAATAAC[A/G]GTGGCCACACTGAGC	8924
rs577142583	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28184336	TGGAGGCCAGCTGTA[C/T]GTGGTCAGTGTGGGA	8924
rs577155638	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28284767	TAAAAATACAAAAAG[G/T]AGCTAGGTGTGATGG	8924
rs577185315	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28115090	GCAGCCGAGGCACAA[C/G]ACAGCCATGGGGAAT	8924
rs577187361	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28158454	ATTTAGGATAGTTAG[C/T]TCTTCTTATTGAATT	8924
rs577191651	snp	C/T	0.0584853	0.160693	intron-variant	HERC2	GRCh38.p7	15:28160029	CCTGGGTATCAGCAG[C/T]GGAGGCTGCAGAACA	8924
rs577212913	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28289416	TATAACATTCTCAAA[C/T]ACATGAAGCAAAACC	8924
rs577229201	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28243374	AAATGAACAACCATT[A/G]AAACAGAAACAAACT	8924
rs577233212	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28201941	ATCATCCCTTCAGTA[A/G]TGAAACACAGCTTTG	8924
rs577239232	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28113916	ACCTACAGCTATGCA[C/T]ACCCCAAGACGCCAC	8924
rs577243393	snp	C/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28156303	AATTCTGTGAAGAAA[C/G]TCATTGGTAGCTTGA	8924
rs577258799	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28189705	TGATAAATATTTGAG[A/G]TGATGGATACATTAT	8924
rs577264486	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28279858	AATAAAATAAAATAA[C/T]GGCACAGATTACACA	8924
rs577295556	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28160360	GGCAGGCAGGCCTCC[C/T]TGAGCTGCGGTGGGC	8924
rs577303574	snp	A/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28280542	TCCGAGGCCACACAG[A/T]GGAGTGCGGCACATG	8924
rs577305895	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28144536	CACGCCTCAGCAGGG[C/G]CTGTGAGAGCACTCA	8924
rs577308589	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28125744	AACTGGCATGATCAC[A/G]GTTCACTGCAGCCTC	8924
rs577313146	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318755	GTATCCAAATAATGT[C/G]TATGATAAAGAAGTC	8924
rs577347816	snp	C/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28119216	GCCTGGCCAACATGG[C/T]GAAATTGTCTCTACT	8924
rs577376535	snp	A/C			utr-variant-3-prime	HERC2	GRCh38.p7	15:28111195	TGCTACAAGGGGACA[A/C]CTGGGAGGGGGGACA	8924
rs577383933	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28273389	TTAAAGAACCAATTT[A/C]TAAAACCACCTTAGA	8924
rs577415385	snp	A/G	0.00438332	0.0466095	intron-variant	HERC2	GRCh38.p7	15:28178272	GTGCTTGCCTCTTCT[A/G]CCAGGCCTGGCCCTG	8924
rs577422098	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28289749	TGGCTCCCTGGAAAA[C/G]GTTCCCTAAGGTGTA	8924
rs577426707	snp	A/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28114400	GGTGGATTTTGTTGA[A/T]CTTGGTATTCTGGTT	8924
rs577447788	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28270494	GCCCCCAGGTTGGGT[C/T]GCCAGGCCTGTGCGC	8924
rs577450455	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28161453	ACATCTCAGGCTCCC[C/T]GGCAGGGCAGAGCAT	8924
rs577467636	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28179364	CACAGGCTACATATA[C/T]GATGGCAGTCCCAGT	8924
rs577470602	snp	A/G	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28145281	GAGTAGGCCGCCCTC[A/G]AGGGAGCAGAGGGCC	8924
rs577507498	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28219229	ACAAAGCACCGGCAT[A/C]TGTGGAGTGGGGCGA	8924
rs577520504	in-del	-/TG	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28159108	TGCCCAGAGATCCGC[-/TG]TTAGTCTGATGGGCT	8924
rs577525275	snp	G/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28298155	TTTGTTTTGTGTTTT[G/T]TGTTTTTTTTTTTTT	8924
rs577527016	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28286315	GGTACTGTACCTAAA[A/G]ACAGTACAAAGTACA	8924
rs577530311	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28180159	CCATGTTTTATCTTT[C/T]ACAATGTATTTTTAC	8924
rs577543388	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28240185	GCACTTTGGGAGGCC[A/G]AGGTGGGCAGATCAC	8924
rs577562277	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28122524	CCCCAGCCCCATGCC[C/T]CTCGCACAGCCCAGA	8924
rs577572136	snp	C/T	1.65985e-05	0.00288079	intron-variant	HERC2	GRCh38.p7	15:28198559	TTAAGGGAATTTTGT[C/T]TCTAAGAAAAAACAA	8924
rs577589963	in-del	-/T	0.16911	0.236552	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28213387	CATGAAGAAAGGCTG[-/T]TTTTTTAAAGGTGTT	8924
rs577599758	snp	A/C	2.28857e-05	0.00338265	intron-variant	HERC2	GRCh38.p7	15:28233364	GTTAACCAGGAAAAG[A/C]CAACTTTAACAACAA	8924
rs577612283	snp	A/G	0.00318978	0.0398085	intron-variant	HERC2	GRCh38.p7	15:28286893	ACACGCTGCAATGTT[A/G]AGAAGCAAGTGTCCA	8924
rs577628214	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28199304	GTCATAAAGGAAGGG[A/G]GCTTTCAAAGATTAC	8924
rs577645477	snp	C/T	0.00478085	0.0486577	intron-variant	HERC2	GRCh38.p7	15:28153613	CTGAGACTGCACCAC[C/T]GCACTCCAGCCTGAG	8924
rs577689851	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28227173	CCAGCTACTCGGGAG[A/G]CTGAGGCATGAGAAG	8924
rs577710729	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316997	GGCCAGGATGACCTC[A/G]ATCTCCTGACCTCAG	8924
rs577736731	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28183334	TCCACCTCAGCCTCC[C/T]GAACAGCTGGCACTA	8924
rs577743304	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28257957	CCAAAGTGCTGGAAT[C/T]ACAAGCGTGAGCCAC	8924
rs577745276	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28142081	CTTTAACTGAAATTC[A/G]CAGTGTCAGTTCACT	8924
rs577747543	snp	C/G/T	8.77253e-05	0.00662238	intron-variant	HERC2	GRCh38.p7	15:28116634	AGGCACAGGCCACAG[C/G/T]GACACAGTCTCAAGC	8924
rs577769279	in-del	-/A	0.0310713	0.120707	intron-variant	HERC2	GRCh38.p7	15:28179245	CAGAATTTTTTTAAC[-/A]AAAAAAAAAGAAAAG	8924
rs577772753	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28219713	TAAGATCTCGTGCTC[A/C]CTGAAATAGCCATTT	8924
rs577773885	snp	A/G	0.00953873	0.0683987	intron-variant	HERC2	GRCh38.p7	15:28234970	GATGGGAGGGCCGAT[A/G]GACTGGAAAGGAGAC	8924
rs577786319	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111664	TGGCTCGAGGACGGA[C/G]GCTTCTCATCAGACA	8924
rs577829478	snp	A/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28311684	GGGCTAGAGACTCAA[A/T]TCTGGGAGTAGTCAA	8924
rs577832145	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28252217	TTGAGTGTAGCCAGA[C/T]GGGCCAGCGCAGGCT	8924
rs577851861	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28267652	ATACATGTACCACAC[A/G]ATACGCATTACTCTG	8924
rs577859102	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28215862	ACAAATCCCTAAAGA[C/T]ATATCCTTATTTTTT	8924
rs577861446	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28259393	AGCCACTGTGTCTGG[C/T]GTAAAATCTTTTAGA	8924
rs577868430	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28306542	TTGTTTTTTTGATTA[C/T]GTCTTTGTCTGGTTT	8924
rs577869151	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28252612	TTGGAAGTTCATCTA[C/T]GTGAACAAGCTGTTG	8924
rs577879529	snp	C/T	0.00279162	0.0372561	intron-variant	HERC2	GRCh38.p7	15:28137718	TATGTCCCTGAGACA[C/T]AACTTATTGAAATAA	8924
rs577905884	snp	A/C	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28216880	TCACATATGCACTCA[A/C]ACTCCTCAACACTAG	8924
rs577916280	snp	A/T	0.00517822	0.0506191	intron-variant	HERC2	GRCh38.p7	15:28165650	AGAGAAAAAAAAAAA[A/T]ACAAAAATTAGCCAG	8924
rs577923858	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28147592	TAGTGAGCCACGATC[A/G]TGCTACCATACTCCA	8924
rs577925606	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28271320	AAATTAAATCATAGT[C/T]CTAATTCTTCTAAAG	8924
rs577926847	snp	C/T	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28159674	TCTTTGCAATGGGTT[C/T]GAACTTCCTCCTTTA	8924
rs577929190	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28143350	TATGTTCACAGCTGT[C/T]GAGACAGATTTTCAG	8924
rs577954630	snp	A/G	0.000399281	0.0141238	intron-variant	LOC107987422, HERC2	GRCh38.p7	15:28315884	CTAGAGCTTGTCTCA[A/G]TGGATCTAGAACTTC	8924
rs577964884	snp	A/T	0.00199481	0.0315187	intron-variant	HERC2	GRCh38.p7	15:28265190	ACCCTTGAAAAAAGG[A/T]TGATCTCACTTAGGA	8924
rs577973362	snp	A/G	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28148321	AGCAGATGCTACCTT[A/G]AGACAAATAGGAAAA	8924
rs578019748	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28248963	GATAATGATGCCCTC[A/G]TGCTTCACTAATGTG	8924
rs578021249	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28253307	CATTGACTTTAGTTT[C/T]GAAAAGAAAAGTTAC	8924
rs578022590	snp	A/G	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28137066	ATGTCTATGGCAGAG[A/G]GGAATAGGTTAGAAC	8924
rs578052846	snp	C/T	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28191529	AGAAAACACTACAGT[C/T]GAGATGGAGAAAGGC	8924
rs578079564	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28315124	CACATTCACTAGGCA[C/T]ATGTGGCTTTTCCAG	8924
rs578081528	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28244946	GGAAGCTAGAACCAT[A/G]GAAAGCATGGTGACT	8924
rs578100069	snp	A/G	0.00119737	0.0244387	intron-variant	HERC2	GRCh38.p7	15:28191888	TGCAGGCTGCTCAAA[A/G]TTCATTTTGAAAATG	8924
rs578107756	snp	C/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28186045	TGCACTCAAAAATTA[C/T]AGGACTGAAGACTAA	8924
rs578110870	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28284362	GAAGAAATAGAAAAT[A/G]CAAAACAAAATGGCA	8924
rs578127101	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28128738	AGGATCCTTTCGCTC[G/T]GCAGGTGAGAAGCCC	8924
rs578186596	snp	A/C	0.000798403	0.0199641	intron-variant	HERC2	GRCh38.p7	15:28172408	ATCAAGACAATATGT[A/C]ATTGCCACCAAAATC	8924
rs578213214	snp	G/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28304653	ACAGGTGTGAGCCAC[G/T]GCACCCGGCCTTTCT	8924
rs578215061	snp	A/T	0.000399281	0.0141238	intron-variant	HERC2	GRCh38.p7	15:28291244	ATACGAATTTTTTTT[A/T]AAGAAACAGAGACCC	8924
rs578217534	snp	C/T	0.00159617	0.0282053	intron-variant	HERC2	GRCh38.p7	15:28296396	GAGAACTGCTTGAAC[C/T]GGGGAGGCAGTGGTT	8924
rs578225791	snp	C/T	0.000399281	0.0141238	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28246897	CCCATTAGCTCTGGA[C/T]CTTGAAGAAGGATTG	8924
rs578236989	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28138287	GGCTTTCAACGTAGA[C/T]GGAACAACCGTCTAT	8924
rs745320944	snp	A/C	1.65836e-05	0.0028795	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28220476	CCTCTGTGTCCGAAT[A/C]CTCTGCTGAGGGCTG	8924
rs745329400	snp	A/G	1.64817e-05	0.00287064	missense	HERC2	GRCh38.p7	15:28135637	GTTGGGGTGGACACC[A/G]ACTCTGTCCCTCCAA	8924
rs745347736	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28123405	CCGTATGGTAATTAG[A/C]CCCTTCAAGATCATC	8924
rs745353929	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28292340	GCTCAGCATGACTAC[A/T]CAACAGGGAAATGCA	8924
rs745367386	in-del	-/T			intron-variant	HERC2	GRCh38.p7	15:28222481	ACTTCTAGGAATTAC[-/T]CCCCCCAAAAAAGCA	8924
rs745372115	snp	A/C	3.29658e-05	0.00405978	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28196508	CATTTCTGATAGCAA[A/C]CCAGTCCAGTGAGAC	8924
rs745376326	snp	C/G/T	0.000527769	0.0162372	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256132	CCGGGCCCGCTCCTC[C/G/T]GCGGTGGGCAGCAGC	8924
rs745390542	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28141187	AGGTTGCAGTGAGCC[A/G]AGACCACGCCATTGC	8924
rs745392759	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28162939	GGTTAAATGCTAAAA[C/T]GTTTTGCTCTAAAGG	8924
rs745402828	snp	C/T	1.64738e-05	0.00286995	missense	HERC2	GRCh38.p7	15:28125098	GGTTGACCTTCTTAC[C/T]CTGAAGGGCAGCTAC	8924
rs745406026	snp	G/T	1.68278e-05	0.00290062	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229342	AACAATCAGTAAGAG[G/T]TTCCCTTTCAAATAA	8924
rs745417857	snp	A/G	4.95593e-05	0.00497767	missense	HERC2	GRCh38.p7	15:28168519	GCGTCGGAAGGGGCC[A/G]CCGAGGAGAACGAGG	8924
rs745442949	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28278384	CATGTCAAAACAAAC[A/G]AACAAAAAAAAATCA	8924
rs745455647	in-del	-/CT			intron-variant	HERC2	GRCh38.p7	15:28216633	GCTCACACACACACA[-/CT]CACTCTCACACCCTC	8924
rs745459730	snp	A/G	3.30786e-05	0.00406672	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28186660	ATCTTCCTCTTCTGC[A/G]CGGATCCGTCCCAGC	8924
rs745464450	snp	A/C/T	3.36741e-05	0.00410319	intron-variant	HERC2	GRCh38.p7	15:28256065	CCTGACCCATGCCCT[A/C/T]TCCTGTTCCTTCCCC	8924
rs745482773	snp	A/G	1.74631e-05	0.00295487	intron-variant	HERC2	GRCh38.p7	15:28117187	AGCAAGCGTGAGGCC[A/G]CTGCCGCAGCAGGAA	8924
rs745491212	snp	C/T	1.66103e-05	0.00288182	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28229262	TACAGCCCAAGCGTA[C/T]AGCTTGCCAAAGGTG	8924
rs745502019	snp	C/T	1.6525e-05	0.00287441	intron-variant	HERC2	GRCh38.p7	15:28146234	TCAACCTCCTGTCCT[C/T]ACCTGACCGCACGGA	8924
rs745517208	snp	A/G	5.00238e-05	0.00500094	intron-variant	HERC2	GRCh38.p7	15:28274886	GAAGCAGAACAACGC[A/G]CCACACCAGGGACCG	8924
rs745517298	snp	C/G	4.89728e-05	0.00494813	missense, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28321396	CATTTGGAGTCGAGG[C/G]GAGCCTGGGCAGCCA	8924
rs745527854	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28259885	ACGCAGGAGAATTGC[A/G]TGAACCCAGGAGGCA	8924
rs745551191	snp	A/G	1.66407e-05	0.00288446	intron-variant	HERC2	GRCh38.p7	15:28263193	TACAAATGCATTTAA[A/G]TAACAACAACTCTGC	8924
rs745563507	snp	G/T	1.92914e-05	0.00310569	intron-variant	HERC2	GRCh38.p7	15:28238245	GGGAAAAAGCAACAT[G/T]AGTTCAATTCAGCTT	8924
rs745570320	snp	C/T	2.16205e-05	0.00328782	intron-variant	HERC2	GRCh38.p7	15:28117218	GCACACAGTCGGGGA[C/T]ATGCGGCACTGGCGA	8924
rs745572391	snp	A/T	1.92261e-05	0.00310044	intron-variant	HERC2	GRCh38.p7	15:28113709	CACTTTACACTTCTG[A/T]CTTCAGTGACACTGA	8924
rs745572958	in-del	-/A	0.0542392	0.155492	intron-variant	HERC2	GRCh38.p7	15:28182525	AGGCTAACCAAACGG[-/A]AAAAAAAAAGAAAAA	8924
rs745577097	snp	A/G	3.55265e-05	0.0042145	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28233273	TCTCAATTCATTAAA[A/G]AGGAATCTCAAACGT	8924
rs745589874	snp	C/T	1.69306e-05	0.00290947	intron-variant	HERC2	GRCh38.p7	15:28142214	TTTGCATCCCAAAAG[C/T]GATTCCAAAATATCA	8924
rs745602986	snp	A/T	3.34689e-05	0.00409064	missense, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28212582	AAGGCCACGGCAGGG[A/T]GCTGGAGAGGACACA	8924
rs745603511	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28219318	AGGCCACCCTCTGCC[A/G]TGGGGCCACCCCTGC	8924
rs745644068	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28150339	TACTGAAAAAACACG[C/T]GGCTTCTAACAGAGA	8924
rs745654241	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28164115	CGCTGTGACCCTGTG[C/T]AGAGCAGGAGTGTGT	8924
rs745654643	snp	A/G	6.87085e-05	0.00586085	intron-variant	HERC2	GRCh38.p7	15:28269482	AACAACAACAACAAT[A/G]AAAAAAGGCTGGGAG	8924
rs745660906	in-del	-/C	6.61463e-05	0.00575055	intron-variant	HERC2	GRCh38.p7	15:28202275	ACACACAGCACAGCA[-/C]GCCACTGTGAGTCAA	8924
rs745665978	snp	C/T	1.64727e-05	0.00286986	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28263000	GTCACCTTTTCCCCA[C/T]GAATAAACTTGGCCA	8924
rs745670018	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28195651	GAGACCAAAGTTAGA[G/T]TCAAGGTTACCAGGG	8924
rs745680360	snp	A/T	1.69418e-05	0.00291043	intron-variant	HERC2	GRCh38.p7	15:28238097	TCCTCTGCATCACTC[A/T]AGGCATACAGCCTCA	8924
rs745689136	snp	A/T	1.74576e-05	0.00295441	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214835	ATAACGACAAGCATT[A/T]AAAAAAATCTGATGA	8924
rs745691418	snp	A/G	3.39507e-05	0.00411997	synonymous-codon	HERC2	GRCh38.p7	15:28132226	TCCACTGCCACAGGC[A/G]ATGTCAACCACACGG	8924
rs745691573	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28190925	CACCTCCCTTGTCAT[C/G]TGTAAATCATCCAAA	8924
rs745706222	snp	C/T	1.64803e-05	0.00287052	synonymous-codon	HERC2	GRCh38.p7	15:28163211	CACACGAGTGTCATC[C/T]GCAATCAGCAGACTG	8924
rs745709062	snp	A/G	3.80691e-05	0.0043627	intron-variant	HERC2	GRCh38.p7	15:28228182	AAGCAAAATCTTGAC[A/G]TTTTCCCAAAGGCGC	8924
rs745731459	snp	G/T	1.65285e-05	0.00287471	missense, downstream-variant-500B	HERC2	GRCh38.p7	15:28174491	TTGTCCACGCCACAC[G/T]GTGGGACGACCCACA	8924
rs745742003	snp	C/T	1.64746e-05	0.00287002	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28201517	AAATCAGCTCGTTTT[C/T]TGTACGTCTGGCTCT	8924
rs745744779	snp	A/C	1.66427e-05	0.00288462	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272943	GGATGGCCAGGGCCA[A/C]GTGCTGGTCCTGCAG	8924
rs745744937	snp	A/G	3.31066e-05	0.00406844	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28269335	ACAGGCAATCTGTGT[A/G]ACTCCCAGGTTGGCC	8924
rs745748871	snp	C/T			missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213831	GGGTGATGCGAGTCA[C/T]AGTGCCTTCTCCAAA	8924
rs745750807	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28245851	GGACAATAAAACTTT[A/C]CTCAGTAAAACTCCT	8924
rs745775753	snp	A/T	2.03419e-05	0.00318913	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28222150	TCCTTGTTTCTTCCA[A/T]AACTGTGGCAGAAGC	8924
rs745777690	snp	C/T	1.66613e-05	0.00288623	intron-variant	HERC2	GRCh38.p7	15:28121468	ATTTAGAATCTGATA[C/T]GGAAAGCATCACTCC	8924
rs745779333	snp	A/G	1.88407e-05	0.0030692	intron-variant	HERC2	GRCh38.p7	15:28132612	GACAGCAGCAGTGAG[A/G]AGCATGCAGCCTCCG	8924
rs745815406	snp	A/C	0.000171849	0.00926795	intron-variant	HERC2	GRCh38.p7	15:28269200	CATCTGTAGGACAGA[A/C]CCTGCCCCGCAAGGG	8924
rs745819269	snp	C/T	1.64895e-05	0.00287132	intron-variant	HERC2	GRCh38.p7	15:28167653	CATTTAAGATTATTT[C/T]ACAATACAAAGTTAA	8924
rs745831017	snp	C/T	1.6492e-05	0.00287154	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28248647	TCCAATGAAGCAGAT[C/T]TTTCACGACTGTGTT	8924
rs745836275	snp	C/T	0.000231661	0.01076	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28257082	TCGTAGAAGATTCAG[C/T]GTTGCCACGGCCACA	8924
rs745837631	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28138029	GATACAATATTCCCT[C/T]AAGCCAAAGCTAATC	8924
rs745846065	snp	A/T	1.66012e-05	0.00288103	intron-variant	HERC2	GRCh38.p7	15:28179117	AGCATAATTTAAAAA[A/T]TTTTTAAGATTAGAA	8924
rs745848340	in-del	-/CACAAAGGTGGA			intron-variant	HERC2	GRCh38.p7	15:28178325	CTAAGACCATCTTCC[-/CACAAAGGTGGA]CACAAAGGACCAGCA	8924
rs745854216	in-del	-/CA	1.66699e-05	0.00288698	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28299553	AGCTTACAGAGTGCT[-/CA]CACTCACATTGCAAT	8924
rs745866455	in-del	-/AACA			intron-variant	HERC2	GRCh38.p7	15:28249135	TGACCCTCTAGAAAG[-/AACA]AACACAGTGTCATTA	8924
rs745886258	snp	C/T	1.64732e-05	0.0028699	synonymous-codon	HERC2	GRCh38.p7	15:28167759	CACTGGGATAAAAGG[C/T]CGAGCGGAGGCTGAG	8924
rs745887590	snp	C/G	3.33717e-05	0.0040847	missense	HERC2	GRCh38.p7	15:28124093	CAACAGAAGGCCCGA[C/G]TCCAGTTTCGTCGAG	8924
rs745888837	snp	A/G			missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28177084	CGATATCCCGGATAC[A/G]CTTGGTTTTCAGGGC	8924
rs745889976	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28238503	TTAAAATATGTGGGG[A/G]CTGGCACAAAACTAA	8924
rs745893650	snp	A/G	9.91441e-05	0.00704004	synonymous-codon	HERC2	GRCh38.p7	15:28144144	GATGCTTCTGTTAGA[A/G]GCAAGGTTGAGTCGG	8924
rs745895518	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28275738	CAGTGAGCCAAGATC[A/G]CGCCACTGCACTCCA	8924
rs745912817	snp	C/G	5.12028e-05	0.00505953	intron-variant	HERC2	GRCh38.p7	15:28280291	GTTCATTCACATCTA[C/G]AAAATAAGACAAGAA	8924
rs745916871	snp	A/T	1.7079e-05	0.00292219	intron-variant	HERC2	GRCh38.p7	15:28179236	TATCTACAACAGAAT[A/T]TTTTTAACAAAAAAA	8924
rs745926160	snp	C/T	8.94815e-05	0.00668825	intron-variant	HERC2	GRCh38.p7	15:28256350	ATTTTCACTTAGAAC[C/T]CCTAAAAATGAGTGA	8924
rs745929433	in-del	-/TGATCGTGTAAT	1.68094e-05	0.00289904	intron-variant	HERC2	GRCh38.p7	15:28142960	TAAAACTCTAAGAAA[-/TGATCGTGTAAT]CAACAGAACAGTATT	8924
rs745939086	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28126533	TGGTATATATACACC[A/G]TGGAATACTACTAGC	8924
rs745941695	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28181925	AATAAGGCAAGTGTG[G/T]ATGCGCACACATGTG	8924
rs745975998	snp	A/G	1.65457e-05	0.00287621	intron-variant	HERC2	GRCh38.p7	15:28229604	CTCTCCAACTGCAAA[A/G]TATCAATGCATACAG	8924
rs745981915	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28242331	TCCAAGAAAAGAATA[C/G]GCAGGAACATTCTCC	8924
rs745983405	snp	A/T	3.29533e-05	0.00405901	synonymous-codon	HERC2	GRCh38.p7	15:28141450	CCCATCAGCCGTCAC[A/T]GCAAAGAGGGTCTGT	8924
rs745986250	in-del	-/GA			intron-variant	HERC2	GRCh38.p7	15:28190410	GTTTACTAAAAATTT[-/GA]GAGAGAGAGAGATAA	8924
rs746006263	snp	A/G	1.64798e-05	0.00287047	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28176458	CCAGACTTGGTGAGC[A/G]CCAGGGAGAACTGAG	8924
rs746016159	snp	A/T	1.64931e-05	0.00287163	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265837	CCCAGCCGGCCGTAG[A/T]TCCCGCGGCCCCAGG	8924
rs746016534	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28112517	AACCCTGGCAGAGAC[A/G]CAGGTCAGGCTGTGC	8924
rs746024804	snp	A/G	1.65367e-05	0.00287543	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28198394	TTTCACAACCCCCAC[A/G]CTCTGATGAGTCACA	8924
rs746028927	in-del	-/CA			intron-variant	HERC2	GRCh38.p7	15:28127483	ATACTGGTGTGAACT[-/CA]CAGTTTTCAACAGAC	8924
rs746029779	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28127674	GAGAAATGGCCAGGT[C/T]GAGGCGTGGGGCATG	8924
rs746034716	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28166623	AAGTCTAGAGCACAG[C/T]TGTGCCAGAAATGAA	8924
rs746048238	snp	A/G	1.64855e-05	0.00287097	intron-variant	HERC2	GRCh38.p7	15:28233629	GTCGAGGAATCTGCA[A/G]TGTACCTAAAGTACA	8924
rs746053625	snp	C/T	3.30475e-05	0.00406481	synonymous-codon	HERC2	GRCh38.p7	15:28113206	GAACCACTGGATCAG[C/T]GATGCGGAAGGCTCG	8924
rs746062183	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28151092	AAAATTAGGGCATAT[C/T]CTAAGATTTTTAAGA	8924
rs746073078	snp	A/T	1.64727e-05	0.00286986	synonymous-codon	HERC2	GRCh38.p7	15:28141579	GTGATTATGTCCCCA[A/T]CCATAAATTGTTCCA	8924
rs746092610	snp	A/G	1.76384e-05	0.00296966	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28218503	CATGTCTTGTCCGTC[A/G]TTCCGCTTTCCACTA	8924
rs746099490	snp	A/G	7.06914e-05	0.0059448	synonymous-codon	HERC2	GRCh38.p7	15:28168584	CAGGGCCCCGACAAC[A/G]GCATCTCTGTCAGGA	8924
rs746106427	snp	C/T			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317108	GACAATTTTTTTTTT[C/T]GAGATGGAGTCTTGC	8924
rs746119660	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28282187	GATGAGGTGAAGCAC[A/G]CCCTATCCCTGCCAG	8924
rs746119676	snp	G/T	1.64808e-05	0.00287057	intron-variant	HERC2	GRCh38.p7	15:28176623	AAGAAACACATATAC[G/T]TCAGGCCAGCGTTTC	8924
rs746129827	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28113995	AACACATGTGCATCC[A/G]CCCCAGGCCCGAGAC	8924
rs746142130	snp	A/G	3.30289e-05	0.00406366	intron-variant	HERC2	GRCh38.p7	15:28198510	GAGGATAGCCTACAG[A/G]TGTCAATAACAAATC	8924
rs746152345	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28182274	CTGAGGGGTAATTTG[A/G]TAATGTCTTTTAGTT	8924
rs746153913	snp	C/G	1.79059e-05	0.00299209	intron-variant	HERC2	GRCh38.p7	15:28218465	AGCGCTGACTCCCTG[C/G]GCCCTCGATCTCTCA	8924
rs746165226	snp	A/C	6.60491e-05	0.00574632	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28248706	ACGGGCAACATCTTT[A/C]AATCTGGCTACAGTC	8924
rs746171864	snp	C/T	1.65367e-05	0.00287543	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28228402	TTGCAGGGGAACCGG[C/T]TGGATACCTAATGAG	8924
rs746182415	snp	C/T	0.00044582	0.0149235	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28270801	AGATCAATGGCAAGC[C/T]CGTTGTCTTGTGGAA	8924
rs746187976	snp	A/G	1.65064e-05	0.00287279	intron-variant	HERC2	GRCh38.p7	15:28146358	ACCTGAAGGACAGGC[A/G]AGCACAAAACATAGC	8924
rs746187983	snp	C/T	4.97789e-05	0.00498868	missense	HERC2	GRCh38.p7	15:28169494	CCTACCTGGCATACA[C/T]GATTTGCAATGCTGT	8924
rs746198078	snp	C/G	2.03295e-05	0.00318816	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274419	CAGGGACTCCTGCAA[C/G]AGCTCACTGCAGAGG	8924
rs746202811	snp	A/C/G	4.98089e-05	0.00499023	intron-variant	HERC2	GRCh38.p7	15:28198582	AAAAACAAAAGCACT[A/C/G]AACAAAGAATGTGCT	8924
rs746210816	snp	A/G	0.0012656	0.0251236	intron-variant	HERC2	GRCh38.p7	15:28255864	CACGTGTGCCTCCAA[A/G]GCCATACCTGGATCT	8924
rs746221689	in-del	-/T			intron-variant	HERC2	GRCh38.p7	15:28184854	GTGACGGAGCAAGAC[-/T]CCGTCTCAAAAAATA	8924
rs746223223	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28154838	TGTTACATATGTACA[A/C]ATGTGCCATGTTGTT	8924
rs746234187	in-del	-/AAA	1.71261e-05	0.00292622	intron-variant	HERC2	GRCh38.p7	15:28262872	CTTTAAAACATTACT[-/AAA]GAAACTGTCCTGAAG	8924
rs746247874	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28120007	CTGGCCCAAAAAGTC[C/T]GCGTGCGGTTTTGAG	8924
rs746253690	snp	A/G	1.64803e-05	0.00287052	synonymous-codon	HERC2	GRCh38.p7	15:28130535	AGATTTGGTAAGGGC[A/G]ACAGAAAACTGGGAT	8924
rs746255078	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28249690	TCTAGCTTTGTTGCC[A/G]GGCTGGAGTGCAGTG	8924
rs746262190	snp	C/G	1.65364e-05	0.0028754	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233167	TTTTCCTTCGTTCTC[C/G]AATTATCTTTTGAGC	8924
rs746267132	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28227260	AGCCTAGGCGACGGA[A/G]TGAGACTCCGTCTCA	8924
rs746275912	snp	A/G	9.83816e-05	0.00701293	missense	HERC2	GRCh38.p7	15:28152680	CAGCCCCTGTACCTG[A/G]TATCTTCACTGTGCC	8924
rs746288175	snp	A/G	1.65529e-05	0.00287683	missense, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28299413	TTACCTTTTCTAGGA[A/G]GGAGCTCTCCGTTCT	8924
rs746290715	snp	C/T	3.30344e-05	0.004064	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28191204	ATCATTTTTAATCTA[C/T]GAACAAGAACATCTG	8924
rs746296524	in-del	-/A	5.0866e-05	0.00504286	intron-variant	HERC2	GRCh38.p7	15:28270907	TTCAGAAATGGTGGG[-/A]AAAAATTAAAGTTAA	8924
rs746300691	snp	A/G	1.6599e-05	0.00288084	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28260909	CCAGCTGTGGACCTC[A/G]CTGTCCTCAGTCAGA	8924
rs746307585	snp	A/G	4.94482e-05	0.00497209	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28177499	AGTTAAAGCCGTCGC[A/G]TGCCGGCCACCTGCA	8924
rs746326041	snp	A/T	2.09387e-05	0.00323557	intron-variant	HERC2	GRCh38.p7	15:28254525	TTCAATATCCTGTAA[A/T]TCATAAAAAGAAATT	8924
rs746336134	in-del	-/AAA					GRCh38.p7	15:28291910	ACTCCGTCTCAAAGG[-/AAA]AAAAAAAAAAAAAAA	8924
rs746355998	snp	A/G	1.85297e-05	0.00304376	missense	HERC2	GRCh38.p7	15:28142900	TCAAACTGCCTTTGC[A/G]AAGCTTCTGGAAGAC	8924
rs746376047	snp	A/C	0.000143916	0.00848158	intron-variant	HERC2	GRCh38.p7	15:28299370	TTATAATGGTCTTTA[A/C]CAAATAAAAAACACT	8924
rs746377652	snp	A/G			intron-variant, utr-variant-5-prime	HERC2, LOC107987422	GRCh38.p7	15:28317664	TGGTGGCAGAAGAGA[A/G]GCAGGAGAGACATCT	8924
rs746381439	snp	A/G	1.69916e-05	0.00291471	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28211039	CTGAACAGCTGGCTG[A/G]GACAGGATCTGCCGC	8924
rs746382849	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28274717	GCATACACTCTCTTT[G/T]TTTTCTTTAAAGCAC	8924
rs746414041	snp	C/G	1.65081e-05	0.00287293	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28260807	GGCAATTCCCACTAT[C/G]TGTTTGGTGTCCAGT	8924
rs746420803	snp	C/T	0.000223439	0.0105674	intron-variant	HERC2	GRCh38.p7	15:28202087	ACAGCGGCCCAGGTG[C/T]GGGCGGTCACATGGG	8924
rs746422755	snp	A/G			synonymous-codon	HERC2	GRCh38.p7	15:28141504	TCTGAGAGTTGCAAG[A/G]GCTTCACAGGGAGTG	8924
rs746442771	snp	A/T	1.77363e-05	0.00297789	intron-variant	HERC2	GRCh38.p7	15:28236946	TGCTGATCAGCAAAA[A/T]GCAAAGATTTTCTTA	8924
rs746443136	snp	A/G	9.88403e-05	0.00702925	synonymous-codon	HERC2	GRCh38.p7	15:28111811	CGAAGCAAAGGAGTC[A/G]ACATCCTCGTTATCT	8924
rs746443137	snp	A/G	4.1898e-05	0.00457681	intron-variant	HERC2	GRCh38.p7	15:28115414	GAGGCCCCGCCTGCC[A/G]CCCCAGGGAGTTACC	8924
rs746473051	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28251528	AATAATGGCCAGGCG[C/T]GGTGGCTCACGCCTG	8924
rs746491340	snp	C/T	1.6601e-05	0.00288101	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28268582	GCAATTTTTACAATG[C/T]TTCTGGAGGCAAGGC	8924
rs746501858	snp	A/C	1.65241e-05	0.00287433	intron-variant	HERC2	GRCh38.p7	15:28175461	GTGTCATGACCCCCA[A/C]GTCCCCCAAGTCAGG	8924
rs746502971	snp	C/T	1.71917e-05	0.00293182	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28234271	TCCAGAGAAGATGGA[C/T]GACTGAAGCCATTCT	8924
rs746508778	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28228977	TACACATCAAAATGT[A/C]AAAATGTTATACTAG	8924
rs746530531	snp	C/T	1.81171e-05	0.00300969	intron-variant	HERC2	GRCh38.p7	15:28248509	GCCTAAAGTAACGAG[C/T]CCCGATCACATACAA	8924
rs746530796	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28175345	GCAAAGCAGGCAGAT[A/G]CACCAGTGGGCAAAA	8924
rs746542360	snp	C/G	1.85765e-05	0.00304761	intron-variant	HERC2	GRCh38.p7	15:28124238	CTCCATGGGGACCTA[C/G]AACACAGAAATGGCC	8924
rs746545181	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28117862	CCGCAGCAGGACCTC[A/G]GCACATCGGAGGGCA	8924
rs746551522	snp	A/G	5.01031e-05	0.0050049	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28220594	GACTCTTATCCATCC[A/G]TCCTCTCCCAGCTCA	8924
rs746562994	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28252553	TCTTAATTAACTCCA[C/T]GAAAGTAAACACGGC	8924
rs746579142	snp	C/T	0.000281819	0.0118672	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272340	CAGTCTCCTGTGCCC[C/T]GCTGTCCCACAGCTG	8924
rs746589172	snp	A/G	3.30071e-05	0.00406232	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28177007	CCGGCCGTACTCGCC[A/G]AGGCCCCAGGTGTAC	8924
rs746590164	snp	A/G	1.67069e-05	0.00289019	intron-variant	HERC2	GRCh38.p7	15:28167867	GAAGTTTAAGTGGAA[A/G]AACTCAGCAACATAA	8924
rs746598599	in-del	-/AA	0.000102506	0.0071584	intron-variant	HERC2	GRCh38.p7	15:28210992	ATTTAAGAACTTTTT[-/AA]AAAGACACCTGTGTG	8924
rs746606606	snp	C/T	1.66563e-05	0.0028858	intron-variant	HERC2	GRCh38.p7	15:28196420	TTCAACAGAAAACCA[C/T]TCGTCCCAAAGCAAA	8924
rs746613976	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28161569	TCACTTTATACTGCA[C/G]ACCTACAGACCAATT	8924
rs746615024	snp	A/G	1.66228e-05	0.0028829	synonymous-codon	HERC2	GRCh38.p7	15:28112032	GGTTGTATTTATCCA[A/G]CACCTGTTGAGCAGA	8924
rs746617325	snp	A/C	1.65608e-05	0.00287752	intron-variant	HERC2	GRCh38.p7	15:28229451	GAAAAAAATATGCTA[A/C]CGTTTTACCCTATAT	8924
rs746645531	snp	C/T	1.66183e-05	0.00288251	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28220500	AGGGCTGTGCAGCAG[C/T]CGGCAGCTCTGCCAG	8924
rs746662298	in-del	AGGATTCCTTG/CAAGGTGGTCGGATCACA			intron-variant	HERC2	GRCh38.p7	15:28139826	AGCACTTTGGGAGGC[AGGATTCCTTG/CAAGGTGGTCGGATCACA]AGGTCAGGAGTTCAA	8924
rs746668494	snp	A/C	2.23666e-05	0.00334407	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28186533	AGTGAGGATCCAGGA[A/C]TGTAGCGGGAGGTAA	8924
rs746671998	snp	A/G	3.29832e-05	0.00406085	missense	HERC2	GRCh38.p7	15:28144706	GATAGACGGTGAAGC[A/G]CCAGCCCCAGCCATT	8924
rs746676953	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28195727	GAGTTTCTGATCGGA[A/G]TGGTGAAAAGTTTTG	8924
rs746687560	snp	A/C/T	4.96507e-05	0.0049823	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272303	AGTGGGGCGCTGGTG[A/C/T]CCTGGGCGGAACGCT	8924
rs746689144	in-del	-/TTT	1.64996e-05	0.0028722	cds-indel, nc-transcript-variant	HERC2	GRCh38.p7	15:28229722	ATCCACTGGCTCTTC[-/TTT]AAGGGCAAATTCAGC	8924
rs746703528	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28119601	TGGGACTACAGGCAC[C/T]CACCACCACACAAGG	8924
rs746703696	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28144500	ACAGCTGGATGGCTG[A/G]GACAGATCTGTGTTC	8924
rs746703861	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28162717	ACATGGTAAAACCCC[A/G]ACTCTACTAAAAATA	8924
rs746709725	snp	C/T	1.66263e-05	0.00288321	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233501	GACTTAGGCAACGTT[C/T]TGTGCTTTACTTGCT	8924
rs746720431	snp	C/T	1.65751e-05	0.00287876	missense	HERC2	GRCh38.p7	15:28117064	GGAGGCTGTCGGGAC[C/T]AAACGAGCTCATCTT	8924
rs746740163	snp	C/T			intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28314142	CTCGACTTATTGCTA[C/T]AATATTGCATATACA	8924
rs746750721	snp	C/G	6.59033e-05	0.00573997	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213864	CATCGTGCATAACTT[C/G]ACCGCCCAGGCGCAG	8924
rs746757241	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28280948	AGAACTTTGAAGTCA[A/G]TATTAGTCAATATTT	8924
rs746758216	snp	A/T	1.64773e-05	0.00287026	intron-variant	HERC2	GRCh38.p7	15:28141704	ACACTCACGATCGAC[A/T]TTACTGCTTGTTTCT	8924
rs746767458	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28112341	CAGGCACGTGACCAC[A/G]GGAGAGCTCTTCATG	8924
rs746785309	snp	C/T	1.65438e-05	0.00287605	missense	HERC2	GRCh38.p7	15:28113617	GAGAGAGGAGGGGAA[C/T]AGGCACAACGCGGGC	8924
rs746790958	snp	A/G	6.61627e-05	0.00575126	intron-variant	HERC2	GRCh38.p7	15:28265603	CCTGTCCAGGGTGGC[A/G]AGAGCTCTACGTACC	8924
rs746794548	snp	C/T	1.67128e-05	0.00289069	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274985	GCGAGCCCCTCCACA[C/T]CTTTGCCCGCAGGCC	8924
rs746797424	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28166227	CACAAGAAAACTACA[C/G]AGCCGTATCCCTTAT	8924
rs746807928	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28133564	CTTCCAGAACTTTTA[A/G]GTTTTACATTTTACA	8924
rs746816681	in-del	-/AC			intron-variant	HERC2	GRCh38.p7	15:28216809	AACAGATGCAAGCTG[-/AC]ACACACTCCCATGCA	8924
rs746830956	snp	A/G/T	4.31204e-05	0.00464313	intron-variant	HERC2	GRCh38.p7	15:28233419	CACAGAATAAAAAGA[A/G/T]TTAAAATCTATCACC	8924
rs746856984	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28113843	CAGCTCGGCACTGCA[C/G]AGCTTCTCCTGACAC	8924
rs746858944	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28219511	CCAGGTGCCATATAC[A/G]TCGCTCCTAACAGGC	8924
rs746861653	snp	A/G	1.69971e-05	0.00291518	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28215740	TGAGAGCGATGCTCC[A/G]CACAAACCCCAGCGT	8924
rs746871370	snp	C/G	3.35132e-05	0.00409334	intron-variant	HERC2	GRCh38.p7	15:28169662	AAGGCACGCCTATAA[C/G]AGGAAAATAAAATTT	8924
rs746878763	snp	C/G	6.71085e-05	0.00579221	intron-variant	HERC2	GRCh38.p7	15:28263208	ATAACAACAACTCTG[C/G]ATTTTAACGAAAAAT	8924
rs746888410	snp	C/T	1.83236e-05	0.00302679	utr-variant-5-prime, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28321435	GATTCAGAGGGCATC[C/T]TTTCTCCAGCTTCCT	8924
rs746889276	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28189136	TTTGTACAGCAAAGG[A/C]CATGCTTAAGATGCA	8924
rs746911051	snp	G/T	3.49168e-05	0.00417818	intron-variant	HERC2	GRCh38.p7	15:28198787	AGAATTAAAATGAAA[G/T]TGGAGATCCAGTCCA	8924
rs746935753	snp	C/T	1.70866e-05	0.00292284	intron-variant	HERC2	GRCh38.p7	15:28142203	TAAATAATGTTTTTG[C/T]ATCCCAAAAGTGATT	8924
rs746956861	snp	C/G	1.64969e-05	0.00287196	intron-variant	HERC2	GRCh38.p7	15:28201432	AAAAACGGATCGAGG[C/G]TCCAGCTTAAGACAA	8924
rs746959635	snp	A/G	1.83923e-05	0.00303246	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174388	AGAAGATACAAATCT[A/G]TGTTACCTAAATAGG	8924
rs746962501	snp	C/T	2.42298e-05	0.00348056	missense	HERC2	GRCh38.p7	15:28132105	TGGGAAATACCTTCA[C/T]AGGCACTTTACAGCC	8924
rs746990193	snp	A/C	1.64882e-05	0.00287121	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28254393	CTGTTTGCCAGAAGA[A/C]TCACAGATCCCCGTA	8924
rs746991643	snp	C/T	7.14184e-05	0.00597529	intron-variant	HERC2	GRCh38.p7	15:28228195	ACATTTTCCCAAAGG[C/T]GCTCAAGCGGGTGCA	8924
rs746997242	in-del	-/CTT			intron-variant	HERC2	GRCh38.p7	15:28216132	GGGCATTTTTAAAAC[-/CTT]CTAAGTATGTGTAGT	8924
rs747000569	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28134912	TCCTGAGTTCAAGCA[A/G]TCTGCCCACCTCAGC	8924
rs747001564	snp	A/G	1.68792e-05	0.00290505	intron-variant	HERC2	GRCh38.p7	15:28273045	AACAAAGCAACCTCC[A/G]GAAAGACAGCATGCT	8924
rs747002057	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28227128	AAAAATATAAAAATT[A/G]GCCAGGTGTGGTGGT	8924
rs747003507	snp	A/G	1.68462e-05	0.00290221	intron-variant	HERC2	GRCh38.p7	15:28191949	CCGCTGCTGTGCCCT[A/G]TTAGATGCTACCTTT	8924
rs747021826	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28190675	GTGTTCAGATGCAAT[A/C]AGCAACCTAAAATGC	8924
rs747022512	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28273335	TTCCAGTTTCAATGA[C/T]GTATAAGACTATACC	8924
rs747023259	snp	A/G	5.05276e-05	0.00502606	synonymous-codon	HERC2	GRCh38.p7	15:28132199	ATCTGTGAGGCAGAG[A/G]GTCTGGGCATCTCCA	8924
rs747024594	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28194963	CGGGAGGCTGATGCA[A/G]GAGAATTGCTTGAGC	8924
rs747042500	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28263555	CTGCTTCTGTTGCCA[A/C]CATGCTGACCGGTGG	8924
rs747042710	snp	A/C	0.000148629	0.0086193	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28192051	CGACACATTCAGGCT[A/C]TTCACCATGCGGGAC	8924
rs747054677	snp	C/G	3.29468e-05	0.00405861	missense	HERC2	GRCh38.p7	15:28121384	CGGGGCCATGCTGAC[C/G]ATCGCGTACCATAGT	8924
rs747054943	snp	C/T	1.65304e-05	0.00287488	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28257158	CCCTCACTCACCTGC[C/T]GAAGCAGGAGATCCA	8924
rs747066371	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28265595	CTCGTGGGCCTGTCC[-/A]GGGTGGCGAGAGCTC	8924
rs747076220	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28159668	TTAACTTCTTTGCAA[C/T]GGGTTCGAACTTCCT	8924
rs747078370	snp	A/G	1.64882e-05	0.00287121	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28178991	CCCAGCCGGCCATTC[A/G]TGGCTTCTCCACAGG	8924
rs747080223	snp	C/T	5.10834e-05	0.00505362	intron-variant	HERC2	GRCh38.p7	15:28248760	GAAAGAAGAGGATTA[C/T]AAAATTAAACAAGAT	8924
rs747084415	in-del	-/C			intron-variant	HERC2	GRCh38.p7	15:28236205	AACAGACCATGAGGG[-/C]AAATGACAACCACTC	8924
rs747086559	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28185380	GTCTGGAGGGCCCCG[A/G]TCACACTAGCAATCC	8924
rs747091697	snp	A/G	1.6617e-05	0.00288239	intron-variant	HERC2	GRCh38.p7	15:28121459	ACAGACAAAATTTAG[A/G]ATCTGATATGGAAAG	8924
rs747093276	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28296232	TGTAAACCCCACACT[C/T]TGGGAGGCCGAGGTG	8924
rs747106354	in-del	-/A			utr-variant-3-prime	HERC2	GRCh38.p7	15:28111632	CCAGTCAGTCTCTCC[-/A]ACTCCCTCCTCCCGC	8924
rs747107263	in-del	-/AG	0.0010673	0.0230762	intron-variant	HERC2	GRCh38.p7	15:28272421	TATTCTAGTAAAAAC[-/AG]ATTAACTTCTTTTCT	8924
rs747108219	snp	A/C	1.6476e-05	0.00287014	intron-variant	HERC2	GRCh38.p7	15:28144005	AGCTGAAATGAGCAG[A/C]GAGAAAGTATCAGAA	8924
rs747110366	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28255846	CTCAGTGCACCACCA[C/G]GTCACGTGTGCCTCC	8924
rs747110968	snp	C/T	5.03639e-05	0.00501791	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229825	ACACCTGTAACAGTA[C/T]TCAACAGCGGCTGCC	8924
rs747131218	snp	A/G	1.71861e-05	0.00293134	intron-variant	HERC2	GRCh38.p7	15:28163318	CAACAATTAACATGA[A/G]GAATGATATGCTAAG	8924
rs747154876	snp	A/G	1.6641e-05	0.00288448	intron-variant	HERC2	GRCh38.p7	15:28202259	CCACACCTAAGAGAG[A/G]CACACACAGCACAGC	8924
rs747158925	snp	A/G	1.65578e-05	0.00287726	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202476	CGGGCGACTGCTTGC[A/G]CCTCTTCACTCTGGC	8924
rs747168586	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28250996	ATCTGCTGTAGAACC[-/A]ATGTCCCATACAGGA	8924
rs747177493	snp	A/G	1.74151e-05	0.0029508	intron-variant	HERC2	GRCh38.p7	15:28116647	AGCGACACAGTCTCA[A/G]GCGGCCGAGAAGCTC	8924
rs747185424	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28141287	AAATATCTTAGAACT[C/T]TAGCTGCTTCCTGCA	8924
rs747189431	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28157704	CAGCTCCTGGCTTCA[C/T]TGATTTTTTGAAGGG	8924
rs747197073	snp	A/G	3.32303e-05	0.00407603	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229757	TTGTACTGAGGAGTG[A/G]AGACTGCGGATAAAG	8924
rs747205316	snp	C/T	1.65759e-05	0.00287883	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233779	CCTACAGTACCTTTC[C/T]ATTTGACACAAAAAG	8924
rs747208939	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28180206	TTAAATACACACATG[C/T]CACTGAGTTACAACT	8924
rs747226955	snp	C/G/T	3.30903e-05	0.00406746	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214148	GTACTTGTTGATGAG[C/G/T]CCATTCCACTGAGTC	8924
rs747249584	snp	G/T	1.82557e-05	0.00302118	intron-variant	HERC2	GRCh38.p7	15:28280318	AGAAAACATCTCACC[G/T]GTGGACAATGTGGCC	8924
rs747252223	snp	C/G	3.31609e-05	0.00407177	intron-variant	HERC2	GRCh38.p7	15:28175685	CATGGTGGAGAGTTA[C/G]AATACGGTTATGGTC	8924
rs747277264	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28126383	AATCCCACCACTAGG[C/T]ACCTACCCAGAAGAA	8924
rs747285095	snp	A/G	0.000115761	0.00760704	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28233728	TTCCACGGGATGCTC[A/G]GGGGGAAACATGATC	8924
rs747298690	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28181657	TCCTCAGCCAGGAGA[C/T]ACTAAGTAATACAAG	8924
rs747299903	snp	A/G	1.65154e-05	0.00287358	intron-variant	HERC2	GRCh38.p7	15:28202329	CATACACAAGCAGAG[A/G]CCAGGAAAACGAAGT	8924
rs747317889	snp	A/G	2.26411e-05	0.00336453	intron-variant	HERC2	GRCh38.p7	15:28246093	AAATAATAAGATTTA[A/G]ATAAGTATTTATCCT	8924
rs747319237	snp	C/G	1.76724e-05	0.00297252	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28218652	AGTGGGGTGAATGTT[C/G]CTTTCAGTTTGTTCG	8924
rs747326434	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28165307	ACAGCCAAGATCGGA[C/G]GTTGGTTATCTAAGG	8924
rs747326443	snp	A/G	8.30048e-05	0.0064417	synonymous-codon	HERC2	GRCh38.p7	15:28116705	CACGGGTGCTCTGGC[A/G]GCCGGGCTGAGCAGG	8924
rs747327955	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28261461	TGGTAAATCTAACAT[A/G]GCCAACACAAAGGGT	8924
rs747337007	snp	C/T	1.66427e-05	0.00288462	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28245906	AGGCCAGGCTAACTC[C/T]TCATGATCATCCCGT	8924
rs747344284	snp	A/G	3.34526e-05	0.00408965	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272224	ACTCACGTGCATGTC[A/G]CCCTCGGAGTGGGGT	8924
rs747349490	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28125905	CAACCTCCGCCTCCC[A/G]GGTTCGAGCGATTCT	8924
rs747360657	in-del	-/AAGAC	1.7203e-05	0.00293278	intron-variant	HERC2	GRCh38.p7	15:28280297	TCACATCTAGAAAAT[-/AAGAC]AAGAAAACATCTCAC	8924
rs747364024	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28204896	ACAGATGTATAATAG[C/T]ATTTCCAGAAAAGAA	8924
rs747372436	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28131600	TTGAGTGGAGCAGAG[A/C]CGCCGACCCCACCAG	8924
rs747408970	snp	C/T	7.04846e-05	0.0059361	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28218520	TCCGCTTTCCACTAA[C/T]ATTCGCAGCAGTCCG	8924
rs747424739	snp	C/T	1.66081e-05	0.00288163	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28255974	TCGACGACCTGGACT[C/T]ATGTTCACTTCATTG	8924
rs747436060	snp	C/T	1.7654e-05	0.00297097	intron-variant	HERC2	GRCh38.p7	15:28272174	TAAAAGTAACTAGAC[C/T]CGAGTGCCACCTAAA	8924
rs747436130	snp	A/G	8.34843e-05	0.00646028	intron-variant	HERC2	GRCh38.p7	15:28274871	TGTTGATGTATTAGG[A/G]AAGCAGAACAACGCG	8924
rs747437971	snp	G/T			intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318042	AGGATAACTCCATTC[G/T]GGACTTATGCTCAAA	8924
rs747446983	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28247324	ATTTTATATCTAGTA[C/T]ACAAATGTTTCCTAA	8924
rs747456737	snp	G/T	1.65026e-05	0.00287246	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28198489	TGTGAGAAGAAGAAC[G/T]TGGTGGAGGATAGCC	8924
rs747478319	snp	A/G	1.64961e-05	0.00287189	intron-variant	HERC2	GRCh38.p7	15:28146350	CCTTCTGCACCTGAA[A/G]GACAGGCAAGCACAA	8924
rs747483943	snp	A/G	2.73153e-05	0.00369553	intron-variant	HERC2	GRCh38.p7	15:28117232	ATATGCGGCACTGGC[A/G]AATGCACGAGGAGGA	8924
rs747485531	snp	C/T	1.64819e-05	0.00287066	synonymous-codon	HERC2	GRCh38.p7	15:28130296	CCTGTGATAATCGCC[C/T]TTGCCCCTGCACACA	8924
rs747491105	snp	C/T	3.36859e-05	0.00410388	intron-variant	HERC2	GRCh38.p7	15:28116975	TCAGGCGACCACTGC[C/T]GGGGACACAGGTGCT	8924
rs747510666	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28173316	CAACTGGAAACAGCC[C/T]AAACATTCATCAACA	8924
rs747514508	snp	C/T	4.68395e-05	0.00483917	missense, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28212555	TCTGTGAAGGGCAGG[C/T]TGTTCACATTAAAGG	8924
rs747525041	in-del	-/TAGG			intron-variant	HERC2	GRCh38.p7	15:28308459	TTCTTGTGGAGTCTT[-/TAGG]TTTTTCCAAATATAA	8924
rs747541727	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28120290	CTGTCCAACAAAGGA[C/T]AAGAGTTTCGTGTCT	8924
rs747542554	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28225477	CTGAGGTGGGCGGAT[C/T]GCGAGGTCAAGAGAT	8924
rs747546285	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28118569	CTAAATAAAATTCCC[A/T]ACAAACAAAACCTTC	8924
rs747551101	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28153658	TCTGTCTCGAAAAAA[C/G]AAAAAGAAAAAAAAG	8924
rs747558429	snp	C/T	1.66866e-05	0.00288842	intron-variant	HERC2	GRCh38.p7	15:28262907	TTTTAAAAGTTTACA[C/T]TTGCACTCACCTTGC	8924
rs747570364	in-del	-/AG			intron-variant	HERC2	GRCh38.p7	15:28185327	GGTGTCTTGGTCAAC[-/AG]AGTTCAGCCAGCACT	8924
rs747591429	snp	C/T	1.67346e-05	0.00289258	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28255895	CTGCAGTAATGGCTG[C/T]GTGTAAGGCTGACTC	8924
rs747609259	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28281930	CCAGAAACAACCCCA[A/G]AGCTCCAAGAGGGCA	8924
rs747615925	snp	C/T	1.65261e-05	0.0028745	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233175	CGTTCTCGAATTATC[C/T]TTTGAGCTATCCTCC	8924
rs747621271	snp	C/T	2.10817e-05	0.0032466	intron-variant	HERC2	GRCh38.p7	15:28230545	AATCATACACTTAAA[C/T]ATTAATTTTAAATTA	8924
rs747639294	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28272029	CAAGGAAGTCAGTGC[G/T]CACTGATCCGAGTCT	8924
rs747642471	snp	A/T	1.69709e-05	0.00291293	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214821	ATAAAAGAAAATTTA[A/T]AACGACAAGCATTAA	8924
rs747644516	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28263530	GCGGACCACCCTCCC[A/G]TTTGCCTGCCTGCTT	8924
rs747646855	snp	A/C	1.65364e-05	0.0028754	stop-gained, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28299420	TTCTAGGAGGGAGCT[A/C]TCCGTTCTGGGTTGA	8924
rs747652007	snp	A/G	1.82231e-05	0.00301848	intron-variant	HERC2	GRCh38.p7	15:28299381	TTTACCAAATAAAAA[A/G]CACTAGTTAAAGGCC	8924
rs747655389	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28199364	TCAAAAACATAACAG[C/T]GGAAACATCACACCC	8924
rs747655399	snp	C/T	4.94328e-05	0.00497131	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28201539	TCTGGCTCTCCGTCA[C/T]AACAGCACCAGTAGA	8924
rs747671034	snp	C/T	1.64827e-05	0.00287073	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28177496	GACAGTTAAAGCCGT[C/T]GCGTGCCGGCCACCT	8924
rs747673663	snp	C/T	4.99031e-05	0.0049949	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28237045	AAGCAGGCCCAGATT[C/T]CTCTCTGTGTCTATC	8924
rs747679349	in-del	-/CTGTC	0.000120878	0.0077733	intron-variant	HERC2	GRCh38.p7	15:28233126	CTTTAATAGTATCTT[-/CTGTC]CTTTTACATTCTTAC	8924
rs747685035	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28133695	AAACCACTTGTTGAA[A/G]ATAGTATATTTTCTC	8924
rs747686190	in-del	-/A	1.66545e-05	0.00288565	intron-variant	HERC2	GRCh38.p7	15:28256005	CTGAAACTGAAATAG[-/A]AAAGTGTGTGCCAAT	8924
rs747690673	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28188917	ACATGACAAAACCCC[A/G]TCTCTATTAAAAATA	8924
rs747701474	snp	A/G	1.64819e-05	0.00287066	synonymous-codon	HERC2	GRCh38.p7	15:28114776	GTCTCGGATGTACAT[A/G]AGTCCAGGAATAAAA	8924
rs747702743	snp	A/G	2.20204e-05	0.00331809	synonymous-codon	HERC2	GRCh38.p7	15:28142857	GTGGAGCAGCTGTTT[A/G]CCACCCCTCACAATA	8924
rs747718911	snp	A/C	1.74215e-05	0.00295134	intron-variant	HERC2	GRCh38.p7	15:28236951	ATCAGCAAAAAGCAA[A/C]GATTTTCTTACTGGC	8924
rs747732552	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28134610	GTTAACAGAGATGCC[C/G]TTGATCAGGTAAAGG	8924
rs747735703	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28250215	AAAACTACCAGCAGC[A/G]TGAGTAAGGACAGAA	8924
rs747741393	snp	A/G	1.70229e-05	0.00291739	intron-variant	HERC2	GRCh38.p7	15:28220674	GTAGAGATCAGTTAG[A/G]AGGGTGCGTAACCTG	8924
rs747744437	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28248892	GTGTCCAATGTATCT[G/T]CAACAAGCGCAACCT	8924
rs747744812	snp	C/T	5.53797e-05	0.00526182	intron-variant	HERC2	GRCh38.p7	15:28202069	TGTTAGAGCGCTAGA[C/T]GGACAGCGGCCCAGG	8924
rs747755299	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28249978	CTAACTCTTATGTCA[A/G]TGTGAAAGCAAATCA	8924
rs747759311	snp	A/C	1.65007e-05	0.00287229	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28248627	GTTGAAAACGCAGTA[A/C]CAAATCCAATGAAGC	8924
rs747762601	snp	A/G	0.000132773	0.00814672	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28174591	GCCATTGCCCTGCTG[A/G]CCGTGGTCGTTGTCA	8924
rs747762972	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28173060	GAGATACCACCATAC[A/G]TCTATCAGTATAACT	8924
rs747771780	snp	C/G/T	0.000155287	0.00881029	intron-variant	HERC2	GRCh38.p7	15:28174649	GAAAAAAGCTTATAA[C/G/T]TTTTCAACATTTCAG	8924
rs747772901	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28118880	TGAACGGGAAGGAGC[C/T]ACCTCTGGCACCCGG	8924
rs747780164	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28119863	AAGAGGTGCTCAGCA[C/T]GTAATGACTTCTTAA	8924
rs747789513	snp	C/T	1.64751e-05	0.00287007	missense	HERC2	GRCh38.p7	15:28111801	GTGTAGAGTCCGAAG[C/T]AAAGGAGTCGACATC	8924
rs747798474	in-del	-/AG			intron-variant	HERC2	GRCh38.p7	15:28168712	CTGAATACATGTAGA[-/AG]AGTTTTGGAAAACTA	8924
rs747812353	snp	C/T	3.29484e-05	0.00405871	synonymous-codon	HERC2	GRCh38.p7	15:28167780	GGAGGCTGAGGGGGC[C/T]GACGGAGTCACTGCA	8924
rs747823062	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28160173	CCAGTTAGGCTACTC[A/G]GGGGTCAGGGACCCA	8924
rs747851013	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28170560	AAACTATAAATCTTT[C/T]AGAGAAAAATAGGAG	8924
rs747875900	snp	A/G	1.64925e-05	0.00287158	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28182419	GGAGCCTTTCAGCCC[A/G]CCCAGCTGGTCCTTG	8924
rs747878097	snp	A/G	0.000164826	0.00907667	synonymous-codon, missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28280100	AGGCAGAGAAATACC[A/G]CTGCTTTTCCACTTA	8924
rs747882830	snp	C/G	0.000264218	0.0114908	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229563	GTTTTAAAATTGTAT[C/G]TATCCCTTCCAGGCG	8924
rs747886274	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28235199	TCCACAACCCACCAC[-/A]ATTCGTTCTTCTGAA	8924
rs747902035	snp	C/T	1.65677e-05	0.00287812	intron-variant	HERC2	GRCh38.p7	15:28167842	TCTAGTCCAAGAGTG[C/T]ACAGTAGGGGAAGTT	8924
rs747905874	snp	C/T	1.67013e-05	0.0028897	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28220610	TCCTCTCCCAGCTCA[C/T]CAATCACGCGGCCTA	8924
rs747922923	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28240515	CATACTCACCTGTTA[A/G]AACTAGATTCATTTT	8924
rs747952734	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28124845	GTGAGCCACCACAAC[C/T]AGCCAAATATCAAGG	8924
rs747957251	snp	A/G	1.65778e-05	0.002879	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272344	CTCCTGTGCCCCGCT[A/G]TCCCACAGCTGAAGC	8924
rs747959499	snp	C/T	1.81671e-05	0.00301384	intron-variant	HERC2	GRCh38.p7	15:28196402	GTCATTTATTAAACT[C/T]AATTCAACAGAAAAC	8924
rs747959673	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28219804	CCTCTTGGATGGTAT[A/T]ACCAAACCCAGCCAT	8924
rs747975480	snp	C/T	1.65419e-05	0.00287588	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229467	CGTTTTACCCTATAT[C/T]GATTCCCTCAGGAAT	8924
rs747979547	snp	C/G	3.2981e-05	0.00406071	intron-variant	HERC2	GRCh38.p7	15:28233614	ATGTACCTCAGGTTA[C/G]TCGAGGAATCTGCAG	8924
rs747987274	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28165200	GAGGGCCAGAGGTCA[C/T]GTAGGGTGACCATGG	8924
rs748007533	snp	C/T			intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214349	GACGGCTACCCACCT[C/T]TAAGTGACGGCACTG	8924
rs748019216	snp	C/T	0.000163178	0.00903119	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256149	CGGTGGGCAGCAGCA[C/T]GGACCAGCCACTCTG	8924
rs748043117	snp	C/T	1.84858e-05	0.00304016	intron-variant	HERC2	GRCh38.p7	15:28275052	GTCAGCAGCAGAGGG[C/T]GCAGATACTACATAA	8924
rs748048857	snp	C/G			downstream-variant-500B	HERC2	GRCh38.p7	15:28110794	AGGCCAATGAAAGCA[C/G]AAGCCAAGGCTGTGC	8924
rs748049398	snp	A/G	1.78398e-05	0.00298657	intron-variant	HERC2	GRCh38.p7	15:28182547	AAAGAAAAAGAAAAG[A/G]GAGGTTATTCAGCAT	8924
rs748053596	in-del	-/ACACACACACAG/ACACACACAG			intron-variant	HERC2	GRCh38.p7	15:28224166	CACACACACACACAC[-/ACACACACACAG/ACACACACAG]AGAGAGAGAGAGAAA	8924
rs748058219	snp	C/T	3.43495e-05	0.0041441	intron-variant	HERC2	GRCh38.p7	15:28113321	GCCGCGTGATGCTTC[C/T]CACCCTGGCATTTCC	8924
rs748059055	in-del	-/C	3.31279e-05	0.00406975	intron-variant	HERC2	GRCh38.p7	15:28144823	CGGGAGGAAAGCGCA[-/C]CCCGGGGTTAGCTTC	8924
rs748061474	snp	A/G	6.59065e-05	0.00574012	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265712	TACCAGCATCGGAAT[A/G]GCCTCGTCCTCACTG	8924
rs748069514	snp	A/C	1.65828e-05	0.00287943	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233523	TTACTTGCTCAATAC[A/C]AAGTGCACCTGCATG	8924
rs748084870	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28296452	CACTCCAGCCTGAGC[G/T]ACAGAACAAGACTCC	8924
rs748097233	snp	A/G	6.63317e-05	0.0057586	synonymous-codon	HERC2	GRCh38.p7	15:28117050	ACGGTGAGGAAGGAG[A/G]AGGCTGTCGGGACCA	8924
rs748118238	snp	C/G	1.65682e-05	0.00287817	intron-variant	HERC2	GRCh38.p7	15:28176808	AGAATCACGCACAGG[C/G]ACGGAGAAAGCAATG	8924
rs748119675	snp	C/T	3.29565e-05	0.00405921	missense	HERC2	GRCh38.p7	15:28141812	ACATCCATGTTTTCG[C/T]TGTCTGCCATTAATT	8924
rs748122837	in-del	-/TGAA			intron-variant	HERC2	GRCh38.p7	15:28217742	GTCAAAGAAACTCAA[-/TGAA]AGAGTCCTTTCAGAG	8924
rs748125345	in-del	-/CACACACA			intron-variant	HERC2	GRCh38.p7	15:28279615	GCAAGACCCCATCTC[-/CACACACA]CACACACACACACAC	8924
rs748127609	snp	A/C	1.65644e-05	0.00287783	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28198628	CATGAATGTACCTAA[A/C]CCAGTAGGTGCCCCC	8924
rs748138765	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28223655	TTTGCAAGCAAAACT[-/A]GGGGGAATTTTTCAT	8924
rs748146401	snp	A/C/T	8.24213e-05	0.00641912	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28270730	TACACAGCGGAGGCA[A/C/T]ACAGGGCGTAGCCAG	8924
rs748153915	snp	C/T	1.65556e-05	0.00287707	missense	HERC2	GRCh38.p7	15:28113592	GTCTCCAGTTCGTAG[C/T]CGGTGAACAGAGAGA	8924
rs748156956	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28187497	CCACCACACCCGGCT[A/T]ATTTTTTGTATTTTT	8924
rs748157404	snp	C/G	2.0188e-05	0.00317704	intron-variant	HERC2	GRCh38.p7	15:28233431	AGAATTAAAATCTAT[C/G]ACCTTAATGAGCGAA	8924
rs748164478	snp	A/G	1.71572e-05	0.00292888	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28215754	CGCACAAACCCCAGC[A/G]TGCACCAGCTCCGGT	8924
rs748180017	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28112099	TTACTTTACTGTGCT[C/G]ATTAGACTCTTCGTG	8924
rs748181272	snp	C/T	1.66015e-05	0.00288105	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28254468	TGAGGCATTCGCTTC[C/T]TGTTCATCAATTTCT	8924
rs748183770	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28223374	AAAGGTGGGCTTGGG[C/T]GGACCAAAAAATGTA	8924
rs748186817	snp	C/G	1.80101e-05	0.00300078	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321478	GCCTGCAAGTAAACA[C/G]ATACGCTGAAGACCT	8924
rs748190497	snp	A/G	1.65403e-05	0.00287574	intron-variant	HERC2	GRCh38.p7	15:28130608	ATCTAGAGGGGGAAA[A/G]GGTTCAATTAGACAG	8924
rs748193583	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28151058	GTAGATGCAGTATAA[G/T]TATTTTAATAAATTC	8924
rs748208313	snp	C/T	4.98965e-05	0.00499457	missense	HERC2	GRCh38.p7	15:28169653	CAGCATCTGAAGGCA[C/T]GCCTATAAGAGGAAA	8924
rs748235507	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28271618	AGCTTGCAGTGAGCC[A/G]AGATCACGCCACTGC	8924
rs748235821	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28158156	GTGCTTTACTTCCAA[C/T]TATGTGGTCAATTTT	8924
rs748236287	snp	A/C	1.75468e-05	0.00296194	intron-variant	HERC2	GRCh38.p7	15:28163077	AATCAGACGGCCCCG[A/C]CCTCCCTGAGACTCA	8924
rs748240475	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28267564	ATGGAGATCAATCTT[C/T]TCTTTTTCACTCGTC	8924
rs748256395	snp	A/T	1.65184e-05	0.00287384	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28228268	ATGCCGGAATTGAGC[A/T]GAAGGTCGAGGTTGT	8924
rs748257375	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28225319	GATTAGAGCAGCCAT[A/G]AATTAAATAGAGAAT	8924
rs748266223	snp	C/G	1.74586e-05	0.00295448	intron-variant	HERC2	GRCh38.p7	15:28238565	AAAATGATATAGGTT[C/G]TAACTTTTAACCAGG	8924
rs748279192	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28138999	AGAAGTGACCTCAGA[A/T]GTGGTGGAAACAGCA	8924
rs748290132	snp	A/C/T	0.000631806	0.0177636	intron-variant	HERC2	GRCh38.p7	15:28210990	AGATTTAAGAACTTT[A/C/T]TAAAAAGACACCTGT	8924
rs748298060	snp	A/G	1.72898e-05	0.00294017	intron-variant	HERC2	GRCh38.p7	15:28274244	AAGAACCAGCCTCAA[A/G]CAGGCCAGCTGTCTG	8924
rs748298242	snp	A/G	2.19272e-05	0.00331106	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174374	CAGAAAAATCTCAGA[A/G]AAGATACAAATCTGT	8924
rs748318895	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28208644	AGCCCCACCACTCAT[C/T]GACAAACCCTGAGCT	8924
rs748326531	snp	G/T	1.64765e-05	0.00287019	missense	HERC2	GRCh38.p7	15:28143883	CATACCAAAGCTCTT[G/T]TTTCCCCATCATTTT	8924
rs748327642	in-del	-/A	2.10396e-05	0.00324335	intron-variant	HERC2	GRCh38.p7	15:28299368	TTTATAATGGTCTTT[-/A]ACCAAATAAAAAACA	8924
rs748354099	snp	C/T	1.64901e-05	0.00287137	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28254405	AGACTCACAGATCCC[C/T]GTATTAATAAGGTCT	8924
rs748360762	snp	C/T	1.6569e-05	0.00287824	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272971	CAGGGGGATGCTTCC[C/T]GGCCCTTTGGTGGCT	8924
rs748362699	snp	C/T	3.303e-05	0.00406373	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28254445	GGAGTCCTGCTTCTA[C/T]GAAATGTTGAGGCAT	8924
rs748378661	snp	C/T	1.76409e-05	0.00296987	intron-variant	HERC2	GRCh38.p7	15:28230342	TTCTATTCAGCCAAC[C/T]TCAGAATCACAGAAA	8924
rs748380126	snp	C/T	3.53794e-05	0.00420577	intron-variant	HERC2	GRCh38.p7	15:28206218	CTGTGGATTAAAAAC[C/T]GTCAAGGCTGCATGG	8924
rs748383571	snp	C/T	1.71484e-05	0.00292812	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28229842	CAACAGCGGCTGCCA[C/T]TTGTCCTAACAAAGG	8924
rs748386216	snp	A/G/T	0.113181	0.209249	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272980	GCTTCCTGGCCCTTT[A/G/T]GTGGCTGGCGTTCCG	8924
rs748388241	snp	A/G	1.67607e-05	0.00289483	missense, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28292998	AGATCTTCTTTCTTT[A/G]TTCCACTTGGTTCGA	8924
rs748402138	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28201972	TTCTGTGCCCGGCAA[C/T]ACCATAGGTTGGTTT	8924
rs748407226	snp	A/G	6.59761e-05	0.00574314	missense	HERC2	GRCh38.p7	15:28163162	CCCTGTCCCCGGCCC[A/G]GCTGCACACTGACAG	8924
rs748421665	in-del	-/TTA	3.41297e-05	0.00413082	intron-variant	HERC2	GRCh38.p7	15:28112084	GAGTACGGCTGCAGT[-/TTA]CTTTACTGTGCTCAT	8924
rs748423829	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28126245	CCCACTAGAGGGCGA[C/T]AAAAACTAACAACAA	8924
rs748435422	snp	G/T	1.6643e-05	0.00288465	synonymous-codon	HERC2	GRCh38.p7	15:28115522	ACTCCCGGTTCGGAT[G/T]GCAATGCCCAGCAAC	8924
rs748446973	snp	C/T	1.65312e-05	0.00287495	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28257110	ACACACTCTTTCTCC[C/T]GGGGCGGGGGCCAGT	8924
rs748452157	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28139564	AGAGTCCTGACCCAG[A/G]GAAACTATGAAATAA	8924
rs748456207	in-del	-/ATAG			intron-variant	HERC2	GRCh38.p7	15:28270245	TCTTTTTATTTATTT[-/ATAG]ATAGATAGATAGATA	8924
rs748460079	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28178233	TGGAGAGGGGGCTGC[A/G]TGGGCAGGAGGGCAC	8924
rs748464195	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28162627	CAGGTTTGGTGCTCA[C/T]TCCTGTAATCCCAGC	8924
rs748468108	snp	C/T	1.71234e-05	0.00292599	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214247	CGAGGCCTGCGGGCG[C/T]ACCCTGCGCCGCCTC	8924
rs748470054	snp	C/G	0.00482303	0.0488697	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202493	CTCTTCACTCTGGCA[C/G]GGCGGATGTGCTGCA	8924
rs748470314	snp	A/G	0.000349956	0.0132233	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28234177	GAGATTTGCTGGCAG[A/G]TGTGCCCCCTGGGGA	8924
rs748477391	snp	C/T	1.65743e-05	0.00287869	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28233788	CCTTTCTATTTGACA[C/T]AAAAAGTCCTGCAAC	8924
rs748478259	snp	G/T	3.30202e-05	0.00406313	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28292922	CCAGCTGTCCAGAAT[G/T]GACTTGGCCCTATAT	8924
rs748493989	snp	C/T	1.65765e-05	0.00287888	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28220463	CCACCAGAGTCATCC[C/T]CTGTGTCCGAATCCT	8924
rs748494736	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28278065	GTTCAAGACCAGCCC[A/G]GGCAACATGGCAAAA	8924
rs748500945	snp	A/C	1.64762e-05	0.00287016	intron-variant	HERC2	GRCh38.p7	15:28143995	TGTGACTGGCAGCTG[A/C]AATGAGCAGAGAGAA	8924
rs748507525	snp	C/G	3.40124e-05	0.00412372	intron-variant	HERC2	GRCh38.p7	15:28266006	ACAAACATGAATGCC[C/G]TTCTTCTTGGTGTTA	8924
rs748508326	in-del	-/CTT			intron-variant	HERC2	GRCh38.p7	15:28216131	GGGCATTTTTAAAAC[-/CTT]CTTCTAAGTATGTGT	8924
rs748511588	in-del	-/GCA	1.71413e-05	0.00292752	cds-indel	HERC2	GRCh38.p7	15:28124165	GCTCGGAGAGGTGGT[-/GCA]GCAGCAGCAGACGGT	8924
rs748514889	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28174951	ATTTTGCAAAGAAAA[A/G]TGACCAAAAACAGTA	8924
rs748515314	snp	C/T	1.65825e-05	0.00287941	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28175602	TTCCACCACCTGTGG[C/T]TTCCGCACGTGCACG	8924
rs748516740	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28211822	GCTGAAGCAGCAATC[A/G]TAGGTCTGTGGGAGC	8924
rs748542231	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28183183	TCATCTATCTCCTGA[C/T]CTGCCCTCAACAGGT	8924
rs748546198	snp	A/C	3.34325e-05	0.00408842	intron-variant	HERC2	GRCh38.p7	15:28112048	CACCTGTTGAGCAGA[A/C]ACATGAAGTGATTAG	8924
rs748549160	snp	G/T	1.64953e-05	0.00287182	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28196544	GGGAAAGTCGACAAT[G/T]ATATCTTTTCCATTG	8924
rs748554843	snp	C/T	1.64917e-05	0.00287151	missense	HERC2	GRCh38.p7	15:28135653	ACTCTGTCCCTCCAA[C/T]GCCTAGTCTGCCACC	8924
rs748557543	snp	C/G/T	3.67338e-05	0.00428553	synonymous-codon, missense	HERC2	GRCh38.p7	15:28113071	CAGCCAGGAGCCTAC[C/G/T]TGGATGACGAAGTCT	8924
rs748580371	snp	C/T	1.64765e-05	0.00287019	synonymous-codon	HERC2	GRCh38.p7	15:28168470	AACAGCCAGCATGCA[C/T]TCTTCTCCATTCATG	8924
rs748582777	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28259819	AAAAAAATACAAAAA[G/T]TAGCCAGGCATGGTA	8924
rs748597437	snp	C/T	1.65045e-05	0.00287263	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265920	GATGTGCACCACGTG[C/T]TTCCCGGCCTGCTTT	8924
rs748602220	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28261189	CCCACAGTCTACAAA[G/T]ATCATAATACTAGGA	8924
rs748616669	snp	A/C/T	6.61445e-05	0.00575052	synonymous-codon	HERC2	GRCh38.p7	15:28168530	GGCCGCCGAGGAGAA[A/C/T]GAGGGGCACTCCACC	8924
rs748623580	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28129606	GGGCCAAGCCTGCAG[C/G]AGGTCTGTCTAAGGA	8924
rs748634836	snp	A/G	0.000132144	0.0081274	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28186668	CTTCTGCACGGATCC[A/G]TCCCAGCAGGATGAG	8924
rs748641339	in-del	-/G	1.65688e-05	0.00287821	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214638	CCAGGGCACAGGGAA[-/G]GTAGACGGCCACCCA	8924
rs748642709	snp	A/G	1.64974e-05	0.00287201	intron-variant	HERC2	GRCh38.p7	15:28141419	CCTTGTGACATAGAA[A/G]AAGAGCTCTTACCTT	8924
rs748652438	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28145019	GCATTCAGCCCCTGT[-/A]ACCAGGTACCCAGGA	8924
rs748675104	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28256440	AATTTCTCAGTTTAT[A/G]TATTTTTAAAAACTG	8924
rs748711694	snp	A/C/T	3.05553e-05	0.00390855	intron-variant	HERC2	GRCh38.p7	15:28115381	GCAGAACAGACTGTG[A/C/T]CTGTTAACAAGACCC	8924
rs748717382	snp	C/G	6.73435e-05	0.00580234	intron-variant	HERC2	GRCh38.p7	15:28256061	ACACCCTGACCCATG[C/G]CCTCTCCTGTTCCTT	8924
rs748722561	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28169724	TTCTATAAAATCTGA[C/T]CTTACAGGTTAGTTC	8924
rs748724099	snp	G/T	1.6659e-05	0.00288604	intron-variant	HERC2	GRCh38.p7	15:28198343	GCGTTAATGAAAAGT[G/T]AACATCAGGAATTTT	8924
rs748736146	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28131729	AGCACTGGCACCCCC[-/A]AGCGCGTGCCGTGGC	8924
rs748736694	snp	C/T	3.30284e-05	0.00406363	intron-variant	HERC2	GRCh38.p7	15:28130139	TCACAGGCCTCAGTC[C/T]TGCGGCACTGAGCCC	8924
rs748768501	snp	C/G/T	3.29904e-05	0.00406132	missense	HERC2	GRCh38.p7	15:28146246	CCTTACCTGACCGCA[C/G/T]GGAGACGATCCTGTT	8924
rs748775184	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28240375	GTGAGCTGAGATCAC[A/G]TCACTACACTCCCGC	8924
rs748783438	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28164849	CATTAAACCCTCAAA[A/C]CAGGAGACTGCCAAA	8924
rs748785395	snp	A/G	3.2969e-05	0.00405998	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213759	GTTTCAGCTGATTCA[A/G]TGGGCAAACGCGACA	8924
rs748796424	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28280652	GCTCACACCTGGAAT[C/T]CCAGCACTTTGGGAG	8924
rs748803103	snp	C/T	3.32408e-05	0.00407668	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28255987	CTTATGTTCACTTCA[C/T]TGCCTGAAACTGAAA	8924
rs748809716	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28250576	GGTATTCTGTGGCTC[C/T]TCGCCAGCATGTAAA	8924
rs748809843	snp	A/G	3.37325e-05	0.00410672	intron-variant	HERC2	GRCh38.p7	15:28186796	TCTGTAGAATCAAGC[A/G]TATTAGATCCTCTAA	8924
rs748816101	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28148343	ATAGGAAAAAAGGAG[C/G]AAATTTTAAAAAAAG	8924
rs748820235	snp	C/T	1.74616e-05	0.00295474	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233259	TTACAAACAGCAGGT[C/T]TCAATTCATTAAAGA	8924
rs748828304	snp	A/G	1.64765e-05	0.00287019	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28263141	GCCCAATTTCCCATA[A/G]TCACCATCTCCCCAA	8924
rs748856451	snp	C/G	1.64789e-05	0.0028704	missense	HERC2	GRCh38.p7	15:28146318	TGGAGCACTGCCGGT[C/G]AAATTCTACCCTGAG	8924
rs748906484	snp	C/T	1.65217e-05	0.00287412	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233185	TTATCTTTTGAGCTA[C/T]CCTCCTCCAACGGGG	8924
rs748910309	snp	C/T	1.75993e-05	0.00296637	intron-variant	HERC2	GRCh38.p7	15:28238072	AACACACAGAGGGTA[C/T]CCCCTGCCATCCTCT	8924
rs748913087	snp	C/T	3.33884e-05	0.00408572	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28269309	GACAGAATCAGGAAA[C/T]GCTTCTCTGCACAGG	8924
rs748922228	snp	C/G	3.29582e-05	0.00405931	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28201458	GACAATTACTCACCT[C/G]AATATTCTCTCTCAC	8924
rs748929948	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28187089	GATGCTTTAACTAAG[A/G]AAGATATTAAATGTC	8924
rs748935454	snp	A/G/T	0.000115318	0.00759261	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28201523	GCTCGTTTTTTGTAC[A/G/T]TCTGGCTCTCCGTCA	8924
rs748944643	snp	A/G	3.29478e-05	0.00405867	missense	HERC2	GRCh38.p7	15:28114646	GCACGTACTCCGCGC[A/G]GTTGTCCAGGGTGAT	8924
rs748957874	snp	C/T	1.64776e-05	0.00287028	missense	HERC2	GRCh38.p7	15:28114771	TCATTGTCTCGGATG[C/T]ACATGAGTCCAGGAA	8924
rs748962242	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28171902	ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA	8924
rs748991795	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28179126	TAAAAATTTTTTAAG[A/G]TTAGAATAATCATAC	8924
rs748994774	snp	A/G	1.66203e-05	0.00288268	intron-variant	HERC2	GRCh38.p7	15:28167668	CACAATACAAAGTTA[A/G]AGAAGAACGCCTCTT	8924
rs748996508	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28138451	TGACCATTCTGAAAA[C/T]CTTAGGGCCCTTAAG	8924
rs748998459	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28173987	TGATTGTGCTGATGC[C/T]TTCATGGATCATACA	8924
rs749025615	in-del	-/AC	3.29582e-05	0.00405931	intron-variant	HERC2	GRCh38.p7	15:28176613	ACCTAGGTTTAAGAA[-/AC]ACATATACTTCAGGC	8924
rs749025739	snp	A/G	2.86932e-05	0.00378758	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28222128	AGCTGCACAGGAGCC[A/G]TTTCCTTCCTTGTTT	8924
rs749051331	snp	A/G	1.78083e-05	0.00298393	intron-variant	HERC2	GRCh38.p7	15:28272853	GGTATTTCCATACAC[A/G]GGCGCTTCCCCAAAG	8924
rs749074909	in-del	-/AAAT			intron-variant	HERC2	GRCh38.p7	15:28177826	AGATGAAAAAAGTAA[-/AAAT]AATTTGTGATTAGAC	8924
rs749075161	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28270153	TTTTAAGTTGAGACA[G/T]GGTTTCTCCAAGTTG	8924
rs749084262	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28138630	TGCTCATTGACAATG[C/T]ACCTGGTCGCCCAAG	8924
rs749087466	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28177219	GATCCACATGTAGTC[A/T]ACACAGGATCCACAG	8924
rs749094353	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28189691	TCACCACAAAAAAGT[A/G]ATAAATATTTGAGGT	8924
rs749104715	snp	C/T	1.6498e-05	0.00287206	missense	HERC2	GRCh38.p7	15:28111767	GTTTCCCCATCTTAG[C/T]GTCCTGTTAAATAAT	8924
rs749108050	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28292464	AACCTTAGTATACCG[C/T]TGCAAGAATATAAAA	8924
rs749116541	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28123661	AGAAACAGCCCAATC[A/G]CCGGCCTTCCTGTGT	8924
rs749117219	snp	A/T	1.64953e-05	0.00287182	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28248639	GTAACAAATCCAATG[A/T]AGCAGATCTTTCACG	8924
rs749118785	snp	A/C	3.29891e-05	0.00406122	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229707	TCTCATTTTTTCCAC[A/C]TCCACTGGCTCTTCT	8924
rs749123510	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28115099	GCACAACACAGCCAT[A/G]GGGAATGAGCTGGCT	8924
rs749134969	snp	C/G	1.76727e-05	0.00297255	intron-variant	HERC2	GRCh38.p7	15:28248522	AGCCCCGATCACATA[C/G]AAGACACTTTCACAT	8924
rs749138133	snp	A/G	9.51937e-05	0.00689839	intron-variant	HERC2	GRCh38.p7	15:28272403	TAAAGGAGAAAAGAT[A/G]TTTATTCTAGTAAAA	8924
rs749156070	snp	A/G	4.94189e-05	0.00497062	synonymous-codon	HERC2	GRCh38.p7	15:28167765	GATAAAAGGCCGAGC[A/G]GAGGCTGAGGGGGCC	8924
rs749158655	in-del	-/TAAAC			intron-variant	HERC2	GRCh38.p7	15:28275906	ACAGTATTGCTACTA[-/TAAAC]TATATTCTCCAAATT	8924
rs749167589	in-del	-/CA			intron-variant	HERC2	GRCh38.p7	15:28169143	AAAACTCAGCCTTCT[-/CA]AGTGAGCGAAGGGGA	8924
rs749173762	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28179250	TTTTTTTAACAAAAA[A/G]AAAAGAAAAGAAAAT	8924
rs749175269	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28178133	CTTACCAACAGAACC[C/T]CCATGTTAAAGTGCT	8924
rs749175507	snp	C/T	2.35663e-05	0.00343258	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28196255	ATGCCTGGTATTGTG[C/T]TTTTTGGTCTTGAAA	8924
rs749178359	in-del	-/A	1.73711e-05	0.00294707	intron-variant	HERC2	GRCh38.p7	15:28179260	AAAAAAAAAGAAAAG[-/A]AAAATTTTACTTGCA	8924
rs749180532	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28237686	ATCTTATTACTTGTC[A/G]ATACCTGGAAAGCTA	8924
rs749202930	snp	A/G	2.98967e-05	0.00386619	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256314	GACTAATGGCAGCAT[A/G]CAACTGAAAGGAGAA	8924
rs749216967	snp	C/T	1.76943e-05	0.00297436	missense	HERC2	GRCh38.p7	15:28124195	GGTTCCTCAGCGCAA[C/T]GATGGGGATCTCCTG	8924
rs749220266	snp	G/T	1.65529e-05	0.00287683	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214009	GCTCGACAGAGACAC[G/T]CACGGAGCTGCCCAA	8924
rs749224517	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28296691	AATTACTGATACATA[-/A]AAAAAAAAAAAAAAA	8924
rs749233515	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28255568	AATCTAATCTCAGGG[A/C]AGGGGAGTATCCTGG	8924
rs749255782	snp	A/G	3.49095e-05	0.00417774	intron-variant	HERC2	GRCh38.p7	15:28144279	GGTTTCACAAGCTAG[A/G]TACCACCCCATAAGA	8924
rs749263149	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28163961	CTATGGAGGTGCCTT[G/T]CCCAGGATGGCCGCC	8924
rs749264138	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28295839	CTGCCCGCTGACATA[C/G]TACTGTCTGTGGCTA	8924
rs749272287	snp	A/C/G	4.94184e-05	0.00497063	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28176496	CTCAATCTGGCACAC[A/C/G]CCCTGTCCATTTAGT	8924
rs749273076	snp	A/T	1.98088e-05	0.00314707	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202406	AGGGCAAACTCGATG[A/T]TCCTTCTGGAAAATC	8924
rs749282697	snp	C/T	3.29544e-05	0.00405908	missense	HERC2	GRCh38.p7	15:28144688	CAGCAGCTGGCATGA[C/T]GGGATAGACGGTGAA	8924
rs749284104	snp	A/G	0.000164946	0.00907996	intron-variant	HERC2	GRCh38.p7	15:28265813	TCATGCAGAGCAGAC[A/G]TACCATGGCCCAGCC	8924
rs749287980	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28192912	TCAGAGTGAACTATG[A/G]AGGGTTTTTGGGTTT	8924
rs749299201	snp	A/G	1.64798e-05	0.00287047	intron-variant	HERC2	GRCh38.p7	15:28176634	ATACTTCAGGCCAGC[A/G]TTTCATATCATTCCT	8924
rs749299438	snp	C/G			intron-variant, utr-variant-5-prime	HERC2, LOC107987422	GRCh38.p7	15:28317804	CTGGGTTTTTATACT[C/G]TATTATAATTACATA	8924
rs749304891	snp	C/G	1.65258e-05	0.00287448	missense	HERC2	GRCh38.p7	15:28113213	TGGATCAGCGATGCG[C/G]AAGGCTCGATGCCTT	8924
rs749311837	snp	A/G	1.66034e-05	0.00288122	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213951	GGTTCTCGGAGTCGG[A/G]GAAGTAGTCCTCTAA	8924
rs749316544	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28244031	AAATTTAAAAATTAG[C/T]CAGGCATGGTGGCGC	8924
rs749320937	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28259572	AAGATAGTATAACAC[A/G]AAGAAAGAAAACCAC	8924
rs749335195	snp	A/G	1.64727e-05	0.00286986	synonymous-codon	HERC2	GRCh38.p7	15:28141603	TGTTCCACTGCCACC[A/G]GCAGAGAGAGTCCAG	8924
rs749339992	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28129563	CAGGGGATCCCTCCC[A/G]AAACCCAGGTTCCCA	8924
rs749340405	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28167583	GGACAGCCGAGGTGA[A/C]TGGGATAGGAATAGA	8924
rs749342969	snp	C/G	0.272182	0.249014	intron-variant	HERC2	GRCh38.p7	15:28238775	GTAAAAAATGACTCT[C/G]TATATACAGAAACCA	8924
rs749351206	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28219461	TAGGCTGGATGCTGG[C/T]GGCCAGCACCACATC	8924
rs749356589	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28243282	GTGCACTATAGCTCT[A/T]AACATGAAAGTTAAG	8924
rs749357270	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28188115	AGTTTTTTTTTTCTT[C/T]AGCAAGAAAAAAAAC	8924
rs749366726	snp	A/G	8.18465e-05	0.0063966	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28202462	CGGCAGAGCGGGAAC[A/G]GGCGACTGCTTGCGC	8924
rs749370723	snp	A/G	0.000119057	0.00771454	intron-variant	HERC2	GRCh38.p7	15:28113309	ATGTCTGTCAGGGCC[A/G]CGTGATGCTTCCCAC	8924
rs749384043	snp	C/G	1.65255e-05	0.00287445	missense	HERC2	GRCh38.p7	15:28169508	ATGATTTGCAATGCT[C/G]TAAGAATATGTGATA	8924
rs749400098	snp	C/T	3.31581e-05	0.00407161	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233529	GCTCAATACCAAGTG[C/T]ACCTGCATGAACTAA	8924
rs749400458	in-del	-/C	1.64974e-05	0.00287201	intron-variant	HERC2	GRCh38.p7	15:28130152	TCCTGCGGCACTGAG[-/C]CCCTACCTACCATCC	8924
rs749405531	snp	A/G	1.79065e-05	0.00299215	intron-variant	HERC2	GRCh38.p7	15:28218444	AGACACAAGCGTGCG[A/G]CCCCCAGCGCTGACT	8924
rs749423546	snp	A/T	1.6476e-05	0.00287014	intron-variant	HERC2	GRCh38.p7	15:28141689	TGCACACAGCCTCTC[A/T]CACTCACGATCGACA	8924
rs749425261	snp	C/T	1.64958e-05	0.00287187	intron-variant	HERC2	GRCh38.p7	15:28130327	AAGGAAGCATGGAAA[C/T]TATGGGGCAAGGTGA	8924
rs749430030	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28284128	AATTTGGGGGCATCA[C/T]GCTGGAGTGCCAAAA	8924
rs749456626	snp	A/G	3.31868e-05	0.00407336	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28198603	AGAATGTGCTCACCT[A/G]TAAGTTCCACATGAA	8924
rs749477792	snp	A/G			missense	HERC2	GRCh38.p7	15:28169590	GAGAAGGGCGATTTG[A/G]CTTAGAATTACTTGC	8924
rs749487917	snp	C/T	1.65367e-05	0.00287543	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28238682	ATCACAGTCCAGAAG[C/T]CTCCATCTTTATTAT	8924
rs749493295	snp	C/G	1.67374e-05	0.00289282	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28215774	CCAGCTCCGGTGTTG[C/G]TCCCTGTACACCAGC	8924
rs749513839	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28285582	CACTAAATAAATGAT[A/G]TATTAGAAACTTGGA	8924
rs749541624	snp	A/C/G	6.60408e-05	0.00574601	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28228276	ATTGAGCAGAAGGTC[A/C/G]AGGTTGTTTGCGCCG	8924
rs749544972	in-del	-/AATATCATGC	1.681e-05	0.00289909	intron-variant	HERC2	GRCh38.p7	15:28142223	CAAAAGTGATTCCAA[-/AATATCATGC]AATACCTCATCAAGA	8924
rs749552300	snp	C/T	0.000395511	0.014057	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28270732	CACAGCGGAGGCATA[C/T]AGGGCGTAGCCAGAC	8924
rs749555303	snp	C/G	3.32602e-05	0.00407786	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274341	CTCCACCACCTCCAG[C/G]CACACAGAGGACACG	8924
rs749559341	snp	A/G	3.30644e-05	0.00406585	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28191209	TTTTAATCTATGAAC[A/G]AGAACATCTGGGAAA	8924
rs749564811	snp	C/T	3.53838e-05	0.00420603	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28254502	TCCTTCTGTGCTTCT[C/T]TTTTGGCTTCAATAT	8924
rs749567711	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28212184	ACAGACTTCTCTTCC[A/G]GGATAAAGGGTGACA	8924
rs749574298	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28274850	AACCGAGTTCGAAAC[C/T]CAGTCTGTTGATGTA	8924
rs749583714	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28192207	ACTGGGGAGAAACAT[C/T]ATGATCAAGAATATT	8924
rs749590139	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28132037	GTGTTTTCCCAGAGG[A/G]GCCCTGGGGGCCCGA	8924
rs749592734	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28258574	CGCCAAAATTTGTAG[G/T]TTTAATTAAAGCACT	8924
rs749601565	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28228597	ACATCTGACTAATAA[A/G]CATTGACACCCACCT	8924
rs749601788	snp	C/T	1.70122e-05	0.00291647	missense	HERC2	GRCh38.p7	15:28142939	AAAGCAGCAAGAGCA[C/T]TACCTGTAAAACTCT	8924
rs749604395	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28117416	TAGTGTGTCTGAACA[A/C]ACACACCTTCCAACA	8924
rs749629934	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28142031	TTAGAAATGTCTAGA[C/G]AGTATCATTCTACCT	8924
rs749639589	snp	A/C/T	0.000122576	0.00782786	intron-variant	HERC2	GRCh38.p7	15:28293073	TTTCAGAATGCCATA[A/C/T]CATTAGTCTCTGCAA	8924
rs749652854	snp	C/T	6.99447e-05	0.00591333	intron-variant	HERC2	GRCh38.p7	15:28260741	ACTGGAAACCAAAAT[C/T]CTCCAAAATACCAAA	8924
rs749655741	snp	C/T	1.82757e-05	0.00302283	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214315	CTGCACCGCTCTTCA[C/T]CAGGGCACAGGGAAA	8924
rs749667609	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28187072	GAGCTTTCTTGAACC[-/A]AGATGCTTTAACTAA	8924
rs749678924	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28161209	CCATCAGAGCTTTAA[C/T]GTTTCAGAATTTCAG	8924
rs749680236	snp	A/C	1.70426e-05	0.00291908	missense, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28293021	TGGTTCGACACTATC[A/C]TCTGCAGAATTAAAA	8924
rs749689822	snp	G/T	6.59359e-05	0.00574139	intron-variant	HERC2	GRCh38.p7	15:28143864	AAATTGTACTAGAAT[G/T]CTCCATACCAAAGCT	8924
rs749713073	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28271836	GCCTGCTCCTCCCTC[-/A]GCTTGTTGTCCACAC	8924
rs749728963	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28291218	GAGGTAGGTACTACT[A/C]TTAACCCCAAATACG	8924
rs749734682	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28196664	TCATACTACATTGTA[C/G]TTATTTGTTTTTTAC	8924
rs749735844	snp	G/T	0.000102074	0.00714328	missense	HERC2	GRCh38.p7	15:28115493	ACAGGCTCGGCAAGG[G/T]TGAGGCTCAGGGGAC	8924
rs749746546	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28235151	CTTAGTGTTCTTTTA[C/G]TGGACATTTAGATTT	8924
rs749769656	in-del	-/T	1.77568e-05	0.00297961	intron-variant	HERC2	GRCh38.p7	15:28237158	AGGAAACAGAATTAA[-/T]TAAAAACATAAAACC	8924
rs749772092	snp	A/G	0.000219242	0.0104677	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28234229	CTCCTCGTTGTAGCT[A/G]TAGTGGATCTGGCTG	8924
rs749775285	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28200224	AAAAATGAAGAAACA[C/T]TGTCTCTACTAAAAA	8924
rs749778346	snp	C/T	1.65693e-05	0.00287826	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272332	CTCATTGTCAGTCTC[C/T]TGTGCCCCGCTGTCC	8924
rs749780321	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28119693	TCCTAGGCTCAAGCA[A/G]TCCATCCACGTCAGC	8924
rs749788850	in-del	-/CTT	0.000301967	0.0122838	cds-indel, nc-transcript-variant	HERC2	GRCh38.p7	15:28230432	GAGGCAAAATGCAAG[-/CTT]CTTCTAAATCACTCT	8924
rs749789527	snp	A/C	1.71784e-05	0.00293069	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214251	GCCTGCGGGCGCACC[A/C]TGCGCCGCCTCAGCG	8924
rs749798857	snp	C/T	1.66443e-05	0.00288477	intron-variant	HERC2	GRCh38.p7	15:28196426	AGAAAACCATTCGTC[C/T]CAAAGCAAATCTAGC	8924
rs749809199	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28145170	CATGGGGACATTTCC[C/T]GGGAAAGCTCTGATA	8924
rs749821923	snp	C/T	7.02506e-05	0.00592624	intron-variant	HERC2	GRCh38.p7	15:28266019	CCCTTCTTCTTGGTG[C/T]TATTTCTTATTAATG	8924
rs749828612	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28183003	GATGTGGCCACATGA[C/G]CATGGAGTTACTTTA	8924
rs749829091	snp	A/C	1.72338e-05	0.00293541	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28175560	GGCCCCGACAGCCAC[A/C]TGCACGATCTTCTTC	8924
rs749842322	snp	C/G	1.71396e-05	0.00292737	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202227	GGAGTGGTCCAGCAG[C/G]CACCCGACCAAGGCT	8924
rs749848043	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28127768	GGGACACACAAAAAG[G/T]GGGCAGAGCCAGCCA	8924
rs749856181	in-del	-/GAA	3.39141e-05	0.00411775	intron-variant	HERC2	GRCh38.p7	15:28257036	CACTTACAAAAGGAG[-/GAA]GAAGAAGGGAAATCA	8924
rs749856736	snp	A/G	1.66676e-05	0.00288679	intron-variant	HERC2	GRCh38.p7	15:28112042	ATCCAACACCTGTTG[A/G]GCAGAAACATGAAGT	8924
rs749871234	snp	C/T	6.62855e-05	0.00575659	intron-variant	HERC2	GRCh38.p7	15:28229428	GTTGCCATAGCTACC[C/T]TAATTAAGAAAAAAA	8924
rs749881360	snp	C/T	4.94425e-05	0.0049718	intron-variant	HERC2	GRCh38.p7	15:28144072	ACTGTAATGGTGGCA[C/T]TTACCTAGGGCACTC	8924
rs749889808	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28202314	AAGCGGGAACCCACA[C/T]ATACACAAGCAGAGG	8924
rs749920864	snp	A/C	6.61124e-05	0.00574907	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28238731	TGCGTATAAGTGTCA[A/C]TTCCTCATTATTTCT	8924
rs749921140	snp	C/T	1.70093e-05	0.00291622	intron-variant	HERC2	GRCh38.p7	15:28275013	GCCGGGAACTGCAGA[C/T]GACACACACGGAACA	8924
rs749928148	snp	A/C	1.64749e-05	0.00287005	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265691	CTTCAGTCCTTTAAG[A/C]CCGGCTACCAGCATC	8924
rs749948950	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28195374	GCTGAGACAGGAGAA[C/T]TGCTTGAACCTAGGA	8924
rs749955606	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28124497	TGGTGTGGAAGAGTT[C/T]GGTGTGGGTTATAAG	8924
rs749960474	snp	A/G	2.20087e-05	0.00331721	intron-variant	HERC2	GRCh38.p7	15:28113045	CGACATCAGCCCAGG[A/G]CCGGCAAGCCCAGCC	8924
rs749978819	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28273708	AGTGCTGACCTCTGC[A/G]AGGAGAGTGAGGAGT	8924
rs749982315	in-del	-/AACT			intron-variant	HERC2	GRCh38.p7	15:28293918	GCGAAGAGAAGAGAG[-/AACT]AACCTTAACCTTGAA	8924
rs749984482	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28255310	ACTGCATCCAGCCTC[A/G]GTGACAGAGCAAGAC	8924
rs749999715	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28291776	CGGGTGTGGTGGTGC[A/C]CGCCTGTAGTCCCAG	8924
rs750000503	snp	A/G	4.97294e-05	0.0049862	synonymous-codon	HERC2	GRCh38.p7	15:28113146	CCAGACGAAGCGAAG[A/G]AAAAGAGAGCGCTCT	8924
rs750000906	snp	A/G	9.26672e-05	0.00680625	intron-variant	HERC2	GRCh38.p7	15:28215821	CAGGAGGGAAAATAG[A/G]CATGCTTGGTAACAA	8924
rs750002878	snp	A/G	1.66568e-05	0.00288585	intron-variant	HERC2	GRCh38.p7	15:28176397	CACCTGCACAAGCAC[A/G]CACAGTGTGACAGGG	8924
rs750010375	snp	A/G	1.65272e-05	0.0028746	intron-variant	HERC2	GRCh38.p7	15:28130129	CCTCTTAGATTCACA[A/G]GCCTCAGTCCTGCGG	8924
rs750011168	in-del	-/AAGC	6.75117e-05	0.00580959	intron-variant	HERC2	GRCh38.p7	15:28117166	GACCTGGAGAGGAGG[-/AAGC]AAGCAAGCAAGCGTG	8924
rs750016015	snp	C/T	1.64773e-05	0.00287026	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28270760	GACGGTCTAAATGGG[C/T]CATGACAACAACCGC	8924
rs750018134	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28261346	TTCAGTGAGGAAGGT[C/T]TCCTAAGAAGAAATC	8924
rs750027877	snp	A/G	1.66924e-05	0.00288893	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28202369	GCTGGATGCATTCCC[A/G]GAAGCACCAGTGAGA	8924
rs750036068	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28140518	ATTTCTATATATCAG[C/T]GGCAATCTTTTTTTG	8924
rs750056710	snp	C/T	1.66366e-05	0.0028841	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28238630	TCCTGTTAACGACTG[C/T]GTCTGGAAGTCCTTT	8924
rs750058947	snp	C/T	9.88338e-05	0.00702902	missense	HERC2	GRCh38.p7	15:28141497	GCACGGGTCTGAGAG[C/T]TGCAAGGGCTTCACA	8924
rs750066945	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28256646	CTCAACCAAAAAAGC[A/T]GCCACAGGTGCAATC	8924
rs750094751	snp	A/C	3.3911e-05	0.00411756	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28215731	CCTGCGGCGTGAGAG[A/C]GATGCTCCGCACAAA	8924
rs750099260	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28303616	TTGATAGGGATTACA[C/T]TGAACCTGTAGATTG	8924
rs750102347	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28292627	ATAAGACCAGCCTGG[A/G]CAACACAGTGAGATT	8924
rs750102404	snp	C/T	1.67846e-05	0.0028969	intron-variant	HERC2	GRCh38.p7	15:28186785	GATCTATAGACTCTG[C/T]AGAATCAAGCATATT	8924
rs750115906	snp	C/T	1.6736e-05	0.0028927	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274293	GGAAAGAACTCACCC[C/T]GTCACGACGGACCTG	8924
rs750116019	snp	A/C/G	3.30029e-05	0.00406209	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28198479	CCAATCTTGATGTGA[A/C/G]AAGAAGAACTTGGTG	8924
rs750124043	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28125436	CTCTCCACAGCCCCT[A/G]TTGGCCACCAGGCCT	8924
rs750128707	snp	A/C/G			intron-variant	HERC2	GRCh38.p7	15:28244626	GCTTTACAGTGAGTA[A/C/G]GCTGCTGATCTGATC	8924
rs750136502	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28164725	AATAATAGAAATACA[A/G]GGTTGCAACCTGGAT	8924
rs750146423	snp	A/C	1.6473e-05	0.00286988	missense	HERC2	GRCh38.p7	15:28130248	TTGGACCTGCCGAGG[A/C]CTTCGAACATGGTCA	8924
rs750157013	snp	A/G	0.124686	0.216325	intron-variant	HERC2	GRCh38.p7	15:28273016	ATCCCTGAAATGAAA[A/G]CAGTGGATGCAGGAA	8924
rs750158226	snp	A/C/T	4.96482e-05	0.00498217	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28254458	TATGAAATGTTGAGG[A/C/T]ATTCGCTTCCTGTTC	8924
rs750158294	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28241544	AAGTAAAAGCAGGCC[A/G]GGCGCAGTGGCTCCC	8924
rs750173093	snp	C/T	1.64784e-05	0.00287035	missense	HERC2	GRCh38.p7	15:28146314	TCTGTGGAGCACTGC[C/T]GGTCAAATTCTACCC	8924
rs750174541	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28260704	AAACTCAGTGGTATT[C/T]TCTACATACTGGTAA	8924
rs750186131	snp	A/G	3.86302e-05	0.00439472	intron-variant	HERC2	GRCh38.p7	15:28210952	TCACTTCCTTTGTCT[A/G]CTTTCTACTGCCCTT	8924
rs750188350	snp	A/G	1.64762e-05	0.00287016	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28191037	CTTTAGTTCAATAAG[A/G]TTATTCAGGGAATTT	8924
rs750192343	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28130705	TGAAAACTTGTACCC[A/G]TGATGAATAATTAGT	8924
rs750195117	snp	C/G	1.71787e-05	0.00293071	intron-variant	HERC2	GRCh38.p7	15:28169441	CACAAAAATGTGAAG[C/G]TCACATAATTGCAGA	8924
rs750212473	snp	A/G	1.7634e-05	0.00296929	intron-variant	HERC2	GRCh38.p7	15:28230320	ATTCCTGTGCTACAT[A/G]CTATGATTCTATTCA	8924
rs750220049	snp	A/T			intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28186159	AAATGGTAAACAATA[A/T]ATATATTTCACCATA	8924
rs750229585	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28169411	AGACATCTGATCAAC[A/G]AAAAGAAAAAAAATC	8924
rs750236374	snp	C/G	1.67835e-05	0.0028968	intron-variant	HERC2	GRCh38.p7	15:28117272	CATGGGCCCCTCCCT[C/G]GTCACACACCTGCTT	8924
rs750239046	snp	C/T	0.000121672	0.00779881	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214265	CCTGCGCCGCCTCAG[C/T]GTGGACTCTGAGGAG	8924
rs750243426	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28119179	GGCGAGTGGATCACC[A/T]GCAGTCAGGAGTTTG	8924
rs750244094	snp	A/G	3.32679e-05	0.00407834	intron-variant	HERC2	GRCh38.p7	15:28254333	CAATACAGCTACTAC[A/G]ATTTACCTAAGAAGC	8924
rs750246262	snp	A/G	1.764e-05	0.00296979	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28257259	TGATGACCAAGCAAA[A/G]CTCTAAGAGGAAACG	8924
rs750274409	snp	A/G	8.6915e-05	0.00659166	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28202600	CAAGCACTGGCAAAC[A/G]GCCAGTGCAGCAGCC	8924
rs750278060	snp	G/T	4.37924e-05	0.00467913	intron-variant	HERC2	GRCh38.p7	15:28117322	CCTGCCGTCTGGGGC[G/T]CTCGACTGTGGACAC	8924
rs750278222	snp	A/T	1.64773e-05	0.00287026	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28177475	CCACGAAAACACTTT[A/T]CCATCGACAGTTAAA	8924
rs750293737	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28116123	CCGACGGTCCACCAC[C/T]GTCAGGCCCTCAATG	8924
rs750304744	in-del	-/TTAA	1.65721e-05	0.0028785	intron-variant	HERC2	GRCh38.p7	15:28229428	GTTGCCATAGCTACC[-/TTAA]TTAAGAAAAAAATAT	8924
rs750319506	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28170779	TAGAAACATCTAGAA[C/T]ATATAATGAACTCTC	8924
rs750326681	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28286705	TATTTACACGGCAGA[C/G]AGAATCATTAAGAAT	8924
rs750330920	snp	A/G	3.29745e-05	0.00406031	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28174546	TTCTAAGCCTTGCAC[A/G]AGTGTGGGCTTCCTG	8924
rs750333831	snp	C/G	1.64738e-05	0.00286995	missense	HERC2	GRCh38.p7	15:28114742	TCATGGCTTCAAACT[C/G]CTCTGAGGTGGCTTC	8924
rs750344246	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28169916	ATGCACTTACAACAG[C/T]TTATGTTATATACAT	8924
rs750356828	snp	A/C/G	6.66095e-05	0.00577071	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229816	TATTTGTGAACACCT[A/C/G]TAACAGTACTCAACA	8924
rs750366498	snp	A/G	1.65042e-05	0.0028726	intron-variant	HERC2	GRCh38.p7	15:28177536	ACAGACACACGGATT[A/G]CCAAAGGGCAGGGAA	8924
rs750375919	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28197807	GAACATTTCACAGAA[C/T]AACTGACAGGACAAG	8924
rs750377684	snp	A/G	0.000202143	0.0100514	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214220	CAGTGTGCTGCTGTG[A/G]GTGGCAGTCAGCGAG	8924
rs750390152	in-del	-/C			intron-variant	HERC2	GRCh38.p7	15:28146842	AGGCACAAGAGTTTT[-/C]CTTCAGGCTGGAAGA	8924
rs750398417	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28225802	TAAAAAAGATTATAA[A/G]AGAACACTGTGAACT	8924
rs750404031	snp	C/G/T	6.60157e-05	0.00574492	missense, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28292906	GTTGCTTGCCCCATA[C/G/T]CCAGCTGTCCAGAAT	8924
rs750404697	in-del	-/TTGAT			intron-variant	HERC2	GRCh38.p7	15:28157982	AACTTTATTTCTGCC[-/TTGAT]TTCGTTATGTACCCA	8924
rs750417830	snp	C/G	3.31241e-05	0.00406952	intron-variant	HERC2	GRCh38.p7	15:28201579	ATAAATACATTCAAA[C/G]AAAAAAACAGGAGAA	8924
rs750420075	snp	G/T			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316369	ACCAGGCCAGGCACA[G/T]TGGCTCATACATGTA	8924
rs750422086	snp	A/G	3.03164e-05	0.00389323	intron-variant	HERC2	GRCh38.p7	15:28115378	CCCGCAGAACAGACT[A/G]TGCCTGTTAACAAGA	8924
rs750423457	snp	C/T	1.65745e-05	0.00287871	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28233773	GCACTGCCTACAGTA[C/T]CTTTCTATTTGACAC	8924
rs750439830	snp	C/T	1.72406e-05	0.00293599	missense	HERC2	GRCh38.p7	15:28132696	TCGCTGTGCCCCAGC[C/T]GGCCGTAGCGGCCTT	8924
rs750465143	snp	A/G	1.65658e-05	0.00287795	intron-variant	HERC2	GRCh38.p7	15:28220426	TGTGGGCTGCCTTGG[A/G]CTAAACACCTTCCTG	8924
rs750466901	snp	A/G	0.000949494	0.021768	intron-variant	HERC2	GRCh38.p7	15:28174633	CACCTGTTTACGAGG[A/G]GAAAAAAGCTTATAA	8924
rs750509942	snp	C/T	2.07605e-05	0.00322177	intron-variant	HERC2	GRCh38.p7	15:28196209	AATATAAACATTCTG[C/T]CATACCTGGTTCATT	8924
rs750512802	snp	A/C	3.43253e-05	0.00414264	intron-variant	HERC2	GRCh38.p7	15:28246070	GAAGGAGAACACCTA[A/C]ATTTAAGAAATAATA	8924
rs750515689	snp	G/T	1.65776e-05	0.00287898	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272264	CTGCAAATGATGCTC[G/T]GGAACCTTTGCAGCA	8924
rs750555488	snp	A/G	3.3618e-05	0.00409974	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272217	TCATGACACTCACGT[A/G]CATGTCGCCCTCGGA	8924
rs750563411	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28208968	AGCATAATGTCTTTC[A/G]ATAGCAGGAGATCAA	8924
rs750568983	snp	A/C/G	5.0343e-05	0.00501691	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229315	AAGGCGGGATCAAAT[A/C/G]AACATCCTTTAAACA	8924
rs750571459	snp	A/G	1.67276e-05	0.00289197	intron-variant	HERC2	GRCh38.p7	15:28256032	CAATTTGAGTGAAAC[A/G]CCATTCCCTCCCAAC	8924
rs750580134	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28144893	AGCAGAATGATTTCC[A/G]TCACGTGTGAAGAGC	8924
rs750585201	snp	G/T	1.66471e-05	0.00288501	intron-variant	HERC2	GRCh38.p7	15:28182387	CCTGCTGGGTCCCAG[G/T]GAGCAGGCCGTACCT	8924
rs750586682	snp	A/G	3.32734e-05	0.00407868	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274921	TGATCGCCAGGCCCT[A/G]CGCAGGAAGGCAAAG	8924
rs750592401	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28223037	CTATAGCCCTGAGTT[A/C]AACTACATGCTGAGT	8924
rs750620862	snp	C/T	3.36502e-05	0.0041017	intron-variant, utr-variant-5-prime, upstream-variant-2KB	HERC2	GRCh38.p7	15:28213707	GTAAAGTCAATTTCC[C/T]TTATCATGCAGTAAC	8924
rs750633771	snp	A/C	0.000103226	0.00718347	intron-variant	HERC2	GRCh38.p7	15:28116877	GCAGGGGAGAAGCAG[A/C]CACTCGAAGTCCCCT	8924
rs750654223	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28184113	GGAGAATCACTTGAG[A/C]CCGGGAGGCAGAGGT	8924
rs750656943	snp	C/T	1.65389e-05	0.00287562	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229223	TTTGGCACTGGCATC[C/T]ATCAAAACATTTCGA	8924
rs750658651	snp	A/G	3.29451e-05	0.00405851	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28263053	ACTGACTTCCACAGC[A/G]GACTTTGACCACATC	8924
rs750663305	snp	A/G	4.02091e-05	0.00448363	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28233324	CTCCTTGTAAGAACG[A/G]CCCTGTTCTTGATGA	8924
rs750667490	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28145828	AGCAGCAGAGATAAG[A/C]CGGACATGTGGCTGC	8924
rs750676079	snp	A/G	3.3399e-05	0.00408637	intron-variant	HERC2	GRCh38.p7	15:28274865	CCAGTCTGTTGATGT[A/G]TTAGGGAAGCAGAAC	8924
rs750676127	snp	C/T	0.000752162	0.0193782	intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28321331	ACATGGAAGCAGAAA[C/T]ACACCAAGAAAAAGA	8924
rs750683881	snp	C/T	0.000509195	0.015948	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202455	CCACGATCGGCAGAG[C/T]GGGAACGGGCGACTG	8924
rs750697674	in-del	-/T			intron-variant	HERC2	GRCh38.p7	15:28179235	TTATCTACAACAGAA[-/T]TTTTTTAACAAAAAA	8924
rs750741801	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28265527	AGGGTGGGTGGCCTC[A/G]TGAGGCCCACTGTAC	8924
rs750743204	snp	A/G	0.000100639	0.00709291	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28215636	CTGCCTCTGCAGCGA[A/G]GTGGCAGTGAAGGGT	8924
rs750750402	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28150184	AATCACGAAAAAAAC[A/G]CACGCGGCTGCTAAC	8924
rs750754891	snp	C/T	1.68692e-05	0.00290419	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233233	TAAACTTAGACATTA[C/T]AGAGAGGTCATTACA	8924
rs750765016	snp	A/C	1.66551e-05	0.00288571	intron-variant	HERC2	GRCh38.p7	15:28113568	CCACCTGGGGGTCGG[A/C]ATACCATCGTCTCCA	8924
rs750765677	snp	C/T	1.65641e-05	0.00287781	missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28299488	ATTTCATTCCACAGA[C/T]CACAGAGCCCATCTC	8924
rs750783080	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28266855	TGACCCAACTGCGTG[C/T]ACTTGTCAAAACCCA	8924
rs750783974	in-del	-/A	1.69628e-05	0.00291224	intron-variant	HERC2	GRCh38.p7	15:28191256	GTGCTTTAGAAAAAC[-/A]AAAAAAACCACATTC	8924
rs750793181	snp	G/T	6.81396e-05	0.00583654	intron-variant	HERC2	GRCh38.p7	15:28262885	CTAAAGAAACTGTCC[G/T]GAAGGGTTTTAAAAG	8924
rs750794053	in-del	-/G			intron-variant	HERC2	GRCh38.p7	15:28302899	CTAATTATATATTCT[-/G]GTTATTAATCCTTTG	8924
rs750806213	snp	A/G	1.64977e-05	0.00287203	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28269402	TAGTATTTCCATCCT[A/G]TTAACCCCCAACCTA	8924
rs750825441	snp	C/G	7.13483e-05	0.00597236	intron-variant	HERC2	GRCh38.p7	15:28237151	CAATCTGAGGAAACA[C/G]AATTAATTAAAAACA	8924
rs750832802	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28190329	CGGCCAACAAAAGTA[G/T]CTTAATTTGTCTTAT	8924
rs750833171	snp	C/T	1.64827e-05	0.00287073	missense	HERC2	GRCh38.p7	15:28169619	GCACCACTTATTTTA[C/T]TACTGGCAGCAGAAG	8924
rs750833709	in-del	-/G			intron-variant	HERC2	GRCh38.p7	15:28114171	CAAGCAGTGGAAGCT[-/G]TGGGTGGTGGTAATG	8924
rs750842370	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28135311	TACGGGTAAGCCTTC[A/G]TATTGGAACATAAAA	8924
rs750853068	snp	A/G	3.29506e-05	0.00405884	missense	HERC2	GRCh38.p7	15:28141776	TGCTCTCTTTTAAAA[A/G]TGTCATGGCTCTCAT	8924
rs750876705	snp	A/G/T	4.99774e-05	0.00499866	stop-gained, synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28198737	TTCGCACACTTCTTC[A/G/T]TACGCTCGGCAGCAT	8924
rs750894362	snp	C/T	1.6964e-05	0.00291233	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28269291	TACACGCGGCCATTG[C/T]GTGACAGAATCAGGA	8924
rs750899160	snp	A/C/T	3.32714e-05	0.00407858	missense	HERC2	GRCh38.p7	15:28113653	CTTCCCGAACAGCAG[A/C/T]CACCTGCTCATCAAA	8924
rs750900670	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28252290	CCAGTCTCGGTGCAC[A/G]GGAACATTCTGGGCA	8924
rs750907285	snp	A/G	3.82183e-05	0.00437123	intron-variant	HERC2	GRCh38.p7	15:28132069	TGCGGTGAGCTGGGA[A/G]AGCACTGGGCAGGGA	8924
rs750910316	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28191472	CCATGTATCTATATA[C/T]TCCTGGCCTAGGGTG	8924
rs750916189	snp	A/G	1.7921e-05	0.00299335	intron-variant	HERC2	GRCh38.p7	15:28198817	ATCATGTACACAGGT[A/G]AAATGAGCCATGATA	8924
rs750923477	snp	A/G	0.00930212	0.0675613	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174350	ATCTATAAGGTTGCT[A/G]TAAACCTACAGAAAA	8924
rs750941083	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28161048	AAAAAAGGATACCTA[C/T]AGCTTTTTAGTTCTT	8924
rs750947260	snp	C/T	3.30142e-05	0.00406276	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28248620	AGCAAACGTTGAAAA[C/T]GCAGTAACAAATCCA	8924
rs750962703	in-del	-/CTGT	1.7227e-05	0.00293482	intron-variant	HERC2	GRCh38.p7	15:28274253	CCTCAAGCAGGCCAG[-/CTGT]CTGCGTGCAGAAGGC	8924
rs750973761	snp	C/T	1.65348e-05	0.00287526	intron-variant	HERC2	GRCh38.p7	15:28229656	CAATGCAGAGAAGCA[C/T]TTCTCATCAAATGTT	8924
rs750978551	snp	A/G	1.65531e-05	0.00287686	intron-variant	HERC2	GRCh38.p7	15:28176801	TAAAAACAGAATCAC[A/G]CACAGGCACGGAGAA	8924
rs750981244	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28115958	CTGGCCAATGGCGAA[C/G]ACCTCACCCCACTCT	8924
rs750987973	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28257035	ACACTTACAAAAGGA[A/G]GAAGAAGAAGGGAAA	8924
rs750988013	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28231551	CCTGGTTAACAATTC[C/T]TCACACATGATATGA	8924
rs750994962	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28157495	TATGTGTCCAGGAAT[G/T]TATCCATTTCTTCTA	8924
rs751003786	snp	A/C	4.94254e-05	0.00497094	missense, utr-variant-5-prime, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28280204	TGAGTCGCAGGGCTG[A/C]GAGGGTGGTGGTGGC	8924
rs751005786	in-del	-/A	1.7988e-05	0.00299895	intron-variant	HERC2	GRCh38.p7	15:28132853	AAAGTCACCAAATAT[-/A]ATGGAAACACATTTT	8924
rs751008760	snp	A/C/T	6.73667e-05	0.00580342	intron-variant	HERC2	GRCh38.p7	15:28220660	CTGAGAAAGCCAAAG[A/C/T]AGAGATCAGTTAGGA	8924
rs751009189	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28244319	CGGGGTGAAGCTCAG[-/A]AACCAAAAGGTACGT	8924
rs751024497	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28150712	TACAGAAAAAACACA[C/T]GCGGCTTCTAACTAA	8924
rs751057853	snp	A/C	1.64743e-05	0.00287	synonymous-codon	HERC2	GRCh38.p7	15:28143948	AAATTCAGTTGTAAG[A/C]AGCTTCCTCAGTCTC	8924
rs751089833	snp	A/G			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28320976	GTTTCTATAGGCCAT[A/G]ATTACTGCAACTTAC	8924
rs751108371	snp	A/G	1.65102e-05	0.00287312	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229544	AAGAAATTCTTGCTC[A/G]CCAGTTTTAAAATTG	8924
rs751139031	snp	A/G	1.64942e-05	0.00287173	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28280090	TGTCCACAGGAGGCA[A/G]AGAAATACCGCTGCT	8924
rs751152791	snp	A/G	3.50478e-05	0.00418601	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202217	CCTGTATGTCGGAGT[A/G]GTCCAGCAGCCACCC	8924
rs751154661	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28137804	CATATTTCTCACTTT[A/G]AGTCAAAAGCTAGAA	8924
rs751158205	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28269020	AAATGAGTTTACAAA[C/T]GGGAATCTCACGATT	8924
rs751162974	snp	A/C	1.77128e-05	0.00297591	intron-variant	HERC2	GRCh38.p7	15:28116614	GTACATTTTAACTCA[A/C]GAGCAGGCACAGGCC	8924
rs751173302	snp	A/T	8.24518e-05	0.00642021	intron-variant	HERC2	GRCh38.p7	15:28265769	TTACTAAGTCCTGTA[A/T]GAGGCCACCTCCTGC	8924
rs751176791	snp	C/T	1.65042e-05	0.0028726	intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28179048	GCAAGGAACGACAGC[C/T]AGGAGAGGACTCTCT	8924
rs751185946	in-del	-/TAGTT			intron-variant	HERC2	GRCh38.p7	15:28231391	AGTGGTCTGGCCAGG[-/TAGTT]TATGCTAATGATGGG	8924
rs751198208	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28121107	TTGCTGACCTGTGTT[C/T]GTGCTTTTGGACTAT	8924
rs751200094	snp	C/T	1.64784e-05	0.00287035	intron-variant	HERC2	GRCh38.p7	15:28144059	GAAGACAGATGTAAC[C/T]GTAATGGTGGCATTT	8924
rs751206213	snp	C/T	3.29984e-05	0.00406179	intron-variant	HERC2	GRCh38.p7	15:28233598	AAGGGCAGGGATGAA[C/T]ATGTACCTCAGGTTA	8924
rs751226628	snp	A/G	1.78093e-05	0.00298401	intron-variant	HERC2	GRCh38.p7	15:28218485	TCGATCTCTCATTCC[A/G]TACATGTCTTGTCCG	8924
rs751236136	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28156712	ACAGGGACAATTTGA[A/C]TTCCTCTTGTTCTAA	8924
rs751242558	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28123029	TGCTACTTTTTATTA[C/T]TGAACAGTAATTGAA	8924
rs751244221	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28271017	TATACTATACATCTA[C/T]ATATTTATGCAGCAT	8924
rs751250858	snp	C/T	0.000840238	0.0204796	intron-variant	HERC2	GRCh38.p7	15:28113030	CCACCCACCGTCGGC[C/T]GACATCAGCCCAGGG	8924
rs751250953	snp	C/T	1.64754e-05	0.00287009	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265703	AAGCCCGGCTACCAG[C/T]ATCGGAATGGCCTCG	8924
rs751252828	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28265561	TCTCACTTCCTCCAG[G/T]GAAGCTGCCATGCGT	8924
rs751255580	snp	C/T	1.6517e-05	0.00287372	intron-variant	HERC2	GRCh38.p7	15:28202302	TCAACAGCCCTGAAG[C/T]GGGAACCCACACATA	8924
rs751259973	snp	C/T	9.3471e-05	0.0068357	intron-variant	HERC2	GRCh38.p7	15:28215826	GGGAAAATAGACATG[C/T]TTGGTAACAAGTCCC	8924
rs751261454	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28177765	AAAATAATACTGATT[A/G]TTAATGGGGTTCCTA	8924
rs751275984	snp	C/T	1.65658e-05	0.00287795	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28270825	TGTGGAAGGGTGAGG[C/T]ACCTCAGGAAACTCT	8924
rs751289939	snp	C/T	3.3112e-05	0.00406877	intron-variant	HERC2	GRCh38.p7	15:28141387	ACCTTTAGCCACAAC[C/T]GCCTCAGGCTCAATG	8924
rs751317705	snp	A/T	0.000131859	0.00811862	synonymous-codon	HERC2	GRCh38.p7	15:28125063	CCAGGCGAGGGTATG[A/T]GCTGAGCCACAGGCC	8924
rs751326087	snp	C/T	1.65647e-05	0.00287786	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28238754	TTATTTCTACAGTTC[C/T]GACCTGTAAAAAATG	8924
rs751332500	snp	C/T	1.69714e-05	0.00291298	intron-variant	HERC2	GRCh38.p7	15:28196596	CAGAAATCACCTGAT[C/T]CATCTTCCTCTTCAC	8924
rs751352652	snp	A/G	3.34219e-05	0.00408777	intron-variant	HERC2	GRCh38.p7	15:28176377	AGGCCCAGGTTCCCT[A/G]CACACACCTGCACAA	8924
rs751365523	in-del	-/AC	2.02856e-05	0.00318471	intron-variant	HERC2	GRCh38.p7	15:28254313	AAATAAATAACATAT[-/AC]AATACAATACAGCTA	8924
rs751368945	snp	A/G			intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318593	GCACCACTGCACTCC[A/G]GCCTGGGAGACAGAG	8924
rs751372329	snp	C/T	1.66394e-05	0.00288434	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28211078	CTGGTGGGAGAGCAG[C/T]GCCCGACCTGCTTTC	8924
rs751378028	in-del	-/AAT			intron-variant	HERC2	GRCh38.p7	15:28180346	CTATCATTTTCCAAC[-/AAT]GACAAAATCACCCAA	8924
rs751392843	in-del	-/C	1.65176e-05	0.00287376	intron-variant	HERC2	GRCh38.p7	15:28268648	ACGAAGAAAAGTAGT[-/C]ATCAGTCCAAGGAAA	8924
rs751395786	snp	C/G	1.64917e-05	0.00287151	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28228299	TTGCGCCGTGCTGCA[C/G]GGTGAGCATGCTGAG	8924
rs751402714	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28259429	ATCTCCAGACTCAGA[C/T]GGGATTCAAAAACAT	8924
rs751409527	snp	A/C	3.41309e-05	0.00413089	intron-variant	HERC2	GRCh38.p7	15:28125245	TAGGGCCAACAAACG[A/C]ATGGCTGCCAGTGTC	8924
rs751415645	snp	A/C	1.68684e-05	0.00290412	intron-variant	HERC2	GRCh38.p7	15:28255843	GATCTCAGTGCACCA[A/C]CAGGTCACGTGTGCC	8924
rs751417735	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28182810	ATCTTAAATACCAAC[A/G]TGAACATGGGTGGGA	8924
rs751420346	snp	C/T	1.66913e-05	0.00288883	intron-variant	HERC2	GRCh38.p7	15:28186769	TAGACACAAAAACCA[C/T]GATCTATAGACTCTG	8924
rs751424947	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28128881	TTCCCAGCTTCCAGG[C/G]GCCACCCCATTCCCC	8924
rs751431101	snp	C/T			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316800	TTATTTTTTTTGAGA[C/T]GGATTCTCGCTCTCT	8924
rs751438038	snp	A/G	3.29533e-05	0.00405901	synonymous-codon	HERC2	GRCh38.p7	15:28146289	GACTGTGAGAGGGTC[A/G]TGGCGCCTCTCTGTG	8924
rs751461055	snp	A/G			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317236	GCTGGGATTACAAGC[A/G]CACACTACCACGCCT	8924
rs751462136	snp	C/T	1.69057e-05	0.00290733	intron-variant	HERC2	GRCh38.p7	15:28177131	TTGTCACAGTTCCTA[C/T]AACAAGATGAAATCA	8924
rs751477040	in-del	-/GGGA					GRCh38.p7	15:28288452	CGTTTGAACCCAGGA[-/GGGA]GGCAGAGGCTGCAGT	8924
rs751483810	snp	A/T	1.80179e-05	0.00300143	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28230463	CTCTTCGTTTCCAAT[A/T]TTTTCTTCATCATCC	8924
rs751488195	in-del	-/G			intron-variant	HERC2	GRCh38.p7	15:28173574	GAGGCCAAGATGGGA[-/G]GATCACTTGAGCTCA	8924
rs751493128	snp	C/T	1.64743e-05	0.00287	missense	HERC2	GRCh38.p7	15:28114630	TAGTTTATCGCCAGC[C/T]GCACGTACTCCGCGC	8924
rs751505548	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28184016	AACACGGTGAAACCT[C/T]ATTTCTACAAAAAAA	8924
rs751514480	snp	A/G	1.64765e-05	0.00287019	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28191013	GTCAGAAGGGTTAAT[A/G]TTGATTGTCTTTAGT	8924
rs751516892	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28114920	CCTCAAGTGCATCTC[A/G]AGGCTGCAAGTGCAT	8924
rs751523024	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28282977	AGGAAGGGATGGGAC[A/G]GGACGGGACTGGATG	8924
rs751555124	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28220138	CAGACACAGGCTCAG[C/T]GCCAACCACATGAGA	8924
rs751562038	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28150265	CCGAAGAAACACACG[C/T]GGCTTCTAACCGAGA	8924
rs751564060	snp	G/T	3.99768e-05	0.00447066	intron-variant	HERC2	GRCh38.p7	15:28257283	GGAAACGCAACAATC[G/T]AAAATGAATCTCCAA	8924
rs751568694	snp	C/T	1.64887e-05	0.00287125	missense	HERC2	GRCh38.p7	15:28142269	CGGGGCAACGGTGTT[C/T]TTTTGTCAAGGGCCA	8924
rs751571660	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28286948	AAAAAATGTGAGGGA[C/T]TGATGGATGAATAGA	8924
rs751591289	snp	A/G	1.76639e-05	0.00297181	intron-variant	HERC2	GRCh38.p7	15:28234308	TGCACACGCAAACAT[A/G]AAAGAGAAACTCAAG	8924
rs751646257	snp	C/T	1.6486e-05	0.00287102	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28268495	CCCAGCCGTCCGCCG[C/T]CCCCACAGCCCCAGG	8924
rs751647092	snp	A/G	8.79902e-05	0.0066323	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214276	TCAGCGTGGACTCTG[A/G]GGAGGAAACCAGGGG	8924
rs751648246	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28174899	AGACACACAGAAGGT[C/G]CTCTCTCTAACTAAG	8924
rs751658082	snp	C/G	1.88407e-05	0.0030692	intron-variant	HERC2	GRCh38.p7	15:28132602	GCCCCCATCTGACAG[C/G]AGCAGTGAGGAGCAT	8924
rs751663156	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28270161	TGAGACAGGGTTTCT[C/T]CAAGTTGGCCAGGCT	8924
rs751667114	snp	A/G	1.69246e-05	0.00290896	intron-variant	HERC2	GRCh38.p7	15:28266000	AAGGGAACAAACATG[A/G]ATGCCCTTCTTCTTG	8924
rs751667906	snp	A/T	3.33023e-05	0.00408044	missense, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28292991	GTCATTCAGATCTTC[A/T]TTCTTTGTTCCACTT	8924
rs751672631	snp	A/G	1.64732e-05	0.0028699	missense	HERC2	GRCh38.p7	15:28114708	TGGCCACTGGCACTT[A/G]GCACTGTGAAGGGCA	8924
rs751690186	in-del	-/TAGT			intron-variant	HERC2	GRCh38.p7	15:28158447	CATAGATATTTAGGA[-/TAGT]TAGTTCTTCTTATTG	8924
rs751704063	snp	A/G	6.61168e-05	0.00574926	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28246787	CCTCCGCGAAGTGCC[A/G]CCAGCTGGTAGAAGC	8924
rs751705631	snp	C/T	4.94564e-05	0.0049725	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28174543	GCCTTCTAAGCCTTG[C/T]ACGAGTGTGGGCTTC	8924
rs751715258	snp	A/C/T	9.93471e-05	0.00704736	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272315	GTGCCCTGGGCGGAA[A/C/T]GCTCATTGTCAGTCT	8924
rs751730445	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28275452	TCTGCTCCTGGCCGC[A/G]GGTGAAGCCCTGCGT	8924
rs751735371	snp	A/G	6.80828e-05	0.0058341	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214242	GTCAGCGAGGCCTGC[A/G]GGCGCACCCTGCGCC	8924
rs751735390	snp	A/G	1.67158e-05	0.00289096	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28220549	TTCTTTCCCCATCCT[A/G]TAGGAGTTGGTGCTG	8924
rs751738072	snp	A/G	1.67005e-05	0.00288963	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28192135	TCCAGAACGGCCACA[A/G]AATACCGCAGACTGA	8924
rs751745989	snp	C/T	1.79845e-05	0.00299865	missense	HERC2	GRCh38.p7	15:28132672	TTCGGCTTCAGCTGG[C/T]CCTCACTGTCGCTGT	8924
rs751750502	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28306351	TTTTATCCTTCATTC[C/T]ATTGATATGATGTAT	8924
rs751751000	snp	A/C/G	3.74127e-05	0.00432495	intron-variant	HERC2	GRCh38.p7	15:28196191	ATATTTGGTGGAAGA[A/C/G]AGAATATAAACATTC	8924
rs751755664	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28148038	CAAGACTGTGTCTCC[-/A]AAAAAAAAAAAAAGA	8924
rs751764900	snp	C/T	1.67629e-05	0.00289503	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111741	GGCTCAGGCTCTCAT[C/T]TCACGAGGACGTTTC	8924
rs751770213	in-del	-/AGA	1.65038e-05	0.00287257	cds-indel, nc-transcript-variant	HERC2	GRCh38.p7	15:28198478	ACCAATCTTGATGTG[-/AGA]AGAAGAACTTGGTGG	8924
rs751777432	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28225244	AAGGAAAAGTAAGAC[A/C]CTGTCTCAAAACAAA	8924
rs751800090	snp	A/G	3.41035e-05	0.00412924	synonymous-codon	HERC2	GRCh38.p7	15:28124160	GAAGAGCTCGGAGAG[A/G]TGGTGCAGCAGCAGC	8924
rs751800923	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28162088	AATCCCAAGCACTTT[C/G]GGAGGCCAAGGTGGG	8924
rs751806857	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28198247	GCAGAAGGCACTGAC[A/T]AGCAAAGGAACACTC	8924
rs751814803	in-del	-/TTTT			intron-variant	HERC2	GRCh38.p7	15:28116217	ATTAAAAGTCTTTTC[-/TTTT]TCTTTTTTTTTTTTT	8924
rs751820151	in-del	-/AA			intron-variant	HERC2	GRCh38.p7	15:28291911	CTCCGTCTCAAAGGA[-/AA]AAAAAAAAAAAAAAA	8924
rs751824995	snp	C/T	4.94181e-05	0.00497057	synonymous-codon	HERC2	GRCh38.p7	15:28167741	GGCTCCCAGGTCATC[C/T]GTCACTGGGATAAAA	8924
rs751826240	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28197946	ACAAACAACCACACA[A/G]TCCCCTATCCTGGTG	8924
rs751826949	snp	A/G	4.96964e-05	0.00498455	intron-variant	HERC2	GRCh38.p7	15:28220443	TAAACACCTTCCTGA[A/G]TCACCCACCAGAGTC	8924
rs751831115	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28291443	TGTCCATGCAAGGAA[A/G]AAAAACCCTGAATAT	8924
rs751862121	snp	A/G	7.12314e-05	0.00596746	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28202393	AGTGAGAGACTTCAG[A/G]GCAAACTCGATGTTC	8924
rs751865830	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28165718	AGGCTGAGGATGGCT[A/T]GAGACCAGGAGGTTG	8924
rs751867372	in-del	-/T			intron-variant	HERC2	GRCh38.p7	15:28218018	GAATTGCAAAATTCG[-/T]TATGTTGAAGCCCTA	8924
rs751884727	snp	A/G	0.000247066	0.0111118	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213825	CCTTTGGGGTGATGC[A/G]AGTCACAGTGCCTTC	8924
rs751886435	snp	A/G	6.6759e-05	0.00577711	synonymous-codon	HERC2	GRCh38.p7	15:28116834	GGACTCGCTGTAGCC[A/G]CCCCCACAGTCATCC	8924
rs751888252	snp	C/G	1.69781e-05	0.00291355	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256098	GCCCACCTGCGCAGG[C/G]CAGGAGAGCAGAGAG	8924
rs751888801	snp	G/T	5.04392e-05	0.00502166	intron-variant	HERC2	GRCh38.p7	15:28182377	AGTGCCCCACCCTGC[G/T]GGGTCCCAGGGAGCA	8924
rs751891639	snp	A/C/G	5.04404e-05	0.00502176	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229335	TCCTTTAAACAATCA[A/C/G]TAAGAGGTTCCCTTT	8924
rs751898740	snp	G/T	3.29451e-05	0.00405851	synonymous-codon	HERC2	GRCh38.p7	15:28141537	AACTTTGACTTTTGC[G/T]CCTTCAATGCCCCCG	8924
rs751910683	snp	C/G	1.64808e-05	0.00287057	missense	HERC2	GRCh38.p7	15:28167806	CTGCAGAGGGGGTCA[C/G]TGCGTCCTCAGAGGA	8924
rs751912780	snp	C/T	0.000171712	0.00926426	intron-variant	HERC2	GRCh38.p7	15:28144260	AACACTGTAAACATC[C/T]CCGGGTTTCACAAGC	8924
rs751930096	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28162050	AAATTAGAAGAAGGC[C/T]GGGCATGGTGGCTCA	8924
rs751938058	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28194493	GAGAATGGCATGAAC[C/T]CGGGAAGCGGAGCTT	8924
rs751962475	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28281681	AGCTTTGCAGCTAAG[A/G]GCTAATAGTTATTTA	8924
rs751962691	snp	A/C	3.29451e-05	0.00405851	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28263002	CACCTTTTCCCCATG[A/C]ATAAACTTGGCCATC	8924
rs751972944	snp	A/G	1.6517e-05	0.00287372	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213743	ACAAGTTCACCTACT[A/G]GTTTCAGCTGATTCA	8924
rs751974950	snp	A/G	3.29565e-05	0.00405921	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28176577	TTTTCCAAAGTCACC[A/G]TCACCCCAGGAAAAT	8924
rs751978078	snp	A/T	5.04562e-05	0.00502251	intron-variant	HERC2	GRCh38.p7	15:28265578	AAGCTGCCATGCGTG[A/T]CCTCGTGGGCCTGTC	8924
rs751984549	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28131731	CACTGGCACCCCCAA[A/G]CGCGTGCCGTGGCAA	8924
rs751990564	snp	C/T	1.71012e-05	0.00292409	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233244	ATTATAGAGAGGTCA[C/T]TACAAACAGCAGGTC	8924
rs751993210	in-del	-/T			intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174229	ATTTTCATTCCAGCA[-/T]TGTATAAATCGCATG	8924
rs752002642	snp	C/T	3.29625e-05	0.00405958	intron-variant	HERC2	GRCh38.p7	15:28144663	TGATCGCCATAAGCC[C/T]CTTCCTTACCAGCAG	8924
rs752007320	snp	C/T	8.97344e-05	0.0066977	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28215662	AGGGTGCGTGCCCTT[C/T]CACGACCTTCATGAG	8924
rs752008067	snp	A/G	6.7659e-05	0.00581592	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28215715	CTGAGGGCGCCGCAT[A/G]CCTGCGGCGTGAGAG	8924
rs752015264	snp	C/T	1.65792e-05	0.00287912	missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28299504	CACAGAGCCCATCTC[C/T]TGTGAATGCAAGCTG	8924
rs752021902	snp	C/G	0.000326637	0.0127754	missense, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28321381	ATATCTGTTTTCAAC[C/G]ATTTGGAGTCGAGGC	8924
rs752052766	snp	A/G	0.000101012	0.00710603	intron-variant	HERC2	GRCh38.p7	15:28116976	CAGGCGACCACTGCC[A/G]GGGACACAGGTGCTC	8924
rs752063015	snp	C/T	1.65176e-05	0.00287376	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28270707	CACCTTATGAGATGT[C/T]GGAGAGCTACACAGC	8924
rs752069516	snp	A/G	0.000115341	0.00759324	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28176715	AGCCAGGGTCTGCGC[A/G]TCTCTACTCCCACAT	8924
rs752074181	snp	G/T	1.67041e-05	0.00288994	intron-variant	HERC2	GRCh38.p7	15:28113286	GGCTGCCACACACCT[G/T]CGGGAGGATGTCTGT	8924
rs752083137	snp	A/G	3.29473e-05	0.00405864	intron-variant	HERC2	GRCh38.p7	15:28141651	ATACACATCAAGTGA[A/G]CATTTGCCATGGGCA	8924
rs752086657	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28243177	TTTTCACCCAAAGGT[C/G]CTGGCACAAAGACAC	8924
rs752096838	snp	A/G	1.64751e-05	0.00287007	missense	HERC2	GRCh38.p7	15:28169595	GGGCGATTTGGCTTA[A/G]AATTACTTGCACCAC	8924
rs752115919	snp	A/G	1.70287e-05	0.00291788	intron-variant	HERC2	GRCh38.p7	15:28169462	TAATTGCAGAATTTC[A/G]AAAATTAGCACAGAA	8924
rs752130443	in-del	-/AC	0.000158178	0.00889179	intron-variant	HERC2	GRCh38.p7	15:28117417	AGTGTGTCTGAACAA[-/AC]ACACCTTCCAACACG	8924
rs752130694	snp	C/T	1.77637e-05	0.00298019	intron-variant	HERC2	GRCh38.p7	15:28237158	AGGAAACAGAATTAA[C/T]TAAAAACATAAAACC	8924
rs752138123	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28167267	ATCAGCAATGCGTGA[A/G]TCCTAATGGAGGCAC	8924
rs752138997	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28259217	CTCCTGCCTTAGCCT[C/G]CTGAGTAGCTGGGAT	8924
rs752139646	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28134118	CAGCATGCCCCTTCA[C/T]GACTTTAGGTTTTTT	8924
rs752152576	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28189601	AATAGTTCCATGACA[C/T]TCCAGAATAAATGGT	8924
rs752156251	snp	C/T	3.32624e-05	0.004078	intron-variant	HERC2	GRCh38.p7	15:28132056	CTGGGGGCCCGACTG[C/T]GGTGAGCTGGGAGAG	8924
rs752159891	snp	A/T	4.96413e-05	0.00498179	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28269433	TGACCTCTTGCAATG[A/T]TCCCTGTAAGATAAG	8924
rs752186829	snp	A/G	1.828e-05	0.00302319	intron-variant	HERC2	GRCh38.p7	15:28152876	GGCCAACAGCCCCAC[A/G]CCTGGTCACCTGCAT	8924
rs752202982	snp	A/G			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28316735	GAAAGCCTGAGAACA[A/G]AATTTATCAAGATAC	8924
rs752213318	snp	A/G	1.68604e-05	0.00290343	intron-variant	HERC2	GRCh38.p7	15:28178838	TTGGTTAACAACGGA[A/G]CAGGAGCAAAGGCCG	8924
rs752216743	snp	C/T	1.65184e-05	0.00287384	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28248711	CAACATCTTTCAATC[C/T]GGCTACAGTCTGAGA	8924
rs752221356	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28216091	AGTGATTCTCCTGCC[C/T]TGCCCTGCCAAATAG	8924
rs752231296	snp	A/G	1.6531e-05	0.00287493	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28198725	GCCAACATCACCTTC[A/G]CACACTTCTTCATAC	8924
rs752231619	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28113469	GAGTGCACTCCCTTC[A/G]GTCAACACACAGGGC	8924
rs752233283	snp	C/T	0.000148465	0.00861454	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28191187	TGTCAGCAGGATCTA[C/T]GATCATTTTTAATCT	8924
rs752242359	snp	A/C	5.38575e-05	0.00518901	intron-variant	HERC2	GRCh38.p7	15:28115403	ACAAGACCCTAGAGG[A/C]CCCGCCTGCCGCCCC	8924
rs752278346	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28157212	GTGTAAAATTCTTTT[C/T]GTTGTGTCTCTGCCA	8924
rs752286727	snp	C/T	1.65466e-05	0.00287628	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229777	TGCGGATAAAGACCC[C/T]GCACATTCTGCTTCA	8924
rs752289895	snp	A/G	0.000145111	0.0085167	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28222122	ACAGGGAGCTGCACA[A/G]GAGCCGTTTCCTTCC	8924
rs752306548	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28206741	GGGAGGCTGACACAG[A/G]AGAATGGCATGAACC	8924
rs752339456	snp	C/T	0.000247449	0.0111204	missense	HERC2	GRCh38.p7	15:28116755	CAGACTCATCCCTCC[C/T]GTTGGGTGTCACGAT	8924
rs752342105	snp	C/T	0.000175771	0.00937308	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256305	CAACCTGGTGACTAA[C/T]GGCAGCATGCAACTG	8924
rs752354044	in-del	-/AAA			intron-variant	HERC2	GRCh38.p7	15:28245547	GCAAGATGTAGTGTC[-/AAA]AAAAAAAAAAAATAT	8924
rs752355192	snp	G/T	3.37524e-05	0.00410793	intron-variant	HERC2	GRCh38.p7	15:28257042	CAAAAGGAGGAAGAA[G/T]AAGGGAAATCATGAA	8924
rs752369289	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28219874	TCACGAAACCTCCTC[C/T]CGCAACCTGGATCTC	8924
rs752370060	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28135422	GATTGTAGCAGCATT[A/C]AAACAAACAAAAACA	8924
rs752374337	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28190429	AGAGAGAGATAATTG[C/T]TGATCTGTAGTATGT	8924
rs752374613	snp	A/C/G/T	4.96327e-05	0.00498142	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28233749	AAACATGATCGGTGT[A/C/G/T]GTCAAATGGCACTGC	8924
rs752377599	snp	C/T	1.6729e-05	0.00289209	missense	HERC2	GRCh38.p7	15:28163116	TAGGCGGTCCCCATG[C/T]CGGAAAGCACCGCGG	8924
rs752382561	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28284661	GGCACAGTGGCTCAC[A/G]CCTGTAATCCTAGCA	8924
rs752384640	snp	C/T	1.64912e-05	0.00287147	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229690	TGTTTTAGTAGGCAC[C/T]TTCTCATTTTTTCCA	8924
rs752389514	snp	A/G	4.97162e-05	0.00498554	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214003	CAGCGAGCTCGACAG[A/G]GACACTCACGGAGCT	8924
rs752399540	in-del	-/TTCTT	4.84614e-05	0.00492223	intron-variant	HERC2	GRCh38.p7	15:28272429	TAAAAACAGATTAAC[-/TTCTT]TTCTTCACAGTTGAT	8924
rs752403993	snp	A/G	3.30109e-05	0.00406256	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28178924	GACCACGTAGCTGCT[A/G]AGAGCTGTGATCTGC	8924
rs752412490	in-del	-/AAC	8.40138e-05	0.00648073	intron-variant	HERC2	GRCh38.p7	15:28269466	GTAAACATTTCCTTT[-/AAC]AACAACAACAACAAT	8924
rs752419184	in-del	-/TTA			intron-variant	HERC2	GRCh38.p7	15:28209354	TTTTTATTTATTTAT[-/TTA]TTTTTTTGAGACAGA	8924
rs752420081	snp	A/G	3.29891e-05	0.00406122	intron-variant	HERC2	GRCh38.p7	15:28265790	CACCTCCTGCTGCAT[A/G]CTCCCACTCATGCAG	8924
rs752428564	snp	G/T	0.000131817	0.00811735	synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28280220	GAGGGTGGTGGTGGC[G/T]GACTGGACGGCCAGG	8924
rs752432424	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28140913	AAAATTGTAATACTT[C/T]TGCATACATGACGTA	8924
rs752443679	snp	A/C	1.76362e-05	0.00296948	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28218573	TCTGCATGATCTCAG[A/C]ATGAACTCCAGCAGA	8924
rs752458809	snp	C/T	1.66963e-05	0.00288927	intron-variant	HERC2	GRCh38.p7	15:28245848	CAAGGACAATAAAAC[C/T]TTCCTCAGTAAAACT	8924
rs752472628	snp	A/G	1.68312e-05	0.00290092	intron-variant	HERC2	GRCh38.p7	15:28135437	AAAACAAACAAAAAC[A/G]AAGACAAATAGAATG	8924
rs752472810	snp	C/T	1.64738e-05	0.00286995	missense	HERC2	GRCh38.p7	15:28143923	GCCTATTTATGTTAA[C/T]TGACTGCCCAAATTC	8924
rs752474472	snp	A/C	3.29821e-05	0.00406078	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233667	CGAGCTCCTTACCTA[A/C]ATCTTCATGTTTTAA	8924
rs752490014	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28290218	ACAGTGAATAGAACA[A/C]GTAGGCAGAAAATTA	8924
rs752492708	in-del	-/CTTA			intron-variant	HERC2	GRCh38.p7	15:28123812	GGAGAGATGCAGCAT[-/CTTA]CTGTTTGCTTTTAAT	8924
rs752502938	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28173700	CCCAGCTATTTGGGA[A/G]GCTGAGGTGGAAGGA	8924
rs752504561	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28210219	GCTCACTGTAAGCTC[C/T]GCCTCCCGGATTCAT	8924
rs752505815	snp	A/C	1.65181e-05	0.00287381	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28196463	AAAAATAACTCACGT[A/C]ACCCCAGGATGAATA	8924
rs752511711	snp	C/T	7.16136e-05	0.00598345	intron-variant	HERC2	GRCh38.p7	15:28113023	GAGCCAGCCACCCAC[C/T]GTCGGCCGACATCAG	8924
rs752515169	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28256870	AAAGTGCTGGGATTA[C/T]AGGCGTGAGCCACCG	8924
rs752524955	snp	A/T	9.89332e-05	0.00703255	synonymous-codon	HERC2	GRCh38.p7	15:28111997	ACAGGTGTAGGACTC[A/T]GGGAGGAAGTGGTCT	8924
rs752525942	snp	A/G	5.10356e-05	0.00505126	intron-variant	HERC2	GRCh38.p7	15:28272204	ACACAAAGTTCCATC[A/G]TGACACTCACGTGCA	8924
rs752531490	snp	G/T	1.76927e-05	0.00297423	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28218496	TTCCATACATGTCTT[G/T]TCCGTCGTTCCGCTT	8924
rs752548693	snp	A/G	1.66322e-05	0.00288371	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28255932	TCCATCAGCCATCAA[A/G]CTGCCCACCAGAAGA	8924
rs752556958	snp	A/G	6.5962e-05	0.00574253	synonymous-codon	HERC2	GRCh38.p7	15:28125054	GCTGGTCGACCAGGC[A/G]AGGGTATGTGCTGAG	8924
rs752560709	snp	C/T	4.94254e-05	0.00497094	missense	HERC2	GRCh38.p7	15:28135608	TAAACACATGCTGAA[C/T]GGATTCAAGCAATGT	8924
rs752580070	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28275357	CATGGGAGACCAGGC[C/T]GGAGAAGAGCTGGAA	8924
rs752614239	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28182736	ACCTTTTAATACTAG[C/T]ACTTAATTTCAGCCT	8924
rs752620575	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28143399	GAACTCAGTATACAC[C/T]GCAACATACGAGAAG	8924
rs752621281	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28258092	AATCATATACAGTTT[C/G]TTCTCCAATCACAAT	8924
rs752627548	snp	C/T	1.65187e-05	0.00287386	synonymous-codon	HERC2	GRCh38.p7	15:28144797	GGACCAGTCGGACCA[C/T]TCTCGGCCTGCGGGA	8924
rs752628904	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28181457	CAGATAAAAACTAAT[G/T]GCACCTTGAAAGGAA	8924
rs752634172	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28225494	CGAGGTCAAGAGATC[A/G]AGACCATCCTGGTCA	8924
rs752642564	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28140183	CAGAAGGAAACATGC[C/T]TAATCTGATCAAGGG	8924
rs752644836	snp	C/T	1.7134e-05	0.00292689	intron-variant	HERC2	GRCh38.p7	15:28117178	GAGGAAGCAAGCAAG[C/T]GTGAGGCCGCTGCCG	8924
rs752651185	snp	C/T	1.65787e-05	0.00287907	missense, splice-acceptor-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28238758	TTCTACAGTTCTGAC[C/T]TGTAAAAAATGACTC	8924
rs752692947	snp	A/G	2.26226e-05	0.00336315	intron-variant	HERC2	GRCh38.p7	15:28260998	AGGGATGCAGATGCA[A/G]CTTCAAGCCTATGAC	8924
rs752695519	snp	C/G/T	8.48938e-05	0.00651464	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28212460	CTGCAAAGGCCTGTT[C/G/T]AGTCGATTTCTTTAT	8924
rs752698888	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28175863	ACCTTAATACCTTAA[C/T]ACATATTTTATGATA	8924
rs752702383	snp	A/G	1.66432e-05	0.00288467	intron-variant	HERC2	GRCh38.p7	15:28196575	GCACTGAAAGCTAGG[A/G]CAGAACAGAAATCAC	8924
rs752705671	snp	C/G	0.000343566	0.0131021	intron-variant	HERC2	GRCh38.p7	15:28234297	ATTCTGGAAAATGCA[C/G]ACGCAAACATGAAAG	8924
rs752711521	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28127406	CGCCAGAAAAGAAAG[A/G]ATCTGCAAGGTTGCC	8924
rs752715125	snp	A/T	1.64893e-05	0.0028713	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28228311	GCAGGGTGAGCATGC[A/T]GAGCATCACCAGGAG	8924
rs752719155	snp	C/T	3.32806e-05	0.00407912	intron-variant	HERC2	GRCh38.p7	15:28146211	CAGGTGGGTAGATCA[C/T]GCCCTGCTCAACCTC	8924
rs752722017	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28255191	AAAATCACAAAACTA[A/G]CCGGGCATGGTGACA	8924
rs752732664	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28272157	GCATGCTAGTCTTGC[G/T]TTAAAAGTAACTAGA	8924
rs752741625	snp	A/G	0.000117908	0.00767723	intron-variant	HERC2	GRCh38.p7	15:28255852	GCACCACCAGGTCAC[A/G]TGTGCCTCCAAAGCC	8924
rs752753358	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28265204	GATGATCTCACTTAG[A/G]AACACAAACATAAAA	8924
rs752755898	snp	A/C	1.67421e-05	0.00289323	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233148	TTTACATTCTTACCT[A/C]TCTTTTTCCTTCGTT	8924
rs752777597	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28134001	TACATTTTATGCTCC[A/G]CTTATCAATTTCTAT	8924
rs752780957	snp	C/T	1.65168e-05	0.00287369	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28260884	AGTGCTGGCACTGGT[C/T]GTTGCTCCCCCAGCT	8924
rs752781536	snp	C/T	8.73538e-05	0.00660827	intron-variant	HERC2	GRCh38.p7	15:28293068	CCGCTTTTCAGAATG[C/T]CATACCATTAGTCTC	8924
rs752784774	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28171383	TGAAAAGAGCTATAC[G/T]TTAAGAAGATACTGA	8924
rs752784852	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28188033	GAGGAAATACAGCTT[A/G]ACCACCACCATAGGG	8924
rs752787208	snp	A/G	1.66369e-05	0.00288412	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28211097	CGACCTGCTTTCAGG[A/G]TGTATAGCTTCAACT	8924
rs752790950	snp	C/G	1.85396e-05	0.00304458	intron-variant	HERC2	GRCh38.p7	15:28113696	GGAAGAAAAAGCTCA[C/G]TTTACACTTCTGTCT	8924
rs752794498	in-del	-/GAT	2.81203e-05	0.00374958	intron-variant	HERC2	GRCh38.p7	15:28221982	CAGAACTGTGCAGAA[-/GAT]AACTAATGTGTGGCT	8924
rs752795612	snp	C/G	1.6617e-05	0.00288239	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274318	GACCTGAGGAACCTG[C/G]TCGCTCTCTCCACCA	8924
rs752802764	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28289239	CATACACAAAGGTTG[-/A]AAGTGAAAAAAGCTA	8924
rs752828767	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28249302	CAGCAGGTGCCGAGG[A/G]CTCAGGGAGTCCAGG	8924
rs752839454	snp	C/G	1.93171e-05	0.00310776	intron-variant	HERC2	GRCh38.p7	15:28117208	GCAGCAGGAAGCACA[C/G]AGTCGGGGATATGCG	8924
rs752843683	snp	C/T	3.295e-05	0.00405881	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28236994	GACAGGAGACAGCGG[C/T]GTGCTCATTGCCAAA	8924
rs752850209	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28161711	GTCCCAGATGGCTCC[A/G]GTCCAGAACATTTCC	8924
rs752853913	snp	C/T	5.12728e-05	0.00506298	intron-variant	HERC2	GRCh38.p7	15:28142195	ACTATAGCTAAATAA[C/T]GTTTTTGCATCCCAA	8924
rs752858588	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28278822	TAACACAAAATATAA[A/G]TTTCATCTGGCAGTC	8924
rs752861668	snp	A/G	1.67114e-05	0.00289057	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28220634	CGGCCTAGGCCTGGA[A/G]GAGGCCCATCCTGAG	8924
rs752865499	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28119522	ACGCTGGTATGATCT[C/T]GGCTCACTACAACCT	8924
rs752873433	snp	C/T	3.31022e-05	0.00406817	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214644	CACAGGGAAGGTAGA[C/T]GGCCACCCACCTCTG	8924
rs752874571	snp	A/G	9.47882e-05	0.00688369	intron-variant	HERC2	GRCh38.p7	15:28268660	AGTCATCAGTCCAAG[A/G]AAAATGAAACCAGCT	8924
rs752878332	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28118379	AGCCATAAGGCTGGA[A/G]GCAGACAGGCTCCTG	8924
rs752879268	snp	C/G	1.65611e-05	0.00287755	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28177089	TCCCGGATACGCTTG[C/G]TTTTCAGGGCCTCGA	8924
rs752893998	snp	A/G			missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274923	ATCGCCAGGCCCTGC[A/G]CAGGAAGGCAAAGGC	8924
rs752908306	snp	A/G	1.66341e-05	0.00288388	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272372	AGCAACAACAGGATG[A/G]CAGACAACATTTGGC	8924
rs752932456	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28226761	AAATTGAACTTCATC[A/C]AAATAAAAAACTTCT	8924
rs752941725	snp	A/G	0.000118204	0.00768688	synonymous-codon	HERC2	GRCh38.p7	15:28132181	GGACCAGACAGTGTC[A/G]TCATCTGTGAGGCAG	8924
rs752946625	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28296946	GAAGCCAGTGATGCA[A/G]CTGCTCTCTCGTTAA	8924
rs752947544	snp	C/T	4.95438e-05	0.00497689	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229509	ATCCACAAAACATCG[C/T]ATACTGCACAGATGG	8924
rs752959610	snp	C/T	1.67801e-05	0.00289651	missense	HERC2	GRCh38.p7	15:28163282	TATTTTGGCTTTCAA[C/T]ATCCTAAGTCAAATG	8924
rs752964669	snp	C/T	1.64776e-05	0.00287028	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28268518	GCCCCAGGAGTACAC[C/T]TCTCCAGTAGCAGCC	8924
rs752975271	snp	A/G	1.67184e-05	0.00289118	missense, downstream-variant-500B	HERC2	GRCh38.p7	15:28174466	ACAGAGGGCGTGGCC[A/G]CATCCACAGTTGTCC	8924
rs752994412	snp	A/G/T			intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28179038	CACAGTCACTGCAAG[A/G/T]AACGACAGCCAGGAG	8924
rs752996193	snp	C/T	6.77955e-05	0.00582178	intron-variant	HERC2	GRCh38.p7	15:28280056	AGGATTCTTTCTTCG[C/T]TTTATTGTTACCTTT	8924
rs753034377	snp	C/T	3.32928e-05	0.00407987	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28192127	AGCTGTTTTCCAGAA[C/T]GGCCACAAAATACCG	8924
rs753036813	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28246900	ATTAGCTCTGGACCT[C/T]GAAGAAGGATTGAGA	8924
rs753043618	snp	C/T	1.64895e-05	0.00287132	synonymous-codon	HERC2	GRCh38.p7	15:28144105	CTGTGCACAAGCTGC[C/T]AGCGAGGCCGCAAGG	8924
rs753046791	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28255093	GTAATCCCAACACTT[C/T]GGGAGGACAAGGTGG	8924
rs753048101	snp	C/T	3.34381e-05	0.00408876	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28220562	CTGTAGGAGTTGGTG[C/T]TGCCTGTGTCCCACT	8924
rs753056580	snp	A/G	1.68818e-05	0.00290527	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111726	AGCGCTCTGCTGCCT[A/G]GCTCAGGCTCTCATC	8924
rs753065591	snp	C/G	1.6477e-05	0.00287024	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28174519	ACAAGCCACGCGTGT[C/G]ATCTTCTGGCCTTCT	8924
rs753079329	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28132014	ACAGTAATGGTGGCT[C/G]TGAGGCTGTGTTTTC	8924
rs753101140	snp	C/T	3.31109e-05	0.00406871	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272322	GGGCGGAACGCTCAT[C/T]GTCAGTCTCCTGTGC	8924
rs753103076	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28245176	CCCCAACTGCACCTT[A/C]TGGAGGCACCAGGAC	8924
rs753126645	snp	A/C	3.29897e-05	0.00406125	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28246803	CCAGCTGGTAGAAGC[A/C]ATGCTGGCGGCCACA	8924
rs753128660	snp	A/G	3.56716e-05	0.00422309	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256184	ACGGCCTGGGCGGCC[A/G]ACTGCACGGTGCTCA	8924
rs753129567	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28168910	GTGAGAGCCTGAGGG[C/G]TGGATAATTGACCAG	8924
rs753148118	snp	C/T	3.29462e-05	0.00405857	missense	HERC2	GRCh38.p7	15:28167725	CTGCAATGATGCTTG[C/T]GGCTCCCAGGTCATC	8924
rs753148722	in-del	-/CTC	1.64735e-05	0.00286993	cds-indel	HERC2	GRCh38.p7	15:28135533	CCCAAGAGTAAACTT[-/CTC]CTTCTGAAGACAGGG	8924
rs753151617	snp	A/G	1.64732e-05	0.0028699	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213835	GATGCGAGTCACAGT[A/G]CCTTCTCCAAACTCA	8924
rs753173937	snp	A/C/T	9.99074e-05	0.00706716	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274951	GGCAAAAGACAGCGC[A/C/T]GCTCGGGATCCCACT	8924
rs753184102	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28164553	TTTTTTTTTATGAGG[G/T]TGTCTTAAAACATGC	8924
rs753196587	snp	C/G	1.67438e-05	0.00289338	intron-variant	HERC2	GRCh38.p7	15:28265585	CATGCGTGTCCTCGT[C/G]GGCCTGTCCAGGGTG	8924
rs753201624	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28279942	AAAACATACAAAAAG[C/G]GAAAGCAAGAATAAA	8924
rs753208263	snp	A/G	1.67089e-05	0.00289035	synonymous-codon	HERC2	GRCh38.p7	15:28116693	CATGCTGCTGTGCAC[A/G]GGTGCTCTGGCGGCC	8924
rs753217330	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28256829	TCGATCTCCTGACCT[C/G]GTGATCCACCCGCCC	8924
rs753218900	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28181128	TTTCCCATTGTAGAT[A/G]GATGTAATTTAAAAT	8924
rs753220508	snp	C/T	0.000541149	0.0164402	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256124	GAGAGTGCCCGGGCC[C/T]GCTCCTCCGCGGTGG	8924
rs753230448	in-del	-/GCC	1.65168e-05	0.00287369	cds-indel	HERC2	GRCh38.p7	15:28168516	GATGCGTCGGAAGGG[-/GCC]GCCGAGGAGAACGAG	8924
rs753235973	snp	A/G/T	3.38709e-05	0.00411516	intron-variant	HERC2	GRCh38.p7	15:28144244	TTAGGGCCTGTGAAT[A/G/T]AACACTGTAAACATC	8924
rs753245733	snp	A/G	4.9423e-05	0.00497082	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28176550	ACAGCCTTCACTTCC[A/G]CCCCGGCCCAGTTTT	8924
rs753257806	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28125769	AGCCTCAACCTCCCC[A/C]GCTCAAGTGATCCTC	8924
rs753260444	snp	A/G	1.65877e-05	0.00287986	intron-variant	HERC2	GRCh38.p7	15:28176415	CAGTGTGACAGGGAG[A/G]ACGTTTACGTACCAT	8924
rs753272218	snp	A/G	1.64969e-05	0.00287196	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28270713	ATGAGATGTCGGAGA[A/G]CTACACAGCGGAGGC	8924
rs753275947	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28148828	ATTCTAGTAAAACTA[C/T]TGATAAAACACACGC	8924
rs753278305	snp	G/T	1.65605e-05	0.0028775	missense	HERC2	GRCh38.p7	15:28113254	CACCGACTTGAGAAG[G/T]TGCAGCGGGATGTCA	8924
rs753279273	snp	A/G	1.64727e-05	0.00286986	missense	HERC2	GRCh38.p7	15:28141521	CTTCACAGGGAGTGG[A/G]AACTTTGACTTTTGC	8924
rs753292061	snp	C/G	1.69009e-05	0.00290692	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202379	TTCCCGGAAGCACCA[C/G]TGAGAGACTTCAGGG	8924
rs753298768	snp	A/G	1.65138e-05	0.00287343	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28254444	TGGAGTCCTGCTTCT[A/G]TGAAATGTTGAGGCA	8924
rs753308541	snp	A/G			missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214744	CATTTCATGTCCCTC[A/G]CCCTTTCGGTCTTGT	8924
rs753313425	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28128242	GCTTGCCAGCTGACT[A/G]GCAGGCAATGTGCTG	8924
rs753339651	snp	A/G	1.71275e-05	0.00292634	intron-variant	HERC2	GRCh38.p7	15:28169446	AAATGTGAAGCTCAC[A/G]TAATTGCAGAATTTC	8924
rs753350608	snp	A/G	0.000152386	0.00872753	missense	HERC2	GRCh38.p7	15:28168565	CGATCATGGCGGCCG[A/G]CATCAGGGCCCCGAC	8924
rs753357781	snp	A/C/T	6.19935e-05	0.00556719	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28238209	CTGGGTCTTCCCCTG[A/C/T]AAACTGAGCTGAAAC	8924
rs753358110	snp	C/T	0.000148291	0.0086095	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28191050	AGGTTATTCAGGGAA[C/T]TTCCACCTAGGAAAA	8924
rs753367848	snp	C/T	3.29462e-05	0.00405857	intron-variant	HERC2	GRCh38.p7	15:28141641	GTCGCCTACAATACA[C/T]ATCAAGTGAGCATTT	8924
rs753373386	snp	C/T	0.0112741	0.0742289	missense, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28321385	CTGTTTTCAACCATT[C/T]GGAGTCGAGGCGAGC	8924
rs753397958	in-del	-/CA	1.66793e-05	0.0028878	intron-variant	HERC2	GRCh38.p7	15:28270686	AGAACACGGTTCTTG[-/CA]CACACACCTTATGAG	8924
rs753407697	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28257963	TGCTGGAATTACAAG[C/T]GTGAGCCACCGCACC	8924
rs753409234	snp	C/T	8.09749e-05	0.00636246	intron-variant	HERC2	GRCh38.p7	15:28117285	CTGGTCACACACCTG[C/T]TTGTGTGGACGCCAG	8924
rs753418763	snp	G/T	1.65784e-05	0.00287905	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272996	GTGGCTGGCGTTCCG[G/T]GAACATCCCTGAAAT	8924
rs753432259	snp	C/T	1.87187e-05	0.00305925	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28215674	CTTCCACGACCTTCA[C/T]GAGCAGCGTGATCCA	8924
rs753443106	snp	C/T	0.000183076	0.00956578	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28228234	AATCAGGCGCAGTGC[C/T]GTCTGCGTGAGGGCC	8924
rs753449701	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28165821	AAACAAAAACAAAAA[A/C]TGATGTATGTACCTA	8924
rs753462745	snp	A/G	0.000116249	0.00762306	intron-variant	HERC2	GRCh38.p7	15:28269443	CAATGATCCCTGTAA[A/G]ATAAGAAAGTAAACA	8924
rs753467838	snp	A/G	1.64808e-05	0.00287057	intron-variant	HERC2	GRCh38.p7	15:28130486	TAGTGGGTTTAAACA[A/G]ACAGAATCTTGCGTA	8924
rs753471549	snp	A/G	3.31961e-05	0.00407394	intron-variant	HERC2	GRCh38.p7	15:28198566	AATTTTGTCTCTAAG[A/G]AAAAACAAAAGCACT	8924
rs753487435	snp	C/T	0.000101666	0.00712899	intron-variant	HERC2	GRCh38.p7	15:28254316	ATAAATAACATATAA[C/T]ACAATACAGCTACTA	8924
rs753495027	snp	C/T	3.30852e-05	0.00406712	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28248720	TCAATCTGGCTACAG[C/T]CTGAGAAGCAATGTT	8924
rs753502684	snp	C/T	0.00011971	0.00773568	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28202519	CTGCACGGCGACAGG[C/T]GTGGTGGCCTCACTG	8924
rs753510844	snp	A/G	1.67256e-05	0.0028918	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272924	TGCACAGCCAGCTCC[A/G]GCAGGATGGCCAGGG	8924
rs753522762	snp	A/C			intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28215162	GATTACAGGCATGAG[A/C]CACTGCGCCCGGCCT	8924
rs753528738	snp	C/T	5.29171e-05	0.00514351	intron-variant	HERC2	GRCh38.p7	15:28222256	TGAGCCAACAAGTAG[C/T]TACAGTGTCCCCTTA	8924
rs753539554	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28166960	GTAGGTAGAAGACAG[A/G]CGGATGAGAAGGGAA	8924
rs753540986	snp	A/G	0.000106095	0.0072826	intron-variant	HERC2	GRCh38.p7	15:28152662	GCAGCTCCCCGCTGG[A/G]GCCAGCCCCTGTACC	8924
rs753548895	snp	C/G	1.64784e-05	0.00287035	intron-variant	HERC2	GRCh38.p7	15:28191132	TTAGGTAAACTAACT[C/G]AATTACCTGACACTA	8924
rs753572356	snp	C/T	1.65274e-05	0.00287462	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28257127	GGGCGGGGGCCAGTC[C/T]GCGGAACCATCCATC	8924
rs753575214	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28257412	ATTCATGGATGTCTA[C/G]CTCACACACTATCAG	8924
rs753578206	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28149472	GAACGTCACCGAGAA[C/T]GGCCACACCAACATA	8924
rs753583620	snp	C/T	1.65924e-05	0.00288027	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28257068	ATGAATACCTGAAGT[C/T]GTAGAAGATTCAGCG	8924
rs753583977	in-del	-/T			intron-variant	HERC2	GRCh38.p7	15:28259444	TGGGATTCAAAAACA[-/T]TTAAAGAAGAAATAA	8924
rs753587449	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28179547	ACCATGATAACAGAC[G/T]ACTGCTACTGGGCTA	8924
rs753591240	snp	A/C	3.33328e-05	0.00408231	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214189	GCGTGCGCAGCAGTG[A/C]CACCACCTCCTCCGC	8924
rs753594827	snp	A/G	4.47878e-05	0.00473201	intron-variant	HERC2	GRCh38.p7	15:28117326	CCGTCTGGGGCGCTC[A/G]ACTGTGGACACCCGA	8924
rs753595308	snp	A/G	6.60949e-05	0.00574831	intron-variant	HERC2	GRCh38.p7	15:28292878	AAAGTGCCAAAATTC[A/G]CAAGATTACCTGGTT	8924
rs753596004	snp	A/C	1.65515e-05	0.00287671	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233754	TGATCGGTGTGGTCA[A/C]ATGGCACTGCCTACA	8924
rs753614688	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28219099	TAATTCTCGAAACAA[C/T]ATTAGCATATAACTC	8924
rs753629222	snp	A/G	2.64918e-05	0.0036394	missense	HERC2	GRCh38.p7	15:28142837	ATTACCTTAAAGAAT[A/G]GGCTGTGGAGCAGCT	8924
rs753632478	snp	A/G	1.65228e-05	0.00287422	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28178913	GCCACCTTCTTGACC[A/G]CGTAGCTGCTGAGAG	8924
rs753633070	snp	G/T	1.75579e-05	0.00296288	intron-variant	HERC2	GRCh38.p7	15:28152851	GAGGAAGCAAGGACA[G/T]GAATGAGGGGGCCAA	8924
rs753637558	snp	A/G	1.65201e-05	0.00287398	intron-variant	HERC2	GRCh38.p7	15:28177556	AGGGCAGGGAACAGA[A/G]AGCCCACAGCATAGC	8924
rs753647385	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28144470	CCACACCAGGTGAGG[A/G]GGAGTGTGAGCCTGA	8924
rs753654108	snp	A/G	0.0153963	0.0863777	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28202137	GGCGGCATCATCCAC[A/G]TCCTCCACCACCTCC	8924
rs753657042	snp	A/G	1.65721e-05	0.0028785	intron-variant	HERC2	GRCh38.p7	15:28201589	TCAAACAAAAAAACA[A/G]GAGAACATGATAAAC	8924
rs753662514	in-del	-/AAGACCCT	0.00143313	0.0267304	intron-variant	HERC2	GRCh38.p7	15:28115389	ACTGTGCCTGTTAAC[-/AAGACCCT]AAGACCCTAGAGGCC	8924
rs753670830	in-del	-/AC			intron-variant	HERC2	GRCh38.p7	15:28245661	TACACACTCATATAT[-/AC]ACACACACACATACA	8924
rs753672960	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28153248	ATCCTAGCTACTCAG[A/G]AGGCTGAGGCAGGAG	8924
rs753682221	snp	A/G	1.65078e-05	0.00287291	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214112	AAAGCTGTGGGTGAT[A/G]GAGCGGAGCTGGGAG	8924
rs753682551	snp	C/T	3.34924e-05	0.00409208	missense	HERC2	GRCh38.p7	15:28115456	CGCGATGGTGAGGCT[C/T]ATCCCAGCCAGCTGC	8924
rs753683654	snp	A/T	2.96195e-05	0.00384823	intron-variant	HERC2	GRCh38.p7	15:28115390	ACTGTGCCTGTTAAC[A/T]AGACCCTAGAGGCCC	8924
rs753692138	snp	A/T	1.8946e-05	0.00307777	intron-variant	HERC2	GRCh38.p7	15:28174643	CGAGGAGAAAAAAGC[A/T]TATAATTTTTCAACA	8924
rs753695406	snp	C/G	5.01525e-05	0.00500737	intron-variant	HERC2	GRCh38.p7	15:28265980	CTCCAAAGGCCTTGG[C/G]GAGAAAGGGAACAAA	8924
rs753700021	snp	C/T	1.67635e-05	0.00289507	missense	HERC2	GRCh38.p7	15:28132733	ATGTGTAGAGGTCCC[C/T]GGCTGCTGTGACACA	8924
rs753717862	snp	C/T	3.35272e-05	0.0040942	intron-variant	HERC2	GRCh38.p7	15:28142989	TTCTATCGCAGGAAT[C/T]CAGGTGCCGGGGAGG	8924
rs753743625	snp	C/G/T	3.30946e-05	0.00406773	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28246037	TGAGCAGAAGCACTA[C/G/T]AGAAACTACTAGTTC	8924
rs753746021	in-del	-/AGG	0.00033134	0.012867	intron-variant	HERC2	GRCh38.p7	15:28201588	TTCAAACAAAAAAAC[-/AGG]AGAACATGATAAACC	8924
rs753749290	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28310452	CCTATCAAAAAAAAA[A/T]TTTAATTTAAATTTA	8924
rs753759577	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28273961	AACCAAGCACCACTC[C/T]GCACTCAGAACAGCA	8924
rs753761512	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28195446	AGCCTGGGCGACAGA[C/G]TGAGACTCTGTCTCA	8924
rs753776822	snp	A/C	2.02006e-05	0.00317803	intron-variant	HERC2	GRCh38.p7	15:28124279	CAGGCACCAAAGGCA[A/C]ACGGGGGCCAGTGTG	8924
rs753777133	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28232169	TTTCATAAGCTTATT[C/G]TTCAAAATGCCCATC	8924
rs753781536	snp	C/T	2.2156e-05	0.00332829	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28175518	CAGCCTTACCTGCCC[C/T]GAGTCCGTGACCGCC	8924
rs753781599	snp	C/T	1.65138e-05	0.00287343	splice-acceptor-variant	HERC2	GRCh38.p7	15:28167828	CTCAGAGGAAACAAT[C/T]TAGTCCAAGAGTGCA	8924
rs753783980	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28197581	ACATGGTGAAACCCC[A/T]TCTCTACTAAAAATA	8924
rs753784290	snp	G/T	1.64961e-05	0.00287189	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265891	ATGGCCGCACTGTAA[G/T]TGCTCCCGCAAGCGA	8924
rs753784400	snp	G/T	1.65844e-05	0.00287957	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272256	CATCCTTCCTGCAAA[G/T]GATGCTCTGGAACCT	8924
rs753798588	in-del	-/AA			intron-variant	HERC2	GRCh38.p7	15:28284919	GAAACTCCGTCTCGG[-/AA]AAAAAAAAAAAAAAA	8924
rs753803641	snp	A/C/G/T	0.000158812	0.00890979	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28218502	ACATGTCTTGTCCGT[A/C/G/T]GTTCCGCTTTCCACT	8924
rs753813346	snp	C/G	3.5302e-05	0.00420116	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28218597	CAGCAGACAGACAAA[C/G]AGTCTGCAGTAAGTT	8924
rs753814832	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28179770	CTAATGTATGTGTTT[C/G]GGTCTTAGTTTTTAA	8924
rs753837474	in-del	-/CA					GRCh38.p7	15:28124566	GCTGGCATGAACATT[-/CA]AGGTTCTTTTGAGAC	8924
rs753841578	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28147311	TTTAAATTTCTATCA[C/T]GAAGTAATAGCTTCA	8924
rs753851438	snp	A/C	2.09159e-05	0.00323381	intron-variant	HERC2	GRCh38.p7	15:28196381	ATAGCAACTGAGTTA[A/C]GAAAGGTCATTTATT	8924
rs753853300	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28140803	CTGGGATTACAGGCA[C/T]GAGCCACCGCACCGG	8924
rs753854771	snp	A/G			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28315520	ATCCTATTAACAGCC[A/G]GGCACGGTTCATGCT	8924
rs753866195	snp	C/T	1.66418e-05	0.00288455	missense	HERC2	GRCh38.p7	15:28168409	GATTCGCTTTTACCT[C/T]TCTCTTTTCTTGCCA	8924
rs753870557	snp	C/T	1.6674e-05	0.00288734	intron-variant	HERC2	GRCh38.p7	15:28245873	AAAACTCCTTTAAGA[C/T]GCCGTACCCATTATG	8924
rs753873582	snp	C/T	1.68983e-05	0.00290669	intron-variant	HERC2	GRCh38.p7	15:28272211	GTTCCATCATGACAC[C/T]CACGTGCATGTCGCC	8924
rs753877945	snp	A/G	4.9423e-05	0.00497082	synonymous-codon	HERC2	GRCh38.p7	15:28111966	AGGAATACCTGGGCA[A/G]CTTCAGCAAGAAGAA	8924
rs753880834	snp	C/G	1.64732e-05	0.0028699	missense	HERC2	GRCh38.p7	15:28135578	TTCCTCCAGAGTTCA[C/G]AGCTACTTTCTTAAT	8924
rs753891806	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28279512	GAAAAATGTCTTTAC[A/G]ATAATGACACAGAGC	8924
rs753894972	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28278984	CAAATTAAAACTCAT[A/C]TGCCCAAAAGCATCT	8924
rs753899704	snp	C/T	6.59957e-05	0.005744	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28228376	CCTGACGGGTTCTCA[C/T]TGGTGATGGTTTGCA	8924
rs753901440	snp	C/T	1.67332e-05	0.00289246	intron-variant	HERC2	GRCh38.p7	15:28229174	AACTATAAAATAACA[C/T]TGATACAATTATTGA	8924
rs753922280	snp	A/G	1.70197e-05	0.00291711	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28212465	AAGGCCTGTTTAGTC[A/G]ATTTCTTTATTTTGT	8924
rs753939364	snp	A/G	1.66946e-05	0.00288912	intron-variant	HERC2	GRCh38.p7	15:28182515	CTTTCTAATGAGGCT[A/G]ACCAAACGGAAAAAA	8924
rs753949170	snp	A/C/T	3.9242e-05	0.00442942	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274414	GCGTCCAGGGACTCC[A/C/T]GCAACAGCTCACTGC	8924
rs753951115	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28146405	CACCCAAAGTAGAAA[C/G]AGTGAAACTAAAACC	8924
rs753956807	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28184235	TATATATACACACAT[A/G]TATGTATGCATGTAT	8924
rs753956820	snp	A/G	1.65348e-05	0.00287526	synonymous-codon	HERC2	GRCh38.p7	15:28125033	TTTGCCAGCACTGGC[A/G]GGCTTGCTGGTCGAC	8924
rs753959898	snp	A/G	1.97474e-05	0.00314218	intron-variant	HERC2	GRCh38.p7	15:28270877	ACAAAAGCTAGAAAG[A/G]AAAAGTAAACAAAAA	8924
rs753967028	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28167517	CAGTAAGCAGTGACA[C/G]GGACCGTGTCCTGCG	8924
rs753977812	in-del	-/CAC			intron-variant	HERC2	GRCh38.p7	15:28134822	ACTACAGGTGTGTGT[-/CAC]CACATCTGGCTAATT	8924
rs753994314	snp	G/T	1.65089e-05	0.00287301	missense	HERC2	GRCh38.p7	15:28144788	CAGCTCGCTGGACCA[G/T]TCGGACCACTCTCGG	8924
rs753999424	snp	C/T	8.32009e-05	0.0064493	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28233216	CAAAGAACTTAACAA[C/T]TTAAACTTAGACATT	8924
rs754008337	snp	A/G	1.66893e-05	0.00288867	synonymous-codon	HERC2	GRCh38.p7	15:28117131	GGGGCCGGCCAGCCC[A/G]CCTTTGCTCCTTGAT	8924
rs754008669	snp	C/T	1.65515e-05	0.00287671	intron-variant	HERC2	GRCh38.p7	15:28176800	TTAAAAACAGAATCA[C/T]GCACAGGCACGGAGA	8924
rs754014400	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28249151	ACAAACACAGTGTCA[C/T]TATTTTTTGTCCAAA	8924
rs754019469	snp	C/T	1.6577e-05	0.00287893	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28176968	TTTGGGCTTTAGCTG[C/T]GTCGTATTATCCCCA	8924
rs754026839	in-del	-/AAG			intron-variant	HERC2	GRCh38.p7	15:28298806	TTCCCCCCCAAAAAA[-/AAG]AAGAAGAAGAAATAC	8924
rs754034972	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28130770	CTCTCAGGAGGCAGG[C/T]GGGACCGTGACTGAC	8924
rs754037631	snp	A/G	1.67013e-05	0.0028897	splice-donor-variant	HERC2	GRCh38.p7	15:28299400	TAGTTAAAGGCCCTT[A/G]CCTTTTCTAGGAGGG	8924
rs754040024	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28132494	TGAGCCAACCCTACA[C/T]CACCATGAAGGCTGT	8924
rs754060261	snp	C/T	1.74036e-05	0.00294983	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28269280	AGGCCTGTGTGTACA[C/T]GCGGCCATTGCGTGA	8924
rs754080333	snp	C/T	1.64757e-05	0.00287012	missense	HERC2	GRCh38.p7	15:28141798	GGCTCTCATGCAGAA[C/T]ATCCATGTTTTCGCT	8924
rs754080787	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28268934	CGTCCCAATTTGCCA[C/G]TATCCCCACGAGGCC	8924
rs754085213	snp	C/G/T	1.65321e-05	0.00287502	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28246778	TGTAAGCCACCTCCG[C/G/T]GAAGTGCCGCCAGCT	8924
rs754087130	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28262409	TTATCTACATACCTT[A/G]GCTTCCATCTCTTGC	8924
rs754091977	snp	A/G	1.67164e-05	0.00289101	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28198741	CACACTTCTTCATAC[A/G]CTCGGCAGCATCTAA	8924
rs754092002	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28116486	CCTCCCAAAGTGCTA[A/G]GGTTATAGGCGTGAG	8924
rs754096318	snp	C/T	1.66366e-05	0.0028841	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28211102	TGCTTTCAGGATGTA[C/T]AGCTTCAACTGCTGG	8924
rs754100264	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28245608	ACACACACACACAGA[C/T]ATATATATACACACA	8924
rs754102243	snp	C/T	1.69255e-05	0.00290903	synonymous-codon	HERC2	GRCh38.p7	15:28113669	CACCTGCTCATCAAA[C/T]TCATGGAGTCTGGAA	8924
rs754106077	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28282818	GCACCTATAATCCCA[A/G]CTACTCGAGAGGCTG	8924
rs754113164	snp	C/T	2.01213e-05	0.00317179	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174367	AAACCTACAGAAAAA[C/T]CTCAGAGAAGATACA	8924
rs754119434	in-del	-/GC	1.71428e-05	0.00292765	frameshift-variant	HERC2	GRCh38.p7	15:28168573	GCGGCCGGCATCAGG[-/GC]CCCGACAACAGCATC	8924
rs754151104	snp	C/T	5.39607e-05	0.00519398	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28222056	TTCCAGTCCACACCT[C/T]TCATGACCCTTGTTC	8924
rs754164290	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28192675	ACCGCAGGAAGACCC[A/G]AGGCGAATGGAGGTG	8924
rs754171780	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28272141	ACACTGCCGTTGACA[A/T]GCATGCTAGTCTTGC	8924
rs754172509	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28253553	AGGGTCTGCTCTTTA[C/T]TCTAACATCTATACT	8924
rs754182095	snp	C/T	1.65244e-05	0.00287436	intron-variant	HERC2	GRCh38.p7	15:28201411	TACTCAAATATTTGC[C/T]GAATGAAAAACGGAT	8924
rs754182620	snp	A/G	1.65195e-05	0.00287393	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214663	CACCCACCTCTGAGT[A/G]ATGGCACGTCAGAGG	8924
rs754199410	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28291639	ACACAAAAAAAAGTA[A/G]GCAAAGAATAAATGT	8924
rs754213327	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28122528	AGCCCCATGCCTCTC[A/G]CACAGCCCAGACTCA	8924
rs754214242	snp	C/T	9.90949e-05	0.0070383	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28177072	AGCTCCCACAGGCGA[C/T]ATCCCGGATACGCTT	8924
rs754235502	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28218941	GTAAGCAGTCCTCCC[A/C]CCTCGACCTCCCAAA	8924
rs754242264	snp	C/T			missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265904	AAGTGCTCCCGCAAG[C/T]GATGTGCACCACGTG	8924
rs754243341	snp	A/G	8.35722e-05	0.00646368	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28220637	CCTAGGCCTGGAGGA[A/G]GCCCATCCTGAGAAA	8924
rs754243569	snp	C/T	1.65389e-05	0.00287562	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28248596	TCTCCTGGATAAAGT[C/T]TACTAATAAGCAAAC	8924
rs754252965	snp	A/T	9.84397e-05	0.007015	intron-variant	HERC2	GRCh38.p7	15:28272430	AAAAACAGATTAACT[A/T]CTTTTCTTCACAGTT	8924
rs754260692	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28162591	AGATGCACAAATCAG[C/T]TATAAAACAGGTAAA	8924
rs754265402	snp	A/C	1.68838e-05	0.00290544	intron-variant	HERC2	GRCh38.p7	15:28176924	ATGGTAAGCTTTCTG[A/C]AAGCAACAAAAATGC	8924
rs754267049	snp	C/T	1.83869e-05	0.00303202	intron-variant	HERC2	GRCh38.p7	15:28236929	GTTCAAAAAAAATAA[C/T]CTGCTGATCAGCAAA	8924
rs754270667	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28188083	AATATGAAGAATGCT[A/C]CAGGAAACAATTACT	8924
rs754278624	snp	C/T	3.36208e-05	0.00409991	synonymous-codon, downstream-variant-500B	HERC2	GRCh38.p7	15:28174459	CTCGTGGACAGAGGG[C/T]GTGGCCACATCCACA	8924
rs754279344	snp	A/C	1.70046e-05	0.00291582	missense	HERC2	GRCh38.p7	15:28132169	CCCGTCCCCCCAGGA[A/C]CAGACAGTGTCGTCA	8924
rs754286436	in-del	-/A	1.64988e-05	0.00287213	intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28179039	ACAGTCACTGCAAGG[-/A]ACGACAGCCAGGAGA	8924
rs754295408	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28277830	CATGTACAGTCGTCC[C/T]TTGGTATCTGTAGGG	8924
rs754302864	snp	C/T	8.3515e-05	0.00646146	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272383	GATGGCAGACAACAT[C/T]TGGCTAAAGGAGAAA	8924
rs754323411	in-del	-/TA			intron-variant	HERC2	GRCh38.p7	15:28163470	CACCAAGCCATGTAC[-/TA]TGTTTTCAAGACCAA	8924
rs754326661	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28298669	GGCGTGGTGGCGGGC[A/G]CCTGTAGTCCCACCT	8924
rs754327449	snp	C/G	2.05063e-05	0.00320199	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256279	CAGACCTAAACCAAG[C/G]AATTCCGGGTCAACC	8924
rs754341273	snp	A/C	4.9423e-05	0.00497082	missense	HERC2	GRCh38.p7	15:28143963	CAGCTTCCTCAGTCT[A/C]TGAAGGGCCCACATT	8924
rs754346660	snp	C/T	1.79101e-05	0.00299244	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256194	CGGCCGACTGCACGG[C/T]GCTCAGCACGCCCGC	8924
rs754366100	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28292785	AATTTTTTATTTACT[A/T]TTTTTAAAATTGTTA	8924
rs754366545	snp	A/G	1.65386e-05	0.00287559	missense	HERC2	GRCh38.p7	15:28163255	AGGCCTGAGGCTCCG[A/G]ACCTGCTGCTTTATT	8924
rs754373712	snp	A/G	1.65097e-05	0.00287308	intron-variant	HERC2	GRCh38.p7	15:28121432	GGAAAGCCGCCTCCT[A/G]AAACACATCAAACAG	8924
rs754382835	snp	A/G	1.65485e-05	0.00287645	intron-variant	HERC2	GRCh38.p7	15:28179071	GACTCTCTTTTCACA[A/G]CATTAAAAACTTTTT	8924
rs754384007	in-del	-/T			intron-variant	HERC2	GRCh38.p7	15:28229021	GTGTCTCCTGCTAAA[-/T]TTTTGAAGTTTTGTT	8924
rs754408388	snp	A/G	3.3211e-05	0.00407485	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28213992	TGCAGACCAAACAGC[A/G]AGCTCGACAGAGACA	8924
rs754418284	snp	C/T	3.32696e-05	0.00407844	missense, synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28280072	TTTATTGTTACCTTT[C/T]TTTGTCCACAGGAGG	8924
rs754418815	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28164876	CAAAAATTAGAAGTT[A/G]ATTCCAGGCACCTAA	8924
rs754431787	snp	C/G	5.27171e-05	0.00513379	intron-variant	HERC2	GRCh38.p7	15:28116624	ACTCAAGAGCAGGCA[C/G]AGGCCACAGCGACAC	8924
rs754435569	snp	C/T	3.29527e-05	0.00405898	synonymous-codon	HERC2	GRCh38.p7	15:28130281	TGATCCATGGCCCAA[C/T]CTGTGATAATCGCCT	8924
rs754442104	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28181269	GAAGTGAAAACTCCA[A/T]GTAAGGCAGTGAGCA	8924
rs754447288	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28163448	AAACGACGGCCCCTA[A/C]AATCTCCACCAAGCC	8924
rs754463224	snp	C/T	1.77231e-05	0.00297678	synonymous-codon	HERC2	GRCh38.p7	15:28124037	TTGCCACTTGAATAC[C/T]TTTCCCTGGGATATC	8924
rs754464130	snp	G/T	1.65075e-05	0.00287289	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28248621	GCAAACGTTGAAAAC[G/T]CAGTAACAAATCCAA	8924
rs754464441	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28241693	GGCATGGTGGCGCAC[A/G]CCTGTAGTCCCAGCT	8924
rs754480011	snp	C/T	1.65721e-05	0.0028785	synonymous-codon	HERC2	GRCh38.p7	15:28113260	CTTGAGAAGGTGCAG[C/T]GGGATGTCAGGGCTG	8924
rs754498111	snp	C/G	0.104141	0.20304	intron-variant	HERC2	GRCh38.p7	15:28272845	ATGCAACAGGTATTT[C/G]CATACACAGGCGCTT	8924
rs754501166	snp	A/G	1.70863e-05	0.00292281	intron-variant	HERC2	GRCh38.p7	15:28169455	GCTCACATAATTGCA[A/G]AATTTCAAAAATTAG	8924
rs754510079	snp	A/C/T	3.6113e-05	0.00424917	intron-variant	HERC2	GRCh38.p7	15:28248510	CCTAAAGTAACGAGC[A/C/T]CCGATCACATACAAG	8924
rs754519373	snp	C/T	1.6519e-05	0.00287388	intron-variant	HERC2	GRCh38.p7	15:28229668	GCATTTCTCATCAAA[C/T]GTTACCTGTTTTAGT	8924
rs754520088	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28281842	CAGCACTTCAAGGGC[C/T]AAGCCCTTCCTGAAG	8924
rs754522648	snp	C/T	1.64817e-05	0.00287064	synonymous-codon	HERC2	GRCh38.p7	15:28146325	CTGCCGGTCAAATTC[C/T]ACCCTGAGTCCTTCT	8924
rs754527443	snp	A/T	1.64784e-05	0.00287035	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28191051	GGTTATTCAGGGAAT[A/T]TCCACCTAGGAAAAA	8924
rs754544288	in-del	-/C			intron-variant	HERC2	GRCh38.p7	15:28167299	GAAAAGAATTCTGCA[-/C]CGTTCCTGTGGTGTC	8924
rs754546559	snp	C/T	1.64789e-05	0.0028704	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28191146	TGAATTACCTGACAC[C/T]ACAACCAGGGACGGC	8924
rs754548333	snp	A/G	2.18081e-05	0.00330206	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256287	AACCAAGGAATTCCG[A/G]GTCAACCTGGTGACT	8924
rs754558049	snp	C/T	8.23181e-05	0.006415	intron-variant	HERC2	GRCh38.p7	15:28117287	GGTCACACACCTGCT[C/T]GTGTGGACGCCAGGC	8924
rs754561083	snp	A/C/G	6.63035e-05	0.00575743	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214001	AACAGCGAGCTCGAC[A/C/G]GAGACACTCACGGAG	8924
rs754568354	snp	C/G	1.64754e-05	0.00287009	missense, utr-variant-5-prime, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28280207	GTCGCAGGGCTGAGA[C/G]GGTGGTGGTGGCTGA	8924
rs754579723	snp	A/G			intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28215202	TTCTGTTCTCATAAC[A/G]CAAGTAATCAAGTGA	8924
rs754583562	snp	C/G			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317275	TGTATTTTTAGTAGA[C/G]ACAGGGTTTCACCAT	8924
rs754588239	snp	A/G	1.77442e-05	0.00297855	intron-variant	HERC2	GRCh38.p7	15:28272397	TTTGGCTAAAGGAGA[A/G]AAGATATTTATTCTA	8924
rs754591672	snp	C/T	1.64939e-05	0.0028717	intron-variant	HERC2	GRCh38.p7	15:28265778	CCTGTAAGAGGCCAC[C/T]TCCTGCTGCATGCTC	8924
rs754593795	in-del	-/ATCT	0.000168755	0.00918417	intron-variant	HERC2	GRCh38.p7	15:28233425	ATAAAAAGAATTAAA[-/ATCT]ATCACCTTAATGAGC	8924
rs754607966	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28265560	ATCTCACTTCCTCCA[A/G]GGAAGCTGCCATGCG	8924
rs754614700	snp	C/T	0.000105535	0.00726337	intron-variant	HERC2	GRCh38.p7	15:28152664	AGCTCCCCGCTGGGG[C/T]CAGCCCCTGTACCTG	8924
rs754619145	snp	C/T	9.88908e-05	0.00703105	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28177493	ATCGACAGTTAAAGC[C/T]GTCGCGTGCCGGCCA	8924
rs754626275	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28121177	CTGACATTCCTGGAA[G/T]CCCCAGCACATCACA	8924
rs754634401	snp	A/G	1.65293e-05	0.00287479	intron-variant	HERC2	GRCh38.p7	15:28177558	GGCAGGGAACAGAAA[A/G]CCCACAGCATAGCTA	8924
rs754636290	snp	A/G	3.60062e-05	0.00424285	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256204	CACGGTGCTCAGCAC[A/G]CCCGCACTGCTGGCC	8924
rs754644626	in-del	-/T	5.30771e-05	0.00515129	frameshift-variant, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28254501	TTCCTTCTGTGCTTC[-/T]TTTTTGGCTTCAATA	8924
rs754647962	snp	A/G	0.000181259	0.00951824	missense	HERC2	GRCh38.p7	15:28114774	TTGTCTCGGATGTAC[A/G]TGAGTCCAGGAATAA	8924
rs754648800	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28134414	GTTTTCTGCAAAAAA[G/T]ACAGTTTTAATTCTC	8924
rs754651088	snp	A/G	1.77659e-05	0.00298038	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28218489	TCTCTCATTCCATAC[A/G]TGTCTTGTCCGTCGT	8924
rs754656900	snp	C/T	1.66696e-05	0.00288696	intron-variant	HERC2	GRCh38.p7	15:28201600	AACAGGAGAACATGA[C/T]AAACCTACTCAAAAA	8924
rs754665884	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28188789	TCTATTTTTGTTTAC[A/G]TGTTAGAAAAAACCC	8924
rs754667098	snp	A/C	5.85892e-05	0.00541213	intron-variant	HERC2	GRCh38.p7	15:28115394	TGCCTGTTAACAAGA[A/C]CCTAGAGGCCCCGCC	8924
rs754695845	in-del	-/C			utr-variant-3-prime	HERC2	GRCh38.p7	15:28111263	TCCTCTGGATGCATT[-/C]AAGTAATACTAATCA	8924
rs754699937	snp	A/G	6.70252e-05	0.00578862	synonymous-codon	HERC2	GRCh38.p7	15:28132734	TGTGTAGAGGTCCCC[A/G]GCTGCTGTGACACAG	8924
rs754700476	snp	A/G	2.32027e-05	0.00340599	synonymous-codon	HERC2	GRCh38.p7	15:28142850	ATGGGCTGTGGAGCA[A/G]CTGTTTGCCACCCCT	8924
rs754721045	snp	C/T	0.00011548	0.00759781	intron-variant	HERC2	GRCh38.p7	15:28233600	GGGCAGGGATGAATA[C/T]GTACCTCAGGTTAGT	8924
rs754721705	snp	G/T	0.000132481	0.00813775	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213936	GGCCCCCCACTTCAG[G/T]GTTCTCGGAGTCGGG	8924
rs754746887	snp	G/T	4.7142e-05	0.00485477	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28196258	CCTGGTATTGTGTTT[G/T]TTGGTCTTGAAACAC	8924
rs754755015	snp	C/T	1.64738e-05	0.00286995	synonymous-codon	HERC2	GRCh38.p7	15:28111862	GGCGGCTGGCTCTCC[C/T]GTAAGTGCGATGCGA	8924
rs754756651	snp	C/T			missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28198464	ACCCGCACTTTATCA[C/T]CAATCTTGATGTGAG	8924
rs754762182	snp	A/G	1.64754e-05	0.00287009	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265704	AGCCCGGCTACCAGC[A/G]TCGGAATGGCCTCGT	8924
rs754768036	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28226684	ATCTTCATCAACCTT[A/G]TATTTGGAAATGGCT	8924
rs754784735	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28172716	CAAAGGTTTTGTAGA[C/T]ACAACATCAAAAGTA	8924
rs754790662	snp	C/T	1.67708e-05	0.00289571	intron-variant	HERC2	GRCh38.p7	15:28142997	CAGGAATCCAGGTGC[C/T]GGGGAGGCTGACCAT	8924
rs754810810	snp	C/T	3.3206e-05	0.00407455	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233511	ACGTTCTGTGCTTTA[C/T]TTGCTCAATACCAAG	8924
rs754811033	snp	A/G	3.31384e-05	0.00407039	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28238756	ATTTCTACAGTTCTG[A/G]CCTGTAAAAAATGAC	8924
rs754813272	snp	C/T	1.92372e-05	0.00310133	intron-variant	HERC2	GRCh38.p7	15:28215841	CTTGGTAACAAGTCC[C/T]TAAAGACAAATCCCT	8924
rs754819490	snp	C/T	1.66935e-05	0.00288903	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202141	GCATCATCCACGTCC[C/T]CCACCACCTCCTCGT	8924
rs754830328	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28273983	AGAACAGCAGCTCCT[A/C]ATCATCACAGAGAGA	8924
rs754842184	snp	C/T	4.94442e-05	0.00497188	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28270776	CATGACAACAACCGC[C/T]GTTTGTCGCAGATCA	8924
rs754852095	snp	G/T			intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318674	TATGTAATAACCACA[G/T]ATATATGCCTGGCAT	8924
rs754854681	snp	A/G	8.71042e-05	0.00659883	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28175519	AGCCTTACCTGCCCC[A/G]AGTCCGTGACCGCCA	8924
rs754857364	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28179792	AGTTTTTAACAAACA[C/T]GTTAAAAAGTAAAAG	8924
rs754860507	snp	A/G	1.82587e-05	0.00302142	intron-variant	HERC2	GRCh38.p7	15:28132878	CATTTTTATTCTTAA[A/G]CATTTTTCAGTGTAT	8924
rs754869365	snp	A/G	1.64909e-05	0.00287144	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28228304	CCGTGCTGCAGGGTG[A/G]GCATGCTGAGCATCA	8924
rs754872030	in-del	-/AG			intron-variant	HERC2	GRCh38.p7	15:28284026	ATATAACTTATACAC[-/AG]AGCCTGAAGGTAATT	8924
rs754896051	snp	A/G	9.94448e-05	0.00705071	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28254463	AATGTTGAGGCATTC[A/G]CTTCCTGTTCATCAA	8924
rs754901092	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28126258	GATAAAAACTAACAA[C/G]AAGCTATCTGTGAAA	8924
rs754907335	snp	G/T	1.93313e-05	0.00310891	intron-variant	HERC2	GRCh38.p7	15:28196388	CTGAGTTAAGAAAGG[G/T]CATTTATTAAACTTA	8924
rs754915831	snp	A/G	1.64751e-05	0.00287007	synonymous-codon	HERC2	GRCh38.p7	15:28111972	ACCTGGGCAGCTTCA[A/G]CAAGAAGAAACAGGT	8924
rs754939899	snp	C/T	1.66217e-05	0.0028828	missense	HERC2	GRCh38.p7	15:28168411	TTCGCTTTTACCTCT[C/T]TCTTTTCTTGCCATG	8924
rs754942125	snp	G/T	1.76334e-05	0.00296924	intron-variant	HERC2	GRCh38.p7	15:28210983	CTTATAAAGATTTAA[G/T]AACTTTTTAAAAAGA	8924
rs754946403	snp	A/C	1.68972e-05	0.0029066	intron-variant	HERC2	GRCh38.p7	15:28273047	CAAAGCAACCTCCAG[A/C]AAGACAGCATGCTTA	8924
rs754956160	snp	A/T	1.81467e-05	0.00301214	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28230473	CCAATTTTTTCTTCA[A/T]CATCCGTAGATTCTG	8924
rs754956277	snp	C/T	1.65485e-05	0.00287645	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28228254	GCGTGAGGGCCAGCA[C/T]GCCGGAATTGAGCAG	8924
rs754978086	snp	A/G	1.6477e-05	0.00287024	missense	HERC2	GRCh38.p7	15:28144690	GCAGCTGGCATGATG[A/G]GATAGACGGTGAAGC	8924
rs754983021	snp	A/G	4.01349e-05	0.00447949	intron-variant	HERC2	GRCh38.p7	15:28257284	GAAACGCAACAATCT[A/G]AAATGAATCTCCAAA	8924
rs754991203	snp	C/T	1.65116e-05	0.00287324	missense	HERC2	GRCh38.p7	15:28144790	GCTCGCTGGACCAGT[C/T]GGACCACTCTCGGCC	8924
rs755007046	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28210252	CATTCTCCTGCGTCA[C/G]CCTCCCAAGTAGCTA	8924
rs755009824	snp	A/G	2.27301e-05	0.00337113	intron-variant	HERC2	GRCh38.p7	15:28234329	GAAACTCAAGTGCAC[A/G]ACTCAAAATAAATAC	8924
rs755011091	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28184242	ACACACATATATGTA[C/T]GCATGTATGTATGGG	8924
rs755013878	in-del	-/A	1.65982e-05	0.00288077	intron-variant	HERC2	GRCh38.p7	15:28198566	AATTTTGTCTCTAAG[-/A]AAAAACAAAAGCACT	8924
rs755016271	snp	C/T	8.43355e-05	0.00649312	intron-variant	HERC2	GRCh38.p7	15:28182522	ATGAGGCTAACCAAA[C/T]GGAAAAAAAAAAGAA	8924
rs755032831	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28125902	CCGCAACCTCCGCCT[C/T]CCGGGTTCGAGCGAT	8924
rs755033754	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28277633	TCAGTTTGATTCGAC[-/A]AACACACAACAGTGC	8924
rs755046770	snp	C/T	1.73809e-05	0.0029479	intron-variant	HERC2	GRCh38.p7	15:28293059	AATCTGTCACCGCTT[C/T]TCAGAATGCCATACC	8924
rs755062921	snp	C/G			missense	HERC2	GRCh38.p7	15:28169607	TTAGAATTACTTGCA[C/G]CACTTATTTTATTAC	8924
rs755069151	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28223429	CAAGAGAGCAACAAA[A/G]GATATTCAATTCCCA	8924
rs755081260	snp	C/T	4.94287e-05	0.00497111	missense	HERC2	GRCh38.p7	15:28141801	TCTCATGCAGAACAT[C/T]CATGTTTTCGCTGTC	8924
rs755097465	snp	A/T	1.65124e-05	0.00287331	missense	HERC2	GRCh38.p7	15:28169643	GCAGAAGAATCAGCA[A/T]CTGAAGGCACGCCTA	8924
rs755099031	snp	A/T	1.66399e-05	0.00288438	synonymous-codon, downstream-variant-500B, nc-transcript-variant	HERC2	GRCh38.p7	15:28186636	AGCTAAGAAAGGAAC[A/T]GCAGCCAAATCTTCC	8924
rs755104493	snp	G/T	1.76393e-05	0.00296974	intron-variant	HERC2	GRCh38.p7	15:28206197	AAAAGTGTTCAAAAT[G/T]TAGTGCTGTGGATTA	8924
rs755110590	snp	C/T	1.71413e-05	0.00292752	synonymous-codon, downstream-variant-500B, nc-transcript-variant	HERC2	GRCh38.p7	15:28186600	GTTGCCTTTCTCATC[C/T]TCCTCCTCTTCATTA	8924
rs755124828	snp	C/G	1.78385e-05	0.00298646	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214291	AGGAGGAAACCAGGG[C/G]AGAAGCTGCTGCACC	8924
rs755141788	snp	C/G	1.65293e-05	0.00287479	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28257165	TCACCTGCCGAAGCA[C/G]GAGATCCAGCTGCTC	8924
rs755142777	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28306587	TATTGGCCTTCTACA[A/G]TAAGTTTGGATGTAT	8924
rs755147772	in-del	-/C			intron-variant	HERC2	GRCh38.p7	15:28136125	CACAAGGGAAAAAAC[-/C]ACCTTTTTTTTTTTT	8924
rs755164619	snp	C/T	0.000100365	0.00708324	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28198742	ACACTTCTTCATACG[C/T]TCGGCAGCATCTAAC	8924
rs755179682	snp	C/G			missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28246806	GCTGGTAGAAGCAAT[C/G]CTGGCGGCCACAGGC	8924
rs755202357	snp	C/T	1.65699e-05	0.00287831	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28176971	GGGCTTTAGCTGTGT[C/T]GTATTATCCCCATGT	8924
rs755212706	snp	A/G	1.67147e-05	0.00289086	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28220552	TTTCCCCATCCTGTA[A/G]GAGTTGGTGCTGCCT	8924
rs755216811	snp	C/T	1.71026e-05	0.00292421	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214245	AGCGAGGCCTGCGGG[C/T]GCACCCTGCGCCGCC	8924
rs755219742	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28287044	TGGTGAATATGTGCG[C/T]GCGCGCTGTAAAATT	8924
rs755252791	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28232724	AAAATGTAACTCTTT[C/T]AGCTTGCCTTTATAA	8924
rs755253597	snp	A/G	3.18203e-05	0.00398862	intron-variant	HERC2	GRCh38.p7	15:28132086	GCACTGGGCAGGGAA[A/G]GAATGGGAAATACCT	8924
rs755254685	snp	C/G	1.73123e-05	0.00294208	intron-variant	HERC2	GRCh38.p7	15:28191926	CAAAACCATCGGTGT[C/G]AAAGTGCCCGCTGCT	8924
rs755256271	snp	A/G	8.26317e-05	0.00642721	intron-variant	HERC2	GRCh38.p7	15:28201414	TCAAATATTTGCTGA[A/G]TGAAAAACGGATCGA	8924
rs755276761	in-del	-/T	4.95839e-05	0.0049789	intron-variant	HERC2	GRCh38.p7	15:28292875	TCCAAAGTGCCAAAA[-/T]TCACAAGATTACCTG	8924
rs755279489	snp	C/G	7.2358e-05	0.00601446	intron-variant	HERC2	GRCh38.p7	15:28246098	ATAAGATTTAAATAA[C/G]TATTTATCCTATAAA	8924
rs755279999	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28148210	ACATAAATCAGACTT[-/A]ACAAAAACCAAAACA	8924
rs755297524	snp	C/T	3.31225e-05	0.00406941	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272284	CCTTTGCAGCAAGGG[C/T]AAAAGTGGGGCGCTG	8924
rs755321980	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28291663	TAAATGTATGGGTTT[C/T]ACTGGGCTGGATAAA	8924
rs755343918	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28253654	TTAATATGAAAACCA[A/G]TAATCACCTACTAAA	8924
rs755343990	in-del	-/T			intron-variant	HERC2	GRCh38.p7	15:28219599	TGTCAAAGATGGTGG[-/T]TATCAGGATCTGAGC	8924
rs755344253	snp	C/T	3.30164e-05	0.00406289	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28192029	GGGATGCCTGGTTCA[C/T]GGAGGACGACACATT	8924
rs755345293	snp	A/C/T	3.2948e-05	0.00405871	missense	HERC2	GRCh38.p7	15:28121366	TGCGGTTCAGCTCCA[A/C/T]GACGGGGCCATGCTG	8924
rs755353698	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28241692	GGGCATGGTGGCGCA[C/T]GCCTGTAGTCCCAGC	8924
rs755373872	snp	A/C	1.69769e-05	0.00291345	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256099	CCCACCTGCGCAGGG[A/C]AGGAGAGCAGAGAGT	8924
rs755391868	snp	A/C	2.2811e-05	0.00337713	intron-variant	HERC2	GRCh38.p7	15:28233366	TAACCAGGAAAAGAC[A/C]ACTTTAACAACAAAT	8924
rs755418556	snp	A/G	1.70589e-05	0.00292047	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202229	AGTGGTCCAGCAGCC[A/G]CCCGACCAAGGCTTC	8924
rs755420366	in-del	-/T	1.65963e-05	0.0028806	intron-variant	HERC2	GRCh38.p7	15:28121454	ATCAAACAGACAAAA[-/T]TTAGAATCTGATATG	8924
rs755424499	snp	A/C	1.75397e-05	0.00296134	intron-variant	HERC2	GRCh38.p7	15:28116630	GAGCAGGCACAGGCC[A/C]CAGCGACACAGTCTC	8924
rs755431466	snp	C/T	6.61332e-05	0.00574998	intron-variant	HERC2	GRCh38.p7	15:28121440	GCCTCCTAAAACACA[C/T]CAAACAGACAAAATT	8924
rs755439392	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28238472	TGATAAGACAGACAT[C/T]GAAGCCACAGATACA	8924
rs755440820	snp	C/T	0.000212868	0.0103145	synonymous-codon, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28321383	ATCTGTTTTCAACCA[C/T]TTGGAGTCGAGGCGA	8924
rs755442234	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28277921	CTGATATAAAATGGT[G/T]TAGTATTTGCATATA	8924
rs755450717	snp	A/G	1.65143e-05	0.00287348	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213744	CAAGTTCACCTACTG[A/G]TTTCAGCTGATTCAA	8924
rs755459449	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28279023	TGCTTCTTTTTGAGA[A/C]AGAATTTCATTCTTG	8924
rs755462370	snp	A/C	1.65392e-05	0.00287564	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229249	TTCGAATGTTCTGTA[A/C]AGCCCAAGCGTACAG	8924
rs755479598	snp	C/T	1.65518e-05	0.00287674	intron-variant	HERC2	GRCh38.p7	15:28175672	CTGAGAGAAGGCCCA[C/T]GGTGGAGAGTTACAA	8924
rs755483096	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28145171	ATGGGGACATTTCCC[A/G]GGAAAGCTCTGATAC	8924
rs755498357	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28147545	CAGGAGGCTAAGGAA[A/G]GGGGATCGCTTGAGC	8924
rs755505384	snp	C/T	3.29652e-05	0.00405974	synonymous-codon	HERC2	GRCh38.p7	15:28135639	TGGGGTGGACACCGA[C/T]TCTGTCCCTCCAATG	8924
rs755508770	snp	A/G	2.06077e-05	0.0032099	intron-variant	HERC2	GRCh38.p7	15:28113053	GCCCAGGGCCGGCAA[A/G]CCCAGCCAGGAGCCT	8924
rs755514197	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28163471	ACCAAGCCATGTACT[A/G]TGTTTTCAAGACCAA	8924
rs755541909	snp	C/T	4.19155e-05	0.00457777	missense, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28212565	GCAGGTTGTTCACAT[C/T]AAAGGCCACGGCAGG	8924
rs755551090	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28211762	GCACCTCCAACCAGA[C/G]ATGTGAATGGGAGAT	8924
rs755551195	snp	C/G	1.71593e-05	0.00292905	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233247	ATAGAGAGGTCATTA[C/G]AAACAGCAGGTCTCA	8924
rs755556500	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28178019	GCCTCAGGATTAAAG[C/G]CATGACCACTCCTAT	8924
rs755562879	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28259611	ATCTCTAATGAGCAT[A/C]AACAGAAAAATCCTC	8924
rs755567710	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28129544	ACACCTACCACCTAG[A/G]GAACAGGGGATCCCT	8924
rs755582126	snp	A/G	1.67967e-05	0.00289794	synonymous-codon	HERC2	GRCh38.p7	15:28116687	GCGGAACATGCTGCT[A/G]TGCACGGGTGCTCTG	8924
rs755595655	snp	C/T	1.65792e-05	0.00287912	synonymous-codon, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28299505	ACAGAGCCCATCTCT[C/T]GTGAATGCAAGCTGG	8924
rs755609440	snp	A/C	1.77197e-05	0.00297649	intron-variant	HERC2	GRCh38.p7	15:28237162	AACAGAATTAATTAA[A/C]AACATAAAACCAAAA	8924
rs755618380	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28255395	AGGAGAATGAACAAA[C/T]AGTACTACACCTATA	8924
rs755618848	snp	A/G	1.68077e-05	0.00289889	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28269298	GGCCATTGCGTGACA[A/G]AATCAGGAAACGCTT	8924
rs755644997	snp	C/G	1.66601e-05	0.00288614	intron-variant	HERC2	GRCh38.p7	15:28176400	CTGCACAAGCACACA[C/G]AGTGTGACAGGGAGG	8924
rs755645938	snp	C/T	1.65269e-05	0.00287457	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28262922	TTTGCACTCACCTTG[C/T]AAGCCTTCTAAGAGT	8924
rs755671297	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28163826	AAGTCTTCTCATTAC[C/T]ACTCGTGTACTTCCC	8924
rs755672294	snp	A/G	4.95823e-05	0.00497882	missense	HERC2	GRCh38.p7	15:28168525	GAAGGGGCCGCCGAG[A/G]AGAACGAGGGGCACT	8924
rs755680296	snp	A/G	2.89666e-05	0.00380558	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28222123	CAGGGAGCTGCACAG[A/G]AGCCGTTTCCTTCCT	8924
rs755690261	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28164731	AGAAATACAGGGTTG[C/T]AACCTGGATAATGCC	8924
rs755708617	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28287449	TGAGTCAATAAGCTG[G/T]GCTTTAATCTGAGCA	8924
rs755710776	snp	A/T	1.79926e-05	0.00299933	intron-variant	HERC2	GRCh38.p7	15:28272847	GCAACAGGTATTTCC[A/T]TACACAGGCGCTTCC	8924
rs755713415	in-del	-/CTC	0.000100984	0.00710505	intron-variant	HERC2	GRCh38.p7	15:28256064	CCTGACCCATGCCCT[-/CTC]CTCCTGTTCCTTCCC	8924
rs755733480	snp	C/T	1.64732e-05	0.0028699	missense	HERC2	GRCh38.p7	15:28130252	ACCTGCCGAGGCCTT[C/T]GAACATGGTCATCTG	8924
rs755747565	snp	A/T	1.6795e-05	0.0028978	intron-variant	HERC2	GRCh38.p7	15:28257048	GAGGAAGAAGAAGGG[A/T]AATCATGAATACCTG	8924
rs755772052	snp	C/T	1.64773e-05	0.00287026	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28191041	AGTTCAATAAGGTTA[C/T]TCAGGGAATTTCCAC	8924
rs755785625	snp	A/G	1.64966e-05	0.00287194	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28248636	GCAGTAACAAATCCA[A/G]TGAAGCAGATCTTTC	8924
rs755787426	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28173064	TACCACCATACGTCT[A/G]TCAGTATAACTAAAA	8924
rs755800378	snp	C/T	2.19469e-05	0.00331255	intron-variant	HERC2	GRCh38.p7	15:28117220	ACACAGTCGGGGATA[C/T]GCGGCACTGGCGAAT	8924
rs755801453	in-del	-/AAT	1.69876e-05	0.00291436	intron-variant	HERC2	GRCh38.p7	15:28269479	TTTAACAACAACAAC[-/AAT]AAAAAAAGGCTGGGA	8924
rs755816058	snp	A/G	3.433e-05	0.00414293	intron-variant	HERC2	GRCh38.p7	15:28177157	AATCAGCTCTCTACA[A/G]TCAATCTGTCCCTTC	8924
rs755818976	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28246648	CCAGAAAATTTAGAG[A/G]GTAAATGCAGGCATG	8924
rs755825307	snp	C/T	7.17283e-05	0.00598824	intron-variant	HERC2	GRCh38.p7	15:28117281	CTCCCTGGTCACACA[C/T]CTGCTTGTGTGGACG	8924
rs755832492	snp	A/G	0.00011537	0.00759418	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214083	AAACCCACCCCTTCG[A/G]AAGGCCTTCCCACAA	8924
rs755841447	snp	C/T	1.64936e-05	0.00287168	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265883	CGGCAGTGATGGCCG[C/T]ACTGTAAGTGCTCCC	8924
rs755842227	snp	C/T	1.648e-05	0.0028705	synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28280223	GGTGGTGGTGGCTGA[C/T]TGGACGGCCAGGGCC	8924
rs755843743	snp	C/T	1.6528e-05	0.00287467	missense	HERC2	GRCh38.p7	15:28142301	AGCAACACGGGAGGC[C/T]ATGCAGTACCTCCGG	8924
rs755846575	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28241572	CCCTCCCGTAATCCC[A/G]TCACTTTGGGAGGCC	8924
rs755864937	snp	A/G	0.000164772	0.00907517	missense	HERC2	GRCh38.p7	15:28146315	CTGTGGAGCACTGCC[A/G]GTCAAATTCTACCCT	8924
rs755879466	snp	C/T	1.64909e-05	0.00287144	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229691	GTTTTAGTAGGCACT[C/T]TCTCATTTTTTCCAC	8924
rs755892407	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28285469	AAGAGGAAGTCTCAA[A/G]GGAAATTTTAAAATA	8924
rs755900411	snp	A/G	6.59087e-05	0.00574021	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28177478	CGAAAACACTTTTCC[A/G]TCGACAGTTAAAGCC	8924
rs755908840	snp	A/G	2.58421e-05	0.0035945	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256307	ACCTGGTGACTAATG[A/G]CAGCATGCAACTGAA	8924
rs755918926	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28116158	GCACGGAAGTCAACA[C/G]CACCTCGTTCGCTTC	8924
rs755928838	snp	C/G	3.29658e-05	0.00405978	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28280101	GGCAGAGAAATACCG[C/G]TGCTTTTCCACTTAA	8924
rs755933898	snp	C/T	1.88304e-05	0.00306837	intron-variant	HERC2	GRCh38.p7	15:28132617	CAGCAGTGAGGAGCA[C/T]GCAGCCTCCGGCCTC	8924
rs755934673	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28255622	ATCTTTCCGGGTAAC[A/G]GGAATGGTCTACATG	8924
rs755952757	snp	G/T	4.33482e-05	0.00465534	intron-variant	HERC2	GRCh38.p7	15:28152660	CTGCAGCTCCCCGCT[G/T]GGGCCAGCCCCTGTA	8924
rs755954587	snp	A/G			missense	HERC2	GRCh38.p7	15:28116689	GGAACATGCTGCTGT[A/G]CACGGGTGCTCTGGC	8924
rs755969205	snp	C/T	1.65192e-05	0.00287391	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229572	TTGTATCTATCCCTT[C/T]CAGGCGAACCTCTGC	8924
rs755969472	snp	A/G	1.64969e-05	0.00287196	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28233683	ATCTTCATGTTTTAA[A/G]AGGCAACATAACAAC	8924
rs755976143	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28286713	CGGCAGAGAGAATCA[C/T]TAAGAATGATTTAGA	8924
rs755980982	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28138099	AGAGGTGAGAAGGCT[A/G]CTGAAGGAAAGTCTG	8924
rs755996017	snp	A/C/T	3.29491e-05	0.00405877	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28201522	AGCTCGTTTTTTGTA[A/C/T]GTCTGGCTCTCCGTC	8924
rs756002942	snp	C/T	3.29924e-05	0.00406142	intron-variant	HERC2	GRCh38.p7	15:28265794	TCCTGCTGCATGCTC[C/T]CACTCATGCAGAGCA	8924
rs756007427	snp	C/G	3.013e-05	0.00388125	intron-variant	HERC2	GRCh38.p7	15:28142821	AAAAAAGAAGTGAAA[C/G]ATTACCTTAAAGAAT	8924
rs756008854	snp	C/T	5.30059e-05	0.00514783	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28218499	CATACATGTCTTGTC[C/T]GTCGTTCCGCTTTCC	8924
rs756018565	snp	C/T	1.64754e-05	0.00287009	missense	HERC2	GRCh38.p7	15:28114765	GTGGCTTCATTGTCT[C/T]GGATGTACATGAGTC	8924
rs756023503	snp	C/T	1.66913e-05	0.00288883	intron-variant	HERC2	GRCh38.p7	15:28245852	GACAATAAAACTTTC[C/T]TCAGTAAAACTCCTT	8924
rs756035498	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28193511	AAATGAAAGAAGAGT[C/T]CCCCCAAAAAGATAG	8924
rs756036400	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28254113	CCATGAAGAAACCCC[A/G]TCTCTACTAAAACTA	8924
rs756038133	snp	C/T	1.65905e-05	0.0028801	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28238761	TACAGTTCTGACCTG[C/T]AAAAAATGACTCTGT	8924
rs756041509	snp	C/T			intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28301435	AAAAAAAAAAGCAGC[C/T]GTTCAAAGACTGATA	8924
rs756054844	snp	A/G	4.94882e-05	0.0049741	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28228367	AGGCTCGGTCCTGAC[A/G]GGTTCTCATTGGTGA	8924
rs756069132	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28123514	CCTGGTGACTTTCAG[A/G]TGCCCTCACTCATGA	8924
rs756076267	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28174640	TTACGAGGAGAAAAA[A/C]GCTTATAATTTTTCA	8924
rs756088992	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28153064	GATCTATGTTAAAAA[C/G]TCGTTGGGGCCAGGC	8924
rs756089113	snp	A/T	1.65446e-05	0.00287612	intron-variant	HERC2	GRCh38.p7	15:28201582	AATACATTCAAACAA[A/T]AAAACAGGAGAACAT	8924
rs756096461	snp	C/T	3.58809e-05	0.00423546	intron-variant	HERC2	GRCh38.p7	15:28218442	CCAGACACAAGCGTG[C/T]GGCCCCCAGCGCTGA	8924
rs756097731	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28271821	CCCAGGGCCCCGCAC[A/G]CCTGCTCCTCCCTCA	8924
rs756107939	snp	A/C/T	4.94192e-05	0.00497067	missense	HERC2	GRCh38.p7	15:28167764	GGATAAAAGGCCGAG[A/C/T]GGAGGCTGAGGGGGC	8924
rs756113580	snp	C/T	1.65397e-05	0.00287569	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111756	CTCACGAGGACGTTT[C/T]CCCATCTTAGTGTCC	8924
rs756124565	snp	A/T	1.64928e-05	0.00287161	missense	HERC2	GRCh38.p7	15:28167818	TCACTGCGTCCTCAG[A/T]GGAAACAATCTAGTC	8924
rs756128722	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28162886	ACAGAGCGAGACTCC[A/G]TCTCAAAAAAACAAA	8924
rs756128964	snp	G/T	1.68318e-05	0.00290096	intron-variant	HERC2	GRCh38.p7	15:28255856	CACCAGGTCACGTGT[G/T]CCTCCAAAGCCATAC	8924
rs756135479	snp	C/T	3.52448e-05	0.00419775	synonymous-codon	HERC2	GRCh38.p7	15:28124190	CAGACGGTTCCTCAG[C/T]GCAATGATGGGGATC	8924
rs756136659	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28139466	CCAAAGTTCCATGAG[A/G]GACTGAATCCTTGCT	8924
rs756145180	snp	C/T	4.99214e-05	0.00499582	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28233153	ATTCTTACCTCTCTT[C/T]TTCCTTCGTTCTCGA	8924
rs756157356	snp	C/T	1.6569e-05	0.00287824	intron-variant	HERC2	GRCh38.p7	15:28182395	GTCCCAGGGAGCAGG[C/T]CGTACCTTGGAGCCT	8924
rs756179048	snp	G/T	1.69507e-05	0.0029112	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28196237	ATTTATTCTGCCAAA[G/T]GTATGCCTGGTATTG	8924
rs756180991	in-del	-/AAAG	1.72368e-05	0.00293566	intron-variant	HERC2	GRCh38.p7	15:28179252	TTTTTAACAAAAAAA[-/AAAG]AAAAGAAAATTTTAC	8924
rs756182697	snp	A/C	6.59533e-05	0.00574215	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28228315	GGTGAGCATGCTGAG[A/C]ATCACCAGGAGGAAG	8924
rs756212651	snp	A/G	1.64789e-05	0.0028704	synonymous-codon	HERC2	GRCh38.p7	15:28144674	AGCCCCTTCCTTACC[A/G]GCAGCTGGCATGATG	8924
rs756219214	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28145145	GTCCAGCACACACCA[G/T]GCCAGGGGCCATGGG	8924
rs756219648	snp	A/G	1.90594e-05	0.00308696	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274407	TCGCAGGGCGTCCAG[A/G]GACTCCTGCAACAGC	8924
rs756221917	snp	A/G	1.64846e-05	0.0028709	stop-gained, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28270784	CAACCGCCGTTTGTC[A/G]CAGATCAATGGCAAG	8924
rs756223210	snp	C/G/T	5.18035e-05	0.00508916	intron-variant	HERC2	GRCh38.p7	15:28116882	GGAGAAGCAGCCACT[C/G/T]GAAGTCCCCTCACAC	8924
rs756225296	snp	A/G	1.96775e-05	0.00313662	intron-variant	HERC2	GRCh38.p7	15:28124273	GCCCCTCAGGCACCA[A/G]AGGCACACGGGGGCC	8924
rs756229862	in-del	-/AA			intron-variant	HERC2	GRCh38.p7	15:28293494	CGAGACTCTGTCTCA[-/AA]AAAAAAAAAAAAAAA	8924
rs756235802	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28307145	CGGCCTGCAAACTTA[C/T]CTATTTCTTCCACGT	8924
rs756236254	snp	C/T	1.73706e-05	0.00294703	intron-variant	HERC2	GRCh38.p7	15:28144276	CCGGGTTTCACAAGC[C/T]AGGTACCACCCCATA	8924
rs756238236	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28277711	ATGACCATCACAGCC[A/G]GTTAGGAAGGAAGAA	8924
rs756256023	snp	A/G	6.60633e-05	0.00574694	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28260885	GTGCTGGCACTGGTC[A/G]TTGCTCCCCCAGCTG	8924
rs756268533	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28132020	ATGGTGGCTCTGAGG[C/G]TGTGTTTTCCCAGAG	8924
rs756270966	snp	A/G	1.67478e-05	0.00289372	intron-variant	HERC2	GRCh38.p7	15:28196357	ACATCCATCACACCT[A/G]TTTGTAAAATAGCAA	8924
rs756276184	snp	A/G	3.38696e-05	0.00411505	intron-variant	HERC2	GRCh38.p7	15:28113304	GGAGGATGTCTGTCA[A/G]GGCCGCGTGATGCTT	8924
rs756284560	snp	C/T			intron-variant	HERC2, LOC107987422	GRCh38.p7	15:28317259	CCACGCCTGACTCTT[C/T]TGTATTTTTAGTAGA	8924
rs756286997	snp	C/T	1.66371e-05	0.00288414	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28211098	GACCTGCTTTCAGGA[C/T]GTATAGCTTCAACTG	8924
rs756302086	snp	C/T	0.000113467	0.0075313	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28230495	TAGATTCTGGCTTCT[C/T]AGGAACTGTGTTTTA	8924
rs756306981	snp	A/G	0.00145238	0.0269087	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28202456	CACGATCGGCAGAGC[A/G]GGAACGGGCGACTGC	8924
rs756309671	snp	C/T	1.662e-05	0.00288266	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274320	CCTGAGGAACCTGGT[C/T]GCTCTCTCCACCACC	8924
rs756315296	snp	A/G	1.67649e-05	0.0028952	intron-variant	HERC2	GRCh38.p7	15:28116988	GCCGGGGACACAGGT[A/G]CTCCAGCACGTGGCA	8924
rs756328637	snp	A/C	1.65457e-05	0.00287621	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214647	AGGGAAGGTAGACGG[A/C]CACCCACCTCTGAGT	8924
rs756331410	snp	A/G	3.29115e-05	0.00405644	intron-variant	HERC2	GRCh38.p7	15:28268662	TCATCAGTCCAAGGA[A/G]AATGAAACCAGCTCA	8924
rs756332351	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28227741	TCAAAAGGCAAAACC[A/C]ACCCAAATGTCCATC	8924
rs756343890	snp	A/T	2.26324e-05	0.00336388	intron-variant	HERC2	GRCh38.p7	15:28257300	AAATGAATCTCCAAA[A/T]GCAGCTGCTGGTCTG	8924
rs756356830	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28297028	CACGAAAGATAAAAA[C/T]GAACAGATGTGACTT	8924
rs756365407	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28244709	TAAGCTCACTCCTTA[A/G]CAAAAGGGGAAGAAT	8924
rs756399507	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28167531	AGGGACCGTGTCCTG[C/T]GGCATTCCCACAAAC	8924
rs756400328	snp	C/T	3.30349e-05	0.00406403	intron-variant	HERC2	GRCh38.p7	15:28176778	TTTCACCTACTCAAT[C/T]ACAAATTTAAAAACA	8924
rs756401108	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28273125	TATTTTTAATATTTA[C/G]GATCAAGTTTCTGAT	8924
rs756419663	snp	A/G	1.64798e-05	0.00287047	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28268545	AGCCAAGGCTAGGTA[A/G]TGGTGACCATCAGAA	8924
rs756421305	snp	C/G	0.000407415	0.0142668	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28234219	CCTCGTCTTTCTCCT[C/G]GTTGTAGCTGTAGTG	8924
rs756428690	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28115073	GCAAGGGTTCCCTCC[C/T]TGCAGCCGAGGCACA	8924
rs756436168	snp	A/G	0.000257903	0.0113527	intron-variant	HERC2	GRCh38.p7	15:28236921	CACTTACAGTTCAAA[A/G]AAAATAATCTGCTGA	8924
rs756439553	snp	C/G	3.34342e-05	0.00408852	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28220572	TGGTGCTGCCTGTGT[C/G]CCACTGGACTCTTAT	8924
rs756456241	snp	C/T	4.94482e-05	0.00497209	missense	HERC2	GRCh38.p7	15:28169620	CACCACTTATTTTAT[C/T]ACTGGCAGCAGAAGA	8924
rs756467466	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28266971	ATGTGGATGGAATGA[A/G]GCCAGCACTCTGCAA	8924
rs756467786	in-del	-/C			intron-variant	HERC2	GRCh38.p7	15:28160877	GCCATCTTGGCACCG[-/C]CCCCCGCTCAGCATT	8924
rs756470889	in-del	-/A	6.5912e-05	0.00574035	intron-variant	HERC2	GRCh38.p7	15:28141719	TTACTGCTTGTTTCT[-/A]AATATAATAACCTGT	8924
rs756474319	snp	G/T	6.6235e-05	0.0057544	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272323	GGCGGAACGCTCATT[G/T]TCAGTCTCCTGTGCC	8924
rs756481425	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28190417	TAAAAATTTGAGAGA[A/G]AGAGATAATTGCTGA	8924
rs756498889	snp	C/T	1.79056e-05	0.00299207	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256191	GGGCGGCCGACTGCA[C/T]GGTGCTCAGCACGCC	8924
rs756516769	snp	A/G	1.65236e-05	0.00287429	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28191205	TCATTTTTAATCTAT[A/G]AACAAGAACATCTGG	8924
rs756522434	snp	C/T	1.65165e-05	0.00287367	intron-variant	HERC2	GRCh38.p7	15:28246910	GACCTTGAAGAAGGA[C/T]TGAGAAATTTTCATT	8924
rs756524583	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28175109	AGTCATAGCGTATGC[C/T]TCTCCAAGCAGAAGA	8924
rs756538317	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28228571	GCAGAAAGCACGGGC[A/G]ATTACTCTAAACATC	8924
rs756540286	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28252396	TGCCAAAGACACCAA[C/T]AGCCCATGAAGCAGC	8924
rs756546399	snp	C/G/T	5.38028e-05	0.00518642	intron-variant	HERC2	GRCh38.p7	15:28163059	CCAACATGGAGGAGG[C/G/T]GGAATCAGACGGCCC	8924
rs756560761	in-del	-/CG	1.65231e-05	0.00287424	frameshift-variant	HERC2	GRCh38.p7	15:28168521	GTCGGAAGGGGCCGC[-/CG]AGGAGAACGAGGGGC	8924
rs756565657	snp	A/G	0.000159096	0.00891756	intron-variant	HERC2	GRCh38.p7	15:28117382	TGTCGCCAGTGATGT[A/G]CCCAGCAGCCCCCAG	8924
rs756582368	in-del	-/G	8.68787e-05	0.00659028	intron-variant	HERC2	GRCh38.p7	15:28220689	GAGGGTGCGTAACCT[-/G]CCCTGGTCCTTCCAT	8924
rs756588350	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28290600	TTCAGACAAGCCTCA[A/G]CATTGAAATCACAGA	8924
rs756596368	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28120491	CAAGTTCTGCACGCT[A/G]TCATCATCAGGGGCC	8924
rs756596954	snp	C/T	1.65012e-05	0.00287234	intron-variant	HERC2	GRCh38.p7	15:28143840	ATTCCCCAAGGGTCA[C/T]AAATCTAGAAATTGT	8924
rs756607168	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28291511	AAAGCTGAAACTGGG[A/G]TGGGCAGTCAGGTGA	8924
rs756610086	snp	A/C	7.37599e-05	0.00607244	intron-variant	HERC2	GRCh38.p7	15:28132074	TGAGCTGGGAGAGCA[A/C]TGGGCAGGGAAAGAA	8924
rs756612640	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28161159	CTTAAGTACTTTATC[A/G]TTTTGGTGATCATGT	8924
rs756624436	snp	C/T	3.29853e-05	0.00406098	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28246807	CTGGTAGAAGCAATG[C/T]TGGCGGCCACAGGCA	8924
rs756654521	snp	A/T	1.68235e-05	0.00290026	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28229340	TAAACAATCAGTAAG[A/T]GGTTCCCTTTCAAAT	8924
rs756667398	in-del	-/TTTA			intron-variant	HERC2	GRCh38.p7	15:28183205	TCAACAGGTTAGGAG[-/TTTA]TTTATTTTTTGTTTG	8924
rs756683751	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28176837	TGGATTTTCCCACAG[A/T]TAAAGCCAACCATGC	8924
rs756711287	snp	C/G	3.29468e-05	0.00405861	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213842	GTCACAGTGCCTTCT[C/G]CAAACTCATCGTGCA	8924
rs756713767	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28289001	TGCCAACCAAGAACA[C/T]GTCAGAAGCAGGAAG	8924
rs756714171	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28181370	ACACTCACAGCTCAC[C/T]GCCCACTGTCCACTT	8924
rs756714220	snp	C/T	0.000524256	0.0161819	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256128	GTGCCCGGGCCCGCT[C/T]CTCCGCGGTGGGCAG	8924
rs756718054	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28224487	TCAGCCGCCCAAAGT[A/G]CTAGGATTACAGCCT	8924
rs756733171	snp	C/T	1.64836e-05	0.0028708	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213760	TTTCAGCTGATTCAA[C/T]GGGCAAACGCGACAC	8924
rs756736818	snp	A/G	1.64947e-05	0.00287177	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28178941	GAGCTGTGATCTGCC[A/G]TGGGATGGGCACCGT	8924
rs756746021	snp	A/G	2.30131e-05	0.00339205	intron-variant	HERC2	GRCh38.p7	15:28233380	CAACTTTAACAACAA[A/G]TATTTCAGCAACTGT	8924
rs756748507	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28191852	TAACGTGAGTACTGA[C/T]AGGTGCTATCAGCAA	8924
rs756758604	snp	C/T	1.64743e-05	0.00287	missense	HERC2	GRCh38.p7	15:28143952	TCAGTTGTAAGCAGC[C/T]TCCTCAGTCTCTGAA	8924
rs756759017	snp	C/T			intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174159	CACACAGAAGGACAG[C/T]GCTGTGAGTTTACCT	8924
rs756763123	snp	C/G	1.67072e-05	0.00289021	intron-variant	HERC2	GRCh38.p7	15:28265588	GCGTGTCCTCGTGGG[C/G]CTGTCCAGGGTGGCG	8924
rs756778169	snp	A/C	1.64868e-05	0.00287109	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28263158	CACCATCTCCCCAAG[A/C]CCACACTTGCCCTAA	8924
rs756809420	snp	C/T	1.66396e-05	0.00288436	splice-acceptor-variant	HERC2	GRCh38.p7	15:28112036	GTATTTATCCAACAC[C/T]TGTTGAGCAGAAACA	8924
rs756813818	snp	A/G	1.74824e-05	0.0029565	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28202218	CTGTATGTCGGAGTG[A/G]TCCAGCAGCCACCCG	8924
rs756823547	snp	C/T	1.64958e-05	0.00287187	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28270714	TGAGATGTCGGAGAG[C/T]TACACAGCGGAGGCA	8924
rs756826766	snp	A/G	8.9156e-05	0.00667608	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28175551	GCAGTGCAGGGCCCC[A/G]ACAGCCACATGCACG	8924
rs756826836	snp	C/T	1.65375e-05	0.0028755	intron-variant	HERC2	GRCh38.p7	15:28179066	GAGAGGACTCTCTTT[C/T]CACAACATTAAAAAC	8924
rs756835034	in-del	-/C	0.283589	0.247733	frameshift-variant, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272969	TGCAGGGGGATGCTT[-/C]CTGGCCCTTTGGTGG	8924
rs756845412	snp	A/T	0.0109963	0.0733297	missense, nc-transcript-variant	HERC2, LOC107987422	GRCh38.p7	15:28321388	TTTTCAACCATTTGG[A/T]GTCGAGGCGAGCCTG	8924
rs756846638	snp	A/G	1.64779e-05	0.00287031	missense	HERC2	GRCh38.p7	15:28135626	ATTCAAGCAATGTTG[A/G]GGTGGACACCGACTC	8924
rs756850497	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28123270	CAAAACATTGCAATT[C/T]TATTAAATCACTAAG	8924
rs756870275	snp	A/G	1.66219e-05	0.00288283	intron-variant	HERC2	GRCh38.p7	15:28269444	AATGATCCCTGTAAG[A/G]TAAGAAAGTAAACAT	8924
rs756870557	snp	C/T	1.64827e-05	0.00287073	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28196502	CAACTCCATTTCTGA[C/T]AGCAACCCAGTCCAG	8924
rs756876591	snp	A/G	1.65323e-05	0.00287505	intron-variant	HERC2	GRCh38.p7	15:28141400	ACTGCCTCAGGCTCA[A/G]TGACCTTGTGACATA	8924
rs756883857	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28253835	GGTGTGGTTGCGGAC[A/G]CCTGTAGTCCCAGCT	8924
rs756901842	in-del	-/CACACACC			intron-variant	HERC2	GRCh38.p7	15:28224141	AAAATTATACACACA[-/CACACACC]CACACACCCACACAC	8924
rs756913592	snp	C/G	0.0567628	0.158617	intron-variant	HERC2	GRCh38.p7	15:28273007	TCCGTGAACATCCCT[C/G]AAATGAAAGCAGTGG	8924
rs756924592	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28237787	CTTCTACATAGTTCT[C/T]CCCAAAAAATACTAC	8924
rs756933047	snp	A/G	3.32646e-05	0.00407814	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28228235	ATCAGGCGCAGTGCC[A/G]TCTGCGTGAGGGCCA	8924
rs756940494	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28124422	GTTTGACTGTAAAAA[A/T]AATTAGTCTATACAA	8924
rs756955127	snp	A/G	1.73773e-05	0.0029476	intron-variant	HERC2	GRCh38.p7	15:28238078	CAGAGGGTATCCCCT[A/G]CCATCCTCTGCATCA	8924
rs756958450	in-del	-/A/AA			intron-variant	HERC2	GRCh38.p7	15:28173791	TGAGACCCTGTCTAC[-/A/AA]AAAAAAAAAAAAAAA	8924
rs756962864	snp	A/G	1.74263e-05	0.00295175	intron-variant	HERC2	GRCh38.p7	15:28196610	TCCATCTTCCTCTTC[A/G]CCAATAAAAACCTGA	8924
rs756972399	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28259477	CTAATTCTACACAAT[A/C]CCTTATAGAAAATGA	8924
rs756976336	snp	C/G	3.31082e-05	0.00406854	intron-variant	HERC2	GRCh38.p7	15:28146227	GCCCTGCTCAACCTC[C/G]TGTCCTTACCTGACC	8924
rs756979066	snp	A/G	0.000147896	0.00859804	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28202525	GGCGACAGGCGTGGT[A/G]GCCTCACTGGAGCTG	8924
rs756984369	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28255245	GAGGCTGAGGTGGCA[A/G]GATCATTTGAGCCTA	8924
rs757001643	snp	C/G	1.66763e-05	0.00288753	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272935	CTCCAGCAGGATGGC[C/G]AGGGCCAAGTGCTGG	8924
rs757008280	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28307465	TATCATTAGGTTATT[C/T]ATTTGAAGTTTTTCT	8924
rs757013411	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28128882	TCCCAGCTTCCAGGG[A/G]CCACCCCATTCCCCA	8924
rs757021937	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28243680	GAAACCACAATGAGA[C/T]ACCAGTGTACACCCA	8924
rs757023044	snp	A/G	3.53245e-05	0.0042025	intron-variant	HERC2	GRCh38.p7	15:28222258	AGCCAACAAGTAGCT[A/G]CAGTGTCCCCTTAAT	8924
rs757032412	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28116922	TAAAGAGAGCCCCAA[A/C]GCTCCCACACCATGT	8924
rs757034529	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28147393	TAGCACTTCGGGAGG[C/G]CGAGGCAGGCAGCTT	8924
rs757052254	snp	C/G	1.66988e-05	0.00288949	intron-variant	HERC2	GRCh38.p7	15:28186770	AGACACAAAAACCAT[C/G]ATCTATAGACTCTGT	8924
rs757066571	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28244503	TGGGAGGGTCCTGCC[A/G]CCATCCAGGCTAAGG	8924
rs757073936	snp	C/T	1.65707e-05	0.00287838	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28229803	CTTCAACCACTTGTA[C/T]TTGTGAACACCTGTA	8924
rs757086244	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28113871	CACTGGGCTCATCTC[A/G]TCCAGCCGACAGGGT	8924
rs757086685	snp	A/C	1.64963e-05	0.00287192	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229712	TTTTTTCCACATCCA[A/C]TGGCTCTTCTTTAAG	8924
rs757088805	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28283258	AAATCCAAACTAAGA[C/T]ATACAATAATCAAAC	8924
rs757091618	snp	C/T	6.60633e-05	0.00574694	intron-variant	HERC2	GRCh38.p7	15:28292885	CAAAATTCACAAGAT[C/T]ACCTGGTTGCTTGCC	8924
rs757107274	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28150292	GAGAACATCACTGAG[A/G]ACGGCCACACGAATG	8924
rs757107769	snp	C/T	1.70438e-05	0.00291918	intron-variant	HERC2	GRCh38.p7	15:28142206	ATAATGTTTTTGCAT[C/T]CCAAAAGTGATTCCA	8924
rs757141755	snp	C/T	4.94303e-05	0.00497119	missense	HERC2	GRCh38.p7	15:28146293	GTGAGAGGGTCGTGG[C/T]GCCTCTCTGTGGAGC	8924
rs757155355	snp	A/G	4.15645e-05	0.00455857	intron-variant	HERC2	GRCh38.p7	15:28117213	AGGAAGCACACAGTC[A/G]GGGATATGCGGCACT	8924
rs757156736	snp	A/G	1.65078e-05	0.00287291	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214113	AAGCTGTGGGTGATG[A/G]AGCGGAGCTGGGAGT	8924
rs757170828	snp	C/T	1.65094e-05	0.00287305	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233702	CAACATAACAACAAG[C/T]GACCGACCTCTTCCA	8924
rs757174088	snp	A/G	5.08444e-05	0.00504179	intron-variant	HERC2	GRCh38.p7	15:28177137	CAGTTCCTACAACAA[A/G]ATGAAATCAGCTCTC	8924
rs757177576	snp	A/G	4.94458e-05	0.00497197	synonymous-codon, utr-variant-5-prime, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28280229	GGTGGCTGACTGGAC[A/G]GCCAGGGCCTGCTGC	8924
rs757184859	snp	A/G	0.000131813	0.00811721	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28177457	TCCATCGTCACCTTC[A/G]CCCCACGAAAACACT	8924
rs757197746	snp	C/G	1.68573e-05	0.00290316	synonymous-codon	HERC2	GRCh38.p7	15:28132205	GAGGCAGAGGGTCTG[C/G]GCATCTCCACTGCCA	8924
rs757200730	in-del	-/TCCTCGTCAGAA	5.62287e-05	0.005302	cds-indel, nc-transcript-variant	HERC2	GRCh38.p7	15:28202150	ACGTCCTCCACCACC[-/TCCTCGTCAGAA]TACTCGTCGGACACC	8924
rs757201608	snp	A/T	1.76524e-05	0.00297084	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28218598	AGCAGACAGACAAAG[A/T]GTCTGCAGTAAGTTA	8924
rs757211472	in-del	-/T	2.91949e-05	0.00382055	intron-variant	HERC2	GRCh38.p7	15:28222020	TTCACATCAAATCTC[-/T]TGAGTACCTGATCGC	8924
rs757228076	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28174900	GACACACAGAAGGTC[C/G]TCTCTCTAACTAAGT	8924
rs757232123	snp	C/T	3.37046e-05	0.00410502	splice-donor-variant, intron-variant	HERC2	GRCh38.p7	15:28272214	CCATCATGACACTCA[C/T]GTGCATGTCGCCCTC	8924
rs757236332	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28228464	ATACAAGAATAAACG[G/T]AACGCAGAAAGCACG	8924
rs757241998	in-del	-/CT			intron-variant	HERC2	GRCh38.p7	15:28135025	AGGATAAGAAGGCCC[-/CT]GTTACTCCAATCTGG	8924
rs757244969	snp	C/T	1.65463e-05	0.00287626	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214012	CGACAGAGACACTCA[C/T]GGAGCTGCCCAATCC	8924
rs757261530	snp	C/T	1.64966e-05	0.00287194	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265892	TGGCCGCACTGTAAG[C/T]GCTCCCGCAAGCGAT	8924
rs757268665	snp	C/G/T	9.8923e-05	0.00703232	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28174545	CTTCTAAGCCTTGCA[C/G/T]GAGTGTGGGCTTCCT	8924
rs757274223	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28150752	TCACCGAGAATGGCC[A/C]CACGAACGTATATTC	8924
rs757291688	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28245683	CACACATACATAAAC[A/C]CACATATATTTGGTT	8924
rs757293165	snp	C/G	3.34348e-05	0.00408855	intron-variant	HERC2	GRCh38.p7	15:28229180	AAAATAACATTGATA[C/G]AATTATTGACTCACC	8924
rs757294366	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28267711	CGGATGCTGTCGGCA[A/G]TGATGCCCTCAACTC	8924
rs757303804	snp	A/G	9.9975e-05	0.00706948	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111746	AGGCTCTCATCTCAC[A/G]AGGACGTTTCCCCAT	8924
rs757338902	snp	A/G	1.64738e-05	0.00286995	missense	HERC2	GRCh38.p7	15:28114738	AGGCTCATGGCTTCA[A/G]ACTCCTCTGAGGTGG	8924
rs757356914	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28160883	TTGGCACCGCCCCCC[A/G]CTCAGCATTATTTTA	8924
rs757359487	snp	C/T	1.64955e-05	0.00287184	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265824	AGACGTACCATGGCC[C/T]AGCCGGCCGTAGTTC	8924
rs757389816	snp	A/G			synonymous-codon	HERC2	GRCh38.p7	15:28169606	CTTAGAATTACTTGC[A/G]CCACTTATTTTATTA	8924
rs757391267	snp	C/G	1.6607e-05	0.00288153	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28255956	CAGAAGATCAATCAT[C/G]AATCGACGACCTGGA	8924
rs757393249	snp	C/T	2.73572e-05	0.00369836	intron-variant	HERC2	GRCh38.p7	15:28270913	AAATGGTGGGAAAAA[C/T]TAAAGTTAACACAAT	8924
rs757396258	snp	C/T	6.59816e-05	0.00574338	intron-variant	HERC2	GRCh38.p7	15:28167636	ATTTCTACTTCTGTG[C/T]ACATTTAAGATTATT	8924
rs757413678	in-del	-/AC			intron-variant	HERC2	GRCh38.p7	15:28113717	CTTCTGTCTTCAGTG[-/AC]ACACTGACTTTATGC	8924
rs757433911	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28275466	CGGGTGAAGCCCTGC[A/G]TGCTTGACCCACCCT	8924
rs757448502	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28143810	TAGAGGTTTAGACTA[C/G]TAAAGCAACATTTTA	8924
rs757456331	snp	C/T	4.95995e-05	0.00497969	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28228399	GGTTTGCAGGGGAAC[C/T]GGCTGGATACCTAAT	8924
rs757477632	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28197725	CACTGCACTCCAGCC[C/T]GGTCAGGGGAGGAGA	8924
rs757483867	snp	A/G	6.58903e-05	0.00573941	missense	HERC2	GRCh38.p7	15:28167742	GCTCCCAGGTCATCC[A/G]TCACTGGGATAAAAG	8924
rs757487314	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28249214	TTCAAGACAAGACTC[A/G]CCTGCATTGCCACAT	8924
rs757488342	snp	C/G	1.68445e-05	0.00290206	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28211117	TAGCTTCAACTGCTG[C/G]CACCGCAGCAGGTCC	8924
rs757491368	snp	A/G	1.72006e-05	0.00293258	missense	HERC2	GRCh38.p7	15:28124165	GCTCGGAGAGGTGGT[A/G]CAGCAGCAGCAGACG	8924
rs757511654	snp	A/G	0.000141046	0.0083966	intron-variant	HERC2	GRCh38.p7	15:28261018	AAGCCTATGACTTCC[A/G]CTGCAAGAAAGATAT	8924
rs757516204	snp	A/G	0.000132538	0.0081395	intron-variant	HERC2	GRCh38.p7	15:28176418	TGTGACAGGGAGGAC[A/G]TTTACGTACCATGTC	8924
rs757520047	snp	A/C	1.65861e-05	0.00287972	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28260906	CCCCCAGCTGTGGAC[A/C]TCGCTGTCCTCAGTC	8924
rs757524101	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28258348	ATGCTGGTGCATGCC[A/G]GTAGTCCCAGCTAAT	8924
rs757549294	snp	C/T	1.66286e-05	0.0028834	missense, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28299404	TAAAGGCCCTTACCT[C/T]TTCTAGGAGGGAGCT	8924
rs757565125	in-del	-/ATT	1.64746e-05	0.00287002	cds-indel	HERC2	GRCh38.p7	15:28169542	CTGCTGTTTGGCCAG[-/ATT]ATTTCCATCCAATGA	8924
rs757574531	snp	C/T	1.71734e-05	0.00293026	intron-variant	HERC2	GRCh38.p7	15:28144261	ACACTGTAAACATCC[C/T]CGGGTTTCACAAGCT	8924
rs757577495	snp	A/G	1.69344e-05	0.00290979	synonymous-codon	HERC2	GRCh38.p7	15:28116858	GTCATCCACAGATTC[A/G]CCTGCAGGGGAGAAG	8924
rs757578315	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28277489	AAAAAGGGGCTTTTT[C/T]AAAATTTTAGGAATT	8924
rs757583117	snp	C/T	3.64159e-05	0.00426692	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28202450	CTGCACCACGATCGG[C/T]AGAGCGGGAACGGGC	8924
rs757596331	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28263223	CATTTTAACGAAAAA[G/T]TTTAAATGACTGCAA	8924
rs757596784	snp	A/T	1.65556e-05	0.00287707	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233162	TCTCTTTTTCCTTCG[A/T]TCTCGAATTATCTTT	8924
rs757604168	in-del	-/AGGCTGGAGTG			intron-variant	HERC2	GRCh38.p7	15:28116257	TACAGAGTGTTGCCC[-/AGGCTGGAGTG]CAATGGTACGATCTC	8924
rs757607420	snp	C/T	2.42462e-05	0.00348174	intron-variant	HERC2	GRCh38.p7	15:28269206	TAGGACAGACCCTGC[C/T]CCGCAAGGGAACACT	8924
rs757634299	snp	C/T	1.65367e-05	0.00287543	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28248597	CTCCTGGATAAAGTT[C/T]ACTAATAAGCAAACG	8924
rs757644718	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28149455	ATGCGGCTCCTAACC[A/G]AGAACGTCACCGAGA	8924
rs757649944	in-del	-/G			intron-variant	HERC2	GRCh38.p7	15:28226126	AAAATACTGCTGAAA[-/G]AAATTAAAGAGGACA	8924
rs757660355	snp	C/G/T	0.000115361	0.00759397	intron-variant	HERC2	GRCh38.p7	15:28144666	TCGCCATAAGCCCCT[C/G/T]CCTTACCAGCAGCTG	8924
rs757673157	snp	G/T	3.32044e-05	0.00407444	intron-variant	HERC2	GRCh38.p7	15:28198577	TAAGAAAAAACAAAA[G/T]CACTGAACAAAGAAT	8924
rs757676082	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28248479	TCTGGGCATATAGGA[A/T]GGACACGTCGAAAAG	8924
rs757684865	snp	C/T	0.000200385	0.0100076	intron-variant	HERC2	GRCh38.p7	15:28230526	AAACATCATTCACTA[C/T]AAAAATCATACACTT	8924
rs757690544	in-del	-/AAAAAAAAAAAAAAAAAAAAAAAAAA					GRCh38.p7	15:28119402	AAGACTCCCTCTCAA[-/AAAAAAAAAAAAAAAAAAAAAAAAAA]AAAAAAAAAAGGCCT	8924
rs757693916	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28188635	ATGAATATTGAAGCA[A/C]GTGCTCCTGAAATAA	8924
rs757700499	snp	A/G	1.66738e-05	0.00288732	synonymous-codon	HERC2	GRCh38.p7	15:28169486	CACAGAAGCCTACCT[A/G]GCATACATGATTTGC	8924
rs757701629	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28189613	ACATTCCAGAATAAA[C/T]GGTAACTACTGTGAA	8924
rs757706883	snp	C/T	1.64923e-05	0.00287156	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28176752	TGGATTACTCTGTGA[C/T]CGAGAAGGACTTTCA	8924
rs757708528	snp	A/G	1.64822e-05	0.00287068	synonymous-codon	HERC2	GRCh38.p7	15:28130299	GTGATAATCGCCTTT[A/G]CCCCTGCACACAAAG	8924
rs757716313	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28157253	TCAGGATGGTGCTGG[C/T]CTCATAAAATGAGTT	8924
rs757718974	snp	A/G	3.35182e-05	0.00409365	intron-variant	HERC2	GRCh38.p7	15:28220653	GCCCATCCTGAGAAA[A/G]CCAAAGTAGAGATCA	8924
rs757734104	snp	C/G	0.000100862	0.00710078	intron-variant	HERC2	GRCh38.p7	15:28152668	CCCCGCTGGGGCCAG[C/G]CCCTGTACCTGGTAT	8924
rs757744232	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28293554	CATGTCTTCCAAAGT[C/G]ATATTCCATCTACTT	8924
rs757770688	snp	C/T	0.000147292	0.00858045	intron-variant	HERC2	GRCh38.p7	15:28236930	TTCAAAAAAAATAAT[C/T]TGCTGATCAGCAAAA	8924
rs757781682	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28173307	TTGTATAGTCAACTG[C/G]AAACAGCCCAAACAT	8924
rs757787117	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28134134	GACTTTAGGTTTTTT[A/G]AAAATTATCTCAGCA	8924
rs757804194	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28188232	CTGGACACTGACTGA[A/C]TATTATATGACATTA	8924
rs757804419	snp	C/T	5.4748e-05	0.00523173	intron-variant	HERC2	GRCh38.p7	15:28248505	AAAAGCCTAAAGTAA[C/T]GAGCCCCGATCACAT	8924
rs757820406	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28180648	ATCTGAACAGTTCCA[C/T]AGTAGAAAGTGAAAA	8924
rs757822447	snp	A/G	8.07967e-05	0.00635545	missense	HERC2	GRCh38.p7	15:28142873	CCACCCCTCACAATA[A/G]GATCTTCATATTCAA	8924
rs757828073	snp	A/G	1.67508e-05	0.00289398	stop-gained, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272385	TGGCAGACAACATTT[A/G]GCTAAAGGAGAAAAG	8924
rs757849858	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28149629	TCACCGAGAACGGCT[A/G]CACGAACGTACATTC	8924
rs757852019	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28257888	ACAGGGTTTCATGGT[A/G]TTAGTCAGGATGGTC	8924
rs757868109	snp	C/T	0.000158165	0.00889144	intron-variant	HERC2	GRCh38.p7	15:28117351	ACCCGAGACCGCTGC[C/T]TCACCCCATTGGGCA	8924
rs757890292	snp	C/G	1.79306e-05	0.00299416	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256195	GGCCGACTGCACGGT[C/G]CTCAGCACGCCCGCA	8924
rs757893230	snp	A/G	8.24926e-05	0.0064218	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28191188	GTCAGCAGGATCTAC[A/G]ATCATTTTTAATCTA	8924
rs757899582	in-del	-/TC	0.000362608	0.01346	frameshift-variant, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28270729	TACACAGCGGAGGCA[-/TC]TACAGGGCGTAGCCA	8924
rs757900398	snp	A/G	1.79477e-05	0.00299558	intron-variant	HERC2	GRCh38.p7	15:28163049	GGAGGGTGGCCCAAC[A/G]TGGAGGAGGTGGAAT	8924
rs757903204	snp	A/G	1.65726e-05	0.00287855	intron-variant	HERC2	GRCh38.p7	15:28229430	TGCCATAGCTACCTT[A/G]ATTAAGAAAAAAATA	8924
rs757906520	snp	A/G			synonymous-codon	HERC2	GRCh38.p7	15:28144698	CATGATGGGATAGAC[A/G]GTGAAGCGCCAGCCC	8924
rs757930995	in-del	-/C	1.6669e-05	0.00288691	intron-variant	HERC2	GRCh38.p7	15:28117262	GGCACCGTGCATGGG[-/C]CCCCTCCCTGGTCAC	8924
rs757940104	snp	A/G	1.65693e-05	0.00287826	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272336	TTGTCAGTCTCCTGT[A/G]CCCCGCTGTCCCACA	8924
rs757955258	snp	C/T	0.000130256	0.00806913	intron-variant	HERC2	GRCh38.p7	15:28215824	GAGGGAAAATAGACA[C/T]GCTTGGTAACAAGTC	8924
rs757955857	in-del	-/ACAA			intron-variant	HERC2	GRCh38.p7	15:28216791	CAGTCACACGTATGC[-/ACAA]ACAGATGCAAGCTGA	8924
rs757955903	snp	A/T	3.29652e-05	0.00405974	intron-variant	HERC2	GRCh38.p7	15:28121327	CTGTCAGACTTGGAG[A/T]GTAATCTCCATGTGC	8924
rs757965969	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28190538	TTATTAACCAAAAAA[C/T]TGCCACTCCGTGACA	8924
rs757983398	snp	A/G	1.68516e-05	0.00290268	intron-variant	HERC2	GRCh38.p7	15:28178841	GTTAACAACGGAGCA[A/G]GAGCAAAGGCCGCCC	8924
rs757992237	snp	A/C	1.65141e-05	0.00287346	intron-variant	HERC2	GRCh38.p7	15:28143829	AGCAACATTTTATTC[A/C]CCAAGGGTCACAAAT	8924
rs757995964	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28252483	TCACTTTAAAACTTT[C/G]CGTGGAACTTTACAT	8924
rs757999942	snp	A/C	3.29473e-05	0.00405864	missense	HERC2	GRCh38.p7	15:28143927	ATTTATGTTAATTGA[A/C]TGCCCAAATTCAGTT	8924
rs758021444	snp	C/T	3.90419e-05	0.00441808	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202166	CCTCGTCAGAATACT[C/T]GTCGGACACCGTGTC	8924
rs758022435	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28147587	GGCTGTAGTGAGCCA[C/T]GATCGTGCTACCATA	8924
rs758030156	snp	A/G	1.70409e-05	0.00291893	intron-variant	HERC2	GRCh38.p7	15:28275014	CCGGGAACTGCAGAC[A/G]ACACACACGGAACAT	8924
rs758030760	snp	C/T	2.05303e-05	0.00320386	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28175526	CCTGCCCCGAGTCCG[C/T]GACCGCCAGGCAGTG	8924
rs758047892	snp	G/T	1.66073e-05	0.00288156	intron-variant	HERC2	GRCh38.p7	15:28265596	TCGTGGGCCTGTCCA[G/T]GGTGGCGAGAGCTCT	8924
rs758049204	snp	A/C	1.6664e-05	0.00288647	intron-variant	HERC2	GRCh38.p7	15:28196415	CTTAATTCAACAGAA[A/C]ACCATTCGTCCCAAA	8924
rs758053461	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28120844	AAGTGGGCACGGCCC[C/T]CCAGCACCATCAGAG	8924
rs758062492	snp	C/T	1.64787e-05	0.00287038	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28270763	GGTCTAAATGGGCCA[C/T]GACAACAACCGCCGT	8924
rs758093331	snp	C/T	4.94238e-05	0.00497086	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213856	TCCAAACTCATCGTG[C/T]ATAACTTGACCGCCC	8924
rs758109699	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28175268	GTCTTTCCACACACT[C/T]TTCACGTGGACTTCA	8924
rs758111308	snp	C/G	1.76055e-05	0.00296689	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202215	GACCTGTATGTCGGA[C/G]TGGTCCAGCAGCCAC	8924
rs758118433	snp	A/G	1.65091e-05	0.00287303	missense	HERC2	GRCh38.p7	15:28168426	CTCTTTTCTTGCCAT[A/G]GATTTGGACTCAGTC	8924
rs758128996	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28143449	TCCTTATTTTTATTC[A/C]TTTATTTATTTTTTT	8924
rs758141150	snp	A/G	1.80322e-05	0.00300262	intron-variant	HERC2	GRCh38.p7	15:28182550	GAAAAAGAAAAGAGA[A/G]GTTATTCAGCATAAA	8924
rs758168078	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28280011	ACTTTCTGAAACAAA[A/C]CAGTCTGAATTTTAT	8924
rs758178267	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28197810	CATTTCACAGAATAA[A/C]TGACAGGACAAGTTT	8924
rs758186578	snp	C/G	1.90707e-05	0.00308788	intron-variant	HERC2	GRCh38.p7	15:28238250	AAAGCAACATGAGTT[C/G]AATTCAGCTTGCCTG	8924
rs758195132	in-del	-/C	3.30983e-05	0.00406793	intron-variant	HERC2	GRCh38.p7	15:28229639	GTGTTATGTATATTA[-/C]CCAATGCAGAGAAGC	8924
rs758205073	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28120752	TGTCACTGGGCCTCT[A/G]ACCCACTCCACTTCT	8924
rs758210761	snp	C/T			intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28313805	GAAGCAGTAAGATAG[C/T]GAGGTCTTCCTAAAG	8924
rs758222873	snp	A/C	1.81516e-05	0.00301255	intron-variant	HERC2	GRCh38.p7	15:28228191	CTTGACATTTTCCCA[A/C]AGGCGCTCAAGCGGG	8924
rs758223161	snp	C/G	1.65012e-05	0.00287234	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28196470	ACTCACGTAACCCCA[C/G]GATGAATACTGGGTA	8924
rs758224239	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28197851	AACATCAGGTAAGGC[C/T]ACTCTGTGACTGATG	8924
rs758244173	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28242035	AACATGGATGAACCT[G/T]GAAGACATGCTAAGT	8924
rs758253364	snp	C/G	0.000116357	0.00762661	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272950	CAGGGCCAAGTGCTG[C/G]TCCTGCAGGGGGATG	8924
rs758258825	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28258107	GTTCTCCAATCACAA[A/T]GGTATTAAACTAGAA	8924
rs758266870	snp	A/C/G	3.30717e-05	0.00406632	intron-variant	HERC2	GRCh38.p7	15:28144808	ACCACTCTCGGCCTG[A/C/G]GGGAGGAAAGCGCAC	8924
rs758267628	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28166207	AATATCCAAACCAAA[G/T]ACATCACAAGAAAAC	8924
rs758283248	in-del	-/TT	5.19125e-05	0.00509447	intron-variant	HERC2	GRCh38.p7	15:28248777	AAATTAAACAAGATA[-/TT]TCTACTAAAAAGAAA	8924
rs758284896	snp	A/G	6.60142e-05	0.0057448	synonymous-codon	HERC2	GRCh38.p7	15:28168506	AGCCATCGCAGATGC[A/G]TCGGAAGGGGCCGCC	8924
rs758286362	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28201652	TAATATTAAAAAGTA[A/G]AGGATGAAATCCTTT	8924
rs758310203	snp	C/G/T	0.00214117	0.0326531	missense	HERC2	GRCh38.p7	15:28125059	TCGACCAGGCGAGGG[C/G/T]ATGTGCTGAGCCACA	8924
rs758334168	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28243191	TGCTGGCACAAAGAC[A/G]CTATGGACAAAATGC	8924
rs758346270	snp	A/G	0.000137045	0.0082767	intron-variant	HERC2	GRCh38.p7	15:28117179	AGGAAGCAAGCAAGC[A/G]TGAGGCCGCTGCCGC	8924
rs758347577	snp	A/G	1.96381e-05	0.00313347	intron-variant	HERC2	GRCh38.p7	15:28117210	AGCAGGAAGCACACA[A/G]TCGGGGATATGCGGC	8924
rs758347994	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28182760	TCAGCCTTTATTTTT[C/G]GTGGAAAACGATGAT	8924
rs758350864	snp	C/T	1.66222e-05	0.00288285	intron-variant	HERC2	GRCh38.p7	15:28146215	TGGGTAGATCATGCC[C/T]TGCTCAACCTCCTGT	8924
rs758354840	snp	C/G	3.29658e-05	0.00405978	missense	HERC2	GRCh38.p7	15:28141819	TGTTTTCGCTGTCTG[C/G]CATTAATTCACGAAT	8924
rs758361517	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28127411	GAAAAGAAAGGATCT[G/T]CAAGGTTGCCATGAG	8924
rs758363700	snp	A/C/G	6.73428e-05	0.00580237	intron-variant	HERC2	GRCh38.p7	15:28265989	CCTTGGGGAGAAAGG[A/C/G]AACAAACATGAATGC	8924
rs758375242	snp	C/T	1.66029e-05	0.00288117	intron-variant	HERC2	GRCh38.p7	15:28233842	GAGCCACCCAGTGAG[C/T]CTTCACAAATCTTAA	8924
rs758383066	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28248347	CTAAAGAATTTAAAT[A/G]TTAAGGCAACAAAAT	8924
rs758402285	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28171670	ATTGTACTTATTTCT[A/T]CATGCTAGCAAAGAG	8924
rs758402374	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28188176	AAACATCATCTGAAT[C/G]AGAAACTGCAAAAGG	8924
rs758419526	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28118499	AATAACTCTGTAATA[A/C]ATTTTTAAGTATAAA	8924
rs758422973	snp	A/T	4.95749e-05	0.00497845	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28257141	CCGCGGAACCATCCA[A/T]CCCCTCACTCACCTG	8924
rs758437597	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28281983	TGCCCTTCTCCCTGA[A/C]ACCCTCCTGCTTATT	8924
rs758440835	snp	C/T	1.71073e-05	0.00292461	intron-variant	HERC2	GRCh38.p7	15:28142197	TATAGCTAAATAATG[C/T]TTTTGCATCCCAAAA	8924
rs758452157	snp	A/C	1.65718e-05	0.00287848	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272269	AATGATGCTCTGGAA[A/C]CTTTGCAGCAAGGGC	8924
rs758452427	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28249414	TTGAGCCATGAGCCA[C/T]TGGAAGATGACAAGA	8924
rs758455627	snp	C/T	1.65756e-05	0.00287881	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233774	CACTGCCTACAGTAC[C/T]TTTCTATTTGACACA	8924
rs758456001	snp	A/G	1.65244e-05	0.00287436	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28176991	TATCCCCATGTCCCA[A/G]CCGGCCGTACTCGCC	8924
rs758464646	snp	C/T	1.68502e-05	0.00290255	synonymous-codon	HERC2	GRCh38.p7	15:28132187	GACAGTGTCGTCATC[C/T]GTGAGGCAGAGGGTC	8924
rs758495414	in-del	-/G			intron-variant	HERC2	GRCh38.p7	15:28135342	CTATTTCTGCCAAAT[-/G]AGTCATTAACATTAT	8924
rs758503392	in-del	-/GG			intron-variant	HERC2	GRCh38.p7	15:28114173	AGCAGTGGAAGCTGT[-/GG]GTGGTGGTAATGACC	8924
rs758518252	snp	A/G	1.65353e-05	0.00287531	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214142	GTTGATGTACTTGTT[A/G]ATGAGCCCATTCCAC	8924
rs758528766	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28164536	TGAAATGTACCTACC[-/A]ATTTTTTTTTATGAG	8924
rs758547189	snp	A/G	8.6722e-05	0.00658434	intron-variant	HERC2	GRCh38.p7	15:28246071	AAGGAGAACACCTAC[A/G]TTTAAGAAATAATAA	8924
rs758550037	snp	A/G	1.909e-05	0.00308944	intron-variant, downstream-variant-500B	HERC2	GRCh38.p7	15:28174378	AAAATCTCAGAGAAG[A/G]TACAAATCTGTGTTA	8924
rs758561920	snp	C/T	1.65671e-05	0.00287807	intron-variant	HERC2	GRCh38.p7	15:28220434	GCCTTGGACTAAACA[C/T]CTTCCTGAGTCACCC	8924
rs758562777	snp	A/G	3.31851e-05	0.00407326	intron-variant	HERC2	GRCh38.p7	15:28121452	ACATCAAACAGACAA[A/G]ATTTAGAATCTGATA	8924
rs758581750	in-del	-/A	1.83256e-05	0.00302696	intron-variant	HERC2	GRCh38.p7	15:28174634	CCTGTTTACGAGGAG[-/A]AAAAAAGCTTATAAT	8924
rs758585160	snp	A/G	3.30191e-05	0.00406306	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28192033	TGCCTGGTTCACGGA[A/G]GACGACACATTCAGG	8924
rs758602776	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28119581	GCCTCAGCCTCCCAA[A/G]TAGCTGGGACTACAG	8924
rs758605836	snp	C/T	6.65447e-05	0.00576783	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274922	GATCGCCAGGCCCTG[C/T]GCAGGAAGGCAAAGG	8924
rs758612885	snp	A/T	1.64749e-05	0.00287005	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28201503	CATCATTACTCAAGA[A/T]ATCAGCTCGTTTTTT	8924
rs758614307	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28227001	AGAAACGGGCTGGGC[A/G]CAGTGGCTCACGCCT	8924
rs758627745	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28163612	GGAGTTTTGGAATGA[A/G]GCTGCATCCTGTATA	8924
rs758629106	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28296202	AAATGTGGGCCGGGC[A/G]TGGTGGCTCACACCT	8924
rs758637405	snp	C/T	1.67908e-05	0.00289743	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272218	CATGACACTCACGTG[C/T]ATGTCGCCCTCGGAG	8924
rs758637624	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28209642	GCCACCGCGCCAGGC[C/G]TATATATCATTTATA	8924
rs758649569	snp	A/G	1.88734e-05	0.00307187	intron-variant	HERC2	GRCh38.p7	15:28132277	CTTCAGAGAAAAGGG[A/G]CTTGGGTTGGCCAAG	8924
rs758650846	snp	A/G	7.06402e-05	0.00594265	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28218616	CTGCAGTAAGTTAAT[A/G]GTGCTGGTAAACATC	8924
rs758658451	snp	A/G	4.98235e-05	0.00499092	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28255964	CAATCATGAATCGAC[A/G]ACCTGGACTTATGTT	8924
rs758667770	snp	C/T	8.37318e-05	0.00646984	intron-variant	HERC2	GRCh38.p7	15:28256037	TGAGTGAAACGCCAT[C/T]CCCTCCCAACACCCT	8924
rs758673330	in-del	-/A	0.0310713	0.120707	intron-variant	HERC2	GRCh38.p7	15:28179244	CAGAATTTTTTTAAC[-/A]AAAAAAAAAAGAAAA	8924
rs758675321	snp	C/G	1.6596e-05	0.00288058	intron-variant	HERC2	GRCh38.p7	15:28179100	TTTGTTTTTTGGTGC[C/G]AAGCATAATTTAAAA	8924
rs758679328	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28262008	GGTGTTGGAACACTG[C/T]CAGGTCCACCTACTT	8924
rs758680377	snp	A/T	1.67781e-05	0.00289634	missense	HERC2	GRCh38.p7	15:28163283	ATTTTGGCTTTCAAC[A/T]TCCTAAGTCAAATGA	8924
rs758688912	snp	A/G	1.69596e-05	0.00291196	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28233237	CTTAGACATTATAGA[A/G]AGGTCATTACAAACA	8924
rs758691403	snp	A/G	1.67301e-05	0.00289219	intron-variant, utr-variant-5-prime, upstream-variant-2KB	HERC2	GRCh38.p7	15:28213715	AATTTCCCTTATCAT[A/G]CAGTAACTAAGCACA	8924
rs758697334	snp	C/T	0.000100185	0.00707691	intron-variant	HERC2	GRCh38.p7	15:28274867	AGTCTGTTGATGTAT[C/T]AGGGAAGCAGAACAA	8924
rs758706329	snp	C/G/T	1.65113e-05	0.00287322	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28228275	AATTGAGCAGAAGGT[C/G/T]GAGGTTGTTTGCGCC	8924
rs758735225	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28306973	CAAGTGGCTGGAATT[-/A]ACAGGCACACAAAAC	8924
rs758739007	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28139897	AACCCCATCTCTACT[-/A]AAAAAAAAAAAAAAA	8924
rs758740909	snp	C/T	9.92047e-05	0.0070422	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28229225	TGGCACTGGCATCCA[C/T]CAAAACATTTCGAAT	8924
rs758746246	snp	A/G	1.69735e-05	0.00291315	intron-variant	HERC2	GRCh38.p7	15:28262890	GAAACTGTCCTGAAG[A/G]GTTTTAAAAGTTTAC	8924
rs758751642	snp	C/T	0.000151353	0.00869792	synonymous-codon	HERC2	GRCh38.p7	15:28124076	TCGGAGAGTGTCGAA[C/T]CCAACAGAAGGCCCG	8924
rs758752584	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28279084	GCAACCTCCACCTCC[C/T]GGGATCAAGCAATTC	8924
rs758765256	snp	A/G	3.31137e-05	0.00406887	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28179210	AGTGTCTCAGAGAAC[A/G]AAGGAACCTTTATCT	8924
rs758776632	snp	A/G/T	3.55241e-05	0.00421439	intron-variant	HERC2	GRCh38.p7	15:28237156	TGAGGAAACAGAATT[A/G/T]ATTAAAAACATAAAA	8924
rs758780862	snp	A/G	1.65853e-05	0.00287964	intron-variant	HERC2	GRCh38.p7	15:28176416	AGTGTGACAGGGAGG[A/G]CGTTTACGTACCATG	8924
rs758785377	snp	A/C	1.65644e-05	0.00287783	missense, utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28299489	TTTCATTCCACAGAC[A/C]ACAGAGCCCATCTCT	8924
rs758798422	snp	A/G	7.0001e-05	0.00591571	intron-variant	HERC2	GRCh38.p7	15:28116635	GGCACAGGCCACAGC[A/G]ACACAGTCTCAAGCG	8924
rs758809724	in-del	-/C	3.78601e-05	0.00435071	intron-variant	HERC2	GRCh38.p7	15:28274473	CACGCGTCAGAGGAG[-/C]CCCCCCCACTCCCCT	8924
rs758814733	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28204465	CTCTACTAAATATAC[-/A]AAAAATTAGCCAGGC	8924
rs758827976	snp	G/T			intron-variant	HERC2	GRCh38.p7	15:28188713	AAAGTGAAACATGAC[G/T]GGCAAAATGTTGATA	8924
rs758829268	snp	A/T	3.29582e-05	0.00405931	missense	HERC2	GRCh38.p7	15:28141439	GCTCTTACCTTCCCA[A/T]CAGCCGTCACAGCAA	8924
rs758831049	in-del	-/CA			intron-variant	HERC2	GRCh38.p7	15:28279617	AAGACCCCATCTCCA[-/CA]CACACACACACACAC	8924
rs758838874	snp	A/C	6.58935e-05	0.00573955	missense, utr-variant-5-prime, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28280182	TCCAAGATCACCAGC[A/C]TCTGCTTGAGTCGCA	8924
rs758859631	snp	A/C	3.30316e-05	0.00406383	intron-variant	HERC2	GRCh38.p7	15:28202327	CACATACACAAGCAG[A/C]GGCCAGGAAAACGAA	8924
rs758861732	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28147724	AGACCAAATACAATA[A/G]AAAGTTATTGTTAGA	8924
rs758867240	snp	A/G	1.68635e-05	0.0029037	intron-variant, upstream-variant-2KB	HERC2	GRCh38.p7	15:28214814	AGATCTGATAAAAGA[A/G]AATTTATAACGACAA	8924
rs758870824	snp	C/G	1.71149e-05	0.00292526	missense	HERC2	GRCh38.p7	15:28168571	TGGCGGCCGGCATCA[C/G]GGCCCCGACAACAGC	8924
rs758871945	in-del	-/AGG			intron-variant	HERC2	GRCh38.p7	15:28304071	TCAGGCAGCTAAGGC[-/AGG]AGGAGGATCGCTTCA	8924
rs758884003	snp	A/G	1.66946e-05	0.00288912	missense	HERC2	GRCh38.p7	15:28116695	TGCTGCTGTGCACGG[A/G]TGCTCTGGCGGCCGG	8924
rs758884781	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28128591	AAGGGTGCATGCTTA[C/T]ATAATTCACCAAAGG	8924
rs758908442	snp	A/G	1.6609e-05	0.0028817	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214176	GTCAGGGAGTGCAGC[A/G]TGCGCAGCAGTGCCA	8924
rs758928277	snp	C/T	1.64874e-05	0.00287113	synonymous-codon	HERC2	GRCh38.p7	15:28144755	GAACTTCCACTTTAA[C/T]TCATCCCCTGGGATG	8924
rs758941971	in-del	-/C			intron-variant	HERC2	GRCh38.p7	15:28244650	CTGATCAAATGAATG[-/C]CCCCTCAACAGTATG	8924
rs758946616	snp	A/G	3.42871e-05	0.00414033	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28202385	GAAGCACCAGTGAGA[A/G]ACTTCAGGGCAAACT	8924
rs758946657	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28148876	ATCACTGAGAACGGC[C/T]ACACAAACGTATATT	8924
rs758961251	snp	A/G	1.65075e-05	0.00287289	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214674	GAGTAATGGCACGTC[A/G]GAGGAGCAGGTAGTG	8924
rs758978348	snp	A/G	4.94279e-05	0.00497107	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28237027	CGAAGCGTGTAATCC[A/G]AGAAGCAGGCCCAGA	8924
rs758982177	snp	C/T	4.94254e-05	0.00497094	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28176554	CCTTCACTTCCGCCC[C/T]GGCCCAGTTTTCCAA	8924
rs758989020	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28182666	AGAAAAAAACCTCAA[A/G]CATGTACAGGAGTAA	8924
rs759002260	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28257974	CAAGCGTGAGCCACC[A/G]CACCTGGCCATACAT	8924
rs759015499	snp	A/C	1.64768e-05	0.00287021	missense	HERC2	GRCh38.p7	15:28141736	ATATAATAACCTGTT[A/C]ATCCACTGCACAAGT	8924
rs759018594	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28276624	CCTATAGTCCCAGCT[A/G]TATGGGAGGCTGAGG	8924
rs759024823	snp	A/G	1.69335e-05	0.00290972	intron-variant	HERC2	GRCh38.p7	15:28257038	CTTACAAAAGGAGGA[A/G]GAAGAAGGGAAATCA	8924
rs759025714	snp	C/G	1.6631e-05	0.00288362	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272238	CGCCCTCGGAGTGGG[C/G]TGCATCCTTCCTGCA	8924
rs759038266	snp	A/T	1.65031e-05	0.00287251	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28198486	TGATGTGAGAAGAAG[A/T]ACTTGGTGGAGGATA	8924
rs759047370	snp	C/T	4.94189e-05	0.00497062	intron-variant	HERC2	GRCh38.p7	15:28141643	CGCCTACAATACACA[C/T]CAAGTGAGCATTTGC	8924
rs759048108	snp	A/C	1.64746e-05	0.00287002	missense	HERC2	GRCh38.p7	15:28169551	TGGCCAGATTTCCAT[A/C]CAATGACAAGAGAAT	8924
rs759048214	in-del	-/AA			intron-variant	HERC2	GRCh38.p7	15:28245548	CAAGATGTAGTGTCA[-/AA]AAAAAAAAAAAATAT	8924
rs759063647	in-del	-/G	1.65888e-05	0.00287996	intron-variant	HERC2	GRCh38.p7	15:28167848	CAAGAGTGCACAGTA[-/G]GGGGAAGTTTAAGTG	8924
rs759076217	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28224421	GAGACAGGGTTTCTC[C/T]ATGTTGCCCAAGTTG	8924
rs759108529	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28259207	TCAAGCGATTCTCCT[A/G]CCTTAGCCTCCTGAG	8924
rs759112915	snp	G/T	8.24056e-05	0.00641841	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28214080	CACAAACCCACCCCT[G/T]CGGAAGGCCTTCCCA	8924
rs759122262	snp	A/G	1.65441e-05	0.00287607	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233744	GGGGGAAACATGATC[A/G]GTGTGGTCAAATGGC	8924
rs759145073	in-del	-/CCTTCTTAGAGATGAAGGAA	1.73402e-05	0.00294445	intron-variant	HERC2	GRCh38.p7	15:28177168	TACAGTCAATCTGTC[-/CCTTCTTAGAGATGAAGGAA]AAAAGACATCTATAC	8924
rs759150665	snp	A/C	1.67691e-05	0.00289556	intron-variant	HERC2	GRCh38.p7	15:28113556	TGCAGGGCAGCCCCA[A/C]CTGGGGGTCGGCATA	8924
rs759177870	snp	C/T	4.10652e-05	0.00453111	intron-variant	HERC2	GRCh38.p7	15:28132054	CCCTGGGGGCCCGAC[C/T]GCGGTGAGCTGGGAG	8924
rs759193685	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28183364	ATAGGCCTGCACCAT[C/T]ATGCCCAGCTAATTT	8924
rs759217095	snp	C/G	0.000281161	0.0118533	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28245978	CAACAGGCCACCCAG[C/G]AGAGGTACAGCTCCA	8924
rs759217101	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28159767	CAGCTTTGTTCCATT[C/G]CTGGTGAGGAGCTGC	8924
rs759221429	snp	C/T	1.64898e-05	0.00287135	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28198703	CTCTGTCCAGCTTGA[C/T]GACTTTGCCAACATC	8924
rs759242196	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28268914	GCTTTAATGAAAACA[C/T]GCCACGTCCCAATTT	8924
rs759242704	snp	G/T	0.00542768	0.051811	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28255921	GACTCCAACCCTCCA[G/T]CAGCCATCAAGCTGC	8924
rs759243796	snp	A/G	8.2741e-05	0.00643146	synonymous-codon	HERC2	GRCh38.p7	15:28113627	GGGAACAGGCACAAC[A/G]CGGGCCATTCCTTCC	8924
rs759244436	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28282851	ACAGAAGAATCATTC[A/G]AACTAGGGAGGCGGC	8924
rs759245537	snp	A/G	3.34851e-05	0.00409163	intron-variant	HERC2	GRCh38.p7	15:28228447	GACATTTCTTGTGAT[A/G]GATACAAGAATAAAC	8924
rs759246413	snp	C/G/T	8.27895e-05	0.00643341	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28191976	CTTTCCTTGCGACCC[C/G/T]GATGACTGCCAGCAG	8924
rs759246983	snp	A/C	3.4574e-05	0.00415762	intron-variant	HERC2	GRCh38.p7	15:28168361	CTAGACACAAAGTAG[A/C]CACCTTTTCCTTTCT	8924
rs759247079	snp	A/C/T			intron-variant	HERC2	GRCh38.p7	15:28150187	CACGAAAAAAACGCA[A/C/T]GCGGCTGCTAACCGA	8924
rs759258781	snp	A/G	1.69562e-05	0.00291167	intron-variant	HERC2	GRCh38.p7	15:28169683	AATAAAATTTGCATT[A/G]TTTTTAAAATCACAG	8924
rs759261532	snp	A/G	6.59565e-05	0.00574229	intron-variant	HERC2	GRCh38.p7	15:28121299	GGTACCCACGAAAGC[A/G]TCACTTCTAAGGCTG	8924
rs759263561	snp	C/T	2.01526e-05	0.00317425	missense	HERC2	GRCh38.p7	15:28132123	GCACTTTACAGCCAT[C/T]GCTGCCTCCCCGGCC	8924
rs759277171	snp	A/G	1.66424e-05	0.0028846	intron-variant	HERC2	GRCh38.p7	15:28256000	CATTGCCTGAAACTG[A/G]AATAGAAAGTGTGTG	8924
rs759278882	snp	A/C/G/T	0.000188035	0.00969466	intron-variant	HERC2	GRCh38.p7	15:28191264	AGAAAAACAAAAAAA[A/C/G/T]CACATTCTCAGTTAG	8924
rs759283691	snp	C/T	1.68153e-05	0.00289955	intron-variant	HERC2	GRCh38.p7	15:28212433	TTTCATCAAGAAGCA[C/T]CATGTACTGACCTGC	8924
rs759284632	snp	G/T			intron-variant, upstream-variant-2KB	HERC2, LOC107987422	GRCh38.p7	15:28318122	AAGAATAAAAAGCTT[G/T]TAAGGTATCATATAT	8924
rs759288574	snp	A/G	1.78624e-05	0.00298846	intron-variant	HERC2	GRCh38.p7	15:28152861	GGACATGAATGAGGG[A/G]GCCAACAGCCCCACA	8924
rs759292224	in-del	-/G			intron-variant	HERC2	GRCh38.p7	15:28189630	GTAACTACTGTGAAT[-/G]TACTACGTATTTCAA	8924
rs759326654	snp	C/T	4.37197e-05	0.00467525	intron-variant	HERC2	GRCh38.p7	15:28260994	GAAGAGGGATGCAGA[C/T]GCAGCTTCAAGCCTA	8924
rs759330534	snp	C/T	0.000115413	0.00759562	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28179017	ACAGGCATACACCTT[C/T]CCTTCCACAGTCACT	8924
rs759337602	snp	A/T	1.64928e-05	0.00287161	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28228360	GGTCCCCAGGCTCGG[A/T]CCTGACGGGTTCTCA	8924
rs759342319	snp	A/G	3.37456e-05	0.00410751	synonymous-codon	HERC2	GRCh38.p7	15:28163106	CACCTGTGGGTAGGC[A/G]GTCCCCATGCCGGAA	8924
rs759352151	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28249229	GCCTGCATTGCCACA[A/T]CTGCCTTGCAAGTCC	8924
rs759353462	snp	C/T	4.94222e-05	0.00497078	missense	HERC2	GRCh38.p7	15:28121396	GACGATCGCGTACCA[C/T]AGTTGCTTGTACTAC	8924
rs759357087	snp	A/G	5.33016e-05	0.00516217	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28202212	CGTGACCTGTATGTC[A/G]GAGTGGTCCAGCAGC	8924
rs759361316	snp	C/T	1.6998e-05	0.00291525	intron-variant	HERC2	GRCh38.p7	15:28115562	CATTCAGGACACAAG[C/T]GACAGAGGACACTTC	8924
rs759377270	in-del	-/ATA	1.83474e-05	0.00302876	cds-indel, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28269262	CAGCGTGTCACTATT[-/ATA]ATAGGCCTGTGTGTA	8924
rs759380051	in-del	-/AA			intron-variant	HERC2	GRCh38.p7	15:28296690	GAATTACTGATACAT[-/AA]AAAAAAAAAAAAAAA	8924
rs759394376	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28236573	TGGGATTACAGGCAT[A/G]AGCCACTGCCTGGCT	8924
rs759396181	snp	A/C	1.64732e-05	0.0028699	synonymous-codon	HERC2	GRCh38.p7	15:28135579	TCCTCCAGAGTTCAC[A/C]GCTACTTTCTTAATA	8924
rs759400744	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28120214	GTGACTGACGTACAG[C/G]TTAGCATTAAACACT	8924
rs759429166	snp	C/T	1.68094e-05	0.00289904	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233146	CTTTTACATTCTTAC[C/T]TCTCTTTTTCCTTCG	8924
rs759440215	snp	C/T	8.25975e-05	0.00642588	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	HERC2	GRCh38.p7	15:28299436	TCCGTTCTGGGTTGA[C/T]TCTGTTCCAGTGTAT	8924
rs759440822	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28290128	CTAAATAATCAGGTA[C/T]GGGTAAGATCTCTGA	8924
rs759442055	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28227978	GTGAGGACTGATGGC[C/T]AAATGGTGTGCATTT	8924
rs759446433	snp	C/T	1.83974e-05	0.00303288	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28274395	CTCGGGAAGTGCTCG[C/T]AGGGCGTCCAGGGAC	8924
rs759447062	snp	C/T	1.65384e-05	0.00287557	intron-variant	HERC2	GRCh38.p7	15:28196458	ACCATAAAAATAACT[C/T]ACGTAACCCCAGGAT	8924
rs759455273	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28161887	TGGTTTTTAAATCAC[C/T]AGGGAAAAGATGAGT	8924
rs759460544	snp	A/T	4.94197e-05	0.00497066	synonymous-codon	HERC2	GRCh38.p7	15:28143915	TCCAAGCAGCCTATT[A/T]ATGTTAATTGACTGC	8924
rs759472074	in-del	-/CT			intron-variant	HERC2	GRCh38.p7	15:28236896	CCTGGCCCTCTCCCA[-/CT]CTTAATGGCACTTAC	8924
rs759480517	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28275118	ACCAATGGTTTTCTT[C/G]AAGTGACAGGATCAC	8924
rs759497952	snp	A/G	1.66405e-05	0.00288443	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28211079	TGGTGGGAGAGCAGC[A/G]CCCGACCTGCTTTCA	8924
rs759498619	snp	A/G	4.95593e-05	0.00497767	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28175620	CCGCACGTGCACGTC[A/G]GAGCCGTGGCCCAAT	8924
rs759498987	snp	A/G	1.95808e-05	0.0031289	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28269249	CCCAGAACACTCACC[A/G]GCGTGTCACTATTAT	8924
rs759499767	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28160690	GCTTCCCAGGTGAGG[C/T]GATGCCTCGCCCTGC	8924
rs759503905	snp	A/T			intron-variant	HERC2	GRCh38.p7	15:28197613	AAAAATTATCCAGGC[A/T]TGGTGGTGGGCACCT	8924
rs759533791	snp	C/T	3.29734e-05	0.00406025	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28246884	CAAGGAACCAACACC[C/T]ATTAGCTCTGGACCT	8924
rs759536330	snp	C/T	1.76696e-05	0.00297228	intron-variant	HERC2	GRCh38.p7	15:28299385	CCAAATAAAAAACAC[C/T]AGTTAAAGGCCCTTA	8924
rs759542663	snp	A/T	1.65002e-05	0.00287225	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28260871	CGCAAGGTGTCAAAG[A/T]GCTGGCACTGGTCGT	8924
rs759548631	snp	A/G	3.29516e-05	0.00405891	intron-variant	HERC2	GRCh38.p7	15:28144018	AGAGAGAAAGTATCA[A/G]AAGTCTGATGGTTTC	8924
rs759560628	snp	C/G			intron-variant	HERC2	GRCh38.p7	15:28288751	TACTAGGGAGGCTGA[C/G]GCAGGAGACTCGCTT	8924
rs759566054	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28276115	ACTTAAACCTGGGAG[-/A]ACAAAGGTTGCAGTG	8924
rs759567478	snp	C/T	1.64781e-05	0.00287033	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28236991	CTCGACAGGAGACAG[C/T]GGTGTGCTCATTGCC	8924
rs759567489	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28129938	GCGCCACCATGCCCA[A/G]CTAATTTTTGTATTT	8924
rs759585667	snp	A/G	2.67269e-05	0.00365551	intron-variant	HERC2	GRCh38.p7	15:28221979	GTACAGAACTGTGCA[A/G]AAGATAACTAATGTG	8924
rs759586689	snp	A/G	4.9788e-05	0.00498914	intron-variant	HERC2	GRCh38.p7	15:28175691	GGAGAGTTACAATAC[A/G]GTTATGGTCTGACAA	8924
rs759588691	snp	A/G	1.6483e-05	0.00287076	intron-variant	HERC2	GRCh38.p7	15:28268635	AAGAAGGAAAAATAC[A/G]AAGAAAAGTAGTCAT	8924
rs759589022	snp	C/T	0.000767754	0.0195777	intron-variant	HERC2	GRCh38.p7	15:28272410	GAAAAGATATTTATT[C/T]TAGTAAAAACAGATT	8924
rs759612895	in-del	-/G			intron-variant	HERC2	GRCh38.p7	15:28194605	CAAAACAAAAAAACA[-/G]GCATGAGCCACTGTG	8924
rs759620286	snp	A/C			intron-variant	HERC2	GRCh38.p7	15:28240870	GAGGTAGACCCTTAC[A/C]TTACGCCACACACAA	8924
rs759626793	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28279719	TCAGGTGGCTGAGGC[A/G]GGAGGATCACTAGAG	8924
rs759638358	snp	G/T	1.84619e-05	0.00303819	intron-variant	HERC2	GRCh38.p7	15:28135715	AAGAAAAAGCAATAG[G/T]AACATCAGTTTTTAA	8924
rs759656981	snp	C/T			missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28257129	GCGGGGGCCAGTCCG[C/T]GGAACCATCCATCCC	8924
rs759661460	snp	C/G	3.31785e-05	0.00407286	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28196569	CCATTGGCACTGAAA[C/G]CTAGGACAGAACAGA	8924
rs759664045	snp	C/T	3.32497e-05	0.00407722	missense, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28213968	AAGTAGTCCTCTAAC[C/T]GGGCCTAGTGCAGAC	8924
rs759678724	snp	C/G	1.66095e-05	0.00288175	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28272362	CCACAGCTGAAGCAA[C/G]AACAGGATGGCAGAC	8924
rs759683313	in-del	-/T			intron-variant	HERC2	GRCh38.p7	15:28171282	ACTGAACATACTATG[-/T]TAATATGTAACAACT	8924
rs759688327	snp	C/G	3.47331e-05	0.00416717	intron-variant	HERC2	GRCh38.p7	15:28280042	ATTTAACTGGCATCA[C/G]GATTCTTTCTTCGCT	8924
rs759694303	snp	A/G	4.94376e-05	0.00497156	synonymous-codon	HERC2	GRCh38.p7	15:28146268	GATCCTGTTGACGCC[A/G]TCCATGACTGTGAGA	8924
rs759694619	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28264901	CTCTGACAAGGTCTG[C/T]CCCGTCAATGGCAGC	8924
rs759712371	snp	C/G/T	3.29556e-05	0.00405918	missense, synonymous-codon	HERC2	GRCh38.p7	15:28125156	GGTTCCGTCTCCCAG[C/G/T]TGTCCCTCATCATTG	8924
rs759721067	in-del	-/AAG	1.97202e-05	0.00314002	intron-variant	HERC2	GRCh38.p7	15:28246085	CATTTAAGAAATAAT[-/AAG]ATTTAAATAAGTATT	8924
rs759744574	in-del	-/AGTAAGAGTTCATCTTTTCC			intron-variant	HERC2	GRCh38.p7	15:28237571	TCAAACTCTGAAAAA[-/AGTAAGAGTTCATCTTTTCC]AGTCACAGAAGATAT	8924
rs759750750	in-del	-/C	1.672e-05	0.00289132	frameshift-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28220568	AGTTGGTGCTGCCTG[-/C]TGTCCCACTGGACTC	8924
rs759770364	in-del	-/A			intron-variant	HERC2	GRCh38.p7	15:28158465	TAGTTCTTCTTATTG[-/A]AATTGATCCCTTTAC	8924
rs759776491	snp	C/T	0.000291742	0.0120742	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256233	CCAGGGTCACCACCG[C/T]CTGCTTCAGGCTGTT	8924
rs759781745	snp	A/G	1.65064e-05	0.00287279	missense	HERC2	GRCh38.p7	15:28142257	TCAAGAAACAGACGG[A/G]GCAACGGTGTTCTTT	8924
rs759782475	snp	C/T	1.64969e-05	0.00287196	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28186708	TTTACAATCGATTCC[C/T]GAGCTCCTGCACTGC	8924
rs759784789	in-del	-/TTTT			intron-variant	HERC2	GRCh38.p7	15:28179238	TCTACAACAGAATTT[-/TTTT]AACAAAAAAAAAAGA	8924
rs759799916	snp	C/G	1.7968e-05	0.00299728	intron-variant	HERC2	GRCh38.p7	15:28117197	AGGCCGCTGCCGCAG[C/G]AGGAAGCACACAGTC	8924
rs759803222	snp	A/G	1.65927e-05	0.00288029	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233546	CCTGCATGAACTAAA[A/G]ATAATGCCACATGAC	8924
rs759840275	snp	C/T	1.64754e-05	0.00287009	missense	HERC2	GRCh38.p7	15:28114618	ACCACCAACCTATAG[C/T]TTATCGCCAGCCGCA	8924
rs759852860	snp	C/G	1.65715e-05	0.00287845	intron-variant	HERC2	GRCh38.p7	15:28229423	ATTTTGTTGCCATAG[C/G]TACCTTAATTAAGAA	8924
rs759872038	snp	A/C	4.94523e-05	0.00497229	intron-variant	HERC2	GRCh38.p7	15:28265748	TTCAAACAGATAGGA[A/C]GGCGGTTACTAAGTC	8924
rs759873703	snp	A/C	1.78599e-05	0.00298824	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256179	GCAGCACGGCCTGGG[A/C]GGCCGACTGCACGGT	8924
rs759875927	snp	C/G	1.65261e-05	0.0028745	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28177076	CCCACAGGCGATATC[C/G]CGGATACGCTTGGTT	8924
rs759877922	snp	A/C	1.69885e-05	0.00291444	intron-variant	HERC2	GRCh38.p7	15:28190930	CCCTTGTCATCTGTA[A/C]ATCATCCAAATGGAA	8924
rs759878586	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28254993	AAAGGAGAACATATG[C/T]TCACTAAAGTACTTG	8924
rs759886060	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28116307	CAACCTCCGCCTCCC[A/G]GGTTCAAGCAATTCT	8924
rs759889002	snp	C/T	1.65255e-05	0.00287445	synonymous-codon, nc-transcript-variant	HERC2	GRCh38.p7	15:28238714	GTTCTCCAAATCAGC[C/T]TTGCGTATAAGTGTC	8924
rs759901732	snp	C/T	1.64749e-05	0.00287005	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28201493	ACAGCATAATCATCA[C/T]TACTCAAGAAATCAG	8924
rs759904083	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28277887	GGCTCCATACCAAAA[C/T]CCTAGGATGCTCAAG	8924
rs759907432	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28139316	CACTCTCTCTTGCTG[A/G]TGCTCCCTCCTGCGC	8924
rs759925957	snp	A/C	1.64732e-05	0.0028699	missense	HERC2	GRCh38.p7	15:28114683	GTGCTTGGAGCTCAA[A/C]TGAATGTCCTGGCCA	8924
rs759933701	snp	C/T	1.6908e-05	0.00290753	synonymous-codon, upstream-variant-2KB, nc-transcript-variant	HERC2	GRCh38.p7	15:28215717	GAGGGCGCCGCATAC[C/T]TGCGGCGTGAGAGCG	8924
rs759940759	snp	A/C/T	6.86336e-05	0.00585773	synonymous-codon, missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28233467	TGCTTGGTAGACAAC[A/C/T]CTACAAACATCCACC	8924
rs759959860	snp	C/T	3.29489e-05	0.00405874	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28265661	ATCCCCACTCCCACA[C/T]GCCACATCGATGACC	8924
rs759964244	snp	A/G	1.65059e-05	0.00287275	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28270708	ACCTTATGAGATGTC[A/G]GAGAGCTACACAGCG	8924
rs759967510	snp	C/T	5.23464e-05	0.00511571	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28215781	CGGTGTTGCTCCCTG[C/T]ACACCAGCCTGTTTG	8924
rs759972326	snp	C/T			missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28238662	TATCATACACCTTCC[C/T]GTCAATCACAGTCCA	8924
rs759989243	snp	G/T	1.68335e-05	0.00290111	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28238605	GTGTAATCTTACCAA[G/T]AATACTATTTCCTGT	8924
rs759989490	snp	C/G	1.6638e-05	0.00288422	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28192124	TTCAGCTGTTTTCCA[C/G]AACGGCCACAAAATA	8924
rs759993755	snp	C/G	2.21668e-05	0.0033291	intron-variant	HERC2	GRCh38.p7	15:28142423	AATGACAAACTCAGG[C/G]AAACTCAGAAATGCA	8924
rs759998605	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28177684	GCTTCCTGGGACATA[C/T]GTGCCAAATAGGTGA	8924
rs760000210	snp	A/G	3.29614e-05	0.00405951	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28270738	GGAGGCATACAGGGC[A/G]TAGCCAGACGGTCTA	8924
rs760015880	snp	C/T	0.000321155	0.0126678	utr-variant-3-prime	HERC2	GRCh38.p7	15:28111721	CAGCGAGCGCTCTGC[C/T]GCCTGGCTCAGGCTC	8924
rs760024594	snp	C/T	1.64784e-05	0.00287035	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28174514	GACCCACAAGCCACG[C/T]GTGTGATCTTCTGGC	8924
rs760037354	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28273567	TTGTGAAATCAACTC[C/T]AAGCCTATGCTCAGG	8924
rs760039855	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28227758	CCCAAATGTCCATCA[A/G]CAGATAAATGAACAA	8924
rs760045824	snp	C/G	6.72653e-05	0.00579898	intron-variant	HERC2	GRCh38.p7	15:28265579	AGCTGCCATGCGTGT[C/G]CTCGTGGGCCTGTCC	8924
rs760046083	snp	C/T	5.21934e-05	0.00510823	missense, nc-transcript-variant	HERC2	GRCh38.p7	15:28206320	GCTGCAAGAGGATCA[C/T]GGGGGGCTGCGGCCC	8924
rs760072627	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28273794	ATTTAAAAACCTTAA[C/T]AAAAATGCATAGCAC	8924
rs760079132	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28168785	TGTTTACTCTGGATC[C/T]TATTTATTTGAAAAA	8924
rs760079208	snp	C/T	1.65042e-05	0.0028726	synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28254435	TTTATCCAGTGGAGT[C/T]CTGCTTCTATGAAAT	8924
rs760084686	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28178681	TATAGACTCTTTCTC[A/G]GAAAAACAGCCTACT	8924
rs760088226	snp	A/C	1.70592e-05	0.0029205	intron-variant	HERC2	GRCh38.p7	15:28274265	CAGCTGTCTGCGTGC[A/C]GAAGGCAAGAAAGGA	8924
rs760094386	snp	A/C/G	0.000135541	0.00823127	missense, synonymous-codon, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28256093	CCCAGGCCCACCTGC[A/C/G]CAGGGCAGGAGAGCA	8924
rs760094924	snp	C/T	3.3195e-05	0.00407387	missense, intron-variant, nc-transcript-variant	HERC2	GRCh38.p7	15:28257218	ACCACAAAAGGGACA[C/T]GGAGGCCAATGGACC	8924
rs760097178	snp	C/G	0.000229981	0.0107209	intron-variant	HERC2	GRCh38.p7	15:28182356	CACGAGGTGTGGCTG[C/G]TGCCGAGTGCCCCAC	8924
rs760100333	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28244819	ACCTCTTGTTTTAAG[C/T]TCCCATGTTAGGGGG	8924
rs760109305	snp	C/T			intron-variant	HERC2	GRCh38.p7	15:28140646	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA	8924
rs760127691	snp	A/G	1.6501e-05	0.00287232	missense	HERC2	GRCh38.p7	15:28116781	ACGATCAGCAGGGGC[A/G]TGAGTCCGTTCTGCA	8924
rs760128455	snp	A/T	1.71452e-05	0.00292785	intron-variant	HERC2	GRCh38.p7	15:28293031	CTATCATCTGCAGAA[A/T]TAAAAATTTTTTAAT	8924
rs760142778	snp	A/G			intron-variant	HERC2	GRCh38.p7	15:28290018	AGGCGGGGTTCAAAG[A/G]GGACGGACCTGCAGG	8924
rs760153487	in-del	-/TC			intron-variant	HERC2	GRCh38.p7	15:28133847	CCATTGATGTATCTG[-/TC]TCTCTCTTTTTGCCA	8924

Page 1 | 2