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

HERC4

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs138206673	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67955856	ACTAAGTGATCATGG[C/T]ATGTGCTCACGAACC	26091
rs138251774	snp	C/T	0.00438332	0.0466095	intron-variant	HERC4	GRCh38.p7	10:68001819	CATATGATATTTGTC[C/T]TTTTGTGTCTTTCAC	26091
rs138255633	snp	A/G	0.00874735	0.0655527	intron-variant	HERC4	GRCh38.p7	10:68062473	TAAAGGACTACCATC[A/G]GCCGGGCACGGTGGC	26091
rs138315876	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68059210	GAACTTGAGTATATA[C/T]TTGTCTACTTCCCTC	26091
rs138359505	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68036661	AACTACATGCCAATA[C/T]TCAAATACACCACTT	26091
rs138365555	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67943792	ACCTTTCTTGAAAAC[C/T]CAAAGGATAAAAAAA	26091
rs138376426	snp	C/G	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:67974950	AATCCCAGAACCTTG[C/G]GAGGCTGAGGTGGTT	26091
rs138377827	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	HERC4	GRCh38.p7	10:68076059	TTGCTAGAATGAATA[G/T]TCAGTACCTAGAAGA	26091
rs138404600	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069397	CAGAAAAGCCAGTAG[C/T]GATAGAAAAGGACAT	26091
rs138435561	snp	A/C	0.00716266	0.059414	intron-variant	HERC4	GRCh38.p7	10:68064630	AAAAACTAAATTGAT[A/C]TATATATGTTCATTG	26091
rs138439185	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68008200	ATAGTTGGGGTAGAG[A/G]TGATGCAAGCACTCC	26091
rs138556630	snp	C/G	0.0228947	0.104514	intron-variant	HERC4	GRCh38.p7	10:67926838	ACCATTCACTAAACT[C/G]TTTTTCACTGTATTA	26091
rs138558717	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67949753	ATCACATAGCTGGGC[A/G]CGGTGGCTCACGCCA	26091
rs138596921	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68001462	ATGCTGGGGGCCATG[C/G]GTTTAACCTCTGGAT	26091
rs138612315	snp	A/G	0.0115144	0.0749975	intron-variant	HERC4	GRCh38.p7	10:67981890	AGGTTGCAGTGAGCC[A/G]AGATCAGGCCACTGT	26091
rs138680161	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68032143	ACCAATGAAAAACTT[C/T]ACATTAACATGACTG	26091
rs138696719	snp	C/T	0.000333778	0.0129142	missense, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68038116	AGTGCAAGTGAATGA[C/T]AGTAACCACAAGCAA	26091
rs138714641	snp	C/G	0.0941369	0.195465	intron-variant	HERC4	GRCh38.p7	10:67931559	CCTCCCAAGTAGCTG[C/G]GATTACAGGTGTGTG	26091
rs138731358	snp	A/T	0.0174175	0.0916809	intron-variant	HERC4	GRCh38.p7	10:68009075	AAAATACTAAAAAAA[A/T]TAGCCAGGTGTGGTG	26091
rs138771419	snp	C/G	0.0119091	0.0762411	intron-variant	HERC4	GRCh38.p7	10:67983589	TAGAGACCATCCTGG[C/G]TAACACGGTGAAACC	26091
rs138922220	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68019994	CCCCACCTTTCATTT[C/T]TTCCTTGTTTCTTTG	26091
rs138953072	in-del	-/A	0.143959	0.226396	intron-variant	HERC4	GRCh38.p7	10:68018221	AAACACAAAGCTGTT[-/A]AACTAGAAAAAAAAA	26091
rs138960073	snp	C/T	0.0115144	0.0749975	intron-variant	HERC4	GRCh38.p7	10:68063240	TTTTAGTTGGAGTCT[C/T]GCTCTGTAACCCAGG	26091
rs138975163	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67931133	GGGACTATAGGCGTG[C/T]GACACTATGCCCAAA	26091
rs138977338	in-del	-/G			intron-variant	HERC4	GRCh38.p7	10:67942269	TGTGAGGATTACATG[-/G]GGATAATATACGTTA	26091
rs138986645	snp	C/T	0.000399281	0.0141238	synonymous-codon	HERC4	GRCh38.p7	10:67956935	TGCTTGGGCATCAAA[C/T]ACAAATGGATATGTA	26091
rs139025183	snp	C/T	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:68051261	AATCATTATAGTCAA[C/T]AGTAATTCTGAAATA	26091
rs139040091	snp	C/T	0.00517822	0.0506191	intron-variant	HERC4	GRCh38.p7	10:67969514	AAGAGCCTCTCTCAA[C/T]GGTACAAGGAATTAG	26091
rs139043842	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68061488	CAGTGAGCCGCAATC[A/G]CGCCACTGCACTCCA	26091
rs139052745	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67966877	TTTTATTTTTTGAGA[C/T]GGAGTCTCACTCTGT	26091
rs139090520	snp	A/T	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:68005004	ATCCAGTTTTCCCAG[A/T]ACCATTTATTGAAAA	26091
rs139169634	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68057772	AGTGCAGTGGTGCAA[C/T]CACTGCAACCACCAC	26091
rs139183973	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67962260	AATTTATCTATGGCC[A/T]GCTTGATAACTATAC	26091
rs139214223	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67982198	TGCGAGGAATCATAT[C/T]ACCTGACTTCAAATT	26091
rs139233393	snp	A/C	0.00676609	0.0577691	intron-variant	HERC4	GRCh38.p7	10:67946848	GGAGGTAGATGTTGC[A/C]TTGAGTCAAGATTGA	26091
rs139249115	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68039287	CACCATCGCACTCCA[A/G]AATGGGCGATAGAGT	26091
rs139254919	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67938986	CACATCCCTTTGCTG[C/T]CTTAATGAAATTGTG	26091
rs139319705	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67934865	TTTTTTCCACTTCTC[A/G]TGCTTTCAATCTTGA	26091
rs139337813	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67951639	CAGCTCTCACAAATG[A/G]TGTCACTTTTCAATC	26091
rs139370130	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68003871	TTTCTTTTGGGTGTA[C/T]ACCCAGCAATGGATC	26091
rs139508405	snp	A/C/T	0.00755907	0.0610114	intron-variant	HERC4	GRCh38.p7	10:67982855	ACAGGCGGCAGGGTG[A/C/T]GGTGGCTCATGCCTG	26091
rs139548183	in-del	-/A	0.0678174	0.1712	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922723	TATTAGAAGATGGTC[-/A]AAAAAAATCCATGGT	26091
rs139549622	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67984991	AAGAAACGCAACCAG[C/T]GTTTGCAGTTTGTAT	26091
rs139603881	snp	C/T	0.0189856	0.0955633	intron-variant	HERC4	GRCh38.p7	10:68066129	GTACACCTCCTCTAT[C/T]AGATTCTTTCATACA	26091
rs139640103	snp	A/T	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:67985426	CAAAATAAAACCTAT[A/T]TAAGTTTGATTATAA	26091
rs139661723	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68070959	TCCTAGGCTCAAAGT[A/G]CATGGCACATCATGT	26091
rs139662542	snp	C/T	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:67933915	AAAGCATCTAAGTAG[C/T]GGAATTAGGATTATA	26091
rs139687526	snp	A/C	0.000944148	0.0217067	intron-variant	HERC4	GRCh38.p7	10:67991240	AATCATAGAATCAGA[A/C]ATTTAATTGTTTACC	26091
rs139743497	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68071548	AATCTCAACCTGAGG[A/C]AGCATTCCAAGCTAA	26091
rs139781632	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67941840	TTTGTATTTTTAGTA[A/G]AGACTGGGTTTCACC	26091
rs139783077	snp	A/G	3.30071e-05	0.00406232	synonymous-codon	HERC4	GRCh38.p7	10:67956938	TTGGGCATCAAATAC[A/G]AATGGATATGTACAG	26091
rs139797574	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67923414	CCATTGCCAAAACAT[C/T]TTGAGAGCCCTTTTT	26091
rs139803461	snp	C/T	0.0505692	0.150756	upstream-variant-2KB	HERC4	GRCh38.p7	10:68076985	ACAAAATTAGCCGGG[C/T]GTGGTGGTGCATTCC	26091
rs139805453	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68017160	AATGTACAGTTGAGT[C/T]TGCCTTCTTGTGTAT	26091
rs139807125	snp	A/C	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67960138	AACTAGAGGTCACTA[A/C]GGGAGCAGGATGTGA	26091
rs139811317	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68054212	AAAGATACTGTAGAG[C/T]TCCATTCTTACACAT	26091
rs139879527	snp	A/C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67965986	AAAGACTTAGCTGCA[A/C/T]AAAAAGATGTACGCA	26091
rs139884964	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68060618	CTTCACCCTATACAA[C/T]GCAGTACCAACTTAT	26091
rs139893117	snp	C/G	0.00517822	0.0506191	intron-variant	HERC4	GRCh38.p7	10:67997026	AAATCATTATGACTT[C/G]AAGAACCCTCTGAGA	26091
rs140003107	snp	C/T	0.00676609	0.0577691	intron-variant	HERC4	GRCh38.p7	10:67935982	CCCTTCTCTTTGTTT[C/T]AATGTCTTCAAGGGA	26091
rs140022071	snp	A/C	0.00398564	0.0444627	intron-variant	HERC4	GRCh38.p7	10:68028998	CAATAAAGCGAGACA[A/C]CATCTCTACAAAAAA	26091
rs140068391	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68043560	GTGCTTCACGCCTAT[A/C]ATCATGAGTACTTTG	26091
rs140092482	snp	C/T	0.00874735	0.0655527	intron-variant	HERC4	GRCh38.p7	10:67940711	CGGTCTCCCAAAATG[C/T]TAGGATTACAGGTGT	26091
rs140094494	snp	C/T	0.00914312	0.0669923	intron-variant	HERC4	GRCh38.p7	10:68035245	GCAACCTCCATCTCC[C/T]GGGTTCAAGTGATTC	26091
rs140107771	snp	A/C	0.00676609	0.0577691	intron-variant	HERC4	GRCh38.p7	10:67964698	TTTACTAAACTCTCT[A/C]TGATCTGGCCCCTGC	26091
rs140140536	snp	A/G	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:67959531	ATTCCTCAGACTTTA[A/G]GACTTTAAAATCTCA	26091
rs140225738	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68052584	GACAAGTCCAGGTTC[C/T]TGTTGCAAAATATTA	26091
rs140225788	snp	A/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67992887	ACGATCCCACAAGCA[A/T]AAGCAGCATTTGGTG	26091
rs140252109	in-del	-/AT			intron-variant	HERC4	GRCh38.p7	10:68027992	TTTTAATTATATATA[-/AT]TATATATATAATAAA	26091
rs140290933	snp	A/C/T	0.0123082	0.0775209	intron-variant	HERC4	GRCh38.p7	10:67955562	AGATTACTTGAGGTC[A/C/T]GGAGTTCAAGACCAG	26091
rs140299294	snp	A/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67973203	GAATGGAAAACATTT[A/T]AAAAAAAAAGGTTTG	26091
rs140305205	snp	C/T	0.0209421	0.100162	intron-variant	HERC4	GRCh38.p7	10:68007683	ATCTGCATTAGTGGA[C/T]ACTCCAAGCCCAGTA	26091
rs140318337	snp	A/G	0.067446	0.170804	intron-variant	HERC4	GRCh38.p7	10:67977727	TGGCTCACGCCTCTA[A/G]TCCCAGCACTTTGGG	26091
rs140329947	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68049480	CAGCCTAGGTGGTGG[A/G]TGTCTGTAATCTCAC	26091
rs140377295	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67994968	GTGCTGGGATTACAG[A/G]TGTGAGCCACTGCAT	26091
rs140377446	snp	C/T	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:68055560	TTAGCACTTTAATTA[C/T]TTAATCTTATTTAAT	26091
rs140451970	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68015444	AGTCGTTCTGTTTAG[C/T]GACATAAGCTAACTA	26091
rs140497661	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68021867	AAAAAAAAATCTCTG[C/T]ATGCAGATGATATGA	26091
rs140517278	snp	A/G	4.98434e-05	0.00499192	synonymous-codon	HERC4	GRCh38.p7	10:67954730	AGCATCTTCTCCAAC[A/G]AATATAACCTAAAAT	26091
rs140522508	snp	C/T	0.00874735	0.0655527	intron-variant	HERC4	GRCh38.p7	10:68072765	GAAATACATAACTTC[C/T]ACTTTGCTTTTAAAG	26091
rs140590467	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68068753	ATATTCTTTTACCTT[C/T]TAAATGTAGCAAAGG	26091
rs140625195	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67930212	AAGTTGTTTCCAGTT[C/T]TTCACTCATTTGCAA	26091
rs140638967	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67936723	GGCAGTTATTTTGAA[A/G]CCTTTTATTTCTTTT	26091
rs140644219	snp	A/G	0.00597247	0.0543191	intron-variant	HERC4	GRCh38.p7	10:68025987	TATATATAATTTCAC[A/G]AAACCTAAAAACGGT	26091
rs140675793	in-del	-/A	0.160609	0.233472	intron-variant	HERC4	GRCh38.p7	10:67973202	GAATGGAAAACATTT[-/A]TAAAAAAAAAAGGTT	26091
rs140706117	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67994536	CTCCCAAGTTCAAGC[A/G]ATTGTCCCACCTCAG	26091
rs140715305	snp	C/T	0.00993419	0.0697739	intron-variant	HERC4	GRCh38.p7	10:68047445	AGACAAGCCATAGCC[C/T]AGGGGAAAACATTTG	26091
rs140793942	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67942920	TTTTCTTTTGAGTTT[A/C]AAATGACAACTTGCT	26091
rs140802600	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67955201	CTGAAACAAGCTAAC[C/T]TCTACCTATTAGTTA	26091
rs140813025	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68049357	GCTAATATTTTATCT[A/G]CATTTTTAAAACTTT	26091
rs140817174	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68001040	CTCCAGGGAGATAAT[A/G]ATCACTAAACCAAAG	26091
rs140842731	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67924089	CCAAACAGAGAAAAG[A/T]GCAATACAGTTGGCC	26091
rs140850588	snp	A/G	0.00914312	0.0669923	intron-variant	HERC4	GRCh38.p7	10:68057173	ACAGTCAAGCACTGT[A/G]TAACAGTGGGTACAC	26091
rs140914390	snp	C/T	0.00953873	0.0683987	intron-variant	HERC4	GRCh38.p7	10:67998864	CTGCCTCAGCCCCAA[C/T]GAGCAGCTGGGACTA	26091
rs140939787	snp	C/T	0.00953873	0.0683987	intron-variant	HERC4	GRCh38.p7	10:67968425	TTGCCCAGGCTGGAA[C/T]ACAGTGGTGTGATCT	26091
rs140959002	snp	C/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68062555	TCAGGAGTTCGAGAC[C/G]AGTATGGTCAACACA	26091
rs141007452	snp	C/T	0.00597247	0.0543191	intron-variant	HERC4	GRCh38.p7	10:67979090	AGAGAGGAACATCTG[C/T]TAAGTTATCAAGACC	26091
rs141042437	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68035882	CCTATGTTCTAAATA[C/T]CCTGAAGTTTTTCTT	26091
rs141051544	snp	A/T	4.96019e-05	0.00497981	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67988712	TGAAGAAAACTGTTG[A/T]AAATTCTTCTTTCAG	26091
rs141077281	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67949103	CTAAAAAATAAAATA[A/T]AATAAAATAAAAATA	26091
rs141087304	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68043812	CAGTGCGAGACTCTG[C/T]CTCAAAAACAAACAA	26091
rs141190346	snp	C/G	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:68023827	AATAAATCAACTTCA[C/G]ATAACTTACAGACCT	26091
rs141192110	snp	C/T	0.00835141	0.0640778	intron-variant	HERC4	GRCh38.p7	10:67987139	TTTAGAATGAGTCCA[C/T]CAAAAAGGTCTTTGA	26091
rs141199852	in-del	-/C			intron-variant	HERC4	GRCh38.p7	10:67930486	TAACTTTTTAAGAAA[-/C]CAGCCACTGTTTCCA	26091
rs141224870	snp	A/G	0.0119091	0.0762411	intron-variant	HERC4	GRCh38.p7	10:68022981	CACAGGAGATAACAT[A/G]TTACACGTATTAAAA	26091
rs141240429	snp	A/C	0.0256215	0.110247	intron-variant	HERC4	GRCh38.p7	10:67931126	GATAGTTGGGACTAT[A/C]GGCGTGCGACACTAT	26091
rs141244713	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67974714	AAGAATTGTTTATAT[A/G]ATTTTCATGTTTTCT	26091
rs141298559	snp	C/T	0.00597247	0.0543191	intron-variant	HERC4	GRCh38.p7	10:68032292	TCAGAGTTAAAGCCA[C/T]TGATAAGACTGTGAT	26091
rs141309259	snp	C/G	0.00636936	0.0560724	intron-variant	HERC4	GRCh38.p7	10:67938694	CTCATGCCTGTAATG[C/G]CAGCACTTCGGGAGG	26091
rs141340509	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68073357	TTGTATTTTTTAAAA[G/T]GTATCATACAGAAAT	26091
rs141398222	snp	A/G	0.00398564	0.0444627	intron-variant	HERC4	GRCh38.p7	10:68019695	GTTAATTTCAACTTC[A/G]GATCTTAGCATGGTA	26091
rs141406021	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67996509	ATGGTCTCTAAGTCC[C/G]TTTCCACTCTTAGCA	26091
rs141454517	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67946568	AAGAAGACAAAGAAG[A/G]TCATTATATAATGAT	26091
rs141461292	snp	C/T	0.00795532	0.062565	intron-variant	HERC4	GRCh38.p7	10:67925870	AGTCATGTGAGTAAG[C/T]CACCTTGGAAGTGAA	26091
rs141514843	snp	C/T	0.0126979	0.078662	intron-variant	HERC4	GRCh38.p7	10:68003306	CTACAGGCCTGCAGG[C/T]GCCTGCCACCATGCC	26091
rs141523125	snp	A/T	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:67926592	CTACACCACTCAGAC[A/T]CATCCTTTCTTCTTT	26091
rs141613140	snp	A/G	0.0170251	0.090679	intron-variant	HERC4	GRCh38.p7	10:67967947	TCTAAATTAAAAGAG[A/G]CTAGAGGAATTCTGG	26091
rs141657078	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	HERC4	GRCh38.p7	10:68075531	TTTGCGAAGACAAAC[C/G]AAGAAGATGTCAACT	26091
rs141664940	snp	A/G	0.00755907	0.0610114	intron-variant	HERC4	GRCh38.p7	10:67981729	TTGGGAGGCCAAGGC[A/G]GGTGGATTACTTGAG	26091
rs141721568	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67989892	TTTTAATTGTTCCTC[C/T]TCCTTTACTTCTTTA	26091
rs141760256	snp	C/T	0.0138799	0.0821421	intron-variant	HERC4	GRCh38.p7	10:68041337	GAATAGGGGAGTAGA[C/T]TTTTAAAAAAATGAA	26091
rs141760333	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67983173	AAAACTACAGTAAGA[C/T]ATCTCACCCCAGTTA	26091
rs141770994	snp	C/T	0.0364509	0.129988	intron-variant	HERC4	GRCh38.p7	10:67984219	GAGGCAGAGAATTGC[C/T]TGAACCTAAGAGGTA	26091
rs141791911	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67985074	AAAAATAATATATTC[A/G]CATAGTAGATAAGGT	26091
rs141792144	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68045100	CCAAGGAGGGCGGAT[C/T]GCTTTAGGTCAGGAG	26091
rs141832778	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:68046683	GTAAATCTTAAAAGA[C/T]AGTCCAGGCGAGGTA	26091
rs141835695	snp	C/T	0.158632	0.232706	intron-variant	HERC4	GRCh38.p7	10:67926267	GGGCATGGTGGCAGG[C/T]GCCTGTAATCCCGGC	26091
rs141878142	snp	C/T	0.000686801	0.0185183	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:67991184	ACCAGAGGAAGAAAA[C/T]GTTCCATCTATCTCA	26091
rs141880530	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67998574	AAAAAGGGGGGGGGG[-/T]ACAGTACTATCCAGT	26091
rs141937506	snp	A/G	0.0178098	0.0926698	intron-variant	HERC4	GRCh38.p7	10:67958323	ATGATCATAAAAACT[A/G]ATTTTACTTCTCTGA	26091
rs141940941	snp	C/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68031678	TATATTTGACAATAA[C/T]GAAGAATAATTATTG	26091
rs141950557	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67975673	CATTCTTAACTCACT[A/G]TATGACTGTCCAATT	26091
rs141997510	snp	A/G	0.0123036	0.0774623	intron-variant	HERC4	GRCh38.p7	10:68038626	GTTTCTTAAGAACCA[A/G]CAGGGATTCTTGTAT	26091
rs142016089	snp	C/G	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:68052702	GTGAAAATTCATATA[C/G]AGTATCATCAACTCC	26091
rs142033941	snp	C/T	0.00557542	0.0525036	intron-variant	HERC4	GRCh38.p7	10:68036649	ACACCCACATAAAAC[C/T]ACATGCCAATATTCA	26091
rs142051189	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67965999	CATAAAAAGATGTAC[A/G]CACCCACATTTATAT	26091
rs142085516	snp	A/G	0.00835141	0.0640778	intron-variant	HERC4	GRCh38.p7	10:68016784	ACCCCCGATCCAACA[A/G]TTACATGAATAAAAC	26091
rs142088977	snp	C/T	0.0256215	0.110247	intron-variant	HERC4	GRCh38.p7	10:67948478	ACCACAATGCAATAC[C/T]ACCTTACTCCCACAA	26091
rs142118011	snp	C/T	0.00517822	0.0506191	intron-variant	HERC4	GRCh38.p7	10:67969735	ACTAGAGGTCTGCAA[C/T]TGCTGGGGGAGGGAG	26091
rs142122704	snp	A/G	0.00755907	0.0610114	intron-variant	HERC4	GRCh38.p7	10:67999511	ATACATCAAAGAAAA[A/G]ACACTTGGGTATAGG	26091
rs142172076	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68017785	TGAGCCACCACGCCC[A/G]GCCTATGTCAATAAG	26091
rs142172335	snp	A/C	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67961236	GAATTTTTAAAATGC[A/C]ATTTCATCATTCTGC	26091
rs142184691	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68061649	TTTGGGAGGCAGAGA[C/T]GGGCAGATCACTTCA	26091
rs142185338	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68020093	CTGTGCATTAGCAGG[A/G]AAAGGTATAGGCTAA	26091
rs142185383	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67965142	ATTTTACCAAATGTT[C/T]GTTGTTCTTGAAATT	26091
rs142186855	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67929556	GAGACAGGGTCTTGC[C/T]TTGCTGCCTATGACA	26091
rs142191960	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68021927	ACACAAAAATTGTTA[A/C]AACTAATAAACTTTG	26091
rs142231582	snp	C/T	8.24504e-05	0.00642016	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:67992219	TATCTCCACAGGAAA[C/T]CTTCCAGAAGGATAG	26091
rs142293022	snp	G/T	0.000153988	0.00877328	synonymous-codon	HERC4	GRCh38.p7	10:67955109	AGGAGACATTCTGCC[G/T]GTGGGCCTGATCAAT	26091
rs142298180	snp	C/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67936374	TACCATATAGCTTAT[C/G]TGAGAATTCTACTTA	26091
rs142319652	in-del	-/AATT			intron-variant	HERC4	GRCh38.p7	10:68065951	CTCATTACAATTTAA[-/AATT]AATTATTGCCTTTTA	26091
rs142398985	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68014781	CTAAGGATGACCCAC[C/T]AATCCACTCTCAGTA	26091
rs142406166	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68016138	GTGTGTGATTATAGT[A/G]TAAAGTGGGGTTCAG	26091
rs142422115	snp	C/G/T	3.29474e-05	0.00405867	missense, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68072964	TTCCATCATCCAGAA[C/G/T]AAACACAGTATGTCT	26091
rs142523834	snp	A/C	0.0134861	0.0810011	intron-variant	HERC4	GRCh38.p7	10:68065673	GAGACCAGCTTGGGC[A/C]AAAGAGTGGAACCCT	26091
rs142538802	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67993878	CTATTCCCATTCCTT[A/C]GTTGACTAATTCTTC	26091
rs142542079	snp	C/T	0.0107246	0.0724382	intron-variant	HERC4	GRCh38.p7	10:68037612	TTCCCCAGTTGCAGC[C/T]ATGAAGAGTTTTTAA	26091
rs142543233	snp	C/T	0.00557542	0.0525036	intron-variant	HERC4	GRCh38.p7	10:67937204	TATGGCAAGTGGCTC[C/T]GAAAAAGAGGAAGGT	26091
rs142543536	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67994065	GTTATCTAGGTTATA[C/T]CAAAAATGAGCTTCA	26091
rs142544726	in-del	-/CT	0.0883596	0.190715	intron-variant	HERC4	GRCh38.p7	10:68004021	CAGCATGTTATTGCC[-/CT]CTTTCAGATAAAAGC	26091
rs142570381	snp	A/G	0.0314385	0.121371	intron-variant	HERC4	GRCh38.p7	10:67939953	TTTTCCCGAGATGGA[A/G]TCTTGCTCTGTCGCC	26091
rs142575625	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68048973	AACAAAACAGTACAA[A/C]CTCTATGAAGAGAAA	26091
rs142640086	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67978938	GTGCCAACTAAAGCA[C/G]ATACAGCTTCTAAGC	26091
rs142686302	snp	C/T	0.0209421	0.100162	intron-variant	HERC4	GRCh38.p7	10:67926975	CTGTACATTATCCGG[C/T]ACACAGTAGAGGCTC	26091
rs142714524	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68056384	CTGAGTTCCTTCTAT[A/G]TGCACCATAGTATTT	26091
rs142719113	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67982121	AACACAATCCTAAAA[C/T]TTACACAGAACCACA	26091
rs142848556	snp	C/T	0.0189856	0.0955633	intron-variant	HERC4	GRCh38.p7	10:68028638	CTAGGACCTTTCACT[C/T]GTTATGGCAAAACAA	26091
rs142940408	snp	C/G/T	0.00319098	0.0398384	intron-variant	HERC4	GRCh38.p7	10:68015868	AGCACTTTGGGAGAC[C/G/T]GAGGCAGGTGGATCA	26091
rs142952211	snp	C/T	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:67942063	ACTGAAACATACTTA[C/T]ACTACTGACACACTG	26091
rs142955574	snp	C/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68035861	GATTAGGTCTAGTAC[C/T]GCTGTCCTATGTTCT	26091
rs142996362	snp	C/G	0.00835141	0.0640778	intron-variant	HERC4	GRCh38.p7	10:67962566	CAGAAAAAGAGAGAT[C/G]ATTAGACATTAGGTA	26091
rs143003395	snp	A/G	0.00676609	0.0577691	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069765	CTTGTGAAGTCAGCT[A/G]GGCACGGTGGCTCAC	26091
rs143005819	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011146	TAGCTCACTGTAAAC[C/T]TTCAACTCCTAAGCT	26091
rs143012471	snp	G/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67957084	TGTTTATTCACTCAT[G/T]TGGTTCTGGAATTAC	26091
rs143083420	snp	C/T	0.00464378	0.0479617	missense	HERC4	GRCh38.p7	10:67932719	CCGCATGAAAAGCAT[C/T]AAATAAGGAAGCCAC	26091
rs143195576	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68007156	CTGTGGGAGTATTTC[A/T]CTCTTTTTTCTTTTG	26091
rs143199207	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68055134	ACCATGTTGCCCAGG[C/G]TGATGGTAACTGATA	26091
rs143222730	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68004242	AGTTGTTGAGTTCAA[C/T]AGAGTTCAACAACTG	26091
rs143235843	in-del	-/T	0.170408	0.236992	intron-variant	HERC4	GRCh38.p7	10:67941716	TAAAGTCTCCCTCTG[-/T]CACCCAGGATGGAGT	26091
rs143263215	in-del	-/C			intron-variant	HERC4	GRCh38.p7	10:67982492	AAAATGATTAATGAT[-/C]TAAATCTAAGACCTC	26091
rs143273799	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68047725	GACAAAACACTGACA[A/C]CACCAGTTGTGATGT	26091
rs143288929	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68061337	AGGAGGTCGATACCA[C/T]CCTGGCTAACATGGT	26091
rs143293939	snp	A/G	0.0123036	0.0774623	intron-variant	HERC4	GRCh38.p7	10:68051056	CGGAGAGTTAAGGGG[A/G]GATTAAACCACATCA	26091
rs143401155	snp	C/T	0.00438332	0.0466095	intron-variant	HERC4	GRCh38.p7	10:67925876	GTGAGTAAGCCACCT[C/T]GGAAGTGAATCTCTA	26091
rs143423277	in-del	-/TAAA			intron-variant	HERC4	GRCh38.p7	10:68022508	CATCTCAAAATAAAT[-/TAAA]AAATAAATAAATAAA	26091
rs143430333	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67933219	ATAGCCTTCTTTTCC[C/T]TGGGTTCCAAGGAAT	26091
rs143437723	in-del	-/AGAAA	0.252983	0.249982	intron-variant	HERC4	GRCh38.p7	10:67945209	CCTGAAAGCAGCAAG[-/AGAAA]AGAAACAACATACAG	26091
rs143460906	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68025154	GATCACTTGAGCCCA[A/G]GAGATTGAGGCTGCA	26091
rs143463156	snp	G/T	0.00993419	0.0697739	intron-variant	HERC4	GRCh38.p7	10:67983742	CAGTGAGCCAAGATC[G/T]CACCACTGCACTCCA	26091
rs143612564	snp	A/G	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:67960984	TCATCACTTTCTTGC[A/G]GATTTGGCGGACCTG	26091
rs143626333	snp	A/G	0.000329669	0.0128345	synonymous-codon	HERC4	GRCh38.p7	10:67954628	GAGCCTGGAATCTTC[A/G]TAATACCTAAACATG	26091
rs143647917	snp	A/C/T	0.00993419	0.0697739	intron-variant	HERC4	GRCh38.p7	10:67982620	GCAAAAGTGGACAAA[A/C/T]GGGATTACATTAAAT	26091
rs143674283	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68019312	AGCCAAAGCATTCTT[A/G]AAGAACAGAAGAATA	26091
rs143684144	snp	C/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68021311	CTAGAATGCAAACCT[C/G]GTTCAACATATGAAA	26091
rs143708253	snp	C/G/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68046554	AGAGAATAAAATAAG[C/G/T]GTCCTAGCCCTCAAT	26091
rs143714687	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68035547	ACATGCATAGAGATA[C/T]TGTAAAAATGCAGAT	26091
rs143728580	in-del	-/AA	0.0138799	0.0821421	intron-variant	HERC4	GRCh38.p7	10:67974761	GTATTCCTAATAGAG[-/AA]AGAGAACAAACACAT	26091
rs143747937	in-del	-/G	0.00835973	0.0641091	intron-variant	HERC4	GRCh38.p7	10:68013448	ATGAACCTTGAGGAC[-/G]TTATGCTTAGTGAAA	26091
rs143748232	snp	C/T	0.0501905	0.150254	upstream-variant-2KB	HERC4	GRCh38.p7	10:68077083	GGTGAGCCTAGAGCG[C/T]GCCATTGCACTCCAG	26091
rs143757534	in-del	-/A	0.0562307	0.157967	intron-variant	HERC4	GRCh38.p7	10:67990524	ACTACAGCAAATATG[-/A]AATGGTGAAGAAGAA	26091
rs143779696	snp	C/T	0.0681886	0.171594	intron-variant	HERC4	GRCh38.p7	10:67931230	ACCTCGTGATCCGCC[C/T]GCCTCGGTGTCCCAA	26091
rs143797020	snp	A/G	0.15698	0.23205	intron-variant	HERC4	GRCh38.p7	10:67972263	ACGGTGGCTCACACC[A/G]GTAATCCCAGCACTT	26091
rs143814018	snp	A/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68008377	GCCTGGGGTCTTTTA[A/T]CTTCAGGGCAGCAGC	26091
rs143815874	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67950672	TGGAAAGGAAGAAGG[A/C]TAGAGTAAATTCTTT	26091
rs143879879	snp	C/T	0.0119091	0.0762411	intron-variant	HERC4	GRCh38.p7	10:68002855	TGTGCATACCTTGGC[C/T]TCCCAAAGTGCTGGG	26091
rs143896818	snp	A/G	0.00874735	0.0655527	intron-variant	HERC4	GRCh38.p7	10:67956604	TAAACTAGTAAAACG[A/G]TTTATAAAGATTGAA	26091
rs143956120	in-del	-/AAAGA			intron-variant	HERC4	GRCh38.p7	10:68025233	ATCACCCCAAAAAGG[-/AAAGA]AAAGAAAAGAAAAAA	26091
rs143963345	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922124	GCACTGCAGCATCAA[C/T]AATTTTGAAAGCTAT	26091
rs143999408	snp	C/T	0.00517822	0.0506191	intron-variant	HERC4	GRCh38.p7	10:67982535	TACTTAAGAAAACAT[C/T]AGGGGAAACTCTCCA	26091
rs144003109	snp	A/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68005201	CTAACAATATCCGCT[A/T]TGTATATCTGGGTTT	26091
rs144011695	snp	A/G	0.00478085	0.0486577	upstream-variant-2KB	HERC4	GRCh38.p7	10:68077297	ATGGTAGGAATGTTC[A/G]CAAAAAATACTCATA	26091
rs144016471	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67959622	ATAAGCCATAAATTG[C/T]TTTTATTTGACAGAA	26091
rs144050041	snp	C/T	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:67954002	TCAAGTCAGGAGTTC[C/T]ACTAAACTGATCCAT	26091
rs144050113	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011596	GAAATCTTTTTACTG[A/G]GCGGTGGGTCTCAAC	26091
rs144100851	snp	A/C	0.0217236	0.101931	intron-variant	HERC4	GRCh38.p7	10:68043379	CTAGGAAAAAGAACA[A/C]AAGAGTTTAAAGAGG	26091
rs144120736	in-del	-/TGT			intron-variant	HERC4	GRCh38.p7	10:67941359	ATACGACTTTACAAC[-/TGT]TTTCTCCCAGACATA	26091
rs144150037	snp	C/T	0.0146672	0.084371	intron-variant	HERC4	GRCh38.p7	10:67928422	CTACCAGCTGTGTAG[C/T]ATCCTCAGTGTTACC	26091
rs144193308	snp	A/G	0.00438332	0.0466095	intron-variant	HERC4	GRCh38.p7	10:67930956	AAGTGCTGGGATTAC[A/G]GGCATGAGACACCAT	26091
rs144194993	snp	A/G	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:67985554	ATTTAAGGGTTCTAC[A/G]TAAAATAGTTTGAAA	26091
rs144218382	in-del	-/G	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:67974337	TTGCACTTAAGAGAA[-/G]AAAAACCACCAAAGA	26091
rs144237681	snp	C/T	0.0119091	0.0762411	intron-variant	HERC4	GRCh38.p7	10:67982962	GTGAAACCCCGTCTC[C/T]AATAAAATACAAAAA	26091
rs144244668	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922396	CTACCTTTTTTTTCT[G/T]TTTATAGAGTCTCAG	26091
rs144262110	snp	A/G	0.00438332	0.0466095	intron-variant	HERC4	GRCh38.p7	10:67935034	GAGGATACTGATTTC[A/G]GTTTCCTCTGAAGTT	26091
rs144284857	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67995954	GTATGAACAGACATC[A/T]TATCTTCCACCTGTA	26091
rs144297137	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68042172	AGGCGCCTGCCTGGC[A/T]AATTTTTTGTATTTT	26091
rs144297476	in-del	-/GTT	0.084364	0.187256	intron-variant	HERC4	GRCh38.p7	10:67961812	AGCATAAGCAAAACA[-/GTT]TCACTCTATGCAAAC	26091
rs144298634	snp	A/T	0.000153988	0.00877328	synonymous-codon	HERC4	GRCh38.p7	10:67954984	TGGCTTCTTGTAATC[A/T]ATGTTCTTTGTTTTC	26091
rs144378779	snp	G/T	0.000115387	0.00759474	intron-variant	HERC4	GRCh38.p7	10:68039504	CTTCAGCAAATCAAA[G/T]TTTGAGCAGGAAAAA	26091
rs144392452	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67964643	AGTTTCCCCTGTTTA[G/T]CATTAACACTTTAGA	26091
rs144393778	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67972916	TATAGAATTATAGTT[A/T]ACTTCCTTAAGAGAA	26091
rs144396685	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:68060330	GCAACCTCTGCTTCC[C/T]GGGTTCAAGCAATTC	26091
rs144467991	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67978348	CCACAGGCCCCTGGT[A/G]ACAGTGGCCAAGGGG	26091
rs144498659	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:67972031	CCAGCCTGGCCAATA[C/T]GGTGAAACCCCATCT	26091
rs144507481	snp	C/T	0.000153988	0.00877328	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67988686	GTATTTCTAAAACCT[C/T]TAATGCAGTATGAAG	26091
rs144538072	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68066417	CTTTTAAGGAAAGTA[C/T]GTGGCTCACTTCTAA	26091
rs144546824	in-del	-/C	0.263535	0.249633	intron-variant	HERC4	GRCh38.p7	10:68002184	TAATTATAAAAAAAA[-/C]ATCAAGTTTATTTAC	26091
rs144565305	snp	G/T	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:67934746	GTTCCTTGATTCCAG[G/T]GTCTGATGTTACTGA	26091
rs144726315	snp	A/G	0.00795532	0.062565	intron-variant	HERC4	GRCh38.p7	10:67950405	CTCAGCCTCCTAAGT[A/G]GCTAGGATTACAGAT	26091
rs144804482	snp	C/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67947308	TAAATAGTAACAAAA[C/G]AGAGCTAGAGAAACT	26091
rs144827497	snp	C/T	0.00517822	0.0506191	intron-variant	HERC4	GRCh38.p7	10:67992071	GCCCAGCTAATTGTA[C/T]TTTTTTGTAGAGACA	26091
rs144835286	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67957267	TCAGTGAATGAGGTT[A/G]CAAATTTGTTCTAAA	26091
rs144839094	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67955280	GTATCCCGTACAGCA[C/T]AAAACTTAATAAACT	26091
rs144852406	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68035958	ATATCACGAAGGCTA[A/G]TAAGTAGTATACTGC	26091
rs144869077	in-del	-/A	0.179425	0.239831	intron-variant	HERC4	GRCh38.p7	10:67979936	ATCTCAAAAAAAAAA[-/A]GAAAAAAAAACCTGT	26091
rs144876625	snp	C/T	0.0209421	0.100162	intron-variant	HERC4	GRCh38.p7	10:68049420	TGTAATCCCAGGACT[C/T]TGGGAGGCTGAGGTG	26091
rs144888944	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68044618	GAAATCAAGGAAAAA[G/T]ATATTGCATTCTAGT	26091
rs144900260	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67951305	GTGCCAGGAAGGAGG[A/C]TAGGATTTGAGCAGA	26091
rs144905243	snp	C/T	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:67949280	CAAAGTGAGACTCTG[C/T]CTCAAAAAAAATAAA	26091
rs144937400	snp	A/G	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:67999126	TCTTGTGTATACCTG[A/G]TATGTTAGATCTCAA	26091
rs144970931	snp	A/G	0.0189856	0.0955633	intron-variant	HERC4	GRCh38.p7	10:68054189	AAGATACCATACTAT[A/G]AAATAAAAAAGATAC	26091
rs145013992	snp	A/G	0.154661	0.231107	intron-variant	HERC4	GRCh38.p7	10:67973940	TAGACCCAGCTACTC[A/G]GGAGGCTGAGGCAGA	26091
rs145089260	snp	A/G	0.00557542	0.0525036	intron-variant	HERC4	GRCh38.p7	10:68073490	ATAAGTACCTTGATG[A/G]AATTAATCACAATTT	26091
rs145121683	in-del	-/AAGTTCTGGATAA			intron-variant, downstream-variant-500B	HERC4	GRCh38.p7	10:67966567	TATTATTTAAAAAGT[-/AAGTTCTGGATAA]AAGTTCTGAAAAAAC	26091
rs145155924	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68023080	AACTGAAACCCTGTA[C/T]ACTTTTGGTGGAAAT	26091
rs145161370	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67985764	GTACCAAAGGTATTT[C/T]CTTATGATGCCATTT	26091
rs145162895	snp	C/T	0.00874735	0.0655527	intron-variant	HERC4	GRCh38.p7	10:68019957	GATGCCTTTCTCTTT[C/T]TTTCTTCTACTCTCC	26091
rs145221350	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67923493	TTTGATTATGATTTC[C/T]TTTTCTATTTGCTTC	26091
rs145260841	snp	C/T	0.00874735	0.0655527	intron-variant	HERC4	GRCh38.p7	10:68071288	ATCTCATCTATACAG[C/T]TGGAGGCTGTTCCTG	26091
rs145281776	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67973884	AAACCCCATCTCTAC[C/T]AAAAATAGAAAAATT	26091
rs145283061	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67928018	TTATCCAGGGAAGGT[C/G]TCTGAGAAGGTATAA	26091
rs145306957	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68017287	AGCCTGAGCAAAGTC[A/C]CCCCAGTGAATAGGC	26091
rs145316105	in-del	-/TTTGGCTTCAAAA	0.154329	0.23097	intron-variant	HERC4	GRCh38.p7	10:67958373	ATCTCCAAAGCACCC[-/TTTGGCTTCAAAA]CTCTATGTTTTCATA	26091
rs145321131	snp	A/G	0.00199481	0.0315187	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069769	TGAAGTCAGCTGGGC[A/G]CGGTGGCTCACGCCT	26091
rs145331292	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67972517	AGAGTCAAACTCTGT[C/T]TCAAAAAAGAGGAAA	26091
rs145430857	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67980188	GCGATCTCGGCTCAC[C/T]ACAACCTTCGCCTTC	26091
rs145440017	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68067069	CAGTCATCTGCTATT[C/T]TGACAAGTTACTTAC	26091
rs145511245	snp	A/C	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67951772	TGAAACACGGGCCAA[A/C]TGACCATATTCCCTG	26091
rs145517090	snp	A/C	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67944636	TGACCAATCATGGAG[A/C]GACTGAGATATATGA	26091
rs145549775	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68000789	CAAGCGAAGGAATGC[C/T]AAAGATTGACAGCAA	26091
rs145582101	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68048101	TCTTTTAATTTCTTG[A/T]AGCAACAGGGTCTCA	26091
rs145584105	snp	G/T	0.0142736	0.0832652	intron-variant	HERC4	GRCh38.p7	10:67987117	TCAAGATGTGAAGAT[G/T]CTAGTATTTAGAATG	26091
rs145584969	snp	G/T	0.00795532	0.062565	intron-variant	HERC4	GRCh38.p7	10:67994983	GTGTGAGCCACTGCA[G/T]CCTATCCTTAATTTC	26091
rs145609152	snp	G/T	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:67997396	TACAAAAGAGCTAAA[G/T]TTCTTTTCAATCATA	26091
rs145662584	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67925463	GATAAAATAATGTTA[C/T]AGGACCATCAAAAGT	26091
rs145664432	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012637	CAATGACCACTGATC[A/G]CAGATCACCATTACA	26091
rs145682624	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68072532	AAGGTAAACACAGAG[C/T]AAATTATGCATTTAA	26091
rs145692244	snp	C/T	0.0193772	0.0965046	intron-variant	HERC4	GRCh38.p7	10:67941760	CTCTGCTCACTGCAA[C/T]GTATGCCTCCTGGGT	26091
rs145764875	snp	C/T	1.65597e-05	0.00287743	missense	HERC4	GRCh38.p7	10:67925148	AAAAAATTTTTATCG[C/T]AGGATGTTCTGCCCA	26091
rs145778674	in-del	-/TATATATATATATATATATATATATATATATATATATAT					GRCh38.p7	10:67927393	CCATATATATATATA[lengthTooLong]TTTTTTTTTTTTTTA	26091
rs145783235	snp	C/T	0.00636936	0.0560724			GRCh38.p7	10:68018657	TAAATATCAACTATT[C/T]CTACATGCCAGTGAT	26091
rs145788604	snp	C/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67983136	GCGCTCAATACCACC[C/G]AACACCAGTGAAATG	26091
rs145804658	in-del	-/C	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68063069	TCTCTACACAGCACT[-/C]TTGTTTATACATCCT	26091
rs145836352	snp	A/G	1.656e-05	0.00287745	missense	HERC4	GRCh38.p7	10:67925147	CAAAAAATTTTTATC[A/G]TAGGATGTTCTGCCC	26091
rs145859134	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67979509	GCCTTAAAGAGGAGA[C/T]AGATGGGGCAGAAAA	26091
rs145873315	snp	C/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67981784	TCAACATGACGAAAC[C/G]CCATCTCTACTAAAA	26091
rs145893546	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68073276	ACAATAATTGCTACA[C/T]GGTAAACATTAAATA	26091
rs145898592	snp	A/G	0.00478085	0.0486577	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069004	TAGATAACAGGGCTT[A/G]TTTTTAAACAGAACA	26091
rs145908882	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67974502	GAATCACTCAGTAAA[C/T]ATATAAATCTAACCA	26091
rs145922405	snp	A/G	0.0158469	0.0875917	intron-variant	HERC4	GRCh38.p7	10:67925573	TCTCTCCTTTTAAAA[A/G]TATGGTACTAAGCAA	26091
rs145963768	snp	C/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68060592	TCTCCAATTATATGG[C/T]TTATGTGTTTCTTCA	26091
rs145968406	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67965781	TATTATATAACTGCT[A/G]CACACATATTAAATT	26091
rs145990147	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68037822	ATATACCGTGTTCTA[A/G]AATTGAAAGGTTCAA	26091
rs146010482	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67944923	GAGCCAAAAGAAAAA[A/G]CAAGAAAGAATGAAG	26091
rs146090632	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67940373	AATTTACTTTCCTAA[A/G]GTGATTATCTGATAT	26091
rs146159666	snp	A/T	4.94254e-05	0.00497094	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68034131	TTGCTTTTTACAGTC[A/T]GTACCTAAACCCAAT	26091
rs146175274	snp	C/T	0.0189856	0.0955633	intron-variant	HERC4	GRCh38.p7	10:68061349	CCATCCTGGCTAACA[C/T]GGTGAAACCCCATCT	26091
rs146198003	snp	C/T	0.000577315	0.0169801	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:67992319	TCATCTGGTGGCCCA[C/T]AGTTCTAAATTTTCA	26091
rs146206021	snp	C/T	0.00755907	0.0610114	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011175	CTCAAGCAATCCTCT[C/T]GCCTAAACCTCCCAA	26091
rs146253779	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67990153	TGGCAAAAGAACTTA[G/T]GAAGCATTTTCATTT	26091
rs146287800	snp	C/T	1.65652e-05	0.0028779	synonymous-codon, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:68032847	AGATCTTAGTGACTT[C/T]AGTAAATTAGGAACA	26091
rs146294383	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68035575	GATTTGATAATATTG[C/T]TCACCCCAAAAAATA	26091
rs146332386	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67985269	CAAGGGCAGAAATCA[C/T]GTCTTTTATCACTAC	26091
rs146336447	snp	G/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68039036	GATGCGGATTACAGG[G/T]GGGTTACTGTAATCC	26091
rs146338188	in-del	-/TT	0.155656	0.231515	intron-variant	HERC4	GRCh38.p7	10:68063128	TCTATTATTTGTGCA[-/TT]TGTTTTCTATTCCCT	26091
rs146353481	snp	C/T	0.0115144	0.0749975	intron-variant	HERC4	GRCh38.p7	10:68064073	CATGGCAAAACTCCA[C/T]CTCTACTAAAAATAC	26091
rs146373956	snp	A/G	0.00398564	0.0444627	intron-variant	HERC4	GRCh38.p7	10:67970079	CCTCAAATTCCTCCA[A/G]TGTTAGAGGCCTCAA	26091
rs146414165	snp	G/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67954349	AATCAGCAGAAGGAA[G/T]AGTCAACATTATTTT	26091
rs146436856	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68008791	AATCGTCCACTGATA[C/T]ATGAATAGATAAACA	26091
rs146452450	snp	C/T	0.000247107	0.0111127	synonymous-codon	HERC4	GRCh38.p7	10:67932651	GACCATTGCTTGTAG[C/T]TCATTAGGCTGAAAG	26091
rs146455883	snp	A/G	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:67959874	TCAGAGCACAGACTC[A/G]TGTAAAGCACCAGAA	26091
rs146471704	snp	A/G	0.00676609	0.0577691	intron-variant	HERC4	GRCh38.p7	10:67961280	TCACTTCAAATATAC[A/G]CAACACTTGAGGCCA	26091
rs146512736	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68005851	GGACTATGGGCATGT[A/G]CCATGATGCCAGGCT	26091
rs146530990	snp	A/T	0.00676609	0.0577691	intron-variant	HERC4	GRCh38.p7	10:68000947	GAGTTTGTGGTAGGT[A/T]GTTACAAGCAACTCT	26091
rs146533332	snp	C/T	0.0126979	0.078662	intron-variant	HERC4	GRCh38.p7	10:68022809	TTAGTATCTAGAATA[C/T]ATAGAGAACTCTGAA	26091
rs146577925	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67935392	CCTCGTGATCCGCCC[A/G]CCTCGGCCTCCCAGA	26091
rs146588699	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68028979	AGTACCAGACCAGCC[C/T]AGGCAATAAAGCGAG	26091
rs146594352	snp	A/G	0.000153988	0.00877328	synonymous-codon, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67988711	ATGAAGAAAACTGTT[A/G]AAAATTCTTCTTTCA	26091
rs146597024	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68015213	TTCTGCTCTACCATC[A/G]TAAGAATAAACCAAG	26091
rs146600902	snp	C/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67956797	CCTTCATTACTGATC[C/G]TAGGAAAATTTCAAA	26091
rs146643270	snp	C/T	0.00438332	0.0466095	intron-variant	HERC4	GRCh38.p7	10:68073306	ATACTTTATAACATG[C/T]TACATAAGTATCATT	26091
rs146698029	snp	A/G/T	0.00159649	0.0282165	intron-variant	HERC4	GRCh38.p7	10:68004874	TCCATTACCTCCACC[A/G/T]GGTCTCTCCGTTGAC	26091
rs146779582	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:67979223	GCTATTTTGAAGAAA[C/T]TCAAAGAAATTCAAG	26091
rs146820265	snp	C/T	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:67982635	CGGGATTACATTAAA[C/T]TAAAAAACTTCTACA	26091
rs146874002	snp	G/T	0.0364509	0.129988	intron-variant	HERC4	GRCh38.p7	10:68029379	TGCCTGTAGTCCCAG[G/T]TACTCAGGAGGCTGA	26091
rs146874406	snp	A/T	0.000528009	0.0162396	synonymous-codon	HERC4	GRCh38.p7	10:67956920	TAACAGAGTAGTTTT[A/T]GCTTGGGCATCAAAT	26091
rs146887700	snp	C/G	0.000116541	0.00763263	missense	HERC4	GRCh38.p7	10:67923092	GGATGACTAGTTTCA[C/G]ACTCTTCATACCAAG	26091
rs146891980	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68023127	ACTATGAGAAACAGT[A/G]TGGCAGTTCCTACAA	26091
rs146896148	in-del	-/ATATAA	0.00795532	0.062565	intron-variant	HERC4	GRCh38.p7	10:67980717	AAAACAGAGTATAAG[-/ATATAA]ATAGAAACAACAAAA	26091
rs146943425	snp	C/T	0.000227314	0.0106586	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:67991144	TTGCCACTTACCTAA[C/T]AGCTAAAAAACTTCC	26091
rs146955008	snp	A/T	0.0189856	0.0955633	intron-variant	HERC4	GRCh38.p7	10:68030881	TTTCCATTTATTCTG[A/T]TTTTAAAAGTTGGTT	26091
rs146964851	in-del	-/T	0.164219	0.234823	intron-variant	HERC4	GRCh38.p7	10:67934632	CTGAGACTGTGCATG[-/T]ATAAAAATGTTTTTA	26091
rs147027018	snp	C/T	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:68058893	TTTTTAAAAGGTATG[C/T]AGTGAGAGTCTACTA	26091
rs147059298	snp	C/T	0.00835141	0.0640778	intron-variant	HERC4	GRCh38.p7	10:68008042	ACTCTTGCCAACTCA[C/T]AGAGGTACTGCCTTG	26091
rs147062714	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68062300	GGATTCCTTATTTCT[A/G]TACTAATGAATATAC	26091
rs147149248	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67977234	TCAGCCACAGCTGGA[C/T]AGGGCACCAGTCAAA	26091
rs147180638	snp	C/T	1.6486e-05	0.00287102	missense	HERC4	GRCh38.p7	10:67954629	AGCCTGGAATCTTCA[C/T]AATACCTAAACATGC	26091
rs147216170	snp	C/T	0.0818113	0.184966	intron-variant	HERC4	GRCh38.p7	10:68061737	TACAAAAAAATTAGC[C/T]GGGCATGGTGGCGGG	26091
rs147218319	snp	C/T	0.000347409	0.0131751	intron-variant	HERC4	GRCh38.p7	10:68025540	CTCTTTTACATAACA[C/T]CTTACCGTCCACAAG	26091
rs147255296	snp	A/G	0.0170251	0.090679	intron-variant	HERC4	GRCh38.p7	10:67950917	ACTTAAAGAAGACAC[A/G]GCTCTTAAGAAAAAT	26091
rs147324195	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67947154	ATAGGACATTTCATC[C/T]AGCAGCTGAAGAATA	26091
rs147325513	snp	C/T	0.00795532	0.062565	intron-variant	HERC4	GRCh38.p7	10:68003230	GGCTCACTTGGCTCA[C/T]TGCAAGCTCCGCCTC	26091
rs147327771	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67997625	CTCAGAATGTGACTG[G/T]ATTTGGAGATAAGGG	26091
rs147361667	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67927003	CTCAATAAATACTTG[C/T]TAATGGGCTTCTTGA	26091
rs147430036	snp	A/G	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:67982137	TTACACAGAACCACA[A/G]AAGACCCAGAATAGT	26091
rs147430704	snp	C/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67923219	TTGGTACAGTCGCTA[C/T]AGCAGAGCTTCACTT	26091
rs147433338	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67978674	GGGTGAGACCCAGTG[C/G]TGTGCTGGCTTCAGG	26091
rs147442213	snp	A/C/G	0.00319074	0.0398324	intron-variant	HERC4	GRCh38.p7	10:68070804	AGGATCAGGACCCCC[A/C/G]CCTTCTACAAAACTA	26091
rs147529890	snp	C/T	0.00557542	0.0525036	intron-variant	HERC4	GRCh38.p7	10:68052498	GTGTTTGTTTGCTTA[C/T]GAACTACATCAAGTA	26091
rs147546679	snp	C/T	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:68047814	AGCCACTTTGGAAAA[C/T]AGTTTGGCAGATTCT	26091
rs147582321	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67942881	TTTCATCTGTATATA[C/T]ACTCTATGCACACAC	26091
rs147584976	snp	A/C	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68036007	GTATGCCTAGTTCAT[A/C]CTAAGGGCTCTAAAA	26091
rs147608223	snp	C/T	0.0260105	0.111035	intron-variant	HERC4	GRCh38.p7	10:68017654	ACCACACCTAGCTAA[C/T]TTTTGTATTTTTAGT	26091
rs147705939	snp	A/C/T	0.000399281	0.0141238	intron-variant, missense	HERC4	GRCh38.p7	10:68067088	CAAGTTACTTACCAA[A/C/T]GTGTGCTGCCATTTC	26091
rs147712732	snp	C/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67937119	TTAAGAAGAGAGTGA[C/G]ATTTCAGACAGAGAA	26091
rs147748456	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67942251	ATTTATCTCATATGG[C/T]TGTTGTGAGGATTAC	26091
rs147793181	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67987134	TAGTATTTAGAATGA[A/G]TCCATCAAAAAGGTC	26091
rs147811510	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68066473	AGAGAAAATCACTGG[C/T]TCCAAGTACTTTAAA	26091
rs147816765	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67973145	TGTTTTCAATGTTTC[C/T]GTAGGTTTGAAGATA	26091
rs147920476	snp	C/G	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:67948060	AGAAAATACTTAAGA[C/G]ACTAATGAAAACACA	26091
rs147984798	snp	C/T	0.0577344	0.159793	intron-variant	HERC4	GRCh38.p7	10:67984195	GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	26091
rs148003522	snp	A/G	0.00835141	0.0640778	intron-variant	HERC4	GRCh38.p7	10:67980343	TCTCCATGTTGGTCA[A/G]GCTGGTCTCGAACTC	26091
rs148067285	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68037551	TTCTTTATTTCTATG[C/T]ATAGAAAGTTCATCT	26091
rs148070047	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67931998	AGCCTTGCTCTGCTG[A/C]CCAGGGTGGAATGCA	26091
rs148073945	snp	C/T	0.38269	0.21188	intron-variant, synonymous-codon	HERC4	GRCh38.p7	10:68070493	CGCCTGTAATCCCAG[C/T]TATTCGGGAGGCTGA	26091
rs148074154	snp	C/T	0.0103295	0.0711199	intron-variant	HERC4	GRCh38.p7	10:67968358	TAAACCAACAGAAAG[C/T]ACAGCTGAGAGGCTA	26091
rs148090966	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68019484	TGACACCATACAGTA[A/G]GAGGGTGAAGAATTT	26091
rs148121254	snp	A/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68046682	TGTAAATCTTAAAAG[A/T]TAGTCCAGGCGAGGT	26091
rs148125272	snp	G/T	0.0103295	0.0711199	intron-variant	HERC4	GRCh38.p7	10:67950638	TTTCTCATTGATGAT[G/T]AAAGTTATATACATA	26091
rs148129699	snp	A/G/T	0.0111196	0.0737302	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011102	GGGTCTTGCTCTGTC[A/G/T]CCCAGGCTGGAGTGC	26091
rs148144872	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68023668	ATGTACTTAATACCA[C/T]GGACTGTATACTTAA	26091
rs148184258	snp	G/T	0.000199591	0.00998777	missense	HERC4	GRCh38.p7	10:67932779	CATCGACAAACTCTT[G/T]CCTAGAAATGAAAAA	26091
rs148251017	snp	C/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67945254	GTACATCTAGCAGTA[C/G]ACTTTTCAATGGAAA	26091
rs148286816	snp	A/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:68015402	GAACTATTAGCTAAA[A/T]AATTATTTTAGGTCA	26091
rs148331938	snp	G/T	0.00676609	0.0577691	intron-variant	HERC4	GRCh38.p7	10:67996025	TTAAAATTCCTCTCC[G/T]CTGGGCACAGTAGCT	26091
rs148348714	snp	A/C	0.00835141	0.0640778	intron-variant	HERC4	GRCh38.p7	10:68060404	CACCATACCCAGCTA[A/C]TTTTTGTATTTTTTT	26091
rs148356352	snp	C/T	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:68074119	TGATGGCGAAATCTG[C/T]AGAACTTTCCAGCAC	26091
rs148401434	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68065128	AAAAAAGTTGAGATA[C/T]AAGAACACATTCCCA	26091
rs148419695	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68048742	AAAGCTGGGGAGGTG[A/G]TGCATGGTAGGGGAC	26091
rs148452741	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67978745	GGGGTGCTTGTGTCA[C/T]TCCACCCCCAGCTCC	26091
rs148456272	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68028280	AGTGTTGTCCTAGCA[A/G]CTTCCAAAGGTAAGC	26091
rs148509520	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68035656	TATAAGGTGCTGTAT[C/G]ATCTACCTATGTTTC	26091
rs148514198	snp	A/G	0.00676609	0.0577691	intron-variant	HERC4	GRCh38.p7	10:67941774	ACGTATGCCTCCTGG[A/G]TTCAAGAGATTCTCC	26091
rs148597938	snp	A/G	0.00517822	0.0506191	intron-variant	HERC4	GRCh38.p7	10:67957506	AGCCTTTAAAGTTAC[A/G]AGAACTGATCTATTA	26091
rs148601321	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922265	CCCATCTATCAGTGT[A/G]TCAGGATTCACAAAG	26091
rs148608861	snp	A/G	0.00517822	0.0506191	intron-variant	HERC4	GRCh38.p7	10:68016439	CTCACTGCAACCTCC[A/G]CCTCCCGGATTCAAG	26091
rs148647741	snp	C/T	0.00517822	0.0506191	intron-variant	HERC4	GRCh38.p7	10:67999463	GTCTCAGAGCCCTAT[C/T]AAAAGGATTCCAACA	26091
rs148652994	snp	G/T	0.093777	0.195178	intron-variant	HERC4	GRCh38.p7	10:67928831	GAGGCTGAGGCAGAA[G/T]AATCGCTTGAACTTG	26091
rs148712124	snp	A/G	3.29837e-05	0.00406088	missense	HERC4	GRCh38.p7	10:67955075	GGATTCACAGATTCA[A/G]TCACTGGGAGAAAAA	26091
rs148724652	in-del	-/AGG	0.138207	0.223612	intron-variant	HERC4	GRCh38.p7	10:67981029	AATGAGTAACAAAAT[-/AGG]AGGAGTGTGTCCTTA	26091
rs148764489	snp	C/T	1.64798e-05	0.00287047	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:68044459	GCTGTCCATCAGAAT[C/T]GAGACCCCAAGCATA	26091
rs148805557	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68003246	TGCAAGCTCCGCCTC[C/T]CGGGTTCATGCCATT	26091
rs148821482	snp	A/G	0.000626783	0.0176918	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:67990930	TCTGCGGATGATCAG[A/G]TTGTATAAGTTTGTG	26091
rs148834054	in-del	-/T	0.0267878	0.112589	intron-variant	HERC4	GRCh38.p7	10:67995894	TCATGTGTCAAGTAA[-/T]TTTCCCCCCCTTATC	26091
rs148834115	snp	A/G	0.0252325	0.109451	intron-variant	HERC4	GRCh38.p7	10:68037126	TTGAGACAGAGTCTC[A/G]CTCTGTCGCCCAGGC	26091
rs148859274	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67951973	GACCTGTCTGTTTCC[A/C]ACAATCTTGTTCTCC	26091
rs148876444	snp	G/T	0.0182019	0.0936463	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012657	TCACCATTACAGATA[G/T]AGTAACAACACAGAA	26091
rs148901885	in-del	-/C			intron-variant	HERC4	GRCh38.p7	10:68070798	TTCTCAGGATCAGGA[-/C]CCCCCCCCTTCTACA	26091
rs148912675	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67960920	CTTTTCCAATGTTTA[C/T]TGACCACTTCTTTCA	26091
rs148923047	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68019259	CCTCGGCCTCCCAAA[A/G]TGCTGAGATTACAGG	26091
rs148974911	snp	C/G	0.029116	0.117091	intron-variant	HERC4	GRCh38.p7	10:68023217	AGAACTGAAAGTGGG[C/G]TCCTGAAGGGATGTT	26091
rs148980435	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67931170	TATATTTAGTAGAGA[C/T]GGGGTTTCACTATGT	26091
rs148986305	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67948201	ATCCTAAGGAACTAA[A/G]AACAAACTATACCCA	26091
rs149036236	snp	C/G	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:67989067	AAATAAAGTGTGAAA[C/G]TCTTGTTGAATTTAT	26091
rs149046431	snp	C/T	1.64776e-05	0.00287028	missense	HERC4	GRCh38.p7	10:67932679	AAGAGCAGAAGGACT[C/T]TTCCTCCACAGACCT	26091
rs149132652	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	HERC4	GRCh38.p7	10:68067212	AAATTCCTCAGATGT[A/G]GGGTCCTACACAAAG	26091
rs149137145	snp	C/T	0.113685	0.209567	intron-variant	HERC4	GRCh38.p7	10:67973917	CTGGGTGCGGTGGCA[C/T]GTGCCTGTAGACCCA	26091
rs149190990	snp	C/T	0.00874735	0.0655527	intron-variant	HERC4	GRCh38.p7	10:67980225	GTCATCAAAACAGCA[C/T]GGTACTGGCATGATT	26091
rs149202490	in-del	-/A	0.0718919	0.175435	intron-variant	HERC4	GRCh38.p7	10:68021850	ATTCAAATTGGAAAG[-/A]AAAAAAAAAATCTCT	26091
rs149245606	snp	C/G	0.00636936	0.0560724	intron-variant	HERC4	GRCh38.p7	10:67944171	GTGCTGGCTTCAGGT[C/G]TGACCCAGTGCAGTC	26091
rs149291370	snp	A/T	0.00993419	0.0697739	intron-variant	HERC4	GRCh38.p7	10:67934667	CACACATTTGATAAT[A/T]TGGATACAGAATTCT	26091
rs149327993	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68027311	CATCACTCAGTTTCA[A/G]TAACTGGCAAAAGGT	26091
rs149348953	snp	C/T	0.000155796	0.00882461	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:68014183	AAAAGCAGAAGTGTG[C/T]TGCCTAGAGTAAAAT	26091
rs149368934	snp	C/G	0.0115144	0.0749975	intron-variant	HERC4	GRCh38.p7	10:68001470	GGCCATGGGTTTAAC[C/G]TCTGGATGGGCTAGA	26091
rs149400454	snp	A/C	0.0146672	0.084371	intron-variant	HERC4	GRCh38.p7	10:68064059	AACAGCCTGGTCAAC[A/C]TGGCAAAACTCCACC	26091
rs149423511	snp	C/T	0.00398564	0.0444627	intron-variant	HERC4	GRCh38.p7	10:68009183	AAACCGAGATTGCAC[C/T]GCTGCACTTCCAGCG	26091
rs149451955	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67977195	AGAGTGGGGAGAACT[C/T]TGTCTTGCATCTTGG	26091
rs149505580	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67982224	AAATTATAGTGCAGC[A/G]GTATAGTAATCAAAA	26091
rs149520798	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67995909	TTTTCCCCCCCTTAT[C/T]TAAAGAACAGTGATG	26091
rs149521850	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68034679	AGGAACTTCTAACTT[A/G]GGATGCCCCAGACTG	26091
rs149576013	snp	A/G	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:68050178	GCCTGGGCAACCAAA[A/G]TGAGACCCTTTCTCA	26091
rs149628768	snp	C/T	0.137867	0.223442	intron-variant	HERC4	GRCh38.p7	10:68059950	TATAATAATATTATA[C/T]TATATTTTGTTTCTC	26091
rs149633054	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67964604	ACACAGCCAACAAAG[A/T]GATCATTCAAAAAGA	26091
rs149678122	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67960177	CAGTAAAAACTCTGG[A/G]CACCAGGGTTCTGGT	26091
rs149685089	snp	C/T	0.000153988	0.00877328	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67988746	GGGGAATACCGATCT[C/T]GTAGAGTTTCAAAAG	26091
rs149734271	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012505	GGAATAGGAAGGCCC[A/G]AGGAGAGGAGAGAGA	26091
rs149750948	in-del	-/AACAT			intron-variant	HERC4	GRCh38.p7	10:67945817	AAACTCAAATCAAAA[-/AACAT]ACGACAGATACACGA	26091
rs149786833	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:67924822	TACAATCCTAGTTTA[C/T]TGTAACCACAGTTTA	26091
rs149787760	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68018381	ATTACTTAGTCTGAT[A/G]GAGGTTATCTATAAA	26091
rs149804935	snp	A/G	0.0170251	0.090679	intron-variant	HERC4	GRCh38.p7	10:68072167	GAAAGCAAAACTCAC[A/G]TAACAATGATACTCC	26091
rs149838408	snp	C/T	0.00874735	0.0655527	intron-variant	HERC4	GRCh38.p7	10:67998973	TGACCTCAGGTGATA[C/T]ACCCATCTCGGCCTC	26091
rs149844890	snp	A/T	0.000759464	0.0194719	missense	HERC4	GRCh38.p7	10:67922971	TGATCAATAGCTTGG[A/T]TCAGTTTAGAGCGTA	26091
rs149894712	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68053767	GACTCAAGTATTTGG[C/T]AGTTCTGTGAATGCC	26091
rs149936767	in-del	-/A	0.435407	0.167703	intron-variant	HERC4	GRCh38.p7	10:68020769	GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	26091
rs149954497	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68061596	AAAGAATAAGCAAAT[A/G]GGCTGGGATCAGTGG	26091
rs149994771	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67946902	ACAAGGCGAGACTCT[A/G]TCTCAAAACAAAACA	26091
rs149995800	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68039295	CACTCCAGAATGGGC[A/G]ATAGAGTAAGACCCT	26091
rs149998782	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67973417	GGCTAAAACAAGGCC[C/G]AATCCCGTAGGAATT	26091
rs150015363	snp	A/G	0.00557542	0.0525036	intron-variant	HERC4	GRCh38.p7	10:68022368	GTCGGGCAAGGTGGC[A/G]CATGCCTGTAATCCC	26091
rs150046476	snp	A/G	0.0111196	0.0737302	intron-variant	HERC4	GRCh38.p7	10:67951663	TTCAATCCTTCATAT[A/G]ATTGCGTCTAGAGCT	26091
rs150112918	snp	A/G	0.00398564	0.0444627	intron-variant	HERC4	GRCh38.p7	10:68020495	GTTTGGGCCGGGCGC[A/G]GTGGCTCACGCCTGT	26091
rs150116306	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	HERC4	GRCh38.p7	10:68075613	TTTGTTTTTTGGTTT[A/G]GTTGTCTTTGTGCTC	26091
rs150117886	snp	A/C	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67943526	TAGCCCAGTTAGCTC[A/C]GCTGGTAAACATAAA	26091
rs150149514	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68001086	TAAGAATGTCCTTTT[A/G]TCAGCCGGGTGCAGT	26091
rs150217701	snp	A/G	0.00517822	0.0506191	intron-variant	HERC4	GRCh38.p7	10:68057230	AATATTATTCAGATT[A/G]GTGTGAAAATAACAG	26091
rs150241832	in-del	-/TTTA/TTTATTTA	0.0271762	0.113356	upstream-variant-2KB	HERC4	GRCh38.p7	10:68076114	TTTTCTTTTCTTATT[-/TTTA/TTTATTTA]TTTATTTATTTATTT	26091
rs150258899	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67931130	GTTGGGACTATAGGC[A/G]TGCGACACTATGCCC	26091
rs150275350	snp	A/G	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:67983097	AAAAAAAAACAAAAC[A/G]AAAACAAACGGGCAT	26091
rs150305648	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68043614	GAGGTCAGGAGTTCG[A/G]GACCAGCCTGGCCAA	26091
rs150325143	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68024673	ATGCATTTGAAGCTA[A/G]TAGTTGATAAAACTA	26091
rs150328621	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67987333	TAAGAAAAAAAAGTA[C/T]TTCTTAAAGGGGGGA	26091
rs150358199	snp	C/T	0.00557542	0.0525036	intron-variant	HERC4	GRCh38.p7	10:67955740	TGTACCACTGCACTA[C/T]AGCCTGGGCGACAAG	26091
rs150364120	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67974081	ATTACTGTACACACA[C/T]ACACACACACACACA	26091
rs150370447	snp	A/G	6.6012e-05	0.00574471	intron-variant, synonymous-codon	HERC4	GRCh38.p7	10:67939600	TACCGTAAAATTAAG[A/G]CAAAATGTTTCCTCT	26091
rs150410211	snp	A/G	0.0111196	0.0737302	intron-variant	HERC4	GRCh38.p7	10:67963236	TTTATTTATTTTTTG[A/G]GATGGAGTCTCACTC	26091
rs150480776	snp	C/T	0.0174175	0.0916809	intron-variant	HERC4	GRCh38.p7	10:68015560	TTTTGCCAGGTGGAG[C/T]TCTCTTTACAACCTG	26091
rs150487516	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67936895	GTATATTCCTGCTGT[A/G]ATGTTTACTATCTAG	26091
rs150489483	snp	A/G	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:68030135	ATTAATTTTAAATTT[A/G]CTGTATTTTTAAAAA	26091
rs150501463	snp	C/T	0.0115144	0.0749975	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012019	ACATTATGGAGATGG[C/T]TTCTTTCCTTAAACT	26091
rs150533751	snp	C/T	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:67926687	TTCATCCAACAAATA[C/T]ATAATGAGTTTTAGT	26091
rs150585699	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67933735	TAGTAACAATCCTAA[C/T]AGCCAACATTTACTG	26091
rs150590528	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67984506	GCTGGGAAGGGTAGT[A/G]GGGAGGCAGGGGCAT	26091
rs150606458	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68047171	TCAGACAAAAGAATA[A/G]CATCCCCAGTTTTTA	26091
rs150637753	snp	C/T	0.000910564	0.0213179	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:68014156	AGAGTAAATTCGTCC[C/T]GATGAAGGAACAAAA	26091
rs150643344	snp	C/T	0.000270205	0.0116202	intron-variant	HERC4	GRCh38.p7	10:67991230	AAGTTTTTTTAATCA[C/T]AGAATCAGAAATTTA	26091
rs150659410	snp	G/T	0.00398564	0.0444627	intron-variant	HERC4	GRCh38.p7	10:68053439	CTCCCGAGTAGCTGG[G/T]ACCACGGACATGAGC	26091
rs150742938	snp	A/C	0.0107246	0.0724382	intron-variant	HERC4	GRCh38.p7	10:67976069	TGCTGGAAAGCAGCC[A/C]CTCCCATCCATTTAC	26091
rs150792900	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68017102	TTTGCTTTTGGTCAA[C/T]GAGATTTCAGTGAAT	26091
rs150800454	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68032350	CCTATGAATAACAGA[G/T]AAATTCATCTCCTCT	26091
rs150852581	snp	C/T	0.00795532	0.062565	intron-variant	HERC4	GRCh38.p7	10:67946838	TATGAACCTGGGAGG[C/T]AGATGTTGCATTGAG	26091
rs150868951	snp	C/T	0.00398564	0.0444627	intron-variant	HERC4	GRCh38.p7	10:68003610	ACCAACAAGTGAGAA[C/T]ATGTGACTGTCTTTC	26091
rs150905967	snp	C/T	0.00676609	0.0577691	intron-variant	HERC4	GRCh38.p7	10:67951414	TCGAAACTCATAGGT[C/T]ATCCCTAAACCCACA	26091
rs150919577	snp	C/T	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:68049255	AGGATATATTATCCA[C/T]TGGGGAAGAAAAAAA	26091
rs150972775	snp	C/T	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:68056899	TGGCAACTGGGTCAA[C/T]GTTGGTGCTACGGGA	26091
rs150975439	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67923643	AGTCACAGCAGCCTC[A/G]ACCTCCTGGGCTCAA	26091
rs150977031	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67961117	AACATGAGCTTCTTT[A/C]ATGATCTACCAGTTT	26091
rs151056898	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67978976	ACATCCAAGTCCTTC[C/T]GAATATCTGGAAAGC	26091
rs151059101	snp	A/G	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:68071293	ATCTATACAGTTGGA[A/G]GCTGTTCCTGGCACT	26091
rs151127412	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68035869	CTAGTACCGCTGTCC[C/T]ATGTTCTAAATACCC	26091
rs151129119	in-del	-/A	0.0115144	0.0749975	intron-variant	HERC4	GRCh38.p7	10:68058285	AGACTAAAGGCAAAG[-/A]AGTACTTCCATGCCT	26091
rs151134683	snp	G/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	HERC4	GRCh38.p7	10:67966540	AATATATAGCACTCC[G/T]TTGCAATGTGTTATT	26091
rs151168656	snp	C/T	4.94197e-05	0.00497066	missense, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68072999	CCACATCCTACATCT[C/T]GGACCCTTTTATTTA	26091
rs151171680	snp	C/G	0.00874735	0.0655527	intron-variant	HERC4	GRCh38.p7	10:67948488	AATACCACCTTACTC[C/G]CACAAGGATAGCCAT	26091
rs151180980	snp	A/C	0.00517822	0.0506191	intron-variant	HERC4	GRCh38.p7	10:68043064	TTGTTATTATTGGAC[A/C]ACCCTCATATAAATT	26091
rs151182500	snp	A/T	0.00438332	0.0466095	intron-variant	HERC4	GRCh38.p7	10:68007307	GAATTTCTCTTTGAT[A/T]TTTCACCATTGTTTT	26091
rs151270005	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68022017	ATGAACAATTTGGAA[G/T]GAAATAAAATTTTAT	26091
rs151272960	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:67929716	GACAGGGTTTTATCA[C/T]GTTGTCCAGGCTGGT	26091
rs151300032	in-del	-/A	0.137527	0.223271	intron-variant	HERC4	GRCh38.p7	10:68052402	ATTTTTAAAACAGTT[-/A]AAATGATCAACCTAA	26091
rs151320563	snp	C/G	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:67936637	TACTCCAGGGTTCCT[C/G]TATCACCCTTGTTGT	26091
rs151336574	snp	C/T	0.00795532	0.062565	intron-variant	HERC4	GRCh38.p7	10:67986853	TATAATATAATACTA[C/T]ATGTGATCTAGAATA	26091
rs180760112	snp	A/T	0.00398564	0.0444627	intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68009990	TTTGAGAAAAAAGTG[A/T]TACATGATATGGGGA	26091
rs180777722	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67991617	AGAGAAACAAAACAG[C/G]TTTTCAAATACAACC	26091
rs180783119	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68068140	GATAGCTTGAGGACT[A/G]GAGTTTGAGACCAGA	26091
rs180783393	snp	A/C	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:68049328	AAGAGGAAGAAGAAA[A/C]CATATTCATATTTGC	26091
rs180786384	snp	C/T	0.000399281	0.0141238	intron-variant, missense, nc-transcript-variant	HERC4	GRCh38.p7	10:68039466	TGACCAGAGAGTCGA[C/T]ACACATGATTTTCGG	26091
rs180789114	snp	A/G	0.0298908	0.118541	upstream-variant-2KB	HERC4	GRCh38.p7	10:68076340	CTCGTTACCTCAGGC[A/G]ATCCACCCGCCTCGG	26091
rs180790495	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68030281	CCCATCTCTACAAAA[A/C]AATACAAAAAATAGC	26091
rs180807264	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68057920	TGCCCAGGCTGGTCT[G/T]GAATTCCTAAGCTCA	26091
rs180813716	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67960235	ATTGTTACACATCTA[A/T]GCCAGGAAAGTAATT	26091
rs180816740	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67974987	TGAGGTCAGGAGTTC[A/G]AGACCAGCCTGGCCA	26091
rs180821052	snp	A/G	0.0678174	0.1712	intron-variant	HERC4	GRCh38.p7	10:68019052	CCCAGGCTGGAGTGC[A/G]ATGGTGCGATCTCGG	26091
rs180829027	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67999899	TAATATATTTATAAA[C/G]GTTCAATAAGAATAT	26091
rs180849924	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67981060	TACTTATCAATAACA[C/T]TGGATGTAAATGAAC	26091
rs180854681	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67967521	AAACTTTAGAAGGTG[A/G]TATCTGGACACGATG	26091
rs180862160	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67978471	AGAACACCAGGTAGA[C/T]GTCTAAGGTTTTTCA	26091
rs180869449	snp	G/T	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:67931809	GCTCTGTCATCCAGG[G/T]TCAAGTGCAGTGGTA	26091
rs180881540	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68005740	ACATGGTCTTGCTCT[A/C]CTGCCCACACTGAAG	26091
rs180883128	snp	A/C	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67949918	CAGCTACTTGGGAGG[A/C]TGAGGCAAGAGAATC	26091
rs180898884	snp	C/G	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:67944751	ATCAGATAAATTTAA[C/G]AGAGTAAAATAAAAA	26091
rs180907284	snp	A/G	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:68043554	GGCACAGTGCTTCAC[A/G]CCTATAATCATGAGT	26091
rs180907477	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67971210	GATGAATTATATCAA[A/G]CATTTAATAAAGAAA	26091
rs180911747	snp	C/T	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:67996007	CTCTATCTGAAAGTG[C/T]CCTTAAAATTCCTCT	26091
rs180913491	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68023404	GAAGGAAATTCTACA[A/G]CATGGGTGAACCTTG	26091
rs180913734	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67985627	GACAGACCAAGTAAG[G/T]CTTCTCTTTTGGCAT	26091
rs180927205	snp	C/T	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:67929721	GGTTTTATCATGTTG[C/T]CCAGGCTGGTCTTGA	26091
rs180932602	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67934891	CTTGAAAAGATGTCA[C/T]TCGTTTCTGGGAAGT	26091
rs180950525	snp	A/G	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:67964136	ATGCAGAACTTCGTC[A/G]AAGTATTGCCAATGG	26091
rs180988745	snp	A/G	0.00398564	0.0444627	intron-variant	HERC4	GRCh38.p7	10:68072213	TTGATTTTAAAATAC[A/G]ATATCCAGGAACAGA	26091
rs181036061	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68053813	CCACAAACTAAAACA[C/T]TGATCATTTTATATA	26091
rs181056683	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68036022	ACTAAGGGCTCTAAA[A/G]AATGTTTAGCGGCTG	26091
rs181061115	snp	A/C	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:68060583	CTAAATTTCTCTCCA[A/C]TTATATGGTTTATGT	26091
rs181067690	snp	C/G	0.00993419	0.0697739	intron-variant	HERC4	GRCh38.p7	10:68013448	ATGAACCTTGAGGAC[C/G]TTATGCTTAGTGAAA	26091
rs181086835	snp	A/G	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:68071020	TATACCTTAACTCCC[A/G]ACCCAGACTCTAAAT	26091
rs181088461	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67978190	CTGAGACAGGAGAAT[C/T]GCTTGAACCCAGGAG	26091
rs181092240	snp	A/G	0.00438332	0.0466095	intron-variant	HERC4	GRCh38.p7	10:67995015	TTTTAATCACTACTC[A/G]AAAAAGTTTGAGAAA	26091
rs181096668	snp	A/G	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:68053253	TAAATACATAATCTC[A/G]TTTTAGGGATGCTTC	26091
rs181100869	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68035974	TAAGTAGTATACTGC[C/T]TATTACTGTATACTG	26091
rs181110830	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68045216	TGATCCCAGCTATTC[A/G]GGAGGCTGAAACAGG	26091
rs181111205	snp	A/G	0.00597247	0.0543191	intron-variant	HERC4	GRCh38.p7	10:68062685	GAATCACATGAACCC[A/G]GGAGGCGGAGGTTGC	26091
rs181173751	snp	A/T	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:68024554	ATTGAATAAAAAACA[A/T]TAATGAGGCCTAATG	26091
rs181179542	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68006580	ATGGGGTTTTGCCAC[A/G]TTGGCCAGGCTAGTC	26091
rs181291682	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67963576	GAGCTAAACACCAAG[A/C]GTTTAGAACTAGTTT	26091
rs181366192	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67929028	CCTTACTTTCTGTCT[A/T]CCAAAACTATTTCTT	26091
rs181375027	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67928694	TTGGGAGGCCGAGGC[A/G]AGTGGATCATGAGGT	26091
rs181503726	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67994771	CTCACTCTGTCGCCC[A/G]GGTTGGAGTGCAGTG	26091
rs181508782	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67944050	AGGGAAGAACACAAG[C/G]TTCGCTGGCTTCACC	26091
rs181520823	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68043848	AAACGATTATGCCCT[A/G]TGTAACTGTGTAAGA	26091
rs181529720	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68023925	AAAATATTTCTTAGA[A/C]AATAAATGGCACTAT	26091
rs181542081	snp	G/T	0.00795532	0.062565	intron-variant	HERC4	GRCh38.p7	10:67943043	TTTGGGGGATAATGT[G/T]TTTCTTAAGTATTTG	26091
rs181549354	snp	C/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67963245	TTTTTGAGATGGAGT[C/G]TCACTCTGTTGCCCA	26091
rs181551370	snp	A/G	0.00438332	0.0466095	intron-variant	HERC4	GRCh38.p7	10:67977930	AGAGTATAGTGAGCC[A/G]AGATTGTGCCACTGC	26091
rs181552018	snp	A/G	0.0115144	0.0749975	intron-variant	HERC4	GRCh38.p7	10:68061413	TGGCAGGCACCTGTA[A/G]TCCCAGCTAATCGGG	26091
rs181570392	snp	A/T	0.00863355	0.0651325	intron-variant	HERC4	GRCh38.p7	10:67939549	GTTAAATAAAAGAGA[A/T]GATAAATAATCAGGC	26091
rs181573405	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67959805	TTATAATGAAAGCTT[A/G]CCACTTTATTGAACA	26091
rs181580415	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67974369	ACAAATAAAGTTGAT[A/C]TAACATACAAACTAA	26091
rs181597917	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67925020	AAGATTAAAACAGGG[C/T]TTTGGAATAATACTA	26091
rs181656689	snp	C/T	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:68006141	TTGTATATGTCTTTA[C/T]AAGTTGCTGTAGTTA	26091
rs181692858	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67971489	TGGTTTAACATCCAA[A/C]TATCAATGAATTTCA	26091
rs181723261	snp	C/G	0.00795532	0.062565	intron-variant	HERC4	GRCh38.p7	10:67935107	TTTGACTGTTTTGGC[C/G]TTTCCTTAAATGTCT	26091
rs181745896	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68014761	AAGAAACCACAGATC[C/T]GAAGCTAAGGATGAC	26091
rs181752757	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68009387	TCCAAAGCACTGGGA[A/T]TACAGGCATGAGCCA	26091
rs181757932	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	HERC4	GRCh38.p7	10:68076895	TTGGGAGGCTGAGGC[A/G]GGTGGATCACCTGAG	26091
rs181762416	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68058807	AGATCTAGCAACAGA[A/G]CCAGGATTTTTATGT	26091
rs181783691	snp	C/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67955544	CGGGAGGCCAATGAG[C/G]GCAGATTACTTGAGG	26091
rs181784892	snp	A/C	0.0115144	0.0749975	intron-variant	HERC4	GRCh38.p7	10:67948961	ACAATTTTTAAAAAG[A/C]ATTAAAAGTTGGCCA	26091
rs181811127	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68048054	CTCCAGGGTAGCTGG[A/G]ACTACAAGCACATGC	26091
rs181817458	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67986638	TGGGATTACAAGCAT[A/G]AGCCATCACGCCCAG	26091
rs181819605	snp	C/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68029485	TGACAGAACAAGACT[C/G]CATCTCAAAAAAAAA	26091
rs181829236	snp	C/T	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:67967864	CTGATTATGAAACTT[C/T]TATAAGAAAACTGGC	26091
rs181834318	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68066434	TGGCTCACTTCTAAT[C/T]ATGTAAAAACACTAA	26091
rs181835398	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67982259	ATGGTACTGGCATGA[A/T]AACAGACACATAAAC	26091
rs181838232	snp	C/G/T	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:68019805	CAGGGTGGGCAATAA[C/G/T]GACTTTGTCTGTTTT	26091
rs181838667	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68001050	ATAATAATCACTAAA[C/T]CAAAGGAATATTCTG	26091
rs181864098	snp	A/G	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:68013326	TTGCTTTATTGCACT[A/G]TTTGCTTCATTGCAG	26091
rs181889839	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68048840	AGAAAGGGTATTTTT[A/T]AAATTTGTTTTTTAA	26091
rs181918023	snp	A/G/T	3.3407e-05	0.00408688	intron-variant	HERC4	GRCh38.p7	10:67990870	AAACAAAATCAACAG[A/G/T]TAATACTGTAAACAT	26091
rs181981595	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:68058611	TTTATTTTTTTGAGA[C/T]GAGAGTTTCACTCTG	26091
rs182001649	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67932035	CAATCTCAGCTCACT[C/G]CAACCTCCGCCTCCC	26091
rs182003810	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68030057	TTTTGCTTTTTAATC[A/G]CATGTAACAGTTTCT	26091
rs182018916	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67950570	CATGAGCCACCACAC[C/G]CAGCCCTACAGGGGA	26091
rs182028300	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67931491	GTGCAGTGGCGCGAT[C/T]TTGGCTCACTGCAAC	26091
rs182140065	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67952412	CCTCAGCTTTCCGAG[C/T]AGCTGGGATTACAGG	26091
rs182140326	snp	C/T	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:68067454	ATAAAACGCAATGAG[C/T]TTCTTTGGTTTAAAT	26091
rs182182185	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67933261	TTACTTTAACAAATG[A/C]CTAAGAGAGGGTACT	26091
rs182206800	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67936972	AATGCATTTATAAGA[A/C]AGAGATGAATAAAAT	26091
rs182208157	snp	C/G	0.00478085	0.0486577	upstream-variant-2KB	HERC4	GRCh38.p7	10:68076747	CTTTTATAAGGACAC[C/G]AGATATTGGATTAGA	26091
rs182216343	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67956817	AAAATTTCAAATATT[C/T]ACTGTCCAGAAACAT	26091
rs182219116	snp	C/T	0.0821764	0.185298	intron-variant	HERC4	GRCh38.p7	10:67972262	CACGGTGGCTCACAC[C/T]GGTAATCCCAGCACT	26091
rs182221466	snp	A/C	4.98666e-05	0.00499308	intron-variant	HERC4	GRCh38.p7	10:67959105	GAGCTTTATTACACC[A/C]AACTTACCTCAGTTA	26091
rs182239537	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67990799	TTTTAAAAGCACATC[A/G]TAAGAGTCTGTGAAA	26091
rs182257730	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68009184	AACCGAGATTGCACC[A/G]CTGCACTTCCAGCGT	26091
rs182263711	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67924204	CTGAATGTGTCAACT[G/T]TTTTTCTTGACATTG	26091
rs182273831	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68040148	GAGGCTTTAGTATTA[G/T]TCATAAAATTTGCCA	26091
rs182322302	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68026295	GAGATGGGGTTTTCC[A/T]GTATTGCCCAGGCTG	26091
rs182335535	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68007386	ATCTTCAGTTTAGTT[A/G]AGATTTCTCAAAACA	26091
rs182347028	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67989123	AAAACTCACCACTAT[A/G]CCTAATATTAAAACC	26091
rs182350064	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68064180	GGAAGCAGAGGTTGC[C/T]GTGAGCCGAGATCAT	26091
rs182356179	snp	C/T	0.0111196	0.0737302	intron-variant	HERC4	GRCh38.p7	10:68045562	AACTTAAAATATTGG[C/T]CCTTAAAATACTGGC	26091
rs182431924	snp	C/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67956045	AGAACACTACAAAAA[C/T]ATTTAGAATACCAAA	26091
rs182436259	snp	C/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67972133	GCAGGAGAATCATTT[C/G]AACCTGGGAGGCAGA	26091
rs182475727	snp	C/T	0.00874735	0.0655527	intron-variant	HERC4	GRCh38.p7	10:68003179	TTTTTTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT	26091
rs182500073	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68037165	AGTGCCGTGATCTTG[A/G]CTCACTGCAACTTCC	26091
rs182501082	snp	C/T	0.00438332	0.0466095	intron-variant	HERC4	GRCh38.p7	10:67973880	GGTGAAACCCCATCT[C/T]TACTAAAAATAGAAA	26091
rs182501853	snp	A/G	0.0115144	0.0749975	intron-variant	HERC4	GRCh38.p7	10:68040846	GTGAGCCAAGATTGC[A/G]CCACTGCACTCCAGC	26091
rs182510498	snp	A/C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68016227	ACTTCATTATACTAC[A/C/T]GGAATGTAAACCTTT	26091
rs182513746	snp	C/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67968870	CTGCTCTCATTAACT[C/G]ATAGAAAAAAATAGA	26091
rs182531564	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68073402	TGACACTTTCTATGA[C/T]CCTTTGCAAAATTTA	26091
rs182535081	snp	C/T	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:68055854	CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA	26091
rs182536195	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67940481	CTGGAGTGAAATGGC[A/G]CAATCTGGGCTCACT	26091
rs182546330	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67938997	GCTGCCTTAATGAAA[C/T]TGTGCATCTTTTACA	26091
rs182561736	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67996672	TTAGCATAGAAAACA[A/T]CTTAGTATTAATATG	26091
rs182613781	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922819	GTAGATTGAACATTC[C/T]GCAAGTAAGAATTAT	26091
rs182637853	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67935521	ACCAAGAAGGAGGGA[A/G]CTATAGACTTTCAGC	26091
rs182639465	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922205	AACTGTGGAGACAGA[A/G]TTCTTCCAGTACTAA	26091
rs182692821	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68056339	AACCAATAAAATACA[C/T]TGATCATGTGTTCAT	26091
rs182724046	snp	A/G	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:68050658	ACTGATAACTTCACT[A/G]TAATTTTTAAAAAGT	26091
rs182753266	snp	C/T	0.00159617	0.0282053	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069817	GGAGGCCAAGGCGGG[C/T]AGATCACAAGGTCAG	26091
rs182757686	snp	G/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:68016631	GCTGGGATTACAGGC[G/T]TGAGCCACTGCACCC	26091
rs182767921	snp	C/G	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:68020595	AAAAACGGTGAAACC[C/G]CGTCTCTACTAAAAA	26091
rs182779459	snp	C/T	0.00993419	0.0697739	intron-variant	HERC4	GRCh38.p7	10:67983743	AGTGAGCCAAGATCG[C/T]ACCACTGCACTCCAG	26091
rs182819674	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67987571	GCAGACCTGGACCCT[C/G]ATATGCTAAAAGAAA	26091
rs182828571	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67965769	TACTCACCCTTCTAT[C/T]ATATAACTGCTGCAC	26091
rs182844085	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67925670	CCCGTGTGTATAAGG[A/G]TACTGTGAATATGAG	26091
rs182859292	snp	A/G	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:67930604	AGAGTGGTAAGTGCT[A/G]CTCTGTTTTTTTATG	26091
rs182957242	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68074528	CCTTTTCTTTAAAAC[A/G]CAGAGGCGTCCTCTC	26091
rs182973823	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67965359	AGAAACAAGGCTCTG[G/T]CTGGTTCACCACTGT	26091
rs182977983	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67979007	CTTTCCAAGAAGCAC[A/G]AAGACACACAAGTCC	26091
rs182986267	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67996344	ACAAGAAACAGTCTT[C/G]ATTAGTGCACTGTTT	26091
rs182986341	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68015063	CCCAGCAAGACTGGA[A/G]ATCTCTTTCTCCATG	26091
rs183000920	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67929882	CAACGGCACGATCTC[C/T]GGCTCACTGCAACCT	26091
rs183004760	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67945594	AACTACCCATATCTT[C/G]AGTATAAAGACTAAA	26091
rs183005372	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67997535	CTCATACTTATTTGA[G/T]TTTTGCCTTCCTGTG	26091
rs183023868	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68037502	ACTGGTAAGAGAGGA[A/G]TGCAAACAAAGCTAA	26091
rs183039537	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67926828	CTCCTTACGCACCAT[C/T]CACTAAACTCTTTTT	26091
rs183050489	snp	A/T	0.0130921	0.0798413	intron-variant	HERC4	GRCh38.p7	10:67940747	ACTGGGCCAGCCAAA[A/T]TTAGTCTTTCAATAG	26091
rs183055270	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67961383	CACGTGCTTTCATAT[C/T]ATATCTATCTTTTTT	26091
rs183062976	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	HERC4	GRCh38.p7	10:68077217	AACCCACAACAGTAT[G/T]TTACAGAAATGAATG	26091
rs183064752	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68021436	GCTTTTCCTGTAAGA[A/T]CAGGAATAAGGATGC	26091
rs183064873	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68068380	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGACAGG	26091
rs183067936	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68049778	TAGCCAGGCATGGGG[A/G]CAAATGCTTGTAGTT	26091
rs183086452	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67984196	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGA	26091
rs183093930	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68003846	ATACCTCTGTGATGT[A/C]CAGATTTCCTTTCTT	26091
rs183099483	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68041333	CTCAGAATAGGGGAG[C/T]AGATTTTTAAAAAAA	26091
rs183105913	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67933674	CATTTTAAAAACAGC[C/T]TTATTTTTATCAAAG	26091
rs183109142	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67952734	AAACCCCGTCTCTAC[G/T]AAAAATATAAAAAAA	26091
rs183128473	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67969199	AAGTTACAAGACAAC[A/C]AAGTAGCCTGAATCC	26091
rs183139965	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67979400	GAAGAAAGAATTAGT[C/G]AGCTGAGGAGACAAA	26091
rs183168203	snp	A/G	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:67946705	TGAGGTCAAGAGATC[A/G]AGACCATCCTGGCCA	26091
rs183169268	snp	C/T	0.00676609	0.0577691	intron-variant	HERC4	GRCh38.p7	10:68040719	AATGGTGAAACCCCG[C/T]CTCTACTAAAAATAC	26091
rs183180341	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68020366	ACCTAAAAGACAAAG[A/G]CTAAATCAAACATCC	26091
rs183189355	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68001964	TCATCTGCTGATGGA[C/T]GTGGGTTGTTTCCAC	26091
rs183192778	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67976297	TATACAAAAAACACA[A/G]TGGCTTTCCCCTCTC	26091
rs183200515	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67992877	TGAACATTAAACGAT[C/T]CCACAAGCATAAGCA	26091
rs183286235	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68064928	GGTGAGTGGAGATCG[C/T]GCCATGCACTCCAGC	26091
rs183328841	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67972453	TTGAATCCGGGAGGC[A/G]GAGGTTGCGGTGAGC	26091
rs183333411	snp	C/T	0.121369	0.214369	intron-variant	HERC4	GRCh38.p7	10:68059569	TATATATCATAATAT[C/T]ATATATCATATTATA	26091
rs183335040	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:68047572	AGTAAAAGACCAAAA[C/T]TGACACCTCACCAAG	26091
rs183358528	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68007644	ATTGAGTGTAATGAT[C/T]TCAATTCTTCAGTCA	26091
rs183362288	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67937571	AGAACCAAAATTTCA[C/T]AGAAAATCGTTTTTG	26091
rs183366317	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68036837	TTATTATTACCAATT[A/G]TATCAATTAGAAACA	26091
rs183432977	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67951627	CCATTTCCTCTGCAG[C/T]TCTCACAAATGGTGT	26091
rs183445623	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67983107	AAAACAAAAACAAAC[A/G]GGCATATGAAAAGGC	26091
rs183576069	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67989500	GATTCCCATATTCTA[A/C]CCCTTGCTTGTTGCT	26091
rs183589369	snp	A/G	0.00438332	0.0466095	intron-variant	HERC4	GRCh38.p7	10:68054527	TTTTGTATTTTTAGT[A/G]GAGATGAGGTTTCAC	26091
rs183594285	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67923310	CACATTCTAATTGCT[C/T]ATCCACACAATATTT	26091
rs183602535	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67957306	CTCCTATGTTAAATG[C/T]GATAGCCAATTCTTA	26091
rs183625457	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68050348	TGTCTTTTCAAAACA[A/T]ACAATAAATAAAATA	26091
rs183638956	snp	C/T	0.00398564	0.0444627	intron-variant	HERC4	GRCh38.p7	10:67930937	TGCCTGCCTCAGCCT[C/T]CCCAAGTGCTGGGAT	26091
rs183639181	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011943	TAGTATACCCACCTT[C/T]GTCAATTACCTCAGC	26091
rs183657440	snp	C/T	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:68032047	ATGAGCCTCTGTGCC[C/T]GGACGTTAATGTCTT	26091
rs183668573	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68059748	CATAATATTATATAT[C/T]ATAATATTATATATC	26091
rs183692947	snp	C/T	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:67968496	TCCTGCCACAGCCTC[C/T]TGAGTAGCTGGGACT	26091
rs183698523	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67934801	ACAGTTTTAGGGTCC[C/G]TTTGACTGAAAATTT	26091
rs183705126	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67992461	AAAACCTATCAAATA[A/G]ATCAGAAAAAACTTA	26091
rs183707549	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67976986	GCAGGCCACAAGGAC[C/T]GCAACTACTAGGTGA	26091
rs183712901	snp	C/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67994112	TTTGATAATTACTAT[C/G]AAATTTTCCGTAAGT	26091
rs183712923	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67954010	GGAGTTCTACTAAAC[G/T]GATCCATCCTTTTCA	26091
rs183733164	snp	C/G/T			intron-variant	HERC4	GRCh38.p7	10:67926328	CTTGAACTTGGGAGA[C/G/T]GGAGGTTGTAGTGAG	26091
rs183755576	snp	G/T	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:67960489	CTCCTGGGTTCAAGC[G/T]ATTCTCCTGCCTCAG	26091
rs183773604	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67947016	AGAGAGACCCCAATA[C/T]AATAATAGCTGGAGA	26091
rs183785526	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069603	GTTATTATGAATCTC[A/G]AGAATAATTTATCCT	26091
rs183826172	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68018487	GTAAACATTATAATG[A/G]TGTCCTAAACAGCAC	26091
rs183848875	snp	A/G	1.65614e-05	0.00287757	intron-variant	HERC4	GRCh38.p7	10:68032774	AGTTTTAGAAGTACA[A/G]TACCTTGGTTAGAGC	26091
rs183895585	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68029136	TGCACTATGACTGTG[C/T]CACTGCACTCCAACT	26091
rs183900296	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68008875	GCAATAAAGCAAATA[C/T]CGCAATAATGCAAGT	26091
rs183909043	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67975261	ATTAAAGTGGACTTC[A/C]TGTACATTGTCTCAT	26091
rs183927097	snp	C/T	0.00398564	0.0444627	intron-variant	HERC4	GRCh38.p7	10:68065948	TAACTCATTACAATT[C/T]AAAATTAATTATTGC	26091
rs183932645	snp	A/G	0.00119737	0.0244387	intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010646	ATTTTCATTGTTGTC[A/G]GCTTCCTCCACCCAC	26091
rs183936510	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67940616	TATAGATGGGGTTTC[C/G]CCATGTTGGTCATAC	26091
rs183938509	snp	C/T	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:67973781	TACATAGGTTGGGCA[C/T]GGTGGCTCATGCCTG	26091
rs183947199	snp	A/C/G	0.000798403	0.0199641	upstream-variant-2KB	HERC4	GRCh38.p7	10:68076039	TTGAAATTGTAAGTT[A/C/G]GGTATTGCTAGAATG	26091
rs183947471	snp	G/T	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:68057568	GGCAGAGGTCAAAGT[G/T]AGCCGAGATCACGCC	26091
rs183947812	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67990683	ATACACAAACTTAAG[C/G]AACGTGGTAATGTTA	26091
rs183957353	snp	A/G	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:68039010	TTTCAAGAAAAAAAG[A/G]GGGGATGCCAGATGC	26091
rs183958235	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68072650	ATTTTCTTTATTGTT[C/T]TATATCGTCATACAA	26091
rs184004070	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67973388	CTAGGTTAGCCATCC[C/T]CAGCCAAGGCTTAGG	26091
rs184008073	snp	C/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67989889	CAGTTTTAATTGTTC[C/T]TCCTCCTTTACTTCT	26091
rs184028827	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67923487	TGCAGTTTTGATTAT[G/T]ATTTCTTTTTCTATT	26091
rs184038658	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67938291	ACTAAAAATACAAAA[A/G]TTAGCTGGGTATGGT	26091
rs184039643	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67957753	CTAATGAAGAATTAA[C/T]ACACCCTAAAACAAT	26091
rs184120040	snp	C/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68026577	GGCCAGATGTGGTGG[C/T]TCACGCCTGTAATCC	26091
rs184233161	snp	A/G	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:68033507	ACTTGTTTCAGTTAC[A/G]ATTTTTTCAAATTCA	26091
rs184239480	snp	C/T	0.00557542	0.0525036	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012587	GTTTGTTGTCTTATA[C/T]AGGTAAGGTTCATGG	26091
rs184260992	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67947539	CCCACTATCATTAAT[A/G]TATACAACAATCCAA	26091
rs184261361	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67967056	AGACGGAGTTTCATC[A/G]TGTTAGCCAGGATGG	26091
rs184285296	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67931125	CGATAGTTGGGACTA[C/T]AGGCGTGCGACACTA	26091
rs184294756	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67941511	AAAATGAATAAACAC[C/T]TGTAAACCAATCACT	26091
rs184321650	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB	HERC4	GRCh38.p7	10:68076359	CACCCGCCTCGGCCT[C/T]CCAAAGTGCTGGAAT	26091
rs184358565	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67961793	AGTAAAGCCAAAGCA[A/G]TGTAAGCATAAGCAA	26091
rs184399579	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67928115	GAAAAGGAAACAAAC[A/G]CCCTAAGACTGGAGT	26091
rs184432147	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68013336	GCACTATTTGCTTCA[A/T]TGCAGTGGTCTGGAA	26091
rs184432351	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68059823	TATAATATTATATAT[C/T]ATAATATTATATATT	26091
rs184441258	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68041740	TAAAATTTGGGTCAA[C/T]TTTTTAAATAAAATG	26091
rs184445040	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68021765	GTGAGCCGAGATCAC[A/G]CCATTGCACTCCAGC	26091
rs184451469	snp	A/C/G	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:67994821	CAACCTCAGCCTCCC[A/C/G]AGTAACTGAGATTAC	26091
rs184458749	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67960558	GCCTAGCTAATTTTG[C/T]ATTTTTAGTAGAGAT	26091
rs184467000	snp	C/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67943121	TTACATACAACCCAG[C/G]CTGTTACATGCTTTT	26091
rs184481251	snp	C/T	0.0314385	0.121371	intron-variant	HERC4	GRCh38.p7	10:67963330	CAAGCCATTCTCCTG[C/T]CTCAGCCTCCTAAGT	26091
rs184488101	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67978046	GTTTGGGAGGCCAAG[A/G]CAGGCAGATCCTTGA	26091
rs184505385	snp	A/G	0.0256215	0.110247	intron-variant	HERC4	GRCh38.p7	10:67928851	GCTTGAACTTGGGAG[A/G]CGGAGGCTGCAGTGA	26091
rs184506783	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67958087	GCTGGGATTACAGGC[A/G]TGAGCCACTGTGCCC	26091
rs184527582	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67923539	TTTAAATCAGAAATT[C/T]ATAATGGGCAGCCAA	26091
rs184563191	snp	A/G	0.00597247	0.0543191	intron-variant	HERC4	GRCh38.p7	10:67998929	ATTTTTAGTAGAAAC[A/G]GGGTTTCACCATGTT	26091
rs184575524	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67931691	TGGCCTCCCAAAGTG[A/C]TGGGATTACAGGCAT	26091
rs184577603	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68065085	TAAAACTTTAAAACA[C/T]GGGAAAATGCTAAAT	26091
rs184586077	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67928286	TAAGGTGATTAGAGG[C/T]GGAGTCCATTTCCAC	26091
rs184589064	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68027301	ACCATATAACCATCA[C/T]TCAGTTTCAATAACT	26091
rs184596905	snp	C/T	0.00398564	0.0444627	intron-variant	HERC4	GRCh38.p7	10:67967133	TGTTGGGATTACAGG[C/T]GTGAGCCACCACGCC	26091
rs184670087	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67938773	AGGTGGTGAAACCCC[A/G]TCTCTACTAAAAATA	26091
rs184683587	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68008271	CAGTACTGGGTCTCA[C/T]CCAAAGCATGTAGAG	26091
rs184685676	snp	A/G	0.0111196	0.0737302	intron-variant	HERC4	GRCh38.p7	10:67980736	AAATAGAAACAACAA[A/G]AAGTTAAAAAGCAGG	26091
rs184718886	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68047856	ATCTACTCTTACCAT[A/G]TGACCCAATTCCTTG	26091
rs184721588	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67949139	AATACAAAAACTAAG[C/T]CAGGCATGGTGGCAT	26091
rs184759346	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68017044	TGGTGGTTGGGCTGT[A/G]TATTATATTCCCCAT	26091
rs184769301	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67980585	AGGTATAAAACTCAA[C/T]AGTATACAGAAAAAT	26091
rs184775063	snp	C/T	0.0460142	0.144533	intron-variant	HERC4	GRCh38.p7	10:67998514	ATCCTGCCACTGCAT[C/T]ACAGCCTGTGCAAAA	26091
rs184788972	snp	C/G	0.000134794	0.00820845	intron-variant	HERC4	GRCh38.p7	10:68038082	GAAATAAAATAAAAA[C/G]TAATGCTTACCTTTA	26091
rs184829572	snp	C/G	0.00438332	0.0466095	intron-variant	HERC4	GRCh38.p7	10:68005104	TTATTTCTGAGTTCT[C/G]TGTTCTGTTCCATTG	26091
rs184863534	snp	G/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68042600	TGCACACCAGCCTGG[G/T]TGACAGAGTGAGACT	26091
rs184874743	snp	C/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68043674	ACAAAAAATTAGCCA[C/G]CTGTGGTGGTGGGCG	26091
rs184879657	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68023582	ATTGTTTAATGGGTA[C/T]AGAGCTTCAGTTTTG	26091
rs184884048	snp	A/G/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68070051	TGTCTCAAACAAAAC[A/G/T]AAACAAAACAAAACA	26091
rs184909082	snp	C/G	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:68061318	GCGGGTGAATCATCA[C/G]GTCAGGAGGTCGATA	26091
rs184931522	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68066843	AGTTATACTGAAGTA[C/T]CAAAGTGGTATCAGA	26091
rs184931977	snp	C/T	0.00795532	0.062565	intron-variant	HERC4	GRCh38.p7	10:68068319	GTGAAACCCTGTCTC[C/T]ACTAAAACTACAAAA	26091
rs184948633	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68049334	AAGAAGAAAACATAT[G/T]CATATTTGCTAATAT	26091
rs184956473	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68031184	AAAGATTAAGAGAAT[G/T]AGCATTTCTTAAAAC	26091
rs184963853	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68060331	CAACCTCTGCTTCCC[A/G]GGTTCAAGCAATTCT	26091
rs184973735	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67985308	TATCTAATATAATAA[C/T]AAGCACATAGTAGGC	26091
rs184978132	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68022163	AACAGCATGGTCATG[C/G]ACTGGAAGACAAATT	26091
rs185181399	snp	C/G	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:67991751	ATAAAAGTTAAGATA[C/G]TGACCATTATAAAAC	26091
rs185201343	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010026	ATCAAGAGCATCACC[A/G]AACTTCACCTTCCCT	26091
rs185269883	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67940215	ACAGGCGTGAGCCAC[C/T]GCACCTGGCCCATTT	26091
rs185276740	snp	A/C	0	0	intron-variant	HERC4	GRCh38.p7	10:67959966	CCCCAGAAGAGAGGG[A/C]ATTGCCCTGGGTTAC	26091
rs185288636	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67974465	ACACTAAAACTAAGG[A/G]ATATCTGAAAGGGAA	26091
rs185305752	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68052732	CAATTCATTGTGTAA[A/G]AGTTCACTTATATGA	26091
rs185324039	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67984739	AGACACGTGCCACCA[C/T]GCTCAATTAATTTTT	26091
rs185361107	snp	A/C	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67953444	GGCAGTAAATGTGTA[A/C]GATAAGTCTGGAACA	26091
rs185386213	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68035674	CTACCTATGTTTCCA[A/G]TCTCTTCTCATATCA	26091
rs185394408	snp	A/G	0.00517822	0.0506191	intron-variant	HERC4	GRCh38.p7	10:68035366	TTTCACCATGGTGGC[A/G]AGGCTGGTCTCGAAC	26091
rs185396824	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67962539	TGAAAAATAATAGGA[C/T]GTGAAAAACTTCAGA	26091
rs185423942	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68070681	TAAAAGATGAAGTTC[C/T]TATCACAGCAACTAC	26091
rs185433109	snp	C/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B	HERC4, POU5F1P5	GRCh38.p7	10:68009545	GCAAGTCTTAAACTT[C/T]TTGTTGATGGAGAGT	26091
rs185437445	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67967723	CATACAAATGATCTA[C/T]GAAGTAAAAATAGTT	26091
rs185449428	snp	C/T	1.65192e-05	0.00287391	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:67990913	ACAGACCTGCTGAGA[C/T]ATCTGCGGATGATCA	26091
rs185453850	snp	C/T	0.00795532	0.062565	intron-variant	HERC4	GRCh38.p7	10:68004294	TTTATATATTCTGGT[C/T]ATTAATTCCTTATCA	26091
rs185470525	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67931968	TTATTTACTTATTTT[C/T]TGTTTTTGAGACAGA	26091
rs185472999	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68071145	ATTAGGGAAACCCAC[C/T]GCCCCAACTTTACAT	26091
rs185473667	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67934137	CTTAAATTTCAATTT[A/G]CTTTGGATTAATCTT	26091
rs185474999	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67950147	GAATTTCCTTAACAC[C/T]ATAAAGGGAATTTGG	26091
rs185479422	snp	A/G	0.00597247	0.0543191	intron-variant	HERC4	GRCh38.p7	10:68053383	ATTACAGCTCACTGC[A/G]GCAGCAACCTCCCAG	26091
rs185485062	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67969767	AGAAACTGCCACACA[A/C]AAAAATCGGAAGCAG	26091
rs185487976	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68035987	GCTTATTACTGTATA[A/C]TGTAGTATGCCTAGT	26091
rs185495764	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67988074	AAATCCATCTTTAAT[A/G]AAACAGCTCAGAGTC	26091
rs185519216	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67942872	TCTTCACGTTTTCAT[C/G]TGTATATATACTCTA	26091
rs185525970	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67936801	TTTCTTTTGCTACTC[C/T]TTCTTTTTGGAATAT	26091
rs185527521	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012850	GCTTTAGTAATTCTC[A/G]CAATATTTCAATATT	26091
rs185528626	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67956388	AGGAATAGGAGATAA[C/T]GGTGACCAACCCCAG	26091
rs185529635	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67977305	ATTTCTAGATACACA[A/G]TGGCCAGAAGGGAAC	26091
rs185533929	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67995211	GCAGGAGAGTAGTTC[C/T]ATCAGGAAACACATA	26091
rs185537998	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67972151	CCTGGGAGGCAGAGG[C/T]TGCAGTGGGCCAAGG	26091
rs185550782	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68013485	AGTCACAAAAAGAAA[C/T]ACTACTATATGATTC	26091
rs185569758	snp	G/T	0.00438332	0.0466095	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922431	AGATTTAAATCATAA[G/T]TTTTAACCTTTAAAA	26091
rs185576765	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68048522	AGGGAGGGATGAACA[A/G]GCAGAGCATAGAGGA	26091
rs185612677	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	HERC4	GRCh38.p7	10:68077068	AGACGGAGGTTTTGC[G/T]GTGAGCCTAGAGCGC	26091
rs185628170	snp	A/T	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:68059303	GTTGATGTGGTTGAG[A/T]GTCCCTATCCATAAA	26091
rs185629212	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	HERC4	GRCh38.p7	10:68075521	AAAGTTGGAGTTTGC[A/G]AAGACAAACGAAGAA	26091
rs185645325	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:68009190	GATTGCACCGCTGCA[C/T]TTCCAGCGTGGGTGA	26091
rs185645644	snp	A/G	0.0103295	0.0711199	intron-variant	HERC4	GRCh38.p7	10:67973910	AAATTAGCTGGGTGC[A/G]GTGGCACGTGCCTGT	26091
rs185661373	snp	C/T	0.00953873	0.0683987	intron-variant	HERC4	GRCh38.p7	10:68051960	AGGCATGAGCCACCG[C/T]GCCCAGCCTCAACTT	26091
rs185683490	snp	C/T	0.0209421	0.100162	intron-variant	HERC4	GRCh38.p7	10:68040820	CTTGAACCCAGGAGG[C/T]GGAAGTTGCAGTGAG	26091
rs185768504	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68029693	TTTATATATTATATA[C/T]ATTTTTATTTATATA	26091
rs185772643	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67959140	ATGGTTGACATCCTA[A/C]GACAGCAGTGCAGAA	26091
rs185778926	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68056887	ATAACCAAAATCTGG[A/C]AACTGGGTCAATGTT	26091
rs185785152	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67990823	TGTGAAACTGCAAAG[C/T]AAATTAGGCTATAAA	26091
rs185957490	snp	A/T	0.00795532	0.062565	intron-variant	HERC4	GRCh38.p7	10:68036905	CTGAAATAGTACATA[A/T]TTTTTTCTGCCTCAG	26091
rs185961778	snp	C/T	0.00874735	0.0655527	intron-variant	HERC4	GRCh38.p7	10:68061710	ATGGTGAAACCACGT[C/T]TCTACTAAAAATACA	26091
rs185965792	snp	G/T	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:68015449	TTCTGTTTAGCGACA[G/T]AAGCTAACTAATACA	26091
rs186079977	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68058600	TAGGTTTTATCTTTA[A/T]TTTTTTGAGACGAGA	26091
rs186089958	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67982101	CATTGATCACAGAAA[C/T]AGGAAACACAATCCT	26091
rs186091411	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67960407	TTTTTTTTTTTGAGA[C/T]GGAGCTTCGATCTTG	26091
rs186100464	snp	C/T	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:68019070	GGTGCGATCTCGGCT[C/T]ACTGCAACCTCCGCC	26091
rs186121195	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67925847	CTATACTGAGGCCTC[C/T]TGCCAACAGTCATGT	26091
rs186187430	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67975017	AAGATGGTGAAACCC[C/T]GTCTCTACTAAAAAT	26091
rs186212511	snp	A/T	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:67996578	AAAATCATTAATACT[A/T]AACGTATTAGAACTT	26091
rs186216778	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68044032	AAAGACTAAAAAAAG[C/G]ACAAGTTAGTGAAAA	26091
rs186219755	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67940506	CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG	26091
rs186223785	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68039816	ATACTAGGCAGATGA[A/T]ACATTGACCTGTTCA	26091
rs186228027	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67999997	TATATTTGAGAACAA[C/T]GGTTACTTAATCCGG	26091
rs186288798	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67971338	AGCAATATGAGAAAT[A/G]AAAATTACAGATCAA	26091
rs186291207	snp	C/T	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:67929781	CAGCCTCCCAAAGTG[C/T]CAGGATTAGAGGTGT	26091
rs186292915	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67944962	CAAGATCTAGAGAAT[C/T]GCCTCAAAAGGGCAA	26091
rs186293873	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67986375	TTTATTTTTTTGAGA[C/T]GGAGTCTCACTCTTT	26091
rs186307819	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68030148	TTACTGTATTTTTAA[A/C]AACATATAAGGCCGG	26091
rs186309421	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68002278	TAAAATCTATTAACA[C/T]ACACGTGACTCAACT	26091
rs186333267	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68067613	AGGAGCAGCTCGTTT[A/T]TAAATTTGTTTTATG	26091
rs186335230	snp	C/G	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:67968655	GCTGGGATTACAGGT[C/G]TGAGCCACCGCGCCT	26091
rs186362677	snp	C/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68006629	GTGATCTGCCCGCCT[C/T]AGCCTCCCAAAGTGG	26091
rs186387933	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68045247	AGACTCGCTTGAATC[C/T]GGGAGATGGAGGTTG	26091
rs186393205	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67978218	GAGATGGAGGAGCTG[A/G]GATTGCGTCACTGCA	26091
rs186419915	snp	A/C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68005860	GCATGTGCCATGATG[A/C/T]CAGGCTAATTTTTAT	26091
rs186443836	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68040302	AAGTATATTCTTCTG[C/T]GTCATTACTGTGTTA	26091
rs186451889	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68020014	TTGTTTCTTTGGGGA[G/T]CCAGGCATTTAAGGT	26091
rs186456482	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67944173	GCTGGCTTCAGGTCT[A/G]ACCCAGTGCAGTCCC	26091
rs186473544	snp	C/T	0.00755907	0.0610114	intron-variant	HERC4	GRCh38.p7	10:68058681	GCAACCTCCACCTCC[C/T]GGGTTCAAGTAATTC	26091
rs186484438	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67967983	AATATGGCAGAATAC[G/T]TTGTATCAGACTACT	26091
rs186488023	snp	C/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67982711	AAACTAATCATCTGA[C/T]AAGGGATTAATAACC	26091
rs186496595	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68001112	GCAGTGGCTCATATG[A/C]GTAATCCCAGCACTT	26091
rs186510975	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67950986	ACCTGGAATGTTTAC[C/T]GTACCAAATGTAAGG	26091
rs186522348	snp	C/T	0.00398564	0.0444627	intron-variant	HERC4	GRCh38.p7	10:67951806	CTGTTCCTTGGGCAG[C/T]TGTATAAAAAACCTT	26091
rs186538197	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68020445	ATGTATGAACAAAAC[A/G]GAAATATCAATCAAA	26091
rs186545754	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67983378	TGCTGAGGAGCTACC[C/G]AAAAGAAACGAAAGC	26091
rs186545960	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68048965	AGTCTAAAAACAAAA[C/T]AGTACAACCTCTATG	26091
rs186555767	snp	C/G	0.000297895	0.0122008	intron-variant	HERC4	GRCh38.p7	10:68025706	AACCCCTTATCATTA[C/G]AAGGCATGATAAAAG	26091
rs186594603	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68055178	CTCTAACATGATGGA[C/G]TTAACAATCATCACA	26091
rs186600792	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68063073	TACACAGCACTCTTG[C/T]TTATACATCCTGTAA	26091
rs186614828	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069875	GTGAAACCCCGTCCC[C/T]ACTAAAAATATAAAA	26091
rs186622629	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68050915	GGCCCAGTAATGTTC[C/T]GTGTAAGAAAGGGAT	26091
rs186649380	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67929054	TTCTTCTCTTGTTCA[C/T]TGCATTTTTATTTTT	26091
rs186660121	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67963585	ACCAAGAGTTTAGAA[C/T]TAGTTTAATGTGTGT	26091
rs186672414	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67939072	ATTTGTTTTATCTAC[A/G]TCATCCAACAGTGAA	26091
rs186681443	snp	C/T	0.00517822	0.0506191	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012794	TCAAAAAACCTTCAA[C/T]TTGTAAAAATTCAGT	26091
rs186750155	snp	A/C	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67952506	CTAGACTGGTCTTGG[A/C]CTCCTGACCTCCACC	26091
rs186757859	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67968961	TAACACTTCACCTAA[C/T]AATTGTACATGAAAT	26091
rs186762201	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67984043	TTGGTGGCTCACGCC[C/T]GTAATCCCAACAGTT	26091
rs186781180	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67933554	ATCTTTGTCTTCCAA[C/G]TAATAAAGGATGATT	26091
rs186857526	snp	C/T	0.00438332	0.0466095	intron-variant	HERC4	GRCh38.p7	10:68072767	AATACATAACTTCTA[C/T]TTTGCTTTTAAAGCT	26091
rs186885344	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67924287	AGGTATTAATAACAT[G/T]TACATTCATGTGTCA	26091
rs186906383	snp	C/T	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:67955758	CCTGGGCGACAAGAG[C/T]GAAACTCCGTCTCAA	26091
rs186912819	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68023973	AATTCATCTACATTA[A/G]TATCTAAAACTTCTG	26091
rs186925653	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67986686	AAACAATACATAAAT[C/T]TTGGAAAACTATCAG	26091
rs186933724	snp	A/G	0.00358779	0.0422022	utr-variant-3-prime	HERC4	GRCh38.p7	10:67921947	TTAAACAGTTTTCAC[A/G]GCATTTTAAAATAAA	26091
rs186998769	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67964563	TTTCTCATGGATTTC[C/T]GTCTTTCATTTCTGT	26091
rs187017038	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67934948	CAGATTTCATTCATT[C/T]CAATTCTTTCAAATG	26091
rs187086424	snp	A/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68033100	GCCAATATGCCAGTA[A/T]GCAAAGGACTCAGAA	26091
rs187091203	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012202	ACTAAAATTCTCTCC[A/G]TATCAGCAATAAGGC	26091
rs187114575	snp	A/C/T	0.00557542	0.0525036	intron-variant	HERC4	GRCh38.p7	10:67971550	ATCTGTTCATCTCAA[A/C/T]AGATGGAAACAATAT	26091
rs187115131	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:68072324	AGGACACTTCATAGT[C/T]ACAAAATCTTTAATA	26091
rs187119388	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68006216	GTGCGCACACCACAA[C/T]GTCTGTGTACTTACT	26091
rs187119468	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67961465	TGCTTGTTCTTGCCA[A/C]ATGTCATGGTGCTGC	26091
rs187125097	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67976486	CTAAAAGCAAACAGG[C/T]GGAAGAGGTGAAGCA	26091
rs187129448	snp	G/T	0.00557542	0.0525036	intron-variant	HERC4	GRCh38.p7	10:67993029	GCTACAAAAGATAGC[G/T]AGAAGGAAATAAAAA	26091
rs187135539	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67927025	GCTTCTTGAATTTTG[A/G]ACTTTCCTTATTTGT	26091
rs187143650	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67940833	TACTTCAGAAATTTA[A/T]CAAGAAGAACAAAAT	26091
rs187149097	snp	A/C	0.00597247	0.0543191	intron-variant	HERC4	GRCh38.p7	10:67935198	TCGCCCAGGCTGGAG[A/C]GCAGTGGCACAATCT	26091
rs187174931	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67996123	CCAGCCTGGACAACA[C/T]GGCAAGACCTCGCCT	26091
rs187176176	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68036295	TGCACTCCAGCCTGG[A/G]TGACAAAGGGAGACT	26091
rs187181578	snp	A/G	0.00835141	0.0640778	intron-variant	HERC4	GRCh38.p7	10:67973607	TATAGTCAAGAATAA[A/G]TAGAGAGGCTGGCAA	26091
rs187201434	snp	C/T	0.0115144	0.0749975	intron-variant	HERC4	GRCh38.p7	10:68037217	CTCCTGCCTCAGCCT[C/T]CCGAGTAGCTGGGAC	26091
rs187205843	snp	C/T	0.00755907	0.0610114	intron-variant	HERC4	GRCh38.p7	10:68016394	AGTCTCACTCTGTTG[C/T]CAGGCTGGAGTGCAG	26091
rs187210279	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68049963	TGTAATCCCAGTACT[C/T]TGGAAGGCTGAGGCA	26091
rs187216310	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	HERC4	GRCh38.p7	10:68076796	TGACCTCATCTTAAC[A/C]TTATTACATCTGCAA	26091
rs187324509	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68073439	ATTAACTAGTTTTGA[C/T]TTCTGGTTATCTTGT	26091
rs187324721	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68055855	CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAA	26091
rs187329293	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68008566	ATGGATGTGGAAAAC[A/G]TCCTTATGTGCTGAA	26091
rs187370771	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67978975	AACATCCAAGTCCTT[C/T]TGAATATCTGGAAAG	26091
rs187373775	snp	C/T	0.0103295	0.0711199	intron-variant	HERC4	GRCh38.p7	10:68054221	GTAGAGCTCCATTCT[C/T]ACACATGTATGCAGA	26091
rs187384715	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68014553	AGTCCAGAGCTGTGG[G/T]CTATGAAAGTCCTCC	26091
rs187423233	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68068722	GATGGAAACCAGCTT[C/T]CTCAAAGGTGAACAA	26091
rs187481491	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68020948	AGTGCAGAGAGCCTA[C/G]GGGAACCATAGGATA	26091
rs187507903	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67962348	AAATATTAGTATGTA[C/T]GCATTATCTTTTTTA	26091
rs187513971	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68059669	TATCATATTATATAT[C/T]ATATTATATATCATA	26091
rs187517475	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67994288	ATTTAGCAGGATGTT[A/T]TTTATTTACTCTTAA	26091
rs187568261	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67932044	CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG	26091
rs187601751	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67965443	GAATAAGCAAATGAA[C/T]AGACCTAAATCTATA	26091
rs187608211	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67923383	CTTAATAAATGTTTG[A/G]TAAGTGAGTATTTTG	26091
rs187612145	snp	C/T	0.00557542	0.0525036	intron-variant	HERC4	GRCh38.p7	10:67979127	GAAAACATGACCTCA[C/T]CAAATGAACAAAATA	26091
rs187625257	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67930227	TTTCACTCATTTGCA[A/C]ATTAAAAAAAAAAGT	26091
rs187641831	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67945968	CAGAACACATTTAAA[A/T]ATGGCAGGAATAGCT	26091
rs187680705	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68064449	ATCTCAGCTACTGGG[A/G]AAGCTGAAGCAGGAG	26091
rs187684035	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68045666	TTTGTCAGGTTTTTT[C/T]ACTAGTATCACAAGT	26091
rs187697301	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67928151	TGGAGGGTTCTAGGC[A/T]CAGCAGAGGTTAATA	26091
rs187719886	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67947082	TCTAACAGAAAATCA[A/G]TGAAGAAACATTGGA	26091
rs187725048	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67989145	ATTAAAACCAGTTTT[C/T]AAAAAATGTTTTGAA	26091
rs187739690	snp	A/T	0.00755907	0.0610114	intron-variant	HERC4	GRCh38.p7	10:68026443	TATACAGATGTTTTT[A/T]AAAAAAACTCCCTAT	26091
rs187746040	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68007561	GTTAGGTATTTATTC[C/T]ATCCTTTGCAGTCCG	26091
rs187754964	snp	A/G	0.00676609	0.0577691	intron-variant	HERC4	GRCh38.p7	10:68003307	TACAGGCCTGCAGGC[A/G]CCTGCCACCATGCCT	26091
rs187755441	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67930950	CTCCCCAAGTGCTGG[A/G]ATTACAGGCATGAGA	26091
rs187756867	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67972365	CATCTCTACTAATAA[C/T]ACAAAATTAGCCGGG	26091
rs187759947	snp	C/T	0.00874735	0.0655527	intron-variant	HERC4	GRCh38.p7	10:67984215	GGCTGAGGCAGAGAA[C/T]TGCTTGAACCTAAGA	26091
rs187760327	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67977016	AGTCCAAGTGCAGAA[A/C]TGGGCCCAGAGCCAG	26091
rs187766705	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68040937	AAAAAGAAGCCAGAA[C/T]AAATTTTGTAAATTA	26091
rs187769088	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68004152	CTTCTTTTGAGAAAT[G/T]CATATTTAGATCTTT	26091
rs187781650	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68021681	GGTGTGGTGGCACAT[A/G]CCTGTAATCCCAGCT	26091
rs187796914	snp	A/C/T	5.05253e-05	0.00502599	intron-variant	HERC4	GRCh38.p7	10:67932802	ATGAAAAAGCACACA[A/C/T]GTACAGATTATAAAA	26091
rs187800848	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67969239	CAAATCCTTACAAAA[A/G]GTAACAGGGTACCAG	26091
rs187911634	snp	C/T	0.108048	0.20579	intron-variant	HERC4	GRCh38.p7	10:68059768	TATTATATATCATAA[C/T]ATTATATATTATAAT	26091
rs187919909	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68041899	TATCAAACTGTTTCA[A/G]TTATATCCTATTGTT	26091
rs187925530	snp	C/T	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:68041427	TTTTAATCTATAATG[C/T]TCCAAATTTTCAGAT	26091
rs187928678	snp	C/T	0.00478085	0.0486577	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069648	CTTTCTCCTTCATTC[C/T]TTATTAGTTATGGAA	26091
rs187960262	snp	C/T	0.00874735	0.0655527	intron-variant	HERC4	GRCh38.p7	10:67940655	AACTCCTGACCTCCA[C/T]GCTGGTCTCAAACTC	26091
rs187979682	snp	A/C	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68071474	TACAGAGAGATGTTC[A/C]GTTATTTCTATGGGG	26091
rs187983891	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68053586	TTGAGCCACAGCACC[C/T]GGCCTGGGGACCATT	26091
rs187988286	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67941649	AGTATTATGTCACTA[A/G]ATGTTCTTCTAAAAC	26091
rs187998347	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68036003	TGTAGTATGCCTAGT[C/T]CATACTAAGGGCTCT	26091
rs188010312	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67946777	CTGGGCATGGTGGCA[C/T]ACACCTGTAGTCCCA	26091
rs188021645	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67979719	AAAACAAGAGCTGGG[C/T]GCAGTAGCTCACACC	26091
rs188138558	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68047887	ATATTTACTCAAACA[C/T]TTATGTCCACATAAA	26091
rs188144990	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67971120	AAACCTGAAATGTCT[A/G]TATTTATTTTTTAAA	26091
rs188155454	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67985526	GGTGAGTATGTTTTA[C/T]CTGTTTGGTTTTATT	26091
rs188164165	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68005710	GCATCTATTAATTTT[C/G]TTTGTTTTTTTGAGA	26091
rs188165911	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68050416	AAGTAGTTAAAGCAA[G/T]GTATTAAAACCATTG	26091
rs188180590	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67934826	AAATTTTGAAATTTC[A/G]TGTATCTTGTCTTGG	26091
rs188253509	snp	A/C/T			intron-variant	HERC4	GRCh38.p7	10:68064936	GAGATCGCGCCATGC[A/C/T]CTCCAGCTTGGGTGA	26091
rs188263617	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67989555	AGTTCTTGTACTGAC[A/G]TTATTACTTCTATAT	26091
rs188264328	snp	A/G	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:67996713	TGACTGGCCAGGCGC[A/G]GTGGCTCACACTTGT	26091
rs188270158	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68026639	ACGAGGTCAGGAGAT[C/T]GAGACCATCCTGGCT	26091
rs188299262	snp	A/G	0.00557542	0.0525036	intron-variant	HERC4	GRCh38.p7	10:67966020	ACATTTATATTAAAA[A/G]TCTGAAATAAAAGTA	26091
rs188326688	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67930689	AGGATGGTATATTAG[A/C]AAGATAGAAAATCAG	26091
rs188349417	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68066276	CATTTGTATGATATA[C/T]TGGGAATACAGAACC	26091
rs188432758	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68027475	CATATATCTGTAACC[A/G]ACAAAAGTATATAAC	26091
rs188456371	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67994880	TATTTAGTACAGATG[A/G]GGTTTCACCATTTTG	26091
rs188457084	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68065845	AGTGACAACAAGATC[C/T]TGTCTAAAAAAACAA	26091
rs188478109	snp	C/T	0.0020032	0.0315846	intron-variant	HERC4	GRCh38.p7	10:68013447	GATGAACCTTGAGGA[C/T]GTTATGCTTAGTGAA	26091
rs188483882	snp	C/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67943699	ATCAAATGAAGGTCT[C/G]TACAGTGAACAAGGA	26091
rs188484253	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67963405	TATTTTTAGTAGAGA[C/T]GGGGTTTCGCCATAT	26091
rs188494321	snp	C/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67978154	AGTGGTGCAGGCCTG[C/T]AGTCCCAGCTACTCA	26091
rs188499863	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67957368	ATGATAAGTAATCTG[C/T]CTATTCCTTCATTTA	26091
rs188517626	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68008004	GACTACATGCACACA[A/C]CACCACGCCCAGCAA	26091
rs188538594	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67972698	GAATATGCAAGATCC[C/T]TGAAAACTACCAAGC	26091
rs188547063	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68047638	ATATTTAACTTATAT[A/G]TTCAACTTATGTCCC	26091
rs188662985	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	HERC4	GRCh38.p7	10:68076216	CACTGGAACTTCCGC[C/T]TTAGCCTCCTGAGTA	26091
rs188677404	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68037606	GCAATCTTCCCCAGT[G/T]GCAGCTATGAAGAGT	26091
rs188700929	snp	A/C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67923526	TTCTGTTATTTTTTT[A/C/T]AAATCAGAAATTTAT	26091
rs188705977	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67997806	CCACCATGACCTGTG[C/T]TCTTGTACGAGGTGG	26091
rs188711808	snp	A/G	0.00835141	0.0640778	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	HERC4	GRCh38.p7	10:68075289	GGAAGAGACTGGGTA[A/G]GAGAAGGCAGAGGGG	26091
rs188718853	snp	C/T	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:67938372	CTTGAACCTGGGAGG[C/T]GGAGGTTGCAATGAG	26091
rs188723203	snp	C/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67957819	GAATCTGCATTTTTT[C/T]TTCCCCCATACAGAG	26091
rs188745189	snp	A/G			upstream-variant-2KB	HERC4	GRCh38.p7	10:68075574	GCTTCGGCGTGCACA[A/G]AGCCTTTTAATGAAG	26091
rs188751420	snp	C/T	0.00517822	0.0506191	intron-variant	HERC4	GRCh38.p7	10:67937083	AAAAGCACCTACAAG[C/T]AGGGGTAGTATTTTG	26091
rs188757672	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68057133	TATATTTGTCCTTGA[C/T]TTTCTTGACATATAA	26091
rs188761546	snp	A/C/T	1.67978e-05	0.00289804	intron-variant	HERC4	GRCh38.p7	10:68038086	TAAAATAAAAACTAA[A/C/T]GCTTACCTTTAGAAA	26091
rs188768923	snp	C/T	0.00636936	0.0560724	intron-variant	HERC4	GRCh38.p7	10:67937806	CTGCCTCAGCCTCCC[C/T]GAGTAGCTGGTACTA	26091
rs188776627	snp	A/G	0.0023933	0.0345097	intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010683	AGCAAGGGCCGCGCC[A/G]CTTACACATGTTCTT	26091
rs188792881	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67980694	AATAACAACTACAAC[A/C]ACTTTTCAAAACAGA	26091
rs188798159	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67939274	GTCTTGTATTTGTCA[A/G]TATCTTTAGCATAAT	26091
rs188802589	snp	C/T	0.00557542	0.0525036	intron-variant	HERC4	GRCh38.p7	10:67998516	CCTGCCACTGCATTA[C/T]AGCCTGTGCAAAAGA	26091
rs188803096	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67976186	TTTACAGAAAAAGTT[C/T]GCAGGTCCTACCCTG	26091
rs188809030	snp	A/G	0.0298908	0.118541	intron-variant	HERC4	GRCh38.p7	10:67952807	CGGGAGGCTGAGGCA[A/G]GAGAATGGCATGAAC	26091
rs188822704	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68017073	ATACCTTAACTTTAG[A/G]TTTGGCCATATAGTT	26091
rs188824638	snp	C/T	0.00874735	0.0655527	intron-variant	HERC4	GRCh38.p7	10:67947664	AACATTCTTTTTAAG[C/T]GTACATGGAACATCT	26091
rs188831179	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67967080	AGGATGGTCTCGATC[G/T]CCTGACCTTGTGATC	26091
rs188839083	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67924306	ATTCATGTGTCACTT[A/G]ACGATGATGATATGT	26091
rs188872646	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67923215	ATATTTGGTACAGTC[A/G]CTACAGCAGAGCTTC	26091
rs188964090	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68016653	ACTGCACCCGGCCCA[A/G]TAAGATGTCTTATAG	26091
rs188976987	snp	C/T	0.00597247	0.0543191	intron-variant	HERC4	GRCh38.p7	10:68060386	GGGATTACAGATGCA[C/T]ACCACCATACCCAGC	26091
rs188991548	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68022791	CAAATATCTGATAAG[A/G]GATTAGTATCTAGAA	26091
rs188993929	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68056510	CAATTTATTAAGTTA[C/T]TGAATTCCATGGGCT	26091
rs189003738	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:68053163	TTGACTTAGCAAATA[C/T]TGAATCATTGCCCCC	26091
rs189007915	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68035703	CAGTCACTCACTATA[A/C]TCTAGCCGTATTGCC	26091
rs189028489	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:67980352	TGGTCAGGCTGGTCT[C/T]GAACTCCCGACCTCA	26091
rs189082562	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67933957	CAACTCCCTGGCAAC[A/G]GCCACTATTAAAGAA	26091
rs189094355	snp	C/T	0.00188245	0.0306216	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:67992660	TGAGAAAATTCTTTT[C/T]ACACAGAAATATTCT	26091
rs189096426	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68032109	AAAAGATAAAGAAAT[C/T]TAACCAGTTTCTAAT	26091
rs189130006	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67961194	AGTTAGGTCGTTTAG[C/T]GCCTCAACATCCTCA	26091
rs189231955	snp	C/T	0.00636936	0.0560724	intron-variant	HERC4	GRCh38.p7	10:68040098	AGTACGTAATGAATA[C/T]ACTGTTAAAGGATAA	26091
rs189260693	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68013645	CTCAAGATGAAAAGA[A/G]TTCTGGAGATTGGTT	26091
rs189270858	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68042673	TTTTAGAAATCTGTT[C/T]ATAGATACTATATGT	26091
rs189271759	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	HERC4	GRCh38.p7	10:68076391	ACAGGCGTGAGCCAC[C/T]GGTCCTGGCCTGTTT	26091
rs189327825	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67943032	CCCACTTATCTTTTG[A/G]GGGATAATGTTTTTC	26091
rs189331932	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67963199	ATTAACTTAATTTGC[C/T]AATTTGTAATGTTAT	26091
rs189368615	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67967854	CAGACAAATCCTGAT[C/T]ATGAAACTTTTATAA	26091
rs189372270	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67928624	TCAGATTCTAGGATA[C/T]AAAATGAGTTGCCTC	26091
rs189378775	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67982151	AAAAGACCCAGAATA[A/G]TCAAAGCTATCTTAA	26091
rs189398557	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68048005	TCATGGCTCACTGCA[A/G]CCTCCCAGGCTCAAG	26091
rs189402239	snp	G/T	0.00438332	0.0466095	intron-variant	HERC4	GRCh38.p7	10:68029484	GTGACAGAACAAGAC[G/T]CCATCTCAAAAAAAA	26091
rs189412362	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68008970	TCACTCCTGTAATCC[C/T]AGCACTTTAAGAGGC	26091
rs189497953	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67969779	ACAAAAAAATCGGAA[A/G]CAGAGTTTGGTTGCC	26091
rs189507448	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68058607	TATCTTTATTTTTTT[C/G]AGACGAGAGTTTCAC	26091
rs189514474	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68004519	TTGTCATAGTTTCAG[A/G]TCTTAGATTTAAGTT	26091
rs189525372	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67988194	TTAATGAATTACATA[C/T]GGTTCCAATTTTAAA	26091
rs189531538	snp	C/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67934183	ATTCACTTTCTACTC[C/G]CCTGTACATCTATTA	26091
rs189547164	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67936919	TATCTAGTAAAGGAA[C/G]AGAAATGTAACATAT	26091
rs189549197	snp	A/T	0.00676609	0.0577691	intron-variant	HERC4	GRCh38.p7	10:68026260	ACCACCACATCTGGC[A/T]AATTTTTTACTTTTT	26091
rs189553089	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67956423	ATGTTTAATACCTTA[C/T]TATTGAAACTTTCTT	26091
rs189557044	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68006710	TGTCTGGGAAGTCTT[C/T]ATTTCTCCTTCACAT	26091
rs189563720	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67972158	GGCAGAGGTTGCAGT[A/G]GGCCAAGGTCTCACC	26091
rs189580227	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922809	ATGAACACTCGTAGA[C/T]TGAACATTCTGCAAG	26091
rs189586946	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68061330	TCAGGTCAGGAGGTC[A/G]ATACCATCCTGGCTA	26091
rs189589800	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67949521	AAAAATCCAACCCTA[C/T]AAACCAATATCCCTT	26091
rs189630118	snp	C/T	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:68043846	AAAAACGATTATGCC[C/T]TATGTAACTGTGTAA	26091
rs189638385	snp	A/C	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68023809	TTATACTGTCCTCCA[A/C]AAAATAAATCAACTT	26091
rs189645229	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67986599	TGACCTCAAGTGATC[C/T]GCTCGCCTCACCACC	26091
rs189743282	snp	A/C	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68018612	TATTAATAAGAGTTT[A/C]GCAAGGTGGTTGTAT	26091
rs189776734	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67980785	AGAGTTTTCATTACT[A/C]TTCTTTTTGCTTATT	26091
rs189781654	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67984830	CTCAAGTGATCCACC[A/G]GCCTCAGCCTCGCAA	26091
rs189788324	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68068364	TGGTGGCACACACCT[A/G]TAGTCCCAGCTACTC	26091
rs189793661	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68021979	CTACACACAAAAATT[A/G]GCTGAATTTCTATAC	26091
rs189796378	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68030047	CCAGCCATAATTTTG[C/T]TTTTTAATCACATGT	26091
rs189802849	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68049371	TACATTTTTAAAACT[C/T]TGGAAAGATAAGTCG	26091
rs189807016	snp	G/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68031922	ATGCCCAGCTAACTT[G/T]CGTATTTTTAGAAGA	26091
rs189809919	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67953568	CCTTGAACAAAGATG[C/G]GACAATATGAGCATC	26091
rs189813506	snp	C/G	0.0158469	0.0875917	intron-variant	HERC4	GRCh38.p7	10:67928872	GCTGCAGTGAGCCAA[C/G]ATTGAGCCACTGCAC	26091
rs189816883	snp	A/C	0.0100823	0.0702816	intron-variant	HERC4	GRCh38.p7	10:67990864	AAAAGAAAACAAAAT[A/C]AACAGATAATACTGT	26091
rs189832863	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	HERC4	GRCh38.p7	10:68067106	GTGCTGCCATTTCTC[C/T]GTAAATTTATCCCCT	26091
rs189845700	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67931716	AGGCATGAGCCATCG[C/T]GCCTGGCTTGGTTAG	26091
rs189853972	snp	A/T	0.00874735	0.0655527	intron-variant	HERC4	GRCh38.p7	10:67959474	GTCTTAAAAAAAAAA[A/T]TTTATGGCTCAGTTT	26091
rs189864354	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67967255	TGAGTGCCTACTATA[C/T]GCAAAATGCTAGTTA	26091
rs189871170	snp	A/G	0.0115144	0.0749975	intron-variant	HERC4	GRCh38.p7	10:67931206	GGCCAGGATGGTCTC[A/G]ATCTCTTAACCTCGT	26091
rs189955698	snp	A/G	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:68067985	TTTTTAAGTTTGTGT[A/G]CAAGGGGGAAGACAA	26091
rs190035271	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67999379	AACCAGAGCAGTTTT[C/T]GTCTGCTCTGATGCT	26091
rs190035627	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68039297	CTCCAGAATGGGCGA[C/T]AGAGTAAGACCCTGT	26091
rs190049219	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68070913	AATCTTACTTTAATT[C/G]TATCCCATAATATTT	26091
rs190050436	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922199	ACTGGCAACTGTGGA[A/G]ACAGAGTTCTTCCAG	26091
rs190052127	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67935381	CGTTGTCGTGACCTC[A/G]TGATCCGCCCGCCTC	26091
rs190059338	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68009266	CGATACTGTAGTCCA[C/T]TGACAAGAGTTGGTT	26091
rs190088372	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68048575	CTACATGATATTACA[A/G]TGATGGATACATGTC	26091
rs190109176	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67974350	AAGAAAAACCACCAA[A/T]GAAACAAATAAAGTT	26091
rs190119964	snp	G/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67925536	CTGTATTCATGAACA[G/T]AAGTCAAACCATTAC	26091
rs190217082	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68049317	ATTTTTTGTGTAAGA[A/G]GAAGAAGAAAACATA	26091
rs190279192	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:67940452	TGAGATGGAGTCTTG[C/T]TCTGTCACCCAGGCT	26091
rs190281285	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68030153	GTATTTTTAAAAACA[A/T]ATAAGGCCGGGTGCA	26091
rs190288040	snp	G/T	0.00557542	0.0525036	intron-variant, downstream-variant-500B	HERC4, POU5F1P5	GRCh38.p7	10:68009622	AATTGCTGAAGGCTG[G/T]GGTAGCTGTGGCAAT	26091
rs190295971	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67959982	ATTGCCCTGGGTTAC[C/T]AGGAGGTGACCTATA	26091
rs190304030	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67974488	AAAGGGAACAAAATG[A/C]ATCACTCAGTAAATA	26091
rs190305910	snp	G/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68000027	GTATGACAAGTCACT[G/T]TTTTTTCTTTTGTAG	26091
rs190326587	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67973852	AGGGCAAGAGATCGA[A/G]ACCATTCAACATGGT	26091
rs190359597	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67938910	GATCACGTCACTGCA[A/C]CCCAGCCTGGGTAAC	26091
rs190377932	snp	C/T	0.00517822	0.0506191	upstream-variant-2KB	HERC4	GRCh38.p7	10:68077216	TAACCCACAACAGTA[C/T]GTTACAGAAATGAAT	26091
rs190406892	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67977748	GCACTTTGGGAGGCC[A/G]AGGCTGGCAAATTAC	26091
rs190442894	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68001589	TTATCATAAAATATA[C/T]ATAAAATTTACAATT	26091
rs190473808	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67968250	TGTGCAAATTCCCCC[A/C]ACATCCTTGGCTAAC	26091
rs190473909	snp	C/T	0.00398564	0.0444627	intron-variant	HERC4	GRCh38.p7	10:68040592	TTCAAATACACTGAA[C/T]AGAAAAGCAAAAGAA	26091
rs190481911	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67940729	GGATTACAGGTGTGG[A/G]CCACTGGGCCAGCCA	26091
rs190482217	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68020214	AGGGGGAGAATCTGA[C/T]TTCCAGTTACCATAT	26091
rs190484062	snp	A/C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67982899	TTGGGAGGCTGAGAC[A/C/G]GGTGGATCGCCTGAG	26091
rs190485994	snp	G/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67961253	TTTCATCATTCTGCA[G/T]ATCAGAAAGGTTCAC	26091
rs190548689	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012853	TTAGTAATTCTCGCA[A/G]TATTTCAATATTTTT	26091
rs190563055	snp	A/G	0.0108986	0.0730104	intron-variant	HERC4	GRCh38.p7	10:67959067	TACTCAGGAGAAAAT[A/G]GAGTATATTTTACTC	26091
rs190566800	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67955454	GAGGGTAAAGAGGGA[A/G]GAGCAAAAACAAACC	26091
rs190583800	snp	A/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68052210	GAAACATATCCACTT[A/T]GTAGATAACGACTTC	26091
rs190590475	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67923986	AGTTATAAATGAGGG[A/C]ACTAAGGCCTGAAAA	26091
rs190602680	snp	C/T	0.00795532	0.062565	upstream-variant-2KB	HERC4	GRCh38.p7	10:68076876	CGCCTGTAATCCCAG[C/T]ACTTTGGGAGGCTGA	26091
rs190606628	snp	A/G	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:68058743	TATCCTAATTTTAGA[A/G]AAGAGAACACCTAGG	26091
rs190623613	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67995611	CACTTTAGATATTCA[A/G]GATATTAACCTTAGG	26091
rs190643519	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67929574	GCTGCCTATGACAGA[A/G]TGCAGTCAGGGCTCA	26091
rs190650662	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67934990	TTTCCATTTTTAATT[A/G]TATGCATCTGGATGT	26091
rs190652150	snp	C/T	0.00795532	0.062565	utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68073163	TCTCTTCTGAAACCC[C/T]GGAAAGTTGGAGGTA	26091
rs190657807	snp	C/G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67964049	CTGAGGTCAATTATT[C/G/T]TCTTTCTTAAAAAAT	26091
rs190713031	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67965457	ATAGACCTAAATCTA[C/T]AGAATGGCTATAAAC	26091
rs190713204	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68055394	GTGTCTTAGTTGACA[A/G]CAAACAATAAAATGT	26091
rs190721375	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68037133	AGAGTCTCGCTCTGT[C/T]GCCCAGGCTGGACTA	26091
rs190722148	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67979159	GGCACCAAAGACAAA[C/T]CTTGGAGAAAAAGAA	26091
rs190726427	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68015452	TGTTTAGCGACATAA[A/G]CTAACTAATACATTA	26091
rs190732990	snp	C/T	0.00398564	0.0444627	intron-variant	HERC4	GRCh38.p7	10:67996663	GCATTACATTTAGCA[C/T]AGAAAACATCTTAGT	26091
rs190741685	snp	C/G	0.0130921	0.0798413	intron-variant	HERC4	GRCh38.p7	10:68063418	TCTCACTACACAGGC[C/G]AGGCTGGTCTTGAAC	26091
rs190790128	snp	C/T	0.00914312	0.0669923	intron-variant	HERC4	GRCh38.p7	10:68035407	GTGATCTGCCCACCT[C/T]GGCCTCCCAAAGTGC	26091
rs190813773	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67994700	GCCTCCCAAAGTGTC[A/G]GAATTACAGGTGTGA	26091
rs190821915	snp	C/T	0.00914312	0.0669923	intron-variant	HERC4	GRCh38.p7	10:67971411	GCAAATTAAATCCAA[C/T]AATATATATAAAGTA	26091
rs190834289	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010083	CCCCCACCCTTTGTG[C/T]TCCCAATTCCTTCCT	26091
rs190854530	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67975111	GGAGAATCGCTTGAA[C/T]CCGGGAGGCAGAGGT	26091
rs190868110	snp	A/G	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:67978469	ACAGAACACCAGGTA[A/G]ACGTCTAAGGTTTTT	26091
rs190892536	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67944651	AGACTGAGATATATG[A/T]CCTTTCAGTCAGACA	26091
rs190980455	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67950527	GTGATCCAACCACCT[C/G]GGCCTCCCAAAGTGC	26091
rs190995310	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68007567	TATTTATTCTATCCT[C/T]TGCAGTCCGTACTTG	26091
rs191000186	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68045549	TAAAACAGAAATTAA[A/C]TTAAAATATTGGCCC	26091
rs191022225	snp	A/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68064474	CAGGAGAATCATCTG[A/T]ACCTGGGAGGCGGAG	26091
rs191024257	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68046530	GTGCTCCAAGCACTG[A/G]AGAGAGAGAGAGAAT	26091
rs191033774	snp	C/T	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:68026524	CTAGCCTGGCCAACA[C/T]GGTGAAACTCTGTCT	26091
rs191091872	snp	A/C	0.0333695	0.124785	intron-variant	HERC4	GRCh38.p7	10:67971975	TCTCAGCACTTTGGG[A/C]GGCTGAGGCAGGCAG	26091
rs191103763	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67946606	TCAATTAAGCAAGAA[C/G]ATATAACAATTACAA	26091
rs191115668	snp	A/G	0.00285197	0.0376544	intron-variant	HERC4	GRCh38.p7	10:67992352	TAAGATTAGTCAGAG[A/G]GAAGAGATATTATAT	26091
rs191188648	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67964946	CCTGGCTAAGTTTTT[C/G]TATTTTTAGTAGAGA	26091
rs191196704	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67978998	CTGGAAAGCCTTTCC[A/G]AGAAGCACGAAGACA	26091
rs191213894	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67929875	TGGAGTGCAACGGCA[C/T]GATCTCCGGCTCACT	26091
rs191218114	snp	A/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67945149	TAAGACTACTTCAAG[A/T]TATTTAATAATCAAA	26091
rs191242510	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67938706	ATGCCAGCACTTCGG[A/G]AGGCCGAGGCGGGTG	26091
rs191323595	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68059519	TATAATATTATATAT[C/T]ATAATAATATTATAT	26091
rs191330632	snp	C/T	0.0115144	0.0749975	intron-variant	HERC4	GRCh38.p7	10:67984050	CTCACGCCCGTAATC[C/T]CAACAGTTTGGGAGG	26091
rs191333950	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67952209	CCCTTGCCTTTTACT[C/T]CCTTCTGTGTTACAT	26091
rs191339197	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68003396	GCCAGGATGGTCTTG[A/G]TCTCCTGACCTCATG	26091
rs191342486	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67930447	CTGGGAGTAGGACTG[C/T]TAGGTCATATAGCAA	26091
rs191348597	snp	C/T	0.00795532	0.062565	intron-variant	HERC4	GRCh38.p7	10:67986951	CTGCTGATATAAATG[C/T]GGACATTCATTTTTC	26091
rs191354126	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67983616	AACCCCGTCTCTACT[A/G]AAAATACAAAATAAA	26091
rs191360016	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68021096	ACATCCATAAGCCCC[A/G]ATGAATTCTACGCAG	26091
rs191361735	snp	G/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67933631	TTTAAAACAAGGATA[G/T]CTAGAAGGACCTAAA	26091
rs191366262	snp	C/G	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:67952622	ATAAATTGGAGGCCG[C/G]GCGCGGTGGCTCACA	26091
rs191372113	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67969076	TGTCCACAATGGAAT[C/T]AAACTAAAATCAGTA	26091
rs191397635	snp	A/T	0.00282069	0.0374485	intron-variant	HERC4	GRCh38.p7	10:67992719	TTAAAAGCCAAGATT[A/T]ACATAACATATTTCA	26091
rs191405271	snp	A/G	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:68047916	AACACCTGCACATGA[A/G]TGTTTTGTTTTTGTT	26091
rs191407343	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67957896	CACGGCAACCTTCGC[C/T]TCTGGGGTTCAAGCG	26091
rs191409525	snp	A/T	0.0126979	0.078662	intron-variant	HERC4	GRCh38.p7	10:68073979	GTGGTAACCGGGATT[A/T]AAAAAATCACCCGTG	26091
rs191413706	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67973703	ACGGATATGGAAAAC[A/G]AGAAGAGTCAAAGAC	26091
rs191415503	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68027996	TATTTTTAATTATAT[A/G]TATATATATATAATA	26091
rs191420226	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67990678	TAACCATACACAAAC[C/T]TAAGCAACGTGGTAA	26091
rs191426125	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68008672	AAAATAATTAACACT[C/T]CTGTATATACCCAAA	26091
rs191426310	snp	C/T	0.0364509	0.129988	intron-variant	HERC4	GRCh38.p7	10:68055947	AGTAGAGGGGGGGTT[C/T]CACCATGTTGGACCA	26091
rs191469207	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069915	GGCATGGTGGCACGC[C/T]CCTATAGTCCCACCT	26091
rs191523450	snp	C/T	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:68040842	TGCAGTGAGCCAAGA[C/T]TGCGCCACTGCACTC	26091
rs191547706	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68032429	TAGGCTGAGCTACAC[A/G]ATATAAATGGGTTTG	26091
rs191552586	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68002980	ACAGGCATACAGTGT[A/G]TAAAAATCACATGAG	26091
rs191574513	snp	A/C	0.00438332	0.0466095	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069309	TGAGACATTAGCTTA[A/C]AAAGTATTTTAAAGT	26091
rs191587820	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67968667	GGTGTGAGCCACCGC[A/G]CCTGGCCAGAGAGGC	26091
rs191625265	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67932903	ACGAAACTGAGAATG[C/T]ATGAGTAGCGTTCAA	26091
rs191637498	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67976204	AGGTCCTACCCTGGA[A/G]TCTTTAGTATTGTGC	26091
rs191653769	snp	G/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68006507	CTCCTGAGTAGCTGG[G/T]ATTACAGGCGCCAGC	26091
rs191655210	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010711	CTTGAAGCTAAGCTG[C/T]TGAGCCTCAAAGAGG	26091
rs191672598	snp	A/G	0.00795532	0.062565	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069695	GCCAACCTATGTAAA[A/G]AAACAATTCTTAGTT	26091
rs191687649	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68045215	GTGATCCCAGCTATT[C/T]GGGAGGCTGAAACAG	26091
rs191705501	snp	C/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67951167	TCAAAACATTATCTC[C/T]TTAAAACTGACTAAA	26091
rs191799752	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68050165	TCACTGCACTCCAGC[C/T]TGGGCAACCAAAGTG	26091
rs191881811	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68050486	CAACATACTAAATAC[C/T]GAAGATAATTTTTGT	26091
rs191881866	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67961515	CTTGGCTGATTTTAA[C/T]CTATTATCCTTTCCC	26091
rs191889705	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67934190	TTCTACTCCCCTGTA[C/T]ATCTATTATATTTAT	26091
rs191890050	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68033141	TTCAAAATTATCTAA[C/T]TGCTTCTAATTTTCC	26091
rs191890095	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67976739	AGCATTTCTGTGCAC[C/T]GGGGAGAGAAAGAAT	26091
rs191890171	snp	C/T	0.00835141	0.0640778	intron-variant	HERC4	GRCh38.p7	10:67940564	AGCTGGGACTACAGG[C/T]GTGGGCCACCACGCC	26091
rs191897661	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012254	TCATGTATTCACCAG[A/G]GTAGCACTTTTAATT	26091
rs191898853	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67993455	GCCCAGTTCAAAGCT[A/G]CAGTATGCTATGACT	26091
rs191935672	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68024446	ACATATACCATATAA[G/T]AAAAGTGCAAAGCAA	26091
rs191968113	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68062422	ATTCTTTCTGCCTCT[C/G]TAAGTCTCCATCATC	26091
rs191992797	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67926628	TCAGGCTAATTTTTA[A/C]CCTTTTAGGGCTCAG	26091
rs192042439	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68021757	AGGTTGCGGTGAGCC[A/G]AGATCACGCCATTGC	26091
rs192045914	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68054347	CAGTTGAAGTATTTA[A/G]TGATTTTTTTTTTTT	26091
rs192061463	snp	A/C	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:68015014	TCCCTCTAACCATAC[A/C]CATATCTTATGCAAT	26091
rs192069466	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67989267	ATATGGTTGAAATAT[C/T]GTGAACCACTACCTT	26091
rs192074447	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67984436	TATTTGTAGGATCTA[A/G]AAATCAAAACAATTT	26091
rs192080583	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68059778	CATAATATTATATAT[C/T]ATAATATTATATATC	26091
rs192084081	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68004274	GTTGAAACAACAGAG[C/T]TGTCTTTATATATTC	26091
rs192085977	snp	C/T	0.00557542	0.0525036	intron-variant	HERC4	GRCh38.p7	10:68041719	ACTTATATTAAACTA[C/T]GATAATAAAATTTGG	26091
rs192098868	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68018195	TACTTGACCAAACTG[A/G]AGTTATTCCAGAAAC	26091
rs192126225	snp	A/T	0.00318978	0.0398085	upstream-variant-2KB	HERC4	GRCh38.p7	10:68075884	CACTCTCCCTGAAAG[A/T]TAGGCTTGAATTGCA	26091
rs192126342	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67980725	GTATAAGATATAAAT[A/G]GAAACAACAAAAAGT	26091
rs192128635	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68057497	TGCGTGGTGGCAGGC[A/G]CCTATAATCCCAGCT	26091
rs192134398	snp	C/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67998841	CCTCCTGGGTTCAAG[C/T]GATTCTCCTGCCTCA	26091
rs192140937	snp	A/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68038639	CAACAGGGATTCTTG[A/T]ATGTTCTACCAACTC	26091
rs192142306	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67966163	TTTGTATTTTTAGTA[C/G]AGATGGGATTTCGTC	26091
rs192172362	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67930701	TAGAAAGATAGAAAA[C/T]CAGCAGATTAATTTC	26091
rs192193769	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67926174	CCAAGCCGGGCAGAT[C/T]ACTTGAGGTCAGGAG	26091
rs192201327	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67960417	TGAGACGGAGCTTCG[A/C]TCTTGTTGCCCAGGC	26091
rs192241672	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67938146	ACAAGCAAAAAATTT[A/G]AAAAATAAAAAAGAG	26091
rs192246400	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67923401	AGTGAGTATTTTGCC[A/G]TTGCCAAAACATTTT	26091
rs192260773	snp	C/T	0.00398564	0.0444627	intron-variant	HERC4	GRCh38.p7	10:67957469	ATATACAAAAAAGTA[C/T]CATTAGTATTACTAT	26091
rs192273898	snp	C/T	0.00874735	0.0655527	intron-variant	HERC4	GRCh38.p7	10:68037315	TGGCCAGGCTGGTCT[C/T]GAACTCCTGAACTCA	26091
rs192294130	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67996757	TGGGAGGCCAAGGTG[G/T]GTGGATCATGAGGTC	26091
rs192337000	snp	A/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012815	AAAATTCAGTATCAA[A/T]AATTGAGTAAAGCTT	26091
rs192345733	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68041057	TATACTGTTGTATTC[C/T]TCTGTTTTCCCAACT	26091
rs192388126	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67977251	GGGCACCAGTCAAAG[C/T]TGTGAAGACTGCTTT	26091
rs192414771	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68036678	CAAATACACCACTTT[C/G]TTAACTCTATGCCTT	26091
rs192415090	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67941736	CAGGATGGAGTGCAG[C/T]GGTGTGATCTCTGCT	26091
rs192454080	snp	A/G	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:68072595	AAAGAGGACCTGCAC[A/G]CTACACACTCTGTAC	26091
rs192477042	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67996204	CTGAGCCCAAGAGGT[C/T]GAGGGTGGAGTGAGC	26091
rs192516421	snp	A/G	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:67923533	ATTTTTTTTAAATCA[A/G]AAATTTATAATGGGC	26091
rs192518302	snp	A/G	0.00636936	0.0560724	intron-variant	HERC4	GRCh38.p7	10:67946918	TCTCAAAACAAAACA[A/G]AACAAAATTACAAAT	26091
rs192537360	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67980023	AGCAGACTTCTCAGG[A/G]CAAACTTTACAGGCC	26091
rs192571396	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68060079	TCTGGAGTCTGACTG[C/T]TCTCACCAAAACACA	26091
rs192589630	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68022078	AGGAATTAACAAGAA[A/G]GCAAAAGATTTGTAA	26091
rs192612554	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67998046	TGGGACTATAGGTGC[A/G]TGCCACCACGCCTAG	26091
rs192638999	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67947121	GCACTACAGACCAAA[C/T]GGATTTAACAGATAT	26091
rs192647430	snp	A/G	0.00398564	0.0444627	intron-variant	HERC4	GRCh38.p7	10:67967016	CCCGCCATCATGACC[A/G]GCTAATTTTTTGTAT	26091
rs192650628	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67980489	ATTTTATCAACACTA[C/G]ACCTGTGGAACAAGA	26091
rs192672168	snp	G/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67931047	CTGGAGTGCAGTGGC[G/T]CAATCTCACTGACTT	26091
rs192690430	snp	C/G	0.0111196	0.0737302	intron-variant	HERC4	GRCh38.p7	10:68016600	TTGTGATCTGCCCGC[C/G]CTGGCCTCCCAAAGT	26091
rs192717925	snp	C/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68035255	TCTCCCGGGTTCAAG[C/T]GATTCTCCTGCCTCA	26091
rs192722934	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67994621	ATTTTTAGTAGAGAC[A/G]GGGTTTCTCCATGTT	26091
rs192746117	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67962448	TAGAATTTATAGTGC[A/G]ACTAACCCATACTAA	26091
rs192760771	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67984885	TGAACCACCGCACCC[A/G]GCCAAACCTAGTATT	26091
rs192764023	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67928175	GTTAATAAGGCTGAG[A/G]CAGAGTGAGAGGAAC	26091
rs192774175	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67953995	ATTTCTTTCAAGTCA[G/T]GAGTTCTACTAAACT	26091
rs192781936	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67927910	GGGAAGGAGCAACCT[A/C]AGTAAAATTATGTCA	26091
rs192784248	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67933921	TCTAAGTAGCGGAAT[A/T]AGGATTATAATCCTT	26091
rs192804597	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67934038	CAGAAATTCCCGCTA[C/T]TAAAAGGCAACTATT	26091
rs192816025	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67969436	CATAGATGCCACTGG[A/G]TGCCCATGAAACAAC	26091
rs192846539	snp	G/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68042496	AGCATAGTGGTGCAC[G/T]CCTATAGTCGCACCT	26091
rs192858056	snp	C/T	0.00755907	0.0610114	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68070478	AGGCATTGTGGTGGG[C/T]GCCTGTAATCCCAGC	26091
rs192891033	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68035590	CTCACCCCAAAAAAT[A/G]TATTTCAGTGCTTTC	26091
rs192909168	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68047854	AAATCTACTCTTACC[A/G]TATGACCCAATTCCT	26091
rs192930670	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67972746	AAGAGTCATTCACCA[C/T]GTTCATGAATCAGAA	26091
rs192941958	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68008175	CTCTCTCTCTGTGCT[A/G]AGATTCTTAATAGTT	26091
rs192962930	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67970349	GTAATCCCAGCACTC[A/G]GGGAGGAGAAGGCAG	26091
rs192972162	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68004705	GAGACTTATAATCAT[A/G]GCAGAAGGCGAAGAG	26091
rs193019371	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67952999	TGGTAACAGCTTACA[C/T]AGCCATGGTCAAAAC	26091
rs193033539	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68056559	AATGTGTGACTTGAA[C/T]TCTTATAAGAGTGAC	26091
rs193067179	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68052550	TTAAAAAAAAGAATA[C/T]TGTCTCACATACAGG	26091
rs193134325	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68016709	ATCAAAATACCAGAT[A/G]CCTACTTACACTTCC	26091
rs193141666	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67957156	AGGCATTGGAATGAA[A/C]CCAATTCCCAATTTT	26091
rs193150903	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67923235	AGCAGAGCTTCACTT[C/T]AACATCTGCTCTAAC	26091
rs193156111	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68065061	ATTCCTAAATATTCC[C/T]AATATTCCTAAAACT	26091
rs193159646	snp	A/C	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68026790	AGAGGTTGCAGTGAG[A/C]CGAGATCACGCCACT	26091
rs193170358	snp	G/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67989677	TAAAATCTAGACAAT[G/T]AGAAAAATTAAAGTG	26091
rs193172903	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67967089	TCGATCTCCTGACCT[C/T]GTGATCTGTCCACCT	26091
rs193219542	snp	A/G	0.00795532	0.062565	upstream-variant-2KB	HERC4	GRCh38.p7	10:68075398	CCCGGCCCCGGCACC[A/G]GCGCCTGCGCCGAAT	26091
rs193222048	snp	C/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68037986	AAAAGGATCAAGAAC[C/G]AGGGCAATCTTGCAG	26091
rs193293549	snp	C/T	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:67937370	CCACTGAAAAATCTC[C/T]GAGAAAGAAATGGCA	26091
rs193296064	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67972378	AATACAAAATTAGCC[A/G]GGCATGGTGGTGCAT	26091
rs199513067	in-del	-/A	0.0209421	0.100162	intron-variant	HERC4	GRCh38.p7	10:67980741	AAACAACAAAAAGTT[-/A]AAAAAGCAGGAGTAC	26091
rs199514878	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67960388	CACTATTAAAAGCCT[-/A]AAATTTTTTTTTTTG	26091
rs199551952	in-del	-/A			upstream-variant-2KB	HERC4	GRCh38.p7	10:68077128	CAAAAAAAAAAAAAA[-/A]GTTCACATTCACAGG	26091
rs199559705	in-del	-/A/GAAAAGAAAAGG	0.0678174	0.1712	intron-variant	HERC4	GRCh38.p7	10:67938458	AAAGAAAAAAAAAAA[-/A/GAAAAGAAAAGG]GAAAAGAAAAGGGAA	26091
rs199563062	in-del	-/A	0.0150606	0.0854603	intron-variant	HERC4	GRCh38.p7	10:67991905	AAAATATCCATGGAT[-/A]TTTTTTTTTGGAGAC	26091
rs199570018	snp	A/T	3.34947e-05	0.00409221	intron-variant	HERC4	GRCh38.p7	10:68032876	CATACCTATCTGAAA[A/T]TTCCAACAAGAGATG	26091
rs199589380	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67995354	GAAGCATTAGTTTCT[A/C]CCTATTATATAGTTA	26091
rs199597530	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67970175	CAGCTTAACTCCTGA[A/C]TAAACTCAAATCCTT	26091
rs199603701	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68041154	AACCACTAATGTTTA[C/G]TAAAAAGTTTATATT	26091
rs199605870	snp	C/T	0.000115757	0.00760691	intron-variant, missense	HERC4	GRCh38.p7	10:67940946	CAACTAACCTCCCAA[C/T]ATCAGGCATTAGTTC	26091
rs199617697	in-del	-/GTGT			intron-variant	HERC4	GRCh38.p7	10:68037898	CCCAAATTCCTAGCA[-/GTGT]GTGTGTGTGTTTGTG	26091
rs199641435	in-del	-/TTATT	0.0263992	0.111815	intron-variant	HERC4	GRCh38.p7	10:67939918	TTTCAACATTTTTCC[-/TTATT]TTATTTTATTTTATT	26091
rs199645377	in-del	-/T/TT			intron-variant	HERC4	GRCh38.p7	10:67986520	ACCATACCCAGCTAA[-/T/TT]TTTTTTTTTGTATTT	26091
rs199652898	in-del	-/AAAG	0.00795532	0.062565	intron-variant	HERC4	GRCh38.p7	10:67990485	AGGAAGGCAGGAAGA[-/AAAG]AAAGAAAAGGAAAAT	26091
rs199665673	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67945621	TAAAACATGAACCAA[A/T]AAAAAATAATAACTA	26091
rs199702213	snp	A/G	0.000580167	0.0170219	intron-variant	HERC4	GRCh38.p7	10:67932572	TCTTTCCATTTAACA[A/G]TATCAGAGATTAGTT	26091
rs199715169	snp	A/C	1.65307e-05	0.0028749	intron-variant	HERC4	GRCh38.p7	10:67992334	CAGTTCTAAATTTTC[A/C]AATAAGATTAGTCAG	26091
rs199727529	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68054537	TTAGTAGAGATGAGG[C/T]TTCACCATGTTGGCC	26091
rs199741484	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67967914	AAGGTAGCAGGGATT[A/G]AAAAAAAAAGGAGCT	26091
rs199788798	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68059905	ATATTATATATTATA[-/A]TAATATTATATATCA	26091
rs199830717	snp	C/T			upstream-variant-2KB	HERC4	GRCh38.p7	10:68076135	TTATTTATTTATTTA[C/T]TTATTTATTGAGACA	26091
rs199839107	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:67984913	ATTTCATAGCACATC[C/T]CATGTACCCCATAAA	26091
rs199842957	in-del	-/TC	0.252983	0.249982	intron-variant	HERC4	GRCh38.p7	10:67941364	ACTTTACAACTGTTT[-/TC]TCCCAGACATAAGCA	26091
rs199849445	in-del	-/A	0.0134861	0.0810011	intron-variant	HERC4	GRCh38.p7	10:67976570	AACAACTATCTACAC[-/A]AAAAAAAGCATCTTC	26091
rs199854984	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67941360	TACGACTTTACAACT[G/T]TTTTCTCCCAGACAT	26091
rs199894309	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68038367	CAAAAAAAAAAAAAT[A/T]AAAGGGGTGAAAAGA	26091
rs199905670	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67938446	CTGTCTCAAAAAAAA[A/G]GAAAAAAAAAAAGAA	26091
rs199939360	snp	C/T	3.30147e-05	0.00406279	missense	HERC4	GRCh38.p7	10:67922983	TGGATCAGTTTAGAG[C/T]GTAGAGTTTCTTTTT	26091
rs199941183	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68057719	TATTATTTTTTTTTT[C/T]CTTTTAAGACAGAGT	26091
rs199974939	in-del	-/T	0.0364509	0.129988	intron-variant	HERC4	GRCh38.p7	10:67997915	TTCTTTGTTCATTTG[-/T]TTTTTGAGACAAAGT	26091
rs199978401	snp	A/G	1.64882e-05	0.00287121	missense	HERC4	GRCh38.p7	10:67955045	TTTTCTCTACGCACC[A/G]CTAGAATTAAGCAGG	26091
rs200017857	in-del	-/A	0.253517	0.249975	intron-variant	HERC4	GRCh38.p7	10:68001373	TGAGACCTTGTATTT[-/A]AAAAAAAAAAAAATT	26091
rs200020130	snp	A/G			upstream-variant-2KB	HERC4	GRCh38.p7	10:68076777	AGCCTACCCTGATCC[A/G]TTATGACCTCATCTT	26091
rs200020429	in-del	-/TTTTTTTTTTT	0.498714	0.0253268	intron-variant	HERC4	GRCh38.p7	10:68051342	AAAATGTTAACACTA[-/TTTTTTTTTTT]TTTTTTTTTTGAGAC	26091
rs200026043	in-del	-/AC/C			intron-variant	HERC4	GRCh38.p7	10:68046991	ACAAACAAAAAAAAA[-/AC/C]CATGAAGAATTTTGG	26091
rs200062764	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68021050	AGTAATAGCCAAAAA[C/T]TCCCAAATATGGGGA	26091
rs200108384	in-del	-/ACACAT			intron-variant	HERC4	GRCh38.p7	10:67974116	CACACACACACACAC[-/ACACAT]ACACACAGGGTCAGG	26091
rs200110206	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68037088	AAATGGAACCTATTT[C/T]TTCTTTTTTTTTTTT	26091
rs200112536	snp	A/G	0.000308981	0.0124256	intron-variant	HERC4	GRCh38.p7	10:67941149	GTCCTCCAAGTTAAA[A/G]TATTAAATTTTCTAA	26091
rs200134764	snp	A/G	0.000198052	0.00994922	missense	HERC4	GRCh38.p7	10:67922984	GGATCAGTTTAGAGC[A/G]TAGAGTTTCTTTTTC	26091
rs200145721	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67982490	TCAAAATGATTAATG[-/A]ATTAAATCTAAGACC	26091
rs200161551	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68002184	TAATTATAAAAAAAA[A/C]ATCAAGTTTATTTAC	26091
rs200162845	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67952910	GTCTCAAAAAAAAAG[A/G]AAAAAAAAAAGACAC	26091
rs200179675	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67925213	CATAATCTTTTATTA[A/G]TATTAAGGGACACAC	26091
rs200230859	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67959464	GCCTGGCTTGGTCTT[-/A]AAAAAAAAAATTTAT	26091
rs200242848	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67990203	AGAAAAAATATTAGA[A/T]TTCTTACCAAGTACT	26091
rs200279919	snp	C/G	0.00199792	0.0315431	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68073001	ACATCCTACATCTCG[C/G]ACCCTTTTATTTATA	26091
rs200295860	in-del	-/C	0.0741063	0.177655	intron-variant	HERC4	GRCh38.p7	10:68041295	ATCTTAACACCAACT[-/C]ATTTCAATTTTGAAA	26091
rs200329439	in-del	-/A	0.02016	0.0983543	intron-variant	HERC4	GRCh38.p7	10:68068194	TTCTCTAACAAACAT[-/A]AAAAAATTGGCCAGG	26091
rs200340001	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68071804	TTTATCCAATAAAAA[A/G]TAAATTACAAATTAA	26091
rs200356340	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68001371	GTGAGACCTTGTATT[-/A]TAAAAAAAAAAAAAA	26091
rs200357240	in-del	-/TCC	0.0333695	0.124785	intron-variant	HERC4	GRCh38.p7	10:67989887	TTCAGTTTTAATTGT[-/TCC]TCCTCCTTTACTTCT	26091
rs200363553	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68025699	AAGACAAAACCCCTT[A/G]TCATTAGAAGGCATG	26091
rs200400095	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67994938	CAAGTGATCTGCCCA[C/T]CTCAGCCTCCCAAAG	26091
rs200407985	in-del	-/ATA	0.344815	0.231323	intron-variant	HERC4	GRCh38.p7	10:68059457	ATAATATTATATATT[-/ATA]ATAATATTATATATT	26091
rs200418082	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68004023	GCATGTTATTGCCCT[C/T]TTTCAGATAAAAGCC	26091
rs200453899	in-del	-/AGAT	0.00398564	0.0444627	intron-variant	HERC4	GRCh38.p7	10:67942969	ATTTGTGATACTGAA[-/AGAT]AATCAGAGATACATA	26091
rs200456575	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67938447	TGTCTCAAAAAAAAA[A/G]AAAAAAAAAAAGAAA	26091
rs200480292	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68007703	CAAGCCCAGTAACAC[-/T]TTTTTTTTTTTTTAA	26091
rs200488939	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68029178	AGACCCCCATCTCAG[-/A]AAAAAAAAAAGTTAC	26091
rs200491012	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67927817	AAGTACTTACTGAGT[A/G]CTCTCCTAGGTGCTG	26091
rs200504485	snp	C/T	6.84193e-05	0.0058485	intron-variant	HERC4	GRCh38.p7	10:68038071	AAAACTGAAGAGAAA[C/T]AAAATAAAAACTAAT	26091
rs200511187	snp	G/T	0.000399281	0.0141238	intron-variant, missense	HERC4	GRCh38.p7	10:67940964	CAGGCATTAGTTCTT[G/T]CAAATCATCCAAGGA	26091
rs200601996	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67993525	TAAAAAAAAAAAAAA[-/A]TTATTCTTAAAAAGA	26091
rs200619987	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67983788	GAAGACTCTGTCTCA[A/C]AAAAAAAAAAAAAAA	26091
rs200620309	in-del	-/TGG	0.00597247	0.0543191	intron-variant	HERC4	GRCh38.p7	10:67934491	TGCTTGTTTGAATCC[-/TGG]TGGTGGTGGTGGTGG	26091
rs200633613	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67995355	AAGCATTAGTTTCTC[C/T]CTATTATATAGTTAT	26091
rs200684660	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68046992	ACAAACAAAAAAAAA[A/C]ATGAAGAATTTTGGA	26091
rs200691965	snp	A/G	1.71123e-05	0.00292504	intron-variant	HERC4	GRCh38.p7	10:68033955	TAAACTATACATAAT[A/G]AGAACCTACCATTTT	26091
rs200693514	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68041155	ACCACTAATGTTTAG[A/T]AAAAAGTTTATATTA	26091
rs200704588	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68054573	TGTCTCAAACTCCTG[A/G]CCTCAAGTGATCCAC	26091
rs200818594	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67996208	GCCCAAGAGGTCGAG[C/G]GTGGAGTGAGCTGTG	26091
rs200827002	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68019482	AGTGACACCATACAG[C/T]AGGAGGGTGAAGAAT	26091
rs200830272	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68021051	GTAATAGCCAAAAAC[C/T]CCCAAATATGGGGAA	26091
rs200888945	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68057720	ATTATTTTTTTTTTT[C/T]TTTTAAGACAGAGTC	26091
rs200895506	in-del	-/C	0.0107246	0.0724382	intron-variant	HERC4	GRCh38.p7	10:68035356	AGAGGCAGGGTTTCA[-/C]CATGGTGGCGAGGCT	26091
rs200895554	in-del	-/C			intron-variant	HERC4	GRCh38.p7	10:67926429	ATAAAAAAAAAAAAA[-/C]AACAAAAAAATTAGT	26091
rs200915628	snp	A/T	0.000860592	0.0207257	intron-variant	HERC4	GRCh38.p7	10:67936254	TTAATTTAAATTTTT[A/T]AAAAAAGTCAATGTC	26091
rs200944873	in-del	-/TAG			intron-variant	HERC4	GRCh38.p7	10:68001482	AACCTCTGGATGGGC[-/TAG]AATTGGTAAATTAAA	26091
rs200950666	in-del	-/TT			intron-variant	HERC4	GRCh38.p7	10:68031787	AACGAGGTCTCACTC[-/TT]TGTCTCCCAGGCTGC	26091
rs200953527	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67999248	CCTTGAAAATAGGCC[C/T]AATCATCATCTTTGG	26091
rs200965850	in-del	-/TC			intron-variant	HERC4	GRCh38.p7	10:68004026	TGTTATTGCCCTCTT[-/TC]AGATAAAAGCCATTT	26091
rs200972691	in-del	-/C	0.00755907	0.0610114	intron-variant	HERC4	GRCh38.p7	10:67976684	GAATCACCAACATCA[-/C]CCCTCTCCCAGCCCC	26091
rs201016658	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67995568	TATCTATTAGCTGTC[-/T]TTTTTTTTTTTCATT	26091
rs201022518	in-del	-/AAAC	0.0314385	0.121371	intron-variant	HERC4	GRCh38.p7	10:67948005	AAACAATACACTCTT[-/AAAC]AACCAAAAGATCAAA	26091
rs201030305	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68050238	TACTTAGAAGGGATA[C/T]AGGCAGAGGGAACAA	26091
rs201033298	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68001472	CCATGGGTTTAACCT[A/C]TGGATGGGCTAGAAT	26091
rs201038182	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67998552	ACTCCACCTCAATTG[-/A]AAAAAAAAAAAGGGG	26091
rs201088115	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68046982	AACAAACAAACAAAC[-/A]AAAAAAAAACATGAA	26091
rs201171016	in-del	-/C	0.266546	0.249452	intron-variant	HERC4	GRCh38.p7	10:68004027	GTTATTGCCCTCTTT[-/C]AGATAAAAGCCATTT	26091
rs201188256	snp	C/T	0.00181226	0.0300474	intron-variant	HERC4	GRCh38.p7	10:67954781	TAGACTGTAAAGAAA[C/T]GAAAGTACATTCTGG	26091
rs201245154	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67967913	CAAGGTAGCAGGGAT[G/T]GAAAAAAAAAGGAGC	26091
rs201272720	in-del	-/CTCT	0.0103295	0.0711199	intron-variant	HERC4	GRCh38.p7	10:68062418	GTCCATTCTTTCTGC[-/CTCT]CTAAGTCTCCATCAT	26091
rs201282248	snp	A/T			upstream-variant-2KB	HERC4	GRCh38.p7	10:68076112	TCTTTTTCTTTTCTT[A/T]TTTTTATTTATTTAT	26091
rs201290017	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68031923	TGCCCAGCTAACTTT[C/T]GTATTTTTAGAAGAG	26091
rs201293007	snp	C/T	1.70667e-05	0.00292114	intron-variant	HERC4	GRCh38.p7	10:67925195	TCTGTATTCTAAAAA[C/T]AACATAATCTTTTAT	26091
rs201305685	snp	A/T	0.00171465	0.0292299	intron-variant	HERC4	GRCh38.p7	10:67966826	GAAAATGTAATTGAC[A/T]TTAAATTTAACCAGT	26091
rs201363246	in-del	-/AG	0.0364509	0.129988	intron-variant	HERC4	GRCh38.p7	10:68038270	CTACTATATGCACAT[-/AG]GTCATATTATTTTTT	26091
rs201367135	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68053311	CTTTTTTTTTTTTTT[-/T]AGACCAGGTCTCTCT	26091
rs201373531	in-del	-/ACAT			intron-variant	HERC4	GRCh38.p7	10:67974118	CACACACACACACAC[-/ACAT]ACACACAGGGTCAGG	26091
rs201374040	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68047201	ATTGACTTCTTAGGG[A/G]AAAAAAAAAAAAGGT	26091
rs201395811	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68041152	CCAACCACTAATGTT[A/T]AGTAAAAAGTTTATA	26091
rs201398469	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67994947	TGCCCACCTCAGCCT[C/T]CCAAAGTGCTGGGAT	26091
rs201424069	in-del	-/T	0.0130921	0.0798413	intron-variant	HERC4	GRCh38.p7	10:68056737	GTACACCAGTAATAG[-/T]CCAGAATGAAAACAA	26091
rs201431244	snp	G/T	0.00143558	0.0267531	intron-variant	HERC4	GRCh38.p7	10:67932575	TTCCATTTAACAATA[G/T]CAGAGATTAGTTTTC	26091
rs201449330	in-del	-/A			intron-variant, downstream-variant-500B	HERC4, POU5F1P5	GRCh38.p7	10:68009457	ATAGCATTGTATCTT[-/A]AAAAAAAAATCCATA	26091
rs201493387	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68025289	AAGCCTTTCGAGTGT[C/G]ATATCAACTACAATA	26091
rs201499570	snp	C/T	0.00107247	0.0231319	synonymous-codon	HERC4	GRCh38.p7	10:67922976	AATAGCTTGGATCAG[C/T]TTAGAGCGTAGAGTT	26091
rs201508924	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67998564	TTGAAAAAAAAAAAA[A/G]GGGGGGGGGTACAGT	26091
rs201530853	in-del	-/TTAG	0.0741063	0.177655	intron-variant	HERC4	GRCh38.p7	10:68026853	CTCAAAAAAAAAAAA[-/TTAG]TTAGGCATGGTAGTG	26091
rs201548872	snp	A/C/G			intron-variant	HERC4	GRCh38.p7	10:67945213	AAAGCAGCAAGAGAA[A/C/G]AGAAACAACATACAG	26091
rs201585460	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68027977	ATTATATATATATTT[A/C]TTATATTTTTAATTA	26091
rs201593981	snp	A/G	0.00299544	0.0385843	intron-variant, synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:68039464	TCTGACCAGAGAGTC[A/G]ACACACATGATTTTC	26091
rs201600809	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68054532	TATTTTTAGTAGAGA[A/T]GAGGTTTCACCATGT	26091
rs201606002	snp	A/G	0.00199792	0.0315431	synonymous-codon	HERC4	GRCh38.p7	10:67954676	TAATTCCCTCATGAT[A/G]AGCAAGAAAAATTCT	26091
rs201611938	in-del	-/ACC			intron-variant	HERC4	GRCh38.p7	10:67932204	CACGTGATCCATCCA[-/ACC]CCTTGGCCTCCCAAA	26091
rs201622271	in-del	-/AAAAG	0.0142736	0.0832652	intron-variant	HERC4	GRCh38.p7	10:67938455	AAAAAAAGAAAAAAA[-/AAAAG]AAAAGAAAAGGGAAA	26091
rs201649863	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68021055	TAGCCAAAAACTCCC[A/C]AATATGGGGAAAGAC	26091
rs201656033	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68007467	TCACTAGTGCCTTAT[A/T]TCATTGGTTTGGTGA	26091
rs201656147	in-del	-/AG/G	0.0970103	0.197722	intron-variant	HERC4	GRCh38.p7	10:68057638	AAAAAAAAAAAAAAA[-/AG/G]GTATAACTAAGTATA	26091
rs201689697	in-del	-/ATA	0.495135	0.0490805	intron-variant	HERC4	GRCh38.p7	10:68059576	ATAATATTATATATC[-/ATA]ATATTATATATCATA	26091
rs201696333	snp	A/T	2.04155e-05	0.00319489	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:67966791	TATAATCTGTCCCAT[A/T]TTCTCATTTACCTAC	26091
rs201707817	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67991641	TACAACCCATCATCC[A/C]AAATACCAACAAAAA	26091
rs201719707	snp	C/T	6.65358e-05	0.00576745	missense	HERC4	GRCh38.p7	10:67954735	CTTCTCCAACAAATA[C/T]AACCTAAAATAGCAC	26091
rs201726576	in-del	-/GTTT	0.0240643	0.107019	intron-variant	HERC4	GRCh38.p7	10:67942523	TTTGTTTGTTTGTTT[-/GTTT]TTGAGATGGAGTTTC	26091
rs201728890	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68038365	TACAAAAAAAAAAAA[A/T]TTAAAGGGGTGAAAA	26091
rs201742135	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67970173	TCCAGCTTAACTCCT[A/G]ACTAAACTCAAATCC	26091
rs201742370	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67995360	TTAGTTTCTCCCTAT[C/T]ATATAGTTATCTTAT	26091
rs201746928	in-del	-/T	0.00953873	0.0683987	intron-variant	HERC4	GRCh38.p7	10:67975353	TAGCATTTAAGAAAG[-/T]AACCAAGGTCACGTA	26091
rs201778980	in-del	-/TATT			upstream-variant-2KB	HERC4	GRCh38.p7	10:68076144	ATTTATTTATTTATT[-/TATT]GAGACAGAGTCTCGC	26091
rs201795706	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68059477	AATATTATATATTAT[-/A]ATATTATATATTATA	26091
rs201796275	in-del	-/TG			intron-variant	HERC4	GRCh38.p7	10:68006379	TTTTGTTTTTGTTTT[-/TG]TTTTTTTTTTTTGAG	26091
rs201811687	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67976033	TGCTACCCACTGTTT[G/T]TTTTTTTTTTAAGTA	26091
rs201819352	in-del	-/ACACACAT			intron-variant	HERC4	GRCh38.p7	10:67974114	CACACACACACACAC[-/ACACACAT]ACACACAGGGTCAGG	26091
rs201823747	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67974249	TAAAGGAGACAACTA[C/T]AAGCTGTGGCAGTAG	26091
rs201846926	snp	C/T	0.000153988	0.00877328	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:68044473	TCGAGACCCCAAGCA[C/T]ACACCTGGCCTTTGT	26091
rs201862671	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67970208	ACTAATACCAGATAG[C/T]AGAGGTGTACCAATT	26091
rs201905120	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68021049	AAGTAATAGCCAAAA[A/C]CTCCCAAATATGGGG	26091
rs201909384	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67974129	ACACACATACACACA[C/G]GGTCAGGAAAACAAG	26091
rs201940897	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68047930	TTTGTTTTTTTTTTT[-/T]GTGAGACAGGGTCTC	26091
rs201942942	in-del	-/A	0.00557542	0.0525036	intron-variant	HERC4	GRCh38.p7	10:68039850	ATTAAGTATTTTAGG[-/A]AAAAAAAAACACTAT	26091
rs201958904	in-del	-/G	0.00769098	0.0615332	intron-variant	HERC4	GRCh38.p7	10:67932789	CTCTTGCCTAGAAAT[-/G]AAAAAGCACACATGT	26091
rs201966338	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68055756	GGCATTACAATATCC[-/T]TTTTTTTTTTTTTGA	26091
rs201978173	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68032884	TCTGAAAATTCCAAC[A/G]AGAGATGTTAATAGT	26091
rs201992424	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68016014	AGGCTGAGGCAGGAG[A/G]ATCACTTGAACCTGG	26091
rs201997393	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67952909	AGTCTCAAAAAAAAA[A/G]AAAAAAAAAAAGACA	26091
rs202072425	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67993249	ACTTGGGAGGCTGAG[A/G]CAGGAGAATCGCTTG	26091
rs202092218	in-del	-/T	0.0916144	0.193427	intron-variant	HERC4	GRCh38.p7	10:68051511	ACCATGCCCAGCTAG[-/T]TTTTTTTTTGGTTTT	26091
rs202129383	snp	C/T	0.0100726	0.0702486	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922920	TAAACTGAATAGTTA[C/T]AACTCCAAAGTTATA	26091
rs202149588	snp	C/T	6.64894e-05	0.00576544	missense	HERC4	GRCh38.p7	10:67923068	ACTCCTCACCACCTC[C/T]TGTGGACTGGATGAC	26091
rs202162838	snp	C/G	6.68293e-05	0.00578015	intron-variant	HERC4	GRCh38.p7	10:68025513	AACAACTGCAGTTTA[C/G]AGACCAAAATGCTCT	26091
rs202190636	in-del	-/G	0.171057	0.237209	intron-variant	HERC4	GRCh38.p7	10:68006380	TTTGTTTTTGTTTTT[-/G]TTTTTTTTTTTGAGA	26091
rs202197664	in-del	-/T			intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069636	ATAAGGCTACCTCTT[-/T]CTCCTTCATTCCTTA	26091
rs202215842	in-del	-/T	0.126909	0.217598	intron-variant	HERC4	GRCh38.p7	10:68001369	GAGTGAGACCTTGTA[-/T]TTTAAAAAAAAAAAA	26091
rs202241159	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68012885	ATTATTATTTTATCT[G/T]TTATGGTGATCTCAT	26091
rs367582019	snp	C/T	0.000100246	0.00707904	intron-variant	HERC4	GRCh38.p7	10:67992177	ATGAGCCACTGTGCC[C/T]GGCCCAAAATGCTTT	26091
rs367603471	snp	C/T	0.000153988	0.00877328	intron-variant	HERC4	GRCh38.p7	10:67932553	CAAGATTTCCATATA[C/T]AAATCTTTCCATTTA	26091
rs367668921	snp	A/G	0.000155988	0.00883004	intron-variant	HERC4	GRCh38.p7	10:67941156	AAGTTAAAATATTAA[A/G]TTTTCTAAGATTACA	26091
rs367683353	in-del	-/ACACAC			intron-variant	HERC4	GRCh38.p7	10:67974074	AAAAAAAATTACTGT[-/ACACAC]ACACACACACACACA	26091
rs367687131	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67938213	TTTGGGAGGCTAACG[C/T]GGGCAGATCACGAGG	26091
rs367689349	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67947943	ATCTGCCCACCTTGG[C/T]CTCCCAAAGTGGTGG	26091
rs367706424	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67968291	GAATGCACAAGGCAC[A/G]AAGTAAGACCTGCTA	26091
rs367708533	snp	A/G	0.00993419	0.0697739	intron-variant	HERC4	GRCh38.p7	10:68063328	AATTCTCCTGCCTCA[A/G]CCTCCCGAGTAGCTG	26091
rs367714852	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68073328	AGTATCATTCAGTTT[C/T]AAAAACCAATCAGTT	26091
rs367718555	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67955923	TTTATTATGGTTCTC[C/T]CTGAGTTCTTGTTCT	26091
rs367724987	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67982246	TAATCAAAAGAGCAT[A/G]GTACTGGCATGAAAA	26091
rs367794313	snp	A/G	6.61037e-05	0.00574869	missense	HERC4	GRCh38.p7	10:67922965	TCATTGTGATCAATA[A/G]CTTGGATCAGTTTAG	26091
rs367839467	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68005614	TCTCTTCCTTCTTTC[A/C]TTCCTTCCTATCTTC	26091
rs367859078	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67983836	GGTGTGGTGGTGTAC[A/G]CCTGCAATCCCAGCT	26091
rs367875304	snp	C/G	1.66172e-05	0.00288242	missense, intron-variant	HERC4	GRCh38.p7	10:67959123	CTTACCTCAGTTAAT[C/G]CATGGTTGACATCCT	26091
rs367885171	in-del	-/AT	0.00159681	0.0282109	intron-variant	HERC4	GRCh38.p7	10:67993958	CAAGGAAATGACCAC[-/AT]GTTAATTTCCTTGAT	26091
rs367913004	snp	G/T	0.0115144	0.0749975	intron-variant	HERC4	GRCh38.p7	10:67989369	CCCACATTCACTATT[G/T]GTAGTTACTAAGTAC	26091
rs367920333	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67979602	TAGAAGACTGTAGAA[C/T]ACCAAGCAGACTTAA	26091
rs367942713	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68038815	TGTATTTTGTCCTTA[A/T]ACTTTCGTAATTTCC	26091
rs367945737	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68031564	AATAAGATTGGCAGG[G/T]ATAATAATCCTTCCT	26091
rs367948645	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	HERC4	GRCh38.p7	10:68076187	GGCTGGAGTGCAATG[A/G]TGCGATCTCAGTTCA	26091
rs367952224	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68029216	AGTTTAAGGGCCAGG[C/T]GCAGTGGCTCACGCC	26091
rs367969936	snp	A/G	0.000153988	0.00877327	intron-variant	HERC4	GRCh38.p7	10:67988621	TATCAATCTGTTAAT[A/G]GGAATGGGGAAAGAG	26091
rs367977434	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68041593	TCTTATACTATCTTG[C/T]CATAATTTTTTAATG	26091
rs367999542	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68020574	GATCGAGACCACCCC[A/G]GCTAAAAAAACGGTG	26091
rs368054284	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67944228	GGCTGGTGTCACCCC[A/T]CCCCCAGCTCCAGAG	26091
rs368071244	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67973125	ACACAGGTTTTAATT[A/G]TATTTGTTTTCAATG	26091
rs368151956	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67926620	TTTGGTCATCAGGCT[A/C]ATTTTTACCCTTTTA	26091
rs368180908	snp	C/T	0.000153988	0.00877328	synonymous-codon	HERC4	GRCh38.p7	10:67954658	GCCGTATTTAGGATC[C/T]AATAATTCCCTCATG	26091
rs368186971	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68023245	GTTTTTATATTCATG[A/T]TCATAGCAACAATAT	26091
rs368215600	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68012988	GGATGCCACAAACCA[C/T]ATCCATATAATAAGA	26091
rs368232102	snp	A/G	0.000467329	0.0152789	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:68014108	GTTGCTTGTTGAACC[A/G]GTTCCCAGCTGCCCA	26091
rs368300745	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67988866	GAACATGCAAATAAA[A/G]TGAATTTTTTAAAAA	26091
rs368333203	snp	A/T	1.74686e-05	0.00295534	intron-variant	HERC4	GRCh38.p7	10:68038052	CAAAAAAGTATCAAG[A/T]AATAAAACTGAAGAG	26091
rs368335790	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67950027	CATCAATCAAAAAAA[-/A]CAAAAAACAAAACAA	26091
rs368426258	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67931620	AGTAGAGACGAGGTT[C/T]CACCATGTTGGCAAG	26091
rs368457290	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68062684	AGAATCACATGAACC[C/T]GGGAGGCGGAGGTTG	26091
rs368490057	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67996764	CCAAGGTGGGTGGAT[C/T]ATGAGGTCAGAAGAT	26091
rs368515835	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67985581	GAAAATCACTGATTT[A/G]GATCAGCACAAATAT	26091
rs368525664	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68015037	TATGCAATATGACTA[C/T]TACAGTTGTTCCCAG	26091
rs368544913	snp	C/G	1.68963e-05	0.00290652	intron-variant	HERC4	GRCh38.p7	10:67932808	AAGCACACATGTACA[C/G]ATTATAAAAATCATG	26091
rs368548157	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67954071	TTCTATAAAGAACCA[C/G]ATGGCAAATATTTTG	26091
rs368585556	snp	C/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68023182	GAACCACCAATTCCA[C/T]TTCTGGGTATATGCC	26091
rs368597602	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68040227	CCAAAATACTAACCT[A/G]AGGCTTGTAACACAC	26091
rs368603224	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68050391	TATAAAAGAAACAGA[C/T]GCTTAGAGTAAGTAG	26091
rs368619891	snp	G/T	0.000104948	0.00724314	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922899	AATAGTTTAATGCTT[G/T]TGCACTAAACTGAAT	26091
rs368624415	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68061579	ATAGGTTTCTGTCAG[C/T]GAAAGAATAAGCAAA	26091
rs368625037	snp	A/C	6.9667e-05	0.00590158	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:68014143	CACCAAGCCCAAAAG[A/C]GTAAATTCGTCCTGA	26091
rs368678077	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68027164	ATATATGCAACTTTA[C/T]ATCCTGCTTTCATCA	26091
rs368700538	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67933254	ACAAAATTTACTTTA[A/C]CAAATGCCTAAGAGA	26091
rs368707784	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67995574	TTAGCTGTCTTTTTT[C/T]TTTTTCATTAATATG	26091
rs368749765	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67978641	GTCAGTAGCCAGGAA[A/G]TTGTTATAACAGGCC	26091
rs368758453	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67971003	AAACCTACAGTCAGA[C/G]TGACCAAGAAAAAGA	26091
rs368761462	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67965501	AAAGTGACTCAGGAG[A/G]AAAGTCAATGAGTCT	26091
rs368766992	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68060759	TCTACCTAGTAACTC[C/T]TCAAAATATAAGGTT	26091
rs368776688	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67994280	CTCAAAAGATTTAGC[A/T]GGATGTTATTTATTT	26091
rs368785710	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68005375	GCTCTTTTTGGTTTC[C/T]ATTTGCATGGAATAT	26091
rs368794669	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68060358	TTCTCCTGCCTTAGT[C/T]TCCCAAGTAGCTGGG	26091
rs368796323	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68060707	AAAATATGAATAGTT[C/T]TATGTTCTGGTACAG	26091
rs368800425	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68051775	GCTCACTGCAACCCC[A/G]CCTCCGAGGCTCAAG	26091
rs368804590	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67999889	CCTTCATTAGTAATA[C/T]ATTTATAAAGGTTCA	26091
rs368805581	snp	A/G	1.65897e-05	0.00288003	intron-variant	HERC4	GRCh38.p7	10:67954939	ATAAAAGTCCCAATT[A/G]TACCACAGAAAATGT	26091
rs368828304	snp	A/G	0.000303644	0.0123179	intron-variant	HERC4	GRCh38.p7	10:67932805	AAAAAGCACACATGT[A/G]CAGATTATAAAAATC	26091
rs368846294	snp	A/G	0.000153065	0.00874695	intron-variant	HERC4	GRCh38.p7	10:67939690	TTCTGAGAGGAAAAA[A/G]TTATTGGATATTTTG	26091
rs368865970	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67998009	GTTCAAGCGATTCTC[C/T]TGCCTCAGCCTCTGG	26091
rs368912891	snp	A/C/T			intron-variant	HERC4	GRCh38.p7	10:67939125	AATGTTAGTATGAAA[A/C/T]AGAAAGGAATGTACC	26091
rs368936258	snp	C/T	1.66554e-05	0.00288573	intron-variant	HERC4	GRCh38.p7	10:67959183	GAGGAAAGAGCAATA[C/T]TAGTGTCCAAATTTA	26091
rs368937936	snp	A/G			upstream-variant-2KB	HERC4	GRCh38.p7	10:68075632	GTCTTTGTGCTCATG[A/G]ATGCTAGCTAGTCTT	26091
rs368964228	snp	A/G	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:68039246	ACTTGGACCTGGGAG[A/G]CAGAGGCTGCAGTGA	26091
rs368988306	snp	C/T	0.000115309	0.00759218	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68072977	AACAAACACAGTATG[C/T]CTGAGTCCACATCCT	26091
rs369027030	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67961188	AATGGAAGTTAGGTC[A/G]TTTAGCGCCTCAACA	26091
rs369044056	snp	G/T	0.000501765	0.0158313	intron-variant	HERC4	GRCh38.p7	10:68034210	CAGTAATGGAAAAAT[G/T]AACCATTTTTCTCAC	26091
rs369096012	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67951026	AAGAATAATGGGGAT[A/G]TGTCAGAAGTACACC	26091
rs369110280	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67940466	GCTCTGTCACCCAGG[C/G]TGGAGTGAAATGGCG	26091
rs369136597	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68015967	AATTAGCTGGGCACG[A/G]TGGCATGCGCCTGTA	26091
rs369176272	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68059843	ATTATATATTATAAT[-/A]ATATTATATATCATA	26091
rs369182071	in-del	-/C			intron-variant	HERC4	GRCh38.p7	10:68004023	GCATGTTATTGCCCT[-/C]TTTCAGATAAAAGCC	26091
rs369185237	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67925521	GAAAATTCCCTTTCT[C/T]TGTATTCATGAACAG	26091
rs369188758	snp	A/T	1.6534e-05	0.00287519	intron-variant, synonymous-codon	HERC4	GRCh38.p7	10:67940950	TAACCTCCCAACATC[A/T]GGCATTAGTTCTTTC	26091
rs369205851	snp	C/T	0.000115922	0.00761233	intron-variant	HERC4	GRCh38.p7	10:67992343	CTGAACACCTGAAA[C/T]	26091
rs369255577	snp	C/T	1.68769e-05	0.00290485	utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68073127	TGTAATTATTTTGGT[C/T]TTCCAGTTTCAATAA	26091
rs369288476	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68068930	ACATACAACTGTTGT[A/G]AGAATTAAATGAGAT	26091
rs369333658	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68056153	AAGACTCCAACATAA[C/T]ACAATACAGTCATAT	26091
rs369370153	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67970185	CCTGACTAAACTCAA[A/C]TCCTTACACTAATAC	26091
rs369383395	snp	A/G	0.00398564	0.0444627	intron-variant	HERC4	GRCh38.p7	10:68064009	GCACTTTGGGAGGGC[A/G]AAGTGGGCAGATCAC	26091
rs369386244	snp	C/G	0.00438332	0.0466095	intron-variant	HERC4	GRCh38.p7	10:68009413	AGCCACTGTGCCAGG[C/G]CAATATACTGTAGTC	26091
rs369417538	snp	C/T			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011296	GCTTCAAGCAATCCT[C/T]TCACTTCACAAATGT	26091
rs369418569	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68046301	AGTAGCAGAAAATGA[C/T]AGGATGACAAGACAG	26091
rs369471006	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68071340	TAGTACACAGTGTCT[A/G]CCTCTAACACTTAAA	26091
rs369524069	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67960803	CTTCACCATGAAGCT[C/T]CCTGGTTTTCCCAGT	26091
rs369534877	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67936291	AAAACTTATAATAAT[A/C]TATTATTATATTCTA	26091
rs369541036	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67929909	ACCTCTGCCTCCTAG[A/G]TTCAAGCGATTCTCC	26091
rs369572767	snp	A/G			intron-variant, missense	HERC4	GRCh38.p7	10:68070521	TGAGGCAGGAGAATT[A/G]CTTGAACCTGGGAGG	26091
rs369584533	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67991214	ACTAAAAAATTTAAA[A/G]AAGTTTTTTTAATCA	26091
rs369598637	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68000977	TAGCAAACTAATATA[A/G]TTGTTTCAACTTTAC	26091
rs369602003	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67959227	AAGGTAGCATTTCAT[A/G]TATTTTGCTACAGCA	26091
rs369615064	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67978457	AGCTGCAGTACAACA[C/G]AACACCAGGTAGACG	26091
rs369641187	snp	A/G	0.000132545	0.0081397	intron-variant	HERC4	GRCh38.p7	10:67992344	TTTTCAAATAAGATT[A/G]GTCAGAGGGAAGAGA	26091
rs369643260	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67994620	TATTTTTAGTAGAGA[C/T]GGGGTTTCTCCATGT	26091
rs369657943	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67924487	ATTCTGTAGGTAACT[C/G]TAACATAACAGTAGG	26091
rs369670268	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68040899	GTCTCAAAAAAAAAA[A/G]AAAGAAAGAAAAAGA	26091
rs369678930	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67979982	AAAAAAACAAATAAC[A/G]TACAATGGTGTGCCA	26091
rs369722875	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68064643	ATATATATATGTTCA[C/T]TGCAGTATTACTTAT	26091
rs369738433	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68038864	TTTGTTTTACCACAA[C/T]GCAACTTTAAAGGCT	26091
rs369759889	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67955982	CAAGTTATTAACTTA[G/T]CGTTTTAACAAAGAC	26091
rs369782527	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67968404	TTGAGACAAAGTCTC[A/G]CTCTCTTGCCCAGGC	26091
rs369813193	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67962973	AAATTAATCTTCTCA[A/C]AACTTTTTAAGGTAG	26091
rs369842022	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67987611	TGGGTAAAGGCAAAC[A/G]TAAGAATGACCTGTT	26091
rs369872461	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68035567	AAAATGCAGATTTGA[C/T]AATATTGCTCACCCC	26091
rs369928682	snp	C/T	0.000153988	0.00877327	intron-variant	HERC4	GRCh38.p7	10:67925053	ATTAGATTCCAGTCT[C/T]ATAAAGTATACAACT	26091
rs369989921	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68067983	GATTTTTAAGTTTGT[A/G]TACAAGGGGGAAGAC	26091
rs370042921	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68000887	AAATTCGGACTTCTA[C/G]TCTGCAGAATAGTGA	26091
rs370064791	snp	A/C/G	0.00279242	0.0372774	intron-variant	HERC4	GRCh38.p7	10:67981698	ATGGTGGTTCACACC[A/C/G]GGTAATCCCAGCACT	26091
rs370086985	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68016461	GGATTCAAGCGAGTC[A/T]CCTGCCTCAGCCTCC	26091
rs370104954	in-del	-/AAAT/AAATAAAT			intron-variant	HERC4	GRCh38.p7	10:68022500	CAAAACTCCATCTCA[-/AAAT/AAATAAAT]AAATAAATAAATAAA	26091
rs370107146	in-del	-/GAG			intron-variant	HERC4	GRCh38.p7	10:67981034	GTAACAAAATAGGAG[-/GAG]TGTGTCCTTACTTAT	26091
rs370234029	snp	C/T			synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:67991148	CACTTACCTAACAGC[C/T]AAAAAACTTCCATTT	26091
rs370254179	snp	C/G	0.00438332	0.0466095	intron-variant	HERC4	GRCh38.p7	10:67945329	GGAAAAAACTTTTAT[C/G]CTAGAATAGTATGTA	26091
rs370266328	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68008699	CAAAAGAACTGAAAG[C/G]AGGATCTCAAAGAGA	26091
rs370271607	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68000592	AAAAAAAAAAAAAAA[A/T]TGTGTGTTGAAATCC	26091
rs370330207	snp	G/T	1.70545e-05	0.0029201	intron-variant	HERC4	GRCh38.p7	10:67957009	ACTTATTAGTACAAG[G/T]TGATTTGTGATATAC	26091
rs370336774	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68047732	CACTGACAACACCAG[C/T]TGTGATGTCAAGGAT	26091
rs370367087	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67969870	AGGCTATACCACAAC[A/C]ACCAAGAACCATTTC	26091
rs370551494	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069913	CGGGCATGGTGGCAC[A/G]CCCCTATAGTCCCAC	26091
rs370564505	in-del	-/TGAATGAGAAAAAATGAATGAGAAA			intron-variant	HERC4	GRCh38.p7	10:68002439	AAAATGAATGAGAAA[-/TGAATGAGAAAAAATGAATGAGAAA]ACAGCATTCAAATAT	26091
rs370582591	snp	A/C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67961827	ATCACTCTATGCAAA[A/C/T]CCTATTCAGAGGAAG	26091
rs370601722	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68055385	CTAACTTATGTGTCT[C/T]AGTTGACAGCAAACA	26091
rs370634872	snp	C/T	0.000153988	0.00877328	missense	HERC4	GRCh38.p7	10:67923002	GAGTTTCTTTTTCTG[C/T]ATATTTTGGAAGATC	26091
rs370655736	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67958245	ATTCTAAACATTCAC[G/T]CTTCAGTATTTTTCA	26091
rs370663208	snp	G/T	5.02105e-05	0.00501026	intron-variant	HERC4	GRCh38.p7	10:67992373	GATATTATATATAAC[G/T]CAAAAACCAAGAAAT	26091
rs370671598	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67983252	GTGGACTAAAGGGAA[C/G]CTTCGTACATTGTTG	26091
rs370678035	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68036032	CTAAAAAATGTTTAG[C/T]GGCTGGGCACAGTGG	26091
rs370684836	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68045218	ATCCCAGCTATTCGG[A/G]AGGCTGAAACAGGAG	26091
rs370692999	in-del	-/ATAA			intron-variant	HERC4	GRCh38.p7	10:68058212	AAGTACCATAAACAA[-/ATAA]TTTTTTAAAATTTTG	26091
rs370705074	snp	C/T			intron-variant, downstream-variant-500B	HERC4	GRCh38.p7	10:67966206	CTGGTCTTGAAATCC[C/T]GAGCTCAGGGAATCC	26091
rs370742107	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68002617	TTTTTTTTTTTTTTT[G/T]AGATGGATTCTCACT	26091
rs370780112	snp	A/G	1.65699e-05	0.00287831	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67988694	AAAACCTTTAATGCA[A/G]TATGAAGAAAACTGT	26091
rs370810058	in-del	-/G	0.0115144	0.0749975	intron-variant	HERC4	GRCh38.p7	10:67987052	TGAACTACAGACAAA[-/G]GAGGTTCTAGTGGTT	26091
rs370829323	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67943498	GACGTACCAATACCC[A/G]CAATATCAGAGGTAG	26091
rs370839726	snp	C/T	3.3994e-05	0.0041226	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:68014128	CCAGCTGCCCATTAC[C/T]ACCAAGCCCAAAAGA	26091
rs370852157	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68063734	CCTGAGGCCAGGAGT[G/T]TGAGACCAGCCTGGT	26091
rs370858454	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68019223	CTGGTCTCAAACTCC[C/T]GACCTCAGGTGATCC	26091
rs370948087	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67978181	CTCAGGAGGCTGAGA[C/T]AGGAGAATCGCTTGA	26091
rs370950067	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68059830	TTATATATCATAATA[C/T]TATATATTATAATAT	26091
rs370971278	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68042108	TGCAACCTCCGCCTC[C/T]CAGGTTCAAGCAATT	26091
rs370993809	snp	A/C	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:67983081	TGCACTGAGCAAAAA[A/C]AAAAAAAAACAAAAC	26091
rs371007369	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68039343	AAAAAAAGAAAGAAA[A/G]AAAAGAAAAAACGGG	26091
rs371011757	in-del	-/T	0.193653	0.243567	intron-variant	HERC4	GRCh38.p7	10:68003163	ACTATATTTTTATAC[-/T]TTTTTTTTTTTGAGA	26091
rs371015969	snp	C/T			intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010645	TATTTTCATTGTTGT[C/T]GGCTTCCTCCACCCA	26091
rs371065989	snp	A/G	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:68009156	TTGAACCCATGAGGT[A/G]AAGGTTGCAGTAAAC	26091
rs371086079	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68070969	AAAGTGCATGGCACA[A/T]CATGTCTAATTTCCA	26091
rs371117405	snp	C/T			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	HERC4	GRCh38.p7	10:68075341	CGGGGGAGGGGCTGG[C/T]CGGAAGTGAACCGCA	26091
rs371154758	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68066359	TGCAACAAGAATCTG[C/T]TAAGTACCCAAATTG	26091
rs371158588	in-del	-/ATT	0.0267878	0.112589	intron-variant	HERC4	GRCh38.p7	10:68065889	TAAAATGTCTGTATA[-/ATT]ACACACAGCATAGGT	26091
rs371193945	in-del	-/GA	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:67966873	TTTTTTTTATTTTTT[-/GA]GACGGAGTCTCACTC	26091
rs371207066	in-del	-/T	0.00279162	0.0372561	intron-variant, downstream-variant-500B	HERC4, POU5F1P5	GRCh38.p7	10:68009467	ATCTTAAAAAAAAAA[-/T]CCATATACCTTAATT	26091
rs371233896	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67972377	TAATACAAAATTAGC[C/T]GGGCATGGTGGTGCA	26091
rs371252161	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67973994	AGAGGTTGCAGTGAG[C/T]CGAGATCACGCCACT	26091
rs371264248	snp	A/T	1.71173e-05	0.00292547	intron-variant	HERC4	GRCh38.p7	10:67932826	TATAAAAATCATGTA[A/T]GAAGAATCCATAATG	26091
rs371353803	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68058805	ACAGATCTAGCAACA[A/G]AGCCAGGATTTTTAT	26091
rs371396605	snp	C/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67957804	AGTTCTTTATAGTCT[C/G]AATCTGCATTTTTTT	26091
rs371398037	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68019437	AGATCACAGAAAGAG[A/G]TCCATGTACATACAA	26091
rs371403729	snp	C/G/T	6.59135e-05	0.00574047	synonymous-codon, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:68044502	GTCATTTAGCGCTAA[C/G/T]GTATGAGCTTCTCCA	26091
rs371439506	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67947735	AATTTTAAAAAGACT[A/G]AAATCATAAAAAATT	26091
rs371439841	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67949846	AACATGGTGAAACCT[C/G]GTCTCTACCAACAAT	26091
rs371472901	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67964003	ACCTAGGTCAGAGAT[A/G]AAGAAAAAAGGAAAT	26091
rs371517446	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68038288	TCATATTATTTTTTT[-/T]CATACAAGCTCAATT	26091
rs371554143	snp	A/G	3.29979e-05	0.00406175	intron-variant, missense	HERC4	GRCh38.p7	10:67939632	TGTCATCTTCTGGAT[A/G]ATCCAGTAACTGTTG	26091
rs371576019	snp	C/T	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:68040523	CTCATCAAAAGTAAT[C/T]CCCTTTGTCACATAA	26091
rs371581986	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68009397	TGGGATTACAGGCAT[G/T]AGCCACTGTGCCAGG	26091
rs371618969	in-del	-/AG			intron-variant	HERC4	GRCh38.p7	10:68039334	AAAAAAAAAAAAAAA[-/AG]AAAGAAAGAAAAGAA	26091
rs371646241	in-del	-/A	0.0973687	0.197999	intron-variant	HERC4	GRCh38.p7	10:68062775	AAAAAAATAATAAAT[-/A]AAAAAATAAAGGACT	26091
rs371654143	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68050136	AGCCTGTGGCTGCAG[C/T]GACCAAGACTGCATC	26091
rs371703905	snp	C/T	0.000197736	0.00994127	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:67992285	CCAGATCTGCTTTGT[C/T]GGATTGGGACATCTG	26091
rs371719117	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68042938	GAAAAGCAGAAATAC[C/G]TTAACATACAGCTTA	26091
rs371721659	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67999400	CTCTGATGCTTGCCT[A/G]AAGACTCTCCTACAA	26091
rs371745774	snp	A/G	0.0283406	0.115616	intron-variant	HERC4	GRCh38.p7	10:68040250	TAACACACATTAAAT[A/G]CTAATATCTTTTACC	26091
rs371777240	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67952714	CAATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT	26091
rs371822144	snp	G/T	0.00953873	0.0683987	intron-variant	HERC4	GRCh38.p7	10:68026706	AAAATAGCCAGGCAT[G/T]GTGGCACAGACCTGG	26091
rs371824618	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68051581	AGCCAGGATGGTCTT[A/G]ATCTCCTGACCTCGT	26091
rs371861416	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68020889	AAACGTAAAGATAGG[A/G]CAGTTGCAATTATTG	26091
rs371864078	snp	C/T	0.000149752	0.00865179	intron-variant	HERC4	GRCh38.p7	10:67959167	AGAATATAACAATAA[C/T]GAGGAAAGAGCAATA	26091
rs371866905	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68067777	ATCAATGCTCATCAT[A/C]TTTAAAAAGAGTTCA	26091
rs371896244	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67983878	TGAAGCAGCAGAATC[A/G]CTTGAACCCGGGAGA	26091
rs371897948	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67971572	AAACAATATCTGATA[A/T]AATTCAAATCCATTT	26091
rs371954165	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67928909	CTGGGCGACAGAGCA[A/G]GACTCCATCTCAAAA	26091
rs371975437	snp	C/T	3.35537e-05	0.00409582	intron-variant	HERC4	GRCh38.p7	10:68032740	ATTATGAAAGAACTA[C/T]GATGAGTAATAATAA	26091
rs371980331	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68020492	AAAGTTTGGGCCGGG[C/T]GCGGTGGCTCACGCC	26091
rs372032135	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67992468	ATCAAATAGATCAGA[A/C]AAAACTTATTCTGTA	26091
rs372038249	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67982594	ATGCCCCACAAGCAC[A/G]TGCAACCAAAGCAAA	26091
rs372046529	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67961000	GATTTGGCGGACCTG[C/T]TGGTGCTGAGAGTAA	26091
rs372048563	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67978714	GTGTAGTCCCAGTGG[C/T]GGTAGCATCGCCACA	26091
rs372056518	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68009167	AGGTGAAGGTTGCAG[A/T]AAACCGAGATTGCAC	26091
rs372192622	snp	A/G	0.000153988	0.00877328	synonymous-codon	HERC4	GRCh38.p7	10:67932654	CATTGCTTGTAGTTC[A/G]TTAGGCTGAAAGAGC	26091
rs372229961	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68067609	TTTAAGGAGCAGCTC[A/G]TTTATAAATTTGTTT	26091
rs372235885	snp	A/G	0.000153988	0.00877327	intron-variant	HERC4	GRCh38.p7	10:67966823	AAAGAAAATGTAATT[A/G]ACATTAAATTTAACC	26091
rs372261160	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67974190	GACTGTCAAGTTACT[C/T]GAGAAACGTTTGCCT	26091
rs372262816	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67958246	TTCTAAACATTCACT[C/T]TTCAGTATTTTTCAT	26091
rs372320471	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68008097	AATTCCCTGGATTAC[C/T]AGGCAGAGTCTCTTG	26091
rs372337559	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68001720	AGAGGGAGGAGGGTA[C/T]GGAGAGTTTCCATTT	26091
rs372346829	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67928285	TTAAGGTGATTAGAG[A/G]TGGAGTCCATTTCCA	26091
rs372353008	snp	C/T	0.000257367	0.011341	intron-variant	HERC4	GRCh38.p7	10:68014211	AATGATAGAAAACTT[C/T]AGACTTAATGTTACC	26091
rs372356997	snp	G/T	0.000104067	0.00721268	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922910	GCTTTTGCACTAAAC[G/T]GAATAGTTATAACTC	26091
rs372389113	snp	C/T	1.65965e-05	0.00288062	missense	HERC4	GRCh38.p7	10:67954725	TCCACAGCATCTTCT[C/T]CAACAAATATAACCT	26091
rs372390549	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68070796	CTTTTCTCAGGATCA[A/G]GACCCCCCCCTTCTA	26091
rs372398240	snp	A/G/T	4.94556e-05	0.00497246	synonymous-codon	HERC4	GRCh38.p7	10:67955026	CATTGCATCTCCTAC[A/G/T]ATATTTTCTCTACGC	26091
rs372483470	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67975358	TTTAAGAAAGTAACC[A/G]AGGTCACGTAAGTAA	26091
rs372493903	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67932071	CAAGAGACTCTCCTG[C/T]CTCAGCCTCCTGAGT	26091
rs372537314	in-del	-/ATAA			intron-variant	HERC4	GRCh38.p7	10:67939551	TAAATAAAAGAGATG[-/ATAA]ATAATCAGGCTAACC	26091
rs372604220	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68037235	GAGTAGCTGGGACTA[C/T]AGGTGTGTGCCACCA	26091
rs372604511	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68046103	ATACAAAAACAAAAA[-/A]GGCAAGCAAGATATG	26091
rs372655436	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67935533	GGAGCTATAGACTTT[A/C]AGCACTTAATCTCCC	26091
rs372682724	in-del	-/A	0.468047	0.122292	intron-variant	HERC4	GRCh38.p7	10:68039153	CTCTACTGAAAATAC[-/A]AAAAAAAAAAAAAAA	26091
rs372703424	snp	C/T	0.000153988	0.00877328	intron-variant	HERC4	GRCh38.p7	10:67990876	AATCAACAGATAATA[C/T]TGTAAACATAATACT	26091
rs372705992	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67980427	CATGAGCCACCGCAC[A/C]CCACCCTGAAAGACA	26091
rs372708849	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68043002	AAAGATGTTGAAACC[A/G]AAGAACTCAAGTAAA	26091
rs372744152	snp	A/G	3.29946e-05	0.00406155	synonymous-codon	HERC4	GRCh38.p7	10:67955095	TGGGAGAAAAAGAGA[A/G]GAGACATTCTGCCTG	26091
rs372790810	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68063767	ACATGGCAAAACCCC[A/G]TCTCTACTAAAAATA	26091
rs372796707	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68072687	GTTTTATAATACTAG[A/T]AGTAAAAAAAAAGAA	26091
rs372809199	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68041699	GTGCAAAGTTATGTG[C/T]TTCCACTTATATTAA	26091
rs372810190	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67990456	GAATACACTTTCAAA[A/G]AAAAAAAAAAAAAAG	26091
rs372818694	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68000931	TATTGTTCAAGCCAC[C/T]GAGTTTGTGGTAGGT	26091
rs372839863	in-del	-/T	0.0131181	0.0799185	intron-variant	HERC4	GRCh38.p7	10:68000026	GGTATGACAAGTCAC[-/T]TTTTTTTCTTTTGTA	26091
rs372850221	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68071640	TAAATTACCATTCAT[C/T]TCTACCAATATGACC	26091
rs372868417	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67993525	GCAAGACCCATCTCT[-/A]AAAAAAAAAAAAATT	26091
rs372871012	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67977417	AGCAGCAATATCCAT[C/G]TACTAGGTACAAAGG	26091
rs372873445	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67987729	CAAAGAAAAAAGTAA[A/G]TCCAGAAAGTTAAGT	26091
rs372896331	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68037604	AAGCAATCTTCCCCA[A/G]TTGCAGCTATGAAGA	26091
rs372916791	snp	C/T	0.00014246	0.00843859	intron-variant	HERC4	GRCh38.p7	10:67992589	CTATTTAATTATTTA[C/T]ATGACTATATTATTA	26091
rs372921266	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68024873	GAATCAACAGATGAA[C/G]CTCAATGTCAAAGAC	26091
rs372924898	in-del	-/C			intron-variant	HERC4	GRCh38.p7	10:68073991	ATTAAAAAAATCACC[-/C]GTGGGCAATCTATAT	26091
rs372930441	snp	A/G	0.000100852	0.00710042	intron-variant	HERC4	GRCh38.p7	10:67941114	CAAATGTCTAAAAAT[A/G]TAAGAAAAAGTAAAC	26091
rs372949748	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67946671	CCCAACACTTTGGGA[A/G]GCCGAGGTGGGCGGA	26091
rs373004094	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67993145	ATGTTAGGAGTTCGA[C/T]GCCAGCCTGGCCAAT	26091
rs373007983	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67962309	ATAGTATGGGAGATC[A/G]ATTTTCTCCTTAGCT	26091
rs373036479	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67955424	TGGTTTTTCTAAAAA[A/G]CATTCACTGGAGGGG	26091
rs373056923	snp	A/G	0.000501084	0.0158206	intron-variant	HERC4	GRCh38.p7	10:67939698	GGAAAAAATTATTGG[A/G]TATTTTGACTATTTT	26091
rs373070903	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67957178	CCCAATTTTAGGGGG[C/T]GACTGTATACTTGAG	26091
rs373093538	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67987300	CCCCTTCCATTTTCT[C/T]GAGGTAAAAGACACA	26091
rs373117786	snp	G/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:67998185	TACAGGTGTGAGCCA[G/T]TGTACCCGGCTGGAA	26091
rs373129001	snp	A/C			downstream-variant-500B	HERC4	GRCh38.p7	10:67921529	ATCTATAGAAGAGTT[A/C]TATGGTTCGCCAATA	26091
rs373222927	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67961764	CAAAGACTTTGGGTT[C/G]TCTCACTATATTAAG	26091
rs373244582	snp	C/T	3.50613e-05	0.00418681	intron-variant	HERC4	GRCh38.p7	10:68038048	CAATCAAAAAAGTAT[C/T]AAGTAATAAAACTGA	26091
rs373280456	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68013607	ATGAAGAGTTGCTGT[G/T]TAATGCATAGAGTTT	26091
rs373336570	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67931018	TGAGATGGAGTCTTG[C/T]TCTGTTGCCTGGGCT	26091
rs373399100	snp	C/T	0.00117305	0.0241898	intron-variant	HERC4	GRCh38.p7	10:67991062	ATAAAAATTTAAAAT[C/T]ATTTCATTTTTTAAT	26091
rs373401588	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67927431	ATATATATATATATA[-/T]TTTTTTTTTTTTTTA	26091
rs373404591	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67936082	TTAGGGTTGTGACAC[A/G]TTTTCTACGTACAGA	26091
rs373438769	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67959853	GTAGAAAGTTTCCAC[A/T]TATGCTCAGAGCACA	26091
rs373480395	snp	C/T	1.65348e-05	0.00287526	missense	HERC4	GRCh38.p7	10:67956898	TCTGTAAGACTGCAT[C/T]GGTCTGTAACAGAGT	26091
rs373486198	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68021948	ATAAACTTTGCAAAG[C/T]AGGAGGATACAAAAT	26091
rs373500078	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68043837	AAACAAACAAAAAAC[G/T]ATTATGCCCTATGTA	26091
rs373512975	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67947865	TTTTTTTTTTTTTGT[A/T]TTTTTAGCAGAGACG	26091
rs373536354	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68062412	AAGCCTGTCCATTCT[C/T]TCTGCCTCTCTAAGT	26091
rs373594642	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67934919	AGTTTTTTTTTTTTT[A/G]ATATTTTCTTTGACA	26091
rs373683302	in-del	-/CAAA			intron-variant	HERC4	GRCh38.p7	10:68036390	GAGTAAACAAACAAA[-/CAAA]AAGGTCAATATGAAA	26091
rs373693404	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67983595	CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCT	26091
rs373735248	snp	C/T			intron-variant, synonymous-codon	HERC4	GRCh38.p7	10:68070562	GGTGAGCCGAGATGG[C/T]GCCATTGCACTCCGG	26091
rs373757940	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68065109	GCTAAATTATTATCG[A/G]GGGAAAAAAGTTGAG	26091
rs373813896	snp	C/T			intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069898	ATATAAAAAATTACC[C/T]GGGCATGGTGGCACG	26091
rs373985461	in-del	-/TCT			intron-variant	HERC4	GRCh38.p7	10:67941364	ACTTTACAACTGTTT[-/TCT]CCCAGACATAAGCAT	26091
rs373991578	snp	A/G			downstream-variant-500B	HERC4	GRCh38.p7	10:67921411	GAAGTGGATGAACAG[A/G]GAAAATGGTATAATA	26091
rs374021742	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67949982	TGAGATTGTGCCACT[C/G]CACTCCAGCCTGGAG	26091
rs374039487	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67993604	ATTTCATAATGCAGA[A/G]TTTTTTTTTTCAATA	26091
rs374051912	snp	A/G	3.31691e-05	0.00407228	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:68014051	TAGACACTGCCCATT[A/G]TAGGGGTACCAATTT	26091
rs374113836	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67932216	TCCACCTTGGCCTCC[C/T]AAAGTCCTGGGGTTA	26091
rs374123894	snp	C/T			intron-variant, missense, nc-transcript-variant	HERC4	GRCh38.p7	10:68039472	GAGAGTCGACACACA[C/T]GATTTTCGGGAAGCA	26091
rs374161271	in-del	-/AGGA	0.0135022	0.0810479	intron-variant	HERC4	GRCh38.p7	10:67945904	AAAAAGGAATGGAAT[-/AGGA]AGGAAGGAAGGAAGG	26091
rs374190892	snp	C/T	0.0111196	0.0737302	intron-variant	HERC4	GRCh38.p7	10:67931212	GATGGTCTCGATCTC[C/T]TAACCTCGTGATCCG	26091
rs374204040	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68055900	GGGATTACAGGCACC[A/G]GCCACCATGCCCGGC	26091
rs374207170	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67952567	GTGAGCCACTGGGCC[C/T]GGCCAAAAAAATACT	26091
rs374256442	snp	C/T	1.68411e-05	0.00290177	intron-variant	HERC4	GRCh38.p7	10:67923160	AAGAAAGAAATCATT[C/T]AGTCAACCACTTCAA	26091
rs374296396	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68051565	AGAGTTTCACCATGT[C/T]AGCCAGGATGGTCTT	26091
rs374296829	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68019845	TGCCCTGATCAATGA[C/T]TGGTGCTTCTGATCA	26091
rs374309116	snp	G/T			intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010563	AACACATTCTCCAGG[G/T]TCTCAATACTGGTTC	26091
rs374377054	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67992443	TCCTGAACACCTGAA[A/G]CAAAAACCTATCAAA	26091
rs374379159	in-del	-/T	0.00795532	0.062565	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069567	CTATTCACTACATTG[-/T]CAGGCCAAGTCCTCC	26091
rs374380236	in-del	-/CCT			intron-variant	HERC4	GRCh38.p7	10:67989894	TTAATTGTTCCTCCT[-/CCT]TTACTTCTTTAATAG	26091
rs374461855	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68041538	TCAAATATGTTTAGT[C/T]TGTATAGTCCAGAAA	26091
rs374497915	snp	C/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67984642	GGCTGGAGTGCAATG[C/G]CACGATTTCGACTCA	26091
rs374508399	snp	G/T	0.000398234	0.0141053	intron-variant	HERC4	GRCh38.p7	10:68044588	TCAAGAAGAGAAATA[G/T]TGCATTCTAGTACAG	26091
rs374524776	in-del	-/G			intron-variant	HERC4	GRCh38.p7	10:67947863	TTTTTTTTTTTTTTT[-/G]TATTTTTAGCAGAGA	26091
rs374532315	snp	C/T			intron-variant, downstream-variant-500B	HERC4	GRCh38.p7	10:67966384	GAAATAAGAGGCAAC[C/T]TCATGGAAAATAAAA	26091
rs374539365	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68033102	CAATATGCCAGTATG[C/T]AAAGGACTCAGAAAT	26091
rs374549105	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68019856	ATGATTGGTGCTTCT[C/G]ATCACCAAGGTGCAG	26091
rs374554453	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67992103	GGTTTTGCCATGTTG[C/T]CCAGGCTGGTCTCCA	26091
rs374564034	snp	C/T	0.000478422	0.0154591	intron-variant	HERC4	GRCh38.p7	10:68038218	ATTCCATTTAACAAA[C/T]TGATCTTGAATGCTA	26091
rs374584005	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68006353	GTTGATGAAACGCCT[C/T]AGCGTTTTTGTTTTT	26091
rs374585007	snp	C/T			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012504	AGGAATAGGAAGGCC[C/T]GAGGAGAGGAGAGAG	26091
rs374585058	snp	C/T	5.6002e-05	0.0052913	intron-variant	HERC4	GRCh38.p7	10:67925236	GGACACACTGGCTAA[C/T]ATATTAGCACATAAA	26091
rs374613927	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67926617	TTCTTTGGTCATCAG[C/G]CTAATTTTTACCCTT	26091
rs374636205	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67927461	AGATAGAGTCTTGCT[C/G]TGTCACCAGGCTGGA	26091
rs374643816	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67991533	TTTTAAACATTTTAT[A/G]TTGGCAGTGAGCCTA	26091
rs374651782	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67927108	ATTTGCTGTTAGTTG[C/T]ACACAAGTTTGAAGA	26091
rs374664842	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68007063	TTTAAATAAACTTTC[C/T]ATCCCTCTCTCTCCT	26091
rs374715597	snp	A/G	0.000153988	0.00877328	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922928	ATAGTTATAACTCCA[A/G]AGTTATATTAAACTG	26091
rs374728105	snp	C/G/T			intron-variant	HERC4	GRCh38.p7	10:67934658	TTTTAAACACACACA[C/G/T]TTGATAATTTGGATA	26091
rs374749560	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68062057	TGAATTATTAATTAC[C/T]TAACAGGTTAGAACT	26091
rs374786475	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67970499	TGGGAGGCTAAAGCA[C/T]GAGAATTGCTTGAAC	26091
rs374822244	snp	A/G	0.000465851	0.0152548	intron-variant	HERC4	GRCh38.p7	10:67959168	GAATATAACAATAAC[A/G]AGGAAAGAGCAATAT	26091
rs374828446	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67926969	TTTCAGCTGTACATT[A/T]TCCGGCACACAGTAG	26091
rs374837877	snp	A/G	1.65512e-05	0.00287669	intron-variant	HERC4	GRCh38.p7	10:67992341	AAATTTTCAAATAAG[A/G]TTAGTCAGAGGGAAG	26091
rs374893667	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68030124	TTGTTCTGGCTATTA[A/T]TTTTAAATTTACTGT	26091
rs374935380	snp	A/C/G	0.000399281	0.0141238	upstream-variant-2KB	HERC4	GRCh38.p7	10:68076630	GATAATCTTTTCCAG[A/C/G]CTTCTCTGCTAGCTT	26091
rs374962215	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68039209	TAGTCCCAGCTACTC[A/G]GGAAGCTGAGGCAGG	26091
rs375028936	snp	C/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68039096	TCACTTGAGGTCAGT[C/G]AGGAGTTTGAGACCA	26091
rs375033055	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68048388	TGGAAGAAATTTACT[G/T]AATAGTAAAAAAGCC	26091
rs375063266	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68068486	AGCAAGACTCCGTTT[A/C]AAAAAAAAAAAAAAA	26091
rs375066190	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68065652	CTGAGGTGCGAGGAT[C/G]ACTTCGAGACCAGCT	26091
rs375087626	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68018027	GTACATTCCTCAATG[C/T]TATTTTATCAGACTA	26091
rs375088843	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67988908	CAAAATCATACTGAC[-/T]TTTTTTCTGAAACAG	26091
rs375109214	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67986472	ATTCTCTTGCCTTAG[C/T]CTCCTGGGTAGTTGG	26091
rs375172170	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68033320	CAAGGTATTCTTTAA[A/T]TCTTTCTGAAAGTAT	26091
rs375188319	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68051650	AGGCGTGAGCCACCA[C/T]GCCCGGCCAATGTTA	26091
rs375198782	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68073760	ACTCTCCCAATTACT[C/T]TTTAGCCCAGAGAGA	26091
rs375257092	in-del	-/TC	0.00636936	0.0560724	upstream-variant-2KB	HERC4	GRCh38.p7	10:68076954	CATGCAGAAACCCTG[-/TC]TCTACTGAAAAAATA	26091
rs375263391	snp	C/T	2.23272e-05	0.00334112	intron-variant	HERC4	GRCh38.p7	10:67925064	GTCTCATAAAGTATA[C/T]AACTAGTTAGAAATA	26091
rs375266020	snp	A/C	3.40518e-05	0.00412611	intron-variant	HERC4	GRCh38.p7	10:68038074	ACTGAAGAGAAATAA[A/C]ATAAAAACTAATGCT	26091
rs375284949	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67983634	AATACAAAATAAAAA[A/T]AAATTAGCCAGGTGT	26091
rs375288107	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68042337	TACGAAAATCTATAA[A/C]CACTAGGCAGGACAC	26091
rs375309228	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67970182	ACTCCTGACTAAACT[A/C]AAATCCTTACACTAA	26091
rs375311812	snp	C/T	0.000153988	0.00877328	intron-variant	HERC4	GRCh38.p7	10:67954587	ATTTAGATGGTTGGA[C/T]ATTTTACCTTATCAG	26091
rs375326411	in-del	-/GA			intron-variant	HERC4	GRCh38.p7	10:68046530	GTGCTCCAAGCACTG[-/GA]GAGAGAGAGAGAATA	26091
rs375336418	snp	A/C/G	0.000377145	0.013727	intron-variant	HERC4	GRCh38.p7	10:67995224	TCCATCAGGAAACAC[A/C/G]TAATTCCTTTGAGAA	26091
rs375344169	snp	A/C/G			intron-variant	HERC4	GRCh38.p7	10:68007776	GCTATTCAAAGGCAC[A/C/G]ATCCCACTACTGATC	26091
rs375365293	in-del	-/C	0.0342848	0.12636	intron-variant	HERC4	GRCh38.p7	10:68070799	TTCTCAGGATCAGGA[-/C]CCCCCCCTTCTACAA	26091
rs375383424	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67923786	AAAGAGTAATGATTT[A/C]TCATCCTTATGACAC	26091
rs375406557	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67929906	GCAACCTCTGCCTCC[C/T]AGGTTCAAGCGATTC	26091
rs375409342	snp	A/G			synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:68025641	ATGGCCCAACTGACC[A/G]TACCCTCCAGCTCCA	26091
rs375464363	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67968403	TTTGAGACAAAGTCT[C/T]GCTCTCTTGCCCAGG	26091
rs375475272	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68040380	TAAAGAATGGGGGAT[A/G]TTGGCTTTGTTTTCT	26091
rs375495657	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67956292	TCATAATATGAATTA[A/G]TTTAAAAAATCCTCT	26091
rs375520062	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67986876	CTAGAATATGAACTT[C/G]TAGATCTAGGGGCAT	26091
rs375527573	in-del	-/ATTT			intron-variant	HERC4	GRCh38.p7	10:67952127	AATTCCACCGTCACA[-/ATTT]ATTTATTTGTCCAAA	26091
rs375527797	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68006624	CTCAGGTGATCTGCC[C/T]GCCTCAGCCTCCCAA	26091
rs375578693	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68003301	TGGGACTACAGGCCT[A/G]CAGGCGCCTGCCACC	26091
rs375583306	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67976322	CCTCTCCAATATTTA[C/T]GTTTATACATATACA	26091
rs375598736	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68035903	AGTTTTTCTTTATAG[C/T]CCTTATCATAGTATG	26091
rs375639953	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67972078	AATTAGCTGAGTGTG[A/G]TGGTGGACACCTGTA	26091
rs375653222	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67935147	GGCTATCGATTTACA[-/T]TTTTTTTTTTTTTTT	26091
rs375700847	in-del	-/T/TT	0.439502	0.163061	intron-variant	HERC4	GRCh38.p7	10:68002599	TTTTTAAATTTTTAC[-/T/TT]TTTTTTTTTTTTTTT	26091
rs375717350	snp	C/T	0.00597247	0.0543191	intron-variant	HERC4	GRCh38.p7	10:67971305	GAAGCCAGAATAAAC[C/T]TGATACCAAAAGCTA	26091
rs375720158	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68028326	TATTGATTTGCAAGA[A/G]GAGAAGATCACTACA	26091
rs375720287	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68071132	AGAGGTATCCCAAAT[G/T]AGGGAAACCCACTGC	26091
rs375767131	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68015959	AATACAAAAATTAGC[C/T]GGGCACGGTGGCATG	26091
rs375797323	snp	A/T	0.000153988	0.00877328	synonymous-codon	HERC4	GRCh38.p7	10:67955074	GGGATTCACAGATTC[A/T]ATCACTGGGAGAAAA	26091
rs375809644	in-del	-/G			intron-variant	HERC4	GRCh38.p7	10:67931174	TTTAGTAGAGACGGG[-/G]TTTCACTATGTTGGT	26091
rs375820989	in-del	-/G			intron-variant	HERC4	GRCh38.p7	10:68039335	AAAAAAAAAAAAAAA[-/G]AAAGAAAGAAAAGAA	26091
rs375821315	snp	C/T	4.94809e-05	0.00497373	missense	HERC4	GRCh38.p7	10:67954986	GCTTCTTGTAATCTA[C/T]GTTCTTTGTTTTCCT	26091
rs375827060	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68000778	GCCAAGGTCTACAAG[C/T]GAAGGAATGCCAAAG	26091
rs375910541	snp	A/G	5.06984e-05	0.00503454	intron-variant	HERC4	GRCh38.p7	10:67992151	ATCTGCCTGGTGCTG[A/G]GATTACAGGCATGAG	26091
rs375943409	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68009318	AGATGAGAGTTAATG[C/T]GGCCCCAGCTGGTCC	26091
rs375992895	in-del	-/C			intron-variant	HERC4	GRCh38.p7	10:67945816	AAACTCAAATCAAAA[-/C]AACATACGACAGATA	26091
rs376043342	in-del	-/G			intron-variant	HERC4	GRCh38.p7	10:67998564	TTGAAAAAAAAAAAA[-/G]GGGGGGGGGTACAGT	26091
rs376125023	snp	C/G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68051780	CTGCAACCCCGCCTC[C/G/T]GAGGCTCAAGTGATC	26091
rs376158813	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68028526	CCCTAGACATGGGAT[C/T]AGACTCTTCTCTAAG	26091
rs376162026	snp	C/G	0.000150632	0.00867717	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:67992609	CTATATTATTACCTG[C/G]GGACTAGAGTAATGT	26091
rs376164208	snp	A/C	3.35914e-05	0.00409812	intron-variant	HERC4	GRCh38.p7	10:67954546	ATACATACAGGTATA[A/C]ATACATGGGTATATA	26091
rs376196716	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67961785	CTATATTAAGTAAAG[C/T]CAAAGCAGTGTAAGC	26091
rs376245578	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68020958	GCCTAGGGGAACCAT[A/G]GGATACCATTAAGCA	26091
rs376299528	snp	A/G	5.01979e-05	0.00500963	missense	HERC4	GRCh38.p7	10:67925111	TTCTTCTTTTCCAAT[A/G]GTAATTCGTGAAATA	26091
rs376301081	snp	A/G	0.000153988	0.00877328	intron-variant	HERC4	GRCh38.p7	10:68038172	ACTTTTAATATTTCT[A/G]GAAAAGAAGAAGACA	26091
rs376375238	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67982918	GGATCGCCTGAGCTC[A/C]GGAGTTCAAGACCAG	26091
rs376377447	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68060319	CTCAATTCACTGCAA[A/C]CTCTGCTTCCCGGGT	26091
rs376428308	snp	A/G			intron-variant, utr-variant-5-prime	HERC4	GRCh38.p7	10:68074753	CTCAACCTGAGAGAA[A/G]CCCATCCCCAGGCAG	26091
rs376433713	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68034300	ATTTTGGGACATTCT[A/G]CCTATCATCAAAAGA	26091
rs376462128	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67938528	TTTATAATATTCAAA[C/T]TGTTCCCTTCTGGAG	26091
rs376468292	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67967766	AATCAAGTCTCCTAA[C/T]CTAAATTTTAGTTTA	26091
rs376478215	snp	C/G	1.71146e-05	0.00292524	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:68014134	GCCCATTACCACCAA[C/G]CCCAAAAGAGTAAAT	26091
rs376523407	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67950281	TACATACAGGGGAGA[-/T]TTTTTTTTTTTTTGA	26091
rs376536363	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68060633	TGCAGTACCAACTTA[C/T]AATGTGTTCTCTTTT	26091
rs376581009	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68035276	TCCTGCCTCAGCCTT[C/T]TGAGTAGCTGGGATT	26091
rs376601683	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67996404	AGCTATTCACAATTC[C/T]GTAAATTGTAATTCT	26091
rs376607008	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67939823	ATACACAATGGCAAA[C/G]TTATAAATGATGCTT	26091
rs376682088	in-del	-/A/AA/AAA/AAAA/AAAAAA	0.273138	0.280998	intron-variant	HERC4	GRCh38.p7	10:67990452	AATGAATACACTTTC[-/A/AA/AAA/AAAA/AAAAAA]AAAGAAAAAAAAAAA	26091
rs376710802	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67973590	CGGCTGAGAGAGTGA[A/G]GTATAGTCAAGAATA	26091
rs376758509	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68024716	GCTATACATACAAGG[C/T]AGAAAAACATTAAGC	26091
rs376813131	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68005110	CTGAGTTCTCTGTTC[C/T]GTTCCATTGGTCCAT	26091
rs376818906	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68035405	TAGTGATCTGCCCAC[C/T]TCGGCCTCCCAAAGT	26091
rs376834364	snp	A/G	0.000153988	0.00877328	intron-variant	HERC4	GRCh38.p7	10:67955142	CCATCTGGAAAACAA[A/G]AGATTAACATTTTAA	26091
rs376855313	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68056693	GGAGCAGGGAGATCA[C/G]TTAAAGAGCTACTGG	26091
rs376857729	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67930540	CCCATCGGCAACATA[C/T]AAATGTTCCTGATGC	26091
rs376858145	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67931111	CTGCCTCAGCCTCTC[A/G]ATAGTTGGGACTATA	26091
rs376866734	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67964002	TACCTAGGTCAGAGA[G/T]GAAGAAAAAAGGAAA	26091
rs376881093	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67939950	TATTTTTCCCGAGAT[A/G]GAGTCTTGCTCTGTC	26091
rs376885465	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67966929	GCACAATCTCAGCTC[A/C]CTGCAAGCTCTGCCT	26091
rs376991330	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67929188	TCCTAATTATTCTTA[A/C]AATCTTATTCCTTAA	26091
rs377012855	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67931667	TGACCTCAGGTGATC[C/T]GCCCACCTTGGCCTC	26091
rs377014016	snp	C/T			utr-variant-3-prime	HERC4	GRCh38.p7	10:67922665	CAAACTCTTAAAATT[C/T]ATGTTAGTAAAACTT	26091
rs377029318	snp	A/C	1.64754e-05	0.00287009	missense	HERC4	GRCh38.p7	10:67932660	TTGTAGTTCATTAGG[A/C]TGAAAGAGCAGAAGG	26091
rs377037886	in-del	-/AAAA			intron-variant	HERC4	GRCh38.p7	10:68018275	AGATTAAAGGAAAAA[-/AAAA]TCATAAATCATTTCA	26091
rs377068058	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67995361	TAGTTTCTCCCTATT[A/C]TATAGTTATCTTATA	26091
rs377101496	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67924316	CACTTAACGATGATG[A/T]TATGTTCTGAGAAAT	26091
rs377113107	snp	C/G/T	6.00263e-05	0.00547816	intron-variant	HERC4	GRCh38.p7	10:68014215	ATAGAAAACTTCAGA[C/G/T]TTAATGTTACCTTCC	26091
rs377141598	snp	A/C/T	5.0289e-05	0.00501422	intron-variant	HERC4	GRCh38.p7	10:68032743	ATGAAAGAACTATGA[A/C/T]GAGTAATAATAAAGA	26091
rs377291219	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68013020	CACAGGCATGCCGCA[C/T]TTTATTGTGCTTTGC	26091
rs377342606	snp	A/C/G	6.61205e-05	0.00574948	synonymous-codon	HERC4	GRCh38.p7	10:67956899	CTGTAAGACTGCATC[A/C/G]GTCTGTAACAGAGTA	26091
rs377355822	snp	A/G	0.000661875	0.0181796	intron-variant	HERC4	GRCh38.p7	10:68032888	AAAATTCCAACAAGA[A/G]ATGTTAATAGTATTT	26091
rs377384992	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67936945	CATATGAAGAACTAA[C/T]TATAATAAAATAATG	26091
rs377390860	snp	C/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67984523	GGAGGCAGGGGCATG[C/G]GTGAGGTTGGGATGG	26091
rs377419044	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67941761	TCTGCTCACTGCAAC[A/G]TATGCCTCCTGGGTT	26091
rs377425758	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68059800	TTATATATCATAATA[C/T]TATATATTATAATAT	26091
rs377448635	snp	A/C	1.66668e-05	0.00288672	intron-variant	HERC4	GRCh38.p7	10:67992364	GAGGGAAGAGATATT[A/C]TATATAACTCAAAAA	26091
rs377472946	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68044071	CAAACCAATATTTAA[C/T]AAATATTTCAATAGC	26091
rs377483234	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67938565	ACCGTAATACTTATG[C/G]ATTTTCTCTTATTTA	26091
rs377484501	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67948536	ACAGTAGATGTTGGC[A/G]TGGATGTGGTGAAAA	26091
rs377496072	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67945584	GTGGTGTATAAACTA[C/T]CCATATCTTGAGTAT	26091
rs377524230	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67975385	GTAACAGAGCCAGAA[A/G]TATAACTCATGCATT	26091
rs377531760	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68040218	CTCTCCTTTCCAAAA[C/T]ACTAACCTAAGGCTT	26091
rs377570108	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68037872	GAATTGATTTATAGA[C/G]ACAACAAAATCCCAA	26091
rs377691762	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68039152	TCTCTACTGAAAATA[A/C]AAAAAAAAAAAAAAA	26091
rs377705248	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68022162	AAACAGCATGGTCAT[A/G]GACTGGAAGACAAAT	26091
rs377711228	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68049240	TATGAAAAGATCCCC[A/G]GGATATATTATCCAT	26091
rs377722745	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67926653	GCTCAGATTAAATGC[C/T]ATCTAATTCATTCAT	26091
rs377729709	snp	C/T	3.33406e-05	0.00408279	intron-variant	HERC4	GRCh38.p7	10:67992363	AGAGGGAAGAGATAT[C/T]ATATATAACTCAAAA	26091
rs377738455	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67991923	TTTTTTTGGAGACAA[G/T]TTCTCACTTTGTTGC	26091
rs377751346	snp	A/G	0.00398564	0.0444627	intron-variant	HERC4	GRCh38.p7	10:67977811	ACATGGAGAAACACT[A/G]TCTCCACAAAAAATA	26091
rs386371694	in-del	-/GAGA			intron-variant	HERC4	GRCh38.p7	10:67963998	CTTTACCTAGGTCAG[-/GAGA]AGATGAAGAAAAAAG	26091
rs386744927	multinucleotide-polymorphism	AACAT/CAAAA			intron-variant	HERC4	GRCh38.p7	10:67945817	AAACTCAAATCAAAA[AACAT/CAAAA]ACGACAGATACACGA	26091
rs386744928	multinucleotide-polymorphism	CA/TG			intron-variant	HERC4	GRCh38.p7	10:67966940	GCTCACTGCAAGCTC[CA/TG]CCTCCCGGGTTCACG	26091
rs386744929	multinucleotide-polymorphism	GC/TT			intron-variant	HERC4	GRCh38.p7	10:67983742	CAGTGAGCCAAGATC[GC/TT]ACCACTGCACTCCAG	26091
rs397700879	in-del	-/ATAG	0	0	intron-variant	HERC4	GRCh38.p7	10:67995359	TAAGATAACTATATA[-/ATAG]ATAGGGAGAAACTAA	26091
rs397703919	in-del	-/A	0	0	intron-variant	HERC4	GRCh38.p7	10:67990470	GAAAAAAAAAAAAAA[-/A]GGAAGGCAGGAAGAA	26091
rs397715777	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67967923	GGATTGAAAAAAAAA[-/A]GGAGCTATTCTAAAT	26091
rs397737437	in-del	-/G/GGAG/GT			intron-variant	HERC4	GRCh38.p7	10:67998573	AAAAAGGGGGGGGGG[-/G/GGAG/GT]TACAGTACTATCCAG	26091
rs397771165	in-del	-/GAGA			intron-variant	HERC4	GRCh38.p7	10:67964001	TACCTAGGTCAGAGA[-/GAGA]TGAAGAAAAAAGGAA	26091
rs397796879	in-del	-/TA	0	0	intron-variant	HERC4	GRCh38.p7	10:68028008	ATATATATATATATA[-/TA]ATAAAAATAAGTCAA	26091
rs397830698	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67983090	AAAAAAAAAAAAAAA[-/A]CAAAACAAAAACAAA	26091
rs397840761	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68073912	AATACAGAAAAAAAA[-/A]CATGCAATTTAAATA	26091
rs397840935	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68025685	ACCTTCCTAAAAAAA[-/A]GACAAAACCCCTTAT	26091
rs397845482	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67937230	AAGGTAAGGTATATT[-/A]AAAAAAATACTGTGT	26091
rs397846989	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67937233	GTAAGGTATATTAAA[-/A]AAAATACTGTGTGAT	26091
rs397847465	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67937232	GGTAAGGTATATTAA[-/A]AAAAATACTGTGTGA	26091
rs398013927	in-del	-/A	0	0	intron-variant	HERC4	GRCh38.p7	10:67970606	CAAAAAAAAAAAAAA[-/A]TCAACAAACAAAACA	26091
rs398013929	in-del	-/A	0	0	intron-variant	HERC4	GRCh38.p7	10:67991042	AAAAGAAAAAAAAAA[-/A]TAGAATAAAAATTTA	26091
rs398013930	in-del	-/A	0	0	intron-variant	HERC4	GRCh38.p7	10:68001386	TAAAAAAAAAAAAAA[-/A]TTCCTCTTGTTTACC	26091
rs398046360	snp	C/T	0.5	0	intron-variant	HERC4	GRCh38.p7	10:67974113	ACACACACACACACA[C/T]ACACACAGGGTCAGG	26091
rs398054473	in-del	-/GGGG			upstream-variant-2KB	HERC4	GRCh38.p7	10:68075434	GGGGGGGGGGGGGGG[-/GGGG]TGGCTGGCCACAGGC	26091
rs398075272	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67991041	GAAAAGAAAAAAAAA[-/A]ATAGAATAAAAATTT	26091
rs527244570	snp	C/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67984329	AAAAAGAGTGACATT[C/G]CTGTGTCATGTGCAA	26091
rs527263977	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67976987	CAGGCCACAAGGACC[A/G]CAACTACTAGGTGAG	26091
rs527299012	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67931613	TATTTTTAGTAGAGA[C/T]GAGGTTTCACCATGT	26091
rs527301600	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68031878	CCTGCCTCAGCCTCC[A/G]GAGTAGCTGGGGATA	26091
rs527306669	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68040635	GTGGCTCAAGCCTGC[A/G]ATCCCAGCATTTTGG	26091
rs527330966	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67983824	AAAAATTAACTGGGT[A/G]TGGTGGTGTACGCCT	26091
rs527372179	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67973995	GAGGTTGCAGTGAGC[C/T]GAGATCACGCCACTG	26091
rs527410718	snp	A/T	0.0115144	0.0749975	intron-variant	HERC4	GRCh38.p7	10:67947315	TAACAAAAGAGAGCT[A/T]GAGAAACTATACTAA	26091
rs527424514	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67938390	AGGTTGCAATGAGCC[A/G]AGATTGCACAACTGC	26091
rs527425330	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68048224	CACACCCAGCCCACA[C/T]AGAAGTTTCTAGCAG	26091
rs527435508	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68001042	CCAGGGAGATAATAA[C/T]CACTAAACCAAAGGA	26091
rs527459234	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68017136	ATGCAAGCAGAAGGC[C/T]TGAAATGGAATGTAC	26091
rs527460057	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67963468	GTGATCTGCCCACCT[C/T]GGCCTCCCAAAGTGC	26091
rs527476604	in-del	-/A	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68033065	ATAAAGGAGGGACTT[-/A]AAGAGTTAAGTGCTA	26091
rs527519809	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67969763	GAGCAGAAACTGCCA[C/T]ACAAAAAAATCGGAA	26091
rs527566653	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67925405	CTTCAAAGAACATGA[C/T]AGGATCATACTATCA	26091
rs527576870	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68023781	TTTAAAAAGTTGATT[A/C]CTTACTTGAACATTA	26091
rs527596577	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68033468	AACTCAATGTAATCA[A/T]GAAAAATAAGTTCCA	26091
rs527596680	in-del	-/AAAAAAAAAAGA			intron-variant	HERC4	GRCh38.p7	10:67996989	CAAGACTCCGTCTCG[-/AAAAAAAAAAGA]AAAAAAAAGAAAATC	26091
rs527626173	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67924710	AGCATCTACTGGATT[C/T]GGGTATCCTTGGCAG	26091
rs527636035	snp	C/T			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011784	GCTTCAACCTAAAGT[C/T]ACCAGATGCATTAGA	26091
rs527636308	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67977507	GCAGCTATGGGGCAA[C/G]ACTCCTGCTTGAGAA	26091
rs527661644	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68049901	GGGAGATAGTAAGAC[G/T]GTCTCAAAACAAAAA	26091
rs527734547	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67948662	ATGGTGGCTCACACC[G/T]GTAATCCCAGCACTT	26091
rs527734598	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67957186	TAGGGGGCGACTGTA[C/T]ACTTGAGAGTCTATA	26091
rs527759452	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68058158	TGAAGGTAAAGGAAT[A/C]CAATCCATTTTATAT	26091
rs527761874	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010273	ACTAAGGAACACAGT[A/G]CAGTGCAGTGCAATG	26091
rs527794095	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68057231	ATATTATTCAGATTG[A/G]TGTGAAAATAACAGC	26091
rs527797905	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67964313	TCTCTTTCACTTTTA[A/G]ATTTTGGTTTCCAAG	26091
rs527806576	in-del	-/CT	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68049738	CAACATAATGAGACC[-/CT]GTCTCTACAAAAAAA	26091
rs527821893	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67962591	TAGGTATAATCATTT[C/T]TCTAAGAGAGAGAGG	26091
rs527859988	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68008160	AGTTTCCCTCTCACT[C/G]TCTCTCTCTGTGCTG	26091
rs527866100	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67979403	GAAAGAATTAGTGAG[C/T]TGAGGAGACAAAAGA	26091
rs527886997	in-del	-/C	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:67978570	AGGGAAGGACACAGG[-/C]CAGGCTGGCTTTGCC	26091
rs527895932	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67926423	ATAAAAAATAAAAAA[A/T]AAAAAAAACAAAAAA	26091
rs527900486	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68034412	CACTTTAAGTTTGAT[G/T]GACTACACAGATGAA	26091
rs527942103	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68033508	CTTGTTTCAGTTACA[A/G]TTTTTTCAAATTCAA	26091
rs527942257	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68042347	TATAAACACTAGGCA[A/G]GACACAGTGGCTTAC	26091
rs527953510	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67932909	CTGAGAATGTATGAG[G/T]AGCGTTCAAACAGGA	26091
rs527987708	snp	C/G			intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069630	TCCTTAATAAGGCTA[C/G]CTCTTTCTCCTTCAT	26091
rs527990644	in-del	-/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67942089	CACTGAAAATGTTTA[-/T]TTTTTTCCCTCATCT	26091
rs527991121	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67994827	CAGCCTCCCGAGTAA[C/T]TGAGATTACAGGCGC	26091
rs528015204	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68050659	CTGATAACTTCACTA[C/T]AATTTTTAAAAAGTT	26091
rs528028775	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68041656	AAACTACATCTTTAT[G/T]GCCAACAATTATTTT	26091
rs528045828	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012011	GTACTTTTACATTAT[A/G]GAGATGGCTTCTTTC	26091
rs528046702	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68026761	GGCAGGAGAATTGCC[A/T]GAACCCGGGAGGCAG	26091
rs528072741	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67965800	ACATATTAAATTACC[C/T]GGGTACAGAAAAGTG	26091
rs528080959	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68019153	AGGCATGTGCCACCA[C/T]GCCCGACTAATTTTG	26091
rs528101155	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68074066	AATTGCAAATAACTC[C/T]AGCACTGCAGATTTT	26091
rs528149035	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67965248	TGAAACCTATCTTTA[C/T]TAAGTCCCCTCATTT	26091
rs528161141	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68020538	TTGGGAGGCCGAGGC[A/G]GGCAGATCACGAGGT	26091
rs528162744	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68026994	ACAAAGCGAGACTCT[A/G]TCACAAAACAAACAA	26091
rs528198109	in-del	-/T	0.00279441	0.0372746	intron-variant	HERC4	GRCh38.p7	10:68038281	ACATAGGTCATATTA[-/T]TTTTTTTCATACAAG	26091
rs528204909	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68073338	AGTTTCAAAAACCAA[C/T]CAGTTGTATTTTTTA	26091
rs528215619	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68026283	TACTTTTTTGTAGAG[A/G]TGGGGTTTTCCTGTA	26091
rs528226306	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67996736	ACACTTGTAATCTCA[A/G]CACTTTGGGAGGCCA	26091
rs528241095	snp	A/G	0.00517822	0.0506191	intron-variant	HERC4	GRCh38.p7	10:67927091	ATTCAAATATGCAAA[A/G]TATTTGCTGTTAGTT	26091
rs528279770	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68063664	AGAGGTAGGTCAGGC[A/G]TGGTGGCTCACACCT	26091
rs528302794	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67942924	CTTTTGAGTTTAAAA[C/T]GACAACTTGCTTTAG	26091
rs528309909	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68005564	TAAGGACTTACTCCT[G/T]ACATTTTAAAATTTG	26091
rs528366105	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67951223	GCAGCACAGCCCCCA[A/G]CCTCATATGCCCTCT	26091
rs528393080	snp	A/C	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:68064983	CTCAAAAAAAAAAAA[A/C]AATCCAAAAAATAGA	26091
rs528395105	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68059733	TTATATATTATATAT[C/T]ATAATATTATATATT	26091
rs528408833	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67958669	AAAGATAATCATACA[A/G]AAAGTTTAACTTTGT	26091
rs528438248	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4	GRCh38.p7	10:68075137	CCCGGCCCCTGGGAA[A/C]CTTTACCGGGTTCCT	26091
rs528474796	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68060927	GCCATCCTAAAAAAA[A/G]AAAAGTCACAAATGT	26091
rs528479207	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67981849	GGGAGGCTGAGACAT[A/G]AGAATCACTTGAATC	26091
rs528482243	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68028364	ATGGATTTTTTTATA[G/T]ATCTGATGTTTTCCA	26091
rs528483631	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67928780	ATAAAAAAATCAGCC[A/G]GGAATAGTGGCATGT	26091
rs528492406	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68031034	ATGGAACAGGTATTT[C/T]AACTTAAATAAAGGG	26091
rs528567769	in-del	-/A	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68002422	TGGTTTCAGGTTGTC[-/A]AAAAAATGAATGAGA	26091
rs528587127	snp	A/C	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67988095	GCTCAGAGTCTACTT[A/C]TTCATATAACTTTGA	26091
rs528611676	in-del	-/GT			intron-variant	HERC4	GRCh38.p7	10:67941360	TACGACTTTACAACT[-/GT]TTTCTCCCAGACATA	26091
rs528617577	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68043800	CAACCCAGGCAACAG[C/T]GCGAGACTCTGTCTC	26091
rs528631819	in-del	-/A	0.271432	0.24908	intron-variant	HERC4	GRCh38.p7	10:67993524	GCAAGACCCATCTCT[-/A]AAAAAAAAAAAAAAT	26091
rs528650689	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069251	ATGGATTGGTCTAGC[A/G]CACTGAAGATTAAAT	26091
rs528688713	snp	G/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68068395	GGGAGGCTGAGACAG[G/T]AGAATCACTTGAACC	26091
rs528786853	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68029098	AGGACTGCTTAAGCC[C/T]AAGAATTCGGTCATA	26091
rs528794676	snp	A/G	0.00517822	0.0506191	upstream-variant-2KB	HERC4	GRCh38.p7	10:68075462	ACAGGCGCCTGCGCA[A/G]TGTGCCGCTTTGCGT	26091
rs528805892	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67966857	ACTCAAGACAGACAA[A/T]TTTTTTTTATTTTTT	26091
rs528826210	snp	A/C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67929400	TGTCTCTATTCACTA[A/C/T]AATTTTTTGTCTTTT	26091
rs528827781	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68033822	CCCACTGCATTCCCC[A/C]AATGGAATTTTTAAA	26091
rs528837059	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67976780	TTAGGCATTGAGCTC[A/T]GCACTGCCCTGTTAC	26091
rs528853905	snp	A/T	1.65031e-05	0.00287251	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67990277	GAATTGCTATTGTTG[A/T]GAAATTGTTGGAATC	26091
rs528864618	snp	G/T	0.00993419	0.0697739	intron-variant	HERC4	GRCh38.p7	10:68002911	AGCCTTATTTTAATT[G/T]TTATGAGTACACAGT	26091
rs528864712	snp	G/T	0	0	intron-variant	HERC4	GRCh38.p7	10:67945763	TATGTAATTGGTGTT[G/T]ACAATATTGGGTTAT	26091
rs528876406	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68015016	CCTCTAACCATACCC[A/G]TATCTTATGCAATAT	26091
rs528879225	snp	G/T			upstream-variant-2KB	HERC4	GRCh38.p7	10:68075474	GCAGTGTGCCGCTTT[G/T]CGTTGCTTTAAGAGG	26091
rs528927791	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67944941	AGAAAGAATGAAGCA[C/T]TCCTACAAGATCTAG	26091
rs528938979	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67998730	AGGGGATGTTCTTCA[A/G]GCTTACCCATGTAGT	26091
rs528955996	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68054480	TGCCTCAGCTAACCA[C/T]GCCCAGCCGGCACCA	26091
rs528976707	snp	C/T	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:68007159	TGGGAGTATTTCACT[C/T]TTTTTTCTTTTGTCA	26091
rs528977086	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67997896	TGCATGGATAGAACA[C/T]ATTTTTCTTTGTTCA	26091
rs528986239	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67952958	TATAAAGAACTCCCA[C/T]GTACCCTTCACTCAG	26091
rs529017692	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67960599	CATGTTGGTTAGGCT[A/G]GTTTCGAACTCCTGA	26091
rs529054227	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67923479	ATACAAAATGCAGTT[A/T]TGATTATGATTTCTT	26091
rs529096764	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67975255	CCTATCATTAAAGTG[C/G]ACTTCATGTACATTG	26091
rs529119566	snp	C/G	1.65072e-05	0.00287286	missense	HERC4	GRCh38.p7	10:67922980	GCTTGGATCAGTTTA[C/G]AGCGTAGAGTTTCTT	26091
rs529155301	in-del	-/AGAGTGGGG			intron-variant	HERC4	GRCh38.p7	10:67977180	AGAAGACTGGAGGGA[-/AGAGTGGGG]AGAACTTTGTCTTGC	26091
rs529155466	snp	G/T	0.00993419	0.0697739	intron-variant	HERC4	GRCh38.p7	10:67930274	AAAACACACATACCA[G/T]AAAGTTTGTATCTTA	26091
rs529163400	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68038906	CATTACAAAACTCAA[C/T]TAACTTTGTATGTAC	26091
rs529183059	snp	A/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67982636	GGGATTACATTAAAT[A/T]AAAAAACTTCTACAC	26091
rs529196381	snp	A/G	1.67181e-05	0.00289115	intron-variant	HERC4	GRCh38.p7	10:67991020	GATCATCATTGCTAA[A/G]AAACAGAAAAGAAAA	26091
rs529217371	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68008918	TGGTTTCATAGTGCA[C/G]ATAAAAGTATGTTTA	26091
rs529218954	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67937404	GGAAGAAATGTTTGA[A/T]TTACCATAGTTCTTT	26091
rs529251830	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68038309	AAGCTCAATTTTAGC[A/G]TACCAAAAATTTATG	26091
rs529253586	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67957586	AGGTAATATATTGAT[C/T]GCTAAGTATTTTAAT	26091
rs529268769	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67923726	CCAGGGCTAATTTTT[A/G]TAGAGATGAGGTTTT	26091
rs529271275	snp	C/G	8.24314e-05	0.00641942	missense	HERC4	GRCh38.p7	10:67955010	TTTTCCTAAGGACTT[C/G]CATTGCATCTCCTAC	26091
rs529282974	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67962311	AGTATGGGAGATCGA[C/T]TTTCTCCTTAGCTAA	26091
rs529291765	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68015900	TTGAGGTCAGGAGTT[C/T]GAGACCAGCATGGCA	26091
rs529309749	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67969227	TCCAAGGATCAACAA[A/G]TCCTTACAAAAGGTA	26091
rs529314154	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68070218	ACAAATTTAAAAAGG[A/G]GTTGGGGAAATGACA	26091
rs529334342	snp	C/T	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:68062558	GGAGTTCGAGACCAG[C/T]ATGGTCAACACAGTG	26091
rs529365209	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68015368	CCCAGTTAAGCCCGG[A/C]CAAAATTACTAAAAC	26091
rs529370182	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67985700	TAAATAACCCAATTA[C/T]TTGCCAGTAAACTCA	26091
rs529378683	snp	C/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68023055	AACAGTGTTGGTGAG[C/G]ATGTAGAGAAACTGA	26091
rs529389311	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67962080	TATTTTAAAGCAGCT[A/T]TAGATTCACAGCAAA	26091
rs529402160	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68022298	TGAGGTCGGGAGTTC[A/G]AGACCAGCCTGACCA	26091
rs529475201	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68049122	ATATACAATAGCAAA[A/C]CACTGGAAATTCTCC	26091
rs529480870	snp	A/G	0.00085759	0.0206896	intron-variant, synonymous-codon	HERC4	GRCh38.p7	10:67941037	ATGGAGGTCCACAAT[A/G]GTACAATTATAAATT	26091
rs529488093	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68001544	AGCTTGAGTACAGTG[A/C]AAAAAGATTATCAAT	26091
rs529506650	snp	C/T	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:67992672	TTTTACACAGAAATA[C/T]TCTTCAGAATCTGTA	26091
rs529516740	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	HERC4	GRCh38.p7	10:67921890	TTTTGACTCTTATAT[A/G]AGAACCACTGAAAGT	26091
rs529520459	snp	C/T	0.00517822	0.0506191	intron-variant	HERC4	GRCh38.p7	10:67939182	GTAGTAATATTCTCA[C/T]ATTACAATAACCTTT	26091
rs529549152	snp	C/T			downstream-variant-500B	HERC4	GRCh38.p7	10:67921746	GAGATGACAATATTC[C/T]TTTCAGTTTTTTTAA	26091
rs529560789	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68013017	GAACACAGGCATGCC[A/G]CATTTTATTGTGCTT	26091
rs529582944	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67947479	GCTGACAGAATCAAA[A/G]CGAGGTATAGACAGT	26091
rs529614049	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67926238	CATCTCTACTGAAAA[A/T]ACAAAAATTAGCTGG	26091
rs529614312	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68071331	TTATACTACTAGTAC[A/G]CAGTGTCTACCTCTA	26091
rs529614893	snp	C/T	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:68056473	TGGTAGGGAAGATCA[C/T]TGTAATGGGAAGACA	26091
rs529619937	in-del	-/A	0.425145	0.178393	intron-variant	HERC4	GRCh38.p7	10:68001373	GAGACCTTGTATTTA[-/A]AAAAAAAAAAAAATT	26091
rs529636979	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67968253	GCAAATTCCCCCCAC[A/C]TCCTTGGCTAACTCT	26091
rs529642111	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67978607	TGATTGTAGAGCGCC[A/C]GCACCTTGAGTGAAG	26091
rs529697107	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67969820	GGGAGGGAACTCTGA[C/T]AAAGGTCCAGGCACA	26091
rs529702289	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68032399	TTATAAGCCAAATGG[A/C]AACTACATTCAAATT	26091
rs529758437	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67978033	GTAATCCCAGCAAGT[G/T]TGGGAGGCCAAGGCA	26091
rs529762390	snp	A/C	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:67939936	ATTTTATTTTATTTT[A/C]TTTTTCCCGAGATGG	26091
rs529772986	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68000598	AAAAAAAAATTGTGT[A/G]TTGAAATCCTAATCC	26091
rs529776036	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67932154	GTAGAGACAGGTTTC[A/G]CCATGTTGGCCAGGC	26091
rs529793334	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67931668	GACCTCAGGTGATCC[G/T]CCCACCTTGGCCTCC	26091
rs529794107	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68029521	AAGAATGCAATTTAA[G/T]ATTTCTTTGTGGATT	26091
rs529820286	snp	A/C	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68010982	ATCTATAGTTAAGTT[A/C]TTCGAATGAAGTCTT	26091
rs529822510	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68029880	ACTACCTGGGATTAC[A/G]GGCGCCTGCCACCAC	26091
rs529830919	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68058284	AAGACTAAAGGCAAA[C/G]AAGTACTTCCATGCC	26091
rs529861408	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67940206	GCTAGGATTACAGGC[A/G]TGAGCCACCGCACCT	26091
rs529892863	in-del	-/G	0.0107246	0.0724382	intron-variant	HERC4	GRCh38.p7	10:67931171	ATATTTAGTAGAGAC[-/G]GGGTTTCACTATGTT	26091
rs529908102	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010389	CCTGAGAAAGGAGAC[C/T]CAGCAGCCTCAAAAT	26091
rs529928382	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68064829	TACAAAAAATTAGCT[G/T]GGAGTGGTGGCACAC	26091
rs529942504	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67996806	GTGAAACCCCGTCTC[C/T]ACTAAAAATAAAAAA	26091
rs529956140	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68060543	CGCGTCCAGCCATAA[A/G]TAATACATTCTAAAT	26091
rs529957076	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67964585	CATTTCTGTCCCGTT[A/C]CCTACACAGCCAACA	26091
rs529996992	snp	A/C/G	0.00398755	0.0445055	intron-variant	HERC4	GRCh38.p7	10:68017238	TATAGTCCCAAGAAC[A/C/G]AGATATGTAACAAAG	26091
rs530010480	in-del	-/A	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67954123	CTGTTGTAATTACTT[-/A]AAACTCTGCCGCTGC	26091
rs530046447	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67941945	ACAGGCGTGAGCCAC[C/T]GTGCCTGGCCAAAAC	26091
rs530070587	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68042016	TCACTTTTCTGATTA[C/T]TCTTTTTTTTTATTT	26091
rs530081924	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68009012	GATCAAATAAGGCCA[A/G]AAGTCTGAGACCAGA	26091
rs530088479	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68042495	AAGCATAGTGGTGCA[C/T]GCCTATAGTCGCACC	26091
rs530097513	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67993984	CTTGATTATTCCTTA[C/G]AAGCAAGCACAATGT	26091
rs530111277	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67950275	CCATGGATACATACA[A/G]GGGAGATTTTTTTTT	26091
rs530146056	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68050047	TCTCCACTAAAAAAA[C/T]AAAACATTAGCCATG	26091
rs530161350	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67994841	ACTGAGATTACAGGC[A/G]CCCACCACCACATCT	26091
rs530199733	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67994353	AAGATGGTTGACTAA[A/T]CTACAGTACATGAAT	26091
rs530248095	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67927985	TGTGCAGGAGAGAGG[A/T]TTGCAATTTTAGATC	26091
rs530275064	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67980064	GGCATGACATTTAAA[A/G]TATTGAAGGGAAAAT	26091
rs530309409	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68066698	TCAGTTACTATGGAC[C/T]TTGGCTTGTAGTACA	26091
rs530313986	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67934607	GAAAAAGGCATCAGA[A/G]GTAAACTCTCTGAGA	26091
rs530334516	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67987000	AAAATACCGACTATA[C/T]AGGGTTTTAAAGTTA	26091
rs530343618	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68027169	TGCAACTTTATATCC[C/T]GCTTTCATCATTTAA	26091
rs530376592	in-del	-/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68045509	ATATCAAAAGATACA[-/T]TGTAGTTAAAATATG	26091
rs530378834	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68026341	GCTCAAGCAATCCTC[A/T]TGCCTTGGCTTCCCG	26091
rs530397070	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68005708	GTGCATCTATTAATT[C/T]TGTTTGTTTTTTTGA	26091
rs530430201	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67979502	GTTACTGGCCTTAAA[A/G]AGGAGATAGATGGGG	26091
rs530472044	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67933766	AGCACTACATGTGCT[A/T]GTTCTTATTCTAAGT	26091
rs530474087	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68034622	TGAGCAAAAAACCCA[C/T]ATAACCCATTGTTTA	26091
rs530481675	snp	A/G	1.9765e-05	0.00314358	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:67966770	TATATAAAATTTATC[A/G]TACTGTATAATCTGT	26091
rs530515332	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68054446	GCAACCTCCACCTCC[C/T]AGGTTCAAGAAATTC	26091
rs530525527	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67951391	GTTTACAGAACAAAT[A/C]CAAAGCCTCGAAACT	26091
rs530536803	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4	GRCh38.p7	10:68074916	CTAACGCCGTCACAC[A/G]CCCCCGAACCCGCTG	26091
rs530540288	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67965932	ATTCAAGTTTTATAA[C/G]ACCATGGTACTATTT	26091
rs530549171	snp	C/T	0.0126979	0.078662	intron-variant	HERC4	GRCh38.p7	10:68063781	CGTCTCTACTAAAAA[C/T]ACAAAAAATTAGCAG	26091
rs530552112	snp	A/T	0.030278	0.119257	intron-variant	HERC4	GRCh38.p7	10:68059843	TATTATATATTATAA[A/T]ATATTATATATCATA	26091
rs530586667	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67989166	ATGTTTTGAAAATTA[C/T]AGTTTCAATTTTTAA	26091
rs530587845	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67958840	TTACATTTTATACTG[C/G]AAGACTTGAGGAGGA	26091
rs530623847	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012034	CTTCTTTCCTTAAAC[G/T]TCACGAACTAATATT	26091
rs530648354	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67988438	TGTTCTGCCCAACTA[C/T]GGATAAGTTATCTAT	26091
rs530648754	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68066621	CATGTATCTACATGG[C/T]GGACTTTATACAACA	26091
rs530697916	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67996801	ATACAGTGAAACCCC[A/G]TCTCTACTAAAAATA	26091
rs530699546	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67981278	TACAAAAGTGTAAGA[A/G]GAGACAAAGAAGGTC	26091
rs530714123	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68036226	GGGAGGCTGAGGCAA[A/G]AGAATGGCGTGAACC	26091
rs530748058	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67951930	GACAAAAAAAAATGC[A/G]TACAACACACTAGCC	26091
rs530748785	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68041787	ATATTAACATCTAGC[C/T]AGAAATGCAGGTCTA	26091
rs530832836	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68029982	TGACCTCGTGATCTG[C/T]CTGCCTTGGCCTCCC	26091
rs530833982	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68052394	TTAGGCTTATTTTTA[A/G]AACAGTTAAAATGAT	26091
rs530837151	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68021025	GAGCAAGAGAGAGAC[C/T]ATTTGAAGAAGTAAT	26091
rs530843338	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68058561	GAATACTCACCATAC[A/G]CTAGGCATTGTTCTT	26091
rs530869771	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68029312	CCTGGCTAACATGGT[A/G]AAACCCCATCTCTAC	26091
rs530899172	snp	A/C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67932254	AAGCCACCACGCCTG[A/C/G]CCTAAGTTATTTTTA	26091
rs530906219	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67967071	GTGTTAGCCAGGATG[A/G]TCTCGATCTCCTGAC	26091
rs530909163	in-del	-/A	0.202959	0.245534	intron-variant	HERC4	GRCh38.p7	10:68009227	AGACTCTGTCTCATT[-/A]AAAAAAAAAAAAGGA	26091
rs530928532	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68068481	AACAGAGCAAGACTC[C/T]GTTTCAAAAAAAAAA	26091
rs530950026	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67930096	CAGGCGTGAGCCACC[A/G]CGCCCGGCCCAGCTG	26091
rs530968679	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67961486	ATGGTGCTGCTCAGA[A/G]AGTCAAAAAGACCCT	26091
rs531055546	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67965063	AGGCGTGAGCCACCA[C/T]ACCTGGCCTAATGCT	26091
rs531097673	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67998804	AGTGCAATGGTGCAA[C/T]CTCAGCTCACTGCAA	26091
rs531104126	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67998404	AATACAAAAATTAGC[C/T]GGGTGTGGTAGCACT	26091
rs531105202	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68007994	AAGTAGGTGGGACTA[C/T]ATGCACACACCACCA	26091
rs531174625	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67983314	AGAACAATTTGGAGG[C/T]TCCTCAAAAAACTAA	26091
rs531189235	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67960761	TAGCACCTGTCACAT[C/T]CCCAGTAGCCTTTCT	26091
rs531190448	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68039027	GGGATGCCAGATGCG[A/G]ATTACAGGTGGGTTA	26091
rs531217766	snp	C/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67938272	ATGGTGAAACCTCAT[C/T]TCTACTAAAAATACA	26091
rs531264766	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67972390	GCCGGGCATGGTGGT[A/G]CATGCCTGTAATCCC	26091
rs531272728	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68013478	ATAAGTGAGTCACAA[A/G]AAGAAACACTACTAT	26091
rs531276078	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68047653	GTTCAACTTATGTCC[C/G]ATGGGAATTACAATT	26091
rs531311959	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68055625	TCACAGATAAAGGCA[C/G]TAAGTTATAAACATT	26091
rs531381728	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67969375	CTTGATAGTATGAAA[A/C]CCCGCAGAGTCCCAG	26091
rs531418987	snp	A/C	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67999540	GGGTTCTGAAGAGAT[A/C]TCTCTTACATAACTT	26091
rs531425239	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67990527	ACAGCAAATATGAAA[C/T]GGTGAAGAAGAAAAA	26091
rs531444625	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67968517	AGCTGGGACTACAGG[C/T]GCCCACCACCACCTC	26091
rs531481088	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67923520	CTTCGTTTCTGTTAT[A/T]TTTTTTAAATCAGAA	26091
rs531513921	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67976125	TTGACTAGTTGCAAC[A/G]AAAACTGTATGGCTC	26091
rs531574524	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67976891	AACTGTGGGTCCCAG[C/T]TGTCAAAATGTGAGT	26091
rs531590841	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68031769	ATGCCTCTTTTTTTT[C/T]GAAACGAGGTCTCAC	26091
rs531596272	snp	A/C	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:67947544	TATCATTAATGTATA[A/C]AACAATCCAAAGATC	26091
rs531608670	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67935646	GTAAATTTCCAATCT[C/T]CTGCCCAGGCCAGAG	26091
rs531632088	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67961898	CCAAGTTATTACCAC[A/G]TAAATGCTCCAACTG	26091
rs531648779	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67963343	TGCCTCAGCCTCCTA[A/C]GTAGCTGGGATTACA	26091
rs531662023	snp	C/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67955690	GCAGGAGAATCACTT[C/G]AACCTGGAAGGCAGA	26091
rs531676821	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68039889	TCAAGTACAATTTTG[C/T]AAATGAAACATTTCA	26091
rs531703812	snp	C/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68001627	CACAATTTAGTGGTA[C/G]CAAGTATATTCACAA	26091
rs531743308	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	HERC4, POU5F1P5	GRCh38.p7	10:68009491	CTTAATTTAAAATCA[C/T]TTTATTGCTAAAAAA	26091
rs531800926	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68063972	CAGAGGCTGGGCATG[A/G]TAGCTCATGCCTGTA	26091
rs531807008	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68046562	AAATAAGCGTCCTAG[C/T]CCTCAATGAGTTTAC	26091
rs531815453	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67984505	AGCTGGGAAGGGTAG[A/T]GGGGAGGCAGGGGCA	26091
rs531828362	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68032632	AAATTTTTTTCAAGA[A/C]TAATCTAAGTCTTTT	26091
rs531832298	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67994151	TACCCTAAGGCCAAA[A/C]ACAAGTTTTAAGAAT	26091
rs531840969	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68016412	GGCTGGAGTGCAGTG[A/G]CGTGATCTTGGCTCA	26091
rs531852219	snp	C/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68072179	CACATAACAATGATA[C/G]TCCTAAATGTAGAAA	26091
rs531852992	in-del	-/CTAT			intron-variant	HERC4	GRCh38.p7	10:68015843	CATGGTGGCTCAGGC[-/CTAT]AATTCCAGCACTTTG	26091
rs531866902	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68040816	ATGGCTTGAACCCAG[A/G]AGGCGGAAGTTGCAG	26091
rs531875312	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67949452	ATCATCACTATCAAA[A/G]TACCAGAAAAGGACC	26091
rs531878491	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68015939	AAAACCCTGTCTCTA[C/T]TAAAAATACAAAAAT	26091
rs531886719	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4	GRCh38.p7	10:68074917	TAACGCCGTCACACG[C/T]CCCCGAACCCGCTGG	26091
rs531897222	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68003052	TCGTGTTACAAATGT[G/T]CCAATAATATATTTA	26091
rs531954426	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67932323	ACTCCTGGCCTCAAG[G/T]GATCCTCCCGCCTAA	26091
rs531955716	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68057967	TGGCCTCCCTAAGTG[C/T]TAGGATTACAGGTGT	26091
rs531998048	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68049852	TGAGGTCAGGGCTAC[A/G]GTGAGCCGTGATTGT	26091
rs532006408	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67940316	ATGAAGGTTATCAGA[A/C]GTAAAAGTCCAAATA	26091
rs532032181	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68026080	TAACCAGAGTGCATA[A/T]ATAGAGCAATTTTTA	26091
rs532052201	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67979282	TTTAACAAAGAGACT[A/G]AAATCATTTAAAAGA	26091
rs532057709	snp	A/C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67948523	AAAAAATAAAAAAAC[A/C/T]GTAGATGTTGGCGTG	26091
rs532068045	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68034269	ATTTCATTTCAAATT[A/T]CATATAAAGAATATT	26091
rs532109354	in-del	-/CA	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:67934250	CATTTCTATATTATT[-/CA]CAGTTAAGCTGTATT	26091
rs532133191	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68028764	CCTATAGTTTTAGAT[C/T]TATCTCTTTTCTCTT	26091
rs532154466	snp	C/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68051075	TAAACCACATCAATT[C/G]ATGATCAGTAGAAAA	26091
rs532175431	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67970921	AGAAATCAATGAAAG[A/G]GAAAACAGAAAAACA	26091
rs532177802	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68072509	GTTTTCCTCCCCCCT[C/G]CCAAAGTAAGGTAAA	26091
rs532185016	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011923	AACATTGAAAATCTG[C/T]TGTTTAGTATACCCA	26091
rs532190525	snp	C/T	0.0240643	0.107019	intron-variant	HERC4	GRCh38.p7	10:68059645	CATAATATTATATAT[C/T]ATATTATATATCATA	26091
rs532191788	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68024964	TGCCAATCAAACTTT[C/T]ATCACATTAATTCTG	26091
rs532209166	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67926351	GTAGTGAGCCAAGAC[C/T]GTGCCATTGCACTCC	26091
rs532270657	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67993604	TTTCATAATGCAGAA[-/T]TTTTTTTTTTCAATA	26091
rs532277166	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68066389	GTAAAACCAAATCTA[C/T]CACACTGCTGATCTT	26091
rs532279263	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68033358	TTATCATTACTAGTT[A/G]TTACTAGATTAATAA	26091
rs532296192	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67932840	ATGAAGAATCCATAA[G/T]GTAGTCATTAAAACT	26091
rs532307870	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68018326	AACATTAAAAACTTA[A/G]CATCCATTCACAATA	26091
rs532308281	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67994909	TGGTCAGGCTGGTCT[C/T]GAACTCCTGACCTCA	26091
rs532314859	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68055159	CTGATACTTTTAAAA[A/G]GATCTCTAACATGAT	26091
rs532348567	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68004260	AGTTCAACAACTGAG[C/T]TGAAACAACAGAGTT	26091
rs532371565	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68027581	TTCCTGATTATTTTA[C/T]TGCATCATGTCACAA	26091
rs532386531	in-del	-/A	0.00616897	0.0551945	intron-variant	HERC4	GRCh38.p7	10:68046133	GACACACACTGTTCC[-/A]AAAAAAAAAAAGAAA	26091
rs532388694	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68043777	GCCGAGATCACACCA[C/T]TGCACTCCAACCCAG	26091
rs532402053	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68034678	AAGGAACTTCTAACT[C/T]AGGATGCCCCAGACT	26091
rs532406345	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68058964	CCACCTCTACACCAA[C/T]AGTTACCAATGTTAT	26091
rs532425290	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68043245	TAGAAAGTTTTGCCA[C/T]GAATCATGGTTTTGA	26091
rs532435098	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68037442	ATATGGCAGATTCTT[C/T]ACTAGCCCATGTTCC	26091
rs532465641	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67965079	ACCTGGCCTAATGCT[G/T]GCTTTTTTCTGTCCT	26091
rs532485099	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67995866	TCTAAACTGACCTTT[C/T]TGTCCCCAATTTTCA	26091
rs532512067	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68051644	GATTACAGGCGTGAG[C/T]CACCATGCCCGGCCA	26091
rs532513822	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67988007	ATCTAAATAGCAACT[C/T]GAGAAAACCAAATGG	26091
rs532526804	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67951082	CTCTCACCAGCCAAG[A/G]TGAGATAGAACTTGA	26091
rs532528171	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67953945	TGATTAAATATTACA[A/T]TGAGGTTTTTACAAC	26091
rs532561269	snp	C/T	0.00517822	0.0506191	upstream-variant-2KB	HERC4	GRCh38.p7	10:68075403	CCCCGGCACCGGCGC[C/T]TGCGCCGAATCTTCC	26091
rs532571737	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68001580	CACAATTTTTTATCA[C/T]AAAATATACATAAAA	26091
rs532572926	snp	A/G	0.000171013	0.0092454	intron-variant	HERC4	GRCh38.p7	10:67966817	CCTACAAAAGAAAAT[A/G]TAATTGACATTAAAT	26091
rs532654155	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67928693	TTTGGGAGGCCGAGG[C/T]GAGTGGATCATGAGG	26091
rs532667254	snp	C/T	0.00914312	0.0669923	intron-variant	HERC4	GRCh38.p7	10:67941979	ACTTTTTAATGGCTG[C/T]ATATTGTATCATAAA	26091
rs532704376	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67935300	ACAGGCACATTCCAC[C/G]ACACCTGGCTAATTT	26091
rs532716380	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67928114	GGAAAAGGAAACAAA[C/T]GCCCTAAGACTGGAG	26091
rs532756131	snp	C/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68020106	GGGAAAGGTATAGGC[C/T]AAGAAAAGACCTCAT	26091
rs532769655	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68053178	TTGAATCATTGCCCC[C/T]GAAGAAAATACAAGG	26091
rs532799979	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68006237	TGTACTTACTATTAT[C/T]GTGAGTTTTGTACCT	26091
rs532800433	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68016537	TTTGTATTTTTAGTA[C/G]AGATGGGGTTTCACC	26091
rs532824714	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67936874	TGGGAGTGGGATGTT[A/G]GATGAGTATATTCCT	26091
rs532841181	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67973036	CAAATGATTCATGAA[A/T]AAAGAATATACACAC	26091
rs532857796	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67980663	TAGAGAGACTATAAA[C/T]AATTAACCAATCAAA	26091
rs532858659	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68061086	ACCAACAGCATTATC[A/G]CAAAAGGTGTATTTC	26091
rs532860754	snp	A/C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68052226	GTAGATAACGACTTC[A/C/G]AATACATCTCTAATA	26091
rs532870126	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68027329	ACTGGCAAAAGGTTG[G/T]TTATTTTGTTTCACT	26091
rs532875818	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68038865	TTGTTTTACCACAAC[A/G]CAACTTTAAAGGCTC	26091
rs532944299	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68063244	AGTTGGAGTCTCGCT[C/T]TGTAACCCAGGCTAG	26091
rs532985926	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67982068	GATTCATTGCAATCC[G/T]TATCAAAATACCAAT	26091
rs533057092	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68060540	CACCGCGTCCAGCCA[C/T]AAATAATACATTCTA	26091
rs533065976	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:67967044	TATTTTTAGTAGAGA[C/T]GGAGTTTCATCGTGT	26091
rs533113866	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67954093	AATATTTTGGGGTTT[C/T]CTGGACATAAGGTCA	26091
rs533153779	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67937339	CTAAAGCTATTATTC[C/T]ACAAGCAATAAAGAG	26091
rs533155492	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68014699	AAAGTAATCTCTATA[G/T]GTACGCACCAAAACT	26091
rs533179598	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68038239	TTGAATGCTATTTAT[A/G]TTATTTATTGATGGC	26091
rs533210921	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67967763	TCCAATCAAGTCTCC[C/T]AATCTAAATTTTAGT	26091
rs533216459	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68046262	AGAAAAAGTCAAGTT[C/T]TCTCCAGAACAATCC	26091
rs533220135	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67945574	CACTCTAATTGTGGT[A/G]TATAAACTACCCATA	26091
rs533230772	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67960796	CTACTACCTTCACCA[C/T]GAAGCTCCCTGGTTT	26091
rs533241792	snp	A/G	0.00398564	0.0444627	intron-variant	HERC4	GRCh38.p7	10:67998560	TCAATTGAAAAAAAA[A/G]AAAGGGGGGGGGGTA	26091
rs533269678	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67975063	GCATGGTGGCGCACG[C/T]CTGTAGTCCCAGCTA	26091
rs533336174	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67968338	TAAATAAAACTCAAA[C/T]CCAATAAACCAACAG	26091
rs533354544	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67946801	AGTCCCAGCTACTCG[A/G]GAGGCTGAGGCAAGA	26091
rs533364276	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:68022265	AACACTTTGGGAGGC[C/T]GAGGTGGGCGGATCA	26091
rs533364857	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069853	CAAGACCATCCTGGC[C/T]AACACGGTGAAACCC	26091
rs533387842	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67989009	TTATAAACCTCCCCC[C/T]GACCAAGTTAAACAA	26091
rs533401625	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67975748	AAAGCACACATTTAA[C/T]AATACTGCTTTTATT	26091
rs533403041	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	HERC4	GRCh38.p7	10:68077124	AAGAGCAAAACTCCA[C/T]CTCAAAAAAAAAAAA	26091
rs533406466	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67957813	TAGTCTGAATCTGCA[-/T]TTTTTTTTCCCCCAT	26091
rs533450098	snp	C/T	0.00993419	0.0697739	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922837	AAGTAAGAATTATAA[C/T]AGTACCTCTGTCACC	26091
rs533457891	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68030492	ATGATATATGTTCAT[A/T]TTTTGGTCCCTTTCT	26091
rs533467041	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68062483	CCATCGGCCGGGCAC[A/G]GTGGCTCACGCCTGT	26091
rs533533257	snp	A/G	0.000135511	0.00823024	intron-variant	HERC4	GRCh38.p7	10:67996168	AAAAATTGGTTAAGC[A/G]TGGTGGCGCATGCCT	26091
rs533555553	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68056350	TACATTGATCATGTG[C/T]TCATTCAACAACCCT	26091
rs533576731	snp	A/G	0.00755907	0.0610114	intron-variant	HERC4	GRCh38.p7	10:67968459	CTCACTGCAAGCTCC[A/G]CCTCTCAGGTTCATG	26091
rs533600730	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67968095	AAAGTAGGCAGAAAC[A/G]GGAATGGACACAAGT	26091
rs533607085	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68021884	TGCAGATGATATGAT[C/T]ATATATGTAGAACAC	26091
rs533622471	snp	A/C	0.000264721	0.0115018	intron-variant	HERC4	GRCh38.p7	10:67954949	CAATTATACCACAGA[A/C]AATGTCAAATTACCT	26091
rs533641665	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68062965	TGCCTAACCTTCCTG[C/T]TCACTATTCTCAAGA	26091
rs533658021	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67949899	TGGCGCACACCTGTA[A/G]TCTCAGCTACTTGGG	26091
rs533688098	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68030268	AACAGGGTGAAACCC[C/T]ATCTCTACAAAAAAA	26091
rs533733160	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67946998	TTACCGCTAAAGAGA[C/G]AGAGAGAGACCCCAA	26091
rs533733499	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67955750	CACTACAGCCTGGGC[A/G]ACAAGAGCGAAACTC	26091
rs533750796	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68000356	GCCCAGGTAGGCACA[C/T]TGCTTGAGCTCAGAA	26091
rs533795575	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67955272	ACCTAACAGTATCCC[A/G]TACAGCATAAAACTT	26091
rs533796239	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68022460	GCCAAGATCATGCCA[C/T]TGCATTCCAGCCTGA	26091
rs533834086	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68031273	GCTGAATTTGAAAAG[C/T]ATTAACATTGTTAGT	26091
rs533883843	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67975532	TTTTTTGTATTTTTG[A/T]AGAGATGGGATTTCA	26091
rs533886010	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67983397	AGAAACGAAAGCAGT[A/G]TATCATACAGGTATT	26091
rs533942236	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67934409	TCCTTGAGCCCTCCA[A/T]CCTCTTGATCTAACC	26091
rs533978156	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67993751	CAACAAAGTTTCTTT[A/T]GAAAAAGATATTCCG	26091
rs534048356	in-del	-/A	0.0115144	0.0749975	intron-variant	HERC4	GRCh38.p7	10:68003270	GCCATTCTCTTGCAC[-/A]AGCCTCCCGAGTAGC	26091
rs534073623	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68016008	CTCAGGAGGCTGAGG[C/T]AGGAGGATCACTTGA	26091
rs534117723	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67971186	CTCCAGGGCCAAAAT[G/T]GTTTCACTGATGAAT	26091
rs534161587	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68032042	CAGGCATGAGCCTCT[A/G]TGCCCGGACGTTAAT	26091
rs534192217	snp	A/G	0.00517822	0.0506191	intron-variant	HERC4	GRCh38.p7	10:67931754	ATCTAGCTGTGTCAC[A/G]GATGACATTTTTGTT	26091
rs534200074	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68067235	ACACAAAGTAAAGTA[G/T]TATTATACATTTCTC	26091
rs534231271	snp	C/T	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:67978259	GGCGACAGGAGACTC[C/T]GTCTCCAAACACAAA	26091
rs534237590	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68035408	TGATCTGCCCACCTC[A/G]GCCTCCCAAAGTGCT	26091
rs534256235	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67932527	AAAATAAAAAATAAT[A/G]CATAAAAAGGCAAGA	26091
rs534358763	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67927378	TTAAGAATAAATACA[C/T]CATATATATATATAT	26091
rs534433217	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68071592	AGGGCCCATTTGTCT[C/T]TGGAGCAGAGACAAT	26091
rs534434261	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67955631	GCAAAATTAGCAGGG[C/T]GTGGTGGTGTGTGCC	26091
rs534442786	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67964677	AATCCAAATTCCTAA[C/T]CCTAGTTTACTAAAC	26091
rs534448755	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68017454	CACAAGAGACCAATA[A/C]AGACATTATAAATTT	26091
rs534464287	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67925817	ATCCCTATATGGAGA[A/G]AAGTACTCATGGTGC	26091
rs534469335	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68032024	CCCAAAGTGCTGGGA[C/T]TACAGGCATGAGCCT	26091
rs534525229	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67934052	ATTAAAAGGCAACTA[C/T]TTAACTCTTTTTGCT	26091
rs534536574	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68032749	GAACTATGATGAGTA[A/C]TAATAAAGAAGTTTT	26091
rs534543722	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67983662	TGTGATGGCAGGCGC[C/G]TGTGGTCCCAGCTGC	26091
rs534578470	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67994527	AACCTCCATCTCCCA[A/G]GTTCAAGCGATTGTC	26091
rs534579323	snp	C/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68042675	TTAGAAATCTGTTTA[C/T]AGATACTATATGTAA	26091
rs534583886	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67942068	AACATACTTACACTA[C/T]TGACACACTGAAAAT	26091
rs534589239	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68059077	AAATGTAGCTCTCTA[C/T]ACATTACTCTCTACA	26091
rs534597878	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67949887	AGCCAGGTATGGTGG[C/T]GCACACCTGTAATCT	26091
rs534615515	snp	C/T	0	0	intron-variant	HERC4	GRCh38.p7	10:68042088	GTGGTGCAATCTCGG[C/T]TCACTGCAACCTCCG	26091
rs534624118	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68051164	AAAAACTATTGAATC[C/T]TTTGATAAATAAGGG	26091
rs534639571	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68058544	CTAGGCAAACACTTA[C/T]TGAATACTCACCATA	26091
rs534663423	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67957307	TCCTATGTTAAATGC[A/G]ATAGCCAATTCTTAC	26091
rs534687740	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68028297	TTCCAAAGGTAAGCA[A/G]TAAGTTTTGCTTATA	26091
rs534727470	snp	C/T	1.65064e-05	0.00287279	missense	HERC4	GRCh38.p7	10:67956913	CGGTCTGTAACAGAG[C/T]AGTTTTTGCTTGGGC	26091
rs534746354	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68074569	GGTAGGGAAATGAGA[A/G]GCAGTTTAGTCCCGT	26091
rs534779970	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67979648	TTGAAGACATTTAAT[A/G]ATCAAACTTCCAAAG	26091
rs534801211	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011317	TCACAAATGTTCTTA[A/G]CAGTAACTGGAATGG	26091
rs534804369	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68025864	GAGAATTCCAGGTAA[C/T]GATGTTTTCACCGTT	26091
rs534834862	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67927688	CCTCAGCCTCCCAAA[G/T]TGCTGGGATTACAGG	26091
rs534884230	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67943282	AAATCTTTCCCCCTC[C/T]TAAAACCCTCTAAAA	26091
rs534889062	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67933391	CTTATGATACAAAAC[C/G]AAACTGTAAAGAAAA	26091
rs534950483	snp	C/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67950630	CAGTAAGGTTTCTCA[C/T]TGATGATGAAAGTTA	26091
rs534952446	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68045679	TTTACTAGTATCACA[A/G]GTTTTTTAAAAGATA	26091
rs534967801	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67930097	AGGCGTGAGCCACCG[C/T]GCCCGGCCCAGCTGT	26091
rs535000654	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68067724	ATTGGAATGACTCAA[A/C]AGTAGAAATTACCAT	26091
rs535053452	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67973969	GAAGAATCACTTGAA[C/T]CCGGGAGGCAGAGGT	26091
rs535062409	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67965472	TAGAATGGCTATAAA[C/T]CTGACCCAGCCTCAA	26091
rs535076753	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68018733	CTAGGAATGGAACTA[C/T]GAAGAGATATGCATG	26091
rs535092249	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68056362	GTGTTCATTCAACAA[C/T]CCTGCCCTGAGTTCC	26091
rs535099225	in-del	-/TTAT	0.00517822	0.0506191	intron-variant	HERC4	GRCh38.p7	10:67997469	ATAGGTAACTAAGTA[-/TTAT]TTCTCAAGCACTTAT	26091
rs535108209	snp	A/G			intron-variant, downstream-variant-500B	HERC4, POU5F1P5	GRCh38.p7	10:68009725	CAGGAGATGCTGCAT[A/G]ATAGCATTTTACCCA	26091
rs535109438	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67929023	TATCTCCTTACTTTC[C/T]GTCTTCCAAAACTAT	26091
rs535131216	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67972406	CATGCCTGTAATCCC[A/T]GCTACTCGGGAGGCT	26091
rs535176462	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67975676	TCTTAACTCACTATA[A/T]GACTGTCCAATTTGC	26091
rs535193928	snp	A/G	6.60578e-05	0.0057467	synonymous-codon, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67988758	TCTTGTAGAGTTTCA[A/G]AAGATGTACCACAAC	26091
rs535194934	in-del	-/ATCT	0.00597247	0.0543191	intron-variant	HERC4	GRCh38.p7	10:68028762	TTCCTATAGTTTTAG[-/ATCT]ATCTCTTTTCTCTTA	26091
rs535205581	in-del	-/CTCT	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:68035702	CAGTCACTCACTATA[-/CTCT]CTCTAGCCGTATTGC	26091
rs535207954	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67944210	GGTGTCTACAAAGGT[A/G]CTGGCTGGTGTCACC	26091
rs535210018	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67952923	AGAAAAAAAAAAAGA[A/C]ACCTAAATTGCACAA	26091
rs535255307	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68052082	CAAGAAAAAAAAAGA[C/G]ACATTTAATTTTTGG	26091
rs535267738	in-del	-/TTAT	0.00398564	0.0444627	intron-variant	HERC4	GRCh38.p7	10:68059718	TTATATATCATAATA[-/TTAT]ATATTATATATCATA	26091
rs535279372	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67960411	TTTTTTTGAGACGGA[A/G]CTTCGATCTTGTTGC	26091
rs535280201	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67959730	ACAGGGAAAAAGGGT[G/T]GGTAAGCAAAAAGAA	26091
rs535327753	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68005125	TGTTCCATTGGTCCA[C/T]GTGTCTGTTTTTATG	26091
rs535347038	snp	G/T	0.00438332	0.0466095	intron-variant	HERC4	GRCh38.p7	10:68021154	GTTCAATCAAAATGC[G/T]GAAAGACAAAGAATC	26091
rs535368499	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67974746	AACTTTTGCCCTGAA[A/G]TATTCCTAATAGAGA	26091
rs535429251	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68028857	ATGTAATATATTGGA[A/G]TTTATTTGCTATTAG	26091
rs535438790	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67990789	TAAAATCTTATTTTA[A/G]AAGCACATCGTAAGA	26091
rs535440360	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67936750	TTTTACTTCTGGAAT[A/T]TTTCTAAAAATATTA	26091
rs535466114	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67989501	ATTCCCATATTCTAC[C/T]CCTTGCTTGTTGCTT	26091
rs535504913	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67960265	TCATCCATGACTCTA[C/T]ATGGAAAGGACAACA	26091
rs535507362	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68045581	TAAAATACTGGCCCT[A/G]CTACCAGTAGCCATC	26091
rs535517164	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68036631	GTCTCCCACTCCCTC[A/C]CAACACCCACATAAA	26091
rs535545155	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68006467	ACCTCCACCTCCCGG[A/G]TTCAAGCAATTCTCC	26091
rs535547243	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68072525	CCAAAGTAAGGTAAA[C/T]ACAGAGTAAATTATG	26091
rs535548840	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68007501	CATGTTTTCCTGGAT[C/T]GTCTTGATGCTTCTA	26091
rs535625123	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67949519	ACAAAAATCCAACCC[C/T]ACAAACCAATATCCC	26091
rs535640215	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68031449	CATTTGTTATCTGAA[C/T]GCCAAAATCAATAAA	26091
rs535660232	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68021716	GGGAGGCTGAGGCAG[A/G]AGAATCGCCTGAACC	26091
rs535683843	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	HERC4	GRCh38.p7	10:68076673	AACAATCCTTGGCAA[C/T]CCTTGTAGAAGCATC	26091
rs535727385	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922307	AGGTTATGTAGTATA[C/T]TCCCTATCTGTGATT	26091
rs535740024	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67930846	CACCACACCTGGCTA[A/G]TTTTTGTATTTTTAG	26091
rs535789980	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	HERC4	GRCh38.p7	10:67921689	TTTAGTGAATACCAT[A/G]AATAGCTTCAACAAT	26091
rs535880448	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68055110	TATTTTTATTAGGGA[C/T]GGGGTTTCACCATGT	26091
rs535898215	in-del	-/TTAG	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:67980286	TACAGACATGCGCCA[-/TTAG]CCATGCCTGGCTAAT	26091
rs535904614	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67954140	AACTCTGCCGCTGCT[A/G]TTGTAGCATGAAAGT	26091
rs535905694	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68023266	GCAACAATATTCACA[A/G]TAAGATAAAACACAA	26091
rs535924032	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68015573	AGTTCTCTTTACAAC[C/T]TGGCAAACTCACACA	26091
rs535944081	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67924762	CCATGTATGCCAAAG[G/T]ATGACTATACTCCAG	26091
rs535945856	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069973	CTTGAACCTGGGAGG[C/T]GGAGGTTGCAGTGAG	26091
rs535970530	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68062076	CAGGTTAGAACTGGG[A/G]GAAGTCTACAGTTGG	26091
rs535977600	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68014757	ACCTAAGAAACCACA[C/G]ATCTGAAGCTAAGGA	26091
rs535978489	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67953570	TTGAACAAAGATGGG[A/G]CAATATGAGCATCAA	26091
rs535991560	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68022645	TTGGCAATGATTTCT[C/T]AGATATGACACCAAA	26091
rs535991595	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68031905	GATAGGTGCCTGCCG[A/C]CATGCCCAGCTAACT	26091
rs536013618	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67994345	TTCCCTACAAGATGG[C/T]TGACTAATCTACAGT	26091
rs536071229	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68057460	GAAACCCTGTCTCTG[C/T]TAAAAATACAAAAAT	26091
rs536078798	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67983530	TGTGCCTGTAATCCC[A/C]GCACTTTGGGATGCT	26091
rs536089155	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67952121	CAATACAATTCCACC[A/G]TCACAATTTATTTAT	26091
rs536089945	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68048732	GAACATCCAGAAAGC[A/T]GGGGAGGTGGTGCAT	26091
rs536118665	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67956775	GCTACCCAAAGTACT[C/T]TGTGTACCTTCATTA	26091
rs536120188	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68039274	TGAGCCAAGATCACA[C/T]CATCGCACTCCAGAA	26091
rs536153333	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	HERC4, POU5F1P5	GRCh38.p7	10:68009639	GTAGCTGTGGCAATT[C/T]CTTAAAATAAGACAG	26091
rs536158683	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68056792	AAACTAAGGACCCAA[C/T]AGTTTAAAGTAATTA	26091
rs536189134	snp	C/T	0.00517822	0.0506191	intron-variant	HERC4	GRCh38.p7	10:67937926	ACCTCCAGTGATCTG[C/T]CCGCCTTGGGCTCCA	26091
rs536261499	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67933187	GAGAGCTTTGGATTC[A/C]GATCATTTGACCAAC	26091
rs536265201	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68016050	AGAGGTTGCAGTGAG[C/T]CAAGATTCTGCCACC	26091
rs536285323	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67942201	GCCTGGTTTAGCAGT[A/C]TAGCCTCTGTGTTTT	26091
rs536298914	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67969480	GAGGGGGGGAAAAAA[A/G]GAAACAAGGCAGAAT	26091
rs536319190	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68041720	CTTATATTAAACTAC[C/G]ATAATAAAATTTGGG	26091
rs536362311	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67968833	TCAACAGAACCATGA[C/T]TATATTTGGAGATTT	26091
rs536379266	snp	A/C			upstream-variant-2KB	HERC4	GRCh38.p7	10:68075981	GATCTCCTAGGCCAG[A/C]CTTAACTTCTTAAAA	26091
rs536387904	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67923880	CAAAGGAAATGTCAC[C/T]GATTTGGACACATAA	26091
rs536399956	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68065910	CACAGCATAGGTTTT[C/T]CTCGCATATAAGGTA	26091
rs536406402	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67963366	GGATTACAGGTGCCC[A/G]CCACGATGCTTGGCT	26091
rs536422497	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67993822	AGAGTATCTATTACC[A/C]AAAATATTGCTTGGC	26091
rs536457881	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68002230	ACCTTTACAAATGTC[A/C]ACCTTCATAGTATCC	26091
rs536464815	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68018605	AGTAAGTTATTAATA[A/C]GAGTTTAGCAAGGTG	26091
rs536487227	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68073387	TTTTTAGGGAAAATA[C/T]GACACTTTCTATGAT	26091
rs536490030	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67964783	TTTCTTTCTTTCTTT[C/T]TTTTTTTTGAAAGGA	26091
rs536490699	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67931511	CTCACTGCAACCTCC[A/G]CTTCCCAGGTTCAAG	26091
rs536531727	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68028249	CATTATTGACCAGTT[-/A]AAAAAAAAAAAAATG	26091
rs536547355	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68001151	CAAGGCAGGAGGATC[A/G]CTTGAATCCAGGAGT	26091
rs536551137	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67969682	TGGGAGGAAAGGTGA[C/T]AAGAACAGTCCTAGG	26091
rs536552113	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67971237	GAAATAATACCAATC[A/T]TAATCAAACTTTTTC	26091
rs536563294	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67991538	AACATTTTATATTGG[C/T]AGTGAGCCTAATCTG	26091
rs536584552	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67926480	GAAGTAGAGAGGAAA[C/T]AGTTTATACTGTGAA	26091
rs536629372	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68024204	TACTCAAGTAAGTCA[C/T]GGAAATGTATATTCA	26091
rs536631051	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68033787	TAGTTCTTTAATGAA[C/T]AAAGGATATTTTGTA	26091
rs536656769	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67995036	GTTTGAGAAACCTAG[C/T]CATTTGTCCTGTACA	26091
rs536744883	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68004428	GTCCACTTTTGCTTT[C/G]GTTGCCTGTGCTTGT	26091
rs536764340	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67981154	GCCTACAAGAAACAC[A/C]CTTCACTTATAAAGA	26091
rs536770090	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67969630	GGGGACGCAAACCCA[C/T]GTCTTGTTGCTGAGG	26091
rs536770455	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67957870	TGGAGTGCAATGGTG[C/T]GATCTAGGCTCACGG	26091
rs536778087	snp	A/C	0.00716266	0.059414	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011273	CCCAGGTTGGTCTCA[A/C]ACTCCTGGCTTCAAG	26091
rs536832115	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68031775	CTTTTTTTTTGAAAC[A/G]AGGTCTCACTCTTTG	26091
rs536833044	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68027815	GTAATCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	26091
rs536874280	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010682	CAGCAAGGGCCGCGC[C/T]GCTTACACATGTTCT	26091
rs536879527	snp	A/C			missense, nc-transcript-variant	HERC4	GRCh38.p7	10:68014048	TGGTAGACACTGCCC[A/C]TTATAGGGGTACCAA	26091
rs536880579	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67997693	TTTAGTATCCTCTTG[C/T]TTTTCAAATTTGCAT	26091
rs536912917	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68017609	CTGTCTCATCAGCCT[A/C]CCCAGAAGCTGGGAT	26091
rs536943500	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68016968	ATAGAGTATGTCACC[C/T]AAAATGATTTAAATT	26091
rs536948701	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68061676	TTCAGGTCAGGAGTT[C/T]GAGACCAGCCTGACC	26091
rs536953478	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68043504	TATGTAATTCATGCT[A/G]TTAGAGTTTTTAATA	26091
rs537006024	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67986730	ATCCTTATAGATAAT[C/T]CTTCATTTGCATATG	26091
rs537040417	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68055618	TTAAGCTTCACAGAT[A/T]AAGGCACTAAGTTAT	26091
rs537042055	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68020761	GCGACAGAGCGAGAC[C/T]CCGTCTCAAAAAAAA	26091
rs537043029	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67942245	TATAGTATTTATCTC[A/G]TATGGTTGTTGTGAG	26091
rs537045636	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68042760	AAAAATGATTTGGTA[C/T]TGAAATTAAAACCAA	26091
rs537045840	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67983373	CCCACTGCTGAGGAG[A/C]TACCCAAAAGAAACG	26091
rs537046011	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68060674	TCAGTTGCAGAGGCT[C/T]ATTCAACTTCCTAAC	26091
rs537074848	snp	A/G	0.00398564	0.0444627	intron-variant	HERC4	GRCh38.p7	10:68012888	ATTATTTTATCTTTT[A/G]TGGTGATCTCATATC	26091
rs537075620	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68051254	AGCATATAATCATTA[C/T]AGTCAACAGTAATTC	26091
rs537082702	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68067882	ATTCAGTAATACACT[A/T]TACATATTTGAATTT	26091
rs537108611	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68020493	AAGTTTGGGCCGGGC[A/G]CGGTGGCTCACGCCT	26091
rs537112153	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68050476	TAATCTTTTTCAACA[G/T]ACTAAATACTGAAGA	26091
rs537158303	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68016915	GAATTACAAAACTGG[A/G]TAACATTAAATCATT	26091
rs537196441	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68019592	CAACAATTACACTGA[C/G]AGAATCTGTCTGAGA	26091
rs537208766	snp	C/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67927112	GCTGTTAGTTGCACA[C/T]AAGTTTGAAGAAAAC	26091
rs537236608	snp	C/T	0.00100475	0.0223912	synonymous-codon	HERC4	GRCh38.p7	10:67936200	ATTTAGAACCAGCTC[C/T]TTCACTTCTGTTGCA	26091
rs537298366	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67944510	AAACCAGACTGTGAA[A/G]ACTACAATAAATACC	26091
rs537315667	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67934925	TTTTTTTTTAATATT[C/T]TCTTTGACAGATTTC	26091
rs537343166	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67979764	ACACGGTGAAACCTC[C/G]TCTCTACTAAAAATA	26091
rs537359593	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68035192	CAGTCTTGCTCTGTC[A/G]CCCAGGTTGGAGTGC	26091
rs537384101	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67983719	ATGAACCCAGGAGGC[A/G]GAGCTTGCAGTGAGC	26091
rs537411941	snp	A/G	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:67967144	CAGGCGTGAGCCACC[A/G]CGCCTGGCCAAGACA	26091
rs537428482	snp	G/T			intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069835	ATCACAAGGTCAGGA[G/T]ATCAAGACCATCCTG	26091
rs537454909	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922428	GTAAGATTTAAATCA[C/T]AATTTTTAACCTTTA	26091
rs537460909	snp	C/T	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:67952346	TGGAGTGCAGTGGCG[C/T]GACCTTGGCTCACTG	26091
rs537469496	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67974847	CTTCAGTATGCATAT[C/T]GAGAAGGGAAGCTAA	26091
rs537483927	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68025227	GACTCTATCACCCCA[A/G]AAAGGAAAGAAAAGA	26091
rs537484375	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67966883	TTTTTGAGACGGAGT[C/T]TCACTCTGTCAACCA	26091
rs537497759	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68029672	AGGACGAATATTTAT[A/C]TAATTTTTATATATT	26091
rs537512654	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012441	TTATGTACTTAGAGG[C/T]CACTGTAGGGTTATT	26091
rs537518441	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67929879	GTGCAACGGCACGAT[C/G]TCCGGCTCACTGCAA	26091
rs537564227	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	HERC4	GRCh38.p7	10:68075269	CCAGGGGTGGGGAGA[C/G]TTGGGGAAGAGACTG	26091
rs537640728	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67945088	GGAAAGGTATCAATA[A/C]TCAAGTACAAGAAGG	26091
rs537648885	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68023511	CAGGAGTTAAATTCA[C/T]AGAGACAGGAAGTAG	26091
rs537651605	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67998018	ATTCTCCTGCCTCAG[C/T]CTCTGGAGTAGCTGG	26091
rs537655929	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:67988977	TAACACAATATCTTA[C/T]GTAACATTTGTAAGG	26091
rs537669000	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68007538	CAGCAATGTCTAAGC[A/G]CTGAAGAGTTAGGTA	26091
rs537677401	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68062316	TACTAATGAATATAC[C/T]AATCTATAGCTAATG	26091
rs537680156	in-del	-/T	0.0019976	0.0315406	intron-variant	HERC4	GRCh38.p7	10:68038281	CATAGGTCATATTAT[-/T]TTTTTTTCATACAAG	26091
rs537700938	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67953301	AGTATAACAATTTTA[A/C]ATTATATCAAAACTA	26091
rs537718996	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68044845	CATTTTGGGAAGAAG[C/T]TAAGGGTTTATAAAG	26091
rs537747609	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68006425	TGTCCGGGCTGGAGT[A/G]CAATGGTGCGATCTC	26091
rs537771055	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069686	ATTTATAAAGCCAAC[C/T]TATGTAAAGAAACAA	26091
rs537798127	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67939883	CACTTTTCTGAATAC[A/G]AAGGCCATGTATCCA	26091
rs537815355	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67975445	GTTGACACCTCCCAG[C/G]TTCAAACAATTCTCC	26091
rs537829741	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68035684	TTCCAATCTCTTCTC[A/C]TATCAGTCACTCACT	26091
rs537855701	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68021333	CATATGAAAATTAAT[A/G]TATGTAATCAATGTA	26091
rs537917287	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68038415	AGTATTTAAGCAAAG[C/T]GAGCTATACTCATAC	26091
rs537955082	in-del	-/AA	0.062036	0.164832	intron-variant	HERC4	GRCh38.p7	10:68046133	ACACACACTGTTCCA[-/AA]AAAAAAAAAAAGAAA	26091
rs537968810	snp	A/C	0.00636936	0.0560724	intron-variant	HERC4	GRCh38.p7	10:67946396	ACACACACACACACA[A/C]AAGACCCAATGATCT	26091
rs538034965	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68055348	TAGTGGGTTCCCTGA[A/T]AAAATCTAAAGTTAA	26091
rs538061299	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68015438	TTTTGGAGTCGTTCT[A/G]TTTAGCGACATAAGC	26091
rs538066089	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68023429	ACCTTGATGACACTA[C/T]GCTGAGTGAGATAAG	26091
rs538098411	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68014818	TCCAACTCCTCAGAA[A/G]AAGTCTCCTTAGGCA	26091
rs538163191	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68006348	CTGCTGTTGATGAAA[C/T]GCCTCAGCGTTTTTG	26091
rs538179803	snp	A/G	3.30066e-05	0.00406229	missense	HERC4	GRCh38.p7	10:67922989	AGTTTAGAGCGTAGA[A/G]TTTCTTTTTCTGTAT	26091
rs538336914	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68016639	TACAGGCTTGAGCCA[C/T]TGCACCCGGCCCAAT	26091
rs538356026	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67969927	AAGCACTGAGTAACA[A/G]GCAATACCAGTTTAC	26091
rs538372885	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68008261	TCACACCTGACAGTA[C/T]TGGGTCTCACCCAAA	26091
rs538375514	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68023921	TAGGAAAATATTTCT[C/T]AGAAAATAAATGGCA	26091
rs538376519	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68063616	TTCTCACTCCTTAAA[A/G]TTAAAGATGTTCTTT	26091
rs538403861	snp	A/G	0.000399281	0.0141238	intron-variant, missense	HERC4	GRCh38.p7	10:68070576	GCGCCATTGCACTCC[A/G]GCCTGGGAAACAAGA	26091
rs538405161	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67925632	AGATGGCCACCAGTG[A/G]GCACTGCCTCCTGGT	26091
rs538438441	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67975739	CCAATTTAAAAAGCA[C/T]ACATTTAATAATACT	26091
rs538460165	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67977299	AACAACATTTCTAGA[C/T]ACACAGTGGCCAGAA	26091
rs538473598	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67946541	AAAACAGATGCAAGA[C/G]AAAAACTATAGAAGA	26091
rs538484293	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68031969	GTTGGCCAGGCTGGT[C/T]TTGAAGTCCTGACCA	26091
rs538510133	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68041250	TCTATTTTCCAGTTA[A/G]GCCACAACTTTCCTA	26091
rs538513333	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67931707	TGGGATTACAGGCAT[A/G]AGCCATCGCGCCTGG	26091
rs538549421	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68049386	TTGGAAAGATAAGTC[A/G]GGCACAGTGGCTCAC	26091
rs538554796	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68003605	CTTCCACCAACAAGT[A/G]AGAACATGTGACTGT	26091
rs538564974	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68058413	GTAATTATGAAAGCA[A/G]TATAGTTTCCCTACA	26091
rs538575331	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67931261	AGTGCTGGCATTACA[C/G]GCATGAGCCACCACA	26091
rs538590132	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68047202	TTGACTTCTTAGGGA[-/A]AAAAAAAAAAAGGTC	26091
rs538592367	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68002786	TGTATTTTTAGTTCA[A/G]ACGGAGTTTCACCAA	26091
rs538592679	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010459	TCTGGCGCCAATTAC[A/G]GAACCACACTCGGAT	26091
rs538613649	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67964896	TCCTGCCTCAGCCTT[C/T]CAAGTAGCTGGGATT	26091
rs538621425	snp	A/G	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:67972364	CCATCTCTACTAATA[A/G]TACAAAATTAGCCGG	26091
rs538625243	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68057580	AGTGAGCCGAGATCA[C/T]GCCACTGCACTCCAG	26091
rs538650766	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67997042	AAGAACCCTCTGAGA[C/T]AGAAATACTGAACTC	26091
rs538658303	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67927227	AGGATGGCTAAAGTT[A/T]TTTTTTCTTTTAAAT	26091
rs538663851	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68064275	AAGAAAGAAATAGGC[C/T]GGGTGCCGTGGCTCA	26091
rs538675256	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67963852	AATATCTATTATGCC[C/T]ATAATGCAAAATTTG	26091
rs538682727	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67979563	AGAACTTCCCAAACA[C/T]AGAAAAAGATATCAA	26091
rs538694807	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68072726	ATAAAGTACTTAGAA[C/T]CATACAAATATACAC	26091
rs538711106	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67933950	TTTGGACCAACTCCC[C/T]GGCAACAGCCACTAT	26091
rs538743320	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67962958	TCACAGGGATCATAT[A/G]AATTAATCTTCTCAA	26091
rs538756559	in-del	-/A	0.181978	0.240568	intron-variant	HERC4	GRCh38.p7	10:68064560	GTGAGATTCTCTCTC[-/A]AAAAAAAAAAAAAAA	26091
rs538763514	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67963229	TTTACTATTTATTTA[A/T]TTTTTGAGATGGAGT	26091
rs538766132	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68031462	AATGCCAAAATCAAT[-/A]AAATATGATATTAGG	26091
rs538781630	in-del	-/T	0.230017	0.2492	intron-variant	HERC4	GRCh38.p7	10:67937682	TTTGTGGAGAGCAAC[-/T]TTTTTTTTTTTTTTT	26091
rs538788299	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67985533	ATGTTTTATCTGTTT[C/G]GTTTTATTTAAGGGT	26091
rs538835612	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67987470	AGAAACAATCTAATT[A/T]ATCTCTTGAATCCTC	26091
rs538848043	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67994486	TGCCCAGGCTGGAGT[A/G]CAGTGGCGCGATCTT	26091
rs538855323	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68059953	AATAATATTATATTA[C/T]ATTTTGTTTCTCTTG	26091
rs538873928	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67960090	TAGGGGCTTGGGCCA[C/T]GTGCTGTCAGTTCTG	26091
rs538881946	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68066642	TTATACAACATAACT[A/T]ATCCAAGTTCCAAGG	26091
rs538884302	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67965990	ACTTAGCTGCATAAA[A/G]AGATGTACGCACCCA	26091
rs538942208	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67949033	CCGAGGAGGATGGAT[C/T]ACAAGGTCAGGAAAT	26091
rs538972368	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68074471	ACAAAATAAGAGTAA[C/T]ACAGGAAAATACCCC	26091
rs539021444	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67980458	AATATTTTCCTAGAC[A/C]AACAAAAGCTGAGGA	26091
rs539021675	snp	C/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67988571	ATTGTTTTTGCCAAT[C/G]TAAATCTTTAATAGA	26091
rs539031821	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67955615	TGTCTCTACTAAAAA[G/T]GCAAAATTAGCAGGG	26091
rs539042405	snp	C/T			intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069780	GGGCACGGTGGCTCA[C/T]GCCTGTAATCCCAGC	26091
rs539049459	snp	A/C/T	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:68005978	TCTGATCTGAGGTTA[A/C/T]CAGGCTTGCAAACAA	26091
rs539049520	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68017728	CCCTGACCTCAGGTG[A/T]TCAGTCTGCCTCGGC	26091
rs539082492	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67987576	CCTGGACCCTGATAT[A/G]CTAAAAGAAAGCCCT	26091
rs539105694	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68061580	TAGGTTTCTGTCAGC[A/G]AAAGAATAAGCAAAT	26091
rs539123364	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67986556	GAGACGGGGTTTCAC[A/C]ATGTTGGCCAGGTTG	26091
rs539134407	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68044958	TAACCTGGGCTGCTT[C/G]ATTTTAACAATAAGA	26091
rs539137663	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67946520	GTCTAATACAAGGTA[C/T]TAGACAAAACAGATG	26091
rs539156639	snp	C/G			intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010347	CCAAAATGGGGCCCT[C/G]AGGCCATAGGAAAGG	26091
rs539177506	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67951442	ACATCCATATGGCAT[C/T]GTGGGATGCCCTCAA	26091
rs539225150	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68004592	GGGGTGTATTCGTCT[A/G]TTTTCATGCTGCTAT	26091
rs539237992	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012132	TAGAATCTTGGTCTG[C/G]ATTAGACTTTGGCTA	26091
rs539265715	snp	A/G	0.00119737	0.0244387	downstream-variant-500B	HERC4	GRCh38.p7	10:67921534	TAGAAGAGTTCTATG[A/G]TTCGCCAATAGTTTT	26091
rs539367053	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68018615	TAATAAGAGTTTAGC[A/G]AGGTGGTTGTATTTA	26091
rs539394415	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68035763	CACACACTTGCTGTT[A/C]TCTCTACCTAAACCT	26091
rs539413533	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68007397	AGTTGAGATTTCTCA[A/C]AACAGCTGTTTTGAA	26091
rs539435354	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68051433	CACTGCAAGCTCTGC[C/T]TCCCGGGTTCGCGCC	26091
rs539437868	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68053717	AAAAGGCAGAGCACT[A/G]CCTTGAACCTCCCCT	26091
rs539457636	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67996848	TAAAAATTAGCTGGG[C/T]GTGGCGGCAGGTGCC	26091
rs539484092	snp	A/G			upstream-variant-2KB	HERC4	GRCh38.p7	10:68075958	CTGATTCATAAAAAC[A/G]AAGTCTGGATCTCCT	26091
rs539535223	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68013734	ATGTTGTGTATATTT[C/T]ACCACAATTTAAAAT	26091
rs539545938	snp	A/C	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:68008466	CTCAAATCAGTCTCC[A/C]CAGAAATTTGAAGGC	26091
rs539604299	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	HERC4	GRCh38.p7	10:68075606	AAATCACTTTGTTTT[G/T]TGGTTTGGTTGTCTT	26091
rs539604376	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68067989	TAAGTTTGTGTACAA[A/G]GGGGAAGACAATAAA	26091
rs539621811	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68038515	CATCAGCTTACAGTT[A/G]GAAACTTGGCAATAC	26091
rs539638868	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68029428	ACCCAAGAGGTGGAC[A/G]TTACAGTGGGCCGAG	26091
rs539684834	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	HERC4	GRCh38.p7	10:68075285	TTGGGGAAGAGACTG[A/G]GTAGGAGAAGGCAGA	26091
rs539700634	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67936911	ATGTTTACTATCTAG[A/T]AAAGGAAGAGAAATG	26091
rs539707885	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68046806	ACCTCGTCTCTACAA[A/G]TAATTTTTTACAAAA	26091
rs539744633	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68045913	ATTCAAATTGTATCT[A/G]GATTACTATCTTGCA	26091
rs539758227	in-del	-/AG	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67982173	CTATCTTAAGCAAAA[-/AG]AACAAAACTGCGAGG	26091
rs539759442	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68027855	TTGAATCCAGGAGAT[A/G]GAAGCCTGAAGTGAG	26091
rs539766900	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:67952561	AGAGGTGTGAGCCAC[C/T]GGGCCCGGCCAAAAA	26091
rs539793444	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68062363	TACCTGGCTCTTTCC[A/G]TTACATTTACTATTT	26091
rs539807838	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68054430	GCAATCTCAGCTCAC[A/G]GCAACCTCCACCTCC	26091
rs539817465	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68060576	TTCAACACTAAATTT[A/C]TCTCCAATTATATGG	26091
rs539821154	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68061818	CCTTGGAGGCGGAGG[C/T]TGCAGTGAGCCGAGA	26091
rs539882662	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069721	TAGTTCCCTCCATTC[C/T]ATGTGCTTTCTGACA	26091
rs539883139	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67960390	CTATTAAAAGCCTAA[A/C]ATTTTTTTTTTTGAG	26091
rs539886723	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67960510	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGATTA	26091
rs539918352	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069122	ATGGTCACCAAATTA[C/T]ACCTATGATTAGATA	26091
rs539926005	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:67967088	CTCGATCTCCTGACC[C/T]TGTGATCTGTCCACC	26091
rs539970189	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922589	AGGTTTTTCACTCAA[C/T]GATTGAAGAAAAATT	26091
rs539983079	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67955310	TGAGCATAAAGAGTA[A/C]CCTTTTGAATGTTTT	26091
rs540012545	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67992002	CTCCTGGGCTCAGCT[C/G]ATCCTCCCACCTCAG	26091
rs540015798	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67937722	GTCTCACTGTGTCAC[C/G]CAGGCTGCAGTACAA	26091
rs540082248	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67945823	AAATCAAAAAACATA[C/T]GACAGATACACGAAA	26091
rs540126639	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68054954	TTTTGAGAGAGTCTC[A/G]CTCTGTTGCCCAGGC	26091
rs540158032	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67954429	GCATCAAATGTATTT[G/T]GACAACTCCAAGTCC	26091
rs540163165	in-del	-/A	0.231189	0.249291	intron-variant	HERC4	GRCh38.p7	10:67962223	AAAGTTTAAATAAGC[-/A]AAAAAAAAAAAAGCC	26091
rs540164724	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67924078	GAAAATGAAGACCAA[A/G]CAGAGAAAAGAGCAA	26091
rs540188288	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67998687	TTATTGTTTCTAATC[C/T]ACATATTCTATGCCA	26091
rs540251462	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68014953	TCTCTTGCCCTAAAC[C/T]TCTTTGCCATTTGTG	26091
rs540263729	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67976651	TATTGCTGAAAAAAA[A/G]AGATACAAAAAAGTC	26091
rs540280651	in-del	-/AG	0.00119737	0.0244387	intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010246	AGTGGCGACAGAAAC[-/AG]GGGGAAAGGCACTAA	26091
rs540283169	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68057421	ACAAGGTCAGGAGTT[C/T]GAGAGCAGCCTGGCC	26091
rs540324860	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67983607	ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA	26091
rs540364352	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	HERC4	GRCh38.p7	10:68077152	AAAAAGTTCACATTC[A/C]CAGGTACTGGAGGTT	26091
rs540365043	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68021391	GAAAAGACACACACA[A/G]TCATCTGAATTGATG	26091
rs540371730	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68013375	ACAATATCTCCAAGG[C/T]ATGCCTGAATTATAT	26091
rs540377878	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68027463	TATCTTCAACAGCAT[A/G]TATCTGTAACCGACA	26091
rs540381136	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68030598	CCTCATTCTGTTTTA[C/T]ACTTCACTGTACTTC	26091
rs540404236	snp	C/T	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:67938711	AGCACTTCGGGAGGC[C/T]GAGGCGGGTGGATCA	26091
rs540443891	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68009341	GCTGGTCCCAAACTC[C/T]TGGCCTCAAGTGATT	26091
rs540470127	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68047250	GTGGGTAAGAGATGT[C/G]AACCAAAAGTTCACA	26091
rs540534635	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68055494	TTTTATATATTTATA[C/T]AGAGGAATACAATTA	26091
rs540562167	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68007603	ACCTGAACTTCTTGG[A/G]AAGGCATTCCAAGTA	26091
rs540564787	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:68060085	GTCTGACTGTTCTCA[C/T]CAAAACACATACTTT	26091
rs540571021	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68015887	GCAGGTGGATCACTT[A/G]AGGTCAGGAGTTCGA	26091
rs540581758	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67969609	AAGCCTTCAGCCACT[A/G]AGGAAGGGGACGCAA	26091
rs540599780	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68038308	CAAGCTCAATTTTAG[C/T]GTACCAAAAATTTAT	26091
rs540607132	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68022988	GATAACATGTTACAC[A/G]TATTAAAATAGGTAT	26091
rs540621953	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68041302	CACCAACTCATTTCA[A/G]TTTTGAAAAATTTAT	26091
rs540637203	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67924235	GTCCCTCAACAATAC[A/G]GTATAACAACTATTT	26091
rs540643858	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68065793	GAACCCAGGGAAGTC[A/G]AGGCTGCATTGAGCC	26091
rs540661735	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68040701	CAAGACCAGCCTGGC[C/T]AAAATGGTGAAACCC	26091
rs540666983	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67940703	ACCTGCCTCGGTCTC[C/T]CAAAATGCTAGGATT	26091
rs540675387	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67993998	ACAAGCAAGCACAAT[C/G]TTTTATTTGTAAAAG	26091
rs540700089	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67931469	GGCTAGGGCTTTTTT[C/T]TGGAGAGTGCAGTGG	26091
rs540700187	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67923402	GTGAGTATTTTGCCA[C/T]TGCCAAAACATTTTG	26091
rs540704346	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68031582	AATAATCCTTCCTTA[C/T]TAAAAGGCAAGTACT	26091
rs540721129	in-del	-/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67975625	AAAGTGCTGGGATTA[-/C]AGGCGTGAGCCACCA	26091
rs540750472	in-del	-/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:67999564	ATAACTTTCAAAACG[-/T]AGCAGTGAAGTACAT	26091
rs540761040	snp	C/T	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:67931027	GTCTTGCTCTGTTGC[C/T]TGGGCTGGAGTGCAG	26091
rs540784439	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68057781	GTGCAATCACTGCAA[C/T]CACCACCTTCTGGGT	26091
rs540854192	snp	A/T	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:68025866	GAATTCCAGGTAATG[A/T]TGTTTTCACCGTTAT	26091
rs540858389	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67950863	AGCAAGAAGTACTAC[A/T]CTTAGCACCCAGAGC	26091
rs540869224	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68063739	GGCCAGGAGTTTGAG[A/G]CCAGCCTGGTCAACA	26091
rs540899582	snp	C/T	1.64757e-05	0.00287012	missense, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68034124	GTGAAGTTTGCTTTT[C/T]ACAGTCAGTACCTAA	26091
rs540903958	snp	C/T	0.00129241	0.0253877	intron-variant	HERC4	GRCh38.p7	10:67996175	GGTTAAGCGTGGTGG[C/T]GCATGCCTGTAGTCT	26091
rs540905978	snp	C/T	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:68070717	TTTGAACTTGTTTCT[C/T]TTCCCTCTGAAACCT	26091
rs540908174	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68063044	CTGTTGCCATCTGCT[C/T]AGTATACTATCTCTA	26091
rs540933405	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67962293	TATACCAAGGGAGTT[C/T]ATAGTATGGGAGATC	26091
rs540938576	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68033069	AAGGAGGGACTTAAG[A/T]GTTAAGTGCTAAACA	26091
rs540970375	snp	G/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67979475	AAAAAAGGCCCAAAA[G/T]GGCAAATCTAAGTTA	26091
rs540979553	snp	C/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68059384	GTCTTCATCATATAG[C/G]TCTTGCACATTTCTT	26091
rs541001061	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67932797	TAGAAATGAAAAAGC[A/G]CACATGTACAGATTA	26091
rs541013985	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67950192	TAACATCCTACTATT[A/G]TACCTTCTCTGAGAG	26091
rs541053140	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67971536	AGGAGAAAAAAATCA[A/T]CTGTTCATCTCAACA	26091
rs541069034	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68066172	TTGATATACTTTATA[C/G]CCTAGGAATACAGAA	26091
rs541069168	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68058781	AGGTTAAGCAATGTG[A/C]CCAAGAAAACAGATC	26091
rs541080448	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67940016	ACTGCAACCTCTGCC[C/T]CCTGGGTTTTTAAAA	26091
rs541105913	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68065434	TCTAAAGGATTCCAG[A/G]ATGTCTTATGGCCAA	26091
rs541113413	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67993142	TTGATGTTAGGAGTT[C/T]GACGCCAGCCTGGCC	26091
rs541136936	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67967287	GTGCTATGGGAGACA[C/G]AAAGATTTGTAAGAT	26091
rs541138504	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67988585	TCTAAATCTTTAATA[A/G]ATTAATGTTAAAATG	26091
rs541142028	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68049053	TTCCAATTCCAGGAA[C/T]TTGTTCTACAGATAT	26091
rs541174787	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67964960	TGTATTTTTAGTAGA[A/G]ACGGGGTTTCACTAT	26091
rs541213920	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68019764	GAACAGCTTCCAGGA[A/G]CAGCCTGTATGCAAC	26091
rs541261803	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67970679	ATTCAGAGAAGACCC[A/C]AATGTTGGAGCTAGG	26091
rs541261898	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67979143	CAAATGAACAAAATA[A/G]GGCACCAAAGACAAA	26091
rs541262361	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67934571	TTGGTAGACAGAACA[C/T]ATCCTCCAGTAACTT	26091
rs541297421	snp	A/G			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011299	TCAAGCAATCCTCTC[A/G]CTTCACAAATGTTCT	26091
rs541334366	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68014726	AACTCCTCTGGAGGT[A/G]CTACAGTGAAAGCAA	26091
rs541349212	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67950919	TTAAAGAAGACACGG[C/T]TCTTAAGAAAAATGC	26091
rs541354428	snp	C/T	0	0	intron-variant	HERC4	GRCh38.p7	10:67995531	CTTCCATTAATTTCC[C/T]TTATTTATTGTTTGT	26091
rs541374301	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68050908	AAAGCCTGGCCCAGT[A/T]ATGTTCCGTGTAAGA	26091
rs541413099	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67960463	CAATCTCGTCTCACC[A/G]CAACCTCTGCCTCCT	26091
rs541457589	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67973468	TATGCCAATGAGTTC[C/T]GGCATGTTTTGTTAC	26091
rs541458896	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011598	AATCTTTTTACTGAG[C/T]GGTGGGTCTCAACAG	26091
rs541464858	snp	C/T	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HERC4	GRCh38.p7	10:68074872	TATGCCGGGCCGGCC[C/T]GCATCCGCCCAGCCC	26091
rs541488161	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68035995	CTGTATACTGTAGTA[A/T]GCCTAGTTCATACTA	26091
rs541496000	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010881	GATGTCCTGGGACTG[A/G]ATGAAGGGTATTTTT	26091
rs541497869	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67991968	AATGGTGTTAATCTC[A/G]GCTCACTGCAGCCTC	26091
rs541516713	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67972758	CCATGTTCATGAATC[A/C]GAAAGGAGAGTAGCA	26091
rs541518934	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67980518	GAAATGCTAAATGGA[A/G]GTCTTCAATCTGAAA	26091
rs541570006	snp	A/G	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:67987659	GCTATGATTTCATCA[A/G]TCAAAATGAAGAGAA	26091
rs541579480	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67965888	ATCTAACTGCTTACC[C/T]ATTTCTGCATTAAAA	26091
rs541587514	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67927956	AATAAAACAGCGAGG[G/T]GAGACAGGATACGTG	26091
rs541618035	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68052890	GGAAAACGAAAGCTA[C/T]AAAAAGAGAAAAATA	26091
rs541645575	snp	A/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67928130	GCCCTAAGACTGGAG[A/T]GTGCCTGGAGGGTTC	26091
rs541679981	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68005683	ATTTCCTTTTTTTTT[A/T]TAATTTTCTGTGCAT	26091
rs541743041	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67994835	CGAGTAACTGAGATT[A/C]CAGGCGCCCACCACC	26091
rs541759390	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68051912	GAGCTCAAGCAACAC[A/G]CCCGCCTCAGCCTCC	26091
rs541768611	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67959405	TTCAGCAATTAAACA[C/T]CCCCATTTGCAGAAT	26091
rs541775775	snp	A/C	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	HERC4	GRCh38.p7	10:68075313	AGAGGGGGAGGTGGC[A/C]ACGCGAGGGAGGCGG	26091
rs541776961	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67993588	AACTTCTGGAGTAAA[C/T]ATTTCATAATGCAGA	26091
rs541778386	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68004643	GTAATTTATAAAGGA[A/C]AGAGGTTTAACTGAC	26091
rs541816193	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68038008	ATCTTGCAGAAAGAT[A/G]AGCAAAGCTGGAGAA	26091
rs541852352	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67966955	TGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT	26091
rs541855226	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68037180	GCTCACTGCAACTTC[C/T]GCCTCCCGGGTTCAA	26091
rs541874142	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68000750	TTTGGATGCAGACAC[A/G]TACAGAGAGAAGGCC	26091
rs541874946	snp	A/G	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:67981862	ATGAGAATCACTTGA[A/G]TCGGGGGGGTGGAGG	26091
rs541875854	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67928550	GTAATTCTGTTGCCC[A/T]TAGTCCAACCTTCAT	26091
rs541877711	in-del	-/A	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:67962787	AGAAAATGTTTCATT[-/A]TAGTGCACATAGAGA	26091
rs541909671	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68071374	TTTAAACCTCAGTAG[A/G]CCTAAGTAACTATAC	26091
rs541920084	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67936348	CTACTAAATTTGAGA[C/T]AAAATTCTGCTACCA	26091
rs541921663	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68028052	GATACATCCCCATTA[A/G]GTTTAATGGTCTTTG	26091
rs541943343	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67935169	TTTTTTTTTTGAGAC[A/G]GAGTCTCGCTCTGTC	26091
rs541952407	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68027029	AAAAACATATAATAT[A/G]TAACTAATTAAATAA	26091
rs541953264	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67997575	ACTGTATCCCCCACC[C/T]AAATAGATCTGTTTG	26091
rs542022464	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67960688	GCACCCAGCCAAAAG[C/T]GTAAATTTTAAACAC	26091
rs542044875	snp	A/C	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68014389	CATAGACAGGCTGCA[A/C]GAGCATGGTCCAGAA	26091
rs542056028	snp	C/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67960023	ATATCATGCCTGATA[C/G]GAGTGTCTTTGTTTG	26091
rs542064248	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68013101	CAACCCTGCATAGAA[C/G]AAGTCTATCAGCACC	26091
rs542083928	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922750	TGGTTCTGTACAATA[A/G]TATTAACAGTTTGTT	26091
rs542093410	snp	A/G	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:67951835	TTCCACAATTCCTTC[A/G]TTCACAAACTTTGGC	26091
rs542115411	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67966997	GTAGCTGGGACTACA[A/G]GCACCCGCCATCATG	26091
rs542123160	in-del	-/T	0.00676609	0.0577691	intron-variant	HERC4	GRCh38.p7	10:68017678	TTTAGTAGAGATGGG[-/T]TTTTTTTGCCATGTT	26091
rs542125027	snp	C/G	0.00557542	0.0525036	intron-variant	HERC4	GRCh38.p7	10:68029898	CGCCTGCCACCACGC[C/G]CGGCTAATTTTTTGT	26091
rs542125082	in-del	-/AA	0.00597247	0.0543191	intron-variant	HERC4	GRCh38.p7	10:68054842	ACTTCCCTATTACTG[-/AA]AAATAACAGTGAAAT	26091
rs542126055	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68068041	AGCTTAGTTATAAGA[C/T]AGTAATTTTTTAAAG	26091
rs542151955	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68020581	ACCACCCCGGCTAAA[A/T]AAACGGTGAAACCCC	26091
rs542162496	snp	A/C	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67982307	TTTGTTTCTAGAGAA[A/C]CTAGAAACAAATCTA	26091
rs542171630	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68056273	CTAATGTAGCTGATG[A/G]TGATCAAGTTCATTA	26091
rs542205213	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67937049	AGTGTGAAAGAACTT[C/G]AGGAAGAAATGCCAT	26091
rs542243662	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67955341	TATACTAATGTATAA[C/T]GTATAACTCATAACA	26091
rs542256995	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68062749	TGGGCAACAGAATGA[C/G]ACTCCATCTCAAAAA	26091
rs542334251	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68062395	TTTCCATCTGGTTAC[A/C]AAAGCCTGTCCATTC	26091
rs542359466	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68074330	TCCTATGTTCCTGTT[A/G]GCAAGTGCCCAAGGT	26091
rs542366924	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67944654	CTGAGATATATGACC[G/T]TTCAGTCAGACAGAG	26091
rs542391395	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68042018	CTTTTCTGATTACTC[-/T]TTTTTTTTTATTTTT	26091
rs542451954	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68040444	GAATGGTAAAACAAG[A/G]CTTCCCATGTTCCAT	26091
rs542471085	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67967394	TGATTAAACTGTATA[C/T]GGTATATATAAACTA	26091
rs542475676	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67938893	AGGTTGCAGTGAGTT[A/G]AGATCACGTCACTGC	26091
rs542537322	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67930061	TCTGCCCGCCTCGGC[C/T]TCCCAAAGTGCTGGG	26091
rs542595815	snp	A/G	0.00090767	0.0212841	intron-variant	HERC4	GRCh38.p7	10:67991045	AGAAAAAAAAAAATA[A/G]AATAAAAATTTAAAA	26091
rs542596302	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68020536	CTTTGGGAGGCCGAG[A/G]CGGGCAGATCACGAG	26091
rs542598114	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68072689	TTTATAATACTAGTA[G/T]TAAAAAAAAAGAAAC	26091
rs542614160	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68071670	CACCTCAATGCCTGA[A/G]ATCATGAAAATCTGG	26091
rs542643448	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67969673	TTCAATTCCTGGGAG[G/T]AAAGGTGACAAGAAC	26091
rs542647993	snp	A/T	0.00517822	0.0506191	intron-variant	HERC4	GRCh38.p7	10:67954501	ATGTTAGGGATCCAG[A/T]AGTAATTCCTTATTT	26091
rs542709747	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67961195	GTTAGGTCGTTTAGC[A/G]CCTCAACATCCTCAG	26091
rs542756589	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68015024	CATACCCATATCTTA[C/T]GCAATATGACTATTA	26091
rs542781432	snp	C/T	0.00874735	0.0655527	intron-variant	HERC4	GRCh38.p7	10:67931964	ACTTTTATTTACTTA[C/T]TTTTTGTTTTTGAGA	26091
rs542795431	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67931510	GCTCACTGCAACCTC[C/T]GCTTCCCAGGTTCAA	26091
rs542830709	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67949412	GATCACAGCAGAGGG[A/G]ATATTTCCTAAATCA	26091
rs542831726	snp	C/T	0.0123036	0.0774623	intron-variant	HERC4	GRCh38.p7	10:68054988	AGTGCAGTGGCACGA[C/T]CTCGGCTCACTGCAA	26091
rs542839321	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68031718	AATTCCCAAGTAGAA[A/G]TATAATGTAGAATTT	26091
rs542840169	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68039684	ACTCAACAAAATGCC[A/G]TTTCTTTGAAATAGC	26091
rs542914311	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010194	TCCCATTCCTAGAAG[A/G]GCAGGCACCTCAGTT	26091
rs542914394	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68031083	TTGGGGATATTAACA[A/G]CTATCTAATTTTGTT	26091
rs542957699	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67926048	GTTATTTTGAAGCCA[A/G]TAAGTTTTGGGGTAA	26091
rs542965030	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68063868	CACTTGAACCTGGGA[A/G]GTGGAGGCTGCAGTG	26091
rs542966759	in-del	-/TA	0.00795532	0.062565	intron-variant	HERC4	GRCh38.p7	10:68059903	CATAATATTATATAT[-/TA]TATAATATTATATAT	26091
rs542966814	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67952951	CAAATAATATAAAGA[A/G]CTCCCATGTACCCTT	26091
rs542993612	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68016378	ATTATTTTTGAGATG[A/G]AGTCTCACTCTGTTG	26091
rs543030835	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68034252	TTAATTTGAAAATAA[C/T]CATTTCATTTCAAAT	26091
rs543065832	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67985962	CTTAATTCTTAACCA[C/T]AGAGCAGAGGGAAGG	26091
rs543119268	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68042171	CAGGCGCCTGCCTGG[C/T]TAATTTTTTGTATTT	26091
rs543132663	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67924309	CATGTGTCACTTAAC[A/G]ATGATGATATGTTCT	26091
rs543148117	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67994099	TTTAGAACAATAATT[G/T]GATAATTACTATCAA	26091
rs543151810	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68023058	AGTGTTGGTGAGGAT[A/G]TAGAGAAACTGAAAC	26091
rs543194811	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67965368	GCTCTGTCTGGTTCA[C/T]CACTGTATTTCCAAT	26091
rs543197673	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68018984	TCATCATCAGCCAAA[C/G]CATTCTTTCTTTTTT	26091
rs543275805	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68057948	TCAGGCAATCCGCCT[A/G]CCTTGGCCTCCCTAA	26091
rs543296826	snp	A/G	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:68073769	ATTACTCTTTAGCCC[A/G]GAGAGAAAATGAAGA	26091
rs543307994	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67956160	CAAGCTTTCTTTTCA[A/T]CCTTTCCTTAATCCT	26091
rs543308551	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68026625	GAGGCAGGTGGATCA[C/T]GAGGTCAGGAGATCG	26091
rs543355620	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68009399	GGATTACAGGCATGA[A/G]CCACTGTGCCAGGCC	26091
rs543363068	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68057023	TGACAGATAAAGATA[A/G]CTAACTGCAATGGCT	26091
rs543389352	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67942730	TGGTCAGGCTGGTCT[C/T]GAACCCCTGACCTCA	26091
rs543406349	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67926253	TACAAAAATTAGCTG[G/T]GCATGGTGGCAGGCG	26091
rs543420811	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67978634	GAAGATAGTCAGTAG[C/T]CAGGAAGTTGTTATA	26091
rs543430398	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67933576	AGGATGATTCTGCAA[C/T]AGGAATAATGGTAAG	26091
rs543440390	snp	A/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68051526	GTTTTTTTTTGGTTT[A/T]TTTTTTGTATTTTTA	26091
rs543472418	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67958999	GATACATATATATCT[A/G]TTTATTTACATTTTT	26091
rs543481234	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67930057	GTGATCTGCCCGCCT[C/T]GGCCTCCCAAAGTGC	26091
rs543483496	snp	C/T	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:67985028	CTGATATGATATATA[C/T]GTTTTTGAAAAGAAA	26091
rs543490323	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67950987	CCTGGAATGTTTACC[A/G]TACCAAATGTAAGGA	26091
rs543517683	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67926543	TTCAGTTCTTCAGAT[A/G]CGTCAGGTCCTTTGG	26091
rs543529947	snp	C/T	0.00517822	0.0506191	intron-variant	HERC4	GRCh38.p7	10:68059474	AATAATATTATATAT[C/T]ATAATATTATATATT	26091
rs543551921	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67958355	ATTCAAAAAGATTTA[A/G]ATATCTCCAAAGCAC	26091
rs543587475	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68049186	TTATGCTCTGCAATT[-/A]AAAAAAAAAAATCAA	26091
rs543589800	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011022	AGTCATCCATGAAGG[C/T]TGGAATAAAATTCTT	26091
rs543600757	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011716	TACAGGCAGAGTAGA[C/T]TTAGCATAATTCCTG	26091
rs543602910	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67973575	TTTATGAATATTATT[C/T]GGCTGAGAGAGTGAG	26091
rs543630507	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67979273	CCAGATAAATTTAAC[A/G]AAGAGACTGAAATCA	26091
rs543651319	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67972445	AGAATCGCTTGAATC[C/T]GGGAGGCGGAGGTTG	26091
rs543653510	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67928646	AGTTGCCTCGGGCCA[A/G]GAGCGGTGGCTCACA	26091
rs543660409	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67935241	AACTCTGCATCCTGG[C/G]TTCAAGAGACTCTTC	26091
rs543669785	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67980604	ATACAGAAAAATACA[C/G]AATATTACAACACTG	26091
rs543674076	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67965061	CCAGGCGTGAGCCAC[C/G]ACACCTGGCCTAATG	26091
rs543683755	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68073192	TACCCTATGTCTGAG[A/G]AAATAGAAAGAAGTT	26091
rs543747026	snp	A/C	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67961590	TGGGAGGCCTCGTAG[A/C]AAATTATCAAACCTA	26091
rs543763604	snp	G/T	0.00557542	0.0525036	intron-variant	HERC4	GRCh38.p7	10:68043747	CTTGAAACCAGGAGG[G/T]GGAGGTTGCAGTGAG	26091
rs543790852	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68043168	AAGTCCCTTAAAAGT[A/G]AACAGCAACAAAAGT	26091
rs543820492	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68060983	GCTAAACTTTCTTCC[A/G]GTTGCTTTTCAGATA	26091
rs543824356	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68005198	GCTCTAACAATATCC[A/G]CTTTGTATATCTGGG	26091
rs543830222	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67967015	ACCCGCCATCATGAC[C/T]GGCTAATTTTTTGTA	26091
rs543836396	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68033055	ATACTATTGTGATAA[A/G]GGAGGGACTTAAGAG	26091
rs543856636	snp	C/G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67938180	AGGTGCTGTGGCTCA[C/G/T]GCCTGTAATCCCAGC	26091
rs543867571	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67957228	TGCAAGTATCTTTTG[C/T]TTAGCATATGTTAAT	26091
rs543872134	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68063836	CCCAGCTACTCAGGA[C/G]GCCAAGGCAAGAGAA	26091
rs543890349	snp	A/C	0.00874735	0.0655527	upstream-variant-2KB	HERC4	GRCh38.p7	10:68075395	CTTCCCGGCCCCGGC[A/C]CCGGCGCCTGCGCCG	26091
rs543892633	snp	C/T	2.0269e-05	0.00318341	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:67966785	ATACTGTATAATCTG[C/T]CCCATTTTCTCATTT	26091
rs543902094	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68019463	TACAACAGCTTATGG[A/C]AACAGTGACACCATA	26091
rs543904283	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67975674	ATTCTTAACTCACTA[A/T]ATGACTGTCCAATTT	26091
rs543920386	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68068263	ACCGAGGTGGGCAGA[C/T]CACCTGAGGTCAGGA	26091
rs543949138	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67981735	GGCCAAGGCGGGTGG[A/G]TTACTTGAGGCCAGG	26091
rs543983132	in-del	-/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68060412	CAGCTAATTTTTGTA[-/T]TTTTTTTTAGTAGAG	26091
rs544019270	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68062597	CTCTACTAAAAATAC[-/A]AAAAAAAAAAAAATT	26091
rs544105855	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67960462	GCAATCTCGTCTCAC[C/T]GCAACCTCTGCCTCC	26091
rs544156506	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069041	TATTTACAAATTATG[A/G]TCACAGAACAGTTTA	26091
rs544166078	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67987042	AGTATTCACATGAAC[C/T]ACAGACAAAGGAGGT	26091
rs544210396	in-del	-/G	0.189261	0.242509	intron-variant	HERC4	GRCh38.p7	10:68003363	ATTTTTAGTAGAGAT[-/G]GGGGTTTCACTGTGT	26091
rs544269706	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	HERC4	GRCh38.p7	10:67921874	CCCTCTTTTTGAAAA[A/G]TTTTGACTCTTATAT	26091
rs544283794	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67974189	GGACTGTCAAGTTAC[A/T]CGAGAAACGTTTGCC	26091
rs544293878	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67975058	GCCAGGCATGGTGGC[A/G]CACGCCTGTAGTCCC	26091
rs544337916	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67990083	CAAGAAAAGGAAAAA[C/T]AGGTTCATTTTTGCC	26091
rs544347008	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68030031	GTGTGAGCCACTGTG[A/C]CCAGCCATAATTTTG	26091
rs544361327	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68020003	TCATTTTTTCCTTGT[G/T]TCTTTGGGGAGCCAG	26091
rs544365060	snp	G/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68028929	TAATTCCAGCATTTT[G/T]GGGGGCTGAGGTGGG	26091
rs544372338	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67945465	CTAAATTGAGTTCTT[C/T]AGTCTGAAAGAAAAG	26091
rs544412506	snp	C/T	0.00398564	0.0444627	intron-variant	HERC4	GRCh38.p7	10:68046167	TACTTAGAAGCATCA[C/T]TTGTTTATATCAAAA	26091
rs544433692	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67953731	CTTTTGAAAAATTGG[A/T]AACTAAATAGAATCC	26091
rs544453238	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68015143	CAGTGTCTCAGTTCC[A/G]AGCCTTTGCCTCACA	26091
rs544458994	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68022907	AGATGTACAAATGGT[C/T]AACAAGTATATAAAA	26091
rs544484617	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68006900	TTGCTGCTTTTGAGA[A/T]CCTTTCTTTATCCCT	26091
rs544494481	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68008031	GCAAAACTGTGACTC[C/T]TGCCAACTCATAGAG	26091
rs544506684	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67968913	GTATAGATGATCTGA[A/G]TAACAATTTAAACCA	26091
rs544517542	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68061568	AAAAAAAAGGAATAG[A/G]TTTCTGTCAGCGAAA	26091
rs544529097	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68062428	TCTGCCTCTCTAAGT[C/T]TCCATCATCTACCTG	26091
rs544563852	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069800	GTAATCCCAGCACTC[C/T]GGGAGGCCAAGGCGG	26091
rs544573080	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68040031	TGTGAAGGCAGACTA[C/T]GTGTTTTATACCCAT	26091
rs544574596	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68030472	CAAACAAATATACAT[A/G]GCATATGATATATGT	26091
rs544583920	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67938950	CTCTGTCTCAAAAAA[A/G]CAAAACAAAACAAAA	26091
rs544591375	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	HERC4	GRCh38.p7	10:68077082	CGGTGAGCCTAGAGC[A/G]CGCCATTGCACTCCA	26091
rs544595914	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68048899	TCATCTGATAAAAAT[A/C]AAAAAGTTTGATAAC	26091
rs544599965	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68071201	TCAAGATGATATAGA[A/T]GTCACAGTGCAATCA	26091
rs544657913	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67947969	GGTGGGATTACAGGC[A/G]TGAGCCACCATGCCC	26091
rs544660760	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68038757	CTCAATTCACAGTTA[C/T]AACAATCATTACTAA	26091
rs544668386	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68039937	AGTACTGTATGTTTT[C/T]TCCTTCAGAGCATTT	26091
rs544671098	snp	C/T	0.00835141	0.0640778	intron-variant	HERC4	GRCh38.p7	10:67938075	GGCATCTTTTGTCAG[C/T]TTTGACAAAACCATA	26091
rs544713301	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68056857	AATTAAAAAACAAGA[A/C]AGTCACTGAGAAAAA	26091
rs544737615	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68063383	CAGCTAATTTTTCTG[G/T]TTTTTTAGTAGAGAC	26091
rs544752347	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68062911	TCACCAAATTAAATT[C/T]AAGCTCCTTAATTTA	26091
rs544755382	in-del	-/CT			intron-variant	HERC4	GRCh38.p7	10:67923766	CCCAGGCTCAAATCA[-/CT]CTTAAAGAGTAATGA	26091
rs544762357	snp	C/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069050	ATTATGGTCACAGAA[C/G]AGTTTAGTACTGTTT	26091
rs544769106	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68071022	TACCTTAACTCCCAA[A/C]CCAGACTCTAAATTT	26091
rs544860448	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68004255	AACAGAGTTCAACAA[C/T]TGAGTTGAAACAACA	26091
rs544862033	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67932016	AGGGTGGAATGCAGT[C/G]GCACAATCTCAGCTC	26091
rs544869167	snp	A/G	0.00279162	0.0372561	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68070017	ACTGCATTCCAGCCT[A/G]GGCAACAGAGTGAGA	26091
rs544875531	snp	C/T			missense	HERC4	GRCh38.p7	10:67923118	CCAAGAATAGGAATG[C/T]GATCACTACCTGTCA	26091
rs544904482	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68040544	TGTCACATAAAAAAG[A/T]TAATGTGTTTAATCA	26091
rs544924222	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67923339	TTTTTCTTTAAAAGT[A/G]TAATCTTAATACTGG	26091
rs544929338	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67942997	ATATGTGCTCATGAA[A/G]TATCTCTCCAGGTAC	26091
rs544946105	in-del	-/TA			intron-variant	HERC4	GRCh38.p7	10:68018906	CCACAAGGCTTTTTT[-/TA]TTTTTTTTTTTTTTG	26091
rs544967826	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67957163	GGAATGAACCCAATT[C/T]CCAATTTTAGGGGGC	26091
rs544996328	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67967050	TAGTAGAGACGGAGT[G/T]TCATCGTGTTAGCCA	26091
rs545028470	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67964206	ATCCCAACCCAAGAA[C/T]GGTATTATCAAGGTT	26091
rs545037424	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68065196	CTCAGGTGACAATAC[C/T]ATTTACCTATGCATG	26091
rs545070961	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67992459	CAAAAACCTATCAAA[C/T]AGATCAGAAAAAACT	26091
rs545075872	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68000445	TTAACTGGGTGTGGT[A/G]GCATGCACCTGTAGT	26091
rs545107533	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67964286	CCTCCTCCTCTGCAG[C/T]ATTCAACAGTCTCTC	26091
rs545108695	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67935441	TGAGTCACTGTGCGG[A/G]GCCTATGGATTTACA	26091
rs545111476	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68056310	GAGTCTATGATCTTC[C/T]TTTCCTAAGACACAA	26091
rs545134013	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67926040	GTTTCATTGTTATTT[C/T]GAAGCCAATAAGTTT	26091
rs545161820	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67970500	GGGAGGCTAAAGCAC[A/G]AGAATTGCTTGAACC	26091
rs545164259	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68023701	ATAGTTAAGGTGGTA[A/C]ATTTTGTTGTATGTA	26091
rs545184587	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:67925360	GAAAAAGAAGAAATA[C/T]GTAAGAATCACCAGA	26091
rs545215005	snp	A/G	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:68024517	CATCAGCAATAGAAT[A/G]AGTATATTATATATG	26091
rs545225514	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67977864	CACATGCCTGTAGTC[C/G]CAGCTACTTGGGAGG	26091
rs545251558	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67995044	AACCTAGTCATTTGT[C/T]CTGTACAACTTTATG	26091
rs545253601	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67941749	AGTGGTGTGATCTCT[G/T]CTCACTGCAACGTAT	26091
rs545292277	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67981926	CTCCAGCCTAGACAA[C/T]ACAGTGAAACTCCAT	26091
rs545300058	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67957618	GTGCAGTAAAATATA[A/G]AGAGTTATGAATTGC	26091
rs545321483	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67984217	CTGAGGCAGAGAATT[C/G]CTTGAACCTAAGAGG	26091
rs545366963	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68003859	GTACAGATTTCCTTT[C/T]TTTTGGGTGTATACC	26091
rs545401871	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68058714	CTGCAGCTACTCTAG[A/G]AGTTTGGCATGATTA	26091
rs545432392	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010237	AGAGCCCAGAGTGGC[A/G]ACAGAAACAGGGGGA	26091
rs545433307	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68064487	TGAACCTGGGAGGCG[A/G]AGGTTGCTGTGAGCC	26091
rs545453865	snp	A/C	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67972479	TGAGCTGAGATCGTG[A/C]CTGCACTCCAGCCTG	26091
rs545462613	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67974016	CACGCCACTGCACTC[C/T]AGCCTGGCAACAGAG	26091
rs545481591	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67947325	GAGCTAGAGAAACTA[C/T]ACTAAGACAAAACAG	26091
rs545504841	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67976524	AAAATGGAAAGCTCC[A/G]CTGATTGTCCCAGCT	26091
rs545526426	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68023555	ACAAGAGAGTATGGA[C/G]AATAGGGAGTCATTG	26091
rs545562425	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68016414	CTGGAGTGCAGTGGC[A/G]TGATCTTGGCTCACT	26091
rs545605598	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68042338	ACGAAAATCTATAAA[C/T]ACTAGGCAGGACACA	26091
rs545610976	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012542	TGGCCAGCTGGTGGA[C/G]CAGTCAGAACATAAA	26091
rs545626241	snp	C/T	1.66352e-05	0.00288398	intron-variant	HERC4	GRCh38.p7	10:67940889	TCTGTACCTTCCCCA[C/T]TTTTTACCTCCCAAA	26091
rs545630701	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68060263	AGTCTTGCTGTGTCA[A/C]CCAGACTGGAGTGCA	26091
rs545643775	snp	C/T	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:67955851	ACTTAACTAAGTGAT[C/T]ATGGTATGTGCTCAC	26091
rs545644149	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68050628	AGCTGACTTTTTAGA[C/T]ATCAAATACACAAAA	26091
rs545649623	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68019736	ACTCCTTACTCCTGT[A/G]TAATGCAGCCATGAA	26091
rs545673470	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67994206	AAATAAGCCAATTAT[C/T]CAACCTAAAATCTTT	26091
rs545687812	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67949459	CTATCAAAATACCAG[A/G]AAAGGACCTTGCACA	26091
rs545728134	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68049853	GAGGTCAGGGCTACA[C/G]TGAGCCGTGATTGTG	26091
rs545733123	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68068616	AGTGAGCTATTATCA[C/T]GCCACTGCACTCTAC	26091
rs545735662	snp	C/T	0.00795532	0.062565	intron-variant	HERC4	GRCh38.p7	10:67931831	GCAGTGGTATAATCA[C/T]GGCTCACTACAGCCT	26091
rs545743749	in-del	-/TTTA	0.401373	0.198963	upstream-variant-2KB	HERC4	GRCh38.p7	10:68076118	CTTTTCTTATTTTTA[-/TTTA]TTTATTTATTTATTT	26091
rs545780854	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68045195	GTGTGTGGTGGTGCA[C/T]GCCTGTGATCCCAGC	26091
rs545781096	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68074003	ACCCGTGGGCAATCT[A/T]TATCTATCTATATCT	26091
rs545790202	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67965705	TTGACTGACAAGAGC[A/G]CCCATCCACAAGGAG	26091
rs545800293	in-del	-/AGGA	0.00240964	0.0346267	intron-variant	HERC4	GRCh38.p7	10:67945907	AGGAATGGAATAGGA[-/AGGA]AGGAAGGAAGGAAGG	26091
rs545811630	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67927866	AAGAGGCAAAAATTC[A/T]GCCCTCATGGTGCTT	26091
rs545830109	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68043787	CACCATTGCACTCCA[A/G]CCCAGGCAACAGTGC	26091
rs545868733	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67934243	TTGTTAACATTTCTA[C/T]ATTATTCACAGTTAA	26091
rs545871978	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67935339	TTTAGTAGAGATGGG[G/T]TTTCACTGCATTAGC	26091
rs545900077	snp	A/C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67942496	ATCTGTTTTCCTCTA[A/C/T]CCCCGTTCCAGTTTG	26091
rs545935405	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67943791	AACCTTTCTTGAAAA[C/G]CCAAAGGATAAAAAA	26091
rs545963227	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68040965	TTAAAAAAATATATA[C/T]ACACACACACATTGG	26091
rs545977232	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67993188	CATCTCTACTAAAAA[C/T]ACAAAAATTAGCCAG	26091
rs545982033	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67929939	CTGCCTCAGCCTCCC[A/G]AGCAGCTGGGATTAC	26091
rs545995573	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68004849	GCATGCAGGAAACCG[A/C]TTCCATGATTCCATT	26091
rs546004535	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68074639	GGGAAAGAGAAATCA[C/T]CTGCACACACCCAAC	26091
rs546005369	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67959383	CTTGAACATAATGAA[A/G]TTTGTTTTCAGCAAT	26091
rs546009324	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68005355	ATATAAGTATAGCTA[C/T]TCCTGCTCTTTTTGG	26091
rs546018224	snp	A/T	0.0240643	0.107019	intron-variant	HERC4	GRCh38.p7	10:68059649	ATATTATATATTATA[A/T]TATATATCATATTAT	26091
rs546045319	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67929342	GCTCTTAGATGCCTC[C/T]TGTGCTACCTCCTCT	26091
rs546055934	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67967047	TTTTAGTAGAGACGG[A/G]GTTTCATCGTGTTAG	26091
rs546058681	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-5-prime	HERC4	GRCh38.p7	10:68067107	TGCTGCCATTTCTCC[A/G]TAAATTTATCCCCTA	26091
rs546059953	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68020877	AGAAAAATCAGCAAA[C/T]GTAAAGATAGGACAG	26091
rs546094956	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68066399	ATCTACCACACTGCT[A/G]ATCTTTTAAGGAAAG	26091
rs546144729	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68029034	AATAAAAAAATTAGC[C/G]AGGCACAGTGGCGCC	26091
rs546159264	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67944594	AGGAAAACATGACCT[C/T]ACCAAACGAACTAAA	26091
rs546178418	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67989032	TTAAACAATATTGTC[C/T]GAAAAGCTCTCAAAA	26091
rs546181754	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67997402	AGAGCTAAAGTTCTT[C/T]TCAATCATATCATCA	26091
rs546204231	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68052783	TGCTGCTCTCTCTGA[C/T]AACGTCTGAATTGTG	26091
rs546234836	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67952829	GGCATGAACCTGGGA[A/G]GCAGAGCTTGCAGTG	26091
rs546247953	in-del	-/TCTATAAAT	0.00597247	0.0543191	downstream-variant-500B	HERC4	GRCh38.p7	10:67921795	AAGAGACTGTGGACC[-/TCTATAAAT]TCATGTAGGAATAGA	26091
rs546262609	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67935832	TATTCTCAGCACCCA[A/G]ACTTTTGTTTTGTGA	26091
rs546267383	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68006065	AATGATAAAAACTTT[A/G]CACTTTATCATCTTT	26091
rs546296284	snp	A/G	0.00557542	0.0525036	intron-variant	HERC4	GRCh38.p7	10:67960184	AACTCTGGGCACCAG[A/G]GTTCTGGTGAGCTTC	26091
rs546324016	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67944086	CTGACTGCAGAGCCC[C/T]AGGGCCTTAAGCAAA	26091
rs546334214	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67996982	GACAGAGCAAGACTC[C/T]GTCTCGAAAAAAAAA	26091
rs546341494	snp	A/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:67951759	TTTCCAACTCCTCTG[A/T]AACACGGGCCAACTG	26091
rs546349206	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67975114	GAATCGCTTGAACCC[A/G]GGAGGCAGAGGTTGT	26091
rs546352910	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67974922	TTGGCTGGGCGCAGT[A/G]GCTCATGCCTGTAAT	26091
rs546355085	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68029772	TTGAGACAGAGTCTC[A/G]CTGTCGACCAGGCTG	26091
rs546362726	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68052567	GTCTCACATACAGGA[C/T]AGACAAGTCCAGGTT	26091
rs546465915	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68026057	ATGCGCTGCAAAAAG[A/C]GTACATGTAACCAGA	26091
rs546471848	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67982088	AAAATACCAATGACA[C/T]TGATCACAGAAATAG	26091
rs546494221	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67936316	ATTCTACCTTTCTCT[C/T]ATTTAATTAAAAAAA	26091
rs546499625	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68054809	AAATAACCAAAGGCT[A/T]CTTCACTCAAGGCAT	26091
rs546570361	snp	A/C	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68007419	TGTTTTGAATTTCTG[A/C]AAAGTCACATGGCTT	26091
rs546593994	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67997809	CCATGACCTGTGCTC[C/T]TGTACGAGGTGGAAG	26091
rs546605513	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67993439	CAGGAGGATGGCGTG[A/T]GCCCAGTTCAAAGCT	26091
rs546660178	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68014701	AGTAATCTCTATATG[A/T]ACGCACCAAAACTCC	26091
rs546673018	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68006268	TTAGTTGATTTGTTA[C/T]TGTTCATTAATGTCC	26091
rs546748929	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68022290	GGATCAACTGAGGTC[A/G]GGAGTTCGAGACCAG	26091
rs546760218	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68005799	GCCTCAACCTCCTGG[C/T]CAAACAATCCTCCTA	26091
rs546762373	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67990629	AATTTAAAAAATCAC[A/G]TGTACAAGTCTCAAT	26091
rs546807482	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922246	GTTCTCTGATCGACA[A/G]TCCCCCATCTATCAG	26091
rs546812168	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68061083	AGAACCAACAGCATT[A/C]TCGCAAAAGGTGTAT	26091
rs546837075	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68048288	CAAGACGTCCTTCAG[C/T]AGGTGAATGGATAAA	26091
rs546837764	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68020626	TACAAAAAATTAGCC[A/G]GGCGTAGTGGCGGGC	26091
rs546854230	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68038276	TATGCACATAGGTCA[C/T]ATTATTTTTTTTCAT	26091
rs546895494	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67936647	TTCCTCTATCACCCT[C/T]GTTGTAAACTTTATC	26091
rs546898159	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68000878	AGCAACTCTAAATTC[A/G]GACTTCTAGTCTGCA	26091
rs546906084	in-del	-/ATC			intron-variant	HERC4	GRCh38.p7	10:68052531	TTTTTCTGCACAAAT[-/ATC]ATTAAAAAAAAGAAT	26091
rs546921688	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069102	TCAATGTGCAAAACA[C/T]AACCATGGTCACCAA	26091
rs546933558	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68008075	GAACTTGGGTAAGAT[C/T]TGGGAGAATTCCCTG	26091
rs546940194	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68037494	TAAGTTAAACTGGTA[A/G]GAGAGGAATGCAAAC	26091
rs546952535	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67964779	TTCTTTCTTTCTTTC[-/T]TTTTTTTTTTTTGAA	26091
rs546982821	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68062517	CCCAGCACTTTGGGA[A/G]CCAAGGCGGGCAGAT	26091
rs546984230	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67932915	ATGTATGAGTAGCGT[C/T]CAAACAGGACAAAAC	26091
rs546988456	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68032302	AGCCATTGATAAGAC[C/T]GTGATCACTGTAACT	26091
rs547007694	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67960841	TGGGCATCTTCAGCA[A/T]TTTTACTTTTCTAAC	26091
rs547020393	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68061820	TTGGAGGCGGAGGTT[A/G]CAGTGAGCCGAGATG	26091
rs547022399	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069854	AAGACCATCCTGGCT[A/T]ACACGGTGAAACCCC	26091
rs547052457	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68005622	TTCTTTCCTTCCTTC[C/T]TATCTTCCTTTTTGT	26091
rs547066261	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68059168	ACTGTGTTTTTAGAA[-/T]TTTCCTAGCTTTTTC	26091
rs547078671	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68021595	GGGCAGATCACCAGT[A/G]GTCAGGAGTTCAAGA	26091
rs547095927	snp	A/G	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:67976499	GGTGGAAGAGGTGAA[A/G]CAATAGGGCAAAATG	26091
rs547109738	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069559	GGTTAAATCTATTCA[C/G]TACATTGTCAGGCCA	26091
rs547131114	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67931656	CCTGGAACTCCTGAC[C/T]TCAGGTGATCCGCCC	26091
rs547140416	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68040451	AAAACAAGGCTTCCC[A/G]TGTTCCATTTTTTCT	26091
rs547156245	snp	A/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67938395	GCAATGAGCCGAGAT[A/T]GCACAACTGCACTCC	26091
rs547166207	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68072542	CAGAGTAAATTATGC[A/G]TTTAAAATCTATCCA	26091
rs547176934	snp	A/G	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:67991405	TTACTGTTTATTCTA[A/G]ACTTTCTTAAATATT	26091
rs547195996	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68064151	TGGAGGCTGAGGGGA[A/G]TCGCTTGAGCCCAGG	26091
rs547201743	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67947355	GACTAATATGATGCA[A/T]AATTGATATGAGACA	26091
rs547207335	snp	A/G	2.7735e-05	0.00372381	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:67992623	GGGGACTAGAGTAAT[A/G]TGAAAAGCTTTGATC	26091
rs547219061	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68047736	GACAACACCAGTTGT[A/G]ATGTCAAGGATGTGA	26091
rs547309737	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67963527	TAATGTTATTTATAA[C/T]TATAAATTTGCTGTG	26091
rs547344864	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68016455	CCTCCCGGATTCAAG[C/T]GAGTCTCCTGCCTCA	26091
rs547345061	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67945868	AATCAAAACATACCA[C/T]CAGAGAAAAGTCACT	26091
rs547374469	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67977962	CTCCAGCCTGGGCAA[C/T]AGAGCCAGACCTTGT	26091
rs547466370	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68058171	ATCCAATCCATTTTA[C/T]ATCGCTCCAATAAAG	26091
rs547494527	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67994322	GTGATTGTGCCCTCT[A/G]TAAACAATTCCCTAC	26091
rs547495272	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67957208	GAGTCTATACAATCA[C/T]ATACTGCAAGTATCT	26091
rs547496065	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67983857	AATCCCAGCTACTCA[G/T]GAGGCTGAAGCAGCA	26091
rs547497498	snp	A/G			upstream-variant-2KB	HERC4	GRCh38.p7	10:68075499	AAGAGGGAAAAGCCA[A/G]ATACAGAAAGTTGGA	26091
rs547536121	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68057325	ATCATTTTGGGAAGG[A/G]CAGGGCTGGTTTTAA	26091
rs547643513	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67977302	AACATTTCTAGATAC[A/T]CAGTGGCCAGAAGGG	26091
rs547666488	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67962633	AAACCAGATAAAGAT[A/C]ATTAACTAAAAGTAT	26091
rs547679896	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67948144	GTAAACACTTAAACT[-/A]AAAAAAAAGGGAATG	26091
rs547772149	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68041695	CTGTGTGCAAAGTTA[C/T]GTGTTTCCACTTATA	26091
rs547798892	snp	A/G	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:67932965	GCTATTATTCTTTCT[A/G]TATAAAAATCAGCTG	26091
rs547818929	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67985362	AAAAAGAAGTCACAC[A/G]GTAGAAGTTCAAAAC	26091
rs547827859	snp	G/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67993810	CCCAAACTGGAAAGA[G/T]TATCTATTACCAAAA	26091
rs547843471	snp	A/G	0.000164861	0.00907764	synonymous-codon	HERC4	GRCh38.p7	10:67954646	ATACCTAAACATGCC[A/G]TATTTAGGATCCAAT	26091
rs547904599	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67957849	GTCTTGCACTGATGC[C/T]GGGGCTGGAGTGCAA	26091
rs547955814	snp	G/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010282	CACAGTGCAGTGCAG[G/T]GCAATGAGGGCTCCC	26091
rs547958047	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68001993	ACCTTTTGGCTATAA[C/T]GTATCACAATTTTTT	26091
rs547970642	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67965270	CCCTCATTTTAATAA[C/T]ACATATTATTAGCTG	26091
rs547987610	snp	A/G	0.000528175	0.0162422	intron-variant, synonymous-codon	HERC4	GRCh38.p7	10:67941067	TGCTAAGCCACAGAT[A/G]ACACCAATCAAATGG	26091
rs547992332	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68018534	AAACACGTTAAGTAT[A/G]AATAATAGAAATAAC	26091
rs548000169	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67927111	TGCTGTTAGTTGCAC[A/G]CAAGTTTGAAGAAAA	26091
rs548002852	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68025381	TAAATAAAATAACAG[C/T]AAAAAAGATGTTTCT	26091
rs548049555	snp	C/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67986421	GCAGTGGTATGATCT[C/G]AGCTCACTGCAACCT	26091
rs548057294	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67996854	TTAGCTGGGCGTGGC[A/G]GCAGGTGCCTGTAGT	26091
rs548062706	snp	A/C	0.0115144	0.0749975	intron-variant	HERC4	GRCh38.p7	10:67926427	AAAATAAAAAAAAAA[A/C]AAAACAAAAAAATTA	26091
rs548072549	snp	A/G			utr-variant-3-prime	HERC4	GRCh38.p7	10:67922444	AATTTTTAACCTTTA[A/G]AAGTCTGTTCAAGTT	26091
rs548091756	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68042382	GTAATCTCAACACTT[C/T]GGGAGGCCAAAGCCG	26091
rs548117796	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68030211	CTGGGAGGCAGAGGC[A/G]GGCAGATCACTTGAG	26091
rs548128907	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68043407	AGGTCAGAATTTGTG[G/T]AAATTTTAAAACTAA	26091
rs548129177	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68033547	AGACTTTAGCATCAA[C/T]GTTAAAAGTGAAGCC	26091
rs548141924	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67958695	TTTGTGACCATTCTG[A/G]GTATCAATTAATCAA	26091
rs548169196	in-del	-/A	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68052537	TGCACAAATATCATT[-/A]AAAAAAAGAATACTG	26091
rs548242605	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68019158	TGTGCCACCACGCCC[A/G]ACTAATTTTGTATTT	26091
rs548251727	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68059136	GAAACTGTCTTTAAA[A/G]AAAGTTAATACGTAT	26091
rs548260533	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68067771	CAAAGAATCAATGCT[A/C]ATCATCTTTAAAAAG	26091
rs548261884	in-del	-/TTGT	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:67965419	TATAACAGATTCTCA[-/TTGT]TTGTTGAATAAGCAA	26091
rs548269261	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67971514	TTTCACAATATTTCT[-/A]AAAAAAAGGAGAAAA	26091
rs548273970	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67975185	CAAGAGCCAAACTCT[A/G]TCTTTAAAAAAAAAA	26091
rs548289469	snp	A/G	0.0267878	0.112589	intron-variant	HERC4	GRCh38.p7	10:68065892	AATGTCTGTATAATT[A/G]CACACAGCATAGGTT	26091
rs548297402	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68036045	AGCGGCTGGGCACAG[A/T]GGCTCACGCCTGTAA	26091
rs548298879	snp	C/G	0.000798403	0.0199641	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	HERC4	GRCh38.p7	10:68075215	GCGACCCGGATGGAG[C/G]GGGCGGGGAAGAACG	26091
rs548309975	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67937580	ATTTCATAGAAAATC[A/G]TTTTTGTTTTTGTTT	26091
rs548379066	in-del	-/G	0.00557542	0.0525036	intron-variant	HERC4	GRCh38.p7	10:68026826	CCAGCCTGGGCGACA[-/G]AAAGACTCCGTCTCA	26091
rs548391583	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67943878	CTATGGATGGGGCCT[A/G]TAGAGTGGGAACAAT	26091
rs548406631	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67928163	GGCTCAGCAGAGGTT[A/C]ATAAGGCTGAGGCAG	26091
rs548410065	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68052315	TGAAAACACTAATGG[C/T]GCATCATTTTACCGA	26091
rs548419296	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68061172	TCAGCTACTAGTGGA[A/G]CCAAAAGCAACTTAT	26091
rs548442420	in-del	-/AAAT	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68021808	GCAAAACTCCACCTC[-/AAAT]AAATAAATAAATAAA	26091
rs548451555	snp	A/C/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68047900	CACTTATGTCCACAT[A/C/G]AACACCTGCACATGA	26091
rs548454551	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67942963	TCTGACTATTTGTGA[C/T]ACTGAAAATCAGAGA	26091
rs548483261	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67944963	AAGATCTAGAGAATC[A/G]CCTCAAAAGGGCAAA	26091
rs548499557	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922044	TTAATGGCATGAGAC[A/C]ACTAAGCATCAGCAC	26091
rs548513258	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67994510	CGATCTTGGTTCACC[A/G]CAACCTCCATCTCCC	26091
rs548545958	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67937560	TCAAATAAAAAAGAA[A/C]CAAAATTTCATAGAA	26091
rs548556914	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67974476	AAGGAATATCTGAAA[A/G]GGAACAAAATGAATC	26091
rs548608298	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67945781	AATATTGGGTTATAA[A/G]CTATTTGCAAGCCTC	26091
rs548608387	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67936768	TCTAAAAATATTACC[A/G]TTCCCACTTATGCAT	26091
rs548615169	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67928782	AAAAAAATCAGCCGG[A/G]AATAGTGGCATGTCT	26091
rs548621596	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67973839	TGGGCAGATCACAAG[A/G]GCAAGAGATCGAGAC	26091
rs548637108	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68066781	GACTGGGCATTACCA[C/T]AGTTAAGTTTCTGTT	26091
rs548641791	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67980858	TGGGTTATAAGATAG[C/T]ATCTGCAAGCCCCAT	26091
rs548651555	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67968272	TTGGCTAACTCTAAA[A/C]CATGAATGCACAAGG	26091
rs548662942	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68038943	CATCCCAGCATCTCC[A/T]TTGGTTCTTTCCCTT	26091
rs548687515	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68054521	CTAATTTTTTGTATT[C/T]TTAGTAGAGATGAGG	26091
rs548705201	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67988171	GGCAGGGAAGAACAA[C/T]AGGCAAATTAATGAA	26091
rs548727818	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67952967	CTCCCATGTACCCTT[C/G]ACTCAGTTTTCTCCA	26091
rs548741605	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67980283	GGATTACAGACATGC[A/G]CCACCATGCCTGGCT	26091
rs548783009	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67975994	CAAACTACAACCTGT[A/G]GGTCAAATGCTACCC	26091
rs548791356	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67960319	TCCCAGACTCTGCCC[C/T]GTGTGTTTCTTCCCT	26091
rs548806368	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67953957	ACATTGAGGTTTTTA[A/C]AACCAATAGCTATTC	26091
rs548822806	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68045603	GTAGCCATCAATTGA[A/C]AAATCAATAAGGAAA	26091
rs548823497	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68035067	TAACTGATTTTTTTA[A/G]GTTGAAACAACAAAA	26091
rs548890710	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67967061	GAGTTTCATCGTGTT[A/G]GCCAGGATGGTCTCG	26091
rs548894111	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67923488	GCAGTTTTGATTATG[A/G]TTTCTTTTTCTATTT	26091
rs548952558	snp	C/T	0.00401202	0.0446084	intron-variant	HERC4	GRCh38.p7	10:68000025	CGGTATGACAAGTCA[C/T]TTTTTTTTCTTTTGT	26091
rs548957402	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67931100	AAGCGATTCTCCTGC[C/T]TCAGCCTCTCGATAG	26091
rs548965452	snp	C/T	1.65021e-05	0.00287241	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67990282	GCTATTGTTGTGAAA[C/T]TGTTGGAATCACTCA	26091
rs548991077	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68058657	GCAGTGGTGCAATCT[C/T]GGCTCACTGCAACCT	26091
rs548992039	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68046601	GAAAAGGAGGTGAGA[C/T]AAAGATTGTGACTAA	26091
rs549003905	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67964259	AATTCACTGTCAATT[C/G]TAAGGTTTCATCCTC	26091
rs549006630	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	HERC4	GRCh38.p7	10:68076702	TCCCTCTTCACCTTG[C/T]TTTCCCTGTGTGTCT	26091
rs549039657	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68015363	AGCAGCCCAGTTAAG[C/G]CCGGCCAAAATTACT	26091
rs549050253	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68052269	TCATTACTTCTGGTT[C/T]TTCTTACACTTCTAT	26091
rs549058443	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67998769	TCATGATGGAGTTTT[A/G]CTCTTGTTGCCCAGG	26091
rs549093849	snp	C/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68008946	TTATACTAGCCTGGG[C/T]GCAGTGGTTCACTCC	26091
rs549147964	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67997942	AAGTCTCGCTCTGTC[A/G]CCAGGCTGGAGTGCA	26091
rs549147981	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68007219	CATGCTAATTCTTTC[C/T]TCTGCTTGATCAATT	26091
rs549168000	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	HERC4	GRCh38.p7	10:68077244	AATGTAGAATGACAA[G/T]ATGCTTAAGCAAGGA	26091
rs549182020	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68015925	ATGGCAAACATGGCA[A/G]AACCCTGTCTCTATT	26091
rs549184869	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68064218	CACTCCAGCCTGGGC[A/G]ACAGAACAAAACCCT	26091
rs549195794	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67932494	GCTTTCCTGTAAAAT[A/G]GTAGTAATAAAGTGT	26091
rs549196957	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68022317	CCAGCCTGACCAACA[C/T]GGAGAAACCCCATCT	26091
rs549211580	in-del	-/ATT	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68050574	TGACTTCAGCAATAC[-/ATT]ATTATAAAAACACAC	26091
rs549226529	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67992688	TCTTCAGAATCTGTA[A/G]TAAAAATGTAAAAAA	26091
rs549264596	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68021749	GGAGGCAGAGGTTGC[A/G]GTGAGCCGAGATCAC	26091
rs549270827	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68043385	AAAAGAACAAAAGAG[A/T]TTAAAGAGGTCAGAA	26091
rs549298787	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67982698	AGGAAATATTTGCAA[A/T]CTAATCATCTGACAA	26091
rs549304616	snp	A/C	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68040717	AAAATGGTGAAACCC[A/C]GTCTCTACTAAAAAT	26091
rs549316256	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68001010	ATTTTAAAGAAAGGT[A/G]TGCCCCTTGCCTGGC	26091
rs549344853	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68024840	TCAAAGACTCTTCTA[C/T]TTATTCCCAAGACCT	26091
rs549356549	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68056494	TGGGAAGACAGCGAT[A/G]CAATTTATTAAGTTA	26091
rs549374092	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67990002	TTATGTTTAATTGAA[C/T]TTCTATATCTAACAT	26091
rs549384798	snp	C/T	1.64885e-05	0.00287123	synonymous-codon	HERC4	GRCh38.p7	10:67955044	ATTTTCTCTACGCAC[C/T]ACTAGAATTAAGCAG	26091
rs549444186	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67961384	ACGTGCTTTCATATC[A/G]TATCTATCTTTTTTA	26091
rs549469084	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68032428	TTAGGCTGAGCTACA[C/T]GATATAAATGGGTTT	26091
rs549485895	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68072430	TTAAAATACTATGAC[A/G]GAGGGATAAAAAGAA	26091
rs549498109	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67972422	GCTACTCGGGAGGCT[A/G]AGACAGAAGAATCGC	26091
rs549524172	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68058852	CAAAAAAAAAAAAAA[A/T]TGAATGGGTAACATA	26091
rs549540176	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67931675	GGTGATCCGCCCACC[A/T]TGGCCTCCCAAAGTG	26091
rs549556215	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67983888	GAATCGCTTGAACCC[A/G]GGAGACGGAGGTTGC	26091
rs549595551	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67947632	TATAGAATACTCTAT[A/C]CAATAAAAGTAGAAT	26091
rs549612038	snp	A/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68058304	ACTTCCATGCCTAGC[A/T]CAATATCAAGGGCAC	26091
rs549637700	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67939211	TTTGCTTCTCTAAAG[C/T]ACTTCTGTAATTGCA	26091
rs549668638	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68048379	GAAAAGACATGGAAG[A/G]AATTTACTTAATAGT	26091
rs549677972	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67949544	TATCCCTTATGACTA[C/T]AGATGTGAAAATTGT	26091
rs549699637	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68000451	GGGTGTGGTGGCATG[C/G]ACCTGTAGTCCCAGC	26091
rs549701137	snp	C/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67947480	CTGACAGAATCAAAG[C/G]GAGGTATAGACAGTT	26091
rs549727950	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68016628	AGTGCTGGGATTACA[C/G]GCTTGAGCCACTGCA	26091
rs549742876	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67933805	ATATTGTCTCATCTA[C/G]TTCTCAACCCCATGA	26091
rs549762267	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010450	GCTTGCCCTTCTGGC[A/G]CCAATTACAGAACCA	26091
rs549802769	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67941946	CAGGCGTGAGCCACC[A/G]TGCCTGGCCAAAACA	26091
rs549804642	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67933200	TCAGATCATTTGACC[A/G]ACTATAGCCTTCTTT	26091
rs549814731	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67969902	GTTCCCTCTCCTCTA[C/T]CAATCTTGAAAGCAC	26091
rs549828481	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68052353	GAGGGCATCCTTCTT[C/T]GCTTCTTAAAGAAAG	26091
rs549847000	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68058456	GTCATTAGGCAAATA[C/T]GAAACAGCATAATAC	26091
rs549866321	snp	G/T	0.000233996	0.010814	intron-variant	HERC4	GRCh38.p7	10:67941144	CACATGTCCTCCAAG[G/T]TAAAATATTAAATTT	26091
rs549887776	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67977224	GGATACCAGCTCAGC[C/T]ACAGCTGGATAGGGC	26091
rs549899416	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68034646	TTGTTTACCTGACAC[C/T]ATACTTGGAAATTTC	26091
rs549913339	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67965977	CTAGTTATTAAAGAC[A/T]TAGCTGCATAAAAAG	26091
rs549972291	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68074406	ATTCTTTTGGGGTAT[A/C]AGAACTCGATAATTC	26091
rs550011830	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67982423	AAAACTGAATATCTG[C/T]ATGAAGAAGAATCAA	26091
rs550081346	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68066622	ATGTATCTACATGGC[A/G]GACTTTATACAACAT	26091
rs550191822	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67954350	ATCAGCAGAAGGAAT[A/C]GTCAACATTATTTTC	26091
rs550192388	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67959589	TTAAAATGCCATATG[A/G]ACACAAAGTAAGAAA	26091
rs550199807	snp	C/T	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:67986516	CACCACCATACCCAG[C/T]TAATTTTTTTTTGTA	26091
rs550211774	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67979915	GCATTCCAGCCTGGG[C/T]GACAGAGCAAGACTC	26091
rs550227120	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67963823	ACAAATAAATTAAAT[A/C]TCTTTTATACTGCAA	26091
rs550235997	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67985510	GTTCAAGGGTGGTTA[C/T]GGTGAGTATGTTTTA	26091
rs550253762	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67958892	TATTGTTGAGGCATC[A/G]TATAGGTGTAATGTT	26091
rs550299203	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67951965	AGTTTCTGGACCTGT[C/T]TGTTTCCAACAATCT	26091
rs550323777	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67994439	TTTTTATTTTTATTT[A/C]TTTCTTTTTTGAGAC	26091
rs550332887	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67951400	ACAAATACAAAGCCT[C/T]GAAACTCATAGGTTA	26091
rs550333138	in-del	-/GCTGTCCACA	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:67976087	CCCATCCATTTACAT[-/GCTGTCCACA]GTGGAGTTGAGAGTT	26091
rs550357342	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68005043	TTTTTCCAATGTATG[C/T]CCTTGGCGCCCTTGT	26091
rs550371271	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67993651	TACATACAGCTCTTT[A/G]TTGGCAGCTATTTGT	26091
rs550374853	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68019288	GGCGTGAGCCACTGC[A/G]CCCGGTCCAGCCAAA	26091
rs550384940	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67989191	TTTTAAACAAAACAT[C/G]CTTTAAATTGTATTG	26091
rs550410751	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67928039	GAAGGTATAAACACA[C/T]AAAGGAGGTGAGAGC	26091
rs550441106	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012038	TTTCCTTAAACTTCA[C/T]GAACTAATATTTGCT	26091
rs550447937	snp	A/G	0.00398564	0.0444627	intron-variant	HERC4	GRCh38.p7	10:67988471	ATGCCTAACAAAGTC[A/G]GGTAAGACCAGAGCT	26091
rs550459516	in-del	-/GC	0.00517822	0.0506191	upstream-variant-2KB	HERC4	GRCh38.p7	10:68075518	AGAAAGTTGGAGTTT[-/GC]GCGAAGACAAACGAA	26091
rs550463815	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68027220	ATATGAGAACATTCA[C/T]TTTTCTTTTTTTATC	26091
rs550490227	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68028539	ATCAGACTCTTCTCT[A/C]AGAAGCCCTGGTTCC	26091
rs550519605	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67951955	CTAGCCTCTCAGTTT[C/T]TGGACCTGTCTGTTT	26091
rs550526865	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67981458	TTCAACACTCCACTT[C/T]TGGCACTGGACAGAG	26091
rs550536538	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68021547	CGTGCAGTGGCTCAT[A/G]CCTGTAATCCCAGCA	26091
rs550542447	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68013542	GTTAAGTCAAATTCA[C/T]AAAGACATAAAGTAG	26091
rs550547662	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68052453	TCATCTGTGTCCTTC[C/T]AATCACCTTTGTAGG	26091
rs550584560	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67933485	GCCACAACATTTTAT[A/G]ATGCTATCTGGTCAA	26091
rs550623740	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67937227	AGGAAGGTAAGGTAT[A/T]TTAAAAAAAATACTG	26091
rs550623934	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67931586	TGTGCCACCACACCC[A/G]ATTAATTTTTGTATT	26091
rs550634287	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68051944	AAAGTGTTGAGATTA[C/T]AGGCATGAGCCACCG	26091
rs550679657	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68002158	ATATGAGCTTAACTG[A/C]AAAAGCCTTTTAATT	26091
rs550700305	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:68068484	AGAGCAAGACTCCGT[C/T]TCAAAAAAAAAAAAA	26091
rs550711425	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67928458	TCCCAAATTGTAAAG[C/T]CTCTCTCCCAAGCTG	26091
rs550712785	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67981958	TCAAAAGAAAAAAAG[A/G]AAAACTATCAAAGAA	26091
rs550724345	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68055630	GATAAAGGCACTAAG[C/T]TATAAACATTTCTGT	26091
rs550739607	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68037240	GCTGGGACTACAGGT[A/G]TGTGCCACCACACCC	26091
rs550800230	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68054803	AGAGAAAAATAACCA[A/G]AGGCTACTTCACTCA	26091
rs550854617	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67943921	CTTGGATGCCAGCAC[A/G]GCCACAGTAGAACAG	26091
rs550900559	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68014585	CTTGGGTATCACCGA[A/G]AAGTTTTAGGCTAAG	26091
rs550905602	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67987589	ATGCTAAAAGAAAGC[C/T]CTGTTCTGGGTAAAG	26091
rs550925813	snp	A/G	0.00159617	0.0282053	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069406	CAGTAGTGATAGAAA[A/G]GGACATACATATACA	26091
rs550932139	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68037770	AGGGAAAACAAAATG[C/T]TAATGGAAAAAATTA	26091
rs550946051	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67967693	ATGTTCTTGGTGATA[C/T]AGCTCAACAAGAAGC	26091
rs551004973	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	HERC4	GRCh38.p7	10:68076392	CAGGCGTGAGCCACC[A/G]GTCCTGGCCTGTTTC	26091
rs551011627	snp	G/T	0.00199481	0.0315187	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922162	TGATTGGTGCTCATA[G/T]TAGCCAATGTTTCTT	26091
rs551029667	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67967076	AGCCAGGATGGTCTC[A/G]ATCTCCTGACCTTGT	26091
rs551032664	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68006480	GGGTTCAAGCAATTC[C/T]CCTGTCTCAGCCTCC	26091
rs551052443	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67974540	CTGGTGTCCAAACAG[A/G]TGCTCAATAAATATG	26091
rs551054549	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68029360	AGCCAGGTGTGGTGA[G/T]GCATGCCTGTAGTCC	26091
rs551072767	snp	G/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68031563	TAATAAGATTGGCAG[G/T]TATAATAATCCTTCC	26091
rs551075898	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68047662	ATGTCCCATGGGAAT[C/T]ACAATTTAAAACAAC	26091
rs551115664	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67929647	AGCCTCCCGAGTAGC[G/T]GGGACTACTGGTGCA	26091
rs551161134	snp	C/T			missense	HERC4	GRCh38.p7	10:67955039	ACAATATTTTCTCTA[C/T]GCACCACTAGAATTA	26091
rs551164067	snp	A/G	0.00318978	0.0398085	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68070382	GAGGCCAAGGCAGGC[A/G]GATCACCTGAGGTCA	26091
rs551194118	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67946794	CACCTGTAGTCCCAG[A/C]TACTCGGGAGGCTGA	26091
rs551202420	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68038419	TTTAAGCAAAGTGAG[C/T]TATACTCATACCTCA	26091
rs551243651	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68061750	GCCGGGCATGGTGGC[A/G]GGTGCCTGTAATCCC	26091
rs551250236	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069899	TATAAAAAATTACCC[A/G]GGCATGGTGGCACGC	26091
rs551270045	snp	C/T	0.00557542	0.0525036	intron-variant	HERC4	GRCh38.p7	10:68015289	CCCAGCTGAGGCCAT[C/T]CTAGACTTCCAGCTC	26091
rs551287593	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67960771	CACATCCCCAGTAGC[C/T]TTTCTAGAACTACTA	26091
rs551337629	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68016597	ACCTTGTGATCTGCC[C/G]GCCCTGGCCTCCCAA	26091
rs551377356	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67992771	TTTTCACATAATCAT[C/G]TTATTTAATAAGGCC	26091
rs551384150	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67976981	ATAGTGCAGGCCACA[A/G]GGACCGCAACTACTA	26091
rs551386433	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68031796	TCACTCTTTGTCTCC[C/T]AGGCTGCAGTGCAGT	26091
rs551467945	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67948594	GGTAAACTAGTACAA[A/C]CACTATGGAAAACAG	26091
rs551469526	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67955725	CCAGTGAGCTGAGAC[C/T]GTACCACTGCACTAC	26091
rs551487418	snp	A/T	5.02172e-05	0.0050106	intron-variant	HERC4	GRCh38.p7	10:67991224	TTAAAAAAGTTTTTT[A/T]AATCATAGAATCAGA	26091
rs551487473	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67982767	TCTATAGAAAAAAAT[C/G]CAATAATCCAATTTA	26091
rs551498623	in-del	-/A	0.0785177	0.181917	intron-variant	HERC4	GRCh38.p7	10:68002175	AAGCCTTTTAATTAT[-/A]AAAAAAAACATCAAG	26091
rs551501162	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68039331	AAAAAAAAAAAAAAA[A/G]AAAGAAAGAAAGAAA	26091
rs551539621	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HERC4, POU5F1P5	GRCh38.p7	10:68009514	CTAAAAAATGCTAAC[A/G]ATCAATTGAGGCTTT	26091
rs551543838	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67957956	GGGATTACAGGTGCC[C/T]GTCACCACACCCGGC	26091
rs551548828	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67990669	CTACCTCTATAACCA[C/T]ACACAAACTTAAGCA	26091
rs551581269	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68015948	TCTCTATTAAAAATA[C/G]AAAAATTAGCTGGGC	26091
rs551581799	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67985180	GCACTCTGCATTTTC[C/G]CTAATCTAGTACTTA	26091
rs551623850	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67951593	TTGTCTAAGGAAACA[A/T]GACTGTCTCCTGAGG	26091
rs551703553	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68022413	CTGAGGCAGGAGAAT[C/T]GCTTGGTCCCGGGAG	26091
rs551703935	in-del	-/T	0.170408	0.236992	intron-variant	HERC4	GRCh38.p7	10:67986519	ACCATACCCAGCTAA[-/T]TTTTTTTTTGTATTT	26091
rs551733722	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67939444	TGTACTATGACTAGC[C/T]AGCATGTAGTAAATG	26091
rs551735229	snp	C/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010593	CGCTTTCTCTTTCAG[C/G]CCTGCACGAGGGTTT	26091
rs551754842	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68020121	TAAGAAAAGACCTCA[C/T]TTTTATACCTCAGGG	26091
rs551791432	snp	C/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67950584	CCCAGCCCTACAGGG[C/G]AGATTTAAGTAAATA	26091
rs551797147	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67947591	ACCTGAACTACATTA[C/T]AAACCAATAAGACCT	26091
rs551821261	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68017320	CCTGAAACAGAACTG[C/T]CCCAGTCAATCTCTA	26091
rs551912388	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67969946	ATACCAGTTTACAAC[G/T]GACAAGAGGAAAGAA	26091
rs551914878	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68042626	AGACTTTGTCTCAAG[A/G]AACAAACAAACAAAA	26091
rs551935377	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67972250	AAAAAGGCCAGGCAC[A/G]GTGGCTCACACCGGT	26091
rs551985831	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68032677	ATTTTTGAAATACCA[A/G]TAACACTCAAGTTAA	26091
rs551997019	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67925691	TGAATATGAGGAATG[C/T]ATGACTTCTGAGACT	26091
rs552016568	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67969554	GAGAAAGGAACAAAG[A/G]CCCGTCACCCTGCCC	26091
rs552029648	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68041469	GCAGGAATTGTAATA[C/T]ATCTTAAAATGAATA	26091
rs552040368	in-del	-/AAAA	0.00145631	0.026945	intron-variant	HERC4	GRCh38.p7	10:68018270	TTAACAGATTAAAGG[-/AAAA]AAAAATCATAAATCA	26091
rs552060164	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67932383	GAGCCACTGTGCCTG[C/G]CCAGATGAGTTTTCT	26091
rs552070918	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67942019	AGTTGCTAAATTTAG[C/T]TGTTTTACTCTCCTT	26091
rs552103933	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67994910	GGTCAGGCTGGTCTC[A/G]AACTCCTGACCTCAA	26091
rs552115162	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68058414	TAATTATGAAAGCAA[C/T]ATAGTTTCCCTACAG	26091
rs552130557	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67950581	ACACCCAGCCCTACA[A/G]GGGAGATTTAAGTAA	26091
rs552136252	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68051114	ACCAAAAAAAAAAAA[A/C]AACAAAGAAAAAACT	26091
rs552142771	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68004270	CTGAGTTGAAACAAC[A/G]GAGTTGTCTTTATAT	26091
rs552165042	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68059009	CTTCCAGGGTTTTTT[C/G]TGTATCTATAAAGCA	26091
rs552168489	snp	A/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68065843	CCAGTGACAACAAGA[A/T]CCTGTCTAAAAAAAC	26091
rs552170914	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67957294	TAAAATTGGGGGCTC[C/T]TATGTTAAATGCGAT	26091
rs552244959	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67973045	CATGAAAAAAGAATA[C/T]ACACACACATATATA	26091
rs552271580	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67948579	CACTGTTGGTGGGAA[A/G]GTAAACTAGTACAAC	26091
rs552287571	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68027385	TATTTTCAAACAAAA[C/T]AAAAAGAACTTGAGT	26091
rs552290587	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68072517	CCCCCCTCCCAAAGT[A/G]AGGTAAACACAGAGT	26091
rs552319636	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67926393	CAAGAGCGAAACTCC[A/T]TCTCAATAAAAAAAA	26091
rs552357759	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68067678	AGAAAGGCAAGCCAA[A/G]TAATCACTACTATGT	26091
rs552390626	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67958993	AAAAATGATACATAT[A/G]TATCTATTTATTTAC	26091
rs552407704	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68033485	AAAAATAAGTTCCAA[C/G]ATCCCAACTTGTTTC	26091
rs552444485	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68066710	GACCTTGGCTTGTAG[A/T]ACAGCATAGCAGTTA	26091
rs552452691	snp	G/T	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:67949794	TGGCTGAGGCAGGTG[G/T]ATCACTTGAGGTCAG	26091
rs552461913	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68060555	TAAATAATACATTCT[A/C]AATATTTCAACACTA	26091
rs552467288	in-del	-/TC	0.00398564	0.0444627	intron-variant	HERC4	GRCh38.p7	10:67964179	CCTTACCTCTAAATT[-/TC]TCTTTACAACATCCC	26091
rs552506560	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67957810	TTATAGTCTGAATCT[A/G]CATTTTTTTTTCCCC	26091
rs552554411	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67980480	AGCTGAGGAATTTTA[C/T]CAACACTAGACCTGT	26091
rs552604853	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68019345	AAGGAGTCACTTTAC[A/C]CCAAATAGAAGAAGT	26091
rs552626950	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68039175	AAAAAAAAAAATTAG[C/T]AGGTGTGGTGGCACG	26091
rs552660454	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68009366	GTGATTCTCTTGCCT[C/T]GGCTTTCCAAAGCAC	26091
rs552668876	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67995922	ATCTAAAGAACAGTG[A/G]TGCCTTGTTTCAATG	26091
rs552681996	in-del	-/ATATATATATATATATATATATATATATATATATATATA			intron-variant	HERC4	GRCh38.p7	10:67927392	ACCATATATATATAT[lengthTooLong]TTTTTTTTTTTTTTT	26091
rs552688774	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67979581	AAAAAGATATCAATA[C/T]CCAAGTAGAAGACTG	26091
rs552704457	snp	A/G	2.46442e-05	0.0035102	intron-variant	HERC4	GRCh38.p7	10:68072846	TAAAATGATATAATT[A/G]TTAAAAATAGCAAAT	26091
rs552744567	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68013041	TGTGCTTTGCTTTAC[C/T]GTGCTTCTCAGATAC	26091
rs552751992	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67977577	GGGTACCAGCTCCAA[C/T]GTAGGAGGGTGAACA	26091
rs552803026	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67934276	TGTATTCTATGGTTA[C/T]CCTTTTTCTCTTAAA	26091
rs552830794	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67973625	GAGAGGCTGGCAATA[A/G]GATTAGGATATTGCT	26091
rs552864924	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68072055	GAAAATACTGAAGTG[C/T]CATTATTGTTACAGT	26091
rs552874808	snp	A/T	0.00438332	0.0466095	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012194	TTCGGACTACTAAAA[A/T]TCTCTCCGTATCAGC	26091
rs552970099	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67995011	TTCCTTTTAATCACT[A/G]CTCGAAAAAGTTTGA	26091
rs552981394	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67928431	GTGTAGCATCCTCAG[C/T]GTTACCTTGTTTCCC	26091
rs552988697	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68051083	ATCAATTGATGATCA[C/G]TAGAAAAACCCAAAG	26091
rs553017368	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68019792	AACTTGTAGAAGCCA[G/T]GGTGGGCAATAACGA	26091
rs553021078	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68006570	TTTAGTAGAGATGGG[C/G]TTTTGCCACGTTGGC	26091
rs553043170	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67943201	AATTAATCTTTCTGT[C/G]CTGTTATGTCTTAAT	26091
rs553045380	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68025877	AATGATGTTTTCACC[A/G]TTATAAAATATTTAG	26091
rs553057640	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68013819	TGACCCACTCTCTGT[A/G]AGTAACTTTTACTTA	26091
rs553075786	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67996229	GTGAGCTGTGATCAC[A/G]CCACTGCAATCCAGC	26091
rs553084375	snp	A/G			missense, nc-transcript-variant	HERC4	GRCh38.p7	10:67992293	GCTTTGTCGGATTGG[A/G]ACATCTGAAGTCATC	26091
rs553087411	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68043612	TTGAGGTCAGGAGTT[C/G]GAGACCAGCCTGGCC	26091
rs553127147	snp	C/T	0.00119737	0.0244387	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922613	AAAAATTAAGCAATA[C/T]TTCCATGCACTCACA	26091
rs553164453	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67997450	TTATTGTCACCGTAG[A/T]AAAATAGGTAACTAA	26091
rs553185281	snp	C/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68052849	CATTATGAACACAGA[C/G]TGAAAAATTCTATAT	26091
rs553188866	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67929974	ACCACACCCAGCTAA[C/T]TTTGTATTTTTAGTA	26091
rs553194783	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68038550	GGAAAGCAAATGTAC[A/C]TTATCTAATTTGTCT	26091
rs553221916	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68060844	AGAAATTACACATAT[G/T]CTGATTGATCAACTG	26091
rs553222225	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68067993	TTTGTGTACAAGGGG[A/G]AAGACAATAAAATAT	26091
rs553224206	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67983835	GGGTGTGGTGGTGTA[C/T]GCCTGCAATCCCAGC	26091
rs553259056	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	HERC4	GRCh38.p7	10:67921545	TATGGTTCGCCAATA[A/G]TTTTTTAAGTTAATC	26091
rs553278601	in-del	-/AC	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:68038509	TTAAATCATCAGCTT[-/AC]AGTTAGAAACTTGGC	26091
rs553297396	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68056490	GTAATGGGAAGACAG[C/T]GATGCAATTTATTAA	26091
rs553298093	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68014851	CAGGGAAGTATTTCA[C/T]TGTGTACCCTATCCA	26091
rs553300659	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68045934	CTATCTTGCATTTTG[G/T]AGAGGGAGGTTAGCC	26091
rs553305051	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67954465	TTATAATTTCTCAAA[C/T]TGTAATAAAGCAGAT	26091
rs553306682	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67945263	GCAGTAGACTTTTCA[A/G]TGGAAACCTTACAGG	26091
rs553314878	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67998225	TTAAGAAACCCCAAA[A/T]GTTCTCAATAAATAA	26091
rs553320377	snp	A/T	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:67928958	TGACAATCCTGTCCC[A/T]CTGGAGGCTTAGAAT	26091
rs553321525	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68062692	ATGAACCCGGGAGGC[A/G]GAGGTTGCAGTGAGC	26091
rs553336876	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	HERC4	GRCh38.p7	10:68074721	AGGCCGGCGGCCGAG[C/G]CTTGGCAGTGCGCGG	26091
rs553338427	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67937795	AAGTGATTCTCCTGC[C/T]TCAGCCTCCCCGAGT	26091
rs553338621	in-del	-/TT			intron-variant	HERC4	GRCh38.p7	10:68018323	AACAACATTAAAAAC[-/TT]AACATCCATTCACAA	26091
rs553339430	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68053775	TATTTGGCAGTTCTG[G/T]GAATGCCCATGTCCA	26091
rs553358301	snp	C/T	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:68062369	GCTCTTTCCGTTACA[C/T]TTACTATTTATTTCC	26091
rs553360275	snp	C/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069936	AGTCCCACCTACTCG[C/G]GAGGCCGAGGCAGGA	26091
rs553395676	snp	C/T	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:68045733	AGCTTAATAAGAAAG[C/T]TATAATCATTGTCTT	26091
rs553432554	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68023170	GAATTGCCATATGAA[C/T]CACCAATTCCACTTC	26091
rs553438438	snp	A/G	0.00517822	0.0506191	intron-variant	HERC4	GRCh38.p7	10:67953478	TGTCATAGTAAGTAC[A/G]CAAGGTAGCAAGGAA	26091
rs553448076	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68040188	TAAATTTGCATAGCA[A/G]TTTATACTCAGTTAC	26091
rs553484912	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68043803	CCCAGGCAACAGTGC[A/G]AGACTCTGTCTCAAA	26091
rs553488135	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68015492	GCAAATTCTTTCAGG[A/G]TAGCTCCAAAGTCAA	26091
rs553501998	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67952440	AGGCATGTACCACCA[C/T]GCCCAGCTAATTTTT	26091
rs553504312	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67968707	AGTAAGAGTTCAAAA[C/T]AAGCATTTCCAGAGG	26091
rs553508413	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67976218	AGTCTTTAGTATTGT[A/G]CTTTAATCAACTGAA	26091
rs553518886	snp	A/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:68022549	AATAAATAAAATTCA[A/T]ATAGATCAAAGACCT	26091
rs553544328	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67953255	AAATAAGTTAGCTTA[A/T]ATGAGTATTCACTTG	26091
rs553571732	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68043618	TCAGGAGTTCGAGAC[C/G]AGCCTGGCCAACATG	26091
rs553581069	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67930359	CCAACCATCTCCAGA[A/G]TTCATTTCATCTAGT	26091
rs553641268	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67936934	GAGAAATGTAACATA[A/T]GAAGAACTAATTATA	26091
rs553652170	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68032016	CTCAGCCTCCCAAAG[G/T]GCTGGGATTACAGGC	26091
rs553654724	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68048675	GATAATGATATATCA[A/G]TGTAGATTTGTTGAT	26091
rs553657933	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67989757	ATCAGATGAGCAATA[A/C]AATCTAGTCTATAGG	26091
rs553687070	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68028391	TCCATTTTTTGCAGT[C/T]ATTATTTCTTCTCGA	26091
rs553691328	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68056564	GTGACTTGAATTCTT[A/G]TAAGAGTGACCAAGG	26091
rs553713184	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67945834	CATACGACAGATACA[C/T]GAAAAATAAAAAAAA	26091
rs553743716	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67961187	CAATGGAAGTTAGGT[C/T]GTTTAGCGCCTCAAC	26091
rs553753531	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67977620	TGGTTCTTAGATGGC[A/G]TTTCTGGACCTGTGC	26091
rs553767913	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68014975	CCATTTGTGGCATAT[G/T]GTTTATAAAAGTGGC	26091
rs553810850	snp	C/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67968114	ATGGACACAAGTAGA[C/G]GATAGAGCTCAAGCA	26091
rs553866012	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	HERC4	GRCh38.p7	10:68076897	GGGAGGCTGAGGCGG[A/G]TGGATCACCTGAGGT	26091
rs553882865	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67976310	CAATGGCTTTCCCCT[C/G]TCCAATATTTATGTT	26091
rs553896158	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67938716	TTCGGGAGGCCGAGG[C/T]GGGTGGATCATGAGG	26091
rs553904374	snp	A/G	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:68038371	AAAAAAAAAATTAAA[A/G]GGGTGAAAAGAACAC	26091
rs553941720	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67984145	CATCTCTACTAAAAA[C/T]ACAAAAAATTAGCCA	26091
rs553943156	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010142	CCCTGGCACAAACTC[C/T]GGGTTCTCTTTCCCT	26091
rs553950556	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67975553	TGGGATTTCACCATA[C/T]TGGCCAGGCTGGTCT	26091
rs553986760	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67939739	ATATATATATATATA[C/T]ACTTCTCATTCCCTC	26091
rs553993336	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68001126	GCGTAATCCCAGCAC[C/T]TTGGGACGTCAAGGC	26091
rs554019645	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67992996	AACCAAAGATGATTT[A/T]AAAAAAATAGAACAA	26091
rs554069343	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67955509	GGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC	26091
rs554080898	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68000395	ACACCCTGGGCAACA[C/T]GGTAAAACCCCAACT	26091
rs554085766	snp	A/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67978304	CCTTGGGCCTCAAGG[A/T]AACACTGGCAGTATT	26091
rs554086061	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67969617	AGCCACTGAGGAAGG[A/G]GACGCAAACCCATGT	26091
rs554089500	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67963993	GAGAAGCTTTACCTA[A/G]GTCAGAGATGAAGAA	26091
rs554106043	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68016774	TCGAAATTTTACCCC[C/T]GATCCAACAGTTACA	26091
rs554112919	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67932545	TAAAAAGGCAAGATT[C/T]CCATATATAAATCTT	26091
rs554119552	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68008392	TCTTCAGGGCAGCAG[C/T]TTCCCTTCTAGTCAA	26091
rs554143745	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68050403	AGACGCTTAGAGTAA[A/G]TAGTTAAAGCAATGT	26091
rs554145115	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68037686	ATAAACAAAAAATGA[A/C]ACCATTCACAACAAC	26091
rs554189565	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68024058	CATCTGTAAAACATA[G/T]GCCCAATAAAGAACT	26091
rs554216577	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68003737	TGTGTATATATACAC[C/T]ACATTTTCTTTATCC	26091
rs554224225	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68042090	GGTGCAATCTCGGCT[C/T]ACTGCAACCTCCGCC	26091
rs554253831	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67931487	GAGAGTGCAGTGGCG[C/T]GATCTTGGCTCACTG	26091
rs554255710	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68002884	GGATTACAAGCCTGA[A/G]CCACCGTGCCTAGCC	26091
rs554296886	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67964682	AAATTCCTAATCCTA[A/G]TTTACTAAACTCTCT	26091
rs554310428	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68050287	GAGCCAAGCTTCTCA[A/C]TGTGTATTTAAATTG	26091
rs554342201	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68017477	ATAAATTTTATGTAA[A/G]TAAGTTTATTTATTT	26091
rs554372291	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68035069	ACTGATTTTTTTAAG[C/T]TGAAACAACAAAATA	26091
rs554375319	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68065031	GGTACATCTAAATGA[C/T]GAAATGTTAATTATA	26091
rs554377317	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68057800	CACCTTCTGGGTTCA[A/G]GCAATTCTCATGCCT	26091
rs554414374	in-del	-/TTTA	0.00770489	0.061588	upstream-variant-2KB	HERC4	GRCh38.p7	10:68076115	TTTTCTTTTCTTATT[-/TTTA]TTTATTTATTTATTT	26091
rs554415882	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68064320	GCAATTTGGGATGTC[A/G]TGGCAGATGGATCAC	26091
rs554499344	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67949951	TTGAACCTGGAAGGT[A/G]GAGTTTGCAGTAAGC	26091
rs554505432	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68051179	CTTTGATAAATAAGG[G/T]CTACAAAATGTTGAA	26091
rs554527079	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67991603	TTGGAAAACAAGCTA[C/G]AGAAACAAAACAGCT	26091
rs554552063	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68066903	AACAGGCCATCAAAT[A/C]GAATGGCAGGGAAAC	26091
rs554567977	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67933399	ACAAAACGAAACTGT[A/G]AAGAAAAAAAGAAGC	26091
rs554614824	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67963370	TACAGGTGCCCGCCA[C/T]GATGCTTGGCTAATT	26091
rs554628218	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68049633	TTGGAAACTAACAAA[C/T]GAACAGGCACAGTGG	26091
rs554666190	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68027693	TTTGGGAGGCTGAGG[C/T]GGGTGGATCATTTGA	26091
rs554683930	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67958289	ACCTCCATCCTATAT[C/T]TGTGGCACTGCCTAG	26091
rs554688774	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67938449	TCTCAAAAAAAAAGA[A/C]AAAAAAAAAGAAAAG	26091
rs554692560	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67949216	TTGAACCCAGGAGGC[A/G]GAGGTTGCAGTGAGC	26091
rs554707504	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67944245	CCCCAGCTCCAGAGA[A/G]CTCAGCATAGAAAGA	26091
rs554730763	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011624	AACAGTGGGCTTAAG[C/T]CCATATTAATATATT	26091
rs554766822	snp	G/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67952215	CCTTTTACTCCCTTC[G/T]GTGTTACATTCACTT	26091
rs554767828	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68018766	CTCTATGATGAAAAT[C/T]TTAAAACATTTTATT	26091
rs554768698	snp	C/T	0.00557542	0.0525036	intron-variant	HERC4	GRCh38.p7	10:68056502	CAGCGATGCAATTTA[C/T]TAAGTTATTGAATTC	26091
rs554768806	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67943326	AATGGTATAAGTCCA[C/T]AGGAAAAAAGAGAAT	26091
rs554787347	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67934097	TTATATTCAAGCTTC[C/T]AACAACACAGTTCTA	26091
rs554790813	in-del	-/G			intron-variant	HERC4	GRCh38.p7	10:68064576	AAAAAAAAAAAAAAA[-/G]AGAGAGAGAGAGAAA	26091
rs554802229	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68073609	ATTTAGCCAACTGCA[C/G]AAACATAACCTTGCA	26091
rs554806726	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67979697	ATCCTGAAAACAGAA[A/G]GAGAAAAAAACAAGA	26091
rs554814065	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67986708	AACTATCAGGGCTGG[C/T]ATTTCAATCCTTATA	26091
rs554830751	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67935187	GTCTCGCTCTGTCGC[C/T]CAGGCTGGAGCGCAG	26091
rs554867099	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68042691	AGATACTATATGTAA[A/C]ATTTACAAAGCTGGC	26091
rs554870118	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67979144	AAATGAACAAAATAA[A/G]GCACCAAAGACAAAT	26091
rs554888375	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67997817	TGTGCTCTTGTACGA[A/G]GTGGAAGAAACATAG	26091
rs554900074	in-del	-/A	0.280953	0.248076	intron-variant	HERC4	GRCh38.p7	10:68018273	ACAGATTAAAGGAAA[-/A]AAAAATCATAAATCA	26091
rs554902452	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67951266	GCTACACCACTACAA[A/T]CTTCCCTATTTATAA	26091
rs554906622	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68043705	CCTGTAATCCCAGCT[A/G]CTCAGGAGGCTGAGG	26091
rs554931720	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67942471	CAAAAGACAGTCAAG[C/T]ATATTGCTAATCTGT	26091
rs554947753	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012322	AGAAGCCTTGCTTTC[A/G]GCCTGTCTGGGCTTT	26091
rs554966472	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67966080	TCTCCCAGGTTCAAG[G/T]GATTCTCATGCCTCA	26091
rs555055569	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67929861	CTTGTTGCCCAGGCT[C/G]GAGTGCAACGGCACG	26091
rs555081154	snp	C/G	0	0	intron-variant	HERC4	GRCh38.p7	10:67973245	TCTAGGCAGAGAGAA[C/G]AGCACCAGCTAAAGA	26091
rs555090798	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	HERC4	GRCh38.p7	10:68075331	GCGAGGGAGGCGGGG[A/G]AGGGGCTGGCCGGAA	26091
rs555099226	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68044746	CTATTCAACAAATAT[A/G]TTCCAAACGTAATTC	26091
rs555118707	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68006745	AGGATATTTTCAGTG[G/T]ATATAATATTCTGGG	26091
rs555121039	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68017444	GTTGTTTGTGCACAA[A/G]AGACCAATACAGACA	26091
rs555138763	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67972415	AATCCCAGCTACTCG[A/G]GAGGCTGAGACAGAA	26091
rs555187765	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67997051	CTGAGATAGAAATAC[C/T]GAACTCAAGCAAAAT	26091
rs555218779	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67967134	GTTGGGATTACAGGC[A/G]TGAGCCACCACGCCT	26091
rs555248182	snp	C/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68014760	TAAGAAACCACAGAT[C/G]TGAAGCTAAGGATGA	26091
rs555280306	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67967004	GGACTACAAGCACCC[A/G]CCATCATGACCGGCT	26091
rs555300020	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68028609	GTGTCCAGATTATAC[A/G]TGGTTCATCACTTCT	26091
rs555314139	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68005164	ATGCTGTAATTTTAT[C/T]GGGGTCTGTCTCTTG	26091
rs555389421	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67929025	TCTCCTTACTTTCTG[C/T]CTTCCAAAACTATTT	26091
rs555392986	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67998999	GCCTCCCAAAATGCT[A/G]GGATTACAGGCATGA	26091
rs555393544	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67981245	GCAGGAGTAGCTACC[A/G]TATCAGAGAAAATAG	26091
rs555432819	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68028896	CTTCTAGCAGTAAGA[C/T]TACAGAATGCACACT	26091
rs555440029	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68053171	GCAAATATTGAATCA[C/T]TGCCCCCGAAGAAAA	26091
rs555442560	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67936091	TGACACGTTTTCTAC[A/G]TACAGAAGAAAATGT	26091
rs555464841	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67988892	AAAAAATCACAATTT[G/T]CAAAATCATACTGAC	26091
rs555468009	snp	A/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67984563	AAAAATAAAAATATT[A/T]AAAAAAAAATGAGTA	26091
rs555479241	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67998460	GCTGAGGCAGGAGAA[C/T]TGCTTGAATCCAGGA	26091
rs555503318	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67955983	AAGTTATTAACTTAT[C/T]GTTTTAACAAAGACC	26091
rs555514233	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68061628	TCACGCCTGTAATCC[C/T]AGCACTTTGGGAGGC	26091
rs555565155	snp	A/G	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:68006517	GCTGGGATTACAGGC[A/G]CCAGCCACCATGCCC	26091
rs555570127	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68031455	TTATCTGAATGCCAA[A/C]ATCAATAAAATATGA	26091
rs555573640	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68062266	TTGCCTCTTAAAAGA[G/T]AATATTTCTCTTCTT	26091
rs555601636	snp	C/T	1.65767e-05	0.00287891	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:68014052	AGACACTGCCCATTA[C/T]AGGGGTACCAATTTC	26091
rs555606643	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67924755	CAATCCCCCATGTAT[A/G]CCAAAGGATGACTAT	26091
rs555612062	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68061489	AGTGAGCCGCAATCG[C/T]GCCACTGCACTCCAG	26091
rs555619369	snp	C/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68007502	ATGTTTTCCTGGATC[C/G]TCTTGATGCTTCTAA	26091
rs555632375	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68068993	AAACTGTTTTTTAGA[C/T]AACAGGGCTTGTTTT	26091
rs555645287	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67927134	GAAGAAAACAGCTTG[A/C]ATTCTAGCATGGAAT	26091
rs555657981	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68030434	TGACAGAGTGAGACC[A/G]TGTCCAAAAACAAAA	26091
rs555685753	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68038700	ATCCTTTTGCTTTAC[A/G]TCTAAATCAGGGACA	26091
rs555701951	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68017257	TATGTAACAAAGCCA[A/C]CCTAGCTGAAACACA	26091
rs555713534	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68056821	TAACTCAAAACGACA[C/G]AGTTAGCTATTTGCA	26091
rs555724218	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922345	GCACAAAGACACTTA[C/T]TCTAGCAAAAAAGAA	26091
rs555747844	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67983546	GCACTTTGGGATGCT[A/G]AGGTGGGCGGATCAC	26091
rs555765010	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67938022	AAAAAATTATGAACA[C/T]GCAATTTTTTTTGGC	26091
rs555802761	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68039280	AAGATCACACCATCG[C/T]ACTCCAGAATGGGCG	26091
rs555828220	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67946005	TGCTGGCTTACATAG[A/C]ACTTAGTGAGGCGGA	26091
rs555866782	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68035778	CTCTCTACCTAAACC[C/T]TTCCCTCATCTTTGT	26091
rs555905720	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67940603	TTTTGTATTTTAGTA[C/T]AGATGGGGTTTCGCC	26091
rs555949564	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68016113	GTCTCAAAAATATAT[A/G]TATATATGTGTGTGT	26091
rs555966040	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68001653	CACAATGTTGTGCAA[C/T]TATCACCACTAATCA	26091
rs555969060	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67939865	TTAGTAAAAGGTTCT[C/T]ATCACTTTTCTGAAT	26091
rs555974596	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67923318	AATTGCTCATCCACA[A/C]AATATTTTTTCTTTA	26091
rs555994650	snp	G/T	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:67927502	ACGATCTTGGCTCAC[G/T]GCAACCTCTGCCTCC	26091
rs556016239	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68048787	AACTCTTTATTTTCT[C/G]CTCAGTTTTGCCCTG	26091
rs556034118	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67930882	ATGGGGTTTCACCAT[G/T]TTGGCCAGGCTGGTC	26091
rs556061218	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67975675	TTCTTAACTCACTAT[A/T]TGACTGTCCAATTTG	26091
rs556098298	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67938608	TCTACTTCTGCCATA[C/T]CCTCATCTATCAATG	26091
rs556187602	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68008545	ACCGGTTGGGGATGT[A/G]ATCATATGGATGTGG	26091
rs556197744	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67952568	TGAGCCACTGGGCCC[A/G]GCCAAAAAAATACTT	26091
rs556218300	in-del	-/AAT	0.00438332	0.0466095	intron-variant	HERC4	GRCh38.p7	10:68022534	ATAAATAAATAAATA[-/AAT]AAATAAAATTCAAAT	26091
rs556224272	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68062845	TCCCTTTCAACCTTT[A/C]CTTTATAAATCCATG	26091
rs556259544	snp	C/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069978	ACCTGGGAGGCGGAG[C/G]TTGCAGTGAGCAGAG	26091
rs556271446	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67969501	AAGGCAGAATATCAA[A/G]AGCCTCTCTCAATGG	26091
rs556273439	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67961990	CTCTGTTTAGCTAGA[A/G]GGCAATATAAAAGGA	26091
rs556327840	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67925942	CCAATATTCTGACTG[C/T]AACTTCATGAGGGAA	26091
rs556335379	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67984200	CCCAGCTACTCGGGA[A/G]GCTGAGGCAGAGAAT	26091
rs556353813	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67948935	CACACCCTCAAAATA[A/G]ATAAATAAATACAAT	26091
rs556435246	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67949960	GAAGGTGGAGTTTGC[A/T]GTAAGCTGAGATTGT	26091
rs556436087	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67964829	CCATGCTGGAGTGCA[A/G]TGGTGCAATCTAAGC	26091
rs556448803	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67993054	TAAAAATCAAGAGTA[C/T]TTATTCTTGGCGAGG	26091
rs556457545	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68003769	TGTCTGTTGATGAAC[A/T]CTTAAATTGATTCCA	26091
rs556505047	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67926492	AAATAGTTTATACTG[G/T]GAACTGTTCTTATCC	26091
rs556505822	in-del	-/AC	0.147656	0.228091	intron-variant	HERC4	GRCh38.p7	10:67996313	AAGACCTTGAAATAG[-/AC]ACCCCCCCTGCCCCA	26091
rs556536912	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68001199	AACATAGTGAGACCC[C/T]GTCTCTACAAAAAAA	26091
rs556544014	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67979027	CACACAAGTCCAAAC[C/T]GCGAAGACTACAATA	26091
rs556547730	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68033796	AATGAATAAAGGATA[C/T]TTTGTATCTTCCCAC	26091
rs556550322	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67986753	TGCATATGGGATAAA[C/G]AAAAAGACTTCTTCA	26091
rs556591330	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67995111	TCCTAACATTTGGCT[C/T]GGTCTTCTGTTCTGT	26091
rs556606499	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68072683	TAAGGTTTTATAATA[C/G]TAGTAGTAAAAAAAA	26091
rs556620094	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68024221	GAAATGTATATTCAA[A/G]TTATGAAATAACAAT	26091
rs556636850	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68035206	CGCCCAGGTTGGAGT[A/G]CAGTGGCGCAATCTT	26091
rs556658752	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67949397	CAAACTCTTCCAAAA[G/T]ATCACAGCAGAGGGA	26091
rs556761960	in-del	-/C	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68042809	CCTTTTATAAAAAAA[-/C]ATTTCCACTGAAATA	26091
rs556769337	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68059218	GTATATATTTGTCTA[C/T]TTCCCTCAAAAGCCA	26091
rs556884724	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67987548	AATCTTCTTAGTAAC[A/T]GTTTACTGCAGACCT	26091
rs556901980	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68017622	CTCCCCAGAAGCTGG[A/G]ATTACAGGTGCATGC	26091
rs556911210	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68052708	ATTCATATAGAGTAT[A/C]ATCAACTCCAATTCA	26091
rs556911500	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67969432	TGTCCATAGATGCCA[C/T]TGGGTGCCCATGAAA	26091
rs556917432	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67935538	TATAGACTTTCAGCA[C/G]TTAATCTCCCTGTTT	26091
rs556947056	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68043511	TTCATGCTGTTAGAG[A/T]TTTTAATATTAAAAC	26091
rs556957973	in-del	-/AACC	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:68065459	GGCCAAGAAAGGCTA[-/AACC]AAAATTCTGCCATGC	26091
rs556965212	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67934227	ATTTTTGGTTCAATA[C/T]TTGTTAACATTTCTA	26091
rs556981581	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67927607	ATTTTCGTATTTTTA[A/G]TAGAGACGGGGGTTT	26091
rs557026467	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67942341	AATAAATGTCAGTTA[C/T]TCTTCCTAGCTAGTA	26091
rs557057856	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68004439	CTTTGGTTGCCTGTG[C/T]TTGTGGGGTATCACT	26091
rs557101351	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67936838	CTTTTATGAAAACCT[A/G]CTATTTATAAAATAC	26091
rs557113758	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67929103	TTTCTATTTTTATTC[A/C]ATTTCTGTCATTCTA	26091
rs557141848	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67973368	TAAGCTGACCTCAAC[C/T]GTCTCTAGGTTAGCC	26091
rs557145055	snp	A/G	0.0377219	0.132053	intron-variant, synonymous-codon	HERC4	GRCh38.p7	10:68070550	GGCAGAGGTTGCGGT[A/G]AGCCGAGATGGCGCC	26091
rs557148797	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67924308	TCATGTGTCACTTAA[C/T]GATGATGATATGTTC	26091
rs557164417	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67928265	GCTGTTATATCATTT[C/T]CATTTTAAGGTGATT	26091
rs557206890	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67980360	CTGGTCTCGAACTCC[C/T]GACCTCAGGTGATAC	26091
rs557208213	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68074644	AGAGAAATCATCTGC[A/C]CACACCCAACCTCGC	26091
rs557217997	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68044939	AAAGAAGAAATCATT[C/T]AAATAACCTGGGCTG	26091
rs557237143	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67975724	CATTGTACAAATAAT[A/C]CAATTTAAAAAGCAC	26091
rs557244738	in-del	-/C			intron-variant	HERC4	GRCh38.p7	10:67984563	AAAATAAAAATATTA[-/C]AAAAAAAAATGAGTA	26091
rs557280196	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67981769	TCAAAACCAGCCCAG[A/T]CAACATGACGAAACC	26091
rs557287456	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67960487	GCCTCCTGGGTTCAA[G/T]CGATTCTCCTGCCTC	26091
rs557294884	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67952375	TGCAACCTCCGTCTA[C/T]TGGGTTCAAGCGATT	26091
rs557303180	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68005994	CAGGCTTGCAAACAA[C/T]ATCTTAACTGATGAC	26091
rs557310054	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67950327	TGTCCCCAGGCTGGA[A/G]TGCAGTGGCATGATC	26091
rs557325002	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68060689	CATTCAACTTCCTAA[C/T]TGAAAATATGAATAG	26091
rs557334872	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67987476	AATCTAATTAATCTC[A/T]TGAATCCTCGGCAAA	26091
rs557349265	in-del	-/A	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68036765	TCTCCAATTATTAAT[-/A]AAAAAATTAATCTTT	26091
rs557355048	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67967215	TTTTCTTAGCTATTT[G/T]TTTCTTCCTACAAAA	26091
rs557381589	snp	G/T	0.00517822	0.0506191	upstream-variant-2KB	HERC4	GRCh38.p7	10:68076086	AAGAAGTTCCACAAA[G/T]AGGCCATCTTTCTTT	26091
rs557410115	in-del	-/T	0.00636936	0.0560724	intron-variant	HERC4	GRCh38.p7	10:68059845	TTATATATTATAATA[-/T]ATTATATATCATAAT	26091
rs557416138	in-del	-/CAAAAA	0.00517822	0.0506191	intron-variant	HERC4	GRCh38.p7	10:68030438	GAGTGAGACCGTGTC[-/CAAAAA]CAAAAACAAAAACAA	26091
rs557440143	snp	A/C	0.00914312	0.0669923	intron-variant	HERC4	GRCh38.p7	10:68046982	AAACAAACAAACAAA[A/C]AAAAAAAAACATGAA	26091
rs557492838	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67975504	ACAGGTGCCCACCAC[C/G]ATGCCCAGCTAATTT	26091
rs557496827	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68030180	TGCAGGATTACACAC[C/T]TGTAATCCCAGCATT	26091
rs557500675	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67955233	AGGTATTCTATAATT[A/C]CTATGCTACTGAATT	26091
rs557518320	snp	A/G	0.00279162	0.0372561	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	HERC4	GRCh38.p7	10:68075274	GGTGGGGAGAGTTGG[A/G]GAAGAGACTGGGTAG	26091
rs557611004	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68013526	AGGTACCTAGCCTAG[C/T]GTTAAGTCAAATTCA	26091
rs557624834	snp	G/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67960988	CACTTTCTTGCGGAT[G/T]TGGCGGACCTGTTGG	26091
rs557631493	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68055956	GGGGTTTCACCATGT[C/T]GGACCAGGCTGGTCT	26091
rs557642007	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67944515	AGACTGTGAAGACTA[C/T]AATAAATACCTAACT	26091
rs557660452	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68026028	CTTTTCAAGGTAGTT[A/C]CTGCCTTACATAAAT	26091
rs557668234	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68062647	TGCCTGTAATCCCAG[A/C]TACTCAGGAGGCTGA	26091
rs557728123	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67997313	TTTATTAAAATAATA[C/T]TCTATGCTTTATGTT	26091
rs557773038	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67956781	CAAAGTACTTTGTGT[A/T]CCTTCATTACTGATC	26091
rs557776041	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67975000	TCGAGACCAGCCTGG[C/T]CAAGATGGTGAAACC	26091
rs557777636	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68021803	ACAAGAGCAAAACTC[C/T]ACCTCAAATAAATAA	26091
rs557779238	snp	C/G	1.65422e-05	0.0028759	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:68014085	TTTACAGTAAAGGGG[C/G]TTTTCCTGTTGCTTG	26091
rs557786830	snp	C/T			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68010926	AGCAATTCAGTCACA[C/T]TTTCAGGCTTTAGTT	26091
rs557800485	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67991602	TTTGGAAAACAAGCT[A/G]GAGAAACAAAACAGC	26091
rs557816012	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68021367	TATCAAATTAACAGA[C/T]TGAAGGAGGAAAAGA	26091
rs557840789	in-del	-/AAAAAATGAATGAGAAATGAATGAG	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68002422	GGTTTCAGGTTGTCA[-/AAAAAATGAATGAGAAATGAATGAG]AAAAAATGAATGAGA	26091
rs557883078	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68052886	TTGTGGAAAACGAAA[A/G]CTACAAAAAGAGAAA	26091
rs557905727	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67946535	TTAGACAAAACAGAT[A/G]CAAGACAAAAACTAT	26091
rs557914013	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67999136	ACCTGGTATGTTAGA[A/T]CTCAAGATTATTAAG	26091
rs557926247	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68016179	TGAACAGAACTACCT[C/T]AAGCTCTAGATTTGA	26091
rs557932807	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67982185	AAAAGAACAAAACTG[C/T]GAGGAATCATATTAC	26091
rs557948724	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68045063	GCTGGCTCACGCCCA[-/T]TAATACCAGCATTTT	26091
rs557963061	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67954365	AGTCAACATTATTTT[C/G]TGGCTAACCATCTCT	26091
rs557976351	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67946949	ATAAATATGCACCCA[C/T]ACTGGACTGCCCAGA	26091
rs558001749	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67981936	GACAACACAGTGAAA[C/T]TCCATCTCAAAAGAA	26091
rs558022834	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68062318	CTAATGAATATACTA[A/C]TCTATAGCTAATGAT	26091
rs558059041	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67924560	ATAATCTTACAGGAC[A/C]ACTATCGTATATATG	26091
rs558076925	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67984021	TGAAGTACTATTCTG[A/G]CCAGGCTTGGTGGCT	26091
rs558086742	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68014883	GAGATGGTTTTACTG[A/C]GGGGACATGGCATCT	26091
rs558087573	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67969535	AAGGAATTAGCTGCC[A/G]CATGAGAAAGGAACA	26091
rs558092223	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68031538	TGAAATTACTTTTGC[A/G]CCAACCTAATAATAA	26091
rs558117255	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68073294	TAAACATTAAATATA[C/T]TTTATAACATGCTAC	26091
rs558145774	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68040289	CTACAGAGACCAGAA[G/T]TATATTCTTCTGCGT	26091
rs558164145	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67931283	GCCACCACACAGGGC[A/C]AGCACTTTCTATTAA	26091
rs558190036	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68031983	TCTTGAAGTCCTGAC[C/T]ACAGGTGATCCACCT	26091
rs558233614	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68039311	ATAGAGTAAGACCCT[C/G]TCTCAAAAAAAAAAA	26091
rs558247259	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68002815	AAGTTGGCCAGGCTG[A/G]TCTCAAACTCCTGAT	26091
rs558259591	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68051505	GCCCGCCACCATGCC[C/T]AGCTAGTTTTTTTTT	26091
rs558271718	in-del	-/TA	0.031825	0.122064	intron-variant	HERC4	GRCh38.p7	10:68049083	ACCTCTGTGTATGTG[-/TA]TATATATATATATTT	26091
rs558309897	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67926121	TAGTACTGGCCGGGC[A/G]CGGTGGCTCACGCCT	26091
rs558345571	snp	A/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67963124	TTACTCTGCTTTCTC[A/T]TCATACATATTTATG	26091
rs558359323	snp	A/G	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:68064276	AGAAAGAAATAGGCC[A/G]GGTGCCGTGGCTCAG	26091
rs558399638	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68063271	CTAGAGTGCAATGGC[A/G]TGATCTCAGCTCACT	26091
rs558402661	snp	C/T	0.000798403	0.0199641	intron-variant, missense	HERC4	GRCh38.p7	10:68070593	CCTGGGAAACAAGAG[C/T]GAAACTCTGTCTCAA	26091
rs558409520	in-del	-/A	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68029179	AGACCCCCATCTCAG[-/A]AAAAAAAAAGTTACA	26091
rs558415580	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68050228	CAAGCGTAGTTACTT[A/G]GAAGGGATATAGGCA	26091
rs558447831	snp	C/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68022933	TAAAAATATGCTCAG[C/G]TCACTAATCATTGGG	26091
rs558448207	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67925040	GAATAATACTATAAT[G/T]AGATTCCAGTCTCAT	26091
rs558468702	in-del	-/AT	0.0433465	0.140692	intron-variant	HERC4	GRCh38.p7	10:68059604	ATATTATATATCATA[-/AT]ATTATATATCATAAT	26091
rs558483293	snp	C/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67957646	TGCCAGTCACACATT[C/T]TTGTAGTTGGAGGAC	26091
rs558506395	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67931709	GGATTACAGGCATGA[A/G]CCATCGCGCCTGGCT	26091
rs558559152	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67948009	AATACACTCTTAAAC[A/C]ACCAAAAGATCAAAG	26091
rs558570093	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67924108	ATACAGTTGGCCCTC[C/T]GTATCTGTGAGCTCT	26091
rs558580906	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68072762	ATGGAAATACATAAC[C/T]TCTACTTTGCTTTTA	26091
rs558591034	snp	C/T	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:68001390	AAAAAAAAAAAATTC[C/T]TCTTGTTTACCCATG	26091
rs558610951	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68056884	AAAATAACCAAAATC[G/T]GGCAACTGGGTCAAT	26091
rs558617941	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67956824	CAAATATTTACTGTC[C/T]AGAAACATCAAAGAA	26091
rs558621828	snp	A/C	0.000799041	0.019972	intron-variant	HERC4	GRCh38.p7	10:67993957	TCAAGGAAATGACCA[A/C]ATGTTAATTTCCTTG	26091
rs558649430	snp	C/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68063650	CTAAATAAATAAACA[C/G]AGGTAGGTCAGGCGT	26091
rs558685526	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67963878	ATTTGCATTTAAAGA[C/T]AGAAAATTAGCCTCA	26091
rs558700970	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67964917	AGCTGGGATTACAGG[C/T]GCCCACCACCATGCC	26091
rs558701240	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67951445	TCCATATGGCATTGT[C/G]GGATGCCCTCAAGTC	26091
rs558704137	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67937971	ACAGACGTGAGCCAC[C/T]GTGCCCGGACAGAAA	26091
rs558747775	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67943054	ATGTTTTTCTTAAGT[A/G]TTTGTATTTGAATTC	26091
rs558762865	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67950913	TTCCACTTAAAGAAG[A/T]CACGGCTCTTAAGAA	26091
rs558763570	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67941305	TAGCATATTTTCTCA[A/G]ACTTAAAAAAAATAT	26091
rs558771756	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67994494	CTGGAGTGCAGTGGC[A/G]CGATCTTGGTTCACC	26091
rs558792439	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67978490	TAAGGTTTTTCACTC[C/T]AGTCCCTGGCTCCCA	26091
rs558807250	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68025819	TTAACAGACAGATGG[C/T]TCTTTCAAAGTAAAA	26091
rs558823109	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67958144	ACTATGCATCATTTA[C/G]TCTTTGCTTTGCCCC	26091
rs558856561	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67942572	GCTGGAGTGCAATGA[C/T]GCGATCTTGGCTCAC	26091
rs558866804	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67995403	AGGATTAATGCTTGA[A/T]CTATTACAATTATTT	26091
rs558893106	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68051445	TGCCTCCCGGGTTCG[C/T]GCCATTCTCCTGCCT	26091
rs558919788	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68062995	ACATCTCAATTACAT[A/G]GACTACTCTTCCCTT	26091
rs558931066	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67990134	AGGGCAGCAGAACTG[C/T]AAATGGCAAAAGAAC	26091
rs558945635	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68026457	TAAAAAAAACTCCCT[A/G]TAAAAACATATAACT	26091
rs558955298	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68004596	TGTATTCGTCTGTTT[C/T]CATGCTGCTATAAAA	26091
rs558956831	snp	A/T	0.00716266	0.059414	intron-variant	HERC4	GRCh38.p7	10:68038513	ATCATCAGCTTACAG[A/T]TAGAAACTTGGCAAT	26091
rs558986355	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010732	CTCAAAGAGGCAGAT[A/G]GTCGTTTGGCTGAAC	26091
rs558992135	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67979969	AAACCTGTCTGAGAA[A/G]AAAACAAATAACATA	26091
rs559025024	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68017780	AGGCATGAGCCACCA[C/T]GCCCGGCCTATGTCA	26091
rs559051880	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67975420	TTTTTTTTGGACAGA[C/G]TCTTGCTCTGTTGAC	26091
rs559055358	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67946022	CTTAGTGAGGCGGAG[A/G]TAGGCAGATCACTTG	26091
rs559090042	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68005117	CTCTGTTCTGTTCCA[C/T]TGGTCCATGTGTCTG	26091
rs559091472	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67965194	GGCTGCTCCTTGTCA[C/T]TCAGATTAGTACTCA	26091
rs559110008	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68059984	CTATTATAATAATTT[G/T]GTTTCTTTTCTTCCA	26091
rs559119481	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68005527	TGGGCAGTTTAGTCC[A/G]TTTACTAAATGTTAT	26091
rs559133723	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68018449	CTGAAAGTTTTCCCA[C/T]AGAAAGGAAACATTA	26091
rs559158736	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012567	CATAAACATTTATCA[A/G]TTAGGTTTGTTGTCT	26091
rs559166272	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68043030	AAATTCTCTTTCAGG[C/T]CCCCATCCAGGTTCA	26091
rs559173588	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67973423	AACAAGGCCCAATCC[C/T]GTAGGAATTAGAATA	26091
rs559184483	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67985596	AGATCAGCACAAATA[A/T]GTAGCGACTAGGCTA	26091
rs559215948	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68063231	TATTTATTTTTTTAG[C/T]TGGAGTCTCGCTCTG	26091
rs559246892	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011978	CATGCTAGACAACTT[A/G]CTGTAGCATATACAT	26091
rs559247748	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67999626	AGAAACAGACATTTC[A/G]TGAAACTGCTAACCC	26091
rs559281078	snp	C/T	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:67995928	AGAACAGTGATGCCT[C/T]GTTTCAATGTGTATG	26091
rs559285854	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67928706	GGCGAGTGGATCATG[A/C]GGTCAGGAGTTCAAG	26091
rs559293451	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68037156	CTGGACTATAGTGCC[A/G]TGATCTTGGCTCACT	26091
rs559302291	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011583	CAGTATTTTGAAAGA[A/G]ATCTTTTTACTGAGC	26091
rs559305068	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67972591	CAAATAATTGGAAAA[C/T]AAAAATTTTAAAAAT	26091
rs559305493	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68049773	AAAATTAGCCAGGCA[C/T]GGGGGCAAATGCTTG	26091
rs559345569	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68026871	GTTAGGCATGGTAGT[A/G]GGTGCCTGTAGTTCC	26091
rs559376203	in-del	-/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67988984	ATATCTTATGTAACA[-/T]TTGTAAGGTTTATAA	26091
rs559381812	snp	C/T	0.000836645	0.0204358	intron-variant	HERC4	GRCh38.p7	10:68059681	TATTATATTATATAT[C/T]ATAATATTATATATT	26091
rs559399337	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68020537	TTTGGGAGGCCGAGG[C/T]GGGCAGATCACGAGG	26091
rs559413399	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68074019	TATCTATCTATATCT[C/T]TGAGACAATTATTTA	26091
rs559416535	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68043794	GCACTCCAACCCAGG[C/T]AACAGTGCGAGACTC	26091
rs559424598	in-del	-/ATA	0.029116	0.117091	intron-variant	HERC4	GRCh38.p7	10:68059921	ATAATATTATATATC[-/ATA]ATATTATATATTATA	26091
rs559450251	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68073310	TTTATAACATGCTAC[A/G]TAAGTATCATTCAGT	26091
rs559462293	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67936325	TTCTCTCATTTAATT[A/T]AAAAAAACTACTAAA	26091
rs559466140	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67928688	AGCACTTTGGGAGGC[C/T]GAGGCGAGTGGATCA	26091
rs559559592	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	HERC4	GRCh38.p7	10:67921998	ATTATAGCAGAAAGT[C/T]ACATGTATTGCATCA	26091
rs559602251	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67951168	CAAAACATTATCTCT[C/T]TAAAACTGACTAAAG	26091
rs559602419	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67959387	AACATAATGAAATTT[A/G]TTTTCAGCAATTAAA	26091
rs559632935	in-del	-/TACCG	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67950983	TAAACCTGGAATGTT[-/TACCG]TACCAAATGTAAGGA	26091
rs559642947	in-del	-/AC	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:68043308	CTCTTTTCATCCTAA[-/AC]ACAGTTTTTTAAAAA	26091
rs559650775	snp	C/T	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:68019842	TGGTGCCCTGATCAA[C/T]GATTGGTGCTTCTGA	26091
rs559651806	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:68021429	AGCACTTGCTTTTCC[C/T]GTAAGATCAGGAATA	26091
rs559664500	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67958654	TATATTAGAAGTGAG[A/G]AAGATAATCATACAA	26091
rs559680519	snp	A/T	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	HERC4	GRCh38.p7	10:68067174	TTTTGAAAGGAACCA[A/T]GAGTTATTGTGTAAT	26091
rs559732033	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67953926	AGCCAACCTCCAGGC[A/G]GAATGATTAAATATT	26091
rs559764440	in-del	-/T	0.00795532	0.062565	intron-variant	HERC4	GRCh38.p7	10:67966857	CTCAAGACAGACAAA[-/T]TTTTTTTTATTTTTT	26091
rs559792536	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67952925	AAAAAAAAAAAGACA[A/C]CTAAATTGCACAAAT	26091
rs559807041	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67996729	GTGGCTCACACTTGT[A/G]ATCTCAGCACTTTGG	26091
rs559810461	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68004749	TTCTTCACAAGGTGG[C/T]AGGAAGAAGTGTCGA	26091
rs559810556	snp	G/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68061674	ACTTCAGGTCAGGAG[G/T]TCGAGACCAGCCTGA	26091
rs559849308	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68061143	CATATATACAACTTA[C/T]AGTTAAAATTACTTC	26091
rs559863028	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68055512	AGGAATACAATTAAC[C/G]TATATAAAGAGCTTA	26091
rs559901740	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67992055	AGGTGTGCACCACCA[C/T]GCCCAGCTAATTGTA	26091
rs559925051	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68036401	CAAACAAAAAGGTCA[A/G]TATGAAAAACTGTCC	26091
rs559925128	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68000795	AAGGAATGCCAAAGA[C/T]TGACAGCAAACCACC	26091
rs559944897	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68020885	CAGCAAACGTAAAGA[C/T]AGGACAGTTGCAATT	26091
rs559945313	snp	A/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:67930919	TCCTGGCCTCAAGTG[A/T]TCTGCCTGCCTCAGC	26091
rs559953113	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	HERC4	GRCh38.p7	10:68075454	GGCTGGCCACAGGCG[C/T]CTGCGCAGTGTGCCG	26091
rs559968572	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67960542	AGGCATGTGCCACCA[C/T]GCCTAGCTAATTTTG	26091
rs559985255	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67967224	CTATTTTTTTCTTCC[C/T]ACAAAAAATAATTAC	26091
rs559986711	snp	C/G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67971688	ACATTTAACATTATA[C/G/T]TTACTATTAAGATAT	26091
rs560002506	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67946634	CAAATATAGGCCAGA[C/T]GCAGTGGCTCACACC	26091
rs560032901	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67967289	GCTATGGGAGACACA[A/G]AGATTTGTAAGATGT	26091
rs560056777	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67974352	GAAAAACCACCAAAG[A/T]AACAAATAAAGTTGA	26091
rs560091665	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67998711	TATGCCAGTAGTTCT[C/T]AAAAGGGGATGTTCT	26091
rs560098062	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68054431	CAATCTCAGCTCACG[A/G]CAACCTCCACCTCCC	26091
rs560117956	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67981837	TCCCAGCTTCTTGGG[A/G]GGCTGAGACATGAGA	26091
rs560118237	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67944349	AAGACCAGGACAGTA[C/T]CTCTTAGTTTGCAAG	26091
rs560178405	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67976676	AAAGTCTTGAATCAC[A/C]AACATCACCCCTCTC	26091
rs560198102	snp	A/G	0.00398564	0.0444627	intron-variant	HERC4	GRCh38.p7	10:67999230	CATAAGAGTCACTGA[A/G]TTCCTTGAAAATAGG	26091
rs560226458	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67973984	CCCGGGAGGCAGAGG[C/T]TGCAGTGAGCCGAGA	26091
rs560232604	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67960220	CTAGAAATACTCTGT[A/G]TTGTTACACATCTAT	26091
rs560256722	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68045770	ACTAAAAGTCTTATG[C/T]TGAAAGTGGTTAAAA	26091
rs560291147	snp	A/C	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67969083	AATGGAATTAAACTA[A/C]AATCAGTAACAGAAA	26091
rs560305428	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68070081	AAAACAAAAACCTCC[C/T]GGGAAATGAACTATG	26091
rs560313147	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:68006339	AGTACAGGTCTGCTG[C/T]TGATGAAACGCCTCA	26091
rs560331112	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67930258	CTTTAAAAATTAAGG[C/G]AAAACACACATACCA	26091
rs560331811	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68023002	CGTATTAAAATAGGT[A/C]TTATAAAAAAAAAAA	26091
rs560343441	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68030651	TATTTAACTCATGGA[C/T]ATTTGGATTTCTTCT	26091
rs560351208	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68000894	GACTTCTAGTCTGCA[C/G]AATAGTGAGCCAATA	26091
rs560383703	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67937383	TCTGAGAAAGAAATG[A/G]CAGTGGGAAGAAATG	26091
rs560431578	snp	A/C	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68038895	CATTTTTAAAACATT[A/C]CAAAACTCAATTAAC	26091
rs560448236	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68049070	TGTTCTACAGATATA[A/C]CTCTGTGTATGTGTA	26091
rs560482669	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68003759	TCTTTATCCATGTCT[C/G]TTGATGAACACTTAA	26091
rs560492247	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67998635	CTGGCACAACCTTAC[C/T]GCTCTAATTCTCACT	26091
rs560492278	snp	C/T			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011684	GTCATCCAGGCTTTG[C/T]TGTTCCATTTATAGA	26091
rs560519637	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67925485	ATCAAAAGTCTGACA[C/T]GGAATTATCTGTGAT	26091
rs560532712	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069858	CCATCCTGGCTAACA[C/T]GGTGAAACCCCGTCC	26091
rs560544525	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67961371	TACTGAACACAGCAC[A/G]TGCTTTCATATCATA	26091
rs560561363	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68042055	GGAGTCTCGCTCTGT[C/T]GCTTAGGCTGGAGTG	26091
rs560562197	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68015327	GATCATCAACTGATC[A/G]TCTAAGTCAGCTAAG	26091
rs560580669	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67947160	CATTTCATCCAGCAG[C/T]TGAAGAATACACATT	26091
rs560584522	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68031667	CTTGAGTTCACTATA[C/T]TTGACAATAACGAAG	26091
rs560598515	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68009095	CAGGTGTGGTGGTGC[A/G]CACCTGAAATCCTAG	26091
rs560621560	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67948249	AAACTAAATATTAAA[A/G]CAGTGATAAATGTAT	26091
rs560676315	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68056901	GCAACTGGGTCAATG[C/T]TGGTGCTACGGGAAA	26091
rs560713915	in-del	-/ATT	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67954310	AAAGTTAATCTGGTG[-/ATT]ATTATTCAATCCTCA	26091
rs560741221	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68048297	CTTCAGTAGGTGAAT[C/G]GATAAACTGTGGTAC	26091
rs560743427	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68071382	TCAGTAGACCTAAGT[A/C]ACTATACTGGCAATT	26091
rs560749122	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67956118	AGGTTTTTAATTTTT[A/T]AAAATATTTTTAGAC	26091
rs560760494	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68025261	GAAAAAAAGGTGGAA[A/G]AGAGAAAGAAAGAAG	26091
rs560762314	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68063744	GGAGTTTGAGACCAG[A/C]CTGGTCAACATGGCA	26091
rs560770953	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68064786	GACCACCCTGGCCAA[A/C]ATGGTGAAACCTTGT	26091
rs560777202	snp	A/G	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:68025891	CGTTATAAAATATTT[A/G]GACACTGAAGAGATA	26091
rs560799875	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68040704	GACCAGCCTGGCCAA[A/C]ATGGTGAAACCCCGT	26091
rs560800953	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68063063	ATACTATCTCTACAC[A/G]GCACTCTTGTTTATA	26091
rs560809754	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67940192	TGGCCTCCCAAAGTG[C/T]TAGGATTACAGGCGT	26091
rs560831649	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67993171	CCAATATAGTGAAAC[A/C]CCATCTCTACTAAAA	26091
rs560836639	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68056392	CTTCTATGTGCACCA[C/T]AGTATTTCACTGTGG	26091
rs560854886	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67977971	GGGCAATAGAGCCAG[A/G]CCTTGTCTCAAAAAA	26091
rs560865818	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68024694	GATAAAACTAAACTA[C/T]TGTATAGCTATACAT	26091
rs560874152	in-del	-/A/AA	0.10953	0.20704	intron-variant	HERC4	GRCh38.p7	10:67938447	GTCTCAAAAAAAAAG[-/A/AA]AAAAAAAAAAAGAAA	26091
rs560875279	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68026667	GCTAAAAAGGTGAAA[C/T]CCTGTCACTACTAAA	26091
rs560900465	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67950977	ACAAGATAAACCTGG[A/C]ATGTTTACCGTACCA	26091
rs560902270	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67941936	GCTGGGATTACAGGC[A/G]TGAGCCACCGTGCCT	26091
rs560915695	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010369	TAGGAAAGGACACTG[A/G]TGCCCCTGAGAAAGG	26091
rs560927588	snp	C/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67964566	CTCATGGATTTCCGT[C/G]TTTCATTTCTGTCCC	26091
rs560942817	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67937931	CAGTGATCTGCCCGC[C/G]TTGGGCTCCAAAAGT	26091
rs560948701	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68054551	GTTTCACCATGTTGG[C/T]CAGGCTTGTCTCAAA	26091
rs560955845	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68059434	GTTTTGTTTCTCTCG[C/T]TATTATAATAATATT	26091
rs560964132	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67950264	GCCTGAAGACTCCAT[A/G]GATACATACAGGGGA	26091
rs560986722	snp	G/T	0.00398564	0.0444627	intron-variant	HERC4	GRCh38.p7	10:68072381	ATGAGAGGAATAAAA[G/T]ATATTTCTAACTAAA	26091
rs561005842	in-del	-/T	0.242775	0.249896	intron-variant	HERC4	GRCh38.p7	10:68047929	AATGTTTTGTTTTTG[-/T]TTTTTTTTTTTGTGA	26091
rs561012443	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67994059	GCAATTGTTATCTAG[A/G]TTATACCAAAAATGA	26091
rs561063224	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67971696	CATTATACTTACTAT[G/T]AAGATATTGAATGCT	26091
rs561065364	in-del	-/TTTTTTTTTT	0.00874735	0.0655527	intron-variant	HERC4	GRCh38.p7	10:67929819	ACACCCAGCTGTGCA[-/TTTTTTTTTT]TTTTTTTTTTGAGAT	26091
rs561080946	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68058235	TTAAAATTTTGGCAT[A/G]GTCTTTGAATAAGAG	26091
rs561091595	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68042474	ACAAAAAATACAAAA[C/T]TGGCCAAGCATAGTG	26091
rs561113756	in-del	-/AT			intron-variant	HERC4	GRCh38.p7	10:67953053	TATATTGCTATCTAC[-/AT]ATATATATATATATT	26091
rs561160357	snp	C/T	5.22899e-05	0.00511294	utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68073155	TAAAAAATTCTCTTC[C/T]GAAACCCCGGAAAGT	26091
rs561195390	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67978598	GCCACCTGGTGATTG[C/T]AGAGCGCCAGCACCT	26091
rs561197121	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67960237	TGTTACACATCTATG[A/C]CAGGAAAGTAATTCA	26091
rs561213652	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67928011	AGATCAGTTATCCAG[A/G]GAAGGTCTCTGAGAA	26091
rs561242500	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67994836	GAGTAACTGAGATTA[C/T]AGGCGCCCACCACCA	26091
rs561247705	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67926198	TCAGGAGTTCCAGAC[C/T]AGCCTGGCCAACATG	26091
rs561260174	snp	A/C	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68033481	CATGAAAAATAAGTT[A/C]CAAGATCCCAACTTG	26091
rs561267640	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67957213	TATACAATCATATAC[C/T]GCAAGTATCTTTTGC	26091
rs561302958	snp	C/G	0.00755907	0.0610114	intron-variant	HERC4	GRCh38.p7	10:68001530	TTTTTATCCTATACA[C/G]CTTGAGTACAGTGCA	26091
rs561327178	snp	C/T			utr-variant-3-prime	HERC4	GRCh38.p7	10:67922025	ATCAACTCACTTTTA[C/T]AATTTAATGGCATGA	26091
rs561330436	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68003981	CCAACTGTATACAAG[C/T]GTTCCCTTTTCTCCA	26091
rs561349262	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HERC4	GRCh38.p7	10:67966597	GTTCTGAAAAAACTT[G/T]CTCATTTCAAAACCA	26091
rs561368719	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68003279	CTTGCACAGCCTCCC[A/G]AGTAGCTGGGACTAC	26091
rs561412438	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67973509	TATGGCAAAAGTTGA[C/T]ACATGGGGAAATAAG	26091
rs561413920	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67933755	AACATTTACTGAGCA[A/C]TACATGTGCTAGTTC	26091
rs561414404	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67957719	CCTGCCCTGACTCAG[A/T]GCCCCTGCTATGAGA	26091
rs561423335	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68027097	AAATCTGTGATAACA[C/T]AATCACAATTAGTAT	26091
rs561436517	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68010963	CTCTTGTTATTTCCA[C/T]CATATCTATAGTTAA	26091
rs561456400	snp	G/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67965426	GATTCTCATTGTTTG[G/T]TGAATAAGCAAATGA	26091
rs561470497	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67964962	TATTTTTAGTAGAGA[C/T]GGGGTTTCACTATGT	26091
rs561505124	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67927980	ATACGTGTGCAGGAG[A/G]GAGGTTTGCAATTTT	26091
rs561521556	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67980056	GAGAGAATGGCATGA[C/T]ATTTAAAGTATTGAA	26091
rs561522309	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67997579	TATCCCCCACCCAAA[A/T]AGATCTGTTTGAAGC	26091
rs561535898	in-del	-/C	0.117232	0.211832	intron-variant	HERC4	GRCh38.p7	10:68070799	TCTCAGGATCAGGAC[-/C]CCCCCCCTTCTACAA	26091
rs561554713	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67967797	TAGGAAATACAAGGG[A/G]TAGAGGAACAAGTTA	26091
rs561558097	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67934599	CTTCCTGAGAAAAAG[C/G]CATCAGAAGTAAACT	26091
rs561569437	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67947902	CACCATGTTGGCCAG[G/T]CTGGTCTCGAATTCC	26091
rs561590465	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68066602	TGCATCTTAGAGAGA[G/T]ATGCATGTATCTACA	26091
rs561606607	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68043112	CTCTCCTTATAATTA[A/G]CTTTCTTTCCATTTA	26091
rs561611602	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68006157	AAGTTGCTGTAGTTA[C/T]TATTATCTTTGATCC	26091
rs561641160	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68019175	CTAATTTTGTATTTT[C/T]AGTAGAGACAGGGTT	26091
rs561656216	snp	A/C	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67980554	AAACATTAATGGGCA[A/C]TAACAAATCATCTAA	26091
rs561661648	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67996002	TCTTTCTCTATCTGA[A/C]AGTGTCCTTAAAATT	26091
rs561680311	snp	A/C	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68074133	GTAGAACTTTCCAGC[A/C]CACTGACTGAATATT	26091
rs561698167	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68029938	AGAGACAGAGTTTCA[A/C]CACGTTGGCCAGGAT	26091
rs561756628	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67979330	GAGCTGAAAAAATGT[A/G]ATTGACATACCGAAG	26091
rs561781753	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HERC4	GRCh38.p7	10:68074888	GCATCCGCCCAGCCC[A/G]GCCTGCCCCTCCCTA	26091
rs561783022	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67953467	CTGGAACATTCTGTC[A/G]TAGTAAGTACACAAG	26091
rs561784523	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68028090	CCATTATTTCATCAG[A/G]GAGTGTAAAATGGTG	26091
rs561814038	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67960093	GGGCTTGGGCCATGT[A/G]CTGTCAGTTCTGCTT	26091
rs561818906	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67944669	TTTCAGTCAGACAGA[G/T]AATTCAAAATAGCTG	26091
rs561838135	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68013109	CATAGAACAAGTCTA[C/T]CAGCACCATTTTTCC	26091
rs561843970	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68019643	AGTCTATGCACGGTT[A/T]GTTATTTCCAAGAGA	26091
rs561868584	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68068082	GCTGCCACAGTAGCT[C/T]ATCCCTATAAATCCC	26091
rs561886817	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68045321	GACAGAGCCAGACCG[A/T]GTCTCAAGATAAAAA	26091
rs561907054	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67930091	GATTACAGGCGTGAG[C/T]CACCGCGCCCGGCCC	26091
rs561948900	snp	A/C	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67982308	TTGTTTCTAGAGAAC[A/C]TAGAAACAAATCTAC	26091
rs561950199	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67997937	AGACAAAGTCTCGCT[C/T]TGTCGCCAGGCTGGA	26091
rs561952337	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68052328	GGCGCATCATTTTAC[C/G]GAGGAGAAAGAGGGC	26091
rs561955812	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68056180	ATATAGTTGCTTTAG[A/T]TCAATTTCTTTCAAA	26091
rs561955936	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68051781	TGCAACCCCGCCTCC[A/G]AGGCTCAAGTGATCC	26091
rs561958023	snp	C/T	0.00517822	0.0506191	intron-variant	HERC4	GRCh38.p7	10:68061722	CGTCTCTACTAAAAA[C/T]ACAAAAAAATTAGCC	26091
rs561960690	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68060949	CACAAATGTCTTCTA[A/G]TAATGTATAGGTAAA	26091
rs561961723	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67957283	CAAATTTGTTCTAAA[A/G]TTGGGGGCTCCTATG	26091
rs561995217	snp	A/C	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67951918	CTTCAATATCCAGAC[A/C]AAAAAAAATGCATAC	26091
rs562001268	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67948991	AGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCAGC	26091
rs562015642	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68009003	AGGTGGGCAGATCAA[A/G]TAAGGCCAGAAGTCT	26091
rs562016098	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67989933	TATACTAAAGGCGAT[A/G]AGGGAAAGGAATACG	26091
rs562028436	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67962324	GATTTTCTCCTTAGC[C/T]AAACAATGAAATATT	26091
rs562028786	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68046895	CCCAAGCAGTTGAAG[C/T]TACAGTGAGCTGTGA	26091
rs562050305	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67976938	ATGGTGGGCTAAAGT[G/T]CTCTGGGGCCCTCAA	26091
rs562055777	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67938701	CTGTAATGCCAGCAC[C/T]TCGGGAGGCCGAGGC	26091
rs562084809	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922099	TTAAATTCAAGGAAA[C/T]AGCTCTAAAGCACTG	26091
rs562139460	snp	A/G	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:67959870	ATGCTCAGAGCACAG[A/G]CTCGTGTAAAGCACC	26091
rs562156227	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68056277	TGTAGCTGATGGTGA[A/T]CAAGTTCATTAAAAC	26091
rs562156530	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67936357	TTGAGATAAAATTCT[G/T]CTACCATATAGCTTA	26091
rs562162217	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67946740	GGTGAAACCTCATCT[C/T]TACTAAAAATACAAA	26091
rs562186284	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67981866	GAATCACTTGAATCG[C/G]GGGGGTGGAGGTTGC	26091
rs562243582	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68055598	ACACCATGAGGAAGT[C/T]ATCCTTAAGCTTCAC	26091
rs562268784	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67968219	AGGAATCCAGAGGAC[A/G]AAGCCCCAAAATCTA	26091
rs562299444	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68007263	CCTCTGATGCATTCT[A/C]CAGGTTGTCAATTAC	26091
rs562311815	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67948622	CAGTGTGGAGATTCC[C/T]TAAAGAACTAAAAGT	26091
rs562337910	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68014440	TTTTAAACAGCCTGG[G/T]TCTATACTGAAATCC	26091
rs562416583	snp	A/C	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:67975014	GCCAAGATGGTGAAA[A/C]CCCGTCTCTACTAAA	26091
rs562429434	in-del	-/CTGT			intron-variant	HERC4	GRCh38.p7	10:68058333	ACAGCAGGAAGACAA[-/CTGT]CTGTTGAATAAATGT	26091
rs562435582	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67938901	GTGAGTTGAGATCAC[A/G]TCACTGCACCCCAGC	26091
rs562440943	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67996711	TTTGACTGGCCAGGC[A/G]CGGTGGCTCACACTT	26091
rs562444976	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68007775	GGCTATTCAAAGGCA[C/T]GATCCCACTACTGAT	26091
rs562445277	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68000433	AAATACAAAAAGTTA[A/T]CTGGGTGTGGTGGCA	26091
rs562484440	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67961228	GTCAGCTTGAATTTT[C/T]AAAATGCAATTTCAT	26091
rs562512964	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67924314	GTCACTTAACGATGA[C/T]GATATGTTCTGAGAA	26091
rs562553356	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67976867	AAAACCCAGCCCTAG[C/T]CAGAGGGGAACTGTG	26091
rs562592522	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68032564	TATCATCACATATAA[C/T]AGTATATCAGAATTC	26091
rs562606351	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67968243	AAATCTATGTGCAAA[C/T]TCCCCCCACATCCTT	26091
rs562625181	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67962373	TTTTTACTACTACAT[A/G]TAAGTAGATATAGAT	26091
rs562627287	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67969716	AGAATCTTATATCAG[C/T]AGGACTAGAGGTCTG	26091
rs562690367	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67969306	ACTACTGTCATATAA[A/G]CAGAAGTAATACACT	26091
rs562753484	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68063953	TCAAATAATAATTAA[G/T]AAACAGAGGCTGGGC	26091
rs562795565	snp	C/T	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:67931105	ATTCTCCTGCCTCAG[C/T]CTCTCGATAGTTGGG	26091
rs562808752	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67993309	GAGATCACCCCACTG[C/T]ACTCCAGCCTGGGCC	26091
rs562830184	snp	C/T	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:68035377	TGGCGAGGCTGGTCT[C/T]GAACTCCTGACCTAG	26091
rs562835650	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68071239	GTCAACATGACCACA[A/G]AGAAGCCTATTCTAG	26091
rs562843461	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68038060	TATCAAGTAATAAAA[C/G]TGAAGAGAAATAAAA	26091
rs562846072	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68001581	ACAATTTTTTATCAT[A/G]AAATATACATAAAAT	26091
rs562882241	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68041382	AACTGACCTACTCTA[C/T]ACCATTAAAAACTAC	26091
rs562894354	in-del	-/A	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68049263	TATCCATTGGGGAAG[-/A]AAAAAAAATAAGATG	26091
rs562896708	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68025999	CACGAAACCTAAAAA[C/T]GGTATCATCTTCACT	26091
rs562933024	in-del	-/GAAA			intron-variant	HERC4	GRCh38.p7	10:67990492	CAGGAAGAAAAGAAA[-/GAAA]AGGAAAATTTTGCAC	26091
rs562947307	snp	A/G			intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069059	ACAGAACAGTTTAGT[A/G]CTGTTTCTAACATGA	26091
rs562984084	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68023584	TGTTTAATGGGTATA[C/G]AGCTTCAGTTTTGCA	26091
rs562992456	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68024920	AAGAACTCAGAATAA[A/G]GAGAATTAGGAGATT	26091
rs563010932	in-del	-/ATA	0.087305	0.189817	intron-variant	HERC4	GRCh38.p7	10:68059682	ATTATATTATATATC[-/ATA]ATATTATATATTATA	26091
rs563015817	snp	C/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68015929	CAAACATGGCAAAAC[C/G]CTGTCTCTATTAAAA	26091
rs563016785	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67986061	ATGATACAAATAAAT[C/T]GTCCCTCGTAGTTCA	26091
rs563037916	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68070355	CTCATGCCTGTAATT[A/C]CAGCACTTCGGGAGG	26091
rs563042099	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67940755	AGCCAAATTTAGTCT[C/T]TCAATAGAAAATTTT	26091
rs563048053	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67977739	CTAATCCCAGCACTT[C/T]GGGAGGCCGAGGCTG	26091
rs563077441	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67985073	TAAAAATAATATATT[C/T]GCATAGTAGATAAGG	26091
rs563107291	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67940267	TTAATGCATTTTATT[C/T]AATAAAAATAAATTT	26091
rs563122043	in-del	-/AAGATCAAAGAAGAAATCACAAGGGAAATTAGAAAATACTTAAGAG	0.171704	0.237423	intron-variant	HERC4	GRCh38.p7	10:67948014	CTCTTAAACAACCAA[lengthTooLong]AAGATCAAAGAAGAA	26091
rs563130662	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67949447	ATGAGATCATCACTA[C/T]CAAAATACCAGAAAA	26091
rs563163089	snp	C/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68057953	CAATCCGCCTGCCTT[C/G]GCCTCCCTAAGTGCT	26091
rs563172544	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68018992	AGCCAAAGCATTCTT[A/T]CTTTTTTTTTTTTTT	26091
rs563173266	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68049234	CATTGTTATGAAAAG[A/T]TCCCCAGGATATATT	26091
rs563201086	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68057170	CTCACAGTCAAGCAC[C/T]GTATAACAGTGGGTA	26091
rs563202071	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010217	CCTCAGTTTGAATGC[A/G]TGGGAGAGCCCAGAG	26091
rs563217338	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67943964	GTTCCTTAAGGTTTC[C/T]GACTCCAAGCCCTGG	26091
rs563222206	snp	C/T	0.00914312	0.0669923	intron-variant	HERC4	GRCh38.p7	10:68033298	GACATATTTTTCTTA[C/T]GCAAAACAAGGTATT	26091
rs563222722	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68064472	AGCAGGAGAATCATC[C/T]GAACCTGGGAGGCGG	26091
rs563238009	snp	C/G/T	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:68052133	AAGTGGAAAAAATTG[C/G/T]CTTCTGAATTCATTT	26091
rs563280311	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67970854	TGTTTCTGCTTTAAG[A/T]ATCTAGAAAAAAAAA	26091
rs563286378	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68062536	AGGCGGGCAGATCAC[A/G]AGGTCAGGAGTTCGA	26091
rs563296410	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68020546	CCGAGGCGGGCAGAT[C/T]ACGAGGTCAGGAGAT	26091
rs563303011	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67933619	ACCAAGTTTTTTTTT[A/G]AAACAAGGATATCTA	26091
rs563313552	snp	C/T	0.00517822	0.0506191	intron-variant	HERC4	GRCh38.p7	10:67934672	ATTTGATAATTTGGA[C/T]ACAGAATTCTAAGTT	26091
rs563335199	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68034257	TTGAAAATAATCATT[G/T]CATTTCAAATTTCAT	26091
rs563352339	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68043191	ACAAAAGTTTAAGTA[G/T]GAGAATCATCAGACT	26091
rs563367089	snp	G/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011050	CTTCCAAACTCTTAT[G/T]GTTGGTATTTTGACT	26091
rs563373671	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68042327	TGATTACTCTTACGA[A/G]AATCTATAAACACTA	26091
rs563378582	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67932828	TAAAAATCATGTATG[A/C]AGAATCCATAATGTA	26091
rs563389080	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68065825	CGATTTAACCACTGT[A/C]CTCCAGTGACAACAA	26091
rs563418955	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68063424	TACACAGGCCAGGCT[A/G]GTCTTGAACTCCTGA	26091
rs563430298	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67958513	GAAAAACATAGCAAC[C/G]AACAAAATGCAAATC	26091
rs563497957	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67965619	CGTGCACTAACCAGA[C/T]TGCCATTCAAAAACT	26091
rs563503305	snp	A/G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67943555	AAGACTCTAAAAGGC[A/G/T]GAGGTATTAGAGTGG	26091
rs563512543	snp	G/T	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:68066374	CTAAGTACCCAAATT[G/T]TAAAACCAAATCTAC	26091
rs563524313	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68073879	TAATTTTAAAACTAA[A/G]TCAATGTGCATAATT	26091
rs563582748	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67928647	GTTGCCTCGGGCCAG[A/G]AGCGGTGGCTCACAC	26091
rs563612130	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67956602	AGTAAACTAGTAAAA[C/T]GGTTTATAAAGATTG	26091
rs563643406	in-del	-/TTAT			intron-variant	HERC4	GRCh38.p7	10:67923516	TTTGCTTCGTTTCTG[-/TTAT]TTTTTTTAAATCAGA	26091
rs563646232	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67935271	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGAACTAC	26091
rs563668101	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67987114	CTATCAAGATGTGAA[A/G]ATTCTAGTATTTAGA	26091
rs563690356	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68028930	AATTCCAGCATTTTG[G/T]GGGGCTGAGGTGGGA	26091
rs563729103	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68026701	GCAAAAAAATAGCCA[A/G]GCATGGTGGCACAGA	26091
rs563734850	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67942753	TGACCTCAGGTGATC[C/T]ACCCGCCTCGGCCTC	26091
rs563739758	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67995787	CTCATATCTTCTTGT[C/T]TTAAGAAGTATTTAC	26091
rs563810554	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68004837	ATTACAAGAACAGCA[C/T]GCAGGAAACCGATTC	26091
rs563815972	in-del	-/ATCTTGAAAAG	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67934874	CTTCTCGTGCTTTCA[-/ATCTTGAAAAG]ATGTCATTCGTTTCT	26091
rs563833710	in-del	-/ATATA			intron-variant	HERC4	GRCh38.p7	10:67927426	TATATATATATATAT[-/ATATA]TTTTTTTTTTTTTTT	26091
rs563850583	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67970699	TTGGAGCTAGGAAAC[A/G]GGGGCTTTAGGAAAA	26091
rs563912697	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67973604	AGGTATAGTCAAGAA[C/T]AAGTAGAGAGGCTGG	26091
rs563943197	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67998334	AGGCAGATCACCTGA[A/G]GTCAGGAGTTTGAGA	26091
rs563955029	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68028200	TTACCTAAAATACAA[C/T]TTGCAAATGAAAGGC	26091
rs563957206	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68008102	CCTGGATTACTAGGC[A/G]GAGTCTCTTGTTCTT	26091
rs563976630	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67945161	AAGATATTTAATAAT[A/C]AAACTCCCAAAGGTC	26091
rs563979555	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67980627	CAACACTGTAATTAT[A/G]GTGTGTAAACTACTC	26091
rs564004935	snp	A/G	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:67987965	CCATAGGTTAGAAAC[A/G]TACGCTTCTCCCTTA	26091
rs564067029	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68067505	GTGTGGGATAATCTG[G/T]TATTTTTATTTTTAA	26091
rs564069784	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68005252	TATTTACAACTGTTA[C/T]ATCCTCTTGTTGTAC	26091
rs564070890	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67974207	AGAAACGTTTGCCTC[A/G]GAGACATAACTGACA	26091
rs564071400	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67952629	GGAGGCCGGGCGCGG[C/T]GGCTCACACCTGTAA	26091
rs564125831	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68061022	TCTGCTCTTTAGGAC[A/C]GCTTTTAGCCTCACC	26091
rs564147265	in-del	-/GT	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68037898	CCCAAATTCCTAGCA[-/GT]GTGTGTGTGTGTTTG	26091
rs564159421	snp	C/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67945557	AAAACAGAATATTAT[C/G]ACACTCTAATTGTGG	26091
rs564162891	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68068287	GTCAGGAGTTCGAGA[A/C]CCCCCTGGCCAACAT	26091
rs564184307	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68021551	CAGTGGCTCATGCCT[A/G]TAATCCCAGCACTTT	26091
rs564219602	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67953758	ATCCTTTCCTATGAA[C/T]TGCACTACTAAGGAA	26091
rs564228721	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68006961	TGAGGTAGTCTTATT[G/T]GGGTTAAATCTGCTT	26091
rs564250509	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67947358	TAATATGATGCAAAA[C/T]TGATATGAGACAAAT	26091
rs564284369	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68046197	ACATTCCCATAAATC[C/T]TAATTATGAAGAAGT	26091
rs564367940	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68045433	ATTAGATATGGTGAG[G/T]AGAGAACTGAAAGGC	26091
rs564369796	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68054282	AACACTGGTTTTTTA[A/T]AATTTTTTTTTCTTT	26091
rs564373051	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68030473	AAACAAATATACATG[A/G]CATATGATATATGTT	26091
rs564389653	in-del	-/CAA	0.0123036	0.0774623	intron-variant	HERC4	GRCh38.p7	10:68035141	TCCTGGTTCCTCTTT[-/CAA]GAGACAACCACTCTT	26091
rs564407545	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68053172	CAAATATTGAATCAT[G/T]GCCCCCGAAGAAAAT	26091
rs564412391	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67997671	TATTAAAATTAGGCT[C/T]TATTTTTTTAGTATC	26091
rs564421274	in-del	-/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:67978912	GAACCACAGCACTAC[-/T]TGGGTGTGGGGTGCC	26091
rs564460025	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68015156	CCGAGCCTTTGCCTC[A/T]CAAGTGGCTTTATAC	26091
rs564504406	snp	A/C	0.00438332	0.0466095	intron-variant	HERC4	GRCh38.p7	10:67932882	TACAATTTCTGCTAC[A/C]TATCTACGAAACTGA	26091
rs564505096	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67931585	GTGTGCCACCACACC[C/G]GATTAATTTTTGTAT	26091
rs564521458	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68008731	ACCTGTACACCTACA[A/T]CCATAGCAGCATTAT	26091
rs564537475	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	HERC4	GRCh38.p7	10:68076456	GAACTGTCTGTGCTA[C/G]AATATGTTCAAGTGT	26091
rs564540589	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68062936	AATTTATTTCTACAA[G/T]CTGACCTCAATTTTG	26091
rs564559727	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68038788	TATGTTAAGTCTTAT[C/T]TTCTTCTGTCTTGTA	26091
rs564574429	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67930206	ACATCTAAGTTGTTT[C/G]CAGTTTTTCACTCAT	26091
rs564574884	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67975061	AGGCATGGTGGCGCA[C/T]GCCTGTAGTCCCAGC	26091
rs564595141	snp	C/T			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012128	GAGTTAGAATCTTGG[C/T]CTGGATTAGACTTTG	26091
rs564596740	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67979803	TTAGCCGGGTGTGGC[A/G]GCGGGCACCTGTAGT	26091
rs564632544	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67955458	GTAAAGAGGGAGGAG[A/C]AAAAACAAACCTTTA	26091
rs564633174	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68048208	TACAGGCATGAGCCA[C/T]CACACCCAGCCCACA	26091
rs564661288	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67946800	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAAG	26091
rs564671969	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67968279	ACTCTAAACCATGAA[C/T]GCACAAGGCACAAAG	26091
rs564696565	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67999648	TGCTAACCCAAGGTC[C/T]AGCAGAATAAGAATT	26091
rs564720651	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68055685	TTAATATTCAAATAT[A/G]ACATAGTTATGTTTC	26091
rs564725944	snp	C/G	0.00318978	0.0398085	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68070033	GGCAACAGAGTGAGA[C/G]TCTGTCTCAAACAAA	26091
rs564778065	snp	A/G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67925361	AAAAAGAAGAAATAC[A/G/T]TAAGAATCACCAGAA	26091
rs564811403	in-del	-/G	0.000347501	0.0131769	intron-variant	HERC4	GRCh38.p7	10:68044399	TTTCTGGTCACCTTT[-/G]TTACCTGGGTACTCT	26091
rs564836773	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68000486	CAGGAGGCTGAGGTG[C/G]GAGGATCGCTTGAGT	26091
rs564867194	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67983759	ACCACTGCACTCCAG[C/G]CTGGGCAACAGAGGA	26091
rs564868483	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68031813	GGCTGCAGTGCAGTG[A/G]TGTGATCTCAACTCA	26091
rs564878878	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67993136	GATCATTTGATGTTA[C/G]GAGTTCGACGCCAGC	26091
rs564935205	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68057642	AAAAAAAAAAAAGTA[C/T]AACTAAGTATATTTA	26091
rs564936812	snp	G/T	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:67969737	TAGAGGTCTGCAATT[G/T]CTGGGGGAGGGAGCA	26091
rs564960902	in-del	-/T	0.226484	0.248892	intron-variant	HERC4	GRCh38.p7	10:67934966	ATTCTTTCAAATGAG[-/T]TTTTTTTTTTTCCAT	26091
rs564985639	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68024776	AAAAAGGTACATTTT[G/T]CTACTTGGGAGTCTG	26091
rs564993232	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68064537	CCAGCCTAGACAATA[A/G]GCAACAGAGTGAGAT	26091
rs565004308	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67993474	TATGCTATGACTGCA[A/T]CTGTGACTAGCCACT	26091
rs565015271	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68032279	AGACAGTGAGAGGTC[A/G]GAGTTAAAGCCATTG	26091
rs565020000	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68028712	TGAGTTCATACTAAC[A/T]CTTGCGATTCAAAGT	26091
rs565024251	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67956402	ATGGTGACCAACCCC[A/G]GGAACATGTTTAATA	26091
rs565083415	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67963406	ATTTTTAGTAGAGAC[A/G]GGGTTTCGCCATATT	26091
rs565093879	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67949463	CAAAATACCAGAAAA[A/G]GACCTTGCACACGCA	26091
rs565129941	snp	C/T	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:67986219	CCTGCTTTTGACTTT[C/T]GTAACTACTGCAAAC	26091
rs565131042	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68003205	TCTGTCACCTAGGCT[C/T]GAGTGCAGTGGCTCA	26091
rs565147896	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67931983	TTGTTTTTGAGACAG[A/T]GCCTTGCTCTGCTGC	26091
rs565153811	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68058050	AAAATCAATGATCAA[A/T]CTAACTTCCATCACG	26091
rs565235274	snp	A/C	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67950092	AGTATCTCCAATATT[A/C]TTTTATGATAAAAAT	26091
rs565362941	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67964263	CACTGTCAATTCTAA[A/G]GTTTCATCCTCCTCC	26091
rs565384643	snp	C/T	0.00119737	0.0244387	intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010600	TCTTTCAGGCCTGCA[C/T]GAGGGTTTCGGCTTT	26091
rs565398119	snp	C/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HERC4, POU5F1P5	GRCh38.p7	10:68009531	TCAATTGAGGCTTTG[C/T]AAGTCTTAAACTTTT	26091
rs565422208	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68017409	ACAAATAAACATTTA[C/T]TATTATATGTCACTG	26091
rs565439069	snp	C/T	3.32414e-05	0.00407671	intron-variant	HERC4	GRCh38.p7	10:67940896	CTTCCCCACTTTTTA[C/T]CTCCCAAACCCTACT	26091
rs565448380	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67994281	TCAAAAGATTTAGCA[C/G]GATGTTATTTATTTA	26091
rs565449757	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68034316	CCTATCATCAAAAGA[A/T]TATAAATATTATTTT	26091
rs565450196	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67933656	CCTAAAATTTTTTCA[C/T]ATCATTTTAAAAACA	26091
rs565457409	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68005954	ATCCTCTTGCCTCCT[C/G]TTTTCTGATCTGATC	26091
rs565479291	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67936575	ATCCAAGTATGAGAA[G/T]GCTATTCAGCTTAGA	26091
rs565485463	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68042345	TCTATAAACACTAGG[A/C]AGGACACAGTGGCTT	26091
rs565494260	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67980334	GAAGGGGTTTCTCCA[C/T]GTTGGTCAGGCTGGT	26091
rs565501299	snp	C/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68003656	ACTTAACATAATGTC[C/G]TCCAGTTCTCATATT	26091
rs565504214	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68034827	CTCCTCTCTCTTTTT[G/T]TTTTTAACCTCACAC	26091
rs565506155	snp	G/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68043384	AAAAAGAACAAAAGA[G/T]TTTAAAGAGGTCAGA	26091
rs565507265	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68047231	TCAGTAATTCGCATG[A/T]CAAGTGGGTAAGAGA	26091
rs565515855	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67932906	AAACTGAGAATGTAT[A/G]AGTAGCGTTCAAACA	26091
rs565560719	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68058462	AGGCAAATATGAAAC[A/G]GCATAATACCACATT	26091
rs565572600	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68041611	TAATTTTTTAATGTA[G/T]ATGTCCAAGAAGCAG	26091
rs565698041	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68065844	CAGTGACAACAAGAT[C/T]CTGTCTAAAAAAACA	26091
rs565739772	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68064933	GTGGAGATCGCGCCA[C/T]GCACTCCAGCTTGGG	26091
rs565746172	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68044917	AAAAGAGTCCAGGTG[-/A]AAAAAAAAAGAAGAA	26091
rs565756269	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68022614	GCAAACAGGGAAATG[C/T]TTCATGACATTGGAT	26091
rs565819021	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67934034	CTGCCAGAAATTCCC[A/G]CTATTAAAAGGCAAC	26091
rs565832900	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67948336	TCAGCAAGAAAAAAA[C/T]AATCCCATCAAAAAG	26091
rs565864032	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68050259	GAGGGAACAATAGCG[C/T]GGTCAAATGTAAGAG	26091
rs565902032	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67994916	GCTGGTCTCGAACTC[C/G]TGACCTCAAGTGATC	26091
rs565913892	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68072618	CTCTGTACCAAAGAT[G/T]TATATACTGCAGGCT	26091
rs565938548	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67951494	GTCCTTGCTCCACCA[A/C]ACCCTTTCACTGTTT	26091
rs565957358	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68051128	AAAACAAAGAAAAAA[C/T]TTGCCACACAAGTCC	26091
rs565991642	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68067711	CCAAAATGCTTTTAT[C/T]GGAATGACTCAACAG	26091
rs566018346	in-del	-/T	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:67992070	GCCCAGCTAATTGTA[-/T]TTTTTTTGTAGAGAC	26091
rs566020299	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68026521	AGACTAGCCTGGCCA[A/T]CATGGTGAAACTCTG	26091
rs566026884	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67980619	GAATATTACAACACT[A/G]TAATTATGGTGTGTA	26091
rs566052001	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68074535	TTTAAAACACAGAGG[A/C]GTCCTCTCGCCAGCA	26091
rs566056984	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67987136	GTATTTAGAATGAGT[C/T]CATCAAAAAGGTCTT	26091
rs566061492	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67982856	CAGGCGGCAGGGTGC[A/G]GTGGCTCATGCCTGT	26091
rs566080179	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68066780	AGACTGGGCATTACC[A/G]TAGTTAAGTTTCTGT	26091
rs566132032	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67980226	TCATCAAAACAGCAC[A/G]GTACTGGCATGATTC	26091
rs566143351	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67959645	TGACAGAAAAAAAAA[C/T]AGTAAAACATAAGGT	26091
rs566205397	in-del	-/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67980553	AAACATTAATGGGCA[-/T]ATAACAAATCATCTA	26091
rs566210978	snp	A/C	4.93559e-05	0.00496745	intron-variant	HERC4	GRCh38.p7	10:67966854	AGTACTCAAGACAGA[A/C]AAATTTTTTTTATTT	26091
rs566227178	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68020164	CAGATAAAACCTACA[A/G]TGATCAAAAACCAAA	26091
rs566268335	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67952146	ATTTATTTGTCCAAA[C/T]CAAGTCCACACAAAG	26091
rs566289959	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4	GRCh38.p7	10:68075119	TGCTCCGCTGCTCCC[C/T]TCCCCGGCCCCTGGG	26091
rs566302743	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67996947	GAGCTGAGACCGCTC[C/T]ACTACACTCTAGCCT	26091
rs566303411	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68005124	CTGTTCCATTGGTCC[A/C]TGTGTCTGTTTTTAT	26091
rs566311524	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67948320	GAACTCAGATAATTA[C/T]TCAGCAAGAAAAAAA	26091
rs566324089	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012849	AGCTTTAGTAATTCT[C/T]GCAATATTTCAATAT	26091
rs566347953	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68045577	CCCTTAAAATACTGG[C/T]CCTACTACCAGTAGC	26091
rs566380705	snp	C/G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67997830	GAGGTGGAAGAAACA[C/G/T]AGTCGGCCCTCTGTA	26091
rs566387813	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67966018	CCACATTTATATTAA[A/C]AATCTGAAATAAAAG	26091
rs566393676	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67952510	ACTGGTCTTGGACTC[C/T]TGACCTCCACCTTGG	26091
rs566397547	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67923600	AGTCTTGCTCAGTTG[C/T]CCAGGCTGGAGTGCA	26091
rs566412672	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68030460	CAAAAACAAAAACAA[A/G]CAAATATACATGGCA	26091
rs566425253	in-del	-/T	0.0115144	0.0749975	intron-variant	HERC4	GRCh38.p7	10:67954387	CCATCTCTTAATTTA[-/T]TTTTGTTAATTTAAA	26091
rs566436052	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67929012	ACTCATCAATTTATC[C/T]CCTTACTTTCTGTCT	26091
rs566444382	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68037527	AGCTAATAAATATGA[A/T]GTTTAGCCTTCTTTA	26091
rs566461652	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68026356	TTGCCTTGGCTTCCC[A/G]AAGTGCTGGGATTAC	26091
rs566462065	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67974756	CTGAAGTATTCCTAA[C/T]AGAGAAAGAGAACAA	26091
rs566480609	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68036613	AAACTGAAGTATGAG[C/T]ATGTCTCCCACTCCC	26091
rs566482590	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67940840	GAAATTTAACAAGAA[C/G]AACAAAATATATTTT	26091
rs566501097	snp	A/G	5.28769e-05	0.00514156	intron-variant	HERC4	GRCh38.p7	10:67988633	AATAGGAATGGGGAA[A/G]GAGGAAAATAAAGGA	26091
rs566517410	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68008096	GAATTCCCTGGATTA[C/G]TAGGCAGAGTCTCTT	26091
rs566553918	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68044673	CACATTCTTCATTTT[A/G]TACAAACAAGCTAAA	26091
rs566613425	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68013858	TTCCTTATGCATTTA[A/C]AAGTAAATATAAGCA	26091
rs566667542	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67968663	TACAGGTGTGAGCCA[A/C]CGCGCCTGGCCAGAG	26091
rs566687370	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68031435	GACTTCAGTGATTAC[A/G]TTTGTTATCTGAATG	26091
rs566698223	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68021107	CCCCAATGAATTCTA[C/T]GCAGGATAAACTCAG	26091
rs566714002	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68030122	ATTTGTTCTGGCTAT[C/T]AATTTTAAATTTACT	26091
rs566731725	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	HERC4	GRCh38.p7	10:68075811	TGGCTGAAGCTACTC[C/T]ACTACCACCACCACC	26091
rs566761171	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67977475	TTCAGGTGAGACTCA[A/G]CACATTCCCTACCAT	26091
rs566820888	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67960880	GCATGGAGAGGATAA[A/G]TAGACTGGCAAGCCT	26091
rs566844105	in-del	-/AA			intron-variant	HERC4	GRCh38.p7	10:68046132	GACACACACTGTTCC[-/AA]AAAAAAAAAAAAGAA	26091
rs566867436	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68014712	TATGTACGCACCAAA[A/G]CTCCTCTGGAGGTAC	26091
rs566872430	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68055026	CTCCTGGGCTCAAGC[A/G]ATTCTCCTGACTCAG	26091
rs566877526	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67954132	ATTACTTAAACTCTG[C/T]CGCTGCTATTGTAGC	26091
rs566931729	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68061981	CTTTAAATTTACAAC[A/G]GTATTATATCACCAT	26091
rs566962733	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67946018	AGCACTTAGTGAGGC[A/G]GAGGTAGGCAGATCA	26091
rs566966644	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67994284	AAAGATTTAGCAGGA[A/T]GTTATTTATTTACTC	26091
rs566967818	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67938508	CAATTTCTCCAAGAG[A/T]CTAATTTATAATATT	26091
rs566969960	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68036598	TTTTTATTTCAGCCT[A/T]AACTGAAGTATGAGT	26091
rs567014972	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67991409	TGTTTATTCTAGACT[C/T]TCTTAAATATTACTT	26091
rs567038411	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68035298	GCTGGGATTACAGGC[A/G]CGTGCCACCATGCCT	26091
rs567076970	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68038944	ATCCCAGCATCTCCA[C/T]TGGTTCTTTCCCTTT	26091
rs567085973	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68055846	AACCTCTGCCTCCTG[A/G]GTTCAAGCGATTCTC	26091
rs567101632	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68016049	CAGAGGTTGCAGTGA[A/G]CCAAGATTCTGCCAC	26091
rs567120207	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67986817	TAGAAATATGATCTT[C/T]TTGATTCCTAGTCCA	26091
rs567128896	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67947808	GGAAATCTGGAAAAT[C/T]CACAAACATATGGAA	26091
rs567133398	snp	C/T			intron-variant, utr-variant-5-prime	HERC4	GRCh38.p7	10:68067194	TATTGTGTAATGCTC[C/T]TGAAATTCCTCAGAT	26091
rs567136552	snp	C/T	0.00874735	0.0655527	intron-variant, missense	HERC4	GRCh38.p7	10:68070498	GTAATCCCAGCTATT[C/T]GGGAGGCTGAGGCAG	26091
rs567147280	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68057390	CAGCACTTTGGGAGG[C/T]CAAAGCGGGTGAATC	26091
rs567182196	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68046940	TCCTTCATGGGCTAT[A/G]GAGGGAGACTGTGTC	26091
rs567185380	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68056676	ATTAATAAGAATGAA[C/T]TGGAGCAGGGAGATC	26091
rs567185381	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68064205	GATCATGCCACTGCA[C/T]TCCAGCCTGGGCGAC	26091
rs567260190	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67990133	CAGGGCAGCAGAACT[G/T]CAAATGGCAAAAGAA	26091
rs567261513	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67969474	AAGGCAGAGGGGGGG[A/G]AAAAAGGAAACAAGG	26091
rs567271314	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68063402	TTTAGTAGAGACGGG[A/G]TCTCACTACACAGGC	26091
rs567289703	in-del	-/ATG			intron-variant	HERC4	GRCh38.p7	10:68025863	TGAGAATTCCAGGTA[-/ATG]ATGTTTTCACCGTTA	26091
rs567322768	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67977100	CTGCTGGCACTACCC[A/C]TCCTTTAACCCAAGG	26091
rs567329979	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68022594	AAACTATAAAACTCT[A/G]AGAAGCAAACAGGGA	26091
rs567338444	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67983482	TCTAAGTGTCCATCA[G/T]TAGGTGAATGAATAA	26091
rs567342630	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67968828	AGAAATCAACAGAAC[C/T]ATGATTATATTTGGA	26091
rs567351021	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68020610	CCGTCTCTACTAAAA[A/C]TACAAAAAATTAGCC	26091
rs567368819	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67983876	GCTGAAGCAGCAGAA[A/T]CGCTTGAACCCGGGA	26091
rs567399173	in-del	-/A	0.00874735	0.0655527	intron-variant	HERC4	GRCh38.p7	10:68070606	GCGAAACTCTGTCTC[-/A]AAAAAAAAAAATAAA	26091
rs567402525	snp	C/G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67940512	GCAACCTCCGCCTCC[C/G/T]GGGTTCAAGCAATTC	26091
rs567402570	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68055988	GAACTCCTCAGGTGA[C/T]CCACTGGCCTCAGTC	26091
rs567404315	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67976328	CAATATTTATGTTTA[C/T]ACATATACAAACTAA	26091
rs567461898	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67948845	AGAATGGCTTGAACA[C/T]GGGAGGCAGAGGTTG	26091
rs567477364	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67962635	ACCAGATAAAGATAA[C/T]TAACTAAAAGTATCA	26091
rs567496388	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68001139	ACTTTGGGACGTCAA[C/G]GCAGGAGGATCACTT	26091
rs567509384	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68064576	AAAAAAAAAAAAAAA[A/G]AGAGAGAGAGAGAAA	26091
rs567511027	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68017707	TTGGCCAGGCTGGTC[A/T]TGAACCCCTGACCTC	26091
rs567516110	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67963559	TCTTAGAGTTCTTTT[A/T]AGAGCTAAACACCAA	26091
rs567545908	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68045139	CAGCCTGGCCAAAAC[A/G]GTGAAACCCCATCTC	26091
rs567565090	snp	C/T	0.00517822	0.0506191	intron-variant	HERC4	GRCh38.p7	10:68016509	AGGCATGTGCCACCA[C/T]GCCCAGCTAATTTTT	26091
rs567572222	snp	G/T	0.000249499	0.0111663	intron-variant	HERC4	GRCh38.p7	10:67932549	AAGGCAAGATTTCCA[G/T]ATATAAATCTTTCCA	26091
rs567590874	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67971228	TTTAATAAAGAAATA[A/G]TACCAATCTTAATCA	26091
rs567605379	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67933127	ATCATGTCACATGCA[A/T]CCCTAAAAGGAATGT	26091
rs567607457	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68058875	GTAACATATTTACAT[G/T]GTTTTTTAAAAGGTA	26091
rs567613874	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67984652	CAATGGCACGATTTC[A/G]ACTCACTGCAACCTC	26091
rs567627082	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68033772	CAGATATACTTTTTA[C/T]AGTTCTTTAATGAAT	26091
rs567642251	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68041011	ACCCTTCCTTTGGGA[C/T]TCTGCTAAAGCATAT	26091
rs567649158	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67985424	TACAAAATAAAACCT[A/C]TATAAGTTTGATTAT	26091
rs567656474	snp	A/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67993811	CCAAACTGGAAAGAG[A/T]ATCTATTACCAAAAA	26091
rs567707248	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68004976	GTCTAGTTTCATTCT[G/T]CTGCATATGGATATC	26091
rs567709647	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010673	CCACTTCTGCAGCAA[C/G]GGCCGCGCCGCTTAC	26091
rs567759970	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67973061	ACACACACATATATA[A/G]AGCAAATGTGACAGC	26091
rs567795292	snp	A/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67952584	GCCAAAAAAATACTT[A/T]TTTTAAAATATCTTA	26091
rs567803644	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68018561	TAACAAAACTGAATT[A/G]ACTCACAGATGGTAT	26091
rs567806142	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68017566	TCAGCTCACTGCAAC[C/T]TCTGCCTCCTGGGAT	26091
rs567828691	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68072606	GCACACTACACACTC[A/T]GTACCAAAGATTTAT	26091
rs567835664	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68065050	ATGTTAATTATATTC[A/C]TAAATATTCCCAATA	26091
rs567896274	snp	C/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68026315	TGCCCAGGCTGGTCT[C/T]GAACTCCTGGGCTCA	26091
rs567944140	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67961705	GTAGTTGACTGAGTT[A/C]CCACGTGTCACCAGC	26091
rs567944281	snp	A/C	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67926428	AAATAAAAAAAAAAA[A/C]AAACAAAAAAATTAG	26091
rs567988249	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68051201	AATGTTGAAATTACA[A/C]ATGTTTGATGCTAAA	26091
rs568009115	snp	C/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67941838	TTTTTGTATTTTTAG[C/T]AGAGACTGGGTTTCA	26091
rs568017203	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67996024	CTTAAAATTCCTCTC[C/T]GCTGGGCACAGTAGC	26091
rs568069305	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68020967	AACCATAGGATACCA[A/T]TAAGCAGACCAACAT	26091
rs568082930	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67950667	TAATATGGAAAGGAA[G/T]AAGGCTAGAGTAAAT	26091
rs568088631	snp	A/T	0.030278	0.119257	intron-variant	HERC4	GRCh38.p7	10:68059842	ATATTATATATTATA[A/T]TATATTATATATCAT	26091
rs568109753	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67957381	TGTCTATTCCTTCAT[G/T]TAACAGATATTGAGT	26091
rs568113261	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68059160	TACGTATTACTGTGT[G/T]TTTAGAATTTTCCTA	26091
rs568128251	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68036211	TAGTCCCAGCTACTA[C/G]GGAGGCTGAGGCAAG	26091
rs568131442	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67957856	ACTGATGCCGGGGCT[A/G]GAGTGCAATGGTGCG	26091
rs568158697	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68020387	TCAAACATCCTAAAG[A/T]TGCTCAAAGAACTAG	26091
rs568165472	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011198	CCTCCCAAGTAGCAT[A/G]TGCCACCACACCTGG	26091
rs568194253	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67965333	TTGCCCAGTAGATTA[C/T]GAATTCCATGAGAAA	26091
rs568204295	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67928174	GGTTAATAAGGCTGA[A/G]GCAGAGTGAGAGGAA	26091
rs568216494	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67935644	AGGTAAATTTCCAAT[C/G]TCCTGCCCAGGCCAG	26091
rs568264595	snp	A/T	0.00636936	0.0560724	intron-variant	HERC4	GRCh38.p7	10:67934918	AAGTTTTTTTTTTTT[A/T]AATATTTTCTTTGAC	26091
rs568272134	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67945048	TTGTTCAAAGAGATA[A/G]TAACAGTGAACATCC	26091
rs568289849	snp	A/C	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68042713	AAAGCTGGCTGACAT[A/C]TCTAAGCCACCTAGA	26091
rs568305879	snp	A/T	0	0	intron-variant	HERC4	GRCh38.p7	10:67951371	CCATCATGTCTTATA[A/T]GCCTGTTTACAGAAC	26091
rs568333637	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68043485	AAATCTGTATATTTT[A/T]ACCTATGTAATTCAT	26091
rs568340539	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	HERC4	GRCh38.p7	10:68075528	GAGTTTGCGAAGACA[A/G]ACGAAGAAGATGTCA	26091
rs568366670	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68061199	TTATACCTATGTCAT[C/T]GCACCTTCTGACTGC	26091
rs568375222	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68052631	CTGTTGAATGAGTAA[C/T]TGGGTAAAAATATCC	26091
rs568389087	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68051906	ACTCGTGAGCTCAAG[C/G]AACACGCCCGCCTCA	26091
rs568396087	snp	C/T	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012858	AATTCTCGCAATATT[C/T]CAATATTTTTCATTA	26091
rs568420920	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68067867	TCGAGTTAGTCTTCC[A/G]TTCAGTAATACACTA	26091
rs568441059	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68019585	ACCTAGACAACAATT[A/G]CACTGACAGAATCTG	26091
rs568444104	in-del	-/T	0.0115144	0.0749975	intron-variant	HERC4	GRCh38.p7	10:67937592	TCGTTTTTGTTTTTG[-/T]TTTTTTTTAATTTTA	26091
rs568448597	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68047940	TTTTGTTTTTTTTTT[G/T]GTGAGACAGGGTCTC	26091
rs568457168	snp	C/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67928813	GTAGTTCCAGCTACT[C/T]GGGAGGCTGAGGCAG	26091
rs568461596	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68074597	CGTCTTTCCCTGAAC[A/G]TGCACCCAGATCAGC	26091
rs568476215	snp	A/G	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:67966878	TTTATTTTTTGAGAC[A/G]GAGTCTCACTCTGTC	26091
rs568495762	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67980874	ATCTGCAAGCCCCAT[G/T]GTAACCTGAAACCAA	26091
rs568532198	snp	C/T			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012856	GTAATTCTCGCAATA[C/T]TTCAATATTTTTCAT	26091
rs568540265	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67966097	ATTCTCATGCCTCAG[C/G]CTTCTGAGTAGCTGG	26091
rs568568488	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67979958	AAAAGAAAAAAAAAC[C/T]TGTCTGAGAAAAAAA	26091
rs568589196	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68006387	TTTGTTTTTTTTTTT[G/T]TTTTGAGACAGTTTC	26091
rs568606004	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67936777	ATTACCATTCCCACT[C/T]ATGCATCTTTTCTTT	26091
rs568606281	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67954535	GAATTAACTTGATAC[A/C]TACAGGTATAAATAC	26091
rs568606318	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67973251	CAGAGAGAACAGCAC[C/T]AGCTAAAGAGACACA	26091
rs568608316	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67945798	TATTTGCAAGCCTCA[C/T]GGTAAACTCAAATCA	26091
rs568610384	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67978410	GGGAGGGATGAGTGG[A/T]AAGGACTATTTTGTG	26091
rs568612787	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67958977	TACAGACTGTATTTT[A/T]AAAAATGATACATAT	26091
rs568643697	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67960321	CCAGACTCTGCCCTG[C/T]GTGTTTCTTCCCTTG	26091
rs568662642	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67997991	ACTGCAACCGCCTCC[C/T]GGGTTCAAGCGATTC	26091
rs568678585	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68013452	ACCTTGAGGACGTTA[C/T]GCTTAGTGAAATAAG	26091
rs568699595	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67997096	GAATATTAAAGAGCA[G/T]AACTAAAGATACAAC	26091
rs568720465	snp	C/T			intron-variant, downstream-variant-500B	HERC4, POU5F1P5	GRCh38.p7	10:68009579	GCCTCATTGTCAACA[C/T]TGATGGCTACTGACT	26091
rs568727772	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67930457	GACTGCTAGGTCATA[C/T]AGCAAATGTATGTTT	26091
rs568752447	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68005945	GCTCAAGCAATCCTC[C/T]TGCCTCCTGTTTTCT	26091
rs568771508	snp	G/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68038381	TTAAAGGGGTGAAAA[G/T]AACACATCTTGGAAA	26091
rs568781073	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67959856	GAAAGTTTCCACATA[A/T]GCTCAGAGCACAGAC	26091
rs568812757	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	HERC4	GRCh38.p7	10:68076738	AATTTCCCTCTTTTA[C/T]AAGGACACCAGATAT	26091
rs568819494	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67967065	TTCATCGTGTTAGCC[A/G]GGATGGTCTCGATCT	26091
rs568865223	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67929876	GGAGTGCAACGGCAC[A/G]ATCTCCGGCTCACTG	26091
rs568892871	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67991440	TCATCCATTTATCCA[A/G]TGTTATCTGCTTTAA	26091
rs568932094	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67990453	AATGAATACACTTTC[A/G]AAGAAAAAAAAAAAA	26091
rs568934592	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069877	GAAACCCCGTCCCTA[C/T]TAAAAATATAAAAAA	26091
rs568977393	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67998796	CAGGCTTAAGTGCAA[C/T]GGTGCAATCTCAGCT	26091
rs568995671	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67989568	ACATTATTACTTCTA[C/T]ATATCTCAGCTCCAC	26091
rs569006237	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67933609	CCTTTCAGAACCAAG[-/T]TTTTTTTTTAAAACA	26091
rs569009102	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68027820	CCCAGCTACTCGGGA[A/G]GCTGAGGCAGGAGAA	26091
rs569053769	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67961403	CTATCTTTTTTAGAA[A/C]GTAGATTAACCACTT	26091
rs569081958	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68023422	TGGGTGAACCTTGAT[A/G]ACACTACGCTGAGTG	26091
rs569097190	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069681	TGTATATTTATAAAG[A/C]CAACCTATGTAAAGA	26091
rs569114769	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68022350	ACTAAAAACACAAAA[A/T]TAGTCGGGCAAGGTG	26091
rs569179318	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67946908	CGAGACTCTGTCTCA[A/G]AACAAAACAAAACAA	26091
rs569213586	snp	C/T	9.57327e-05	0.00691789	intron-variant	HERC4	GRCh38.p7	10:67992697	TCTGTAATAAAAATG[C/T]AAAAAATTAAAAGCC	26091
rs569233872	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67938680	GCCAGGTGCAGTGGC[A/T]CATGCCTGTAATGCC	26091
rs569239065	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67997638	TGTATTTGGAGATAA[A/G]GGCATTAAAGAGGTG	26091
rs569253458	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67955666	ATCCCAGCTACTCAG[C/G]AGGCTGAGGCAGGAG	26091
rs569261824	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68008951	CTAGCCTGGGCGCAG[C/T]GGTTCACTCCTGTAA	26091
rs569271114	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68008190	GAGATTCTTAATAGT[C/T]GGGGTAGAGGTGATG	26091
rs569286336	snp	A/T	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:68063213	TTTATTTATTTACTT[A/T]ATTATTTATTTTTTT	26091
rs569291764	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68062611	ACAAAAAAAAAAAAA[A/T]TAGCCGGGTGTGGTG	26091
rs569310573	snp	A/C	0.0244538	0.107838	intron-variant, upstream-variant-2KB	HERC4	GRCh38.p7	10:68074992	TGACGGGGGGCGGCC[A/C]CTGCCCAGAGAGCAA	26091
rs569320434	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67924987	GTGCAGATAGTTCTG[C/T]TTCAAAAAAATTACT	26091
rs569321669	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67983146	CCACCGAACACCAGT[G/T]AAATGCAAATCAAAA	26091
rs569325670	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:68055912	ACCGGCCACCATGCC[C/T]GGCTAATTTTTGTAT	26091
rs569364320	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67995588	TTTTTTTCATTAATA[C/T]GTATGGACACTTTAG	26091
rs569409606	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67983902	CGGGAGACGGAGGTT[A/G]CAGTGAGCTGAGACT	26091
rs569428924	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67984504	AAGCTGGGAAGGGTA[G/T]TGGGGAGGCAGGGGC	26091
rs569509400	snp	A/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	HERC4, POU5F1P5	GRCh38.p7	10:68009918	CCATAAAATATAAAT[A/G]GATGAGGAGTATTTT	26091
rs569529880	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68064254	CAAAACATAAAAAAT[A/G]ATTAAAAGAAAGAAA	26091
rs569567249	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67939267	AGAGGATGTCTTGTA[A/T]TTGTCAATATCTTTA	26091
rs569567673	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68058328	AGGGCACAGCAGGAA[C/G]ACAACTGTCTGTTGA	26091
rs569617917	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68071431	ACTTTCTACTTGCCC[G/T]ATGGCCTTTCAGAAA	26091
rs569674943	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68053055	AGAAACCACATCATT[C/T]TTCCACTTATTAGTC	26091
rs569676399	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67963627	TAATATGTAAGTGAA[C/T]ACTGGGCTTCTTAAG	26091
rs569701831	snp	A/G	0.00636936	0.0560724	intron-variant	HERC4	GRCh38.p7	10:68040339	AAACTATCCCCTTTC[A/G]TCTTCATATAAATGT	26091
rs569720369	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68013868	ATTTACAAGTAAATA[C/T]AAGCAAATCAAACAA	26091
rs569737505	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67969906	CCTCTCCTCTACCAA[A/T]CTTGAAAGCACTGAG	26091
rs569763044	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68055551	GCACTAAGCTTAGCA[C/T]TTTAATTACTTAATC	26091
rs569765588	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67978103	CAACATGGTGAAACC[C/T]CATCTCTACTAAAAA	26091
rs569798872	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67969504	GCAGAATATCAAGAG[C/T]CTCTCTCAATGGTAC	26091
rs569810048	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67941965	CTGGCCAAAACATGA[A/C]TTTTTAATGGCTGCA	26091
rs569813762	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68042509	ACGCCTATAGTCGCA[A/C]CTACTAGGGAGGCTG	26091
rs569858715	snp	C/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67994477	CACTCTTGTTGCCCA[C/G]GCTGGAGTGCAGTGG	26091
rs569871790	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68016408	GCCAGGCTGGAGTGC[A/G]GTGGCGTGATCTTGG	26091
rs569872152	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68002465	AATATTTCCAACTAA[G/T]TAGTAAATTAACATC	26091
rs569881775	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68047578	AGACCAAAACTGACA[A/C]CTCACCAAGGAAGAT	26091
rs569918203	snp	A/G			downstream-variant-500B	HERC4	GRCh38.p7	10:67921678	TCATAGTCTTATTTA[A/G]TGAATACCATAAATA	26091
rs569926414	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:67958028	TGGCCAGGCTAGTCT[C/T]GAACTCCTGACCTCA	26091
rs569954850	snp	C/T	0.000798403	0.0199641	intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010452	TTGCCCTTCTGGCGC[C/T]AATTACAGAACCACA	26091
rs569971415	in-del	-/CG	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:67996987	AGCAAGACTCCGTCT[-/CG]AAAAAAAAAAGAAAA	26091
rs569975458	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68064887	TGAGACAGGAGAATC[A/G]CTTGAATCCAGGAGG	26091
rs569979862	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67926497	GTTTATACTGTGAAC[C/T]GTTCTTATCCAGCCG	26091
rs569986544	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67965440	GTTGAATAAGCAAAT[A/G]AATAGACCTAAATCT	26091
rs570000206	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67927221	GAAAAGAGGATGGCT[A/G]AAGTTTTTTTTTCTT	26091
rs570008818	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67964619	TGATCATTCAAAAAG[A/G]TCAGATTAAGTTTCC	26091
rs570011532	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67979028	ACACAAGTCCAAACC[A/G]CGAAGACTACAATAA	26091
rs570018190	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68073408	TTTCTATGATCCTTT[A/G]CAAAATTTAAAACAT	26091
rs570027458	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67979510	CCTTAAAGAGGAGAT[A/G]GATGGGGCAGAAAAT	26091
rs570039881	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68026441	AATATACAGATGTTT[A/T]TAAAAAAAACTCCCT	26091
rs570050798	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68033867	CACCTCTATACCAGG[A/G]AAGATACATTTCTCT	26091
rs570077434	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68067338	TTCTCAAAGTAAAGC[A/G]TTCAAAGCAAGCCTC	26091
rs570120305	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67986546	ATTTTTAGTGGAGAC[A/G]GGGTTTCACCATGTT	26091
rs570121388	in-del	-/ATA	0.301429	0.244653	intron-variant	HERC4	GRCh38.p7	10:68059520	ATAATATTATATATC[-/ATA]ATAATATTATATATC	26091
rs570129637	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68001134	CCAGCACTTTGGGAC[A/G]TCAAGGCAGGAGGAT	26091
rs570147995	in-del	-/CT	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67944022	TGGGACTGAGGGGAA[-/CT]CTCTGCACTGAAGGG	26091
rs570161626	snp	C/T			intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069748	GACACAAGTTTAAAG[C/T]TCTTGTGAAGTCAGC	26091
rs570168371	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67994889	CAGATGGGGTTTCAC[C/T]ATTTTGGTCAGGCTG	26091
rs570197954	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011570	TGTCAATAAGCAGCA[A/G]TATTTTGAAAGAAAT	26091
rs570209629	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68066630	ACATGGCGGACTTTA[C/T]ACAACATAACTAATC	26091
rs570221526	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012130	GTTAGAATCTTGGTC[C/T]GGATTAGACTTTGGC	26091
rs570222185	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68065932	TATAAGGTAATTATC[A/G]TAACTCATTACAATT	26091
rs570261516	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67958917	AATGTTAACAGAATT[C/T]CATTTTCTTCAGAAA	26091
rs570285822	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68020533	GCACTTTGGGAGGCC[A/G]AGGCGGGCAGATCAC	26091
rs570307743	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67982056	TAGCAATCTACAGAT[C/T]CATTGCAATCCTTAT	26091
rs570308178	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68019291	GTGAGCCACTGCGCC[C/T]GGTCCAGCCAAAGCA	26091
rs570314111	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67944031	GGGGAACTCTCTGCA[C/T]TGAAGGGAAGAACAC	26091
rs570347379	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67996840	AAATAAAATAAAAAT[C/T]AGCTGGGCGTGGCGG	26091
rs570360986	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67972348	CCAACATGGAGAAAC[C/T]CCATCTCTACTAATA	26091
rs570387234	snp	C/T	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:67952120	TCAATACAATTCCAC[C/T]GTCACAATTTATTTA	26091
rs570392890	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67925591	TGGTACTAAGCAACA[C/T]TAAAAATTTTCTGAG	26091
rs570402522	snp	A/C	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:68001324	TTGCAGTGAGCTGTG[A/C]TCATGTCACAGCACT	26091
rs570402594	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67969030	GTCTTCATACATTTA[A/C]AAGAATCCAAAGTAT	26091
rs570406759	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68060529	CAGGCGTGAGCCACC[A/G]CGTCCAGCCATAAAT	26091
rs570422793	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67934980	GTTTTTTTTTTTTCC[A/G]TTTTTAATTGTATGC	26091
rs570431403	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67988492	GACCAGAGCTCCAAA[A/G]GACAGGTTTATTACT	26091
rs570469926	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68014691	TTCTGAGGAAAGTAA[C/T]CTCTATATGTACGCA	26091
rs570545842	snp	C/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68005097	TATGAATTTATTTCT[C/G]AGTTCTCTGTTCTGT	26091
rs570564791	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68037246	ACTACAGGTGTGTGC[C/T]ACCACACCCAGCTAA	26091
rs570589895	snp	C/T	0.000798403	0.0199641	downstream-variant-500B	HERC4	GRCh38.p7	10:67921532	TATAGAAGAGTTCTA[C/T]GGTTCGCCAATAGTT	26091
rs570592875	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68021079	GAAAGACATGAATCT[A/G]AACATCCATAAGCCC	26091
rs570616532	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67973909	AAAATTAGCTGGGTG[C/T]GGTGGCACGTGCCTG	26091
rs570720057	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68036529	GTTCCTAACTGCCTA[C/T]AGAAGTCCAAATTCC	26091
rs570730355	snp	C/T	0.00597247	0.0543191	intron-variant	HERC4	GRCh38.p7	10:68046798	ATAGTGAGACCTCGT[C/T]TCTACAAATAATTTT	26091
rs570757241	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67935775	TTCTTATAAGAGTTC[C/T]AGCATTTCCCCAAAC	26091
rs570838905	snp	A/G	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069504	TCTGTGTGGTCCCTA[A/G]AAAGTCCAGAACAGA	26091
rs570868975	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67960342	TCTTCCCTTGGCTGA[C/T]TTTTGTTCTCAGATG	26091
rs570890452	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67974559	TCAATAAATATGAGA[C/T]GAATGGATGGACAGA	26091
rs570917394	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67937654	GGAAAATGCTTTTCT[C/G]TTGTTATCTGGATTT	26091
rs570937014	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67923193	CAAAAAGATACAGTA[C/G]CAAGTAATATTTGGT	26091
rs570948744	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67977917	GCCTGGGAGGTAGAG[A/G]GTATAGTGAGCCGAG	26091
rs570957905	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68009398	GGGATTACAGGCATG[A/G]GCCACTGTGCCAGGC	26091
rs570961351	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	HERC4	GRCh38.p7	10:68075591	GCCTTTTAATGAAGA[A/G]AATCACTTTGTTTTT	26091
rs570985794	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67966907	TCAACCAGGCTGGAG[G/T]GCAGTGGCACAATCT	26091
rs570989115	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68006261	TGTACCTTTAGTTGA[C/T]TTGTTATTGTTCATT	26091
rs570990608	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67998858	ATTCTCCTGCCTCAG[C/T]CCCAACGAGCAGCTG	26091
rs571043850	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68047681	ATTTAAAACAACATA[A/C]CACTACACACCTATT	26091
rs571058653	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67975444	TGTTGACACCTCCCA[A/G]GTTCAAACAATTCTC	26091
rs571098911	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68061795	CTGAAGCAGGAGAAT[C/T]GCTTGAACCTTGGAG	26091
rs571100399	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68039499	AGCAGCTTCAGCAAA[C/T]CAAAGTTTGAGCAGG	26091
rs571111672	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67962540	GAAAAATAATAGGAC[A/G]TGAAAAACTTCAGAA	26091
rs571111731	snp	A/G	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:67945230	GAAACAACATACAGT[A/G]GAGCTCCAGTACATC	26091
rs571113318	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67955235	GTATTCTATAATTCC[C/T]ATGCTACTGAATTAA	26091
rs571126288	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68022437	CCGGGAGGCAGAGGT[C/T]GCAGTGAGCCAAGAT	26091
rs571145025	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67998148	GTGATCCACCTGCCT[C/T]GGCCTCCCAAAGTGC	26091
rs571162481	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68031245	AACATTAGGATGAAT[A/G]GTTATCTGAAAGGCT	26091
rs571167149	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68053684	AAAGGCCACTTGTTT[A/G]TAATGACAGCTAGAA	26091
rs571167603	snp	C/T	0.00119737	0.0244387	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68070413	GGAGTTCGAGACCAG[C/T]CTGGCCAACATGGTA	26091
rs571173542	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67961586	GTTCTGGGAGGCCTC[A/G]TAGCAAATTATCAAA	26091
rs571210036	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67960781	GTAGCCTTTCTAGAA[C/T]TACTACCTTCACCAT	26091
rs571277046	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67975526	AGCTAATTTTTTGTA[C/T]TTTTGTAGAGATGGG	26091
rs571280706	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67965850	TGGCTAGCAAATAAG[A/G]GTAGTAAACCTAAAT	26091
rs571285561	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67963163	TAGAATTCTTCATCA[C/T]TACAACATTCTCCAT	26091
rs571309040	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67997000	CTCGAAAAAAAAAAG[-/A]AAAAAAAAGAAAATC	26091
rs571319720	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67983382	GAGGAGCTACCCAAA[A/C]GAAACGAAAGCAGTA	26091
rs571373376	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68063267	CAGGCTAGAGTGCAA[C/T]GGCATGATCTCAGCT	26091
rs571381193	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67982845	AAAATACCAAACAGG[C/T]GGCAGGGTGCGGTGG	26091
rs571467297	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67987200	TGAGACTGAAGTTAC[C/T]GAGCTAGGCAGGTAA	26091
rs571467761	in-del	-/TT			intron-variant	HERC4	GRCh38.p7	10:68037111	TTTTTTTTTTTTTTT[-/TT]GAGACAGAGTCTCGC	26091
rs571476176	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68062670	GAGGCTGAGGCAGGA[A/G]AATCACATGAACCCG	26091
rs571479926	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68016703	AAACTGATCAAAATA[C/T]CAGATACCTACTTAC	26091
rs571484568	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67969409	GTTGGCACTCACTCA[C/T]AGCCTCTTGTCCATA	26091
rs571498519	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67978972	GACAACATCCAAGTC[C/T]TTCTGAATATCTGGA	26091
rs571513519	snp	C/T	0.000798403	0.0199641	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069213	CTGAATTTGAAAGTA[C/T]AAAAAAACAACAATT	26091
rs571514558	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68008285	ACCCAAAGCATGTAG[A/G]GACTAATTCCTGTCT	26091
rs571564561	snp	G/T	0.0267878	0.112589	intron-variant	HERC4	GRCh38.p7	10:67939535	CCTAAGACACGGCTG[G/T]TAAATAAAAGAGATG	26091
rs571627312	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67947608	AACCAATAAGACCTA[A/T]CAGACATATATAGAA	26091
rs571663014	snp	A/G	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:68045789	AAGTGGTTAAAACTG[A/G]ATCAATCAGGGTTTC	26091
rs571671235	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68007702	CAAGCCCAGTAACAC[-/T]TTTTTTTTTTTTTTA	26091
rs571672668	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68001093	GTCCTTTTGTCAGCC[A/G]GGTGCAGTGGCTCAT	26091
rs571673667	snp	C/T			intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010345	CACCAAAATGGGGCC[C/T]TGAGGCCATAGGAAA	26091
rs571680920	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68056529	ATTCCATGGGCTGTA[C/T]TTGGTAGTACACAAA	26091
rs571756815	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68023968	TAATAAATTCATCTA[C/T]ATTAATATCTAAAAC	26091
rs571763371	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68048570	CTATTCTACATGATA[C/T]TACAATGATGGATAC	26091
rs571794430	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010038	ACCGAACTTCACCTT[C/G]CCTCCAACCAGTTGC	26091
rs571833140	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67926406	CCATCTCAATAAAAA[A/C]AATAAAAAATAAAAA	26091
rs571844031	snp	A/T	1.67837e-05	0.00289682	intron-variant	HERC4	GRCh38.p7	10:68032736	ATTAATTATGAAAGA[A/T]CTATGATGAGTAATA	26091
rs571862976	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68036404	ACAAAAAGGTCAATA[C/T]GAAAAACTGTCCTCA	26091
rs571895793	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67925703	ATGTATGACTTCTGA[C/G]ACTAAATCATAAAAA	26091
rs571931235	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67926122	AGTACTGGCCGGGCG[C/T]GGTGGCTCACGCCTA	26091
rs571948578	snp	A/C	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:67940005	GATTTTGGCTCACTG[A/C]AACCTCTGCCCCCTG	26091
rs571957395	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67932447	TCATATACCGTTCAA[A/G]TCCATTCATTGTGGA	26091
rs571959610	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67953658	CCTAATGATACTTGA[A/C]AGCAAAACACAAAAA	26091
rs571968579	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67993997	TACAAGCAAGCACAA[C/T]GTTTTATTTGTAAAA	26091
rs571970578	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67976482	ATCCCTAAAAGCAAA[C/T]AGGTGGAAGAGGTGA	26091
rs571994603	snp	C/T	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:67931666	CTGACCTCAGGTGAT[C/T]CGCCCACCTTGGCCT	26091
rs571995664	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67993140	ATTTGATGTTAGGAG[A/T]TCGACGCCAGCCTGG	26091
rs572000426	snp	A/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68041954	ATCCATCCACTGGCA[A/T]TAAAAATGGGTTTTG	26091
rs572100457	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67957683	CTTCTACCATCTACC[C/T]AGTAAAACAATATCT	26091
rs572105379	snp	G/T	0.000147852	0.00859676	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68070443	AAAACCCCATCTCCA[G/T]TAAAATATGAAAAGT	26091
rs572124436	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67970786	GGCATAAAAGAAAAT[C/T]TATAGCATTAAATGA	26091
rs572125796	snp	A/T	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67970544	TTGCAGTGAGCTGAG[A/T]TTGCACCACTGCACT	26091
rs572135717	in-del	-/A	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67987321	AAAGACACAGCTAAG[-/A]AAAAAAAAGTATTTC	26091
rs572146166	in-del	-/A	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68059873	AATATTATATATTAT[-/A]ATAATATTATATATC	26091
rs572152337	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68024650	AAGAATACTTACAGT[G/T]TGATTACATGCATTT	26091
rs572179469	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68065425	AAAGCCCATTCTAAA[A/G]GATTCCAGAATGTCT	26091
rs572181671	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68073496	ACCTTGATGAAATTA[A/G]TCACAATTTTTTCTA	26091
rs572187082	snp	A/G	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:68040710	CCTGGCCAAAATGGT[A/G]AAACCCCGTCTCTAC	26091
rs572216638	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68064318	CAGCAATTTGGGATG[C/T]CGTGGCAGATGGATC	26091
rs572249382	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68013179	ATAAAGCATATTTAT[A/T]AACTAACATATACAC	26091
rs572301523	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68048619	TAAAATCCATTTAAT[A/G]TGTAACACTAAAAAT	26091
rs572308995	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67978495	TTTTTCACTCTAGTC[C/T]CTGGCTCCCAGACAG	26091
rs572309142	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67985597	GATCAGCACAAATAT[A/G]TAGCGACTAGGCTAG	26091
rs572327033	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68003409	TGATCTCCTGACCTC[A/T]TGATCTGCCCGCCTC	26091
rs572328462	snp	C/G	0.0107246	0.0724382	intron-variant	HERC4	GRCh38.p7	10:68068470	CCAGCCTGGGTAACA[C/G]AGCAAGACTCCGTTT	26091
rs572335640	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68058753	TTAGAGAAGAGAACA[C/T]CTAGGCACAGAAAGG	26091
rs572337853	snp	A/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67965470	TATAGAATGGCTATA[A/T]ACCTGACCCAGCCTC	26091
rs572344757	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67940674	GGTCTCAAACTCCTG[A/C]CCTCAGGTGATCCAC	26091
rs572376547	in-del	-/A	0.00438332	0.0466095	intron-variant	HERC4	GRCh38.p7	10:68025482	TCTCTGAAACAATTC[-/A]AATAAGCAATCCCTA	26091
rs572388359	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68018714	AATACCATTAAAGAC[A/G]CACCTAGGAATGGAA	26091
rs572435522	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67958233	GTATTTTATTACATT[C/G]TAAACATTCACTCTT	26091
rs572443449	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68051146	CCACACAAGTCCATT[-/A]AAAAAAACTATTGAA	26091
rs572512708	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010741	GCAGATGGTCGTTTG[A/G]CTGAACATATTCCCA	26091
rs572536070	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67996248	CTGCAATCCAGCCTG[A/G]GCAGCCTTCTTCTTC	26091
rs572543106	snp	C/G	3.30382e-05	0.00406423	missense, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68034186	CAGAAGACTTCACTT[C/G]CTGTAAAACAGTAAT	26091
rs572566937	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68052026	GAAAAAAAAGTATCA[G/T]TGTGTTCCTATCAGT	26091
rs572604680	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67942587	CGCGATCTTGGCTCA[C/T]GGCAACCTCCACCTC	26091
rs572628040	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67979974	TGTCTGAGAAAAAAA[C/T]AAATAACATACAATG	26091
rs572636325	snp	G/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68074578	ATGAGAAGCAGTTTA[G/T]TCCCGTCTTTCCCTG	26091
rs572652083	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68051457	TCGCGCCATTCTCCT[A/G]CCTCAGCCTCCTGAG	26091
rs572692153	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68043058	TCATAGTTGTTATTA[C/T]TGGACAACCCTCATA	26091
rs572718678	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68028696	CTTGGAGAAAAATAA[A/G]TGAGTTCATACTAAC	26091
rs572730563	snp	A/G			upstream-variant-2KB	HERC4	GRCh38.p7	10:68077226	CAGTATGTTACAGAA[A/G]TGAATGTAGAATGAC	26091
rs572738189	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68013069	TACTGTGATTTTTAC[A/C]AATTGAAGGTTTGGG	26091
rs572747441	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68059306	GATGTGGTTGAGTGT[A/C]CCTATCCATAAATGT	26091
rs572789198	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68004617	TGCTATAAAAAATTG[C/G]CTGAGACTGGGTAAT	26091
rs572792598	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68062715	CAGTGAGCTGGGATC[A/G]CACCACTGCACTCCA	26091
rs572794243	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-5-prime	HERC4	GRCh38.p7	10:68074805	GCCAGGGAGCCACAG[A/C]CCTGCCCTCGCCCCA	26091
rs572876404	snp	A/C	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67987641	TTCCCTAGGAAATAC[A/C]TGGCTATGATTTCAT	26091
rs572893026	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67943223	TGTCTTAATTCTGTT[A/T]AAGTTTATAAAGTTC	26091
rs572899202	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67928468	TAAAGCCTCTCTCCC[A/C]AGCTGTCTTTTGCTG	26091
rs572917926	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68028623	CATGGTTCATCACTT[C/T]TAGGACCTTTCACTC	26091
rs572935152	snp	C/T	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67934351	TCCAAAAGAAATATC[C/T]ATTTCCTCTAGATTC	26091
rs573000592	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68035358	AGGCAGGGTTTCACC[A/G]TGGTGGCGAGGCTGG	26091
rs573006348	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67966948	CAAGCTCTGCCTCCC[C/G]GGTTCACGCCATTCT	26091
rs573030523	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68020570	AGGAGATCGAGACCA[C/T]CCCGGCTAAAAAAAC	26091
rs573046658	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67959400	TTGTTTTCAGCAATT[A/G]AACACCCCCATTTGC	26091
rs573058592	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67923302	TTTTGAGACACATTC[G/T]AATTGCTCATCCACA	26091
rs573065464	snp	A/G	0.000798403	0.0199641	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	HERC4	GRCh38.p7	10:68075303	AGGAGAAGGCAGAGG[A/G]GGAGGTGGCCACGCG	26091
rs573083505	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67963853	ATATCTATTATGCCC[A/G]TAATGCAAAATTTGC	26091
rs573101358	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68030283	CATCTCTACAAAAAA[A/G]TACAAAAAATAGCCG	26091
rs573107935	snp	G/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	HERC4	GRCh38.p7	10:67966436	CTTGTAGGTTTTTTT[G/T]GTCTTGTTTTGTTTT	26091
rs573123009	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922685	TAGTAAAACTTTAAT[A/G]TATTCATAATACTTG	26091
rs573141225	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67989882	GTTTGTTCAGTTTTA[A/T]TTGTTCCTCCTCCTT	26091
rs573148901	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68068008	GAAGACAATAAAATA[C/T]GCTGTCTTCATTGTA	26091
rs573182227	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68058952	CCACTTCTTTTCCCA[C/T]CTCTACACCAACAGT	26091
rs573182600	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67998256	TAATAATACAATTAA[A/C]AATCATACAGGCCAG	26091
rs573189958	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68029884	CCTGGGATTACAGGC[A/G]CCTGCCACCACGCCC	26091
rs573236364	snp	C/T	0.00874735	0.0655527	intron-variant	HERC4	GRCh38.p7	10:67989086	TGTTGAATTTATATT[C/T]TTGGTTTCCTAAGTT	26091
rs573240060	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68045217	GATCCCAGCTATTCG[G/T]GAGGCTGAAACAGGA	26091
rs573274406	snp	A/G			utr-variant-3-prime	HERC4	GRCh38.p7	10:67922229	GTACTAAATATTAAT[A/G]AGTTCTCTGATCGAC	26091
rs573277609	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67945279	TGGAAACCTTACAGG[C/T]CAGGAGAATGGCATG	26091
rs573301524	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67997531	TCCTCTCATACTTAT[A/T]TGATTTTTGCCTTCC	26091
rs573309404	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67954490	GCAGATCTTATATGT[C/T]AGGGATCCAGTAGTA	26091
rs573325106	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68021961	AGCAGGAGGATACAA[A/G]ATCTACACACAAAAA	26091
rs573325199	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67967847	AAACAATCAGACAAA[C/T]CCTGATTATGAAACT	26091
rs573325923	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68052882	TTAATTGTGGAAAAC[A/G]AAAGCTACAAAAAGA	26091
rs573347192	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	HERC4	GRCh38.p7	10:68076954	CATGCAGAAACCCTG[C/T]CTCTACTGAAAAAAT	26091
rs573366278	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68062393	TATTTCCATCTGGTT[A/C]CCAAAGCCTGTCCAT	26091
rs573383248	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67967306	GATTTGTAAGATGTG[A/G]TATCTGCATTCAGTA	26091
rs573401984	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67936024	AAAGGCAGATTATTT[A/C]CTCACTAACCACTCA	26091
rs573405767	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67930757	TAACCTTGCACTTTC[C/T]GTCACTCTGCCTCCC	26091
rs573423848	snp	C/T	0.00279162	0.0372561	intron-variant	HERC4	GRCh38.p7	10:68061481	GAGCTTGCAGTGAGC[C/T]GCAATCGCGCCACTG	26091
rs573444028	snp	A/G	0.00517822	0.0506191	intron-variant	HERC4	GRCh38.p7	10:67998314	GCATTTTGGGAGGCC[A/G]AGGCAGGCAGATCAC	26091
rs573446547	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67982898	TTTGGGAGGCTGAGA[C/T]GGGTGGATCGCCTGA	26091
rs573472863	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67975650	CCACCATGCTCAGCC[A/G]ACACATGCATTCTTA	26091
rs573494852	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67984774	TTTTTAGTAGAGATG[A/G]GGTTTCACCATGTTG	26091
rs573537948	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67974969	GCTGAGGTGGTTGGA[C/T]CATGAGGTCAGGAGT	26091
rs573551170	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67955608	GAAATCCTGTCTCTA[C/T]TAAAAATGCAAAATT	26091
rs573556556	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68031935	TTTCGTATTTTTAGA[A/G]GAGACAGAGTTTCAC	26091
rs573557418	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68055515	AATACAATTAACGTA[C/T]ATAAAGAGCTTATGT	26091
rs573558445	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67996171	AATTGGTTAAGCGTG[A/G]TGGCGCATGCCTGTA	26091
rs573631603	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68008398	GGGCAGCAGCTTCCC[C/T]TCTAGTCAAAAAATT	26091
rs573633663	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67999283	ATTATTATTCTTACT[C/G]TGAATCTTCATCAGA	26091
rs573638798	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67953079	ATATTTAAAGGAGGA[C/T]AGCCCATACATTTTC	26091
rs573643003	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67946696	GGCGGATCATGAGGT[C/T]AAGAGATCGAGACCA	26091
rs573645399	snp	C/T	0.00159617	0.0282053	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069959	AGGCAGGAGAATCGC[C/T]TGAACCTGGGAGGCG	26091
rs573648929	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68056254	AAATTTTAAATTTTT[C/T]GCTCTAATGTAGCTG	26091
rs573656741	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069768	GTGAAGTCAGCTGGG[C/T]ACGGTGGCTCACGCC	26091
rs573689328	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67968188	CCAGACAGTGAGGAA[C/T]AAAAAAATCAAAGAA	26091
rs573740468	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67983686	CAGCTGCTCGGGAGG[C/T]TGAGGCAGGAGAACA	26091
rs573746361	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67979428	AAAAGAAAAAAGAAT[A/G]AAAAACAATAAGGCA	26091
rs573757422	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67977719	AGGCATGGTGGCTCA[C/T]GCCTCTAATCCCAGC	26091
rs573803643	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68047983	AGGCTGAAGTGCAGC[A/G]GCATAATCATGGCTC	26091
rs573838637	snp	A/C	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:67939752	TATACTTCTCATTCC[A/C]TCTTGGTAAAATCCT	26091
rs573850043	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67969546	TGCCACATGAGAAAG[A/G]AACAAAGGCCCGTCA	26091
rs573850698	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68002891	AAGCCTGAGCCACCG[C/T]GCCTAGCCTTATTTT	26091
rs573918276	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67988560	CTATAATATGCATTG[C/T]TTTTGCCAATCTAAA	26091
rs573918460	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68016354	ACATATTTCTTTTTT[A/T]AAAATTTTATTATTT	26091
rs573937224	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68019722	GGTAGCAGTTACCCA[C/G]TCCTTACTCCTGTGT	26091
rs573982322	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67991913	CATGGATATTTTTTT[C/T]TGGAGACAAGTTCTC	26091
rs574048889	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68017896	CTCATAGCCACTAAA[A/G]AAATTGAAGAATGTT	26091
rs574049748	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67935759	ACTAGTTTCTAACTG[C/T]TTCTTATAAGAGTTC	26091
rs574085307	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68023568	GAGAATAGGGAGTCA[C/T]TGTTTAATGGGTATA	26091
rs574103133	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67984147	TCTCTACTAAAAATA[C/T]AAAAAATTAGCCAGT	26091
rs574105304	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68040409	CTTTGTTTTAGCTTT[C/T]AGAAATTAAAAAATA	26091
rs574129712	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:67989755	AGATCAGATGAGCAA[C/T]AAAATCTAGTCTATA	26091
rs574172280	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68032051	GCCTCTGTGCCCGGA[A/C]GTTAATGTCTTTTTA	26091
rs574195120	in-del	-/ATA/ATAATA	0.30945	0.272783	intron-variant	HERC4	GRCh38.p7	10:68059657	ATTATATTATATATC[-/ATA/ATAATA]ATATTATATATTATA	26091
rs574219209	snp	A/G	0.000798403	0.0199641	intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010143	CCTGGCACAAACTCC[A/G]GGTTCTCTTTCCCTA	26091
rs574221147	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67956124	TTAATTTTTTAAAAT[A/G]TTTTTAGACTATTAA	26091
rs574249262	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67964006	TAGGTCAGAGATGAA[G/T]AAAAAAGGAAATATT	26091
rs574255655	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68016775	CGAAATTTTACCCCC[A/G]ATCCAACAGTTACAT	26091
rs574278143	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68071662	AATATGACCACCTCA[A/G]TGCCTGAGATCATGA	26091
rs574283444	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:67963277	GCTGGAGTGCAGTGG[C/T]GTGATCTCAACTCAT	26091
rs574324176	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68067944	GAAAATAGAACTCTC[G/T]ATCTTCTTATCAGTT	26091
rs574331432	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67933475	TGTTTTGCTAGCCAC[A/G]ACATTTTATGATGCT	26091
rs574347928	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68064382	ATCATGGTGAAACCC[C/T]ATCTCTACTAAAAAT	26091
rs574358787	snp	A/G	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67985961	CCTTAATTCTTAACC[A/G]TAGAGCAGAGGGAAG	26091
rs574380265	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68035160	AGACAACCACTCTTT[C/T]TTTTTTTTTTTTGAG	26091
rs574389493	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68025935	ATTTGCATTGCCTTT[C/T]ATTATCATTATACTG	26091
rs574394794	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67985022	ATCTTGCTGATATGA[C/T]ATATACGTTTTTGAA	26091
rs574396560	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68007097	ACCTCCTCTTTAAGG[C/T]CAGTAACCCTTAGAT	26091
rs574397402	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68042161	GCTGGGATTACAGGC[A/G]CCTGCCTGGCTAATT	26091
rs574404732	in-del	-/C	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68050914	TGGCCCAGTAATGTT[-/C]CGTGTAAGAAAGGGA	26091
rs574428610	snp	C/T	0.000115347	0.00759343	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68034146	AGTACCTAAACCCAA[C/T]TGGCCATATTTATTC	26091
rs574436130	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68050290	CCAAGCTTCTCAATG[A/T]GTATTTAAATTGCTT	26091
rs574468394	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68060153	GGATTCAGCACAGTA[C/G]CTGGCATATAATGGA	26091
rs574505450	snp	C/T	0	0	intron-variant	HERC4	GRCh38.p7	10:67941643	TACATGAGTATTATG[C/T]CACTAAATGTTCTTC	26091
rs574540948	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68018845	TACAAAGATAACAAC[A/T]TTTCCCCAAATTAAC	26091
rs574542609	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67927692	AGCCTCCCAAAGTGC[C/T]GGGATTACAGGCATG	26091
rs574555480	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68018013	ATTAGAAAACAAAGG[C/T]ACATTCCTCAATGTT	26091
rs574558102	snp	C/T	0.0248432	0.108648	intron-variant	HERC4	GRCh38.p7	10:68059471	TATAATAATATTATA[C/T]ATTATAATATTATAT	26091
rs574563267	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68073731	ATTTAAAGCAATTTT[A/C]CACAATTTAAACGAC	26091
rs574565816	snp	A/C	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67927716	AGGCATGAGCCACTG[A/C]GCCCGGCCGCTACAA	26091
rs574568241	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67949910	TGTAATCTCAGCTAC[C/T]TGGGAGGCTGAGGCA	26091
rs574606432	snp	C/G	0.00517822	0.0506191	intron-variant	HERC4	GRCh38.p7	10:67979729	CTGGGCGCAGTAGCT[C/G]ACACCTATAATCCCA	26091
rs574679146	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67965008	TGAACTCCTGACCTC[A/G]TGATCTGCCCACCTC	26091
rs574683465	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67972436	TGAGACAGAAGAATC[A/G]CTTGAATCCGGGAGG	26091
rs574700125	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68073978	GTGGTAACCGGGATT[-/A]AAAAAAATCACCCGT	26091
rs574714667	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68065984	AATTTCATCAAAATG[-/A]AAAAAAAAAAATCCA	26091
rs574742227	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67971849	GCCAAATGAATCAAT[C/T]TATAAGAGAATTACC	26091
rs574776762	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67943523	AGGTAGCCCAGTTAG[C/T]TCAGCTGGTAAACAT	26091
rs574839586	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67942705	CAGTAGAAATGGGGT[C/T]TCTCCATGTTGGTCA	26091
rs574856408	snp	C/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011667	CTGTAAACAGATGAG[C/T]TGTCATCCAGGCTTT	26091
rs574877220	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68066275	ACATTTGTATGATAT[A/G]TTGGGAATACAGAAC	26091
rs574918666	snp	A/G	0.00398564	0.0444627	intron-variant	HERC4	GRCh38.p7	10:67988925	TTTTTCTGAAACAGT[A/G]GTTGTTAAACCTGAG	26091
rs574928628	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68004739	GCAAAGCACCTTCTT[C/T]ACAAGGTGGCAGGAA	26091
rs574929827	snp	A/C	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67928631	CTAGGATATAAAATG[A/C]GTTGCCTCGGGCCAG	26091
rs574930435	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68045254	CTTGAATCTGGGAGA[C/T]GGAGGTTGCAGTAAG	26091
rs574950579	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67974003	AGTGAGCCGAGATCA[C/T]GCCACTGCACTCTAG	26091
rs574957832	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68044822	CTCAGAATATCAAGT[G/T]ACCTGAACATTTTGG	26091
rs575017347	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67973514	CAAAAGTTGATACAT[A/G]GGGAAATAAGGTTTT	26091
rs575024178	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67965571	TGTCTAGAAGCAACC[C/T]GATTCCGGAAGGTGG	26091
rs575037257	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68043731	TGAGGCAGGTGAATC[A/G]CTTGAAACCAGGAGG	26091
rs575061671	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67947348	CAAAACAGACTAATA[C/T]GATGCAAAATTGATA	26091
rs575072271	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67951568	CTAAACTCCAAATTT[C/T]TTCCCCTTTTTGTCT	26091
rs575148933	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68013174	AAGCAATAAAGCATA[C/T]TTATAAACTAACATA	26091
rs575162659	snp	A/C	0.000798403	0.0199641	downstream-variant-500B	HERC4	GRCh38.p7	10:67921859	CCTTCCCTGAACCAT[A/C]CCTCTTTTTGAAAAA	26091
rs575169055	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68068241	TGTAATCCCAGCACT[A/T]TGGGAGACCGAGGTG	26091
rs575171495	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67974837	GACTGTCAGGCTTCA[A/G]TATGCATATCGAGAA	26091
rs575172228	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67944076	TCACCACCTGCTGAC[C/T]GCAGAGCCCTAGGGC	26091
rs575187522	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67934414	GAGCCCTCCATCCTC[G/T]TGATCTAACCCAAGT	26091
rs575188718	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67967143	ACAGGCGTGAGCCAC[C/T]ACGCCTGGCCAAGAC	26091
rs575209102	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67969472	ACAAGGCAGAGGGGG[A/G]GAAAAAAGGAAACAA	26091
rs575209260	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67935729	GTTGTTTTAAATCCA[A/G]TGTTAGCATGGGAAA	26091
rs575226495	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	HERC4	GRCh38.p7	10:68075393	CACTTCCCGGCCCCG[A/G]CACCGGCGCCTGCGC	26091
rs575241145	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67938334	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	26091
rs575253799	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67941309	TATTTTCTCAGACTT[-/A]AAAAAAAATATATCT	26091
rs575294701	in-del	-/TTCT	0.0115144	0.0749975	intron-variant	HERC4	GRCh38.p7	10:68054303	TTTTTTCTTTTCTTC[-/TTCT]TTGTTTTATTAAACA	26091
rs575315992	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67967055	GAGACGGAGTTTCAT[C/T]GTGTTAGCCAGGATG	26091
rs575340529	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67989968	ACAGTTTTTAACTTT[C/T]CTAATACTGTCTCTG	26091
rs575344254	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68057144	TTGATTTTCTTGACA[C/T]ATAAATTTCTCTCAC	26091
rs575350766	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68007529	CTAAATTTTCAGCAA[C/T]GTCTAAGCGCTGAAG	26091
rs575351762	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67999082	AATATGTCTAGGCTT[C/G]ATCCTACACTTGCTG	26091
rs575360309	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67953685	AAAAATGAATTATTA[C/T]CAGTGGACTATGCTA	26091
rs575393285	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68006760	GATATAATATTCTGG[A/G]ATAAATGTTATTTTC	26091
rs575403045	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68015813	ATCTAGGTAAAAATA[C/T]ATATTTTGGCCAGGC	26091
rs575406425	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67931141	AGGCGTGCGACACTA[C/T]GCCCAAATTTTTGTA	26091
rs575408498	snp	A/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68028912	TACAGAATGCACACT[A/T]GTAATTCCAGCATTT	26091
rs575415427	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68061512	CACTCCAGCCTGGGC[A/G]ACAGAGCAAGACTCC	26091
rs575423657	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67960455	CAATGGTGCAATCTC[A/G]TCTCACCGCAACCTC	26091
rs575445045	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68022900	CTCCTAAAGATGTAC[A/G]AATGGTCAACAAGTA	26091
rs575484212	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67960203	CTGGTGAGCTTCTTT[A/G]GCTAGAAATACTCTG	26091
rs575526884	snp	C/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:68022158	AAAGAAACAGCATGG[C/T]CATGGACTGGAAGAC	26091
rs575605024	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67981049	AGTGTGTCCTTACTT[-/A]ATCAATAACATTGGA	26091
rs575611458	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68056839	TTAGCTATTTGCAAA[A/G]GAAATTAAAAAACAA	26091
rs575614395	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68060951	CAAATGTCTTCTAAT[A/G]ATGTATAGGTAAAGT	26091
rs575636559	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67982398	AGTCTCTTCAATAAA[C/T]GGTACTGGGAAAACT	26091
rs575642074	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67952792	GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	26091
rs575676621	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67946230	TCTAGCCTGGGTGAC[A/T]GAGCAAGACCCTATG	26091
rs575699705	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68056278	GTAGCTGATGGTGAT[C/T]AAGTTCATTAAAACA	26091
rs575712874	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68054280	TTAACACTGGTTTTT[A/T]ATAATTTTTTTTTCT	26091
rs575715909	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68016117	CAAAAATATATGTAT[A/G]TATGTGTGTGTGATT	26091
rs575717867	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67978999	TGGAAAGCCTTTCCA[A/G]GAAGCACGAAGACAC	26091
rs575739731	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68070008	GATCGTGCCACTGCA[C/T]TCCAGCCTGGGCAAC	26091
rs575739866	snp	A/C	0.00597247	0.0543191	intron-variant	HERC4	GRCh38.p7	10:68046139	CACTGTTCCAAAAAA[A/C]AAAAAGAAAAAATAC	26091
rs575752720	snp	A/G	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:68028577	GGAGAATCTACAACA[A/G]TCAAGGGATTATCAT	26091
rs575768823	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68047077	TCCATTTGAGGAAAT[C/T]TGAATTACTTGTTAT	26091
rs575800568	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68029235	GTGGCTCACGCCTAT[A/C]ATCCTAGCATTTTGG	26091
rs575823102	snp	A/G	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069779	TGGGCACGGTGGCTC[A/G]CGCCTGTAATCCCAG	26091
rs575840648	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67923321	TGCTCATCCACACAA[C/T]ATTTTTTCTTTAAAA	26091
rs575848412	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68055230	TTAAAGAAACAAACA[A/G]AACTAAAACATCAAT	26091
rs575856590	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67945435	ATCAACATGAGACCT[A/G]TTCAAGAAGAAAAAC	26091
rs575869255	snp	C/G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67975698	CCAATTTGCTTGATC[C/G/T]TGTGGCTTAGCATTG	26091
rs575869347	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68026355	CTTGCCTTGGCTTCC[C/T]GAAGTGCTGGGATTA	26091
rs575885653	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68030458	AACAAAAACAAAAAC[A/G]AACAAATATACATGG	26091
rs575887637	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67985759	AGCAGGTACCAAAGG[C/T]ATTTTCTTATGATGC	26091
rs575891490	snp	C/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68049385	TTTGGAAAGATAAGT[C/G]GGGCACAGTGGCTCA	26091
rs575912483	snp	C/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67983578	AGGTCAGGAGATAGA[C/G]ACCATCCTGGCTAAC	26091
rs575949948	in-del	-/A	0.00755907	0.0610114	intron-variant	HERC4	GRCh38.p7	10:67984266	AGATCACGCCACTGT[-/A]ACTCCACCCTGGACG	26091
rs575950376	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68001288	GAGGTGAAAGGACTG[C/T]TTGAGCCTGGGAGGC	26091
rs575967685	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67968236	AGCCCCAAAATCTAT[C/G]TGCAAATTCCCCCCA	26091
rs576001025	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68000442	AAGTTAACTGGGTGT[A/G]GTGGCATGCACCTGT	26091
rs576018801	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67964163	ATGGTTGTTACTGCT[C/T]CCTTACCTCTAAATT	26091
rs576053947	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68063497	ACAGGCATGAGCCAC[C/T]GCACTCAGCCTTGTC	26091
rs576061617	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68062910	TTCACCAAATTAAAT[C/T]CAAGCTCCTTAATTT	26091
rs576090806	in-del	-/AAGATAATAAC	0.00438332	0.0466095	intron-variant	HERC4	GRCh38.p7	10:67947497	GGTATAGACAGTTCT[-/AAGATAATAAC]AAGATAATAACTGGT	26091
rs576091618	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67952573	CACTGGGCCCGGCCA[A/G]AAAAATACTTATTTT	26091
rs576094480	snp	C/T	0.000399281	0.0141238	intron-variant, missense	HERC4	GRCh38.p7	10:68070573	ATGGCGCCATTGCAC[C/T]CCGGCCTGGGAAACA	26091
rs576109930	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67925320	TTTTCTGGACATTTA[A/C]AATTTGAAGCTATTA	26091
rs576118250	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68045077	CATAATACCAGCATT[C/T]TGGGAGGCCAAGGAG	26091
rs576123401	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68001704	AAAACAGAAACCCAT[C/T]AAATGGAAACTCTCC	26091
rs576179262	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67962898	GCAACAATAATCACC[A/G]TTTTATAAAGACTTA	26091
rs576206653	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68041083	CAACTTAATGTGTAG[C/T]GGCAATATAGGCAGA	26091
rs576207977	snp	C/T			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68010954	GTTCTAGTTCTCTTG[C/T]TATTTCCACCATATC	26091
rs576216407	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68040543	TTGTCACATAAAAAA[G/T]ATAATGTGTTTAATC	26091
rs576234316	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67982957	ACACGGTGAAACCCC[A/G]TCTCTAATAAAATAC	26091
rs576241160	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67962047	CTTGTGGGACTTTTT[C/T]TGAAAAAAGAACTTT	26091
rs576284511	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67984822	CTCCTGACCTCAAGT[G/T]ATCCACCGGCCTCAG	26091
rs576300648	snp	C/T	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:67957557	ACACTTTATAGACAA[C/T]TACTTATCCTGGCAG	26091
rs576331787	snp	C/T	0.000399281	0.0141238	intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010236	GAGAGCCCAGAGTGG[C/T]GACAGAAACAGGGGG	26091
rs576332964	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67947955	TGGCCTCCCAAAGTG[A/G]TGGGATTACAGGCAT	26091
rs576349273	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67957079	TTCTTTGTTTATTCA[C/T]TCATGTGGTTCTGGA	26091
rs576362058	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67964882	GGTTCAAGCAATTCT[C/T]CTGCCTCAGCCTTCC	26091
rs576419263	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68008010	ATGCACACACCACCA[C/T]GCCCAGCAAAACTGT	26091
rs576419998	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68073409	TTCTATGATCCTTTG[C/T]AAAATTTAAAACATA	26091
rs576424484	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67993064	GAGTATTTATTCTTG[A/G]CGAGGCACAGTGGCT	26091
rs576429935	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68020747	GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC	26091
rs576436222	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67970490	CCAGCAACTTGGGAG[A/G]CTAAAGCACGAGAAT	26091
rs576470944	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67925967	AGGGAACCCTGAGCC[A/C]AAACTACTCAGCTAA	26091
rs576518113	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68025764	TCCAAATCTTTAATA[A/T]AAACTCAGTTTTTTC	26091
rs576532802	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67986069	AATAAATCGTCCCTC[A/G]TAGTTCATATCTACA	26091
rs576539467	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68059219	TATATATTTGTCTAC[G/T]TCCCTCAAAAGCCAT	26091
rs576550929	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67995273	TTTTTGTGGTGGTAG[G/T]AGGCATTGATGCTCA	26091
rs576602762	snp	C/T	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012521	AGGAGAGGAGAGAGA[C/T]AGGACTGGCCAGCTG	26091
rs576604422	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68024293	GGTGATAAGTACAAG[A/G]GCATCAGGAATTCTC	26091
rs576625760	in-del	-/A	0.000356026	0.0133374	intron-variant	HERC4	GRCh38.p7	10:67923179	CAACCACTTCAAAAC[-/A]AAAAGATACAGTAGC	26091
rs576661269	in-del	-/CT			downstream-variant-500B	HERC4	GRCh38.p7	10:67921444	AGGTATGTGGAAACA[-/CT]CTCATGGGGAAGAAT	26091
rs576724290	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68019049	TTGCCCAGGCTGGAG[C/T]GCAATGGTGCGATCT	26091
rs576750511	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67979877	GAGAGGTGGAGCTTG[C/T]GGTGAGCCGAGATAG	26091
rs576793495	snp	C/T	0	0	intron-variant	HERC4	GRCh38.p7	10:68035243	TTGCAACCTCCATCT[C/T]CCGGGTTCAAGTGAT	26091
rs576833657	in-del	-/A	0.025576	0.110154	intron-variant	HERC4	GRCh38.p7	10:68018273	CAGATTAAAGGAAAA[-/A]AAAAATCATAAATCA	26091
rs576858825	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67927832	GCTCTCCTAGGTGCT[A/G]GGAATACAGCAGTGA	26091
rs576896292	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68063527	CATACATTTTAAAAA[C/T]TTTCATTTACAAATA	26091
rs576912374	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67950776	AAGTCTATGGATGCA[C/T]GTGTGTATACACACA	26091
rs576937093	snp	A/C	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67934240	TATTTGTTAACATTT[A/C]TATATTATTCACAGT	26091
rs576974288	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67929883	AACGGCACGATCTCC[A/G]GCTCACTGCAACCTC	26091
rs576999799	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68060400	ACACCACCATACCCA[A/G]CTAATTTTTGTATTT	26091
rs577044046	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68037812	AAATGGACAAATATA[C/G]CGTGTTCTAGAATTG	26091
rs577048138	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67929287	AGATCTGTGTAACCA[C/T]TGCCACAATTAGGAT	26091
rs577057037	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68042333	CTCTTACGAAAATCT[A/G]TAAACACTAGGCAGG	26091
rs577057160	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68051384	GAGTCTCGCTCTGTC[A/G]CCCAGGCTGGAGTGC	26091
rs577058061	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68027831	GGGAGGCTGAGGCAG[A/G]AGAATCACTTGAATC	26091
rs577059451	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67935016	GATGTCACGCATCAT[C/T]CTGAGGATACTGATT	26091
rs577080796	snp	C/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68045874	GACTGAACCAAAGAG[C/G]CTGAAATTCCTATCT	26091
rs577082370	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67980451	AAAGACAAATATTTT[C/T]CTAGACAAACAAAAG	26091
rs577085992	snp	G/T	0.00199481	0.0315187	intron-variant	HERC4	GRCh38.p7	10:67972463	GAGGCGGAGGTTGCG[G/T]TGAGCTGAGATCGTG	26091
rs577094210	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68035749	CAATGGCCAGTTCTC[A/G]CACACTTGCTGTTCT	26091
rs577101505	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:68026751	GGGAGGCTGAGGCAG[A/G]AGAATTGCCTGAACC	26091
rs577146046	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68003760	CTTTATCCATGTCTG[A/T]TGATGAACACTTAAA	26091
rs577170483	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67952409	CTGCCTCAGCTTTCC[A/G]AGTAGCTGGGATTAC	26091
rs577181299	snp	A/G	0.000399281	0.0141238	intron-variant, splice-donor-variant	HERC4	GRCh38.p7	10:68074648	AAATCATCTGCACAC[A/G]CCCAACCTCGCAGCC	26091
rs577216364	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68006043	AAAACAAATAAGCAA[A/G]GAGAAAAATGATAAA	26091
rs577224574	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68060729	CTGGTACAGGTAACA[C/T]CAACCACTCAGGCTT	26091
rs577252776	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68005267	TATCCTCTTGTTGTA[C/T]TAATCCTTTTATCAT	26091
rs577313271	snp	C/T	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68060237	TTTTTGTTTGCTTGT[C/T]TTTGAGACAGAGTCT	26091
rs577344241	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67974342	CTTAAGAGAAGAAAA[A/G]CCACCAAAGAAACAA	26091
rs577372615	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67943765	ACTAAAACACAGACA[A/C]CCAGGGTTACAACCT	26091
rs577377768	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67959902	GAATCTTCAGAAATA[G/T]GTTACTAAATTTGTG	26091
rs577407231	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67946038	TAGGCAGATCACTTG[-/A]GCCCAGGAATTTGAG	26091
rs577440379	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67959357	ACCTTGTGATCATAA[A/T]ATGATTGAGGCTTGA	26091
rs577478058	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67954404	TTTGTTAATTTAAAA[C/T]GTGTGGTAAGCATCA	26091
rs577478909	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67973424	ACAAGGCCCAATCCC[A/G]TAGGAATTAGAATAA	26091
rs577505530	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67944588	CCACCCAGGAAAACA[A/T]GACCTCACCAAACGA	26091
rs577542442	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:67960993	TCTTGCGGATTTGGC[A/G]GACCTGTTGGTGCTG	26091
rs577555029	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67989730	CAGAACAGTAAGAGA[C/T]AGAAGTGCAAGATCA	26091
rs577580970	in-del	-/TTTC			intron-variant	HERC4	GRCh38.p7	10:67964048	GCTGAGGTCAATTAT[-/TTTC]TTTCTTAAAAAATTA	26091
rs577581179	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67995279	TGGTGGTAGTAGGCA[C/T]TGATGCTCATTCACT	26091
rs577590932	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67976600	CCTGAGAACCAAAAA[C/T]CAGGTGAGCACTCAT	26091
rs577622404	snp	A/G	0.00119737	0.0244387	intron-variant	HERC4	GRCh38.p7	10:67967249	AATTACTGAGTGCCT[A/G]CTATATGCAAAATGC	26091
rs577628754	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67929938	CCTGCCTCAGCCTCC[C/T]GAGCAGCTGGGATTA	26091
rs577681601	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67974920	ATTTGGCTGGGCGCA[G/T]TGGCTCATGCCTGTA	26091
rs577684898	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68014898	AGGGGACATGGCATC[C/T]CCAGGTCTCACCCTT	26091
rs577697970	snp	G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68029711	TTTTATTTATATAAT[G/T]TACATATAATTTTTA	26091
rs577698183	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67927453	TTTTTTTTAGATAGA[A/G]TCTTGCTCTGTCACC	26091
rs577727806	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:68000196	TTTGCCTGTACTAAC[A/G]GGGGCGATGCTGAGG	26091
rs577768036	snp	C/T	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:68009327	TTAATGTGGCCCCAG[C/T]TGGTCCCAAACTCCT	26091
rs577787702	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68056121	GAAGAGGAAAGAAGG[C/G]GTAAAGGTGAAATAT	26091
rs577809293	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67999168	TGTATCTCAAGATTT[C/T]GTTTTTGTCTATAAA	26091
rs577856572	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68016190	ACCTTAAGCTCTAGA[C/T]TTGATGTAAGAGCTC	26091
rs577895789	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68015871	ACTTTGGGAGACCGA[C/G]GCAGGTGGATCACTT	26091
rs577930833	snp	C/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67977321	TGGCCAGAAGGGAAC[C/G]CACTGCCTCGAAAAG	26091
rs577936352	snp	C/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68032041	ACAGGCATGAGCCTC[C/T]GTGCCCGGACGTTAA	26091
rs577980546	snp	C/T	0.0023933	0.0345097	intron-variant	HERC4	GRCh38.p7	10:67981832	TGTAATCCCAGCTTC[C/T]TGGGAGGCTGAGACA	26091
rs578022458	snp	A/G	0.00159617	0.0282053	intron-variant	HERC4	GRCh38.p7	10:68023552	GCCACAAGAGAGTAT[A/G]GAGAATAGGGAGTCA	26091
rs578043419	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67924150	TTGAACCGACTGCAA[A/G]TCGAAAATATTTTCA	26091
rs578076680	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:67946988	GCAAATATTATTACC[A/G]CTAAAGAGAGAGAGA	26091
rs578085998	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68056562	GTGTGACTTGAATTC[C/T]TATAAGAGTGACCAA	26091
rs578087892	snp	A/G	0.00478085	0.0486577	intron-variant	HERC4	GRCh38.p7	10:67931436	AGACTGAGGCAGAAC[A/G]AAAACCCATTCAGCT	26091
rs578139860	snp	A/G	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68039360	AAAGAAAAAACGGGG[A/G]ATGGGGAGGTACACA	26091
rs578153242	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68025948	TTCATTATCATTATA[C/T]TGTCTTGCTGAATTC	26091
rs578163997	snp	C/G/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68038837	GTAATTTCCTTCCCC[C/G/T]CTTTCCTGAGTTTTG	26091
rs578165472	snp	G/T	0.00358779	0.0422022	intron-variant	HERC4	GRCh38.p7	10:68047935	TTTGTTTTTGTTTTT[G/T]TTTTTGTGAGACAGG	26091
rs578197071	snp	A/G	0.000798403	0.0199641	intron-variant	HERC4	GRCh38.p7	10:67969011	ATCCTGGACCATACA[A/G]TAAGTCTTCATACAT	26091
rs578197116	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68053783	AGTTCTGTGAATGCC[A/C]ATGTCCAGGAATGAC	26091
rs578197733	snp	G/T	0.00676609	0.0577691	intron-variant	HERC4	GRCh38.p7	10:67993282	CCCAGGAGGCGGAGG[G/T]TGCAGTGAGCCGAGA	26091
rs578206930	snp	A/T	0.000399281	0.0141238	intron-variant	HERC4	GRCh38.p7	10:68063674	CAGGCGTGGTGGCTC[A/T]CACCTGTAAACCCAG	26091
rs578243444	snp	A/T	0.00318978	0.0398085	intron-variant	HERC4	GRCh38.p7	10:68070618	TCTCAAAAAAAAAAA[A/T]AAAAATAAAAATAAA	26091
rs578252998	snp	C/T	0.000399281	0.0141238	intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68070050	CTGTCTCAAACAAAA[C/T]GAAACAAAACAAAAC	26091
rs745307394	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67941764	GCTCACTGCAACGTA[C/T]GCCTCCTGGGTTCAA	26091
rs745328979	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67988627	TCTGTTAATAGGAAT[A/G]GGGAAAGAGGAAAAT	26091
rs745343043	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68056999	AGGAGTTGTTTTTGC[-/A]TTTTGTTTTGACAGA	26091
rs745352137	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68055045	CTCCTGACTCAGGCT[C/T]CTGAGTAGCTGGGAT	26091
rs745365899	snp	A/C	1.64798e-05	0.00287047	missense, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68034040	CAGAAAGGGTGAGTA[A/C]AAAACTATGGGCTCC	26091
rs745367811	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68005560	TTAATAAGGACTTAC[C/T]CCTGACATTTTAAAA	26091
rs745392144	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67970855	GTTTCTGCTTTAAGA[A/C]TCTAGAAAAAAAAAG	26091
rs745401647	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67955502	ACAGGCTGGGCGCAG[C/T]GGCTCACGCCTGTAA	26091
rs745404665	snp	C/T	3.30671e-05	0.00406602	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:68032823	ACAACAAATATAAAC[C/T]ATTTTCTGAGATCTT	26091
rs745440006	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68053449	GCTGGGACCACGGAC[A/G]TGAGCTACCACACCC	26091
rs745453978	in-del	-/G			intron-variant	HERC4	GRCh38.p7	10:67938939	ACAGAGCAAGACTCT[-/G]TCTCAAAAAAACAAA	26091
rs745465955	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68017648	CATGCCACCACACCT[A/C]GCTAATTTTTGTATT	26091
rs745484793	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67928500	GTAGGAGAGGGGACA[A/T]GCATGGTCCAATTAT	26091
rs745502342	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67969265	ACCAGAATTGGCTCA[C/T]TTGTGGCAGAGAGAA	26091
rs745514516	in-del	-/A	1.91075e-05	0.00309085	intron-variant	HERC4	GRCh38.p7	10:67991107	AAGACAATAAATTTG[-/A]AAATTTCAGCATATT	26091
rs745514559	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68034847	TAACCTCACACATAT[A/C]CAGTCTATCATATAT	26091
rs745525085	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67933904	TTTAAAGTTATAAAG[C/G]ATCTAAGTAGCGGAA	26091
rs745525097	in-del	-/A	1.66327e-05	0.00288376	intron-variant	HERC4	GRCh38.p7	10:68034204	GTAAAACAGTAATGG[-/A]AAAATTAACCATTTT	26091
rs745547582	snp	C/T			intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069268	ACTGAAGATTAAATA[C/T]ATTTGTTAGCTATAA	26091
rs745548730	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68016359	TTTCTTTTTTAAAAA[C/T]TTTATTATTTTTGAG	26091
rs745552503	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68033385	ATAACTCACTTTTGT[A/C]CATTTCAGTCATTAC	26091
rs745584499	in-del	-/AAAAAG			intron-variant	HERC4	GRCh38.p7	10:67924046	TTTTAGTCTTGAAGC[-/AAAAAG]AAAAAGAAAAAGAAA	26091
rs745624493	snp	C/T	1.72797e-05	0.00293931	utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68073151	TCAATAAAAAATTCT[C/T]TTCTGAAACCCCGGA	26091
rs745663995	in-del	-/GTAAAAGAAATCA			intron-variant	HERC4	GRCh38.p7	10:67994007	CACAATGTTTTATTT[-/GTAAAAGAAATCA]GTAAATACCTGTCCA	26091
rs745668552	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67978881	ACCATCAAGGCAGTA[A/C]CTTTATGAGTCTGCC	26091
rs745681617	snp	A/C	1.67105e-05	0.0028905	intron-variant	HERC4	GRCh38.p7	10:67954565	CATGGGTATATACAC[A/C]GAAGTAATTTAGATG	26091
rs745682630	in-del	-/AGA			intron-variant	HERC4	GRCh38.p7	10:67973641	GATTAGGATATTGCT[-/AGA]AGATTTAAAGTCTCT	26091
rs745692304	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67992899	GCATAAGCAGCATTT[C/G]GTGAAGTTTACAAGC	26091
rs745749829	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68027108	AACACAATCACAATT[A/G]GTATTCTTCAGTTCA	26091
rs745756564	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67978193	AGACAGGAGAATCGC[G/T]TGAACCCAGGAGATG	26091
rs745780768	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67993128	GGTGGGAGGATCATT[G/T]GATGTTAGGAGTTCG	26091
rs745793831	snp	A/C			upstream-variant-2KB	HERC4	GRCh38.p7	10:68076300	AGAGACAAGGTTTCG[A/C]CATATTGGCCAGGCT	26091
rs745821827	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68042485	AAAATTGGCCAAGCA[C/T]AGTGGTGCACGCCTA	26091
rs745825516	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68017374	TAGCCAAAGGCCTGG[C/T]TTTACTGAACCACAG	26091
rs745853634	in-del	-/G			intron-variant	HERC4	GRCh38.p7	10:67965585	CTGATTCCGGAAGGT[-/G]GGAGTATCCTAAAAA	26091
rs745870692	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68006347	TCTGCTGTTGATGAA[A/G]CGCCTCAGCGTTTTT	26091
rs745872927	snp	C/T	1.65239e-05	0.00287431	intron-variant, missense	HERC4	GRCh38.p7	10:67939648	ATCCAGTAACTGTTG[C/T]ATGCTTCTGCAAAAT	26091
rs745958405	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67974819	CCATGGAGGGGCATA[A/G]GGGACTGTCAGGCTT	26091
rs745966264	in-del	-/CTTT			intron-variant	HERC4	GRCh38.p7	10:68045709	ACCATTTAAAATTAA[-/CTTT]CTTTCAGCTTAATAA	26091
rs745967370	snp	C/T	1.65154e-05	0.00287358	synonymous-codon, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67988753	ACCGATCTTGTAGAG[C/T]TTCAAAAGATGTACC	26091
rs745970922	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67974469	TAAAACTAAGGAATA[C/T]CTGAAAGGGAACAAA	26091
rs745974295	snp	C/T	1.65877e-05	0.00287986	synonymous-codon, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67988690	TTCTAAAACCTTTAA[C/T]GCAGTATGAAGAAAA	26091
rs745979496	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67939195	CATATTACAATAACC[C/T]TTTGCTTCTCTAAAG	26091
rs746012378	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68021537	TAAAATGCTGCGTGC[A/T]GTGGCTCATGCCTGT	26091
rs746016380	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67932219	ACCTTGGCCTCCCAA[A/G]GTCCTGGGGTTACAG	26091
rs746024936	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67996412	ACAATTCTGTAAATT[A/G]TAATTCTACTTAGAA	26091
rs746042363	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68028643	ACCTTTCACTCGTTA[C/T]GGCAAAACAAAAACA	26091
rs746100570	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68037514	GGAATGCAAACAAAG[C/T]TAATAAATATGATGT	26091
rs746149175	snp	G/T	1.64803e-05	0.00287052	synonymous-codon, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:68044529	TCCACATGAAACAGC[G/T]ACAATATTTTGGGCA	26091
rs746161871	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67952297	ATCCAAACAGCTAAA[C/T]ATGACTAAAGAGAGT	26091
rs746180938	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67949055	TCAGGAAATCGAGAT[C/T]ATCCTGGCTAACACA	26091
rs746181402	snp	C/T	3.37986e-05	0.00411074	intron-variant	HERC4	GRCh38.p7	10:67956859	TTAAAAAAAAAAACC[C/T]TCTCAAATAATATTT	26091
rs746191911	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67997673	TTAAAATTAGGCTTT[-/A]TTTTTTTAGTATCCT	26091
rs746208264	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68032273	TACCCAAGACAGTGA[G/T]AGGTCAGAGTTAAAG	26091
rs746220767	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67981672	TTCAAAAAAACTGAA[A/G]TAGGCCAGGCATGGT	26091
rs746236227	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67930271	GGCAAAACACACATA[C/G]CATAAAGTTTGTATC	26091
rs746242089	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67997466	AAAATAGGTAACTAA[A/G]TATTATTTCTCAAGC	26091
rs746259558	snp	C/G	1.64939e-05	0.0028717	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:67992315	GAAGTCATCTGGTGG[C/G]CCACAGTTCTAAATT	26091
rs746276275	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68046618	AAGATTGTGACTAAA[C/T]GCTAAGATAAACATA	26091
rs746315267	snp	A/G			intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010616	GAGGGTTTCGGCTTT[A/G]CATATCTCCTGAATA	26091
rs746340073	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67983264	GAACCTTCGTACATT[C/G]TTGGTGAGAATGTAA	26091
rs746349509	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67961140	ACCAGTTTTTGGCCA[C/T]GGAACTCATTTTGTC	26091
rs746368133	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68060530	AGGCGTGAGCCACCG[C/T]GTCCAGCCATAAATA	26091
rs746393290	snp	C/T			intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010267	AAAGGCACTAAGGAA[C/T]ACAGTGCAGTGCAGT	26091
rs746427700	snp	A/G	1.66518e-05	0.00288542	intron-variant	HERC4	GRCh38.p7	10:67959065	ATTACTCAGGAGAAA[A/G]TGGAGTATATTTTAC	26091
rs746439422	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67960393	TTAAAAGCCTAAAAT[A/T]TTTTTTTTTGAGACG	26091
rs746467454	snp	C/T	1.96419e-05	0.00313378	intron-variant	HERC4	GRCh38.p7	10:67991043	AAAGAAAAAAAAAAA[C/T]AGAATAAAAATTTAA	26091
rs746479287	in-del	-/AA	0.478764	0.100831	intron-variant	HERC4	GRCh38.p7	10:67991032	TAAAAAACAGAAAAG[-/AA]AAAAAAAAATAGAAT	26091
rs746523956	snp	A/T	3.51939e-05	0.00419473	intron-variant	HERC4	GRCh38.p7	10:68034237	TCACATGCAAAAAAT[A/T]TAATTTGAAAATAAT	26091
rs746532367	in-del	-/TAAA			intron-variant	HERC4	GRCh38.p7	10:68063636	AGATGTTCTTTTTCC[-/TAAA]TAAATAAACAGAGGT	26091
rs746602127	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68015132	AGCAGAAACAACAGT[A/G]TCTCAGTTCCGAGCC	26091
rs746608186	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67945490	GAAAAGAACTTTAAT[C/G]AGCAATATCATGTGA	26091
rs746618837	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68041084	AACTTAATGTGTAGC[A/G]GCAATATAGGCAGAA	26091
rs746636958	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67981537	ATAGACCAAATGGAC[C/T]AAACACATATTTACA	26091
rs746642750	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67947481	TGACAGAATCAAAGC[A/G]AGGTATAGACAGTTC	26091
rs746644769	in-del	-/CA	4.11066e-05	0.00453339	frameshift-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67966796	TCTGTCCCATTTTCT[-/CA]TTTACCTACAAAAGA	26091
rs746681996	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68038674	ATTATGAAACCTATT[C/T]CTTACAAGCTATCCT	26091
rs746684356	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68030873	GGTATGTCTTTCCAT[C/T]TATTCTGTTTTTAAA	26091
rs746720760	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67996421	TAAATTGTAATTCTA[C/T]TTAGAAGCAAAACAG	26091
rs746731866	snp	G/T			upstream-variant-2KB	HERC4	GRCh38.p7	10:68076136	TATTTATTTATTTAT[G/T]TATTTATTGAGACAG	26091
rs746734867	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67926972	CAGCTGTACATTATC[C/T]GGCACACAGTAGAGG	26091
rs746741329	snp	C/T	1.66946e-05	0.00288912	intron-variant	HERC4	GRCh38.p7	10:67954753	CCTAAAATAGCACAA[C/T]GCAAACACCAAATAG	26091
rs746774893	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67941961	GTGCCTGGCCAAAAC[A/G]TGACTTTTTAATGGC	26091
rs746806435	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67973564	ACCAGTTGTATTTTA[C/T]GAATATTATTCGGCT	26091
rs746807972	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67976673	AAAAAAGTCTTGAAT[C/T]ACCAACATCACCCCT	26091
rs746851626	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67941517	AATAAACACCTGTAA[A/G]CCAATCACTCAGGAA	26091
rs746859012	in-del	-/AA			intron-variant	HERC4	GRCh38.p7	10:68061532	GCAAGACTCCGTCTC[-/AA]AAAAAAAAAAAAAAA	26091
rs746861634	snp	A/G			intron-variant, utr-variant-5-prime	HERC4	GRCh38.p7	10:68074815	CACAGCCCTGCCCTC[A/G]CCCCACGCCCCTCAC	26091
rs746866530	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68065021	AATAAATTTTGGTAC[A/T]TCTAAATGATGAAAT	26091
rs746891948	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67989656	ATAAAGGCCAGGAAA[C/T]AGAGATAAAATCTAG	26091
rs746904219	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67994412	CAAAAGTTAAGTTTC[C/T]TTAATTTCCTTTTTT	26091
rs746912997	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68005413	CATCCCTTTATTTTC[A/G]GTGTATGTGTGTCTT	26091
rs746919500	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68062502	GCTCACGCCTGTAAT[C/T]CCAGCACTTTGGGAG	26091
rs746951416	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68053421	TGATCCTCCTGCTTC[A/C]GCCTCCCGAGTAGCT	26091
rs746979863	snp	C/T	1.77215e-05	0.00297665	intron-variant	HERC4	GRCh38.p7	10:67988614	TGAACAGTATCAATC[C/T]GTTAATAGGAATGGG	26091
rs747005413	snp	A/T	1.64901e-05	0.00287137	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:68025557	TTACCGTCCACAAGC[A/T]ATCTCAGTGACAATG	26091
rs747017350	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67953979	TAGCTATTCTATCTA[A/C]ATTTCTTTCAAGTCA	26091
rs747022336	in-del	AGGG/TCACA			intron-variant	HERC4	GRCh38.p7	10:67967821	CAAGTTAAATAAACA[AGGG/TCACA]ATGAGGAAACAATCA	26091
rs747050232	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67938002	ACAGTCTTAAAATTT[C/T]CTTGAAAAAATTATG	26091
rs747072916	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68071835	GGCAGAAGAAAATAC[A/C]CTAAGACCTTAACCA	26091
rs747088957	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68037260	CCACCACACCCAGCT[A/C]ATTTTTTGTATTTTT	26091
rs747098882	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67923893	ACCGATTTGGACACA[C/T]AAATTCTGACAACTT	26091
rs747105574	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67952854	GCAGTGAGCCGAGAG[C/T]GCGCCACTGTACTCC	26091
rs747132596	in-del	-/A			upstream-variant-2KB	HERC4	GRCh38.p7	10:68077127	GCAAAACTCCATCTC[-/A]AAAAAAAAAAAAAAG	26091
rs747144570	snp	A/G	1.65718e-05	0.00287848	intron-variant	HERC4	GRCh38.p7	10:68044580	TACAGAAATCAAGAA[A/G]AGAAATATTGCATTC	26091
rs747145301	snp	A/G			intron-variant, utr-variant-5-prime	HERC4	GRCh38.p7	10:68074718	CAGAGGCCGGCGGCC[A/G]AGGCTTGGCAGTGCG	26091
rs747202842	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68072142	TCATTAACTTTTAGT[C/T]ATCATAATTGAAAGC	26091
rs747210875	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67965910	GCATTAAAATTTTAT[G/T]TGCCTAATTCAAGTT	26091
rs747235049	snp	C/G	2.85189e-05	0.00377606	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:67992616	ATTACCTGGGGACTA[C/G]AGTAATGTGAAAAGC	26091
rs747242850	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67955459	TAAAGAGGGAGGAGC[-/A]AAAACAAACCTTTAA	26091
rs747248358	in-del	-/AGA			intron-variant	HERC4	GRCh38.p7	10:68031158	CTACTATCTTCTGAG[-/AGA]AGAATACAAAAGATT	26091
rs747249911	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67999170	TATCTCAAGATTTCG[C/T]TTTTGTCTATAAATG	26091
rs747268435	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68000104	CTCAAGCAATCCTCC[C/T]GCCTCAACCTCTCAA	26091
rs747298473	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67965145	TTACCAAATGTTCGT[A/T]GTTCTTGAAATTCTC	26091
rs747304971	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68018054	ACTAGAAAACCTTCA[C/T]AATAAAACCTGGTGA	26091
rs747309252	snp	A/G	1.66446e-05	0.00288479	intron-variant	HERC4	GRCh38.p7	10:67959175	ACAATAACGAGGAAA[A/G]AGCAATATTAGTGTC	26091
rs747328455	snp	C/T	1.64944e-05	0.00287175	intron-variant	HERC4	GRCh38.p7	10:67932591	CAGAGATTAGTTTTC[C/T]CCTACCTTTTCCAGT	26091
rs747378846	in-del	-/A	1.72777e-05	0.00293914	intron-variant	HERC4	GRCh38.p7	10:67925201	TTCTAAAAACAACAT[-/A]ATCTTTTATTAGTAT	26091
rs747395098	snp	A/G	1.66488e-05	0.00288515	intron-variant	HERC4	GRCh38.p7	10:67959070	TCAGGAGAAAATGGA[A/G]TATATTTTACTCTAA	26091
rs747404290	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68058601	AGGTTTTATCTTTAT[G/T]TTTTTGAGACGAGAG	26091
rs747422589	snp	G/T	0.000833681	0.0203996	intron-variant	HERC4	GRCh38.p7	10:67996092	AGGAGGATCACTTGA[G/T]CCCAGGAGTTCAAGA	26091
rs747427541	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67964965	TTTTAGTAGAGACGG[C/G]GTTTCACTATGTTGG	26091
rs747441080	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67974694	TATTGTTAATTTTTC[A/G]TAAAAAGAATTGTTT	26091
rs747456851	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68008328	TATTCAAAGCCCAAG[G/T]GCTCTTTAGTCAGCA	26091
rs747458360	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68022505	ACTCCATCTCAAAAT[A/C]AATAAATAAATAAAT	26091
rs747474175	in-del	-/G	3.32768e-05	0.00407888	intron-variant	HERC4	GRCh38.p7	10:68044388	TAAGGACCTCTTTCT[-/G]GGTCACCTTTGTTAC	26091
rs747481052	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68068200	AACAAACATAAAAAA[-/A]TTGGCCAGGCCTGGT	26091
rs747484412	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68073231	TTCAAAGAAAAAAGG[A/T]TGTATAATTGCTCTT	26091
rs747553863	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67931096	GTTCAAGCGATTCTC[C/T]TGCCTCAGCCTCTCG	26091
rs747578872	snp	A/C	1.6476e-05	0.00287014	missense, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68034087	ATGAAAGGGATTCCA[A/C]GCAAAGACTTAAGCA	26091
rs747595221	snp	C/T	1.64977e-05	0.00287203	missense	HERC4	GRCh38.p7	10:67954976	ACCTTGAGTGGCTTC[C/T]TGTAATCTATGTTCT	26091
rs747605825	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67973576	TTATGAATATTATTC[A/G]GCTGAGAGAGTGAGG	26091
rs747650587	in-del	-/AGAGATTA	1.6516e-05	0.00287362	intron-variant	HERC4	GRCh38.p7	10:67932577	CCATTTAACAATATC[-/AGAGATTA]GTTTTCCCCTACCTT	26091
rs747684551	snp	C/T	1.67455e-05	0.00289352	intron-variant	HERC4	GRCh38.p7	10:67954766	AATGCAAACACCAAA[C/T]AGACTGTAAAGAAAT	26091
rs747694163	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68044764	CCAAACGTAATTCTC[A/G]TTGTGGTAAACCACA	26091
rs747723125	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68056052	CACGCCTGGCCCTTT[C/T]CTTTTAAAGAAGTAC	26091
rs747724991	snp	C/T	1.68542e-05	0.0029029	missense	HERC4	GRCh38.p7	10:67925106	ACTGTTTCTTCTTTT[C/T]CAATGGTAATTCGTG	26091
rs747748690	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67994979	ACAGGTGTGAGCCAC[C/T]GCATCCTATCCTTAA	26091
rs747782628	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67944649	AGAGACTGAGATATA[C/T]GACCTTTCAGTCAGA	26091
rs747799831	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68043230	AAAAATAAAGGAAAC[C/T]AGAAAGTTTTGCCAT	26091
rs747833089	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67955236	TATTCTATAATTCCT[A/G]TGCTACTGAATTAAC	26091
rs747836944	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67993435	GAGGCAGGAGGATGG[C/T]GTGAGCCCAGTTCAA	26091
rs747841419	snp	C/T	1.65195e-05	0.00287393	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67988779	GTACCACAACTTCCT[C/T]AAAAAGTTCTACTAT	26091
rs747863345	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68043710	AATCCCAGCTACTCA[A/G]GAGGCTGAGGCAGGT	26091
rs747870763	snp	A/G	1.77571e-05	0.00297964	intron-variant	HERC4	GRCh38.p7	10:67956834	CTGTCCAGAAACATC[A/G]AAGAAACAATTAAAA	26091
rs747876854	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67958285	GTTTACCTCCATCCT[A/G]TATTTGTGGCACTGC	26091
rs747881616	snp	A/G	1.65759e-05	0.00287883	intron-variant	HERC4	GRCh38.p7	10:68032771	AGAAGTTTTAGAAGT[A/G]CAATACCTTGGTTAG	26091
rs747891701	in-del	-/TT			intron-variant	HERC4	GRCh38.p7	10:68073529	TTTTGCTTTAAATAA[-/TT]TCAATGGGAACAAGA	26091
rs747897415	snp	C/G	1.65097e-05	0.00287308	missense	HERC4	GRCh38.p7	10:67922999	GTAGAGTTTCTTTTT[C/G]TGTATATTTTGGAAG	26091
rs747897938	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68046761	ACTTGAACCCAGGAG[-/T]TTTGAGACCAGCCTG	26091
rs747918556	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68038945	TCCCAGCATCTCCAT[C/T]GGTTCTTTCCCTTTG	26091
rs747968162	snp	A/G	1.64765e-05	0.00287019	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:68025583	CAATGCTTCCCATAA[A/G]TTCAAAAACTTTCCT	26091
rs747969865	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67987568	ACTGCAGACCTGGAC[C/G]CTGATATGCTAAAAG	26091
rs748009317	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67952419	TTTCCGAGTAGCTGG[A/G]ATTACAGGCATGTAC	26091
rs748030875	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68052170	GACATAGGCAAAACC[A/T]GAAAAGATAAAGTGC	26091
rs748036840	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68015965	AAAATTAGCTGGGCA[C/T]GGTGGCATGCGCCTG	26091
rs748038320	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68050531	AGCCCCATCAAATTA[C/T]TGGGATACTAACTTT	26091
rs748049964	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67967742	GTAAAAATAGTTTAA[A/C]CCAAATCCAATCAAG	26091
rs748094829	snp	C/T			intron-variant, downstream-variant-500B	HERC4	GRCh38.p7	10:67966326	ACAATAATGCATTCT[C/T]AGGAGTTCCAGTATG	26091
rs748098770	snp	C/T	1.6528e-05	0.00287467	intron-variant, missense	HERC4	GRCh38.p7	10:67940955	TCCCAACATCAGGCA[C/T]TAGTTCTTTCAAATC	26091
rs748103470	snp	C/T	1.71572e-05	0.00292888	intron-variant	HERC4	GRCh38.p7	10:67939694	GAGAGGAAAAAATTA[C/T]TGGATATTTTGACTA	26091
rs748108321	in-del	-/AAC	3.32613e-05	0.00407793	intron-variant	HERC4	GRCh38.p7	10:67959159	AGCAGTGCAGAATAT[-/AAC]AATAACGAGGAAAGA	26091
rs748116935	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68067604	TATATTTTAAGGAGC[A/G]GCTCGTTTATAAATT	26091
rs748120034	snp	A/C	0.00159668	0.0282097	intron-variant	HERC4	GRCh38.p7	10:67996165	ATTAAAAATTGGTTA[A/C]GCGTGGTGGCGCATG	26091
rs748144003	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67981299	AAAGAAGGTCACTAT[A/G]TAATGATAAAGTGGT	26091
rs748186150	snp	C/T	1.65979e-05	0.00288074	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67990220	TCTTACCAAGTACTT[C/T]CAGTGGTGCCTTTTC	26091
rs748194719	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67934905	TTCGTTTCTGGGAAG[-/T]TTTTTTTTTTTTTAA	26091
rs748220488	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68048529	GATGAACAGGCAGAG[A/C]ATAGAGGATTTTGAG	26091
rs748221387	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67999994	TGTTATATTTGAGAA[C/G]AACGGTTACTTAATC	26091
rs748241178	snp	C/T	1.69983e-05	0.00291528	utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68073137	TTGGTCTTCCAGTTT[C/T]AATAAAAAATTCTCT	26091
rs748255928	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67927481	ACCAGGCTGGAATAC[A/C]GTGGCACGATCTTGG	26091
rs748280124	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67964697	GTTTACTAAACTCTC[C/T]ATGATCTGGCCCCTG	26091
rs748291353	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67963448	TCTAGAACTTCTGAC[C/G]TCAGGTGATCTGCCC	26091
rs748292294	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68047620	AAGCAGGCATACAAA[C/T]AGATATTTAACTTAT	26091
rs748300000	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68046309	AAAATGATAGGATGA[C/T]AAGACAGGTAAGTAA	26091
rs748306314	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68020488	AAAAAAAGTTTGGGC[C/T]GGGCGCGGTGGCTCA	26091
rs748311485	snp	A/G			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012432	TCTTTTCACTTATGT[A/G]CTTAGAGGCCACTGT	26091
rs748329413	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68063955	AAATAATAATTAAGA[A/C]ACAGAGGCTGGGCAT	26091
rs748329447	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68048146	CTGGTCATGAACTCC[C/T]GGGCTCAAGTGCTCC	26091
rs748330061	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67953086	AAGGAGGATAGCCCA[C/T]ACATTTTCAAAAGAT	26091
rs748330082	snp	A/T			utr-variant-3-prime	HERC4	GRCh38.p7	10:67922047	ATGGCATGAGACAAC[A/T]AAGCATCAGCACCAT	26091
rs748352245	snp	C/T	3.30415e-05	0.00406444	missense	HERC4	GRCh38.p7	10:67932742	GAAGCCACTGATTTA[C/T]TGAATATGTAATCCA	26091
rs748384585	snp	A/T	2.20107e-05	0.00331736	intron-variant	HERC4	GRCh38.p7	10:67966835	ATTGACATTAAATTT[A/T]ACCAGTACTCAAGAC	26091
rs748385823	snp	C/T	4.52714e-05	0.00475748	intron-variant, downstream-variant-500B	HERC4	GRCh38.p7	10:67966618	TTCAAAACCAAGCAA[C/T]TGTTTCTTTTTTTAT	26091
rs748443424	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67977998	AAAAGCCCTTGGGCT[A/G]GGCATGGTGGCTCAC	26091
rs748467507	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67928176	TTAATAAGGCTGAGG[C/T]AGAGTGAGAGGAACA	26091
rs748469130	in-del	-/AAG	1.70536e-05	0.00292002	intron-variant	HERC4	GRCh38.p7	10:68038176	TTAATATTTCTAGAA[-/AAG]AAGAAGACAGATCAA	26091
rs748473068	snp	C/G	1.64822e-05	0.00287068	missense	HERC4	GRCh38.p7	10:67936171	TTTTGTTTGTTAACA[C/G]CTGTGTCTGCACCAT	26091
rs748523482	snp	C/T	1.64806e-05	0.00287054	intron-variant	HERC4	GRCh38.p7	10:68038055	AAAAGTATCAAGTAA[C/T]AAAACTGAAGAGAAA	26091
rs748532987	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68019795	TTGTAGAAGCCAGGG[G/T]GGGCAATAACGACTT	26091
rs748623912	in-del	-/TCAC			intron-variant	HERC4	GRCh38.p7	10:67967821	CAAGTTAAATAAACA[-/TCAC]AATGAGGAAACAATC	26091
rs748640601	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67935766	TCTAACTGCTTCTTA[G/T]AAGAGTTCTAGCATT	26091
rs748652288	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67971799	TTAGTTAATAAAATA[C/T]GCCAAGAAAATAACA	26091
rs748669492	snp	C/T	0.000491047	0.0156615	intron-variant	HERC4	GRCh38.p7	10:68038209	GACCAGTTAATTCCA[C/T]TTAACAAATTGATCT	26091
rs748682077	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67944448	TTACAACACCCAAGT[C/T]CCTCTAAATACCTGG	26091
rs748699656	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68000650	TTATTTGGAAATAAG[A/G]TCACTGCAGATATAA	26091
rs748740321	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67984829	CCTCAAGTGATCCAC[C/T]GGCCTCAGCCTCGCA	26091
rs748755387	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67996829	ATAAAAAAATAAAAT[-/A]AAATAAAAATTAGCT	26091
rs748762171	in-del	-/AATC			utr-variant-3-prime	HERC4	GRCh38.p7	10:67922544	ACAAAATGAAAAAAT[-/AATC]AAATGACTATTGCAG	26091
rs748768500	snp	A/G	4.99031e-05	0.0049949	synonymous-codon	HERC4	GRCh38.p7	10:67925119	TTCCAATGGTAATTC[A/G]TGAAATACTTCCCAA	26091
rs748774173	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67958065	GCCCACCTCGGCCTC[C/T]CAAAGTGCTGGGATT	26091
rs748785500	snp	A/G	1.64738e-05	0.00286995	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:68025606	ACTTTCCTTGGGTTT[A/G]TTTCATGACTGGTAG	26091
rs748802005	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67993253	GGGAGGCTGAGACAG[G/T]AGAATCGCTTGAACC	26091
rs748843703	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67984549	GATGGCTAATAGATA[A/C]AAATAAAAATATTAA	26091
rs748864349	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68061334	GTCAGGAGGTCGATA[C/T]CATCCTGGCTAACAT	26091
rs748885603	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68042508	CACGCCTATAGTCGC[A/G]CCTACTAGGGAGGCT	26091
rs748917757	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67973344	TGGATTCAACATGCA[C/G]TTGGGAAATAAGCTG	26091
rs748940917	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68071605	CTCTGGAGCAGAGAC[A/G]ATCATCAAATGCGTA	26091
rs748970065	snp	C/T	1.65102e-05	0.00287312	intron-variant, synonymous-codon	HERC4	GRCh38.p7	10:67940995	TGGCTTCTTTTTCAG[C/T]AGTTTCTTATATAAA	26091
rs748975493	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67979702	GAAAACAGAAAGAGA[A/G]AAAAACAAGAGCTGG	26091
rs748980054	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68005735	TTGAGACATGGTCTT[A/G]CTCTACTGCCCACAC	26091
rs748982053	snp	A/G	1.65312e-05	0.00287495	synonymous-codon, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:68032796	GGTTAGAGCAGCAGT[A/G]TGATCTTCTCCACAA	26091
rs749005251	snp	A/C	0.000398916	0.0141173	intron-variant	HERC4	GRCh38.p7	10:67932562	CATATATAAATCTTT[A/C]CATTTAACAATATCA	26091
rs749014076	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68019743	ACTCCTGTGTAATGC[A/G]GCCATGAACAGCTTC	26091
rs749020700	snp	C/T	3.91573e-05	0.00442461	intron-variant	HERC4	GRCh38.p7	10:67990448	TTTAAAATGAATACA[C/T]TTTCAAAGAAAAAAA	26091
rs749030564	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67991718	AGAAAGAAATAATAC[-/T]CAAGTCTTCCACAAA	26091
rs749108962	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68000905	TGCAGAATAGTGAGC[C/G]AATAAATTTGTATTG	26091
rs749114808	snp	A/G			utr-variant-3-prime	HERC4	GRCh38.p7	10:67922804	CTTCCATGAACACTC[A/G]TAGATTGAACATTCT	26091
rs749129496	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67966048	GTAAACACATAATCG[A/G]CTCACTGCAACCTCC	26091
rs749144646	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68016755	CTTAGATCTCACTCA[A/G]TAGTCGAAATTTTAC	26091
rs749147238	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67965206	TCATTCAGATTAGTA[C/T]TCATACTTCATTAGA	26091
rs749179829	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68013585	CAGGCACTAGGAAGA[C/G]GAGGGAATGAAGAGT	26091
rs749181954	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68030266	CCAACAGGGTGAAAC[A/C]CCATCTCTACAAAAA	26091
rs749278390	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68041498	TAACAAGAAAATAAA[C/T]TGTATTTTTGACCAA	26091
rs749296095	snp	C/T	1.68349e-05	0.00290123	intron-variant	HERC4	GRCh38.p7	10:68072872	CAAATTTTAAAAACA[C/T]TTCAACTTACCTGGT	26091
rs749320647	snp	A/C	7.07039e-05	0.00594533	intron-variant	HERC4	GRCh38.p7	10:67966845	AATTTAACCAGTACT[A/C]AAGACAGACAAATTT	26091
rs749369317	in-del	-/CTG			intron-variant	HERC4	GRCh38.p7	10:68008227	CTCCCATGGCCACCA[-/CTG]CTAAGACTGTGCTAG	26091
rs749383654	snp	A/G			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68010993	AGTTCTTCGAATGAA[A/G]TCTTGAGCCCCTCAG	26091
rs749400156	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67977812	CATGGAGAAACACTA[C/T]CTCCACAAAAAATAC	26091
rs749410210	snp	G/T	2.24686e-05	0.00335169	intron-variant, downstream-variant-500B	HERC4	GRCh38.p7	10:67966625	CCAAGCAATTGTTTC[G/T]TTTTTTATTAGATAC	26091
rs749445855	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68060822	ATAGCTAAGCAATAC[C/T]TGGATTAGAAATTAC	26091
rs749447632	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68022550	ATAAATAAAATTCAA[A/C]TAGATCAAAGACCTA	26091
rs749448609	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67958407	GTTTTCATAATTTTA[C/T]GTGCTAATTCTATTT	26091
rs749456774	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68024928	AGAATAAGGAGAATT[A/G]GGAGATTATTGGTTT	26091
rs749482314	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68074630	ATGGGGACTGGGAAA[C/G]AGAAATCATCTGCAC	26091
rs749502389	snp	C/T	4.9498e-05	0.00497459	intron-variant, missense	HERC4	GRCh38.p7	10:67939617	AAAATGTTTCCTCTA[C/T]GTCATCTTCTGGATA	26091
rs749537161	in-del	ATTACTGTACACACAC/GTACAGTAT			intron-variant	HERC4	GRCh38.p7	10:67974066	AAAAAAAAAAAAAAA[ATTACTGTACACACAC/GTACAGTAT]ACACACACACACACA	26091
rs749537472	snp	A/C	3.29587e-05	0.00405934	synonymous-codon	HERC4	GRCh38.p7	10:67936182	AACAGCTGTGTCTGC[A/C]CCATTTAGAACCAGC	26091
rs749603652	snp	C/T			intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68070155	CAGAAGACTTTAAAA[C/T]AAATAAGATCCAACA	26091
rs749610400	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67935525	AGAAGGAGGGAGCTA[C/T]AGACTTTCAGCACTT	26091
rs749642598	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67955667	TCCCAGCTACTCAGG[A/C]GGCTGAGGCAGGAGA	26091
rs749664734	snp	C/T	0.000219756	0.01048	intron-variant	HERC4	GRCh38.p7	10:68039372	GGGGATGGGGAGGTA[C/T]ACAATATGTTTCTTA	26091
rs749675774	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67984539	GTGAGGTTGGGATGG[C/T]TAATAGATAAAAATA	26091
rs749682239	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67925528	CCCTTTCTCTGTATT[C/T]ATGAACAGAAGTCAA	26091
rs749695691	snp	C/T			intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069477	TATAATAAAGGAATT[C/T]AGTTAAATCTTTCTG	26091
rs749708972	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67999947	AATATAATTGAAAAA[A/C]ATCTATTATGCAACC	26091
rs749777392	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67949176	GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	26091
rs749792515	snp	A/T	1.76375e-05	0.00296958	intron-variant	HERC4	GRCh38.p7	10:67956843	AACATCAAAGAAACA[A/T]TTAAAAAAAAAAACC	26091
rs749797144	snp	C/T			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012008	TCAGTACTTTTACAT[C/T]ATGGAGATGGCTTCT	26091
rs749830827	snp	G/T	1.64795e-05	0.00287045	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:67992290	TCTGCTTTGTCGGAT[G/T]GGGACATCTGAAGTC	26091
rs749841685	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68047425	AATCTATCAAGAGAG[G/T]AAGAAGACAAGCCAT	26091
rs749859393	snp	A/G	2.00246e-05	0.00316416	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:67966779	TTTATCATACTGTAT[A/G]ATCTGTCCCATTTTC	26091
rs749880389	snp	C/T	1.64931e-05	0.00287163	missense	HERC4	GRCh38.p7	10:67954989	TCTTGTAATCTATGT[C/T]CTTTGTTTTCCTAAG	26091
rs749880741	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67973055	GAATATACACACACA[C/T]ATATAAAGCAAATGT	26091
rs749901822	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67945055	AAGAGATAATAACAG[G/T]GAACATCCCAAACCT	26091
rs749905264	snp	C/T	3.29859e-05	0.00406102	synonymous-codon	HERC4	GRCh38.p7	10:67932705	GACCTTATGAAAGCC[C/T]GCATGAAAAGCATCA	26091
rs749944966	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67935447	ACTGTGCGGGGCCTA[C/T]GGATTTACATTTTAA	26091
rs749956974	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67973202	TGAATGGAAAACATT[A/T]AAAAAAAAAAGGTTT	26091
rs749974513	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67985602	GCACAAATATGTAGC[G/T]ACTAGGCTAGACAGA	26091
rs749988015	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68035284	CAGCCTTCTGAGTAG[C/G]TGGGATTACAGGCGC	26091
rs750017747	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68067677	AAGAAAGGCAAGCCA[A/C]GTAATCACTACTATG	26091
rs750023800	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68049409	TGGCTCACATCTGTA[A/C]TCCCAGGACTTTGGG	26091
rs750063363	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68048121	ACAGGGTCTCACTAT[C/G]TTGCCCAGGCTGGTC	26091
rs750073838	in-del	-/AGTC			intron-variant	HERC4	GRCh38.p7	10:68017283	ACACAGCCTGAGCAA[-/AGTC]ACCCCAGTGAATAGG	26091
rs750104101	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68012967	ATGTTACTATTGCAA[G/T]TGTTTGGATGCCACA	26091
rs750112410	snp	C/T	1.66158e-05	0.0028823	intron-variant	HERC4	GRCh38.p7	10:68034201	GCTGTAAAACAGTAA[C/T]GGAAAAATTAACCAT	26091
rs750164893	snp	A/T	0.000175128	0.00935591	intron-variant	HERC4	GRCh38.p7	10:67991211	CTCACTAAAAAATTT[A/T]AAAAAGTTTTTTTAA	26091
rs750175497	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68024690	AGTTGATAAAACTAA[A/C]CTATTGTATAGCTAT	26091
rs750213450	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67929279	ACATGTGCAGATCTG[C/T]GTAACCACTGCCACA	26091
rs750233277	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68008719	TCTCAAAGAGATACC[G/T]GTACACCTACATCCA	26091
rs750238070	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68044339	CAAAGATAAGCAGAA[C/T]AATTTAGATTAACAA	26091
rs750248628	snp	A/G	1.67066e-05	0.00289016	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68038139	ACAAGCAACCTGTAC[A/G]ATCTGGATATCTGAC	26091
rs750255738	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67944329	GATTCTTCCAAATCT[A/T]ATCCAAGACCAGGAC	26091
rs750273096	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68021698	CTGTAATCCCAGCTA[C/T]TTGGGAGGCTGAGGC	26091
rs750321229	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68007647	GAGTGTAATGATCTC[A/C]ATTCTTCAGTCACTG	26091
rs750328075	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68043553	AGGCACAGTGCTTCA[A/C]GCCTATAATCATGAG	26091
rs750329201	snp	C/T	1.65564e-05	0.00287714	missense	HERC4	GRCh38.p7	10:67955130	CCTGATCAATAGCCA[C/T]CTGGAAAACAAAAGA	26091
rs750384005	snp	C/T	1.64885e-05	0.00287123	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:67992222	CTCCACAGGAAACCT[C/T]CCAGAAGGATAGCTC	26091
rs750393198	snp	A/C			upstream-variant-2KB	HERC4	GRCh38.p7	10:68076524	CAGATTCGGTGGCTT[A/C]AAACAACAGAAATTT	26091
rs750418058	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68056385	TGAGTTCCTTCTATG[C/T]GCACCATAGTATTTC	26091
rs750432313	snp	A/G			downstream-variant-500B	HERC4	GRCh38.p7	10:67921831	AGAAACAAGTCATCC[A/G]AAATTTAAGAGACCT	26091
rs750450933	snp	A/G	1.71196e-05	0.00292567	intron-variant	HERC4	GRCh38.p7	10:68032897	ACAAGAGATGTTAAT[A/G]GTATTTTAAAAATCA	26091
rs750460567	snp	C/T	1.70435e-05	0.00291915	intron-variant	HERC4	GRCh38.p7	10:67990196	TTTCAAAAGAAAAAA[C/T]ATTAGAATTCTTACC	26091
rs750473018	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67955736	AGACTGTACCACTGC[A/T]CTACAGCCTGGGCGA	26091
rs750475300	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67940920	CCCTACTACTTTTTG[A/T]CTTTTTTTTCCAACT	26091
rs750483908	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68004945	GGTGGGGGCACAAAG[C/T]CTAACCATATGAGGG	26091
rs750488626	snp	A/G	1.65323e-05	0.00287505	synonymous-codon, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:68032817	TTCTCCACAACAAAT[A/G]TAAACTATTTTCTGA	26091
rs750490482	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68040077	CTACTATAGTGCCTA[A/C]TTAATAGTACGTAAT	26091
rs750498325	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67966947	GCAAGCTCTGCCTCC[C/T]GGGTTCACGCCATTC	26091
rs750547799	in-del	-/A	6.72122e-05	0.00579669	intron-variant	HERC4	GRCh38.p7	10:67988876	TAAAATGAATTTTTT[-/A]AAAAAATCACAATTT	26091
rs750547966	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67934550	TTCTTGGTTTAATTC[C/G]TTGTTTTGGTAGACA	26091
rs750572948	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67929689	GGGCCAATTTTTGTA[-/T]TTTTTTGTAGAGACA	26091
rs750599390	in-del	-/CTTT			intron-variant	HERC4	GRCh38.p7	10:67964763	ATGCTGGCTGTTTTC[-/CTTT]CTTTCTTTCTTTCTT	26091
rs750621504	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68004282	AACAGAGTTGTCTTT[A/C]TATATTCTGGTTATT	26091
rs750636447	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68016836	AGAGCTAAGAATAAC[C/T]ATTCAAATCATGTAT	26091
rs750641328	in-del	-/A	0.00535802	0.0514811	intron-variant	HERC4	GRCh38.p7	10:67956846	ATCAAAGAAACAATT[-/A]AAAAAAAAAACCCTC	26091
rs750644867	snp	A/G	1.69818e-05	0.00291387	intron-variant	HERC4	GRCh38.p7	10:67941122	TAAAAATATAAGAAA[A/G]AGTAAACACATGTCC	26091
rs750662252	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67933515	AATAATGAGAATGGA[C/T]ACTAGAAGATTTCAC	26091
rs750679197	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67967454	GGGACCTTAATAATA[A/G]TAGCAGCTAATGCTT	26091
rs750686860	in-del	-/A			downstream-variant-500B	HERC4	GRCh38.p7	10:67921665	CACCCAATAGCGGTC[-/A]TAGTCTTATTTAGTG	26091
rs750688814	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68068582	GGAGGATCACTTGAG[A/C]CCAGGAGTCCAAGGC	26091
rs750720722	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67964198	TTTACAACATCCCAA[C/T]CCAAGAATGGTATTA	26091
rs750726646	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68032636	TTTTTTCAAGAATAA[C/T]CTAAGTCTTTTTTCC	26091
rs750732816	snp	C/G	2.05751e-05	0.00320735	intron-variant	HERC4	GRCh38.p7	10:67990425	GACAAAAAGTAAAAC[C/G]TACTTCATTTAAAAT	26091
rs750739345	snp	C/T	4.94352e-05	0.00497143	missense, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68073057	GTACAATTTCTTCAT[C/T]AATTCCACCCAAACC	26091
rs750769396	snp	G/T	3.29946e-05	0.00406155	synonymous-codon	HERC4	GRCh38.p7	10:67954669	GATCCAATAATTCCC[G/T]CATGATGAGCAAGAA	26091
rs750785688	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68063484	AAGTGCTGTGATTAC[A/G]GGCATGAGCCACCGC	26091
rs750805244	snp	A/G			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011944	AGTATACCCACCTTC[A/G]TCAATTACCTCAGCT	26091
rs750906843	snp	C/G	1.67975e-05	0.00289802	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:68014035	ACTTACCAATATCTG[C/G]TAGACACTGCCCATT	26091
rs750909937	snp	C/T			intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069996	GCAGTGAGCAGAGAT[C/T]GTGCCACTGCATTCC	26091
rs750934605	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68024648	CAAAGAATACTTACA[A/G]TGTGATTACATGCAT	26091
rs750949361	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67990552	GAAAAAAGAAAGACA[A/G]TGTCTTACAATGAAT	26091
rs750972125	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68041598	TACTATCTTGCCATA[A/G]TTTTTTAATGTATAT	26091
rs751010795	in-del	-/AT			intron-variant	HERC4	GRCh38.p7	10:67953055	TATTGCTATCTACAT[-/AT]ATATATATATATTTA	26091
rs751025171	snp	A/T	3.3129e-05	0.00406982	intron-variant	HERC4	GRCh38.p7	10:67939561	AGATGATAAATAATC[A/T]GGCTAACCTATGTCC	26091
rs751028485	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67949974	CAGTAAGCTGAGATT[G/T]TGCCACTGCACTCCA	26091
rs751055483	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67948104	TATAGGATGCAAAAA[C/T]AGTGTTCAGAGGGAA	26091
rs751064525	snp	A/G	1.69235e-05	0.00290886	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68038166	TGACAAACTTTTAAT[A/G]TTTCTAGAAAAGAAG	26091
rs751069366	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68016131	TATATGTGTGTGTGA[C/T]TATAGTATAAAGTGG	26091
rs751096067	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67999054	GTTTTATAAAAATAA[A/G]ATAAAAAATAAAAAT	26091
rs751097405	in-del	-/AT			intron-variant	HERC4	GRCh38.p7	10:68057110	AAACATCCATGTAAT[-/AT]ATATATATATATTTG	26091
rs751100177	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67977923	GAGGTAGAGAGTATA[A/G]TGAGCCGAGATTGTG	26091
rs751113602	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68042894	ACAAATCAGATCAAG[C/T]CATAAAATTTTGAAA	26091
rs751120282	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67963870	AATGCAAAATTTGCA[C/T]TTAAAGATAGAAAAT	26091
rs751156673	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68047141	AAAAAAATCAGACAA[A/C]AAATAGTATTCATCT	26091
rs751157681	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67962534	GAATATGAAAAATAA[C/T]AGGACGTGAAAAACT	26091
rs751186922	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68000201	CTGTACTAACAGGGG[C/G]GATGCTGAGGATACC	26091
rs751219832	snp	A/C			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011722	CAGAGTAGATTTAGC[A/C]TAATTCCTGAGGGCC	26091
rs751221942	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68068330	CTCTACTAAAACTAC[-/A]AAAAAAATTAGCCAG	26091
rs751234131	snp	A/T	1.64852e-05	0.00287094	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:67992227	CAGGAAACCTTCCAG[A/T]AGGATAGCTCAGCCA	26091
rs751292742	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67933592	AGGAATAATGGTAAG[C/T]TGCCTTTCAGAACCA	26091
rs751293636	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67957596	TTGATTGCTAAGTAT[G/T]TTAATAGTGCAGTAA	26091
rs751297240	snp	G/T	3.32204e-05	0.00407542	intron-variant	HERC4	GRCh38.p7	10:68044391	AGGACCTCTTTCTGG[G/T]CACCTTTGTTACCTG	26091
rs751330884	snp	C/T	1.66868e-05	0.00288845	intron-variant	HERC4	GRCh38.p7	10:67955158	AGATTAACATTTTAA[C/T]AGCAATGCTACAATA	26091
rs751369018	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68056255	AATTTTAAATTTTTC[C/G]CTCTAATGTAGCTGA	26091
rs751376087	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68020232	CCAGTTACCATATTA[C/T]TAAATGTCCAGTTTT	26091
rs751386994	snp	C/G/T			intron-variant	HERC4	GRCh38.p7	10:67997819	TGCTCTTGTACGAGG[C/G/T]GGAAGAAACATAGTC	26091
rs751402836	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68019224	TGGTCTCAAACTCCC[C/G]ACCTCAGGTGATCCA	26091
rs751427614	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67985361	TAAAAAGAAGTCACA[C/T]GGTAGAAGTTCAAAA	26091
rs751443112	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67960543	GGCATGTGCCACCAC[A/G]CCTAGCTAATTTTGT	26091
rs751471787	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67970418	CCAATGTGGTGAAAC[C/G]CTGTCCCTACTGAAA	26091
rs751491290	in-del	-/ATA			intron-variant	HERC4	GRCh38.p7	10:68025308	TCAACTACAATAAAT[-/ATA]ATATTACATATACAC	26091
rs751497343	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68036071	TGTAATCCCAGCACT[C/T]TGGGAGGCTGAGGCG	26091
rs751531254	snp	C/T	2.26027e-05	0.00336167	intron-variant	HERC4	GRCh38.p7	10:67925062	CAGTCTCATAAAGTA[C/T]ACAACTAGTTAGAAA	26091
rs751542646	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67935268	CTTCTGCCTCAGCCT[C/T]CCGAGTAGCTGGAAC	26091
rs751555729	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68017536	TTGCCCAGGCTGGAG[A/T]GCAGTGGTGCAATCT	26091
rs751556600	snp	C/T	5.27533e-05	0.00513555	intron-variant	HERC4	GRCh38.p7	10:67941139	GTAAACACATGTCCT[C/T]CAAGTTAAAATATTA	26091
rs751556800	in-del	-/CAA	3.48961e-05	0.00417694	intron-variant	HERC4	GRCh38.p7	10:68032911	TAGTATTTTAAAAAT[-/CAA]AACTCATCTAGATGT	26091
rs751578801	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67983898	AACCCGGGAGACGGA[A/G]GTTGCAGTGAGCTGA	26091
rs751587435	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67980241	GGTACTGGCATGATT[C/G]TCCTGTCTCAGCCTC	26091
rs751595759	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68015542	TTTTCAAATTTCTTT[C/T]GTTTTTGCCAGGTGG	26091
rs751609138	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68068297	CGAGACCCCCCTGGC[C/T]AACATGGTGAAACCC	26091
rs751621688	snp	G/T	1.64917e-05	0.00287151	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:67990966	AAAGCCTAGCAGCAT[G/T]CATATCAACCCCTGA	26091
rs751628363	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68035912	TTATAGCCCTTATCA[C/T]AGTATGTAATTATAT	26091
rs751630882	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67968286	ACCATGAATGCACAA[C/G]GCACAAAGTAAGACC	26091
rs751645732	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68002466	ATATTTCCAACTAAG[C/T]AGTAAATTAACATCA	26091
rs751690590	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67931678	GATCCGCCCACCTTG[G/T]CCTCCCAAAGTGCTG	26091
rs751756872	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68014468	TCCCTTACAATAAAC[A/G]ATTCAGCACCAGAGT	26091
rs751772503	in-del	-/TGAA			intron-variant	HERC4	GRCh38.p7	10:68061307	GGAGGCCAAGGCGGG[-/TGAA]TGAATCATCAGGTCA	26091
rs751783124	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67980657	CTTAAGTAGAGAGAC[C/T]ATAAACAATTAACCA	26091
rs751793897	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67979720	AAACAAGAGCTGGGC[A/G]CAGTAGCTCACACCT	26091
rs751824179	snp	A/C/G	3.30569e-05	0.00406541	missense	HERC4	GRCh38.p7	10:67954696	AGAAAAATTCTTTGC[A/C/G]CACCCCTCCTGCATC	26091
rs751827867	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68054015	ATGTTTAAAACCACC[-/A]GAGATTAAGTTTCAA	26091
rs751852387	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67977556	GGGGACTTTGTCTTG[C/T]ACCTTGGGTACCAGC	26091
rs751875078	snp	A/C	1.66363e-05	0.00288407	utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68073110	CCCCAGCACAACATG[A/C]TTGTAATTATTTTGG	26091
rs751879551	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67961003	TTGGCGGACCTGTTG[C/G]TGCTGAGAGTAAGAG	26091
rs751900800	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68018948	CAACCTATGCTAAAA[-/T]TTATATGAAAGTAAT	26091
rs751917374	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67991446	ATTTATCCAATGTTA[C/T]CTGCTTTAAAACATG	26091
rs751928099	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67926247	TGAAAATACAAAAAT[C/T]AGCTGGGCATGGTGG	26091
rs751944381	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67990204	GAAAAAATATTAGAA[C/T]TCTTACCAAGTACTT	26091
rs751969647	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68024044	AAAACATGGAAAGAC[A/T]TCTGTAAAACATATG	26091
rs752019817	in-del	-/ATA			intron-variant	HERC4	GRCh38.p7	10:68059888	ATAATATTATATATC[-/ATA]ATAATATTATATATT	26091
rs752020911	snp	C/T	5.18417e-05	0.00509099	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922914	TTGCACTAAACTGAA[C/T]AGTTATAACTCCAAA	26091
rs752028227	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68074216	ACGTAGACTTTTAAA[C/T]ACATCGCGTTACTAA	26091
rs752029690	in-del	-/AT	3.45483e-05	0.00415607	intron-variant	HERC4	GRCh38.p7	10:67941132	AGAAAAAGTAAACAC[-/AT]GTCCTCCAAGTTAAA	26091
rs752034596	snp	A/G	1.65603e-05	0.00287747	intron-variant	HERC4	GRCh38.p7	10:67936128	AATCTTATTACTCCC[A/G]CTGTTGCTGCTAAAA	26091
rs752037546	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68038663	CCAACTCTCAAATTA[A/T]GAAACCTATTCCTTA	26091
rs752046538	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68039931	TCTCACAGTACTGTA[C/T]GTTTTTTCCTTCAGA	26091
rs752064875	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67987464	GAGAAAAGAAACAAT[C/G]TAATTAATCTCTTGA	26091
rs752105220	snp	A/G	1.67321e-05	0.00289236	intron-variant	HERC4	GRCh38.p7	10:68044613	GTACAGAAATCAAGG[A/G]AAAAGATATTGCATT	26091
rs752128311	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68052535	TCTGCACAAATATCA[C/T]TAAAAAAAAGAATAC	26091
rs752175825	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68061277	CACAGTAATTAAGAA[C/T]AGGTTTGACACTTTG	26091
rs752182682	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67924507	ATAACAGTAGGTATT[C/T]GTGTATCTAAACATA	26091
rs752186130	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68021350	ATGTAATCAATGTAA[C/T]ATATCAAATTAACAG	26091
rs752190655	snp	A/G	1.648e-05	0.0028705	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:67992273	TTCATTCACTGTCCA[A/G]ATCTGCTTTGTCGGA	26091
rs752252958	snp	C/T			intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010430	TGCATAATCACTGCT[C/T]GATTGCTTGCCCTTC	26091
rs752263167	snp	A/G	4.94368e-05	0.00497152	synonymous-codon, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:68044460	CTGTCCATCAGAATC[A/G]AGACCCCAAGCATAC	26091
rs752266420	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67975730	ACAAATAATCCAATT[C/T]AAAAAGCACACATTT	26091
rs752284482	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67960907	GCCTTTTCTTTATCT[C/T]TTCCAATGTTTATTG	26091
rs752296402	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68045131	TTCAAGACCAGCCTG[G/T]CCAAAACGGTGAAAC	26091
rs752299245	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68074044	TATTTAAAGATTGGC[A/G]GGGGGGAATTGCAAA	26091
rs752370451	snp	C/T	1.65438e-05	0.00287605	missense	HERC4	GRCh38.p7	10:67956958	GATATGTACAGATTG[C/T]AACAGGGATATCTGC	26091
rs752426245	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68017185	GTGTATTTGTCTCCA[A/T]CAGAAGAATACCCAG	26091
rs752435948	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68039784	AATTACTAAACATTT[A/G]CTGTTATTGTTTATG	26091
rs752458270	snp	A/G	3.33907e-05	0.00408586	intron-variant	HERC4	GRCh38.p7	10:67992368	GAAGAGATATTATAT[A/G]TAACTCAAAAACCAA	26091
rs752483097	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67933610	CCTTTCAGAACCAAG[A/T]TTTTTTTTAAAACAA	26091
rs752489434	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68068729	ACCAGCTTCCTCAAA[C/G]GTGAACAAATATTCT	26091
rs752495002	snp	C/T	1.66161e-05	0.00288232	missense, intron-variant	HERC4	GRCh38.p7	10:67959126	ACCTCAGTTAATCCA[C/T]GGTTGACATCCTAAG	26091
rs752513189	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67968805	CAGAGCTTGAAAATA[C/T]ATGAAAGAGAAATCA	26091
rs752531937	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67978118	CCATCTCTACTAAAA[A/G]TACAAAAATTAGCCA	26091
rs752555042	snp	A/C/T	0.000375988	0.0137067	intron-variant	HERC4	GRCh38.p7	10:67990446	CATTTAAAATGAATA[A/C/T]ACTTTCAAAGAAAAA	26091
rs752576364	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67926165	TTTGGGTGTCCAAGC[C/T]GGGCAGATCACTTGA	26091
rs752587093	in-del	-/TAGAAG	1.66258e-05	0.00288316	intron-variant	HERC4	GRCh38.p7	10:68032764	ATAATAAAGAAGTTT[-/TAGAAG]TACAATACCTTGGTT	26091
rs752589484	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68028612	TCCAGATTATACATG[A/G]TTCATCACTTCTAGG	26091
rs752615182	snp	C/T	1.64768e-05	0.00287021	missense, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68034141	CAGTCAGTACCTAAA[C/T]CCAATTGGCCATATT	26091
rs752639005	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68030522	TTACAGAAAGCTGTT[A/C]CATACACCTTGCTCT	26091
rs752643963	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68057221	CTAAGCCAAAATATT[A/C]TTCAGATTGGTGTGA	26091
rs752656231	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68046945	CATGGGCTATAGAGG[A/G]AGACTGTGTCTCCAG	26091
rs752664679	in-del	-/TG			utr-variant-3-prime	HERC4	GRCh38.p7	10:67922450	TAACCTTTAAAAGTC[-/TG]TTCAAGTTCAATTAC	26091
rs752670245	snp	C/T	3.54183e-05	0.00420807	intron-variant	HERC4	GRCh38.p7	10:68032918	TTAAAAATCAAAACT[C/T]ATCTAGATGTGTTTC	26091
rs752676962	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67948828	TGGGAGGCTGAGGCA[A/C]AAGAATGGCTTGAAC	26091
rs752684777	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67933798	TCTTAAAATATTGTC[G/T]CATCTAGTTCTCAAC	26091
rs752700066	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68065802	GAAGTCGAGGCTGCA[C/T]TGAGCCACGATTTAA	26091
rs752706779	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68031975	CAGGCTGGTCTTGAA[A/G]TCCTGACCACAGGTG	26091
rs752719744	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67996357	TTGATTAGTGCACTG[-/T]TTAGGATTATCTCCA	26091
rs752731519	snp	C/T	1.66297e-05	0.0028835	intron-variant	HERC4	GRCh38.p7	10:67954931	GCTTCTGAATAAAAG[C/T]CCCAATTATACCACA	26091
rs752735396	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67997073	AAGCAAAATGTCACT[C/T]TGTTGCAGAATATTA	26091
rs752765387	snp	A/G			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012237	TTTCACTTTCTTACC[A/G]TTCATGTATTCACCA	26091
rs752796145	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68044215	GAAAATATAGAGTAT[A/C]TAAAAATAGCAAATC	26091
rs752844938	snp	C/T	1.67486e-05	0.00289379	intron-variant	HERC4	GRCh38.p7	10:68025495	TTCAATAAGCAATCC[C/T]TAAACAACTGCAGTT	26091
rs752904958	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68028385	ATGTTTTCCATTTTT[A/T]GCAGTCATTATTTCT	26091
rs752932531	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67978710	TCCAGTGTAGTCCCA[A/G]TGGTGGTAGCATCGC	26091
rs752940642	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67994210	AAGCCAATTATTCAA[C/T]CTAAAATCTTTTTTC	26091
rs752967547	snp	C/T	1.65364e-05	0.0028754	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67988710	TATGAAGAAAACTGT[C/T]GAAAATTCTTCTTTC	26091
rs752968980	in-del	-/AAAAA			intron-variant	HERC4	GRCh38.p7	10:67972530	GTCTCAAAAAAGAGG[-/AAAAA]AAAAAAAAAAAAAAA	26091
rs752974560	snp	A/T	1.65641e-05	0.00287781	missense	HERC4	GRCh38.p7	10:67922954	AACTGAAGCCTTCAT[A/T]GTGATCAATAGCTTG	26091
rs753022403	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67993065	AGTATTTATTCTTGG[C/T]GAGGCACAGTGGCTC	26091
rs753022579	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67944106	CCTTAAGCAAACAAA[C/G]GCAGTAGCCAGGCAG	26091
rs753067726	snp	A/T	6.59e-05	0.00573983	missense, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68034127	AAGTTTGCTTTTTAC[A/T]GTCAGTACCTAAACC	26091
rs753070433	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67972311	CAGATCACCTGAGGT[C/T]GGGAGTTCAAGACCA	26091
rs753077113	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68003808	CTATTATGAATAGTG[C/T]TGCAATAAACATGAG	26091
rs753083615	in-del	-/GTT			intron-variant	HERC4	GRCh38.p7	10:67941360	TACGACTTTACAACT[-/GTT]TTCTCCCAGACATAA	26091
rs753095922	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68038310	AGCTCAATTTTAGCG[C/T]ACCAAAAATTTATGC	26091
rs753103831	in-del	-/G			intron-variant	HERC4	GRCh38.p7	10:67964110	TTTTTTTTTTTTTTT[-/G]CTCCTCTTCAATGCA	26091
rs753129307	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67951779	CGGGCCAACTGACCA[C/T]ATTCCCTGCAACTGT	26091
rs753145893	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67953087	AGGAGGATAGCCCAT[A/G]CATTTTCAAAAGATC	26091
rs753160715	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68002199	CATCAAGTTTATTTA[C/T]AATAAAAAGCACTGG	26091
rs753169249	snp	C/T	1.66175e-05	0.00288244	intron-variant	HERC4	GRCh38.p7	10:67940898	TCCCCACTTTTTACC[C/T]CCCAAACCCTACTAC	26091
rs753180198	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68049739	AACATAATGAGACCC[A/T]GTCTCTACAAAAAAA	26091
rs753201457	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67929007	AAGTCACTCATCAAT[G/T]TATCTCCTTACTTTC	26091
rs753218059	snp	A/C	1.6531e-05	0.00287493	intron-variant	HERC4	GRCh38.p7	10:67939580	TAACCTATGTCCTTC[A/C]ATCTTACCGTAAAAT	26091
rs753250802	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68014279	CAAAAGAGGTAATTT[C/T]TCTTTTCAAAAAATT	26091
rs753301580	snp	A/G	1.66421e-05	0.00288458	intron-variant	HERC4	GRCh38.p7	10:67988849	TTCTGTTATTAAAAA[A/G]TGAACATGCAAATAA	26091
rs753314665	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68073857	AATACTAACATTCCA[A/G]CCTCACTAATTTTAA	26091
rs753326184	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67960073	GACAATGTGACTTAT[G/T]ATAGGGGCTTGGGCC	26091
rs753334614	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67975661	AGCCGACACATGCAT[G/T]CTTAACTCACTATAT	26091
rs753354557	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68058099	AAAAAAAAGGCATCT[A/T]TAATTCTTTTCTTTT	26091
rs753394099	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67934462	CACAGTTATTGATCC[C/T]TCAGAAAGAATCTTT	26091
rs753407587	snp	A/T	3.94688e-05	0.00444216	intron-variant	HERC4	GRCh38.p7	10:67992557	TGGGTTTTTAAAATT[A/T]GTCAAAATTATTGGA	26091
rs753448045	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68047582	CAAAACTGACACCTC[A/G]CCAAGGAAGATAAAC	26091
rs753478593	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68036672	AATATTCAAATACAC[C/G]ACTTTCTTAACTCTA	26091
rs753487159	snp	A/G	4.98898e-05	0.00499424	intron-variant	HERC4	GRCh38.p7	10:67959157	ACAGCAGTGCAGAAT[A/G]TAACAATAACGAGGA	26091
rs753552505	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68067446	CGGGAGTTATAAAAC[A/G]CAATGAGCTTCTTTG	26091
rs753593155	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68062842	CTCTCCCTTTCAACC[-/T]TTCCTTTATAAATCC	26091
rs753604399	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67985784	TGATGCCATTTGGAG[C/T]ACTGAAAACAATTTT	26091
rs753616203	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67947034	TAATAGCTGGAGACT[G/T]CAACACTCCACTTAC	26091
rs753625242	snp	A/C	1.64795e-05	0.00287045	missense, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68034150	CCTAAACCCAATTGG[A/C]CATATTTATTCTGTC	26091
rs753636808	snp	C/T	1.64754e-05	0.00287009	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:68025593	CATAAGTTCAAAAAC[C/T]TTCCTTGGGTTTATT	26091
rs753642226	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67996853	ATTAGCTGGGCGTGG[C/T]GGCAGGTGCCTGTAG	26091
rs753648030	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68045905	ATACAGAAATTCAAA[C/T]TGTATCTAGATTACT	26091
rs753652704	snp	C/T	4.95839e-05	0.0049789	missense	HERC4	GRCh38.p7	10:67954695	AAGAAAAATTCTTTG[C/T]GCACCCCTCCTGCAT	26091
rs753668393	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67923425	ACATTTTGAGAGCCC[A/T]TTTTTGGAAAAGCCA	26091
rs753690593	snp	C/T	1.65946e-05	0.00288046	synonymous-codon	HERC4	GRCh38.p7	10:67954724	ATCCACAGCATCTTC[C/T]CCAACAAATATAACC	26091
rs753691720	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67979865	TGGCGTGAACCTGAG[A/T]GGTGGAGCTTGCGGT	26091
rs753735161	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67995901	TCAAGTAATTTTCCC[A/C]CCCTTATCTAAAGAA	26091
rs753749500	snp	A/C	3.53707e-05	0.00420525	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:67991174	CATTTAGGCAACCAG[A/C]GGAAGAAAACGTTCC	26091
rs753760284	in-del	-/C			intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010202	CTAGAAGGGCAGGCA[-/C]CTCAGTTTGAATGCA	26091
rs753762536	snp	C/T	1.66996e-05	0.00288956	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68038136	ACCACAAGCAACCTG[C/T]ACAATCTGGATATCT	26091
rs753811940	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67943855	TGACAGGTCCCCACC[C/T]AATTATTCTATGGAT	26091
rs753819321	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68008832	TAAGCATACCTCAAA[C/G]ATATTTAGGGTTTGG	26091
rs753833576	snp	A/T	8.30186e-05	0.00644223	splice-acceptor-variant	HERC4	GRCh38.p7	10:67991017	AGTGATCATCATTGC[A/T]AAAAAACAGAAAAGA	26091
rs753833921	snp	A/G	1.65386e-05	0.00287559	intron-variant	HERC4	GRCh38.p7	10:68044568	AACAACCTGCTCTAC[A/G]GAAATCAAGAAGAGA	26091
rs753838599	snp	G/T			upstream-variant-2KB	HERC4	GRCh38.p7	10:68076988	AAATTAGCCGGGCGT[G/T]GTGGTGCATTCCTGT	26091
rs753856487	in-del	-/G			intron-variant	HERC4	GRCh38.p7	10:67935629	TCAATTTCTCCAGAA[-/G]GGTAAATTTCCAATC	26091
rs753863839	snp	C/T	1.7079e-05	0.00292219	intron-variant	HERC4	GRCh38.p7	10:67923191	AACAAAAAGATACAG[C/T]AGCAAGTAATATTTG	26091
rs753898674	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68026416	GAAATTTTTAGCATA[C/T]AGCTGCTATAATATA	26091
rs753903774	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67957466	TTAATATACAAAAAA[G/T]TACCATTAGTATTAC	26091
rs753908427	snp	C/T	3.33045e-05	0.00408058	intron-variant	HERC4	GRCh38.p7	10:68025523	GTTTAGAGACCAAAA[C/T]GCTCTTTTACATAAC	26091
rs753951446	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68056047	GCCACCACGCCTGGC[C/T]CTTTTCTTTTAAAGA	26091
rs753978426	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67992873	ATGATGAACATTAAA[C/T]GATCCCACAAGCATA	26091
rs754029040	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67984129	CAACGTGGTGAAACC[C/G]CATCTCTACTAAAAA	26091
rs754050418	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68015525	CAAACTAACACCTTT[C/G]GTTTTCAAATTTCTT	26091
rs754087269	snp	A/T	1.68267e-05	0.00290053	intron-variant	HERC4	GRCh38.p7	10:67988877	TAAAATGAATTTTTT[A/T]AAAAATCACAATTTT	26091
rs754111479	snp	A/C	1.66007e-05	0.00288098	intron-variant	HERC4	GRCh38.p7	10:67940913	TCCCAAACCCTACTA[A/C]TTTTTGACTTTTTTT	26091
rs754131381	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67986220	TGCTTTTGACTTTTG[-/T]TAACTACTGCAAACA	26091
rs754146912	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67951765	ACTCCTCTGAAACAC[A/G]GGCCAACTGACCATA	26091
rs754154157	snp	A/C	3.77074e-05	0.00434192	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:68014162	AATTCGTCCTGATGA[A/C]GGAACAAAAGCAGAA	26091
rs754161048	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68005130	CATTGGTCCATGTGT[C/T]TGTTTTTATGCCAAT	26091
rs754177289	snp	C/T	3.35818e-05	0.00409753	intron-variant	HERC4	GRCh38.p7	10:68032737	TTAATTATGAAAGAA[C/T]TATGATGAGTAATAA	26091
rs754177379	snp	C/T	3.30376e-05	0.0040642	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67988740	CAGAAGGGGGAATAC[C/T]GATCTTGTAGAGTTT	26091
rs754181106	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67944557	AGACACCAATGAACA[C/T]CCACAAACATCACAA	26091
rs754192921	snp	C/T			intron-variant, downstream-variant-500B	HERC4, POU5F1P5	GRCh38.p7	10:68009733	GCTGCATGATAGCAT[C/T]TTACCCACGGAACTG	26091
rs754214205	snp	C/T	0.000150356	0.00866923	intron-variant	HERC4	GRCh38.p7	10:67990409	CTGCCACCTATATTT[C/T]GACAAAAAGTAAAAC	26091
rs754232920	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67950551	AAAGTGCTGGGATTA[C/T]AGGCATGAGCCACCA	26091
rs754295974	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68040254	ACACATTAAATGCTA[A/G]TATCTTTTACCATTA	26091
rs754319201	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68013077	TTTTTACAAATTGAA[A/G]GTTTGGGGCAACCCT	26091
rs754324865	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67964437	ATTTTCCTTTTGTCT[C/G]CAAGATTCCCTTTTA	26091
rs754334922	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68065645	TGGGAGTCTGAGGTG[C/T]GAGGATCACTTCGAG	26091
rs754336675	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68048440	ACATGATCCCAACTA[C/T]ATGACAAGCTGGAAA	26091
rs754351903	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67979342	TGTAATTGACATACC[A/G]AAGAATGTCTCAGAG	26091
rs754373150	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67978487	GTCTAAGGTTTTTCA[C/T]TCTAGTCCCTGGCTC	26091
rs754378244	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68028289	CTAGCAACTTCCAAA[A/G]GTAAGCAATAAGTTT	26091
rs754424501	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68063530	ACATTTTAAAAACTT[C/T]CATTTACAAATATCT	26091
rs754445247	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67928015	CAGTTATCCAGGGAA[C/G]GTCTCTGAGAAGGTA	26091
rs754491541	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68058142	TTGTATCTTTAAAGT[C/T]TGAAGGTAAAGGAAT	26091
rs754508178	snp	A/G	2.76407e-05	0.00371747	intron-variant	HERC4	GRCh38.p7	10:67991232	GTTTTTTTAATCATA[A/G]AATCAGAAATTTAAT	26091
rs754514187	snp	A/C	1.65479e-05	0.0028764	intron-variant	HERC4	GRCh38.p7	10:67939567	TAAATAATCAGGCTA[A/C]CCTATGTCCTTCCAT	26091
rs754514543	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67951050	GTACACCAAAGAGTA[C/G]AGCCGGCTCCAAGGG	26091
rs754530787	snp	A/G	1.65209e-05	0.00287405	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:68044407	CACCTTTGTTACCTG[A/G]GTACTCTGATGCATT	26091
rs754573887	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68073262	CAAGTGCTAGGCTAC[-/A]AATAATTGCTACATG	26091
rs754584092	snp	A/C	1.72591e-05	0.00293756	intron-variant	HERC4	GRCh38.p7	10:68038191	AAGAAGAAGACAGAT[A/C]AAGACCAGTTAATTC	26091
rs754610964	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67973212	CATTTAAAAAAAAAA[-/T]GGTTTGAAGGAGAAC	26091
rs754612918	snp	A/G	3.30153e-05	0.00406283	missense	HERC4	GRCh38.p7	10:67954967	TGTCAAATTACCTTG[A/G]GTGGCTTCTTGTAAT	26091
rs754624695	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67958227	TAAATTGTATTTTAT[C/T]ACATTCTAAACATTC	26091
rs754630867	snp	C/T	3.29674e-05	0.00405988	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:67992232	AACCTTCCAGAAGGA[C/T]AGCTCAGCCATTTCT	26091
rs754652750	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67947195	TCTACAACATACGGA[G/T]GGACCATATATGTTA	26091
rs754660816	snp	A/G	0.000355935	0.0133357	intron-variant, missense	HERC4	GRCh38.p7	10:68070555	AGGTTGCGGTGAGCC[A/G]AGATGGCGCCATTGC	26091
rs754671198	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67973872	TTCAACATGGTGAAA[A/C]CCCATCTCTACTAAA	26091
rs754688762	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67975751	GCACACATTTAATAA[C/T]ACTGCTTTTATTTTC	26091
rs754706086	snp	C/T	1.64879e-05	0.00287118	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:68025559	ACCGTCCACAAGCAA[C/T]CTCAGTGACAATGCT	26091
rs754732216	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68068901	AAATGCGGACCATGA[A/T]ACCTGCCTTAGCTAC	26091
rs754734855	snp	G/T	1.68122e-05	0.00289928	intron-variant	HERC4	GRCh38.p7	10:67955176	CAATGCTACAATAAA[G/T]CTACTGTGACTGAAA	26091
rs754756689	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67982138	TACACAGAACCACAA[A/T]AGACCCAGAATAGTC	26091
rs754757037	in-del	-/AAAT	1.68527e-05	0.00290277	intron-variant	HERC4	GRCh38.p7	10:67956864	AAAAAAAACCCTCTC[-/AAAT]AATATTTTACCTGCA	26091
rs754761793	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67998093	TAGTAGAGAGGGGGT[A/T]CCACCATGTTGGCCA	26091
rs754788973	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67967595	ATTAATTACAAAGAT[A/T]AAAACAAATCTTTAC	26091
rs754832860	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67931071	CTGACTTGAACCCTC[C/T]GCTTCCCGGGTTCAA	26091
rs754844702	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67980877	TGCAAGCCCCATGGT[A/G]ACCTGAAACCAAAAG	26091
rs754882298	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68014926	CTTGTTTCTATCAGG[C/T]CTTAGATCTTGTCTC	26091
rs754903616	snp	A/G	1.67632e-05	0.00289505	intron-variant	HERC4	GRCh38.p7	10:68032744	TGAAAGAACTATGAT[A/G]AGTAATAATAAAGAA	26091
rs754905676	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67947061	TTACAGCACTGGACA[G/T]ATCATTCTAACAGAA	26091
rs754929404	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67996134	AACATGGCAAGACCT[C/T]GCCTCTACAAAAAAA	26091
rs754953372	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68045914	TTCAAATTGTATCTA[C/G]ATTACTATCTTGCAT	26091
rs754957192	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68028581	AATCTACAACAATCA[A/G]GGGATTATCATTGTG	26091
rs754961301	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67996189	GCGCATGCCTGTAGT[C/T]TGAGCCCAAGAGGTC	26091
rs754986389	snp	A/T	1.78121e-05	0.00298425	intron-variant	HERC4	GRCh38.p7	10:67925216	AATCTTTTATTAGTA[A/T]TAAGGGACACACTGG	26091
rs754990944	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68008170	TCACTCTCTCTCTCT[C/G]TGCTGAGATTCTTAA	26091
rs754999419	snp	C/T	1.66699e-05	0.00288698	utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68073114	AGCACAACATGCTTG[C/T]AATTATTTTGGTCTT	26091
rs755009217	snp	C/T			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012058	TAATATTTGCTAGCT[C/T]CAAGCTTTTCTTCTG	26091
rs755015019	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68063774	AAAACCCCGTCTCTA[C/T]TAAAAATACAAAAAA	26091
rs755018215	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67960809	CATGAAGCTCCCTGG[C/T]TTTCCCAGTTCAAAC	26091
rs755028194	snp	A/G			intron-variant, utr-variant-5-prime	HERC4	GRCh38.p7	10:68074771	CATCCCCAGGCAGAT[A/G]AGACATTCCAGCCCC	26091
rs755043057	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67928848	ATCGCTTGAACTTGG[A/G]AGGCGGAGGCTGCAG	26091
rs755058063	snp	G/T	1.64939e-05	0.0028717	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:67990979	ATTCATATCAACCCC[G/T]GAAAATCTGGTACCT	26091
rs755096980	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68026489	AAGCAGGTGGATCAC[C/T]TGAGCTCAAGAGTTT	26091
rs755106937	snp	A/G			upstream-variant-2KB	HERC4	GRCh38.p7	10:68077210	CAAATTTAACCCACA[A/G]CAGTATGTTACAGAA	26091
rs755115790	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67942501	TTTTCCTCTACCCCC[A/G]TTCCAGTTTGTTTGT	26091
rs755116099	snp	C/T	0.000444346	0.0148988	intron-variant	HERC4	GRCh38.p7	10:67996121	GACCAGCCTGGACAA[C/T]ATGGCAAGACCTCGC	26091
rs755146741	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68041992	AAAAGTATAACCTAA[C/T]GCGAATCTTCACTTT	26091
rs755153856	in-del	-/AGG			intron-variant	HERC4	GRCh38.p7	10:67998562	ATTGAAAAAAAAAAA[-/AGG]AGGGGGGGGGGTACA	26091
rs755179555	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68033767	TTGTCCAGATATACT[C/T]TTTATAGTTCTTTAA	26091
rs755181858	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67992941	CCTGCACCAAGAAAA[A/C]AAGCTTTTTCTAATC	26091
rs755217621	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68003068	CCAATAATATATTTA[-/T]TTTTAAATGTACAAT	26091
rs755273062	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68071629	ATGCGTATCAGTAAA[C/T]TACCATTCATTTCTA	26091
rs755277504	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67985948	CTGAGGAAATTCCCC[C/T]TAATTCTTAACCATA	26091
rs755278309	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67941394	CATATTCATGTCATT[C/T]GACATTAAGTTAATA	26091
rs755331046	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67960836	AAACTTGGGCATCTT[C/T]AGCATTTTTACTTTT	26091
rs755341434	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68037004	TTTATCTGTGCTTCC[C/T]CATGGTTCCTAGTGC	26091
rs755342317	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67951771	CTGAAACACGGGCCA[A/T]CTGACCATATTCCCT	26091
rs755343029	in-del	-/AAA			intron-variant	HERC4	GRCh38.p7	10:67972532	CTCAAAAAAGAGGAA[-/AAA]AAAAAAAAAAAAAAA	26091
rs755357703	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68036317	GGGAGACTCCATCTC[-/A]AAAAAAAAAAAAAAA	26091
rs755363565	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68000504	GGATCGCTTGAGTCT[A/G]GGAGGTGGAGGCTGC	26091
rs755384955	snp	A/G	1.65647e-05	0.00287786	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:68014054	ACACTGCCCATTATA[A/G]GGGTACCAATTTCCT	26091
rs755393880	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67965604	GTATCCTAAAAACAG[C/T]GTGCACTAACCAGAT	26091
rs755431077	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68049720	GTTCGAAACCAGCCT[C/T]GGCAACATAATGAGA	26091
rs755453631	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67967280	TAGTTAAGTGCTATG[A/G]GAGACACAAAGATTT	26091
rs755454337	snp	A/G			intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010678	TCTGCAGCAAGGGCC[A/G]CGCCGCTTACACATG	26091
rs755485423	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68013089	GAAGGTTTGGGGCAA[C/T]CCTGCATAGAACAAG	26091
rs755493388	in-del	-/GAT			intron-variant	HERC4	GRCh38.p7	10:67924309	CATGTGTCACTTAAC[-/GAT]GATGATATGTTCTGA	26091
rs755500731	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68057945	AGCTCAGGCAATCCG[C/G]CTGCCTTGGCCTCCC	26091
rs755520085	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68051102	AAAAACCCAAAGACC[-/A]AAAAAAAAAAAAAAC	26091
rs755524349	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68048462	AGCTGGAAAAGACAA[C/G]GATGGAGACAGTAAA	26091
rs755530901	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68018635	GGTTGTATTTAAAAT[A/C]AATATGTAAATATCA	26091
rs755532061	snp	C/T	1.6504e-05	0.00287258	missense	HERC4	GRCh38.p7	10:67936153	CTAAAATTCACTTAC[C/T]GATTTTGTTTGTTAA	26091
rs755551513	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67964554	AAATATAGCTTTCTC[A/G]TGGATTTCCGTCTTT	26091
rs755568103	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67973183	TAAAAATCAAAAAGG[A/C]AAGTGAATGGAAAAC	26091
rs755594605	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67937052	GTGAAAGAACTTGAG[A/G]AAGAAATGCCATCTG	26091
rs755595150	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68020957	AGCCTAGGGGAACCA[C/T]AGGATACCATTAAGC	26091
rs755599027	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68071402	TACTGGCAATTTCTA[C/T]GTGCTGGCTTTTTAC	26091
rs755649130	snp	A/T	3.34225e-05	0.0040878	intron-variant	HERC4	GRCh38.p7	10:67992371	GAGATATTATATATA[A/T]CTCAAAAACCAAGAA	26091
rs755659900	in-del	-/AAT			intron-variant	HERC4	GRCh38.p7	10:68022533	ATAAATAAATAAATA[-/AAT]AATAAATAAAATTCA	26091
rs755666986	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67941670	CTTCTAAAACACAAC[-/T]TTTTTTTTTTTTTTT	26091
rs755679166	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68019410	GGGCAGGCATATAGA[C/T]TGAAAAATTAGAGAT	26091
rs755684668	snp	A/C	1.7725e-05	0.00297694	intron-variant	HERC4	GRCh38.p7	10:67956836	GTCCAGAAACATCAA[A/C]GAAACAATTAAAAAA	26091
rs755754932	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67929269	AGTTCTAAGCACATG[C/T]GCAGATCTGTGTAAC	26091
rs755756603	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68019311	CAGCCAAAGCATTCT[C/T]AAAGAACAGAAGAAT	26091
rs755760615	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67985641	GGCTTCTCTTTTGGC[A/G]TACCAGCATGTCTAT	26091
rs755763484	snp	C/T			intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68070028	GCCTGGGCAACAGAG[C/T]GAGACTCTGTCTCAA	26091
rs755774061	in-del	-/AATTTG	1.76624e-05	0.00297168	intron-variant	HERC4	GRCh38.p7	10:68034238	ACATGCAAAAAATTT[-/AATTTG]AATTTGAAAATAATC	26091
rs755776666	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67954514	AGTAGTAATTCCTTA[C/T]TTACTGAATTAACTT	26091
rs755809675	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68016640	ACAGGCTTGAGCCAC[C/T]GCACCCGGCCCAATA	26091
rs755816147	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67950081	TTACACAAAAGAGTA[C/T]CTCCAATATTCTTTT	26091
rs755845935	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68066075	CATTTTTCTACTAAC[A/G]TTATCCAAGCCCAAA	26091
rs755886023	in-del	-/TTCT			intron-variant	HERC4	GRCh38.p7	10:68056378	CCTGCCCTGAGTTCC[-/TTCT]ATGTGCACCATAGTA	26091
rs755897186	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68074013	AATCTATATCTATCT[A/G]TATCTCTGAGACAAT	26091
rs755942398	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67939891	TGAATACAAAGGCCA[C/T]GTATCCAACTATTTT	26091
rs755977167	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68002011	ATCACAATTTTTTGA[G/T]GAAACTAAATTGCAG	26091
rs756030139	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68030685	CTTTTGCCATTAAAA[A/G]GTCACAGTAAATGGT	26091
rs756064570	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68057973	CCCTAAGTGCTAGGA[C/T]TACAGGTGTGAGCCA	26091
rs756084598	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67976116	AGTTGAGAGTTGACT[A/G]GTTGCAACAAAAACT	26091
rs756105176	snp	C/G			downstream-variant-500B	HERC4	GRCh38.p7	10:67921869	ACCATCCCTCTTTTT[C/G]AAAAATTTTGACTCT	26091
rs756134733	snp	A/G	1.65477e-05	0.00287638	missense	HERC4	GRCh38.p7	10:67922957	TGAAGCCTTCATTGT[A/G]ATCAATAGCTTGGAT	26091
rs756183290	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68024665	GTGATTACATGCATT[C/T]GAAGCTAATAGTTGA	26091
rs756186679	snp	C/G	1.66239e-05	0.00288299	intron-variant	HERC4	GRCh38.p7	10:67954933	TTCTGAATAAAAGTC[C/G]CAATTATACCACAGA	26091
rs756203212	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67926761	ACTTACCTTGTGGAG[C/T]TCACCGTCTAGTAAG	26091
rs756224669	snp	C/G	1.65345e-05	0.00287524	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67988811	TTGAGGAATAGTGGA[C/G]GTTCAAGTACTGACC	26091
rs756245101	snp	C/T	2.21958e-05	0.00333128	intron-variant	HERC4	GRCh38.p7	10:67966837	TGACATTAAATTTAA[C/T]CAGTACTCAAGACAG	26091
rs756246047	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67958050	CTGACCTCATGATCC[A/G]CCCACCTCGGCCTCC	26091
rs756266007	in-del	-/CC			intron-variant	HERC4	GRCh38.p7	10:67978296	AAAAAACCCCTTGGG[-/CC]TCAAGGAAACACTGG	26091
rs756293145	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67927971	GGAGACAGGATACGT[G/T]TGCAGGAGAGAGGTT	26091
rs756295052	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67982588	TTCCTAATGCCCCAC[-/A]AGCACATGCAACCAA	26091
rs756300696	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67944224	TGCTGGCTGGTGTCA[C/T]CCCTCCCCCAGCTCC	26091
rs756313107	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68053003	CAGAAGGATGCTATA[C/T]ACTGATAGTTTATTT	26091
rs756386151	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68033445	TTGTAAGTCAAATAC[C/T]GGCATTCAACTCAAT	26091
rs756388959	in-del	-/A/AA	0.268358	0.24967	intron-variant	HERC4	GRCh38.p7	10:67956845	ATCAAAGAAACAATT[-/A/AA]AAAAAAAAAAACCCT	26091
rs756402288	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67953608	AATAACTGCAGTGAA[C/T]TGAAAAACATCAAGT	26091
rs756433315	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67949081	ACACAGTGAAACCCC[A/G]TTTCTACTAAAAAAT	26091
rs756479529	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68036654	CACATAAAACTACAT[G/T]CCAATATTCAAATAC	26091
rs756481839	in-del	-/GA			intron-variant	HERC4	GRCh38.p7	10:67951301	ACCAGTGCCAGGAAG[-/GA]GGCTAGGATTTGAGC	26091
rs756485896	snp	A/G	1.77307e-05	0.00297742	intron-variant	HERC4	GRCh38.p7	10:68038217	AATTCCATTTAACAA[A/G]TTGATCTTGAATGCT	26091
rs756494341	snp	A/G	3.30207e-05	0.00406316	intron-variant, missense	HERC4	GRCh38.p7	10:67939589	TCCTTCCATCTTACC[A/G]TAAAATTAAGACAAA	26091
rs756504642	snp	C/T			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011963	ATTACCTCAGCTAGA[C/T]ATGCTAGACAACTTG	26091
rs756509007	snp	C/T	1.64784e-05	0.00287035	synonymous-codon, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:68044493	CTGGCCTTTGTCATT[C/T]AGCGCTAACGTATGA	26091
rs756526135	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67999930	GTCCCCTTTCCTACT[A/G]CAATATAATTGAAAA	26091
rs756581643	in-del	-/CT			intron-variant	HERC4	GRCh38.p7	10:68042778	AAATTAAAACCAAAA[-/CT]CTCTTGGCACTCTTC	26091
rs756613467	in-del	-/GGG			intron-variant	HERC4	GRCh38.p7	10:67967825	TAAATAAACATCACA[-/GGG]ATGAGGAAACAATCA	26091
rs756627471	snp	A/G	1.66123e-05	0.00288199	intron-variant	HERC4	GRCh38.p7	10:67940904	CTTTTTACCTCCCAA[A/G]CCCTACTACTTTTTG	26091
rs756642179	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67993657	CAGCTCTTTGTTGGC[A/C]GCTATTTGTCAGTAA	26091
rs756644599	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67977731	TCACGCCTCTAATCC[C/T]AGCACTTTGGGAGGC	26091
rs756658251	snp	G/T			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68010909	TTTTATCCTAAGATT[G/T]CAGCAATTCAGTCAC	26091
rs756673754	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68064060	ACAGCCTGGTCAACA[C/T]GGCAAAACTCCACCT	26091
rs756683544	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68062088	GGGAGAAGTCTACAG[A/T]TGGAATGTCAGCCTA	26091
rs756717741	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68035042	CTGCACTAAATAACT[G/T]ATACACTAATAACTG	26091
rs756721458	in-del	-/TGGG	1.75228e-05	0.00295991	intron-variant	HERC4	GRCh38.p7	10:68032911	AGTATTTTAAAAATC[-/TGGG]AAAACTCATCTAGAT	26091
rs756729050	snp	C/T	1.71776e-05	0.00293061	intron-variant	HERC4	GRCh38.p7	10:67957022	AGTTGATTTGTGATA[C/T]ACTTACTGTGGATGC	26091
rs756783478	snp	C/T	1.6633e-05	0.00288378	intron-variant	HERC4	GRCh38.p7	10:67959161	CAGTGCAGAATATAA[C/T]AATAACGAGGAAAGA	26091
rs756801990	snp	C/T	0.000186968	0.00966691	intron-variant	HERC4	GRCh38.p7	10:67995313	GGTTGAAAAATTAAG[C/T]GTTAGCATTACTTCA	26091
rs756809443	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68033282	CATGATATCCTAATA[C/T]GACATATTTTTCTTA	26091
rs756837120	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67933636	AACAAGGATATCTAG[A/C]AGGACCTAAAATTTT	26091
rs756855479	snp	C/T			downstream-variant-500B	HERC4	GRCh38.p7	10:67921683	GTCTTATTTAGTGAA[C/T]ACCATAAATAGCTTC	26091
rs756863154	snp	C/T	6.72099e-05	0.00579659	intron-variant	HERC4	GRCh38.p7	10:68033962	TACATAATGAGAACC[C/T]ACCATTTTCATCATT	26091
rs756904936	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67947495	CGAGGTATAGACAGT[G/T]CTAAGATAATAACTG	26091
rs756906444	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67999256	ATAGGCCTAATCATC[A/G]TCTTTGGAAACATTA	26091
rs756928807	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67928946	AGAGTTGCCTCCTGA[C/T]AATCCTGTCCCTCTG	26091
rs756964151	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68043439	TATGAGTTAATGTAT[C/T]ATTTATGTATCTGAA	26091
rs756982399	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67927060	ATGATTTATCTTAAT[C/T]ACTGAACTCTCAATA	26091
rs756992996	in-del	-/AAAT			intron-variant	HERC4	GRCh38.p7	10:68068673	TCAAAAAAATATAAA[-/AAAT]AAAAAACCCTCAGAA	26091
rs756996494	snp	A/G			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011799	CACCAGATGCATTAG[A/G]CCCTAAAAGAGAGTC	26091
rs756996564	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67997433	TCTGTATTTATTTTT[A/C]TTTATTGTCACCGTA	26091
rs757010306	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68047689	CAACATACCACTACA[A/C]ACCTATTAGAACGGC	26091
rs757019007	snp	C/G	1.64811e-05	0.00287059	missense	HERC4	GRCh38.p7	10:67932688	AGGACTTTTCCTCCA[C/G]AGACCTTATGAAAGC	26091
rs757046681	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67957661	CTTGTAGTTGGAGGA[C/T]GACCTACTTCTACCA	26091
rs757060970	snp	C/T	0.000315408	0.0125541	intron-variant	HERC4	GRCh38.p7	10:67990450	TAAAATGAATACACT[C/T]TCAAAGAAAAAAAAA	26091
rs757100294	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67993066	GTATTTATTCTTGGC[A/G]AGGCACAGTGGCTCA	26091
rs757119042	in-del	-/CTTT			intron-variant	HERC4	GRCh38.p7	10:68063110	GCATATTTTAATTGC[-/CTTT]CTATTATTTGTGCAT	26091
rs757145750	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68006238	GTACTTACTATTATC[A/G]TGAGTTTTGTACCTT	26091
rs757152321	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68005451	GAAGTGTGTTTCTTT[A/G]CAGGGAGCAGATCAC	26091
rs757167641	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68056302	TAAAACAAGAGTCTA[C/T]GATCTTCCTTTCCTA	26091
rs757178838	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67970474	GCACATGCCTGTAAT[C/T]CCAGCAACTTGGGAG	26091
rs757218259	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68004781	CAAAGTGGGGTAGAG[C/G]CCCTTATAAAACAAT	26091
rs757259675	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68071159	CTGCCCCAACTTTAC[A/T]TTACCAAATAATGGT	26091
rs757308081	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67987301	CCCTTCCATTTTCTC[C/G]AGGTAAAAGACACAG	26091
rs757311641	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68038691	TTACAAGCTATCCTT[C/T]TGCTTTACGTCTAAA	26091
rs757326415	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67935357	TCACTGCATTAGCCA[G/T]GATGGTCTCGTTGTC	26091
rs757339649	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68004057	TTAACCAGAGTGAGA[C/T]AATACCTCATTTTAG	26091
rs757350240	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68002485	AAATTAACATCAATG[A/G]AAAAATAATCAGCTC	26091
rs757354919	snp	C/T	7.36549e-05	0.00606811	intron-variant	HERC4	GRCh38.p7	10:67925046	TACTATAATTAGATT[C/T]CAGTCTCATAAAGTA	26091
rs757377354	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68052094	AGAGACATTTAATTT[C/T]TGGAGGCACAAAAAG	26091
rs757377501	snp	A/G	1.65187e-05	0.00287386	synonymous-codon, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67988741	AGAAGGGGGAATACC[A/G]ATCTTGTAGAGTTTC	26091
rs757394711	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67961571	AACAATTTTCAGTGA[A/G]TTCTGGGAGGCCTCG	26091
rs757400248	in-del	-/AATT			intron-variant	HERC4	GRCh38.p7	10:68043919	AATAATTATATGATG[-/AATT]AATTAAATTGGGCTC	26091
rs757404552	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67926473	CAGGTAGGAAGTAGA[A/G]AGGAAATAGTTTATA	26091
rs757414512	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67953454	GTGTAAGATAAGTCT[A/G]GAACATTCTGTCATA	26091
rs757435185	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68014582	CCACTTGGGTATCAC[C/T]GAGAAGTTTTAGGCT	26091
rs757467336	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68067397	CAAATCTATCATCCA[A/C]ATCTTTCTCTTCCTT	26091
rs757467582	snp	A/G	0.000132578	0.00814071	intron-variant	HERC4	GRCh38.p7	10:68025534	AAAATGCTCTTTTAC[A/G]TAACACCTTACCGTC	26091
rs757504366	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67967191	CTAAAGAAAAAAATG[A/C]TTTGGGGATTTTCTT	26091
rs757509857	in-del	-/G			intron-variant	HERC4	GRCh38.p7	10:68051521	AGCTAGTTTTTTTTT[-/G]GTTTTTTTTTTGTAT	26091
rs757536945	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67930651	GTATACAGTATCTAA[C/G]TAATTATAAATGCAT	26091
rs757558385	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67961031	GAGGTCTTCTGTACC[C/T]GACCATTGCGTTTCT	26091
rs757579737	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67982945	CCAGCCTGGGCAACA[C/T]GGTGAAACCCCGTCT	26091
rs757592876	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67965968	GGATAGTGTCTAGTT[A/T]TTAAAGACTTAGCTG	26091
rs757612911	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67977567	CTTGTACCTTGGGTA[A/C]CAGCTCCAACGTAGG	26091
rs757641084	snp	C/T	3.31851e-05	0.00407326	intron-variant	HERC4	GRCh38.p7	10:67940917	AAACCCTACTACTTT[C/T]TGACTTTTTTTTCCA	26091
rs757660888	snp	A/G	3.90373e-05	0.00441782	intron-variant	HERC4	GRCh38.p7	10:67992570	TTTGTCAAAATTATT[A/G]GAGCTATTTAATTAT	26091
rs757668469	snp	C/T			intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010609	CCTGCACGAGGGTTT[C/T]GGCTTTGCATATCTC	26091
rs757669110	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67940849	CAAGAAGAACAAAAT[A/G]TATTTTTTCATAGAA	26091
rs757679030	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68074223	CTTTTAAACACATCG[C/G]GTTACTAAATATCAT	26091
rs757709847	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68039973	TACTAACCACAGGTA[C/T]CTATTCATTTAATAT	26091
rs757774575	in-del	-/CTGT			intron-variant	HERC4	GRCh38.p7	10:67951961	TCTCAGTTTCTGGAC[-/CTGT]CTGTTTCCAACAATC	26091
rs757779144	snp	G/T			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	HERC4	GRCh38.p7	10:68075222	GGATGGAGCGGGCGG[G/T]GAAGAACGGGAGGCA	26091
rs757785920	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68022764	AACCCACAGAATGAA[A/T]GAAAATATCTGCAAA	26091
rs757794571	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67988608	TTAAAATGAACAGTA[C/T]CAATCTGTTAATAGG	26091
rs757820311	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67997173	GAAGCTATAAAATGG[A/T]TAACATCTTAGCAAA	26091
rs757837855	in-del	-/ATA			intron-variant	HERC4	GRCh38.p7	10:68040544	TGTCACATAAAAAAG[-/ATA]ATGTGTTTAATCATT	26091
rs757842724	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68063467	TTGTGTCAGCCTCCC[-/A]AAAGTGCTGTGATTA	26091
rs757848606	snp	A/G	4.94866e-05	0.00497402	synonymous-codon	HERC4	GRCh38.p7	10:67932708	CTTATGAAAGCCCGC[A/G]TGAAAAGCATCAAAT	26091
rs757978456	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68017505	TTATTTTTTTGAGAC[-/A]AGAGTTTTCGCTCTG	26091
rs757987097	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67947316	AACAAAAGAGAGCTA[A/G]AGAAACTATACTAAG	26091
rs757990578	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67996360	ATTAGTGCACTGTTT[A/C]GGATTATCTCCACCT	26091
rs758025294	snp	A/G	2.05505e-05	0.00320544	intron-variant	HERC4	GRCh38.p7	10:67991026	CATTGCTAAAAAACA[A/G]AAAAGAAAAAAAAAA	26091
rs758035768	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68067851	CTATAAACTCTGCCA[A/G]TCGAGTTAGTCTTCC	26091
rs758047368	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67973308	ACTGCTAAAGAGAAT[A/G]AGCGGCACATGGAGC	26091
rs758058940	snp	C/T	1.67725e-05	0.00289585	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68038154	AATCTGGATATCTGA[C/T]AAACTTTTAATATTT	26091
rs758065612	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68054657	CCATTTTATGATTCT[C/G]ACTTTTTAAAGATAA	26091
rs758066519	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67993539	TAAAAAAAAAAAAAA[A/T]TATTCTTAAAAAGAA	26091
rs758073528	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67994216	ATTATTCAACCTAAA[A/G]TCTTTTTTCTAAATA	26091
rs758080180	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68009083	AAAAAAATTAGCCAG[G/T]TGTGGTGGTGCGCAC	26091
rs758102703	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67996045	GCACAGTAGCTCATA[C/T]CTGTAATCCCAGCAC	26091
rs758108171	in-del	-/G			intron-variant	HERC4	GRCh38.p7	10:67988159	CTGGGAAGAAGGGCA[-/G]GGGAAGAACAATAGG	26091
rs758111049	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68064929	GTGAGTGGAGATCGC[A/G]CCATGCACTCCAGCT	26091
rs758122716	snp	C/T	1.65853e-05	0.00287964	intron-variant	HERC4	GRCh38.p7	10:67954940	TAAAAGTCCCAATTA[C/T]ACCACAGAAAATGTC	26091
rs758125569	snp	C/T	3.32884e-05	0.00407959	missense	HERC4	GRCh38.p7	10:67925118	TTTCCAATGGTAATT[C/T]GTGAAATACTTCCCA	26091
rs758139261	snp	C/T	2.42733e-05	0.00348369	intron-variant	HERC4	GRCh38.p7	10:67991220	AAATTTAAAAAAGTT[C/T]TTTTAATCATAGAAT	26091
rs758232643	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68005145	CTGTTTTTATGCCAA[C/T]ATTATGCTGTAATTT	26091
rs758247257	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67957544	TATTAGACATTAGAC[A/C]CTTTATAGACAATTA	26091
rs758268103	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68017343	AATCTCTAGCCTAAA[A/T]AAAAGCTGCTCCAGA	26091
rs758269709	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68015966	AAATTAGCTGGGCAC[A/G]GTGGCATGCGCCTGT	26091
rs758300239	in-del	-/ATAATTT	1.72931e-05	0.00294045	intron-variant	HERC4	GRCh38.p7	10:68032908	AATAGTATTTTAAAA[-/ATAATTT]ATCAAAACTCATCTA	26091
rs758323405	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67933611	CTTTCAGAACCAAGT[G/T]TTTTTTTAAAACAAG	26091
rs758324705	in-del	-/G			intron-variant	HERC4	GRCh38.p7	10:67978762	CCACCCCCAGCTCCA[-/G]GTGCCTCAGAACAGA	26091
rs758324884	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67932441	TCTAATTCATATACC[A/G]TTCAAATCCATTCAT	26091
rs758366961	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67982236	AGCGGTATAGTAATC[A/G]AAAGAGCATGGTACT	26091
rs758402837	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68068763	ACCTTCTAAATGTAG[A/C]AAAGGAAAAGATTTG	26091
rs758405367	snp	A/T	1.70359e-05	0.0029185	intron-variant	HERC4	GRCh38.p7	10:67990440	CTACTTCATTTAAAA[A/T]GAATACACTTTCAAA	26091
rs758407884	snp	C/T	1.65927e-05	0.00288029	intron-variant	HERC4	GRCh38.p7	10:67955139	TAGCCATCTGGAAAA[C/T]AAAAGATTAACATTT	26091
rs758410670	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68050342	ATATATTGTCTTTTC[A/G]AAACAAACAATAAAT	26091
rs758421693	snp	C/T	3.4263e-05	0.00413888	intron-variant	HERC4	GRCh38.p7	10:68032899	AAGAGATGTTAATAG[C/T]ATTTTAAAAATCAAA	26091
rs758438003	in-del	-/AT			intron-variant	HERC4	GRCh38.p7	10:67953054	TATATTGCTATCTAC[-/AT]ATATATATATATTTA	26091
rs758439105	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68000687	AAGGTCATAATGGAG[C/T]AGGGTAGGTCCATAA	26091
rs758439167	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68014350	TCATTAACAGACTTA[A/C]TCTATAGAATGAATT	26091
rs758440317	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68049810	CCACTACTCAGGGAA[C/T]TGAGGTGGGAGGATC	26091
rs758489314	in-del	-/TACT			intron-variant	HERC4	GRCh38.p7	10:68046152	AAAAAAAAGAAAAAA[-/TACT]TAGAAGCATCATTTG	26091
rs758511469	snp	A/G	0.000181802	0.00953246	intron-variant, missense	HERC4	GRCh38.p7	10:68070563	GTGAGCCGAGATGGC[A/G]CCATTGCACTCCGGC	26091
rs758518015	snp	A/G	1.68749e-05	0.00290468	intron-variant	HERC4	GRCh38.p7	10:67990202	AAGAAAAAATATTAG[A/G]ATTCTTACCAAGTAC	26091
rs758521592	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68063964	TTAAGAAACAGAGGC[C/T]GGGCATGGTAGCTCA	26091
rs758530732	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68065862	GTCTAAAAAAACAAA[A/G]CAAAACTCCAATAAA	26091
rs758530821	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68013305	TGATTTGCTTTATTA[C/T]GATATTTGCTTTATT	26091
rs758534789	in-del	-/ATG			intron-variant	HERC4	GRCh38.p7	10:68053892	AGAATCAATAGCTTT[-/ATG]AAGAGCGACAAGTAT	26091
rs758563078	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68029473	CTCCAGACTGGGTGA[C/T]AGAACAAGACTCCAT	26091
rs758571894	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67937852	ATGCCTGGCTCATTT[G/T]TGTATCTTTAGTAGA	26091
rs758615684	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68031073	ATATTTTACTTTGGG[G/T]ATATTAACAACTATC	26091
rs758698052	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67964768	GGCTGTTTTCCTTTC[-/T]TTCTTTCTTTCTTTT	26091
rs758707769	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68058569	ACCATACGCTAGGCA[C/T]TGTTCTTTGCACTGT	26091
rs758720681	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67978733	AGCATCGCCACAGGG[G/T]TGCTTGTGTCACTCC	26091
rs758722233	in-del	-/AT			intron-variant	HERC4	GRCh38.p7	10:68054630	TTACAGGCATGAGAC[-/AT]ATATATCTGTCCCAT	26091
rs758723483	snp	A/C/G	3.29478e-05	0.00405867	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68072980	AAACACAGTATGTCT[A/C/G]AGTCCACATCCTACA	26091
rs758723798	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67929019	AATTTATCTCCTTAC[C/T]TTCTGTCTTCCAAAA	26091
rs758730391	snp	C/T	0.000969462	0.0219953	intron-variant	HERC4	GRCh38.p7	10:67996087	AAGGTAGGAGGATCA[C/T]TTGAGCCCAGGAGTT	26091
rs758733384	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68074095	TTTCAAGAATAGGAA[C/T]GGATAGTCTGATGGC	26091
rs758745290	snp	C/G	1.70568e-05	0.0029203	intron-variant	HERC4	GRCh38.p7	10:67941124	AAAATATAAGAAAAA[C/G]TAAACACATGTCCTC	26091
rs758750606	in-del	-/TT			intron-variant	HERC4	GRCh38.p7	10:68003329	ACCATGCCTGACTAA[-/TT]TTTTTTTTTTTTTTT	26091
rs758760510	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67987124	GTGAAGATTCTAGTA[C/T]TTAGAATGAGTCCAT	26091
rs758780478	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67988515	TTATTACTTCTTTTA[A/G]GAGAAAGTATAGATA	26091
rs758787083	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67953276	TATTCACTTGGTGGT[A/G]TAACAATAGAGTATA	26091
rs758802746	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68054351	TGAAGTATTTAATGA[-/T]TTTTTTTTTTTTTTT	26091
rs758820049	snp	C/T	3.38839e-05	0.00411592	intron-variant	HERC4	GRCh38.p7	10:67992595	AATTATTTACATGAC[C/T]ATATTATTACCTGGG	26091
rs758847630	snp	C/T	3.29625e-05	0.00405958	missense, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68073066	CTTCATCAATTCCAC[C/T]CAAACCTAGCTGCCC	26091
rs758852226	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68013268	TATAACTTTTATATG[C/T]ACTAGGATACCAAAA	26091
rs758879911	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68021372	AATTAACAGATTGAA[A/G]GAGGAAAAGACACAC	26091
rs758880265	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68038638	CCAACAGGGATTCTT[G/T]TATGTTCTACCAACT	26091
rs758907780	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68016016	GCTGAGGCAGGAGGA[A/T]CACTTGAACCTGGAA	26091
rs758912004	snp	C/G/T			intron-variant	HERC4	GRCh38.p7	10:67947980	AGGCATGAGCCACCA[C/G/T]GCCCAGTCTAAACAA	26091
rs758916636	snp	A/G	3.30055e-05	0.00406222	synonymous-codon, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67990278	AATTGCTATTGTTGT[A/G]AAATTGTTGGAATCA	26091
rs758924655	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68002238	AAATGTCAACCTTCA[C/T]AGTATCCTCGTCACT	26091
rs758966892	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68037219	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	26091
rs758977599	snp	C/G			upstream-variant-2KB	HERC4	GRCh38.p7	10:68075768	TCAACTGGAGCCAGT[C/G]TGAGGATGTGAGATG	26091
rs758989899	snp	A/T	1.66266e-05	0.00288323	intron-variant	HERC4	GRCh38.p7	10:67940894	ACCTTCCCCACTTTT[A/T]ACCTCCCAAACCCTA	26091
rs759018745	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67961354	TCTCCAATATTTCTT[-/A]ATACTGAACACAGCA	26091
rs759049959	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67987982	ACGCTTCTCCCTTAG[A/G]TCATGTCTCATCTAA	26091
rs759051726	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68023829	TAAATCAACTTCAGA[A/T]AACTTACAGACCTCC	26091
rs759057313	in-del	-/C			intron-variant	HERC4	GRCh38.p7	10:67950832	AAGAACCCAGTAGAA[-/C]TACTGACTCTCCGGA	26091
rs759067651	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67940505	GCTCACTGCAACCTC[C/T]GCCTCCTGGGTTCAA	26091
rs759094274	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68073858	ATACTAACATTCCAA[C/T]CTCACTAATTTTAAA	26091
rs759110932	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68049458	TTAAGGCCAGGAGTT[-/A]AGAGACCAGCCTAGG	26091
rs759119216	snp	A/G	1.65688e-05	0.00287821	synonymous-codon, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67988831	AAGTACTGACCACCA[A/G]TTTTCTGTTATTAAA	26091
rs759140078	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68003732	TCCATTGTGTATATA[C/T]ACACCACATTTTCTT	26091
rs759157441	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67938621	TATCCTCATCTATCA[A/G]TGGCTTTGCATGTGA	26091
rs759164786	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67967972	TTCTGGTACTAAATA[C/T]GGCAGAATACTTTGT	26091
rs759173097	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68039697	CCATTTCTTTGAAAT[A/C]GCAAAATCAAACACT	26091
rs759179711	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67979408	AATTAGTGAGCTGAG[A/G]AGACAAAAGAAAAAA	26091
rs759204967	snp	C/T	1.66299e-05	0.00288352	intron-variant	HERC4	GRCh38.p7	10:68044599	AATATTGCATTCTAG[C/T]ACAGAAATCAAGGAA	26091
rs759253572	snp	A/T	4.94972e-05	0.00497455	intron-variant, missense	HERC4	GRCh38.p7	10:67941036	AATGGAGGTCCACAA[A/T]GGTACAATTATAAAT	26091
rs759261401	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67948693	TGGGAGGCTGAGGTA[C/G]GGGAATAACCTGAGG	26091
rs759262414	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68038304	CATACAAGCTCAATT[C/T]TAGCGTACCAAAAAT	26091
rs759278496	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68052370	CTTCTTAAAGAAAGA[C/G]TTTCATTTTTAGGCT	26091
rs759288987	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68000768	CAGAGAGAAGGCCAA[C/G]GTCTACAAGCGAAGG	26091
rs759293968	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68046914	AGTGAGCTGTGATCA[C/T]GCCACTGTATTCCTT	26091
rs759316140	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68030298	ATACAAAAAATAGCC[A/G]GGTGTGATCGTGCAT	26091
rs759320638	snp	G/T			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011174	GCTCAAGCAATCCTC[G/T]TGCCTAAACCTCCCA	26091
rs759362895	snp	C/T	1.65061e-05	0.00287277	synonymous-codon	HERC4	GRCh38.p7	10:67956941	GGCATCAAATACAAA[C/T]GGATATGTACAGATT	26091
rs759372374	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68001933	ATAGAGGTATACAAT[-/A]TTTTTTTTCACTCAT	26091
rs759414307	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68025417	TACTATGACTCCTCA[A/G]TGGCAAAATAGGTAT	26091
rs759415449	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67963622	TTATATAATATGTAA[A/G]TGAACACTGGGCTTC	26091
rs759416860	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67963547	ATTTGCTGTGGTCTT[-/A]AGAGTTCTTTTAAGA	26091
rs759432031	snp	C/T	1.64757e-05	0.00287012	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68072938	ATCATTACATCCACA[C/T]GTGTACACTGTTCCA	26091
rs759435078	snp	C/T	1.66211e-05	0.00288275	splice-donor-variant, intron-variant	HERC4	GRCh38.p7	10:67959112	ATTACACCAAACTTA[C/T]CTCAGTTAATCCATG	26091
rs759471801	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68039911	AACATTTCAAAATAC[C/T]ACATTCTCACAGTAC	26091
rs759495860	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68003330	CCATGCCTGACTAAT[-/T]TTTTTTTTTTTTTTT	26091
rs759505235	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67961723	ACGTGTCACCAGCGA[C/T]ATTATTGGAGGATTT	26091
rs759578144	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68057397	TTGGGAGGCCAAAGC[A/G]GGTGAATCACAAGGT	26091
rs759587641	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67926116	AATATTAGTACTGGC[C/T]GGGCGCGGTGGCTCA	26091
rs759596264	in-del	-/TTC			intron-variant	HERC4	GRCh38.p7	10:68016345	AATAATAATACATAT[-/TTC]TTTTTTAAAAATTTT	26091
rs759602945	snp	C/T	1.75474e-05	0.00296199	intron-variant	HERC4	GRCh38.p7	10:67991137	TAAAGAATTGCCACT[C/T]ACCTAACAGCTAAAA	26091
rs759639793	snp	C/T	5.02088e-05	0.00501018	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68038094	AAACTAATGCTTACC[C/T]TTAGAAAGTGCAAGT	26091
rs759645971	in-del	-/AAA			intron-variant	HERC4	GRCh38.p7	10:68066914	AATCGAATGGCAGGG[-/AAA]AAACAATCTGTGCAC	26091
rs759671225	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67993947	TCCATTCTTTTCAAG[A/G]AAATGACCACATGTT	26091
rs759673487	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67943868	CCTAATTATTCTATG[A/G]ATGGGGCCTGTAGAG	26091
rs759677317	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68008349	TTAGTCAGCAAGTGA[C/T]AAATCCTGTCAGGCC	26091
rs759710104	snp	A/T	1.64836e-05	0.0028708	missense	HERC4	GRCh38.p7	10:67936218	CACTTCTGTTGCACC[A/T]AAGTTTTCAACTGTG	26091
rs759711409	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67973626	AGAGGCTGGCAATAG[A/G]ATTAGGATATTGCTA	26091
rs759713877	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67929952	CCGAGCAGCTGGGAT[G/T]ACAGGCACCACACCC	26091
rs759759567	snp	C/G	1.66527e-05	0.00288549	missense	HERC4	GRCh38.p7	10:67923094	ATGACTAGTTTCAGA[C/G]TCTTCATACCAAGAA	26091
rs759763044	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67957525	ACTGATCTATTATTA[C/T]CATTATTAGACATTA	26091
rs759777237	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67988176	GGAAGAACAATAGGC[-/A]AATTAATGAATTACA	26091
rs759781167	in-del	-/AC	1.64738e-05	0.00286995	frameshift-variant, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68072967	CATCATCCAGAACAA[-/AC]ACAGTATGTCTGAGT	26091
rs759783806	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68068136	GGAGGATAGCTTGAG[A/G]ACTGGAGTTTGAGAC	26091
rs759795598	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68056097	TGAACTGCTAAAATT[A/G]GTTGCTTTGAAGAGG	26091
rs759806133	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67994900	TCACCATTTTGGTCA[C/G]GCTGGTCTCGAACTC	26091
rs759819210	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68072119	TCATCTGAATTTACC[A/G]CCTGAAATCATTAAC	26091
rs759844892	snp	A/C	1.66496e-05	0.00288522	intron-variant	HERC4	GRCh38.p7	10:67954926	ACATAGCTTCTGAAT[A/C]AAAGTCCCAATTATA	26091
rs759845213	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67969312	GTCATATAAGCAGAA[A/G]TAATACACTAAAATT	26091
rs759846904	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68063406	GTAGAGACGGGGTCT[C/T]ACTACACAGGCCAGG	26091
rs759854763	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67986548	TTTTAGTGGAGACGG[G/T]GTTTCACCATGTTGG	26091
rs759870767	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68015365	CAGCCCAGTTAAGCC[C/T]GGCCAAAATTACTAA	26091
rs759918538	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68001808	ATCAGTAGACTCATA[A/T]GATATTTGTCCTTTT	26091
rs759925457	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68020840	CACTAGAGAGATTTG[A/T]AGGCAGATTTCAGCA	26091
rs759961489	snp	C/T			utr-variant-3-prime	HERC4	GRCh38.p7	10:67922769	TAACAGTTTGTTCAT[C/T]TTCCTTTAATATTTT	26091
rs759969325	snp	A/G	1.72018e-05	0.00293268	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922919	CTAAACTGAATAGTT[A/G]TAACTCCAAAGTTAT	26091
rs759973508	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67931488	AGAGTGCAGTGGCGC[A/G]ATCTTGGCTCACTGC	26091
rs760025530	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67944873	AAGTGATTAGTGAGC[C/T]TGAAGACAGGCTATT	26091
rs760036722	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67980310	GGCTAATTTTGTATT[C/T]TTAGTAGAGAAGGGG	26091
rs760045977	snp	A/C/G	1.64893e-05	0.0028713	synonymous-codon	HERC4	GRCh38.p7	10:67954619	AAACCAAATGAGCCT[A/C/G]GAATCTTCATAATAC	26091
rs760048656	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68029093	GTGGGAGGACTGCTT[A/C]AGCCCAAGAATTCGG	26091
rs760061617	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67946784	TGGTGGCACACACCT[A/G]TAGTCCCAGCTACTC	26091
rs760137616	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67981654	AAAACAAGTCTTAAA[A/C]CATTCAAAAAAACTG	26091
rs760141353	snp	C/T	1.6641e-05	0.00288448	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:68025674	AGTAAACACTCCACC[C/T]TCCTAAAAAAAGACA	26091
rs760204623	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68037860	AAGATTTTCCTTGAA[C/T]TGATTTATAGAGACA	26091
rs760213833	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67925595	ACTAAGCAACACTAA[A/G]AATTTTCTGAGGTAG	26091
rs760218751	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68003526	TACCCCACTACCCTT[C/T]CCAGCCTCTGGTAAC	26091
rs760247896	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67986835	GATTCCTAGTCCAGC[A/G]CCTATAATATAATAC	26091
rs760253672	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67924691	AATTTATACAAGAAA[C/G]TTGAGCATCTACTGG	26091
rs760281738	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67951693	TAAGGTAGGTCTCCT[C/T]GCTCTTGCTCTTCTG	26091
rs760283718	snp	C/T			intron-variant, downstream-variant-500B	HERC4	GRCh38.p7	10:67966448	TTTTGTCTTGTTTTG[C/T]TTTGTTTTACAGTGT	26091
rs760294694	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68050894	AAAAATTCACTTACA[A/G]AGCCTGGCCCAGTAA	26091
rs760299068	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67955931	GGTTCTCCCTGAGTT[A/C]TTGTTCTAAAATGGA	26091
rs760335708	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68001473	CATGGGTTTAACCTC[C/T]GGATGGGCTAGAATT	26091
rs760391588	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67960608	TAGGCTGGTTTCGAA[C/T]TCCTGACCTCGTGAT	26091
rs760407276	in-del	-/A	1.68139e-05	0.00289943	intron-variant	HERC4	GRCh38.p7	10:67932789	TCTTGCCTAGAAATG[-/A]AAAAAGCACACATGT	26091
rs760413737	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68066702	TTACTATGGACCTTG[C/G]CTTGTAGTACAGCAT	26091
rs760414010	in-del	-/C			intron-variant, downstream-variant-500B	HERC4, POU5F1P5	GRCh38.p7	10:68009682	CTACACTGATTGACT[-/C]TTCTTTTCATAAAAG	26091
rs760472570	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68057120	TGTAATATATATATA[-/T]ATTTGTCCTTGATTT	26091
rs760495383	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68045705	AGATACCATTTAAAA[G/T]TAACTTTCTTTCAGC	26091
rs760506237	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67940089	ACCGCCACCATGCCC[A/G]GCTAATTTTTGTATT	26091
rs760512133	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68073733	TTAAAGCAATTTTCC[A/T]CAATTTAAACGACTC	26091
rs760517955	in-del	-/GTCTGACCCA			intron-variant	HERC4	GRCh38.p7	10:67944169	CTGTGCTGGCTTCAG[-/GTCTGACCCA]GTGCAGTCCCAGTAG	26091
rs760519384	snp	A/T	1.74473e-05	0.00295353	intron-variant	HERC4	GRCh38.p7	10:68013994	CAAGAACTTCAATAT[A/T]TGAAGGAAAGCTTTA	26091
rs760530158	snp	A/C	1.94869e-05	0.00312139	intron-variant, downstream-variant-500B	HERC4	GRCh38.p7	10:67966651	GATACATATACATAA[A/C]AATGAAATCACAAAT	26091
rs760541133	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68008746	TCCATAGCAGCATTA[C/T]TCACAATAGCCAAAA	26091
rs760545279	snp	A/G	1.64787e-05	0.00287038	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68034145	CAGTACCTAAACCCA[A/G]TTGGCCATATTTATT	26091
rs760548332	snp	C/T	3.32358e-05	0.00407637	splice-acceptor-variant, intron-variant	HERC4	GRCh38.p7	10:67959138	CCATGGTTGACATCC[C/T]AAGACAGCAGTGCAG	26091
rs760578688	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68004381	GTTTCCTTTGCTGTG[C/T]AGAAGCTTTTTAATT	26091
rs760628986	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68060044	GCTTTAATTTCAACT[G/T]TGGCAGAATTACTTA	26091
rs760674807	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67993203	TACAAAAATTAGCCA[C/G]GCGTGGTGGTGTGTG	26091
rs760693080	in-del	-/A	0.000143592	0.00847204	intron-variant	HERC4	GRCh38.p7	10:67992697	CTGTAATAAAAATGT[-/A]AAAAAATTAAAAGCC	26091
rs760694487	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68055924	GCCCGGCTAATTTTT[A/G]TATTTTTAGTAGAGG	26091
rs760707321	snp	C/T			intron-variant, splice-acceptor-variant	HERC4	GRCh38.p7	10:68070601	ACAAGAGCGAAACTC[C/T]GTCTCAAAAAAAAAA	26091
rs760721646	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68015428	GGTCACTAGGTTTTG[C/G]AGTCGTTCTGTTTAG	26091
rs760729075	snp	C/T	3.30737e-05	0.00406642	intron-variant	HERC4	GRCh38.p7	10:67992337	TTCTAAATTTTCAAA[C/T]AAGATTAGTCAGAGG	26091
rs760732872	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67938470	AAAAGAAAAGAAAAG[A/G]GAAAAGAAAACTGAA	26091
rs760745642	snp	A/G	1.651e-05	0.0028731	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:67992205	TTTTCTTACTTGGCT[A/G]TCTCCACAGGAAACC	26091
rs760768134	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67985577	TTTGAAAATCACTGA[-/T]TTTAGATCAGCACAA	26091
rs760815992	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68006067	TGATAAAAACTTTAC[A/T]CTTTATCATCTTTTC	26091
rs760841772	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67985050	GAAAAGAAATGTTAA[C/T]GTTAGAATAAAAATA	26091
rs760853867	in-del	-/T	1.79858e-05	0.00299876	intron-variant	HERC4	GRCh38.p7	10:67990166	TATGAAGCATTTTCA[-/T]TTAAAGAGAAAAGGT	26091
rs760872867	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67933591	TAGGAATAATGGTAA[A/G]TTGCCTTTCAGAACC	26091
rs760900186	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68018433	ACTTAACTATGAAAT[A/C]CTGAAAGTTTTCCCA	26091
rs760908710	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67947295	CAGTTATTCCATGTA[A/C]ATAGTAACAAAAGAG	26091
rs760916990	snp	A/T			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012573	CATTTATCAATTAGG[A/T]TTGTTGTCTTATATA	26091
rs760927220	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67934634	GAGACTGTGCATGTA[C/T]AAAAATGTTTTTAAA	26091
rs760940404	snp	A/T	1.66355e-05	0.002884	intron-variant	HERC4	GRCh38.p7	10:67988850	TCTGTTATTAAAAAG[A/T]GAACATGCAAATAAA	26091
rs760992927	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68028997	GCAATAAAGCGAGAC[A/C]CCATCTCTACAAAAA	26091
rs760993563	snp	C/T	3.37952e-05	0.00411053	intron-variant	HERC4	GRCh38.p7	10:67923168	AATCATTCAGTCAAC[C/T]ACTTCAAAACAAAAA	26091
rs761008260	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67972435	CTGAGACAGAAGAAT[C/T]GCTTGAATCCGGGAG	26091
rs761033358	in-del	-/ATATATATATATATATATATATATATATATATATATATT			intron-variant	HERC4	GRCh38.p7	10:67927394	CATATATATATATAT[lengthTooLong]TTTTTTTTTTTTTAG	26091
rs761099073	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68043802	ACCCAGGCAACAGTG[C/T]GAGACTCTGTCTCAA	26091
rs761102860	in-del	-/G			intron-variant	HERC4	GRCh38.p7	10:68051042	ACACAATTAGAAAAC[-/G]GAGAGTTAAGGGGGG	26091
rs761116551	snp	C/T			synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:67992645	GCTTTGATCTCCCCC[C/T]GAGAAAATTCTTTTT	26091
rs761183575	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67993744	GAAAGGGCAACAAAG[C/T]TTCTTTTGAAAAAGA	26091
rs761201643	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67937681	TTTGTGGAGAGCAAC[-/T]TTTTTTTTTTTTTTT	26091
rs761203775	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68023576	GGAGTCATTGTTTAA[C/T]GGGTATAGAGCTTCA	26091
rs761222916	snp	A/T	1.72166e-05	0.00293394	intron-variant	HERC4	GRCh38.p7	10:68014015	GAAAGCTTTAATATG[A/T]CAGAACTTACCAATA	26091
rs761233762	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67943692	CAAAGGGATCAAATG[A/G]AGGTCTGTACAGTGA	26091
rs761269749	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68047925	ACATGAATGTTTTGT[C/T]TTTGTTTTTTTTTTT	26091
rs761289844	snp	A/C/T	3.31105e-05	0.00406871	synonymous-codon, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67990335	AAGATAAAACCTCAA[A/C/T]GCTTCAACATCAGGT	26091
rs761359986	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68063335	CTGCCTCAGCCTCCC[A/G]AGTAGCTGAGACTAC	26091
rs761365270	in-del	-/CTAA			intron-variant	HERC4	GRCh38.p7	10:68015453	GTTTAGCGACATAAG[-/CTAA]CTAATACATTACCCA	26091
rs761392192	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67965405	ATCAGTGCCTGTTAT[A/G]TAACAGATTCTCATT	26091
rs761395341	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68000277	GGATTGAACTGGGTC[C/T]CCTAAAACTTTGTAT	26091
rs761397786	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68013800	CCATCTTCTAGTTCC[A/C]ATATGACCCACTCTC	26091
rs761405605	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67979033	AGTCCAAACCGCGAA[C/G]ACTACAATAAATACG	26091
rs761421198	snp	C/T	1.88952e-05	0.00307364	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:67966748	CTATCAATTCTTGTA[C/T]TTCATGTATATAAAA	26091
rs761441441	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67943554	AAAGACTCTAAAAGG[C/T]GGAGGTATTAGAGTG	26091
rs761501938	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67978346	CCCCACAGGCCCCTG[A/G]TGACAGTGGCCAAGG	26091
rs761517354	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67973861	GATCGAGACCATTCA[A/G]CATGGTGAAACCCCA	26091
rs761533762	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67928663	AGCGGTGGCTCACAC[C/T]TGTAATCCCAGCACT	26091
rs761575321	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68021665	AATACAAAATTAGTC[A/G]GGTGTGGTGGCACAT	26091
rs761600974	snp	C/T	0.000462963	0.0152075	intron-variant	HERC4	GRCh38.p7	10:68039507	CAGCAAATCAAAGTT[C/T]GAGCAGGAAAAAGGA	26091
rs761613881	in-del	-/AA			intron-variant	HERC4	GRCh38.p7	10:67975171	TCCAGCCTGGGTGAC[-/AA]GAGCCAAACTCTGTC	26091
rs761626942	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68073534	CTTTAAATAATTTCA[A/G]TGGGAACAAGAAATA	26091
rs761629139	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67945896	ACTTTCACAAAAAGG[-/A]ATGGAATAGGAAGGA	26091
rs761640289	snp	A/T	3.35492e-05	0.00409554	intron-variant	HERC4	GRCh38.p7	10:67936249	ATCTATTAATTTAAA[A/T]TTTTAAAAAAAGTCA	26091
rs761662720	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68057438	AGAGCAGCCTGGCCA[A/G]CATGGTGAAACCCTG	26091
rs761663524	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68020521	CCTGTAATCCCAGCA[C/T]TTTGGGAGGCCGAGG	26091
rs761667826	snp	A/G	1.67019e-05	0.00288975	missense, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68038137	CCACAAGCAACCTGT[A/G]CAATCTGGATATCTG	26091
rs761672497	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67939367	CTGTTTTCAGTGTTC[G/T]TCATCTGTAAACCAG	26091
rs761725525	in-del	-/AAAT			intron-variant	HERC4	GRCh38.p7	10:68022504	ACTCCATCTCAAAAT[-/AAAT]AAATAAATAAATAAA	26091
rs761735522	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67982034	GTTAAAATGTCCATA[A/C]CACCTATAGCAATCT	26091
rs761742668	in-del	-/TTTGGCTTCAAAA			intron-variant	HERC4	GRCh38.p7	10:67958372	ATCTCCAAAGCACCC[-/TTTGGCTTCAAAA]TTTGGCTTCAAAACT	26091
rs761753334	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68036155	CCACCTCTACTAAAA[A/G]AAAACGCAAAAAATT	26091
rs761756623	in-del	-/GACA			intron-variant	HERC4	GRCh38.p7	10:67928194	AGTGAGAGGAACAAT[-/GACA]GGAGATGAGGCAAGG	26091
rs761780887	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68016761	TCTCACTCAATAGTC[A/G]AAATTTTACCCCCGA	26091
rs761795466	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67982946	CAGCCTGGGCAACAC[A/G]GTGAAACCCCGTCTC	26091
rs761814390	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67936671	CTTTATCACAGACAG[G/T]TTTTCCAGTTATGTA	26091
rs761826877	snp	C/T	1.71781e-05	0.00293066	intron-variant	HERC4	GRCh38.p7	10:67925198	GTATTCTAAAAACAA[C/T]ATAATCTTTTATTAG	26091
rs761826993	in-del	-/AAT	1.80794e-05	0.00300656	intron-variant	HERC4	GRCh38.p7	10:67941148	TGTCCTCCAAGTTAA[-/AAT]ATTAAATTTTCTAAG	26091
rs761848143	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67985462	TTATTTCACATTTTA[A/C]TTAAAGTTTAGTATT	26091
rs761881180	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67997987	GCTCACTGCAACCGC[C/G]TCCCGGGTTCAAGCG	26091
rs761895079	snp	A/G	1.66258e-05	0.00288316	intron-variant	HERC4	GRCh38.p7	10:67959097	CTAAACATGAGCTTT[A/G]TTACACCAAACTTAC	26091
rs761964640	in-del	-/A			downstream-variant-500B	HERC4	GRCh38.p7	10:67921634	GAATTGTGAATTCTG[-/A]AAGAATTTTTTAAAG	26091
rs762053468	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68032479	CTTAATGAACTAAAA[C/T]GGAATAATTTTATTC	26091
rs762059057	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68042646	AACAAACAAAAATCT[A/G]TAAACACCAATTTTT	26091
rs762067289	snp	A/C/T	3.37685e-05	0.00410893	intron-variant	HERC4	GRCh38.p7	10:67941117	ATGTCTAAAAATATA[A/C/T]GAAAAAGTAAACACA	26091
rs762087163	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67936081	CTTAGGGTTGTGACA[C/T]GTTTTCTACGTACAG	26091
rs762093385	snp	A/C	1.648e-05	0.0028705	missense	HERC4	GRCh38.p7	10:67932609	TACCTTTTCCAGTTC[A/C]TTCCAATCATAATTT	26091
rs762104514	in-del	-/AAT			intron-variant	HERC4	GRCh38.p7	10:68018074	AAACCTGGTGAAAAG[-/AAT]AATAAGAAAAAAATT	26091
rs762116186	snp	C/T	1.64757e-05	0.00287012	missense, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68034117	AGCTGCGGTGAAGTT[C/T]GCTTTTTACAGTCAG	26091
rs762122334	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67947825	ACAAACATATGGAAA[C/T]TAAACAATACACTCT	26091
rs762127101	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68046777	TTTGAGACCAGCCTG[A/G]GCAACATAGTGAGAC	26091
rs762143100	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68031755	CTGATTAGAAGTTAA[C/T]GCCTCTTTTTTTTTG	26091
rs762150675	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68053310	ATTTAAGCACTACAC[-/T]TTTTTTTTTTTTTTA	26091
rs762204600	snp	A/T			upstream-variant-2KB	HERC4	GRCh38.p7	10:68076598	GTAAGCTTGGTTCTC[A/T]CTTGGGGTCTCTGAG	26091
rs762207224	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68026000	ACGAAACCTAAAAAC[A/G]GTATCATCTTCACTT	26091
rs762210722	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68042425	AGTCCAGGAATTTAA[A/G]ACCAGCTGGGCAACA	26091
rs762212901	in-del	-/A			utr-variant-3-prime	HERC4	GRCh38.p7	10:67922730	AGATGGTCAAAAAAA[-/A]TCCATGGTTCTGTAC	26091
rs762235476	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67968947	TGCACTCACTGTCAT[-/A]ACACTTCACCTAATA	26091
rs762244426	snp	C/T	3.29478e-05	0.00405867	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68073004	TCCTACATCTCGGAC[C/T]CTTTTATTTATAAAG	26091
rs762253779	snp	C/T	4.94841e-05	0.00497389	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:67990940	ATCAGGTTGTATAAG[C/T]TTGTGGAATAAAAGC	26091
rs762258323	in-del	-/C			intron-variant	HERC4	GRCh38.p7	10:68057259	GCAAATGCAAAATAA[-/C]GAGTACAGAAGTATG	26091
rs762273844	snp	A/G	3.81112e-05	0.00436511	intron-variant	HERC4	GRCh38.p7	10:67990413	CACCTATATTTTGAC[A/G]AAAAGTAAAACCTAC	26091
rs762289338	in-del	-/TTAA	3.06734e-05	0.00391609	intron-variant	HERC4	GRCh38.p7	10:67991243	CATAGAATCAGAAAT[-/TTAA]TTGTTTACCCTTTCT	26091
rs762312075	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67996873	GGTGCCTGTAGTCCC[A/G]GCTACTTGGGAGGCT	26091
rs762319939	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68054065	CCTCATTAGTTGTTA[A/C]AAATACAGATTTCCC	26091
rs762345510	in-del	-/G			intron-variant	HERC4	GRCh38.p7	10:68051490	GCTGGGACTACAAGC[-/G]CCCGCCACCATGCCC	26091
rs762358501	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68018993	CCAAAGCATTCTTTC[-/T]TTTTTTTTTTTTTTT	26091
rs762369696	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67962199	TTTAAAAAGTGTTAT[C/T]ACTACTAAGAAAGTT	26091
rs762374150	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67955628	AATGCAAAATTAGCA[C/G]GGCGTGGTGGTGTGT	26091
rs762377484	in-del	-/G	1.67485e-05	0.00289378	intron-variant	HERC4	GRCh38.p7	10:67988868	ACATGCAAATAAAAT[-/G]AATTTTTTAAAAAAT	26091
rs762415816	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68018171	CCCAGCACCAAACAA[A/G]AAGGATAATACTTGA	26091
rs762438636	snp	C/T	1.72919e-05	0.00294035	intron-variant	HERC4	GRCh38.p7	10:67988653	AAAATAAAGGAATGA[C/T]TGGACATACCCTATG	26091
rs762459994	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67969790	GGAAGCAGAGTTTGG[G/T]TGCCACAGGAAGAGG	26091
rs762471571	in-del	-/TCTG			intron-variant	HERC4	GRCh38.p7	10:68024976	TTTCATCACATTAAT[-/TCTG]TCTTAATTAACTGGT	26091
rs762480167	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67997446	TTATTTATTGTCACC[A/G]TAGTAAAATAGGTAA	26091
rs762488030	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67941971	AAAACATGACTTTTT[A/C]ATGGCTGCATATTGT	26091
rs762508594	snp	A/G			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	HERC4	GRCh38.p7	10:68075247	GAGGCAAGCGGGGCG[A/G]AGAGCACCAGGGGTG	26091
rs762528071	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67978253	AGCCTGGGCGACAGG[A/C]GACTCCGTCTCCAAA	26091
rs762555807	snp	A/G	1.91635e-05	0.00309538	intron-variant	HERC4	GRCh38.p7	10:67936283	TCAGACTCAAAACTT[A/G]TAATAATCTATTATT	26091
rs762581731	snp	A/G			downstream-variant-500B	HERC4	GRCh38.p7	10:67921403	TACCTCAAGAAGTGG[A/G]TGAACAGGGAAAATG	26091
rs762617087	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68025805	ACTGTCTTCACAATT[C/T]AACAGACAGATGGCT	26091
rs762635669	snp	G/T	1.65302e-05	0.00287486	synonymous-codon, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67988804	TACTATCTTGAGGAA[G/T]AGTGGAGGTTCAAGT	26091
rs762636101	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67989964	GGTGACAGTTTTTAA[C/T]TTTCCTAATACTGTC	26091
rs762654940	in-del	-/AT			intron-variant	HERC4	GRCh38.p7	10:67939723	ATTTTACTTATGGAT[-/AT]ATATATATATATATA	26091
rs762659992	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68029883	ACCTGGGATTACAGG[C/T]GCCTGCCACCACGCC	26091
rs762745344	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68000210	CAGGGGCGATGCTGA[A/G]GATACCCTCTGTGCA	26091
rs762766244	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67936449	CATGATTAATTACAA[A/T]TTACCAAGTTTGGTA	26091
rs762803507	snp	C/T	1.64879e-05	0.00287118	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:67992223	TCCACAGGAAACCTT[C/T]CAGAAGGATAGCTCA	26091
rs762810193	snp	A/C	3.32138e-05	0.00407502	intron-variant	HERC4	GRCh38.p7	10:68044592	GAAGAGAAATATTGC[A/C]TTCTAGTACAGAAAT	26091
rs762850556	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68014576	AGTCCTCCACTTGGG[C/T]ATCACCGAGAAGTTT	26091
rs762860549	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67935011	ATCTGGATGTCACGC[A/G]TCATTCTGAGGATAC	26091
rs762860732	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67951258	TTCTACCTGCTACAC[C/G]ACTACAAACTTCCCT	26091
rs762864637	snp	A/C	1.64743e-05	0.00287	intron-variant	HERC4	GRCh38.p7	10:68044354	CAATTTAGATTAACA[A/C]ATTTATTTTAAAAGA	26091
rs762910041	snp	C/T			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011937	GTTGTTTAGTATACC[C/T]ACCTTCGTCAATTAC	26091
rs762939826	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67996686	ATCTTAGTATTAATA[C/T]GAAAATCATTTTGAC	26091
rs762941061	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67928639	TAAAATGAGTTGCCT[C/T]GGGCCAGGAGCGGTG	26091
rs762948573	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67949834	ACCAGCCTGGCCAAC[A/G]TGGTGAAACCTCGTC	26091
rs762964572	snp	A/G	1.64757e-05	0.00287012	missense	HERC4	GRCh38.p7	10:67932634	TAATTTGTATTTCCA[A/G]TGACCATTGCTTGTA	26091
rs762997212	in-del	-/TAAA			intron-variant	HERC4	GRCh38.p7	10:67927176	TTCAACTGTTTGAAT[-/TAAA]TAAAGTCTGTGAGCA	26091
rs763004912	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67963732	CCTAGGGTACCCTGG[C/T]TGGTGTGTGAGGGTT	26091
rs763019424	snp	A/G			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012749	GCTGTTGGAAAAATG[A/G]TGCCAACTGACTTGC	26091
rs763025239	snp	C/T	6.62833e-05	0.0057565	missense	HERC4	GRCh38.p7	10:67932767	AATCCACATAAGCAT[C/T]GACAAACTCTTGCCT	26091
rs763119567	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67980380	TCAGGTGATACACCC[A/G]CGTCAGTCTCCCAAA	26091
rs763127559	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67945194	GGATAAAGAAAGGAT[A/C]CTGAAAGCAGCAAGA	26091
rs763140742	snp	A/T	0.000134932	0.00821267	intron-variant	HERC4	GRCh38.p7	10:68038081	AGAAATAAAATAAAA[A/T]CTAATGCTTACCTTT	26091
rs763179571	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68053901	AGCTTTATGAAGAGC[A/G]ACAAGTATATCCACA	26091
rs763183579	in-del	-/GAGGTT			intron-variant	HERC4	GRCh38.p7	10:67981873	TGAATCGGGGGGGTG[-/GAGGTT]GAGGTTGCAGTGAGC	26091
rs763193250	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67969217	GTAGCCTGAATCCAA[C/G]GATCAACAAATCCTT	26091
rs763235747	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68060275	TCACCCAGACTGGAG[C/T]GCAGTGACACAAATA	26091
rs763245391	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67993306	GCCGAGACTGCGCCA[C/T]TGCACTCCAGCCTGG	26091
rs763250159	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68044242	AATCAATCAATAGCT[A/C]AATCAACATCATAAG	26091
rs763260970	snp	A/G	1.8917e-05	0.00307541	intron-variant	HERC4	GRCh38.p7	10:67991110	ACAATAAATTTGAAA[A/G]TTTCAGCATATTAAA	26091
rs763270771	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68008511	GATAGTTTGGCAGGC[A/G]GGAGAATGGGTGCTG	26091
rs763286883	snp	A/G	1.64925e-05	0.00287158	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:67990954	GTTTGTGGAATAAAA[A/G]CCTAGCAGCATTCAT	26091
rs763294275	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68004835	TTATTACAAGAACAG[A/C]ATGCAGGAAACCGAT	26091
rs763294280	in-del	-/CT			intron-variant	HERC4	GRCh38.p7	10:67926093	ACTAAAATATCTCCC[-/CT]GTCAAAAATATTAGT	26091
rs763317281	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67979133	ATGACCTCACCAAAT[A/G]AACAAAATAAGGCAC	26091
rs763321755	in-del	-/G			intron-variant	HERC4	GRCh38.p7	10:68007690	TAGTGGACACTCCAA[-/G]GCCCAGTAACACTTT	26091
rs763328642	in-del	-/GGTTTTAG	3.32196e-05	0.00407537	intron-variant	HERC4	GRCh38.p7	10:67988846	TTTTCTGTTATTAAA[-/GGTTTTAG]AAGTGAACATGCAAA	26091
rs763339420	in-del	-/T	3.31876e-05	0.00407341	intron-variant	HERC4	GRCh38.p7	10:67940922	CTACTACTTTTTGAC[-/T]TTTTTTTCCAACTAA	26091
rs763341346	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68043950	CTCACTGCTATGTAC[A/C]AAGTGGAAAGTGACT	26091
rs763348728	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67923872	AGGAGTATCAAAGGA[A/T]ATGTCACCGATTTGG	26091
rs763356414	snp	A/C	3.36095e-05	0.00409922	intron-variant	HERC4	GRCh38.p7	10:67954784	ACTGTAAAGAAATGA[A/C]AGTACATTCTGGAGA	26091
rs763368735	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68039791	AAACATTTACTGTTA[C/T]TGTTTATGCATACTA	26091
rs763394469	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68015480	TTACCCAGATTGGCA[A/G]ATTCTTTCAGGGTAG	26091
rs763401280	snp	C/T	1.6654e-05	0.00288561	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:68014045	ATCTGGTAGACACTG[C/T]CCATTATAGGGGTAC	26091
rs763416424	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68052445	TTTCTACATCATCTG[G/T]GTCCTTCCAATCACC	26091
rs763442803	snp	C/T	1.6517e-05	0.00287372	missense	HERC4	GRCh38.p7	10:67954689	ATGAGCAAGAAAAAT[C/T]CTTTGCGCACCCCTC	26091
rs763451516	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68016681	TAGTACTGACTACCT[A/G]GAAGTCAAACTGATC	26091
rs763468052	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67998932	TTTAGTAGAAACGGG[A/G]TTTCACCATGTTGGT	26091
rs763488853	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67963786	CAAGGTTCATTTCCT[A/G]AAGAATCAATTTTCC	26091
rs763498294	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67933056	ATGGGCAGAATGATG[C/T]AAATGGCTATGAAAA	26091
rs763504506	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68068209	AAAAAAATTGGCCAG[A/G]CCTGGTGGCTCATGC	26091
rs763514150	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67968196	TGAGGAATAAAAAAA[C/T]CAAAGAAAGGAATCC	26091
rs763517288	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68049684	GGGAGGCTGAGGCGG[C/G]AGGATGGCTTGAATC	26091
rs763519056	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67976696	TCACCCCTCTCCCAG[C/T]CCCTGGCAGAGGCAT	26091
rs763524415	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67995897	TGTGTCAAGTAATTT[-/T]CCCCCCCTTATCTAA	26091
rs763534504	snp	C/T	1.65853e-05	0.00287964	missense	HERC4	GRCh38.p7	10:67923037	AGATTAAAACAAGTA[C/T]GGGAAACTGGGAGAT	26091
rs763539527	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68032404	AGCCAAATGGAAACT[A/G]CATTCAAATTAGGCT	26091
rs763580164	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68066040	AGCTCATTAATATAG[-/T]TTTCCTCATTAGTGT	26091
rs763608456	snp	A/G			upstream-variant-2KB	HERC4	GRCh38.p7	10:68076470	AGAATATGTTCAAGT[A/G]TGTGTATTCGTGTCC	26091
rs763622222	snp	C/G	0.000104904	0.00724162	utr-variant-3-prime	HERC4	GRCh38.p7	10:67922901	TAGTTTAATGCTTTT[C/G]CACTAAACTGAATAG	26091
rs763740983	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68020158	CTGACACAGATAAAA[A/C]CTACAATGATCAAAA	26091
rs763779468	snp	A/G	8.314e-05	0.00644695	intron-variant	HERC4	GRCh38.p7	10:67959153	TAAGACAGCAGTGCA[A/G]AATATAACAATAACG	26091
rs763813179	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68004480	TTGCCCAGACCAATG[C/T]CCTGGAGAGTTTCCT	26091
rs763816266	snp	A/G			downstream-variant-500B	HERC4	GRCh38.p7	10:67921533	ATAGAAGAGTTCTAT[A/G]GTTCGCCAATAGTTT	26091
rs763817128	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68074178	GAAAGACACAAATAA[C/T]AGAGTCCACTTCATC	26091
rs763818518	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67977503	CATGGCAGCTATGGG[A/G]CAAGACTCCTGCTTG	26091
rs763820717	in-del	-/G			intron-variant	HERC4	GRCh38.p7	10:68061670	GATCACTTCAGGTCA[-/G]GAGTTCGAGACCAGC	26091
rs763822918	snp	A/G			intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010531	TCTGCTGCAGTGTGG[A/G]CTTCAGGCGCTGCAG	26091
rs763833129	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67956263	TAAAGCAAACTTACT[C/G]TAACCCTTTAAAGTC	26091
rs763834892	snp	C/T	0.000186411	0.00965249	intron-variant	HERC4	GRCh38.p7	10:67995285	TAGTAGGCATTGATG[C/T]TCATTCACTGTAGGT	26091
rs763840487	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67926266	TGGGCATGGTGGCAG[A/G]CGCCTGTAATCCCGG	26091
rs763867133	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68047469	ACATTTGCAAAAGAT[A/C]CAGCTGATAAAGAAG	26091
rs763867657	in-del	-/G			intron-variant	HERC4	GRCh38.p7	10:68030366	GAATCACTTGAACCT[-/G]GGAGGCAGAGGTTGC	26091
rs763932380	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67970382	GGATCACCTGAAGTC[A/C]GGAGTTCAAGACCAC	26091
rs763966769	snp	A/G	1.64974e-05	0.00287201	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:67990995	GAAAATCTGGTACCT[A/G]TTCTATAGTGATCAT	26091
rs763972365	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67936512	TAAAACTTTAGAATT[A/G]TTACTATAAAATATT	26091
rs763979691	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68018750	AAGAGATATGCATGA[A/C]CTCTATGATGAAAAT	26091
rs763994701	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68071092	AGGCTGTGGTGTAAT[C/T]GGGACAACAATGAGG	26091
rs764004451	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67985345	TTTGCAAAATGAATT[G/T]TAAAAAGAAGTCACA	26091
rs764006103	snp	A/C			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	HERC4	GRCh38.p7	10:68075252	AAGCGGGGCGGAGAG[A/C]ACCAGGGGTGGGGAG	26091
rs764043540	snp	A/G	1.7447e-05	0.0029535	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:67966692	ACCTACCATTCCATA[A/G]GCCTGCTGTTGGACC	26091
rs764045686	snp	A/G	1.64751e-05	0.00287007	synonymous-codon	HERC4	GRCh38.p7	10:67932666	TTCATTAGGCTGAAA[A/G]AGCAGAAGGACTTTT	26091
rs764076353	in-del	-/TAATTTATCTGGGAAAAAAGACTTAGATTAT	1.74293e-05	0.00295201	intron-variant	HERC4	GRCh38.p7	10:68032909	ATAGTATTTTAAAAA[lengthTooLong]TCAAAACTCATCTAG	26091
rs764100326	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68000249	TAGCTCAGCAGGTTT[C/G]GGGTATTCCTATGGA	26091
rs764132953	snp	A/C	8.46676e-05	0.00650589	intron-variant	HERC4	GRCh38.p7	10:67923181	ACCACTTCAAAACAA[A/C]AAGATACAGTAGCAA	26091
rs764177140	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68015485	CAGATTGGCAAATTC[G/T]TTCAGGGTAGCTCCA	26091
rs764224178	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67931592	ACCACACCCGATTAA[G/T]TTTTGTATTTTTAGT	26091
rs764237154	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67946982	TATGAAGCAAATATT[A/G]TTACCGCTAAAGAGA	26091
rs764241113	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67947406	TTCATCAAGAAGATA[C/T]AACAATTACAAATAG	26091
rs764246895	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67960532	CTGGGATTATAGGCA[A/T]GTGCCACCACGCCTA	26091
rs764257921	snp	C/T	1.65625e-05	0.00287766	synonymous-codon	HERC4	GRCh38.p7	10:67925155	TTTTATCGTAGGATG[C/T]TCTGCCCAATATTCC	26091
rs764301983	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67974686	TGTATGCTTATTGTT[A/G]ATTTTTCGTAAAAAG	26091
rs764388084	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68039881	TCTGAGTATCAAGTA[C/T]AATTTTGCAAATGAA	26091
rs764404760	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67990066	AAAAGACTAGACAAA[A/C]GCAAGAAAAGGAAAA	26091
rs764437252	snp	C/T	1.65564e-05	0.00287714	intron-variant, missense	HERC4	GRCh38.p7	10:67941090	TCAAATGGAACAAAT[C/T]ACTGTCTTCAAATGT	26091
rs764455278	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67936249	ATCTATTAATTTAAA[-/T]TTTTAAAAAAAGTCA	26091
rs764466837	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68059067	AAAAAACCCAAAATG[C/T]AGCTCTCTATACATT	26091
rs764468743	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68044314	AATGAGATGTCAACT[C/T]TTACAGGCCCAAAGA	26091
rs764479058	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68042062	CGCTCTGTCGCTTAG[G/T]CTGGAGTGCAGTGGT	26091
rs764495033	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68004847	CAGCATGCAGGAAAC[C/T]GATTCCATGATTCCA	26091
rs764504651	snp	A/G/T			intron-variant	HERC4	GRCh38.p7	10:68016733	CACTTCCTGTTTAGG[A/G/T]TAAGTCCTTAGATCT	26091
rs764555224	snp	A/T	0.000134415	0.00819693	intron-variant	HERC4	GRCh38.p7	10:67988876	ATAAAATGAATTTTT[A/T]AAAAAATCACAATTT	26091
rs764584839	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68004001	CCTTTTCTCCATATC[C/T]TTGCCAGCATGTTAT	26091
rs764591313	snp	C/T	3.32579e-05	0.00407773	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:68032863	AGTAAATTAGGAACA[C/T]ACCTATCTGAAAATT	26091
rs764620867	in-del	-/G/GG/GGG			upstream-variant-2KB	HERC4	GRCh38.p7	10:68075418	TGCGCCGAATCTTCC[-/G/GG/GGG]GGGGGGGGGGGGGGG	26091
rs764622693	in-del	-/T	3.31876e-05	0.00407341	intron-variant	HERC4	GRCh38.p7	10:67940921	CTACTACTTTTTGAC[-/T]TTTTTTTTCCAACTA	26091
rs764629871	snp	A/G	0.000186759	0.0096615	intron-variant	HERC4	GRCh38.p7	10:67995298	TGCTCATTCACTGTA[A/G]GTTGAAAAATTAAGT	26091
rs764636367	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68064079	AAAACTCCACCTCTA[C/G]TAAAAATACAAAAAT	26091
rs764645336	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67972750	GTCATTCACCATGTT[C/T]ATGAATCAGAAAGGA	26091
rs764654165	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68068283	TGAGGTCAGGAGTTC[A/G]AGACCCCCCTGGCCA	26091
rs764683073	snp	A/T	1.66078e-05	0.00288161	intron-variant	HERC4	GRCh38.p7	10:67940909	TACCTCCCAAACCCT[A/T]CTACTTTTTGACTTT	26091
rs764728754	snp	A/G	1.76052e-05	0.00296686	intron-variant	HERC4	GRCh38.p7	10:67988635	TAGGAATGGGGAAAG[A/G]GGAAAATAAAGGAAT	26091
rs764729181	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68060130	AAGACTTTTGGATAA[C/T]GAATAAAGGATTCAG	26091
rs764730151	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68051962	GCATGAGCCACCGCG[C/T]CCAGCCTCAACTTTT	26091
rs764766134	snp	A/G	8.46002e-05	0.0065033	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:68014028	TGACAGAACTTACCA[A/G]TATCTGGTAGACACT	26091
rs764819735	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68073991	ATTAAAAAAATCACC[C/T]GTGGGCAATCTATAT	26091
rs764870170	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68034513	GTCTCATTTTTATTT[C/T]ATAGTTTCTCCCAAG	26091
rs764874595	snp	C/T	1.69046e-05	0.00290723	intron-variant	HERC4	GRCh38.p7	10:67932810	GCACACATGTACAGA[C/T]TATAAAAATCATGTA	26091
rs764899432	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67938658	CAGTTATTTAACATC[A/C]CTTTTGGCCAGGTGC	26091
rs764902053	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67975716	TGGCTTAGCATTGTA[A/C]AAATAATCCAATTTA	26091
rs764917310	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68022201	TGTCAATGCTACCCA[A/G]AAGAATGTACAGACT	26091
rs764959312	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68039779	GCTCAAATTACTAAA[C/T]ATTTACTGTTATTGT	26091
rs764997152	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67936253	ATTAATTTAAATTTT[A/T]AAAAAAAGTCAATGT	26091
rs765003086	snp	C/T	1.67066e-05	0.00289016	missense, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68038138	CACAAGCAACCTGTA[C/T]AATCTGGATATCTGA	26091
rs765033024	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67929228	CAGTAAAACTGGCTA[C/T]ATTCTGGGGTGTATA	26091
rs765042464	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67983661	GTGTGATGGCAGGCG[C/T]CTGTGGTCCCAGCTG	26091
rs765043288	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68052388	TCATTTTTAGGCTTA[C/T]TTTTAAAACAGTTAA	26091
rs765050822	in-del	-/TGG			intron-variant	HERC4	GRCh38.p7	10:67934494	TTGTTTGAATCCTGG[-/TGG]TGGTGGTGGTGGTTG	26091
rs765065296	in-del	-/A	3.81003e-05	0.00436448	intron-variant	HERC4	GRCh38.p7	10:68025679	ACACTCCACCTTCCT[-/A]AAAAAAGACAAAACC	26091
rs765068215	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67982208	CATATTACCTGACTT[C/G]AAATTATAGTGCAGC	26091
rs765076281	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67924899	TTCCATTTTACTTCA[C/T]AGAATGAATCAATGC	26091
rs765096885	snp	A/G	3.32038e-05	0.00407441	intron-variant	HERC4	GRCh38.p7	10:67954936	TGAATAAAAGTCCCA[A/G]TTATACCACAGAAAA	26091
rs765099654	snp	C/G			missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:68032812	TGATCTTCTCCACAA[C/G]AAATATAAACTATTT	26091
rs765111430	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67947140	TTTAACAGATATTTA[C/T]AGGACATTTCATCCA	26091
rs765113510	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67943099	GTATTACTCTGTGTC[A/G]TATTTGTTACATACA	26091
rs765115659	snp	A/T	4.37503e-05	0.00467688	intron-variant	HERC4	GRCh38.p7	10:67991208	TATCTCACTAAAAAA[A/T]TTAAAAAAGTTTTTT	26091
rs765162351	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68022870	AAATGGGAAAAACAC[-/T]TTTAATTGACATTTC	26091
rs765166433	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67926117	ATATTAGTACTGGCC[A/G]GGCGCGGTGGCTCAC	26091
rs765202157	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68046915	GTGAGCTGTGATCAC[A/G]CCACTGTATTCCTTC	26091
rs765212549	snp	A/T			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011243	TTTTTGTAGAGACAG[A/T]GTCTCACTACATTGC	26091
rs765226804	snp	A/C	0.000240558	0.0109645	intron-variant	HERC4	GRCh38.p7	10:68039528	GGAAAAAGGAGAGTT[A/C]CTCTGATTCCATATT	26091
rs765227782	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68061229	CAAAAGCTTTGTTTC[C/T]AGTAAGACCTGGAGG	26091
rs765233541	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68029351	CAGAAAATTAGCCAG[A/G]TGTGGTGATGCATGC	26091
rs765272794	snp	C/T	4.94303e-05	0.00497119	missense	HERC4	GRCh38.p7	10:67932623	CCTTCCAATCATAAT[C/T]TGTATTTCCAATGAC	26091
rs765282981	snp	C/T			intron-variant, missense	HERC4	GRCh38.p7	10:67940973	GTTCTTTCAAATCAT[C/T]CAAGGATGGCTTCTT	26091
rs765284574	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67961821	CAAAACATCACTCTA[C/T]GCAAACCCTATTCAG	26091
rs765322893	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67930011	GGGTTTCTCCATGTT[C/G]GTCAGGGTGGTCTTG	26091
rs765339067	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68030767	TGCTACATCAAAATG[C/T]GTATTTGTATGTGAT	26091
rs765343278	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67944918	CAGAGGAGCCAAAAG[A/G]AAAAACAAGAAAGAA	26091
rs765362350	snp	A/T	5.20233e-05	0.00509989	intron-variant	HERC4	GRCh38.p7	10:67925202	TCTAAAAACAACATA[A/T]TCTTTTATTAGTATT	26091
rs765372198	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67995292	CATTGATGCTCATTC[A/G]CTGTAGGTTGAAAAA	26091
rs765401991	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67923584	TTTTTTTTTTGAGAC[A/G]AGTCTTGCTCAGTTG	26091
rs765408241	snp	A/T	1.69934e-05	0.00291486	intron-variant	HERC4	GRCh38.p7	10:68032890	AATTCCAACAAGAGA[A/T]GTTAATAGTATTTTA	26091
rs765461453	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67993948	CCATTCTTTTCAAGG[A/G]AATGACCACATGTTA	26091
rs765467400	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67987028	TTAAATATATCTAGA[A/G]TATTCACATGAACTA	26091
rs765495648	snp	A/G	1.98277e-05	0.00314856	intron-variant	HERC4	GRCh38.p7	10:67990418	ATATTTTGACAAAAA[A/G]TAAAACCTACTTCAT	26091
rs765496779	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67953077	ATATATTTAAAGGAG[A/G]ATAGCCCATACATTT	26091
rs765534566	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68003784	ACTTAAATTGATTCC[A/G]AATACTGGCTATTAT	26091
rs765536176	in-del	-/ATC			intron-variant	HERC4	GRCh38.p7	10:67932574	TTTCCATTTAACAAT[-/ATC]AGAGATTAGTTTTCC	26091
rs765544548	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67990548	AGAAGAAAAAAGAAA[A/G]ACAATGTCTTACAAT	26091
rs765628721	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68015408	TTAGCTAAATAATTA[C/T]TTTAGGTCACTAGGT	26091
rs765639894	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68042483	ACAAAATTGGCCAAG[C/T]ATAGTGGTGCACGCC	26091
rs765647668	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68018048	TATCAGACTAGAAAA[C/T]CTTCATAATAAAACC	26091
rs765676364	snp	A/G	3.29794e-05	0.00406061	synonymous-codon	HERC4	GRCh38.p7	10:67954660	CGTATTTAGGATCCA[A/G]TAATTCCCTCATGAT	26091
rs765677568	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67928990	CAATTTTCCTCTGCT[C/T]TAAGTCACTCATCAA	26091
rs765722367	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68040649	CAATCCCAGCATTTT[C/G]GGAGGCCAAGGCGAG	26091
rs765764303	snp	C/T	4.94809e-05	0.00497373	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:67990944	GGTTGTATAAGTTTG[C/T]GGAATAAAAGCCTAG	26091
rs765765141	snp	A/C/T			intron-variant	HERC4	GRCh38.p7	10:67977160	TTCTCCTTCCACTTG[A/C/T]GGAGAGAAGACTGGA	26091
rs765765831	snp	C/T	8.23689e-05	0.00641698	missense, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68073005	CCTACATCTCGGACC[C/T]TTTTATTTATAAAGA	26091
rs765785136	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67965652	TGTACTTTTTTAGTG[C/T]TTACTAGACATATTC	26091
rs765787506	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68042880	ATGTATACGTTACAA[C/T]AAATCAGATCAAGCC	26091
rs765794026	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67938494	AACTGAAGGTTTTAC[A/C]ATTTCTCCAAGAGTC	26091
rs765839510	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68072654	TCTTTATTGTTTTAT[A/G]TCGTCATACAAAATA	26091
rs765850085	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67980335	AAGGGGTTTCTCCAT[C/G]TTGGTCAGGCTGGTC	26091
rs765919324	in-del	-/AG			intron-variant, frameshift-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:68039431	CCTGATTCTGCCATA[-/AG]AGAGTCCGGAGCAAA	26091
rs765940116	snp	C/G	1.67992e-05	0.00289816	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67988671	GACATACCCTATGTA[C/G]TATTTCTAAAACCTT	26091
rs765963591	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67925846	GCTATACTGAGGCCT[A/C]CTGCCAACAGTCATG	26091
rs765976651	snp	A/G	1.93996e-05	0.00311439	intron-variant	HERC4	GRCh38.p7	10:67939706	TTATTGGATATTTTG[A/G]CTATTTTACTTATGG	26091
rs765990167	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67937091	CTACAAGTAGGGGTA[A/G]TATTTTGAAAGATTA	26091
rs766026736	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68046831	ACAAAATTAGCCAAG[C/T]GTGGTGGCACACATC	26091
rs766042292	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67951701	GTCTCCTTGCTCTTG[C/T]TCTTCTGTGTTTCTA	26091
rs766049959	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68001532	TTTATCCTATACAGC[C/T]TGAGTACAGTGCAAA	26091
rs766080602	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67933517	TAATGAGAATGGATA[C/T]TAGAAGATTTCACTA	26091
rs766099500	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67963365	GGGATTACAGGTGCC[C/T]GCCACGATGCTTGGC	26091
rs766108047	snp	C/T	1.66496e-05	0.00288522	intron-variant	HERC4	GRCh38.p7	10:68044387	GTTAAGGACCTCTTT[C/T]TGGTCACCTTTGTTA	26091
rs766121151	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67997477	CTAAGTATTATTTCT[C/T]AAGCACTTATGATTA	26091
rs766126973	snp	A/G	1.6486e-05	0.00287102	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:67992226	ACAGGAAACCTTCCA[A/G]AAGGATAGCTCAGCC	26091
rs766149884	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67980771	CAAAGTTAAGGTGTA[C/G]AGTTTTCATTACTCT	26091
rs766161426	snp	C/T	1.68553e-05	0.00290299	missense, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68038161	ATATCTGACAAACTT[C/T]TAATATTTCTAGAAA	26091
rs766197214	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68030118	GCACATTTGTTCTGG[C/T]TATTAATTTTAAATT	26091
rs766200204	snp	C/T			intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010029	AAGAGCATCACCGAA[C/T]TTCACCTTCCCTCCA	26091
rs766201956	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67995778	CATCCTCAACTCATA[C/T]CTTCTTGTCTTAAGA	26091
rs766226021	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68045894	AATTCCTATCTATAC[A/G]GAAATTCAAATTGTA	26091
rs766241498	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67960026	TCATGCCTGATAGGA[A/G]TGTCTTTGTTTGCCT	26091
rs766251691	snp	A/T	1.66432e-05	0.00288467	intron-variant	HERC4	GRCh38.p7	10:67955147	TGGAAAACAAAAGAT[A/T]AACATTTTAACAGCA	26091
rs766267201	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67960672	ACAGGCGTCAGCCAC[C/T]GCACCCAGCCAAAAG	26091
rs766287957	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67985977	TAGAGCAGAGGGAAG[A/G]AATTTAGGCAGCTGT	26091
rs766336785	in-del	-/AA			intron-variant	HERC4	GRCh38.p7	10:68066755	TACAATATATAACAG[-/AA]AAGAGAAAAGACTGG	26091
rs766341091	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67983829	TTAACTGGGTGTGGT[C/G]GTGTACGCCTGCAAT	26091
rs766342354	snp	C/T	1.66266e-05	0.00288323	intron-variant	HERC4	GRCh38.p7	10:68044595	GAGAAATATTGCATT[C/T]TAGTACAGAAATCAA	26091
rs766352875	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67923385	TAATAAATGTTTGAT[A/G]AGTGAGTATTTTGCC	26091
rs766362980	snp	C/T	1.658e-05	0.00287919	intron-variant	HERC4	GRCh38.p7	10:67992347	TCAAATAAGATTAGT[C/T]AGAGGGAAGAGATAT	26091
rs766369879	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68073800	TTCTCTTACCAAACC[A/G]TAATCTTAAATCACC	26091
rs766378575	in-del	-/A	0.00335632	0.0408276	intron-variant	HERC4	GRCh38.p7	10:67996143	AGACCTCGCCTCTAC[-/A]AAAAAAATTAAAAAT	26091
rs766416116	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67939458	CTAGCATGTAGTAAA[G/T]GCTCAATAAATGTTA	26091
rs766436032	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67975658	CTCAGCCGACACATG[C/G]ATTCTTAACTCACTA	26091
rs766458998	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67957455	TCTTCATTTACTTAA[C/T]ATACAAAAAAGTACC	26091
rs766472806	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68041702	CAAAGTTATGTGTTT[C/T]CACTTATATTAAACT	26091
rs766487876	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68056034	ATTACAAGCGTAAGC[C/T]ACCACGCCTGGCCCT	26091
rs766514516	in-del	-/AAAAA			intron-variant	HERC4	GRCh38.p7	10:68049590	GTGAGACACTGCCAC[-/AAAAA]AAAAAAAAAAAAAAA	26091
rs766520547	snp	A/T	6.70893e-05	0.00579139	intron-variant	HERC4	GRCh38.p7	10:67990444	TTCATTTAAAATGAA[A/T]ACACTTTCAAAGAAA	26091
rs766526113	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67969986	AATCCCTCTAAGGAG[C/T]AGGCATGCAAAGTGG	26091
rs766534132	snp	A/G	1.64923e-05	0.00287156	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:67990961	GAATAAAAGCCTAGC[A/G]GCATTCATATCAACC	26091
rs766545571	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67942493	CTAATCTGTTTTCCT[C/T]TACCCCCGTTCCAGT	26091
rs766559188	snp	C/T	1.78033e-05	0.00298351	intron-variant	HERC4	GRCh38.p7	10:67991129	CAGCATATTAAAGAA[C/T]TGCCACTTACCTAAC	26091
rs766577497	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68070876	CAATAGAATTAAATG[G/T]AAGCCTTCATTTTCT	26091
rs766579731	in-del	-/AC	2.11383e-05	0.00325095	intron-variant	HERC4	GRCh38.p7	10:67990427	CAAAAAGTAAAACCT[-/AC]TTCATTTAAAATGAA	26091
rs766593740	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68000435	ATACAAAAAGTTAAC[A/T]GGGTGTGGTGGCATG	26091
rs766625071	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67928814	TAGTTCCAGCTACTC[A/G]GGAGGCTGAGGCAGA	26091
rs766637165	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67996314	GACCTTGAAATAGAC[-/A]ACCCCCCCTGCCCCA	26091
rs766676669	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67926221	CCAACATGGTGAAAC[C/T]CCATCTCTACTGAAA	26091
rs766681697	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68013027	ATGCCGCATTTTATT[A/G]TGCTTTGCTTTACTG	26091
rs766690830	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68018524	ACAATTATATAAACA[C/T]GTTAAGTATAAATAA	26091
rs766694851	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68005051	ATGTATGTCCTTGGC[A/G]CCCTTGTCCAAAATG	26091
rs766703203	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67965436	GTTTGTTGAATAAGC[A/T]AATGAATAGACCTAA	26091
rs766714938	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67929835	TTTTTTTTTTGAGAT[A/G]GAGTTTCACTCTTGT	26091
rs766742853	in-del	-/TTTG			intron-variant	HERC4	GRCh38.p7	10:67976423	CCTCTGATATATATT[-/TTTG]TTTATCTTACTTAAA	26091
rs766769602	in-del	-/ATAA			intron-variant	HERC4	GRCh38.p7	10:68018532	ATAAACACGTTAAGT[-/ATAA]ATAATAGAAATAACA	26091
rs766791333	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67964336	TTTCCAAGACTCTCC[C/T]AGTTTTCCCTCTACC	26091
rs766829084	snp	A/C	1.68323e-05	0.00290101	intron-variant	HERC4	GRCh38.p7	10:67954790	AAGAAATGAAAGTAC[A/C]TTCTGGAGACCCTAG	26091
rs766846321	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68028264	TAAAAAAAAAAAAAT[A/G]AGTGTTGTCCTAGCA	26091
rs766848402	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67994310	TACTCTTAAAATGTG[A/G]TTGTGCCCTCTATAA	26091
rs766851084	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68065426	AAGCCCATTCTAAAG[A/G]ATTCCAGAATGTCTT	26091
rs766867003	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67923980	GGCATCAGTTATAAA[C/T]GAGGGAACTAAGGCC	26091
rs766906997	in-del	-/GCTAACATTACACAAGACA			intron-variant	HERC4	GRCh38.p7	10:67953893	TCTAGGCACTAAGCT[-/GCTAACATTACACAAGACA]GCCAACCTCCAGGCA	26091
rs766910954	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67971233	TAAAGAAATAATACC[-/A]ATCTTAATCAAACTT	26091
rs766919475	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67951645	TCACAAATGGTGTCA[C/G]TTTTCAATCCTTCAT	26091
rs766948665	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68036389	TGAGTAAACAAACAA[A/G]CAAAAAGGTCAATAT	26091
rs766964158	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68044036	ACTAAAAAAAGGACA[A/C]GTTAGTGAAAAACAT	26091
rs766991663	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68018755	ATATGCATGACCTCT[A/G]TGATGAAAATTTTAA	26091
rs767023000	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67943707	AAGGTCTGTACAGTG[A/T]ACAAGGAGAATCCTA	26091
rs767035462	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67935373	GATGGTCTCGTTGTC[A/G]TGACCTCGTGATCCG	26091
rs767040874	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68045129	AGTTCAAGACCAGCC[G/T]GGCCAAAACGGTGAA	26091
rs767081670	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67965415	GTTATATAACAGATT[A/C]TCATTGTTTGTTGAA	26091
rs767096591	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68001278	TTAGGAGGCTGAGGT[C/G]AAAGGACTGCTTGAG	26091
rs767123688	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67950036	AAAAAAACAAAAAAC[A/C]AAACAAAAAACAAAA	26091
rs767188163	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68000294	CTAAAACTTTGTATA[C/T]TGGGCAAGGCACGGT	26091
rs767195481	snp	A/G	1.84082e-05	0.00303377	intron-variant	HERC4	GRCh38.p7	10:67925230	ATTAAGGGACACACT[A/G]GCTAATATATTAGCA	26091
rs767201099	snp	A/G	1.67033e-05	0.00288987	intron-variant	HERC4	GRCh38.p7	10:68044609	TCTAGTACAGAAATC[A/G]AGGAAAAAGATATTG	26091
rs767280522	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67924469	AGCATGTTACTGTAC[C/T]GAATTCTGTAGGTAA	26091
rs767315093	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67977940	GAGCCGAGATTGTGC[C/T]ACTGCACTCCAGCCT	26091
rs767367228	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67973001	TTAAGTATTAAAGGA[C/T]GATATCTACATTTTA	26091
rs767389405	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68007576	TATCCTTTGCAGTCC[A/G]TACTTGTTTGTACCT	26091
rs767389695	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67936776	TATTACCATTCCCAC[G/T]TATGCATCTTTTCTT	26091
rs767397947	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68071208	GATATAGATGTCACA[A/G]TGCAATCATCACAAT	26091
rs767411376	in-del	-/TGG			intron-variant	HERC4	GRCh38.p7	10:67934492	TGCTTGTTTGAATCC[-/TGG]TGGTGGTGGTGGTTG	26091
rs767442396	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68072320	AATCAGGACACTTCA[C/T]AGTCACAAAATCTTT	26091
rs767450699	snp	C/T	3.29506e-05	0.00405884	synonymous-codon	HERC4	GRCh38.p7	10:67932645	TCCAATGACCATTGC[C/T]TGTAGTTCATTAGGC	26091
rs767477230	snp	C/T	3.52516e-05	0.00419816	intron-variant	HERC4	GRCh38.p7	10:68032916	TTTTAAAAATCAAAA[C/T]TCATCTAGATGTGTT	26091
rs767488387	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67963580	TAAACACCAAGAGTT[C/T]AGAACTAGTTTAATG	26091
rs767490830	snp	C/T	5.10087e-05	0.00504993	intron-variant	HERC4	GRCh38.p7	10:67992705	AAAAATGTAAAAAAT[C/T]AAAAGCCAAGATTTA	26091
rs767490985	snp	A/G	1.65138e-05	0.00287343	synonymous-codon	HERC4	GRCh38.p7	10:67956944	ATCAAATACAAATGG[A/G]TATGTACAGATTGTA	26091
rs767498811	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67972220	GCTCTGTCTCAAAGG[-/A]AAAAAAAAAAAAAAA	26091
rs767574054	in-del	-/AATT	0.000167524	0.00915062	intron-variant	HERC4	GRCh38.p7	10:67988869	CATGCAAATAAAATG[-/AATT]TTTTAAAAAATCACA	26091
rs767587356	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68004876	CATTACCTCCACCGG[C/G]TCTCTCCGTTGACAC	26091
rs767588528	snp	C/T			intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069687	TTTATAAAGCCAACC[C/T]ATGTAAAGAAACAAT	26091
rs767592707	in-del	-/A	1.64901e-05	0.00287137	frameshift-variant	HERC4	GRCh38.p7	10:67954658	CCGTATTTAGGATCC[-/A]AATAATTCCCTCATG	26091
rs767603981	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67969793	AGCAGAGTTTGGTTG[A/C]CACAGGAAGAGGGGA	26091
rs767624660	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68015842	GCATGGTGGCTCAGG[C/T]CTATAATTCCAGCAC	26091
rs767636273	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68040063	ATAATGCCTGGCACC[C/T]ACTATAGTGCCTAAT	26091
rs767645112	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67927968	AGGGGAGACAGGATA[C/T]GTGTGCAGGAGAGAG	26091
rs767645691	in-del	-/TTG			upstream-variant-2KB	HERC4	GRCh38.p7	10:68075599	ATGAAGAAAATCACT[-/TTG]TTTTTTGGTTTGGTT	26091
rs767645756	in-del	-/G			intron-variant	HERC4	GRCh38.p7	10:67977541	TGGAGGAAAAGTAAA[-/G]GGGACTTTGTCTTGT	26091
rs767653372	snp	A/C	1.66371e-05	0.00288414	intron-variant	HERC4	GRCh38.p7	10:67954929	TAGCTTCTGAATAAA[A/C]GTCCCAATTATACCA	26091
rs767665848	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67948535	AACAGTAGATGTTGG[A/C]GTGGATGTGGTGAAA	26091
rs767677124	snp	C/G	3.31609e-05	0.00407177	intron-variant	HERC4	GRCh38.p7	10:67954942	AAAGTCCCAATTATA[C/G]CACAGAAAATGTCAA	26091
rs767698816	in-del	-/TTTGT			intron-variant	HERC4	GRCh38.p7	10:68067618	CAGCTCGTTTATAAA[-/TTTGT]TTTATGAACAGAGAG	26091
rs767729246	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67995103	GTGGTTTCTCCTAAC[A/G]TTTGGCTTGGTCTTC	26091
rs767748530	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68016835	CAGAGCTAAGAATAA[A/C]TATTCAAATCATGTA	26091
rs767806775	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68026013	ACGGTATCATCTTCA[A/C]TTTTCAAGGTAGTTA	26091
rs767835359	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68023006	TAAAATAGGTATTAT[-/A]AAAAAAAAAAAGAAA	26091
rs767843056	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68032521	TTAAGCAGTATTTCA[C/T]ATAAAGCTGAGAAAT	26091
rs767848054	snp	A/G	1.66101e-05	0.0028818	intron-variant	HERC4	GRCh38.p7	10:67988846	GTTTTCTGTTATTAA[A/G]AAGTGAACATGCAAA	26091
rs767886364	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67969458	TGAAACAACTGGAAA[C/T]AAGGCAGAGGGGGGG	26091
rs767887562	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68042817	AAAAAAACATTTCCA[C/T]TGAAATACTAAATGG	26091
rs767890896	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68041444	CCAAATTTTCAGATG[C/T]TAAAATTAGGCAGGA	26091
rs767926262	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67977688	CCACAAGCTGACTAA[A/C]GAGCCCTTAAGGACC	26091
rs767935956	snp	A/C	4.957e-05	0.00497821	intron-variant	HERC4	GRCh38.p7	10:68025693	TAAAAAAAGACAAAA[A/C]CCCTTATCATTAGAA	26091
rs767946610	snp	C/G	1.65545e-05	0.00287697	intron-variant	HERC4	GRCh38.p7	10:67939568	AAATAATCAGGCTAA[C/G]CTATGTCCTTCCATC	26091
rs767959590	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68063766	AACATGGCAAAACCC[C/T]GTCTCTACTAAAAAT	26091
rs767968193	snp	A/T	3.64571e-05	0.00426933	intron-variant	HERC4	GRCh38.p7	10:68014236	GTTACCTTCCAACAA[A/T]TTACAATGACAAAAG	26091
rs767982612	snp	C/G	1.6664e-05	0.00288647	missense	HERC4	GRCh38.p7	10:67923107	GACTCTTCATACCAA[C/G]AATAGGAATGCGATC	26091
rs768004420	snp	G/T			upstream-variant-2KB	HERC4	GRCh38.p7	10:68076606	GGTTCTCTCTTGGGG[G/T]CTCTGAGAGATAATC	26091
rs768017957	snp	A/C	5.01534e-05	0.00500741	intron-variant	HERC4	GRCh38.p7	10:67954759	ATAGCACAATGCAAA[A/C]ACCAAATAGACTGTA	26091
rs768059455	snp	C/T			intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069250	AATGGATTGGTCTAG[C/T]GCACTGAAGATTAAA	26091
rs768069289	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68054137	AATGCAGAGTATACC[C/T]AAAATCCATGCCTAA	26091
rs768073843	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67942195	GCTCCAGCCTGGTTT[A/G]GCAGTCTAGCCTCTG	26091
rs768074206	snp	C/T			missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67990296	ATTGTTGGAATCACT[C/T]ATCAGGGGACATTCT	26091
rs768095071	snp	G/T	1.65375e-05	0.0028755	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67988709	GTATGAAGAAAACTG[G/T]TGAAAATTCTTCTTT	26091
rs768132262	snp	A/G	0.000121628	0.00779739	intron-variant	HERC4	GRCh38.p7	10:68014002	TCAATATATGAAGGA[A/G]AGCTTTAATATGACA	26091
rs768137829	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68040017	TAAACAGTAAGTTCT[A/G]TGAAGGCAGACTATG	26091
rs768138191	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67943395	TCAAAATATGAAAAG[C/T]AGACAAATGGCTGGT	26091
rs768162094	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67929444	TAAATGGAGCCATAC[A/G]GTATGCAACCATTTG	26091
rs768163781	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67940859	AAAATATATTTTTTC[A/G]TAGAAGGAAAGCTTT	26091
rs768164538	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68052159	CATTTTTCAGAGACA[C/T]AGGCAAAACCTGAAA	26091
rs768189607	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67983502	TGAATGAATAAGGCC[A/G]GGTGCAGTGGCTTGT	26091
rs768211350	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67944595	GGAAAACATGACCTC[A/G]CCAAACGAACTAAAT	26091
rs768222539	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67993260	TGAGACAGGAGAATC[A/G]CTTGAACCCAGGAGG	26091
rs768235595	snp	C/G			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012752	GTTGGAAAAATGGTG[C/G]CAACTGACTTGCTCA	26091
rs768312680	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68006757	GTGGATATAATATTC[C/T]GGGATAAATGTTATT	26091
rs768339527	snp	A/C	1.97607e-05	0.00314324	intron-variant	HERC4	GRCh38.p7	10:67991044	AAGAAAAAAAAAAAT[A/C]GAATAAAAATTTAAA	26091
rs768383923	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68037524	CAAAGCTAATAAATA[C/T]GATGTTTAGCCTTCT	26091
rs768421569	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67995567	TATCTATTAGCTGTC[-/T]TTTTTTTTTTTTCAT	26091
rs768429451	in-del	-/CAA			intron-variant	HERC4	GRCh38.p7	10:68057196	GGGTACACAGTTTAT[-/CAA]CAACACACTAAGCCA	26091
rs768444945	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68066141	TATTAGATTCTTTCA[C/T]ACATATCCCAAGCAC	26091
rs768455832	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68065795	ACCCAGGGAAGTCGA[C/G]GCTGCATTGAGCCAC	26091
rs768457591	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68035558	GATATTGTAAAAATG[C/T]AGATTTGATAATATT	26091
rs768475091	snp	C/T	1.77178e-05	0.00297634	intron-variant	HERC4	GRCh38.p7	10:67988620	GTATCAATCTGTTAA[C/T]AGGAATGGGGAAAGA	26091
rs768495353	in-del	-/CAA			intron-variant	HERC4	GRCh38.p7	10:68032880	CCTATCTGAAAATTC[-/CAA]CAAGAGATGTTAATA	26091
rs768499937	in-del	-/TCCTGGACCATAC			intron-variant	HERC4	GRCh38.p7	10:67968997	CTAAGATAGACCAAA[-/TCCTGGACCATAC]AATAAGTCTTCATAC	26091
rs768510768	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68003328	ACCATGCCTGACTAA[-/T]TTTTTTTTTTTTTTT	26091
rs768561810	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67952345	CTGGAGTGCAGTGGC[A/G]CGACCTTGGCTCACT	26091
rs768577749	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67997835	GGAAGAAACATAGTC[A/G]GCCCTCTGTATCCAT	26091
rs768581975	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68017515	TGAGACAGAGTTTTC[A/G]CTCTGTTGCCCAGGC	26091
rs768582797	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67928640	AAAATGAGTTGCCTC[A/G]GGCCAGGAGCGGTGG	26091
rs768634602	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67971671	ACCCCCACCCCCCAC[C/T]GACATTTAACATTAT	26091
rs768653894	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67951513	CTTTCACTGTTTGTT[C/G]TGGAACTCACAATCT	26091
rs768667357	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67965256	ATCTTTACTAAGTCC[C/T]CTCATTTTAATAATA	26091
rs768670278	snp	A/G	3.3036e-05	0.0040641	missense	HERC4	GRCh38.p7	10:67936228	GCACCAAAGTTTTCA[A/G]CTGTGATCTATTAAT	26091
rs768675896	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67952889	TGGGCGACAGAGGGA[A/G]ACTCAGTCTCAAAAA	26091
rs768685366	in-del	-/T	1.7748e-05	0.00297887	intron-variant	HERC4	GRCh38.p7	10:67925214	ATAATCTTTTATTAG[-/T]ATTAAGGGACACACT	26091
rs768699670	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68064270	ATTAAAAGAAAGAAA[G/T]AGGCCGGGTGCCGTG	26091
rs768723474	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68013665	GGAGATTGGTTACAT[A/T]ATAACGTGAATATGC	26091
rs768820749	snp	A/T	0.000127289	0.00797672	intron-variant	HERC4	GRCh38.p7	10:68072853	ATATAATTATTAAAA[A/T]TAGCAAATTTTAAAA	26091
rs768828177	snp	A/C	3.32768e-05	0.00407888	intron-variant	HERC4	GRCh38.p7	10:67959084	AGTATATTTTACTCT[A/C]AACATGAGCTTTATT	26091
rs768836265	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67978596	TTGCCACCTGGTGAT[C/T]GTAGAGCGCCAGCAC	26091
rs768837065	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67923371	ACAAAGGAAGTGCTT[-/A]ATAAATGTTTGATAA	26091
rs768845415	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68055553	ACTAAGCTTAGCACT[G/T]TAATTACTTAATCTT	26091
rs768857187	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67961400	TATCTATCTTTTTTA[C/G]AAAGTAGATTAACCA	26091
rs768864156	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68019748	TGTGTAATGCAGCCA[C/T]GAACAGCTTCCAGGA	26091
rs768873315	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68025092	AATTAGCTGGGCATG[A/G]TAGTGCATGCCTGCA	26091
rs768876860	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68046735	ACTTGCAGAAGCCAA[A/G]GTGGGAGGATCACTT	26091
rs768889638	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67976548	CCCAGCTGCATGGAC[A/G]CCAATTTAACAACTA	26091
rs768890048	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67949385	AACACCAATTCTCAA[A/G]CTCTTCCAAAAGATC	26091
rs768914387	in-del	-/ATATATATATATATATATATATATATATATATATATATAT			intron-variant	HERC4	GRCh38.p7	10:67927380	AAGAATAAATACACC[lengthTooLong]ATATATATATATTTT	26091
rs768915833	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68051341	AAAATGTTAACACTA[-/T]TTTTTTTTTTTTTTT	26091
rs768916942	in-del	-/ATACTACATAG	1.66305e-05	0.00288357	intron-variant	HERC4	GRCh38.p7	10:67988848	TTCTGTTATTAAAAA[-/ATACTACATAG]GTGAACATGCAAATA	26091
rs768928910	snp	A/C			intron-variant, downstream-variant-500B	HERC4, POU5F1P5	GRCh38.p7	10:68009652	TTTCTTAAAATAAGA[A/C]AGCAACAAAGTTTGC	26091
rs768942782	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67999442	GTTTGTGTTTTCAAC[A/G]AAGGAGTCTCAGAGC	26091
rs768968483	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68060846	AAATTACACATATGC[C/T]GATTGATCAACTGTA	26091
rs769007833	snp	A/G	1.65239e-05	0.00287431	missense	HERC4	GRCh38.p7	10:67932727	AAAGCATCAAATAAG[A/G]AAGCCACTGATTTAT	26091
rs769024542	snp	C/G	1.64936e-05	0.00287168	intron-variant	HERC4	GRCh38.p7	10:67932592	AGAGATTAGTTTTCC[C/G]CTACCTTTTCCAGTT	26091
rs769036704	snp	A/G			intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68070246	ACACAAATCATTAAC[A/G]AATTATTCCAAATAT	26091
rs769065590	in-del	-/TTTT	4.6805e-05	0.00483739	intron-variant	HERC4	GRCh38.p7	10:67991218	AAAAATTTAAAAAAG[-/TTTT]TTTAATCATAGAATC	26091
rs769086674	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68055378	ATATACACTAACTTA[C/T]GTGTCTTAGTTGACA	26091
rs769096208	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68053925	ATCCACACTGAAAAA[G/T]TTTAATACTGAGGTC	26091
rs769104091	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67934298	TCTCTTAAAAAGAAC[C/T]TCTGTTTTCTTTAGT	26091
rs769126814	snp	C/T			intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069593	CCTCCAGTAGGTTAT[C/T]ATGAATCTCGAGAAT	26091
rs769133070	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67984637	GCCCAGGCTGGAGTG[C/T]AATGGCACGATTTCG	26091
rs769186805	snp	C/T	1.65343e-05	0.00287521	missense	HERC4	GRCh38.p7	10:67923016	GTATATTTTGGAAGA[C/T]CCAGAAGATTAAAAC	26091
rs769192103	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67949273	GGGGTGACAAAGTGA[A/G]ACTCTGTCTCAAAAA	26091
rs769204616	snp	C/T			missense, nc-transcript-variant	HERC4	GRCh38.p7	10:68033976	CTACCATTTTCATCA[C/T]TAAGACCTAGCTGAC	26091
rs769211771	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67969775	CCACACAAAAAAATC[A/G]GAAGCAGAGTTTGGT	26091
rs769217841	snp	C/T	4.95291e-05	0.00497615	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:67990919	CTGCTGAGATATCTG[C/T]GGATGATCAGGTTGT	26091
rs769250181	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67989749	AGTGCAAGATCAGAT[A/G]AGCAATAAAATCTAG	26091
rs769256834	snp	C/T			missense	HERC4	GRCh38.p7	10:67932622	TCCTTCCAATCATAA[C/T]TTGTATTTCCAATGA	26091
rs769268871	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67955510	GGCGCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA	26091
rs769290488	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68025418	ACTATGACTCCTCAG[C/T]GGCAAAATAGGTATT	26091
rs769299894	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67982907	CTGAGACGGGTGGAT[C/T]GCCTGAGCTCAGGAG	26091
rs769301523	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68053699	GTAATGACAGCTAGA[A/G]CAAAAAGGCAGAGCA	26091
rs769301795	snp	C/T	4.94262e-05	0.00497098	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68034107	AGACTTAAGCAGCTG[C/T]GGTGAAGTTTGCTTT	26091
rs769319266	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67991791	CACATTTCAAGGCCA[A/G]TCCTAAAATGGCTAC	26091
rs769337334	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67928525	AATTATTCTTTAAAA[C/T]GGCTTTAAAGTAATT	26091
rs769338240	snp	A/T			utr-variant-3-prime	HERC4	GRCh38.p7	10:67922544	ACAAAATGAAAAAAT[A/T]ATCAAATGACTATTG	26091
rs769339794	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67956603	GTAAACTAGTAAAAC[A/G]GTTTATAAAGATTGA	26091
rs769369947	snp	C/T	9.88484e-05	0.00702954	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:68025592	CCATAAGTTCAAAAA[C/T]TTTCCTTGGGTTTAT	26091
rs769370356	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68055063	GAGTAGCTGGGATTA[C/T]ACAAGTGTGCCGCCA	26091
rs769371603	in-del	-/TA			intron-variant	HERC4	GRCh38.p7	10:67933104	AAGTTATTGAGAATT[-/TA]TATATATATCATGTC	26091
rs769375571	in-del	-/ACAGGACA			intron-variant	HERC4	GRCh38.p7	10:68058426	CAATATAGTTTCCCT[-/ACAGGACA]ATATACAGTCATTAG	26091
rs769378974	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67985091	ATAGTAGATAAGGTT[C/T]AATCAGCCATCATTT	26091
rs769429158	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67988576	TTTTGCCAATCTAAA[C/T]CTTTAATAGATTAAT	26091
rs769442828	snp	C/T	1.64974e-05	0.00287201	missense	HERC4	GRCh38.p7	10:67954979	TTGAGTGGCTTCTTG[C/T]AATCTATGTTCTTTG	26091
rs769443595	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68004812	CAGATCTTGTGAGAA[A/C]TCACTCATTATTACA	26091
rs769444632	snp	C/T	1.65474e-05	0.00287636	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67990229	GTACTTTCAGTGGTG[C/T]CTTTTCTAGGTTCAC	26091
rs769509992	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68047763	GTGAAGCAACAGGAA[C/T]TCTCCTTCACTGCTG	26091
rs769510333	in-del	-/TTAGAG			intron-variant	HERC4	GRCh38.p7	10:67981395	ACAAAGCAAATATTA[-/TTAGAG]TTAAAGAGAGAAATA	26091
rs769569731	snp	A/T	1.65817e-05	0.00287933	intron-variant	HERC4	GRCh38.p7	10:68044584	GAAATCAAGAAGAGA[A/T]ATATTGCATTCTAGT	26091
rs769573609	snp	C/T	1.65247e-05	0.00287438	intron-variant, synonymous-codon	HERC4	GRCh38.p7	10:67940959	AACATCAGGCATTAG[C/T]TCTTTCAAATCATCC	26091
rs769574959	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68049084	ACCTCTGTGTATGTG[C/T]ATATATATATATTTG	26091
rs769589474	snp	C/T			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011410	GTAACTACAGCCTTA[C/T]GAAATGTATTTCTTA	26091
rs769603334	snp	A/T	6.86448e-05	0.00585813	intron-variant	HERC4	GRCh38.p7	10:67939695	AGAGGAAAAAATTAT[A/T]GGATATTTTGACTAT	26091
rs769608115	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68064048	AGGAGTTCTAGAACA[C/G]CCTGGTCAACATGGC	26091
rs769617441	in-del	-/ATT			intron-variant	HERC4	GRCh38.p7	10:67956667	TTAATATATAAAATG[-/ATT]ATAGGTTAAGTTATT	26091
rs769691049	snp	A/G	1.65198e-05	0.00287395	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67988782	CCACAACTTCCTTAA[A/G]AAGTTCTACTATCTT	26091
rs769698696	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67949532	CCTACAAACCAATAT[C/G]CCTTATGACTATAGA	26091
rs769698817	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67965161	GTTCTTGAAATTCTC[A/T]CTGCCCTGATCTTAA	26091
rs769701921	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68063179	TTCATCATGTTGTAA[C/T]AGAAAGCTTGTCATA	26091
rs769706363	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68045192	TGGGTGTGTGGTGGT[G/T]CACGCCTGTGATCCC	26091
rs769712208	in-del	-/ATAATATTATATATCATAATATTATATATTAT			intron-variant	HERC4	GRCh38.p7	10:68059874	ATATTATATATTATA[lengthTooLong]ATAATATTATATATC	26091
rs769725733	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68009384	CTTTCCAAAGCACTG[G/T]GATTACAGGCATGAG	26091
rs769768765	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67942823	CTCCTGTTCCAGTTT[A/G]AACTGCCATTTGCAG	26091
rs769783840	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67963687	ATCCCTCCAAATGTT[A/C]TGAATCCTTTCAAAA	26091
rs769790448	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67978222	TGGAGGAGCTGAGAT[G/T]GCGTCACTGCACTCC	26091
rs769823359	snp	A/C	1.66241e-05	0.00288302	intron-variant	HERC4	GRCh38.p7	10:67959103	ATGAGCTTTATTACA[A/C]CAAACTTACCTCAGT	26091
rs769826464	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67946644	CCAGACGCAGTGGCT[C/T]ACACCTGTAATCCCA	26091
rs769833479	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68068962	CTCCATTTGAAAGAA[C/T]GTTGTAAAACACAAA	26091
rs769850446	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67960426	GCTTCGATCTTGTTG[C/G]CCAGGCTGGAGTGCA	26091
rs769871615	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67974037	GGCAACAGAGAGAGA[C/T]TCTGTCTCAAAAAAA	26091
rs769890370	snp	G/T	2.2638e-05	0.0033643	intron-variant, downstream-variant-500B	HERC4	GRCh38.p7	10:67966620	CAAAACCAAGCAATT[G/T]TTTCTTTTTTTATTA	26091
rs769928903	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67993209	AATTAGCCAGGCGTG[C/G]TGGTGTGTGCCTGTA	26091
rs769935151	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68060596	CAATTATATGGTTTA[C/T]GTGTTTCTTCACCCT	26091
rs769954509	snp	C/G/T	6.61456e-05	0.00575057	synonymous-codon	HERC4	GRCh38.p7	10:67932756	ATTGAATATGTAATC[C/G/T]ACATAAGCATCGACA	26091
rs769968282	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68008419	TCAAAAAATTTTTTG[C/T]TGTTTTTATATGGGA	26091
rs770001248	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68038775	CAATCATTACTAATA[C/T]GTTAAGTCTTATTTT	26091
rs770001587	in-del	-/TTTAT			intron-variant	HERC4	GRCh38.p7	10:68017338	AGTCAATCTCTAGCC[-/TTTAT]TAAATAAAAGCTGCT	26091
rs770009086	snp	C/T	1.64754e-05	0.00287009	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68034119	CTGCGGTGAAGTTTG[C/T]TTTTTACAGTCAGTA	26091
rs770023973	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67973770	AAAAATTACTGTACA[C/T]AGGTTGGGCACGGTG	26091
rs770026925	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68058907	GCAGTGAGAGTCTAC[A/T]ATGTATGTTCTCCAT	26091
rs770046375	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68073646	TATAATTAAGCTTTC[-/T]TAATACCTACCTCCA	26091
rs770052151	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68021561	TGCCTGTAATCCCAG[A/C]ACTTTGGGAGGCCAA	26091
rs770058816	snp	C/T	0.000320256	0.0126501	intron-variant	HERC4	GRCh38.p7	10:67996167	TAAAAATTGGTTAAG[C/T]GTGGTGGCGCATGCC	26091
rs770059814	snp	A/G	1.648e-05	0.0028705	synonymous-codon	HERC4	GRCh38.p7	10:67936176	TTTGTTAACAGCTGT[A/G]TCTGCACCATTTAGA	26091
rs770077313	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67979004	AGCCTTTCCAAGAAG[C/G]ACGAAGACACACAAG	26091
rs770097195	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68046310	AAATGATAGGATGAC[A/C]AGACAGGTAAGTAAG	26091
rs770168735	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67968043	GACAATACATTAAAG[A/G]ACAACTACTGTACTT	26091
rs770188325	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68031253	GATGAATGGTTATCT[A/G]AAAGGCTGAATTTGA	26091
rs770194759	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67925412	GAACATGATAGGATC[A/G]TACTATCATCTTCAA	26091
rs770195010	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67932998	TCCATGAGGCATTCA[G/T]TTATTCTTAGGCTAT	26091
rs770203362	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68068175	GCAACATAGGGAGAC[A/C]CCCTTCTCTAACAAA	26091
rs770239780	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68031537	ATGAAATTACTTTTG[C/T]GCCAACCTAATAATA	26091
rs770259143	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67982768	CTATAGAAAAAAATG[C/T]AATAATCCAATTTAA	26091
rs770263052	snp	A/G	0.000173586	0.00931466	intron-variant	HERC4	GRCh38.p7	10:67991094	TGATATACTATTTAA[A/G]ACAATAAATTTGAAA	26091
rs770368944	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67993344	ATAAGACTCCACCTC[-/A]AAAAAAAAAAAAAAA	26091
rs770370521	in-del	-/AT	1.94007e-05	0.00311448	intron-variant	HERC4	GRCh38.p7	10:67991042	AAAAGAAAAAAAAAA[-/AT]AGAATAAAAATTTAA	26091
rs770372696	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67999897	AGTAATATATTTATA[A/C]AGGTTCAATAAGAAT	26091
rs770385786	snp	C/G	3.37724e-05	0.00410914	intron-variant	HERC4	GRCh38.p7	10:67992152	TCTGCCTGGTGCTGG[C/G]ATTACAGGCATGAGC	26091
rs770392917	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68003720	GCTGAATAGTATTCC[A/G]TTGTGTATATATACA	26091
rs770403646	snp	A/G			intron-variant, missense, nc-transcript-variant	HERC4	GRCh38.p7	10:68039480	ACACACATGATTTTC[A/G]GGAAGCAGCTTCAGC	26091
rs770430356	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68004714	AATCATGGCAGAAGG[C/T]GAAGAGGAAGCAAAG	26091
rs770459100	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67935227	CTCGGCTCACTGCAA[A/C]CTCTGCATCCTGGGT	26091
rs770467016	in-del	-/AC			intron-variant	HERC4	GRCh38.p7	10:68049008	GCAATATCTAACAAA[-/AC]ACATGCATTCACCCT	26091
rs770480902	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68015142	ACAGTGTCTCAGTTC[C/G]GAGCCTTTGCCTCAC	26091
rs770522454	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68003900	TCATCTGATAGTTCT[A/T]TTTTCAGTTTTTTTA	26091
rs770524474	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68034531	AGTTTCTCCCAAGAG[G/T]CACTCATTCAAGCTC	26091
rs770527997	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68057624	GTGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAG	26091
rs770530172	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67938750	GGAGTTCGAGACCAG[A/C]CTGGCCAAGGTGGTG	26091
rs770535399	snp	C/T	1.65002e-05	0.00287225	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67990268	TACCAAAGGGAATTG[C/T]TATTGTTGTGAAATT	26091
rs770544423	snp	A/C	1.64749e-05	0.00287005	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:68025645	CCCAACTGACCATAC[A/C]CTCCAGCTCCAAAAG	26091
rs770577676	snp	C/T	8.29456e-05	0.0064394	missense	HERC4	GRCh38.p7	10:67925127	GTAATTCGTGAAATA[C/T]TTCCCAAAAAATTTT	26091
rs770600292	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68052329	GCGCATCATTTTACC[A/G]AGGAGAAAGAGGGCA	26091
rs770613500	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67961640	TCCCCAAACTCACAA[C/T]TGGTATCAGAAGTGA	26091
rs770658893	in-del	-/AGAC	7.09832e-05	0.00595706	intron-variant	HERC4	GRCh38.p7	10:67966847	TTTAACCAGTACTCA[-/AGAC]AGACAAATTTTTTTT	26091
rs770660493	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68060901	TTTAAGATCTACTTT[A/T]TCCTCGTTATGCCAT	26091
rs770699714	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68062805	TACCATCACAGCCTA[A/G]CTATTTCTTTACCTC	26091
rs770707791	snp	G/T	3.89567e-05	0.00441326	intron-variant	HERC4	GRCh38.p7	10:67992686	ATTCTTCAGAATCTG[G/T]AATAAAAATGTAAAA	26091
rs770710059	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68026659	CCATCCTGGCTAAAA[A/C]GGTGAAACCCTGTCA	26091
rs770710959	snp	A/G	1.67911e-05	0.00289746	intron-variant	HERC4	GRCh38.p7	10:67954547	TACATACAGGTATAA[A/G]TACATGGGTATATAC	26091
rs770727449	snp	C/T	1.64993e-05	0.00287218	intron-variant, missense	HERC4	GRCh38.p7	10:67941023	AAAGCCAAAGGAAAA[C/T]GGAGGTCCACAATGG	26091
rs770727886	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68056928	GAAAGGAAAAGATCC[-/T]AAAGTGAATTTAAGG	26091
rs770734757	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68056816	GTAATTAACTCAAAA[C/T]GACACAGTTAGCTAT	26091
rs770753801	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67931401	AAAAATCATAACTGC[A/G]TTTCATGATGGTTTT	26091
rs770758506	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68040308	ATTCTTCTGCGTCAT[G/T]ACTGTGTTAAAGAAA	26091
rs770763580	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68066786	GGCATTACCATAGTT[A/C]AGTTTCTGTTCGTTT	26091
rs770792981	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67959946	GTTGTGAGGAATTAA[-/T]TTTACCCCAGAAGAG	26091
rs770809927	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68014832	AAAAGTCTCCTTAGG[A/C]AAGCAGGGAAGTATT	26091
rs770831260	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67978068	GATCCTTGAGGTCAG[A/G]AGTTTGAGACCAGCC	26091
rs770831811	snp	A/G			intron-variant, upstream-variant-2KB	HERC4	GRCh38.p7	10:68074906	CTGCCCCTCCCTAAC[A/G]CCGTCACACGCCCCC	26091
rs770848516	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68059673	ATATTATATATTATA[A/T]TATATATCATAATAT	26091
rs770862881	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67924085	AAGACCAAACAGAGA[A/G]AAGAGCAATACAGTT	26091
rs770916232	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67938023	AAAAATTATGAACAT[C/G]CAATTTTTTTTGGCA	26091
rs770921123	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67976895	GTGGGTCCCAGTTGT[C/T]AAAATGTGAGTTCCT	26091
rs770922008	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68071849	CACTAAGACCTTAAC[A/C]ACAAAGAAAGGATGA	26091
rs770939332	in-del	-/AACT			intron-variant	HERC4	GRCh38.p7	10:68043417	TTGTGTAAATTTTAA[-/AACT]AAGTATGAGTTAATG	26091
rs770949625	snp	A/C	1.69893e-05	0.00291451	utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68073138	TGGTCTTCCAGTTTC[A/C]ATAAAAAATTCTCTT	26091
rs770955171	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68037376	GCTGGGATTACAGGC[A/G]TGAGCCACTGCGCCC	26091
rs770971001	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67973598	AGAGTGAGGTATAGT[A/C]AAGAATAAGTAGAGA	26091
rs770973100	snp	A/G	6.62987e-05	0.00575717	synonymous-codon	HERC4	GRCh38.p7	10:67932768	ATCCACATAAGCATC[A/G]ACAAACTCTTGCCTA	26091
rs771002928	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67989660	AGGCCAGGAAATAGA[C/G]ATAAAATCTAGACAA	26091
rs771003134	snp	C/T	1.65157e-05	0.0028736	missense, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68072895	TACCTGGTTTCTTTC[C/T]GGATTTTTCATGACC	26091
rs771010638	snp	C/T	1.64795e-05	0.00287045	missense	HERC4	GRCh38.p7	10:67936183	ACAGCTGTGTCTGCA[C/T]CATTTAGAACCAGCT	26091
rs771021344	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67948870	AGGTTGCAGTGAGCC[A/G]AGACTGTGCCACTGC	26091
rs771044889	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68026220	CCCACCTCAGCCTCC[A/T]AAGTAGCTGGGAGTG	26091
rs771082646	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68007135	TTTGAAGCTATTTTC[C/T]AGATCCTGTGGGAGT	26091
rs771099324	snp	C/T	0.000108395	0.0073611	intron-variant, synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:68039437	TCTGCCATAAGAGAG[C/T]CCGGAGCAAATTCTG	26091
rs771117837	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67929917	CTCCTAGGTTCAAGC[A/G]ATTCTCCTGCCTCAG	26091
rs771160657	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67985058	ATGTTAATGTTAGAA[C/T]AAAAATAATATATTC	26091
rs771169898	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68035813	TTCATTTCAACTCTC[C/T]CCCAGCAGGAGCCTT	26091
rs771174512	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68019938	CCAAGGAATTCAAAG[A/G]GCTGATGCCTTTCTC	26091
rs771177168	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67927969	GGGGAGACAGGATAC[C/G]TGTGCAGGAGAGAGG	26091
rs771191016	snp	A/G	2.36326e-05	0.0034374	intron-variant	HERC4	GRCh38.p7	10:67966847	TTTAACCAGTACTCA[A/G]GACAGACAAATTTTT	26091
rs771200673	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68000809	ATTGACAGCAAACCA[C/T]CAGAAACTAGGAAAG	26091
rs771224316	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68030927	ATGCAGTTTTCCTAA[A/G]GTAGGTTTTGTACAG	26091
rs771233790	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68022126	TGGTGGAAAGACATT[-/A]AGAGACAAATAAATG	26091
rs771263348	snp	C/T	1.68781e-05	0.00290495	intron-variant	HERC4	GRCh38.p7	10:67992157	CTGGTGCTGGGATTA[C/T]AGGCATGAGCCACTG	26091
rs771282161	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67944835	ATCAGTGTCTGTCAA[C/T]AGTGGAACTGACCAA	26091
rs771300741	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67980250	ATGATTCTCCTGTCT[C/T]AGCCTCCCAAGTAGC	26091
rs771300990	snp	A/C	1.64817e-05	0.00287064	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:67992295	TTTGTCGGATTGGGA[A/C]ATCTGAAGTCATCTG	26091
rs771310028	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68044973	GATTTTAACAATAAG[A/G]TCATAACTGACACAT	26091
rs771321352	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67946674	AACACTTTGGGAGGC[C/T]GAGGTGGGCGGATCA	26091
rs771334891	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67981418	AAAGAGAGAAATAGA[A/C]CTCAGTACAGTAATA	26091
rs771380586	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67995133	CTGTTCTGTAAATTG[A/G]TGGTTGAATCTAGAC	26091
rs771395351	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67996440	GAAGCAAAACAGTGA[C/T]AGAGCTACAACTGTG	26091
rs771422643	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67960391	ATTAAAAGCCTAAAA[-/T]TTTTTTTTTTTGAGA	26091
rs771457069	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67974775	GAAAGAGAACAAACA[C/G]ATATATAACACCATT	26091
rs771457096	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67974769	AATAGAGAAAGAGAA[C/T]AAACACATATATAAC	26091
rs771468416	snp	A/G			utr-variant-3-prime	HERC4	GRCh38.p7	10:67922703	TTCATAATACTTGCT[A/G]TGTTTATTAGAAGAT	26091
rs771483273	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68009321	TGAGAGTTAATGTGG[C/T]CCCAGCTGGTCCCAA	26091
rs771527533	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68073255	TGCTCTTTCAAGTGC[C/T]AGGCTACAATAATTG	26091
rs771550154	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68050857	AATGAAGAGAAATAA[A/G]TGAATCCAGCAAAAC	26091
rs771558684	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68015042	AATATGACTATTACA[G/T]TTGTTCCCAGCAAGA	26091
rs771566868	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68008334	AAGCCCAAGGGCTCT[G/T]TAGTCAGCAAGTGAT	26091
rs771623243	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68028767	ATAGTTTTAGATCTA[C/T]CTCTTTTCTCTTAAG	26091
rs771635499	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67995008	AATTTCCTTTTAATC[A/G]CTACTCGAAAAAGTT	26091
rs771640859	in-del	-/T			intron-variant, downstream-variant-500B	HERC4	GRCh38.p7	10:67966624	CCAAGCAATTGTTTC[-/T]TTTTTTTATTAGATA	26091
rs771644923	in-del	-/G			intron-variant	HERC4	GRCh38.p7	10:67981698	ATGGTGGTTCACACC[-/G]GGTAATCCCAGCACT	26091
rs771646617	snp	C/T			intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010296	GTGCAATGAGGGCTC[C/T]CATAGCCTGGGGTAC	26091
rs771646915	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68067791	TCTTTAAAAAGAGTT[C/T]AACATAAACCACAAT	26091
rs771652083	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67970684	GAGAAGACCCAAATG[C/T]TGGAGCTAGGAAACA	26091
rs771666541	in-del	-/AT			intron-variant	HERC4	GRCh38.p7	10:68057109	TCAAACATCCATGTA[-/AT]ATATATATATATTTG	26091
rs771669668	snp	A/T	1.66601e-05	0.00288614	intron-variant	HERC4	GRCh38.p7	10:67954573	TATACACAGAAGTAA[A/T]TTAGATGGTTGGACA	26091
rs771709146	snp	A/G			upstream-variant-2KB	HERC4	GRCh38.p7	10:68075855	TGTACAGTGTTGGCT[A/G]CCATCACTTTCTACA	26091
rs771712769	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68044780	TTGTGGTAAACCACA[A/G]ATAAATATATCATAG	26091
rs771727209	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67979123	CCAGGAAAACATGAC[C/T]TCACCAAATGAACAA	26091
rs771730432	in-del	-/AGA	1.64754e-05	0.00287009	cds-indel	HERC4	GRCh38.p7	10:67932670	TTAGGCTGAAAGAGC[-/AGA]AGGACTTTTCCTCCA	26091
rs771733743	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67975487	CCTAAGTAGCTGGGA[C/T]TACAGGTGCCCACCA	26091
rs771800131	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67946045	ATCACTTGAGCCCAG[C/G]AATTTGAGACCAGCC	26091
rs771808585	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68023466	ACCAAAAGACAAACA[C/T]TGTAAGAGTCTACCT	26091
rs771839142	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68006344	AGGTCTGCTGTTGAT[G/T]AAACGCCTCAGCGTT	26091
rs771848001	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67953754	TAGAATCCTTTCCTA[C/T]GAATTGCACTACTAA	26091
rs771867953	snp	A/C	1.66333e-05	0.00288381	synonymous-codon	HERC4	GRCh38.p7	10:67954736	TTCTCCAACAAATAT[A/C]ACCTAAAATAGCACA	26091
rs771896969	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68038980	GTCATGTTACTGTTT[C/T]TCCTGAATGAATGTT	26091
rs771897154	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68052178	CAAAACCTGAAAAGA[C/T]AAAGTGCTAGACAGA	26091
rs771957306	in-del	-/C			intron-variant	HERC4	GRCh38.p7	10:68002183	TAATTATAAAAAAAA[-/C]CATCAAGTTTATTTA	26091
rs771974088	snp	A/T	1.7468e-05	0.00295528	intron-variant	HERC4	GRCh38.p7	10:68013989	TTTAACAAGAACTTC[A/T]ATATATGAAGGAAAG	26091
rs771986691	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68037739	AAGTCTAATCGAAGG[C/T]GTATAAGACCTGTCC	26091
rs772038340	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67950744	TCTTCAACATATATA[C/T]AGCTCTAAATATAGA	26091
rs772043043	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67993027	AAGCTACAAAAGATA[A/G]CTAGAAGGAAATAAA	26091
rs772049554	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67987636	CCTGTTTCCCTAGGA[A/G]ATACATGGCTATGAT	26091
rs772049746	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68004552	TATTCCATTTGTACA[C/T]GCTTTTTGTATACAG	26091
rs772064040	snp	C/T	1.69954e-05	0.00291503	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:68014127	CCCAGCTGCCCATTA[C/T]CACCAAGCCCAAAAG	26091
rs772071050	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68048602	TGTCATTATACATCT[C/G]TTAAAATCCATTTAA	26091
rs772077832	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67952438	ACAGGCATGTACCAC[A/C]ACGCCCAGCTAATTT	26091
rs772098391	snp	C/T	6.30497e-05	0.00561435	intron-variant, downstream-variant-500B	HERC4	GRCh38.p7	10:67966640	TTTTTTTATTAGATA[C/T]ATATACATAAAAATG	26091
rs772133982	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67934474	TCCTTCAGAAAGAAT[C/G]TTTGCTTGTTTGAAT	26091
rs772137622	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68003163	ACTATATTTTTATAC[C/T]TTTTTTTTTTTGAGA	26091
rs772180623	snp	A/C			utr-variant-3-prime	HERC4	GRCh38.p7	10:67922138	ATAATTTTGAAAGCT[A/C]TAACCCAGTGATTGG	26091
rs772181495	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67998922	TTTTTATATTTTTAG[C/T]AGAAACGGGGTTTCA	26091
rs772188741	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68020134	CATTTTTATACCTCA[C/G]GGTGACTCCTGACAC	26091
rs772219083	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68018302	CATTTCAATAAATAC[A/G]GAAAAAACAACATTA	26091
rs772271979	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67996313	AAGACCTTGAAATAG[-/A]CACCCCCCCTGCCCC	26091
rs772282803	snp	A/C			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012566	ACATAAACATTTATC[A/C]ATTAGGTTTGTTGTC	26091
rs772283734	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68008105	GGATTACTAGGCAGA[A/G]TCTCTTGTTCTTCTC	26091
rs772288645	snp	C/T	1.6643e-05	0.00288465	intron-variant	HERC4	GRCh38.p7	10:67939670	CTGCAAAATAATATA[C/T]ATGTTTCTGAGAGGA	26091
rs772297323	snp	A/C	3.30017e-05	0.00406199	synonymous-codon, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:68044556	GGCATCCAGGGCAAC[A/C]ACCTGCTCTACAGAA	26091
rs772299476	snp	A/C/G	0.000399068	0.0141203	intron-variant	HERC4	GRCh38.p7	10:67992184	ACTGTGCCTGGCCCA[A/C/G]AATGCTTTTCTTACT	26091
rs772305196	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68034388	CTAGAAGAACATTCA[A/G]TATTAGTACACTTTA	26091
rs772330836	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68047679	CAATTTAAAACAACA[A/T]ACCACTACACACCTA	26091
rs772352568	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68043730	CTGAGGCAGGTGAAT[C/T]GCTTGAAACCAGGAG	26091
rs772373779	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67963472	TCTGCCCACCTCGGC[C/G]TCCCAAAGTGCTGGG	26091
rs772375210	snp	C/T	1.68545e-05	0.00290292	intron-variant	HERC4	GRCh38.p7	10:67956862	AAAAAAAAAACCCTC[C/T]CAAATAATATTTTAC	26091
rs772390297	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67996478	TTTTGTTTAACATGG[A/C]AAATGAGTAGTTTTG	26091
rs772444059	in-del	-/T	0.000230747	0.0107387	intron-variant	HERC4	GRCh38.p7	10:68039504	TTCAGCAAATCAAAG[-/T]TTTGAGCAGGAAAAA	26091
rs772446019	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68056995	GAAAAGGAGTTGTTT[C/T]TGCATTTTGTTTTGA	26091
rs772477391	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68067043	TTCAGATTCAACTTA[C/T]AGCTGTTCACCAGTC	26091
rs772482803	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67971969	CTGTAATCTCAGCAC[C/T]TTGGGAGGCTGAGGC	26091
rs772535133	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68007056	TTAGCTCTTTAAATA[A/G]ACTTTCTATCCCTCT	26091
rs772543125	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67962375	TTTACTACTACATGT[A/G]AGTAGATATAGATGT	26091
rs772552321	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67935495	CAGAAAAGGATCTTT[C/T]ACTATACGGTACCAA	26091
rs772569499	snp	C/G	1.65375e-05	0.0028755	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:68032829	AATATAAACTATTTT[C/G]TGAGATCTTAGTGAC	26091
rs772576805	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68006375	TTGTTTTTGTTTTTG[-/T]TTTTTTTTTTTTTTT	26091
rs772581075	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68050861	AAGAGAAATAAATGA[A/C]TCCAGCAAAACAAAC	26091
rs772598491	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68071774	TAAAAATCTATTTTA[C/T]GAATGTCACTATCAT	26091
rs772604811	in-del	-/G	6.63515e-05	0.00575946	intron-variant	HERC4	GRCh38.p7	10:67992351	ATAAGATTAGTCAGA[-/G]GGAAGAGATATTATA	26091
rs772607589	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68015121	TTGCTTTGGCCAGCA[A/G]AAACAACAGTGTCTC	26091
rs772651653	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67955867	ATGGTATGTGCTCAC[A/G]AACCAAGGATTTGAC	26091
rs772653262	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67986333	CACTGTCTTATGAAT[A/G]TATAATAACTTACAT	26091
rs772670203	snp	C/G	2.08045e-05	0.00322519	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:68014175	GAAGGAACAAAAGCA[C/G]AAGTGTGCTGCCTAG	26091
rs772730676	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67983344	ACAATAGAGCTACCA[C/G]ATGATCTAGCAATCC	26091
rs772838033	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67965419	TATAACAGATTCTCA[C/T]TGTTTGTTGAATAAG	26091
rs772840921	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68031578	GTATAATAATCCTTC[C/T]TTACTAAAAGGCAAG	26091
rs772844602	snp	A/T	1.73733e-05	0.00294726	intron-variant	HERC4	GRCh38.p7	10:68044353	ACAATTTAGATTAAC[A/T]AATTTATTTTAAAAG	26091
rs772847954	snp	A/G	1.65222e-05	0.00287417	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67988790	TCCTTAAAAAGTTCT[A/G]CTATCTTGAGGAATA	26091
rs772878393	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68013957	TCGCAGAAATCTTCA[G/T]GATTTAAGAGCAACA	26091
rs772889912	snp	A/T	1.65707e-05	0.00287838	synonymous-codon	HERC4	GRCh38.p7	10:67923033	CAGAAGATTAAAACA[A/T]GTATGGGAAACTGGG	26091
rs772929457	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68066659	TCCAAGTTCCAAGGT[A/T]AGCCACCAAATCAAT	26091
rs772932461	snp	A/C	3.51179e-05	0.00419019	intron-variant	HERC4	GRCh38.p7	10:67988639	AATGGGGAAAGAGGA[A/C]AATAAAGGAATGATT	26091
rs772933815	snp	G/T	6.87853e-05	0.00586412	intron-variant	HERC4	GRCh38.p7	10:67939696	GAGGAAAAAATTATT[G/T]GATATTTTGACTATT	26091
rs772955980	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68056636	ACAGAGAAACTGAAA[G/T]ATACCTTGGAAAGAT	26091
rs772977435	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67963305	CATTGCAACCTCCAC[C/T]TCCCGGGTTCAAGCC	26091
rs773003809	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67960604	TGGTTAGGCTGGTTT[C/T]GAACTCCTGACCTCG	26091
rs773012819	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68014233	AATGTTACCTTCCAA[C/T]AATTTACAATGACAA	26091
rs773021301	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68065214	TTACCTATGCATGAT[G/T]GCATTATAGTTTTTA	26091
rs773030064	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67938389	GAGGTTGCAATGAGC[C/T]GAGATTGCACAACTG	26091
rs773055227	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68059147	TAAAAAAAGTTAATA[C/T]GTATTACTGTGTTTT	26091
rs773092175	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67975529	TAATTTTTTGTATTT[C/T]TGTAGAGATGGGATT	26091
rs773098351	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68021748	AGGAGGCAGAGGTTG[C/T]GGTGAGCCGAGATCA	26091
rs773118469	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67940076	GGGATTACAGGCGAC[C/T]GCCACCATGCCCGGC	26091
rs773127819	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67929795	GCCAGGATTAGAGGT[C/G]TGAGACACCACACCC	26091
rs773140804	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68073605	CAAAATTTAGCCAAC[A/T]GCAGAAACATAACCT	26091
rs773177887	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67947134	AATGGATTTAACAGA[-/T]ATTTATAGGACATTT	26091
rs773199849	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67969875	ATACCACAACAACCA[A/G]GAACCATTTCTGTTC	26091
rs773206624	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67953830	GCTAATAAATGAAAA[A/G]GAAATATTAGAGTAG	26091
rs773218099	snp	C/T			intron-variant, downstream-variant-500B	HERC4	GRCh38.p7	10:67966624	ACCAAGCAATTGTTT[C/T]TTTTTTTATTAGATA	26091
rs773237079	snp	A/C	1.65146e-05	0.0028735	intron-variant, missense	HERC4	GRCh38.p7	10:67940976	CTTTCAAATCATCCA[A/C]GGATGGCTTCTTTTT	26091
rs773237216	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68052183	CCTGAAAAGATAAAG[C/T]GCTAGACAGATGAAA	26091
rs773246576	snp	C/T			intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069782	GCACGGTGGCTCACG[C/T]CTGTAATCCCAGCAC	26091
rs773275844	snp	G/T	3.29881e-05	0.00406115	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:67990945	GTTGTATAAGTTTGT[G/T]GAATAAAAGCCTAGC	26091
rs773287184	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67971974	ATCTCAGCACTTTGG[A/G]AGGCTGAGGCAGGCA	26091
rs773298676	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67927853	ACAGCAGTGAACAAA[A/G]AGGCAAAAATTCTGC	26091
rs773311105	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67969036	ATACATTTAAAAGAA[A/T]CCAAAGTATACAACA	26091
rs773345558	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67928779	AATAAAAAAATCAGC[C/T]GGGAATAGTGGCATG	26091
rs773349202	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68003248	CAAGCTCCGCCTCCC[A/G]GGTTCATGCCATTCT	26091
rs773359752	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68047703	ACACCTATTAGAACG[G/T]CCACAAGACAAAACA	26091
rs773390965	snp	G/T	1.64762e-05	0.00287016	synonymous-codon	HERC4	GRCh38.p7	10:67932624	CTTCCAATCATAATT[G/T]GTATTTCCAATGACC	26091
rs773405085	in-del	-/AT			intron-variant	HERC4	GRCh38.p7	10:67941618	TTAAGATTTTATCTC[-/AT]TTTCTAATTACATGA	26091
rs773426774	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68018383	TACTTAGTCTGATAG[A/G]GGTTATCTATAAAAA	26091
rs773447663	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68046376	CATCAGCTATAAAGA[C/T]AGCAATGTAAAGTCA	26091
rs773487394	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67998217	ATATTTTTTTAAGAA[A/G]CCCCAAAAGTTCTCA	26091
rs773514616	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68034430	CTACACAGATGAACC[A/G]GTGAATCACATAACA	26091
rs773517904	in-del	-/TT			intron-variant	HERC4	GRCh38.p7	10:68018900	AAAACCCCACAAGGC[-/TT]TTTTTTTTTTTTTTT	26091
rs773533501	in-del	-/CAG			intron-variant	HERC4	GRCh38.p7	10:67976692	ACATCACCCCTCTCC[-/CAG]CAGCCCCTGGCAGAG	26091
rs773543337	in-del	-/AT			intron-variant	HERC4	GRCh38.p7	10:68007487	TGGTTTGGTGAGGTC[-/AT]GTTTTCCTGGATCGT	26091
rs773544800	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67953424	TGGTAATGTTGGTAC[C/T]GTTAGGCAGTAAATG	26091
rs773556241	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67995051	TCATTTGTCCTGTAC[A/G]ACTTTATGCAGACTG	26091
rs773557069	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68064970	GCAAGGCTCCATCTC[-/A]AAAAAAAAAAAAAAA	26091
rs773578515	in-del	-/AAG			intron-variant	HERC4	GRCh38.p7	10:68066010	ATCCAGGGGAACAGA[-/AAG]AAGGTCAACCATGAG	26091
rs773578780	snp	C/T	1.64909e-05	0.00287144	intron-variant	HERC4	GRCh38.p7	10:67991105	TTAAGACAATAAATT[C/T]GAAAATTTCAGCATA	26091
rs773598051	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67950314	CACAGTCTTGCTCTG[C/T]CCCCAGGCTGGAGTG	26091
rs773647110	in-del	-/TAAGGAC	5.14231e-05	0.0050704	intron-variant	HERC4	GRCh38.p7	10:68044370	TTTATTTTAAAAGAT[-/TAAGGAC]TGTTAAGGACCTCTT	26091
rs773670095	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67944750	TATCAGATAAATTTA[A/G]CAGAGTAAAATAAAA	26091
rs773677202	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68043872	TGTAAGACTAAAACA[C/T]TGATGAGGCACTGCT	26091
rs773678655	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67965383	CCACTGTATTTCCAA[C/T]ACCTAAATCAGTGCC	26091
rs773699091	in-del	-/T	1.66355e-05	0.002884	intron-variant	HERC4	GRCh38.p7	10:67932551	GGCAAGATTTCCATA[-/T]ATAAATCTTTCCATT	26091
rs773711575	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68003802	TACTGGCTATTATGA[A/G]TAGTGCTGCAATAAA	26091
rs773736842	in-del	-/A	0.000167535	0.00915093	intron-variant	HERC4	GRCh38.p7	10:67992375	TATTATATATAACTC[-/A]AAAACCAAGAAATTC	26091
rs773742189	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67938859	TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGG	26091
rs773755217	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68055839	TCATTGCAACCTCTG[C/G]CTCCTGGGTTCAAGC	26091
rs773761792	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67943564	AAAGGCGGAGGTATT[A/C]GAGTGGGGTTGAAAC	26091
rs773793086	snp	A/C			missense	HERC4	GRCh38.p7	10:67923054	GGAAACTGGGAGATA[A/C]TCCTCACCACCTCCT	26091
rs773806237	snp	G/T	3.30721e-05	0.00406632	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67988812	TGAGGAATAGTGGAG[G/T]TTCAAGTACTGACCA	26091
rs773860168	snp	A/G	1.68012e-05	0.00289833	intron-variant	HERC4	GRCh38.p7	10:67954783	GACTGTAAAGAAATG[A/G]AAGTACATTCTGGAG	26091
rs773866949	snp	C/T	1.65326e-05	0.00287507	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:68032818	TCTCCACAACAAATA[C/T]AAACTATTTTCTGAG	26091
rs773936246	in-del	-/AAA/AAAAAAA			intron-variant	HERC4	GRCh38.p7	10:68061879	AGCGAGACTCCATTT[-/AAA/AAAAAAA]AAAAAAAAAAAAAAA	26091
rs773979901	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67978260	GCGACAGGAGACTCC[A/G]TCTCCAAACACAAAC	26091
rs773981885	snp	G/T	1.64993e-05	0.00287218	intron-variant, missense	HERC4	GRCh38.p7	10:67941028	CAAAGGAAAATGGAG[G/T]TCCACAATGGTACAA	26091
rs773998868	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68063334	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGAGACTA	26091
rs774080178	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68031924	GCCCAGCTAACTTTC[A/G]TATTTTTAGAAGAGA	26091
rs774090979	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68042572	AGGCTGCAGTGAGCT[C/G]TGAGCATGCCACTGC	26091
rs774101479	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68017182	CTTGTGTATTTGTCT[C/T]CATCAGAAGAATACC	26091
rs774106162	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67966012	ACGCACCCACATTTA[C/T]ATTAAAAATCTGAAA	26091
rs774133157	snp	C/T	3.32458e-05	0.00407698	intron-variant	HERC4	GRCh38.p7	10:68044596	AGAAATATTGCATTC[C/T]AGTACAGAAATCAAG	26091
rs774135892	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67973853	GGGCAAGAGATCGAG[A/G]CCATTCAACATGGTG	26091
rs774154787	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67951543	TACCATTTGGAAAAC[C/T]GCTTGTATCCTAAAC	26091
rs774185411	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67929460	GTATGCAACCATTTG[A/C]AACTGGCTTCTTTCA	26091
rs774223535	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68000251	GCTCAGCAGGTTTGG[A/G]GTATTCCTATGGATT	26091
rs774233716	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67986657	CATCACGCCCAGCCC[A/G]TACTGTATAATGTAA	26091
rs774244585	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67947296	AGTTATTCCATGTAA[A/G]TAGTAACAAAAGAGA	26091
rs774284632	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67928651	CCTCGGGCCAGGAGC[A/G]GTGGCTCACACCTGT	26091
rs774330294	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68046438	AGTCAAAGATAGCAA[C/T]GTAAAGTCAAAGGTA	26091
rs774340574	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67936625	CATGACAACTGCTAC[C/T]CCAGGGTTCCTCTAT	26091
rs774341825	snp	G/T			intron-variant, downstream-variant-500B	HERC4	GRCh38.p7	10:67966199	GCCGAGGCTGGTCTT[G/T]AAATCCCGAGCTCAG	26091
rs774374274	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67949354	TCAGATTCTACCAAA[C/T]ATTTAAAGGAGAATT	26091
rs774423542	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67982940	CAAGACCAGCCTGGG[A/C]AACACGGTGAAACCC	26091
rs774434912	snp	A/G	1.66718e-05	0.00288715	intron-variant	HERC4	GRCh38.p7	10:67954915	GAAAATTTTAAACAT[A/G]GCTTCTGAATAAAAG	26091
rs774436729	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67961432	TTCTTTGCTCCCTAT[C/T]TGTCACCTTTCATAA	26091
rs774446595	snp	C/T	8.53898e-05	0.00653358	intron-variant	HERC4	GRCh38.p7	10:67992689	CTTCAGAATCTGTAA[C/T]AAAAATGTAAAAAAT	26091
rs774453477	snp	C/G	3.52827e-05	0.00420001	intron-variant	HERC4	GRCh38.p7	10:67991133	ATATTAAAGAATTGC[C/G]ACTTACCTAACAGCT	26091
rs774466860	in-del	-/CAC			cds-indel	HERC4	GRCh38.p7	10:67922866	CCTTGCTGAATTCAT[-/CAC]CACAAGAAAAACACA	26091
rs774472918	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68039356	AAGAAAAGAAAAAAC[A/G]GGGGATGGGGAGGTA	26091
rs774482278	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68060885	CAATTGTGGGAAGCA[A/G]TTTAAGATCTACTTT	26091
rs774500007	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68013725	GTAAATTTTATGTTG[C/T]GTATATTTTACCACA	26091
rs774511138	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67997934	TTGAGACAAAGTCTC[A/G]CTCTGTCGCCAGGCT	26091
rs774518986	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67996323	AATAGACACCCCCCC[-/T]GCCCCACAAGAAACA	26091
rs774522987	snp	C/G			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011055	AAACTCTTATTGTTG[C/G]TATTTTGACTTCCTC	26091
rs774554873	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67943570	GGAGGTATTAGAGTG[A/G]GGTTGAAACTAGGAT	26091
rs774555550	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67946987	AGCAAATATTATTAC[C/T]GCTAAAGAGAGAGAG	26091
rs774574081	snp	A/G	0.00021699	0.0104138	intron-variant, synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:68039440	GCCATAAGAGAGTCC[A/G]GAGCAAATTCTGACC	26091
rs774581312	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68032455	GTTTGATGCATATAT[A/C]ATGGCAAGCTTAATG	26091
rs774583547	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68047601	AGGAAGATAAACAAA[C/T]GGCAAGCAGGCATAC	26091
rs774603384	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68005798	AGCCTCAACCTCCTG[A/G]TCAAACAATCCTCCT	26091
rs774631780	snp	A/C	1.67758e-05	0.00289614	intron-variant	HERC4	GRCh38.p7	10:67992169	TTACAGGCATGAGCC[A/C]CTGTGCCTGGCCCAA	26091
rs774654454	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68053994	ATCATTTCAACTCTT[C/T]AGTACATGTTTAAAA	26091
rs774673244	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68046742	GAAGCCAAGGTGGGA[A/G]GATCACTTGAACCCA	26091
rs774693183	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68018136	ATAAGTAAGAGTCAA[C/T]AGAATATTCACAAAT	26091
rs774693219	snp	C/T	1.65116e-05	0.00287324	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:68025672	AAAGTAAACACTCCA[C/T]CTTCCTAAAAAAAGA	26091
rs774713139	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68006960	TTGAGGTAGTCTTAT[G/T]TGGGTTAAATCTGCT	26091
rs774757845	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67991218	AAAAATTTAAAAAAG[-/T]TTTTTTAATCATAGA	26091
rs774761545	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68045400	AAATTTTTTAAAGAT[A/C]TCATAAATAAAGCAT	26091
rs774772489	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67993400	GGCACATGTCTGTAG[C/T]CCCAGCTACTTGGGA	26091
rs774786919	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67955767	CAAGAGCGAAACTCC[A/G]TCTCAAAAATAAAAA	26091
rs774791649	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67965838	GTATACACAAATGGC[-/T]TAGCAAATAAGAGTA	26091
rs774801881	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67978225	AGGAGCTGAGATTGC[C/G]TCACTGCACTCCAGC	26091
rs774813610	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68028753	AGGTTTTAATTCCTA[C/T]AGTTTTAGATCTATC	26091
rs774813765	snp	C/G	1.65072e-05	0.00287286	intron-variant, missense	HERC4	GRCh38.p7	10:67941064	AATTGCTAAGCCACA[C/G]ATAACACCAATCAAA	26091
rs774826210	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67942993	ATACATATGTGCTCA[A/T]GAAATATCTCTCCAG	26091
rs774827747	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68020827	GAAATAAAAAATACA[C/T]TAGAGAGATTTGAAG	26091
rs774829979	snp	A/G	1.64863e-05	0.00287104	synonymous-codon	HERC4	GRCh38.p7	10:67955017	AAGGACTTCCATTGC[A/G]TCTCCTACAATATTT	26091
rs774853765	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67934455	AAATCGACACAGTTA[C/T]TGATCCTTCAGAAAG	26091
rs774858406	in-del	-/AA	1.67273e-05	0.00289195	intron-variant	HERC4	GRCh38.p7	10:67988863	AGTGAACATGCAAAT[-/AA]AATGAATTTTTTAAA	26091
rs774896473	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67971604	TAATAAACACTCTCA[A/G]CAAATGAGAAATGGA	26091
rs774984161	snp	C/T	1.6577e-05	0.00287893	stop-gained	HERC4	GRCh38.p7	10:67925131	TTCGTGAAATACTTC[C/T]CAAAAAATTTTTATC	26091
rs775032319	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67967114	CCACCTTGGCCTCCC[A/C]AAGTGTTGGGATTAC	26091
rs775035538	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67941900	ACCTCAGGTGATCTG[C/T]TCACGTCAGCCTCCC	26091
rs775085684	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68000897	TTCTAGTCTGCAGAA[G/T]AGTGAGCCAATAAAT	26091
rs775093689	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67977273	GACTGCTTTCCAGAC[A/T]GTAGCTCCTGAACAA	26091
rs775115154	in-del	-/TTGTTCTAAAATGGAATA			intron-variant	HERC4	GRCh38.p7	10:67955932	GTTCTCCCTGAGTTC[-/TTGTTCTAAAATGGAATA]TCCCATGGTAAAATC	26091
rs775143416	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68025515	CAACTGCAGTTTAGA[A/G]ACCAAAATGCTCTTT	26091
rs775145436	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68042501	AGTGGTGCACGCCTA[C/T]AGTCGCACCTACTAG	26091
rs775154829	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68006448	GCGATCTCAGCTCAC[C/T]GCAACCTCCACCTCC	26091
rs775162348	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67941935	TGCTGGGATTACAGG[C/T]GTGAGCCACCGTGCC	26091
rs775189627	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67989963	GGGTGACAGTTTTTA[A/T]CTTTCCTAATACTGT	26091
rs775208137	snp	C/G	1.65715e-05	0.00287845	intron-variant	HERC4	GRCh38.p7	10:67954585	TAATTTAGATGGTTG[C/G]ACATTTTACCTTATC	26091
rs775231001	snp	A/G			missense, nc-transcript-variant	HERC4	GRCh38.p7	10:67991185	CCAGAGGAAGAAAAC[A/G]TTCCATCTATCTCAC	26091
rs775254394	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68049118	CACTATATACAATAG[C/T]AAAACACTGGAAATT	26091
rs775312751	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67935009	GCATCTGGATGTCAC[A/G]CATCATTCTGAGGAT	26091
rs775351605	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68035213	GTTGGAGTGCAGTGG[C/T]GCAATCTTCACTCAT	26091
rs775353453	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68051352	ACTATTTTTTTTTTT[-/T]TTTTTTTTTTGAGAC	26091
rs775367381	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68059969	ATTTTGTTTCTCTTG[C/T]TATTATAATAATTTG	26091
rs775370771	in-del	-/CT			intron-variant	HERC4	GRCh38.p7	10:68008158	GAAGTTTCCCTCTCA[-/CT]CTCTCTCTCTGTGCT	26091
rs775381176	snp	A/G	1.74659e-05	0.0029551	intron-variant	HERC4	GRCh38.p7	10:68013990	TTAACAAGAACTTCA[A/G]TATATGAAGGAAAGC	26091
rs775381203	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67951054	ACCAAAGAGTAGAGC[C/T]GGCTCCAAGGGGCTC	26091
rs775441031	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67927154	TAGCATGGAATTTAT[A/G]GAATTTATTCAACTG	26091
rs775471104	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67949744	TAAAAAAGCATCACA[G/T]AGCTGGGCGCGGTGG	26091
rs775473364	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67965179	GCCCTGATCTTAAAG[A/G]GCTGCTCCTTGTCAT	26091
rs775494070	in-del	-/ATAAAA			intron-variant	HERC4	GRCh38.p7	10:67984546	TGGGATGGCTAATAG[-/ATAAAA]ATAAAAATATTAAAA	26091
rs775504541	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67946898	GGTGACAAGGCGAGA[C/T]TCTGTCTCAAAACAA	26091
rs775559309	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67963700	TTCTGAATCCTTTCA[A/G]AAACACTGCTAAAAG	26091
rs775570600	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67974964	GGGAGGCTGAGGTGG[C/T]TGGATCATGAGGTCA	26091
rs775579341	snp	C/T	4.12244e-05	0.00453988	intron-variant, downstream-variant-500B	HERC4	GRCh38.p7	10:67966642	TTTTTATTAGATACA[C/T]ATACATAAAAATGAA	26091
rs775597253	in-del	-/AG			intron-variant	HERC4	GRCh38.p7	10:67945827	CAAAAAACATACGAC[-/AG]ATACACGAAAAATAA	26091
rs775646105	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67976429	ATATATATTTTTGTT[A/T]ATCTTACTTAAAATT	26091
rs775646814	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67996637	TTATTTGAAGATGAG[C/G]AATATTGAGTGCATT	26091
rs775684450	snp	A/G	1.65679e-05	0.00287814	synonymous-codon	HERC4	GRCh38.p7	10:67956890	TACCTGCATCTGTAA[A/G]ACTGCATCGGTCTGT	26091
rs775715781	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68052418	AAATGATCAACCTAA[C/T]GAAAATTTTCATTTC	26091
rs775756895	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67968106	AAACAGGAATGGACA[A/C]AAGTAGAGGATAGAG	26091
rs775779451	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67933046	TCATTTCCTAATGGG[C/T]AGAATGATGCAAATG	26091
rs775789996	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68058968	CTCTACACCAACAGT[C/T]ACCAATGTTATTACT	26091
rs775803687	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68068194	TTCTCTAACAAACAT[A/T]AAAAAATTGGCCAGG	26091
rs775814517	snp	A/T			intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069507	GTGTGGTCCCTAAAA[A/T]GTCCAGAACAGAAAC	26091
rs775820354	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68032346	TTGGCCTATGAATAA[C/G]AGAGAAATTCATCTC	26091
rs775826526	snp	C/G	1.65329e-05	0.0028751	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67990322	ATTCTGGTAGAGTAA[C/G]ATAAAACCTCAATGC	26091
rs775842070	in-del	-/TATT			intron-variant	HERC4	GRCh38.p7	10:67934382	ATTCAAAATACTAGA[-/TATT]TATTTCTCTCCTTGA	26091
rs775847783	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68016456	CTCCCGGATTCAAGC[A/G]AGTCTCCTGCCTCAG	26091
rs775865796	in-del	-/T			intron-variant, utr-variant-5-prime	HERC4	GRCh38.p7	10:68067132	CCCCTAAGATGAGGA[-/T]AATTCTTGCAAATTG	26091
rs775877895	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68057422	CAAGGTCAGGAGTTC[A/G]AGAGCAGCCTGGCCA	26091
rs775889856	snp	A/C	1.64969e-05	0.00287196	intron-variant	HERC4	GRCh38.p7	10:67932590	TCAGAGATTAGTTTT[A/C]CCCTACCTTTTCCAG	26091
rs775900109	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68046696	GATAGTCCAGGCGAG[A/G]TAGCTCACATCTATA	26091
rs775900750	in-del	-/TG			intron-variant	HERC4	GRCh38.p7	10:67924486	AATTCTGTAGGTAAC[-/TG]TAACATAACAGTAGG	26091
rs775924467	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67928487	TGTCTTTTGCTGGGT[A/G]GGAGAGGGGACATGC	26091
rs775926774	snp	C/T	1.65337e-05	0.00287517	intron-variant	HERC4	GRCh38.p7	10:68025698	AAAGACAAAACCCCT[C/T]ATCATTAGAAGGCAT	26091
rs775936231	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67930504	GCCACTGTTTCCAAA[A/G]TGACTATACCACTTT	26091
rs775942313	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67995115	AACATTTGGCTTGGT[C/T]TTCTGTTCTGTAAAT	26091
rs775974780	in-del	-/AT	1.65924e-05	0.00288027	intron-variant	HERC4	GRCh38.p7	10:67939665	TGCTTCTGCAAAATA[-/AT]ATATATGTTTCTGAG	26091
rs775984496	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67947979	CAGGCATGAGCCACC[A/G]TGCCCAGTCTAAACA	26091
rs775997856	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68039579	ATTTAGTGAAGTTAT[A/G]CTCTTAACTACAAAA	26091
rs776024681	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68004715	ATCATGGCAGAAGGC[A/G]AAGAGGAAGCAAAGC	26091
rs776034951	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67985029	TGATATGATATATAC[A/G]TTTTTGAAAAGAAAT	26091
rs776113794	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68031383	AATAACGAAAAAGGA[C/T]GAGTAAAATTTAAGA	26091
rs776125256	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67981723	AGCACTTTGGGAGGC[C/T]AAGGCGGGTGGATTA	26091
rs776181199	in-del	-/G	1.76918e-05	0.00297415	intron-variant	HERC4	GRCh38.p7	10:67988627	TCTGTTAATAGGAAT[-/G]GGGAAAGAGGAAAAT	26091
rs776205216	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67959713	AAAATAGAAAGTACA[A/G]GACAGGGAAAAAGGG	26091
rs776224418	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67987968	TAGGTTAGAAACATA[C/T]GCTTCTCCCTTAGGT	26091
rs776230077	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67930671	TATAAATGCATAAAT[C/T]AGAGGATGGTATATT	26091
rs776233282	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68016232	ATTATACTACTGGAA[G/T]GTAAACCTTTTTCTT	26091
rs776239778	snp	A/G	1.76558e-05	0.00297113	intron-variant	HERC4	GRCh38.p7	10:67988630	GTTAATAGGAATGGG[A/G]AAAGAGGAAAATAAA	26091
rs776255290	snp	A/C	3.34739e-05	0.00409095	intron-variant	HERC4	GRCh38.p7	10:67954764	ACAATGCAAACACCA[A/C]ATAGACTGTAAAGAA	26091
rs776258768	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67962959	CACAGGGATCATATA[A/G]ATTAATCTTCTCAAA	26091
rs776259612	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67952942	TAAATTGCACAAATA[A/G]TATAAAGAACTCCCA	26091
rs776288835	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68062891	AACTATGAGTGAATA[G/T]ATATTCACCAAATTA	26091
rs776312303	snp	C/T	3.50281e-05	0.00418483	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:67966701	TCCATAGGCCTGCTG[C/T]TGGACCCAGTTGATA	26091
rs776323034	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68015237	AACCAAGGTTAGCAG[C/T]TAAAGGATGATCTAC	26091
rs776359963	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68052366	TTTGCTTCTTAAAGA[A/C]AGACTTTCATTTTTA	26091
rs776400981	snp	C/T	3.45465e-05	0.00415597	intron-variant	HERC4	GRCh38.p7	10:68014011	GAAGGAAAGCTTTAA[C/T]ATGACAGAACTTACC	26091
rs776403228	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67983576	CAAGGTCAGGAGATA[A/G]AGACCATCCTGGCTA	26091
rs776434596	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68038754	TTACTCAATTCACAG[C/T]TATAACAATCATTAC	26091
rs776449592	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68068107	AATCCCAGCAATTTG[A/G]GGAAGCCAGGACAGG	26091
rs776453619	in-del	-/AAAG			intron-variant	HERC4	GRCh38.p7	10:68064259	CATAAAAAATAATTA[-/AAAG]AAAGAAATAGGCCGG	26091
rs776510872	snp	C/G			intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010072	AAACTCCCCTGCCCC[C/G]ACCCTTTGTGTTCCC	26091
rs776515342	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67963562	TAGAGTTCTTTTAAG[A/T]GCTAAACACCAAGAG	26091
rs776526166	snp	A/G	2.75433e-05	0.00371091	synonymous-codon, nc-transcript-variant	HERC4	GRCh38.p7	10:67992630	AGAGTAATGTGAAAA[A/G]CTTTGATCTCCCCCT	26091
rs776561693	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68061027	TCTTTAGGACCGCTT[C/T]TAGCCTCACCTCTTT	26091
rs776585698	in-del	-/AA			intron-variant	HERC4	GRCh38.p7	10:67923374	AAGGAAGTGCTTAAT[-/AA]ATGTTTGATAAGTGA	26091
rs776588144	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68025202	TACTCCAGACTGGGT[A/G]ACAGAGCAAGACTCT	26091
rs776611121	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67961704	TGTAGTTGACTGAGT[C/T]CCCACGTGTCACCAG	26091
rs776620920	snp	C/T	9.62325e-05	0.00693592	intron-variant	HERC4	GRCh38.p7	10:68039506	TCAGCAAATCAAAGT[C/T]TGAGCAGGAAAAAGG	26091
rs776630618	in-del	-/A	0.00416015	0.0454177	intron-variant	HERC4	GRCh38.p7	10:68070607	GCGAAACTCTGTCTC[-/A]AAAAAAAAAATAAAA	26091
rs776677439	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68020000	CTTTCATTTTTTCCT[C/T]GTTTCTTTGGGGAGC	26091
rs776690754	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67939366	ACTGTTTTCAGTGTT[A/C]TTCATCTGTAAACCA	26091
rs776710805	snp	A/G	9.99967e-05	0.00707024	intron-variant	HERC4	GRCh38.p7	10:67936238	TTTCAACTGTGATCT[A/G]TTAATTTAAATTTTT	26091
rs776723590	snp	A/G	1.66363e-05	0.00288407	intron-variant	HERC4	GRCh38.p7	10:67959090	TTTTACTCTAAACAT[A/G]AGCTTTATTACACCA	26091
rs776744027	snp	G/T			missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67990288	GTTGTGAAATTGTTG[G/T]AATCACTCATCAGGG	26091
rs776751227	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68070962	TAGGCTCAAAGTGCA[C/T]GGCACATCATGTCTA	26091
rs776755891	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68040616	AAAAGAAAGGCTGGG[C/T]GTGGTGGCTCAAGCC	26091
rs776765538	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68035950	GAATGACTATATCAC[A/G]AAGGCTAGTAAGTAG	26091
rs776768191	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67971870	GAGAATTACCAGAAC[C/T]AAGAATTTATCAAGA	26091
rs776772536	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68057353	TAAAAGTATAACTAA[C/T]GGTGGCTCATGCCTG	26091
rs776800231	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67966936	CTCAGCTCACTGCAA[C/G]CTCTGCCTCCCGGGT	26091
rs776818116	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67972683	ATAAAATTTTTAAAA[C/G]AATATGCAAGATCCT	26091
rs776821361	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68020149	GGGTGACTCCTGACA[C/T]AGATAAAACCTACAA	26091
rs776822434	snp	C/T	1.64906e-05	0.00287142	synonymous-codon	HERC4	GRCh38.p7	10:67932597	TTAGTTTTCCCCTAC[C/T]TTTTCCAGTTCCTTC	26091
rs776824148	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67986530	GCTAATTTTTTTTTG[G/T]ATTTTTAGTGGAGAC	26091
rs776844820	in-del	-/CA	1.67304e-05	0.00289222	intron-variant	HERC4	GRCh38.p7	10:68025506	ATCCCTAAACAACTG[-/CA]GTTTAGAGACCAAAA	26091
rs776860789	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68007230	TTTCTTCTGCTTGAT[C/T]AATTCTGCTGTTGAG	26091
rs776915046	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67946722	GACCATCCTGGCCAA[C/T]ATGGTGAAACCTCAT	26091
rs776936233	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68072022	CCTAATTAATAAACT[A/G]ATAAAATAACTGCCA	26091
rs776992115	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67981633	ACACACCATATGTTA[C/T]GTCATAAAACAAGTC	26091
rs777009104	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67960364	TCTCAGATGGAACTT[G/T]CTATTTGTCACTATT	26091
rs777069308	snp	C/T	8.23744e-05	0.0064172	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68034116	CAGCTGCGGTGAAGT[C/T]TGCTTTTTACAGTCA	26091
rs777070253	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68029061	CGCCCGTAGCTCCAG[C/T]TACTCAGGAGACTGA	26091
rs777090357	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67940894	CCTTCCCCACTTTTT[-/A]ACCTCCCAAACCCTA	26091
rs777094319	snp	A/G			intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069818	GAGGCCAAGGCGGGC[A/G]GATCACAAGGTCAGG	26091
rs777101907	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67931409	TAACTGCATTTCATG[A/G]TGGTTTTCCTAAGAC	26091
rs777107806	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68066866	GTATCAGAATGTAAG[C/G]ATCTTGGTAAAATAA	26091
rs777124292	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68042420	CCTTGAGTCCAGGAA[C/T]TTAAGACCAGCTGGG	26091
rs777143685	in-del	-/AAAT			intron-variant	HERC4	GRCh38.p7	10:67926413	AATAAAAAAAATAAA[-/AAAT]AAAAAAAAAAAAAAA	26091
rs777246502	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68030581	ATTCCACAGCATAAA[C/T]ACCTCATTCTGTTTT	26091
rs777247282	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68043807	GGCAACAGTGCGAGA[C/T]TCTGTCTCAAAAACA	26091
rs777251174	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67995142	AAATTGGTGGTTGAA[A/T]CTAGACAGGTTTCAA	26091
rs777274740	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67996385	CCACCTTTCACTGTC[G/T]TTGAGCTATTCACAA	26091
rs777284248	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67982425	AACTGAATATCTGTA[C/T]GAAGAAGAATCAAAC	26091
rs777340772	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67993915	TATTATTTGTGACCA[C/T]GGCTGCTATAGAATT	26091
rs777342706	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68008346	TCTTTAGTCAGCAAG[C/T]GATAAATCCTGTCAG	26091
rs777358311	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68046138	ACACTGTTCCAAAAA[A/G]AAAAAAGAAAAAATA	26091
rs777379642	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67997201	AAAGTTAACTCAATT[C/T]AGAAGGACCTGCTCC	26091
rs777399825	snp	C/T	1.6534e-05	0.00287519	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:68032789	ATACCTTGGTTAGAG[C/T]AGCAGTATGATCTTC	26091
rs777411422	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:67996823	CTAAAAATAAAAAAA[-/T]AAAATAAAATAAAAA	26091
rs777430886	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68040247	TTGTAACACACATTA[A/C]ATGCTAATATCTTTT	26091
rs777445719	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68044814	ATAATCAACTCAGAA[A/T]ATCAAGTGACCTGAA	26091
rs777457810	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68019366	TAGAAGAAGTTATTA[A/T]GGTGTCTATATAGTG	26091
rs777467860	snp	A/G	1.76089e-05	0.00296718	intron-variant	HERC4	GRCh38.p7	10:67956842	AAACATCAAAGAAAC[A/G]ATTAAAAAAAAAAAC	26091
rs777471744	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68058430	ATAGTTTCCCTACAG[A/G]ACAATATACAGTCAT	26091
rs777490186	in-del	-/TTTTT	2.27177e-05	0.00337021	intron-variant, downstream-variant-500B	HERC4	GRCh38.p7	10:67966625	CCAAGCAATTGTTTC[-/TTTTT]TTATTAGATACATAT	26091
rs777492030	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67947470	AAGGCAAAAGCTGAC[A/G]GAATCAAAGCGAGGT	26091
rs777508486	snp	C/T	3.3264e-05	0.0040781	intron-variant	HERC4	GRCh38.p7	10:67932551	GGCAAGATTTCCATA[C/T]ATAAATCTTTCCATT	26091
rs777509218	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68016737	TCCTGTTTAGGTTAA[A/G]TCCTTAGATCTCACT	26091
rs777511292	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67956089	ACAGAATAAAAATGG[C/T]TACCAAGATTTGAAG	26091
rs777548615	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68017493	TAAGTTTATTTATTT[A/G]TTTTTTTGAGACAGA	26091
rs777579990	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67946552	AAGACAAAAACTATA[G/T]AAGAAGACAAAGAAG	26091
rs777594165	snp	C/T	3.4246e-05	0.00413785	intron-variant	HERC4	GRCh38.p7	10:67957015	TAGTACAAGTTGATT[C/T]GTGATATACTTACTG	26091
rs777599181	snp	A/C/G	3.40236e-05	0.00412442	intron-variant	HERC4	GRCh38.p7	10:68033957	AACTATACATAATGA[A/C/G]AACCTACCATTTTCA	26091
rs777600974	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67955335	TGTTTTTATACTAAT[A/G]TATAATGTATAACTC	26091
rs777645010	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68043325	ACAGTTTTTTAAAAA[A/T]CTTAAATTTAAAATC	26091
rs777666162	in-del	-/CTTT			intron-variant	HERC4	GRCh38.p7	10:67951862	TGGCACTATCTTATG[-/CTTT]CTTTCTCTACCACTA	26091
rs777679405	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67951961	TCTCAGTTTCTGGAC[C/G]TGTCTGTTTCCAACA	26091
rs777688991	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67969001	GATAGACCAAATCCT[A/G]GACCATACAATAAGT	26091
rs777721044	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67948718	CTGAGGTCAGGAGTT[C/T]AAGACCAGCCTGGCC	26091
rs777723498	snp	A/C	0.00137504	0.0261845	intron-variant	HERC4	GRCh38.p7	10:67990447	ATTTAAAATGAATAC[A/C]CTTTCAAAGAAAAAA	26091
rs777730217	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68049855	GGTCAGGGCTACAGT[A/G]AGCCGTGATTGTGCC	26091
rs777734518	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68051320	ACACACAGACAAAAC[A/T]TATGGCAAAATGTTA	26091
rs777748384	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67925780	GGGGAAACCAGTTGT[A/C]ATTTCATGAGGATAT	26091
rs777768570	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67986348	ATATAATAACTTACA[C/T]ATATTGTATTATTTA	26091
rs777774929	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68002396	AAATATATATGAAAA[A/G]AAGGACATTTTGGTT	26091
rs777793228	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67929713	AGAGACAGGGTTTTA[A/T]CATGTTGTCCAGGCT	26091
rs777831233	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68004668	ACTGACTCACAGTTC[A/C]GCATAGCTGGGGTGG	26091
rs777840919	snp	C/G	1.65217e-05	0.00287412	synonymous-codon, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67988732	TCTTCTTTCAGAAGG[C/G]GGAATACCGATCTTG	26091
rs777848065	snp	A/T	3.73587e-05	0.0043218	intron-variant	HERC4	GRCh38.p7	10:68072859	TTATTAAAAATAGCA[A/T]ATTTTAAAAACATTT	26091
rs777858629	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68000730	TGTCCTTATAAAAGG[C/G]GGAATTTGGATGCAG	26091
rs777870358	in-del	-/TT			utr-variant-3-prime	HERC4	GRCh38.p7	10:67922517	ATTTTATTACAAAAC[-/TT]AACATTATTTACAAA	26091
rs777909124	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68068871	TCTCTTTTAACCTCA[A/G]TGTCCTCATCTGTAA	26091
rs777920833	snp	C/T			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68012577	TATCAATTAGGTTTG[C/T]TGTCTTATATAGGTA	26091
rs777929941	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68022442	AGGCAGAGGTTGCAG[G/T]GAGCCAAGATCATGC	26091
rs777966921	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67950841	GTAGAACTACTGACT[A/C]TCCGGAAGCAAGAAG	26091
rs777981447	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68048446	TCCCAACTATATGAC[A/G]AGCTGGAAAAGACAA	26091
rs777987733	snp	C/T			synonymous-codon	HERC4	GRCh38.p7	10:67925125	TGGTAATTCGTGAAA[C/T]ACTTCCCAAAAAATT	26091
rs778025858	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68005923	TAGGCTGATCTCAAA[C/T]TCCTGGGCTCAAGCA	26091
rs778032310	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68013325	TTTGCTTTATTGCAC[C/T]ATTTGCTTCATTGCA	26091
rs778091404	snp	C/T	8.91246e-05	0.0066749	intron-variant	HERC4	GRCh38.p7	10:67966838	GACATTAAATTTAAC[C/T]AGTACTCAAGACAGA	26091
rs778109918	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68064008	AGCACTTTGGGAGGG[C/T]GAAGTGGGCAGATCA	26091
rs778124034	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68028405	TCATTATTTCTTCTC[A/G]ATATCCAGTGAAAGC	26091
rs778141344	snp	A/C	1.67002e-05	0.00288961	intron-variant	HERC4	GRCh38.p7	10:68025517	ACTGCAGTTTAGAGA[A/C]CAAAATGCTCTTTTA	26091
rs778142950	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67965143	TTTTACCAAATGTTC[A/G]TTGTTCTTGAAATTC	26091
rs778150283	snp	A/G/T	5.05619e-05	0.00502781	intron-variant	HERC4	GRCh38.p7	10:67992153	CTGCCTGGTGCTGGG[A/G/T]TTACAGGCATGAGCC	26091
rs778156892	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67960236	TTGTTACACATCTAT[A/G]CCAGGAAAGTAATTC	26091
rs778162660	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67937962	GCTGGGATTACAGAC[A/G]TGAGCCACTGTGCCC	26091
rs778173127	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67929180	ACTAGAAGTCCTAAT[A/T]ATTCTTAAAATCTTA	26091
rs778173357	snp	A/G			intron-variant, downstream-variant-500B	HERC4, POU5F1P5	GRCh38.p7	10:68009715	TTCTCTATACCAGGA[A/G]ATGCTGCATGATAGC	26091
rs778191040	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68071816	AAAATAAATTACAAA[G/T]TAAGGCAGAAGAAAA	26091
rs778199474	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68037220	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	26091
rs778277616	snp	C/G			missense, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68073089	AGCTGCCCAAAGGAT[C/G]CATTTCCCCAGCACA	26091
rs778310346	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68038659	TCTACCAACTCTCAA[A/G]TTATGAAACCTATTC	26091
rs778316302	in-del	-/G			intron-variant	HERC4	GRCh38.p7	10:67944345	TCCAAGACCAGGACA[-/G]GTACCTCTTAGTTTG	26091
rs778326091	snp	C/T	1.66344e-05	0.0028839	intron-variant	HERC4	GRCh38.p7	10:67959164	TGCAGAATATAACAA[C/T]AACGAGGAAAGAGCA	26091
rs778334721	snp	A/G	1.64798e-05	0.00287047	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:67992286	CAGATCTGCTTTGTC[A/G]GATTGGGACATCTGA	26091
rs778371832	snp	A/G	3.29554e-05	0.00405914	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:68044497	CCTTTGTCATTTAGC[A/G]CTAACGTATGAGCTT	26091
rs778377456	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68043624	GTTCGAGACCAGCCT[A/G]GCCAACATGGTGAAC	26091
rs778401673	in-del	-/GC			intron-variant	HERC4	GRCh38.p7	10:67923598	GAGTCTTGCTCAGTT[-/GC]GCCCAGGCTGGAGTG	26091
rs778405411	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67970423	GTGGTGAAACCCTGT[C/G]CCTACTGAAAATACA	26091
rs778448649	snp	C/T	1.64836e-05	0.0028708	missense	HERC4	GRCh38.p7	10:67932694	TTTCCTCCACAGACC[C/T]TATGAAAGCCCGCAT	26091
rs778456961	snp	C/T	3.29696e-05	0.00406001	missense, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68034019	GTCCCCATCCAAAGA[C/T]AGCTCCAGAAAGGGT	26091
rs778485266	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68058336	GCAGGAAGACAACTG[C/T]CTGTTGAATAAATGT	26091
rs778486288	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68044620	AATCAAGGAAAAAGA[C/T]ATTGCATTCTAGTTT	26091
rs778493872	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68021252	AATTCAGCAGCACAC[C/T]AAAAGGGTTACATAC	26091
rs778516639	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68008964	AGTGGTTCACTCCTG[C/T]AATCCCAGCACTTTA	26091
rs778529810	snp	C/T	0.000457352	0.0151151	intron-variant	HERC4	GRCh38.p7	10:67990451	AAAATGAATACACTT[C/T]CAAAGAAAAAAAAAA	26091
rs778536573	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67953646	AACCTATGAATACCT[A/C]ATGATACTTGAAAGC	26091
rs778545259	in-del	-/AG			intron-variant	HERC4	GRCh38.p7	10:67937110	TTTGAAAGATTAAGA[-/AG]AGAGTGAGATTTCAG	26091
rs778572963	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68056491	TAATGGGAAGACAGC[A/G]ATGCAATTTATTAAG	26091
rs778575068	snp	C/T	3.29538e-05	0.00405904	synonymous-codon, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68072932	TCCTAGATCATTACA[C/T]CCACATGTGTACACT	26091
rs778600528	snp	A/G	1.66073e-05	0.00288156	intron-variant	HERC4	GRCh38.p7	10:68034199	TTGCTGTAAAACAGT[A/G]ATGGAAAAATTAACC	26091
rs778622603	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67967667	CACCAATACTGGAAC[A/T]ATGAAATATTATGTT	26091
rs778681582	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68031931	TAACTTTCGTATTTT[C/T]AGAAGAGACAGAGTT	26091
rs778717434	snp	A/G					GRCh38.p7	10:67974565	AATATGAGACGAATG[A/G]ATGGACAGATAAAAC	26091
rs778724296	snp	C/G/T	3.44064e-05	0.00414756			GRCh38.p7	10:67991024	ATCATTGCTAAAAAA[C/G/T]AGAAAAGAAAAAAAA	26091
rs778733430	snp	A/G					GRCh38.p7	10:67968751	TTCATAATAATAAAA[A/G]GATTAATTCACCAAG	26091
rs778778430	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68068710	CAATAAAATACTGAT[A/G]GAAACCAGCTTCCTC	26091
rs778790064	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67999984	TTATCTGAAGTGTTA[C/T]ATTTGAGAACAACGG	26091
rs778791897	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67934141	AATTTCAATTTGCTT[C/T]GGATTAATCTTTAAT	26091
rs778820148	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67981161	AGAAACACACTTCAC[G/T]TATAAAGACAAACAG	26091
rs778843141	snp	C/G			intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069124	GGTCACCAAATTATA[C/G]CTATGATTAGATACA	26091
rs778857940	in-del	-/AAT	1.68252e-05	0.0029004	intron-variant	HERC4	GRCh38.p7	10:67956865	AAAAAAACCCTCTCA[-/AAT]AATATTTTACCTGCA	26091
rs778869907	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68063803	AATTAGCAGGGCATG[C/T]TGACGGGCATCTGTA	26091
rs778870865	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68015901	TGAGGTCAGGAGTTC[A/G]AGACCAGCATGGCAA	26091
rs778884957	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68002890	CAAGCCTGAGCCACC[A/G]TGCCTAGCCTTATTT	26091
rs778896755	in-del	-/C			intron-variant	HERC4	GRCh38.p7	10:67955233	AGGTATTCTATAATT[-/C]CTATGCTACTGAATT	26091
rs778938386	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68045508	TAATATCAAAAGATA[C/G]ATGTAGTTAAAATAT	26091
rs778975092	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68014946	GATCTTGTCTCTTGC[C/G]CTAAACCTCTTTGCC	26091
rs778980538	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68030343	CTACTTGGGAGGCTG[A/C]GGCATGAGAATCACT	26091
rs779013886	snp	C/T	3.43637e-05	0.00414496	utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68073149	TTTCAATAAAAAATT[C/T]TCTTCTGAAACCCCG	26091
rs779071732	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68026581	AGATGTGGTGGCTCA[C/T]GCCTGTAATCCCAGC	26091
rs779094478	snp	A/T	1.64838e-05	0.00287083	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:67992306	GGGACATCTGAAGTC[A/T]TCTGGTGGCCCACAG	26091
rs779106463	snp	C/T	1.64779e-05	0.00287031	synonymous-codon, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:68044511	CGCTAACGTATGAGC[C/T]TCTCCACATGAAACA	26091
rs779125269	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67926930	CTATCTTATTTCCTG[A/C]CCTCTCTTCAATCTC	26091
rs779137169	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68026377	CTGGGATTACAGGCA[G/T]GAGCCACCATGCATG	26091
rs779161986	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68025107	GTAGTGCATGCCTGC[A/G]GTCCCAGCTACTCAA	26091
rs779179504	snp	C/T	1.65162e-05	0.00287365	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67988748	GGAATACCGATCTTG[C/T]AGAGTTTCAAAAGAT	26091
rs779203896	in-del	-/TGG			intron-variant	HERC4	GRCh38.p7	10:67945521	AGGAGCAAAACTCAC[-/TGG]TAATAGTAAATACAC	26091
rs779215523	in-del	-/C			intron-variant	HERC4	GRCh38.p7	10:67983787	GAAGACTCTGTCTCA[-/C]AAAAAAAAAAAAAAA	26091
rs779216169	snp	C/T	1.65444e-05	0.00287609	intron-variant, synonymous-codon	HERC4	GRCh38.p7	10:67940941	TTTTCCAACTAACCT[C/T]CCAACATCAGGCATT	26091
rs779221328	in-del	-/AAATA	3.44453e-05	0.00414988	intron-variant	HERC4	GRCh38.p7	10:68038068	AATAAAACTGAAGAG[-/AAATA]AAATAAAAACTAATG	26091
rs779243447	snp	A/T			upstream-variant-2KB	HERC4	GRCh38.p7	10:68076092	TTCCACAAATAGGCC[A/T]TCTTTCTTTTTCTTT	26091
rs779289359	snp	A/C	3.39934e-05	0.00412256	intron-variant	HERC4	GRCh38.p7	10:67956856	CAATTAAAAAAAAAA[A/C]CCCTCTCAAATAATA	26091
rs779304311	snp	C/T	1.65119e-05	0.00287327	intron-variant, synonymous-codon	HERC4	GRCh38.p7	10:67939645	ATAATCCAGTAACTG[C/T]TGCATGCTTCTGCAA	26091
rs779308367	snp	A/G	1.79078e-05	0.00299226	intron-variant	HERC4	GRCh38.p7	10:67990173	CATTTTCATTTAAAG[A/G]GAAAAGGTTTCAAAA	26091
rs779319182	in-del	-/ACACA			intron-variant	HERC4	GRCh38.p7	10:67974114	CACACACACACACAC[-/ACACA]CATACACACAGGGTC	26091
rs779378106	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67986052	GTTTCTTGAATGATA[C/T]AAATAAATCGTCCCT	26091
rs779395092	snp	A/C	3.73448e-05	0.00432099	intron-variant	HERC4	GRCh38.p7	10:67992581	TATTGGAGCTATTTA[A/C]TTATTTACATGACTA	26091
rs779429957	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68037005	TTATCTGTGCTTCCC[C/T]ATGGTTCCTAGTGCT	26091
rs779445585	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67944864	AAGAAAAAGAAGTGA[C/T]TAGTGAGCTTGAAGA	26091
rs779458904	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68000629	CCAATATCTCAGAAT[A/G]TGATCTTATTTGGAA	26091
rs779458914	snp	C/T	1.72237e-05	0.00293455	intron-variant	HERC4	GRCh38.p7	10:67957024	TTGATTTGTGATATA[C/T]TTACTGTGGATGCTG	26091
rs779465576	snp	C/T			intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010717	GCTAAGCTGTTGAGC[C/T]TCAAAGAGGCAGATG	26091
rs779481908	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67956644	AATGAAAGAGGCTTA[C/T]ACAATTTTTAATATA	26091
rs779500365	snp	G/T	1.65987e-05	0.00288082	intron-variant	HERC4	GRCh38.p7	10:67936108	ACAGAAGAAAATGTC[G/T]ACTGAATCTTATTAC	26091
rs779501052	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67948011	TACACTCTTAAACAA[C/G]CAAAAGATCAAAGAA	26091
rs779514957	in-del	-/TC			intron-variant	HERC4	GRCh38.p7	10:68038471	ATAATTCAGATATTT[-/TC]TTTCATTATAAAAAC	26091
rs779517593	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68049731	GCCTCGGCAACATAA[C/T]GAGACCCTGTCTCTA	26091
rs779531252	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68055127	GGGTTTCACCATGTT[A/G]CCCAGGCTGATGGTA	26091
rs779559355	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67993143	TGATGTTAGGAGTTC[A/G]ACGCCAGCCTGGCCA	26091
rs779559495	snp	A/G	1.66699e-05	0.00288698	intron-variant	HERC4	GRCh38.p7	10:67954746	AATATAACCTAAAAT[A/G]GCACAATGCAAACAC	26091
rs779572373	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68006357	ATGAAACGCCTCAGC[A/G]TTTTTGTTTTTGTTT	26091
rs779576088	snp	A/G	0.000171836	0.0092676	intron-variant	HERC4	GRCh38.p7	10:67991029	TGCTAAAAAACAGAA[A/G]AGAAAAAAAAAAATA	26091
rs779579656	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67958059	TGATCCGCCCACCTC[A/G]GCCTCCCAAAGTGCT	26091
rs779598268	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67935507	TTTCACTATACGGTA[C/T]CAAGAAGGAGGGAGC	26091
rs779623868	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68051692	TCAACTTTTCTTTTC[-/T]TTTTTTTTTTTTTTT	26091
rs779624225	in-del	-/TCA			intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68009972	GTGTCCCAGTCTTCT[-/TCA]TTTGAGAAAAAAGTG	26091
rs779624886	snp	A/G			intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68070086	AAAAACCTCCTGGGA[A/G]ATGAACTATGTTTAT	26091
rs779626842	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68056457	CATCCAGGAGATGAC[A/G]TGGTAGGGAAGATCA	26091
rs779641651	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68035466	CAGCCTGGGACAATC[A/G]CTCTTACCAATTACT	26091
rs779649847	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68040971	AAATATATACACACA[A/C]ACACATTGGAGATAA	26091
rs779655175	snp	G/T	3.36078e-05	0.00409912	intron-variant	HERC4	GRCh38.p7	10:68034216	TGGAAAAATTAACCA[G/T]TTTTCTCACATGCAA	26091
rs779688892	in-del	-/AA	0.00101905	0.0225496	intron-variant	HERC4	GRCh38.p7	10:67956846	ATCAAAGAAACAATT[-/AA]AAAAAAAAACCCTCT	26091
rs779693799	in-del	-/AAAAC			intron-variant	HERC4	GRCh38.p7	10:67938946	AGACTCTGTCTCAAA[-/AAAAC]AAAACAAAACAAAAC	26091
rs779746325	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67974045	GAGAGACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	26091
rs779748758	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68017758	CCTCCCAAAGTGCTG[A/G]GATTACAGGCATGAG	26091
rs779761542	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67973263	CACCAGCTAAAGAGA[C/T]ACAATCTGTATGTAA	26091
rs779762298	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67979752	TAATCCCAGCTAACA[C/T]GGTGAAACCTCGTCT	26091
rs779778853	snp	C/T			utr-variant-3-prime	HERC4	GRCh38.p7	10:67921941	TCTTTATTAAACAGT[C/T]TTCACGGCATTTTAA	26091
rs779812242	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68066095	CCAAGCCCAAATAAA[C/T]TCTTATATAAACATT	26091
rs779902261	snp	A/G	2.30752e-05	0.00339663	intron-variant	HERC4	GRCh38.p7	10:67925059	TTCCAGTCTCATAAA[A/G]TATACAACTAGTTAG	26091
rs779903310	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67994324	GATTGTGCCCTCTAT[A/T]AACAATTCCCTACAA	26091
rs779911722	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67970579	CCTGGGTGACAGAGC[A/G]AGACTCTGTCTCAAA	26091
rs779932233	snp	A/G			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68010973	TTCCACCATATCTAT[A/G]GTTAAGTTCTTCGAA	26091
rs779963212	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67994675	AACCTCAGGTGATCC[A/G]CCCACCTCAGCCTCC	26091
rs779968467	in-del	-/T	2.35624e-05	0.00343229	intron-variant	HERC4	GRCh38.p7	10:67925055	TAGATTCCAGTCTCA[-/T]AAAGTATACAACTAG	26091
rs780009817	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68006208	GATGAGTAGTGCGCA[A/C]ACCACAATGTCTGTG	26091
rs780036413	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67990643	CGTGTACAAGTCTCA[A/G]TTTAAACTCTCTACC	26091
rs780045027	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68026324	TGGTCTCGAACTCCT[A/G]GGCTCAAGCAATCCT	26091
rs780058465	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67944380	AGACACAGTGATATT[A/G]GGCTTGGGGTGCCCC	26091
rs780061423	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67961263	CTGCAGATCAGAAAG[A/G]TTCACTTCAAATATA	26091
rs780109071	snp	C/G	1.656e-05	0.00287745	missense, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68073100	GGATGCATTTCCCCA[C/G]CACAACATGCTTGTA	26091
rs780115746	snp	A/G			synonymous-codon, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:68044550	ATTTTGGGCATCCAG[A/G]GCAACAACCTGCTCT	26091
rs780127580	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67937951	GCTCCAAAAGTGCTG[C/G]GATTACAGACGTGAG	26091
rs780134536	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68024680	TGAAGCTAATAGTTG[A/G]TAAAACTAAACTATT	26091
rs780164691	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68072202	TGTAGAAATATTTGA[-/T]TTTAAAATACAATAT	26091
rs780250442	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67927974	GACAGGATACGTGTG[C/T]AGGAGAGAGGTTTGC	26091
rs780317317	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67999120	TGATATTCTTGTGTA[C/T]ACCTGGTATGTTAGA	26091
rs780347536	snp	A/G	0.000204243	0.0101035	intron-variant	HERC4	GRCh38.p7	10:68072840	CAAATTTAAAATGAT[A/G]TAATTATTAAAAATA	26091
rs780350625	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67941241	AGTTCATCCTCATTA[C/T]TGTCTCCCTGGGATA	26091
rs780354734	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68074606	CTGAACGTGCACCCA[A/G]ATCAGCTCATGGGGA	26091
rs780366479	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68028861	AATATATTGGAATTT[A/G]TTTGCTATTAGCAAA	26091
rs780366481	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67950475	GAGACAGGGTTTCAC[C/T]ATGTTGGCCAGGCTG	26091
rs780380067	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67959203	GTCCAAATTTAACTA[C/T]TTCTATTCAAGGTAG	26091
rs780437790	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68057726	TTTTTTTTTCTTTTA[A/G]GACAGAGTCTTGTTC	26091
rs780437810	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:67934182	CATTCACTTTCTACT[A/C]CCCTGTACATCTATT	26091
rs780444217	snp	C/G	1.66557e-05	0.00288575	intron-variant	HERC4	GRCh38.p7	10:67959068	ACTCAGGAGAAAATG[C/G]AGTATATTTTACTCT	26091
rs780446104	snp	C/T	0.000908678	0.0212958	intron-variant	HERC4	GRCh38.p7	10:67996089	GGTAGGAGGATCACT[C/T]GAGCCCAGGAGTTCA	26091
rs780448968	snp	C/G	1.73893e-05	0.00294862	intron-variant	HERC4	GRCh38.p7	10:67941134	AAAAAGTAAACACAT[C/G]TCCTCCAAGTTAAAA	26091
rs780482595	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68033536	CAAAATGTTTAAGAC[C/T]TTAGCATCAATGTTA	26091
rs780497553	in-del	-/AAAA			intron-variant	HERC4	GRCh38.p7	10:67972531	TCTCAAAAAAGAGGA[-/AAAA]AAAAAAAAAAAAAAA	26091
rs780526412	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67964935	CCACCACCATGCCTG[A/G]CTAAGTTTTTGTATT	26091
rs780549962	snp	C/G	1.65015e-05	0.00287237	missense	HERC4	GRCh38.p7	10:67932715	AAGCCCGCATGAAAA[C/G]CATCAAATAAGGAAG	26091
rs780567405	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68048210	CAGGCATGAGCCACC[A/T]CACCCAGCCCACACA	26091
rs780568889	snp	A/G	3.32845e-05	0.00407936	intron-variant	HERC4	GRCh38.p7	10:67959170	ATATAACAATAACGA[A/G]GAAAGAGCAATATTA	26091
rs780577656	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67962513	CAGAAAGATGTGAAC[C/T]GGCAAGAATATGAAA	26091
rs780599177	snp	C/T			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011987	CAACTTGCTGTAGCA[C/T]ATACATCAGTACTTT	26091
rs780637392	in-del	-/TA	1.80201e-05	0.00300162	intron-variant	HERC4	GRCh38.p7	10:68033944	AAAGTACACTTAAAC[-/TA]TATACATAATGAGAA	26091
rs780640566	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67955437	AAACATTCACTGGAG[A/G]GGAGGGTAAAGAGGG	26091
rs780647373	snp	A/G			intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069137	TACCTATGATTAGAT[A/G]CACAGTAAGAAAAGG	26091
rs780689130	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:67924464	TGTACAGCATGTTAC[A/T]GTACTGAATTCTGTA	26091
rs780689132	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68005466	GCAGGGAGCAGATCA[C/G]TGGGTCTTGTTTTTT	26091
rs780704009	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68017585	GCCTCCTGGGATCAA[A/G]TGATTCTCCTGTCTC	26091
rs780704481	snp	C/T	3.29538e-05	0.00405904	missense, utr-variant-5-prime, nc-transcript-variant	HERC4	GRCh38.p7	10:68034073	CTGCTGCAACTTGCA[C/T]GAAAGGGATTCCAAG	26091
rs780711742	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:68016390	ATGGAGTCTCACTCT[G/T]TTGCCAGGCTGGAGT	26091
rs780726941	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67926767	CTTGTGGAGCTCACC[A/G]TCTAGTAAGAGGCGT	26091
rs780744210	snp	A/C			intron-variant, utr-variant-3-prime	HERC4	GRCh38.p7	10:68069926	ACGCCCCTATAGTCC[A/C]ACCTACTCGGGAGGC	26091
rs780775720	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67984473	TGGAGACACAGAGTA[A/G]AAGAATGGTTACCAG	26091
rs780791570	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68033371	TTGTTACTAGATTAA[A/T]AACTCACTTTTGTCC	26091
rs780801543	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67983978	AAAAAAAAAGAACGA[A/G]TACAGAAAATGTGGT	26091
rs780840364	in-del	-/T	5.90697e-05	0.00543427	intron-variant	HERC4	GRCh38.p7	10:67991043	AAAGAAAAAAAAAAA[-/T]AGAATAAAAATTTAA	26091
rs780841600	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68070992	AATTTCCAGTTCTCT[C/G]CAGTTGTTCATGTAT	26091
rs780862226	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68026914	CGCTGAGGCAGAATC[A/G]CTTGAACCCAGGAGG	26091
rs780921031	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67933642	GATATCTAGAAGGAC[C/G]TAAAATTTTTTCACA	26091
rs780935078	snp	C/G	1.78064e-05	0.00298377	intron-variant	HERC4	GRCh38.p7	10:67956833	ACTGTCCAGAAACAT[C/G]AAAGAAACAATTAAA	26091
rs780991360	snp	C/T	1.648e-05	0.0028705	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:68025573	ATCTCAGTGACAATG[C/T]TTCCCATAAGTTCAA	26091
rs781010891	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67932913	GAATGTATGAGTAGC[A/G]TTCAAACAGGACAAA	26091
rs781025020	snp	G/T	1.648e-05	0.0028705	missense, nc-transcript-variant	HERC4	GRCh38.p7	10:67992247	TAGCTCAGCCATTTC[G/T]GAATTAGAGCTTCAT	26091
rs781028972	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67942757	CTCAGGTGATCCACC[C/T]GCCTCGGCCTCCCAA	26091
rs781085572	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68068941	TTGTGAGAATTAAAT[A/G]AGATACTCCATTTGA	26091
rs781107293	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67925273	ATGGTCCAGTAGTTT[C/G]CAACTTGTGCAATTC	26091
rs781112024	snp	C/T	1.73773e-05	0.0029476	synonymous-codon	HERC4	GRCh38.p7	10:67925095	CTTACACAGAAACTG[C/T]TTCTTCTTTTCCAAT	26091
rs781116818	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67956467	CATCTTCTTCCTAAC[A/G]AGATCAAATGCTTCC	26091
rs781121549	in-del	-/AAAAAAAAAAGA			intron-variant	HERC4	GRCh38.p7	10:67996988	CAAGACTCCGTCTCG[-/AAAAAAAAAAGA]AAAAAAAAAAGAAAA	26091
rs781135567	snp	G/T			intron-variant	HERC4	GRCh38.p7	10:67998278	ACAGGCCAGGCATGG[G/T]GGCTCATGCCTGTAA	26091
rs781139713	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68043539	AACAATGATTAGCCA[A/G]GCACAGTGCTTCACG	26091
rs781156711	snp	A/C			upstream-variant-2KB	HERC4	GRCh38.p7	10:68077021	TCCCATCTCCTCAGG[A/C]GGCTGAGGCAGGAGA	26091
rs781192397	snp	C/T	3.30355e-05	0.00406407	missense, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67988776	GATGTACCACAACTT[C/T]CTTAAAAAGTTCTAC	26091
rs781201023	snp	A/G			synonymous-codon, intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67988666	GATTGGACATACCCT[A/G]TGTAGTATTTCTAAA	26091
rs781228276	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68056382	CCCTGAGTTCCTTCT[A/G]TGTGCACCATAGTAT	26091
rs781234205	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68042442	CCAGCTGGGCAACAT[A/G]GTGAAACTCTGTCTC	26091
rs781259493	snp	C/T	1.65329e-05	0.0028751	stop-gained, nc-transcript-variant	HERC4	GRCh38.p7	10:68014060	CCCATTATAGGGGTA[C/T]CAATTTCCTTTTACA	26091
rs781291811	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67987343	AAGTATTTCTTAAAG[A/G]GGGGAATAAAGATAA	26091
rs781335936	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67996274	TCTTCTTCTTTACAA[A/G]ATATATTGTCAGGGA	26091
rs781392935	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68048052	GCCTCCAGGGTAGCT[C/G]GGACTACAAGCACAT	26091
rs781393215	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67939189	TATTCTCATATTACA[A/G]TAACCTTTTGCTTCT	26091
rs781402035	snp	C/G	1.65332e-05	0.00287512	synonymous-codon	HERC4	GRCh38.p7	10:67954700	AAATTCTTTGCGCAC[C/G]CCTCCTGCATCCACA	26091
rs781421678	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68073277	CAATAATTGCTACAT[A/G]GTAAACATTAAATAT	26091
rs781425392	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67967594	TATTAATTACAAAGA[C/T]AAAAACAAATCTTTA	26091
rs781430914	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68067401	TCTATCATCCACATC[C/T]TTCTCTTCCTTAGAA	26091
rs781433218	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68050272	CGTGGTCAAATGTAA[A/G]AGCCAAGCTTCTCAA	26091
rs781436396	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68037388	GGCGTGAGCCACTGC[A/G]CCCAGCAAACCTATT	26091
rs781453920	snp	A/G	2.18472e-05	0.00330501	intron-variant	HERC4	GRCh38.p7	10:67966829	AATGTAATTGACATT[A/G]AATTTAACCAGTACT	26091
rs781463225	snp	A/C	2.28001e-05	0.00337632	intron-variant, downstream-variant-500B	HERC4	GRCh38.p7	10:67966615	CATTTCAAAACCAAG[A/C]AATTGTTTCTTTTTT	26091
rs781467103	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68002805	GAGTTTCACCAAGTT[A/G]GCCAGGCTGGTCTCA	26091
rs781481767	snp	G/T	0.000142096	0.0084278	intron-variant	HERC4	GRCh38.p7	10:67996135	ACATGGCAAGACCTC[G/T]CCTCTACAAAAAAAA	26091
rs781497002	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68058157	CTGAAGGTAAAGGAA[C/T]CCAATCCATTTTATA	26091
rs781575296	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67952244	TTGTTAAAACCAAAA[C/T]GTGATTAAAATCAAC	26091
rs781580167	snp	A/G	1.65116e-05	0.00287324	missense	HERC4	GRCh38.p7	10:67932730	GCATCAAATAAGGAA[A/G]CCACTGATTTATTGA	26091
rs781586026	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67947601	CATTATAAACCAATA[A/G]GACCTATCAGACATA	26091
rs781615262	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67991571	ATGCCTTTGGGATTT[C/T]CAGAAAAATTATAGT	26091
rs781617616	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68022999	ACACGTATTAAAATA[A/G]GTATTATAAAAAAAA	26091
rs781680419	snp	C/T	1.64893e-05	0.0028713	synonymous-codon	HERC4	GRCh38.p7	10:67936161	CACTTACCGATTTTG[C/T]TTGTTAACAGCTGTG	26091
rs781695308	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68060503	CTCGACCTCCCAAAG[C/T]TCTGGGAATACAGGC	26091
rs781700684	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67935055	CTCTGAAGTTTTGTC[C/T]TTCAACCTGCATGGT	26091
rs781708994	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68024197	GAAAAGGTACTCAAG[C/T]AAGTCATGGAAATGT	26091
rs781716875	snp	A/G			intron-variant, nc-transcript-variant	HERC4, POU5F1P5	GRCh38.p7	10:68010610	CTGCACGAGGGTTTC[A/G]GCTTTGCATATCTCC	26091
rs781755098	snp	A/C	1.75059e-05	0.00295849	intron-variant	HERC4	GRCh38.p7	10:68038206	CAAGACCAGTTAATT[A/C]CATTTAACAAATTGA	26091
rs781757559	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67965169	AATTCTCTCTGCCCT[A/G]ATCTTAAAGGGCTGC	26091
rs781759798	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68009363	CAAGTGATTCTCTTG[C/T]CTTGGCTTTCCAAAG	26091
rs781777799	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68074270	CCTTATTCTGTAGCA[C/G]TCATCCACATTCTTA	26091
rs796103788	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67970846	ATGATCAATGTTTCT[C/G]CTTTAAGAATCTAGA	26091
rs796131082	in-del	AA/C			intron-variant	HERC4	GRCh38.p7	10:67962226	GTTTAAATAAGCAAA[AA/C]AAAAAAAGCCTATAA	26091
rs796170655	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67981904	CGAGATCAGGCCACT[A/G]TACTTACTCCAGCCT	26091
rs796174518	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68016644	GCTTGAGCCACTGCA[C/T]CCGGCCCAATAAGAT	26091
rs796179056	multinucleotide-polymorphism	AT/GC			intron-variant	HERC4	GRCh38.p7	10:67936494	TAAGCATTTGTTGTG[AT/GC]TAAAACTTTAGAATT	26091
rs796210475	in-del	-/ATA			intron-variant	HERC4	GRCh38.p7	10:68059562	ATCATAATATATATC[-/ATA]ATATTATATATCATA	26091
rs796221884	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68051691	TTCAACTTTTCTTTT[C/T]TTTTTTTTTTTTTTT	26091
rs796235895	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67985572	AAATAGTTTGAAAAT[C/G]ACTGATTTAGATCAG	26091
rs796236171	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67960254	AGGAAAGTAATTCAT[C/T]CATGACTCTACATGG	26091
rs796248097	in-del	-/AC			intron-variant	HERC4	GRCh38.p7	10:68046991	AACAAACAAAAAAAA[-/AC]ATGAAGAATTTTGGA	26091
rs796264047	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67979355	CCGAAGAATGTCTCA[A/G]AGTCTTTTAATAGGA	26091
rs796277433	in-del	-/AT			intron-variant	HERC4	GRCh38.p7	10:67976389	TGACTCTTGCAGAAT[-/AT]GATTCACATCCCACT	26091
rs796327217	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68038809	CTGTCTTGTATTTTG[C/T]CCTTATACTTTCGTA	26091
rs796373874	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67998130	TCTTGATCTCTTGAC[C/T]TTGTGATCCACCTGC	26091
rs796395455	snp	A/T			intron-variant	HERC4	GRCh38.p7	10:68002958	GGGATACATGAGACA[A/T]TGTGATACAGGCATA	26091
rs796400979	in-del	-/T			intron-variant	HERC4	GRCh38.p7	10:68003346	TTTTTTTTTTTTTTT[-/T]GTATTTTTAGTAGAG	26091
rs796407005	in-del	-/ATA			intron-variant	HERC4	GRCh38.p7	10:68059615	ATAATATTATATATC[-/ATA]ATAATATTATATATC	26091
rs796417072	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67962235	AAGCAAAAAAAAAAA[-/A]GCCTATAAAAATTTA	26091
rs796441089	in-del	-/AT			intron-variant	HERC4	GRCh38.p7	10:67939722	CTATTTTACTTATGG[-/AT]ATATATATATATATA	26091
rs796464618	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67930267	TTAAGGCAAAACACA[C/T]ATACCATAAAGTTTG	26091
rs796478847	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68047191	CCCAGTTTTTATTGA[C/T]TTCTTAGGGAAAAAA	26091
rs796479705	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67982621	CAAAAGTGGACAAAC[A/G]GGATTACATTAAATT	26091
rs796535253	in-del	-/ACACACACAT			intron-variant	HERC4	GRCh38.p7	10:67974112	CACACACACACACAC[-/ACACACACAT]ACACACAGGGTCAGG	26091
rs796538719	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68064535	CTCCAGCCTAGACAA[C/T]AGGCAACAGAGTGAG	26091
rs796551680	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68047213	GGGAAAAAAAAAAAA[-/A]GGTCAGTAATTCGCA	26091
rs796555137	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67928920	GCAAGACTCCATCTC[-/A]AAAAAAAAAAAGAGT	26091
rs796555556	in-del	-/TATAATATTATA			intron-variant	HERC4	GRCh38.p7	10:68059488	TATAATATTATATAT[-/TATAATATTATA]TATAACATTATATAT	26091
rs796556681	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:68061528	ACAGAGCAAGACTCC[A/G]TCTCAAAAAAAAAAA	26091
rs796637048	in-del	-/AT			intron-variant	HERC4	GRCh38.p7	10:68059553	ATATTATATATCATA[-/AT]ATATATCATAATATT	26091
rs796638689	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:68002345	CCATCAATAGATAAA[C/G]AAGAAGACAATTCTG	26091
rs796649008	snp	C/T			intron-variant, upstream-variant-2KB	HERC4, POU5F1P5	GRCh38.p7	10:68011991	TTGCTGTAGCATATA[C/T]ATCAGTACTTTTACA	26091
rs796652540	in-del	-/AAAC			intron-variant	HERC4	GRCh38.p7	10:68036379	ACCACAAAGCTGAGT[-/AAAC]AAACAAACAAAAAGG	26091
rs796673214	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:67950047	AACAAAACAAAAAAC[-/A]AAAAAAAAAGGAAAA	26091
rs796709189	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67984821	ACTCCTGACCTCAAG[C/T]GATCCACCGGCCTCA	26091
rs796720245	snp	A/C			intron-variant, nc-transcript-variant	HERC4	GRCh38.p7	10:67988050	ATACCTACCAACTGT[A/C]AGGGATGAAAATCCA	26091
rs796871214	in-del	-/A			intron-variant	HERC4	GRCh38.p7	10:68018340	ACATCCATTCACAAT[-/A]AAAAAAAACTAGGAA	26091
rs796872835	in-del	-/GT			intron-variant	HERC4	GRCh38.p7	10:67998573	AAAAAAGGGGGGGGG[-/GT]ACAGTACTATCCAGT	26091
rs796884826	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:68059242	AAAGCCATTTGACAT[C/T]TTCATTGAGATCATA	26091
rs796918747	snp	C/G			intron-variant	HERC4	GRCh38.p7	10:67925494	CTGACATGGAATTAT[C/G]TGTGATAATCAGAAA	26091
rs796919259	snp	A/G			intron-variant	HERC4	GRCh38.p7	10:67961366	TCTTATACTGAACAC[A/G]GCACGTGCTTTCATA	26091
rs796919447	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68000499	TGGGAGGATCGCTTG[A/C]GTCTGGGAGGTGGAG	26091
rs796974332	snp	A/C			intron-variant	HERC4	GRCh38.p7	10:68071033	CCAACCCAGACTCTA[A/C]ATTTCTCAAGACAAA	26091
rs797000830	snp	C/T			intron-variant	HERC4	GRCh38.p7	10:67932336	AGTGATCCTCCCGCC[C/T]AAGCACCCCAAAGTG	26091

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