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

AHCTF1

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs146496899	snp	A/G	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246867499	ATTTCACTTTTAAAG[A/G]TTTTTAAAAATTCTT	25909
rs146535830	snp	C/G	0.00755907	0.0610114	intron-variant	AHCTF1	GRCh38.p7	1:246914953	TTATTTACCTGAATG[C/G]CAATAGTCTACTTGT	25909
rs146554120	snp	C/T	0.0130921	0.0798413	intron-variant	AHCTF1	GRCh38.p7	1:246920654	GGGCGCCTGTAGTTC[C/T]AGCTACTCGGGAGGC	25909
rs146587251	snp	C/T	0.0345262	0.126772	intron-variant	AHCTF1	GRCh38.p7	1:246873574	ATACTAGAGACAATA[C/T]ACTAGTCAATTTCTC	25909
rs146607238	snp	C/T	0.0024552	0.034951	intron-variant	AHCTF1	GRCh38.p7	1:246863895	AGCCATCTAGTTTGA[C/T]TGTGAACGCTAGATG	25909
rs146651670	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246861567	ACTGAAAGGTTCCTA[C/T]TAACCTACAGTGGAC	25909
rs146653142	snp	C/G/T	0.00795532	0.062565	intron-variant	AHCTF1	GRCh38.p7	1:246929789	CCGGGCGCGGTGGCT[C/G/T]ACGCCTGTAATCCCA	25909
rs146669369	snp	C/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246864501	AAATTCATTAACATG[C/T]AAAATATCCATTCAC	25909
rs146669497	snp	A/G	3.35903e-05	0.00409805	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877268	TCAACCTATTGCAAT[A/G]TTGCCGCAAAAAATT	25909
rs146672252	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933027	AGCAGCCTCGAACTC[A/G]TGGGCTCAAATGATC	25909
rs146716812	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246868846	GTGTGTGTGTTTTTT[G/T]TTTTTTTTTTTTTTT	25909
rs146724486	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246878871	TATTCCCTAAAAATT[C/T]ACATCTGAAATTGCC	25909
rs146724760	in-del	-/TTGCAGTGAGCCGAGA	0.34101	0.232846	intron-variant	AHCTF1	GRCh38.p7	1:246854236	CCTGGGAGGCGGAGC[-/TTGCAGTGAGCCGAGA]TTGCACCACTGCACT	25909
rs146736366	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246845366	AAGCATATGATTCTT[-/A]AAAAAAAAGAAAAAT	25909
rs146740751	in-del	-/ATT	0.0898077	0.191933	cds-indel, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839708	GTTTCTAGATAATCA[-/ATT]ATTAATAGTCCATTC	25909
rs146772110	snp	A/G	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246880435	TGGTCATGGTGGCAC[A/G]TGCCTATAATCCCAG	25909
rs146772616	snp	G/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246875923	AGCAATATCTCCAAG[G/T]CATGCCTGTATGTGT	25909
rs146780498	snp	C/T	5.06205e-05	0.00503068	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853247	AGAGACAATAGGACC[C/T]TCAGAGATAGTGAGC	25909
rs146791176	snp	A/G	0.00557542	0.0525036	intron-variant	AHCTF1	GRCh38.p7	1:246879006	CCAAAATCTAGAAAC[A/G]TTAAAAGCAGAACAT	25909
rs146824779	snp	G/T	0.0030839	0.0391464	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840993	GCACTTTCTTTTTCT[G/T]TGTTTCTGAAAAAAA	25909
rs146913959	snp	A/C/G	0.0248531	0.10867	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849641	CTTGGAACTTCTGAC[A/C/G]CTGGAGAAAATAAAG	25909
rs146950666	snp	C/T	0.00318978	0.0398085	intron-variant	AHCTF1	GRCh38.p7	1:246880997	CAGACTGAAAACCCA[C/T]CCTGTGGCAAACTCT	25909
rs147054466	snp	C/T	0.0166325	0.0896639	intron-variant	AHCTF1	GRCh38.p7	1:246899689	AACAAACCTATTACA[C/T]AGCAAAACAAGAAAA	25909
rs147084849	snp	A/G	0.00835141	0.0640778	intron-variant	AHCTF1	GRCh38.p7	1:246843239	TCTGTTGGGAGGAAT[A/G]CCTGTCTCCTCTAAC	25909
rs147100873	snp	A/C	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246846423	AAGGAGTGAATACTC[A/C]TAAGAACCCCTGTAA	25909
rs147113268	snp	C/T	1.66493e-05	0.0028852	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900169	ATATCCAAGATGCCA[C/T]GTGGAGAAGTCCTAC	25909
rs147139190	snp	A/G	0.00755907	0.0610114	intron-variant	AHCTF1	GRCh38.p7	1:246913756	AGATGAAATAACCTG[A/G]GGCTTAGAAAGTCAG	25909
rs147140439	snp	A/T	0.00700672	0.058773	synonymous-codon, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843876	GATGACAAACTGAGA[A/T]GATAAATCCGAAACT	25909
rs147142698	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246916923	TATTATTCTATCCCT[A/G]AAGAGTTCACAGTCC	25909
rs147143321	snp	C/G	3.29951e-05	0.00406159	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850919	CTCACTAAAGGTATT[C/G]TTTCATGAATGGACT	25909
rs147232579	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246928661	ATAAATCAGTTTTCT[A/G]TGTGAAATACACAAA	25909
rs147238273	snp	A/G	4.99654e-05	0.00499802	missense, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246842718	TGTTTTGTTTTTGAC[A/G]TCCTGATTCGTTTCG	25909
rs147242943	snp	A/C	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246860249	CTCCAGCCTGGGCAA[A/C]AGAGTGAGACTCTGT	25909
rs147246074	snp	G/T	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246862844	TAACCAAATTATGTA[G/T]CAGAATCCTCTGAAG	25909
rs147249071	snp	A/C	0.0517044	0.152246	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246931781	GGCCACCTCAGAGCC[A/C]CACGCCCCCGAGAGT	25909
rs147351671	snp	C/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246873101	ACTAGGTTCGACTTA[C/T]TCCTATAAGCCAGTC	25909
rs147355371	snp	A/G	0.00163586	0.0285527	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877181	TGTCTGTAAATGGTA[A/G]CTTCAGTAAATCTTC	25909
rs147399261	snp	G/T	3.30753e-05	0.00406652	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877178	CAGTGTCTGTAAATG[G/T]TAACTTCAGTAAATC	25909
rs147455910	snp	C/G/T	0.000104242	0.0072188	intron-variant	AHCTF1	GRCh38.p7	1:246891945	TAAAAGAAAAGATAA[C/G/T]TTTCCATACAGTAAA	25909
rs147459267	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246896778	GGTTTAATATCACAG[C/G]AACCTATTAATTTCA	25909
rs147575288	in-del	-/A	0.0126979	0.078662	intron-variant	AHCTF1	GRCh38.p7	1:246874174	ACTCCAGTTTCTAGT[-/A]TATACAAGTAGACAT	25909
rs147620319	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246903304	AGACGCGTATGTCCT[C/T]TTATAAAAATCACCC	25909
rs147643285	snp	C/T	0.0883596	0.190715	intron-variant	AHCTF1	GRCh38.p7	1:246928057	GTGCGGTGGCTCACG[C/T]CTGTAATCCCAAGGC	25909
rs147650038	snp	A/T	0.0603597	0.1629	intron-variant	AHCTF1	GRCh38.p7	1:246909124	ATTTATATATATATA[A/T]AATTCAGCCAGGTGA	25909
rs147658943	snp	C/T	0.0358925	0.129066	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877229	GACAGACTTCATACA[C/T]GTGCTTCAGTAACTC	25909
rs147722911	snp	G/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246853025	TAGATTTGAACTACT[G/T]TGTCTTGAAACAACT	25909
rs147723200	snp	G/T	0.000477408	0.0154427	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916301	AGGCTGTTCATTGAC[G/T]CCACTGAATCTGTAA	25909
rs147739591	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246925605	AGCCTGGGCAAGATC[C/T]TGTTTCTAAAAATAT	25909
rs147752536	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246858400	ATTCAAAAAAAGTAG[A/G]TAAGAAAACTGAAGC	25909
rs147755684	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246927331	TCTCTACTAAAAACA[A/G]GAAATGTAGCAGCCA	25909
rs147811792	snp	C/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246909827	CTATCCTGTACACTG[C/T]AGGACGCTAAGCCAC	25909
rs147859788	snp	A/G	0.00318978	0.0398085	intron-variant	AHCTF1	GRCh38.p7	1:246869679	ACAGCATGGTTTACC[A/G]AATATTTTAAGCCTA	25909
rs147898082	in-del	-/TT	0.0596104	0.162024	intron-variant	AHCTF1	GRCh38.p7	1:246921008	AGGCAGGAGAATCGC[-/TT]TTGAACCTGGGAGAA	25909
rs147918616	snp	C/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246927460	TGCCACTACACTCCA[C/G]CCTCAGCAACACAGC	25909
rs147931881	snp	C/T	3.31565e-05	0.0040715	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850313	ATCATTCTGCTAGGA[C/T]TTGTTACCGTACTAA	25909
rs147935233	snp	A/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246928768	AGCAAACATTTCTAT[A/T]AACCACTTTGTATGC	25909
rs147936400	snp	C/G	0.00755907	0.0610114	intron-variant	AHCTF1	GRCh38.p7	1:246884692	TTATTATGTAAATGA[C/G]AAATACACTGATTAG	25909
rs147966769	snp	C/T	0.000177399	0.00941638	intron-variant	AHCTF1	GRCh38.p7	1:246888545	AAAAATTAAGACTTA[C/T]TTAATATCACTGTTA	25909
rs147968469	snp	A/T	0.000153988	0.00877328	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850104	TTCTAGGTATGGCAG[A/T]CATATCAAATTCTGC	25909
rs147981044	snp	A/G	0.00413666	0.0452904	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850807	TTTGGAGGAAACCAC[A/G]TCATCAACCTGGCTG	25909
rs148019871	snp	C/T	0.00230211	0.033849	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916339	ATCGCTCTCCTGTTA[C/T]AGAGTTTACTACCTC	25909
rs148056251	snp	A/C	0.00716266	0.059414	intron-variant	AHCTF1	GRCh38.p7	1:246931056	TTAAATCTCCTTGAT[A/C]TGACCAATCGGGTGA	25909
rs148060665	snp	C/T	0.14933	0.228835	intron-variant	AHCTF1	GRCh38.p7	1:246922952	TGCACCACTGCACTC[C/T]AGCCTGGGCGACAGA	25909
rs148103547	snp	A/G	9.88419e-05	0.00702931	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849746	TTAGTGAAGGAAGCT[A/G]TGGCGAGCAATCTTT	25909
rs148129004	snp	C/G	0.00795532	0.062565	intron-variant	AHCTF1	GRCh38.p7	1:246872103	AACCTAGGGTGGTCT[C/G]TAACTAAATATGGTC	25909
rs148243382	snp	C/T	0.00116933	0.0241516	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902615	TACTCGTCTGTCCCC[C/T]CAAAGGGAACATGCC	25909
rs148267610	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246895427	TGTGTGTGTGTATGT[A/G]TGTGAAGAGTAACAG	25909
rs148290282	snp	C/T	0.0107246	0.0724382	intron-variant	AHCTF1	GRCh38.p7	1:246904773	GAATTTTACTACTAG[C/T]TGATCCCTTTTAATA	25909
rs148319631	snp	C/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246867986	TTTTTTTCTTTTAGA[C/T]CAGTCTTGCTGTGTC	25909
rs148340536	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838693	ATGTTGTTCTGTCAA[C/G]CAAGTCTTGATCGAC	25909
rs148341363	snp	A/C/G	0.0360663	0.129354	intron-variant	AHCTF1	GRCh38.p7	1:246912378	ATCTCAGCTACTCAG[A/C/G]AGGCTGAGGCAGGAG	25909
rs148366852	snp	C/T	1.79464e-05	0.00299548	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246885643	TGCCATGACAAAGGT[C/T]TTGCAGTAGCTGGAT	25909
rs148394860	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246907992	TATTTAAAAATTCTC[C/T]CAGTACATCTCAAAT	25909
rs148424307	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868827	TATTGTGCTTTGCTT[A/C]ATTGTGTGTGTGTTT	25909
rs148463078	snp	G/T	0.0225045	0.103662	intron-variant	AHCTF1	GRCh38.p7	1:246914424	CAGGCTGTAACTTAC[G/T]ACAGACAAAAGCCTG	25909
rs148581930	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246863598	TGATAGAAGAAATAA[C/T]AGCATAATGATATCA	25909
rs148584080	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932655	TCATGGCCAAAAATG[C/T]TCGCGCAGCCTAGCC	25909
rs148587670	in-del	-/TTAGT	0.293807	0.246132	downstream-variant-500B	AHCTF1	GRCh38.p7	1:246839004	ATGATACTAAGCACC[-/TTAGT]TTAACCAATGCTTTG	25909
rs148600466	snp	A/T	0.00755907	0.0610114	splice-acceptor-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843930	CTCTATTTTTTTAGC[A/T]AAAAAAAGTTGAAAA	25909
rs148636241	snp	C/T	0.00517822	0.0506191	intron-variant	AHCTF1	GRCh38.p7	1:246902203	AAGACAACCAAGGCA[C/T]GTATGCCATACATGG	25909
rs148657554	snp	C/T	0.0126979	0.078662	intron-variant	AHCTF1	GRCh38.p7	1:246873501	GTACTAGAGACAATA[C/T]ACTAGTCAATTTCTC	25909
rs148727145	snp	C/G/T	0.000233063	0.0107926	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246862043	AGACCTTCCAGGTGA[C/G/T]GGAGAGGGAGATGCT	25909
rs148778024	snp	A/C/T	1.66363e-05	0.00288407	synonymous-codon, missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246860960	ATCTTTATCTCCATC[A/C/T]TTTTCAGTTTGTTCA	25909
rs148792915	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246897246	TGAACCCAGGAGGTT[A/G]GAGGTTGCAGTGAGC	25909
rs148853953	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246927482	CAACACAGCCTGACT[A/G]TCTCAAAAAGAAAAA	25909
rs148902945	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246899190	ACTTCATTTCCTCAT[A/C]AGCTTTCTGAGGAGA	25909
rs148921577	snp	C/T	0.00676609	0.0577691	intron-variant	AHCTF1	GRCh38.p7	1:246879320	CATAGCATACGGTAA[C/T]TGAGAGGAGGATTAA	25909
rs148954903	snp	A/C/G/T	0.0968282	0.198216	intron-variant	AHCTF1	GRCh38.p7	1:246869066	GGCCAGGATGGTCTC[A/C/G/T]ATCTCCTGACCTCGT	25909
rs149009595	snp	C/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246925052	CACATTGTTACTATG[C/T]TGTTTTCCCCTCTGA	25909
rs149058862	snp	A/G	0.0162398	0.0886349	intron-variant	AHCTF1	GRCh38.p7	1:246929189	CGAGGTGGGCAGATC[A/G]TCTGAGCTCAGGAGT	25909
rs149130949	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246845765	GGAGTTCAAAAGGCC[C/T]AGGTTCAAACCCAAC	25909
rs149164047	snp	C/T	0.0592355	0.161582	intron-variant	AHCTF1	GRCh38.p7	1:246904329	TCCTTCCTCAATGGT[C/T]ATACTCTACTTAAAC	25909
rs149188418	in-del	-/AAAG	0.0341408	0.126114	intron-variant	AHCTF1	GRCh38.p7	1:246918169	TTTCTTCTTCCACAT[-/AAAG]AAACTATAATATATA	25909
rs149219566	snp	C/T	0.000395537	0.0140575	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851121	TATCATTTTCCCCAC[C/T]GCATACAAGTTTTTC	25909
rs149221187	snp	C/T	0.0322114	0.122752	intron-variant	AHCTF1	GRCh38.p7	1:246883809	AGACTTTTTCCAACT[C/T]AAGAGAAATAAGGTT	25909
rs149239782	in-del	-/TT	0.0588605	0.161139	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933785	CTTTTGGAAATGTAA[-/TT]TTCTTTTTTCTGTAA	25909
rs149252201	snp	A/C	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246847348	CATAAGTAGGGGGAC[A/C]AAAGCAGAATATATG	25909
rs149307588	snp	A/T	0.00914312	0.0669923	intron-variant	AHCTF1	GRCh38.p7	1:246857179	AACATAAACTGACAC[A/T]CTCACCAATCTGCTT	25909
rs149320039	snp	A/C/G	0.000249847	0.0111746	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850784	ATACGTTGACCTCTC[A/C/G]TACGAGTTTTGGAGG	25909
rs149380779	snp	A/C	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246859713	CCTGAGTAGCTAGGA[A/C]TACAAGTGCATGCTA	25909
rs149383055	snp	A/G	0.0433465	0.140692	intron-variant	AHCTF1	GRCh38.p7	1:246928118	CATCCTGGCTAACAC[A/G]GTGAAACCCCATCTC	25909
rs149412849	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246915398	ATAAGGCCATTCACA[A/G]TCTAAAACCTAACGT	25909
rs149419984	snp	C/T	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246901038	AGGAAATAGGAAGAA[C/T]GGGGAATAAGAGAGA	25909
rs149429737	in-del	-/TACTACTGA	0.154661	0.231107	downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838899	GTACATTGTTTACCT[-/TACTACTGA]TACTAAGTATCTTTC	25909
rs149437187	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246863293	GAGAACCCAGGGACA[A/G]TGGGGAGGGGTGAGG	25909
rs149453680	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246895051	AAAAGGTCAATTTTT[-/T]GAAAGACAAAGTGAC	25909
rs149466120	snp	A/G	0.0193772	0.0965046	intron-variant	AHCTF1	GRCh38.p7	1:246881428	TTAAAACCATGCAAC[A/G]AACAAACTTGATCAT	25909
rs149538294	snp	A/T	1.6842e-05	0.00290184	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851359	CTGAAGCTTAAGTGT[A/T]CCAGAGGGATATAAC	25909
rs149543044	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246926749	AATCCCAGCTACTTT[A/G]GGAGGCTGAGGCAGG	25909
rs149594899	snp	C/T	0.0535932	0.154675	intron-variant	AHCTF1	GRCh38.p7	1:246890247	AGTGAGAAAATGATC[C/T]GTCATGAAAGTCTAA	25909
rs149611336	in-del	-/CTTT			intron-variant	AHCTF1	GRCh38.p7	1:246857963	TGCTAACACTTTCTT[-/CTTT]CTTTTTTTTTTTTTG	25909
rs149623746	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246876294	TCCAAAAAATCTTCC[C/G]CCTACCTACATATCC	25909
rs149645831	snp	C/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246897079	AGCACTTTGGGAGGC[C/T]GAGGAGGGCAGATCA	25909
rs149650242	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246848391	GATAATTTCTTTGTA[-/T]TTTTTTTTAGTAGTG	25909
rs149690307	snp	C/T	0.000412919	0.0143628	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246904023	GATGCAAACTCAAAA[C/T]ATCCCCTTCACTGAA	25909
rs149713465	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246870279	TGAGGCCCTCTCTAC[-/A]AAAAATACCCAGGCA	25909
rs149732454	snp	C/T	0.00438332	0.0466095	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839901	TCCCAACCTCAATAA[C/T]CTGTGCCTGAGGTCC	25909
rs149783282	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246851871	CTTTTCTAAATAGCA[C/T]GATCCCCGTAAGGTT	25909
rs149784740	snp	A/T	0.0170251	0.090679	intron-variant	AHCTF1	GRCh38.p7	1:246924463	TAAAATCAATAATTA[A/T]AGAATTTTAAAACAT	25909
rs149818118	in-del	-/GTACT			intron-variant	AHCTF1	GRCh38.p7	1:246927570	AAACACCTACGTTCA[-/GTACT]GTACAAAATTAAACA	25909
rs149818912	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246893377	GAATAACTTAACTTA[C/T]ATTGTGAAAAGCTAT	25909
rs149835592	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246858430	CCTAAGGTTATACTG[C/T]GTATCCCAGCTCATG	25909
rs149892420	snp	A/G	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246869360	TGTTCATGTGAAAGG[A/G]GGAGTCACATGTCTA	25909
rs149899496	snp	C/T	0.000843735	0.0205221	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850293	TAGTACTTCTCAATT[C/T]TCTGATCATTCTGCT	25909
rs149944020	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246919759	GTTATTTTCAGGTTC[A/G]TTGCTCCAAGCAATC	25909
rs149947550	snp	C/T	0.00557542	0.0525036	intron-variant	AHCTF1	GRCh38.p7	1:246873455	TCTCCTGCATCATAG[C/T]GAAGGGAAAGAATCC	25909
rs149979310	snp	A/G	0.0178098	0.0926698	intron-variant	AHCTF1	GRCh38.p7	1:246927315	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAACA	25909
rs149995687	snp	C/T	0.0142736	0.0832652	intron-variant	AHCTF1	GRCh38.p7	1:246883284	GACTTTTAGTTCAAA[C/T]TTCCCAAATGTAACC	25909
rs150032385	snp	A/G	0.00716266	0.059414	intron-variant	AHCTF1	GRCh38.p7	1:246929079	AGGTACATATGCTGT[A/G]AGATCCCAGTAAAAA	25909
rs150088180	snp	C/G	0.00438332	0.0466095	intron-variant	AHCTF1	GRCh38.p7	1:246886143	CAAGACCAGCCTGGT[C/G]AACATGGTGAAACCT	25909
rs150104510	snp	C/T	0.327445	0.237702	intron-variant	AHCTF1	GRCh38.p7	1:246847107	GCTTGGCCAACATGG[C/T]GAAACCCTGTCTCTA	25909
rs150123190	snp	A/G/T	4.04132e-05	0.00449503	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861259	CTGCACATTTTTTAG[A/G/T]TGTAGTAAATACTTC	25909
rs150139369	snp	A/G	0.000904334	0.021245	intron-variant	AHCTF1	GRCh38.p7	1:246931103	TGAGCCCCGAGTCCA[A/G]CTTCTTCCCCGCCAG	25909
rs150290650	snp	A/G	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246866061	ATATGATGTACCCAC[A/G]GATGTTATCTATTCT	25909
rs150298389	snp	C/G	0.00175125	0.0295391	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246855821	GGACTTCTGGGTGAA[C/G]ATTTTCCTTTAGAAA	25909
rs150299020	snp	C/T	0.0138799	0.0821421	intron-variant	AHCTF1	GRCh38.p7	1:246926531	CTTTTCCAATTTAAG[C/T]ACACTACAGAGAACA	25909
rs150348172	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246895679	CATACTGTGGGCAAA[C/T]GTGCTAAAGGGGGTG	25909
rs150394496	snp	C/T	0.00115354	0.0239883	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850143	TCAACTGAGATGACT[C/T]AAGGTTGGAGTCTTC	25909
rs150403067	snp	A/G			missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900119	GTGGATATGAAGGAG[A/G]GACTCCTCTATTTAA	25909
rs150420552	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246870219	GAGGCCAAGGTGGGA[A/G]GATCACTTGAGGCCA	25909
rs150473634	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246875933	CCAAGGCATGCCTGT[A/G]TGTGTTAGCGAAAGT	25909
rs150504092	snp	C/T	9.89674e-05	0.00703377	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246903970	TAAGATTTGTCCTGA[C/T]GCCAAACACTTTCTA	25909
rs150543674	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246872325	GGAAAAGACTGACAA[A/G]AAGACTTTACAGTGA	25909
rs150565789	snp	A/G	0.00953873	0.0683987	intron-variant	AHCTF1	GRCh38.p7	1:246923228	GAGACCAGCCTGACT[A/G]ACATGATGAAACCCC	25909
rs150578707	in-del	-/TTCAA	0.00941842	0.0679743	intron-variant	AHCTF1	GRCh38.p7	1:246899420	AAGATCTGACTTCAG[-/TTCAA]TTAAGAAATCACTAG	25909
rs150596968	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246877577	AAGACAAAAAACTAA[C/T]GTGGCCTGGATAGAG	25909
rs150612389	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246900724	CTTGTTTTCAGTTAA[C/T]ACTTGAGCAACGTTG	25909
rs150619640	snp	C/T	0.000264275	0.0114921	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246888179	CTTAAAAGGATACAA[C/T]AGAGTGTTTGGCTGC	25909
rs150710000	snp	G/T	0.000247641	0.0111247	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850260	GCTTATTTCCTGTAT[G/T]TTCAGAAGCATCTAA	25909
rs150742902	in-del	-/TA	0.0228947	0.104514	intron-variant	AHCTF1	GRCh38.p7	1:246912839	ATATGCCAAGAACAC[-/TA]TGTTAGATCCTACAT	25909
rs150752133	snp	A/G	0.0130921	0.0798413	intron-variant	AHCTF1	GRCh38.p7	1:246912539	AGTCAAAATTTTTTC[A/G]GGTCAAATACTCCTT	25909
rs150761910	snp	A/C/T	0.000115495	0.00759843	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849889	AGAGCTCATCACCAT[A/C/T]GAAAGTTCCTCGTTT	25909
rs150768350	in-del	-/GC	0.394171	0.204242	intron-variant	AHCTF1	GRCh38.p7	1:246927870	TAGCTGGGCGCGGTA[-/GC]GCGCTGTAGTCCCAG	25909
rs150772980	snp	C/T	0.00318978	0.0398085	intron-variant	AHCTF1	GRCh38.p7	1:246859678	CCTCCTGGGTCCAAG[C/T]GATCCTCCCCTCTCA	25909
rs150790555	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246844236	TTAATCCGTACTGCT[C/G]CTCAAGCATTCTGGG	25909
rs150807473	snp	A/G	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246918504	AAAATCTGGTTACAA[A/G]ATACATATTGGCCAG	25909
rs150822349	snp	C/T	0.0528381	0.153711	intron-variant	AHCTF1	GRCh38.p7	1:246868253	CCTGCCTTAGCCTCC[C/T]GAGTAGCTGGGACTA	25909
rs150874772	snp	C/T	0.0520825	0.152737	intron-variant	AHCTF1	GRCh38.p7	1:246869134	AGGCGTGAGCCACCA[C/T]GCCCGGCCGTGTGTT	25909
rs150972308	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246870045	ATTAAAAGGAGTTTG[C/T]AAGAAGGTGATTCCA	25909
rs150987118	in-del	-/AGAT	0.00517822	0.0506191	intron-variant	AHCTF1	GRCh38.p7	1:246869910	AGCTATAGCTGTCAC[-/AGAT]AGATAGTGATTCCTC	25909
rs150987151	snp	A/G	3.29777e-05	0.00406051	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246855799	CTTCGTCCAACACTG[A/G]TACCTTGGACTTCTG	25909
rs151038417	snp	C/G	1.64852e-05	0.00287094	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861040	TGAAAACAGTCTCTT[C/G]AAGGTCTTCCGGTGA	25909
rs151093519	snp	A/G	0.00914312	0.0669923	intron-variant	AHCTF1	GRCh38.p7	1:246892589	GCCTCCCAAAGTCCT[A/G]GGATTACAGGCATGA	25909
rs151129973	snp	A/C	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246902776	GTTCACACAATACAA[A/C]GAAAACAATTTAGAC	25909
rs151137571	in-del	-/AAATA	0.372592	0.217879	intron-variant	AHCTF1	GRCh38.p7	1:246843712	AAATCATTAAAATTT[-/AAATA]AAATAATTTTATTAA	25909
rs151148585	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246889554	GTCATTCTAAAGCAC[C/T]GGTTCCCACAATTGC	25909
rs151269714	in-del	-/TACTGA	0.0755793	0.179102	downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838902	CATTGTTTACCTTAC[-/TACTGA]TACTAAGTATCTTTC	25909
rs151285382	snp	A/G	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246914724	TGAACTTTTGAAAGT[A/G]TCTATCGCTACTCCC	25909
rs151288253	snp	A/G	0.00755907	0.0610114	intron-variant	AHCTF1	GRCh38.p7	1:246897623	ACTGTGCTGAATACT[A/G]TAAGCAACTGTAACA	25909
rs151296376	snp	C/T	9.90949e-05	0.0070383	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246899468	CCTTCTGAAAGCCAG[C/T]ACAAGTTAAATGAAC	25909
rs151336952	snp	A/G/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246920824	GGCACGGTGCCTCAC[A/G/T]CCTATAATCCCAGCA	25909
rs180712612	snp	A/G	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246918658	GGGCGACAGAGCAAA[A/G]TCCAGTCTTAAAAAC	25909
rs180729263	snp	C/T	0.0596104	0.162024	intron-variant	AHCTF1	GRCh38.p7	1:246930005	TGCAGTGAGCCAAGA[C/T]TGTGCCACTGCACTC	25909
rs180970667	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246896613	GCATAGAACTTTCTT[C/T]AGAAGTAATAAAAAT	25909
rs180975219	snp	A/G	0.00398564	0.0444627	intron-variant	AHCTF1	GRCh38.p7	1:246878381	CAGCCTGGCAGACAG[A/G]GCAAGATTCTGTCTC	25909
rs181009716	snp	A/C	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246842871	TAGAGCCAAACACTG[A/C]TGAATTCAAACTCGC	25909
rs181022038	snp	C/T	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246861791	CTTAGCCAATGGCCC[C/T]AGTGTTTCTTTCAGA	25909
rs181049550	snp	C/T			intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842454	AGGTGTGGTGGTGGG[C/T]ACCTGTAGTCCCAGC	25909
rs181151873	snp	G/T	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246877862	ATTTAAATGAAGGAG[G/T]GTTTCTTACACAGAA	25909
rs181167824	snp	A/G/T	8.2485e-05	0.00642157	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861089	TAAGGTAGTCTCATC[A/G/T]GATGTGATTGAAACA	25909
rs181168192	snp	G/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246896172	GGCGGTTTCTCAGTA[G/T]GCTAAACATAGACTT	25909
rs181204573	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246873083	GCCCTCAGATCAGGC[A/G]CTACTAGGTTCGACT	25909
rs181212014	snp	A/G	0.000149911	0.0086564	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900099	ATTAAAAAACTGCTC[A/G]GGAGGTGGATATGAA	25909
rs181213354	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246858633	AGGAGTTCGAGACCA[A/G]CCTGGCCAACATGGT	25909
rs181213986	snp	A/C	0.00755907	0.0610114	intron-variant	AHCTF1	GRCh38.p7	1:246924208	GTGTTTAACTTTAAA[A/C]AATTTATAAAGAAAT	25909
rs181218878	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246892021	CACTCAAAAGAATTA[C/T]TCTATTCATTATGAG	25909
rs181257988	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246929932	TGGCGTGCGCCTGTA[A/G]TCCCAGCTACTCAGG	25909
rs181261627	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839717	TAATCAATTATTAAT[A/G]GTCCATTCATTACAC	25909
rs181264158	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246852152	CATTTTCCCACTCCC[C/G]AAACATTCAGTGAGA	25909
rs181264780	snp	A/G	0.0217236	0.101931	intron-variant	AHCTF1	GRCh38.p7	1:246869091	CCTCGTGATCCGCCC[A/G]CCTTGGCCTCCCAAA	25909
rs181270182	snp	C/T	0.00478085	0.0486577	intron-variant	AHCTF1	GRCh38.p7	1:246906906	TTATTAAGCTGTTAC[C/T]TTACACAGATGATGA	25909
rs181304177	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246912742	TTCTATTTTAGGATG[C/T]TATTTTGTGAGAAAG	25909
rs181308771	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246886663	ATGGACACAGAGGGC[C/T]GATGGTATACAAGAG	25909
rs181337564	snp	C/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246916049	ATTGTAAATGTTGCG[C/G]GTCAGTGAAATTTCA	25909
rs181351945	snp	A/C	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246846685	AGATGAAATGCCAAT[A/C]TGAAAAAAAAAGAAA	25909
rs181358439	snp	A/G	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246881406	AATTATTCAGGACAC[A/G]GAAAGATTAAAACCA	25909
rs181398266	snp	A/G	0.0174175	0.0916809	intron-variant	AHCTF1	GRCh38.p7	1:246927095	AGGAGGGAGAATGGC[A/G]TGAACCCGGGAGGCG	25909
rs181469028	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246866793	CAATCACAATTTCAT[C/G]TTGGATACAAAACTT	25909
rs181484078	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246901741	GAGAATTGGTTGAGC[A/C]CAGAAGGTCAAGGCT	25909
rs181492346	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246882601	ATCATTATCCAACCT[C/G]AGTTAAAAGGACAGC	25909
rs181492771	snp	C/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246921511	AATGCAGCACAAAGG[C/G]ATGAGTAGTTTTAAA	25909
rs181522177	snp	A/C/T	0.035	0.128084	intron-variant	AHCTF1	GRCh38.p7	1:246926990	CCATCCTGGCTAACA[A/C/T]GGTGAAATCCCGTCT	25909
rs181712276	snp	C/T	0.00716266	0.059414	intron-variant	AHCTF1	GRCh38.p7	1:246868285	AGGAATGTGCCACCA[C/T]GCTAATTTTTGTATT	25909
rs181717914	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246847451	AATGGTGATTCTTTC[A/G]ATGGCTGGATTATAT	25909
rs181820068	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246927564	CACATGAAACACCTA[C/T]GTTCAGTACTGTACA	25909
rs181830472	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246856518	ACTAGTTAGCCAAGA[C/T]AGTGAATATGCACCC	25909
rs181863748	snp	C/T	0.00517822	0.0506191	intron-variant	AHCTF1	GRCh38.p7	1:246893369	TCTACTAAGAATAAC[C/T]TAACTTACATTGTGA	25909
rs181867609	snp	A/C	0.00318978	0.0398085	intron-variant	AHCTF1	GRCh38.p7	1:246890826	GAAAAGAAGGTTAAG[A/C]ATAAATTAAATTAAG	25909
rs181903693	snp	A/G	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246846908	AGGTGCAGCCACCAC[A/G]TGCCCAAATCATTAA	25909
rs181928886	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246885944	GTAATCTCCGCACTT[C/T]GGGAGGCCAAGACAA	25909
rs181934968	snp	C/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246923567	ATGGTAAAAAGCTAT[C/T]TGGATATTTCAATTC	25909
rs181937950	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246906524	GAAGTGGAGGTTGCA[A/G]TGAGCCAAGATCGTG	25909
rs181990187	snp	A/G	0.00557542	0.0525036	intron-variant	AHCTF1	GRCh38.p7	1:246869026	ACTTTTTCTATTTTT[A/G]GTAGAGACGGGGTTT	25909
rs182073822	snp	A/G	0.000581693	0.0170443	intron-variant	AHCTF1	GRCh38.p7	1:246867850	TTAAGTGCATCTCTA[A/G]CAAACGGGAATTTAA	25909
rs182082990	snp	A/G	0.0123036	0.0774623	intron-variant	AHCTF1	GRCh38.p7	1:246901355	AAAAAAACAAAAACA[A/G]GCCAGGTGCGGTGGC	25909
rs182086025	snp	C/T	0.00318978	0.0398085	intron-variant	AHCTF1	GRCh38.p7	1:246869421	GCCAGTTAGCCAAGT[C/T]GTAAATGCAAAAAAG	25909
rs182092266	snp	A/G	0.0119091	0.0762411	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932013	GAGGGGAGAACCGGC[A/G]GGAGATCGCGGCTGC	25909
rs182105118	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838757	TTCTATCTACATCTA[A/G]GAAGCCTTCAAGATC	25909
rs182116179	snp	A/G	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246872257	AATAATACTCAGATC[A/G]GGCTCCCTTGTGACT	25909
rs182119624	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246911645	TGCGCCACCACACCT[A/G]GCTAATTTTATATTT	25909
rs182142878	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246878784	ACTTTTGTTGTTCTG[G/T]AACTAGAGTATTTCC	25909
rs182169249	snp	C/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246919009	ATATCTTTTGCAGGA[C/T]AGAAATAATATAGGC	25909
rs182170969	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246919895	ATGCCTGTAACACCA[A/C]TTTGGGAGGCCAAGG	25909
rs182359090	snp	C/T	0.0566069	0.158427	intron-variant	AHCTF1	GRCh38.p7	1:246882142	AGCTGGGACTACAGG[C/T]GTGCACCACCTCGCC	25909
rs182396126	snp	A/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246921278	TTTGAGAGAGAAAGC[A/G]GAAGAATATACGAGG	25909
rs182419335	snp	A/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246862269	GCGGATCACCAGGTC[A/G]GGAGATCGAGACCAT	25909
rs182425396	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246896876	GAGGGAATTACATAA[C/T]GGTCCACAAAACCTA	25909
rs182432605	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246930658	GTTCAAGCGATCCTC[A/C]CGCCTCAGCCTCTCA	25909
rs182436998	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246863307	AATGGGGAGGGGTGA[A/G]GGAGAAATAAAGCTT	25909
rs182444981	snp	A/G/T	4.9504e-05	0.00497493	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246888190	ACAATAGAGTGTTTG[A/G/T]CTGCTTCAGTAACGC	25909
rs182446433	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246924815	AAGTCATCAAAAGTA[G/T]AAGTTTGCTTTTTAT	25909
rs182467447	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246897543	ACACAAACTTAGATG[A/G]TGTAGTCAACTACAT	25909
rs182584442	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246896976	GTCTGCTACTAACAT[C/T]ATTACCTATAGTTTA	25909
rs182595360	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246878928	ATCATTGTAACTTGG[A/G]TGTAGAAGAGTGTTC	25909
rs182659630	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246845347	ACACAGTAGGTGTAT[A/T]TATAAGCATATGATT	25909
rs182664647	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246862646	TATACGTAAGTCTAC[A/G]AAACATAAAACTGCA	25909
rs182676473	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246844870	AATATAATTACAGAC[A/G]AGCACAGTTCAGTTT	25909
rs182678161	snp	A/C	0.000951873	0.0217952	intron-variant	AHCTF1	GRCh38.p7	1:246907506	GTACAAGCTATATGC[A/C]AAAAAACTACCTATA	25909
rs182698462	snp	C/T	0.00597247	0.0543191	intron-variant	AHCTF1	GRCh38.p7	1:246879742	CTGAGGCAGGAAAAT[C/T]GGCTTGAACCCAGGA	25909
rs182702045	snp	C/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246859864	CAGCCTGAACATTTA[C/T]TTTCATTGTCCAGTG	25909
rs182712900	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246875605	ACTTCACTGTGTCAT[C/T]GTAAGAAACTGTCAC	25909
rs182714808	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246841073	GCTTCCCAACATGTT[A/G]AGAAAAACCTTAGGG	25909
rs182716933	snp	A/G	0.0111196	0.0737302	intron-variant	AHCTF1	GRCh38.p7	1:246922794	GAGACCATCCTGGAT[A/G]ACACGGTGAAACCCT	25909
rs182718588	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246903342	TAATGCTTGATATGT[C/T]AGAGCAACAAAGTGG	25909
rs182792508	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246884079	AAATGAAAAAAAAAT[G/T]TATATGCTGGTTTCC	25909
rs182811610	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246894117	GCTGAGGCAGGAGGA[C/T]GACTTGGGCTCAAAA	25909
rs182814086	snp	A/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246922092	GGGCTGGGCACAGTG[A/G]CTCACGCCTGTAATC	25909
rs182826139	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246913890	TCCTAAGAGTAAAAA[C/T]TAATCATTCCAGAAA	25909
rs182906051	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246870262	TAGCCTGGGCGACAT[A/G]GTGAGGCCCTCTCTA	25909
rs182909280	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246909715	ATAAGGAAAAATCAT[A/G]ATGTGTGCAGGGTTC	25909
rs183003094	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246848033	AAAACATAGGTCTAA[A/C]CACACTTTTCTAACA	25909
rs183038891	snp	C/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246882815	GCCACAGTTGTGATG[C/G]TATGTCCATATATAT	25909
rs183160573	snp	C/G	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246868747	GAAAGGCTTACATTT[C/G]TTGGGTTACAGAGCA	25909
rs183185973	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246889615	TTAAAGTACTGATTC[A/C]CAGGTGATTCAGGTG	25909
rs183189293	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246853685	TCTGGGCTTTGATAC[A/C]ACTAGGATAAAGAAT	25909
rs183221658	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246848533	TATAAGGTCCTGAAC[A/T]GCTTTGCTGAAATTC	25909
rs183225743	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246925809	GTTTAAAGCCAGGCA[C/T]GGTGGCTCCCAGCAC	25909
rs183236322	snp	C/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246873830	TCCCCTCCACAAAAA[C/T]GTTCCCTGTGTCACC	25909
rs183267333	snp	C/T	0.00438332	0.0466095	intron-variant	AHCTF1	GRCh38.p7	1:246869781	ACCCAGGAGCCCTGA[C/T]GATGTACAGGGAGAC	25909
rs183277579	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246852964	TTTTTTGAACCCATA[C/T]TTTTATAAATAAGTT	25909
rs183278800	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246889114	TACCATAAAGCCCAG[C/T]GTAGTGAAAATAATG	25909
rs183286893	snp	C/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246868400	TGCTGGGATTACAGG[C/T]GTGAGCCACTGCGCC	25909
rs183315071	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246902419	AATTCCGTTAATTAC[C/T]ATTCCAATTTTCTGA	25909
rs183317877	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246893815	TAGTAAATTAAACTC[C/T]TAAGACCAAAAGACA	25909
rs183319280	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246927873	CTGGGCGCGGTAGCG[C/T]GCTGTAGTCCCAGCT	25909
rs183420176	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246925259	TCCATGATCCCTATA[C/T]TTCAATCAAAATCAT	25909
rs183426083	snp	G/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246908683	ACAAGGTCAGGAGAT[G/T]GAGACCATCCTGGCT	25909
rs183433112	snp	A/G	0.00636936	0.0560724	intron-variant	AHCTF1	GRCh38.p7	1:246928091	TGGATCACGAGGTCA[A/G]GAGATCGAGACCATC	25909
rs183540050	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840120	AAGGTTGCAAGTGAG[C/T]AGTGAACCGGTCAAT	25909
rs183542698	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246874423	AACTTGCTAAACCTT[C/T]TGACTTATCTGTCCC	25909
rs183602106	snp	A/G	0.000247519	0.011122	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246889994	CAAACTTCTGTCGAC[A/G]ACTGGTGTAGTAGTT	25909
rs183618308	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246910171	CGAAAATGATACCAC[A/T]TGAAAGCACAGTTAA	25909
rs183686187	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246870717	CTAAAAGAGGGTATA[A/T]AACCTCAAAAAAAAA	25909
rs183691939	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246855327	GCTCATTGGATTAAA[A/C]AAAAAATTCCATATA	25909
rs183784916	snp	C/T	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246903154	AAACCCGTTTCTATA[C/T]GCCTCCAACATTAGG	25909
rs183822958	snp	C/G	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839953	AAACCTGAATATTAA[C/G]GGATTTCTGTGGTTC	25909
rs183850010	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246928640	AGATACTAAAAACAG[A/C]ATACTATAAATCAGT	25909
rs183853630	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246885925	GGCACGGTGGCTCAC[A/G]CCTGTAATCTCCGCA	25909
rs183898548	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246846470	TTCATTCTAGGAGGA[A/G]GAAACAAGGCTCATA	25909
rs183915973	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246866267	AACTTCTATTATTGC[C/T]CCCCGCAACCTCAGA	25909
rs183923158	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246899671	TTCATCCTAAGAATA[A/G]ATAACAAACCTATTA	25909
rs183940591	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246881209	ATTAACAAGTATTCA[A/T]AATAAAGAAGGTTAC	25909
rs183980650	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246882998	GAGTCCAAAGATTTT[A/G]CTCTTAACATCTTTG	25909
rs183993127	snp	A/C/T	0.0182236	0.0938726	intron-variant	AHCTF1	GRCh38.p7	1:246922753	TTTGGGAGGCCAAGG[A/C/T]GGGCGGATCACGAGG	25909
rs184044269	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246859119	TGCTATTTATGGGCA[C/T]GGTCCTAAAGTTCTT	25909
rs184092347	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246916630	CTGCACTCCAGCCTG[C/T]GTGACAGAGCAAGAC	25909
rs184099934	snp	C/T	0.00755907	0.0610114	intron-variant	AHCTF1	GRCh38.p7	1:246867025	AACTTCACTCCTGTC[C/T]ACTAAGCAGTCTGAA	25909
rs184101022	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246929938	GCGCCTGTAATCCCA[A/G]CTACTCAGGAGGCTG	25909
rs184125630	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246926274	TCCTTTATAGCAACA[C/T]AGGCTAACGTATTTC	25909
rs184136551	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246900536	ATCACCTCAACAGAA[C/T]TATAGCAAGATTTTC	25909
rs184154525	snp	A/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246861370	TAAGCTACCCATCCC[A/T]ATCATACCCATACTT	25909
rs184155920	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246896245	AGAAACAAAAATACA[C/T]GCCCAAACAAAAATT	25909
rs184166984	snp	A/G	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246878301	ATTCAGTAGGCTAAG[A/G]TGGGAGGATTGCTTG	25909
rs184229649	snp	C/T			intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842236	GCTTAATTTCCTTTT[C/T]GTAAAATTAAGGGTC	25909
rs184229946	snp	A/G	0.00318978	0.0398085	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932634	TTCTAGCATCCTCCT[A/G]TGCTTTCATGGCCAA	25909
rs184231153	snp	A/G	0.00835141	0.0640778	intron-variant	AHCTF1	GRCh38.p7	1:246868876	TTGAGATGGAGTCTC[A/G]CTCTGTCACCCAGGT	25909
rs184240348	snp	A/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246849461	CTCAAACTTTGAAAC[A/G]TGAAACCTTTAAACT	25909
rs184265555	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246846706	AAAAAAGAAATATTA[C/T]GTTTAAGATTTTGAA	25909
rs184265883	snp	A/T	0.0325976	0.123435	intron-variant	AHCTF1	GRCh38.p7	1:246881531	GTCTTACCAAAAAAA[A/T]TTTTTTTAAATAGAA	25909
rs184289545	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246921160	TGACATTTATATAAG[C/G]TTAAAAAGACACGCA	25909
rs184383099	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246920642	GAGCGTGGTGGCGGG[C/T]GCCTGTAGTTCCAGC	25909
rs184398832	snp	A/G	0.00874735	0.0655527	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933334	AGACAGGGTTTCACC[A/G]TGTTGGCCAGGATGG	25909
rs184401387	snp	C/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246905270	TTTGGGAGGCTGAGG[C/T]GGGCAGATCATGAGG	25909
rs184538425	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246923392	TGCACTCCAGCCTAG[C/G]TGACAGCAAGACTCT	25909
rs184736382	snp	A/C	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246846095	CGATATATGAATGTC[A/C]TGTATCTAGTATGGC	25909
rs184839925	snp	C/T	0.0158469	0.0875917	intron-variant	AHCTF1	GRCh38.p7	1:246894917	CCACACCACGGAGCA[C/T]GTCATTTCAGGTAAT	25909
rs184854150	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246914470	CAGTATACAAAACAT[C/T]ACTCAGTGTTTCTAA	25909
rs184863324	snp	A/G	0.00170055	0.0291099	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850274	TTTTCAGAAGCATCT[A/G]AATTAGTACTTCTCA	25909
rs184882761	snp	A/G	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839739	TCATTACACACTATC[A/G]ATTACCTGTTATAAA	25909
rs184910478	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246873429	TACTAGAGACAATAC[A/G]CTAGTCAATTTCTCC	25909
rs184922441	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246892724	GCACTCTCAAACTCC[C/T]GGGCTCAAGTGTTCC	25909
rs184938859	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246885070	CAATTTGGCGCCCCT[C/T]CCTTTTATTCAAGGT	25909
rs184991582	snp	A/G	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246895602	AAGAAGGTAGGTATG[A/G]CTGTAACGGCAGCAT	25909
rs184999493	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246929879	CAATATGGTGAAACC[C/T]CGTCTCTACTAAAAA	25909
rs185020099	snp	C/T	0.00478085	0.0486577	intron-variant	AHCTF1	GRCh38.p7	1:246926949	GGAGGCTAAGGCGGG[C/T]GGATCACGAGGTCAG	25909
rs185036978	snp	C/T	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246927156	GCACTCCAGCCTGGG[C/T]GACAGAGCGAGACTC	25909
rs185038690	snp	A/G	0.0134861	0.0810011	intron-variant	AHCTF1	GRCh38.p7	1:246912835	AACAATATGCCAAGA[A/G]CACTATGTTAGATCC	25909
rs185059329	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246860809	ACAGTACCTGGCTAG[A/G]ATGCTTTTCTTATGG	25909
rs185069810	snp	A/G	0.000186651	0.00965871	intron-variant	AHCTF1	GRCh38.p7	1:246904059	AATTAACGAAGACAC[A/G]CTAAATATATTAATA	25909
rs185087376	snp	C/T	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876971	ATTAATCTTCAGAGT[C/T]TGGTTCAGCTTCAAG	25909
rs185088150	snp	C/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246890778	ACTGTGTGTCAGGCA[C/T]AGGATGAAGATACAA	25909
rs185088223	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246907815	ACAGCATTAAAAGCA[A/G]ATATGTCATCCATTA	25909
rs185111717	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246910672	ATTAATATAACCACT[A/G]TGCAAGAGCAGATTC	25909
rs185115457	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246915681	ACCAAGTTCAATTTA[C/T]TCATCCTGGGAATCT	25909
rs185139212	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246852597	CAAGGATGCATGGGG[C/T]GGGGGTGTCAATCCT	25909
rs185156779	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869482	GTGAACACATGAATG[A/G]AGAAGTCAATGCCTG	25909
rs185156945	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246918893	CAGAAAAAAGAAAAA[C/G]TGATTGGTGTCTTTT	25909
rs185164100	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246930071	AAAAAAAAAGATGTA[G/T]CTGTACCTATGAAAA	25909
rs185168576	snp	C/T	0.00557542	0.0525036	intron-variant	AHCTF1	GRCh38.p7	1:246888288	CAGTCATTCATTCAT[C/T]CATGCTTCTTGTTTT	25909
rs185236694	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246912220	TGGTGGCTCACACCT[A/G]TAATCCCAGCACTTG	25909
rs185360018	snp	A/G	0.00597247	0.0543191	intron-variant	AHCTF1	GRCh38.p7	1:246927020	TCTACTAAAAATACA[A/G]AAACAAAATTAGCAG	25909
rs185481876	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246841700	AGGTAAACCATCCCA[C/T]TTCCCTTTCCTACTT	25909
rs185492707	snp	C/T	0.00517822	0.0506191	intron-variant	AHCTF1	GRCh38.p7	1:246876364	TTTTATCAATCCTTA[C/T]CCATCAATAAATTCC	25909
rs185593558	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246859946	AATTATAGAAACTTA[A/G]AACTGGTGGATAAGT	25909
rs185625524	snp	A/T	0.000399281	0.0141238	intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842589	TCTGTCTCAAAAAAA[A/T]TAAATAAAAATAAAA	25909
rs185705768	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246880846	TTCTCTTGCTTCCTA[C/T]AGAAGACAATAATGA	25909
rs185736704	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246920498	TTAAACCAGCCGGGC[A/G]TGGTGGCTCACGCCT	25909
rs185852705	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246898032	AGTTATGGCCTATTG[A/G]GTATTAGGAATAGGA	25909
rs185871975	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246871721	TGCATTTTTTTTTGA[A/G]GCCTCCTGACTGCAG	25909
rs185910751	snp	A/C/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246869056	TCACCATGTTGGCCA[A/C/G]GATGGTCTCGATCTC	25909
rs185922053	snp	A/G	0.0715223	0.175059	intron-variant	AHCTF1	GRCh38.p7	1:246862353	GGCGGGGTGGCGGGC[A/G]CCTGTAGTCCCAGCT	25909
rs185924135	snp	G/T	0.00517822	0.0506191	intron-variant	AHCTF1	GRCh38.p7	1:246886113	AGGTGGGCAGATCAG[G/T]TGAGGTCAGGAGTTC	25909
rs185927135	snp	C/T	1.65581e-05	0.00287728	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902544	ATTCACGCCTTCCTC[C/T]CTGTCACCATGAGAT	25909
rs185939446	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246924023	GCAAAAGAGAGATCC[A/G]AGGTACAAGTCATTA	25909
rs185941658	snp	A/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246844267	GAGGGAAAGCATTAA[A/T]CCTATATGTAACCTG	25909
rs185947811	snp	C/G	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246906565	CCAGCCTGGGCAACA[C/G]AGTGAGACCCCACCC	25909
rs186019261	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246842977	ATTCCTACAATTCAA[C/T]TAATCTCCAAGTTAT	25909
rs186023684	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246878446	TGAAACAATGAATTA[C/T]GATGTAGCCCTATAT	25909
rs186037126	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246882906	ATGAGGAAACTCAGG[C/T]TCAGAGAGGATAACT	25909
rs186065934	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246922419	AACAGTATTCTGTTG[C/T]GGTTTTTTGGGTTGT	25909
rs186087215	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246924924	CAAAACCCTCATGAG[A/G]GTCCTATACTCAAGC	25909
rs186156007	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246861910	ACTTGTCAGAGCTAA[C/T]ACATTCTTATTAAAA	25909
rs186159570	snp	C/T	0.0513262	0.151752	intron-variant	AHCTF1	GRCh38.p7	1:246868340	TGGCCAGGCTGGTCT[C/T]GAACTCCTGACCTCA	25909
rs186170215	snp	C/T	0.0174175	0.0916809	intron-variant	AHCTF1	GRCh38.p7	1:246896738	ATATCTCAATAAAGC[C/T]GATATTTTGAAAATC	25909
rs186176782	snp	C/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246882634	AATAAACCCACCTAA[C/G]AAAGAGGAAAAATTA	25909
rs186183900	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246922045	TGGTATATTTTAGAC[A/T]TTGTTACATATCCAT	25909
rs186187248	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246902281	TTCAGACTAGGGATC[A/G]CCTGTTTTGAGAACT	25909
rs186278955	snp	A/C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839224	ATGATCTACATTCAC[A/C/G]GAGGGGGGAAAAAAA	25909
rs186397371	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246913013	TACTTGAGAACATAT[G/T]AACACCTGATCAACA	25909
rs186414551	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246927648	AAAGTAATTTACTAA[C/G]TTTCAATTCCTTTCC	25909
rs186442971	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246857482	TCTGCCTCAATTTAC[C/T]GTGTCTCTGTATATT	25909
rs186471654	snp	A/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246887767	AACATTAGCACAAAA[A/T]TATTATCACAAAGAC	25909
rs186494073	snp	C/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246924382	ATTCACAAAACATTA[C/G]TGCCGTTTATTTTTG	25909
rs186523367	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246852255	ACTAAAAGAACTGGA[A/G]CTTTACTCATCTATT	25909
rs186590574	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246882243	ACCTCGTGATCCACC[C/T]GCCTCAGCCTCCCAA	25909
rs186593933	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246847280	GGTAACAACAGCCAA[A/T]CTCCATCTCAAAAAA	25909
rs186595371	snp	C/T	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246868100	CCCAAGTAGATGGGA[C/T]TACAGGCATGGCCAC	25909
rs186674151	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246869116	CCCAAAGTGCTGGAT[G/T]ACAGGCGTGAGCCAC	25909
rs186689763	snp	C/T	0.00835141	0.0640778	intron-variant	AHCTF1	GRCh38.p7	1:246907411	AATGCCATGAAAAAT[C/T]AGTCATCTCAATCAT	25909
rs186693546	snp	A/G	0.00517822	0.0506191	intron-variant	AHCTF1	GRCh38.p7	1:246928235	ATGAACCCGGGAGGC[A/G]GACCTGGCAGTGAGC	25909
rs186711914	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246896960	GGGACAAAACAGAAA[C/T]GTCTGCTACTAACAT	25909
rs186720154	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246930901	CAGATAGTATGAACC[C/T]CGTAAGCTTTGAGAA	25909
rs186748646	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246859922	AGAATGAAATTCTTA[A/T]TTTCTGAGAATTATA	25909
rs186759246	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246875678	AGCCATCAACATTGA[G/T]ACAAGATCCTTTATT	25909
rs186766834	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246841499	ATAAAATGCATTCAC[A/G]TGTGCTTTTATTGAA	25909
rs186771516	snp	C/G/T	0.000610833	0.0174657	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851330	AACTGTTGGTCAATA[C/G/T]TATCAAAATTGTACT	25909
rs186777873	snp	A/G	0.00636936	0.0560724	intron-variant	AHCTF1	GRCh38.p7	1:246894443	GCCGAGCGTAGTGGC[A/G]GGCAGGAGAATGGCG	25909
rs186792622	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246914184	TTTCCTTCAGTTTCC[C/T]ATTAATTCATAAAAA	25909
rs186810407	snp	G/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246872438	CACAAAAAGACAAAT[G/T]AGGTGGTCAGAGCTT	25909
rs186815694	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246878828	GGCTTATACAGGCCA[A/G]CAACTCAAGAAGTAC	25909
rs186818267	snp	C/G			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932359	GGACTCTCTTGTCAC[C/G]TAATCGTGTGGCCCT	25909
rs186829124	snp	A/G	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246926781	GAATCACTTGAACCC[A/G]GGAGGCGGAGATTGC	25909
rs186937330	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246919221	AGCCTAGGACAAAGA[C/G]AACTAATAAGCTCAT	25909
rs187039849	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246931832	TGCAGACCGCTCAGC[A/G]GCTAAAACGCAGTCG	25909
rs187040324	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246891279	CTCCAAAATGCTAAA[A/G]TAAGTAAGTCACTCC	25909
rs187265771	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246862966	AACAAATTACTGAAT[C/T]CCATTAGATCATAAT	25909
rs187287311	snp	C/G	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246845047	AACAATGTGTGGCAG[C/G]GTAGGTGGTAAGTGC	25909
rs187290811	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246897080	GCACTTTGGGAGGCC[A/G]AGGAGGGCAGATCAC	25909
rs187301522	snp	C/T	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246878991	TCATTTTTCCCTAAA[C/T]CAAAATCTAGAAACG	25909
rs187305429	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246919777	GCTCCAAGCAATCCA[C/T]GGAAACAACCACATA	25909
rs187323713	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246893505	ACAGTGCAACTGTAT[A/C]CCTACTAGTACTTTT	25909
rs187328040	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246859202	TTCAGTGGACTCTCA[C/T]CTTAAACTACTTAAG	25909
rs187329758	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246921441	AATACTCAACAAAAA[C/T]AAACTCAAAGGATAA	25909
rs187334222	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246846267	TATAGTATACCTATA[A/C]CCAGTCTTCTCGGCA	25909
rs187342418	snp	C/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246889209	ATTCCTTCACTCGAA[C/T]ATCTATTGCTGAGTG	25909
rs187348029	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246881053	TATGCATTATGAAAT[A/G]CACGGTGGAGACCAC	25909
rs187354153	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246864982	CAACTTTAAGATTCT[A/G]CTACAAGGTTTTCCG	25909
rs187355551	snp	A/G	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246909009	ACAGTTTCACTCTCC[A/G]ATTTCCGTTACCTGT	25909
rs187362828	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246925320	AATCCAAAGTCCAAA[G/T]GATAACACACAAAAA	25909
rs187393305	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246884363	TGTAGATCTTACCCT[C/T]TTATCCGTAGAAGTA	25909
rs187399426	snp	A/T	0.0232847	0.105357	intron-variant	AHCTF1	GRCh38.p7	1:246922797	ACCATCCTGGATAAC[A/T]CGGTGAAACCCTGTC	25909
rs187401056	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246903539	TTCAATATAAGAATC[C/G]CTTTTCACAGCCAGG	25909
rs187566134	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868499	GCCTCAAGTGATCCT[C/T]CCTCCTCGGCCTCTC	25909
rs187579199	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246901408	TGGGGAGGCCGAGGC[A/G]GGTGGATCATGAGGT	25909
rs187592476	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840674	GAGTTACTTTACTTA[C/T]TGAAGACCTTCTGTT	25909
rs187596244	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246873961	AACACAGACTTACTA[C/T]GCTGACATAAGATCT	25909
rs187599383	snp	C/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246880486	GGAGAATCACTTGAA[C/T]CCGGGAGGTGGAGGT	25909
rs187607280	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246920004	ATAAATTAGCCGGGC[A/G]TGGAGGCATACGCTT	25909
rs187662148	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246845379	TTAAAAAAAAGAAAA[A/G]TAGAGTTGATATCAG	25909
rs187665741	snp	A/G	0	0	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839991	AGCTCCTTCACAGCA[A/G]TATTATAAAAATTTG	25909
rs187705607	snp	A/G	0.00557542	0.0525036	intron-variant	AHCTF1	GRCh38.p7	1:246848257	ATTATTTGGCCCCCC[A/G]GGCTGGAATACAGTG	25909
rs187782843	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246929623	GTTAACATATGAGGA[C/T]AGACAGTAGCATATA	25909
rs187843206	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246889685	TGTTATATGCTTTGT[A/G]ATTTTGTCACTGCAA	25909
rs187847727	snp	C/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246925924	AAAATAATTAGCCAG[C/G]TGTGGTGGCGCCTGC	25909
rs187865569	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246848588	GTCAACTACATGGCT[A/G]GGTGTGGTGGCTCAC	25909
rs187883865	snp	A/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246897824	TGTCTCTACCAAAAA[A/G]AAAAAGGGCTAAGCA	25909
rs187886155	snp	C/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246868781	AATAAAAAAGTACCA[C/T]GTGATGAATGAGTAC	25909
rs187897007	snp	C/G	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246903155	AACCCGTTTCTATAC[C/G]CCTCCAACATTAGGT	25909
rs187904910	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246883267	TGCAGCTTAACTTCT[C/T]GGACTTTTAGTTCAA	25909
rs187955343	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246863845	CGTATCAGTTATAAA[C/T]TGCTTATTTTTCTCC	25909
rs188067542	snp	C/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246896465	ACAAAAGACTTCATA[C/T]TATTTGACCCATTTA	25909
rs188072806	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246861410	TTTTTACCCAAATTC[A/T]CTCCTTAATAAAAAT	25909
rs188076710	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246878380	CCAGCCTGGCAGACA[A/G]AGCAAGATTCTGTCT	25909
rs188081396	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246917349	TGGTAACTTCTAAAT[C/T]TGAGATGTCCATCAA	25909
rs188101913	snp	A/G	0.0130921	0.0798413	intron-variant	AHCTF1	GRCh38.p7	1:246929973	AGGAGAATCGCTTGA[A/G]CCTGGGAGACGGAGG	25909
rs188119537	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246909782	TGGAATGTATCCCTC[A/G]CAGATAAGGGGGAAC	25909
rs188124954	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246854338	ACATACTTCTGGACC[C/T]AACAAGTCCATGGTT	25909
rs188287011	snp	A/G	0.000214297	0.010349	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246855788	AGATGTTAATCCTTC[A/G]TCCAACACTGGTACC	25909
rs188296183	snp	G/T	0.00438332	0.0466095	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932944	GTGCTTTTTAAATTT[G/T]TTTATTTTTGAGACA	25909
rs188299946	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246870718	TAAAAGAGGGTATAA[A/G]ACCTCAAAAAAAAAA	25909
rs188314650	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246890355	GCAAGAAATGTTCAC[C/T]ACAAATCAAAATCTA	25909
rs188329084	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246910213	GGAACATTCTATCAG[A/G]TAACTTCAGCAAGTC	25909
rs188352840	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246869845	CATTCTGTAACCCTG[A/G]ATCACAGTAATCGCA	25909
rs188370119	snp	A/G	0.00398564	0.0444627	intron-variant	AHCTF1	GRCh38.p7	1:246898396	AATAATCAAATTTAA[A/G]ATTAATTAATTACAC	25909
rs188398068	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246913120	TTTTTATAGATAGGA[A/G]GATATCTTTTATTTT	25909
rs188399805	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839402	TCATTTAACAAGTTC[A/G]TTTAAATAAGTTCAA	25909
rs188403784	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246866585	AAAATTCAGAGTCTT[G/T]TAATGATTATTTATA	25909
rs188408747	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246870276	TAGTGAGGCCCTCTC[C/T]ACAAAAAATACCCAG	25909
rs188410138	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246858518	GTGTTGTATGAAACC[C/T]CACCCACCACAAACA	25909
rs188420758	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246881342	ACATCCACCATTAGC[A/G]TCAGCAACTCTGCAT	25909
rs188425011	snp	C/G	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246920728	TGAGCCGAGATCGCA[C/G]CACTGCACTCCAGCC	25909
rs188434258	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246899848	TAATTCCTTTATAAA[A/G]CATATAAATACTAAA	25909
rs188448163	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933868	AGGTATTGGACCAAG[C/T]TGTGATAGAAACAGT	25909
rs188468889	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246874826	TAAAAAGTTACAAAA[A/C]AACCTGACCTCCGGC	25909
rs188573798	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246920526	CCTGTAACCCCAGCA[A/C]TTTGGGAGGCTGAGG	25909
rs188627042	snp	A/G	5.09628e-05	0.00504765	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853228	CCTGGTTAAGCCTGC[A/G]CTCAGAGACAATAGG	25909
rs188628781	snp	C/G/T	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246922778	ACGAGGTCAGGAGAT[C/G/T]GAGACCATCCTGGAT	25909
rs188651412	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246895041	TTTAAAAAAAAAAAG[A/G]TCAATTTTTTGAAAG	25909
rs188662158	snp	A/G	0.00597247	0.0543191	intron-variant	AHCTF1	GRCh38.p7	1:246868938	CAAGTTCTGCCTCCC[A/G]GGTTCACGCCATTCT	25909
rs188666437	snp	C/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246894024	GCCTAGGCAATATAG[C/T]GAGACCATGTCTCTA	25909
rs188674087	snp	A/G	0.00438332	0.0466095	intron-variant	AHCTF1	GRCh38.p7	1:246927908	GGGAGGCTGAGGCAG[A/G]AGAATCGCTTGAACC	25909
rs188912240	snp	C/T	0.000100299	0.00708093	intron-variant	AHCTF1	GRCh38.p7	1:246876921	TCCTTATTCTCTTAT[C/T]CCCCATAATAAGACA	25909
rs188923148	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246914582	TCAGTGAGGAGTAGC[A/G]AATCTAAGTTTACAT	25909
rs188943142	snp	A/G	0.00119737	0.0244387	intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842411	ACATGATAAAATGCC[A/G]TCTCTACTAAAAATA	25909
rs188964345	snp	A/G	0.00636936	0.0560724	intron-variant	AHCTF1	GRCh38.p7	1:246877489	AATGTCAGTAAAATG[A/G]CACGTTTAAAGAATT	25909
rs188976481	snp	A/C/T	1.64868e-05	0.00287109	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861022	TTTTGGGCTTAGAGG[A/C/T]CGTGAAAACAGTCTC	25909
rs188988862	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246911387	TTTTGCTCATCAATT[A/C]TTTTCATTTAAACTT	25909
rs188999284	snp	C/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246901700	GTGTGTGCCGGCAGT[C/T]CCAGTTACTTGGGAG	25909
rs189008391	snp	A/G	0.00478085	0.0486577	intron-variant	AHCTF1	GRCh38.p7	1:246926950	GAGGCTAAGGCGGGC[A/G]GATCACGAGGTCAGG	25909
rs189073335	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246904120	TTAGTTTGCTTGCAA[C/T]GTTGAGTGCATGTGA	25909
rs189171214	snp	A/C	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246868948	CTCCCGGGTTCACGC[A/C]ATTCTCCTGCCTCAG	25909
rs189212609	snp	A/T	0.00597247	0.0543191	intron-variant	AHCTF1	GRCh38.p7	1:246846746	CATATACATATATAT[A/T]TTTTTTGGGGGGATG	25909
rs189243217	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246906642	GAGAGTTGAGATACA[C/T]TTCCTATAAGATAAA	25909
rs189251390	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246924152	ACTATCAAACTGAAA[C/T]CTGTGGTAAAATAAC	25909
rs189341214	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246921277	ATTTGAGAGAGAAAG[C/T]GGAAGAATATACGAG	25909
rs189350958	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246885938	ACGCCTGTAATCTCC[A/G]CACTTTGGGAGGCCA	25909
rs189357861	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246923491	ATATAGGCTAGTAAT[A/G]GACAAACAGGTCAAC	25909
rs189364695	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246905998	GTGGATGCATTCATG[C/T]CTGTGTAAACTGGTC	25909
rs189375706	snp	A/C/T			intron-variant	AHCTF1	GRCh38.p7	1:246927034	AGAAACAAAATTAGC[A/C/T]GGGCGTGGTGACGGG	25909
rs189379174	snp	A/C	0.0126979	0.078662	intron-variant	AHCTF1	GRCh38.p7	1:246923176	TCCCAGCACTTTGGG[A/C]GGCCGAGGTGGGCAG	25909
rs189445466	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246885349	CACTGTATTTTCAAT[C/G]TGAATTTGATGCAGA	25909
rs189451209	snp	A/G	0.000115497	0.00759837	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850231	CAGCTGCTTGTCACT[A/G]GATTTATCATCTTGC	25909
rs189465346	snp	G/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246891559	TAATAATCATTAACT[G/T]CAGAATTTCCCAAGC	25909
rs189505574	snp	A/G	8.28998e-05	0.00643763	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867311	GCAGCTCTGGAGCTG[A/G]GAGCGAATACACTAT	25909
rs189614656	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246900612	ACGCATTTCTATCAT[G/T]TGTATGTAAGACCAG	25909
rs189625267	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246852308	GATGAGTATGGATAA[C/T]GATGACATTTTTATG	25909
rs189727244	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246872711	TCGCACTATCATGGG[C/T]GCTGAAAGGGAATGG	25909
rs189737862	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246912415	TTGAACACGGGAGGC[A/G]GAGGTTGCAGTGAGC	25909
rs189746436	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839872	TTTCTCCTTTTCTAC[A/G]TCTACTCACTCTCTC	25909
rs189863713	snp	C/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246873598	ATTTCTCCTGCATCA[C/T]AGCAAAGGGAAAGAA	25909
rs189878097	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246858884	ATAATGCTATGAACA[C/T]TCTTTTAACAGCTAC	25909
rs189898503	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246912866	TACATTGCTGGGTAA[C/T]TTCATATTGGCTGAT	25909
rs189899676	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246872049	AGATGAACTATTAAT[A/G]ACAAAAAAAAAAAAA	25909
rs189906202	snp	A/C	0.00478085	0.0486577	intron-variant	AHCTF1	GRCh38.p7	1:246927369	CTGCATACGCTTGTC[A/C]TCCCGACTACTTGGG	25909
rs189979929	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246846629	AAAGCAATTCAAATA[A/C]CCAACAGAAGAGGGT	25909
rs189986694	snp	A/G	0	0	downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838658	AATCCATTGTAGCCC[A/G]TTCAGGACCAGGTCT	25909
rs190017354	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246851535	ACCCTTGGCTGTGTG[C/T]CTTTTAAAACATAAA	25909
rs190050935	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246882786	CATGGTTAATTTGCA[C/T]GTAAAACAGCCACGC	25909
rs190062366	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246922057	GACTTTGTTACATAT[C/T]CATGTTGAAAACATA	25909
rs190062580	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246875368	TCCTTACTTAGAAGC[C/T]AAATAATAAAAAGTC	25909
rs190141871	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246886282	GCTGCAGTGAGACAA[C/G]ATCGTGCCACTGCAC	25909
rs190143995	snp	A/G	0.00318978	0.0398085	intron-variant	AHCTF1	GRCh38.p7	1:246890825	AGAAAAGAAGGTTAA[A/G]CATAAATTAAATTAA	25909
rs190144338	snp	A/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246915765	GGTAAAAACATTTTA[A/T]AAATTGAATAGTAAT	25909
rs190181851	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246921471	AGTAAAAAAGTAAAC[C/T]AGAAAGCCCCCAAAA	25909
rs190222228	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246856331	TTCCTTTAATATTCT[A/C]ATCTGACCTTTCTCA	25909
rs190276696	snp	A/G	0.0573587	0.15934	intron-variant	AHCTF1	GRCh38.p7	1:246869080	CGATCTCCTGACCTC[A/G]TGATCCGCCCGCCTT	25909
rs190284983	snp	G/T	0.00180009	0.0299467	intron-variant	AHCTF1	GRCh38.p7	1:246895826	TTTTACTTGTTATCA[G/T]AATCTTACCTTCTGT	25909
rs190302654	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246879314	AAAAGACATAGCATA[C/T]GGTAATTGAGAGGAG	25909
rs190307524	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246919810	CTCTGGAATCTCAAA[G/T]AATTCTTAAAGAATT	25909
rs190315672	snp	C/T	0.00755907	0.0610114	intron-variant	AHCTF1	GRCh38.p7	1:246897521	CAATCATGGTAAGAG[C/T]GTACTTACACAAACT	25909
rs190330401	snp	C/T	0.00318978	0.0398085	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246931926	CGGCCCCGCTCTGCG[C/T]ATTACCCTGCGCCGA	25909
rs190391748	snp	G/T	0.021333	0.101051	intron-variant	AHCTF1	GRCh38.p7	1:246929922	CCGGGTGTGGTGGCG[G/T]GCGCCTGTAATCCCA	25909
rs190518781	snp	A/G	0.00716266	0.059414	intron-variant	AHCTF1	GRCh38.p7	1:246860089	ATATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	25909
rs190558581	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246868283	ACAGGAATGTGCCAC[A/C]ACGCTAATTTTTGTA	25909
rs190558770	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246847286	AACAGCCAAACTCCA[C/T]CTCAAAAAAAAAAAA	25909
rs190571948	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246882352	AAGGTCAGGTACCAC[A/G]TGGATCACATTATGT	25909
rs190699404	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246869517	CAAAGGACAGGGTGA[C/T]TCTGCTGTTAGTGGT	25909
rs190711324	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246852665	TATGACTAAAAAAAC[C/T]TTTCATTTGAACCAG	25909
rs190714025	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246869225	CCATTTTTCCAACAG[C/T]GTGTACTTACTCCAC	25909
rs190717664	snp	C/T	0.0103295	0.0711199	intron-variant	AHCTF1	GRCh38.p7	1:246888293	ATTCATTCATTCATG[C/T]TTCTTGTTTTCCCAA	25909
rs190725384	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246907451	CATTAATCTACCCAC[A/C]CTTTTCTCACTATGC	25909
rs190725635	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246925200	GCAGTAGCTTTTTAC[A/G]AAGTGTATTCAGAAG	25909
rs190729662	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246908539	AAATTATTCTTTACA[C/T]TGACAGAACATAAAA	25909
rs190731597	snp	C/T	0.00438332	0.0466095	intron-variant	AHCTF1	GRCh38.p7	1:246845248	ATATAAAAATGTTTT[C/T]TGTGGGTACACAGTA	25909
rs190783816	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246841714	ACTTCCCTTTCCTAC[G/T]TTTTCTGCAAAAACC	25909
rs190787258	snp	C/T	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246862582	ATATCAATAGAAATA[C/T]TTATTCCAGATTTCT	25909
rs190797902	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246878917	TAGACGGTGGAATCA[C/T]TGTAACTTGGGTGTA	25909
rs190806283	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246844447	GAGAAAGTGCCAGGT[A/G]CAGTGGCTCACAATT	25909
rs190814904	snp	A/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246896974	ACGTCTGCTACTAAC[A/T]TTATTACCTATAGTT	25909
rs190889533	snp	C/T	0.0107246	0.0724382	intron-variant	AHCTF1	GRCh38.p7	1:246922645	GCAATCCTCCTGCCT[C/T]GGCCTCCCAAAGTGC	25909
rs190937167	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246848497	TGAGCCACCGTGACC[A/G]GCCAAGTCATCTACT	25909
rs190953927	snp	A/C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246882956	TTCACAAAGTGGCAT[A/C/T]GTTTAGATTTAAATC	25909
rs190964992	snp	A/G	0.0119091	0.0762411	intron-variant	AHCTF1	GRCh38.p7	1:246927864	AAAAATTAGCTGGGC[A/G]CGGTAGCGCGCTGTA	25909
rs190966275	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246863138	AAAAATACTATACTG[A/C]ATATTTTAAATTATT	25909
rs190979521	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246888037	TCTGAGCCCAAACAA[C/G]AGATCCTGGGTTAAC	25909
rs191013572	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246894114	GAGGCTGAGGCAGGA[G/T]GATGACTTGGGCTCA	25909
rs191021623	snp	A/G	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246927994	ACAGAGCAAGACTCC[A/G]CCACCAAAAAATTAA	25909
rs191071031	snp	C/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246868367	CTCATGTGATCCACC[C/T]GCCTTGGCCTCCCAA	25909
rs191211409	snp	G/T	0.00398564	0.0444627	intron-variant	AHCTF1	GRCh38.p7	1:246868729	AACAGTCAAATCTTC[G/T]AAGAAAGGCTTACAT	25909
rs191217193	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246902774	TTGTTCACACAATAC[A/G]AAGAAAACAATTTAG	25909
rs191269569	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246913855	CTTAAACAGCTACTC[C/T]AGGATTCTATGGCCT	25909
rs191300745	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246847810	TTACTGAGATGTTTG[C/T]TAAGCTCTAACAAAA	25909
rs191481947	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246924385	CACAAAACATTAGTG[C/T]CGTTTATTTTTGTGT	25909
rs191491397	snp	A/G	0.00478085	0.0486577	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840001	CAGCAATATTATAAA[A/G]ATTTGTTCAGACATC	25909
rs191537632	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246876253	CTGTAATTCTATATT[C/T]ACCATTTAAAATAAA	25909
rs191539806	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246914451	CCTGGCTCTTTCTCT[A/G]TATCAGTATACAAAA	25909
rs191557274	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246928416	ATTCGACAAGGTCAC[A/G]GTGCCTTTGGACTAA	25909
rs191599931	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246859936	AATTTCTGAGAATTA[C/T]AGAAACTTAAAACTG	25909
rs191616291	snp	C/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246859833	TGCTGGTATTACAGG[C/T]GTGAGCCACTTTACC	25909
rs191629276	snp	G/T	0.00500552	0.0497765	intron-variant	AHCTF1	GRCh38.p7	1:246841037	GTAAGAATAAACACA[G/T]TATGCTATAAAATAA	25909
rs191651108	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246922808	TAACACGGTGAAACC[C/T]TGTCTCTACTAAAAA	25909
rs191686839	snp	C/T	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246921009	AGGCAGGAGAATCGC[C/T]TGAACCTGGGAGAAG	25909
rs191696447	snp	G/T	0.00755907	0.0610114	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933882	GTTGTGATAGAAACA[G/T]TTAAAAAGAGTACTG	25909
rs191784203	snp	A/G	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246859232	GATGCAGATTTTTAT[A/G]TAAGTATGTAGTTTT	25909
rs191786121	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246919590	TGGTGGCACACACCT[A/G]TAGTCTCACCTACTC	25909
rs191798900	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246896840	AAAAGGAATCCCATG[A/G]ATGTAAGTTGAACAG	25909
rs191802152	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246930618	GGGTCTCGCCATGTT[C/G]CTCAGGCTGGTCTCA	25909
rs191840221	snp	C/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246870414	TGTGACAGACAAAGA[C/T]CTTGTCTCTTAAAAA	25909
rs191842864	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246855165	GATTAAATGAGTTAA[C/T]AGACACAAGATGATC	25909
rs191877319	snp	C/T	6.32798e-05	0.00562458	intron-variant	AHCTF1	GRCh38.p7	1:246862197	CATTAAAAGTGCTTA[C/T]AGGCCGGGCGCGGTG	25909
rs192004954	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246913089	CAATAAAAAAGATTT[A/T]AAAATACCTTTTTTT	25909
rs192026887	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246849219	CTTAGTAAAAAGCTA[C/T]TGGTGTTTCCCTTCA	25909
rs192092296	snp	C/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246918927	AAAATCACTTCTTCA[C/G]TAAAGGGGGAGAAAG	25909
rs192176344	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246843693	AAATAATAAACAAAA[C/T]TTAAAATCATTAAAA	25909
rs192178517	snp	G/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246878628	GTAATGATCAATCTG[G/T]CAGTTAAAATTTTTG	25909
rs192209774	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246865254	TGCCAAAGTGGCTCA[C/T]CTGAGAATAACCAGA	25909
rs192216242	snp	A/G	0.00225249	0.0334839	intron-variant	AHCTF1	GRCh38.p7	1:246899424	TCTGACTTCAGTTCA[A/G]TTAAGAAATCACTAG	25909
rs192224437	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246925478	TTTAAACTGTGGCCA[A/G]ACATGATGGCTTATG	25909
rs192224759	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246881139	GGAGTAAAGTAAAAA[C/G]ACTGGGGAAATATAC	25909
rs192235151	snp	C/T	0.0123036	0.0774623	intron-variant	AHCTF1	GRCh38.p7	1:246920580	TCGAGACCATCCTGG[C/T]TAACAAGGTGAAACC	25909
rs192282630	snp	A/G/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246846304	TCCCTATGTAAAAAC[A/G/T]AAGTTTAGAATATAA	25909
rs192356034	snp	C/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246893526	TAGTACTTTTTAGCC[C/T]TATTTTTGCACTAAC	25909
rs192374185	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246855948	TTCAGAGAATTCAAT[A/G]CAACTCAAGCTCATT	25909
rs192383171	snp	A/C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246871160	ACTTGACATGGTGGC[A/C/T]ACCAAAAGGCCCCCA	25909
rs192453653	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246885877	GCAGACTGAACTAAG[G/T]GCAGATAGAAAACAT	25909
rs192469264	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246923273	TACAAAAATTAGCTG[G/T]GCATGGTGACATGCG	25909
rs192484331	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246890591	GAAATATTAGTCAGT[A/G]ACCATATTAAAAGGA	25909
rs192499008	snp	A/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246910591	TATGGGAACTCTTGT[A/T]TTCTTCTAACTATCT	25909
rs192506408	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246926814	TCAGCCGACACTGCA[C/T]CATTGCACTCCAGCC	25909
rs192547227	snp	A/C	0.0138799	0.0821421	intron-variant	AHCTF1	GRCh38.p7	1:246868944	CTGCCTCCCGGGTTC[A/C]CGCCATTCTCCTGCC	25909
rs192556235	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246868875	TTTGAGATGGAGTCT[C/T]GCTCTGTCACCCAGG	25909
rs192568024	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246903182	AGGTTCAGAAAAGTC[A/G]GTTCTAGAGACAGGT	25909
rs192572159	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246883858	TTAGTGTTTGTTTAC[C/T]ATATGGCAAAGGTAA	25909
rs192578090	snp	A/C	0.0433465	0.140692	intron-variant	AHCTF1	GRCh38.p7	1:246922792	TCGAGACCATCCTGG[A/C]TAACACGGTGAAACC	25909
rs192744256	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246910156	TAATTTGCAGAAAAT[C/T]GAAAATGATACCACA	25909
rs192775568	snp	C/G/T	0.0418435	0.138591	intron-variant	AHCTF1	GRCh38.p7	1:246868967	CTCCTGCCTCAGCCT[C/G/T]CTGAGTAGCTGGGAC	25909
rs192780663	snp	C/T	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246905030	ACATTCAAGTAAGTC[C/T]GCACAATTTCTTCTG	25909
rs192812338	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246841615	TTTTAGTGCTTTCTG[A/T]AAAATAATTGCAGGA	25909
rs192835030	snp	C/G	0.000399281	0.0141238	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850122	TATCAAATTCTGCTT[C/G]AACAGTCAACTGAGA	25909
rs192835938	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246884393	ACATGCTATTTAACC[A/G]AAGAGAACCAAGAAA	25909
rs192955815	snp	C/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246889841	AATAAAATAGTAATG[C/G]TAATAGCAAATTCTG	25909
rs192957816	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246925934	GCCAGGTGTGGTGGC[A/G]CCTGCCTGTAGTCCC	25909
rs192996276	snp	C/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246889563	AAGCACTGGTTCCCA[C/G]AATTGCCATGCATCA	25909
rs192999096	snp	C/T	3.92249e-05	0.00442842	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853297	CAAGGACATCAGCCA[C/T]AGCTGAAAGAAAAAT	25909
rs193020663	snp	C/G	6.59315e-05	0.0057412	intron-variant	AHCTF1	GRCh38.p7	1:246863907	TGATTGTGAACGCTA[C/G]ATGCGTAAATACTAA	25909
rs193024688	snp	A/G	0.00438332	0.0466095	intron-variant	AHCTF1	GRCh38.p7	1:246897890	GGGCTGGGGTGGGAA[A/G]ATCGCTTAAGCCCAA	25909
rs193078851	snp	A/C	0.000798403	0.0199641	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932542	ATCTTGGCTCACTAC[A/C]ACCTGTGCTCCCGCT	25909
rs193112182	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246842061	GCCTCCCAAAGTGCT[C/G]GGATTACAGGCGTGA	25909
rs193119424	snp	G/T	3.33483e-05	0.00408327	intron-variant	AHCTF1	GRCh38.p7	1:246876930	TCTTATCCCCCATAA[G/T]AAGACAACTTTAATC	25909
rs193122083	snp	A/G	0.00438332	0.0466095	intron-variant	AHCTF1	GRCh38.p7	1:246915285	CAGTGAGCTGAGATC[A/G]TGCCACTGCACTCCA	25909
rs193190820	snp	C/T			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933056	TCCTCCTACCTCAGC[C/T]CTCCAAGTAGCTGGG	25909
rs193203753	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246870232	GAGGATCACTTGAGG[C/T]CATGAGTTTGAGAAT	25909
rs193205214	snp	G/T	0.00438332	0.0466095	intron-variant	AHCTF1	GRCh38.p7	1:246845656	CATGCAAAAATAGCC[G/T]CCACCATTTTTTCCA	25909
rs193211316	snp	C/T	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246880842	ACTATTCTCTTGCTT[C/T]CTACAGAAGACAATA	25909
rs193243252	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246920029	ACGCTTGTAATTCCA[G/T]CTACTCAGGAGGCTG	25909
rs193253623	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246929828	GGAGGCCAAGGCGGG[C/T]GGATCACGAGGTCAG	25909
rs193268311	snp	C/G/T	0.00795532	0.062565	intron-variant	AHCTF1	GRCh38.p7	1:246860126	TTAGCCAGTCATGGT[C/G/T]GGGGGCGACTATAGT	25909
rs193278154	snp	A/G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246895476	GGATGAATTCCTAGA[A/G/T]AATTTTGCTGAGTAA	25909
rs199542478	snp	C/T	8.25212e-05	0.00642291	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850939	ATGAATGGACTGTTC[C/T]ATTGTATCTGAAGTA	25909
rs199556608	snp	C/G	0.00226712	0.0335919	intron-variant	AHCTF1	GRCh38.p7	1:246876199	CATTCTATTAAACAT[C/G]AAAATTGGTAAAAAA	25909
rs199608908	in-del	-/GC			intron-variant	AHCTF1	GRCh38.p7	1:246860198	CTGGTTGGGGGGGGG[-/GC]GGAGGTTGCAGTGAG	25909
rs199612083	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246891484	GAAAAAATTTATGAG[-/T]TCTTTGAATAAAAAA	25909
rs199635904	snp	C/T	0.00178324	0.0298067	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246904025	TGCAAACTCAAAACA[C/T]CCCCTTCACTGAAAC	25909
rs199638572	snp	A/C	0.000153988	0.00877328	missense, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843796	CATGCATTTCTTACC[A/C]GTTCATCTTCAAGCT	25909
rs199639157	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246892810	CTAATTAAAAAAAAG[A/T]TTTTTTTTTGGTTTT	25909
rs199686540	in-del	-/TT	0.00557542	0.0525036	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839246	GGAAAAAAAGTACAC[-/TT]ATTAAAAACAGGTAC	25909
rs199694321	snp	A/G	6.66678e-05	0.00577317	intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842684	TCAAGAACAGAACAG[A/G]AAGTCATACTTGCTT	25909
rs199729275	in-del	-/CT/T			intron-variant	AHCTF1	GRCh38.p7	1:246903662	TGAGACCCCCCCCCC[-/CT/T]TCCGTCTCTGCTAAA	25909
rs199732006	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246869028	TTTTTCTATTTTTAG[C/T]AGAGACGGGGTTTCA	25909
rs199739670	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246903743	ACTCCAGAGGCTGAG[A/G]CAGAGAATTGCTTGA	25909
rs199771528	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246911210	CATATTGACTTGAAG[A/G]GAGTTTTAATTACGA	25909
rs199837370	snp	A/G/T			intron-variant	AHCTF1	GRCh38.p7	1:246904191	TTTTATAAAAATGTA[A/G/T]TCCTTTGAAATAATA	25909
rs199870359	in-del	-/A	0.00993419	0.0697739	intron-variant	AHCTF1	GRCh38.p7	1:246884068	AGGTACATGCAAATG[-/A]AAAAAAAAATTTATA	25909
rs199923661	in-del	-/A			intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842589	CTGTCTCAAAAAAAA[-/A]TAAATAAAAATAAAA	25909
rs199987898	in-del	-/ATAAATAAATAC			intron-variant	AHCTF1	GRCh38.p7	1:246923421	CTGTCCCAAAAATAA[-/ATAAATAAATAC]ATAAATAAATACATA	25909
rs200010862	snp	C/T	0.00199806	0.0315443	intron-variant	AHCTF1	GRCh38.p7	1:246855727	CAAAATTATTATACA[C/T]ACATTTATTGTCATT	25909
rs200042860	in-del	-/G	0.0737376	0.17729	intron-variant	AHCTF1	GRCh38.p7	1:246869111	GCCTCCCAAAGTGCT[-/G]GGATTACAGGCGTGA	25909
rs200059115	snp	A/T	0.43221	0.171171	intron-variant	AHCTF1	GRCh38.p7	1:246864592	AAAGACTAGACTGAC[A/T]TGGGAGGCCGAGGCG	25909
rs200085237	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246896097	GACGTGTTAAAACTG[C/G]AACTCTCATACACTG	25909
rs200147070	snp	C/T	0.000215077	0.0103678	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246891838	ACTATATTAAGATTG[C/T]TAAGAAGCAAATAGC	25909
rs200147170	in-del	-/TTAA			intron-variant	AHCTF1	GRCh38.p7	1:246899949	TAAGTTATCCATATG[-/TTAA]CTAACAGTGAGATAC	25909
rs200148859	in-del	-/GG			intron-variant	AHCTF1	GRCh38.p7	1:246910786	CTTTTTCAGAGAAGA[-/GG]GATTAGATTTTGCCA	25909
rs200165532	in-del	-/ATTT			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933152	TTTATTTATTTATTT[-/ATTT]GAGACGGAGTCTCGC	25909
rs200166495	in-del	-/TTAT			intron-variant	AHCTF1	GRCh38.p7	1:246845970	AACAACACATCTTAC[-/TTAT]TCCCTGGGTGATGTG	25909
rs200171102	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868066	CTCCTGGGTTCAAGC[A/G]ATTCTCCTGCCTCAG	25909
rs200194769	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246928227	AGAATGGCATGAACC[C/T]GGGAGGCGGACCTGG	25909
rs200231734	in-del	-/TCTT			intron-variant	AHCTF1	GRCh38.p7	1:246845964	CTCTAGAACAACACA[-/TCTT]ACTTATTCCCTGGGT	25909
rs200254086	in-del	-/AATT	0.0130921	0.0798413	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839753	CGATTACCTGTTATA[-/AATT]ATTTTACAACACTTA	25909
rs200283654	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246852394	GTTTTTTATCCAAAT[A/T]TCTATAAATAATTAG	25909
rs200284512	in-del	-/TAGAG	0.00755907	0.0610114	intron-variant	AHCTF1	GRCh38.p7	1:246913522	ATAGATTTAAGACTA[-/TAGAG]TAAATTTGCATTTGA	25909
rs200325446	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246871709	CATGCCTACAGTGCA[-/T]TTTTTTTTTGAGGCC	25909
rs200338789	snp	C/G/T	0.00067552	0.018367	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246907587	TTCCAAAGTGCTAGA[C/G/T]AGCCATCAGAAAAAC	25909
rs200355866	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246875045	AGGCCAACAACTTAT[G/T]TTATAGATAAACCAG	25909
rs200363705	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246920582	GAGACCATCCTGGCT[A/G]ACAAGGTGAAACCCT	25909
rs200512569	snp	C/T	0.0039921	0.0444985	intron-variant	AHCTF1	GRCh38.p7	1:246930947	TCTCAAAACAAAACA[C/T]CCAAACCAAAACAGT	25909
rs200513694	in-del	-/G	0.0596104	0.162024	intron-variant	AHCTF1	GRCh38.p7	1:246922435	GTTTTTTGGGTTGTT[-/G]TTTTTTTTTTGACAG	25909
rs200537262	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246908323	AAATTCACAGGGATA[A/C]AAAAAAAAAAAAAAA	25909
rs200562886	in-del	-/C			intron-variant	AHCTF1	GRCh38.p7	1:246860199	TGGTTGGGGGGGGGG[-/C]GGAGGTTGCAGTGAG	25909
rs200582408	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246883729	CATTTTGAGTGGTTG[G/T]TTTTATTTCTGTATT	25909
rs200604228	in-del	-/A	0.0225045	0.103662	intron-variant	AHCTF1	GRCh38.p7	1:246882476	CCGTAATGAAAATTT[-/A]AAAGATACTTAGAAC	25909
rs200641823	snp	C/T	4.2983e-05	0.00463569	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851442	TTTCTTGTTCAATCA[C/T]CTAAATGAATTAAAG	25909
rs200680433	in-del	-/AG			intron-variant	AHCTF1	GRCh38.p7	1:246910783	TGTCTTTTTCAGAGA[-/AG]AGAGATTAGATTTTG	25909
rs200701729	snp	C/T	0.000197821	0.0099434	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877045	ATTCATGATTCTGAA[C/T]GCTGGCACTGGACTG	25909
rs200702767	snp	C/T	0.000449749	0.0149891	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246891031	AGATGAGGTGGGAAA[C/T]CACAAACTTATTGCT	25909
rs200743124	in-del	-/AC			intron-variant	AHCTF1	GRCh38.p7	1:246847294	ACTCCATCTCAAAAA[-/AC]AAAAAAACAAACAAA	25909
rs200751034	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246852484	TTTGGTATAATAGAA[-/T]TTTTTTTTTTAAAAA	25909
rs200762494	snp	G/T	0.00199798	0.0315436	intron-variant	AHCTF1	GRCh38.p7	1:246849602	AAACTGTTTTGCAGA[G/T]AAAGAAAAGTACCTT	25909
rs200792896	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246864886	AAAAAAAAAAAAAAA[A/T]AAAGACTAGACTGAC	25909
rs200888196	in-del	-/AC			downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838886	AGTATCTTTCTGAGT[-/AC]ATTGTTTACCTTACT	25909
rs200903359	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246892808	AGCTAATTAAAAAAA[A/G]GATTTTTTTTTGGTT	25909
rs200912155	snp	A/G	3.30819e-05	0.00406692	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246918276	TTTCCACGAAGCACA[A/G]ATTCTAATGTTATTT	25909
rs201013631	snp	A/C/T	0.161924	0.233971	intron-variant	AHCTF1	GRCh38.p7	1:246852389	AGTTGGTTTTTTATC[A/C/T]AAATTTCTATAAATA	25909
rs201021519	snp	A/C	0.00019858	0.00996246	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849956	ACATCAACATTTTCA[A/C]TTTTAGCTGGGGTAT	25909
rs201022449	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246862720	AAAAGTGCCAATTAG[A/T]AAGATAAATTACTTA	25909
rs201045015	in-del	-/T	0.0127029	0.0786772	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839513	TTCAACAAGGCAGCG[-/T]TAACATCCATCACTA	25909
rs201109397	snp	C/T	0.000667234	0.018253	intron-variant	AHCTF1	GRCh38.p7	1:246887187	TAATTCATGAAAGTT[C/T]ATGCTGTAAGTGAAT	25909
rs201113359	snp	A/G	3.29538e-05	0.00405904	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246898288	GATTATAACCATCAG[A/G]AATGAGTTCATTGAG	25909
rs201117355	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246884365	TAGATCTTACCCTCT[C/T]ATCCGTAGAAGTACA	25909
rs201139530	in-del	-/G	0.0566069	0.158427	intron-variant	AHCTF1	GRCh38.p7	1:246911847	AATCAAATTTTTTCA[-/G]GTCTGATTTTGCATA	25909
rs201150652	in-del	-/TTC			intron-variant	AHCTF1	GRCh38.p7	1:246857958	CAGACTGCTAACACT[-/TTC]TTCTTCTTTTTTTTT	25909
rs201179961	snp	A/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246928006	TCCGCCACCAAAAAA[A/T]TAATTAATTAATTAA	25909
rs201238439	snp	A/C	0.00199798	0.0315436	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850661	TCAGAAGCTTCAGAA[A/C]TTTCTTTTGCCTTCC	25909
rs201253679	in-del	-/TCCT			intron-variant	AHCTF1	GRCh38.p7	1:246906860	TTTGATTTTTAAAAA[-/TCCT]TTTTTTTCCCTCTCA	25909
rs201266735	snp	C/T	1.65389e-05	0.00287562	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246890056	GACAACTGCACAGAA[C/T]CATCTAGATTTTTAA	25909
rs201276411	snp	C/T	0.000160571	0.00895878	intron-variant	AHCTF1	GRCh38.p7	1:246867827	CTGTAAAATGAAGAA[C/T]GCTGGAATTAAGTGC	25909
rs201308457	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246906768	CACAAATTAACTTAG[A/C]TACAAAGTATCAATA	25909
rs201321125	in-del	-/A	0.00113992	0.0238466	intron-variant	AHCTF1	GRCh38.p7	1:246841001	TTTTCTGTGTTTCTG[-/A]AAAAAAAAAGATATG	25909
rs201338008	in-del	-/AAC/AC/C			intron-variant	AHCTF1	GRCh38.p7	1:246847305	AAAAAAAAAAACAAA[-/AAC/AC/C]CAAAAAAAAAACTGA	25909
rs201346302	in-del	-/ATATAC			intron-variant	AHCTF1	GRCh38.p7	1:246846725	AAGATTTTGAAATAT[-/ATATAC]ATATACATATACATA	25909
rs201354601	snp	A/C	0.330482	0.236691	intron-variant	AHCTF1	GRCh38.p7	1:246867905	CACCCCCCCCCCCAC[A/C]CACACACACACACAC	25909
rs201407224	snp	A/G	3.29516e-05	0.00405891	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851250	TGCTTTGAGCCACAA[A/G]AAGTTCCCCATCTAC	25909
rs201421761	snp	A/C	0.00636936	0.0560724	intron-variant	AHCTF1	GRCh38.p7	1:246920586	CCATCCTGGCTAACA[A/C]GGTGAAACCCTGTCT	25909
rs201449234	in-del	-/AA	0.425586	0.17796	intron-variant	AHCTF1	GRCh38.p7	1:246930052	GCAAGACCCCGTCTC[-/AA]AAAAAAAAAAAGATG	25909
rs201481584	snp	C/T	0.00183889	0.0302665	intron-variant	AHCTF1	GRCh38.p7	1:246903938	AAACCCATAGTCCAA[C/T]GACCATTTACCTCAT	25909
rs201498481	snp	C/T	0.00478085	0.0486577	intron-variant	AHCTF1	GRCh38.p7	1:246920920	GTGAATCCACATCTC[C/T]ACTAATAATACCAAA	25909
rs201559540	in-del	-/TAT	0.222035	0.248431	downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838988	TGTTTACCTTACTAC[-/TAT]GATACTAAGCACCTT	25909
rs201638378	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246869236	ACAGCGTGTACTTAC[C/T]CCACTGACTAACTGT	25909
rs201652739	in-del	-/A	0.00874735	0.0655527	intron-variant	AHCTF1	GRCh38.p7	1:246921663	CCAATGAATCCTAGG[-/A]ACTACCAAAAAAGAG	25909
rs201657362	snp	A/C	0.00181402	0.0300619	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900134	GGACTCCTCTATTTA[A/C]ACTTCTCTCATGTAC	25909
rs201673996	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246869915	ATAGCTGTCACAGAT[-/A]AGTGATTCCTCTGAG	25909
rs201677476	snp	A/C/T	3.30246e-05	0.0040634	intron-variant	AHCTF1	GRCh38.p7	1:246877120	AAACTACCAATTTAT[A/C/T]TTGAATTTCTGACAA	25909
rs201706489	in-del	-/TCTT	0.0205511	0.0992634	intron-variant	AHCTF1	GRCh38.p7	1:246915517	TTTTCCATGCTAGTC[-/TCTT]TATCTAAAATGTCCA	25909
rs201718431	in-del	-/TAAC	0.0290542	0.116974	intron-variant	AHCTF1	GRCh38.p7	1:246899950	AAGTTATCCATATGT[-/TAAC]TAACAGTGAGATACA	25909
rs201746803	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246852393	GGTTTTTTATCCAAA[A/T]TTCTATAAATAATTA	25909
rs201761552	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246854968	TGATCGGCTTTTTAC[A/T]TGTTAGACAATTCTC	25909
rs201763321	in-del	-/ACTA	0.0209421	0.100162	intron-variant	AHCTF1	GRCh38.p7	1:246926666	TTCAAGACCAGCCTC[-/ACTA]ACAGGGTGAAATCCC	25909
rs201767677	snp	A/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246894400	ACACGGTGAAACCCC[A/G]TCTCTACTAAAAAAT	25909
rs201781867	snp	A/C	0.268452	0.249318	intron-variant	AHCTF1	GRCh38.p7	1:246847308	AAAAAAAAACAAACA[A/C]AAAAAAAACTGAAAA	25909
rs201805140	snp	A/C	0.00199792	0.0315431	intron-variant	AHCTF1	GRCh38.p7	1:246888378	TCTAAATGATAGCAC[A/C]TTACTGCAAACCTAC	25909
rs201815383	in-del	-/CGGGG			downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838618	GTGGGCGGGGCGGGG[-/CGGGG]GGAAGACCTCATATA	25909
rs201853355	snp	A/C/T	0.000179009	0.00945918	missense, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843863	AAGCAGGAGGTGAGA[A/C/T]GACAAACTGAGAAGA	25909
rs201868046	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246892809	GCTAATTAAAAAAAA[A/G]ATTTTTTTTTGGTTT	25909
rs201879215	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246852390	GTTGGTTTTTTATCC[A/T]AATTTCTATAAATAA	25909
rs201904837	snp	C/T	0.00199802	0.0315439	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246918286	GCACAGATTCTAATG[C/T]TATTTCGTCTTCTCC	25909
rs201947289	in-del	-/TG	0.00716266	0.059414	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933585	TATTTTTGTAGAGAC[-/TG]TGTCTTGCTGTGTTG	25909
rs201962947	snp	A/G	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246922779	CGAGGTCAGGAGATC[A/G]AGACCATCCTGGATA	25909
rs201974813	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246848713	TCTACAAATACAAAA[A/T]ATTAGCCAGGCCTGT	25909
rs201984673	snp	C/G	2.01888e-05	0.0031771	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861258	ACTGCACATTTTTTA[C/G]GTGTAGTAAATACTT	25909
rs202058646	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246920523	ACGCCTGTAACCCCA[A/G]CACTTTGGGAGGCTG	25909
rs202069305	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246917544	ACAGAATAGTGGCTA[A/C]TTAGAAAAAAGTTTT	25909
rs202106757	snp	C/T	0.00034628	0.0131537	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867730	ATTTTAGATAACACA[C/T]TGTTGATGAAAACAG	25909
rs202199548	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246864913	TGACAACCCACACCC[A/C]CCACCACAACCAAAA	25909
rs202231152	snp	A/G	1.65545e-05	0.00287697	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246894713	TCCACGTCCATTCAA[A/G]AACAAAGCGCAAATT	25909
rs267598462	snp	A/G	1.64876e-05	0.00287116	AHCTF1	1	allele_origin=G(germline)/A(somatic)	1:246850151	GATGACTCAAGGTTG[A/G]AGTCTTCTCTCACAT	25909
rs367564374	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246922617	CATGATGGTCTTGAA[C/T]TCCTGGGTTCCAGCA	25909
rs367585265	in-del	-/C	0.00795532	0.062565	intron-variant	AHCTF1	GRCh38.p7	1:246886685	ATACAAGAGGATGTG[-/C]ATAGGGTATATGCAA	25909
rs367665479	snp	C/T	0.000535854	0.0163597	intron-variant	AHCTF1	GRCh38.p7	1:246867855	TGCATCTCTAACAAA[C/T]GGGAATTTAATAAAA	25909
rs367694906	snp	C/T	0.000383107	0.013835	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850783	GATACGTTGACCTCT[C/T]GTACGAGTTTTGGAG	25909
rs367723662	snp	C/T	0.000332419	0.0128879	intron-variant	AHCTF1	GRCh38.p7	1:246887194	TGAAAGTTTATGCTG[C/T]AAGTGAATAGACTTA	25909
rs367757339	snp	A/G	4.94368e-05	0.00497152	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902626	CCCCTCAAAGGGAAC[A/G]TGCCACCTGTCAGGT	25909
rs367757583	snp	G/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246885807	TAAGCTGAAAAAATC[G/T]ACTTTAATCTGTGCT	25909
rs367758846	snp	A/G/T	6.59374e-05	0.00574151	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861043	AAACAGTCTCTTCAA[A/G/T]GTCTTCCGGTGACGG	25909
rs367764687	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246899605	AGACTGCAAGGCAAG[G/T]TGTCAAATTATTACA	25909
rs367765009	snp	C/T	0.000153988	0.00877328	intron-variant	AHCTF1	GRCh38.p7	1:246907777	AAACCACAAATTAGA[C/T]AAATGAAGTTAAAAA	25909
rs367768011	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246924130	ATTCTCACAGAAGAG[A/G]ATCAATACTATCAAA	25909
rs367769249	snp	G/T	1.81253e-05	0.00301037	missense, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843857	TCCTTAAAGCAGGAG[G/T]TGAGATGACAAACTG	25909
rs367799840	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246920643	AGCGTGGTGGCGGGC[A/G]CCTGTAGTTCCAGCT	25909
rs367848739	snp	C/T	0.000153988	0.00877328	intron-variant	AHCTF1	GRCh38.p7	1:246857848	AGAATATTATTTATG[C/T]TAAATATTTAGTGAT	25909
rs367872349	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246923998	CCCAAAGGCGTAGAA[C/T]ATAAATCTGGCAAAA	25909
rs367920072	snp	C/T	4.99147e-05	0.00499549	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900396	AAAAAGCCCCAAATA[C/T]ACAGAAGGCTTTCCC	25909
rs367924006	snp	A/G	0.00398564	0.0444627	intron-variant	AHCTF1	GRCh38.p7	1:246869096	TGATCCGCCCGCCTT[A/G]GCCTCCCAAAGTGCT	25909
rs367958551	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246861777	GATGATGGGTTTGGC[C/T]TAGCCAATGGCCCTA	25909
rs367972100	multinucleotide-polymorphism	AA/GG			intron-variant	AHCTF1	GRCh38.p7	1:246919871	TCACAGAGCCAGGCA[AA/GG]GTGGCTCATGCCTGT	25909
rs368025192	in-del	-/T	0.00716266	0.059414	intron-variant	AHCTF1	GRCh38.p7	1:246877740	GCTTGGTAGTAGATG[-/T]TTTTTGGTTGATTTG	25909
rs368063328	in-del	-/GTTTTAC			intron-variant	AHCTF1	GRCh38.p7	1:246892295	ATCAAATTCTAATTT[-/GTTTTAC]TTTTTTTTTTTTTTT	25909
rs368072334	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246920724	GCAGTGAGCCGAGAT[C/T]GCACCACTGCACTCC	25909
rs368107849	snp	C/T	6.61781e-05	0.00575193	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246891850	TTGCTAAGAAGCAAA[C/T]AGCATTGCTGGATAG	25909
rs368119622	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246843236	TACTCTGTTGGGAGG[A/G]ATGCCTGTCTCCTCT	25909
rs368120677	snp	A/G	1.66338e-05	0.00288386	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850795	TCTCGTACGAGTTTT[A/G]GAGGAAACCACGTCA	25909
rs368123846	snp	A/G	0.000275824	0.0117404	intron-variant	AHCTF1	GRCh38.p7	1:246862203	AAGTGCTTATAGGCC[A/G]GGCGCGGTGGCTCAC	25909
rs368127317	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246874248	GACCATCTTTGAGGT[G/T]GGCCTCTGTCTCCCT	25909
rs368212406	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246930435	AGACAACGTAGACTT[C/T]CCATAGCGCTTGGCA	25909
rs368230093	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246848423	AGCCAGGATGGTCTC[A/G]ATCTCCTGATCTCGT	25909
rs368246638	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246869256	TGACTAACTGTTCCC[C/T]CGCGTCTCTCCCTTT	25909
rs368307524	snp	A/C	1.65792e-05	0.00287912	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840950	CAAGGGGGAAATCAG[A/C]CGAATTTCTATGGGA	25909
rs368320933	snp	A/G	1.65002e-05	0.00287225	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861123	CTGTTTCCTTTGCTC[A/G]CATCCAGTTTCTCTA	25909
rs368370413	snp	A/G	1.64841e-05	0.00287085	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851107	AATTTGTCCATGATT[A/G]TCATTTTCCCCACTG	25909
rs368383090	snp	G/T	1.65573e-05	0.00287721	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246918305	TTCGTCTTCTCCAAG[G/T]GCTTGAAGAGTCACT	25909
rs368385143	snp	A/G	0.00795532	0.062565	intron-variant	AHCTF1	GRCh38.p7	1:246929881	ATATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	25909
rs368425692	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246867891	TGAAAGAATGATTAC[-/A]CCCCCCCCCCCACAC	25909
rs368425839	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246848795	GCACATGTTGCAGTG[A/T]GCCGAGATCATGCCA	25909
rs368431815	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246855266	ATCCTATCTTCCTCA[C/T]CTCTGTATAGCCAGG	25909
rs368445746	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246918106	GCTTATAGATGTTAT[A/G]TATGTAACTGTAGAT	25909
rs368523532	snp	A/G	1.65312e-05	0.00287495	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867757	ACAGATCTTGTCAAC[A/G]CAGTTCCTGTTACAA	25909
rs368537882	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246900886	GATGAACCTTAGCTG[A/G]GAAGGACTTATCCAG	25909
rs368548624	snp	C/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246927730	CTGTTCATGGCCGGG[C/T]GCGGTAGCTCAAGCC	25909
rs368558758	snp	A/G/T	3.43284e-05	0.00414286	intron-variant	AHCTF1	GRCh38.p7	1:246899526	ATCTAAAAAAAAGAT[A/G/T]TAAAAAATAATCCAC	25909
rs368600987	snp	C/T	5.00931e-05	0.0050044	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246885548	TACCACTGGACACTG[C/T]TGGCTTCATTGTCTG	25909
rs368629914	snp	G/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246928052	GCCGGGTGCGGTGGC[G/T]CACGCCTGTAATCCC	25909
rs368632848	snp	C/T			missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246905590	AGCAATTCCGAGGAT[C/T]ATTCTCAGGTTCTTG	25909
rs368654840	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868916	GTGGTGTGATCTCGG[C/T]TCACTGCAAGTTCTG	25909
rs368702933	snp	A/C/T			intron-variant	AHCTF1	GRCh38.p7	1:246877662	TCAGTGGGAAGCGTG[A/C/T]GAAAGACTGAGATCT	25909
rs368716204	in-del	-/AAAAA	0.0228903	0.104504	intron-variant	AHCTF1	GRCh38.p7	1:246845366	AAGCATATGATTCTT[-/AAAAA]AAAGAAAAATAGAGT	25909
rs368742330	snp	C/T	0.000304961	0.0123445	intron-variant	AHCTF1	GRCh38.p7	1:246904058	AAATTAACGAAGACA[C/T]GCTAAATATATTAAT	25909
rs368754778	snp	A/G	3.8552e-05	0.00439027	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861226	CTTTGCTCTTCAGCC[A/G]TTCAGTTTCCACTGG	25909
rs368769884	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246883832	ATAAGGTTTAGAAAT[C/T]AAACTATTTATTAGT	25909
rs368778976	snp	C/T	0.0225045	0.103662	intron-variant	AHCTF1	GRCh38.p7	1:246868905	GTTGGAGTGCAGTGG[C/T]GTGATCTCGGCTCAC	25909
rs368802357	snp	C/T	3.30447e-05	0.00406464	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246905645	TTGTCCACTTTCCAA[C/T]TGTATGTAATATCTG	25909
rs368802989	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246928404	TTATTCCTGGGCATT[C/T]GACAAGGTCACAGTG	25909
rs368823025	snp	A/C/T	3.4329e-05	0.00414289	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877298	TCCAGGCTTCAACCA[A/C/T]ACACCTGAAAGCAGT	25909
rs368827923	snp	A/C	1.71714e-05	0.00293008	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246862128	AATCCAGAAGTAGTA[A/C]CTGACATGGCCAAAC	25909
rs368902281	snp	C/T	1.65034e-05	0.00287253	intron-variant	AHCTF1	GRCh38.p7	1:246877101	AAAGAACAAAATAGA[C/T]TGTAAACTACCAATT	25909
rs368941568	snp	A/C	0.104504	0.2033	intron-variant	AHCTF1	GRCh38.p7	1:246867901	ATTACACCCCCCCCC[A/C]CACACACACACACAC	25909
rs368950744	snp	C/T	0.00024729	0.0111168	intron-variant	AHCTF1	GRCh38.p7	1:246895934	GTTCTTCCTAAACCA[C/T]GCATTACAGAAAGGA	25909
rs368970530	snp	C/G	1.67939e-05	0.0028977	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916348	CTGTTATAGAGTTTA[C/G]TACCTCAAGTTGTGG	25909
rs368992959	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246849173	CCAGTTTGTGGGCAA[C/T]AGTGAATATGGATTG	25909
rs368999735	snp	C/T	1.65551e-05	0.00287702	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850064	ACATCTTCAGATGGA[C/T]TGATTTTTCTTGGTC	25909
rs369048405	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246926465	AAATGTTTAATAAAG[C/T]TTTTCAAATTTAACA	25909
rs369072844	snp	C/T	4.94344e-05	0.00497139	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246898299	TCAGGAATGAGTTCA[C/T]TGAGTGATGGACCTG	25909
rs369090058	in-del	-/ACAT			intron-variant	AHCTF1	GRCh38.p7	1:246864522	TCCATTCACCTACAT[-/ACAT]GTAATATATATAATG	25909
rs369090958	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246866336	CAGAAAAAAAAATCC[A/G]AACTATTGGTAGAAA	25909
rs369099199	snp	C/T	3.2969e-05	0.00405998	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246855782	TTCAACAGATGTTAA[C/T]CCTTCGTCCAACACT	25909
rs369119391	snp	A/G	8.70193e-05	0.00659561	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853206	TCTTTTAAGTTCAGC[A/G]CTACTTCCTGGTTAA	25909
rs369166034	snp	C/G/T	0.000764551	0.0195369	intron-variant	AHCTF1	GRCh38.p7	1:246889923	CTATTCTGAGAAACT[C/G/T]TGACTTCTTACAGAT	25909
rs369212124	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246902436	TTCCAATTTTCTGAA[C/T]TGCCAGGAGTATGAA	25909
rs369213429	snp	A/G/T	0.00024652	0.0110996	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876087	GGCTTAGCTCGTTCA[A/G/T]TGGCTAATTTTCGAT	25909
rs369259650	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246891258	CCAAAATGATGTCAA[A/G]CAAACCTCCAAAATG	25909
rs369278200	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246893798	TCCATCATCAGTATA[C/T]TTAGTAAATTAAACT	25909
rs369343018	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246910794	AGAGAAGAGATTAGA[C/T]TTTGCCACAACAAAC	25909
rs369355157	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246911479	CTATCTATGAAGATT[C/T]TTTTTTTTTTTTTTT	25909
rs369427665	snp	A/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246888825	TAAGGAAGGAGGATC[A/G]TTGGAGCCCAGGAGT	25909
rs369433989	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246916017	TAAGAGTAACACATT[C/T]ACATAAAAGTATACA	25909
rs369507349	snp	C/T	1.64844e-05	0.00287087	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849660	GAGAAAATAAAGGCT[C/T]ATTGTTTGGTTCAGA	25909
rs369528671	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246915717	ATATTTTCCATAATG[C/T]TCCAATCCAAGACTA	25909
rs369612509	snp	A/C	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246918508	TCTGGTTACAAAATA[A/C]ATATTGGCCAGATGC	25909
rs369612701	snp	C/T	0.00636936	0.0560724	intron-variant	AHCTF1	GRCh38.p7	1:246869034	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT	25909
rs369643786	snp	C/T	0.410399	0.191761	intron-variant	AHCTF1	GRCh38.p7	1:246897884	TTGCGGGGGCTGGGG[C/T]GGGAAGATCGCTTAA	25909
rs369646906	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246844225	GTCTATTTCTTTTAA[G/T]CCGTACTGCTCCTCA	25909
rs369650473	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246848216	TGTATCAGTACAACA[A/G]GTCATCTACTTTATT	25909
rs369678601	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246886890	ATCACCAATTTCATA[C/T]ATCAAGGCCAAATCT	25909
rs369696763	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246908374	AAGCCTACCCTCCCC[A/C]CCTACAAAAGACCTT	25909
rs369757901	snp	C/T	0.000165096	0.00908408	intron-variant	AHCTF1	GRCh38.p7	1:246888358	CCCTCCCCAGCTTTG[C/T]AGACTCTAAATGATA	25909
rs369759637	snp	A/C/T	8.23708e-05	0.00641712	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849826	TGATACTGAGTGCAA[A/C/T]GAACGTTTTTGGCTT	25909
rs369797943	snp	C/T	1.64808e-05	0.00287057	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864004	CTTTTAATTGCGAAC[C/T]TGAGGGCAGTGAACG	25909
rs369798428	snp	C/T	6.59729e-05	0.005743	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876999	AAGGCAGGCACATAA[C/T]TGGCACGCTGCAAAT	25909
rs369839183	snp	A/C	0.000153988	0.00877327	intron-variant	AHCTF1	GRCh38.p7	1:246900485	CTGGAAGAAAAAGAT[A/C]ATTTTTAAAAACAGA	25909
rs369872645	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246906163	GATGAGTTAGAAACT[A/G]AAGAGTTCCCATAAA	25909
rs369881206	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246896713	ATATCTGAACTGCAC[A/G]GTGTATGAAATATCT	25909
rs369897027	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246879955	AATTAGCACCAAACT[A/G]AAGTGAAAAAAGTAT	25909
rs369907900	in-del	-/CAAAAAA			intron-variant	AHCTF1	GRCh38.p7	1:246848708	CTGTCTCTACAAATA[-/CAAAAAA]TTAGCCAGGCCTGTA	25909
rs369910717	snp	A/C	0.000179424	0.00946993	intron-variant	AHCTF1	GRCh38.p7	1:246891959	AGTTTCCATACAGTA[A/C]ATCTAAATAAATTAG	25909
rs369954768	snp	C/T	8.65314e-05	0.0065771	intron-variant	AHCTF1	GRCh38.p7	1:246867384	TAACTTCTGATGTAT[C/T]ACAAGGAGCACTGAT	25909
rs369978816	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246908346	AAAAAAAAAGAGGGG[G/T]GGGGCAAGGGGGAAG	25909
rs369984833	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246925665	CTGTCCCCTCCCAAT[C/T]TCATACTGAAATGTG	25909
rs369995299	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246846807	TCACCTGGGCTGGAG[C/T]ACAGTGGTGTGATGG	25909
rs369995931	snp	A/G	0.000101612	0.00712712	intron-variant	AHCTF1	GRCh38.p7	1:246907779	ACCACAAATTAGACA[A/G]ATGAAGTTAAAAAAC	25909
rs370055569	in-del	-/AA			intron-variant	AHCTF1	GRCh38.p7	1:246880567	GTGAGACTCCAGCTC[-/AA]AAAAAAAAAAAAAAA	25909
rs370081948	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246921636	ACACACCGATTCCCT[A/G]AGTCAGGAAGTCCAA	25909
rs370087175	snp	C/T	0.0479149	0.147179	intron-variant	AHCTF1	GRCh38.p7	1:246868969	CCTGCCTCAGCCTGC[C/T]GAGTAGCTGGGACTA	25909
rs370105401	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246929755	CGTTTTGCTTCCTCT[G/T]AAAATATATCTGTAC	25909
rs370118612	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246929404	ACAAAGTGAGACTCC[A/G]TCTCAAAAAAATAAA	25909
rs370142896	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246898665	ACACACACACACACA[C/G]GAAAACTCCTGCAGT	25909
rs370145552	snp	A/C	4.97682e-05	0.00498815	intron-variant	AHCTF1	GRCh38.p7	1:246900333	GAAAAAAAAAGAATC[A/C]TACCTTAACGAATCT	25909
rs370165641	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246924168	CTGTGGTAAAATAAC[A/G]GGATAACAGCCACTT	25909
rs370220535	in-del	-/AT			intron-variant	AHCTF1	GRCh38.p7	1:246912840	TATGCCAAGAACACT[-/AT]GTTAGATCCTACATT	25909
rs370281990	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246854490	GTTAAGCATGTAACA[G/T]CTACACTACAAAACA	25909
rs370291964	snp	C/T	0.000164902	0.00907876	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246913278	CAAGTCATCCAAACA[C/T]AGGTCAACAAGAAGG	25909
rs370302054	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246909781	TTGGAATGTATCCCT[C/T]GCAGATAAGGGGGAA	25909
rs370331065	snp	C/T	1.78784e-05	0.00298979	intron-variant	AHCTF1	GRCh38.p7	1:246857849	GAATATTATTTATGC[C/T]AAATATTTAGTGATT	25909
rs370331510	snp	C/T	0.000100189	0.00707703	intron-variant	AHCTF1	GRCh38.p7	1:246902693	GTAACATAAAATACA[C/T]GCAAATATTAATCTG	25909
rs370390882	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246927045	TAGCAGGGCGTGGTG[A/G]CGGGAACCTGTAGTC	25909
rs370392677	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246904674	ACAAAGTGAAGATAC[C/T]AAATCAACCCTGTAG	25909
rs370396851	snp	A/G	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246873239	ACTCATTACTCTTCT[A/G]TAAAAGAAAAAAATC	25909
rs370404844	snp	A/G	8.26125e-05	0.00642646	intron-variant	AHCTF1	GRCh38.p7	1:246877146	GACAAGTTTACATCG[A/G]TAAGTAATTACCTGC	25909
rs370406323	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246854571	AAATGTCTTAAATAT[A/G]TTACATGAGAAAAGA	25909
rs370448826	snp	A/T	1.86565e-05	0.00305416	intron-variant	AHCTF1	GRCh38.p7	1:246861911	CTTGTCAGAGCTAAT[A/T]CATTCTTATTAAAAA	25909
rs370453312	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246907432	TCTCAATCATTCATT[C/G]AATCATTAATCTACC	25909
rs370475593	snp	C/G	0.000324867	0.0127408	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850614	GTATTTGCTGGTTCT[C/G]AGATAGTCCTCTGAC	25909
rs370510911	in-del	-/TC			intron-variant	AHCTF1	GRCh38.p7	1:246846842	TGCAACCTCAACCTC[-/TC]CCGGGCTCAAGCCAT	25909
rs370532111	snp	C/T	6.61649e-05	0.00575135	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246891830	AGCTCAAGACTATAT[C/T]AAGATTGCTAAGAAG	25909
rs370568528	snp	A/G	1.75459e-05	0.00296186	intron-variant	AHCTF1	GRCh38.p7	1:246918219	TTACAAATCAATTGT[A/G]TTAGTAAATGTTCAG	25909
rs370593480	snp	A/T	3.3083e-05	0.00406699	intron-variant	AHCTF1	GRCh38.p7	1:246895822	AACATTTTACTTGTT[A/T]TCAGAATCTTACCTT	25909
rs370639205	snp	A/C/G	0.000165678	0.00910009	missense, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840823	ACAGCATTTTTCTGC[A/C/G]TAAAATTTGCTTTGG	25909
rs370684422	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246871741	CCTGACTGCAGACTA[A/T]AAGGAGGTTAATAAT	25909
rs370800805	snp	G/T	0.000153988	0.00877328	intron-variant	AHCTF1	GRCh38.p7	1:246862160	TTTAGCTTTCTATAG[G/T]AAAGAGCAAATGGAA	25909
rs370808320	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246867075	AAGTATACTACTACC[C/T]GATGTAAAATTTCCT	25909
rs370829910	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246922861	GGTGGCAGGCGCCTG[C/T]AGTCCCAGCTACTCG	25909
rs370847036	in-del	-/G			intron-variant	AHCTF1	GRCh38.p7	1:246903855	AAAAAAAAAAAAAAA[-/G]AATCACTTTTCAATA	25909
rs370907992	snp	A/C	0.000153988	0.00877328	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246891011	AACCACTTGTGCATA[A/C]TGACAGATGAGGTGG	25909
rs371036535	snp	A/C	5.49486e-05	0.0052413	intron-variant	AHCTF1	GRCh38.p7	1:246877342	TAGTTTTAGAAAAAG[A/C]TATTTAAATGTACAA	25909
rs371058434	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246904316	CTTTCTCAAATATTC[C/T]TTCCTCAATGGTTAT	25909
rs371074920	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246903430	ATTGTAGAGGAAAAC[A/G]GTATCTGAGAAGTTA	25909
rs371075057	snp	C/T	0.0126979	0.078662	intron-variant	AHCTF1	GRCh38.p7	1:246872265	TCAGATCGGGCTCCC[C/T]TGTGACTCCACTAAC	25909
rs371095250	snp	G/T	7.03977e-05	0.00593245	intron-variant	AHCTF1	GRCh38.p7	1:246849595	AGATGAAAAACTGTT[G/T]TGCAGAGAAAGAAAA	25909
rs371099999	snp	C/G	1.66427e-05	0.00288462	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900198	ACTTACAACAGACTC[C/G]AATGACCACAGTGCA	25909
rs371100178	snp	C/T	1.65111e-05	0.0028732	missense, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840897	GTCACTTCTGTAGTT[C/T]TTCTTGGTTTGCTCT	25909
rs371107812	snp	C/G	0.000346761	0.0131628	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246857753	CGGGCTTAAGTGATT[C/G]AATTCTGAAAATGCC	25909
rs371134556	snp	A/G	3.34874e-05	0.00409177	intron-variant	AHCTF1	GRCh38.p7	1:246891730	TCGTTTCTCTTAGTC[A/G]AGAAGTAAAATTTAA	25909
rs371134950	in-del	-/G			intron-variant	AHCTF1	GRCh38.p7	1:246864462	AGAAAACAGGACAAG[-/G]CTTCCCTGGCAATCT	25909
rs371157124	snp	A/C/T	1.66067e-05	0.00288151	synonymous-codon, missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850741	TGCTGATGCTTCCTG[A/C/T]TGTGCTGATTTGACA	25909
rs371220461	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246929921	GCCGGGTGTGGTGGC[A/G]TGCGCCTGTAATCCC	25909
rs371230164	snp	A/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246881291	TGTACCTAATATTCA[A/G]AATACAAAAAGCTGG	25909
rs371294351	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246897409	TAGATATCAAATAAA[C/T]ATACAAAAATGAATT	25909
rs371298272	snp	A/C	0.00279162	0.0372561	downstream-variant-500B	AHCTF1	GRCh38.p7	1:246839034	CTTTGATCATCAGAT[A/C]CATGGTTGCTACAAG	25909
rs371304548	snp	C/T	1.77915e-05	0.00298252	intron-variant	AHCTF1	GRCh38.p7	1:246913192	TTGCATCAGAATATC[C/T]AGGTGCTCCATTTTT	25909
rs371333425	snp	A/C	2.07372e-05	0.00321996	intron-variant	AHCTF1	GRCh38.p7	1:246885459	TTATTAACAGATACG[A/C]TAAAGACTTTATAGT	25909
rs371353448	snp	C/T			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932433	GCTTGCATTCTGTAT[C/T]TTCTGTTCTGTGCTC	25909
rs371361209	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246885867	ATCCATATCTGCAGA[A/C]TGAACTAAGTGCAGA	25909
rs371454614	snp	C/T	0.0182019	0.0936463	intron-variant	AHCTF1	GRCh38.p7	1:246878472	TATATAAGGAAAATA[C/T]GTATTAACTTGGAAA	25909
rs371541290	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246922331	CACCACTGCACTCCA[C/G]CGCGGGTGACAGAGC	25909
rs371546935	snp	A/C/T	0.000183131	0.00956757	missense, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246842727	TTTGACGTCCTGATT[A/C/T]GTTTCGCTTTTGGCT	25909
rs371558157	snp	A/G	0.000100341	0.00708241	intron-variant	AHCTF1	GRCh38.p7	1:246887370	GGTCTTTTAAAAAGC[A/G]GATTAAGGACAATAA	25909
rs371642091	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246910397	ACATCAATTTGATTA[C/T]AGTCTAGATAACACA	25909
rs371688669	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246863090	GAACCTAGCTGTAGA[A/G]AATACAAAGTGTGAT	25909
rs371688921	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246847058	TTGGGAGGCCAAGGC[A/G]GGTGGATTATCTGAG	25909
rs371700285	snp	C/G/T	0.000136738	0.00826754	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867273	TGATGCTTTTGAAAT[C/G/T]GGTGTTCCAAAAAAT	25909
rs371700914	snp	A/C/T	3.32018e-05	0.00407431	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246891897	ATCCATGAAATGACA[A/C/T]GAACCATCAAATAAT	25909
rs371701056	snp	C/T	8.24804e-05	0.00642132	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851059	TACTTTTTGGGACTT[C/T]TGGTCACTAGTTACG	25909
rs371712513	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246883881	AAAGGTAAAGGAAAT[G/T]AGAACCTGGCAAATC	25909
rs371714111	in-del	-/G	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246901115	AAGGCCAGGTGGGCA[-/G]ATCAATTGAGCCCAG	25909
rs371786127	snp	C/T	4.02059e-05	0.00448345	intron-variant	AHCTF1	GRCh38.p7	1:246876002	GTATCTTTTTTGATC[C/T]AATAGATTATGATAT	25909
rs371835166	snp	A/G	1.66466e-05	0.00288496	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900244	TGTAGATATTCTCCT[A/G]ACCTAAAAGAAAATT	25909
rs371877843	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246842916	ACTCCTTTTCTCATA[C/T]CTTTTAGTAGAAACC	25909
rs371888208	snp	C/T			synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246863984	GGAGATGGCCTGAGG[C/T]GATCCTTTTAATTGC	25909
rs371948895	snp	C/T	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849637	TTTCCTTGGAACTTC[C/T]GACGCTGGAGAAAAT	25909
rs371969768	snp	G/T	0.0166325	0.0896639	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932873	AGGTAGAGTAGGGAT[G/T]TTAAGAAGATGCTCT	25909
rs372036407	snp	C/T	1.64988e-05	0.00287213	intron-variant	AHCTF1	GRCh38.p7	1:246888237	ATCAAGTACTGCCTA[C/T]AAAACAAAGGGATAA	25909
rs372037901	snp	C/T	0.00013084	0.0080872	intron-variant	AHCTF1	GRCh38.p7	1:246907501	AATGAGTACAAGCTA[C/T]ATGCAAAAAAACTAC	25909
rs372046386	snp	A/G	3.30134e-05	0.00406271	intron-variant	AHCTF1	GRCh38.p7	1:246863875	CTTGCTACTTGAAAA[A/G]TAAGAGCCATCTAGT	25909
rs372049828	snp	C/T	4.95872e-05	0.00497907	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246904027	CAAACTCAAAACATC[C/T]CCTTCACTGAAACAG	25909
rs372066381	snp	C/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246922720	GGGCGCAGTGGCTCA[C/T]GCCTGTAATCCCAGC	25909
rs372085829	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246843268	ACCTCGGTCTATAAA[A/G]TATTTGAAGTAATTG	25909
rs372110145	snp	C/T	1.6498e-05	0.00287206	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861126	TTTCCTTTGCTCACA[C/T]CCAGTTTCTCTAAAC	25909
rs372154266	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246881862	AACCAAAAAAAAAAA[A/C]AAAAAAAAAAGAAGA	25909
rs372163053	snp	A/C	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876140	ATACTGGTCTAATAT[A/C]GAATTTCGAGCCAGT	25909
rs372257932	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246904391	CAGCTTCCTTTGCAG[C/T]TAAGTGCAGTACCCT	25909
rs372299704	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246869117	CCAAAGTGCTGGATT[A/G]CAGGCGTGAGCCACC	25909
rs372302506	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246901600	CTGCACTGGACAGAG[C/T]GAGACTCCATCTCAA	25909
rs372302812	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246920813	AAAAGCATCCAGGCA[C/T]GGTGCCTCACGCCTA	25909
rs372323719	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246908401	CCTTATATTGAACAA[C/T]TGGAGTAACTAGGTA	25909
rs372344061	snp	C/T	3.40524e-05	0.00412614	intron-variant	AHCTF1	GRCh38.p7	1:246904061	TTAACGAAGACACGC[C/T]AAATATATTAATACA	25909
rs372392410	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246868946	GCCTCCCGGGTTCAC[A/G]CCATTCTCCTGCCTC	25909
rs372396900	snp	C/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246905421	AGAATGGCATGAATC[C/T]GGGAGGCGGAGGTTG	25909
rs372453230	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246898687	TCCTGCAGTCTACTC[C/T]TCTTTATCTAATGTG	25909
rs372460109	snp	C/T	3.45644e-05	0.00415704	intron-variant	AHCTF1	GRCh38.p7	1:246916415	AAGAAAAAAAAATTG[C/T]CTATTTTAATATTGT	25909
rs372534833	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246924823	AAAAGTAGAAGTTTG[C/T]TTTTTATTATCCAAA	25909
rs372542632	snp	A/G	6.61365e-05	0.00575012	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246891798	CTCAGTGATCTCTCG[A/G]GCTTCTGATGCAAAA	25909
rs372545499	snp	A/G	1.64947e-05	0.00287177	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864033	CGGGATACTAGGTAC[A/G]AAGGAGATTTCATGG	25909
rs372609681	snp	A/T	3.30393e-05	0.0040643	intron-variant	AHCTF1	GRCh38.p7	1:246877142	TTCTGACAAGTTTAC[A/T]TCGGTAAGTAATTAC	25909
rs372613414	snp	C/G	3.29516e-05	0.00405891	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851275	ATCTACTTCAGCAAT[C/G]TCACATTCAGCAGTG	25909
rs372617142	snp	A/G	4.9923e-05	0.0049959	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246918341	AAATGGCAGGAGACC[A/G]CTAGTCACTTGAGCT	25909
rs372654933	snp	C/T	1.85789e-05	0.0030478	intron-variant	AHCTF1	GRCh38.p7	1:246861918	GAGCTAATACATTCT[C/T]ATTAAAAAATGTCTT	25909
rs372686736	snp	C/G/T	5.10341e-05	0.00505123	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853262	TTCAGAGATAGTGAG[C/G/T]GAGGAGTTTCCACCA	25909
rs372688283	snp	G/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246846081	AAGTGGGAATCAAAC[G/T]ATATATGAATGTCAT	25909
rs372696795	snp	C/T	0.0158469	0.0875917	intron-variant	AHCTF1	GRCh38.p7	1:246868927	TCGGCTCACTGCAAG[C/T]TCTGCCTCCCGGGTT	25909
rs372742919	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246926840	CAGCCTGGGCAACAA[A/G]AGCGAAACCCCGTTT	25909
rs372748732	snp	C/G	7.00109e-05	0.00591612	intron-variant	AHCTF1	GRCh38.p7	1:246877310	CCATACACCTGAAAG[C/G]AGTATTTATCAAAGT	25909
rs372793971	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246917389	TACATTAGTTGGATA[C/T]GTAAGTTTATAGCTA	25909
rs372843367	in-del	-/GT			intron-variant	AHCTF1	GRCh38.p7	1:246895411	CAATATGCGTTTGGG[-/GT]GTGTGTGTGTATGTG	25909
rs372858806	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246862020	CTAGTTTCTTTAAGT[C/T]GTTGAGGAGACCTTC	25909
rs372860043	snp	A/G	0.000153988	0.00877328	intron-variant	AHCTF1	GRCh38.p7	1:246889939	TGACTTCTTACAGAT[A/G]TAATTTCTAAAATTG	25909
rs372869051	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246925748	GGACCCCTCATGAAT[A/G]GGTTGGTGTCCTCTC	25909
rs372869333	snp	C/T	0.00398564	0.0444627	intron-variant	AHCTF1	GRCh38.p7	1:246868907	TGGAGTGCAGTGGTG[C/T]GATCTCGGCTCACTG	25909
rs372894439	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246922851	AGCCGGGCGTGGTGG[C/T]AGGCGCCTGTAGTCC	25909
rs372902458	snp	C/T	0.000204915	0.01012	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916296	ACAGGAGGCTGTTCA[C/T]TGACTCCACTGAATC	25909
rs372908744	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246845614	CTCCATTTCAAATAT[A/G]TAAGGAAATACAAAA	25909
rs372932409	snp	G/T	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246907027	AGGGATTCAGTCATT[G/T]TGCAAACATCATACA	25909
rs372967955	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246909779	TCTTGGAATGTATCC[C/T]TCGCAGATAAGGGGG	25909
rs373007431	snp	A/G	3.38226e-05	0.0041122	intron-variant	AHCTF1	GRCh38.p7	1:246902511	CATGACATATTTCAA[A/G]TACTTTAACTAACCT	25909
rs373012684	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246868248	ATTTTCCTGCCTTAG[C/T]CTCCCGAGTAGCTGG	25909
rs373043560	snp	C/T	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246891912	CGAACCATCAAATAA[C/T]GGCACACCTTTCAAG	25909
rs373146844	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246908902	GACTCCGTCTCAAAA[A/G]AAAAAAAAAAAAAAG	25909
rs373188474	snp	A/G	0.00517822	0.0506191	intron-variant	AHCTF1	GRCh38.p7	1:246869035	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	25909
rs373226573	snp	A/G	3.29592e-05	0.00405938	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246863938	CCTTAACTACAAGAG[A/G]AGTTTCAAGCAAATG	25909
rs373338270	snp	C/T	9.9167e-05	0.00704086	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850085	TTTCTTGGTCTACCA[C/T]GTTTTCTAGGTATGG	25909
rs373347700	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246921791	ATCCTTAACAAATAC[A/G]AAATATGTTTTTAGA	25909
rs373392871	snp	C/T	0.000216557	0.0104034	intron-variant	AHCTF1	GRCh38.p7	1:246900270	AAATTTAAAACATTA[C/T]TAAGTCATTGGTCAG	25909
rs373415930	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246879083	AATCTCACAACAAGG[C/T]TGATTTCCCTAATGC	25909
rs373438051	snp	A/G	1.64882e-05	0.00287121	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877055	CTGAACGCTGGCACT[A/G]GACTGCAAAAATTTC	25909
rs373456600	snp	A/C	1.69804e-05	0.00291374	intron-variant	AHCTF1	GRCh38.p7	1:246907784	AAATTAGACAAATGA[A/C]GTTAAAAAACTAGAA	25909
rs373464644	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246905983	GTTAGAATTACTCAA[C/G]TGGATGCATTCATGT	25909
rs373492917	snp	C/T	1.64942e-05	0.00287173	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246888448	ATCTCGTTTCCACAA[C/T]TTCTCAATTCGCTCT	25909
rs373496461	snp	C/T	6.59055e-05	0.00574007	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849856	TTGACTTTCAGTCTT[C/T]TTTGTAAGTTTTTTC	25909
rs373549632	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246880622	CTACACCCAGTTGAT[C/T]AGACAAACTAGCAGG	25909
rs373566595	in-del	-/A			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932169	TCATTTACAAAAAAA[-/A]TCGGGTCTCTCCGCC	25909
rs373573414	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246908609	CCAAGAATCTTAGGC[C/T]GGGCACGGTGGCTCA	25909
rs373619574	snp	A/C/G	4.95711e-05	0.0049783	missense, synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246860992	TTACATTAGTAGTTA[A/C/G]TGCAGTGGAAGAGCT	25909
rs373667317	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246894492	AGCCTGCAGTGAGCC[A/G]AGATCGCGCCACTGC	25909
rs373708166	in-del	-/ATTA			utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839754	GATTACCTGTTATAA[-/ATTA]TTTTACAACACTTAT	25909
rs373718195	snp	C/T	3.29522e-05	0.00405894	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246907622	AGCAAGCTGATTTGT[C/T]CTGCTTATGTAACTA	25909
rs373736823	snp	A/T	1.67978e-05	0.00289804	intron-variant	AHCTF1	GRCh38.p7	1:246913434	AACATAATACGTGAT[A/T]TGCTTTTCTTCTGCA	25909
rs373744452	snp	A/G	1.76805e-05	0.0029732	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851396	AATGAAAGATTCCTA[A/G]CCTCTTCTCCTGAAT	25909
rs373838472	snp	A/G	0.000635728	0.0178174	intron-variant	AHCTF1	GRCh38.p7	1:246855846	TAGAAAAAGAAATAC[A/G]TACCTTAGTGTGTAA	25909
rs373852389	snp	C/T	0.067446	0.170804	intron-variant	AHCTF1	GRCh38.p7	1:246897919	AAGAGGTTGAGGCTA[C/T]AGTGAGCCATGACCA	25909
rs373884656	snp	G/T	3.30497e-05	0.00406494	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246857774	TGAAAATGCCTCTGC[G/T]GCAACTAAGAGATCC	25909
rs373887485	snp	A/T			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933116	ACGTCCCATTAATTT[A/T]TTTATTTTATTTATT	25909
rs373892396	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246921138	GCAGCAGAAAATACA[C/T]GCAAAATGACATTTA	25909
rs373895205	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246892973	AAAACACTTACTATG[C/T]TTTGTATGTTAATTA	25909
rs373896111	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246927292	TTGGTTAGAGACCAG[C/T]CTGGCCAACATGGTG	25909
rs373897626	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246877553	GCAAAGTAGACAAAA[-/A]ATTCAAAGAAGACAA	25909
rs373898965	in-del	-/TTC			intron-variant	AHCTF1	GRCh38.p7	1:246929550	GAGTGGAAACATCTC[-/TTC]CACAGAATGAGTCCA	25909
rs373919412	snp	A/C/G			intron-variant	AHCTF1	GRCh38.p7	1:246899085	CAAGAGCGAAACTCC[A/C/G]TCTCAAAAAGAGAAA	25909
rs373928660	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246920706	ACCTGGGAGGCGGAG[C/T]TTGCAGTGAGCCGAG	25909
rs373929379	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246919032	ATATAGGCATAAAGT[G/T]GTCTTTCATTTAGAA	25909
rs373950211	in-del	-/GACTAGACTGAC			intron-variant	AHCTF1	GRCh38.p7	1:246864890	AAAAAAAAAAAAAAA[-/GACTAGACTGAC]AACCCACACCCACCA	25909
rs373954182	snp	A/C	1.65181e-05	0.00287381	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864056	TTTCATGGAGCTTTG[A/C]TGAATAAACTCCGAA	25909
rs373975739	snp	G/T	4.94246e-05	0.0049709	intron-variant	AHCTF1	GRCh38.p7	1:246867637	AACAAGCAGCATGAC[G/T]ATGAAACGTGTAAGA	25909
rs373981950	in-del	-/AACAA			intron-variant	AHCTF1	GRCh38.p7	1:246866644	TTTTGTCTTTGATAA[-/AACAA]TCAAAAATTTCCAAA	25909
rs373985621	snp	C/T	8.25566e-05	0.00642429	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246913384	GCACTGGCTCCTCCA[C/T]GATTAATTATAGGTT	25909
rs374006698	snp	C/T	0.000153988	0.00877328	missense, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840873	CTGTTCCTTCCAAGA[C/T]CTGTTCCTGTCACTT	25909
rs374026609	snp	C/T	8.33757e-05	0.00645608	intron-variant	AHCTF1	GRCh38.p7	1:246903930	GGTAATATAAACCCA[C/T]AGTCCAATGACCATT	25909
rs374030684	snp	C/G	0.00014845	0.00861411	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861090	AAGGTAGTCTCATCG[C/G]ATGTGATTGAAACAC	25909
rs374068053	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246927630	AGCACTGGCAACCTA[C/T]AAAAAGTAATTTACT	25909
rs374148720	in-del	-/G			intron-variant	AHCTF1	GRCh38.p7	1:246868846	GTGTGTGTGTTTTTT[-/G]TTTTTTTTTTTTTTT	25909
rs374195541	snp	C/G	0.000153988	0.00877328	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867745	TTGTTGATGAAAACA[C/G]ATCTTGTCAACACAG	25909
rs374213766	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246846356	TATGGTAACAGTATA[A/C]AGGGCAGAGGAAGAC	25909
rs374217782	snp	C/T	1.68258e-05	0.00290045	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900455	AGACTGAAACACTAG[C/T]GTCAGGCGATAGAGC	25909
rs374222002	snp	A/C/T	3.32117e-05	0.00407492	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850321	GCTAGGACTTGTTAC[A/C/T]GTACTAACTTTTAGA	25909
rs374263217	snp	A/G/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246868914	CAGTGGTGTGATCTC[A/G/T]GCTCACTGCAAGTTC	25909
rs374265942	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246913055	TATGCAAGAAGTATC[C/T]ACTGTGCTCAGGTCC	25909
rs374271779	snp	A/G			utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840014	AAAATTTGTTCAGAC[A/G]TCTCATCCTATCAAT	25909
rs374274680	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246898935	TCTACTAAAAATACA[A/G]AATATTAGCCGGGCG	25909
rs374281941	snp	C/T	2.20233e-05	0.00331831	intron-variant	AHCTF1	GRCh38.p7	1:246862201	AAAAGTGCTTATAGG[C/T]CGGGCGCGGTGGCTC	25909
rs374319977	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246868915	AGTGGTGTGATCTCG[A/G]CTCACTGCAAGTTCT	25909
rs374352059	snp	A/C/T	1.7051e-05	0.0029198	intron-variant	AHCTF1	GRCh38.p7	1:246899522	TGGCATCTAAAAAAA[A/C/T]GATTTAAAAAATAAT	25909
rs374422640	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246924072	CCTCCTATCTATTGA[A/G]TACAGAAAGGACTAC	25909
rs374435402	snp	A/G	0.00517822	0.0506191	intron-variant	AHCTF1	GRCh38.p7	1:246869052	GGTTTCACCATGTTG[A/G]CCAGGATGGTCTCGA	25909
rs374471218	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246931567	CAACCCCCTCCCTCC[C/G]TTCCCCCTACCTGAA	25909
rs374482635	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246913816	GCATAAAACGCAAAC[C/G]TAAATTGTTCTCATT	25909
rs374560518	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246855230	GCTTCCCCTGAATCC[A/C]ACTGTAAGCTCCTTA	25909
rs374602603	snp	A/C/G	5.00124e-05	0.00500041	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850773	TCACGTTTTGGATAC[A/C/G]TTGACCTCTCGTACG	25909
rs374602983	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246868384	CCTTGGCCTCCCAAA[C/G]TGCTGGGATTACAGG	25909
rs374608822	snp	C/G	0.0558544	0.157504	intron-variant	AHCTF1	GRCh38.p7	1:246903660	TGGTGAGACCCCCCC[C/G]CCTCCGTCTCTGCTA	25909
rs374610979	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246922078	TGAAAACATATACAG[A/G]GCTGGGCACAGTGGC	25909
rs374627296	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246843250	GAATGCCTGTCTCCT[C/T]TAACCTCGGTCTATA	25909
rs374687125	snp	C/T	1.66502e-05	0.00288527	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850787	CGTTGACCTCTCGTA[C/T]GAGTTTTGGAGGAAA	25909
rs374710464	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246856127	TATTTAAGCCAATTT[C/T]TAATAATCTGTGGCC	25909
rs374720542	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246878700	TGCACTGCCCTATAC[A/G]TTCTGTGAATACAAA	25909
rs374757952	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246854639	ACATTTACTAAACTT[C/T]AGGTACCAAGCGCTA	25909
rs374798878	snp	C/T	1.65392e-05	0.00287564	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877184	CTGTAAATGGTAACT[C/T]CAGTAAATCTTCCAT	25909
rs374800499	snp	A/G	1.65195e-05	0.00287393	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246888480	CTAACTGAGAAACCA[A/G]TCCATCAATCATCAA	25909
rs374821852	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246882143	GCTGGGACTACAGGC[A/G]TGCACCACCTCGCCC	25909
rs374904963	snp	A/G	0.0146672	0.084371	intron-variant	AHCTF1	GRCh38.p7	1:246858147	TGTATTTTTAGTAGA[A/G]ACGGGGTTTCACTGT	25909
rs374928501	snp	A/C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246929779	TCTGTACCAGCCGGG[A/C/T]GCGGTGGCTCACGCC	25909
rs374936055	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246869413	CCTCTTATGCCAGTT[A/T]GCCAAGTTGTAAATG	25909
rs374963100	in-del	-/TTT			intron-variant	AHCTF1	GRCh38.p7	1:246857957	TCAGACTGCTAACAC[-/TTT]TTTCTTCTTTTTTTT	25909
rs375008404	snp	G/T	3.29473e-05	0.00405864	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246898227	CTTAAACTGGAAGGC[G/T]GAACATCAACAAATC	25909
rs375048035	snp	G/T	0.00049613	0.0157423	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246918261	TTACCTGCAGCAAAC[G/T]TTCCACGAAGCACAG	25909
rs375082870	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869036	TTTTTAGTAGAGACG[A/G]GGTTTCACCATGTTG	25909
rs375097328	snp	A/T	0.000138882	0.00833196	intron-variant	AHCTF1	GRCh38.p7	1:246891942	GAATAAAAGAAAAGA[A/T]AAGTTTCCATACAGT	25909
rs375099156	snp	C/T	3.2993e-05	0.00406145	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851060	ACTTTTTGGGACTTT[C/T]GGTCACTAGTTACGG	25909
rs375132592	snp	C/T	3.50238e-05	0.00418458	intron-variant	AHCTF1	GRCh38.p7	1:246913463	CAAAGTAAGAAAATA[C/T]AATTAACACAATAAA	25909
rs375145421	snp	A/G	0.000355556	0.0133286	intron-variant	AHCTF1	GRCh38.p7	1:246843756	AAAAAAAAAAAGTAT[A/G]TTTTAACAAACATAC	25909
rs375161879	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246884137	TTATTCAACAGTTAC[C/T]ACATTTAGCTTCTTT	25909
rs375170246	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246879815	CCTGGGTGACAAAGT[C/G]AGACTCTGTTCCCCC	25909
rs375232044	snp	A/G	2.12836e-05	0.00326211	intron-variant	AHCTF1	GRCh38.p7	1:246885449	CAATTCCATTTTATT[A/G]ACAGATACGATAAAG	25909
rs375284074	snp	C/T	1.7107e-05	0.00292459	intron-variant	AHCTF1	GRCh38.p7	1:246857640	ACTTCTGGTTCATAA[C/T]TTCATTAAACTTCTT	25909
rs375306954	snp	C/T	0.0146672	0.084371	intron-variant	AHCTF1	GRCh38.p7	1:246847420	ATGTATCTGGAACGA[C/T]ATACAGGAAAACGTG	25909
rs375335803	snp	A/G	1.9297e-05	0.00310614	intron-variant	AHCTF1	GRCh38.p7	1:246918413	AAACATTATTATGAC[A/G]CATTTGTAGACAATA	25909
rs375354441	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246863225	GGTATCTTTTATTCA[A/G]CTTGAAAAATAAGGA	25909
rs375362186	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849738	GGGATGATTTAGTGA[A/G]GGAAGCTGTGGCGAG	25909
rs375362581	snp	C/T	4.9534e-05	0.0049764	intron-variant	AHCTF1	GRCh38.p7	1:246888283	TTATACAGTCATTCA[C/T]TCATTCATGCTTCTT	25909
rs375402511	snp	C/T	1.64876e-05	0.00287116	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849658	TGGAGAAAATAAAGG[C/T]TCATTGTTTGGTTCA	25909
rs375441020	snp	A/G	1.66774e-05	0.00288763	intron-variant	AHCTF1	GRCh38.p7	1:246876929	CTCTTATCCCCCATA[A/G]TAAGACAACTTTAAT	25909
rs375462884	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246900496	GATAATTTTTAAAAA[-/A]CAGAATAAAGAATCT	25909
rs375470134	snp	A/G	1.68567e-05	0.00290312	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850382	TCTACAGATCTTTTA[A/G]TTCTTCTAGGAGTCC	25909
rs375479517	in-del	-/TTA			cds-indel, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839712	CTAGATAATCAATTA[-/TTA]ATAGTCCATTCATTA	25909
rs375482777	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246872038	TAGATTCAGAAAGAT[A/G]AACTATTAATGACAA	25909
rs375513578	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246901238	CCCAGCTACTCAGGA[A/G]GCTGAGGTGGGAGGA	25909
rs375529420	snp	G/T	0.000100334	0.00708217	intron-variant	AHCTF1	GRCh38.p7	1:246891742	GTCAAGAAGTAAAAT[G/T]TAATAAAACACTCAT	25909
rs375584455	snp	A/C/G	0.000258618	0.0113687	intron-variant	AHCTF1	GRCh38.p7	1:246907797	GAAGTTAAAAAACTA[A/C/G]AAACAGCATTAAAAG	25909
rs375589160	snp	C/T	6.61857e-05	0.00575226	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864084	GAACACTGAGAAGGC[C/T]GGGGGACAGGCTGAA	25909
rs375615157	in-del	-/CTGG	0.00795532	0.062565	intron-variant	AHCTF1	GRCh38.p7	1:246922554	CTCGTGCCACCATGC[-/CTGG]CTAATTTTTTTTTTT	25909
rs375642977	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246872352	GTGATGCCCCAGGAC[C/T]CAAAAACTTCAGGTA	25909
rs375643011	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246893776	TTACCTAGCACATTC[C/T]GCTTACTCCATCATC	25909
rs375657308	snp	C/T	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246929867	GACCAGCCTGGCCAA[C/T]ATGGTGAAACCCCGT	25909
rs375680762	snp	A/C			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933866	CAAGGTATTGGACCA[A/C]GTTGTGATAGAAACA	25909
rs375715157	snp	A/G/T	0.0213452	0.101169	intron-variant	AHCTF1	GRCh38.p7	1:246868990	GCTGGGACTACAGGC[A/G/T]CCCGCCACCATGCCT	25909
rs375722416	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246845544	TAACTCTCTTCTAGG[C/T]TACCTGAAAAAACGA	25909
rs375728771	snp	A/G	0.000183626	0.00958014	intron-variant	AHCTF1	GRCh38.p7	1:246905506	TGTCTCCAAAAAAAC[A/G]AAACAAAACAAAACA	25909
rs375742788	snp	A/G	1.65507e-05	0.00287664	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849949	TTTTCCAACATCAAC[A/G]TTTTCACTTTTAGCT	25909
rs375761312	snp	C/G	0.00358779	0.0422022	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932403	CGAGTGATAATCTTT[C/G]TCCCATAATTGGCAG	25909
rs375765269	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246926180	AGGTAGGCAGCTGCT[A/G]GTGTCATGCCTGCAC	25909
rs375868677	snp	C/T	3.38003e-05	0.00411084	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916326	CTGTAAGCAGACAAT[C/T]GCTCTCCTGTTATAG	25909
rs375884310	snp	C/T	0.0174175	0.0916809	intron-variant	AHCTF1	GRCh38.p7	1:246868993	GGGACTACAGGCGCC[C/T]GCCACCATGCCTGGC	25909
rs375886381	snp	C/T	4.79145e-05	0.00489438	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867336	CACTATAGGAGATGG[C/T]TCTTCTATTTTAGAA	25909
rs375910854	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246872051	ATGAACTATTAATGA[A/C]AAAAAAAAAAAAAAA	25909
rs375932279	in-del	-/ATA			intron-variant	AHCTF1	GRCh38.p7	1:246916555	ATCATTACAATAATA[-/ATA]GTCATTCAGTGGCGT	25909
rs375932948	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246847104	CTAGCTTGGCCAACA[C/T]GGCGAAACCCTGTCT	25909
rs375933399	snp	A/G	0.00953873	0.0683987	intron-variant	AHCTF1	GRCh38.p7	1:246922852	GCCGGGCGTGGTGGC[A/G]GGCGCCTGTAGTCCC	25909
rs375978705	snp	C/T	0.000122003	0.0078094	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861262	CACATTTTTTAGGTG[C/T]AGTAAATACTTCTAA	25909
rs375999683	snp	C/G	0.000120355	0.00775647	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851376	CAGAGGGATATAACT[C/G]ATTAAATGAAAGATT	25909
rs376018203	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246907945	TTATCTATTTAAATG[C/T]CACAATTTAAAAAAC	25909
rs376044622	in-del	-/GATTTTAAAGTACT			intron-variant	AHCTF1	GRCh38.p7	1:246889596	ATTACAGCCGGCACA[-/GATTTTAAAGTACT]GATTCCCAGGTGATT	25909
rs376048859	snp	C/T	0.000407747	0.0142726	intron-variant	AHCTF1	GRCh38.p7	1:246916123	AGAGAAATGTCCAGG[C/T]ATCTTAAACAGTACC	25909
rs376055634	snp	C/T	1.66488e-05	0.00288515	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246885539	TAACATCGTTACCAC[C/T]GGACACTGTTGGCTT	25909
rs376061981	snp	C/T	4.94662e-05	0.00497299	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867726	TCCAATTTTAGATAA[C/T]ACATTGTTGATGAAA	25909
rs376073830	snp	A/C	0.000699872	0.0186935	intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842681	CAATCAAGAACAGAA[A/C]AGAAAGTCATACTTG	25909
rs376126499	snp	C/G	0.000403234	0.0141935	intron-variant	AHCTF1	GRCh38.p7	1:246867851	TAAGTGCATCTCTAA[C/G]AAACGGGAATTTAAT	25909
rs376171651	snp	C/T	0.000131946	0.0081213	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850214	CTAACATGTTTAATA[C/T]GCAGCTGCTTGTCAC	25909
rs376196185	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246897185	GGGTGTGGTGGCACA[C/T]GCCTCTAGTTCCAGC	25909
rs376217768	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246909071	TAATTCTATATCTAT[A/C]TATATCTATATCTAT	25909
rs376245355	snp	A/C	0.00318978	0.0398085	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839177	TTTAAAATATATGTA[A/C]AGTTCATTTAGAACA	25909
rs376278917	snp	C/T	1.69642e-05	0.00291236	intron-variant	AHCTF1	GRCh38.p7	1:246887396	AATAAAATACAACAA[C/T]AAAAACCTCCTACGT	25909
rs376323714	snp	C/T	3.40426e-05	0.00412554	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246918366	TGAGCTCTTAAGTCT[C/T]GCATACTTCCACTGT	25909
rs376427862	snp	A/G	1.66801e-05	0.00288787	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246862052	AGGTGATGGAGAGGG[A/G]GATGCTAAAGGTGTT	25909
rs376474185	snp	C/T	0.0244538	0.107838	intron-variant	AHCTF1	GRCh38.p7	1:246922798	CCATCCTGGATAACA[C/T]GGTGAAACCCTGTCT	25909
rs376513733	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246925086	CCTTTTATATAGCTT[A/G]ATAAAACTAGTTTAA	25909
rs376522295	snp	A/G	0.000297015	0.0121827	intron-variant	AHCTF1	GRCh38.p7	1:246877099	AAAAAGAACAAAATA[A/G]ATTGTAAACTACCAA	25909
rs376540570	snp	C/T	5.19458e-05	0.0050961	intron-variant	AHCTF1	GRCh38.p7	1:246860871	GGACATTAATAACAA[C/T]TTTGAGTATTCAGAA	25909
rs376540753	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246909886	GTAGCACCAGCAGTA[A/G]CAATCAAAAATGTCT	25909
rs376628761	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246868266	CCCGAGTAGCTGGGA[A/C]TACAGGAATGTGCCA	25909
rs376641485	snp	C/T	2.10617e-05	0.00324506	intron-variant	AHCTF1	GRCh38.p7	1:246885457	TTTTATTAACAGATA[C/T]GATAAAGACTTTATA	25909
rs376646297	snp	A/C/G	5.20877e-05	0.0051031	synonymous-codon, missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840977	GGGAGGAGGTGACCA[A/C/G]GCACTTTCTTTTTCT	25909
rs376685608	snp	A/G	0.000153988	0.00877328	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861201	TTCAGGAAAAAAGAT[A/G]TGGTCCTATCTTTGC	25909
rs376766906	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246922722	GCGCAGTGGCTCACG[A/C]CTGTAATCCCAGCAC	25909
rs376772059	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246894979	AATCATGAGGAGCGA[C/T]GGCAAGCACAAACTA	25909
rs376781120	snp	C/G	8.24858e-05	0.00642153	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246855747	TTATTGTCATTTGCT[C/G]TAATTGCAGGGGTGT	25909
rs376786479	snp	C/T	0.000442951	0.0148755	intron-variant	AHCTF1	GRCh38.p7	1:246876020	TAGATTATGATATTC[C/T]TCAATGAAATTCTTA	25909
rs376794190	snp	A/G	4.94214e-05	0.00497074	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246907688	CTGGAAACACAGATG[A/G]CGCCCTTGTCTCATT	25909
rs376798744	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246896435	AACCTTGAAAACATG[C/T]TAAATGAGACAGTCA	25909
rs376806951	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246844796	AATTAAAAGCATTTA[C/T]CACACAGACTTTTTT	25909
rs376837343	in-del	-/C			intron-variant	AHCTF1	GRCh38.p7	1:246882792	AATTTGCACGTAAAA[-/C]CAGCCACGCCACAGT	25909
rs376837878	in-del	-/AAATTTGTTGAATACTAA			intron-variant	AHCTF1	GRCh38.p7	1:246877432	TGAAAAGTACTTTAA[-/AAATTTGTTGAATACTAA]GTACTGCATAATAAT	25909
rs376844732	snp	G/T	6.59228e-05	0.00574083	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246895911	TGCTGACAATATAGC[G/T]TCTAACTGTTCTTCC	25909
rs376888811	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246841214	AATTTTTTCATTTTC[A/G]ATCAGAATATTTACA	25909
rs376933748	snp	G/T	0.000153988	0.00877328	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246907561	CTTACTCTCTTTTCA[G/T]GCTTTTCATGTTCCA	25909
rs376943640	snp	A/T	3.59357e-05	0.0042387	intron-variant	AHCTF1	GRCh38.p7	1:246885706	CATGAAAAATGTTAA[A/T]TATAAATATAATCCT	25909
rs377050688	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246923899	CCAGGTCTGGAAGTC[C/T]CTAACTACATACTAT	25909
rs377075707	snp	C/T			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932666	AATGCTCGCGCAGCC[C/T]AGCCTAATCTTTTTA	25909
rs377088513	snp	A/G			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932960	TTTATTTTTGAGACA[A/G]TGTCTCGCTCTGTCG	25909
rs377097885	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246888627	ATCAAAGAGAGAAGA[A/G]GCTGGGCATGGTGGC	25909
rs377099713	in-del	-/GTTT			downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838891	CTTTCTGAGTACATT[-/GTTT]ACCTTACTACTGATA	25909
rs377251787	snp	A/G	0.000177456	0.00941787	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850451	GTTTCTTCAACTGCT[A/G]GTTCCAACAGCTGAG	25909
rs377257919	snp	A/G	3.30273e-05	0.00406356	missense, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840891	GTTCCTGTCACTTCT[A/G]TAGTTTTTCTTGGTT	25909
rs377315376	snp	C/T	3.37177e-05	0.00410582	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246894745	GTGGCAGAATTTGGT[C/T]GTTCTTATTTGTAAA	25909
rs377345070	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246868171	TCTTGCTCTGTAGCC[C/G]AGGCTGGAGTGCAGT	25909
rs377357876	in-del	-/CT	0.00676609	0.0577691	intron-variant	AHCTF1	GRCh38.p7	1:246874607	TTCCTTCCCTTCACC[-/CT]GTTTAACATTAACTT	25909
rs377375258	snp	A/G	0.00011536	0.00759387	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864000	GATCCTTTTAATTGC[A/G]AACTTGAGGGCAGTG	25909
rs377388249	in-del	-/C	0.00993419	0.0697739	intron-variant	AHCTF1	GRCh38.p7	1:246919478	CAGCACTTTGGGAGG[-/C]TGAGGCAGGCGGATC	25909
rs377390554	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246930051	GCAAGACCCCGTCTC[-/A]AAAAAAAAAAAAAGA	25909
rs377508264	snp	A/G	0.000155988	0.00883004	intron-variant	AHCTF1	GRCh38.p7	1:246843968	TCTGTATCTTTATAT[A/G]TGTGTGTATATATAT	25909
rs377558015	snp	C/T	3.32851e-05	0.00407939	intron-variant	AHCTF1	GRCh38.p7	1:246900299	AGCTACACATACAAA[C/T]ACAAAGAGAAAGGAG	25909
rs377563134	snp	A/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246899033	GGCAGAGGTTGCAAT[A/G]AGCCGAGATGGTGTC	25909
rs377572505	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246846459	GCACTACCACATTCA[C/T]TCTAGGAGGAGGAAA	25909
rs377574206	snp	C/T	7.03346e-05	0.00592979	intron-variant	AHCTF1	GRCh38.p7	1:246916434	TTTTAATATTGTATA[C/T]ACACAAAACATGCAA	25909
rs377608299	snp	C/T	1.65203e-05	0.002874	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246899479	CCAGTACAAGTTAAA[C/T]GAACAACTCCCGAGT	25909
rs377630628	snp	C/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246919557	TCTCTACTAAAAATA[C/T]AAAAAATTAGCCAGG	25909
rs377632340	snp	G/T			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933529	TCAGCCTCTCAACGT[G/T]CTGGGATTACAGACA	25909
rs377658506	snp	G/T	1.86586e-05	0.00305434	intron-variant	AHCTF1	GRCh38.p7	1:246891103	TTACTTACAAAAAAA[G/T]CAAGATGCTCCACAG	25909
rs377664267	snp	C/G	1.64947e-05	0.00287177	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850703	CTGACTGACTGCCCT[C/G]GCATCTTAGGAGTAG	25909
rs377665424	in-del	-/GTTTA			downstream-variant-500B	AHCTF1	GRCh38.p7	1:246839007	ATACTAAGCACCTTA[-/GTTTA]ACCAATGCTTTGATC	25909
rs377698455	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246853644	TCCTTGTAGAGTAAT[C/T]ACAGAATTACATGAG	25909
rs377764344	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246908654	GCACTTTGGAAGGCC[A/G]AGGTGGGCGGATCAC	25909
rs386354762	in-del	-/A	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246877554	CAAAGTAGACAAAAA[-/A]TTCAAAGAAGACAAA	25909
rs386354763	in-del	-/A	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246879848	CCCGCCAAAAAAAAA[-/A]GGGAGAACTAATTTA	25909
rs386370367	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246879842	CCCAACCCCGCCAAA[-/A]AAAAAAGGGAGAACT	25909
rs386641780	multinucleotide-polymorphism	GC/TG			intron-variant	AHCTF1	GRCh38.p7	1:246868905	GTTGGAGTGCAGTGG[GC/TG]TGATCTCGGCTCACT	25909
rs386641781	multinucleotide-polymorphism	CA/TG			intron-variant	AHCTF1	GRCh38.p7	1:246869001	AGGCGCCCGCCACCA[CA/TG]CCTGGCTAACTTTTT	25909
rs386641783	in-del	AGG/GA			intron-variant	AHCTF1	GRCh38.p7	1:246882480	TAATGAAAATTTAAA[AGG/GA]TACTTAGAACAGAAT	25909
rs386641784	in-del	CC/TCT			intron-variant	AHCTF1	GRCh38.p7	1:246891485	AAAAAATTTATGAGT[CC/TCT]TTGAATAAAAAATAC	25909
rs386641785	in-del	CGGG/TGGGAAGATCGCTTAAGCCCAAGAGGTTGAGGCTACAGTGAGCCATGAC			intron-variant	AHCTF1	GRCh38.p7	1:246897884	TTGCGGGGGCTGGGG[lengthTooLong]CATGCCACTGCATTC	25909
rs386641786	multinucleotide-polymorphism	CG/TC			intron-variant	AHCTF1	GRCh38.p7	1:246903154	AAACCCGTTTCTATA[CG/TC]CCTCCAACATTAGGT	25909
rs386641787	in-del	C/TAAAT			intron-variant	AHCTF1	GRCh38.p7	1:246906707	AAATGGAGAAACAAA[C/TAAAT]TGACAACTTAAGGGC	25909
rs386641788	multinucleotide-polymorphism	CA/TG			intron-variant	AHCTF1	GRCh38.p7	1:246920694	AGAATGGCATGAACC[CA/TG]GGAGGCGGAGCTTGC	25909
rs386641789	multinucleotide-polymorphism	CCA/GCG			intron-variant	AHCTF1	GRCh38.p7	1:246929778	ATCTGTACCAGCCGG[CCA/GCG]CGGTGGCTCACGCCT	25909
rs386641790	in-del	ATCT/CCCAAGATGTGCTTTTATTTTA			intron-variant	AHCTF1	GRCh38.p7	1:246931022	AGGAAGGCAAAGCAC[ATCT/CCCAAGATGTGCTTTTATTTTA]AATCTCCTTGATCTG	25909
rs397701939	in-del	-/TTTAA/TTTAC			intron-variant	AHCTF1	GRCh38.p7	1:246854967	TGATCGGCTTTTTAC[-/TTTAA/TTTAC]ATGTTAGACAATTCT	25909
rs397730569	in-del	-/GAG	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246910787	TTTTTCAGAGAAGAG[-/GAG]ATTAGATTTTGCCAC	25909
rs397776307	in-del	-/AAAATA			intron-variant	AHCTF1	GRCh38.p7	1:246929435	ATAAAAATAAAAATA[-/AAAATA]CAGTGAAAACATTGG	25909
rs397792946	in-del	-/AAAA/AAAAC/AAAC			intron-variant	AHCTF1	GRCh38.p7	1:246848865	AACAAACAACACAAA[-/AAAA/AAAAC/AAAC]CCCCCTACATTTTGT	25909
rs397821330	in-del	-/CTG			intron-variant	AHCTF1	GRCh38.p7	1:246842870	TAGAGCCAAACACTG[-/CTG]ATGAATTCAAACTCG	25909
rs397844557	in-del	-/A	0.476746	0.10529	intron-variant	AHCTF1	GRCh38.p7	1:246868612	CTTTTGGTAAGTGGT[-/A]AAAAAAAAAAAAAAA	25909
rs397860206	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246841974	TTTTTTTTTTTTTTT[-/T]CAGTAGAGACAGGGT	25909
rs397953618	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246924396	GTGCCGTTTATTTTT[-/T]GTGTGATGCAAATTT	25909
rs397973850	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246880587	AAAAAAAAAAAAAAA[-/A]TTCCACTTTAAACTG	25909
rs397983634	in-del	-/A	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246843751	TTTGTAAAAAAAAAA[-/A]GTATGTTTTAACAAA	25909
rs397983635	in-del	-/G	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246860198	CTGGTTGGGGGGGGG[-/G]CGGAGGTTGCAGTGA	25909
rs397983636	in-del	-/T	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246870079	TTCATGAATAACTTT[-/T]GAGGGCTTCAAGACT	25909
rs397983640	in-del	-/T	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246892819	AAAAGATTTTTTTTT[-/T]GGTTTTGCAGAGACG	25909
rs397983642	in-del	-/A	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246908745	AAAAAAAAAAAAAAA[-/A]TTAGCCGGGCATGGC	25909
rs397983644	in-del	-/A	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246919717	CAAAAAAAAAAAAAA[-/A]TCCTCAAGAGAAGAA	25909
rs397983645	in-del	-/AAA	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246920168	AAAAAAAAAAAAAAA[-/AAA]GAAAAGAAGCTCACA	25909
rs397983646	in-del	-/A	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246926066	AAAAAAAAAAAAAAA[-/A]GGCCTGGTACCTCCT	25909
rs398074826	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246870078	TTTCATGAATAACTT[-/T]TGAGGGCTTCAAGAC	25909
rs398090056	in-del	-/TTATA			intron-variant	AHCTF1	GRCh38.p7	1:246875046	GGCCAACAACTTATA[-/TTATA]GATAAACCAGAATGA	25909
rs527242743	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246911731	TCAAGTGATCCACCC[A/G]CCTTGGCCTCCCAAA	25909
rs527259881	snp	G/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246870214	TTTTGGAGGCCAAGG[G/T]GGGAGGATCACTTGA	25909
rs527382500	snp	G/T	0.00517822	0.0506191	intron-variant	AHCTF1	GRCh38.p7	1:246904187	TAATTTTTATAAAAA[G/T]GTAGTCCTTTGAAAT	25909
rs527417305	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246904983	AGAGAGCAGGGTACT[G/T]AGAAGGTTCCAAGGC	25909
rs527428514	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246868858	TTTGTTTTTTTTTTT[G/T]TTTTGAGATGGAGTC	25909
rs527430851	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246898411	GATTAATTAATTACA[C/T]TTAAAATTTAAGTAA	25909
rs527454255	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246898987	CTAGCTATTCAGGTG[A/G]CGGAGGCAGAAGAAT	25909
rs527480152	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246862676	ATCCATCTTTCTAAA[A/C]GCATTATTTCCAACT	25909
rs527489102	snp	C/G/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246892390	TGCAATCTCAATCTC[C/G/T]GCTCACTGCAACCTC	25909
rs527526293	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246849152	AGATGAGGGCATGTA[A/G]ATGCGCCAGTTTGTG	25909
rs527529078	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246901862	AAAACTTTAAAAAGA[C/T]GTGAGCTCATGACAA	25909
rs527539411	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246929880	AATATGGTGAAACCC[C/T]GTCTCTACTAAAAAT	25909
rs527548077	in-del	-/AAAG	0.00318978	0.0398085	intron-variant	AHCTF1	GRCh38.p7	1:246845371	TATGATTCTTAAAAA[-/AAAG]AAAAATAGAGTTGAT	25909
rs527553101	snp	A/G	8.23784e-05	0.00641735	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849804	TCATTTCATCTGTGC[A/G]TTCTTCTGATACTGA	25909
rs527678940	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246905446	AGGTTGCAGTGAGCC[A/G]AAATCACGCCACTGC	25909
rs527685517	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869280	TCCCTTTCCCCGAGG[A/G]CCTCCCTTATTCCTT	25909
rs527699910	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246878976	TGCACAGAAATATAG[C/T]CATTTTTCCCTAAAC	25909
rs527705438	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246870748	AAAAAAAAGCCCTAG[A/G]CTATTTAATTTCTCA	25909
rs527715489	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246926063	AAAAAAAAAAAAAAA[A/G]AAAGGCCTGGTACCT	25909
rs527740931	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246903152	TGAAACCCGTTTCTA[C/T]ACGCCTCCAACATTA	25909
rs527741879	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246871694	TGCTTTCTCTGTAAT[A/C]CATGCCTACAGTGCA	25909
rs527777392	snp	C/T	0.00398564	0.0444627	intron-variant	AHCTF1	GRCh38.p7	1:246920545	GGGAGGCTGAGGCGG[C/T]GAATCATGAGGTCAG	25909
rs527806848	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246913024	ATATGAACACCTGAT[C/G]AACAAAACAGTATCT	25909
rs527837906	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246906003	TGCATTCATGTCTGT[G/T]TAAACTGGTCCTAAG	25909
rs527888948	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246853401	CTGCACTTGAATAGT[C/G]TATTAATAAACTATC	25909
rs527918600	snp	C/T	1.65315e-05	0.00287498	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864072	TGAATAAACTCCGAA[C/T]ACTGAGAAGGCCGGG	25909
rs527946192	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246864490	TCTATTTACTAAAAT[C/T]CATTAACATGCAAAA	25909
rs527956977	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246858304	AGCTCAAGAGCCCCC[A/C]TTAACCTCTCGCTTT	25909
rs528013816	snp	A/G	1.65861e-05	0.00287972	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900343	GAATCATACCTTAAC[A/G]AATCTGGCATTTGTG	25909
rs528063428	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246894299	AACTTCAGGCCAGGC[A/G]CGGTGGCTCACGCCT	25909
rs528066384	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246920086	AGGCAGTTGCAGTGA[A/G]CCGAGATTGTGCAAC	25909
rs528088826	snp	C/T	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246858687	AAAATTGGCTGGGCA[C/T]GGTGGCACGTGCCTG	25909
rs528116595	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246931068	GATCTGACCAATCGG[A/G]TGAGCTGGAACCTCA	25909
rs528127298	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246931603	CGGGTGAGCGCGCCG[C/T]CGCGGGCCGAGTCCA	25909
rs528135003	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246916517	ATATTATCTCCACAT[G/T]GAAATCTTTTAATCA	25909
rs528165475	snp	A/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246852034	GGAATGGTCCTTGCA[A/G]TTACCTTTTGGTAAG	25909
rs528191338	snp	A/C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246927002	ACAAGGTGAAATCCC[A/C/G]TCTCTACTAAAAATA	25909
rs528240848	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246880244	TATATATATAAAATA[C/T]ATAATAGGCATTATA	25909
rs528294028	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246865299	TTTGGAGCCCAGAAA[C/T]AAAAACTTGTAGTTG	25909
rs528316991	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246873261	AAAAAAATCTTAACC[A/G]GTGATAAATCACCAT	25909
rs528340336	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246862971	ATTACTGAATCCCAT[C/T]AGATCATAATAAATT	25909
rs528345511	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869043	TAGAGACGGGGTTTC[A/G]CCATGTTGGCCAGGA	25909
rs528351849	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246874054	TCACTCCTGTCCTGA[A/C]ACAATCACCATTAAT	25909
rs528361259	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246922427	TCTGTTGCGGTTTTT[C/T]GGGTTGTTTTTTTTT	25909
rs528369865	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246914780	CTCTTCCATACACCA[A/G]CCATGCATTCAACTG	25909
rs528471387	snp	C/T	0.00597247	0.0543191	intron-variant	AHCTF1	GRCh38.p7	1:246869079	TCGATCTCCTGACCT[C/T]GTGATCCGCCCGCCT	25909
rs528478549	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246865843	CCCTGAGACCAAATA[G/T]TCTTTCAGAACTAAC	25909
rs528488358	snp	C/T			synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246903961	TACCTCATATAAGAT[C/T]TGTCCTGATGCCAAA	25909
rs528524232	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246885281	TTGGTCCTGCAGAGC[C/T]CATGTATATGAAAAG	25909
rs528570879	snp	A/G	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246905403	CTCGGGAGGCTGAGC[A/G]AGAGAATGGCATGAA	25909
rs528629758	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246902157	CTGCCAGGAAAAAGC[A/G]ATGACACTAAAGAAG	25909
rs528659861	snp	C/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246888748	GACCCCAGTTCTAAA[C/G]AAAATATAAAAACTA	25909
rs528665408	snp	A/C	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246896358	TATGGTATGCTCATA[A/C]AACAGAATATTATAC	25909
rs528693993	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246896911	GGCATGACTCTAAAC[A/G]GAGACTCACTGAAGC	25909
rs528702836	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246853630	CAGACAACCAGCTAT[C/T]CTTGTAGAGTAATTA	25909
rs528753166	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246927930	GCTTGAACCTGGGAG[A/G]CAGAGGTTGCAATAA	25909
rs528759613	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246847273	CAGCCTGGGTAACAA[C/T]AGCCAAACTCCATCT	25909
rs528812461	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246928088	AGGTGGATCACGAGG[C/T]CAGGAGATCGAGACC	25909
rs528818678	snp	G/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246922314	GCAGTAAGCAGAGAT[G/T]GCACCACTGCACTCC	25909
rs528830532	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246899681	GAATAGATAACAAAC[C/T]TATTACACAGCAAAA	25909
rs528831515	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246882083	GCTCACTGCAAGCTC[C/T]GCCTCCTGGGTTCAC	25909
rs528881071	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246857529	AACTACTAAATGACA[C/T]ATAACTGCACAACTA	25909
rs528955164	snp	A/G	8.33382e-05	0.00645462	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850769	ACATTCACGTTTTGG[A/G]TACGTTGACCTCTCG	25909
rs528964573	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246844092	ATGTTGGCAGAGAAA[C/T]GACAGAAAAATCCCA	25909
rs528985358	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246893534	TTTAGCCTTATTTTT[A/G]CACTAACTGGACATG	25909
rs528992602	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246926464	AAAATGTTTAATAAA[C/G]TTTTTCAAATTTAAC	25909
rs529005024	snp	A/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246894209	CCATGTCTCAAAAAA[A/G]AAAATTACTTTTATC	25909
rs529028951	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246886160	ACATGGTGAAACCTC[A/G]TCTCTACTAAAAATG	25909
rs529068212	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246886901	CATATATCAAGGCCA[A/C]ATCTTGCCTTCCATG	25909
rs529089515	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246908607	ATCCAAGAATCTTAG[A/G]CCGGGCACGGTGGCT	25909
rs529090895	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246880048	TTAGTGGGAGAGGAC[A/G]TATAGGCATTTGTTG	25909
rs529098780	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246844829	TTTTTTTTAACTATA[A/G]GGCCCCCATATTAAA	25909
rs529228497	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246872479	CATCATCTTGAGGTT[C/T]TGGCTTACTCCAACC	25909
rs529229231	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246913829	ACCTAAATTGTTCTC[A/C]TTTTAAAGCTCTTAA	25909
rs529266507	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246906938	TAGGAAGGTACTTCT[C/G]AAAGAACTCATATTA	25909
rs529271528	snp	C/G	0.43221	0.171171	intron-variant	AHCTF1	GRCh38.p7	1:246864594	AGACTAGACTGACTT[C/G]GGAGGCCGAGGCGGG	25909
rs529307691	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246865751	TCAAGACTTAATAGT[G/T]TAAAGGTTCTGAGAA	25909
rs529315551	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246854411	CACAAGAATATTCAC[C/T]GCAGAAACAGCAAAA	25909
rs529332728	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246878046	ACCCAATGATCCCAA[A/T]GCAAAGAATACAGTC	25909
rs529368565	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246851809	AAACAGAAACAACCC[C/G]CAAACTGTGTTTTAA	25909
rs529403161	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246901165	GCAACACAGCAAAAA[A/C]CTCATCTCTACAAAA	25909
rs529415955	in-del	-/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246875652	AGTAGTCACCATGCT[-/G]ATCAGTCAGCAGCCA	25909
rs529419649	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246901594	GTGCAACTGCACTGG[A/G]CAGAGCGAGACTCCA	25909
rs529420324	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246908630	CGGTGGCTCACGCCT[A/G]TAATCTCAGCACTTT	25909
rs529428003	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246927190	CTCAAAAAAAAAAAA[A/G]GAAAGAAATAGGCCA	25909
rs529435715	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246910812	TGCCACAACAAACAG[C/T]TCACACAATGGGATA	25909
rs529444043	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246866418	AAAATACCATCTTAC[A/C]AGAGTAAATAAAGGG	25909
rs529479892	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246859825	TCCCGAAGTGCTGGT[A/G]TTACAGGCGTGAGCC	25909
rs529524216	in-del	-/TCAAT	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246857472	CACCAGAGTTCTGCC[-/TCAAT]TCAATTTACCGTGTC	25909
rs529534864	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246887996	AAACAAAATTTTTCA[C/T]ATAGTTTTAGGTTGA	25909
rs529549845	snp	C/T	0.00159617	0.0282053	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246931872	CCGCGCTTCTGGGTC[C/T]TTCCCCTTGCAACGC	25909
rs529562509	in-del	-/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246911929	TTTTATCACTTGCAG[-/T]TTTTTTTGTTTTTGT	25909
rs529572167	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246846397	GTCCTAGAGTGGTCA[C/T]TGCTTTGTTAAAGGA	25909
rs529573143	snp	G/T	5.01073e-05	0.00500511	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246888513	AATCGGGATTCCACT[G/T]CCCTCTGCAATCAGG	25909
rs529608809	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246881469	ATATTTGACATTTCA[C/T]CTATTAAATGGAGAA	25909
rs529610844	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246889310	TTTCTAATTGTGAAT[A/G]GCGGCAGCACTTACT	25909
rs529629265	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246927413	GGAATCGCTTGAACC[A/G]GGGAGGTGGAGGTAG	25909
rs529646966	snp	A/C/T	0.00517997	0.0506535	intron-variant	AHCTF1	GRCh38.p7	1:246882036	GGAGTCTTGCTCTGT[A/C/T]GCCCAGGCTGGAGTG	25909
rs529719084	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246922558	TGCCACCATGCCTGG[C/T]TAATTTTTTTTTTTT	25909
rs529765839	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246880864	AAGACAATAATGATG[C/T]TAGGAAGAACAATAA	25909
rs529781459	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246893775	GTTACCTAGCACATT[C/T]CGCTTACTCCATCAT	25909
rs529782106	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246915465	CTCAGCCATTCTAAA[C/T]CAAGTCTAGTTTCCC	25909
rs529793286	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246875132	CCTTACCATGACATG[A/C]GACCTATATACTGAC	25909
rs529797292	snp	C/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839823	TTGCTTAATTGCACA[C/G]AGTTGTACTGTAGAG	25909
rs529826196	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246909101	TCTATCTATCTATCT[A/G]TCTATCTATTTATAT	25909
rs529913705	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246845369	CATATGATTCTTAAA[A/G]AAAAGAAAAATAGAG	25909
rs529916101	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869433	AGTTGTAAATGCAAA[A/G]AAGAACCTGAAGGAA	25909
rs529971980	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246902955	TAAACTGGAATAACC[A/G]TCAAAATTATATATG	25909
rs529975470	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246842985	AATTCAACTAATCTC[C/T]AAGTTATCATCAGTT	25909
rs529975762	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246860657	CTGAACACTCCCACC[A/G]TGCCTGGCTAATTTT	25909
rs529975930	snp	A/C/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246867897	AATGATTACACCCCC[A/C/G]CCCCCACACACACAC	25909
rs530026674	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246927143	AGATCGTGCCACTGC[A/G]CTCCAGCCTGGGCGA	25909
rs530107612	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246847688	TACTTTTTGTAGAGA[C/T]GGGGTTTTTTTGGCC	25909
rs530145691	snp	C/G	1.74154e-05	0.00295083	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840756	ATTTAATAATCCACA[C/G]TATTCTGATGACTTT	25909
rs530147836	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246928771	AAACATTTCTATAAA[C/T]CACTTTGTATGCAAT	25909
rs530183820	snp	A/T	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246855107	GTTGAGAGCATGGGC[A/T]CTAGAGTCAGATAAC	25909
rs530201223	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246897619	TGTTACTGTGCTGAA[C/T]ACTGTAAGCAACTGT	25909
rs530224202	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246848305	TGCAAGCTCTGCCTC[C/T]CAGGTTCACACCATT	25909
rs530240690	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246890503	AACAAATATAGCACA[A/G]GTCAAATACCAAAAA	25909
rs530264011	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246882695	TGTACATTTATGATC[C/G]TAAGACTGAATAATC	25909
rs530312892	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246918192	TATAATATATACTTA[C/T]TATTATTTATCTTAC	25909
rs530322992	snp	C/T	0.000701895	0.0187204	intron-variant	AHCTF1	GRCh38.p7	1:246876920	TTCCTTATTCTCTTA[C/T]CCCCCATAATAAGAC	25909
rs530324709	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246881765	ATCGCTTGAACCTGG[A/G]AGGCAGAGGTTGCAG	25909
rs530382245	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246869143	CCACCACGCCCGGCC[A/G]TGTGTTTTGTTTTTT	25909
rs530409010	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246924487	AAAACATATATATAT[A/G]AAATAAAAATGCAAC	25909
rs530460357	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246868977	AGCCTGCTGAGTAGC[C/T]GGGACTACAGGCGCC	25909
rs530473003	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932299	GTGGTAGTCTTCGCT[A/G]GGGGTCGCGCCGGGC	25909
rs530483687	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246921783	CTGAAAGGATCCTTA[A/G]CAAATACGAAATATG	25909
rs530533019	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839329	CATACGTTGCATCCA[C/T]GTTTATTGTGCTACT	25909
rs530539292	in-del	-/AGTAGCTGGGACTAC			intron-variant	AHCTF1	GRCh38.p7	1:246868971	TGCCTCAGCCTGCTG[-/AGTAGCTGGGACTAC]AGGCGCCCGCCACCA	25909
rs530542038	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246922505	ATCAGAGCTCAATGC[A/T]GCCTCAATCTCCTGG	25909
rs530558713	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246845733	ATTCTTTACCCATCT[C/T]TTGTTTTGAGGATTA	25909
rs530559505	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246881427	ATTAAAACCATGCAA[C/T]GAACAAACTTGATCA	25909
rs530605377	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246874177	CCAGTTTCTAGTATA[C/T]ACAAGTAGACATGCC	25909
rs530641988	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246928288	AGCCTGGGCGACAGA[C/G]CGAGACTCCGTCTCA	25909
rs530658735	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246915316	GCCTGCTGACAGAGC[A/G]ACTCTGTCTCAAAAA	25909
rs530662204	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246873397	CAAAGGGAAAGAATC[C/T]GTCCCAATACTAAAT	25909
rs530693930	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246916047	AAATTGTAAATGTTG[C/T]GGGTCAGTGAAATTT	25909
rs530726178	snp	C/G/T	0.000100202	0.0070775	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246860933	TGAAGGAGTTACTTC[C/G/T]GATGCAAATACATCT	25909
rs530730609	snp	A/C	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246909631	AGTGGTCATGCTGGC[A/C]ATTCAGATATGCCAA	25909
rs530737770	snp	C/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246885290	CAGAGCCCATGTATA[C/T]GAAAAGCTGACCTTC	25909
rs530768062	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246902229	CATGGCTCAAAAAAT[A/T]CACGGGTAAACTTCA	25909
rs530783547	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246866789	CTTGCAATCACAATT[A/T]CATCTTGGATACAAA	25909
rs530796841	snp	A/C	0.00755907	0.0610114	intron-variant	AHCTF1	GRCh38.p7	1:246883783	CTAGTTTTCTGGGGA[A/C]TGGAAAATTGAGACT	25909
rs530814285	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246908830	GTGAATCCGGGAGGC[A/C]GAGCTTGCCGTGAGC	25909
rs530836421	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246860408	CTAAATTTCACGGCC[A/C]AATAAAAAATGTAAC	25909
rs530885571	in-del	-/A	0.00438332	0.0466095	intron-variant	AHCTF1	GRCh38.p7	1:246869914	ATAGCTGTCACAGAT[-/A]AGTGATTCCTCTGAG	25909
rs530917521	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246867228	TGTCTCTAAGAATGA[G/T]TTAATAAACTCTTAC	25909
rs530918956	in-del	-/CATATTTATG	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246924517	TTTAAAAATACAGTA[-/CATATTTATG]CATATTTATGTAGCC	25909
rs530922496	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246859947	ATTATAGAAACTTAA[A/C]ACTGGTGGATAAGTT	25909
rs530956268	snp	C/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246869065	TGGCCAGGATGGTCT[C/T]GATCTCCTGACCTCG	25909
rs531000218	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246922034	TAAAGATACATTGGT[A/G]TATTTTAGACTTTGT	25909
rs531019800	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246896424	TAATACAGATGAACC[C/T]TGAAAACATGCTAAA	25909
rs531037589	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246854519	CACTATTAGAGCTGT[C/T]AAAAAGAACAGGATT	25909
rs531049330	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246847562	GAGTGCAGGGGCACA[C/T]GATCATGGCTCACTG	25909
rs531052781	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246889475	ACACTTAGGAAATAA[A/C]AGATCTAGAATTTTA	25909
rs531056807	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246896805	TTCATTCATTACAGG[A/C]GCAAATTAAAAGATG	25909
rs531066843	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246862471	GGCGACAGAGCAAGA[C/T]TCCGTCTCAAAAAAA	25909
rs531091423	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246889770	CTTTGTCTATTACCT[C/T]TACTTCATTTCAAAG	25909
rs531097061	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246882132	CCTCCTGAGTAGCTG[A/G]GACTACAGGCGTGCA	25909
rs531119756	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246927957	ATAAGCCAAGATCAC[A/G]CCACTGCACTCCAGC	25909
rs531147087	snp	C/T	3.51642e-05	0.00419295	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876081	TGATAAGGCTTAGCT[C/T]GTTCAATGGCTAATT	25909
rs531177375	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839925	GAGGTCCTGTGAGAA[C/T]TTGCCAGTTTTAAAA	25909
rs531191952	in-del	-/G	0.00757112	0.0610593	intron-variant	AHCTF1	GRCh38.p7	1:246846752	ATATATATATTTTTT[-/G]GGGGGGATGGGGGTG	25909
rs531219727	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869797	GATGTACAGGGAGAC[A/G]AATGCTGTTAGCAGG	25909
rs531229670	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246867926	ACACACACACATTAC[A/G]TGGTAATACTAGCTA	25909
rs531232916	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246917254	AATTGGATTTCCTTG[C/T]TGATGAATGAGACAC	25909
rs531284858	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246899601	TAACAGACTGCAAGG[C/T]AAGGTGTCAAATTAT	25909
rs531313078	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246876787	AATTACGTGGTAATA[C/T]CCTGTTCCCAATTCT	25909
rs531319982	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246903679	CCGTCTCTGCTAAAT[A/G]TACAAAAAAATTAGC	25909
rs531341971	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246845574	ATTTATTTCACTTTT[C/T]GTAATCTTCACCTAA	25909
rs531345472	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	AHCTF1	GRCh38.p7	1:246839070	AGAATATCATTCATG[C/T]GCTATCCTAAAATGT	25909
rs531355327	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246897756	GATGCCAAGGTGGGA[A/G]GGTAACTTGAGGCCT	25909
rs531403920	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246861812	TTCTTTCAGAACTAA[C/T]CTTTTCTTATTTCAT	25909
rs531409222	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246847310	AAAAAAACAAACAAA[A/C]AAAAAACTGAAAATG	25909
rs531460154	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246927220	AGGCACTGTGGCTCA[C/G]ACCTGTCATCTCAGC	25909
rs531489828	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246904150	ACAAAACTAAAATCA[C/T]TGTGAAAAATTTAGT	25909
rs531491950	snp	A/C			missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900228	AAAATAAGAGCAATT[A/C]TGTAGATATTCTCCT	25909
rs531495595	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246890789	GGCATAGGATGAAGA[C/T]ACAAAGTAAGGAAAA	25909
rs531562139	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246884416	CCAAGAAAATGTAAC[A/T]TTCAGAGTGCTGACA	25909
rs531597731	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246885131	ATGTTTTTCTTAACA[C/T]TGGAAGACCAATAAA	25909
rs531598786	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246855927	TTTTGGTGATGTAAA[A/C]TGAGGTTCAGAGAAT	25909
rs531599964	snp	C/T	1.6498e-05	0.00287206	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850918	GCTCACTAAAGGTAT[C/T]GTTTCATGAATGGAC	25909
rs531607771	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246848512	GGCCAAGTCATCTAC[C/T]TTATTTATAAGGTCC	25909
rs531610625	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246877502	TGACACGTTTAAAGA[A/T]TTTTATGCTGCTTTT	25909
rs531628308	snp	A/G	0.00032943	0.0128299	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246898249	CAACAAATCTTGGGG[A/G]AAGAAGGCCAGCTAC	25909
rs531639802	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246849110	ATACAGTCCTTAGCT[C/T]GTGACAATGAAGGAT	25909
rs531656656	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246919342	TCCACATTGACCATG[C/G]CTCTGAGTCTCTTAC	25909
rs531779587	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246929869	CCAGCCTGGCCAATA[C/T]GGTGAAACCCCGTCT	25909
rs531780657	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842400	CAGCCTGGCCAACAT[A/G]ATAAAATGCCGTCTC	25909
rs531827419	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246841475	GTGGTATTAGCCATA[A/G]TGTCTTAAATAAAAT	25909
rs531862353	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246912885	ATATTGGCTGATAAG[C/G]CTCAAGATTTCTTAT	25909
rs531871998	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246878266	GCTGGGCATGGTGGT[G/T]TGTGCCTGTAGTCCC	25909
rs531910217	snp	A/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246870611	GGAATTTTACATTTA[A/T]AAGAGAAAAGTATAA	25909
rs531926072	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246899151	CAGGCACTATACCAC[A/T]GTGCTAGGTGCCTTC	25909
rs531975558	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246893328	GCGCCATGTCTTCCT[A/G]ACGAACTTGATTGGT	25909
rs532001185	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869198	ACCCTGTGTCCAGCA[A/T]GTCTACTGGCACCAT	25909
rs532011719	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246885910	GAAAAAATAAGGCTG[G/T]GCACGGTGGCTCACG	25909
rs532037010	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246869506	ATGCCTGGCTTCAAA[A/G]GACAGGGTGACTCTG	25909
rs532043369	in-del	-/C	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246884358	AATTTGTAGATCTTA[-/C]CCCTCTTATCCGTAG	25909
rs532047442	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246905913	ATGCATTTATGTGTG[C/T]GTGTAACTGGTCCTA	25909
rs532087008	snp	C/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246885325	TATGCAGGTTTTACA[C/T]CCCATGAACACTGTA	25909
rs532091281	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246917160	CACAGAGTAGCCGCA[C/G]TGGGTGGAAGACGAC	25909
rs532133843	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246903134	GGGCCTTTACTGATT[C/T]CCTGAAACCCGTTTC	25909
rs532177334	snp	C/G	0.000117425	0.00766151	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916357	AGTTTACTACCTCAA[C/G]TTGTGGACCACAAGC	25909
rs532179526	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840252	ATTTGAGGTAGATTA[A/C]ACAAAATTTGTGAAA	25909
rs532198828	snp	A/C	0.499631	0.0135733	intron-variant	AHCTF1	GRCh38.p7	1:246867903	TACACCCCCCCCCCC[A/C]CACACACACACACAC	25909
rs532236432	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246861359	AAGTCTAGTCCTAAG[C/T]TACCCATCCCAATCA	25909
rs532269794	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246897096	AGGAGGGCAGATCAC[C/T]TGAGGTCAGGAGTTT	25909
rs532271611	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246903595	AGCACTTTGGGAGTT[C/T]GAGGTGGGTGGATCA	25909
rs532291262	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246910745	AGAACAGGGCCCCCA[A/C]CCCCAAATCACTTCT	25909
rs532305750	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246897653	ACAATATGAAGTATA[C/T]GTGTATTTAAACACA	25909
rs532365579	snp	C/T	0.0123036	0.0774623	intron-variant	AHCTF1	GRCh38.p7	1:246868151	TTTTTTTTTTTGAGA[C/T]GGAGTCTTGCTCTGT	25909
rs532376052	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246890704	CATTTTCAGGAGCTA[C/T]GTTTTCTCAAATTTG	25909
rs532394440	snp	A/G	0.0174175	0.0916809	intron-variant	AHCTF1	GRCh38.p7	1:246922900	AGGCAGGAGAATGGC[A/G]TGAACCCAGGAGGCG	25909
rs532414695	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246883417	AAACTTTGTTTTCTT[A/G]AATAAGTCCCTGTAA	25909
rs532416126	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246854650	ACTTCAGGTACCAAG[C/T]GCTACACAAAACACT	25909
rs532427201	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246924052	TACCGTTTCTCAGCA[C/T]TCCCCCTCCTATCTA	25909
rs532476869	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246841498	AATAAAATGCATTCA[C/T]GTGTGCTTTTATTGA	25909
rs532549043	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246891437	GGCATTTAAATGAAA[C/T]TGGCTTGTTTTTGTT	25909
rs532596096	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246929365	AGTGAGCCAAGATCA[C/T]GCCATTGCACTCTAG	25909
rs532735254	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246868397	AAGTGCTGGGATTAC[A/G]GGCGTGAGCCACTGC	25909
rs532750301	snp	C/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246868989	AGCTGGGACTACAGG[C/T]GCCCGCCACCATGCC	25909
rs532772929	snp	G/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246847699	GAGATGGGGTTTTTT[G/T]GGCCATGTTGTTGCA	25909
rs532812942	snp	A/T	3.32674e-05	0.0040783	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900219	CCACAGTGCAAAATA[A/T]GAGCAATTATGTAGA	25909
rs532830618	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246857450	TTGGTCTTCAACAAA[A/C]ACAGAATCACCAGAG	25909
rs532869171	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246858087	GCCTCCGCCCCCCGA[A/G]TAGCTGGCACTACAG	25909
rs532869215	snp	C/G	0.00028111	0.0118523	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849989	CTTGTAGATCTCCTT[C/G]TAATGCTGGGAGCTT	25909
rs532894904	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246905099	TAACTTTTAAAATAA[C/T]TTCAACTACTACTCA	25909
rs532932126	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868807	AGTACAGGTCTACCT[C/T]ATTTTATTGTGCTTT	25909
rs532956445	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246885431	TGCCACTGTCTATCT[C/T]ATCAATTCCATTTTA	25909
rs532970100	snp	C/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246862865	TCCTCTGAAGATTTC[C/G]TATAATGAATACAAA	25909
rs533017761	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246843403	GCAGACTCATGGCAG[A/G]TAATTCAATAAATGC	25909
rs533093844	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246899626	AATTATTACATGTAA[C/T]AAATCTTTAAATAAA	25909
rs533094204	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246892545	AGGCTGGCCTCGAAC[A/T]CCTGACCTCAGGTGA	25909
rs533140055	in-del	-/T	0.0115144	0.0749975	intron-variant	AHCTF1	GRCh38.p7	1:246858661	GTGAAACCCCGCCTC[-/T]TAATAATACAAAAAT	25909
rs533151748	in-del	-/AA	0.000838954	0.0204639	intron-variant	AHCTF1	GRCh38.p7	1:246855713	AATAATCCTGAAGTC[-/AA]AATTATTATACATAC	25909
rs533154569	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246878328	CTTGATCCTAGGAGG[A/T]CAAGGCTGCAGTGAG	25909
rs533158805	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246879902	AATAATGAACTACTA[C/T]GCAATAGTTAAAAAG	25909
rs533162268	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246886091	ATCCCAGCACTTTGG[C/G]AGGCTGAGGTGGGCA	25909
rs533169441	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868943	TCTGCCTCCCGGGTT[C/T]ACGCCATTCTCCTGC	25909
rs533215428	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868991	CTGGGACTACAGGCG[C/T]CCGCCACCATGCCTG	25909
rs533221198	in-del	-/TTG			intron-variant	AHCTF1	GRCh38.p7	1:246911901	TGGCTCTTCCATTTC[-/TTG]TTAAGTATAGTTTTT	25909
rs533223102	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246926344	ACATGTAACATTGTG[C/T]TTTACTATATTCTGT	25909
rs533231401	snp	A/G	0.000273947	0.0117004	intron-variant	AHCTF1	GRCh38.p7	1:246843978	TATATATGTGTGTAT[A/G]TATATAAACACAATA	25909
rs533304944	snp	C/T	5.9783e-05	0.00546698	intron-variant	AHCTF1	GRCh38.p7	1:246900509	AAACAGAATAAAGAA[C/T]CTCAAAGTAAAATCA	25909
rs533320448	snp	A/G	0.000431023	0.014674	intron-variant	AHCTF1	GRCh38.p7	1:246907534	ATAATCAAATAAGGG[A/G]AAAAAGTTATACTTA	25909
rs533398574	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246920963	TGGCCATGGTGGCGC[A/T]TGCCTGTAATCTCAG	25909
rs533413608	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246897423	ATATACAAAAATGAA[C/T]TGCATTTTTCCATAT	25909
rs533424108	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246859217	TCTTAAACTACTTAA[A/G]ATGCAGATTTTTATG	25909
rs533473864	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246894906	TTCTCAGTGCACCAC[A/G]CCACGGAGCACGTCA	25909
rs533491894	in-del	-/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246869153	CGGCCGTGTGTTTTG[-/T]TTTTTTAAACAAATT	25909
rs533517033	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246897347	AACAAACAAATAAAC[G/T]AAAAAAGTCTATTAT	25909
rs533561859	snp	G/T	1.85824e-05	0.00304809	intron-variant	AHCTF1	GRCh38.p7	1:246861917	AGAGCTAATACATTC[G/T]TATTAAAAAATGTCT	25909
rs533561959	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246864561	TTCATTTTGCCTTTA[C/T]GGTTCTGATTACAAT	25909
rs533600675	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246855489	GGATGCATTTGGCTG[C/T]GGACTAGTAATCTAA	25909
rs533601614	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246858713	GCCTGTAATCCCAGC[A/T]ACTCGGGAGGCTGAG	25909
rs533630525	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246851560	CATAAATTATATTTA[A/G]TATGGCATATACTTA	25909
rs533668533	snp	A/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246852195	AATAACCTAGAAATT[A/T]GGATTCCCACTTACA	25909
rs533721555	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246898439	TAAAATTTAAAGATA[A/G]CAAGTGGAAATTATG	25909
rs533745456	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246884547	TGGTATAAAATAAGT[C/T]TAGTAAGGAATTTCA	25909
rs533747523	snp	A/C/G	3.29789e-05	0.00406061	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877066	CACTGGACTGCAAAA[A/C/G]TTTCACTAAACATTC	25909
rs533816458	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246918534	GATGCGGAGGCTCAC[A/G]CCTTTAAGTCCCAGC	25909
rs533818821	snp	A/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842531	AGGTTGCAGTGAGCC[A/G]AAATCACACCACTGC	25909
rs533821417	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246898743	TACAGCATTCATCCA[C/T]ATCTGGACGATTATC	25909
rs533839659	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246928542	TAAAATCAATTTTTT[A/T]AAACTCAAGATTGGG	25909
rs533852139	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246911552	GCAATGGCGCAATCT[C/T]GGCTCACTGCAGCCT	25909
rs533887274	snp	G/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246870042	CACATTAAAAGGAGT[G/T]TGTAAGAAGGTGATT	25909
rs533919454	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246842085	GGCGTGAGCCACCAC[A/G]CCCGACCTCCCATGT	25909
rs533919527	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246890857	GAGAAAAATAAGTGA[A/G]GTGGAAGAAAAGAAA	25909
rs533956185	snp	A/C	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246929075	ATAGAGGTACATATG[A/C]TGTGAGATCCCAGTA	25909
rs533988088	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246848547	CTGCTTTGCTGAAAT[G/T]CAAATATTAAACTGT	25909
rs533993175	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868868	TTTTTTTTTTGAGAT[A/G]GAGTCTCGCTCTGTC	25909
rs534010434	snp	A/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246904616	GGAAAAAATTTTTTT[A/T]AAATATGGATGTTGC	25909
rs534028587	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246841646	TTTTAAAGTGTATAA[C/T]TGTTTTTTACTAATA	25909
rs534035660	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246924955	CTTAGTTGCTCTTAT[A/G]TACACAAATGGACCC	25909
rs534046734	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246901098	TAATCCCAGCACTTT[G/T]GAAGGCCAGGTGGGC	25909
rs534082934	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246899226	AGCTTGAGGTTCACG[C/T]AGCTAGCATCTACAT	25909
rs534179482	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246870296	AAAATACCCAGGCAC[A/G]GTTGCAGTCTCAGCC	25909
rs534229361	snp	A/G	1.65381e-05	0.00287555	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850819	CACGTCATCAACCTG[A/G]CTGACATTCATAGTC	25909
rs534240773	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246862534	CAACTGAGTCACAAT[A/G]GTGGTTATATTCTCA	25909
rs534244460	snp	C/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246912161	ATGAAAAGAGCTACA[C/G]TGATATTCTAGGCTT	25909
rs534255131	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246869029	TTTTCTATTTTTAGT[A/G]GAGACGGGGTTTCAC	25909
rs534256072	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246893659	ATAACGACATCTATC[C/T]ATGGAGGACAGCAGT	25909
rs534256134	in-del	-/AG			intron-variant	AHCTF1	GRCh38.p7	1:246848025	CTCCATGCAAAACAT[-/AG]GTCTAACCACACTTT	25909
rs534292712	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246886318	CCTGGGTGACAGAGC[A/G]AGACTCCATCTCAAA	25909
rs534298671	snp	A/G	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246930534	AAGTAAACCACTCTA[A/G]TTTCTTCTCTCCTAA	25909
rs534319392	in-del	-/AAGTA			intron-variant	AHCTF1	GRCh38.p7	1:246859233	TGCAGATTTTTATGT[-/AAGTA]AAGTATGTAGTTTTA	25909
rs534355308	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246844255	AAGCATTCTGGGGAG[A/G]GAAAGCATTAATCCT	25909
rs534382479	snp	C/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246856785	TTTCTCAGGCGTAAA[C/G]CATGTGATTTAGTTC	25909
rs534538497	snp	A/G	0.0115144	0.0749975	intron-variant	AHCTF1	GRCh38.p7	1:246868997	CTACAGGCGCCCGCC[A/G]CCATGCCTGGCTAAC	25909
rs534544869	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246885746	GACAAAGTAGGTAAA[C/T]CTAACACTAAAAACC	25909
rs534559843	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246913894	AAGAGTAAAAACTAA[C/T]CATTCCAGAAAAATT	25909
rs534568398	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246864903	AAGACTAGACTGACA[A/G]CCCACACCCACCACC	25909
rs534573041	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246878749	TGGTACCCACTGTTG[A/G]CAGATCAGGGCCATC	25909
rs534579122	snp	A/G	0.00795532	0.062565	intron-variant	AHCTF1	GRCh38.p7	1:246930976	GTCAACCAGTGGCAA[A/G]AGAAACCGTCCTGTT	25909
rs534608881	snp	A/C	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246879287	AAAAAATATCTGGTA[A/C]ACTGTGTTGATAAAA	25909
rs534617037	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246920678	GGGAGGCTGAGGCAG[A/G]AGAATGGCATGAACC	25909
rs534722576	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246913483	AACACAATAAATTTA[A/G]GTTAAAGCAGGTTAT	25909
rs534727851	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246859476	CCATTTCTACTTGAC[C/T]CACTGTTTGATCTTC	25909
rs534733257	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246859628	GGGCTGGAGTTCAGT[A/G]GCGCAATCACGGCTC	25909
rs534739599	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246876662	TACCACACAATGATC[C/T]TTGTACTATGTAACT	25909
rs534755568	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246871911	CTAAAAAGACAACAC[A/G]AACATGTGAACTTTA	25909
rs534795072	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246872526	AGAACTGCCTTCATT[A/T]ACAAAGTTACTTAGG	25909
rs534803758	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246895165	GCATGATTCTGAGCT[C/G]TCTCTACCCTCTAAA	25909
rs534812893	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246845876	CTCCTGTGGCCAATG[A/C]AAACCATGGCTGGGT	25909
rs534814535	snp	C/T	1.65405e-05	0.00287576	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246918267	GCAGCAAACTTTCCA[C/T]GAAGCACAGATTCTA	25909
rs534833665	snp	C/T	0.00716266	0.059414	intron-variant	AHCTF1	GRCh38.p7	1:246864362	CGTCGTCCTCCTTCC[C/T]TTTACCTATATTTAC	25909
rs534860397	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246906407	ACAAGGTGAAAATCC[A/G]TCTCTAAAAAAAAAA	25909
rs534882207	snp	A/C/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839353	TGCTACTTGCGCAAA[A/C/G]GAATTGTTTACTGAA	25909
rs534921674	in-del	-/AA	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246929527	AGGACATGAGCAAAG[-/AA]ACATCAGAGTGGAAA	25909
rs534939657	in-del	-/TCAT	1.65388e-05	0.00287561	intron-variant	AHCTF1	GRCh38.p7	1:246888275	GTGGATCTTATACAG[-/TCAT]TCATTCATTCATTCA	25909
rs534952095	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246861354	CAGTTAAGTCTAGTC[C/G]TAAGCTACCCATCCC	25909
rs534963381	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246864263	AATCCAAAGTGCTAC[C/G]ATGCATTCAAAAAGT	25909
rs534973079	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246901257	GAGGTGGGAGGATCG[C/T]TTGAACCTGGGAAGC	25909
rs534976380	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246894521	GCACTATAGCCTGGC[A/G]ACAGAGCAAGACTCA	25909
rs535013397	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246915643	TCTTCTCCCACTAGA[A/C]TATAAGCTCTCTAAA	25909
rs535024624	snp	C/T	0.000152219	0.00872274	intron-variant, utr-variant-5-prime, upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246931269	GCGGCCCCGGCCGTC[C/T]GTAAAGGGACCCGAC	25909
rs535032396	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246874407	CACTGTAGCCTTGCT[A/T]AACTTGCTAAACCTT	25909
rs535063943	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246917849	AATGAAATCAGAAAA[A/C]GAGATTTTCTGAAAA	25909
rs535085900	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246845325	TATAAAAATGTTTTT[C/T]GTGGGTACACAGTAG	25909
rs535116869	snp	A/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246887596	CAGCACCACAAAGGA[A/G]ATAAAGCGTATTTTT	25909
rs535190603	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246904402	GCAGCTAAGTGCAGT[A/G]CCCTGTGGTAAAGTT	25909
rs535279258	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246927424	AACCGGGGAGGTGGA[A/G]GTAGCTGTGAGCTGA	25909
rs535293705	snp	A/C/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246915058	CACCACTGGCCGGGC[A/C/G]TGGTGGCTCATGCCT	25909
rs535295727	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246871846	ACAAAAAAATAAAAA[A/G]TAAAAATTTGAGGTT	25909
rs535297103	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246893961	GTAATACCAACACTT[C/T]GGAAGGCCCAGGCAG	25909
rs535304313	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839404	ATTTAACAAGTTCAT[G/T]TAAATAAGTTCAATA	25909
rs535364032	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246890357	AAGAAATGTTCACTA[C/T]AAATCAAAATCTAAG	25909
rs535375841	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246869062	TGTTGGCCAGGATGG[C/T]CTCGATCTCCTGACC	25909
rs535394286	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246892694	TGGAGTGCAATGGTA[C/T]GATCACAGCTCACTG	25909
rs535394308	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246884912	CAGAGTACCATTACT[A/G]AATACAAATTCTCAA	25909
rs535405377	snp	A/C	0.00874735	0.0655527	intron-variant	AHCTF1	GRCh38.p7	1:246868947	CCTCCCGGGTTCACG[A/C]CATTCTCCTGCCTCA	25909
rs535405472	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246863831	CAGCACTCCCCAAGC[A/G]TATCAGTTATAAATT	25909
rs535429285	in-del	-/GTAG			intron-variant	AHCTF1	GRCh38.p7	1:246927564	ACATGAAACACCTAC[-/GTAG]GTTCAGTACTGTACA	25909
rs535484767	snp	A/G	0.00119737	0.0244387	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246931821	GGCTGTAGGCCTGCA[A/G]ACCGCTCAGCGGCTA	25909
rs535486433	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246925673	TCCCAATCTCATACT[A/G]AAATGTGATCCCCAG	25909
rs535493006	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246926945	TTTGGGAGGCTAAGG[C/T]GGGCGGATCACGAGG	25909
rs535535680	snp	C/T	0.000217248	0.01042	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246885530	GGTGAAGGATAACAT[C/T]GTTACCACTGGACAC	25909
rs535575182	snp	C/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246900539	ACCTCAACAGAATTA[C/T]AGCAAGATTTTCTCA	25909
rs535581690	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246851677	TTTAACTAGAAATTC[-/T]ACATTTCCCTAGCTA	25909
rs535587769	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246886625	CTGATCTACAGTTGA[C/T]TGAAGCCACGGATGT	25909
rs535606254	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246871011	AGTGACTGCGCTCCC[A/G]CTGTAGCCTTGCTTA	25909
rs535624154	snp	C/T	3.31175e-05	0.00406911	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246887343	ATACATAATATCAAG[C/T]AGCAAATAAATGGTC	25909
rs535667245	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246851578	TGGCATATACTTATG[A/G]GTTTACTTTACAAAA	25909
rs535669100	snp	C/T	0.0146672	0.084371	intron-variant	AHCTF1	GRCh38.p7	1:246922764	AAGGAGGGCGGATCA[C/T]GAGGTCAGGAGATCG	25909
rs535697511	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246912707	AGTATTTCATTTTCT[C/T]TGAATCTGAATAGAA	25909
rs535698202	snp	A/T			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933338	AGGGTTTCACCATGT[A/T]GGCCAGGATGGTCTT	25909
rs535733833	snp	C/T	1.64855e-05	0.00287097	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246913299	AACAAGAAGGATCTG[C/T]CCAACATCAGTGACC	25909
rs535735735	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246905432	AATCCGGGAGGCGGA[A/G]GTTGCAGTGAGCCGA	25909
rs535739030	snp	C/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246880478	CTGAGGCAGGAGAAT[C/T]ACTTGAACCCGGGAG	25909
rs535773551	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246906281	GAGCAAATTCAAAGA[C/T]GAGCTGACAAACTGG	25909
rs535774762	snp	C/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246881056	GCATTATGAAATGCA[C/T]GGTGGAGACCACAAT	25909
rs535788696	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246922022	TGCCTGAGAGAATAA[A/T]GATACATTGGTATAT	25909
rs535802148	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246899966	AACTAACAGTGAGAT[A/G]CAAACAGATAACACT	25909
rs535840495	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246873459	CTGCATCATAGCGAA[A/G]GGAAAGAATCCGTCC	25909
rs535845380	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246841844	TCACCCAGGCTGGAG[C/T]GCAGTGGCGTGATCT	25909
rs535862446	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246858428	AGCCTAAGGTTATAC[A/T]GCGTATCCCAGCTCA	25909
rs535891301	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246914881	TTCTGTATGTGTTCT[A/G]AATCTGCCCCATCTT	25909
rs535900280	snp	C/T	4.94858e-05	0.00497398	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851073	TTTGGTCACTAGTTA[C/T]GGCAGATGGCAAATT	25909
rs535920845	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246930714	CACTGCGCCCAGCCA[A/G]AGACAGTTCTTAAAA	25909
rs535972925	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246864211	TTCACTGGTAACTAT[C/G]ATAGCCACATGCAAA	25909
rs536016821	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246922704	ATAGTATCAATAGGC[C/T]GGGCGCAGTGGCTCA	25909
rs536037532	snp	A/G	0.000399281	0.0141238	intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246931206	CGCTTCCCTCGGGGA[A/G]AGGCCCGCCAACGAG	25909
rs536099250	snp	A/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246921446	TCAACAAAAACAAAC[A/T]CAAAGGATAAGTAAA	25909
rs536110036	snp	A/G	0.00159617	0.0282053	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932900	CTCTTTTATCAGGAA[A/G]GTTTCTACTTTTCTG	25909
rs536110311	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246875684	CAACATTGAGACAAG[A/T]TCCTTTATTAGCAAA	25909
rs536155349	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246896077	ACAATAACAAGCATG[C/G]TAAGGACGTGTTAAA	25909
rs536162159	snp	C/T	0.000798403	0.0199641	downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838987	TTGTTTACCTTACTA[C/T]TATGATACTAAGCAC	25909
rs536177331	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246872918	CCATATTAACCTAGA[A/G]ACCGGGTTCACCTTA	25909
rs536226995	snp	A/C	0.00119737	0.0244387	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933427	GTGAGCCACCGCGCC[A/C]GGCCTTATTTTTTAT	25909
rs536283277	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839608	CCAATTTCTCATTAT[C/T]TGTATTATTTGGTAG	25909
rs536287433	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246927986	GCCTGGCGACAGAGC[A/G]AGACTCCGCCACCAA	25909
rs536357115	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246916829	AGATCCCAAGCCTGT[C/T]TAACTCCAAAACTCA	25909
rs536391378	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246875593	TTGACATGGCCAACT[C/T]CACTGTGTCATCGTA	25909
rs536396387	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246866028	ATCAATTACATAAAT[C/T]AGCACTTCAGCCTTA	25909
rs536414298	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246924790	CTAAAAAGTTATGTT[G/T]GAGATTTCCAAGTCA	25909
rs536438127	in-del	-/A	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246841822	TTGAGACAGAGTCTC[-/A]AGTCTGTCACCCAGG	25909
rs536459570	snp	A/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246888050	AACAGATCCTGGGTT[A/T]ACACCTCTTCTTAAG	25909
rs536467115	snp	A/C	1.64751e-05	0.00287007	intron-variant	AHCTF1	GRCh38.p7	1:246867632	AGATTAACAAGCAGC[A/C]TGACTATGAAACGTG	25909
rs536467912	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246852621	CAATCCTGTGTAACT[A/G]TATCCATATATTTTC	25909
rs536470162	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246860028	GCACTCTGGGAGTCC[A/G]AGGCAGGCAGATCAC	25909
rs536529886	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246866982	GCAGGTAACAAGGAA[A/C]GTAAGTTAATAGTTT	25909
rs536583600	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246888947	TTGACCCTAGTTAGC[A/G]TGATGAGAACTACAG	25909
rs536609093	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246880331	GCACTTTGGGAGCCC[A/G]AGGCGGGCAGATCAC	25909
rs536619589	snp	A/C	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246881769	CTTGAACCTGGGAGG[A/C]AGAGGTTGCAGTGAG	25909
rs536626832	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246926912	GGCCGCGGTGGCACA[C/T]GCCTGTAATCCCAGC	25909
rs536627847	snp	A/G	0.00438332	0.0466095	intron-variant	AHCTF1	GRCh38.p7	1:246848957	GTGTCTTAACTTTTT[A/G]GACATGTTTAAAGCA	25909
rs536637019	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246891985	ATTAGAATCACAATG[C/T]AAAATTTCTCAAACT	25909
rs536641959	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246868911	GTGCAGTGGTGTGAT[C/T]TCGGCTCACTGCAAG	25909
rs536644053	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246853939	AGGACGACGAAAAAC[C/G]ACTTTACAGGCTTCT	25909
rs536654879	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246882233	CGATCTCCTGACCTC[A/G]TGATCCACCCGCCTC	25909
rs536691629	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246922749	GCACTTTGGGAGGCC[A/G]AGGAGGGCGGATCAC	25909
rs536701969	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246898075	ACCTAAGACCACAAC[G/T]GCTGATCACCCAGAG	25909
rs536703171	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246909161	TCATGCCTGTAATCC[C/T]AGCACTTTGGGAGGC	25909
rs536759025	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246924053	ACCGTTTCTCAGCAC[-/T]CCCCCTCCTATCTAT	25909
rs536767910	snp	A/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246923086	AGGAGAATGAAGAAG[A/T]AGTTATTTAATCAAA	25909
rs536824683	snp	A/G	3.68915e-05	0.00429469	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876136	TTCCATACTGGTCTA[A/G]TATAGAATTTCGAGC	25909
rs536871159	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869562	ACTTTAAATTAAAGG[C/G]AATCACCATTCCAAA	25909
rs536873977	snp	A/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246865921	AGTGGTATTTAAAAA[A/T]TTGATTTATGTAACT	25909
rs536877254	in-del	-/A	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246907267	TGACCAAAACGTTGT[-/A]AAAGTTACAAAGTCA	25909
rs536892450	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246910093	TACTCAGCACTTCCA[A/G]ACTACCTTGCCAAAA	25909
rs536895019	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246870053	GAGTTTGTAAGAAGG[G/T]GATTCCATCTTTCAT	25909
rs536909644	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246859561	AAAACATTTTTTGAT[C/T]ACTAAAATAATATTT	25909
rs536922964	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246901295	GCAGTGAGACGAGAT[C/T]GTGCAAGTGCACTCC	25909
rs536928123	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246902759	CTCCAAATTTAAAGA[C/T]TGTTCACACAATACA	25909
rs536969059	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246903202	TAGAGACAGGTATGT[A/G]AGGGTGAACAAAATA	25909
rs536974934	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246843789	ATAAAATCATGCATT[C/T]CTTACCAGTTCATCT	25909
rs537009029	snp	C/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246872120	AACTAAATATGGTCA[C/T]AGATCATCACATTAT	25909
rs537060692	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932796	CCCAGCGCCAAACAT[A/G]TTTCAAACAGATAGG	25909
rs537093550	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246873882	AATACTACTTACTGT[A/G]TAAGTCCTACTAAAC	25909
rs537111799	snp	C/T	0.00318978	0.0398085	intron-variant	AHCTF1	GRCh38.p7	1:246854625	ATTTCTAACAGCTAA[C/T]ATTTACTAAACTTCA	25909
rs537123404	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246927573	CACCTACGTTCAGTA[C/T]TGTACAAAATTAAAC	25909
rs537152529	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246907199	ACATTAAAAAGGTAC[A/G]ATCAAAATACAGTAA	25909
rs537174491	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246881700	AAAATTAGGTGGGCA[C/T]GATGGCGGGCACCTG	25909
rs537213049	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246874478	GGGGGAGCACTTACC[C/T]AAATGCTAGGACCAC	25909
rs537250888	snp	A/G	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246869114	CTCCCAAAGTGCTGG[A/G]TTACAGGCGTGAGCC	25909
rs537276345	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246858956	ATGTAGGCCAGGACC[A/G]GTGGCGCATGCCTGT	25909
rs537313689	snp	A/G	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246915702	CTGGGAATCTAACAT[A/G]TATTTTCCATAATGC	25909
rs537355035	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246895223	CAATAAGGTCTCTAG[A/G]TTAGATAAAAGTCTT	25909
rs537367523	in-del	-/T	0.0923359	0.194016	intron-variant	AHCTF1	GRCh38.p7	1:246891487	AAAATTTATGAGTTC[-/T]TTGAATAAAAAATAC	25909
rs537373241	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246879186	AGGTCACAAAAGAAA[C/T]AGCTCTTTAAAAAAA	25909
rs537387112	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869245	ACTTACTCCACTGAC[C/T]AACTGTTCCCCCGCG	25909
rs537399062	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246888098	CAACCTTGCAATTAG[A/G]TATGTCAGGTTTCCA	25909
rs537422924	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246924276	CTTTCAGTTTTCTTA[C/T]GAAATTAACTATTTC	25909
rs537433831	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246867542	GCCAACATAAAGAGT[C/T]TTTCTTTTTTACATA	25909
rs537465278	snp	C/T	3.33161e-05	0.00408129	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246860950	ATGCAAATACATCTT[C/T]ATCTCCATCCTTTTC	25909
rs537506045	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246854168	GCCAGGCGTGGTGGC[A/G]GGCACCTGTAGTCCC	25909
rs537523130	snp	C/G	0.000399281	0.0141238	downstream-variant-500B	AHCTF1	GRCh38.p7	1:246839090	TCCTAAAATGTTGTA[C/G]CAACACATTTTAATG	25909
rs537525250	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246896551	ATGTAAGGCTGGGTA[C/G]GATGGGGCAGGCAGG	25909
rs537545350	snp	A/T	0.00478085	0.0486577	intron-variant	AHCTF1	GRCh38.p7	1:246881211	TAACAAGTATTCATA[A/T]TAAAGAAGGTTACCA	25909
rs537636156	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246903550	AATCGCTTTTCACAG[C/T]CAGGTGCGGTGGCTC	25909
rs537638993	snp	A/T	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246889476	CACTTAGGAAATAAC[A/T]GATCTAGAATTTTAA	25909
rs537667800	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246915731	GCTCCAATCCAAGAC[A/T]ATTGTCGCAAATTTA	25909
rs537683208	snp	C/T	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246928337	AATTACTTCTGCTTG[C/T]CTGTCTTCTCCACTA	25909
rs537698570	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246922802	CCTGGATAACACGGT[G/T]AAACCCTGTCTCTAC	25909
rs537700397	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246923258	CATCTTTACTAAAAA[C/T]ACAAAAATTAGCTGG	25909
rs537705094	snp	A/G	0.00398564	0.0444627	intron-variant	AHCTF1	GRCh38.p7	1:246916571	TAGTCATTCAGTGGC[A/G]TGAACCTGGGAGGTG	25909
rs537713121	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246909239	ATATGGTGAAACCTC[A/G]GCTCTACTAAAAAAA	25909
rs537742814	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246882829	GGTATGTCCATATAT[A/G]TAGCTCATAAAATTG	25909
rs537759708	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246917659	TCAAGAGAGAAATGA[C/T]TGATACATATGTTTT	25909
rs537779408	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246876431	TAAAAACAATGGTTA[C/T]TAAGCATCCATGTGT	25909
rs537950963	snp	C/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246912050	ACTGGCAGTTTTAAT[C/T]GGTTTTTTTATACAC	25909
rs537977194	snp	C/G	1.64914e-05	0.00287149	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246903997	TCTATTACCAAAGGC[C/G]AGCTGCAGCAGATGC	25909
rs538038542	snp	C/T	6.9006e-05	0.00587352	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246862135	AAGTAGTAACTGACA[C/T]GGCCAAACTTTTAGC	25909
rs538042010	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246854837	TCGGGTTCAGCCCCC[C/T]GCACTCTTCAGGCAC	25909
rs538073728	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246847862	ACTATATTCCTCCAG[C/G]TCCTGAGGAGTGTAT	25909
rs538108525	snp	C/G/T	0.000895268	0.0211394	missense, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840951	AAGGGGGAAATCAGC[C/G/T]GAATTTCTATGGGAG	25909
rs538159056	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246926895	ACAAAAGTGTATGGC[C/T]GGGCCGCGGTGGCAC	25909
rs538242316	in-del	-/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246852917	TTATTAAAGGATGTG[-/T]TTTTATATTCCACAA	25909
rs538298602	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246909120	ATCTATTTATATATA[C/T]ATAAAATTCAGCCAG	25909
rs538326577	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246901863	AAACTTTAAAAAGAC[G/T]TGAGCTCATGACAAC	25909
rs538367703	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246883054	ATTATTTGTAAGGGT[A/G]CAAATTAATAAACAA	25909
rs538389332	snp	A/G	0.0479149	0.147179	intron-variant	AHCTF1	GRCh38.p7	1:246868350	GGTCTTGAACTCCTG[A/G]CCTCATGTGATCCAC	25909
rs538409265	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246929643	AGTAGCATATACTTA[C/T]TGTAGAGACCTTTGA	25909
rs538411214	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246929912	CAAAAATTAGCCGGG[C/T]GTGGTGGCGTGCGCC	25909
rs538426373	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868570	CATTTTGTTTCATTA[C/T]AGCTATGCTGGATTT	25909
rs538426654	snp	A/G	0.00438332	0.0466095	intron-variant	AHCTF1	GRCh38.p7	1:246870952	AAGAAGACAAACAAT[A/G]CAACTGAGCCTTCGA	25909
rs538463554	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246858651	TGGCCAACATGGTGA[A/C]ACCCCGCCTCTAATA	25909
rs538472186	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246904493	AAAATATCCTTTATG[C/G]CTTCATCCTGGTCTC	25909
rs538508710	snp	G/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246898696	CTACTCCTCTTTATC[G/T]AATGTGAAAGAGATT	25909
rs538554576	snp	C/T	0.00755907	0.0610114	intron-variant	AHCTF1	GRCh38.p7	1:246889601	AGCCGGCACAGATTT[C/T]AAAGTACTGATTCCC	25909
rs538631897	snp	A/G	0.00318978	0.0398085	intron-variant	AHCTF1	GRCh38.p7	1:246922856	GGCGTGGTGGCAGGC[A/G]CCTGTAGTCCCAGCT	25909
rs538674983	in-del	-/A	0.00636936	0.0560724	intron-variant	AHCTF1	GRCh38.p7	1:246920369	TTTGAAAAAATTTCT[-/A]AAAAATGAAAAATTA	25909
rs538692617	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246923175	ATCCCAGCACTTTGG[A/G]AGGCCGAGGTGGGCA	25909
rs538748809	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246859798	GTCTAGGCTGGTCTC[A/G]AACTCCTGGGCTCCC	25909
rs538760118	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246910662	AGACTCATATATTAA[C/T]ATAACCACTGTGCAA	25909
rs538772345	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246920968	ATGGTGGCGCATGCC[-/T]GTAATCTCAGCTACT	25909
rs538791539	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246883250	TGGGTGTTGGACTAT[C/T]ATGCAGCTTAACTTC	25909
rs538834493	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246867980	ATTAATTTTTTTTCT[C/T]TTAGACCAGTCTTGC	25909
rs538995624	snp	A/C	0.00993419	0.0697739	intron-variant	AHCTF1	GRCh38.p7	1:246882792	TAATTTGCACGTAAA[A/C]CAGCCACGCCACAGT	25909
rs539008709	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246875708	TAGCAAAAGGATTAC[A/G]ACTCACAGAAGGCTC	25909
rs539034069	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246855645	ATCTGAATAACACAA[C/T]AGATTATTTTGTTCT	25909
rs539062848	snp	C/G	1.65141e-05	0.00287346	missense, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840889	CTGTTCCTGTCACTT[C/G]TGTAGTTTTTCTTGG	25909
rs539072674	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246856194	TTTCTATGAACTCAG[A/T]AGAGGCAAGGTTCAA	25909
rs539072857	snp	A/G	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246848608	TGGTGGCTCACGCCT[A/G]TAATCCCAACACTTT	25909
rs539184570	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869608	AAAAATGATGGGAAA[C/T]CTACTATGCCTGTCT	25909
rs539206612	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246912312	AACCCCATCTCTACT[-/A]AAAAAAAAAAAAATA	25909
rs539249174	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246870365	AAGGTCAAGGCTACA[A/G]TGAGCTATGATTATA	25909
rs539255684	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246854874	GTCTCCTCTTCCAAC[A/G]TATCGGGAGAAATGG	25909
rs539264305	snp	A/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246911109	GAGAAATGGTTCTGA[A/T]CACAATCCAGAGACT	25909
rs539298063	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246903859	AAAAAAAAAAAGAAT[C/T]ACTTTTCAATATCTT	25909
rs539304749	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246868897	TCACCCAGGTTGGAG[C/T]GCAGTGGTGTGATCT	25909
rs539356998	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246897912	TAAGCCCAAGAGGTT[A/G]AGGCTACAGTGAGCC	25909
rs539368916	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246867525	TTCTTCTCAGAAACA[C/T]AGCCAACATAAAGAG	25909
rs539393137	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246898549	TTAGCAAAAGGTAGC[C/T]TATATATTTTTATGA	25909
rs539423732	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868880	GATGGAGTCTCGCTC[C/T]GTCACCCAGGTTGGA	25909
rs539487454	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246904664	CTATCAAGACACAAA[A/G]TGAAGATACTAAATC	25909
rs539492454	snp	C/G	0.00398564	0.0444627	intron-variant	AHCTF1	GRCh38.p7	1:246929778	ATCTGTACCAGCCGG[C/G]CGCGGTGGCTCACGC	25909
rs539499022	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246864179	AATTTAGTATCCCAT[C/T]TAATCAGACCTCTAT	25909
rs539526357	snp	A/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842590	CTGTCTCAAAAAAAA[A/T]AAATAAAAATAAAAT	25909
rs539526689	snp	A/G	0.00438332	0.0466095	intron-variant	AHCTF1	GRCh38.p7	1:246927872	GCTGGGCGCGGTAGC[A/G]CGCTGTAGTCCCAGC	25909
rs539528488	snp	A/G	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246906208	AAAATTGACCAAGAG[A/G]TGATAGTGTTAGAGA	25909
rs539584099	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246877623	GGTGTGACAGAGGAA[C/T]ATCAGGTTTTTAAGA	25909
rs539599198	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246893836	CCAAAAGACAAGTTA[C/T]AATCCTAAAACCTGC	25909
rs539628220	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246925101	GATAAAACTAGTTTA[A/C]TGATGAACTGAAGTT	25909
rs539635710	snp	A/C	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246858378	ATTAACTTACTTAAT[A/C]CTCAACATTCAAAAA	25909
rs539689764	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246913604	CCATTACTCAATACA[C/T]AGAAAAATCACGCAG	25909
rs539701445	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246875984	CAGAAAAGTAATCAT[C/T]CAGTATCTTTTTTGA	25909
rs539764191	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246873522	TCAATTTCTCCTGCA[A/T]CACAGTGAAGGGAAA	25909
rs539801856	snp	A/G			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933450	TTTTTTATTTTTTGT[A/G]GAGACTGTCTCACTG	25909
rs539812932	snp	A/C	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246921578	AATCCCCCCAAAAAT[A/C]TAGTACTAATAGGAA	25909
rs539863948	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246905402	ACTCGGGAGGCTGAG[C/T]GAGAGAATGGCATGA	25909
rs539917470	snp	C/T			intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842218	GATAATCTTTTCTGA[C/T]GAGCTTAATTTCCTT	25909
rs539919650	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246922924	GGAGGCGGAGTTTGC[A/T]GTGAGCCGAGATTGC	25909
rs539938508	snp	G/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246884147	GTTACCACATTTAGC[G/T]TCTTTATTTTGTTCT	25909
rs540007291	in-del	-/ATAATG			intron-variant	AHCTF1	GRCh38.p7	1:246916965	TAAGACATAACTAGC[-/ATAATG]ATAGGAAGTCTCAGA	25909
rs540008984	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246876565	CCCAAGCACACAGAG[C/T]AAATGAAGAATTAGT	25909
rs540024963	snp	A/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246869463	AATTAAAAGTGCTAC[A/G]TCAGTGAACACATGA	25909
rs540048092	snp	A/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246917149	ACAAGGAGAAGCACA[A/G]AGTAGCCGCACTGGG	25909
rs540056502	snp	A/C	0.02016	0.0983543	intron-variant	AHCTF1	GRCh38.p7	1:246867899	TGATTACACCCCCCC[A/C]CCCACACACACACAC	25909
rs540065218	snp	C/T	3.29587e-05	0.00405934	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850891	CAATTTAGTGGGACA[C/T]ATTATGTTTTGGCTC	25909
rs540081152	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246895340	GCTACAAAAGCATGA[C/T]GGCTTATCATCAAAT	25909
rs540104199	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246844292	AACCTGAGCTAGTCT[G/T]TGCCATAACTACTGC	25909
rs540114709	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246886523	ATACCATGTAAATAA[C/T]TGTTATAGTGTAACA	25909
rs540187346	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246889687	TTATATGCTTTGTAA[C/T]TTTGTCACTGCAACT	25909
rs540228112	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246927880	CGGTAGCGCGCTGTA[C/G]TCCCAGCTACTTGGG	25909
rs540250770	snp	G/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246847493	AGAGTTTTCAGTAAG[G/T]AGGCATGTATTGTTT	25909
rs540258721	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839826	CTTAATTGCACACAG[C/T]TGTACTGTAGAGAAC	25909
rs540295293	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840191	GCCTTTAAGCTTGCC[A/G]AATAAGAGATGCCAA	25909
rs540325068	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246848415	GTAGTGTTAGCCAGG[A/G]TGGTCTCGATCTCCT	25909
rs540400834	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246925906	GAAATCTCATCTCTA[C/T]GAAAAATAATTAGCC	25909
rs540423488	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246929265	ATACAAAAAATTAGC[C/G]GAGTGTGGCGGCGCG	25909
rs540435586	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246924588	CTTGTCATTCTTATT[C/G]TCTCCACATCTTAGT	25909
rs540452970	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246917743	TGCAATATCTTTCAT[C/T]AGAACAAGATCCATA	25909
rs540495342	snp	A/C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246925330	CCAAAGGATAACACA[A/C/T]AAAAAGCATTTTTTG	25909
rs540500286	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246849530	GGGAAAAATTCCCTA[C/T]AAAACCATTTTTAGG	25909
rs540535301	snp	A/G	0.00318978	0.0398085	intron-variant	AHCTF1	GRCh38.p7	1:246842854	CCTGAGACAAGGAAT[A/G]CTAGAGCCAAACACT	25909
rs540570087	snp	A/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246884994	GCATACTAAACCCTC[A/G]GCTGTCCAGGCAGGA	25909
rs540611011	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246861680	AATTAGGAGGTTTGA[A/C]TCCTACTCCCAATTC	25909
rs540617691	in-del	-/TCTT	0.00119737	0.0244387	downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838875	CTACGATACTAAGTA[-/TCTT]TCTGAGTACATTGTT	25909
rs540711845	in-del	-/ACAA	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246893160	AAAACATGAGCTCTG[-/ACAA]ACATTTTCCTCTTAA	25909
rs540714202	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246920258	CTTCAGATATTGAAA[C/T]TACCAGAGATTAGAA	25909
rs540808172	snp	G/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246899897	CCTTTATAAAACATA[G/T]AAATACTAAGTTTCT	25909
rs540809075	snp	A/G	0.0178098	0.0926698	intron-variant	AHCTF1	GRCh38.p7	1:246868906	TTGGAGTGCAGTGGT[A/G]TGATCTCGGCTCACT	25909
rs540814665	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246848933	GATGGGATCTATTCA[C/G]CCACACCAGTGTCTT	25909
rs540840495	snp	C/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246858045	GCTCACTGCAAGCTC[C/T]GCCTCCCAGGTTCAC	25909
rs540883028	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246858456	TCATGACGCATACTC[A/C]GTAAGTAGCTGAGCT	25909
rs540928507	snp	C/T	3.32662e-05	0.00407824	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877244	TGTGCTTCAGTAACT[C/T]CTCTATATTCAACCT	25909
rs541026001	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246886664	TGGACACAGAGGGCC[A/G]ATGGTATACAAGAGG	25909
rs541052028	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246912355	AGGCATGGTGGCGTG[C/T]GCCTGTAATCTCAGC	25909
rs541083912	snp	C/T	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246895609	TAGGTATGGCTGTAA[C/T]GGCAGCATGAGGGAT	25909
rs541093029	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246844596	CAATGTGGTGGTGCA[C/T]GCCTGTGGTGTCAGC	25909
rs541111401	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246881546	TTTTTTTTAAATAGA[A/G]GCAGGGTCAGCTGGG	25909
rs541124601	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246879836	CTGTTCCCCCAACCC[C/T]GCCAAAAAAAAAGGG	25909
rs541133029	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246905459	CCGAAATCACGCCAC[C/T]GCACTCCAGCCTGGA	25909
rs541141857	in-del	-/A	0.49706	0.0382258	intron-variant	AHCTF1	GRCh38.p7	1:246881838	GCAAGGCTCCGTCTC[-/A]AAAAAAAAAACCAAA	25909
rs541161458	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246880577	CAGCTCAAAAAAAAA[A/C]AAAAAAAAAATTCCA	25909
rs541163326	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246872318	CACGCCAGGAAAAGA[A/C]TGACAAGAAGACTTT	25909
rs541196599	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246911274	CCACAAAATACACTA[C/T]GAAACAAAAGCCTAT	25909
rs541201566	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246873049	AAAGCCATCATTCCT[C/G]AGTGAATCCTGCACC	25909
rs541269835	snp	A/G	0.000381961	0.0138143	intron-variant	AHCTF1	GRCh38.p7	1:246899550	AATCCACTTACATAT[A/G]TTTAAAATGGCATTA	25909
rs541271095	snp	A/G	2.55073e-05	0.00357113	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850549	TTCTAGTATGTCCTG[A/G]TTAACTTCTTTCTTT	25909
rs541276696	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869025	AACTTTTTCTATTTT[C/T]AGTAGAGACGGGGTT	25909
rs541296229	snp	C/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246893358	TTTAAAAATCCTCTA[C/T]TAAGAATAACTTAAC	25909
rs541331381	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246900988	AGAGACATCAACAGG[A/T]GAAGAAGAAAGTAAA	25909
rs541342755	in-del	-/T	0.308931	0.249744	intron-variant	AHCTF1	GRCh38.p7	1:246848390	GATAATTTCTTTGTA[-/T]TTTTTTTTAGTAGTG	25909
rs541399332	snp	C/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246865322	TGTAGTTGCAGTACC[C/T]TCCTTGTCATTCTAT	25909
rs541444798	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246926770	CTGAGGCAGGAGAAT[C/T]ACTTGAACCCGGGAG	25909
rs541446107	snp	C/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246901828	GTGAGACCCCTGTCT[C/G]TAAATAAATAAACAA	25909
rs541508402	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246926954	CTAAGGCGGGCGGAT[C/T]ACGAGGTCAGGAGAT	25909
rs541556255	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868446	TTTTAGTAGAGACAG[C/G]GTTTCACCATGTTGG	25909
rs541594533	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246868761	TCTTGGGTTACAGAG[C/T]AGCCAATAAAAAAGT	25909
rs541594586	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246862276	ACCAGGTCAGGAGAT[A/C]GAGACCATCCTGGCT	25909
rs541603466	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246913616	ACATAGAAAAATCAC[A/G]CAGTTGGACTAACAA	25909
rs541620784	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246921520	CAAAGGGATGAGTAG[C/T]TTTAAATTATAGATA	25909
rs541636517	snp	A/C	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246881100	CAAGAGAGGTAAACA[A/C]CCAACCACTGATTTC	25909
rs541716653	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246908247	CATTACCAATGACAG[C/G]ACATTTTGGGCATCA	25909
rs541735430	snp	A/C	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246901043	ATAGGAAGAATGGGG[A/C]ATAAGAGAGAGCATG	25909
rs541763787	snp	A/C	8.27506e-05	0.00643183	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877204	AAATCTTCCATCAAG[A/C]CCATTTCCTGACAGA	25909
rs541781154	snp	C/T	0.00143753	0.0267712	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246899490	TAAATGAACAACTCC[C/T]GAGTTTAACAAACAA	25909
rs541792335	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246868965	TTCTCCTGCCTCAGC[C/G]TGCTGAGTAGCTGGG	25909
rs541794090	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246928257	GCAGTGAGCCGACAT[C/T]GCGCCACTGCACTGT	25909
rs541816014	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246893281	TATTTCATGACAACA[C/G]TTTCATAAGTATAGT	25909
rs541902567	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246870163	AGAAGCAGAGCCTAG[C/G]CCAGGCATGATGGCT	25909
rs541919623	snp	C/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246911672	ATTTTTTAGTAGAGA[C/T]GGGGTTTCTCCATGT	25909
rs541956166	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246912316	CCCATCTCTACTAAA[A/G]AAAAAAAAATACAAA	25909
rs541958506	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246924628	CAAAAAAATTTATGT[C/G]AAAAAAACATTTCAA	25909
rs542016318	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246896835	GTTCAAAAAGGAATC[C/G]CATGAATGTAAGTTG	25909
rs542036794	snp	A/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246926614	TCATCCCAGCACTTC[A/G]GAAAGCTGAGGTGGG	25909
rs542067808	in-del	-/TATA	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246907096	ACCTAGGCTAGATGG[-/TATA]TATAGCCTGTTGCTC	25909
rs542093008	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246898913	GCCAACATGGTGAAA[A/C]CCCATCTCTACTAAA	25909
rs542125118	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246906616	AGAGCTGATAAAAGG[A/G]TAACAGCAAAGAGAG	25909
rs542128984	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246905292	ATCATGAGGTCAGGA[A/G]TTCAAGACCAGCCTG	25909
rs542153870	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246857092	AATCATACTGATTAG[C/T]ACAGCTGACTTTCCG	25909
rs542190722	snp	A/T	1.6476e-05	0.00287014	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849785	TCATTTGTTTCTTTA[A/T]GTGTCATTTCATCTG	25909
rs542206071	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246863148	TACTGAATATTTTAA[A/G]TTATTGAAACCTAAT	25909
rs542235757	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246929870	CAGCCTGGCCAATAT[A/G]GTGAAACCCCGTCTC	25909
rs542305190	snp	C/G	1.71199e-05	0.00292569	missense, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843905	CTAATTCTTTCAGCT[C/G]TGCAGGAACCTCTAT	25909
rs542343884	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246900868	GCATTAAGGCTTTAT[C/T]ATGATGAACCTTAGC	25909
rs542382513	snp	C/T	0.000414068	0.0143827	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246894721	CATTCAAGAACAAAG[C/T]GCAAATTAGTGGCAG	25909
rs542418042	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932149	AGCAGGGCCTGGAAG[A/G]GCGGATCATTTACAA	25909
rs542445145	snp	C/T	0.00517822	0.0506191	intron-variant	AHCTF1	GRCh38.p7	1:246896537	GTAGATTAGTCATTA[C/T]GTAAGGCTGGGTAGG	25909
rs542446621	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246868919	GTGTGATCTCGGCTC[A/C]CTGCAAGTTCTGCCT	25909
rs542459511	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246870393	ATACCACTGTACTAG[A/G]GCATCTGTGACAGAC	25909
rs542473421	snp	A/G	0.00358779	0.0422022	downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838663	ATTGTAGCCCATTCA[A/G]GACCAGGTCTTTGCA	25909
rs542569750	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246910040	ACTAATTGAAACTAC[C/T]AGACACTATGTGTCT	25909
rs542623955	snp	A/C	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246858625	ACGAGGTCAGGAGTT[A/C]GAGACCAGCCTGGCC	25909
rs542624831	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246864458	CTAAAGAAAACAGGA[C/G]AAGGCTTCCCTGGCA	25909
rs542651331	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246865195	GTCTATCTTATGGTT[C/G]TATTTCCTAGTGGTA	25909
rs542652311	snp	A/C/G	6.6565e-05	0.00576877	intron-variant	AHCTF1	GRCh38.p7	1:246900305	ACATACAAATACAAA[A/C/G]AGAAAGGAGAGAGAA	25909
rs542663246	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869073	ATGGTCTCGATCTCC[C/T]GACCTCGTGATCCGC	25909
rs542687675	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246915206	GTGGTGGTGCACGCC[C/T]GTAGTCCCAGCTACT	25909
rs542689070	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246894245	AATGTAAAAAGAAAT[A/G]ATTTTCTTTTGGGAC	25909
rs542734687	in-del	-/TTTA	0.0707826	0.174302	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933121	CATTAATTTTTTTAT[-/TTTA]TTTATTTATTTATTT	25909
rs542754130	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246866457	TAACTAAATTTAGTC[C/T]AAAAAAAGAAAAATC	25909
rs542788495	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246859002	GAGGCTGAGGCAAGA[C/G]AAGAGGTTGCAGGAG	25909
rs542792961	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246867171	GTCTATAAAATGTTA[A/C]AGATAATTAAAAATT	25909
rs542800491	snp	A/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246887671	AAATTTCTAAAGATC[A/T]AGCAAAAGATGGCAG	25909
rs542854914	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246921172	AAGGTTAAAAAGACA[C/T]GCAGAACTAAGCAAA	25909
rs542865078	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246846087	GAATCAAACGATATA[C/T]GAATGTCATGTATCT	25909
rs542906059	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246853540	CAGGAAACATTAATA[C/T]GACGACCAACTGCTT	25909
rs542933106	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246896336	CATTAATTGTAGATA[A/G]ACAAATTATGGTATG	25909
rs542937639	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246880857	CCTACAGAAGACAAT[A/G]ATGATGCTAGGAAGA	25909
rs542940649	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246873245	TACTCTTCTGTAAAA[C/G]AAAAAAATCTTAACC	25909
rs542975631	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246889312	TCTAATTGTGAATAG[C/T]GGCAGCACTTACTAC	25909
rs542978299	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246916857	TCATGCTTTAACTAC[C/T]AAGGCTTAAACGATT	25909
rs542987360	in-del	-/A	0.350863	0.22875	intron-variant	AHCTF1	GRCh38.p7	1:246843742	ATTAAAACATTTGTA[-/A]AAAAAAAAAGTATGT	25909
rs543003373	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246912872	GCTGGGTAATTTCAT[A/G]TTGGCTGATAAGGCT	25909
rs543040131	snp	A/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246913576	GAAATCTTCAGCTAT[A/T]CTAGGAATTACACCA	25909
rs543098732	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246868195	GTGCAGTGGCACAAT[C/G]TTGGCTCACTGCAAC	25909
rs543098808	snp	G/T			utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840179	AGACTTTAAAGAGCC[G/T]TTAAGCTTGCCGAAT	25909
rs543113223	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246908648	ATCTCAGCACTTTGG[A/G]AGGCCAAGGTGGGCG	25909
rs543119616	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246867061	TGAACAAAAATTTTA[A/G]GTATACTACTACCTG	25909
rs543152719	snp	A/T	6.65779e-05	0.00576927	intron-variant	AHCTF1	GRCh38.p7	1:246900255	TCCTGACCTAAAAGA[A/T]AATTTAAAACATTAC	25909
rs543153544	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246909359	GAGGCAGAGGTTGCA[A/G]TGAGCCGAGATTGCG	25909
rs543159227	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246864743	TACTCGGGAGGCTGA[C/G]GCAGGAGAATGGCGT	25909
rs543200628	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246864382	CCTATATTTACTGAG[A/C]TCTTACTATGTGCCT	25909
rs543237330	snp	A/G/T	0.00319074	0.0398324	intron-variant	AHCTF1	GRCh38.p7	1:246858558	TTTCTGGCCAGGCAC[A/G/T]GAGGCTCATACCTGT	25909
rs543256124	in-del	-/CTT			intron-variant	AHCTF1	GRCh38.p7	1:246884328	TCTATTATTAAACTT[-/CTT]TTCTTCTGCCTGAAA	25909
rs543271264	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246844778	AATTGGTTTAAAATA[A/G]GGAATTAAAAGCATT	25909
rs543273134	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246851816	AACAACCCCCAAACT[A/G]TGTTTTAATGGTATT	25909
rs543287909	snp	A/C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246902059	AACAGAGCTCTGAAA[A/C/T]GTTAAGCAATTTGTC	25909
rs543347732	snp	A/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246911880	TAAGTTTTGTTCAGA[A/T]GATTTTGGCTCTTCC	25909
rs543414896	snp	A/G	0.000477889	0.0154504	intron-variant	AHCTF1	GRCh38.p7	1:246863912	GTGAACGCTAGATGC[A/G]TAAATACTAACCTTA	25909
rs543437329	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246878512	TTTTTAAAAAGCAAG[C/T]TAAAAACAGTATGAA	25909
rs543453026	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868971	TGCCTCAGCCTGCTG[A/T]GTAGCTGGGACTACA	25909
rs543492204	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246910742	CCTAGAACAGGGCCC[C/G]CACCCCCAAATCACT	25909
rs543498806	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246849400	AAATAAATCTGTTAC[A/G]TGAGTTACAGGATTT	25909
rs543538057	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869033	CTATTTTTAGTAGAG[A/G]CGGGGTTTCACCATG	25909
rs543556187	snp	A/G	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246870246	GCCATGAGTTTGAGA[A/G]TAGCCTGGGCGACAT	25909
rs543581333	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246865587	GTTTGCTCACTTTTA[C/T]ACTGAGCTATCCCAA	25909
rs543619435	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246866370	AGAATGTCGGTAATA[A/G]CGACTTTCATTTAAA	25909
rs543659382	snp	C/T	3.29837e-05	0.00406088	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877005	GGCACATAATTGGCA[C/T]GCTGCAAATGGTGCA	25909
rs543662653	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246860053	GATCACGAGGTCAGG[A/G]GTTCGAGACCAGCCT	25909
rs543665047	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246926793	CCCGGGAGGCGGAGA[C/T]TGCAGTCAGCCGACA	25909
rs543680568	snp	A/C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246894179	ACTGTACTCCTGCCT[A/C/G]GGCAAAAAGTGAGAC	25909
rs543694000	in-del	-/TAAGA	0.00953873	0.0683987	intron-variant	AHCTF1	GRCh38.p7	1:246911791	GCCCAGCTCTTCTAT[-/TAAGA]TATTTTAAAGTGCAT	25909
rs543710393	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246895567	ACAAAATTCTTGCCA[A/G]GGGTTAAGGATGGGG	25909
rs543716351	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246894564	GAAAAGAGTTTACAA[C/T]TTCAAAATGATTAAA	25909
rs543719605	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246879934	AAATCCTTTATGTAA[C/T]TATAAAATTAGCACC	25909
rs543720529	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246886810	ACTGTATTTTAAAGA[A/C]TAAAAGCTTTATAAA	25909
rs543721576	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246901497	GGCATGGTGGCGGGT[A/G]CTTGTAGCCCCAGCT	25909
rs543781560	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246895433	TGTGTATGTGTGTGA[A/C]GAGTAACAGTGATAC	25909
rs543784456	snp	C/T	3.31131e-05	0.00406884	missense, synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246891780	AACAAAGAGCGTACC[C/T]CTCTCAGTGATCTCT	25909
rs543810135	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246859750	CCAGCTAATTTTTTT[A/G]TATTTTTTGTAGAGA	25909
rs543849781	snp	G/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246852935	TTATATTCCACAAAA[G/T]ATTTATACACTTATT	25909
rs543884107	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246889255	GCAGGTATGGTCCCT[A/G]TTTCCTTTTCTTTTC	25909
rs543900599	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246907770	AGATCTAAAACCACA[A/G]ATTAGACAAATGAAG	25909
rs543908057	snp	A/G	1.65468e-05	0.00287631	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246907756	CAGTTAGAACTTCAA[A/G]ATCTAAAACCACAAA	25909
rs543947162	in-del	-/A	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246921222	CATGACAAAACTATG[-/A]AAAAAAACAAAGAAA	25909
rs543972371	in-del	-/ATG			intron-variant	AHCTF1	GRCh38.p7	1:246921897	TGAGAGGCAGCAAGA[-/ATG]ATGATGTCAAAGTAC	25909
rs543988551	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246881897	TCTCCTACGTTGCCC[A/G]GCCTGATCCTGGGCT	25909
rs544006153	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246921798	ACAAATACGAAATAT[C/G]TTTTTAGACAAAAAA	25909
rs544051683	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246868936	TGCAAGTTCTGCCTC[C/T]CGGGTTCACGCCATT	25909
rs544110138	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246881287	CTTATGTACCTAATA[C/T]TCAAAATACAAAAAG	25909
rs544134062	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246842884	TGATGAATTCAAACT[C/T]GCCAAATGCAAAATT	25909
rs544152405	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246880658	GATAAACTTAATTTA[C/T]GATTTACCAAGTATT	25909
rs544181065	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246860212	GGCGGAGGTTGCAGT[A/G]AGCCGAGATCACGCC	25909
rs544220033	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246853497	AAGGTAAATTTCACA[A/T]TTAAAAATGATAACT	25909
rs544247738	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246910675	AATATAACCACTGTG[A/C]AAGAGCAGATTCTCT	25909
rs544286361	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246847016	TGAAGGCTGGGCACA[A/G]TGGCTCATGCCTATA	25909
rs544351663	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246882308	GGCCTATTATTACTT[C/T]TAAACAGAGCAAGTC	25909
rs544384555	snp	A/C/T			intron-variant	AHCTF1	GRCh38.p7	1:246845152	CTTCAGCTACTGGGA[A/C/T]AGTCAAGAGTTCTAT	25909
rs544414828	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839763	TTATAAATTATTTTA[C/T]AACACTTATTTATTG	25909
rs544423098	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246854593	GAGAAAAGAAAGTTG[C/T]TTTTTTGATAATGAT	25909
rs544433668	snp	A/G	0.00557542	0.0525036	intron-variant	AHCTF1	GRCh38.p7	1:246922910	ATGGCATGAACCCAG[A/G]AGGCGGAGTTTGCAG	25909
rs544452497	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840129	AGTGAGCAGTGAACC[A/G]GTCAATCTAACCTGG	25909
rs544453844	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246905194	GTTCTATTTTTGACT[A/G]ATTTTTAAAGATTGT	25909
rs544484095	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246928751	TATTGCAACATGTAC[C/G]AAGCAAACATTTCTA	25909
rs544545407	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246923882	ATAACCCCAGGAAAA[C/T]TCCAGGTCTGGAAGT	25909
rs544546775	snp	C/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246869393	ACTTTAAATCAAAAG[C/G]TAGACCTCTTATGCC	25909
rs544611103	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246876829	GAACTGAGGATTCTC[C/T]AAGTTCAAGGTAATG	25909
rs544645239	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246901440	AGGAGATGGCTAACA[C/T]GGTGAAACCCTGTCT	25909
rs544653037	in-del	-/AA	0.401711	0.198705	intron-variant	AHCTF1	GRCh38.p7	1:246843741	TATTAAAACATTTGT[-/AA]AAAAAAAAAGTATGT	25909
rs544738016	snp	G/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246861612	TCAAAAACATATAAC[G/T]AGTTAGAAACAACAC	25909
rs544773660	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246855086	ACCAGGAACAAAGGC[A/G]TAACAGTTGAGAGCA	25909
rs544774711	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246890496	TATTCTAAACAAATA[C/T]AGCACAAGTCAAATA	25909
rs544800676	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246927362	GCCACGGCTGCATAC[A/G]CTTGTCATCCCGACT	25909
rs544813018	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246922436	GTTTTTTGGGTTGTT[G/T]TTTTTTTTTGACAGG	25909
rs544814170	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932212	GTGGGGAGAAAGACT[A/G]CGAGTCCCACAGTGC	25909
rs544829859	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246902448	GAACTGCCAGGAGTA[C/T]GAAATCTAGAAAATA	25909
rs544865242	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246846206	CTAAGATAATTTCTT[C/T]GCTATGTTTCAATAA	25909
rs544905250	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839287	ATATTCACCAAATTG[C/T]GTTGGTTTAAAAAAG	25909
rs544916943	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246883182	AGTGTTTGATGGTTT[A/C]AATATTAAAACTTTT	25909
rs544917646	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246915627	TAGTCTTATTCATTT[A/G]TCTTCTCCCACTAGA	25909
rs544937640	snp	A/G	0.00438332	0.0466095	intron-variant	AHCTF1	GRCh38.p7	1:246884038	TAGCAACACTTTAAC[A/G]TCACTAAACAGTGAG	25909
rs544952974	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246921022	GCTTGAACCTGGGAG[A/G]AGGAGGTTGCAGTGA	25909
rs544963368	in-del	-/ACTG	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246869239	GCGTGTACTTACTCC[-/ACTG]ACTAACTGTTCCCCC	25909
rs545037170	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246859716	GAGTAGCTAGGAATA[A/C]AAGTGCATGCTATCG	25909
rs545047099	in-del	-/AAAT	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246923415	AAGACTCTGTCCCAA[-/AAAT]AAATAAATAAATACA	25909
rs545073615	snp	A/G	0.000109242	0.00738979	intron-variant	AHCTF1	GRCh38.p7	1:246867193	TTAAAAATTACAATT[A/G]TAACTATCATCTAAC	25909
rs545086786	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246863374	GGAGATAGTATGTTT[A/G]AAAAAAAAAAAACAA	25909
rs545187046	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932939	CATATGTGCTTTTTA[A/C]ATTTTTTTATTTTTG	25909
rs545204419	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246882007	ACTTTTTTTTTTGTT[G/T]TTTTTTTTGAGATGG	25909
rs545211803	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246854456	GTGATTGGCCCAAAT[G/T]TTCAGCAATAAGCAA	25909
rs545248756	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246847520	GTTTTTGTTTTGAGA[C/T]GTGGTCTTGCTCTGT	25909
rs545256461	snp	A/C	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839699	AAGCAGTTCGTTTCT[A/C]GATAATCAATTATTA	25909
rs545276966	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246881820	CCCAGCCTGGGTAAC[A/G]GAGCAAGGCTCCGTC	25909
rs545347964	snp	A/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246874846	TGACCTCCGGCTCTC[A/G]GCCCTCAAGAATGAG	25909
rs545349787	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246873699	AGAATCTGTCCTATA[A/C]TGAATATACTAGAGA	25909
rs545352662	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246889758	CAACACCACTTTCTT[C/T]GTCTATTACCTTTAC	25909
rs545389939	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246882565	ACTTTTGTATTACAA[A/G]GAAAAAAGGCTGAAA	25909
rs545410452	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246864607	TTGGGAGGCCGAGGC[A/G]GGTGGATCATGAGGT	25909
rs545413473	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246916979	CATAATGATAGGAAG[C/T]CTCAGAACCTCTTCT	25909
rs545430867	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869358	AGTGTTCATGTGAAA[A/G]GAGGAGTCACATGTC	25909
rs545451160	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246910113	CCTTGCCAAAATACT[A/G]AACCTTCATCTATAA	25909
rs545484245	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246876707	CTACATCTTCCTCTT[C/G]TTTTCCCTGAGTGAA	25909
rs545519091	snp	C/T	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246877151	GTTTACATCGGTAAG[C/T]AATTACCTGCTCAGT	25909
rs545535994	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246884867	TACAAAGAATTCCAA[A/T]ACTCAAACAACCAAT	25909
rs545557792	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246870083	TGAATAACTTTTGAG[A/G]GCTTCAAGACTTCAG	25909
rs545653398	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868221	GCAACCTCTGCCTGC[A/C]AGACTCAAGTGATTT	25909
rs545669849	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246910759	ACCCCCAAATCACTT[A/C]TGCTTCTGATGTCTT	25909
rs545692719	snp	A/T	8.23784e-05	0.00641735	intron-variant	AHCTF1	GRCh38.p7	1:246898197	AACAATAGAGTTAAA[A/T]ATCATCTCACTTGGC	25909
rs545769234	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246847239	GGTTGCAGTGAGCCA[A/G]GATCACACCATTGCA	25909
rs545799428	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246869978	AAAGGATTCACCATT[A/C]TAGATGCCATTCAGC	25909
rs545802508	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246848845	ACAGAGTGAGACTCT[A/G]CCTCAAACAAACAAC	25909
rs545830589	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246869126	TGGATTACAGGCGTG[A/T]GCCACCACGCCCGGC	25909
rs545832052	snp	A/G	0.00478085	0.0486577	intron-variant	AHCTF1	GRCh38.p7	1:246898872	GCAGGCGGATCATCT[A/G]AGGTCAGGAGTTCGA	25909
rs545836289	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246891465	GTTTTGAAATTGCAA[A/C]ACAGAAAAAATTTAT	25909
rs545864005	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246862619	AAAATACAAAATTCT[C/T]CCAGAGCTTTTTATA	25909
rs545866503	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246918004	CAAACATAGATAATA[C/T]TAAGATACAAAACAC	25909
rs545873322	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246892175	CTCATAACCAGCACA[A/C]ATCAAAAGACAGGGA	25909
rs545986245	snp	A/C	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246925434	AGATGATATAGAAGT[A/C]CTAGCTCTAAGAGAA	25909
rs546006224	snp	C/G/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246911632	GGGATTAGAGGCATG[C/G/T]GCCACCACACCTGGC	25909
rs546009836	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246918640	GCCACTTCACTCCAG[C/G]ATGGGCGACAGAGCA	25909
rs546042676	snp	C/T	1.76024e-05	0.00296663	intron-variant	AHCTF1	GRCh38.p7	1:246904082	TATTAATACATTAAA[C/T]ATCTCTTACTGTCCA	25909
rs546059618	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246926270	ATATTCCTTTATAGC[A/G]ACACAGGCTAACGTA	25909
rs546096486	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246901365	AAACAGGCCAGGTGC[A/G]GTGGCTCACGCCTGT	25909
rs546160394	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246887056	TATTCTTGCCTTCTA[A/T]AATAGTGCTTGGTAA	25909
rs546204855	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246855900	GCTTTAGTCCTACCA[A/C]CTAACCTGTCATTTT	25909
rs546222713	in-del	-/ACAAAACAC			intron-variant	AHCTF1	GRCh38.p7	1:246920192	CTCACAGTCCAAATA[-/ACAAAACAC]ACAAAACACACAAGG	25909
rs546238144	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246874327	TCTATCTTCAGACAA[A/G]TACGTGTCCCTCTGA	25909
rs546241650	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246849048	TATATGTGCTCCCTT[G/T]GGGGAGAGATCACCC	25909
rs546243446	snp	C/T	0.00398564	0.0444627	intron-variant	AHCTF1	GRCh38.p7	1:246856948	ACCCTTACTACTACT[C/T]GATAACTGAAGCTGT	25909
rs546274565	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246922593	GAAATAAGGTCTCAC[G/T]ATGTTGCCCATGATG	25909
rs546280276	snp	A/G	4.94328e-05	0.00497131	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849683	GGTTCAGAAAGGTCC[A/G]GCAACAAGATGGCCT	25909
rs546281609	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246928684	TACACAAATTCCTGC[A/T]GTAACTGAATTCCAC	25909
rs546291771	snp	G/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246885113	CTAGATAAAAGGTGT[G/T]GTATGTTTTTCTTAA	25909
rs546294141	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246916633	CACTCCAGCCTGCGT[G/T]ACAGAGCAAGACTTC	25909
rs546314204	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246929863	TCAAGACCAGCCTGG[C/T]CAATATGGTGAAACC	25909
rs546376796	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869093	TCGTGATCCGCCCGC[C/T]TTGGCCTCCCAAAGT	25909
rs546383693	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246928786	CCACTTTGTATGCAA[C/T]GGTACTTTTTTTCTT	25909
rs546448150	snp	A/C	1.96126e-05	0.00313144	missense, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843824	GCTTGTTCTTATTGG[A/C]TGTGTTTTTTTGTCT	25909
rs546544557	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246896499	GAAATGTCTAGAATA[A/G]GTCAATCTATAAAGA	25909
rs546546201	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246871415	CCCAGGAACTGCTCC[C/G]ACACAAATACTCAAC	25909
rs546583730	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246922791	ATCGAGACCATCCTG[A/G]ATAACACGGTGAAAC	25909
rs546626384	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933546	TGGGATTACAGACAT[A/G]AGCCACCATGCCCAG	25909
rs546654130	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246904609	AGGGTGGGGAAAAAA[A/T]TTTTTTAAAATATGG	25909
rs546666663	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246930978	CAACCAGTGGCAAAA[A/G]AAACCGTCCTGTTTC	25909
rs546692591	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246885445	TCATCAATTCCATTT[G/T]ATTAACAGATACGAT	25909
rs546723274	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246928820	GACTAATAAAAAGAC[A/G]AATTGTCATTTAAAT	25909
rs546723316	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246923095	AAGAAGAAGTTATTT[A/C]ATCAAATAATACCAA	25909
rs546745763	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246866911	TTCAATGAGCTACCC[A/G]AGATTAATCTGTAAT	25909
rs546755428	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246875777	AAATTAAGGTATGTA[C/T]ACTGGTTTTAAGAAT	25909
rs546786225	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246924006	CGTAGAATATAAATC[C/T]GGCAAAAGAGAGATC	25909
rs546821920	snp	C/G			downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838829	TTCCCTTACTACTAT[C/G]ATACTAAGTATCTGA	25909
rs546857311	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246917491	CTGCCACTTACCTGT[A/G]TAACTGGGATCAAAT	25909
rs546867513	snp	A/C/G	0.00119752	0.0244452	intron-variant	AHCTF1	GRCh38.p7	1:246841440	TTTCTCACATAGATA[A/C/G]GCCAGTTTATATGTA	25909
rs546883274	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246863284	ATCCAAACAGAGAAC[C/G]CAGGGACAATGGGGA	25909
rs546886375	in-del	-/AC			intron-variant	AHCTF1	GRCh38.p7	1:246898408	TAAGATTAATTAATT[-/AC]ACTTAAAATTTAAGT	25909
rs546951819	snp	C/T	1.71352e-05	0.00292699	intron-variant	AHCTF1	GRCh38.p7	1:246861947	TTTTCTCCCAATTAT[C/T]ATCAAACTTACCCCA	25909
rs546954676	snp	C/T	0.000399281	0.0141238	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861247	TTTCCACTGGAACTG[C/T]ACATTTTTTAGGTGT	25909
rs546982841	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246922335	ACTGCACTCCAGCGC[A/G]GGTGACAGAGCAAGA	25909
rs546992531	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246855535	AGCCACAGAATGCCT[C/T]ACAAGCAACCCACTG	25909
rs546997624	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246854633	CAGCTAACATTTACT[A/G]AACTTCAGGTACCAA	25909
rs547022079	snp	A/C	1.65228e-05	0.00287422	missense, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840870	TTTCTGTTCCTTCCA[A/C]GACCTGTTCCTGTCA	25909
rs547071717	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246911807	AAGATATTTTAAAGT[C/G]CATGTATGACCATTA	25909
rs547101507	snp	A/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246882697	TACATTTATGATCCT[A/T]AGACTGAATAATCAA	25909
rs547165407	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246857290	ACAAACTTAGAGTCA[C/T]GTATTGAACAAATGG	25909
rs547225408	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246911074	GCTATAAAGTCCAAC[G/T]GCTTCCAATTCTCAA	25909
rs547263776	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246877605	GAGCTGAATGGTTGG[C/T]GTGGTGTGACAGAGG	25909
rs547269923	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246869858	TGGATCACAGTAATC[A/G]CAATTTTCAAGATAT	25909
rs547286727	snp	C/T	3.29891e-05	0.00406122	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849886	CTTAGAGCTCATCAC[C/T]ATCGAAAGTTCCTCG	25909
rs547298234	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868323	AAAGGGTTTCACCAT[C/G]TTGGCCAGGCTGGTC	25909
rs547315407	snp	C/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246892464	TAGCTGGGATTACAG[C/G]CATGTGCCACAACAC	25909
rs547321311	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246922855	GGGCGTGGTGGCAGG[A/C]GCCTGTAGTCCCAGC	25909
rs547338108	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246870811	TGGCTGTGTATCAAA[C/T]ACCTCCTCCTCAGAA	25909
rs547432218	in-del	-/A	0.00398564	0.0444627	intron-variant	AHCTF1	GRCh38.p7	1:246903683	CTCTGCTAAATATAC[-/A]AAAAAATTAGCCAGG	25909
rs547443701	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246904241	TCTAATCAACTAAAT[C/T]GATGCTGTTTGCATA	25909
rs547468350	in-del	-/A	0.00318978	0.0398085	intron-variant	AHCTF1	GRCh38.p7	1:246887448	ACAAAATGTAGCATT[-/A]AAAGAGACTTGAAAT	25909
rs547484221	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246920563	ATCATGAGGTCAGGA[A/G]ATCGAGACCATCCTG	25909
rs547484959	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246871700	CTCTGTAATCCATGC[C/T]TACAGTGCATTTTTT	25909
rs547575076	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246929596	TTCTGGAATAGCAAA[A/G]GCATAAAATTTGTTA	25909
rs547577611	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246906080	TGCCCTACAAAGAGA[C/T]GAGATACTGCCACGA	25909
rs547585109	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246854570	AAAATGTCTTAAATA[C/T]ATTACATGAGAAAAG	25909
rs547609662	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246884564	AGTAAGGAATTTCAG[A/C]TCCAAGCAATTTCTC	25909
rs547646193	snp	A/G	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246908707	CCTGGCTAACACGGT[A/G]AAACCCAGTCTCTAC	25909
rs547653574	snp	C/T	6.6486e-05	0.00576529	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900387	ATTTATATCAAAAAG[C/T]CCCAAATATACAGAA	25909
rs547707369	snp	G/T			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932512	CTGTTGCCCAGGCTG[G/T]AGTGCTGTGGCACGA	25909
rs547709309	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246906525	AAGTGGAGGTTGCAG[A/T]GAGCCAAGATCGTGC	25909
rs547749980	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246925579	AAGCTATGATCAGGC[C/T]ACTGCACTCCAGCCT	25909
rs547750705	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246867929	CACACACATTACGTG[A/G]TAATACTAGCTAAAA	25909
rs547767445	snp	C/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246920015	GGGCGTGGAGGCATA[C/T]GCTTGTAATTCCAGC	25909
rs547783515	snp	A/G	0.00318978	0.0398085	intron-variant	AHCTF1	GRCh38.p7	1:246912484	GAGACGCCGTCTCCA[A/G]AAAAAAAAAACAAAA	25909
rs547788463	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868254	CTGCCTTAGCCTCCC[A/G]AGTAGCTGGGACTAC	25909
rs547819324	snp	A/C	8.28562e-05	0.00643593	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246857788	CTGCAACTAAGAGAT[A/C]CTTTGTTTCTGCATC	25909
rs547990470	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246896470	AGACTTCATATTATT[C/T]GACCCATTTATATGA	25909
rs548036734	snp	A/G	0.0134861	0.0810011	intron-variant	AHCTF1	GRCh38.p7	1:246868884	GAGTCTCGCTCTGTC[A/G]CCCAGGTTGGAGTGC	25909
rs548037969	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246893670	TATCCATGGAGGACA[A/G]CAGTGATGCATTTTT	25909
rs548062404	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246891513	AATACATATAACTTA[A/C]TTTGAAACTTTACTG	25909
rs548062458	snp	C/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246883540	CCTTTTGCAAAATTA[C/T]CAGTTCAAAAATTTA	25909
rs548072731	snp	A/G	0.00398564	0.0444627	intron-variant	AHCTF1	GRCh38.p7	1:246847754	AGTTAAAATTAGTAG[A/G]TACAGAAATGAAAAA	25909
rs548099510	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246884442	TGACACAGAAGTGGT[A/G]ATTGGTTCATGTATA	25909
rs548117279	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246930543	ACTCTAATTTCTTCT[C/G]TCCTAAGAGACTCTA	25909
rs548134730	snp	A/G	1.64917e-05	0.00287151	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246898315	TGAGTGATGGACCTG[A/G]TTTCTTTAAAAAAGT	25909
rs548149121	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246858689	AATTGGCTGGGCATG[A/G]TGGCACGTGCCTGTA	25909
rs548149162	snp	C/T	1.64914e-05	0.00287149	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850842	TCATAGTCATTGTGC[C/T]TGTTTCCTGAGCAGT	25909
rs548205223	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246918105	AGCTTATAGATGTTA[C/T]ATATGTAACTGTAGA	25909
rs548233469	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246912092	ATTAGTTATGTTCAT[C/T]ATAAACTACATAAAA	25909
rs548234416	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246849114	AGTCCTTAGCTCGTG[A/G]CAATGAAGGATGGCC	25909
rs548238413	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246903700	AAAAATTAGCCAGGC[A/G]TGGTGGCGGGCACCT	25909
rs548241470	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246910895	AGATGTATAAGAAAC[C/T]GGTTAAGTCTGGGGA	25909
rs548273008	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246897802	CCTAGGCAACATAGC[A/G]AGACCCTGTCTCTAC	25909
rs548273195	in-del	-/AATTCAA			intron-variant	AHCTF1	GRCh38.p7	1:246926291	GGCTAACGTATTTCT[-/AATTCAA]ACTTTGAATCCAGGT	25909
rs548298681	snp	C/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246925553	TAAGACCAGGAGTTG[C/T]AGGTTGCAGTAAGCT	25909
rs548342591	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246849517	TTGAGGGGGGAAGGG[A/G]AAAAATTCCCTATAA	25909
rs548345276	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246855417	TCAACCTTGGCCTTA[A/C]GTTATCACAAACAAA	25909
rs548351031	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246919984	TCTCTACTAAAAATA[A/C]AAAAATAAATTAGCC	25909
rs548368459	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246912453	ACGCCACTGCACTCC[A/G]GCCTGGCAACAGAGC	25909
rs548390189	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246878275	GGTGGTGTGTGCCTG[C/T]AGTCCCAGCTATTCA	25909
rs548409075	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246905226	TGTATCAGGCCAGTC[A/G]TGGTGACTCACACCT	25909
rs548410265	snp	A/G	0.00557542	0.0525036	intron-variant	AHCTF1	GRCh38.p7	1:246912323	CTACTAAAAAAAAAA[A/G]AATACAAAAATTAGC	25909
rs548522949	snp	A/G	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246877541	AAATAATAAAAAAGC[A/G]AAGTAGACAAAAATT	25909
rs548533981	in-del	-/TGAC			intron-variant	AHCTF1	GRCh38.p7	1:246869513	CTTCAAAGGACAGGG[-/TGAC]TGACTCTGCTGTTAG	25909
rs548534247	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246929482	TGAAATTTGAGTATT[A/T]AAAAAAGGAAAGATG	25909
rs548536803	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246882084	CTCACTGCAAGCTCC[A/G]CCTCCTGGGTTCACG	25909
rs548584313	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246919376	GAAAGACAACATTTT[C/G]TTTCATACAAATGTG	25909
rs548590031	snp	C/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246930428	AGTACAGAGACAACG[C/T]AGACTTCCCATAGCG	25909
rs548594824	in-del	-/AAGA			intron-variant	AHCTF1	GRCh38.p7	1:246900993	CATCAACAGGAGAAG[-/AAGA]AAGTAAAAATCTGAA	25909
rs548607907	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246869230	TTTCCAACAGCGTGT[A/G]CTTACTCCACTGACT	25909
rs548657803	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246870284	CCCTCTCTACAAAAA[A/C]TACCCAGGCACGGTT	25909
rs548676248	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246879315	AAAGACATAGCATAC[A/G]GTAATTGAGAGGAGG	25909
rs548680632	snp	A/G	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246858283	TTCTTCTAATTCTCT[A/G]AACCTAGCTCAAGAG	25909
rs548729151	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868573	TTTGTTTCATTATAG[C/G]TATGCTGGATTTAGG	25909
rs548740734	snp	A/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246912474	GCAACAGAGCGAGAC[A/G]CCGTCTCCAAAAAAA	25909
rs548748821	snp	G/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246893616	AGATTAATAAAACTG[G/T]CAAGAAGGAAAATGA	25909
rs548767769	snp	G/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246868853	TGTTTTTTGTTTTTT[G/T]TTTTTTTTTGAGATG	25909
rs548875259	snp	A/G	0.0126979	0.078662	intron-variant	AHCTF1	GRCh38.p7	1:246868994	GGACTACAGGCGCCC[A/G]CCACCATGCCTGGCT	25909
rs548904047	snp	A/G	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246857530	ACTACTAAATGACAT[A/G]TAACTGCACAACTAA	25909
rs548911220	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246846063	CTACACTTTACTGGG[G/T]TGAAGTGGGAATCAA	25909
rs548912398	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246921151	CACGCAAAATGACAT[C/T]TATATAAGGTTAAAA	25909
rs548932136	snp	C/G	0.43221	0.171171	intron-variant	AHCTF1	GRCh38.p7	1:246864595	GACTAGACTGACTTG[C/G]GAGGCCGAGGCGGGT	25909
rs548943647	snp	C/T	1.64901e-05	0.00287137	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864025	GCAGTGAACGGGATA[C/T]TAGGTACAAAGGAGA	25909
rs548968818	snp	A/C	0.046775	0.145601	intron-variant	AHCTF1	GRCh38.p7	1:246865763	AGTTTAAAGGTTCTG[A/C]GAAATCTTTTTAAGG	25909
rs548972275	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246912352	GCCAGGCATGGTGGC[A/G]TGTGCCTGTAATCTC	25909
rs549004631	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246872487	TGAGGTTCTGGCTTA[C/T]TCCAACCAATCCAGA	25909
rs549041580	snp	C/T	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246868995	GACTACAGGCGCCCG[C/T]CACCATGCCTGGCTA	25909
rs549107673	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246859382	TACTAGTGTTCCCCT[C/G]GCCCTCTTGTTAACC	25909
rs549121711	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246879267	TACCCATGAGATGAA[A/G]AGACAAAAAATATCT	25909
rs549181627	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246901221	TGGCATGCACCTGTA[C/G]TCCCAGCTACTCAGG	25909
rs549214030	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246888026	ATCACAGGCCATCTG[A/G]GCCCAAACAACAGAT	25909
rs549218484	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246895107	ATAAAAACAATTACA[A/T]ACAAACTATTCTAGA	25909
rs549227379	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246898148	ATACATTTTTACTGT[A/T]ATAGAAAGCTAATAA	25909
rs549270211	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246882285	TACAGGCATGAGCCA[C/T]CGCACCTGGCCTATT	25909
rs549292303	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246852347	AACTTCCCAAATCCT[A/C]AACAAATTTCTATAA	25909
rs549305502	snp	A/G/T	0.00438332	0.0466095	intron-variant	AHCTF1	GRCh38.p7	1:246858811	TCTCAAAAAAAAAAA[A/G/T]AAATAAATACAAATT	25909
rs549391126	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246900565	TCTCATAAATTAAGC[C/G]GTTTAATTCATATTT	25909
rs549405737	in-del	-/A	0.494358	0.0528145	intron-variant	AHCTF1	GRCh38.p7	1:246847306	AAAAAAAAAACAAAC[-/A]AAAAAAAAAACTGAA	25909
rs549500393	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246905140	GAAAGAATTGTGTTG[C/T]CTTCACTAAAAAAGA	25909
rs549546776	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246843495	AAAACACCCAGGTAA[A/T]TCTGATGGACACTAG	25909
rs549550920	snp	C/T	0.00070835	0.0188062	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850625	TTCTGAGATAGTCCT[C/T]TGACATCAGAATAGA	25909
rs549555916	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246931889	TCCCCTTGCAACGCT[C/G]CCTGCTCGCCTCGGA	25909
rs549585429	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246844026	ATGTGTTTTAGAAAG[A/G]TGCAAACGTCCCCAA	25909
rs549607674	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246846415	CTTTGTTAAAGGAGT[C/G]AATACTCATAAGAAC	25909
rs549621095	snp	A/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246927113	AACCCGGGAGGCGGA[A/G]CTTGCAGTGAGCCAA	25909
rs549635392	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246922103	AGTGGCTCACGCCTG[C/T]AATCCCAGCACTTTG	25909
rs549649890	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	AHCTF1	GRCh38.p7	1:246839019	TTAGTTTAACCAATG[C/T]TTTGATCATCAGATA	25909
rs549681750	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246871750	AGACTATAAGGAGGT[G/T]AATAATATTAAAAAC	25909
rs549683977	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246906036	TCATATTTGATGTAC[A/C]CTCCTACATACTGCT	25909
rs549698389	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246930221	GCTCACTGCAACCCT[C/T]GAACTCTCAGTTTGA	25909
rs549729262	snp	G/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246927416	ATCGCTTGAACCGGG[G/T]AGGTGGAGGTAGCTG	25909
rs549743131	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246854116	CACCCTGGCTAACAC[A/G]GTGAAACCCTGTCTC	25909
rs549788768	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246879107	CTAATGCATACAAAG[C/T]GGCTATAAATCAGTA	25909
rs549855644	snp	A/C	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246868992	TGGGACTACAGGCGC[A/C]CGCCACCATGCCTGG	25909
rs549857001	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246842898	TCGCCAAATGCAAAA[C/T]TGACTCCTTTTCTCA	25909
rs549872357	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246872311	GGGGTGGCACGCCAG[G/T]AAAAGACTGACAAGA	25909
rs549873447	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246929919	TAGCCGGGTGTGGTG[A/G]CGTGCGCCTGTAATC	25909
rs549920617	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246847391	CTGCAGGTTTTTAAA[C/T]ACCAACCATACATAT	25909
rs549923160	snp	A/G			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933227	CAACCTCCGCCTCCC[A/G]GGTTCAAGAGGTTCT	25909
rs549936851	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246925630	AAATATAAAAAATAA[A/G]CCTAATGTGGTTTGT	25909
rs550016016	snp	A/T	4.04187e-05	0.0044953	intron-variant	AHCTF1	GRCh38.p7	1:246900513	AGAATAAAGAATCTC[A/T]AAGTAAAATCACCTC	25909
rs550038550	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246894311	GGCGCGGTGGCTCAC[A/G]CCTGTAATCCCAGCA	25909
rs550077374	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246858740	TGAGGCAGAGGTTGC[A/G]GTGAGCCGAGATCAC	25909
rs550082448	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246887856	CAGCACAGAGGTTAA[C/T]GCCATTGATAGTGAC	25909
rs550082799	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246906368	GTGGATCACAAGGTC[A/G]GGAGTTCGAGACCAG	25909
rs550141534	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246865956	ACTTGTTAGAGCTAA[-/T]TTTTTTTTACCATAA	25909
rs550154386	in-del	-/GG	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246877628	GACAGAGGAACATCA[-/GG]TTTTTAAGAAGTGAC	25909
rs550164080	snp	A/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246921867	TCAGGTAGAATAGAG[A/T]TCAGATAGAAGGTCT	25909
rs550175289	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246920991	CAGCTACTCAGGAGG[C/T]TGAGGCAGGAGAATC	25909
rs550189054	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246875401	ATTGACCAAAACCTG[A/C]CTTCTTGTAGAGTAG	25909
rs550204117	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246846808	CACCTGGGCTGGAGC[A/G]CAGTGGTGTGATGGC	25909
rs550219454	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246914853	CAAATGATCAATGAG[C/T]GTCCATGTTTCCTTC	25909
rs550234672	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246913790	AGTTATTCAAGCCAT[A/G]AAATCATTACGCATA	25909
rs550297891	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246927071	TAGTCCCAGGTACCC[A/G]GGAGGCTGAGGAGGG	25909
rs550306158	in-del	-/C	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246928125	GCTAACACGGTGAAA[-/C]CCCATCTCTACTAAA	25909
rs550330443	snp	G/T	0.000399281	0.0141238	downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838934	TTTCTGAGTATATCA[G/T]TTACCTTACTATGAT	25909
rs550358275	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246915353	AAAAAATTACTTCAC[C/T]GTTGATTTCAAAGGA	25909
rs550398192	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246873445	CTAGTCAATTTCTCC[C/T]GCATCATAGCGAAGG	25909
rs550400162	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246874331	TCTTCAGACAAATAC[A/G]TGTCCCTCTGAGGCA	25909
rs550405553	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246851564	AATTATATTTAATAT[A/G]GCATATACTTATGGG	25909
rs550433746	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246909641	CTGGCAATTCAGATA[C/T]GCCAAAGAGAAGCTG	25909
rs550543839	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246845092	CATTTGTTATTTCAA[G/T]AATATCATTTACAAA	25909
rs550552540	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246927373	ATACGCTTGTCATCC[C/T]GACTACTTGGGAAGC	25909
rs550575657	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246901805	CCTGGACTGGCCTGG[C/G]CATCAGAGTGAGACC	25909
rs550576490	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246845747	TCTTGTTTTGAGGAT[A/T]AAGGAGTTCAAAAGG	25909
rs550577452	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933360	GATGGTCTTGAACTC[C/T]TGACCTCGTGATCCA	25909
rs550615273	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246922521	GCCTCAATCTCCTGG[A/G]CTCTAGCAATCTCTC	25909
rs550633113	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246860000	GGCGCGGTGGCTCAC[C/G]CCTGTAATCCCAGCA	25909
rs550663886	snp	A/C/G			intron-variant	AHCTF1	GRCh38.p7	1:246925555	AGACCAGGAGTTGTA[A/C/G]GTTGCAGTAAGCTAT	25909
rs550668340	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246874200	GACATGCCAACAAAT[C/T]ACGATAAAATTTCAG	25909
rs550671733	snp	C/G	3.43956e-05	0.00414688	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853216	TCAGCGCTACTTCCT[C/G]GTTAAGCCTGCGCTC	25909
rs550727418	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869050	GGGGTTTCACCATGT[C/T]GGCCAGGATGGTCTC	25909
rs550744844	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246847616	GTGATCCTCCTGCCT[C/G]AGCCTCCCAAGTAGC	25909
rs550750308	snp	C/T	0.0123036	0.0774623	intron-variant	AHCTF1	GRCh38.p7	1:246869088	TGACCTCGTGATCCG[C/T]CCGCCTTGGCCTCCC	25909
rs550785866	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840698	TTCTGTTTACATAAA[A/C]ATTTACAATAATTTA	25909
rs550807773	snp	C/T	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246927831	AACATGGTGAAACCC[C/T]GTCTCTACTAAAAAT	25909
rs550826337	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246927969	CACGCCACTGCACTC[C/G]AGCCTGGCGACAGAG	25909
rs550864385	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246902232	GGCTCAAAAAATACA[C/T]GGGTAAACTTCATTC	25909
rs550906757	snp	A/G	9.90802e-05	0.00703778	intron-variant	AHCTF1	GRCh38.p7	1:246895970	ATGGAAAGAAAGAGG[A/G]TGTGAGATCATAGGC	25909
rs550921635	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246860423	AAATAAAAAATGTAA[C/T]ACATAAGTTCTCCTC	25909
rs550960873	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246853723	TTTTGGCAGAAAGCA[C/T]TCAAATAGGTACAAA	25909
rs550994077	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246900538	CACCTCAACAGAATT[A/G]TAGCAAGATTTTCTC	25909
rs551095891	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246917788	TTAGTATGGTTCTCT[C/G]ATGTATTACACAATC	25909
rs551096776	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246921221	AACATGACAAAACTA[C/T]GAAAAAAACAAAGAA	25909
rs551115640	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246889801	GAACTAAGTAGGTTA[C/T]TCGTGTACTTTTTTA	25909
rs551116619	snp	C/T			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932631	TTTTTCTAGCATCCT[C/T]CTGTGCTTTCATGGC	25909
rs551124026	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246918164	TGCTTTTTCTTCTTC[C/T]ACATAAAGAAACTAT	25909
rs551128848	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246887144	TTTAATACCAAATTT[A/T]AATTATGTGTATTTT	25909
rs551158893	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246922970	CCTGGGCGACAGAGC[A/G]AGACTCTGTCTCAAA	25909
rs551159893	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246921750	ACCAAAAGTAACTGC[C/G]AACATAATTATATAT	25909
rs551250064	snp	A/G	1.75925e-05	0.00296579	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876086	AGGCTTAGCTCGTTC[A/G]ATGGCTAATTTTCGA	25909
rs551254802	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246917306	ATCAAGTACAGACTC[C/T]GAATTTCTGCTTGAG	25909
rs551263477	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246858108	GGCACTACAGATGCC[C/T]GCCACCATGCCCTGC	25909
rs551288892	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246869546	GTTAATGTAGCTGAT[A/G]ACTTTAAATTAAAGG	25909
rs551302347	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246914838	TCTCAATTCCTCATC[A/C]AAATGATCAATGAGT	25909
rs551339399	snp	C/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246907946	TATCTATTTAAATGC[C/G]ACAATTTAAAAAACA	25909
rs551359374	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246909078	ATATCTATATATATC[A/T]ATATCTATCTATCTA	25909
rs551375933	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869044	AGAGACGGGGTTTCA[C/T]CATGTTGGCCAGGAT	25909
rs551401503	in-del	-/A	0.277867	0.248442	intron-variant	AHCTF1	GRCh38.p7	1:246858799	GCGAAACTCTGTCTC[-/A]AAAAAAAAAAAAAAA	25909
rs551407428	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246845693	TCTATTATAGCACAG[A/G]TGAGACTTTCTTGAG	25909
rs551433871	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246887806	TCAAATAATGCCTAA[A/G]GTAGTATCACGCTAA	25909
rs551438614	in-del	-/C	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246916673	AATAATAATAATAGT[-/C]ATTCAGTAAAAGCCA	25909
rs551497296	snp	G/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246912550	TTTCGGGTCAAATAC[G/T]CCTTTTCTAAAAATT	25909
rs551508378	snp	G/T	4.06413e-05	0.00450766	intron-variant	AHCTF1	GRCh38.p7	1:246853059	CCAAAACTGAAAGAC[G/T]GATAAAGAAGTAAAA	25909
rs551516154	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246872528	AACTGCCTTCATTTA[A/C]AAAGTTACTTAGGGG	25909
rs551529844	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246914216	TAATTAGGTATGATA[C/T]ATGATAAAATGTTTG	25909
rs551536958	snp	A/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246853656	AATTACAGAATTACA[A/T]GAGGAACATGCAATC	25909
rs551551076	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246873270	TTAACCGGTGATAAA[C/T]CACCATATAAAAAAA	25909
rs551654589	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246912408	GAATTGCTTGAACAC[A/G]GGAGGCGGAGGTTGC	25909
rs551704985	snp	A/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839500	AAGTCAGTGAAATTT[A/T]CAACAAGGCAGCGTA	25909
rs551709168	snp	C/T	0.000482567	0.0155258	intron-variant	AHCTF1	GRCh38.p7	1:246875997	ATTCAGTATCTTTTT[C/T]GATCCAATAGATTAT	25909
rs551727525	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246866587	AATTCAGAGTCTTGT[A/G]ATGATTATTTATAAT	25909
rs551730148	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246881542	AAAATTTTTTTTAAA[A/T]AGAAGCAGGGTCAGC	25909
rs551741951	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246908752	AAAAAAAAATTAGCC[A/G]GGCATGGCGGCGTGC	25909
rs551787847	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246901285	AGCAGAGGTTGCAGT[C/G]AGACGAGATCGTGCA	25909
rs551861782	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246895766	AAAATAACTAAGAAA[A/G]AAATATAACAAATAG	25909
rs551899529	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246909805	GGGGGAACTACCCTG[A/C]AGAGGGCTATCCTGT	25909
rs551911099	snp	A/C	0.0228947	0.104514	intron-variant	AHCTF1	GRCh38.p7	1:246896372	ACAACAGAATATTAT[A/C]CAGCCATAAAAGGGG	25909
rs551912057	snp	C/T	0.0023933	0.0345097	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933288	ACAGGTGTGCGCCAC[C/T]ATGCCCAGCTGATTT	25909
rs551914230	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246920442	AATGAGAGTGAATCA[C/T]AGCTACATGCAACAA	25909
rs551975307	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246927931	CTTGAACCTGGGAGG[A/C]AGAGGTTGCAATAAG	25909
rs551989638	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246889350	GGTTGTCCAATGAGC[C/T]AGGCACTGCACTAGA	25909
rs552001621	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868987	GTAGCTGGGACTACA[A/G]GCGCCCGCCACCATG	25909
rs552004315	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839890	TACTCACTCTCTCCC[A/C]ACCTCAATAATCTGT	25909
rs552026840	snp	C/T	0.00914312	0.0669923	intron-variant	AHCTF1	GRCh38.p7	1:246882122	CCTGCCTCAGCCTCC[C/T]GAGTAGCTGGGACTA	25909
rs552052789	snp	C/T	0.00517822	0.0506191	intron-variant	AHCTF1	GRCh38.p7	1:246927172	GACAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA	25909
rs552057863	snp	G/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246890770	GTATGAGCACTGTGT[G/T]TCAGGCATAGGATGA	25909
rs552112047	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246903655	CAAGATGGTGAGACC[C/T]CCCCCCCTCCGTCTC	25909
rs552178801	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246916480	TTACATACAACTATA[C/T]GTTCATTACATAAAA	25909
rs552196153	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246869429	CCAAGTTGTAAATGC[-/A]AAAAAAGAACCTGAA	25909
rs552200780	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246910351	ATTCCAATCCAAACA[A/G]TCCAAATGTAAAAAG	25909
rs552214636	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246918481	CACCAACAAAATAAA[C/G]AAAAACTAAAATCTG	25909
rs552215648	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246917173	CACTGGGTGGAAGAC[A/G]ACACCTGCTAGGTGA	25909
rs552259591	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246903156	ACCCGTTTCTATACG[C/T]CTCCAACATTAGGTT	25909
rs552264087	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246843258	GTCTCCTCTAACCTC[A/G]GTCTATAAAGTATTT	25909
rs552289844	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246929386	TGCACTCTAGCTTGG[G/T]CTACAAAGTGAGACT	25909
rs552355316	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246870065	AGGTGATTCCATCTT[C/T]CATGAATAACTTTTG	25909
rs552379009	snp	C/T	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246926581	GAAATAGGGGCCAGG[C/T]GCGGTGGCTCACACC	25909
rs552406535	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246877436	AAGTACTTTAAAAAT[C/T]TGTTGAATACTAAGT	25909
rs552413228	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246854682	TACATGCAAGGGGCT[G/T]AATCCTGACAACTCT	25909
rs552469509	snp	C/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246928970	TCAAGAAGATAACCT[C/T]CTTCCTGACTTTAAG	25909
rs552506204	snp	A/G	0.00716266	0.059414	intron-variant	AHCTF1	GRCh38.p7	1:246919436	AATCCTCAAGAGGCC[A/G]GGCGTGGTGGCTCAC	25909
rs552520354	snp	A/G	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246848121	GTGACGAGGGGAGAG[A/G]AGGATCCCCTATAGC	25909
rs552530112	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246907481	CTAACTTTCAAATAT[C/T]AGTAAATGAGTACAA	25909
rs552532258	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246928933	TACTTTTAAAACACC[A/G]TGTTAGTAAAGGAAT	25909
rs552564781	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246908094	AGAACTACTACCTAA[A/G]TACCTTCCTTGGAGC	25909
rs552570011	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246884681	TGTAATAATCATTAT[A/T]ATGTAAATGACAAAT	25909
rs552589908	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246848496	GTGAGCCACCGTGAC[C/T]GGCCAAGTCATCTAC	25909
rs552619830	snp	A/G	6.64088e-05	0.00576194	intron-variant	AHCTF1	GRCh38.p7	1:246876946	AAGACAACTTTAATC[A/G]TACCATAACATTAAT	25909
rs552721597	snp	G/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246869912	GCTATAGCTGTCACA[G/T]ATAGTGATTCCTCTG	25909
rs552722456	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932174	TTACAAAAAAATCGG[A/G]TCTCTCCGCCTCCGA	25909
rs552740578	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246901830	GAGACCCCTGTCTCT[A/C]AATAAATAAACAAAT	25909
rs552758230	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246870256	TGAGAATAGCCTGGG[C/T]GACATAGTGAGGCCC	25909
rs552794824	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246856516	GAACTAGTTAGCCAA[A/G]ATAGTGAATATGCAC	25909
rs552808551	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246904275	TAGGAGATATCTTAT[C/G]TAGCAAAGACTGATT	25909
rs552836382	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932912	GAAAGTTTCTACTTT[G/T]CTGTTACCTTTCATA	25909
rs552867179	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246862463	CCAGCCTGGGCGACA[A/G]AGCAAGACTCCGTCT	25909
rs552896494	snp	A/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246927731	TGTTCATGGCCGGGC[A/G]CGGTAGCTCAAGCCT	25909
rs552901416	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868544	GAGGTGTGAGCCACC[A/G]GCCTGGCCTACATTT	25909
rs552913914	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246898553	CAAAAGGTAGCTTAT[A/C]TATTTTTATGAACTG	25909
rs552917477	snp	A/G	1.64961e-05	0.00287189	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246888204	GGCTGCTTCAGTAAC[A/G]CCGTCTAATAGGTAC	25909
rs552929147	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839670	CTTCACATTAAAATA[C/T]TAAAAGCCCACGAAA	25909
rs553052423	snp	A/G	0.00318978	0.0398085	intron-variant	AHCTF1	GRCh38.p7	1:246922750	CACTTTGGGAGGCCA[A/G]GGAGGGCGGATCACG	25909
rs553089426	snp	C/T	0.00478085	0.0486577	intron-variant	AHCTF1	GRCh38.p7	1:246921706	AACAGTAGTAGAAAC[C/T]GCAATTCTGGAATAT	25909
rs553094916	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246915802	ATTTTTATAAACTTC[A/G]AGTGTCCTCATAGAA	25909
rs553128463	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246895613	TATGGCTGTAACGGC[A/T]GCATGAGGGATCCTG	25909
rs553168577	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246869124	GCTGGATTACAGGCG[C/T]GAGCCACCACGCCCG	25909
rs553249694	in-del	-/C	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246929801	GCTCACGCCTGTAAT[-/C]CCAGCACTCTGGGAG	25909
rs553268887	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246842136	TTTCATGCTATTAAT[A/G]TATAAAGAAATCCAC	25909
rs553271709	snp	G/T	0.00320191	0.0398836	intron-variant	AHCTF1	GRCh38.p7	1:246846752	CATATATATATTTTT[G/T]GGGGGGATGGGGGTG	25909
rs553276755	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246861499	CCCTAATTGGTAATA[C/T]ACCAGTATTTTCAGA	25909
rs553286912	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246854348	GGACCCAACAAGTCC[A/G]TGGTTAGGAATCTAC	25909
rs553306231	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246881770	TTGAACCTGGGAGGC[A/G]GAGGTTGCAGTGAGC	25909
rs553307622	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246910597	AACTCTTGTATTCTT[C/T]TAACTATCTGAAGAT	25909
rs553315605	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246854919	AATTCAGGAAAGACA[C/T]TTTAAATGGTTAATT	25909
rs553330090	in-del	-/TTAC	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246867442	GGGTTTTCATTCGTT[-/TTAC]TTTGTACAGTTCTGC	25909
rs553340594	snp	A/C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246896712	AATATCTGAACTGCA[A/C/T]GGTGTATGAAATATC	25909
rs553370946	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246890637	AGGAAAACTGAGTTA[C/T]AGAAACTATAGTTCT	25909
rs553379521	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246867946	AATACTAGCTAAAAA[C/T]TTTAATTATATATAT	25909
rs553415484	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246882921	CTCAGAGAGGATAAC[C/T]GAACTGCCTTTGATC	25909
rs553434436	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246920825	GCACGGTGCCTCACG[C/T]CTATAATCCCAGCAC	25909
rs553445475	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869286	TCCCCGAGGACCTCC[C/T]TTATTCCTTGAGACT	25909
rs553494492	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246867649	GACTATGAAACGTGT[A/G]AGAAAACATACCTAT	25909
rs553495870	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246918030	AACACATGAGATTTT[C/T]AATAAGGAAAAATTA	25909
rs553570105	in-del	-/TAGA	0.00358779	0.0422022	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839698	AAAGCAGTTCGTTTC[-/TAGA]TAATCAATTATTAAT	25909
rs553581557	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246910105	CCAAACTACCTTGCC[A/C]AAATACTAAACCTTC	25909
rs553586331	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246883716	ATCTCACAAATAGCA[C/T]TTTGAGTGGTTGTTT	25909
rs553589400	snp	C/T	0.00398564	0.0444627	intron-variant	AHCTF1	GRCh38.p7	1:246872291	CTAACCCAAGCTGTC[C/T]AGCTGGGGTGGCACG	25909
rs553636677	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246860774	GCCTCCCAAAGTGCT[A/G]AGATTAACTAGCATG	25909
rs553658305	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246903250	CCTCCGATCTCCTCA[A/G]GAATTCAGCCAGATA	25909
rs553704259	snp	C/T	0.0154538	0.0865337	intron-variant	AHCTF1	GRCh38.p7	1:246929976	AGAATCGCTTGAACC[C/T]GGGAGACGGAGGTTG	25909
rs553723051	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246897400	AAAGTTATGTAGATA[C/T]CAAATAAATATACAA	25909
rs553755798	snp	A/G	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246890289	GGGGCTTAAAATCCT[A/G]GAAACTGTTCTAAAT	25909
rs553763391	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246904636	ATGGATGTTGCCCTC[A/G]ACCATGAGAGGCCTA	25909
rs553800538	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246898859	TCGGGAGGCCGAGGC[A/G]GGCGGATCATCTGAG	25909
rs553820367	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246919489	GAGGCTGAGGCAGGC[A/G]GATCACAAGGTTAGG	25909
rs553842687	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868672	GGACATGTGCCTTCA[A/G]CTGAAATAGGAGTTC	25909
rs553858912	snp	A/C	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246912193	CTTTAAAAATCAAGA[A/C]TGTGCCGGGTGTGGT	25909
rs553872535	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246841055	TGCTATAAAATAAAA[C/T]TGGCTTCCCAACATG	25909
rs553882206	snp	C/T	0.000777174	0.0196973	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246918284	AAGCACAGATTCTAA[C/T]GTTATTTCGTCTTCT	25909
rs553904778	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246851846	TCCCCAAATTACCTA[A/T]CTATCCACACTTTTC	25909
rs553914408	snp	C/T	4.95552e-05	0.00497747	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246913255	TCAACTTCATTTTGA[C/T]TGCATGACAAGTCAT	25909
rs553934518	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246918581	GCAGGCGGATGAACT[C/G]ATCCCAGAAGTTCGA	25909
rs553967215	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246873443	CACTAGTCAATTTCT[C/G]CTGCATCATAGCGAA	25909
rs553970951	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246924360	TTTAAACAGAGATAT[C/T]TGAAATATTCACAAA	25909
rs553974106	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246909946	CAAAATTCACCCCCT[A/G]CTGAGAACCACTAGT	25909
rs553974463	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246862543	CACAATAGTGGTTAT[A/C]TTCTCATCTCATCTC	25909
rs554036982	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246907102	GGCTAGATGGTATAG[C/T]CTGTTGCTCTTAGTC	25909
rs554037057	snp	G/T			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933401	CCTCCCAAAGTGCTG[G/T]GATTATAGGCGTGAG	25909
rs554057878	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868377	CCACCCGCCTTGGCC[C/T]CCCAAAGTGCTGGGA	25909
rs554069657	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246925827	TGGCTCCCAGCACTT[G/T]GGGAGGCTGAGGCAG	25909
rs554074041	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246911554	AATGGCGCAATCTCG[A/G]CTCACTGCAGCCTCC	25909
rs554101909	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246892954	CCTAATCTCTAATAC[G/T]TTTAAAACACTTACT	25909
rs554138480	snp	A/G	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246885774	ACCACAAAAATCCAG[A/G]TAAGACTCGTTTAAA	25909
rs554170758	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246862207	GCTTATAGGCCGGGC[A/G]CGGTGGCTCACGCCT	25909
rs554255633	in-del	-/GT			utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839110	ACATTTTAATGAGCA[-/GT]GTTTTTATTCAAGCT	25909
rs554255767	snp	G/T	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246890177	GTTAACCCACAGGGT[G/T]GGTATATTTAGGTAA	25909
rs554292846	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246929844	GGATCACGAGGTCAG[A/G]AGTTCAAGACCAGCC	25909
rs554336031	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246892138	GACTATGAACTCAAA[C/T]CATCTATATCTAGAG	25909
rs554336903	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246897283	CACGTCACTGCACTC[C/T]AGTCTGGGCAACAGA	25909
rs554364072	snp	A/G	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246922711	CAATAGGCTGGGCGC[A/G]GTGGCTCACGCCTGT	25909
rs554392378	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246882866	TACCAGCATGAAGTT[A/T]TAGAGAAATGCAAAG	25909
rs554410222	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246854841	GTTCAGCCCCCTGCA[C/G]TCTTCAGGCACCGTC	25909
rs554412399	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246928070	CGCCTGTAATCCCAA[A/G]GCAGGTGGATCACGA	25909
rs554549376	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246889065	TGGTCCATCCAGCCA[A/G]TGACCATTCTATTTT	25909
rs554552698	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246854191	GTAGTCCCAGCTACT[C/T]GGGAGACTGAGGCAG	25909
rs554564072	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246911403	TTTTCATTTAAACTT[A/C]ACATAAAAATTTTAT	25909
rs554581310	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246896566	GGATGGGGCAGGCAG[A/G]AAGGTAAGGGAAAAG	25909
rs554588297	snp	C/T	1.64904e-05	0.00287139	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877014	TTGGCACGCTGCAAA[C/T]GGTGCACTAAAAGGA	25909
rs554616820	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246889486	ATAACAGATCTAGAA[C/T]TTTAAAATATGCCTA	25909
rs554625253	snp	A/C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246870001	CATTCAGCACATTCA[A/C/T]AATTCCTGGGAGGAG	25909
rs554688513	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933957	AAGAGATCTCTTCAA[A/G]CAGAAACCACCCTCT	25909
rs554702140	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246868913	GCAGTGGTGTGATCT[C/T]GGCTCACTGCAAGTT	25909
rs554707668	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246894977	TTAATCATGAGGAGC[A/G]ACGGCAAGCACAAAC	25909
rs554747558	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246847454	GGTGATTCTTTCGAT[A/G]GCTGGATTATATACT	25909
rs554782185	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840170	GACTAATTAAGACTT[C/T]AAAGAGCCTTTAAGC	25909
rs554834471	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246876543	AAAAGCAAGACTCAG[A/T]GTGTGTCCCAAGCAC	25909
rs554869556	snp	C/T	0.00228352	0.0337127	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877270	AACCTATTGCAATGT[C/T]GCCGCAAAAAATTCC	25909
rs554869863	snp	C/T	0.00517822	0.0506191	intron-variant	AHCTF1	GRCh38.p7	1:246856725	CTTTCATACTGGCTT[C/T]TACTTTTTCCATGCA	25909
rs554889383	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246929820	GCACTCTGGGAGGCC[A/G]AGGCGGGCGGATCAC	25909
rs554898776	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246898816	TTTCAGGCCAGGCAC[A/G]GTGGCTCACGCTCAT	25909
rs554937308	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246892053	TTTATAAAGACAAGC[C/T]AGAAATGGCAAAACC	25909
rs554963187	in-del	-/AA			intron-variant	AHCTF1	GRCh38.p7	1:246926047	GAGACCCTGTCTTTA[-/AA]AAAAAAAAAAAAAAA	25909
rs555034902	in-del	-/TG	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246891708	CTAAGACATGGGAAA[-/TG]TGTTATTCGTTTCTC	25909
rs555045486	snp	C/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246868227	TCTGCCTGCCAGACT[C/G]AAGTGATTTTCCTGC	25909
rs555091550	snp	A/T	0.0479149	0.147179	intron-variant	AHCTF1	GRCh38.p7	1:246868356	GAACTCCTGACCTCA[A/T]GTGATCCACCCGCCT	25909
rs555113444	snp	A/G	1.64871e-05	0.00287111	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246855793	TTAATCCTTCGTCCA[A/G]CACTGGTACCTTGGA	25909
rs555141999	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246898045	TGGGTATTAGGAATA[A/G]GAATTTTAAACCAAA	25909
rs555203135	snp	A/C	0.00517822	0.0506191	intron-variant	AHCTF1	GRCh38.p7	1:246920175	AAAAAAAAAGAAAAG[A/C]AGCTCACAGTCCAAA	25909
rs555269712	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246864344	ATTTTTAAAAAGAGT[C/T]TGCGTCGTCCTCCTT	25909
rs555312138	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246884934	AATTCTCAATTTGTC[A/G]ACTCTATCACTTCAT	25909
rs555379081	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246876458	GTGTCAGGCAACATT[A/C]TACTTCACACACATC	25909
rs555407233	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246886635	GTTGATTGAAGCCAC[A/G]GATGTAGAATCCATG	25909
rs555426521	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246870422	ACAAAGACCTTGTCT[C/T]TTAAAAAAACAAAAA	25909
rs555433194	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246852877	ACTATGGGCACCCGC[C/T]ACAGCACCCACCTCC	25909
rs555433291	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246881384	ACAAAACAGACTAGG[-/A]AAAAAAAATTATTCA	25909
rs555450441	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246887410	ACAAAAACCTCCTAC[A/G]TATATATTTACAATA	25909
rs555451494	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246877945	TTTTTTTTAATGCCA[C/G]TGTTCAACTCATACC	25909
rs555468349	snp	C/T	0.000617846	0.0175653	intron-variant	AHCTF1	GRCh38.p7	1:246900015	ACGTATACATTTACA[C/T]ACTTTTGTGCATTAC	25909
rs555478272	snp	A/T	0.000399281	0.0141238	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851096	GGCAAATTTGCAATT[A/T]GTCCATGATTATCAT	25909
rs555506890	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246893966	ACCAACACTTTGGAA[A/G]GCCCAGGCAGGAGGA	25909
rs555591245	snp	A/G	1.70618e-05	0.00292072	intron-variant	AHCTF1	GRCh38.p7	1:246899523	GGCATCTAAAAAAAA[A/G]ATTTAAAAAATAATC	25909
rs555618531	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246905434	TCCGGGAGGCGGAGG[C/T]TGCAGTGAGCCGAAA	25909
rs555618588	snp	C/T	1.68875e-05	0.00290576	intron-variant	AHCTF1	GRCh38.p7	1:246913441	TACGTGATTTGCTTT[C/T]CTTCTGCAAAGTAAG	25909
rs555623651	snp	C/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246844499	GCTGAGGTAGGAGGA[C/T]GGCTTAAGGCCAGGA	25909
rs555626225	in-del	-/GAGGCAGAAGAATCACCTGAACCCAG	0.0126979	0.078662	intron-variant	AHCTF1	GRCh38.p7	1:246909317	GCTACTTGGGAGGCT[-/GAGGCAGAAGAATCACCTGAACCCAG]GAGGCAGAAGAATCA	25909
rs555655328	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246906299	GCTGACAAACTGGCA[C/G]CCGGGCGTGGTAGCT	25909
rs555656253	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246864219	TAACTATGATAGCCA[C/T]ATGCAAATACAGTCA	25909
rs555688685	in-del	-/G	0.00318978	0.0398085	intron-variant	AHCTF1	GRCh38.p7	1:246921292	CGGAAGAATATACGA[-/G]GGACTCTGAAGTAGT	25909
rs555690001	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246917428	CACAGTTTAAGAAAG[C/T]AGCATGGTACAGTGG	25909
rs555704643	snp	C/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246921447	CAACAAAAACAAACT[C/G]AAAGGATAAGTAAAA	25909
rs555709344	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246848686	GCCTGGCCAACATGG[C/T]GAAATGCTGTCTCTA	25909
rs555711242	snp	C/T	0.00438332	0.0466095	intron-variant	AHCTF1	GRCh38.p7	1:246854106	AGATCGAGACCACCC[C/T]GGCTAACACGGTGAA	25909
rs555750081	snp	C/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246848436	TCGATCTCCTGATCT[C/T]GTGATCCACCCGCCT	25909
rs555772012	snp	A/C	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246872937	GGGTTCACCTTAAGA[A/C]TCAAAAATCCAAATC	25909
rs555810907	snp	C/G	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246869018	CCTGGCTAACTTTTT[C/G]TATTTTTAGTAGAGA	25909
rs555883756	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246930804	TTACGTTTTGTTCTA[C/T]GAAGAACCCAGTTCT	25909
rs555942778	snp	G/T	0.000726375	0.0190436	intron-variant, utr-variant-5-prime, upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246931236	GTCCATCGCGTGGGA[G/T]AACAGTGGGAAAGGG	25909
rs555945023	snp	A/G	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246926724	ACCAGGTGTGGTGGC[A/G]CATGCCTATAATCCC	25909
rs555983296	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246870408	AGCATCTGTGACAGA[A/C]AAAGACCTTGTCTCT	25909
rs555990403	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246877857	AGATCATTTAAATGA[A/C]GGAGTGTTTCTTACA	25909
rs556019564	in-del	-/ACT			intron-variant	AHCTF1	GRCh38.p7	1:246884182	GTAAATCTTATTGAA[-/ACT]ACAATTTTGATCTCA	25909
rs556020281	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246870956	AGACAAACAATACAA[A/C]TGAGCCTTCGAAAAA	25909
rs556031325	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246896218	AATTCCACACCTAGG[C/T]ATATACCAAAAAGAA	25909
rs556050644	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246873470	CGAAGGGAAAGAATC[C/T]GTCCCAATACTAAAT	25909
rs556079169	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246929137	CAGTGGGCTGGGTGC[A/G]GTGGTTCACGCCTGT	25909
rs556132703	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246899652	ATAAACTTTTCTAGG[C/T]ATTTTCATCCTAAGA	25909
rs556136510	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246841822	TTTGAGACAGAGTCT[C/T]AGTCTGTCACCCAGG	25909
rs556184458	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246901519	GCCCCAGCTACTTAG[C/G]GGGCTGAAGCAGGAG	25909
rs556210791	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246924387	CAAAACATTAGTGCC[A/G]TTTATTTTTGTGTGA	25909
rs556359070	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246929920	AGCCGGGTGTGGTGG[C/T]GTGCGCCTGTAATCC	25909
rs556378764	snp	C/T	0.000176081	0.00938134	intron-variant	AHCTF1	GRCh38.p7	1:246857839	ATACAAATAAGAATA[C/T]TATTTATGCTAAATA	25909
rs556385847	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246886539	TGTTATAGTGTAACA[C/T]CTAGGGAATAATGAC	25909
rs556395703	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246920089	CAGTTGCAGTGAGCC[A/G]AGATTGTGCAACTGC	25909
rs556416104	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246912247	CTTGGGAGGCCAAGG[C/T]GGGCGGATCACAAGG	25909
rs556437164	snp	C/T	0.00557542	0.0525036	intron-variant	AHCTF1	GRCh38.p7	1:246930659	TTCAAGCGATCCTCC[C/T]GCCTCAGCCTCTCAA	25909
rs556438963	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246906954	AAAGAACTCATATTA[C/T]ACAAACACAGCCATG	25909
rs556456915	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246912685	TACAAGCATTTAAAG[C/G]AGAAAAAGTATTTCA	25909
rs556468722	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246920799	AATTATTAAACAATA[A/C]AAGCATCCAGGCACG	25909
rs556522084	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246913577	AAATCTTCAGCTATA[C/T]TAGGAATTACACCAT	25909
rs556560775	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246914314	CCCAGGCATTTTGGA[C/T]AGGGGATTCTCAACC	25909
rs556598431	snp	A/G	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246872203	GATCTAAAAGATAAA[A/G]CAGATCAAGGATCTA	25909
rs556643290	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246861643	AATATAAGGTAAAAA[C/G]AAAGATAAAAGAAGG	25909
rs556658509	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246930006	GCAGTGAGCCAAGAT[C/T]GTGCCACTGCACTCC	25909
rs556728227	snp	C/T	4.96118e-05	0.0049803	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850284	CATCTAAATTAGTAC[C/T]TCTCAATTTTCTGAT	25909
rs556740844	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246907297	ATGCTTTACTAGCAT[A/G]TTAAACACATGACTG	25909
rs556765007	snp	G/T	0.000399281	0.0141238	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850893	ATTTAGTGGGACACA[G/T]TATGTTTTGGCTCAC	25909
rs556800453	snp	A/G			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246931836	GACCGCTCAGCGGCT[A/G]AAACGCAGTCGCTGC	25909
rs556837986	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246880334	CTTTGGGAGCCCGAG[A/G]CGGGCAGATCACGAG	25909
rs556844378	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246926913	GCCGCGGTGGCACAC[A/G]CCTGTAATCCCAGCA	25909
rs556845538	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246858962	GCCAGGACCGGTGGC[A/G]CATGCCTGTAATCCA	25909
rs556872080	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246900729	TTTCAGTTAATACTT[C/G]AGCAACGTTGAGGTA	25909
rs556909009	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246846078	TTGAAGTGGGAATCA[A/G]ACGATATATGAATGT	25909
rs556951238	snp	A/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246868983	CTGAGTAGCTGGGAC[A/T]ACAGGCGCCCGCCAC	25909
rs556959381	in-del	-/TT	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246876705	CTCTACATCTTCCTC[-/TT]GTTTTCCCTGAGTGA	25909
rs556997629	in-del	-/AAAAC	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246866642	AATTTTGTCTTTGAT[-/AAAAC]AATCAAAAATTTCCA	25909
rs557006429	in-del	-/CT	0.00318978	0.0398085	intron-variant	AHCTF1	GRCh38.p7	1:246920763	TGACAGAGCAAAACA[-/CT]GTCTCAAAAAAAAAA	25909
rs557078431	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246921008	GAGGCAGGAGAATCG[C/T]TTGAACCTGGGAGAA	25909
rs557080972	snp	A/G	0.000803535	0.020028	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839513	TTTCAACAAGGCAGC[A/G]TAACATCCATCACTA	25909
rs557117270	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246908043	TTTAGGGTTAACAAC[C/T]ATAAATAAAACTGAT	25909
rs557120961	snp	A/G/T	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246881243	ATAATAATTTTAAAA[A/G/T]TCATTTTAAAAAAGA	25909
rs557124294	snp	A/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246865173	CTTCTCGATTTCCTA[A/T]TAAACAGTCTATCTT	25909
rs557150704	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246865928	TTTAAAAAATTGATT[C/T]ATGTAACTTTTTACT	25909
rs557159367	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246873569	TAAATATACTAGAGA[A/C]AATACACTAGTCAAT	25909
rs557226262	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869261	AACTGTTCCCCCGCG[C/T]CTCTCCCTTTCCCCG	25909
rs557262592	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246867585	TAGGCAAAGAGAGTG[C/G]ATTGTTGATGAACGC	25909
rs557293266	snp	A/G/T	0.00159649	0.0282165	intron-variant	AHCTF1	GRCh38.p7	1:246926549	ACTACAGAGAACATC[A/G/T]AAACACTCTATTATT	25909
rs557300680	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246913098	AGATTTTAAAATACC[-/T]TTTTTTTTTTTATAG	25909
rs557318167	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246920268	TGAAATTACCAGAGA[G/T]TAGAAAGTAAATGTC	25909
rs557329819	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246901994	GTGATTTAATCCTCA[C/T]AACTACCCTTTGCAA	25909
rs557356657	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246920702	ATGAACCTGGGAGGC[A/G]GAGCTTGCAGTGAGC	25909
rs557363641	snp	C/T	0.000131796	0.00811668	intron-variant	AHCTF1	GRCh38.p7	1:246867644	AGCATGACTATGAAA[C/T]GTGTAAGAAAACATA	25909
rs557415850	in-del	-/TAAG	0.00119737	0.0244387	downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838869	CCCTTACTACGATAC[-/TAAG]TATCTTTCTGAGTAC	25909
rs557424396	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246864703	AAATTAGCCGGGCGC[A/G]GTGGCGGGCGCCTGT	25909
rs557436498	snp	C/G	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246888885	CTGCAGCCTGGGCAA[C/G]AGAGACCCTGTCTCT	25909
rs557450253	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246874558	GAAACGGCCACCCAA[A/C]AAAATATAAAACCCA	25909
rs557487247	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246922806	GATAACACGGTGAAA[C/T]CCTGTCTCTACTAAA	25909
rs557489543	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246891732	GTTTCTCTTAGTCAA[C/G]AAGTAAAATTTAATA	25909
rs557531007	in-del	-/TAC	0.00755907	0.0610114	intron-variant	AHCTF1	GRCh38.p7	1:246889606	GCACAGATTTTAAAG[-/TAC]TGATTCCCAGGTGAT	25909
rs557571183	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246915740	CAAGACTATTGTCGC[A/T]AATTTAAAAGGTAAA	25909
rs557607783	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246909283	TTGGCCGCACATGGT[C/G]GTGTGCAACTGTAGT	25909
rs557629134	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246864378	TTTACCTATATTTAC[C/T]GAGCTCTTACTATGT	25909
rs557630126	in-del	-/AAG			intron-variant	AHCTF1	GRCh38.p7	1:246843750	ATTTGTAAAAAAAAA[-/AAG]TATGTTTTAACAAAC	25909
rs557643676	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246906433	AAAAAAATACAAAAA[A/C]TAGCTGGGTTCAGTG	25909
rs557646597	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246909964	GAGAACCACTAGTTT[A/C]AAGTTGATGACAGAC	25909
rs557684873	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246909718	AGGAAAAATCATAAT[A/G]TGTGCAGGGTTCAGT	25909
rs557772693	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246852753	CATGAAAACCAGTTT[A/G]TTTATTTATTTATTT	25909
rs557812241	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246906648	TGAGATACACTTCCT[A/G]TAAGATAAATTACTC	25909
rs557817726	snp	C/G	0.000153151	0.0087494	intron-variant, utr-variant-5-prime, upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246931275	CCGGCCGTCCGTAAA[C/G]GGACCCGACTGCCGG	25909
rs557833335	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246873082	AGCCCTCAGATCAGG[A/C]GCTACTAGGTTCGAC	25909
rs557865093	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246872096	TCCCAAAAACCTAGG[A/G]TGGTCTCTAACTAAA	25909
rs557886675	snp	C/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246868999	ACAGGCGCCCGCCAC[C/T]ATGCCTGGCTAACTT	25909
rs557895592	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246887604	CAAAGGAGATAAAGC[A/G]TATTTTTATGAAGTC	25909
rs557970533	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246873528	TCTCCTGCATCACAG[C/T]GAAGGGAAAGAATCC	25909
rs557999988	snp	C/T	3.33139e-05	0.00408116	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900138	TCCTCTATTTAAACT[C/T]CTCTCATGTACTAAT	25909
rs558046139	snp	C/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246869097	GATCCGCCCGCCTTG[C/G]CCTCCCAAAGTGCTG	25909
rs558080917	snp	A/C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246922786	AGGAGATCGAGACCA[A/C/T]CCTGGATAACACGGT	25909
rs558093643	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246915095	CCAGCACTTTGGGAG[C/G]CTAAGGCAGGTGGAT	25909
rs558147399	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246931932	CGCTCTGCGCATTAC[C/T]CTGCGCCGACAAAAC	25909
rs558166538	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246901882	GCTCATGACAACATG[C/T]GCTTTTCACATATTT	25909
rs558183131	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246896151	AGCCACTCTGCAAAG[C/T]AGTTTGGCGGTTTCT	25909
rs558189602	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246866271	TCTATTATTGCTCCC[C/T]GCAACCTCAGAGCCA	25909
rs558196828	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246926956	AAGGCGGGCGGATCA[C/T]GAGGTCAGGAGATCG	25909
rs558198692	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246888054	GATCCTGGGTTAACA[A/C]CTCTTCTTAAGAAAA	25909
rs558209220	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246895215	TGGGATTTCAATAAG[C/G]TCTCTAGGTTAGATA	25909
rs558237378	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246881143	TAAAGTAAAAAGACT[A/G]GGGAAATATACATAC	25909
rs558297807	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246901290	AGGTTGCAGTGAGAC[A/G]AGATCGTGCAAGTGC	25909
rs558309245	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246927164	GCCTGGGCGACAGAG[C/T]GAGACTCTGTCTCAA	25909
rs558309507	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246921559	CTAAGATATGCCTAA[G/T]CAGAATCCCCCCAAA	25909
rs558320309	snp	C/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246896544	AGTCATTATGTAAGG[C/T]TGGGTAGGATGGGGC	25909
rs558355086	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246898900	CGAGACCAGCCTGGC[A/C]AACATGGTGAAACCC	25909
rs558361900	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246908443	CTCTGAAAATTAGTA[C/T]TTAAGAAACACTAAA	25909
rs558372239	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246922177	TCAGCCCAACCAGTA[C/T]GGTGAAACCCCATCT	25909
rs558417670	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246913615	TACATAGAAAAATCA[C/T]GCAGTTGGACTAACA	25909
rs558420011	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246927805	GTCAAGAGACCCAGA[C/G]CATCCTGGCCAACAT	25909
rs558463322	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246889169	TTTCTGTTTCATCAC[C/T]TGGGTTAGTCTTTTA	25909
rs558486819	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246866952	AACAACCCTCATTTA[C/G]AGGTCTACTAACAAG	25909
rs558500066	snp	A/C	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246881861	AAACCAAAAAAAAAA[A/C]CAAAAAAAAAAGAAG	25909
rs558513389	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246917013	CCTATTAGTCATGTT[A/T]GGATTTTACCCTGCC	25909
rs558552411	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246917582	TCCAATGAAGTCATC[A/G]TACAATGCCTGGCAT	25909
rs558607049	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246928267	GACATCGCGCCACTG[C/T]ACTGTAGCCTGGGCG	25909
rs558628182	snp	C/G	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246893905	TGCTGCAAAATCTTG[C/G]TCAAAAATTACTTTT	25909
rs558662453	snp	C/T	1.65138e-05	0.00287343	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840890	TGTTCCTGTCACTTC[C/T]GTAGTTTTTCTTGGT	25909
rs558662773	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246879108	TAATGCATACAAAGC[G/T]GCTATAAATCAGTAA	25909
rs558696949	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246919170	GGGAACCCTGATCTT[A/C]TTCTGGGCACTCTAA	25909
rs558702869	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246910116	TGCCAAAATACTAAA[C/T]CTTCATCTATAACCA	25909
rs558731070	snp	A/G	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246928040	AAATACTGTTCGGCC[A/G]GGTGCGGTGGCTCAC	25909
rs558745198	snp	A/C	0.00755907	0.0610114	intron-variant	AHCTF1	GRCh38.p7	1:246889602	GCCGGCACAGATTTT[A/C]AAGTACTGATTCCCA	25909
rs558759040	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246854159	AAAAAATTAGCCAGG[C/T]GTGGTGGCGGGCACC	25909
rs558818846	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246855051	CTGCTGAAGCTTGCC[A/G]TATACCCCATTCATA	25909
rs558884765	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246911285	ACTATGAAACAAAAG[C/G]CTATCAAGCCTACTT	25909
rs558897806	snp	C/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246875736	CTCAGATGATCCTTA[C/G]CATTTTTTAGCAATA	25909
rs558903673	snp	A/C/T	3.31957e-05	0.00407394	intron-variant	AHCTF1	GRCh38.p7	1:246900324	AAGGAGAGAGAAAAA[A/C/T]AAAGAATCATACCTT	25909
rs558972488	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246910665	CTCATATATTAATAT[A/C]ACCACTGTGCAAGAG	25909
rs558983340	snp	C/T	1.67882e-05	0.00289721	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246862071	GCTAAAGGTGTTGAT[C/T]GAAGAGTAGACCTCA	25909
rs559013335	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246855045	ACTAGTCTGCTGAAG[C/T]TTGCCGTATACCCCA	25909
rs559013750	snp	A/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246845070	GTAAGTGCTCTACAG[A/T]TGTTTGCATTTGTTA	25909
rs559032029	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246931597	ACGGGGCGGGTGAGC[A/G]CGCCGCCGCGGGCCG	25909
rs559053589	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246915173	CATCTCTACTAAAAA[C/T]ACAAAAATTAGCTGG	25909
rs559075160	snp	G/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246869633	CTGTCTTCTATCAAT[G/T]GAAAAAGCCTAGATG	25909
rs559152757	snp	A/G	0.0509478	0.151255	intron-variant	AHCTF1	GRCh38.p7	1:246868341	GGCCAGGCTGGTCTT[A/G]AACTCCTGACCTCAT	25909
rs559174020	snp	A/G	2.87129e-05	0.00378888	intron-variant	AHCTF1	GRCh38.p7	1:246851472	GATAAGAGACTGGTT[A/G]AAGAATTTTAATACA	25909
rs559230978	snp	C/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246897467	TTAATGATGGGGATA[C/T]ATTCCGATGAATGTT	25909
rs559302152	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246891219	TCTTGAACTAATTCA[C/T]CTTTGTATTTAGTTT	25909
rs559355413	snp	C/T	0.00478085	0.0486577	intron-variant	AHCTF1	GRCh38.p7	1:246894836	AAGCATGGCAGACAG[C/T]ACCCTAACCGAGTGA	25909
rs559390473	snp	A/G	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246869037	TTTTAGTAGAGACGG[A/G]GTTTCACCATGTTGG	25909
rs559426181	snp	C/G	0.000399281	0.0141238	intron-variant, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851980	AATTCCTAAGGCTTT[C/G]AAGTTCAGTACCTCT	25909
rs559480201	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246853029	TTTGAACTACTGTGT[A/C]TTGAAACAACTAAAC	25909
rs559482166	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246860281	TCAAAAATTAAATAA[A/G]TAAAAATTGCAATAA	25909
rs559487889	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246887758	TAAGTAACTAACATT[A/T]GCACAAAAATATTAT	25909
rs559489165	in-del	-/GA	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246894099	GTCCAAGCTACTCAG[-/GA]GGCTGAGGCAGGAGG	25909
rs559525845	in-del	-/ATAG	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246882441	TAAAACTTCTAAATC[-/ATAG]ATAGGGAAAATAAAC	25909
rs559541673	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246915190	CAAAAATTAGCTGGG[C/T]GTGGTGGTGCACGCC	25909
rs559545726	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246852656	TATGATCTTATGACT[-/A]AAAAAAACCTTTCAT	25909
rs559604446	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246873559	GTCCCAATAATAAAT[A/G]TACTAGAGACAATAC	25909
rs559640010	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246869226	CATTTTTCCAACAGC[A/G]TGTACTTACTCCACT	25909
rs559652130	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246873260	GAAAAAAATCTTAAC[C/T]GGTGATAAATCACCA	25909
rs559663632	snp	G/T	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246915221	TGTAGTCCCAGCTAC[G/T]CAGGAGGCTAAGGCA	25909
rs559684935	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246845449	GGCAGAAATGGCAAT[C/G]GCTAGGTCTACTGGT	25909
rs559712478	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246859973	AAGTTAAAAATTGCA[A/G]TAATTTGGCAGGGCG	25909
rs559728735	snp	A/G	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246860257	TGGGCAACAGAGTGA[A/G]ACTCTGTCTCAAAAA	25909
rs559736321	snp	A/G	0.00398564	0.0444627	intron-variant	AHCTF1	GRCh38.p7	1:246869075	GGTCTCGATCTCCTG[A/G]CCTCGTGATCCGCCC	25909
rs559784944	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246866525	TGTACTTCTGGCCTC[A/C]GTTGTTTGTATGACC	25909
rs559822556	in-del	-/A	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246858629	GGTCAGGAGTTCGAG[-/A]CCAGCCTGGCCAACA	25909
rs559874918	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246881602	AGCACTTTGGGAGGC[C/T]GAGGCGGGCGGATCA	25909
rs559896963	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840195	TTAAGCTTGCCGAAT[A/G]AGAGATGCCAACATT	25909
rs559910266	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246896338	TTAATTGTAGATAAA[C/T]AAATTATGGTATGCT	25909
rs559948660	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246881489	TAAATGGAGAATACA[C/T]TGAGTACTTATCAGT	25909
rs559973618	snp	C/T	0.00199481	0.0315187	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933157	TTTATTTATTTGAGA[C/T]GGAGTCTCGCTCTGT	25909
rs559985033	in-del	-/TT	0.0146672	0.084371	intron-variant	AHCTF1	GRCh38.p7	1:246869143	CACCACGCCCGGCCG[-/TT]TGTGTTTTGTTTTTT	25909
rs560053448	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246917869	TTTTCTGAAAATTTT[A/C]TAACATCTAGGGCCC	25909
rs560056357	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246903570	TGCGGTGGCTCACAC[C/T]TGTAATCCCAGCACT	25909
rs560065741	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839847	TGTAGAGAACAGGGC[A/G]TGTGTTGTTTTTCTC	25909
rs560086695	snp	C/G	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246868896	GTCACCCAGGTTGGA[C/G]TGCAGTGGTGTGATC	25909
rs560090179	snp	C/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246910736	CACTGTCCTAGAACA[C/G]GGCCCCCACCCCCAA	25909
rs560098533	in-del	-/A	0.309399	0.242841	intron-variant	AHCTF1	GRCh38.p7	1:246845370	TATGATTCTTAAAAA[-/A]AAAGAAAAATAGAGT	25909
rs560127584	snp	A/G	0.00398564	0.0444627	intron-variant	AHCTF1	GRCh38.p7	1:246898151	CATTTTTACTGTAAT[A/G]GAAAGCTAATAACGT	25909
rs560131762	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246903145	GATTCCCTGAAACCC[A/G]TTTCTATACGCCTCC	25909
rs560164791	snp	A/G	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246928086	GCAGGTGGATCACGA[A/G]GTCAGGAGATCGAGA	25909
rs560173430	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868125	GGCCACCAAGCCCGG[C/G]TAATTTTTTTTTTTT	25909
rs560191260	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246927157	CACTCCAGCCTGGGC[G/T]ACAGAGCGAGACTCT	25909
rs560191505	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246928848	AATGTAAACTACCAG[C/T]GGACCCAGAAACTTC	25909
rs560257366	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246910275	GAAAGAGGATTGCTG[C/T]ACGTTCAAGGAGACT	25909
rs560264469	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246924774	CATTAAGTCACAAAA[A/C]CTAAAAAGTTATGTT	25909
rs560276265	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246922937	GCAGTGAGCCGAGAT[C/T]GCACCACTGCACTCT	25909
rs560339923	snp	A/C	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246891348	GCTACACTTTCATTT[A/C]GCTAATTCCAGAACT	25909
rs560462159	snp	C/T	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861260	TGCACATTTTTTAGG[C/T]GTAGTAAATACTTCT	25909
rs560480961	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246855183	ACACAAGATGATCAG[A/G]CCAATTCTGGGCATA	25909
rs560503025	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246920000	AAAAATAAATTAGCC[A/G]GGCGTGGAGGCATAC	25909
rs560543120	snp	C/T	0.0012598	0.0250662	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246888501	CAATCATCAAGCAAT[C/T]GGGATTCCACTTCCC	25909
rs560551915	snp	A/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246890699	GAACTCATTTTCAGG[A/G]GCTATGTTTTCTCAA	25909
rs560565502	snp	A/G	1.66671e-05	0.00288674	intron-variant	AHCTF1	GRCh38.p7	1:246855838	TTTTCCTTTAGAAAA[A/G]GAAATACATACCTTA	25909
rs560567798	snp	A/C/G			intron-variant	AHCTF1	GRCh38.p7	1:246916477	CATTTACATACAACT[A/C/G]TATGTTCATTACATA	25909
rs560585240	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246881456	CATGGGGACAAATAT[A/G]TTTGACATTTCACCT	25909
rs560585323	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246889260	TATGGTCCCTATTTC[C/T]TTTTCTTTTCTCTTC	25909
rs560601656	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246925596	CTGCACTCCAGCCTG[A/G]GCAAGATCCTGTTTC	25909
rs560622113	snp	G/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246882001	ATTATTACTTTTTTT[G/T]TTGTTTTTTTTTTTG	25909
rs560670894	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246919801	CCACATATCCTCTGG[A/C]ATCTCAAAGAATTCT	25909
rs560680848	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246863229	TCTTTTATTCAACTT[A/G]AAAAATAAGGATTCC	25909
rs560689304	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246853510	CATTTAAAAATGATA[A/C]CTGATAAACGGTATC	25909
rs560693230	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246927398	GGAAGCTGAGGCATG[A/G]GAATCGCTTGAACCG	25909
rs560717556	snp	A/G	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246896180	CTCAGTATGCTAAAC[A/G]TAGACTTACCACACG	25909
rs560733683	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246878110	AGTATAAGAATATAC[A/G]GTAAGAGCCAGGCAT	25909
rs560735966	snp	C/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246880862	AGAAGACAATAATGA[C/T]GCTAGGAAGAACAAT	25909
rs560748774	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246918995	ATCAAGTTTGGTACA[C/T]ATCTTTTGCAGGATA	25909
rs560754349	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246917103	TTATGCATGTTTTTA[A/C]ATGTTACTCCAGCTG	25909
rs560767295	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246874734	CCTATCCTGAGAGAT[A/C]CTGAAATATATTTAA	25909
rs560836134	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246846345	GGGACAGAAAGTATG[A/G]TAACAGTATAAAGGG	25909
rs560836444	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933024	CACAGCAGCCTCGAA[C/T]TCGTGGGCTCAAATG	25909
rs560848869	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868538	GGGATAGAGGTGTGA[A/G]CCACCGGCCTGGCCT	25909
rs560872835	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246847047	ATCCCAGCACTTTGG[A/G]AGGCCAAGGCGGGTG	25909
rs560876836	snp	C/T	0.0189856	0.0955633	intron-variant	AHCTF1	GRCh38.p7	1:246922914	CATGAACCCAGGAGG[C/T]GGAGTTTGCAGTGAG	25909
rs560880463	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246864756	GAGGCAGGAGAATGG[C/T]GTGAACCCGGGAAGC	25909
rs560891713	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246911813	TTTTAAAGTGCATGT[A/G]TGACCATTATTTCTG	25909
rs560946356	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246892528	GTTTCACCATGTTGG[C/T]CAGGCTGGCCTCGAA	25909
rs561003895	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839808	CTACATCAAGTACCA[C/T]TGCTTAATTGCACAC	25909
rs561050067	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246875111	CCCCAGGAGGTGCTA[C/T]GACTTCCTTACCATG	25909
rs561142902	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246903462	GAATGCTACCTGGGT[A/G]AATAGGTAAAACAGA	25909
rs561151664	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246841374	ATGTCAGAAATGTCA[A/G]TGATCAAACACAGCA	25909
rs561181213	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246867895	AGAATGATTACACCC[C/G]CCCCCCCACACACAC	25909
rs561184928	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246869135	GGCGTGAGCCACCAC[A/G]CCCGGCCGTGTGTTT	25909
rs561219934	snp	C/T	0.000131823	0.00811752	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861216	GTGGTCCTATCTTTG[C/T]TCTTCAGCCATTCAG	25909
rs561227259	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246886359	AAAAATAAAAAATAA[C/T]AGTATAATGATAAAA	25909
rs561251338	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246855102	TAACAGTTGAGAGCA[C/T]GGGCTCTAGAGTCAG	25909
rs561289624	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246844809	ACCACACAGACTTTT[-/T]TTTTTTTTTTTTAAC	25909
rs561314444	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246902921	ACACAGAAGCCCTCA[C/T]GCACTACTGGTTGGT	25909
rs561366581	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840414	GTAAAAAGAAATATC[A/G]ATACTTCAATCATCC	25909
rs561421275	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246924677	AAAATATATGAGTTA[C/T]CATTTTCTGTTCAGG	25909
rs561422443	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246854598	AAGAAAGTTGCTTTT[C/T]TGATAATGATCATTT	25909
rs561457573	snp	A/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246890497	ATTCTAAACAAATAT[A/T]GCACAAGTCAAATAC	25909
rs561459577	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246862308	ACACGGTGAAACCCC[A/G]TCTCTACTAAAAATA	25909
rs561472911	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246924481	AATTTTAAAACATAT[A/G]TATATAAAATAAAAA	25909
rs561493192	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246918869	ACCTCACCACCACCA[A/T]CCTCCCTACAGAAAA	25909
rs561493827	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246883194	TTTAAATATTAAAAC[C/T]TTTTCAGCCATTTCA	25909
rs561496569	snp	A/C	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246862657	CTACGAAACATAAAA[A/C]TGCATCCATCTTTCT	25909
rs561578273	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246870176	AGGCCAGGCATGATG[A/G]CTCATGCCTGTAATC	25909
rs561637753	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869827	GCATGAAAACACAAC[A/G]TCCATTCTGTAACCC	25909
rs561653534	snp	A/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246918132	TAGATGTTACATATT[A/T]AAGATCACTCAGGTT	25909
rs561672513	snp	A/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246911673	TTTTTTAGTAGAGAC[A/G]GGGTTTCTCCATGTT	25909
rs561752237	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246898917	ACATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	25909
rs561774175	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246885931	GTGGCTCACGCCTGT[A/T]ATCTCCGCACTTTGG	25909
rs561785416	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246892384	CAGTGGTGCAATCTC[A/C]ATCTCCGCTCACTGC	25909
rs561808779	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246904181	TTTCGGTAATTTTTA[C/T]AAAAATGTAGTCCTT	25909
rs561847294	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246904982	AAGAGAGCAGGGTAC[A/T]TAGAAGGTTCCAAGG	25909
rs561860295	snp	C/T	1.64768e-05	0.00287021	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849801	GTGTCATTTCATCTG[C/T]GCGTTCTTCTGATAC	25909
rs561874548	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246855974	TCATTCTGAACAATA[A/C]TATAAAATTTAAAAG	25909
rs561878959	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246905779	AGAATAAGTGATCTG[C/T]GGGCCATGGCCAAGT	25909
rs562024548	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246875429	TAGTTTGTTACTCAC[C/T]AGGCATTTAGAAAAT	25909
rs562036679	snp	C/T	0.00517822	0.0506191	intron-variant	AHCTF1	GRCh38.p7	1:246927169	GGCGACAGAGCGAGA[C/T]TCTGTCTCAAAAAAA	25909
rs562037432	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246930024	GCCACTGCACTCCAG[C/G]CTGGGCAACAGAGCA	25909
rs562042629	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246871615	CTACCTCTGTGAACC[C/T]TGACTAGATGAGCCT	25909
rs562043281	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246860079	AGCCTGGCCAATATG[A/G]TGAAACCCCGTCTCT	25909
rs562069211	snp	A/G	0.000188999	0.00971924	missense, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843911	CTTTCAGCTGTGCAG[A/G]AACCTCTATTTTTTT	25909
rs562078405	snp	A/G	3.56608e-05	0.00422245	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850415	TTTGTAACAGATGAA[A/G]CCTTAACTTCTTTTT	25909
rs562086653	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246925557	ACCAGGAGTTGTAGG[C/T]TGCAGTAAGCTATGA	25909
rs562103173	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246893314	AAAAACACTAGAAAG[C/T]GCCATGTCTTCCTAA	25909
rs562157365	snp	A/G	0.00517822	0.0506191	intron-variant	AHCTF1	GRCh38.p7	1:246845822	TTCAAAGAGAGCTCT[A/G]ATTTGCAGCATTTGC	25909
rs562279053	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246896945	TTATATTTAATACCA[C/G]GGACAAAACAGAAAC	25909
rs562297831	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868409	TACAGGCGTGAGCCA[C/T]TGCGCCTGGCAATTT	25909
rs562309670	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246913603	ACCATTACTCAATAC[A/G]TAGAAAAATCACGCA	25909
rs562318858	snp	A/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246841192	GAGTTCAGGTTTCAT[A/T]AAGGGGAATTTTTTC	25909
rs562355764	snp	A/C/G	0.000132241	0.00813047	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864069	TGCTGAATAAACTCC[A/C/G]AACACTGAGAAGGCC	25909
rs562369179	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246896162	AAAGCAGTTTGGCGG[C/T]TTCTCAGTATGCTAA	25909
rs562388345	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246876778	ACGTAAAAGAATTAC[C/G]TGGTAATACCCTGTT	25909
rs562422793	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246923812	TTCACAAAATCCAGA[C/G]AATTCTAACATCCTT	25909
rs562430351	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246922800	ATCCTGGATAACACG[A/G]TGAAACCCTGTCTCT	25909
rs562437381	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246917205	CGAATAGAGAAAAGT[A/G]GGTTGACTGGAGATT	25909
rs562542569	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246898885	CTGAGGTCAGGAGTT[C/T]GAGACCAGCCTGGCC	25909
rs562542571	snp	C/T	0.0923359	0.194016	intron-variant	AHCTF1	GRCh38.p7	1:246891485	AAAAAATTTATGAGT[C/T]CTTTGAATAAAAAAT	25909
rs562586241	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246893497	TTTCACTTACAGTGC[A/G]ACTGTATCCCTACTA	25909
rs562633843	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246862231	CACGCCTGTAATCCC[A/T]GCACTTTGGGAGGCA	25909
rs562647414	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246921923	AAAGTACTGGTATAT[A/T]CACAGAAAAAAATCT	25909
rs562670547	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246855901	CTTTAGTCCTACCAC[C/G]TAACCTGTCATTTTG	25909
rs562750633	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246912420	CACGGGAGGCGGAGG[C/T]TGCAGTGAGCAGGGA	25909
rs562760215	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246920483	TGTCAGAATATATTA[C/T]TAAACCAGCCGGGCG	25909
rs562812120	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246885130	TATGTTTTTCTTAAC[A/G]TTGGAAGACCAATAA	25909
rs562858915	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246856988	GTATCCTCTACAACG[A/G]TGTTATTCAAAAGTG	25909
rs562870666	snp	A/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246929417	CCGTCTCAAAAAAAT[A/T]AAAATAAAAATAAAA	25909
rs562873969	snp	G/T	0.00119737	0.0244387	intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842365	GGCAGGCGGATCACT[G/T]GAGACCAGGAGTTTG	25909
rs563054154	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246925890	GCCTGGGCCACATGG[A/C]GAAATCTCATCTCTA	25909
rs563055863	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246870315	GCAGTCTCAGCCACT[C/T]GGAAAGCTGAGGCAG	25909
rs563092117	snp	A/C/T	0.000131839	0.00811815	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246863999	CGATCCTTTTAATTG[A/C/T]GAACTTGAGGGCAGT	25909
rs563094999	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246869139	TGAGCCACCACGCCC[A/G]GCCGTGTGTTTTGTT	25909
rs563109798	snp	C/T	0.000399281	0.0141238	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851186	TCAGATGATGCAAAA[C/T]CACCTGGCTCAACTT	25909
rs563118985	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246905830	ACACGGCACAAGACA[C/T]CAAGACTATGGTCAT	25909
rs563144134	snp	A/T	0.00755907	0.0610114	intron-variant	AHCTF1	GRCh38.p7	1:246844821	TTTTTTTTTTTTTTT[A/T]AACTATAGGGCCCCC	25909
rs563144703	snp	A/G/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246878889	ATCTGAAATTGCCTC[A/G/T]TGCTTCTCTTACTAG	25909
rs563154609	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868817	TACCTCATTTTATTG[C/T]GCTTTGCTTCATTGT	25909
rs563225195	snp	A/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246931459	CCCGGCCTAGGCCCG[A/G]CGCTCGCGGGGCAGA	25909
rs563230390	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246858239	GCTGGGATTACAGGC[A/G]TGAGCCACTGCACCC	25909
rs563283633	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246845511	ACAAAAGTATTTCTA[C/T]GAAAATTATACATTC	25909
rs563319898	snp	A/G	0.000798403	0.0199641	downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838601	AGCAGCAAGTTGTAG[A/G]AGTGGGCGGGGCGGG	25909
rs563359285	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246919351	ACCATGGCTCTGAGT[C/T]TCTTACTCAGAAAGA	25909
rs563360966	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246915911	TTTTTACTCTGGAAC[A/G]TTTTAACCAATAAGA	25909
rs563366137	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246864383	CTATATTTACTGAGC[A/T]CTTACTATGTGCCTG	25909
rs563383895	in-del	-/TT			intron-variant	AHCTF1	GRCh38.p7	1:246868848	GTGTGTGTTTTTTGT[-/TT]TTTTTTTTTTTTTGA	25909
rs563410946	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246880040	AAAAGGGTTTAGTGG[A/G]AGAGGACATATAGGC	25909
rs563417229	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246926805	AGATTGCAGTCAGCC[A/G]ACACTGCACCATTGC	25909
rs563430166	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246860761	TCCTCCAGCCTCAGC[C/T]TCCCAAAGTGCTGAG	25909
rs563453463	snp	C/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246928163	AAAAAATTAGCCGGG[C/T]GTGGTGGTGGGCACC	25909
rs563457069	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246865700	GGACTGTGCAACAAA[A/C]GCTACCTACCAAGTC	25909
rs563463291	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246869067	GCCAGGATGGTCTCG[A/G]TCTCCTGACCTCGTG	25909
rs563467098	snp	C/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246894197	CAAAAAGTGAGACCA[C/T]GTCTCAAAAAAAAAA	25909
rs563494825	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246866371	GAATGTCGGTAATAA[C/T]GACTTTCATTTAAAA	25909
rs563548738	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246887650	ACAAGAAACAAAGAT[A/G]TACGCAAATTTCTAA	25909
rs563549532	in-del	-/A	0.00159617	0.0282053	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932162	GGGCGGATCATTTAC[-/A]AAAAAAATCGGGTCT	25909
rs563559405	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246911886	TTGTTCAGATGATTT[C/T]GGCTCTTCCATTTCT	25909
rs563645165	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246926988	GACCATCCTGGCTAA[C/G]AAGGTGAAATCCCGT	25909
rs563657289	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246921627	GATTTACAGACACAC[C/T]GATTCCCTGAGTCAG	25909
rs563683822	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246859293	TAACCTTGTTAAAAA[C/T]GTGTGTAGGGTAAGA	25909
rs563750796	snp	C/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246873205	ATATTCAAACTTTCT[C/T]CCTTATAGAACTCTC	25909
rs563808117	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246896872	CACAGAGGGAATTAC[A/T]TAATGGTCCACAAAA	25909
rs563815668	snp	A/G	1.65974e-05	0.0028807	intron-variant	AHCTF1	GRCh38.p7	1:246907761	AGAACTTCAAGATCT[A/G]AAACCACAAATTAGA	25909
rs563875061	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246859751	CAGCTAATTTTTTTA[C/T]ATTTTTTGTAGAGAT	25909
rs563966995	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246895573	TTCTTGCCAGGGGTT[A/G]AGGATGGGGCAGAAA	25909
rs563972611	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246868801	TGAATGAGTACAGGT[C/T]TACCTCATTTTATTG	25909
rs563978508	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932420	CCCATAATTGGCAGC[C/T]TGCATTCTGTATTTT	25909
rs564026255	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246883019	AACATCTTTGCTACA[A/G]TAAGTGCTGTTTCAA	25909
rs564039185	snp	C/T	7.37944e-05	0.00607386	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850558	GTCCTGATTAACTTC[C/T]TTCTTTCTCCTTCCT	25909
rs564092239	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246903018	GTTCTCACAGAAATT[A/C]TTGCTCTAGAATAGT	25909
rs564094653	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246905031	CATTCAAGTAAGTCC[A/G]CACAATTTCTTCTGA	25909
rs564179835	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246886058	TAAACAAAAAAAGTG[C/T]AGTGGCTCATGCCTA	25909
rs564201665	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246930117	AGAAAACAAAAGTCT[C/T]AAAACTGATGTATAA	25909
rs564225696	snp	C/T	4.94694e-05	0.00497316	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246905583	AAGTAACAGCAATTC[C/T]GAGGATCATTCTCAG	25909
rs564251523	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246899608	CTGCAAGGCAAGGTG[G/T]CAAATTATTACATGT	25909
rs564255285	snp	C/G/T	0.000320775	0.0126607	intron-variant	AHCTF1	GRCh38.p7	1:246843969	CTGTATCTTTATATA[C/G/T]GTGTGTATATATATA	25909
rs564302045	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246892532	CACCATGTTGGCCAG[C/G]CTGGCCTCGAACTCC	25909
rs564364697	snp	A/C/G	1.66443e-05	0.00288477	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900400	AGCCCCAAATATACA[A/C/G]AAGGCTTTCCCTGTC	25909
rs564368244	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246857262	AGTATGTTTCAAATG[G/T]TCGTTAAAAAACACA	25909
rs564398610	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246900992	ACATCAACAGGAGAA[A/G]AAGAAAGTAAAAATC	25909
rs564411863	snp	G/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246926262	AGTTTCACATATTCC[G/T]TTATAGCAACACAGG	25909
rs564425974	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246920571	GTCAGGAGATCGAGA[A/C]CATCCTGGCTAACAA	25909
rs564444203	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246930903	GATAGTATGAACCTC[C/G]TAAGCTTTGAGAACA	25909
rs564455937	snp	C/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246926940	AGCACTTTGGGAGGC[C/T]AAGGCGGGCGGATCA	25909
rs564471818	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246913664	CTTACTGATACGCCA[C/G]GCATTGTGTTACCTG	25909
rs564475556	snp	A/G	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246844615	TGTGGTGTCAGCTAC[A/G]TGGGAGGCTGAGGCA	25909
rs564486797	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246920947	CAAAAAAAAAATCAG[C/T]TGGCCATGGTGGCGC	25909
rs564498034	snp	A/G	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246886679	GATGGTATACAAGAG[A/G]ATGTGCATAGGGTAT	25909
rs564506827	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246906731	AACTTAAGGGCCAAA[C/T]AGGCATCTATTTAAC	25909
rs564528268	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246907460	ACCCACCCTTTTCTC[A/C]CTATGCTAACTTTCA	25909
rs564533724	snp	G/T	0.00398564	0.0444627	intron-variant	AHCTF1	GRCh38.p7	1:246879853	CCAAAAAAAAAGGGA[G/T]AACTAATTTAAAATA	25909
rs564536966	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246894880	AGGGAGGCAACTTGG[A/G]AAAATGGACTTTCTC	25909
rs564555160	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246921581	CCCCCCAAAAATATA[A/G]TACTAATAGGAAGAA	25909
rs564569167	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246864517	AAAATATCCATTCAC[C/T]TACATGTAATATATA	25909
rs564591272	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246930584	CTCACAAAAAAACAG[C/T]TTAAAAAAAAAAAAG	25909
rs564616388	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246920292	AAATGTCTAATATAT[C/T]TGTGTAAATCAGCGA	25909
rs564688347	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246914502	TCTGAAAGCTGTAAC[C/T]TCATCACTTTTTCTT	25909
rs564688944	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246855519	AGACTTTGAATATTA[A/G]AGCCACAGAATGCCT	25909
rs564690951	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246922479	CACCCAGGCTGGAGT[A/G]CAGTGGCATTATCAG	25909
rs564724191	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246901154	GACCAGCCCAGGCAA[C/T]ACAGCAAAAACCTCA	25909
rs564747241	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246915286	AGTGAGCTGAGATCG[C/T]GCCACTGCACTCCAG	25909
rs564753383	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246922757	GGAGGCCAAGGAGGG[C/T]GGATCACGAGGTCAG	25909
rs564754467	snp	A/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246858690	ATTGGCTGGGCATGG[A/T]GGCACGTGCCTGTAA	25909
rs564762038	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246887810	ATAATGCCTAAGGTA[A/G]TATCACGCTAACTTA	25909
rs564800869	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246880957	AATAAGGAATGCATG[A/G]GGGTTCTTGGCAATA	25909
rs564807194	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246927046	AGCAGGGCGTGGTGA[C/T]GGGAACCTGTAGTCC	25909
rs564824158	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246845716	TTCTTGAGTGTATGT[C/T]AATTCTTTACCCATC	25909
rs564827505	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246895363	CATCAAATGGTTCAG[A/G]AAAAAAACTATTCTC	25909
rs564865739	snp	C/T	0.000399281	0.0141238	downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838816	CTGAGTATATTGTTT[C/T]CCTTACTACTATGAT	25909
rs564882553	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246915962	AGTTCCTTGAATAAC[A/G]TATCATCTTTAACCT	25909
rs564973357	snp	G/T	0.00279162	0.0372561	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932285	GTGCGCAGTTGGGAG[G/T]GGTAGTCTTCGCTGG	25909
rs565001167	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246881408	TTATTCAGGACACAG[A/T]AAGATTAAAACCATG	25909
rs565004581	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246846228	TTTCAATAAAATAAA[A/G]GACCACCTCTAGCCT	25909
rs565005318	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246868025	TGGAGGGCAGTGGCA[C/T]GATCTCGGCTCACTG	25909
rs565034015	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246927363	CCACGGCTGCATACG[C/T]TTGTCATCCCGACTA	25909
rs565051406	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246866593	GAGTCTTGTAATGAT[C/T]ATTTATAATCATTAT	25909
rs565066569	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839298	ATTGCGTTGGTTTAA[A/G]AAAGTATTAACTTGA	25909
rs565078282	snp	C/T	0.00795532	0.062565	intron-variant	AHCTF1	GRCh38.p7	1:246908760	ATTAGCCGGGCATGG[C/T]GGCGTGCGCCTGTAG	25909
rs565096716	snp	A/C	0.00318978	0.0398085	intron-variant	AHCTF1	GRCh38.p7	1:246847294	AACTCCATCTCAAAA[A/C]AAAAAAACAAACAAA	25909
rs565096790	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246854496	CATGTAACATCTACA[A/C]TACAAAACACTATTA	25909
rs565135345	in-del	-/TTGT	0.00517822	0.0506191	downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838889	ATCTTTCTGAGTACA[-/TTGT]TTACCTTACTACTGA	25909
rs565177797	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246865836	TCTTCAACCCTGAGA[A/C]CAAATATTCTTTCAG	25909
rs565185172	snp	A/C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869132	ACAGGCGTGAGCCAC[A/C/T]ACGCCCGGCCGTGTG	25909
rs565217176	snp	A/G	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867744	ATTGTTGATGAAAAC[A/G]GATCTTGTCAACACA	25909
rs565233790	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246847538	GGTCTTGCTCTGTTG[C/T]CCAGGCTGGAGTGCA	25909
rs565239057	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933290	AGGTGTGCGCCACCA[C/T]GCCCAGCTGATTTTT	25909
rs565267315	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246909621	AAAGCACAAGAGTGG[C/T]CATGCTGGCAATTCA	25909
rs565270121	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246848209	CTCAAACTGTATCAG[C/T]ACAACAAGTCATCTA	25909
rs565286210	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246843728	AATAAAATAATTTTA[G/T]TAAAACATTTGTAAA	25909
rs565323960	snp	C/T	5.34402e-05	0.00516887	intron-variant	AHCTF1	GRCh38.p7	1:246867203	CAATTGTAACTATCA[C/T]CTAACATTGTGTCTC	25909
rs565362563	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246860404	TTTTCTAAATTTCAC[A/G]GCCAAATAAAAAATG	25909
rs565416701	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246925485	TGTGGCCAGACATGA[G/T]GGCTTATGCCTGTAC	25909
rs565448434	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246883157	GAAGGGTGAGTCCGG[A/G]GAGAGTGTTAGTGTT	25909
rs565476823	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246896757	ATTTTGAAAATCACT[C/G]AGTCTGGTTTAATAT	25909
rs565510367	snp	A/C/T			intron-variant	AHCTF1	GRCh38.p7	1:246885721	ATATAAATATAATCC[A/C/T]ATACATTTAGACAAA	25909
rs565511856	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246889761	CACCACTTTCTTTGT[C/G]TATTACCTTTACTTC	25909
rs565547451	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246874839	AAAAACCTGACCTCC[G/T]GCTCTCAGCCCTCAA	25909
rs565581835	snp	A/G	0.000158579	0.00890306	intron-variant	AHCTF1	GRCh38.p7	1:246876008	TTTTTGATCCAATAG[A/G]TTATGATATTCTTCA	25909
rs565606579	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840591	TAAGCCATATTTACA[C/T]ATATAAATGTATGAA	25909
rs565646183	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246893658	AATAACGACATCTAT[A/C]CATGGAGGACAGCAG	25909
rs565647307	snp	C/G	0.43221	0.171171	intron-variant	AHCTF1	GRCh38.p7	1:246864596	ACTAGACTGACTTGG[C/G]AGGCCGAGGCGGGTG	25909
rs565661051	snp	A/T	0.000122095	0.00781233	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246885602	GCTCGCCCTGACTCA[A/T]GAATGCCTGAATAAT	25909
rs565675860	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246920663	TAGTTCCAGCTACTC[C/G]GGAGGCTGAGGCAGG	25909
rs565697875	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246886314	CCAGCCTGGGTGACA[A/G]AGCGAGACTCCATCT	25909
rs565701351	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246861753	CTTCCGAGTCCTATT[A/T]ATCTGTAAGATGATG	25909
rs565712480	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246913476	TATAATTAACACAAT[A/C]AATTTAAGTTAAAGC	25909
rs565728376	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246871890	AACAACCTAAAGACA[A/C]AGCTACTAAAAAGAC	25909
rs565735005	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246879283	AGACAAAAAATATCT[A/G]GTACACTGTGTTGAT	25909
rs565753193	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246852322	ACGATGACATTTTTA[G/T]GAGTTAAGAAACTTC	25909
rs565771335	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246868954	GGTTCACGCCATTCT[C/T]CTGCCTCAGCCTGCT	25909
rs565784632	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246858830	TAAATACAAATTTCT[A/C]TTTGAGACTGCCTAA	25909
rs565784723	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246865795	ATTTTCTAAATGAAA[C/T]GTTAAATATTGCATT	25909
rs565812572	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246873452	ATTTCTCCTGCATCA[C/T]AGCGAAGGGAAAGAA	25909
rs565821328	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246859388	TGTTCCCCTGGCCCT[A/C]TTGTTAACCAAACTG	25909
rs565823182	snp	G/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246854707	AACTCTAGGAAATGG[G/T]TCTTATTAATATTCC	25909
rs565870384	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246880212	TTATTATCAAAAACA[A/G]TATGTTATTTGTTAT	25909
rs565931696	snp	C/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246868996	ACTACAGGCGCCCGC[C/T]ACCATGCCTGGCTAA	25909
rs565942844	snp	A/T	5.03926e-05	0.00501934	intron-variant	AHCTF1	GRCh38.p7	1:246913435	ACATAATACGTGATT[A/T]GCTTTTCTTCTGCAA	25909
rs565953181	snp	C/G	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246913877	CTATGGCCTCTTCTC[C/G]TAAGAGTAAAAACTA	25909
rs565989494	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246881530	AGTCTTACCAAAAAA[A/T]TTTTTTTTAAATAGA	25909
rs566006509	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246906988	CACTTAACAAAAGGG[A/G]ATCTGTTCTGAGAAA	25909
rs566019791	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246906554	GCCACTGCACTCCAG[C/T]CTGGGCAACAGAGTG	25909
rs566026651	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246851626	CAGACTTTCTCATTC[A/G]GTCAAAATAACTACA	25909
rs566042366	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246907831	ATATGTCATCCATTA[G/T]TCAAGCTGCAAATGA	25909
rs566044153	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246900584	TAATTCATATTTCAC[G/T]TGATTCATCAAAACG	25909
rs566082956	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246901250	GGAGGCTGAGGTGGG[A/G]GGATCGCTTGAACCT	25909
rs566122356	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246874345	CGTGTCCCTCTGAGG[C/T]ATGTATTCCTCTACA	25909
rs566143051	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246909016	CACTCTCCAATTTCC[A/G]TTACCTGTAGTAAAC	25909
rs566159877	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246888702	TCAACTCAAGGTCAG[A/G]AGTTCGAGACCAGCC	25909
rs566179074	snp	A/C	0.000798403	0.0199641	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246931914	CTCGGACAGCGCCGG[A/C]CCCGCTCTGCGCATT	25909
rs566203399	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246895109	AAAAACAATTACATA[C/T]AAACTATTCTAGATC	25909
rs566225758	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246845839	TTTGCAGCATTTGCT[A/G]ATTTCTAAGGTATAA	25909
rs566317024	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246902383	GCAAGAAATATCTAG[C/T]ATCTCATATAGAACT	25909
rs566351542	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246896533	GAAAGTAGATTAGTC[A/T]TTATGTAAGGCTGGG	25909
rs566352318	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246927417	TCGCTTGAACCGGGG[A/T]GGTGGAGGTAGCTGT	25909
rs566357878	snp	C/T	0.000399281	0.0141238	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916349	TGTTATAGAGTTTAC[C/T]ACCTCAAGTTGTGGA	25909
rs566407863	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246848799	ATGTTGCAGTGAGCC[A/G]AGATCATGCCATTGT	25909
rs566409610	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839403	CATTTAACAAGTTCA[C/T]TTAAATAAGTTCAAT	25909
rs566411191	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246869171	TTTTAAACAAATTGA[A/G]GGTCTGTGGCAACCC	25909
rs566494064	snp	A/G	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246928255	TGGCAGTGAGCCGAC[A/G]TCGCGCCACTGCACT	25909
rs566496645	snp	A/G	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246909749	ACTAGCTGTGGTTTC[A/G]GCATCCACTGGGGTT	25909
rs566580911	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246860070	TTCGAGACCAGCCTG[A/G]CCAATATGGTGAAAC	25909
rs566603667	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246901029	ACTACTATAAGGAAA[C/T]AGGAAGAATGGGGAA	25909
rs566604021	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246923138	AAAAAAGATAGGCTG[A/G]GCACGGTGGCCCATG	25909
rs566663364	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246924040	GGTACAAGTCATTAC[C/T]GTTTCTCAGCACTCC	25909
rs566663407	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246926329	CTAGCACTTAATAAT[A/C]CATGTAACATTGTGC	25909
rs566670176	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246882981	TAAATCCAAATCTAT[C/T]TGAGTCCAAAGATTT	25909
rs566714504	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246847749	AAAAAAGTTAAAATT[A/G]GTAGGTACAGAAATG	25909
rs566717919	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246860725	TGACCAGGCTGGTCT[G/T]GAACTCCTGGGCTCA	25909
rs566719147	snp	C/T	0.00755907	0.0610114	intron-variant	AHCTF1	GRCh38.p7	1:246889600	CAGCCGGCACAGATT[C/T]TAAAGTACTGATTCC	25909
rs566752065	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933552	TACAGACATGAGCCA[A/C]CATGCCCAGCCTATT	25909
rs566754833	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246854096	TGAGGTCAGGAGATC[A/G]AGACCACCCTGGCTA	25909
rs566757833	in-del	-/ATCTAT	0.00159617	0.0282053	cds-indel, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839268	AAACAGGTACCACAC[-/ATCTAT]ATTCACCAAATTGCG	25909
rs566769452	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246882790	GTTAATTTGCACGTA[A/C]AACAGCCACGCCACA	25909
rs566795697	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246854638	AACATTTACTAAACT[C/T]CAGGTACCAAGCGCT	25909
rs566814455	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246869258	ACTAACTGTTCCCCC[A/G]CGTCTCTCCCTTTCC	25909
rs566820563	snp	A/G	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840028	CATCTCATCCTATCA[A/G]TATTAGGCACATACA	25909
rs566867209	snp	A/G	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246882244	CCTCGTGATCCACCC[A/G]CCTCAGCCTCCCAAA	25909
rs566924472	snp	A/G	4.96266e-05	0.00498105	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246918285	AGCACAGATTCTAAT[A/G]TTATTTCGTCTTCTC	25909
rs566929561	in-del	-/TA			intron-variant	AHCTF1	GRCh38.p7	1:246880224	CAATATGTTATTTGT[-/TA]TATATATATATATAA	25909
rs566961773	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246911092	TTCCAATTCTCAAAA[C/T]TGAGAAATGGTTCTG	25909
rs566965571	in-del	-/GCCTCCCA	0.00835141	0.0640778	intron-variant	AHCTF1	GRCh38.p7	1:246848453	GATCCACCCGCCTTG[-/GCCTCCCA]GCCTCCCAAAGTGCT	25909
rs566990494	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246917535	CTCAGTTACACAGAA[C/T]AGTGGCTACTTAGAA	25909
rs567023113	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868338	GTTGGCCAGGCTGGT[C/T]TTGAACTCCTGACCT	25909
rs567051639	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246915418	AAACCTAACGTTTCT[A/G]GCCCCCTATTCTTCC	25909
rs567059110	snp	C/T	8.30834e-05	0.00644475	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861971	TACCCCAGGAATCCA[C/T]TTTGGGTGGACATCT	25909
rs567064643	snp	C/G/T	0.000618223	0.0175718	intron-variant	AHCTF1	GRCh38.p7	1:246876922	CCTTATTCTCTTATC[C/G/T]CCCATAATAAGACAA	25909
rs567086295	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246867948	TACTAGCTAAAAATT[G/T]TAATTATATATATAT	25909
rs567089503	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246908926	AAAAAAGAATCTTAA[C/T]GAATGAAACAATTAG	25909
rs567100943	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869886	TATAATTTAGAAATA[C/T]ATTTCATAAAGCTAT	25909
rs567220750	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246903818	ACTCCAGCCTGGGCG[A/C]CAGAGCGAGACTCTG	25909
rs567222853	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246859176	CTAAGTAAAGATATC[A/G]TAGTCCAAACTTCAG	25909
rs567223967	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246874298	AAGCCAAATAACATT[A/G]ACTATTAAATGTCTC	25909
rs567225387	snp	G/T	0.00398564	0.0444627	intron-variant	AHCTF1	GRCh38.p7	1:246921971	CAATAATAATGGCTG[G/T]GTGGAGTTTAAATAA	25909
rs567251881	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246881017	TGGCAAACTCTCTAA[A/T]CATGCTAGACCAAAT	25909
rs567270390	in-del	-/GAG			intron-variant	AHCTF1	GRCh38.p7	1:246879324	GCATACGGTAATTGA[-/GAG]GAGGATTAAGTTGTC	25909
rs567359580	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933421	ATAGGCGTGAGCCAC[C/T]GCGCCCGGCCTTATT	25909
rs567379852	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869090	ACCTCGTGATCCGCC[C/T]GCCTTGGCCTCCCAA	25909
rs567431372	snp	A/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246928164	AAAAATTAGCCGGGC[A/G]TGGTGGTGGGCACCT	25909
rs567451599	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839966	AAGGGATTTCTGTGG[C/T]TCAATAGCAAGCTCC	25909
rs567460838	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246901810	ACTGGCCTGGGCATC[A/G]GAGTGAGACCCCTGT	25909
rs567474886	in-del	-/AATATTT	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246863138	AAAAATACTATACTG[-/AATATTT]TAAATTATTGAAACC	25909
rs567528111	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246860008	GGCTCACGCCTGTAA[C/T]CCCAGCACTCTGGGA	25909
rs567531980	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246896478	TATTATTTGACCCAT[A/T]TATATGAAATGTCTA	25909
rs567593409	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246895981	GAGGGTGTGAGATCA[C/T]AGGCAAGTTCTGGTT	25909
rs567691421	in-del	-/AAAT	0.00914312	0.0669923	intron-variant	AHCTF1	GRCh38.p7	1:246871837	GCCAGGGTCACAAAA[-/AAAT]AAAAAATAAAAATTT	25909
rs567697384	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246909423	AAAAAAAAAAAAAAA[-/A]TTTGCATGCTGCTCT	25909
rs567730698	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246922977	GACAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA	25909
rs567755757	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868258	CTTAGCCTCCCGAGT[A/G]GCTGGGACTACAGGA	25909
rs567765030	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246861481	TAATGGTGGCTAATG[C/T]TTCCCTAATTGGTAA	25909
rs567779894	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246893852	AATCCTAAAACCTGC[C/T]ATTGTAGGCATATCA	25909
rs567811541	in-del	-/TTATTA	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246848231	AGTCATCTACTTTAT[-/TTATTA]TTATTATTATTTGGC	25909
rs567812846	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246916798	CCCAAAGTCAAAAAG[C/T]AGCACAGGCAGAAGT	25909
rs567826493	snp	C/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246869560	TGACTTTAAATTAAA[C/G]GCAATCACCATTCCA	25909
rs567848254	in-del	-/A	0.00874735	0.0655527	intron-variant	AHCTF1	GRCh38.p7	1:246841277	TGTTTCAAATGTATG[-/A]AAAAAATACTGCTGG	25909
rs567853335	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246917330	GCTTGAGCAACCAGA[C/T]GAATGGTAACTTCTA	25909
rs567875042	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869276	TCTCTCCCTTTCCCC[A/G]AGGACCTCCCTTATT	25909
rs567927540	snp	A/C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246883632	TGACTTTCTAGCAAC[A/C/T]CTGAAGTCATTCTCT	25909
rs567964295	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246884541	TAAAAGTGGTATAAA[A/G]TAAGTCTAGTAAGGA	25909
rs567966330	snp	A/G	0.000461544	0.0151842	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877046	TTCATGATTCTGAAC[A/G]CTGGCACTGGACTGC	25909
rs568026532	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246910920	TGGGGAAGCTGCAGA[A/C]CAATATTTATGCTGT	25909
rs568054756	snp	C/G	0.0356815	0.128715	intron-variant, upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246931473	GGCGCTCGCGGGGCA[C/G]AAGCCCCGCCGCCGC	25909
rs568068241	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246903781	TGGCGGAGGTTGCAG[C/T]GAGCCAAGATTGCAC	25909
rs568077097	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246855435	TATCACAAACAAACA[C/T]GAAATAACTCTTCTG	25909
rs568105801	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246897807	GCAACATAGCGAGAC[C/G]CTGTCTCTACCAAAA	25909
rs568115885	snp	G/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246848538	GGTCCTGAACTGCTT[G/T]GCTGAAATTCAAATA	25909
rs568201204	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246851582	ATATACTTATGGGTT[C/T]ACTTTACAAAATTAT	25909
rs568203468	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246912134	TGTATCTATTTCTGA[C/G]CTGCTCCATAAATGA	25909
rs568243525	snp	A/C	0.0130921	0.0798413	intron-variant	AHCTF1	GRCh38.p7	1:246912463	ACTCCAGCCTGGCAA[A/C]AGAGCGAGACGCCGT	25909
rs568260320	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246891529	TTTGAAACTTTACTG[A/C]AAATACATTAATCTT	25909
rs568262591	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246906174	AACTGAAGAGTTCCC[A/C]TAAACTGCTAAAAAA	25909
rs568275417	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246924942	CCTATACTCAAGCCT[C/T]AGTTGCTCTTATATA	25909
rs568315557	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246919405	TGTGGCCAGAATTCA[A/C]GCTAGGTTATATGGA	25909
rs568333706	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246849119	TTAGCTCGTGACAAT[G/T]AAGGATGGCCTCACT	25909
rs568353997	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246841641	CAGGATTTTAAAGTG[C/T]ATAATTGTTTTTTAC	25909
rs568363176	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246929523	ATGAAGGACATGAGC[A/G]AAGAAACATCAGAGT	25909
rs568390148	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246870295	AAAAATACCCAGGCA[C/T]GGTTGCAGTCTCAGC	25909
rs568393004	snp	C/T	0.000798403	0.0199641	intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842530	GAGGTTGCAGTGAGC[C/T]GAAATCACACCACTG	25909
rs568407206	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246927262	CCAAGGCGGGAGAAT[A/G]GCTGAGGTCAGGAGT	25909
rs568417707	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246929967	TGAGGCAGGAGAATC[A/G]CTTGAACCTGGGAGA	25909
rs568537121	in-del	-/TAAG			downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838952	ACCTTACTATGATAC[-/TAAG]TATCTCTCTGAGTAC	25909
rs568551864	snp	C/T	0.00914312	0.0669923	intron-variant	AHCTF1	GRCh38.p7	1:246868867	TTTTTTTTTTTGAGA[C/T]GGAGTCTCGCTCTGT	25909
rs568562904	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246899224	AAAGCTTGAGGTTCA[C/T]GTAGCTAGCATCTAC	25909
rs568577564	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246862526	GATGGGGTCAACTGA[A/G]TCACAATAGTGGTTA	25909
rs568591563	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246867925	CACACACACACATTA[C/G]GTGGTAATACTAGCT	25909
rs568657066	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246896546	TCATTATGTAAGGCT[C/G]GGTAGGATGGGGCAG	25909
rs568689987	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246841863	GTGGCGTGATCTTGG[C/T]TCACTGCAACCTCCG	25909
rs568694307	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246897184	CGGGTGTGGTGGCAC[A/G]CGCCTCTAGTTCCAG	25909
rs568702972	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246892801	CCTGCCCAGCTAATT[A/T]AAAAAAAGATTTTTT	25909
rs568767405	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246910358	TCCAAACAATCCAAA[A/T]GTAAAAAGATGCTTT	25909
rs568793109	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246858300	ACCTAGCTCAAGAGC[A/C]CCCCTTAACCTCTCG	25909
rs568889247	in-del	-/TAAAAATTTGTTGAATAC	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246877429	AATTGAAAAGTACTT[-/TAAAAATTTGTTGAATAC]TAAGTACTGCATAAT	25909
rs568913541	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246860820	CTAGGATGCTTTTCT[C/T]ATGGTGGAAAAAATT	25909
rs568983267	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246889244	TGATGCAACGTGCAG[A/G]TATGGTCCCTATTTC	25909
rs568991953	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246854167	AGCCAGGCGTGGTGG[C/T]GGGCACCTGTAGTCC	25909
rs569039446	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246911290	GAAACAAAAGCCTAT[C/G]AAGCCTACTTCTTTG	25909
rs569041254	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246919280	TACATCAGCCTAAAG[A/G]TGAGCAAGAACAATA	25909
rs569064730	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246928937	TTTAAAACACCGTGT[G/T]AGTAAAGGAATGCAA	25909
rs569079503	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246911999	AGTGCAGTGGCGTGA[C/T]CTCGGTTCACTGCAG	25909
rs569126251	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246924111	CCAACACCCAGCCCA[A/G]GCCATTCTCACAGAA	25909
rs569127578	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246928282	CACTGTAGCCTGGGC[A/G]ACAGAGCGAGACTCC	25909
rs569149673	in-del	-/GG			intron-variant	AHCTF1	GRCh38.p7	1:246860195	AACCTGGTTGGGGGG[-/GG]GGCGGAGGTTGCAGT	25909
rs569156812	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246883517	CTCCTGGGCAATAAA[C/T]ATGGCTGCCTTTTGC	25909
rs569166324	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246847825	CTAAGCTCTAACAAA[A/G]TAACTCTCACTTTTG	25909
rs569193007	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246923598	AGAGCAGACATGTGG[A/C]CTCTTCAATCAACAT	25909
rs569266035	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246849453	TAACTGAACTCAAAC[A/T]TTGAAACATGAAACC	25909
rs569346868	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869921	GTCACAGATAGTGAT[G/T]CCTCTGAGAGATCCG	25909
rs569367242	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246922674	GCTGGGATTACAGGT[A/G]TGAGACACCTATCAA	25909
rs569376880	snp	G/T	0.0479149	0.147179	intron-variant	AHCTF1	GRCh38.p7	1:246868348	CTGGTCTTGAACTCC[G/T]GACCTCATGTGATCC	25909
rs569404964	snp	A/G/T	4.94934e-05	0.0049744	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850106	CTAGGTATGGCAGAC[A/G/T]TATCAAATTCTGCTT	25909
rs569438474	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246843537	CCTTCCACAAACAGG[G/T]AATTTAAACTGTAAC	25909
rs569477043	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246844033	TTAGAAAGATGCAAA[C/T]GTCCCCAAACCTGGA	25909
rs569496651	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246898691	GCAGTCTACTCCTCT[A/T]TATCTAATGTGAAAG	25909
rs569513818	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868551	GAGCCACCGGCCTGG[C/G]CTACATTTTGTTTCA	25909
rs569551703	snp	A/C	0.00716266	0.059414	intron-variant	AHCTF1	GRCh38.p7	1:246862944	CTTGGCCTCTAAAGG[A/C]CTAGTAAACAAATTA	25909
rs569580539	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246900578	GCGGTTTAATTCATA[C/T]TTCACTTGATTCATC	25909
rs569616673	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246899104	CAAAAAGAGAAAAGT[A/G]TTTTTCAAAATTCTT	25909
rs569654018	snp	A/G	0.000399281	0.0141238	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246891899	CCATGAAATGACACG[A/G]ACCATCAAATAATGG	25909
rs569661012	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246925646	CCTAATGTGGTTTGT[A/G]TAACTGTCCCCTCCC	25909
rs569666018	snp	A/G	0.00438332	0.0466095	intron-variant	AHCTF1	GRCh38.p7	1:246929780	CTGTACCAGCCGGGC[A/G]CGGTGGCTCACGCCT	25909
rs569683930	snp	G/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246929857	AGAAGTTCAAGACCA[G/T]CCTGGCCAATATGGT	25909
rs569691068	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246892625	TGTGCCCGACCTAAT[C/T]TGCTTTACTTCTAAT	25909
rs569727186	snp	C/T	0.000805737	0.0200554	intron-variant	AHCTF1	GRCh38.p7	1:246885466	CAGATACGATAAAGA[C/T]TTTATAGTTTCAAAA	25909
rs569738929	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246930222	CTCACTGCAACCCTC[C/G]AACTCTCAGTTTGAG	25909
rs569749711	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246878610	AGATATACACTAAGA[A/G]TGGTAATGATCAATC	25909
rs569768638	in-del	-/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246859826	CCCGAAGTGCTGGTA[-/T]TACAGGCGTGAGCCA	25909
rs569786874	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246870961	AACAATACAACTGAG[C/T]CTTCGAAAAACTAAA	25909
rs569793409	snp	A/T	0.43221	0.171171	intron-variant	AHCTF1	GRCh38.p7	1:246864593	AAGACTAGACTGACT[A/T]GGGAGGCCGAGGCGG	25909
rs569837684	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246920117	TGCACTCCAGCCTGA[C/T]GACACAGTGAGACTC	25909
rs569843891	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246912935	ATTTACTTAAGAATA[C/G]ATCTTATTCAGGTAT	25909
rs569867497	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246879143	AATCCCAACAACACA[C/G]GAAAAAAAGCCAAAG	25909
rs569893721	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246894442	AGCCGAGCGTAGTGG[C/T]GGGCAGGAGAATGGC	25909
rs569905133	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246871841	GGGTCACAAAAAAAT[A/C]AAAAATAAAAATTTG	25909
rs569930622	snp	A/G	0.000197954	0.00994676	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246887307	AGATTCAATGGGAGT[A/G]TCTGTTTTGTTGGGA	25909
rs569936812	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246894947	TGCTGCCGCCAAAAA[C/T]GCAAAAACTGTCATT	25909
rs569952182	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246879029	CAGAACATTTTTGTA[-/T]AAAGAAAAATAGAGG	25909
rs569958040	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246912705	AAAGTATTTCATTTT[A/C]TTTGAATCTGAATAG	25909
rs569959238	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246889843	TAAAATAGTAATGGT[A/G]ATAGCAAATTCTGAT	25909
rs569974633	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246887931	GTGTCTTGGACACAT[C/T]TAAGTGTCTGATAAA	25909
rs569996751	snp	C/G	8.26112e-05	0.00642641	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246913253	CTTCAACTTCATTTT[C/G]ATTGCATGACAAGTC	25909
rs570008911	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246876290	AATATCCAAAAAATC[C/T]TCCCCCTACCTACAT	25909
rs570128804	snp	A/T	0.00438332	0.0466095	intron-variant	AHCTF1	GRCh38.p7	1:246852496	AGAATTTTTTTTTTA[A/T]AAAAACTAAGTCTTA	25909
rs570148415	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246858748	AGGTTGCGGTGAGCC[A/G]AGATCACACCACTGC	25909
rs570159320	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246855589	AGAATACTTCTACAC[C/T]AGGAAAGCTGACCAG	25909
rs570182819	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246851570	ATTTAATATGGCATA[C/T]ACTTATGGGTTTACT	25909
rs570194416	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246848606	TGTGGTGGCTCACGC[C/T]TGTAATCCCAACACT	25909
rs570232842	snp	C/G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246849244	CCTTCAAAACAATTT[C/G/T]GGGTTGTGGATATCA	25909
rs570246672	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246852263	AACTGGAACTTTACT[C/T]ATCTATTTGGCAGTG	25909
rs570299748	snp	A/C	0.000137922	0.00830312	intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246931182	ACAGGACAGGCTCAG[A/C]ACGCCGGCCGCTTCC	25909
rs570344092	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246877615	GTTGGTGTGGTGTGA[C/T]AGAGGAACATCAGGT	25909
rs570394474	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246845762	TAAGGAGTTCAAAAG[G/T]CCTAGGTTCAAACCC	25909
rs570410826	snp	A/G	3.31345e-05	0.00407016	intron-variant	AHCTF1	GRCh38.p7	1:246891775	GATAAAACAAAGAGC[A/G]TACCTCTCTCAGTGA	25909
rs570421488	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246870849	TTCTTGAAAATGGCC[A/G]GATTCTGTCACATAT	25909
rs570436573	snp	C/G	0.00318978	0.0398085	intron-variant	AHCTF1	GRCh38.p7	1:246920312	TAAATCAGCGATTTA[C/G]CTTGATAAGAAACTG	25909
rs570535005	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246872195	AGATACCTGATCTAA[A/C]AGATAAAACAGATCA	25909
rs570593701	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246929907	AAATACAAAAATTAG[A/C]CGGGTGTGGTGGCGT	25909
rs570598742	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246869536	GCTGTTAGTGGTTAA[C/T]GTAGCTGATGACTTT	25909
rs570601060	snp	A/T	0.00517822	0.0506191	intron-variant	AHCTF1	GRCh38.p7	1:246884715	CTGATTAGAGAACAT[A/T]AAAATCTGCAAAAGG	25909
rs570628060	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246925053	ACATTGTTACTATGT[G/T]GTTTTCCCCTCTGAC	25909
rs570636545	snp	A/G	0.00517822	0.0506191	intron-variant	AHCTF1	GRCh38.p7	1:246927173	ACAGAGCGAGACTCT[A/G]TCTCAAAAAAAAAAA	25909
rs570647315	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246870242	TGAGGCCATGAGTTT[C/G]AGAATAGCCTGGGCG	25909
rs570661578	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246903363	AACAAAGTGGAATTA[A/T]TTTTCCTGGGTACCA	25909
rs570697582	snp	A/T	0.0111196	0.0737302	intron-variant	AHCTF1	GRCh38.p7	1:246899865	ATATAAATACTAAAT[A/T]TCTCCAAGTCATAAT	25909
rs570768132	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246905398	AGCTACTCGGGAGGC[A/T]GAGCGAGAGAATGGC	25909
rs570794200	snp	G/T	0.00835141	0.0640778	intron-variant	AHCTF1	GRCh38.p7	1:246930434	GAGACAACGTAGACT[G/T]CCCATAGCGCTTGGC	25909
rs570800761	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246868878	GAGATGGAGTCTCGC[C/T]CTGTCACCCAGGTTG	25909
rs570827268	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246863472	TCTCAGCTAATAACT[C/T]AGGAGATGGGAAAAG	25909
rs570842934	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246846535	GCAGAAATGAGAGAT[A/C]TCAATCCCAAGTTTC	25909
rs570924995	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246887073	ATAGTGCTTGGTAAA[G/T]GTACTGATTAAACTG	25909
rs570972942	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246906094	ACGAGATACTGCCAC[A/G]AGACTTTTCAGCTGT	25909
rs570988052	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246883050	TAACATTATTTGTAA[A/G]GGTGCAAATTAATAA	25909
rs571048327	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246916664	ATCTCAAATAATAAT[A/G]ATAATAGTCATTCAG	25909
rs571110488	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246863497	GAAAAGGCAGTTTAA[A/G]GAGGGATAAACCAAA	25909
rs571142241	snp	G/T	1.64898e-05	0.00287135	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850843	CATAGTCATTGTGCT[G/T]GTTTCCTGAGCAGTC	25909
rs571153702	snp	C/T			synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246913368	TAAATGCTGAGTGCT[C/T]GCACTGGCTCCTCCA	25909
rs571182332	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246851556	AAAACATAAATTATA[C/T]TTAATATGGCATATA	25909
rs571217534	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246887153	AAATTTAAATTATGT[A/G]TATTTTCTAAAATTC	25909
rs571243890	in-del	-/AAA	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246920142	GACTCTGTCCCCCGC[-/AAA]AAAAAAAAAAAAAAA	25909
rs571252508	snp	C/G	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246880312	GCTCACGCCTGTAAT[C/G]CCAGCACTTTGGGAG	25909
rs571326097	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246907119	TGTTGCTCTTAGTCT[A/G]CTAACCTGTACAGCA	25909
rs571333962	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246872567	TGCCTTGGAAATTAA[A/G]TAGAGGAGGTTACAC	25909
rs571371166	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246873325	TAGTCCCTTTTATTA[C/T]TGTGGCTGATGGTCT	25909
rs571373007	snp	A/G	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246869000	CAGGCGCCCGCCACC[A/G]TGCCTGGCTAACTTT	25909
rs571390907	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246914845	TCCTCATCCAAATGA[C/T]CAATGAGTGTCCATG	25909
rs571395363	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246865109	TTTAAACTCAAAAGT[C/G]GGGTTTTCAGGTGGT	25909
rs571398206	snp	C/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246845954	GCAGTAGTAGCTCTA[C/G]AACAACACATCTTAC	25909
rs571442050	snp	A/G			downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838891	CTTTCTGAGTACATT[A/G]TTTACCTTACTACTG	25909
rs571498743	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246865916	TCTATAGTGGTATTT[A/T]AAAAATTGATTTATG	25909
rs571512366	snp	C/T	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246869045	GAGACGGGGTTTCAC[C/T]ATGTTGGCCAGGATG	25909
rs571535629	snp	C/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246859522	CACAGTAGGAGCTAA[C/G]AGGAATACATACTTC	25909
rs571541144	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246874454	ATAAAAGGAAGGGAA[C/T]AGCTAGCTGGGGGAG	25909
rs571560737	snp	A/C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246922531	CCTGGGCTCTAGCAA[A/C/T]CTCTCGTCTCGTGCC	25909
rs571585569	snp	C/G	0.00318978	0.0398085	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932008	AGAGGGAGGGGAGAA[C/G]CGGCGGGAGATCGCG	25909
rs571612551	in-del	-/G	0.00398564	0.0444627	intron-variant	AHCTF1	GRCh38.p7	1:246926896	CAAAAGTGTATGGCC[-/G]GGCCGCGGTGGCACA	25909
rs571649723	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246895222	TCAATAAGGTCTCTA[A/G]GTTAGATAAAAGTCT	25909
rs571671165	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246888826	AAGGAAGGAGGATCG[C/T]TGGAGCCCAGGAGTT	25909
rs571716514	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246927956	AATAAGCCAAGATCA[C/T]GCCACTGCACTCCAG	25909
rs571772679	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839507	TGAAATTTTCAACAA[A/G]GCAGCGTAACATCCA	25909
rs571781121	snp	C/G	0.00914312	0.0669923	intron-variant	AHCTF1	GRCh38.p7	1:246882123	CTGCCTCAGCCTCCT[C/G]AGTAGCTGGGACTAC	25909
rs571885337	in-del	-/TT			intron-variant	AHCTF1	GRCh38.p7	1:246899118	TATTTTTCAAAATTC[-/TT]TTTTTTTTTCCTGTG	25909
rs571886017	in-del	-/AT	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246879038	TTTGTATAAAGAAAA[-/AT]AGAGGATAAGATGAA	25909
rs571907782	snp	C/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246919773	CGTTGCTCCAAGCAA[C/T]CCACGGAAACAACCA	25909
rs571953173	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246867498	CATTTCACTTTTAAA[A/G]GTTTTTAAAAATTCT	25909
rs571954819	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246869125	CTGGATTACAGGCGT[C/G]AGCCACCACGCCCGG	25909
rs571962811	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246870438	TTAAAAAAACAAAAA[A/C]AGACTAAAGATGTGA	25909
rs571979893	snp	C/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246858009	GTGTCGCCCAGGCTG[C/G]AGTGCAGTGGCGCTA	25909
rs572018579	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246894203	GTGAGACCATGTCTC[-/A]AAAAAAAAAATTACT	25909
rs572020820	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246858448	ATCCCAGCTCATGAC[A/G]CATACTCAGTAAGTA	25909
rs572053842	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246862297	CATCCTGGCTAACAC[A/G]GTGAAACCCCGTCTC	25909
rs572086643	snp	C/T	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246878699	TTGCACTGCCCTATA[C/T]GTTCTGTGAATACAA	25909
rs572134617	snp	C/T			synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246863954	AGTTTCAAGCAAATG[C/T]AATTCTGAAGCCCTG	25909
rs572143382	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246901973	TGGGATGGGTAAGTT[C/T]GCTGTGTGATTTAAT	25909
rs572143526	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246912715	ATTTTCTTTGAATCT[A/G]AATAGAATTACTTCT	25909
rs572171568	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246912326	CTAAAAAAAAAAAAA[C/T]ACAAAAATTAGCCAG	25909
rs572206700	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246926977	CAGGAGATCGAGACC[A/C]TCCTGGCTAACAAGG	25909
rs572243785	snp	C/T	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246905440	AGGCGGAGGTTGCAG[C/T]GAGCCGAAATCACGC	25909
rs572283485	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246848785	AACCCAGGGGGCACA[G/T]GTTGCAGTGAGCCGA	25909
rs572284221	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246880519	CAGTGAGCCGAGATC[A/G]CGCCACTGCACTCCA	25909
rs572371912	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246893983	CCCAGGCAGGAGGAT[C/T]GCTTGAGGCCAGGAG	25909
rs572376811	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246910157	AATTTGCAGAAAATC[A/G]AAAATGATACCACAT	25909
rs572439269	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246907484	ACTTTCAAATATTAG[C/T]AAATGAGTACAAGCT	25909
rs572440851	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246907202	TTAAAAAGGTACAAT[C/G]AAAATACAGTAAAAT	25909
rs572453159	snp	G/T	3.29745e-05	0.00406031	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851097	GCAAATTTGCAATTT[G/T]TCCATGATTATCATT	25909
rs572467199	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246845252	AAAAATGTTTTTTGT[A/G]GGTACACAGTAGGTG	25909
rs572483540	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246844583	TTAAAAGATTAGCCA[A/G]TGTGGTGGTGCACGC	25909
rs572488842	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246887458	GCATTAAAAGAGACT[G/T]GAAATGCCTGTTTTT	25909
rs572500107	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246930887	TAAAACTTTGCACAC[A/G]GATAGTATGAACCTC	25909
rs572515145	snp	A/G	0.00597247	0.0543191	intron-variant	AHCTF1	GRCh38.p7	1:246901414	GGCCGAGGCGGGTGG[A/G]TCATGAGGTCAGGAG	25909
rs572560433	snp	A/G	0.000293988	0.0121205	intron-variant, utr-variant-5-prime, upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246931244	CGTGGGAGAACAGTG[A/G]GAAAGGGTCGCGGCC	25909
rs572593939	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246855053	GCTGAAGCTTGCCGT[A/G]TACCCCATTCATAAT	25909
rs572654295	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246869020	TGGCTAACTTTTTCT[A/G]TTTTTAGTAGAGACG	25909
rs572687166	snp	A/C			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933417	GATTATAGGCGTGAG[A/C]CACCGCGCCCGGCCT	25909
rs572709885	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246900943	AGTGCTTGGATGGTG[C/G]CTGTGGAATGGAAAG	25909
rs572729816	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246927348	AAATGTAGCAGCCAG[C/T]CACGGCTGCATACGC	25909
rs572742989	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869058	ACCATGTTGGCCAGG[A/C]TGGTCTCGATCTCCT	25909
rs572783870	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246866071	CCCACGGATGTTATC[A/T]ATTCTGCCTTATTTC	25909
rs572883508	snp	A/G	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246926941	GCACTTTGGGAGGCT[A/G]AGGCGGGCGGATCAC	25909
rs572934926	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246914834	TTCTTCTCAATTCCT[C/T]ATCCAAATGATCAAT	25909
rs572936477	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246896087	GCATGGTAAGGACGT[A/G]TTAAAACTGGAACTC	25909
rs572941535	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246895425	GGTGTGTGTGTGTAT[G/T]TGTGTGAAGAGTAAC	25909
rs572954643	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246895233	TCTAGGTTAGATAAA[A/C]GTCTTAATTTTCTTG	25909
rs572974922	snp	C/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246888981	TCAAGGAGAGTTAGT[C/G]GGATAAGCCCTTAAT	25909
rs572976808	snp	A/G	3.29913e-05	0.00406135	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246888207	TGCTTCAGTAACGCC[A/G]TCTAATAGGTACATA	25909
rs572983733	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932915	AGTTTCTACTTTTCT[C/G]TTACCTTTCATATGT	25909
rs573036716	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246846828	GGTGTGATGGCTCAC[C/T]GCAACCTCAACCTCC	25909
rs573079808	snp	C/T	0.000798403	0.0199641	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839681	AATATTAAAAGCCCA[C/T]GAAAGCAGTTCGTTT	25909
rs573106940	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246879141	AAAATCCCAACAACA[C/T]AGGAAAAAAAGCCAA	25909
rs573120138	snp	A/C	0.000175512	0.00936619	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853280	GGAGTTTCCACCATC[A/C]CCAAGGACATCAGCC	25909
rs573133006	snp	A/G	3.29679e-05	0.00405991	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861033	GAGGCCGTGAAAACA[A/G]TCTCTTCAAGGTCTT	25909
rs573150454	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246915875	AAAAAAAGAGTATCA[A/G]AACATTACATGTCAT	25909
rs573210526	snp	C/T	0.00318978	0.0398085	intron-variant	AHCTF1	GRCh38.p7	1:246854957	CCTAAAATGGGTGAT[C/T]GGCTTTTTACATGTT	25909
rs573213082	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869298	TCCCTTATTCCTTGA[A/G]ACTGACAATATCCAA	25909
rs573221699	snp	G/T	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246869127	GGATTACAGGCGTGA[G/T]CCACCACGCCCGGCC	25909
rs573253633	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246906593	CCCCCCAAAAAAATA[A/G]AAAAAAAAGAGCTGA	25909
rs573253691	snp	A/G	0.00597247	0.0543191	intron-variant	AHCTF1	GRCh38.p7	1:246914369	AAAAGAAAATATCTG[A/G]TATCAATGATTCATG	25909
rs573268651	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246868917	TGGTGTGATCTCGGC[C/T]CACTGCAAGTTCTGC	25909
rs573283319	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246909551	GTTCTCAGATCAACT[A/G]TCGCAGTATTGCAGT	25909
rs573291908	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246875606	CTTCACTGTGTCATC[A/G]TAAGAAACTGTCACA	25909
rs573292261	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246910111	TACCTTGCCAAAATA[C/T]TAAACCTTCATCTAT	25909
rs573351269	snp	G/T	0.000131804	0.00811695	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867699	TATAGGTTCTTTGCT[G/T]GCCCAAACTTCTCCA	25909
rs573434409	in-del	-/TCAA	0.0525931	0.153397	intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842653	CAGAGCGAGACTGTC[-/TCAA]TCAATCAATCAATCA	25909
rs573448373	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246902771	AGATTGTTCACACAA[C/T]ACAAAGAAAACAATT	25909
rs573488669	snp	C/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246903255	GATCTCCTCAGGAAT[C/T]CAGCCAGATAAATAG	25909
rs573545734	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246872822	AGAGGGCAGTAAAAC[A/G]TGCTGTAGATTTTTA	25909
rs573644256	snp	C/T	4.99422e-05	0.00499686	intron-variant	AHCTF1	GRCh38.p7	1:246900293	TTGGTCAGCTACACA[C/T]ACAAATACAAAGAGA	25909
rs573678661	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868984	TGAGTAGCTGGGACT[A/G]CAGGCGCCCGCCACC	25909
rs573693075	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246855445	AAACACGAAATAACT[A/C]TTCTGAGTCCAAGAA	25909
rs573715503	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246864423	TTCAAATGAAGATGA[A/G]CTGCCAATGATTTAA	25909
rs573723235	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246874241	AGACTGAGACCATCT[C/T]TGAGGTGGGCCTCTG	25909
rs573754104	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246865190	AAACAGTCTATCTTA[C/T]GGTTGTATTTCCTAG	25909
rs573754294	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246852973	CCCATATTTTTATAA[A/G]TAAGTTTTTATATAG	25909
rs573787655	snp	A/G	0.00119737	0.0244387	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839551	TAAAAGGCCGCACTC[A/G]CACTGCTTTCACACT	25909
rs573793093	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246859612	TCTCATTCTCTTGCC[C/T]GGGCTGGAGTTCAGT	25909
rs573827406	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246851867	CACACTTTTCTAAAT[A/G]GCACGATCCCCGTAA	25909
rs573881869	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246887653	AGAAACAAAGATATA[C/T]GCAAATTTCTAAAGA	25909
rs573947202	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246847289	GCCAAACTCCATCTC[-/A]AAAAAAAAAAAACAA	25909
rs573962642	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246916745	ATCACACCTCAATGT[A/G]GAGATAAGGCAGCTA	25909
rs573969347	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246867597	GTGGATTGTTGATGA[A/G]CGCTGTTGATGTCCA	25909
rs574002820	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246874676	TTCCAAATTAAAAAA[A/C]ATTCAACTACAGCTG	25909
rs574015563	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246922333	CCACTGCACTCCAGC[A/G]CGGGTGACAGAGCAA	25909
rs574019766	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246905208	TAATTTTTAAAGATT[A/G]TATGTATCAGGCCAG	25909
rs574031205	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869071	GGATGGTCTCGATCT[C/T]CTGACCTCGTGATCC	25909
rs574083479	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246917581	CTCCAATGAAGTCAT[C/T]GTACAATGCCTGGCA	25909
rs574095694	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246881768	GCTTGAACCTGGGAG[A/G]CAGAGGTTGCAGTGA	25909
rs574135725	snp	A/G			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932344	GCTGCGATTGCAGGC[A/G]GACTCTCTTGTCACG	25909
rs574142458	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869122	GTGCTGGATTACAGG[C/T]GTGAGCCACCACGCC	25909
rs574146068	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246914663	GAAGACAAAAATAAA[C/T]ATAATGAGTGTATAC	25909
rs574155585	in-del	-/AC	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246868715	TACACTAGTAAATAA[-/AC]AGTCAAATCTTCTAA	25909
rs574158472	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246915202	GGGCGTGGTGGTGCA[C/T]GCCTGTAGTCCCAGC	25909
rs574231838	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246861939	AAAATGTCTTTTCTC[A/C]CAATTATTATCAAAC	25909
rs574234875	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246882355	GTCAGGTACCACATG[C/G]ATCACATTATGTGAT	25909
rs574236102	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246909344	ATCACCTGAACCCAG[C/G]AGGCAGAGGTTGCAG	25909
rs574277181	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246902745	TAAAATTAAATATTC[C/T]CCAAATTTAAAGATT	25909
rs574286082	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246853520	TGATAACTGATAAAC[A/G]GTATCAGGAAACATT	25909
rs574289533	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246884193	TGAAACTACAATTTT[A/G]ATCTCATAAAAAATC	25909
rs574305943	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246846940	AATTTTTCTTTTGTA[C/G]AGATGGGGTCCCACT	25909
rs574316233	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246896570	GGGGCAGGCAGGAAG[G/T]TAAGGGAAAAGGAGT	25909
rs574378586	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246909968	ACCACTAGTTTAAAG[C/T]TGATGACAGACTTTA	25909
rs574396670	snp	A/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246854286	CCTGGGTGACAGAGC[A/G]AGACTCTGTTTCAAA	25909
rs574435293	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246847480	ATACTTCTATTTTAG[A/C]GTTTTCAGTAAGTAG	25909
rs574443710	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246911480	TATCTATGAAGATTC[A/T]TTTTTTTTTTTTTTT	25909
rs574475429	snp	C/T	0.0402882	0.136092	intron-variant	AHCTF1	GRCh38.p7	1:246922919	ACCCAGGAGGCGGAG[C/T]TTGCAGTGAGCCGAG	25909
rs574504008	snp	C/T	0.0123036	0.0774623	intron-variant	AHCTF1	GRCh38.p7	1:246921713	GTAGAAACCGCAATT[C/T]TGGAATATCTTCAGA	25909
rs574552672	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246924563	GGCAAAAATCAACCT[A/G]ACGTTCTTTCTTGTC	25909
rs574563584	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246876550	AGACTCAGAGTGTGT[A/C]CCAAGCACACAGAGT	25909
rs574598386	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869676	TTGACAGCATGGTTT[A/G]CCGAATATTTTAAGC	25909
rs574605860	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840190	AGCCTTTAAGCTTGC[C/T]GAATAAGAGATGCCA	25909
rs574620859	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246917732	GAAAAGTCTTCTGCA[A/G]TATCTTTCATTAGAA	25909
rs574644404	snp	C/T	7.70604e-05	0.00620679	intron-variant	AHCTF1	GRCh38.p7	1:246841015	TGAAAAAAAAAGATA[C/T]GATCAAGTAAGAATA	25909
rs574690239	snp	C/T	0.00438332	0.0466095	intron-variant	AHCTF1	GRCh38.p7	1:246918533	AGATGCGGAGGCTCA[C/T]GCCTTTAAGTCCCAG	25909
rs574719674	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246929263	AAATACAAAAAATTA[A/G]CCGAGTGTGGCGGCG	25909
rs574765828	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246870013	TCATAATTCCTGGGA[A/G]GAGTCAAACTATGCA	25909
rs574774746	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246841933	AGCTGGGACTACAGG[C/T]ACCCACCACCACGCC	25909
rs574782924	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246929824	TCTGGGAGGCCAAGG[C/T]GGGCGGATCACGAGG	25909
rs574793164	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246925323	CCAAAGTCCAAAGGA[A/T]AACACACAAAAAGCA	25909
rs574820623	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246928234	CATGAACCCGGGAGG[C/T]GGACCTGGCAGTGAG	25909
rs574849186	snp	C/T	1.6489e-05	0.00287128	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246855800	TTCGTCCAACACTGG[C/T]ACCTTGGACTTCTGG	25909
rs574863498	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246898111	ATTACACTACTTCAC[C/T]TATTTTTGCAGAAAT	25909
rs574900740	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246896084	CAAGCATGGTAAGGA[C/T]GTGTTAAAACTGGAA	25909
rs574902460	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246891331	AATACACTTTCACCT[C/T]AGCTACACTTTCATT	25909
rs574902808	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246896160	GCAAAGCAGTTTGGC[A/G]GTTTCTCAGTATGCT	25909
rs574922326	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246861670	AAGGACTAAAAATTA[A/G]GAGGTTTGAATCCTA	25909
rs574941743	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246898826	GGCACGGTGGCTCAC[A/G]CTCATAATCCCAACA	25909
rs574949000	in-del	-/AAGTGCAGAACTGGG	0.0103295	0.0711199	intron-variant	AHCTF1	GRCh38.p7	1:246854776	AGAGACACAGCCCTT[-/AAGTGCAGAACTGGG]AAGTGCAGAACTGGG	25909
rs574959357	snp	C/T	0.000156685	0.00884975	intron-variant	AHCTF1	GRCh38.p7	1:246862202	AAAGTGCTTATAGGC[C/T]GGGCGCGGTGGCTCA	25909
rs574982540	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246906956	AGAACTCATATTATA[A/C]AAACACAGCCATGTG	25909
rs574996620	snp	A/G	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246905253	ACCTGTAATCCCAGC[A/G]CTTTGGGAGGCTGAG	25909
rs575036323	in-del	-/T	0.415399	0.187465	intron-variant	AHCTF1	GRCh38.p7	1:246844805	ATTTACCACACAGAC[-/T]TTTTTTTTTTTTTTT	25909
rs575081507	snp	A/G	0.00755907	0.0610114	intron-variant	AHCTF1	GRCh38.p7	1:246889604	CGGCACAGATTTTAA[A/G]GTACTGATTCCCAGG	25909
rs575089279	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246884105	TTTCCAACCCAGTAC[C/T]AGAACTCTTAACCCA	25909
rs575103170	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246901892	ACATGTGCTTTTCAC[A/G]TATTTAACTGGATCT	25909
rs575173036	snp	A/G	0.0142736	0.0832652	intron-variant	AHCTF1	GRCh38.p7	1:246860192	TTGAACCTGGTTGGG[A/G]GGGGGGCGGAGGTTG	25909
rs575179923	snp	A/G	0.0107246	0.0724382	intron-variant	AHCTF1	GRCh38.p7	1:246922908	GAATGGCATGAACCC[A/G]GGAGGCGGAGTTTGC	25909
rs575194597	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246917639	CATTCAAGAGAATGG[C/T]GCTGTCAAGAGAGAA	25909
rs575249532	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246884962	CATTCTTCCTCTCTA[C/T]TCCTGACTCCTTTTC	25909
rs575297225	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246868275	CTGGGACTACAGGAA[C/T]GTGCCACCACGCTAA	25909
rs575381379	snp	A/C	0.0275645	0.114116	intron-variant	AHCTF1	GRCh38.p7	1:246881863	ACCAAAAAAAAAAAC[A/C]AAAAAAAAAGAAGAA	25909
rs575411359	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246875752	CATTTTTTAGCAATA[C/T]TGCATTTCAAAATTA	25909
rs575420104	snp	C/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246875018	CCTACTTTGTTAAAA[C/T]CATCTCCTGACAGGC	25909
rs575429415	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246846972	AGTTGCCCAGGCTGG[C/T]TGGATTTTGAAGAAT	25909
rs575462897	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246919381	ACAACATTTTCTTTC[A/G]TACAAATGTGTGGCC	25909
rs575509009	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246848256	TATTATTTGGCCCCC[C/T]GGGCTGGAATACAGT	25909
rs575588773	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246841852	GCTGGAGTGCAGTGG[C/T]GTGATCTTGGCTCAC	25909
rs575656789	snp	A/C	1.64999e-05	0.00287222	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861148	TCTCTAAACTTTGTG[A/C]CCCCTCATCCATTTC	25909
rs575666954	in-del	-/TTAT	0.00597247	0.0543191	intron-variant	AHCTF1	GRCh38.p7	1:246918195	AATATATACTTATTA[-/TTAT]TTATCTTACAAATCA	25909
rs575667145	in-del	-/T	0.00279162	0.0372561	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933067	AGCCCTCCAAGTAGC[-/T]TGGGACTATGGGCAT	25909
rs575678159	snp	C/T	0.00398564	0.0444627	intron-variant	AHCTF1	GRCh38.p7	1:246903347	CTTGATATGTTAGAG[C/T]AACAAAGTGGAATTA	25909
rs575682340	in-del	-/A	0.00318978	0.0398085	intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842271	AAATCTAATTTTGAG[-/A]AAAAAAATGGATAAA	25909
rs575683207	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246870150	GAGAACTAGAATGAG[A/C]AGCAGAGCCTAGGCC	25909
rs575686912	snp	C/T	0.00318978	0.0398085	intron-variant	AHCTF1	GRCh38.p7	1:246902818	AATCATGGAAAAAGG[C/T]TCTAAAATTTTACAT	25909
rs575708288	snp	C/T	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246869373	GGAGGAGTCACATGT[C/T]TAGGACTTTAAATCA	25909
rs575734575	snp	A/C	1.737e-05	0.00294698	intron-variant	AHCTF1	GRCh38.p7	1:246867818	GTCTAGAAACTGTAA[A/C]ATGAAGAACGCTGGA	25909
rs575744512	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246869649	GAAAAAGCCTAGATG[A/G]AAACACATCTGTTGA	25909
rs575751647	snp	A/G	0.00557542	0.0525036	intron-variant	AHCTF1	GRCh38.p7	1:246925891	CCTGGGCCACATGGC[A/G]AAATCTCATCTCTAC	25909
rs575786129	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246855068	ATACCCCATTCATAA[G/T]GTACCAGGAACAAAG	25909
rs575786872	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246864741	GCTACTCGGGAGGCT[A/G]AGGCAGGAGAATGGC	25909
rs575855369	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246928742	CAACAATTATATTGC[A/C]ACATGTACCAAGCAA	25909
rs575871414	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246929146	GGGTGCGGTGGTTCA[C/T]GCCTGTAATCCCAGC	25909
rs575874515	snp	A/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246897468	TAATGATGGGGATAC[A/T]TTCCGATGAATGTTT	25909
rs575891177	in-del	-/CC	0.00755907	0.0610114	intron-variant	AHCTF1	GRCh38.p7	1:246889614	TTTAAAGTACTGATT[-/CC]CAGGTGATTCAGGTG	25909
rs575911125	snp	A/C	0.00318978	0.0398085	intron-variant	AHCTF1	GRCh38.p7	1:246877593	GTGGCCTGGATAGAG[A/C]TGAATGGTTGGTGTG	25909
rs575931393	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246863782	TCCGTTTTTAGAAGA[C/T]GTGAAAACATAAAAG	25909
rs575934055	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246883162	GTGAGTCCGGGGAGA[A/G]TGTTAGTGTTTGATG	25909
rs575962224	snp	A/G	0.000399281	0.0141238	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877201	AGTAAATCTTCCATC[A/G]AGCCCATTTCCTGAC	25909
rs575991943	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246892265	AACTGTCTTCATTCT[A/G]AAATCCTTCTTTAAA	25909
rs575992273	snp	A/T	0.0111196	0.0737302	intron-variant	AHCTF1	GRCh38.p7	1:246865936	ATTGATTTATGTAAC[A/T]TTTTACTTGTTAGAG	25909
rs576022426	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246899685	AGATAACAAACCTAT[C/T]ACACAGCAAAACAAG	25909
rs576024774	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246906882	TTTTCCCTCTCAACT[A/G]AGAATTCTTTATTAA	25909
rs576030140	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246893140	AATTGAGTTTAATTT[C/T]TTACAAAACATGAGC	25909
rs576048129	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246891225	ACTAATTCATCTTTG[C/T]ATTTAGTTTACTTTG	25909
rs576090521	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246896673	AGAATTCTGTGAATT[A/C]AAATCACTGAACTGT	25909
rs576113682	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246873839	CAAAAACGTTCCCTG[C/T]GTCACCTTGACTAAC	25909
rs576117924	snp	C/G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246849399	AAAATAAATCTGTTA[C/G/T]GTGAGTTACAGGATT	25909
rs576170531	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246893916	CTTGGTCAAAAATTA[C/G]TTTTGGCTGGATGTA	25909
rs576176798	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246870117	AGAAAACAACTGCAG[A/G]TATGGGGGAAAGAGC	25909
rs576186021	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246870413	CTGTGACAGACAAAG[A/G]CCTTGTCTCTTAAAA	25909
rs576219030	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246911663	TAATTTTATATTTTT[C/T]AGTAGAGACGGGGTT	25909
rs576220958	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246919649	ACCCAGGAGGTGGAG[A/G]TTGCAGTGAGCCTCA	25909
rs576239928	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246860002	CGCGGTGGCTCACGC[C/T]TGTAATCCCAGCACT	25909
rs576259660	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246912304	ATATGGTGAAACCCC[A/G]TCTCTACTAAAAAAA	25909
rs576260540	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246857010	TCAAAAGTGCGGACA[A/T]GCAATCTGTGTCAGT	25909
rs576289524	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246898905	CCAGCCTGGCCAACA[C/T]GGTGAAACCCCATCT	25909
rs576298817	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246880855	TTCCTACAGAAGACA[A/G]TAATGATGCTAGGAA	25909
rs576362170	in-del	-/GTA			intron-variant	AHCTF1	GRCh38.p7	1:246877730	GAAGAGTAGAGCTTG[-/GTA]GTAGATGTTTTTTGG	25909
rs576423699	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246857868	TATTTAGTGATTACT[A/G]ATAGTCTTGCATTAT	25909
rs576440146	snp	C/T			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933789	GAAATGTAATTTTCT[C/T]TTTTCTGTAATTTTT	25909
rs576454925	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246852842	AGGATCCTCCCTCCT[C/T]AAACTCCCAAGTAGC	25909
rs576458752	snp	A/C	3.37046e-05	0.00410502	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850381	TTCTACAGATCTTTT[A/C]ATTCTTCTAGGAGTC	25909
rs576465385	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246844159	AATGCTTCAAACTAA[A/G]AAGTGCTACAATATA	25909
rs576474243	snp	C/T	3.30087e-05	0.00406242	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850941	GAATGGACTGTTCCA[C/T]TGTATCTGAAGTAAT	25909
rs576565701	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246930013	GCCAAGATTGTGCCA[C/T]TGCACTCCAGCCTGG	25909
rs576592058	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246879488	AGCATTGTTTAAAAT[A/G]GCTAAAGGTTGAAAC	25909
rs576624513	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869765	GATAATGCCCCTGGT[C/T]ACCCAGGAGCCCTGA	25909
rs576634025	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246930713	CCACTGCGCCCAGCC[A/C]AAGACAGTTCTTAAA	25909
rs576634168	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246868933	CACTGCAAGTTCTGC[C/T]TCCCGGGTTCACGCC	25909
rs576698199	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246914155	TAACTAGTCATCCAT[A/G]TTTTATACTTGTCTT	25909
rs576701636	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246868368	TCATGTGATCCACCC[A/G]CCTTGGCCTCCCAAA	25909
rs576744929	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246890348	TTTGAAAGCAAGAAA[C/T]GTTCACTACAAATCA	25909
rs576809294	snp	C/G	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246848206	GGGCTCAAACTGTAT[C/G]AGTACAACAAGTCAT	25909
rs576831934	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246883779	TGTGCTAGTTTTCTG[A/G]GGACTGGAAAATTGA	25909
rs576833228	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246898862	GGAGGCCGAGGCAGG[A/C]GGATCATCTGAGGTC	25909
rs576892207	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246917957	ACTTCCTAATTATAA[A/G]GAAAAACTAGTTGCA	25909
rs576894632	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246841710	TCCCACTTCCCTTTC[C/T]TACTTTTTCTGCAAA	25909
rs576918696	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246895404	GAACAGACAATATGC[A/G]TTTGGGGTGTGTGTG	25909
rs577004784	snp	C/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246892968	CTTTTAAAACACTTA[C/G]TATGCTTTGTATGTT	25909
rs577031674	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868380	CCCGCCTTGGCCTCC[C/T]AAAGTGCTGGGATTA	25909
rs577054500	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246925375	GTAAATGTTCTATTT[C/T]TTAGGCTGGGTGAGT	25909
rs577061112	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246880911	AAGGCTAGGCTAGCA[C/T]GTTGGCAGTAAAAGA	25909
rs577070008	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246862218	GGGCGCGGTGGCTCA[C/T]GCCTGTAATCCCTGC	25909
rs577073671	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868700	TTCTTTCATTATGCA[C/T]ACACTAGTAAATAAA	25909
rs577101372	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246924212	TTAACTTTAAAAAAT[G/T]TATAAAGAAATATTT	25909
rs577114479	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246925870	AGCCCAGGAATTTGA[C/T]ACCAGCCTGGGCCAC	25909
rs577138816	snp	A/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246904699	CTGTAGTGAACTCAA[A/G]CACGAAGCATGCAGT	25909
rs577248790	in-del	-/CAT	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246846567	TATCCCTTCCAATCC[-/CAT]CATCTCATTCTAGCA	25909
rs577351838	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246855882	TCCCATCTGCTTTAA[C/G]CTGCTTTAGTCCTAC	25909
rs577389594	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246858061	GCCTCCCAGGTTCAC[A/G]CCATTCTCCTGCCTC	25909
rs577390789	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246856896	ACCATTTATAATGTT[G/T]TAAGTTATATTTTGT	25909
rs577523820	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246912871	TGCTGGGTAATTTCA[C/T]ATTGGCTGATAAGGC	25909
rs577532215	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246851814	GAAACAACCCCCAAA[C/T]TGTGTTTTAATGGTA	25909
rs577536725	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246878146	CTCATGCCTGTAATC[A/C]CAACACTTTGGGAGG	25909
rs577654282	in-del	-/A	0.00120651	0.0245316	intron-variant	AHCTF1	GRCh38.p7	1:246852494	TAGAATTTTTTTTTT[-/A]AAAAAAACTAAGTCT	25909
rs577659031	snp	C/T	1.64912e-05	0.00287147	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246905635	ATACAGGAACTTGTC[C/T]ACTTTCCAATTGTAT	25909
rs577670378	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246864381	ACCTATATTTACTGA[A/G]CTCTTACTATGTGCC	25909
rs577698450	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246906472	ATGTAATCCCAGCTA[C/G]TTGGGAGGCTGAGGC	25909
rs577709306	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246871295	AAAACAGAGACACCA[C/T]TCGCTTACTGATGGG	25909
rs577714473	in-del	-/CTGGTAACTCTCATGTGATTCCTTCTCATG			intron-variant	AHCTF1	GRCh38.p7	1:246856543	GCACCCAGGTTCTCA[lengthTooLong]CTGGTAACTCTCATG	25909
rs577813788	snp	C/G	0.00438332	0.0466095	intron-variant	AHCTF1	GRCh38.p7	1:246869030	TTTCTATTTTTAGTA[C/G]AGACGGGGTTTCACC	25909
rs577874301	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246844737	AGGAAGATATTCCAT[A/G]GAAAAATAAAAATGG	25909
rs577884110	snp	C/T	6.65458e-05	0.00576788	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900210	CTCCAATGACCACAG[C/T]GCAAAATAAGAGCAA	25909
rs577891160	snp	A/C	0.000399281	0.0141238	intron-variant, utr-variant-5-prime, upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246931335	GCCGCCATGTGCCGC[A/C]GCTCCTCCGGTCCGA	25909
rs577907246	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246886719	CTATGCCATTTTATA[C/T]AAGAGACATGAGCCT	25909
rs577918968	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246900688	TTAAAAAGTAGTCAC[A/T]CATCAGAAGTTATAT	25909
rs577920863	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246894161	CTGAGCCATGAACTC[A/G]CCACTGTACTCCTGC	25909
rs577975446	snp	A/G	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246862341	AAAAATTAGGCAGGC[A/G]GGGTGGCGGGCGCCT	25909
rs577994202	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246926978	AGGAGATCGAGACCA[C/T]CCTGGCTAACAAGGT	25909
rs578031491	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246894556	CAAAAAAAGAAAAGA[C/G]TTTACAACTTCAAAA	25909
rs578150552	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246922189	GTATGGTGAAACCCC[A/G]TCTCTACTAAAAATA	25909
rs578184158	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246915148	CAGCCTGGCCAACAG[A/G]GTGAAACCCCATCTC	25909
rs578190718	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246908481	CCTGCCTGTTCTGTA[A/G]ACATTGTGTTTCAGA	25909
rs578211073	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246909184	TGGGAGGCTGAGGCA[A/G]GCAGATCATGAAGTC	25909
rs578218312	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246901493	GCTGGGCATGGTGGC[A/G]GGTGCTTGTAGCCCC	25909
rs745308809	snp	A/G	1.64743e-05	0.00287	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849820	TTCTTCTGATACTGA[A/G]TGCAATGAACGTTTT	25909
rs745353272	snp	C/T	1.66579e-05	0.00288595	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900096	TGGATTAAAAAACTG[C/T]TCGGGAGGTGGATAT	25909
rs745356540	snp	A/G	1.65031e-05	0.00287251	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246889992	CTCAAACTTCTGTCG[A/G]CGACTGGTGTAGTAG	25909
rs745364337	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246845575	TTTATTTCACTTTTC[A/G]TAATCTTCACCTAAG	25909
rs745387102	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246859753	GCTAATTTTTTTATA[C/T]TTTTTGTAGAGATGG	25909
rs745393529	snp	C/T	1.9517e-05	0.0031238	intron-variant	AHCTF1	GRCh38.p7	1:246876015	TCCAATAGATTATGA[C/T]ATTCTTCAATGAAAT	25909
rs745399680	snp	C/T	5.24654e-05	0.00512152	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861200	GTTCAGGAAAAAAGA[C/T]GTGGTCCTATCTTTG	25909
rs745410574	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246907262	TGTTGTTGACCAAAA[C/T]GTTGTAAAGTTACAA	25909
rs745421117	snp	C/T	1.75167e-05	0.0029594	intron-variant	AHCTF1	GRCh38.p7	1:246899534	AAAAGATTTAAAAAA[C/T]AATCCACTTACATAT	25909
rs745421350	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246894222	AAAAAAATTACTTTT[A/C]TCACTTTAATGTAAA	25909
rs745427412	in-del	-/C			intron-variant	AHCTF1	GRCh38.p7	1:246911479	CTATCTATGAAGATT[-/C]TTTTTTTTTTTTTTT	25909
rs745471437	snp	A/T	1.66671e-05	0.00288674	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246905657	CAATTGTATGTAATA[A/T]CTGAAACAAATTAGT	25909
rs745520896	snp	A/C/G	8.23684e-05	0.00641706	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849723	GAGTCCTGCTGCTGC[A/C/G]GGATGATTTAGTGAA	25909
rs745530686	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246895234	CTAGGTTAGATAAAA[C/G]TCTTAATTTTCTTGA	25909
rs745554095	snp	C/T	1.65622e-05	0.00287764	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850812	AGGAAACCACGTCAT[C/T]AACCTGGCTGACATT	25909
rs745562552	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246846332	TAAATAGGCACAAGG[G/T]ACAGAAAGTATGGTA	25909
rs745585236	snp	A/T	1.81338e-05	0.00301108	intron-variant	AHCTF1	GRCh38.p7	1:246867830	TAAAATGAAGAACGC[A/T]GGAATTAAGTGCATC	25909
rs745601363	snp	A/G	1.66081e-05	0.00288163	intron-variant	AHCTF1	GRCh38.p7	1:246842786	ATCTTTCTATGGGTT[A/G]AACATTTTAAAAGGT	25909
rs745619250	snp	C/T	5.17451e-05	0.00508624	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850401	TTCTAGGAGTCCTTT[C/T]TGTAACAGATGAAAC	25909
rs745623814	snp	A/C	3.53432e-05	0.00420361	intron-variant	AHCTF1	GRCh38.p7	1:246877318	CTGAAAGCAGTATTT[A/C]TCAAAGTTTAGTTTT	25909
rs745634334	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246869246	CTTACTCCACTGACT[A/G]ACTGTTCCCCCGCGT	25909
rs745639711	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246854823	AGGAACCCACACATT[C/G]GGGTTCAGCCCCCTG	25909
rs745645765	snp	G/T	1.77307e-05	0.00297742	intron-variant	AHCTF1	GRCh38.p7	1:246864163	ACTGAAAAAACAAAA[G/T]AATTTAGTATCCCAT	25909
rs745652905	snp	C/G	3.31384e-05	0.00407039	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902673	TTCACAGTATTCTAA[C/G]CCCTGTAACATAAAA	25909
rs745674759	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246905693	TCATATTTTTAAGTT[-/A]TTTTTTAGAAAGGAA	25909
rs745678766	snp	C/T	1.65996e-05	0.00288089	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877233	GACTTCATACATGTG[C/T]TTCAGTAACTCCTCT	25909
rs745707771	snp	C/G	1.64803e-05	0.00287052	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902596	CATCCCAACAATTTG[C/G]TATTACTCGTCTGTC	25909
rs745724348	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246868482	CTGGTCTCAAACTCC[A/G]GGCCTCAAGTGATCC	25909
rs745732093	snp	A/G	0.000265098	0.0115099	intron-variant	AHCTF1	GRCh38.p7	1:246890071	TCATCTAGATTTTTA[A/G]GAGTTGGAAAAAAAG	25909
rs745741965	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246888583	TCAAAGCAACCAGCA[C/T]CAAAATATTAAAAGT	25909
rs745798503	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246916512	TTTACATATTATCTC[C/G]ACATTGAAATCTTTT	25909
rs745805835	snp	A/C			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933891	GAAACAGTTAAAAAG[A/C]GTACTGCTTTTGCAG	25909
rs745817083	snp	G/T	3.55032e-05	0.00421311	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853190	TTCTACTTCATGATC[G/T]TCTTTTAAGTTCAGC	25909
rs745825077	snp	C/T	3.46891e-05	0.00416453	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840765	TCCACACTATTCTGA[C/T]GACTTTACAAATAGG	25909
rs745839202	snp	C/G	1.6825e-05	0.00290038	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916201	GGTCATAAAGACAGA[C/G]AACACTCCCTTCTGT	25909
rs745870521	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246929850	CGAGGTCAGAAGTTC[A/G]AGACCAGCCTGGCCA	25909
rs745935425	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246841878	CTCACTGCAACCTCC[A/G]CCTCCTGGGTTCAAG	25909
rs745953082	snp	A/T	1.67156e-05	0.00289093	intron-variant	AHCTF1	GRCh38.p7	1:246913427	CCTAGAAAACATAAT[A/T]CGTGATTTGCTTTTC	25909
rs745954810	in-del	-/TTGCAGTGAGCCGAGA			intron-variant	AHCTF1	GRCh38.p7	1:246854235	CCTGGGAGGCGGAGC[-/TTGCAGTGAGCCGAGA]TTGCAGTGAGCCGAG	25909
rs745966646	snp	C/T	3.30748e-05	0.00406649	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246888489	AAACCAGTCCATCAA[C/T]CATCAAGCAATCGGG	25909
rs745989774	snp	C/T	1.64849e-05	0.00287092	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246913306	AGGATCTGTCCAACA[C/T]CAGTGACCACAGCTG	25909
rs746000634	in-del	-/AT			intron-variant	AHCTF1	GRCh38.p7	1:246854968	TGATCGGCTTTTTAC[-/AT]GTTAGACAATTCTCT	25909
rs746008613	snp	C/T	1.64773e-05	0.00287026	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246898291	TATAACCATCAGGAA[C/T]GAGTTCATTGAGTGA	25909
rs746071853	snp	C/T	3.29669e-05	0.00405984	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851169	CTGCTTTAGGTAACA[C/T]ATCAGATGATGCAAA	25909
rs746104489	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246910018	TCACCATGTGAATCC[A/G]CTGATCACTAATTGA	25909
rs746122214	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246924566	AAAAATCAACCTAAC[A/G]TTCTTTCTTGTCATT	25909
rs746129399	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246923695	GTGACACATTGCTTT[A/G]CATTCCTCCCCTAGT	25909
rs746152606	snp	A/G	1.64857e-05	0.00287099	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851103	TTGCAATTTGTCCAT[A/G]ATTATCATTTTCCCC	25909
rs746153217	in-del	-/A	0.000119253	0.00772091	intron-variant	AHCTF1	GRCh38.p7	1:246905497	CGAGACTCTGTCTCC[-/A]AAAAAAACAAAACAA	25909
rs746166496	snp	A/G	3.3976e-05	0.00412151	intron-variant	AHCTF1	GRCh38.p7	1:246857661	TAAACTTCTTTCTAA[A/G]AGTATTTGAATTTCT	25909
rs746167533	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246914708	AAAACAGCTAGTAGG[A/T]TGAACTTTTGAAAGT	25909
rs746177702	snp	A/G	1.95946e-05	0.00313	intron-variant	AHCTF1	GRCh38.p7	1:246918421	TTATGACACATTTGT[A/G]GACAATATACTTGAT	25909
rs746188781	snp	A/T	1.65726e-05	0.00287855	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850732	AGCAACATCTGCTGA[A/T]GCTTCCTGTTGTGCT	25909
rs746219072	snp	A/C	1.65121e-05	0.00287329	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864051	GGAGATTTCATGGAG[A/C]TTTGCTGAATAAACT	25909
rs746227895	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246912848	GAACACTATGTTAGA[A/T]CCTACATTGCTGGGT	25909
rs746232246	in-del	-/G			utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839227	ATCTACATTCACGGA[-/G]GGGGGAAAAAAAGTA	25909
rs746235389	snp	C/T	1.67733e-05	0.00289592	intron-variant	AHCTF1	GRCh38.p7	1:246864129	AGTCTGTAATCAGAA[C/T]GCGCATTTATTGAGT	25909
rs746241299	in-del	-/TTTCCTGAT	0.000418155	0.0144535	cds-indel, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850356	TTATAATTTCAACAC[-/TTTCCTGAT]TTTCTACAGATCTTT	25909
rs746242151	snp	C/G	1.65086e-05	0.00287298	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246855812	TGGTACCTTGGACTT[C/G]TGGGTGAAGATTTTC	25909
rs746257524	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246912294	ATCCTGGCCAATATG[A/G]TGAAACCCCATCTCT	25909
rs746328158	in-del	-/A			splice-acceptor-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843930	TCTATTTTTTTAGCT[-/A]AAAAAAAGTTGAAAA	25909
rs746345149	snp	A/C	0.000200093	0.0100003	intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842659	GAGACTGTCTCAATC[A/C]ATCAATCAATCAAGA	25909
rs746398092	snp	C/G	1.75542e-05	0.00296256	missense, synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840979	GAGGAGGTGACCAAG[C/G]ACTTTCTTTTTCTGT	25909
rs746406227	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246900654	TGCATTTTGACTGTT[C/T]CTCAATTTTAAGGCC	25909
rs746412004	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246929370	GCCAAGATCACGCCA[C/T]TGCACTCTAGCTTGG	25909
rs746416283	snp	A/T	1.64885e-05	0.00287123	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850165	GGAGTCTTCTCTCAC[A/T]TCTGATGGACTAACT	25909
rs746449054	snp	A/G	1.64792e-05	0.00287042	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246863969	TAATTCTGAAGCCCT[A/G]GAGATGGCCTGAGGC	25909
rs746463611	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246927568	TGAAACACCTACGTT[A/C]AGTACTGTACAAAAT	25909
rs746476506	snp	A/G	3.53632e-05	0.0042048	intron-variant	AHCTF1	GRCh38.p7	1:246891079	TAAAGAAGAGTTAAC[A/G]TCAGTTGTTTACTTA	25909
rs746480416	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246880986	TACAGCAAAGACAGA[A/C]TGAAAACCCATCCTG	25909
rs746493325	snp	C/T	1.66338e-05	0.00288386	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877245	GTGCTTCAGTAACTC[C/T]TCTATATTCAACCTA	25909
rs746530827	snp	A/G	1.66726e-05	0.00288722	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246862050	CCAGGTGATGGAGAG[A/G]GAGATGCTAAAGGTG	25909
rs746533513	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246914271	GAACATCCAAATCCA[A/T]AAGTCCAAAATCTAA	25909
rs746543111	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246846732	TTGAAATATATATAC[A/G]TATACATATATATAT	25909
rs746550814	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246880511	GGAGGTTACAGTGAG[A/C]CGAGATCGCGCCACT	25909
rs746557110	snp	A/G	1.66228e-05	0.0028829	intron-variant	AHCTF1	GRCh38.p7	1:246890090	TTGGAAAAAAAGCTG[A/G]TAATAATCCCCAAAT	25909
rs746600292	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246879728	AGCTACTTGCGAGAC[C/T]GAGGCAGGAAAATCG	25909
rs746606806	snp	C/G	1.66546e-05	0.00288566	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900120	TGGATATGAAGGAGG[C/G]ACTCCTCTATTTAAA	25909
rs746632307	snp	C/T	1.71149e-05	0.00292526	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840777	TGATGACTTTACAAA[C/T]AGGTGTACATTAAAA	25909
rs746649401	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246917017	TTAGTCATGTTTGGA[C/T]TTTACCCTGCCTGCA	25909
rs746687719	snp	A/G	3.29489e-05	0.00405874	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849831	CTGAGTGCAATGAAC[A/G]TTTTTGGCTTTGACT	25909
rs746737038	snp	A/T	1.90134e-05	0.00308323	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876162	CGAGCCAGTGATCTC[A/T]CCCGCAAACGAGGAT	25909
rs746741909	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246903092	AGGCTATGAGACTTC[A/G]CCCATAAAAATGCAA	25909
rs746749291	snp	G/T	1.87675e-05	0.00306324	intron-variant	AHCTF1	GRCh38.p7	1:246843956	GAAAAAACTGTATCT[G/T]TATCTTTATATATGT	25909
rs746763370	snp	A/G/T	3.31946e-05	0.00407387	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246860975	CTTTTCAGTTTGTTC[A/G/T]GTTACATTAGTAGTT	25909
rs746784410	in-del	-/TC	5.65254e-05	0.00531597	intron-variant	AHCTF1	GRCh38.p7	1:246894628	ATTTTAATATTAAAT[-/TC]TGTCCTACATCTAGA	25909
rs746793008	snp	C/T	1.64811e-05	0.00287059	intron-variant	AHCTF1	GRCh38.p7	1:246898175	ATAACGTGATCCAAC[C/T]AAAAGAAACAATAGA	25909
rs746802871	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246857212	CCATACTTTGAATAC[A/G]TCATCTGGTAAAGTG	25909
rs746819261	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246856033	TTACCCATTTTCTAA[C/T]GTTTTACTCTTTTGG	25909
rs746859756	snp	A/G	4.94727e-05	0.00497332	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246903999	TATTACCAAAGGCCA[A/G]CTGCAGCAGATGCAA	25909
rs746905854	snp	A/G	1.82241e-05	0.00301856	synonymous-codon, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843855	GCTCCTTAAAGCAGG[A/G]GGTGAGATGACAAAC	25909
rs746931903	snp	A/C	2.49972e-05	0.00353525	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850554	GTATGTCCTGATTAA[A/C]TTCTTTCTTTCTCCT	25909
rs746944451	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246904740	AGCATAGATTCCAGA[C/G]CCACATCATCTGAAT	25909
rs747017810	snp	C/T	1.6554e-05	0.00287693	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246918253	CATTATGTTTACCTG[C/T]AGCAAACTTTCCACG	25909
rs747049667	snp	C/G/T	4.95793e-05	0.00497871	synonymous-codon, missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864065	GCTTTGCTGAATAAA[C/G/T]TCCGAACACTGAGAA	25909
rs747061573	in-del	-/CTC	3.29603e-05	0.00405944	cds-indel, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851202	CACCTGGCTCAACTT[-/CTC]CTTCTTCACCTTCCA	25909
rs747070990	snp	A/C	1.68972e-05	0.0029066	intron-variant	AHCTF1	GRCh38.p7	1:246916129	ATGTCCAGGTATCTT[A/C]AACAGTACCTACCCT	25909
rs747071652	snp	C/T	0.000162838	0.00902179	intron-variant	AHCTF1	GRCh38.p7	1:246891963	TCCATACAGTAAATC[C/T]AAATAAATTAGAATC	25909
rs747079897	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246899942	AATTTCCTAAGTTAT[C/T]CATATGTTAACTAAC	25909
rs747097475	snp	C/T	1.65157e-05	0.0028736	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902559	CCTGTCACCATGAGA[C/T]CGAAATTTCTCTATA	25909
rs747098059	snp	A/G	1.77303e-05	0.00297739	intron-variant	AHCTF1	GRCh38.p7	1:246900476	GCGATAGAGCTGGAA[A/G]AAAAAGATAATTTTT	25909
rs747098665	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246844228	TATTTCTTTTAATCC[A/G]TACTGCTCCTCAAGC	25909
rs747108992	snp	G/T	1.65124e-05	0.00287331	intron-variant	AHCTF1	GRCh38.p7	1:246877123	CTACCAATTTATCTT[G/T]AATTTCTGACAAGTT	25909
rs747140014	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246910985	TCAGTGAAGCCTAAA[C/T]AGTTGTAATCATAAA	25909
rs747152873	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246866411	TCCATTTAAAATACC[A/G]TCTTACCAGAGTAAA	25909
rs747199866	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246855606	GGAAAGCTGACCAGA[A/G]AGAGGAATAACTGAG	25909
rs747245098	snp	A/G	1.67368e-05	0.00289277	intron-variant	AHCTF1	GRCh38.p7	1:246913429	TAGAAAACATAATAC[A/G]TGATTTGCTTTTCTT	25909
rs747264288	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246912026	GCAGCCTCCCCTCCC[A/G]CTTCCACCACTGGCA	25909
rs747265367	snp	C/T	3.3042e-05	0.00406447	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246889968	TGTTTTACTATACCT[C/T]GATAAACGCTCAAAC	25909
rs747271989	snp	A/G	1.65089e-05	0.00287301	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851329	AAACTGTTGGTCAAT[A/G]GTATCAAAATTGTAC	25909
rs747275720	snp	A/G	4.95086e-05	0.00497512	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850931	ATTGTTTCATGAATG[A/G]ACTGTTCCATTGTAT	25909
rs747308530	snp	C/T	1.75965e-05	0.00296613	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876058	GAAAAACTGATGATG[C/T]TGACAGATGATAAGG	25909
rs747316822	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246870724	AGGGTATAAAACCTC[A/C]AAAAAAAAAAAAAAA	25909
rs747321221	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246930263	AAACGTTCCCCCCGC[C/T]TCAGCCTCCCAAGTA	25909
rs747326267	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246871741	CTGACTGCAGACTAT[-/A]AAGGAGGTTAATAAT	25909
rs747329452	in-del	-/ACAC			intron-variant	AHCTF1	GRCh38.p7	1:246898634	AAAACACACACACAC[-/ACAC]ACACACACACACACA	25909
rs747368544	snp	A/G	1.64768e-05	0.00287021	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246907607	ATCAGAAAAACCTAC[A/G]GCAAGCTGATTTGTC	25909
rs747403104	snp	A/C	1.64969e-05	0.00287196	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246887304	GAAAGATTCAATGGG[A/C]GTGTCTGTTTTGTTG	25909
rs747419980	snp	G/T	1.88149e-05	0.0030671	intron-variant	AHCTF1	GRCh38.p7	1:246905676	AAACAAATTAGTATA[G/T]TTCATATTTTTAAGT	25909
rs747442353	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246901819	GGCATCAGAGTGAGA[C/T]CCCTGTCTCTAAATA	25909
rs747465807	snp	A/G	1.7009e-05	0.0029162	intron-variant	AHCTF1	GRCh38.p7	1:246857820	TCTAAATTGCCTATA[A/G]GTCATACAAATAAGA	25909
rs747536430	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246906374	CACAAGGTCAGGAGT[C/T]CGAGACCAGTCTGAC	25909
rs747546536	snp	A/G	1.65343e-05	0.00287521	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850822	GTCATCAACCTGGCT[A/G]ACATTCATAGTCATT	25909
rs747557376	snp	A/G	0.000162774	0.00902	intron-variant, utr-variant-5-prime, upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246931295	CCGACTGCCGGCGCA[A/G]GACGCGAACCACCAG	25909
rs747582142	snp	C/T	1.67206e-05	0.00289137	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246885552	ACTGGACACTGTTGG[C/T]TTCATTGTCTGAATA	25909
rs747582879	in-del	-/C	3.35233e-05	0.00409396	intron-variant	AHCTF1	GRCh38.p7	1:246855849	AAAAAGAAATACATA[-/C]CTTAGTGTGTAAGAA	25909
rs747587376	snp	A/C	1.66355e-05	0.002884	missense, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246842748	GCTTTTGGCTTTCCC[A/C]GAGTTTCTACTGATT	25909
rs747596138	snp	A/G/T	8.80153e-05	0.00663333	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850583	CTTCCTCTCCTAGGC[A/G/T]TAACAGAATTTTGAG	25909
rs747597500	snp	C/T	5.00897e-05	0.00500423	intron-variant	AHCTF1	GRCh38.p7	1:246857680	ATTTGAATTTCTCTC[C/T]ATTAACTTACCCTTC	25909
rs747603129	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246911143	GTTATAAAATTATCC[C/T]TGTGCACCTACTGAT	25909
rs747639401	in-del	-/TCAA	0.0525931	0.153397	intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842652	CAGAGCGAGACTGTC[-/TCAA]TCAATCAATCAATCA	25909
rs747656296	snp	A/C	1.6525e-05	0.00287441	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246904026	GCAAACTCAAAACAT[A/C]CCCTTCACTGAAACA	25909
rs747664719	snp	C/G	1.75041e-05	0.00295833	utr-variant-5-prime, missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246918376	AGTCTCGCATACTTC[C/G]ACTGTAAATATTTTT	25909
rs747683525	snp	A/G	1.654e-05	0.00287571	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246891790	GTACCTCTCTCAGTG[A/G]TCTCTCGGGCTTCTG	25909
rs747688439	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246908682	CACAAGGTCAGGAGA[C/T]TGAGACCATCCTGGC	25909
rs747717897	snp	A/G	2.1067e-05	0.00324547	intron-variant	AHCTF1	GRCh38.p7	1:246885454	CCATTTTATTAACAG[A/G]TACGATAAAGACTTT	25909
rs747732737	snp	A/G	1.66291e-05	0.00288345	intron-variant	AHCTF1	GRCh38.p7	1:246900312	AATACAAAGAGAAAG[A/G]AGAGAGAAAAAAAAA	25909
rs747736400	snp	C/T	3.61579e-05	0.00425178	intron-variant	AHCTF1	GRCh38.p7	1:246891091	AACATCAGTTGTTTA[C/T]TTACAAAAAAATCAA	25909
rs747744982	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246904884	CACTCCTTAGTCCTT[C/T]GCTGAGTACCCACCC	25909
rs747745047	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246847185	TCCCAGCTACTGGGG[A/G]GGCTGAGGCAGGAGA	25909
rs747748138	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246874548	TGGTGGTCATGAAAC[A/G]GCCACCCAAAAAAAT	25909
rs747799982	snp	C/T			utr-variant-5-prime, missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246918373	TTAAGTCTCGCATAC[C/T]TCCACTGTAAATATT	25909
rs747803449	snp	A/G	1.68357e-05	0.00290131	missense, synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840967	GAATTTCTATGGGAG[A/G]AGGTGACCAAGCACT	25909
rs747883397	snp	A/T	1.90569e-05	0.00308676	intron-variant	AHCTF1	GRCh38.p7	1:246862186	TGGAATTACACCATT[A/T]AAAGTGCTTATAGGC	25909
rs747899069	snp	C/G	1.64784e-05	0.00287035	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851227	ACCTTCCAATATCAA[C/G]GTAAAGTTGCTTTGA	25909
rs747933406	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246844407	GTTCCAGCCAAAGGA[A/C]CAGAAAAGTTCATCT	25909
rs747947036	in-del	-/GCGGG			downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838607	AAGTTGTAGAAGTGG[-/GCGGG]GCGGGGCGGGGGGAA	25909
rs747960854	snp	A/G	1.64855e-05	0.00287097	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861041	GAAAACAGTCTCTTC[A/G]AGGTCTTCCGGTGAC	25909
rs747966604	in-del	-/AT	4.94336e-05	0.00497135	intron-variant	AHCTF1	GRCh38.p7	1:246898186	CAACCAAAAGAAACA[-/AT]AGAGTTAAAAATCAT	25909
rs747968451	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246877505	CACGTTTAAAGAATT[G/T]TATGCTGCTTTTTAG	25909
rs747975206	in-del	-/ATCT			intron-variant	AHCTF1	GRCh38.p7	1:246871632	GACTAGATGAGCCTC[-/ATCT]TCAGGACAGGCTAAG	25909
rs747994051	in-del	-/AAAACAAAAC	1.67594e-05	0.00289472	intron-variant	AHCTF1	GRCh38.p7	1:246905501	GACTCTGTCTCCAAA[-/AAAACAAAAC]AAAACAAAACAAAGT	25909
rs748040755	snp	A/G	4.97203e-05	0.00498575	intron-variant	AHCTF1	GRCh38.p7	1:246905530	CAAAACAAAGTTTGT[A/G]TGAGACCTACCTATC	25909
rs748045156	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246892409	CACTGCAACCTCTAC[C/T]TCCCAGGTTCAAGGG	25909
rs748058979	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246865302	GGAGCCCAGAAATAA[A/G]AACTTGTAGTTGCAG	25909
rs748068412	snp	C/T	3.29864e-05	0.00406105	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849652	TGACGCTGGAGAAAA[C/T]AAAGGCTCATTGTTT	25909
rs748071561	snp	C/G/T			intron-variant	AHCTF1	GRCh38.p7	1:246926970	ACGAGGTCAGGAGAT[C/G/T]GAGACCATCCTGGCT	25909
rs748091418	snp	A/G	1.64743e-05	0.00287	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867663	TAAGAAAACATACCT[A/G]TTGAAAGGTGTGGTG	25909
rs748100554	in-del	-/GA			intron-variant	AHCTF1	GRCh38.p7	1:246861878	GGTATTTAAAAACTT[-/GA]TTTATCTAACTTTTT	25909
rs748173691	snp	G/T	1.95372e-05	0.00312541	missense, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843828	GTTCTTATTGGATGT[G/T]TTTTTTTGTCTGCTC	25909
rs748192239	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246918511	GTTACAAAATACATA[-/T]TTGGCCAGATGCGGA	25909
rs748209865	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246862479	GCAAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAG	25909
rs748220523	snp	A/G	3.30639e-05	0.00406581	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246887332	TTGGGAAAGGAATAC[A/G]TAATATCAAGTAGCA	25909
rs748233484	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246855205	CTGGGCATAGACATT[C/T]AAGGTGTCTGCTTCC	25909
rs748241395	in-del	-/CAGT	1.64762e-05	0.00287016	intron-variant	AHCTF1	GRCh38.p7	1:246877310	CCATACACCTGAAAG[-/CAGT]ATTTATCAAAGTTTA	25909
rs748241505	snp	A/C	0.000197827	0.00994356	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246895860	CCATCTTCGGATATA[A/C]CCAGTCAAAAGTCCC	25909
rs748262742	snp	C/T	1.64996e-05	0.0028722	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902569	TGAGATCGAAATTTC[C/T]CTATACTCTGGCATC	25909
rs748270702	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246901182	TCATCTCTACAAAAA[A/G]ATACAAAAATTAGCC	25909
rs748273425	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246853835	AGGAAAAAATATTTC[C/T]ACACTTTCAATGGAA	25909
rs748273760	in-del	-/TC	1.67987e-05	0.00289811	intron-variant	AHCTF1	GRCh38.p7	1:246857674	AAAAGTATTTGAATT[-/TC]TCTCCATTAACTTAC	25909
rs748294594	snp	A/G	8.24463e-05	0.00642	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902647	CCTGTCAGGTCCAGG[A/G]TGTATCTTTCTTCAC	25909
rs748305600	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246886744	GAGCCTCTGTAAATT[C/T]TGGTATGTTTCTGGA	25909
rs748333026	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246853925	TGTTTGGCAAAAAGA[C/G]GACGACGAAAAACCA	25909
rs748349335	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246920306	TTTGTGTAAATCAGC[A/G]ATTTAGCTTGATAAG	25909
rs748369982	snp	G/T	0.0020254	0.0317584	missense, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246842752	TTGGCTTTCCCAGAG[G/T]TTCTACTGATTGTGC	25909
rs748377419	snp	A/G	6.63328e-05	0.00575865	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877228	TGACAGACTTCATAC[A/G]TGTGCTTCAGTAACT	25909
rs748408002	snp	A/G	1.65405e-05	0.00287576	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849908	AGTTCCTCGTTTGGC[A/G]CTAAAATGGATTTTC	25909
rs748420187	snp	C/T	1.66944e-05	0.0028891	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246862055	TGATGGAGAGGGAGA[C/T]GCTAAAGGTGTTGAT	25909
rs748423421	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246930293	AGGCGCGCGACTAGA[A/G]GCGCCACCAATTCCC	25909
rs748426126	snp	C/T	6.61201e-05	0.00574941	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864068	TTGCTGAATAAACTC[C/T]GAACACTGAGAAGGC	25909
rs748430743	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246859914	CAGAGAGTAGAATGA[A/C]ATTCTTAATTTCTGA	25909
rs748465551	snp	A/G			downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838864	TGTTTCCCTTACTAC[A/G]ATACTAAGTATCTTT	25909
rs748484392	snp	C/G	3.34941e-05	0.00409218	intron-variant	AHCTF1	GRCh38.p7	1:246876907	AAAGCCTCCAGTTTT[C/G]CTTATTCTCTTATCC	25909
rs748537598	snp	C/T	1.92959e-05	0.00310605	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876167	CAGTGATCTCTCCCG[C/T]AAACGAGGATCACGA	25909
rs748571347	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246871931	TGTGAACTTTACAAA[C/T]GACCCTGATCCCAGA	25909
rs748572951	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246888257	CAAAGGGATAAAACC[G/T]TCAGTGGATCTTATA	25909
rs748580216	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246921155	CAAAATGACATTTAT[A/G]TAAGGTTAAAAAGAC	25909
rs748610843	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246909723	AAATCATAATGTGTG[C/T]AGGGTTCAGTACTAG	25909
rs748640066	snp	C/T	1.64751e-05	0.00287007	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246907636	TCCTGCTTATGTAAC[C/T]AAGAGTTGAAACAGC	25909
rs748652890	snp	A/G	1.64914e-05	0.00287149	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851084	GTTACGGCAGATGGC[A/G]AATTTGCAATTTGTC	25909
rs748659437	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246921064	GGCATTGCACTCCAG[A/C]CTGGGCAACAAGAGT	25909
rs748666315	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246922239	GCAGTATGTGCCCGT[A/G]GTCCCAGCTACTCAG	25909
rs748688909	snp	A/C/G	4.94265e-05	0.00497104	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849850	TTGGCTTTGACTTTC[A/C/G]GTCTTTTTTGTAAGT	25909
rs748692431	in-del	-/GC			intron-variant	AHCTF1	GRCh38.p7	1:246860804	GAGCCACAGTACCTG[-/GC]TAGGATGCTTTTCTT	25909
rs748704163	snp	A/G	1.66665e-05	0.00288669	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246860945	TTCTGATGCAAATAC[A/G]TCTTTATCTCCATCC	25909
rs748720600	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246858447	TATCCCAGCTCATGA[C/T]GCATACTCAGTAAGT	25909
rs748737238	snp	C/T	4.96973e-05	0.00498459	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246905650	CACTTTCCAATTGTA[C/T]GTAATATCTGAAACA	25909
rs748740387	snp	C/T	3.30098e-05	0.00406249	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850944	TGGACTGTTCCATTG[C/T]ATCTGAAGTAATTTC	25909
rs748742490	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246889510	ATGCCTAGTCAATCT[C/T]CCAAGCTAATGTTCA	25909
rs748765217	snp	A/T	1.74318e-05	0.00295222	intron-variant	AHCTF1	GRCh38.p7	1:246867819	TCTAGAAACTGTAAA[A/T]TGAAGAACGCTGGAA	25909
rs748797163	snp	A/C	1.65034e-05	0.00287253	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246898328	TGATTTCTTTAAAAA[A/C]GTCAAAGTCTGTAAC	25909
rs748798833	in-del	-/A	1.92721e-05	0.00310414	intron-variant	AHCTF1	GRCh38.p7	1:246907505	GTACAAGCTATATGC[-/A]AAAAAAACTACCTAT	25909
rs748810136	snp	C/T	1.64746e-05	0.00287002	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867686	GTGTGGTGCTATTTA[C/T]AGGTTCTTTGCTTGC	25909
rs748832449	in-del	-/AT			intron-variant	AHCTF1	GRCh38.p7	1:246862719	AAAAGTGCCAATTAG[-/AT]TAAGATAAATTACTT	25909
rs748841123	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246905129	ACTAATTCACTGAAA[C/G]AATTGTGTTGCCTTC	25909
rs748845661	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246844578	AATTTTTAAAAGATT[A/G]GCCAATGTGGTGGTG	25909
rs748850182	snp	A/G	1.65277e-05	0.00287464	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246905550	ACCTACCTATCTTGT[A/G]TAGACTGAACAGCCC	25909
rs748860563	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246870598	TCCAGGGATTATAGG[A/T]ATTTTACATTTAAAA	25909
rs748896913	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246859660	CTGCATCCCCAACCT[C/T]GACCTCCTGGGTCCA	25909
rs748915510	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246926283	GCAACACAGGCTAAC[A/G]TATTTCTAATTCAAA	25909
rs748969270	snp	C/T			missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850724	TTAGGAGTAGCAACA[C/T]CTGCTGATGCTTCCT	25909
rs748997494	snp	A/G	1.64887e-05	0.00287125	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246855801	TCGTCCAACACTGGT[A/G]CCTTGGACTTCTGGG	25909
rs749008373	snp	C/T	1.68758e-05	0.00290476	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246885571	ATTGTCTGAATATAT[C/T]TGAGGGCTTGTCTGT	25909
rs749008578	in-del	-/CTTCTCTCACATCTGATGGACTAA	4.94605e-05	0.0049727	cds-indel, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850155	ACTCAAGGTTGGAGT[-/CTTCTCTCACATCTGATGGACTAA]CTTCTCTCCCTCTGA	25909
rs749036247	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246926986	GAGACCATCCTGGCT[A/G]ACAAGGTGAAATCCC	25909
rs749043981	snp	A/T	3.30535e-05	0.00406518	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851335	TTGGTCAATAGTATC[A/T]AAATTGTACTGAAGC	25909
rs749046482	snp	C/T	8.24559e-05	0.00642037	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850200	TCCCTCTGACCCTTC[C/T]AACATGTTTAATACG	25909
rs749063191	snp	A/T	2.44412e-05	0.00349571	intron-variant	AHCTF1	GRCh38.p7	1:246851459	TAAATGAATTAAAGA[A/T]AAGAGACTGGTTAAA	25909
rs749085095	snp	C/T	1.67167e-05	0.00289103	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916165	GAAGAACAACTGCTT[C/T]AACTACTTTTGATAT	25909
rs749111022	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246845514	AAAGTATTTCTACGA[A/C]AATTATACATTCTAT	25909
rs749115287	snp	A/G	1.66261e-05	0.00288319	intron-variant	AHCTF1	GRCh38.p7	1:246861333	GAAAAAAATTAGTAA[A/G]TATCACAGTTAAGTC	25909
rs749131586	snp	G/T	4.95201e-05	0.0049757	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246889984	GATAAACGCTCAAAC[G/T]TCTGTCGACGACTGG	25909
rs749136991	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246868469	CATGTTGGCCAGACT[A/G]GTCTCAAACTCCGGG	25909
rs749148447	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246895030	GGCCTAATTCCTTTA[A/T]AAAAAAAAAGGTCAA	25909
rs749173898	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246877734	AGTAGAGCTTGGTAG[C/T]AGATGTTTTTTGGTT	25909
rs749215652	snp	C/T	1.64743e-05	0.00287	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849713	TTGCTAGACCGAGTC[C/T]TGCTGCTGCGGGATG	25909
rs749240210	in-del	-/C			intron-variant	AHCTF1	GRCh38.p7	1:246875928	TATCTCCAAGGCATG[-/C]CTGTATGTGTTAGCG	25909
rs749243963	snp	C/T	1.65121e-05	0.00287329	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861157	TTTGTGACCCCTCAT[C/T]CATTTCTTGATGCTC	25909
rs749273645	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246913659	GAGAGCTTACTGATA[C/T]GCCAGGCATTGTGTT	25909
rs749304075	snp	A/G			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932527	GAGTGCTGTGGCACG[A/G]TCTTGGCTCACTACA	25909
rs749304732	in-del	-/TC			intron-variant	AHCTF1	GRCh38.p7	1:246908260	AGGACATTTTGGGCA[-/TC]AAAAACAATAAAATT	25909
rs749318042	snp	A/C	1.64882e-05	0.00287121	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851092	AGATGGCAAATTTGC[A/C]ATTTGTCCATGATTA	25909
rs749336183	snp	C/T	1.66252e-05	0.00288311	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246860965	TATCTCCATCCTTTT[C/T]AGTTTGTTCAGTTAC	25909
rs749365487	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246886907	TCAAGGCCAAATCTT[A/G]CCTTCCATGGTTCCC	25909
rs749378492	snp	C/T			downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838990	TTTACCTTACTACTA[C/T]GATACTAAGCACCTT	25909
rs749395017	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246854588	TACATGAGAAAAGAA[A/G]GTTGCTTTTTTGATA	25909
rs749397589	snp	A/G	3.29647e-05	0.00405971	intron-variant	AHCTF1	GRCh38.p7	1:246898165	TAGAAAGCTAATAAC[A/G]TGATCCAACCAAAAG	25909
rs749406446	in-del	-/C	1.95082e-05	0.00312309	frameshift-variant, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246885676	AACAAAAGATCCAAA[-/C]CACTCTGGAAATAAC	25909
rs749408331	in-del	-/TTGTTTAC	1.7814e-05	0.00298441	intron-variant	AHCTF1	GRCh38.p7	1:246891084	AAGAGTTAACATCAG[-/TTGTTTAC]TTACAAAAAAATCAA	25909
rs749427189	in-del	-/TA			intron-variant	AHCTF1	GRCh38.p7	1:246909078	ATATCTATATATATC[-/TA]TATCTATCTATCTAT	25909
rs749438002	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246894794	AAGATTATTAATTAC[A/T]AACAGAGTTCTAAAT	25909
rs749444646	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246873195	TACTCTTGATATATT[C/T]AAACTTTCTCCCTTA	25909
rs749448420	snp	C/T	1.64795e-05	0.00287045	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246895896	ACTAGTCTGAATTGC[C/T]GCTGACAATATAGCT	25909
rs749450421	snp	A/C	1.64893e-05	0.0028713	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246903977	TGTCCTGATGCCAAA[A/C]ACTTTCTATTACCAA	25909
rs749498949	snp	G/T	1.85273e-05	0.00304357	intron-variant	AHCTF1	GRCh38.p7	1:246843949	AAAAGTTGAAAAAAC[G/T]GTATCTGTATCTTTA	25909
rs749533245	snp	C/G	2.07514e-05	0.00322107	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867291	TGTTCCAAAAAATGC[C/G]TCAGGCAGCTCTGGA	25909
rs749535591	snp	A/C			utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840612	AATGTATGAAGTCTT[A/C]ATATAAAATAGAAAA	25909
rs749540526	snp	A/G			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933627	AGTGCATGGCTATTC[A/G]CAGGCACTATGGCCT	25909
rs749543190	snp	A/G			synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246888502	AATCATCAAGCAATC[A/G]GGATTCCACTTCCCT	25909
rs749552372	snp	C/G	1.91496e-05	0.00309426	missense, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843836	TGGATGTGTTTTTTT[C/G]TCTGCTCCTTAAAGC	25909
rs749557651	snp	A/C	1.71684e-05	0.00292983	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840974	TATGGGAGGAGGTGA[A/C]CAAGCACTTTCTTTT	25909
rs749574538	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246841550	ACAGCATAAACAAGA[C/T]ACTGTGTAACAAATA	25909
rs749583750	snp	A/G	3.4822e-05	0.0041725	intron-variant	AHCTF1	GRCh38.p7	1:246860856	ATAAACTTTATTGAG[A/G]GACATTAATAACAAT	25909
rs749584903	in-del	-/G			intron-variant	AHCTF1	GRCh38.p7	1:246904190	TTTTATAAAAATGTA[-/G]GTCCTTTGAAATAAT	25909
rs749618289	snp	A/G/T			intron-variant	AHCTF1	GRCh38.p7	1:246862567	TCATCTCCAATAAAC[A/G/T]TATCAATAGAAATAT	25909
rs749618388	in-del	-/TTGTT	1.66618e-05	0.00288628	frameshift-variant, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246842702	GTCATACTTGCTTGC[-/TTGTT]TTGTTTTTGACGTCC	25909
rs749625852	snp	A/G	3.29853e-05	0.00406098	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877001	GGCAGGCACATAATT[A/G]GCACGCTGCAAATGG	25909
rs749630994	snp	C/G/T	5.13249e-05	0.00506559	intron-variant	AHCTF1	GRCh38.p7	1:246855689	TCTTCACTCAAAACA[C/G/T]AAAAATGGAATAATC	25909
rs749684159	snp	G/T	1.95785e-05	0.00312871	intron-variant	AHCTF1	GRCh38.p7	1:246862191	TTACACCATTAAAAG[G/T]GCTTATAGGCCGGGC	25909
rs749753377	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246881334	GAACTGAGACATCCA[C/T]CATTAGCGTCAGCAA	25909
rs749756762	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246848090	AAAATCGAAGATCCA[A/G]TTAAAAATTTTCTGA	25909
rs749757853	snp	A/G	1.64857e-05	0.00287099	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246913292	ATAGGTCAACAAGAA[A/G]GATCTGTCCAACATC	25909
rs749768710	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246928417	TTCGACAAGGTCACA[A/G]TGCCTTTGGACTAAC	25909
rs749795710	snp	A/G	1.65143e-05	0.00287348	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840920	TTTGCTCTTGACTCC[A/G]TCAGCTGGGCTAGCC	25909
rs749835821	snp	C/T	4.94548e-05	0.00497242	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851160	CTGTGTTAGCTGCTT[C/T]AGGTAACACATCAGA	25909
rs749835998	snp	A/G	3.31082e-05	0.00406854	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849941	AAAGCTGGTTTTCCA[A/G]CATCAACATTTTCAC	25909
rs749880184	snp	A/G	3.40344e-05	0.00412505	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853263	TCAGAGATAGTGAGC[A/G]AGGAGTTTCCACCAT	25909
rs749886223	snp	G/T	1.64985e-05	0.0028721	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851051	AAAGTGTCTACTTTT[G/T]GGGACTTTTGGTCAC	25909
rs749891546	snp	G/T	1.86218e-05	0.00305132	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876146	GTCTAATATAGAATT[G/T]CGAGCCAGTGATCTC	25909
rs749933821	snp	C/T	1.64746e-05	0.00287002	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246907703	GCGCCCTTGTCTCAT[C/T]ACACTTTCTCTAATG	25909
rs749950409	in-del	-/CTC	1.65007e-05	0.00287229	cds-indel, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246888462	ACTTCTCAATTCGCT[-/CTC]CTAACTGAGAAACCA	25909
rs749966562	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246888962	ATGATGAGAACTACA[A/G]ACATCAAGGAGAGTT	25909
rs749968334	snp	C/G	1.65002e-05	0.00287225	intron-variant	AHCTF1	GRCh38.p7	1:246895958	GAAAGGAAAGAAATG[C/G]AAAGAAAGAGGGTGT	25909
rs750016817	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246928428	ACAGTGCCTTTGGAC[-/T]TAACAGGTCCTAAAT	25909
rs750027057	snp	C/G	1.67203e-05	0.00289134	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246860925	TGTAGGTCTGAAGGA[C/G]TTACTTCTGATGCAA	25909
rs750099909	in-del	-/TCTTTATGTTG	1.78438e-05	0.0029869	intron-variant	AHCTF1	GRCh38.p7	1:246867827	TGTAAAATGAAGAAC[-/TCTTTATGTTG]GCTGGAATTAAGTGC	25909
rs750100103	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246883155	CAGAAGGGTGAGTCC[A/G]GGGAGAGTGTTAGTG	25909
rs750108240	snp	G/T	5.00271e-05	0.0050011	intron-variant	AHCTF1	GRCh38.p7	1:246895786	ATAACAAATAGCAAG[G/T]TGATAACTTTAAAAA	25909
rs750111395	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246923928	ATGCCACAGGACCTG[A/T]GAAGAGGGCCATGTT	25909
rs750113737	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246909560	TCAACTGTCGCAGTA[C/T]TGCAGTGCTTGTGTT	25909
rs750124737	snp	C/T	3.49034e-05	0.00417738	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853278	GAGGAGTTTCCACCA[C/T]CACCAAGGACATCAG	25909
rs750128073	snp	C/T	1.65935e-05	0.00288036	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246857792	AACTAAGAGATCCTT[C/T]GTTTCTGCATCTTCT	25909
rs750150213	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246861793	TAGCCAATGGCCCTA[C/G]TGTTTCTTTCAGAAC	25909
rs750157810	snp	A/G	1.65012e-05	0.00287234	intron-variant	AHCTF1	GRCh38.p7	1:246863888	AAGTAAGAGCCATCT[A/G]GTTTGATTGTGAACG	25909
rs750193849	snp	A/G	1.67399e-05	0.00289304	intron-variant	AHCTF1	GRCh38.p7	1:246918234	ATTAGTAAATGTTCA[A/G]TGACATTATGTTTAC	25909
rs750195258	in-del	-/C	0.000120755	0.00776937	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840773	ATTCTGATGACTTTA[-/C]AAATAGGTGTACATT	25909
rs750206531	snp	A/C	1.66532e-05	0.00288554	intron-variant	AHCTF1	GRCh38.p7	1:246900295	GGTCAGCTACACATA[A/C]AAATACAAAGAGAAA	25909
rs750209176	snp	C/G/T	3.31577e-05	0.00407161	intron-variant	AHCTF1	GRCh38.p7	1:246891773	TTGATAAAACAAAGA[C/G/T]CGTACCTCTCTCAGT	25909
rs750230045	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246848902	AACCATTAACACTTT[C/T]ACAGAGAGTTACTCT	25909
rs750243290	snp	A/C/T	3.29507e-05	0.00405887	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246898272	CCAGCTACAAGACAT[A/C/T]GATTATAACCATCAG	25909
rs750245602	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246923110	AATCAAATAATACCA[-/A]AAAAAAAAAAAAAAA	25909
rs750259513	snp	A/G	1.69146e-05	0.0029081	intron-variant	AHCTF1	GRCh38.p7	1:246913221	TTGGTTTCAAGTAAA[A/G]AACTGATTACCTGAT	25909
rs750262279	snp	A/G	1.72047e-05	0.00293293	intron-variant	AHCTF1	GRCh38.p7	1:246891063	AAGTCTATCAGTCCT[A/G]TAAAGAAGAGTTAAC	25909
rs750274819	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246863454	AAGTTGAGTGCTGTG[A/G]TTTCTCAGCTAATAA	25909
rs750276606	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246846845	CAACCTCAACCTCCC[A/G]GGCTCAAGCCATCCT	25909
rs750328148	in-del	-/AAAT			intron-variant	AHCTF1	GRCh38.p7	1:246845376	TCTTAAAAAAAAGAA[-/AAAT]AAATAGAGTTGATAT	25909
rs750352407	snp	A/G	1.65422e-05	0.0028759	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849968	TCACTTTTAGCTGGG[A/G]TATTTCTTGTAGATC	25909
rs750377497	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246928890	AAATTTCTTACCAAC[A/T]TAATTCAAACATTTT	25909
rs750408583	in-del	-/CTGA			intron-variant	AHCTF1	GRCh38.p7	1:246927476	CCTCAGCAACACAGC[-/CTGA]CTGTCTCAAAAAGAA	25909
rs750428516	snp	A/G	4.77829e-05	0.00488765	intron-variant	AHCTF1	GRCh38.p7	1:246876214	CAAAATTGGTAAAAA[A/G]TTTAACCTTCAAAAT	25909
rs750441271	snp	A/G	0.000100239	0.0070788	intron-variant	AHCTF1	GRCh38.p7	1:246900024	TTTACATACTTTTGT[A/G]CATTACTTTTCTTAA	25909
rs750454838	in-del	-/TA			intron-variant	AHCTF1	GRCh38.p7	1:246909067	AGATAATTCTATATC[-/TA]TATATATATCTATAT	25909
rs750459242	snp	A/T	1.64827e-05	0.00287073	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851309	TTGTTATCAGCTAAG[A/T]CACAAAACTGTTGGT	25909
rs750468056	snp	C/T	1.65784e-05	0.00287905	intron-variant	AHCTF1	GRCh38.p7	1:246889943	TTCTTACAGATGTAA[C/T]TTCTAAAATTGTTTT	25909
rs750506512	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246919072	CCCAGAATGACTACT[C/T]CCATTATAAACAACC	25909
rs750508648	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246870261	ATAGCCTGGGCGACA[C/T]AGTGAGGCCCTCTCT	25909
rs750510027	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246905405	CGGGAGGCTGAGCGA[C/G]AGAATGGCATGAATC	25909
rs750519336	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246857006	TTATTCAAAAGTGCG[C/G]ACATGCAATCTGTGT	25909
rs750535535	snp	A/G			utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840197	AAGCTTGCCGAATAA[A/G]AGATGCCAACATTAT	25909
rs750591278	snp	A/G	1.64836e-05	0.0028708	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246905616	TCTTGAAAAGTGACA[A/G]CATATACAGGAACTT	25909
rs750623456	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246925725	GGAGGTGTCTGGGTC[A/G]TGGGAGAGGACCCCT	25909
rs750623731	snp	C/G	3.29506e-05	0.00405884	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849688	AGAAAGGTCCGGCAA[C/G]AAGATGGCCTTGCTA	25909
rs750627497	snp	G/T			missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246862095	GACCTCAGGATGGAC[G/T]GAGGAGTGAACTCAG	25909
rs750634497	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246893516	GTATCCCTACTAGTA[C/T]TTTTTAGCCTTATTT	25909
rs750663479	snp	C/G/T	9.99978e-05	0.0070704	missense, synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850774	CACGTTTTGGATACG[C/G/T]TGACCTCTCGTACGA	25909
rs750671480	snp	C/T	2.00749e-05	0.00316813	intron-variant	AHCTF1	GRCh38.p7	1:246876000	CAGTATCTTTTTTGA[C/T]CCAATAGATTATGAT	25909
rs750710937	snp	A/G	3.32629e-05	0.00407803	intron-variant	AHCTF1	GRCh38.p7	1:246887193	ATGAAAGTTTATGCT[A/G]TAAGTGAATAGACTT	25909
rs750719857	snp	C/T	1.66835e-05	0.00288816	intron-variant	AHCTF1	GRCh38.p7	1:246902691	CTGTAACATAAAATA[C/T]ACGCAAATATTAATC	25909
rs750720380	snp	A/G	1.67304e-05	0.00289222	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867793	TTTGGAACTGCTGAT[A/G]ATGGTTTGGGTCTAG	25909
rs750747706	snp	C/G	1.65509e-05	0.00287666	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864088	ACTGAGAAGGCCGGG[C/G]GACAGGCTGAACAAC	25909
rs750750298	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246878169	TTGGGAGGCCAGGGT[A/G]GGCAGATCACTTGAG	25909
rs750768183	in-del	-/AAAT	2.98681e-05	0.00386435	intron-variant	AHCTF1	GRCh38.p7	1:246853339	TACATTTAAACTGAA[-/AAAT]AAATAAATCCACACA	25909
rs750770271	snp	A/G	1.71132e-05	0.00292511	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916285	CAGCTAAAACTACAG[A/G]AGGCTGTTCATTGAC	25909
rs750775634	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246874547	ATGGTGGTCATGAAA[C/T]GGCCACCCAAAAAAA	25909
rs750794098	snp	C/G	0.000115349	0.00759349	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902622	CTGTCCCCTCAAAGG[C/G]AACATGCCACCTGTC	25909
rs750825292	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246911878	TTTAAGTTTTGTTCA[C/G]ATGATTTTGGCTCTT	25909
rs750828165	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246901694	GTGGTGGTGTGTGCC[A/G]GCAGTCCCAGTTACT	25909
rs750851570	snp	C/T	1.66413e-05	0.0028845	synonymous-codon, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246842741	TCGTTTCGCTTTTGG[C/T]TTTCCCAGAGTTTCT	25909
rs750855690	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246926706	ACTAAATACAGAAAA[C/G]TAACCAGGTGTGGTG	25909
rs750864401	snp	C/T	3.35475e-05	0.00409544	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850365	CAACACTTTCCTGAT[C/T]TTCTACAGATCTTTT	25909
rs750919421	snp	C/T	2.01428e-05	0.00317348	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853098	TTTTTTACATGAATT[C/T]CTTGAGTATCAGGAG	25909
rs750924356	snp	C/T	1.83994e-05	0.00303305	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851418	CTCCTGAATCTTGAG[C/T]TTCAAGCTTTTCTTG	25909
rs750941605	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246912826	ACAAACATAAACAAT[A/C]TGCCAAGAACACTAT	25909
rs750942522	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246871565	AAACAAGGTATACAG[C/T]GCTGTCCTCACTTGG	25909
rs750975661	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246852125	GAACATTACCACCCA[C/G]CTAGACAATGACATT	25909
rs750981675	snp	C/T	3.55859e-05	0.00421802	intron-variant	AHCTF1	GRCh38.p7	1:246862157	ACTTTTAGCTTTCTA[C/T]AGTAAAGAGCAAATG	25909
rs750982197	snp	C/G	1.65051e-05	0.00287267	intron-variant	AHCTF1	GRCh38.p7	1:246877108	AAAATAGATTGTAAA[C/G]TACCAATTTATCTTG	25909
rs750990107	snp	A/G	1.65053e-05	0.0028727	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246890028	AATTACAGGGTAGTT[A/G]TAGCATAACCTTGAC	25909
rs751002835	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246928986	CTTCCTGACTTTAAG[G/T]AGTTTACAATCTAGA	25909
rs751039101	snp	C/G	6.21022e-05	0.005572	intron-variant	AHCTF1	GRCh38.p7	1:246876237	TTCAAAATGTTAGGT[C/G]CTGTAATTCTATATT	25909
rs751048463	snp	A/G	1.66405e-05	0.00288443	intron-variant	AHCTF1	GRCh38.p7	1:246900303	ACACATACAAATACA[A/G]AGAGAAAGGAGAGAG	25909
rs751050073	snp	C/T	3.30759e-05	0.00406655	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849983	GTATTTCTTGTAGAT[C/T]TCCTTCTAATGCTGG	25909
rs751073668	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246863579	CAAAGAACTAAATAG[C/T]ATTTGATAGAAGAAA	25909
rs751091206	snp	C/G	1.6507e-05	0.00287284	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246913381	CTTGCACTGGCTCCT[C/G]CATGATTAATTATAG	25909
rs751094813	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246898463	AATTATGAAAGACTA[C/T]ATTTCCTGCAAGAAA	25909
rs751106321	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246908505	TTTCAGAGTGACCAG[-/A]AAGCCCTAATTAATG	25909
rs751116630	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246925438	GATATAGAAGTACTA[C/G]CTCTAAGAGAATAAA	25909
rs751119655	snp	A/G	6.59446e-05	0.00574177	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246888403	ACCTACATGCAGACT[A/G]GCAGGAGGATATTTT	25909
rs751161621	snp	A/G	1.64846e-05	0.0028709	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851130	CCCCACTGCATACAA[A/G]TTTTTCTTCAGTTGC	25909
rs751176388	in-del	-/ATTTA			intron-variant	AHCTF1	GRCh38.p7	1:246870751	AAAAAGCCCTAGGCT[-/ATTTA]ATTTCTCAGGGACAG	25909
rs751184939	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246910601	CTTGTATTCTTCTAA[A/C]TATCTGAAGATGTCT	25909
rs751251729	multinucleotide-polymorphism	AT/GC			intron-variant	AHCTF1	GRCh38.p7	1:246869087	CTGACCTCGTGATCC[AT/GC]CCGCCTTGGCCTCCC	25909
rs751274435	snp	A/G	1.85903e-05	0.00304874	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246885662	CAGTAGCTGGATGAA[A/G]CAAAAGATCCAAACC	25909
rs751275830	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246849004	TATTACTGCAGATAT[A/G]TTGTATATCTGTTTG	25909
rs751280371	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246870367	GGTCAAGGCTACAAT[A/G]AGCTATGATTATACC	25909
rs751285402	snp	A/G	1.6498e-05	0.00287206	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850679	TCTTTTGCCTTCCTA[A/G]TTTTCTTCCTGACTG	25909
rs751287332	snp	A/G	1.68366e-05	0.00290138	intron-variant	AHCTF1	GRCh38.p7	1:246855856	AATACATACCTTAGT[A/G]TGTAAGAAGATCCCA	25909
rs751312983	in-del	-/TG	7.06826e-05	0.00594444	intron-variant	AHCTF1	GRCh38.p7	1:246849591	ACTGAGATGAAAAAC[-/TG]TTTTGCAGAGAAAGA	25909
rs751317888	snp	C/T	1.64963e-05	0.00287192	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246888223	TCTAATAGGTACATA[C/T]CAAGTACTGCCTATA	25909
rs751320115	in-del	-/TTACC			downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838893	TTCTGAGTACATTGT[-/TTACC]TTACTACTGATACTA	25909
rs751325576	snp	C/G	1.65562e-05	0.00287712	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246891869	ATTGCTGGATAGACT[C/G]TATAGTTTGTGGATC	25909
rs751337087	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246885892	TGCAGATAGAAAACA[A/T]TTGAAAAAATAAGGC	25909
rs751345811	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246851545	GTGTGCCTTTTAAAA[A/C]ATAAATTATATTTAA	25909
rs751362444	snp	C/G/T	3.36006e-05	0.00409871	missense, synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246918358	TAGTCACTTGAGCTC[C/G/T]TAAGTCTCGCATACT	25909
rs751388025	snp	C/T	1.66305e-05	0.00288357	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246885538	ATAACATCGTTACCA[C/T]TGGACACTGTTGGCT	25909
rs751414007	snp	A/C	0.000133449	0.00816742	intron-variant, missense, utr-variant-5-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246931148	GCCAGGCCCAAGCGC[A/C]TGTGGAACACACGCC	25909
rs751431703	in-del	-/AAAACAAAGAAA			intron-variant	AHCTF1	GRCh38.p7	1:246891628	CTGTAGCTTTTCATT[-/AAAACAAAGAAA]CAAACAAAAACCCTA	25909
rs751449296	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246858149	TATTTTTAGTAGAGA[C/T]GGGGTTTCACTGTTT	25909
rs751449578	snp	C/G/T	1.64939e-05	0.0028717	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246905577	GCCCACAAGTAACAG[C/G/T]AATTCCGAGGATCAT	25909
rs751465750	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246871110	CCAAATGCTAGGACC[A/C]CTAAAAAAGGTGGTG	25909
rs751484045	snp	C/T	1.64841e-05	0.00287085	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246855783	TCAACAGATGTTAAT[C/T]CTTCGTCCAACACTG	25909
rs751496666	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246891111	AAAAAAATCAAGATG[C/T]TCCACAGTTTTCAAA	25909
rs751521719	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246920368	GATTTGAAAAAATTT[C/T]TAAAAATGAAAAATT	25909
rs751527009	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246919427	TTATATGGAAATCCT[C/G]AAGAGGCCGGGCGTG	25909
rs751553846	snp	C/T	1.64836e-05	0.0028708	intron-variant	AHCTF1	GRCh38.p7	1:246863904	GTTTGATTGTGAACG[C/T]TAGATGCGTAAATAC	25909
rs751554306	snp	A/G	1.71408e-05	0.00292747	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246890958	GTAAATATTTTACCT[A/G]TGCCTTCTGGTAAAA	25909
rs751573964	snp	C/T	3.33367e-05	0.00408255	missense, stop-lost, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840959	AATCAGCCGAATTTC[C/T]ATGGGAGGAGGTGAC	25909
rs751584930	in-del	-/A	0.00113992	0.0238466	intron-variant	AHCTF1	GRCh38.p7	1:246841002	TTTTCTGTGTTTCTG[-/A]AAAAAAAAGATATGA	25909
rs751596748	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246881811	CCACTGCACCCCAGC[C/T]TGGGTAACAGAGCAA	25909
rs751600674	snp	C/G	1.65682e-05	0.00287817	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877216	AAGCCCATTTCCTGA[C/G]AGACTTCATACATGT	25909
rs751603752	snp	C/T	1.70749e-05	0.00292184	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916297	CAGGAGGCTGTTCAT[C/T]GACTCCACTGAATCT	25909
rs751614611	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246887898	AGTATTTTAGAGCAA[C/G]TGTTGTTAACTTTTT	25909
rs751625418	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246845202	ATGATTCTTTAAAAA[A/C]ATGTTTTTTGTGGGT	25909
rs751633142	snp	A/G	1.82048e-05	0.00301697	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853129	GGCTGTCAGAAATTG[A/G]AAGCTTTTCTTCTGG	25909
rs751643886	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246859214	TCATCTTAAACTACT[C/T]AAGATGCAGATTTTT	25909
rs751673109	snp	C/T	3.30186e-05	0.00406303	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246890038	TAGTTGTAGCATAAC[C/T]TTGACAACTGCACAG	25909
rs751751409	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246893632	CAAGAAGGAAAATGA[G/T]TTGCCACAATAATAA	25909
rs751758088	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246879930	AAGCAAATCCTTTAT[A/G]TAATTATAAAATTAG	25909
rs751803469	snp	C/T	1.66134e-05	0.00288208	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861973	CCCCAGGAATCCATT[C/T]TGGGTGGACATCTTC	25909
rs751816772	snp	A/G	4.29415e-05	0.00463345	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851441	TTTTCTTGTTCAATC[A/G]CCTAAATGAATTAAA	25909
rs751821443	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246845856	TTTCTAAGGTATAAA[C/T]GTGCCTCCTGTGGCC	25909
rs751864283	snp	A/T	3.41711e-05	0.00413333	intron-variant	AHCTF1	GRCh38.p7	1:246867369	ATGAAAATAAAAATT[A/T]AACTTCTGATGTATC	25909
rs751873184	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246910459	TTATGTAATAAAATA[C/T]CCCTATTTGCTTTAA	25909
rs751879303	snp	C/T	1.66966e-05	0.00288929	intron-variant	AHCTF1	GRCh38.p7	1:246900044	ACTTTTCTTAAGAGG[C/T]AATGTTAAGGAAATA	25909
rs751891708	snp	A/C	1.66952e-05	0.00288917	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246860938	GAGTTACTTCTGATG[A/C]AAATACATCTTTATC	25909
rs751903122	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246902376	CTGGAGAGCAAGAAA[C/T]ATCTAGTATCTCATA	25909
rs751938802	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246853681	GCAATCTGGGCTTTG[A/C]TACAACTAGGATAAA	25909
rs751941316	snp	C/G	1.65214e-05	0.0028741	intron-variant	AHCTF1	GRCh38.p7	1:246895974	AAAGAAAGAGGGTGT[C/G]AGATCATAGGCAAGT	25909
rs751945332	in-del	-/TT	4.99122e-05	0.00499536	intron-variant	AHCTF1	GRCh38.p7	1:246889922	ACTATTCTGAGAAAC[-/TT]TGACTTCTTACAGAT	25909
rs751945573	snp	C/G	1.64819e-05	0.00287066	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902635	GGGAACATGCCACCT[C/G]TCAGGTCCAGGGTGT	25909
rs751958521	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246914667	ACAAAAATAAACATA[A/G]TGAGTGTATACTGCA	25909
rs751974412	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246888103	TTGCAATTAGATATG[C/T]CAGGTTTCCACTACT	25909
rs751977393	snp	A/G	5.08091e-05	0.00504004	intron-variant	AHCTF1	GRCh38.p7	1:246903916	GAAAACAACAAAATG[A/G]TAATATAAACCCATA	25909
rs751982201	in-del	-/T	1.65015e-05	0.00287237	intron-variant	AHCTF1	GRCh38.p7	1:246877101	AAAGAACAAAATAGA[-/T]TGTAAACTACCAATT	25909
rs751990889	snp	C/T	2.00672e-05	0.00316752	missense, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843817	TCTTCAAGCTTGTTC[C/T]TATTGGATGTGTTTT	25909
rs752024333	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246903195	TCGGTTCTAGAGACA[C/G]GTATGTGAGGGTGAA	25909
rs752030285	snp	C/T	5.1343e-05	0.00506645	synonymous-codon, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843903	AACTAATTCTTTCAG[C/T]TGTGCAGGAACCTCT	25909
rs752039964	snp	A/C	1.67866e-05	0.00289707	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850371	TTTCCTGATTTTCTA[A/C]AGATCTTTTAATTCT	25909
rs752056188	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246855123	CTAGAGTCAGATAAC[A/T]ACTATGTCATAGTAT	25909
rs752056968	snp	A/G	2.99999e-05	0.00387286	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867248	TAAACTCTTACCTAG[A/G]AATTTTTTGTGATGC	25909
rs752099901	snp	G/T			downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838753	ATGCTTCTATCTACA[G/T]CTAGGAAGCCTTCAA	25909
rs752108126	snp	A/G	1.66034e-05	0.00288122	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864115	CAACCAAATCTAGCA[A/G]TCTGTAATCAGAATG	25909
rs752156514	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246849343	ATTAAAAGTCACTTA[C/T]AATTTATAAAACTCA	25909
rs752173216	in-del	-/AAAAAAACAAAACAA			intron-variant	AHCTF1	GRCh38.p7	1:246901614	GCGAGACTCCATCTC[-/AAAAAAACAAAACAA]AAAAAAACAAAACAC	25909
rs752175047	snp	C/T	1.74695e-05	0.00295541	intron-variant	AHCTF1	GRCh38.p7	1:246916427	TTGCCTATTTTAATA[C/T]TGTATATACACAAAA	25909
rs752175571	in-del	-/TCC	0.000132103	0.00812612	cds-indel, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849896	ATCACCATCGAAAGT[-/TCC]TCGTTTGGCACTAAA	25909
rs752175697	snp	A/T	1.65603e-05	0.00287747	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246891877	ATAGACTGTATAGTT[A/T]GTGGATCCATGAAAT	25909
rs752204222	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246865822	CATTAGGTCTCAGGT[C/T]TTCAACCCTGAGACC	25909
rs752224289	snp	G/T	1.68969e-05	0.00290657	intron-variant	AHCTF1	GRCh38.p7	1:246902512	ATGACATATTTCAAG[G/T]ACTTTAACTAACCTT	25909
rs752228896	snp	C/T	1.66813e-05	0.00288797	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900414	AGAAGGCTTTCCCTG[C/T]CCATATATATTCACC	25909
rs752260137	snp	C/T	1.6483e-05	0.00287076	intron-variant	AHCTF1	GRCh38.p7	1:246863911	TGTGAACGCTAGATG[C/T]GTAAATACTAACCTT	25909
rs752270952	snp	C/G	1.64917e-05	0.00287151	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850118	GACATATCAAATTCT[C/G]CTTGAACAGTCAACT	25909
rs752272755	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246930746	CTACAGGTTCTTTAG[A/G]ATATTCTGAGAATAA	25909
rs752328787	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246919606	TAGTCTCACCTACTC[C/G]GGAGGCTGAAGCAGG	25909
rs752356538	snp	C/T	1.65211e-05	0.00287407	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246913394	CTCCATGATTAATTA[C/T]AGGTTCAATAGCTGT	25909
rs752357903	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246886312	CTCCAGCCTGGGTGA[C/G]AGAGCGAGACTCCAT	25909
rs752372720	snp	G/T	3.29587e-05	0.00405934	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850894	TTTAGTGGGACACAT[G/T]ATGTTTTGGCTCACT	25909
rs752382325	snp	C/T			missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853245	TCAGAGACAATAGGA[C/T]CTTCAGAGATAGTGA	25909
rs752398166	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246845528	AAAATTATACATTCT[-/A]TAACTCTCTTCTAGG	25909
rs752410972	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246904366	TGCCTAAAGTTCTAT[-/A]AACATCTCCCAGCTT	25909
rs752412028	snp	A/G	1.6691e-05	0.00288881	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246899508	GTTTAACAAACAAGT[A/G]GCATCTAAAAAAAAG	25909
rs752425265	snp	C/T	1.64741e-05	0.00286998	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849707	ATGGCCTTGCTAGAC[C/T]GAGTCCTGCTGCTGC	25909
rs752428674	snp	C/T	6.61496e-05	0.00575069	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849990	TTGTAGATCTCCTTC[C/T]AATGCTGGGAGCTTC	25909
rs752434013	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246859429	GTTTGTCAGTATAGT[C/T]CACCATGCTCTGTGT	25909
rs752440524	snp	C/T	3.30808e-05	0.00406686	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246887211	AGTGAATAGACTTAC[C/T]TCATAGTCATTATGA	25909
rs752444713	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246871241	ACAAACCATGACTCA[A/G]ACATTAATGGTCTAG	25909
rs752454417	snp	C/T	1.64958e-05	0.00287187	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876994	GCTTCAAGGCAGGCA[C/T]ATAATTGGCACGCTG	25909
rs752478555	in-del	-/G			intron-variant	AHCTF1	GRCh38.p7	1:246874911	AGACAGAGTCTCCCA[-/G]GATTATAGAAATTTA	25909
rs752493268	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246886533	AATAATTGTTATAGT[A/G]TAACATCTAGGGAAT	25909
rs752521461	snp	A/C	1.80719e-05	0.00300593	intron-variant	AHCTF1	GRCh38.p7	1:246907524	AAAACTACCTATAAT[A/C]AAATAAGGGAAAAAA	25909
rs752525155	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246906010	ATGTCTGTGTAAACT[A/G]GTCCTAAGAGTCATA	25909
rs752533366	in-del	-/T/TT			intron-variant	AHCTF1	GRCh38.p7	1:246852388	AGTTGGTTTTTTATC[-/T/TT]CAAATTTCTATAAAT	25909
rs752561949	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246908065	AAAACTGATTTATTT[A/C]TTTATTGAAATTTAG	25909
rs752572727	snp	G/T	1.64988e-05	0.00287213	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246905638	CAGGAACTTGTCCAC[G/T]TTCCAATTGTATGTA	25909
rs752649856	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246907009	TTCTGAGAAATGCTC[A/G]TCAGGGATTCAGTCA	25909
rs752673510	snp	C/T	1.71267e-05	0.00292627	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877295	AATTCCAGGCTTCAA[C/T]CATACACCTGAAAGC	25909
rs752677585	snp	A/G/T	8.93606e-05	0.00668381	intron-variant	AHCTF1	GRCh38.p7	1:246885485	ATAGTTTCAAAAGAT[A/G/T]TACTTACCTATTAAA	25909
rs752692575	in-del	-/T	0.000201558	0.0100368	intron-variant	AHCTF1	GRCh38.p7	1:246853081	GAAGTAAAAAATTAA[-/T]TTTTTTTACATGAAT	25909
rs752692676	snp	G/T	1.76599e-05	0.00297147	intron-variant	AHCTF1	GRCh38.p7	1:246894641	ATTCTGTCCTACATC[G/T]AGACCTCTAATACTT	25909
rs752720979	snp	C/T	3.41431e-05	0.00413163	intron-variant	AHCTF1	GRCh38.p7	1:246855870	TGTGTAAGAAGATCC[C/T]ATCTGCTTTAACCTG	25909
rs752725201	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246860259	GGCAACAGAGTGAGA[A/C]TCTGTCTCAAAAATT	25909
rs752738277	snp	G/T	0.000140125	0.00836915	intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246931199	CGCCGGCCGCTTCCC[G/T]CGGGGAAAGGCCCGC	25909
rs752739097	snp	A/C	2.39725e-05	0.00346203	intron-variant	AHCTF1	GRCh38.p7	1:246885691	CCACTCTGGAAATAA[A/C]ATGAAAAATGTTAAA	25909
rs752739878	snp	C/T	1.79406e-05	0.00299499	intron-variant	AHCTF1	GRCh38.p7	1:246918215	TATCTTACAAATCAA[C/T]TGTATTAGTAAATGT	25909
rs752756043	snp	A/G	1.65179e-05	0.00287379	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246903954	GACCATTTACCTCAT[A/G]TAAGATTTGTCCTGA	25909
rs752758644	snp	C/G	5.56127e-05	0.00527288	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850521	GTAATTCTTGTTCCA[C/G]AGAACTGGTGTTTTC	25909
rs752773695	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246896401	GGATGAAGTACTGAT[A/G]CTTGCTATAATACAG	25909
rs752782414	snp	A/G	2.60122e-05	0.0036063	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867260	TAGAAATTTTTTGTG[A/G]TGCTTTTGAAATTGG	25909
rs752808083	in-del	-/TTA			intron-variant	AHCTF1	GRCh38.p7	1:246848234	CATCTACTTTATTTA[-/TTA]TTATTATTATTTGGC	25909
rs752835319	snp	C/T	3.45095e-05	0.00415374	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877302	GGCTTCAACCATACA[C/T]CTGAAAGCAGTATTT	25909
rs752836580	snp	C/T	1.66935e-05	0.00288903	intron-variant	AHCTF1	GRCh38.p7	1:246891751	TAAAATTTAATAAAA[C/T]ACTCATTTGATAAAA	25909
rs752871710	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246914801	CATTCAACTGAGCAA[C/G]CAGTTCAGGAACCTT	25909
rs752889133	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246907354	AAAAATAAAGCTAAA[G/T]TCATGTGCTAAGTCA	25909
rs752906596	snp	C/G/T	5.39353e-05	0.00519281	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853170	CTTTCTTTTAGTACA[C/G/T]CAACTTCTACTTCAT	25909
rs752916069	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246869184	GAAGGTCTGTGGCAA[C/T]CCTGTGTCCAGCAAG	25909
rs752919329	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246916088	CACACCTATATAACC[A/T]GCAGGGGTTCAGTTT	25909
rs752921619	snp	A/G	1.65438e-05	0.00287605	missense, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840838	GTAAAATTTGCTTTG[A/G]ATAGGAAGACAGTTT	25909
rs752933675	in-del	-/AAT			intron-variant	AHCTF1	GRCh38.p7	1:246916655	CAAGACTTCATCTCA[-/AAT]AATAATAATAATAGT	25909
rs752972627	snp	C/T	1.70261e-05	0.00291766	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916306	GTTCATTGACTCCAC[C/T]GAATCTGTAAGCAGA	25909
rs752975071	snp	A/G			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932015	GGGGAGAACCGGCGG[A/G]AGATCGCGGCTGCAG	25909
rs752975503	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246927780	GAGGCCGAGGCTGGC[A/G]GATCACAAGGTCAAG	25909
rs753005586	snp	C/T	1.64933e-05	0.00287165	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861083	ATACTCTAAGGTAGT[C/T]TCATCGGATGTGATT	25909
rs753006968	snp	A/T	1.71563e-05	0.0029288	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246862126	AAAATCCAGAAGTAG[A/T]AACTGACATGGCCAA	25909
rs753021392	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246845078	TCTACAGATGTTTGC[A/G]TTTGTTATTTCAAGA	25909
rs753034362	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246889206	GTGATTCCTTCACTC[A/G]AATATCTATTGCTGA	25909
rs753051830	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246896843	AGGAATCCCATGAAT[G/T]TAAGTTGAACAGGCA	25909
rs753092353	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246923982	GGGAGAAAGGTGAAG[A/G]CCCAAAGGCGTAGAA	25909
rs753094812	snp	A/G	0.000247355	0.0111183	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246913277	ACAAGTCATCCAAAC[A/G]TAGGTCAACAAGAAG	25909
rs753101948	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246856655	TTGCAATAAATAACA[A/T]TAGTTTTCATTAAAA	25909
rs753118573	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246855358	TTTGTTAATTTCCCT[A/G]GAGAATATTCAGTCA	25909
rs753121506	in-del	-/ATACAA	1.66551e-05	0.00288571	intron-variant	AHCTF1	GRCh38.p7	1:246900292	ATTGGTCAGCTACAC[-/ATACAA]ATACAAAGAGAAAGG	25909
rs753121638	snp	G/T	0.000164745	0.00907442	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246898273	CAGCTACAAGACATC[G/T]ATTATAACCATCAGG	25909
rs753128486	snp	A/G	1.65015e-05	0.00287237	intron-variant	AHCTF1	GRCh38.p7	1:246888248	CCTATAAAACAAAGG[A/G]ATAAAACCTTCAGTG	25909
rs753158523	snp	C/T			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933495	GTCTCTACTCCTGGG[C/T]TCAAGAGATCCTCCT	25909
rs753158977	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246891138	CAAAATTAATCACTT[A/G]GTAATTTACATAATT	25909
rs753168710	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246903287	CAGCCATCTAAAAGC[C/T]CAGACGCGTATGTCC	25909
rs753188962	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246859387	GTGTTCCCCTGGCCC[C/T]CTTGTTAACCAAACT	25909
rs753197946	snp	A/G	3.30049e-05	0.00406219	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861005	TAGTGCAGTGGAAGA[A/G]CTTTTGGGCTTAGAG	25909
rs753213247	in-del	-/A	3.31763e-05	0.00407272	intron-variant	AHCTF1	GRCh38.p7	1:246890078	ATTTTTAAGAGTTGG[-/A]AAAAAAAGCTGGTAA	25909
rs753214869	snp	A/G	8.24273e-05	0.00641926	intron-variant	AHCTF1	GRCh38.p7	1:246898160	TGTAATAGAAAGCTA[A/G]TAACGTGATCCAACC	25909
rs753224879	snp	C/T	3.51723e-05	0.00419343	intron-variant	AHCTF1	GRCh38.p7	1:246849596	GATGAAAAACTGTTT[C/T]GCAGAGAAAGAAAAG	25909
rs753237268	in-del	-/TAGT			intron-variant	AHCTF1	GRCh38.p7	1:246898516	TTAACCAATGCTTGC[-/TAGT]TGTGAATACTACTAT	25909
rs753254380	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246879766	CCCAGGAGGCAGAGG[C/T]TGCAGTGAGCCAAAA	25909
rs753279915	snp	C/G/T	5.17088e-05	0.0050845	synonymous-codon, missense, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843915	CAGCTGTGCAGGAAC[C/G/T]TCTATTTTTTTAGCT	25909
rs753302170	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246899364	GAAACAACTGTCAAT[A/G]TCACTAAGTAAAACT	25909
rs753304186	in-del	-/AAAAC	3.44364e-05	0.00414934	intron-variant	AHCTF1	GRCh38.p7	1:246864154	TTGAGTTATACTGAA[-/AAAAC]AAAAGAATTTAGTAT	25909
rs753307240	snp	C/G	1.72519e-05	0.00293695	intron-variant	AHCTF1	GRCh38.p7	1:246894648	CCTACATCTAGACCT[C/G]TAATACTTACATAGT	25909
rs753314812	snp	A/G	1.64914e-05	0.00287149	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246887267	GTTTAACTTGGCCCC[A/G]AGAAATGGCAAATAC	25909
rs753352721	snp	G/T	0.000105442	0.00726015	intron-variant	AHCTF1	GRCh38.p7	1:246894790	AATAAAGATTATTAA[G/T]TACAAACAGAGTTCT	25909
rs753359905	in-del	-/AATTTCTTGAGT	2.0919e-05	0.00323405	cds-indel, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853093	AATTTTTTTTACATG[-/AATTTCTTGAGT]AATTTCTTGAGTATC	25909
rs753360431	snp	A/T	1.6684e-05	0.00288821	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902526	GTACTTTAACTAACC[A/T]TCATTCACGCCTTCC	25909
rs753371292	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246871449	TACTGATAAAATGTA[A/T]TCTAGTCAAAAGGAC	25909
rs753384522	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246921953	TAAACACTGACTACA[A/C]AACAATAATAATGGC	25909
rs753446458	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246902273	CACACTAGTTCAGAC[A/T]AGGGATCGCCTGTTT	25909
rs753463689	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246896412	TGATACTTGCTATAA[C/T]ACAGATGAACCTTGA	25909
rs753486272	in-del	-/TATG			intron-variant	AHCTF1	GRCh38.p7	1:246884655	CTTTCTCACAGTTAC[-/TATG]TATGTGAGACTGTAA	25909
rs753494296	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246872690	ACTGACTAAAGCTCC[C/T]TCCCATCGCACTATC	25909
rs753499425	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246922705	TAGTATCAATAGGCT[A/G]GGCGCAGTGGCTCAC	25909
rs753508974	snp	A/T	1.65012e-05	0.00287234	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850233	GCTGCTTGTCACTGG[A/T]TTTATCATCTTGCTT	25909
rs753530062	snp	A/T	1.65792e-05	0.00287912	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861989	TGGGTGGACATCTTC[A/T]TCCACAAATGAAATT	25909
rs753534476	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246920919	GGTGAATCCACATCT[C/G]TACTAATAATACCAA	25909
rs753539284	snp	C/G	1.65405e-05	0.00287576	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864081	TCCGAACACTGAGAA[C/G]GCCGGGGGACAGGCT	25909
rs753541025	snp	C/T	1.70414e-05	0.00291898	intron-variant	AHCTF1	GRCh38.p7	1:246857656	TTCATTAAACTTCTT[C/T]CTAAAAGTATTTGAA	25909
rs753557086	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246846203	ATTCTAAGATAATTT[A/C]TTCGCTATGTTTCAA	25909
rs753558183	snp	A/G	5.00446e-05	0.00500198	intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842644	GGGTGGGGACAGAGC[A/G]AGACTGTCTCAATCA	25909
rs753602111	snp	A/G	3.29473e-05	0.00405864	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246907690	GGAAACACAGATGGC[A/G]CCCTTGTCTCATTAC	25909
rs753605642	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246896701	TGTACACTTGAAATA[A/T]CTGAACTGCACGGTG	25909
rs753619447	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246913063	AAGTATCCACTGTGC[G/T]CAGGTCCAGACAATA	25909
rs753632271	snp	A/C	1.83296e-05	0.00302729	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876128	AAGGATTTTTCCATA[A/C]TGGTCTAATATAGAA	25909
rs753642595	snp	A/C/T	3.29849e-05	0.00406098	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849884	TTCTTAGAGCTCATC[A/C/T]CCATCGAAAGTTCCT	25909
rs753660728	snp	C/T	1.66413e-05	0.0028845	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900185	GTGGAGAAGTCCTAC[C/T]TACAACAGACTCCAA	25909
rs753679734	in-del	-/ATA			intron-variant	AHCTF1	GRCh38.p7	1:246911062	TTAATTTTTTGTGCT[-/ATA]AAGTCCAACTGCTTC	25909
rs753693530	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246860403	CTTTTCTAAATTTCA[C/T]GGCCAAATAAAAAAT	25909
rs753694936	snp	A/G	4.94947e-05	0.00497443	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851045	TATGGTAAAGTGTCT[A/G]CTTTTTGGGACTTTT	25909
rs753704921	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246928304	CGAGACTCCGTCTCA[-/A]AAAAAAAAAAAAAAA	25909
rs753711735	snp	A/G	5.00254e-05	0.00500102	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900072	ATACATACCAAAATT[A/G]TAAGTGCTTGGATTA	25909
rs753735512	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246898137	GAAATTATCTAATAC[A/G]TTTTTACTGTAATAG	25909
rs753746962	snp	A/T	3.37365e-05	0.00410696	intron-variant	AHCTF1	GRCh38.p7	1:246907541	AATAAGGGAAAAAAG[A/T]TATACTTACTCTCTT	25909
rs753783368	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246869317	GACAATATCCAAAGC[C/T]AACTAATAACCCTAC	25909
rs753785226	in-del	-/TGAAG			intron-variant	AHCTF1	GRCh38.p7	1:246914617	CATAAAAATACTATA[-/TGAAG]TGATTAATACTATTA	25909
rs753793042	snp	C/T	8.23798e-05	0.00641741	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849803	GTCATTTCATCTGTG[C/T]GTTCTTCTGATACTG	25909
rs753802207	in-del	-/ACAA			intron-variant	AHCTF1	GRCh38.p7	1:246870942	ACCCTTTTAAAGAAG[-/ACAA]ACAAACAATACAACT	25909
rs753816151	snp	C/T	1.65441e-05	0.00287607	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867761	ATCTTGTCAACACAG[C/T]TCCTGTTACAACTTG	25909
rs753829363	snp	C/T	1.97924e-05	0.00314576	intron-variant	AHCTF1	GRCh38.p7	1:246876009	TTTTGATCCAATAGA[C/T]TATGATATTCTTCAA	25909
rs753832156	in-del	-/G	1.69372e-05	0.00291004	intron-variant	AHCTF1	GRCh38.p7	1:246900319	GAGAAAGGAGAGAGA[-/G]AAAAAAAAGAATCAT	25909
rs753846197	snp	C/T	1.64808e-05	0.00287057	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850901	GGACACATTATGTTT[C/T]GGCTCACTAAAGGTA	25909
rs753861669	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246927280	TGAGGTCAGGAGTTG[A/G]TTAGAGACCAGTCTG	25909
rs753874920	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246847093	GGCGTTTGAGACTAG[C/G]TTGGCCAACATGGCG	25909
rs753883456	in-del	-/TTTA			intron-variant	AHCTF1	GRCh38.p7	1:246893007	TTAGAGGTTTTTATT[-/TTTA]TTTTTTAAAAAACCC	25909
rs753888818	snp	C/T	1.64765e-05	0.00287019	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246898284	CATCGATTATAACCA[C/T]CAGGAATGAGTTCAT	25909
rs753891876	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246844204	AAGCAGGTACAGAAC[C/T]GTTTAGTCTATTTCT	25909
rs753907727	snp	A/T	1.64904e-05	0.00287139	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861017	AGAGCTTTTGGGCTT[A/T]GAGGCCGTGAAAACA	25909
rs753940784	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246889376	CTAGATGTCCTGCAC[A/G]TACTATTTTATTTAG	25909
rs753960874	snp	A/G	1.64757e-05	0.00287012	intron-variant	AHCTF1	GRCh38.p7	1:246867626	CAGTAAAGATTAACA[A/G]GCAGCATGACTATGA	25909
rs753977798	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246872052	TGAACTATTAATGAC[-/A]AAAAAAAAAAAAAAA	25909
rs754014894	snp	C/T	3.31307e-05	0.00406992	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849633	TTGCTTTCCTTGGAA[C/T]TTCTGACGCTGGAGA	25909
rs754023078	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246904379	TATAACATCTCCCAG[C/T]TTCCTTTGCAGCTAA	25909
rs754027689	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246903316	CCTCTTATAAAAATC[A/G]CCCTATGGCTTAATG	25909
rs754035939	snp	C/G	5.13782e-05	0.00506818	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850548	TTTCTAGTATGTCCT[C/G]ATTAACTTCTTTCTT	25909
rs754040479	snp	C/T	1.77272e-05	0.00297713	intron-variant	AHCTF1	GRCh38.p7	1:246916438	AATATTGTATATACA[C/T]AAAACATGCAATAAC	25909
rs754068157	snp	C/T	5.02374e-05	0.0050116	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850653	AGATGTTTTCAGAAG[C/T]TTCAGAAATTTCTTT	25909
rs754116711	in-del	-/CG			intron-variant	AHCTF1	GRCh38.p7	1:246927871	AGCTGGGCGCGGTAG[-/CG]CGCTGTAGTCCCAGC	25909
rs754132668	snp	C/T	1.76577e-05	0.00297129	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851394	TAAATGAAAGATTCC[C/T]AGCCTCTTCTCCTGA	25909
rs754134696	snp	A/G	1.64898e-05	0.00287135	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850131	CTGCTTGAACAGTCA[A/G]CTGAGATGACTCAAG	25909
rs754188356	snp	G/T	1.65016e-05	0.00287238	intron-variant	AHCTF1	GRCh38.p7	1:246877097	CTAAAAAGAACAAAA[G/T]AGATTGTAAACTACC	25909
rs754213273	snp	C/G	3.34465e-05	0.00408927	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900431	CATATATATTCACCT[C/G]CCAGGTAAAGACTGA	25909
rs754220071	snp	C/G	1.66073e-05	0.00288156	intron-variant	AHCTF1	GRCh38.p7	1:246913416	AATAGCTGTTACCTA[C/G]AAAACATAATACGTG	25909
rs754220238	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246857345	TCCCCTGTGCTCTAC[C/T]GTGTCTACCTACAAG	25909
rs754238130	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246911775	AGGCATGAGCCACGG[C/T]GCCCAGCTCTTCTAT	25909
rs754239466	snp	A/G	1.66377e-05	0.00288419	intron-variant	AHCTF1	GRCh38.p7	1:246889915	GATGAACACTATTCT[A/G]AGAAACTTTGACTTC	25909
rs754285823	in-del	-/CCGCCG			intron-variant, upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246931479	CGCGGGGCAGAAGCC[-/CCGCCG]CCGCCGCCGCCGCCG	25909
rs754286535	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246891312	AAAATAGACATTTTA[C/G]GTAAATACACTTTCA	25909
rs754292006	snp	C/G			missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876979	TCAGAGTTTGGTTCA[C/G]CTTCAAGGCAGGCAC	25909
rs754301581	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246874968	TCCTGCTATTTAGCC[A/G]GTTTCTTCCTAAACC	25909
rs754331331	snp	C/G	1.64773e-05	0.00287026	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851292	CACATTCAGCAGTGT[C/G]TTTGTTATCAGCTAA	25909
rs754342974	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246854959	TAAAATGGGTGATCG[C/G]CTTTTTACATGTTAG	25909
rs754351955	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246876765	CATAAATGGCATACG[-/T]TAAAAGAATTACGTG	25909
rs754368961	snp	A/G	3.30104e-05	0.00406252	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246888467	TCAATTCGCTCTCCT[A/G]ACTGAGAAACCAGTC	25909
rs754397667	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246912563	ACTCCTTTTCTAAAA[A/T]TTAAGAGTAAAAAAC	25909
rs754424057	snp	A/G	1.64833e-05	0.00287078	intron-variant	AHCTF1	GRCh38.p7	1:246863906	TTGATTGTGAACGCT[A/G]GATGCGTAAATACTA	25909
rs754425825	in-del	-/ATT	9.27136e-05	0.00680795	intron-variant	AHCTF1	GRCh38.p7	1:246918402	TTTTTAAAAGAAAAC[-/ATT]ATTATGACACATTTG	25909
rs754436495	in-del	-/ATAAA	1.67525e-05	0.00289413	intron-variant	AHCTF1	GRCh38.p7	1:246841044	TAAACACATTATGCT[-/ATAAA]ATAAAATTGGCTTCC	25909
rs754461811	snp	A/T	2.20909e-05	0.0033234	intron-variant	AHCTF1	GRCh38.p7	1:246853310	CATAGCTGAAAGAAA[A/T]ATGAGTGAATTTTTT	25909
rs754483583	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246863767	ATAAATTTAATTAGC[C/T]CCGTTTTTAGAAGAT	25909
rs754485817	snp	C/T	1.6743e-05	0.0028933	missense, synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840961	TCAGCCGAATTTCTA[C/T]GGGAGGAGGTGACCA	25909
rs754492023	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246898537	TGAATACTACTATTA[C/G]CAAAAGGTAGCTTAT	25909
rs754533644	snp	G/T	1.6537e-05	0.00287545	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849987	TTCTTGTAGATCTCC[G/T]TCTAATGCTGGGAGC	25909
rs754545901	snp	C/T	3.73148e-05	0.00431926	intron-variant	AHCTF1	GRCh38.p7	1:246862179	GAGCAAATGGAATTA[C/T]ACCATTAAAAGTGCT	25909
rs754546438	in-del	-/GAC			intron-variant	AHCTF1	GRCh38.p7	1:246928977	GATAACCTTCTTCCT[-/GAC]TTTAAGGAGTTTACA	25909
rs754567541	snp	C/T	1.65037e-05	0.00287256	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876981	AGAGTTTGGTTCAGC[C/T]TCAAGGCAGGCACAT	25909
rs754575175	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246869796	TGATGTACAGGGAGA[C/T]GAATGCTGTTAGCAG	25909
rs754595276	snp	C/T	1.6638e-05	0.00288422	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900212	CCAATGACCACAGTG[C/T]AAAATAAGAGCAATT	25909
rs754603037	snp	A/C	1.65726e-05	0.00287855	intron-variant	AHCTF1	GRCh38.p7	1:246876238	TCAAAATGTTAGGTG[A/C]TGTAATTCTATATTT	25909
rs754609584	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246918144	ATTTAAGATCACTCA[C/G]GTTCTGCTTTTTCTT	25909
rs754662506	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246929061	TAAATGCTACTACAA[C/T]AGAGGTACATATGCT	25909
rs754688323	snp	C/T			synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900243	ATGTAGATATTCTCC[C/T]GACCTAAAAGAAAAT	25909
rs754697487	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246919454	CGTGGTGGCTCACGC[C/T]TGTAATCCCAGCACT	25909
rs754737894	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246859989	TAATTTGGCAGGGCG[C/T]GGTGGCTCACGCCTG	25909
rs754753473	snp	A/C	0.000135584	0.00823247	intron-variant, missense, utr-variant-5-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246931166	TGGAACACACGCCAA[A/C]ACAGGACAGGCTCAG	25909
rs754758485	snp	A/G	1.65029e-05	0.00287248	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849645	GAACTTCTGACGCTG[A/G]AGAAAATAAAGGCTC	25909
rs754779208	snp	A/G	4.94719e-05	0.00497328	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850690	CCTAGTTTTCTTCCT[A/G]ACTGACTGCCCTGGC	25909
rs754802806	in-del	-/TATG			intron-variant	AHCTF1	GRCh38.p7	1:246883376	AACAAATTAGGTGAT[-/TATG]TATGACCGCAGGAGA	25909
rs754804757	snp	A/G	1.68664e-05	0.00290395	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867802	GCTGATAATGGTTTG[A/G]GTCTAGAAACTGTAA	25909
rs754813273	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246880201	ATGTAAATAGCTTAT[G/T]ATCAAAAACAATATG	25909
rs754833295	in-del	-/CTC			cds-indel, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246913376	GAGTGCTTGCACTGG[-/CTC]CTCCATGATTAATTA	25909
rs754845976	snp	A/G	1.87149e-05	0.00305893	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246885665	TAGCTGGATGAAACA[A/G]AAGATCCAAACCACT	25909
rs754850462	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246870416	TGACAGACAAAGACC[C/T]TGTCTCTTAAAAAAA	25909
rs754853038	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246859259	TTTTACAGCTTTAGA[A/G]TTAGGAGTTACCTTT	25909
rs754857774	snp	C/T	1.64751e-05	0.00287007	intron-variant	AHCTF1	GRCh38.p7	1:246867639	CAAGCAGCATGACTA[C/T]GAAACGTGTAAGAAA	25909
rs754868510	snp	A/C	1.66776e-05	0.00288765	intron-variant	AHCTF1	GRCh38.p7	1:246905510	TCCAAAAAAACAAAA[A/C]AAAACAAAACAAAGT	25909
rs754869890	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246893727	TATCAATATGTTAAA[C/T]AGAAAGTGAGTTAAG	25909
rs754889894	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246905805	CAAGTCATCTTATCT[A/G]CAAAAATACACACGG	25909
rs754895393	snp	C/G	1.65578e-05	0.00287726	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246891874	TGGATAGACTGTATA[C/G]TTTGTGGATCCATGA	25909
rs754899492	in-del	-/TTGCAGAGAAAG	1.76111e-05	0.00296736	intron-variant	AHCTF1	GRCh38.p7	1:246849595	AGATGAAAAACTGTT[-/TTGCAGAGAAAG]AAAAGTACCTTTTGC	25909
rs754936188	snp	C/T	0.00016484	0.00907704	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246855787	CAGATGTTAATCCTT[C/T]GTCCAACACTGGTAC	25909
rs755033364	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246894857	AACCGAGTGAACATC[A/G]ACACTTCAGGGAGGC	25909
rs755035822	snp	C/T	1.66062e-05	0.00288146	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864116	AACCAAATCTAGCAG[C/T]CTGTAATCAGAATGC	25909
rs755054696	snp	C/T	1.65817e-05	0.00287933	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877225	TCCTGACAGACTTCA[C/T]ACATGTGCTTCAGTA	25909
rs755091329	snp	A/T	1.66098e-05	0.00288177	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861974	CCCAGGAATCCATTT[A/T]GGGTGGACATCTTCT	25909
rs755107773	snp	A/G	1.65116e-05	0.00287324	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246890041	TTGTAGCATAACCTT[A/G]ACAACTGCACAGAAT	25909
rs755132680	snp	C/T	3.6003e-05	0.00424266	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853159	GTAAGTCAACACTTT[C/T]TTTTAGTACACCAAC	25909
rs755134725	snp	G/T	1.65288e-05	0.00287474	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850278	CAGAAGCATCTAAAT[G/T]AGTACTTCTCAATTT	25909
rs755148487	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246914680	TAATGAGTGTATACT[G/T]CACCCTACCCAAAAA	25909
rs755152162	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246929324	TGAGGCACAAGAATC[A/G]CTTGAGCCCTGGAGG	25909
rs755159572	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246877314	ACACCTGAAAGCAGT[A/T]TTTATCAAAGTTTAG	25909
rs755177349	snp	C/G	1.68119e-05	0.00289926	intron-variant	AHCTF1	GRCh38.p7	1:246916134	CAGGTATCTTAAACA[C/G]TACCTACCCTTCCAG	25909
rs755259731	snp	A/G	1.66913e-05	0.00288883	intron-variant	AHCTF1	GRCh38.p7	1:246900054	AGAGGTAATGTTAAG[A/G]AAATACATACCAAAA	25909
rs755274594	snp	A/C	3.30246e-05	0.0040634	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246913259	CTTCATTTTGATTGC[A/C]TGACAAGTCATCCAA	25909
rs755301955	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246920987	ATCTCAGCTACTCAG[C/G]AGGCTGAGGCAGGAG	25909
rs755317905	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246893124	CAAAACTCAATTTAT[A/G]AATTGAGTTTAATTT	25909
rs755343472	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246931061	TCTCCTTGATCTGAC[C/T]AATCGGGTGAGCTGG	25909
rs755351100	snp	G/T	1.65285e-05	0.00287471	intron-variant	AHCTF1	GRCh38.p7	1:246895976	AGAAAGAGGGTGTGA[G/T]ATCATAGGCAAGTTC	25909
rs755356634	snp	A/G	1.6674e-05	0.00288734	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246860943	ACTTCTGATGCAAAT[A/G]CATCTTTATCTCCAT	25909
rs755411706	snp	C/G/T	0.000142438	0.00843806	missense, synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867252	CTCTTACCTAGAAAT[C/G/T]TTTTGTGATGCTTTT	25909
rs755445761	in-del	-/CTT	1.6507e-05	0.00287284	cds-indel, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246889983	TGATAAACGCTCAAA[-/CTT]CTGTCGACGACTGGT	25909
rs755463546	snp	G/T			downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838815	TCTGAGTATATTGTT[G/T]CCCTTACTACTATGA	25909
rs755483516	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246888119	CAGGTTTCCACTACT[C/G]TTGAAATTTTATAAT	25909
rs755490389	in-del	-/TGT	3.30617e-05	0.00406568	cds-indel, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877166	TAATTACCTGCTCAG[-/TGT]CTGTAAATGGTAACT	25909
rs755497281	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246872760	CACTATATAGAAGAG[C/T]TTGCTTGGCATGATT	25909
rs755502009	snp	A/C	3.29777e-05	0.00406051	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246895855	GTTATCCATCTTCGG[A/C]TATAACCAGTCAAAA	25909
rs755524776	snp	C/T	9.88843e-05	0.00703081	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902636	GGAACATGCCACCTG[C/T]CAGGTCCAGGGTGTA	25909
rs755526487	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246922094	GCTGGGCACAGTGGC[G/T]CACGCCTGTAATCCC	25909
rs755527541	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246901581	GTGAGCTGAGATCGT[C/G]CAACTGCACTGGACA	25909
rs755532977	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246855317	TCACAAAAATGCTCA[C/T]TGGATTAAAAAAAAA	25909
rs755547499	snp	A/G			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933368	TGAACTCTTGACCTC[A/G]TGATCCACCTGCCTC	25909
rs755557828	snp	C/T	1.75529e-05	0.00296246	intron-variant	AHCTF1	GRCh38.p7	1:246855879	AGATCCCATCTGCTT[C/T]AACCTGCTTTAGTCC	25909
rs755569767	snp	A/T	1.99249e-05	0.00315627	missense, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843819	TTCAAGCTTGTTCTT[A/T]TTGGATGTGTTTTTT	25909
rs755581451	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246921135	AAAGCAGCAGAAAAT[A/G]CACGCAAAATGACAT	25909
rs755592653	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246892397	TCAATCTCCGCTCAC[G/T]GCAACCTCTACCTCC	25909
rs755596515	in-del	-/TTCT/TTT			intron-variant	AHCTF1	GRCh38.p7	1:246857961	ACTGCTAACACTTTC[-/TTCT/TTT]TTCTTTTTTTTTTTT	25909
rs755618028	snp	A/G	2.53913e-05	0.00356301	intron-variant	AHCTF1	GRCh38.p7	1:246885694	CTCTGGAAATAACAT[A/G]AAAAATGTTAAATAT	25909
rs755618031	in-del	-/C/T	0.000201558	0.0100368	intron-variant	AHCTF1	GRCh38.p7	1:246853080	GAAGTAAAAAATTAA[-/C/T]TTTTTTTTACATGAA	25909
rs755619681	snp	A/G	1.75268e-05	0.00296025	intron-variant	AHCTF1	GRCh38.p7	1:246894643	TCTGTCCTACATCTA[A/G]ACCTCTAATACTTAC	25909
rs755630613	snp	C/T	1.64961e-05	0.00287189	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850708	TGACTGCCCTGGCAT[C/T]TTAGGAGTAGCAACA	25909
rs755631830	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246884676	GAGACTGTAATAATC[A/C]TTATTATGTAAATGA	25909
rs755660997	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246929208	GAGCTCAGGAGTTCG[A/C]GATCACCCTGGGCAA	25909
rs755661466	snp	C/T	0.000165126	0.0090849	intron-variant	AHCTF1	GRCh38.p7	1:246841040	AGAATAAACACATTA[C/T]GCTATAAAATAAAAT	25909
rs755672914	in-del	-/CTT	1.65389e-05	0.00287562	cds-indel, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849986	TTTCTTGTAGATCTC[-/CTT]CTAATGCTGGGAGCT	25909
rs755673039	snp	A/G	1.65627e-05	0.00287769	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246891880	GACTGTATAGTTTGT[A/G]GATCCATGAAATGAC	25909
rs755738258	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246906023	CTGGTCCTAAGAGTC[A/C]TATTTGATGTACACT	25909
rs755739389	snp	A/G	8.32577e-05	0.00645151	intron-variant	AHCTF1	GRCh38.p7	1:246900320	GAGAAAGGAGAGAGA[A/G]AAAAAAAGAATCATA	25909
rs755750960	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246889041	GTCAGTCAAGGTGAG[G/T]TCCCCATGTGGTCCA	25909
rs755757058	snp	C/T	1.6691e-05	0.00288881	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900420	CTTTCCCTGTCCATA[C/T]ATATTCACCTGCCAG	25909
rs755775483	snp	C/G	1.65293e-05	0.00287479	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246913400	GATTAATTATAGGTT[C/G]AATAGCTGTTACCTA	25909
rs755779938	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246920907	CCTGGCCAACATGGT[A/G]AATCCACATCTCTAC	25909
rs755786671	snp	A/C/G	5.07227e-05	0.00503579	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840969	ATTTCTATGGGAGGA[A/C/G]GTGACCAAGCACTTT	25909
rs755808040	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246919630	AAGCAGGAGAATCAC[C/T]TGAACCCAGGAGGTG	25909
rs755811275	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246871292	CTAAAAACAGAGACA[C/T]CACTCGCTTACTGAT	25909
rs755832750	snp	C/T			utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840201	TTGCCGAATAAGAGA[C/T]GCCAACATTATAGTT	25909
rs755838313	in-del	-/GT			intron-variant	AHCTF1	GRCh38.p7	1:246923743	TGTGCGTGCATGCGT[-/GT]GTGTGTGTGTGCGCG	25909
rs755854248	snp	C/T	1.6492e-05	0.00287154	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850119	ACATATCAAATTCTG[C/T]TTGAACAGTCAACTG	25909
rs755865627	snp	A/C	1.64765e-05	0.00287019	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849798	TATGTGTCATTTCAT[A/C]TGTGCGTTCTTCTGA	25909
rs755895293	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246893941	GATGTAGTGGCTCAC[A/G]CCTTGTAATACCAAC	25909
rs755918895	snp	A/G	0.000115311	0.00759224	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849708	TGGCCTTGCTAGACC[A/G]AGTCCTGCTGCTGCG	25909
rs755925372	snp	A/G	4.69462e-05	0.00484467	intron-variant	AHCTF1	GRCh38.p7	1:246861298	TATCATCTGCAGCCT[A/G]TAAAGTAAGATTTTG	25909
rs755946408	snp	C/T	0.00104848	0.0228723	intron-variant	AHCTF1	GRCh38.p7	1:246867815	TGGGTCTAGAAACTG[C/T]AAAATGAAGAACGCT	25909
rs755976686	snp	A/G	1.98963e-05	0.00315401	intron-variant	AHCTF1	GRCh38.p7	1:246876007	TTTTTTGATCCAATA[A/G]ATTATGATATTCTTC	25909
rs755981311	snp	C/T	0.000285225	0.0119386	intron-variant, synonymous-codon, utr-variant-5-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246931218	GGAAAGGCCCGCCAA[C/T]GAGTCCATCGCGTGG	25909
rs755996260	snp	A/G	3.30082e-05	0.00406239	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246887226	CTCATAGTCATTATG[A/G]TCTATCAACCAAAAC	25909
rs756001393	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246879166	AGCCAAAGATTTTAA[C/T]AGGCAGGTCACAAAA	25909
rs756032571	snp	A/G	1.7051e-05	0.0029198	intron-variant	AHCTF1	GRCh38.p7	1:246899520	AGTGGCATCTAAAAA[A/G]AAGATTTAAAAAATA	25909
rs756034691	snp	A/G	1.73168e-05	0.00294246	intron-variant	AHCTF1	GRCh38.p7	1:246907533	TATAATCAAATAAGG[A/G]AAAAAAGTTATACTT	25909
rs756064105	in-del	-/G			intron-variant	AHCTF1	GRCh38.p7	1:246860190	GCTTGAACCTGGTTG[-/G]GGGGGGGGCGGAGGT	25909
rs756089086	snp	C/G	1.65051e-05	0.00287267	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246905641	GAACTTGTCCACTTT[C/G]CAATTGTATGTAATA	25909
rs756101765	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246845395	TAGAGTTGATATCAG[A/G]TATCAGAAATATATA	25909
rs756163414	snp	C/G/T	5.53193e-05	0.00525901	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850523	AATTCTTGTTCCACA[C/G/T]AACTGGTGTTTTCTA	25909
rs756176438	snp	C/G			intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842524	GAGGCAGAGGTTGCA[C/G]TGAGCCGAAATCACA	25909
rs756205801	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246902409	GAACTGAATAAATTC[C/T]GTTAATTACTATTCC	25909
rs756231317	in-del	-/A			utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840328	GTAACAGCCAAAAAC[-/A]AAAAAAATACATTTT	25909
rs756239288	snp	A/G	1.73426e-05	0.00294466	intron-variant	AHCTF1	GRCh38.p7	1:246877306	TCAACCATACACCTG[A/G]AAGCAGTATTTATCA	25909
rs756247847	snp	C/T	1.6516e-05	0.00287362	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246903955	ACCATTTACCTCATA[C/T]AAGATTTGTCCTGAT	25909
rs756255457	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246903294	CTAAAAGCCCAGACG[C/T]GTATGTCCTCTTATA	25909
rs756277027	snp	G/T	1.92665e-05	0.00310369	missense, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843833	TATTGGATGTGTTTT[G/T]TTGTCTGCTCCTTAA	25909
rs756279015	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246927105	ATGGCGTGAACCCGG[A/G]AGGCGGAGCTTGCAG	25909
rs756300836	snp	A/G	1.64991e-05	0.00287215	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902651	TCAGGTCCAGGGTGT[A/G]TCTTTCTTCACAGTA	25909
rs756303119	snp	A/T	5.10347e-05	0.00505121	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916310	ATTGACTCCACTGAA[A/T]CTGTAAGCAGACAAT	25909
rs756309731	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246868419	AGCCACTGCGCCTGG[A/C]AATTTTTGTATTTTT	25909
rs756343520	snp	C/G			missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916380	CCACAAGCCAAGCAA[C/G]CAAGTCCATTTTTCC	25909
rs756360999	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246845244	GTATATATAAAAATG[-/T]TTTTTGTGGGTACAC	25909
rs756387863	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246869209	AGCAAGTCTACTGGC[A/G]CCATTTTTCCAACAG	25909
rs756404764	snp	A/G	1.65395e-05	0.00287567	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849999	TCCTTCTAATGCTGG[A/G]AGCTTCTTTCTTCTT	25909
rs756408014	snp	C/T	1.66838e-05	0.00288818	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246891034	TGAGGTGGGAAACCA[C/T]AAACTTATTGCTTAA	25909
rs756414195	snp	A/C/G	1.67708e-05	0.00289571	intron-variant	AHCTF1	GRCh38.p7	1:246902706	CACGCAAATATTAAT[A/C/G]TGATTCTAGGCAAAA	25909
rs756417679	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246889323	ATAGCGGCAGCACTT[A/C]CTACTCTTTGCGGTT	25909
rs756440164	snp	A/G	1.6476e-05	0.00287014	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851278	TACTTCAGCAATGTC[A/G]CATTCAGCAGTGTCT	25909
rs756445387	snp	A/G			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933527	CCTCAGCCTCTCAAC[A/G]TGCTGGGATTACAGA	25909
rs756445992	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246917433	TTTAAGAAAGTAGCA[C/T]GGTACAGTGGGGTCT	25909
rs756471351	snp	C/T	1.69407e-05	0.00291034	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850388	GATCTTTTAATTCTT[C/T]TAGGAGTCCTTTTTG	25909
rs756482422	snp	C/G	8.2479e-05	0.00642127	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246888451	TCGTTTCCACAACTT[C/G]TCAATTCGCTCTCCT	25909
rs756531391	in-del	-/A	0.000305105	0.0123475	intron-variant	AHCTF1	GRCh38.p7	1:246900318	AGAGAAAGGAGAGAG[-/A]AAAAAAAAAGAATCA	25909
rs756535737	snp	C/T	1.6476e-05	0.00287014	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246898278	ACAAGACATCGATTA[C/T]AACCATCAGGAATGA	25909
rs756550334	snp	C/T	1.65002e-05	0.00287225	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861009	GCAGTGGAAGAGCTT[C/T]TGGGCTTAGAGGCCG	25909
rs756573900	in-del	-/ATAG			intron-variant	AHCTF1	GRCh38.p7	1:246923862	GAAATGAAGGGGGAA[-/ATAG]ATAGATAACCCCAGG	25909
rs756578879	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246907482	TAACTTTCAAATATT[A/G]GTAAATGAGTACAAG	25909
rs756587618	snp	C/T	1.67293e-05	0.00289212	intron-variant	AHCTF1	GRCh38.p7	1:246876915	CAGTTTTCCTTATTC[C/T]CTTATCCCCCATAAT	25909
rs756596455	snp	G/T	4.95111e-05	0.00497525	intron-variant	AHCTF1	GRCh38.p7	1:246888262	GGATAAAACCTTCAG[G/T]GGATCTTATACAGTC	25909
rs756629135	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246862206	TGCTTATAGGCCGGG[C/T]GCGGTGGCTCACGCC	25909
rs756651823	in-del	-/CAA	3.34694e-05	0.00409067	intron-variant	AHCTF1	GRCh38.p7	1:246890110	AATCCCCAAATATCT[-/CAA]CAATACATATTAATA	25909
rs756651916	snp	A/C	1.64827e-05	0.00287073	intron-variant	AHCTF1	GRCh38.p7	1:246898163	AATAGAAAGCTAATA[A/C]CGTGATCCAACCAAA	25909
rs756690647	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246924057	TTTCTCAGCACTCCC[C/T]CTCCTATCTATTGAG	25909
rs756727492	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246917046	CAATGTAAAGTCATA[A/G]AGGTGACTATCTGAT	25909
rs756754128	snp	A/G	1.97241e-05	0.00314032	intron-variant	AHCTF1	GRCh38.p7	1:246876011	TTGATCCAATAGATT[A/G]TGATATTCTTCAATG	25909
rs756767919	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246887941	CACATTTAAGTGTCT[C/G]ATAAAAGCCAAGTAC	25909
rs756798263	snp	G/T	3.29913e-05	0.00406135	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850914	TTTGGCTCACTAAAG[G/T]TATTGTTTCATGAAT	25909
rs756809314	snp	A/G	1.64906e-05	0.00287142	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246887269	TTAACTTGGCCCCAA[A/G]AAATGGCAAATACAG	25909
rs756817653	snp	C/T			downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838649	TATAAGGTCAATCCA[C/T]TGTAGCCCATTCAGG	25909
rs756841281	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246930966	AACCAAAACAGTCAA[C/T]CAGTGGCAAAAGAAA	25909
rs756851524	snp	C/T	4.97739e-05	0.00498844	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850806	TTTTGGAGGAAACCA[C/T]GTCATCAACCTGGCT	25909
rs756861258	snp	A/G	0.000165656	0.00909949	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246905651	ACTTTCCAATTGTAT[A/G]TAATATCTGAAACAA	25909
rs756865996	in-del	-/GACT	1.64887e-05	0.00287125	frameshift-variant, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850173	CTCTCACATCTGATG[-/GACT]AACTTCTCTCCCTCT	25909
rs756867330	in-del	-/CT			intron-variant	AHCTF1	GRCh38.p7	1:246927169	GGCGACAGAGCGAGA[-/CT]CTGTCTCAAAAAAAA	25909
rs756870314	snp	A/G	1.73534e-05	0.00294558	intron-variant	AHCTF1	GRCh38.p7	1:246891941	AGAATAAAAGAAAAG[A/G]TAAGTTTCCATACAG	25909
rs756870671	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246895151	AAACAAAATACAAAG[C/T]ATGATTCTGAGCTCT	25909
rs756879765	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246871608	TAACAGCCTACCTCT[A/G]TGAACCCTGACTAGA	25909
rs756885510	in-del	-/TCT	3.5598e-05	0.00421873	cds-indel, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853188	ACTTCTACTTCATGA[-/TCT]TCTTTTAAGTTCAGC	25909
rs756889770	snp	C/T	1.66485e-05	0.00288513	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246894675	TAGTCTGTCAAATTC[C/T]TCTTTTGTGAGAACC	25909
rs756914771	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246860421	CCAAATAAAAAATGT[A/G]ACACATAAGTTCTCC	25909
rs756917277	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246907194	CTTAAACATTAAAAA[G/T]GTACAATCAAAATAC	25909
rs756944550	snp	C/T	1.6643e-05	0.00288465	missense, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246842737	TGATTCGTTTCGCTT[C/T]TGGCTTTCCCAGAGT	25909
rs756944974	snp	C/T	3.32441e-05	0.00407688	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902534	ACTAACCTTCATTCA[C/T]GCCTTCCTCCCTGTC	25909
rs756950637	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246867598	TGGATTGTTGATGAA[C/T]GCTGTTGATGTCCAG	25909
rs756952978	snp	A/C/T	0.00058517	0.0170965	intron-variant, utr-variant-5-prime, upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246931242	CGCGTGGGAGAACAG[A/C/T]GGGAAAGGGTCGCGG	25909
rs756954436	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246869330	GCCAACTAATAACCC[-/T]ACAAAGACCTCAAGT	25909
rs756957007	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246852548	TCAGAGTGTACAGAT[A/G]TTCAACACCAGCCAG	25909
rs756983877	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246921994	TTAAATAAACCATAC[A/G]GAGTCTTCTTACTGC	25909
rs756995556	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246896716	TCTGAACTGCACGGT[A/G]TATGAAATATCTCAA	25909
rs757037085	snp	A/C	1.65302e-05	0.00287486	missense, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840849	TTTGGATAGGAAGAC[A/C]GTTTCTTTCTGTTCC	25909
rs757086714	snp	C/G	1.66646e-05	0.00288652	intron-variant	AHCTF1	GRCh38.p7	1:246861337	AAAATTAGTAAATAT[C/G]ACAGTTAAGTCTAGT	25909
rs757109050	snp	G/T	1.65811e-05	0.00287929	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246862010	AAATGAAATTCTAGT[G/T]TCTTTAAGTCGTTGA	25909
rs757139638	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246846207	TAAGATAATTTCTTC[A/G]CTATGTTTCAATAAA	25909
rs757160395	snp	C/T	1.67556e-05	0.0028944	intron-variant	AHCTF1	GRCh38.p7	1:246907544	AAGGGAAAAAAGTTA[C/T]ACTTACTCTCTTTTC	25909
rs757167462	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246842803	ACATTTTAAAAGGTT[A/G]AGTATTAAACACGAA	25909
rs757173810	snp	A/C/G	0.000116496	0.00763122	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900188	GAGAAGTCCTACTTA[A/C/G]AACAGACTCCAATGA	25909
rs757184477	snp	C/T	1.64743e-05	0.00287	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246907698	AGATGGCGCCCTTGT[C/T]TCATTACACTTTCTC	25909
rs757187820	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246880747	TCCCAGTTTCCCCCA[C/T]AGCAGGAAAATACTT	25909
rs757226973	snp	C/T	1.66746e-05	0.00288739	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900073	TACATACCAAAATTA[C/T]AAGTGCTTGGATTAA	25909
rs757227077	in-del	-/TTC			intron-variant	AHCTF1	GRCh38.p7	1:246845701	AGCACAGATGAGACT[-/TTC]TTGAGTGTATGTCAA	25909
rs757249410	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246916454	AAAACATGCAATAAC[A/G]GTTAGCTCATTTACA	25909
rs757250019	in-del	-/GAA			intron-variant	AHCTF1	GRCh38.p7	1:246904932	TCTCCAAGTATATTT[-/GAA]GAATAAGAGAGCAGG	25909
rs757264547	snp	A/G	1.64841e-05	0.00287085	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851162	GTGTTAGCTGCTTTA[A/G]GTAACACATCAGATG	25909
rs757287157	snp	C/T	3.30513e-05	0.00406504	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849640	CCTTGGAACTTCTGA[C/T]GCTGGAGAAAATAAA	25909
rs757302709	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246915062	ACTGGCCGGGCGTGG[C/T]GGCTCATGCCTGTAA	25909
rs757316981	snp	C/T			missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246855786	ACAGATGTTAATCCT[C/T]CGTCCAACACTGGTA	25909
rs757335600	snp	A/G/T	3.29898e-05	0.00406128	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861091	AGGTAGTCTCATCGG[A/G/T]TGTGATTGAAACACT	25909
rs757375264	in-del	-/AAC	1.70653e-05	0.00292102	intron-variant	AHCTF1	GRCh38.p7	1:246903904	ATATTTAAAATAGAA[-/AAC]AACAAAATGGTAATA	25909
rs757377288	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246859686	GTCCAAGCGATCCTC[C/T]CCTCTCAGTGTCCTG	25909
rs757386569	snp	A/C	1.77745e-05	0.00298109	intron-variant	AHCTF1	GRCh38.p7	1:246904085	TAATACATTAAACAT[A/C]TCTTACTGTCCAAGT	25909
rs757390474	in-del	-/AACA			intron-variant	AHCTF1	GRCh38.p7	1:246857952	TGTTATCAGACTGCT[-/AACA]AACACTTTCTTCTTT	25909
rs757402469	snp	G/T	1.66551e-05	0.00288571	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246918343	ATGGCAGGAGACCAC[G/T]AGTCACTTGAGCTCT	25909
rs757430495	in-del	-/AAAAG	3.41309e-05	0.00413089	intron-variant	AHCTF1	GRCh38.p7	1:246891931	ACACCTTTCAAGAAT[-/AAAAG]AAAAGATAAGTTTCC	25909
rs757436317	snp	G/T	1.64819e-05	0.00287066	intron-variant	AHCTF1	GRCh38.p7	1:246898169	AAGCTAATAACGTGA[G/T]CCAACCAAAAGAAAC	25909
rs757439221	snp	A/G	3.3168e-05	0.00407221	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867772	ACAGTTCCTGTTACA[A/G]CTTGCTTTGGAACTG	25909
rs757478321	snp	C/T	1.66167e-05	0.00288237	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850662	CAGAAGCTTCAGAAA[C/T]TTCTTTTGCCTTCCT	25909
rs757483821	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246922810	ACACGGTGAAACCCT[A/G]TCTCTACTAAAAATA	25909
rs757489801	snp	A/G	1.6489e-05	0.00287128	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246903978	GTCCTGATGCCAAAC[A/G]CTTTCTATTACCAAA	25909
rs757492844	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246910695	GCAGATTCTCTCATT[C/G]TTATAAAGGGGGAAA	25909
rs757493168	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246874731	CAACCTATCCTGAGA[A/G]ATCCTGAAATATATT	25909
rs757496520	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246849109	AATACAGTCCTTAGC[A/T]CGTGACAATGAAGGA	25909
rs757513653	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246889413	ACTGACTTTATAACT[C/T]ATATAACAAGCAGGA	25909
rs757552610	snp	C/T	1.65089e-05	0.00287301	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864046	ACAAAGGAGATTTCA[C/T]GGAGCTTTGCTGAAT	25909
rs757556837	snp	G/T	1.85379e-05	0.00304444	intron-variant	AHCTF1	GRCh38.p7	1:246843950	AAAGTTGAAAAAACT[G/T]TATCTGTATCTTTAT	25909
rs757569758	snp	C/T			intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842652	ACAGAGCGAGACTGT[C/T]TCAATCAATCAATCA	25909
rs757581822	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246925570	GGTTGCAGTAAGCTA[C/T]GATCAGGCCACTGCA	25909
rs757625854	snp	A/G	1.67382e-05	0.00289289	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900438	ATTCACCTGCCAGGT[A/G]AAGACTGAAACACTA	25909
rs757631720	snp	C/T	1.7117e-05	0.00292544	intron-variant	AHCTF1	GRCh38.p7	1:246916101	CCAGCAGGGGTTCAG[C/T]TTTGAAAGAGAAATG	25909
rs757635067	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246924219	TAAAAAATTTATAAA[C/G]AAATATTTACATTAA	25909
rs757636628	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246870817	TGTATCAAATACCTC[C/T]TCCTCAGAACCAAAA	25909
rs757637018	in-del	-/TA			intron-variant	AHCTF1	GRCh38.p7	1:246862720	AAAAGTGCCAATTAG[-/TA]AGATAAATTACTTAA	25909
rs757739903	snp	A/T	3.29587e-05	0.00405934	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246863951	AGGAGTTTCAAGCAA[A/T]TGTAATTCTGAAGCC	25909
rs757767844	in-del	-/ACAAAAA			intron-variant	AHCTF1	GRCh38.p7	1:246848706	GCTGTCTCTACAAAT[-/ACAAAAA]ACAAAAAATTAGCCA	25909
rs757788540	snp	A/C/G	1.64795e-05	0.00287045	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246863935	TAACCTTAACTACAA[A/C/G]AGGAGTTTCAAGCAA	25909
rs757836741	snp	A/C	2.49237e-05	0.00353004	intron-variant	AHCTF1	GRCh38.p7	1:246876220	TGGTAAAAAATTTAA[A/C]CTTCAAAATGTTAGG	25909
rs757838911	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246911781	GAGCCACGGCGCCCA[A/G]CTCTTCTATTAAGAT	25909
rs757847395	snp	C/T	1.64773e-05	0.00287026	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851295	ATTCAGCAGTGTCTT[C/T]GTTATCAGCTAAGTC	25909
rs757864826	snp	A/G	3.33506e-05	0.0040834	intron-variant	AHCTF1	GRCh38.p7	1:246913422	TGTTACCTAGAAAAC[A/G]TAATACGTGATTTGC	25909
rs757898761	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246851898	GGTTGAAGAACAATT[C/G]ACCTACATAAGCTCC	25909
rs757949928	in-del	-/AG			intron-variant	AHCTF1	GRCh38.p7	1:246848905	CATTAACACTTTTAC[-/AG]AGAGTTACTCTGATG	25909
rs757967887	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246860573	GCTTTCCTTCTGAGA[C/T]AGGGTCTTGCTCTGT	25909
rs757968395	snp	A/G	1.64751e-05	0.00287007	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246907706	CCCTTGTCTCATTAC[A/G]CTTTCTCTAATGTGT	25909
rs757970163	snp	C/T	3.73741e-05	0.00432269	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876147	TCTAATATAGAATTT[C/T]GAGCCAGTGATCTCT	25909
rs757985160	in-del	-/TCAAT			intron-variant	AHCTF1	GRCh38.p7	1:246911381	TATTGCTTTTGCTCA[-/TCAAT]TCTTTTCATTTAAAC	25909
rs757989663	snp	C/T	3.29891e-05	0.00406122	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246887300	TTGGGAAAGATTCAA[C/T]GGGAGTGTCTGTTTT	25909
rs757991360	snp	G/T	1.64966e-05	0.00287194	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851058	CTACTTTTTGGGACT[G/T]TTGGTCACTAGTTAC	25909
rs758016958	snp	C/G	1.70688e-05	0.00292132	intron-variant	AHCTF1	GRCh38.p7	1:246887402	ATACAACAACAAAAA[C/G]CTCCTACGTATATAT	25909
rs758022590	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246863831	AGCACTCCCCAAGCG[-/T]TATCAGTTATAAATT	25909
rs758046033	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246880956	TAATAAGGAATGCAT[G/T]GGGGTTCTTGGCAAT	25909
rs758126238	snp	A/G	1.65699e-05	0.00287831	intron-variant	AHCTF1	GRCh38.p7	1:246895815	AATACCAAACATTTT[A/G]CTTGTTATCAGAATC	25909
rs758126748	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246866584	AAAAATTCAGAGTCT[C/T]GTAATGATTATTTAT	25909
rs758135670	snp	A/C	1.67122e-05	0.00289064	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246860929	GGTCTGAAGGAGTTA[A/C]TTCTGATGCAAATAC	25909
rs758136091	snp	C/T	5.5439e-05	0.00526464	intron-variant	AHCTF1	GRCh38.p7	1:246857866	AATATTTAGTGATTA[C/T]TGATAGTCTTGCATT	25909
rs758140455	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246910589	TTTATGGGAACTCTT[A/G]TATTCTTCTAACTAT	25909
rs758172343	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246916996	TCAGAACCTCTTCTC[C/T]GCCTATTAGTCATGT	25909
rs758191634	snp	A/T	1.6498e-05	0.00287206	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850920	TCACTAAAGGTATTG[A/T]TTCATGAATGGACTG	25909
rs758208623	in-del	-/AAAAAGTGCTTATAT			intron-variant	AHCTF1	GRCh38.p7	1:246862487	CCGTCTCAAAAAAAA[-/AAAAAGTGCTTATAT]AAAAAAGTGCTTATA	25909
rs758208803	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246857036	TCAGTCTCGCAATGA[A/G]ACAAGGACCTCTTGC	25909
rs758224918	snp	C/G	0.000121098	0.00778038	intron-variant	AHCTF1	GRCh38.p7	1:246891068	TATCAGTCCTGTAAA[C/G]AAGAGTTAACATCAG	25909
rs758259236	snp	A/G	1.67019e-05	0.00288975	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246885531	GTGAAGGATAACATC[A/G]TTACCACTGGACACT	25909
rs758260839	snp	G/T	1.76555e-05	0.0029711	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246862153	CCAAACTTTTAGCTT[G/T]CTATAGTAAAGAGCA	25909
rs758262461	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246882677	AGGATTTTTTGGCTT[G/T]CTTGTACATTTATGA	25909
rs758280312	snp	A/C	3.32806e-05	0.00407912	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900199	CTTACAACAGACTCC[A/C]ATGACCACAGTGCAA	25909
rs758282811	snp	A/C/T	6.64114e-05	0.00576211	intron-variant	AHCTF1	GRCh38.p7	1:246918243	TGTTCAGTGACATTA[A/C/T]GTTTACCTGCAGCAA	25909
rs758285704	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246886631	TACAGTTGATTGAAG[C/G]CACGGATGTAGAATC	25909
rs758314453	snp	A/T	1.64789e-05	0.0028704	intron-variant	AHCTF1	GRCh38.p7	1:246877323	AGCAGTATTTATCAA[A/T]GTTTAGTTTTAGAAA	25909
rs758316645	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246918053	AAAAATTAACTATAA[C/T]CCCCCCAATCAGAGG	25909
rs758320250	in-del	-/TT	1.65252e-05	0.00287443	frameshift-variant, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840932	CCGTCAGCTGGGCTA[-/TT]GCCAAGGGGGAAATC	25909
rs758346249	snp	A/C/G	4.97998e-05	0.00498977	missense, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840952	AGGGGGAAATCAGCC[A/C/G]AATTTCTATGGGAGG	25909
rs758364897	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246869698	ATTTTAAGCCTACTG[C/T]TGAGAACTGTTCAGA	25909
rs758376059	snp	C/T	1.64887e-05	0.00287125	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850171	TTCTCTCACATCTGA[C/T]GGACTAACTTCTCTC	25909
rs758383074	in-del	-/CT			intron-variant	AHCTF1	GRCh38.p7	1:246930169	AGCAACAGGTTCTCG[-/CT]CTGTCACACAGGCTG	25909
rs758425751	snp	A/C	1.65086e-05	0.00287298	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851326	ACAAAACTGTTGGTC[A/C]ATAGTATCAAAATTG	25909
rs758453114	in-del	-/G			intron-variant	AHCTF1	GRCh38.p7	1:246911275	CACAAAATACACTAT[-/G]AAACAAAAGCCTATC	25909
rs758468293	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246903432	TGTAGAGGAAAACGG[C/T]ATCTGAGAAGTTAAG	25909
rs758471853	snp	C/T	1.65097e-05	0.00287308	intron-variant	AHCTF1	GRCh38.p7	1:246877116	TTGTAAACTACCAAT[C/T]TATCTTGAATTTCTG	25909
rs758471964	snp	A/G	1.65064e-05	0.00287279	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246890033	CAGGGTAGTTGTAGC[A/G]TAACCTTGACAACTG	25909
rs758473094	snp	C/G	1.88329e-05	0.00306857	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851424	AATCTTGAGCTTCAA[C/G]CTTTTCTTGTTCAAT	25909
rs758476757	snp	C/G/T	3.34662e-05	0.0040905	intron-variant	AHCTF1	GRCh38.p7	1:246913428	CTAGAAAACATAATA[C/G/T]GTGATTTGCTTTTCT	25909
rs758495293	in-del	-/TC			intron-variant	AHCTF1	GRCh38.p7	1:246887051	TTTATATTCTTGCCT[-/TC]TCTAAAATAGTGCTT	25909
rs758504910	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246905464	ATCACGCCACTGCAC[G/T]CCAGCCTGGACAACA	25909
rs758504963	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246892012	AACTCCTATCACTCA[A/G]AAGAATTATTCTATT	25909
rs758524817	snp	A/G	1.65633e-05	0.00287774	intron-variant	AHCTF1	GRCh38.p7	1:246889950	AGATGTAATTTCTAA[A/G]ATTGTTTTACTATAC	25909
rs758562770	snp	C/T	1.64836e-05	0.0028708	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246905619	TGAAAAGTGACAGCA[C/T]ATACAGGAACTTGTC	25909
rs758571381	snp	A/G/T	0.000142023	0.00842582	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861261	GCACATTTTTTAGGT[A/G/T]TAGTAAATACTTCTA	25909
rs758579118	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246907400	CACATTGATTTAATG[C/T]CATGAAAAATTAGTC	25909
rs758581335	in-del	-/TC			intron-variant	AHCTF1	GRCh38.p7	1:246875160	GACATAGTAACTAAG[-/TC]TACACAACTGGGACC	25909
rs758597231	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246911931	TTTATCACTTGCAGT[G/T]TTTTTGTTTTTGTTT	25909
rs758605367	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246926742	TGCCTATAATCCCAG[C/T]TACTTTGGGAGGCTG	25909
rs758621810	in-del	-/AAAAC	0.277778	0.248452	intron-variant	AHCTF1	GRCh38.p7	1:246905501	GACTCTGTCTCCAAA[-/AAAAC]AAAACAAAACAAAAC	25909
rs758648190	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246900841	TTCACTACCTAAAAC[A/G]GATGCTTTTGGGCAT	25909
rs758655616	snp	C/T			missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876180	CGCAAACGAGGATCA[C/T]GATCATTCTATTAAA	25909
rs758657807	snp	A/G	1.64773e-05	0.00287026	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246898292	ATAACCATCAGGAAT[A/G]AGTTCATTGAGTGAT	25909
rs758664218	snp	C/T	1.66192e-05	0.00288259	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246857798	GAGATCCTTTGTTTC[C/T]GCATCTTCTAAATTG	25909
rs758681386	snp	C/T	1.64754e-05	0.00287009	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849693	GGTCCGGCAACAAGA[C/T]GGCCTTGCTAGACCG	25909
rs758709757	snp	C/G	4.07166e-05	0.00451183	missense, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843813	TTCATCTTCAAGCTT[C/G]TTCTTATTGGATGTG	25909
rs758717529	snp	C/G	1.65712e-05	0.00287843	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864103	GGACAGGCTGAACAA[C/G]CAAATCTAGCAGTCT	25909
rs758732012	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246866047	ACTTCAGCCTTACTA[C/T]ATGATGTACCCACGG	25909
rs758763048	snp	C/T	9.98303e-05	0.00706436	missense, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246842745	TTCGCTTTTGGCTTT[C/T]CCAGAGTTTCTACTG	25909
rs758780543	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246899655	AACTTTTCTAGGTAT[C/T]TTCATCCTAAGAATA	25909
rs758784240	in-del	-/A	7.04655e-05	0.0059353	intron-variant	AHCTF1	GRCh38.p7	1:246876208	AACATCAAAATTGGT[-/A]AAAAAATTTAACCTT	25909
rs758826780	in-del	-/ATCC			intron-variant	AHCTF1	GRCh38.p7	1:246893741	TAGAAAGTGAGTTAA[-/ATCC]GTACAGAAACTTCTG	25909
rs758863614	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246871297	AACAGAGACACCACT[C/T]GCTTACTGATGGGAG	25909
rs758878604	snp	C/G	1.65165e-05	0.00287367	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864055	ATTTCATGGAGCTTT[C/G]CTGAATAAACTCCGA	25909
rs758917844	snp	A/G	5.09221e-05	0.00504564	intron-variant	AHCTF1	GRCh38.p7	1:246916124	GAGAAATGTCCAGGT[A/G]TCTTAAACAGTACCT	25909
rs758925793	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246852127	ACATTACCACCCACC[G/T]AGACAATGACATTTT	25909
rs758931642	snp	C/T	1.64958e-05	0.00287187	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850109	GGTATGGCAGACATA[C/T]CAAATTCTGCTTGAA	25909
rs758937842	in-del	AAAAAAAAAAAAAA/T			intron-variant	AHCTF1	GRCh38.p7	1:246909399	CCAGCCTCTCAAAAA[AAAAAAAAAAAAAA/T]AAAAAAAAAATTTGC	25909
rs758940402	snp	A/G	1.65474e-05	0.00287636	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902547	CACGCCTTCCTCCCT[A/G]TCACCATGAGATCGA	25909
rs758941358	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246886456	TAAGTAATCTACAGA[C/T]GATTTAAAGATCAAG	25909
rs758957942	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246901719	GTTACTTGGGAGACC[A/G]AGATGGGAGAATTGG	25909
rs758986571	snp	G/T	1.64757e-05	0.00287012	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851267	AGTTCCCCATCTACT[G/T]CAGCAATGTCACATT	25909
rs758987725	snp	A/G	1.65111e-05	0.0028732	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246913383	TGCACTGGCTCCTCC[A/G]TGATTAATTATAGGT	25909
rs759040712	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246930181	TCGCTCTGTCACACA[C/G]GCTGAGTGCAGCGGC	25909
rs759045210	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246901722	ACTTGGGAGACCGAG[A/G]TGGGAGAATTGGTTG	25909
rs759047411	snp	A/G	1.65979e-05	0.00288074	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851348	TCAAAATTGTACTGA[A/G]GCTTAAGTGTTCCAG	25909
rs759056251	snp	C/T	1.66026e-05	0.00288115	intron-variant	AHCTF1	GRCh38.p7	1:246898372	AGGCATCAATCAATG[C/T]TCAATTTGAATAATC	25909
rs759063345	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246899389	AAAACTTAAATCCAT[A/C]AATCAACTATATTCT	25909
rs759082090	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246876764	AACATAAATGGCATA[C/T]GTAAAAGAATTACGT	25909
rs759094026	snp	C/T			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932461	CTCCCACTTTTCTTT[C/T]TTTCTTTTTCTTTTT	25909
rs759126391	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246844709	AGCCTGGGTAACAGA[C/G]TGAAAAGCTAACAGG	25909
rs759150696	snp	G/T	1.77881e-05	0.00298223	intron-variant	AHCTF1	GRCh38.p7	1:246888546	AAAATTAAGACTTAT[G/T]TAATATCACTGTTAA	25909
rs759152189	snp	C/T	3.29641e-05	0.00405968	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849663	AAAATAAAGGCTCAT[C/T]GTTTGGTTCAGAAAG	25909
rs759164168	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246851548	TGCCTTTTAAAACAT[A/G]AATTATATTTAATAT	25909
rs759206319	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246877961	TGTTCAACTCATACC[C/G]CACCGACAGGATTAT	25909
rs759207132	snp	C/G	1.64874e-05	0.00287113	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246888404	CCTACATGCAGACTA[C/G]CAGGAGGATATTTTC	25909
rs759208911	in-del	-/TTCAGT	1.71315e-05	0.00292668	intron-variant	AHCTF1	GRCh38.p7	1:246916096	TATAACCAGCAGGGG[-/TTCAGT]TTTGAAAGAGAAATG	25909
rs759223506	snp	A/G			utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839261	TTATTAAAAACAGGT[A/G]CCACACATCTATATT	25909
rs759235603	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246913941	AAAAACAACAAAAAA[G/T]ATATTTTAAGTCCTC	25909
rs759251600	snp	A/C/G	6.59429e-05	0.00574177	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861057	AGGTCTTCCGGTGAC[A/C/G]GTGCATCCTGATACT	25909
rs759255909	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246901342	AGACCCTGTCTCTAA[A/C]AAAACAAAAACAGGC	25909
rs759257715	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246930552	TCTTCTCTCCTAAGA[A/G]ACTCTATCAGTGAAA	25909
rs759261775	in-del	-/AAC			intron-variant	AHCTF1	GRCh38.p7	1:246921228	CAAAACTATGAAAAA[-/AAC]AAAGAAAAAATAAAC	25909
rs759273373	snp	A/G	1.6531e-05	0.00287493	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864070	GCTGAATAAACTCCG[A/G]ACACTGAGAAGGCCG	25909
rs759293843	in-del	-/A	3.54566e-05	0.00421035	intron-variant	AHCTF1	GRCh38.p7	1:246853070	GACTGATAAAGAAGT[-/A]AAAAAATTAATTTTT	25909
rs759297998	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246886043	AAACAAAAGTAAGTT[C/T]AAACAAAAAAAGTGC	25909
rs759316810	snp	C/T	1.67167e-05	0.00289103	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246894740	AATTAGTGGCAGAAT[C/T]TGGTTGTTCTTATTT	25909
rs759358995	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246854215	GAGGCAGGAGAATAG[C/T]GTGAGCCTGGGAGGC	25909
rs759364965	in-del	-/A	7.45261e-05	0.00610389	intron-variant	AHCTF1	GRCh38.p7	1:246861911	CTTGTCAGAGCTAAT[-/A]CATTCTTATTAAAAA	25909
rs759399151	snp	A/C			synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916148	AGTACCTACCCTTCC[A/C]GGAAGAACAACTGCT	25909
rs759399677	snp	G/T	1.6896e-05	0.0029065	intron-variant	AHCTF1	GRCh38.p7	1:246855862	TACCTTAGTGTGTAA[G/T]AAGATCCCATCTGCT	25909
rs759443498	in-del	-/C			intron-variant	AHCTF1	GRCh38.p7	1:246854625	ATTTCTAACAGCTAA[-/C]ATTTACTAAACTTCA	25909
rs759452268	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246902128	CTTGGCTTAAAAAAC[C/T]GATGCAAAAAAAACT	25909
rs759467078	snp	A/G			utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839580	CTGTCAACACTTTGC[A/G]TAGGCATTTTCACCA	25909
rs759476253	snp	A/C	1.66601e-05	0.00288614	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900405	CAAATATACAGAAGG[A/C]TTTCCCTGTCCATAT	25909
rs759481949	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246908015	TCTCAAATATTATCT[A/C]AGATAGAATTTTTTT	25909
rs759499255	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246917234	TTCAACTTAGAGGGA[A/G]AACTAATTGGATTTC	25909
rs759505841	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246931008	CCCAGGTAGGAAAAA[A/G]GAAGGCAAAGCACCC	25909
rs759510273	snp	C/T	1.69654e-05	0.00291246	intron-variant	AHCTF1	GRCh38.p7	1:246913445	TGATTTGCTTTTCTT[C/T]TGCAAAGTAAGAAAA	25909
rs759524712	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246907064	TAACACAAACCTAGA[A/T]GAGATAGCCTACTAT	25909
rs759528795	snp	A/G	3.34868e-05	0.00409173	intron-variant	AHCTF1	GRCh38.p7	1:246891731	CGTTTCTCTTAGTCA[A/G]GAAGTAAAATTTAAT	25909
rs759545917	snp	C/T	0.000765455	0.0195484	missense, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840930	ACTCCGTCAGCTGGG[C/T]TAGCCAAGGGGGAAA	25909
rs759584965	snp	A/T	2.83821e-05	0.00376699	intron-variant	AHCTF1	GRCh38.p7	1:246841020	AAAAAAGATATGATC[A/T]AGTAAGAATAAACAC	25909
rs759596600	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246873471	GAAGGGAAAGAATCC[A/G]TCCCAATACTAAATG	25909
rs759619263	snp	C/G			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246931998	GAAAGGGCGGAGAGG[C/G]AGGGGAGAACCGGCG	25909
rs759656970	snp	C/T	3.38828e-05	0.00411585	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853258	GACCTTCAGAGATAG[C/T]GAGCGAGGAGTTTCC	25909
rs759676665	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246860133	GTCATGGTGGGGGGC[A/G]ACTATAGTCCCAGCT	25909
rs759685774	snp	A/G	3.42395e-05	0.00413746	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246862121	CTCAGAAAATCCAGA[A/G]GTAGTAACTGACATG	25909
rs759700229	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246845055	GTGGCAGGGTAGGTG[G/T]TAAGTGCTCTACAGA	25909
rs759702424	snp	A/C	1.6599e-05	0.00288084	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246890984	TAAAAGCCCAGAATG[A/C]GAGAACCAAAGAACC	25909
rs759719454	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246847176	CACCTGTAATCCCAG[A/C]TACTGGGGAGGCTGA	25909
rs759734529	snp	A/G	2.02702e-05	0.0031835	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876181	GCAAACGAGGATCAC[A/G]ATCATTCTATTAAAC	25909
rs759735557	snp	G/T	1.6651e-05	0.00288535	intron-variant	AHCTF1	GRCh38.p7	1:246900258	TGACCTAAAAGAAAA[G/T]TTAAAACATTACTAA	25909
rs759740089	snp	G/T	1.65688e-05	0.00287821	missense, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840824	CAGCATTTTTCTGCG[G/T]AAAATTTGCTTTGGA	25909
rs759755437	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246928524	AATAGGCATGTTAAA[C/T]AATAAAATCAATTTT	25909
rs759788378	snp	A/G	1.76201e-05	0.00296812	intron-variant	AHCTF1	GRCh38.p7	1:246907802	TAAAAAACTAGAAAC[A/G]GCATTAAAAGCAAAT	25909
rs759803378	snp	G/T	1.64817e-05	0.00287064	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849873	TTGTAAGTTTTTTCT[G/T]AGAGCTCATCACCAT	25909
rs759816995	in-del	-/TAAAT			utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840716	TTACAATAATTTATA[-/TAAAT]TATTTTCTTCCAAAC	25909
rs759817313	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246880036	TGTTAAAAGGGTTTA[C/G]TGGGAGAGGACATAT	25909
rs759818901	snp	A/G	1.64993e-05	0.00287218	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246905570	CTGAACAGCCCACAA[A/G]TAACAGCAATTCCGA	25909
rs759872976	snp	C/G	1.6477e-05	0.00287024	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867703	GGTTCTTTGCTTGCC[C/G]AAACTTCTCCAATTT	25909
rs759888265	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246868506	GTGATCCTCCCTCCT[C/T]GGCCTCTCAAAGTGC	25909
rs759899385	in-del	-/ACA			intron-variant	AHCTF1	GRCh38.p7	1:246879074	TCATTATTAAATCTC[-/ACA]ACAAGGTTGATTTCC	25909
rs759902833	snp	C/T	1.6473e-05	0.00286988	intron-variant	AHCTF1	GRCh38.p7	1:246885471	ACGATAAAGACTTTA[C/T]AGTTTCAAAAGATGT	25909
rs759971265	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246879487	TAGCATTGTTTAAAA[C/T]GGCTAAAGGTTGAAA	25909
rs759978109	in-del	-/A	1.66604e-05	0.00288616	frameshift-variant, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900086	ATAAGTGCTTGGATT[-/A]AAAAAACTGCTCGGG	25909
rs759984160	snp	C/T	1.72722e-05	0.00293867	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850637	CCTCTGACATCAGAA[C/T]AGATGTTTTCAGAAG	25909
rs759987050	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246917282	CACAGGGAGGTGAGT[A/C]AAACAAGAATCAAGT	25909
rs760018955	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246881418	CACAGAAAGATTAAA[A/G]CCATGCAACGAACAA	25909
rs760044674	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246903214	TGTGAGGGTGAACAA[A/C]ATACAGCTATTAGCA	25909
rs760095640	in-del	-/CA			intron-variant	AHCTF1	GRCh38.p7	1:246870723	GAGGGTATAAAACCT[-/CA]AAAAAAAAAAAAAAA	25909
rs760109268	snp	A/C	1.64993e-05	0.00287218	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850229	CGCAGCTGCTTGTCA[A/C]TGGATTTATCATCTT	25909
rs760156275	snp	G/T	1.68408e-05	0.00290175	intron-variant	AHCTF1	GRCh38.p7	1:246902515	ACATATTTCAAGTAC[G/T]TTAACTAACCTTCAT	25909
rs760173356	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246895616	GGCTGTAACGGCAGC[A/G]TGAGGGATCCTGGTG	25909
rs760177980	snp	C/T	1.69321e-05	0.0029096	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916214	GAGAACACTCCCTTC[C/T]GTTTCTTCCAATCCT	25909
rs760179640	snp	C/T	4.27451e-05	0.00462285	intron-variant	AHCTF1	GRCh38.p7	1:246853051	CAACTAAACCAAAAC[C/T]GAAAGACTGATAAAG	25909
rs760182402	snp	A/G	1.66782e-05	0.0028877	intron-variant	AHCTF1	GRCh38.p7	1:246855719	CCTGAAGTCAAAATT[A/G]TTATACATACATTTA	25909
rs760182454	snp	A/C/G	0.000198739	0.00996663	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850494	TTTTTGATTCCCTAC[A/C/G]TGTAGTGATCTGTAA	25909
rs760183202	snp	C/T	1.65012e-05	0.00287234	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246890002	TGTCGACGACTGGTG[C/T]AGTAGTTCTGAATTA	25909
rs760231960	snp	A/G			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932899	GCTCTTTTATCAGGA[A/G]AGTTTCTACTTTTCT	25909
rs760232052	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246903046	AGTTCTTAGACTTTT[A/G]GCTTATTGATACCTT	25909
rs760237399	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246863746	GTTAACTTTAAGCAG[G/T]AAGGGATAAATTTAA	25909
rs760242005	snp	A/C	1.65348e-05	0.00287526	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864074	AATAAACTCCGAACA[A/C]TGAGAAGGCCGGGGG	25909
rs760277708	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246854898	GAAATGGGCACAGAA[A/C]ACAAAAATTCAGGAA	25909
rs760281122	snp	G/T	8.54037e-05	0.00653411	intron-variant	AHCTF1	GRCh38.p7	1:246913452	CTTTTCTTCTGCAAA[G/T]TAAGAAAATATAATT	25909
rs760344070	snp	C/T	1.64933e-05	0.00287165	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877070	GGACTGCAAAAATTT[C/T]ACTAAACATTCCTAA	25909
rs760348708	snp	A/T	9.89952e-05	0.00703476	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851030	ATAGGTTCAGGCACA[A/T]ATGGTAAAGTGTCTA	25909
rs760373255	snp	A/G	1.8053e-05	0.00300436	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876110	TTTTCGATGGACTCT[A/G]GGAAGGATTTTTCCA	25909
rs760388922	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246887817	CTAAGGTAGTATCAC[G/T]CTAACTTATAATGTA	25909
rs760403673	snp	A/C	5.20784e-05	0.00510259	intron-variant	AHCTF1	GRCh38.p7	1:246860866	TTGAGGGACATTAAT[A/C]ACAATTTTGAGTATT	25909
rs760415927	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246869248	TACTCCACTGACTAA[C/G]TGTTCCCCCGCGTCT	25909
rs760419144	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246930794	CCCAAAGGATTTACG[C/T]TTTGTTCTATGAAGA	25909
rs760421537	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246856915	GTTATATTTTGTGTC[A/G]GTTAATTTTACTGAA	25909
rs760450121	in-del	-/AATC			intron-variant	AHCTF1	GRCh38.p7	1:246887690	AAAAGATGGCAGCTT[-/AATC]AAACATCATCTAGCT	25909
rs760456492	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246879115	TACAAAGCGGCTATA[A/T]ATCAGTAAGAAAAAT	25909
rs760457826	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246869988	CCATTCTAGATGCCA[C/T]TCAGCACATTCATAA	25909
rs760500570	snp	C/T	1.66092e-05	0.00288172	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246887354	CAAGTAGCAAATAAA[C/T]GGTCTTTTAAAAAGC	25909
rs760531819	snp	C/T	1.64798e-05	0.00287047	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850896	TAGTGGGACACATTA[C/T]GTTTTGGCTCACTAA	25909
rs760549438	in-del	-/AGG	1.64963e-05	0.00287192	cds-indel, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864035	GGATACTAGGTACAA[-/AGG]AGATTTCATGGAGCT	25909
rs760553770	snp	C/T	5.78185e-05	0.00537642	intron-variant	AHCTF1	GRCh38.p7	1:246894777	ACAAAAGGGAAAAAA[C/T]AAAGATTATTAATTA	25909
rs760583281	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246872489	AGGTTCTGGCTTACT[C/T]CAACCAATCCAGAGT	25909
rs760589163	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246888800	CTGTAGTCCTAGCCA[C/T]TCAGGAGGATAAGGA	25909
rs760598784	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246861475	AAAAGTTAATGGTGG[C/G]TAATGTTTCCCTAAT	25909
rs760655294	snp	C/G	1.77316e-05	0.0029775	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246885630	AATCTTTGAATGTTG[C/G]CATGACAAAGGTTTT	25909
rs760662305	snp	A/G	1.64803e-05	0.00287052	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902605	AATTTGGTATTACTC[A/G]TCTGTCCCCTCAAAG	25909
rs760686203	snp	C/T	1.65809e-05	0.00287926	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246918323	TTGAAGAGTCACTTC[C/T]GGAAATGGCAGGAGA	25909
rs760686791	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246923451	AATAAATACATAAAA[C/T]AATTATAATAACTGA	25909
rs760694972	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246890122	TCTCAACAATACATA[A/T]TAATATTTTACTGTA	25909
rs760722141	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246881970	CAGGCATGAGCCACC[A/G]TGCCTGGCCTTTATT	25909
rs760727763	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246863159	TTAAATTATTGAAAC[C/G]TAATCTTTTCAACTT	25909
rs760736790	snp	C/G	1.6522e-05	0.00287414	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246857770	ATTCTGAAAATGCCT[C/G]TGCTGCAACTAAGAG	25909
rs760765068	snp	A/G	1.66032e-05	0.0028812	intron-variant	AHCTF1	GRCh38.p7	1:246867202	ACAATTGTAACTATC[A/G]TCTAACATTGTGTCT	25909
rs760767548	snp	G/T	1.69934e-05	0.00291486	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850646	TCAGAATAGATGTTT[G/T]CAGAAGCTTCAGAAA	25909
rs760790737	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246897795	AGACCAGCCTAGGCA[A/G]CATAGCGAGACCCTG	25909
rs760820555	snp	C/T	3.2981e-05	0.00406071	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246855754	CATTTGCTCTAATTG[C/T]AGGGGTGTAGGTTTC	25909
rs760835234	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246865949	ACTTTTTACTTGTTA[C/G]AGCTAATTTTTTTTT	25909
rs760863464	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246847403	AAATACCAACCATAC[A/G]TATGTATCTGGAACG	25909
rs760867412	in-del	-/CTGTAT	1.82814e-05	0.0030233	intron-variant	AHCTF1	GRCh38.p7	1:246843948	AAAAAGTTGAAAAAA[-/CTGTAT]CTGTATCTTTATATA	25909
rs760873512	snp	A/C	1.65474e-05	0.00287636	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246891840	TATATTAAGATTGCT[A/C]AGAAGCAAATAGCAT	25909
rs760890525	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246883183	GTGTTTGATGGTTTA[A/T]ATATTAAAACTTTTT	25909
rs760902458	snp	A/G	1.65872e-05	0.00287981	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900345	ATCATACCTTAACGA[A/G]TCTGGCATTTGTGCA	25909
rs760930694	snp	A/C	3.32386e-05	0.00407654	intron-variant	AHCTF1	GRCh38.p7	1:246891764	AACACTCATTTGATA[A/C]AACAAAGAGCGTACC	25909
rs760940178	snp	C/T	1.80651e-05	0.00300536	intron-variant	AHCTF1	GRCh38.p7	1:246899547	AATAATCCACTTACA[C/T]ATATTTAAAATGGCA	25909
rs760949448	snp	A/G	1.64933e-05	0.00287165	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246913365	ATGTAAATGCTGAGT[A/G]CTTGCACTGGCTCCT	25909
rs760949626	snp	C/T	1.81965e-05	0.00301628	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840984	GGTGACCAAGCACTT[C/T]CTTTTTCTGTGTTTC	25909
rs760977040	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246917507	TAACTGGGATCAAAT[A/T]AATGATTTCATTCTC	25909
rs760978804	snp	C/G	1.66515e-05	0.00288539	intron-variant	AHCTF1	GRCh38.p7	1:246900280	CATTACTAAGTCATT[C/G]GTCAGCTACACATAC	25909
rs760993765	snp	A/G	8.26289e-05	0.0064271	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850086	TTCTTGGTCTACCAC[A/G]TTTTCTAGGTATGGC	25909
rs761003741	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246886317	GCCTGGGTGACAGAG[C/T]GAGACTCCATCTCAA	25909
rs761020927	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246919693	TCGGTGACAGAGCAA[C/G]ACTCCATCTCAAAAA	25909
rs761049721	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246876633	CCCTTACTGCTGGCC[-/T]CTACGTCTTCCTCTA	25909
rs761052117	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246848831	TCCAGCCTGGGCGAC[-/A]AGAGTGAGACTCTAC	25909
rs761065908	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246918801	ATTCCCTAGATTCTT[C/T]AAACACTAGTTCAGT	25909
rs761089835	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246905247	ACTCACACCTGTAAT[C/G]CCAGCACTTTGGGAG	25909
rs761094648	snp	C/T			synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246857693	TCCATTAACTTACCC[C/T]TCATAGACTGATGGT	25909
rs761095728	snp	C/T	0.000337901	0.0129937	intron-variant	AHCTF1	GRCh38.p7	1:246888568	CACTGTTAATTAATA[C/T]CAAAGCAACCAGCAT	25909
rs761120104	snp	C/G	3.87732e-05	0.00440285	intron-variant	AHCTF1	GRCh38.p7	1:246867847	GAATTAAGTGCATCT[C/G]TAACAAACGGGAATT	25909
rs761127937	snp	A/G	3.29783e-05	0.00406055	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246905584	AGTAACAGCAATTCC[A/G]AGGATCATTCTCAGG	25909
rs761128061	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246846389	GAAGCTATGTCCTAG[A/C]GTGGTCATTGCTTTG	25909
rs761142676	in-del	-/A	0.000503031	0.0158513	intron-variant	AHCTF1	GRCh38.p7	1:246916402	ATTTTTCCCTAGAAG[-/A]AAAAAAAAATTGCCT	25909
rs761180882	snp	A/G	1.71231e-05	0.00292597	intron-variant	AHCTF1	GRCh38.p7	1:246904066	GAAGACACGCTAAAT[A/G]TATTAATACATTAAA	25909
rs761194849	snp	A/T	0.000133849	0.00817963	intron-variant	AHCTF1	GRCh38.p7	1:246887179	AATTCTAGTAATTCA[A/T]GAAAGTTTATGCTGT	25909
rs761247682	snp	C/T	1.64923e-05	0.00287156	intron-variant	AHCTF1	GRCh38.p7	1:246867233	CTAAGAATGATTTAA[C/T]AAACTCTTACCTAGA	25909
rs761258194	snp	A/G	1.64806e-05	0.00287054	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849669	AAGGCTCATTGTTTG[A/G]TTCAGAAAGGTCCGG	25909
rs761268096	in-del	-/TC	5.06598e-05	0.00503263	intron-variant	AHCTF1	GRCh38.p7	1:246867215	TCATCTAACATTGTG[-/TC]TCTAAGAATGATTTA	25909
rs761271805	in-del	-/AAAC			intron-variant	AHCTF1	GRCh38.p7	1:246854658	ACCAAGCGCTACACA[-/AAAC]AAACACTTTACATGC	25909
rs761278131	snp	A/G	2.25966e-05	0.00336122	intron-variant	AHCTF1	GRCh38.p7	1:246894798	TTATTAATTACAAAC[A/G]GAGTTCTAAATTGTT	25909
rs761289993	in-del	-/AAG			intron-variant	AHCTF1	GRCh38.p7	1:246877471	CATAATAATCTTGCT[-/AAG]AATGTCAGTAAAATG	25909
rs761318779	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246890161	TTTACAGCAACCCCT[A/G]GTTAACCCACAGGGT	25909
rs761353051	snp	C/T	0.000368596	0.0135706	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867333	ATACACTATAGGAGA[C/T]GGTTCTTCTATTTTA	25909
rs761363639	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246856262	TCAGAATAAGAGACC[A/C]ATGAAACCTGTATTA	25909
rs761368770	snp	C/G			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933046	GCTCAAATGATCCTC[C/G]TACCTCAGCCCTCCA	25909
rs761371486	in-del	-/TCAT	1.65388e-05	0.00287561	intron-variant	AHCTF1	GRCh38.p7	1:246888276	GTGGATCTTATACAG[-/TCAT]TCATTCATTCATGCT	25909
rs761374481	snp	A/G	1.67371e-05	0.0028928	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246860921	TTTCTGTAGGTCTGA[A/G]GGAGTTACTTCTGAT	25909
rs761375620	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246856740	CTACTTTTTCCATGC[A/T]GGCCTGGCAAAAATT	25909
rs761375838	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246920478	ATGAATGTCAGAATA[C/T]ATTATTAAACCAGCC	25909
rs761380015	snp	A/G	1.64982e-05	0.00287208	intron-variant	AHCTF1	GRCh38.p7	1:246895951	CATTACAGAAAGGAA[A/G]GAAATGGAAAGAAAG	25909
rs761448300	snp	A/G	0.000105416	0.00725925	intron-variant	AHCTF1	GRCh38.p7	1:246843784	TACAAATAAAATCAT[A/G]CATTTCTTACCAGTT	25909
rs761453221	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246869272	CGCGTCTCTCCCTTT[C/T]CCCGAGGACCTCCCT	25909
rs761499711	snp	C/T	1.66635e-05	0.00288643	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850337	GTACTAACTTTTAGA[C/T]CATTTATAATTTCAA	25909
rs761501192	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246874102	ATTTAGTATTTTATA[A/G]TCTTTTTTAATATTA	25909
rs761533846	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246894581	TCAAAATGATTAAAA[A/G]TTATGTACTTAAGAC	25909
rs761541791	snp	A/T	1.6507e-05	0.00287284	intron-variant	AHCTF1	GRCh38.p7	1:246888369	TTTGTAGACTCTAAA[A/T]GATAGCACATTACTG	25909
rs761546332	snp	C/G	1.71176e-05	0.00292549	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916245	ATTAATAATCCAGTT[C/G]TCTTCTGCCAAGAGA	25909
rs761568392	snp	C/G	1.76537e-05	0.00297095	intron-variant	AHCTF1	GRCh38.p7	1:246913197	TCAGAATATCCAGGT[C/G]CTCCATTTTTGGTTT	25909
rs761580630	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246875262	ACACTCCCTTACATA[A/C]AATGACACAACCTCT	25909
rs761599612	snp	C/T	1.6884e-05	0.00290547	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916394	AGCAAGTCCATTTTT[C/T]CCTAGAAGAAAAAAA	25909
rs761602641	in-del	-/TCTT			downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838917	TACTGATACTAAGTA[-/TCTT]TCTGAGTATATCATT	25909
rs761605943	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246906478	TCCCAGCTACTTGGG[A/T]GGCTGAGGCAGGAGA	25909
rs761634146	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246869061	ATGTTGGCCAGGATG[G/T]TCTCGATCTCCTGAC	25909
rs761645860	in-del	-/TAT			cds-indel, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839611	ATTTCTCATTATCTG[-/TAT]TATTTGGTAGAAAAA	25909
rs761680907	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246869329	GCCAACTAATAACCC[-/T]TACAAAGACCTCAAG	25909
rs761693307	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246922282	GGAGAATTGCTTGAA[C/T]CCAGGAGGCAGAGGT	25909
rs761729681	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246885893	GCAGATAGAAAACAT[C/T]TGAAAAAATAAGGCT	25909
rs761741960	snp	C/T	0.000409836	0.0143091	intron-variant, utr-variant-5-prime, upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246931356	TCCGGTCCGAGATTA[C/T]GTAACGAAGCCCGGC	25909
rs761749767	snp	A/G	1.64974e-05	0.00287201	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246888199	TGTTTGGCTGCTTCA[A/G]TAACGCCGTCTAATA	25909
rs761798794	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246928819	TGACTAATAAAAAGA[C/T]GAATTGTCATTTAAA	25909
rs761802779	in-del	-/G			intron-variant	AHCTF1	GRCh38.p7	1:246847920	CCCTGCCAATAAAAT[-/G]TTTTTCATTTTAACT	25909
rs761815444	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246911190	GAAGGATGTTTTAAC[A/G]CCACCATATTGACTT	25909
rs761816867	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246919177	CTGATCTTATTCTGG[A/G]CACTCTAAGATCCAG	25909
rs761871138	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246857902	TTTTTAAAAAGTTGT[C/T]GGGTCTGCTTTTTTG	25909
rs761875794	in-del	-/CAACTTCTT	0.000258065	0.0113563	intron-variant	AHCTF1	GRCh38.p7	1:246931101	GCTGAGCCCCGAGTC[-/CAACTTCTT]CCCCGCCAGGACTAC	25909
rs761884141	snp	C/G	1.65154e-05	0.00287358	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246857734	AAGCTTCAGTTCCTT[C/G]AACCGGGCTTAAGTG	25909
rs761895894	snp	C/T	1.65765e-05	0.00287888	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246860983	TTTGTTCAGTTACAT[C/T]AGTAGTTAGTGCAGT	25909
rs761898045	snp	C/T	1.64991e-05	0.00287215	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851048	GGTAAAGTGTCTACT[C/T]TTTGGGACTTTTGGT	25909
rs761900985	snp	C/T	1.64776e-05	0.00287028	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849682	TGGTTCAGAAAGGTC[C/T]GGCAACAAGATGGCC	25909
rs761918399	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246917646	GAGAATGGCGCTGTC[A/G]AGAGAGAAATGACTG	25909
rs761966900	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246870195	ATGCCTGTAATCCCA[A/G]TACTTTTGGAGGCCA	25909
rs762009426	snp	C/G	1.6483e-05	0.00287076	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246905610	TCAGGTTCTTGAAAA[C/G]TGACAGCATATACAG	25909
rs762029865	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246870925	TACAAGAGCTGGAGT[C/T]AGACCCTTTTAAAGA	25909
rs762038185	snp	A/T	1.91419e-05	0.00309363	intron-variant	AHCTF1	GRCh38.p7	1:246894613	TAAACCAAGGTTAGT[A/T]TTTTAATATTAAATT	25909
rs762045595	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246885361	AATCTGAATTTGATG[C/T]AGAACCCACTAATAC	25909
rs762057201	in-del	-/T	2.41999e-05	0.00347841	intron-variant	AHCTF1	GRCh38.p7	1:246851458	TAAATGAATTAAAGA[-/T]TAAGAGACTGGTTAA	25909
rs762073550	snp	C/G	0.000146483	0.00855686	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246885655	GGTTTTGCAGTAGCT[C/G]GATGAAACAAAAGAT	25909
rs762104686	snp	C/T			missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850259	TGCTTATTTCCTGTA[C/T]TTTCAGAAGCATCTA	25909
rs762122830	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246905326	AACATGGTGAAACCC[C/T]GTCTCTACTGAAAAT	25909
rs762149312	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246918898	AAAAGAAAAAGTGAT[A/T]GGTGTCTTTTAGAAA	25909
rs762154451	snp	G/T	2.74179e-05	0.00370246	intron-variant	AHCTF1	GRCh38.p7	1:246890911	CAAAATTATAAAGAT[G/T]CAGAATGTTTTAATT	25909
rs762171853	snp	C/G/T	3.33257e-05	0.0040819	missense, splice-donor-variant, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246842697	AGAAAGTCATACTTG[C/G/T]TTGCTTGTTTTGTTT	25909
rs762203443	snp	C/G	1.65012e-05	0.00287234	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246890010	ACTGGTGTAGTAGTT[C/G]TGAATTACAGGGTAG	25909
rs762221394	snp	C/T	1.65408e-05	0.00287578	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877185	TGTAAATGGTAACTT[C/T]AGTAAATCTTCCATC	25909
rs762224336	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246912692	ATTTAAAGGAGAAAA[A/C]GTATTTCATTTTCTT	25909
rs762237172	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246845098	TTATTTCAAGAATAT[A/C]ATTTACAAACCCTTG	25909
rs762248231	snp	A/G	1.82417e-05	0.00302002	intron-variant	AHCTF1	GRCh38.p7	1:246861929	TTCTTATTAAAAAAT[A/G]TCTTTTCTCCCAATT	25909
rs762258506	snp	G/T	1.88802e-05	0.00307242	intron-variant	AHCTF1	GRCh38.p7	1:246899560	CATATATTTAAAATG[G/T]CATTAATAGAACAAA	25909
rs762259468	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246894301	CTTCAGGCCAGGCGC[A/G]GTGGCTCACGCCTGT	25909
rs762263196	snp	A/C	3.29506e-05	0.00405884	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849755	GAAGCTGTGGCGAGC[A/C]ATCTTTCTTCCTGCT	25909
rs762288950	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246893383	CTTAACTTACATTGT[A/G]AAAAGCTATCTATAG	25909
rs762292886	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246929509	GATGGCACTCCAGGA[C/T]GAAGGACATGAGCAA	25909
rs762294871	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246858960	AGGCCAGGACCGGTG[A/G]CGCATGCCTGTAATC	25909
rs762305656	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246927008	TGAAATCCCGTCTCT[A/G]CTAAAAATACAGAAA	25909
rs762311921	snp	C/G	1.65165e-05	0.00287367	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246899470	TTCTGAAAGCCAGTA[C/G]AAGTTAAATGAACAA	25909
rs762318810	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246906578	CAGAGTGAGACCCCA[C/T]CCCCCAAAAAAATAG	25909
rs762360142	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246845632	AGGAAATACAAAAAT[A/G]TACTATCACATGCAA	25909
rs762362885	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246865506	CTTTTCTTCTAGATT[C/G]TCTTCTTTCTCTATC	25909
rs762365458	in-del	-/CAAATTTCTATAAATAATTAGAAGAGTTGGTTTTTTATC			intron-variant	AHCTF1	GRCh38.p7	1:246852350	TTCCCAAATCCTAAA[lengthTooLong]CAAATTTCTATAAAT	25909
rs762372372	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246927369	TGCATACGCTTGTCA[-/T]TCCCGACTACTTGGG	25909
rs762383722	snp	C/G	3.3089e-05	0.00406736	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246860988	TCAGTTACATTAGTA[C/G]TTAGTGCAGTGGAAG	25909
rs762451436	in-del	-/A	3.47102e-05	0.0041658	intron-variant	AHCTF1	GRCh38.p7	1:246888529	CCTCTGCAATCAGGG[-/A]AAAAATTAAGACTTA	25909
rs762455348	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246876588	GAATTAGTCTGACCC[C/T]TGAAGTCCAATGATC	25909
rs762458531	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246872752	TTTCCAATCACTATA[C/T]AGAAGAGCTTGCTTG	25909
rs762483210	snp	C/T	1.64849e-05	0.00287092	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861048	GTCTCTTCAAGGTCT[C/T]CCGGTGACGGTGCAT	25909
rs762509252	snp	A/T	3.29685e-05	0.00405995	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851126	TTTTCCCCACTGCAT[A/T]CAAGTTTTTCTTCAG	25909
rs762515808	snp	G/T	1.65012e-05	0.00287234	intron-variant	AHCTF1	GRCh38.p7	1:246888380	TAAATGATAGCACAT[G/T]ACTGCAAACCTACAT	25909
rs762536224	in-del	-/ATTT			utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839389	TTTAGCTCTTTATTC[-/ATTT]AACAAGTTCATTTAA	25909
rs762545424	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246896215	TCCAATTCCACACCT[A/G]GGTATATACCAAAAA	25909
rs762548417	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246903618	GTGGATCACGAGGTC[A/G]GGAGTTCAAGACCAG	25909
rs762577727	snp	A/G	2.49884e-05	0.00353463	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867343	GGAGATGGTTCTTCT[A/G]TTTTAGAACTATGAA	25909
rs762607957	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246863502	GGCAGTTTAAAGAGG[A/G]ATAAACCAAAGTAGC	25909
rs762612214	snp	A/G	7.72171e-05	0.0062131	intron-variant	AHCTF1	GRCh38.p7	1:246841002	TTTTCTGTGTTTCTG[A/G]AAAAAAAAGATATGA	25909
rs762647514	snp	A/G	1.65046e-05	0.00287264	intron-variant	AHCTF1	GRCh38.p7	1:246895962	GGAAAGAAATGGAAA[A/G]AAAGAGGGTGTGAGA	25909
rs762653425	snp	C/T	3.30983e-05	0.00406793	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246891856	AGAAGCAAATAGCAT[C/T]GCTGGATAGACTGTA	25909
rs762663729	in-del	-/TT			intron-variant	AHCTF1	GRCh38.p7	1:246868847	TGTGTGTGTTTTTTG[-/TT]TTTTTTTTTTTTTTG	25909
rs762669685	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246920352	AAGGAAAAATCAAGT[A/G]GATTTGAAAAAATTT	25909
rs762681626	snp	C/G	1.64876e-05	0.00287116	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877050	TGATTCTGAACGCTG[C/G]CACTGGACTGCAAAA	25909
rs762716957	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246845365	AAGCATATGATTCTT[-/A]AAAAAAAAGAAAAAT	25909
rs762719950	snp	C/T	1.71185e-05	0.00292557	synonymous-codon, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843897	ATCCGAAACTAATTC[C/T]TTCAGCTGTGCAGGA	25909
rs762722568	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246865435	TTACTCTGTATCAAA[C/T]ACAGCTTTTAGATTT	25909
rs762732890	snp	A/T	1.75409e-05	0.00296145	intron-variant	AHCTF1	GRCh38.p7	1:246888534	TGCAATCAGGGAAAA[A/T]TTAAGACTTATTTAA	25909
rs762732976	in-del	-/C			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933425	GCGTGAGCCACCGCG[-/C]CCGGCCTTATTTTTT	25909
rs762737502	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246928513	CAGAGACAAGAAATA[A/G]GCATGTTAAACAATA	25909
rs762826227	in-del	-/T	4.25677e-05	0.00461324	intron-variant	AHCTF1	GRCh38.p7	1:246843980	ATATGTGTGTATATA[-/T]TATAAACACAATAAA	25909
rs762831399	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246883358	TAGAGATGTAGGTAT[C/T]TGAACAAATTAGGTG	25909
rs762848050	in-del	-/GCTCTA			intron-variant	AHCTF1	GRCh38.p7	1:246889661	AACGTTTGTGGCACT[-/GCTCTA]GCTCTAAATGTTATA	25909
rs762869372	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246930414	GATCCAAAAATCACA[C/G]TACAGAGACAACGTA	25909
rs762880584	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246920456	ACAGCTACATGCAAC[A/G]ATATGAATGAATGTC	25909
rs762889999	snp	A/G	1.68545e-05	0.00290292	intron-variant	AHCTF1	GRCh38.p7	1:246913223	GGTTTCAAGTAAAGA[A/G]CTGATTACCTGATGC	25909
rs762892446	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246885782	AATCCAGATAAGACT[C/T]GTTTAAATATAAGCT	25909
rs762918430	snp	A/G	1.65015e-05	0.00287237	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246913374	CTGAGTGCTTGCACT[A/G]GCTCCTCCATGATTA	25909
rs762938117	snp	C/T	1.66593e-05	0.00288607	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900147	TAAACTTCTCTCATG[C/T]ACTAATATATCCAAG	25909
rs762941404	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246919130	TTTTAGCCATCTGAG[C/T]TGGTTAGCTATGAAA	25909
rs762993619	snp	A/T	6.58946e-05	0.0057396	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246907661	AACAGCTGTTCCTGT[A/T]GGACTTACTAACTGG	25909
rs763016540	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246879832	GACTCTGTTCCCCCA[A/G]CCCCGCCAAAAAAAA	25909
rs763028950	snp	C/T	1.64762e-05	0.00287016	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849782	TGCTCATTTGTTTCT[C/T]TATGTGTCATTTCAT	25909
rs763029053	snp	C/T	4.95119e-05	0.00497529	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850985	GTGTCTTTAATTACA[C/T]CTAGTAAATTTTCTG	25909
rs763029669	snp	C/T	1.65381e-05	0.00287555	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849978	CTGGGGTATTTCTTG[C/T]AGATCTCCTTCTAAT	25909
rs763088155	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246871017	TGCGCTCCCACTGTA[C/G]CCTTGCTTAAGTTGC	25909
rs763118695	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246841482	TAGCCATAGTGTCTT[-/A]AATAAAATGCATTCA	25909
rs763133784	in-del	-/AAT			intron-variant	AHCTF1	GRCh38.p7	1:246916657	GACTTCATCTCAAAT[-/AAT]AATAATAATAATAGT	25909
rs763143098	snp	C/T	1.67049e-05	0.00289002	intron-variant	AHCTF1	GRCh38.p7	1:246900027	ACATACTTTTGTGCA[C/T]TACTTTTCTTAAGAG	25909
rs763217676	in-del	-/AA			intron-variant	AHCTF1	GRCh38.p7	1:246928303	GCGAGACTCCGTCTC[-/AA]AAAAAAAAAAAAAAA	25909
rs763222353	snp	C/T	1.64779e-05	0.00287031	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850875	TAAATGCAGATTTGA[C/T]CAATTTAGTGGGACA	25909
rs763228246	snp	C/T	3.35435e-05	0.0040952	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850368	CACTTTCCTGATTTT[C/T]TACAGATCTTTTAAT	25909
rs763253810	snp	A/C	0.000525072	0.0161945	intron-variant, utr-variant-5-prime, upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246931377	GAAGCCCGGCGCCCG[A/C]GAGCCTGCCGTACCC	25909
rs763282193	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246846701	TGAAAAAAAAAGAAA[C/T]ATTACGTTTAAGATT	25909
rs763339244	snp	C/T	5.57585e-05	0.00527978	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850479	GAGATGATTTTAATC[C/T]TTTTGATTCCCTACC	25909
rs763340545	snp	G/T	3.39098e-05	0.00411749	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877283	GTTGCCGCAAAAAAT[G/T]CCAGGCTTCAACCAT	25909
rs763397698	snp	G/T	1.99193e-05	0.00315583	intron-variant	AHCTF1	GRCh38.p7	1:246890943	ATACTTATAGATTAA[G/T]TAAATATTTTACCTA	25909
rs763400989	snp	C/T	5.13185e-05	0.00506523	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916289	TAAAACTACAGGAGG[C/T]TGTTCATTGACTCCA	25909
rs763406673	snp	A/C	1.88457e-05	0.00306961	intron-variant	AHCTF1	GRCh38.p7	1:246891104	TACTTACAAAAAAAT[A/C]AAGATGCTCCACAGT	25909
rs763417017	snp	C/G	1.66183e-05	0.00288251	missense, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840811	TCCCAAGAAATTACA[C/G]CATTTTTCTGCGTAA	25909
rs763417553	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246915603	TTAAAGTATTCACTA[C/T]ATTTATGCTAGTCTT	25909
rs763452006	snp	C/T	3.29582e-05	0.00405931	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902607	TTTGGTATTACTCGT[C/T]TGTCCCCTCAAAGGG	25909
rs763456092	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246902234	CTCAAAAAATACACG[A/G]GTAAACTTCATTCAA	25909
rs763472697	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246914595	GCGAATCTAAGTTTA[C/T]ATTCCTCATAAAAAT	25909
rs763488686	snp	A/G	3.8678e-05	0.00439744	intron-variant	AHCTF1	GRCh38.p7	1:246843765	AAGTATGTTTTAACA[A/G]ACATACAAATAAAAT	25909
rs763501523	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246881404	AAAATTATTCAGGAC[A/T]CAGAAAGATTAAAAC	25909
rs763511375	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246930891	ACTTTGCACACAGAT[A/G]GTATGAACCTCGTAA	25909
rs763517206	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246914418	TTGTTTCAGGCTGTA[A/C]CTTACTACAGACAAA	25909
rs763534209	snp	C/T	1.7333e-05	0.00294384	intron-variant	AHCTF1	GRCh38.p7	1:246894646	GTCCTACATCTAGAC[C/T]TCTAATACTTACATA	25909
rs763542495	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246853408	TGAATAGTGTATTAA[C/T]AAACTATCACAATGC	25909
rs763546245	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246854471	GTTCAGCAATAAGCA[A/G]TTAGTTAAGCATGTA	25909
rs763577728	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246879906	ATGAACTACTATGCA[A/G]TAGTTAAAAAGCAAA	25909
rs763579498	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246872784	CATGATTGAACCTTC[A/G]AAGTGTGCTGCTGTC	25909
rs763598043	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246903634	GGAGTTCAAGACCAG[A/C]CTGGCCAAGATGGTG	25909
rs763598864	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246852175	CAGTGAGATGACAGA[C/T]TGGAAATAACCTAGA	25909
rs763611636	snp	A/G	1.89414e-05	0.00307739	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853110	ATTTCTTGAGTATCA[A/G]GAGGGCTGTCAGAAA	25909
rs763622332	snp	A/G	1.67899e-05	0.00289736	stop-gained, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246862072	CTAAAGGTGTTGATC[A/G]AAGAGTAGACCTCAG	25909
rs763625624	snp	A/G	0.000182705	0.00955609	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850322	CTAGGACTTGTTACC[A/G]TACTAACTTTTAGAT	25909
rs763635578	snp	A/G			synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246887355	AAGTAGCAAATAAAT[A/G]GTCTTTTAAAAAGCG	25909
rs763670830	in-del	-/CA			intron-variant	AHCTF1	GRCh38.p7	1:246887844	TGTATTCATTTCCAG[-/CA]CAGAGGTTAATGCCA	25909
rs763675525	snp	A/C	1.64953e-05	0.00287182	intron-variant	AHCTF1	GRCh38.p7	1:246877085	CACTAAACATTCCTA[A/C]AAAGAACAAAATAGA	25909
rs763691860	in-del	-/AAC			intron-variant	AHCTF1	GRCh38.p7	1:246847304	CAAAAAAAAAAAACA[-/AAC]AAAAAAAAAACTGAA	25909
rs763738233	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246854907	ACAGAAAACAAAAAT[C/T]CAGGAAAGACACTTT	25909
rs763745535	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246870712	TCTAGCTAAAAGAGG[A/G]TATAAAACCTCAAAA	25909
rs763768365	snp	C/T	6.61573e-05	0.00575102	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877182	GTCTGTAAATGGTAA[C/T]TTCAGTAAATCTTCC	25909
rs763794044	snp	A/C	1.72065e-05	0.00293308	intron-variant	AHCTF1	GRCh38.p7	1:246913455	TTCTTCTGCAAAGTA[A/C]GAAAATATAATTAAC	25909
rs763794750	snp	A/C	1.67956e-05	0.00289784	intron-variant	AHCTF1	GRCh38.p7	1:246902518	TATTTCAAGTACTTT[A/C]ACTAACCTTCATTCA	25909
rs763810529	snp	C/G	6.59642e-05	0.00574262	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864028	GTGAACGGGATACTA[C/G]GTACAAAGGAGATTT	25909
rs763818920	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246872625	AAAGGTCAAGCATAG[A/T]AATAAAACATAAGGA	25909
rs763826400	snp	C/T	4.95029e-05	0.00497484	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246890005	CGACGACTGGTGTAG[C/T]AGTTCTGAATTACAG	25909
rs763845650	snp	A/G	1.70046e-05	0.00291582	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916225	CTTCTGTTTCTTCCA[A/G]TCCTATTAATAATCC	25909
rs763853907	in-del	-/TTAA	3.63861e-05	0.00426518	intron-variant	AHCTF1	GRCh38.p7	1:246888558	TATTTAATATCACTG[-/TTAA]TTAATATCAAAGCAA	25909
rs763889081	snp	A/G	3.29598e-05	0.00405941	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850897	AGTGGGACACATTAT[A/G]TTTTGGCTCACTAAA	25909
rs763908611	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246887865	GGTTAATGCCATTGA[C/T]AGTGACCACTTGGTG	25909
rs763914192	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246860283	AAAAATTAAATAAAT[A/G]AAAATTGCAATAATT	25909
rs763929025	snp	C/T	3.29473e-05	0.00405864	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246907689	TGGAAACACAGATGG[C/T]GCCCTTGTCTCATTA	25909
rs763936920	snp	C/T	1.64917e-05	0.00287151	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849880	TTTTTTCTTAGAGCT[C/T]ATCACCATCGAAAGT	25909
rs763940327	snp	C/T	1.6501e-05	0.00287232	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246888191	CAATAGAGTGTTTGG[C/T]TGCTTCAGTAACGCC	25909
rs763942410	snp	A/G	1.81217e-05	0.00301007	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876115	GATGGACTCTAGGAA[A/G]GATTTTTCCATACTG	25909
rs763960554	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246916758	GTAGAGATAAGGCAG[C/T]TAAACCTGAATACTG	25909
rs763966450	snp	G/T	3.87087e-05	0.00439919	intron-variant	AHCTF1	GRCh38.p7	1:246894781	AAGGGAAAAAATAAA[G/T]ATTATTAATTACAAA	25909
rs763983669	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246921871	GTAGAATAGAGATCA[A/G]ATAGAAGGTCTGAGA	25909
rs763992055	snp	A/G	1.64985e-05	0.0028721	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851039	GGCACATATGGTAAA[A/G]TGTCTACTTTTTGGG	25909
rs763995889	snp	C/G/T	5.01688e-05	0.00500822	intron-variant	AHCTF1	GRCh38.p7	1:246887369	TGGTCTTTTAAAAAG[C/G/T]GGATTAAGGACAATA	25909
rs764039376	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246891455	GCTTGTTTTTGTTTT[C/G]AAATTGCAAAACAGA	25909
rs764042394	in-del	-/T	1.69861e-05	0.00291424	intron-variant	AHCTF1	GRCh38.p7	1:246864139	CAGAATGCGCATTTA[-/T]TGAGTTATACTGAAA	25909
rs764048702	snp	G/T	1.64917e-05	0.00287151	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246887262	AATAAGTTTAACTTG[G/T]CCCCAAGAAATGGCA	25909
rs764058879	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246910292	CGTTCAAGGAGACTT[C/G]AGACTTAACTGTCAA	25909
rs764060029	snp	C/G			missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246887252	AAAACCCCTGAATAA[C/G]TTTAACTTGGCCCCA	25909
rs764080781	snp	C/G	1.66109e-05	0.00288187	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246918332	CACTTCTGGAAATGG[C/G]AGGAGACCACTAGTC	25909
rs764107980	snp	A/T	1.7268e-05	0.00293832	intron-variant	AHCTF1	GRCh38.p7	1:246904073	CGCTAAATATATTAA[A/T]ACATTAAACATCTCT	25909
rs764118284	snp	G/T	1.67764e-05	0.00289619	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850652	TAGATGTTTTCAGAA[G/T]CTTCAGAAATTTCTT	25909
rs764126844	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246881771	TGAACCTGGGAGGCA[G/T]AGGTTGCAGTGAGCC	25909
rs764135701	snp	C/T	8.26084e-05	0.00642631	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246857771	TTCTGAAAATGCCTC[C/T]GCTGCAACTAAGAGA	25909
rs764149032	snp	A/T	1.64765e-05	0.00287019	intron-variant	AHCTF1	GRCh38.p7	1:246867615	CTGTTGATGTCCAGT[A/T]AAGATTAACAAGCAG	25909
rs764169631	snp	A/G	8.24463e-05	0.00642	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246855755	ATTTGCTCTAATTGC[A/G]GGGGTGTAGGTTTCA	25909
rs764193424	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246859565	CATTTTTTGATCACT[A/G]AAATAATATTTTTTT	25909
rs764195885	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246870126	CTGCAGATATGGGGG[A/G]AAGAGCAAGAGAACT	25909
rs764216964	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246879887	TGGTACAGCCATCCA[A/T]ATAATGAACTACTAT	25909
rs764235487	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246910297	AAGGAGACTTGAGAC[C/T]TAACTGTCAAATGCA	25909
rs764256014	snp	A/G	1.66056e-05	0.00288141	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849629	CCTTTTGCTTTCCTT[A/G]GAACTTCTGACGCTG	25909
rs764287241	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246931100	GGCTGAGCCCCGAGT[A/C]CAACTTCTTCCCCGC	25909
rs764296899	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246927972	GCCACTGCACTCCAG[C/T]CTGGCGACAGAGCAA	25909
rs764298253	snp	A/C	3.81643e-05	0.00436815	intron-variant	AHCTF1	GRCh38.p7	1:246888569	ACTGTTAATTAATAT[A/C]AAAGCAACCAGCATC	25909
rs764308177	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246891276	AACCTCCAAAATGCT[A/G]AAATAAGTAAGTCAC	25909
rs764331907	snp	A/G	1.7731e-05	0.00297744	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246885632	TCTTTGAATGTTGCC[A/G]TGACAAAGGTTTTGC	25909
rs764378835	in-del	-/TG	1.85393e-05	0.00304455	intron-variant	AHCTF1	GRCh38.p7	1:246843949	AAAAGTTGAAAAAAC[-/TG]TATCTGTATCTTTAT	25909
rs764381152	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246847748	GAAAAAAGTTAAAAT[C/T]AGTAGGTACAGAAAT	25909
rs764383704	snp	C/T	3.47017e-05	0.00416529	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853275	AGCGAGGAGTTTCCA[C/T]CATCACCAAGGACAT	25909
rs764386876	snp	C/T	5.01895e-05	0.00500921	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246885527	TGAGGTGAAGGATAA[C/T]ATCGTTACCACTGGA	25909
rs764396291	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246904331	CTTCCTCAATGGTTA[C/T]ACTCTACTTAAACAC	25909
rs764410761	snp	C/T	1.65353e-05	0.00287531	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246913403	TAATTATAGGTTCAA[C/T]AGCTGTTACCTAGAA	25909
rs764430639	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246869588	CCAAAATTCCTAAGG[C/T]CCTTAAAAATGATGG	25909
rs764433187	snp	A/T			utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839876	TCCTTTTCTACATCT[A/T]CTCACTCTCTCCCAA	25909
rs764437889	snp	C/T	4.94694e-05	0.00497316	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850125	CAAATTCTGCTTGAA[C/T]AGTCAACTGAGATGA	25909
rs764438231	snp	A/G	1.65847e-05	0.0028796	intron-variant	AHCTF1	GRCh38.p7	1:246891771	ATTTGATAAAACAAA[A/G]AGCGTACCTCTCTCA	25909
rs764450621	in-del	-/ACACACACACACACAC			intron-variant	AHCTF1	GRCh38.p7	1:246898630	TGACAAAACACACAC[-/ACACACACACACACAC]ACACACACACACACA	25909
rs764459458	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246861743	TTACTTGGTGCTTCC[G/T]AGTCCTATTTATCTG	25909
rs764470769	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246917573	TTACACCACTCCAAT[A/G]AAGTCATCGTACAAT	25909
rs764486093	in-del	-/A	1.81866e-05	0.00301546	intron-variant	AHCTF1	GRCh38.p7	1:246918391	ACTGTAAATATTTTT[-/A]AAAAGAAAACATTAT	25909
rs764492933	snp	C/G	1.64768e-05	0.00287021	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851285	GCAATGTCACATTCA[C/G]CAGTGTCTTTGTTAT	25909
rs764568360	snp	C/T	8.26153e-05	0.00642657	intron-variant	AHCTF1	GRCh38.p7	1:246899448	TCACTAGTTGTTACC[C/T]ACCTCCTTCTGAAAG	25909
rs764582411	snp	G/T	1.65004e-05	0.00287227	intron-variant	AHCTF1	GRCh38.p7	1:246895956	CAGAAAGGAAAGAAA[G/T]GGAAAGAAAGAGGGT	25909
rs764588456	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246888906	CCCTGTCTCTAAAAA[C/G]AGAGAGAGAGGAGAG	25909
rs764604537	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246856305	ATAAATCCTGGAATA[C/T]GATGACAGTGTTCCT	25909
rs764623442	snp	A/C	1.64765e-05	0.00287019	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246898279	CAAGACATCGATTAT[A/C]ACCATCAGGAATGAG	25909
rs764623548	snp	A/G	3.2975e-05	0.00406035	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246905587	AACAGCAATTCCGAG[A/G]ATCATTCTCAGGTTC	25909
rs764626395	snp	A/G	1.64781e-05	0.00287033	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849677	TTGTTTGGTTCAGAA[A/G]GGTCCGGCAACAAGA	25909
rs764648316	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246875912	GGAACCAAACCAGCA[A/G]TATCTCCAAGGCATG	25909
rs764655820	in-del	-/TC			downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838879	GATACTAAGTATCTT[-/TC]TGAGTACATTGTTTA	25909
rs764680152	snp	G/T			utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840603	ACATATATAAATGTA[G/T]GAAGTCTTAATATAA	25909
rs764694962	in-del	-/A	0.000305105	0.0123475	intron-variant	AHCTF1	GRCh38.p7	1:246900319	AGAGAAAGGAGAGAG[-/A]AAAAAAAAGAATCAT	25909
rs764718593	in-del	-/A	1.64988e-05	0.00287213	intron-variant	AHCTF1	GRCh38.p7	1:246888385	ATAGCACATTACTGC[-/A]AAACCTACATGCAGA	25909
rs764733957	snp	A/T	5.0396e-05	0.00501951	intron-variant	AHCTF1	GRCh38.p7	1:246887383	GCGGATTAAGGACAA[A/T]AAAATACAACAACAA	25909
rs764789289	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246869456	TGAAGGAAATTAAAA[C/G]TGCTACGTCAGTGAA	25909
rs764801267	snp	A/G	2.08435e-05	0.00322821	missense, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843808	ACCAGTTCATCTTCA[A/G]GCTTGTTCTTATTGG	25909
rs764806558	snp	C/G	1.65507e-05	0.00287664	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864085	AACACTGAGAAGGCC[C/G]GGGGACAGGCTGAAC	25909
rs764834680	snp	C/T	1.64982e-05	0.00287208	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851050	TAAAGTGTCTACTTT[C/T]TGGGACTTTTGGTCA	25909
rs764861038	snp	G/T			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933066	TCAGCCCTCCAAGTA[G/T]CTGGGACTATGGGCA	25909
rs764884470	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246911368	ATTCATTTTTAGTTA[C/T]TGCTTTTGCTCATCA	25909
rs764885624	snp	G/T	1.67267e-05	0.0028919	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246860923	TCTGTAGGTCTGAAG[G/T]AGTTACTTCTGATGC	25909
rs764913640	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246875275	TACAATGACACAACC[C/T]CTCCCCTCTCCATAA	25909
rs764919563	in-del	-/A	3.0254e-05	0.00388923	intron-variant	AHCTF1	GRCh38.p7	1:246867362	TAGAACTATGAAAAT[-/A]AAAATTTAACTTCTG	25909
rs764927947	snp	C/G	2.25005e-05	0.00335406	intron-variant	AHCTF1	GRCh38.p7	1:246894799	TATTAATTACAAACA[C/G]AGTTCTAAATTGTTG	25909
rs764937763	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246882434	TGTAAATTAAAACTT[C/T]TAAATCATAGATAGG	25909
rs764965859	snp	A/G	1.65312e-05	0.00287495	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840850	TTGGATAGGAAGACA[A/G]TTTCTTTCTGTTCCT	25909
rs764966694	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246925554	AAGACCAGGAGTTGT[A/G]GGTTGCAGTAAGCTA	25909
rs764969740	snp	G/T	1.68159e-05	0.0028996	intron-variant	AHCTF1	GRCh38.p7	1:246902713	ATATTAATCTGATTC[G/T]AGGCAAAAAGTCACT	25909
rs765024399	snp	A/G	3.29478e-05	0.00405867	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246898246	CATCAACAAATCTTG[A/G]GGAAAGAAGGCCAGC	25909
rs765040922	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246923897	CTCCAGGTCTGGAAG[A/T]CCCTAACTACATACT	25909
rs765073811	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246847464	TCGATGGCTGGATTA[C/T]ATACTTCTATTTTAG	25909
rs765076053	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246863342	GTTTCAATCCAGAAC[A/G]TTAGTCAAGGGGCTA	25909
rs765078510	snp	C/G	6.87628e-05	0.00586316	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246862129	ATCCAGAAGTAGTAA[C/G]TGACATGGCCAAACT	25909
rs765108189	snp	C/G	1.65438e-05	0.00287605	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849967	TTCACTTTTAGCTGG[C/G]GTATTTCTTGTAGAT	25909
rs765112366	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246910556	ATGTTGAAAATTAAC[G/T]TGAATTTGGGTGATG	25909
rs765123555	snp	C/T	7.04655e-05	0.0059353	intron-variant	AHCTF1	GRCh38.p7	1:246876208	AAACATCAAAATTGG[C/T]AAAAAATTTAACCTT	25909
rs765134003	snp	G/T	1.64743e-05	0.00287	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246907699	GATGGCGCCCTTGTC[G/T]CATTACACTTTCTCT	25909
rs765135473	snp	A/T	1.64836e-05	0.0028708	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851111	TGTCCATGATTATCA[A/T]TTTCCCCACTGCATA	25909
rs765175799	snp	C/T			missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916387	CCAAGCAAGCAAGTC[C/T]ATTTTTCCCTAGAAG	25909
rs765214331	snp	C/T	1.76263e-05	0.00296864	intron-variant	AHCTF1	GRCh38.p7	1:246913198	CAGAATATCCAGGTG[C/T]TCCATTTTTGGTTTC	25909
rs765236917	in-del	-/CAT			intron-variant	AHCTF1	GRCh38.p7	1:246887697	GGCAGCTTAATCAAA[-/CAT]CATCTAGCTTATAAA	25909
rs765241767	snp	A/G	0.0002147	0.0103588	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246899472	CTGAAAGCCAGTACA[A/G]GTTAAATGAACAACT	25909
rs765269937	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246848747	CCCAGCTACTAGGGA[A/G]GCTGAGGTAGGAGAA	25909
rs765302345	snp	C/T	4.48029e-05	0.0047328	intron-variant	AHCTF1	GRCh38.p7	1:246905696	TATTTTTAAGTTATT[C/T]TTTAGAAAGGAAAAA	25909
rs765328409	snp	C/G	0.000666356	0.018241	intron-variant, missense, utr-variant-5-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246931146	TGGCCAGGCCCAAGC[C/G]CATGTGGAACACACG	25909
rs765334727	snp	C/T	1.64749e-05	0.00287005	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849759	CTGTGGCGAGCAATC[C/T]TTCTTCCTGCTCATT	25909
rs765350660	snp	C/T	6.65557e-05	0.00576831	intron-variant	AHCTF1	GRCh38.p7	1:246887192	CATGAAAGTTTATGC[C/T]GTAAGTGAATAGACT	25909
rs765371434	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246858982	CCTGTAATCCAGCTA[C/T]TTGGGAGGCTGAGGC	25909
rs765373073	snp	C/T	3.29674e-05	0.00405988	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246905614	GTTCTTGAAAAGTGA[C/T]AGCATATACAGGAAC	25909
rs765387503	in-del	-/AAAG	3.97354e-05	0.00445714	intron-variant	AHCTF1	GRCh38.p7	1:246853063	AACTGAAAGACTGAT[-/AAAG]AAGTAAAAAATTAAT	25909
rs765388200	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246929819	AGCACTCTGGGAGGC[C/T]AAGGCGGGCGGATCA	25909
rs765401686	snp	A/T	3.82212e-05	0.0043714	intron-variant	AHCTF1	GRCh38.p7	1:246894614	AAACCAAGGTTAGTA[A/T]TTTAATATTAAATTC	25909
rs765439191	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246917764	AAGATCCATAAGAGA[A/G]AGCCTTCTTTAGTAT	25909
rs765442060	snp	G/T			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932014	AGGGGAGAACCGGCG[G/T]GAGATCGCGGCTGCA	25909
rs765502906	snp	C/T	1.67511e-05	0.00289401	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850359	TAATTTCAACACTTT[C/T]CTGATTTTCTACAGA	25909
rs765507816	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246869012	CCATGCCTGGCTAAC[-/T]TTTTTCTATTTTTAG	25909
rs765521877	snp	G/T	1.66252e-05	0.00288311	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867780	TGTTACAACTTGCTT[G/T]GGAACTGCTGATAAT	25909
rs765523282	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246859373	TCTCCCATTTACTAG[C/T]GTTCCCCTGGCCCTC	25909
rs765583218	snp	A/G	1.85262e-05	0.00304348	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246885659	TTGCAGTAGCTGGAT[A/G]AAACAAAAGATCCAA	25909
rs765591066	snp	C/T	1.65452e-05	0.00287616	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877196	ACTTCAGTAAATCTT[C/T]CATCAAGCCCATTTC	25909
rs765628964	snp	C/T	3.30098e-05	0.00406249	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850246	GGATTTATCATCTTG[C/T]TTATTTCCTGTATTT	25909
rs765694726	snp	A/G	1.70813e-05	0.00292239	intron-variant	AHCTF1	GRCh38.p7	1:246916112	TCAGTTTTGAAAGAG[A/G]AATGTCCAGGTATCT	25909
rs765712841	snp	A/T	1.65026e-05	0.00287246	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246890016	GTAGTAGTTCTGAAT[A/T]ACAGGGTAGTTGTAG	25909
rs765721900	snp	A/G	1.83913e-05	0.00303238	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851417	TCTCCTGAATCTTGA[A/G]CTTCAAGCTTTTCTT	25909
rs765746489	snp	A/C	3.29533e-05	0.00405901	intron-variant	AHCTF1	GRCh38.p7	1:246867610	GAACGCTGTTGATGT[A/C]CAGTAAAGATTAACA	25909
rs765747691	snp	A/G	1.71525e-05	0.00292847	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916272	GAGAATTCTTTCACA[A/G]CTAAAACTACAGGAG	25909
rs765761592	snp	C/T	1.65935e-05	0.00288036	intron-variant	AHCTF1	GRCh38.p7	1:246889938	TTGACTTCTTACAGA[C/T]GTAATTTCTAAAATT	25909
rs765788804	snp	A/G	1.7376e-05	0.00294749	intron-variant	AHCTF1	GRCh38.p7	1:246861942	ATGTCTTTTCTCCCA[A/G]TTATTATCAAACTTA	25909
rs765805897	snp	C/T	1.64765e-05	0.00287019	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851254	TTGAGCCACAAAAAG[C/T]TCCCCATCTACTTCA	25909
rs765834434	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246878164	ACACTTTGGGAGGCC[A/G]GGGTGGGCAGATCAC	25909
rs765927841	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246896223	CACACCTAGGTATAT[A/T]CCAAAAAGAAACAAA	25909
rs765951256	snp	C/G	1.64844e-05	0.00287087	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851127	TTTCCCCACTGCATA[C/G]AAGTTTTTCTTCAGT	25909
rs765970221	snp	G/T	1.65378e-05	0.00287552	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849982	GGTATTTCTTGTAGA[G/T]CTCCTTCTAATGCTG	25909
rs765976475	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246910592	ATGGGAACTCTTGTA[C/T]TCTTCTAACTATCTG	25909
rs765984023	snp	A/G	5.38677e-05	0.0051895	intron-variant	AHCTF1	GRCh38.p7	1:246876228	AATTTAACCTTCAAA[A/G]TGTTAGGTGCTGTAA	25909
rs766003906	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246863572	AATAAACCAAAGAAC[G/T]AAATAGCATTTGATA	25909
rs766006266	snp	C/T	1.65356e-05	0.00287533	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246860990	AGTTACATTAGTAGT[C/T]AGTGCAGTGGAAGAG	25909
rs766016028	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246923944	GAAGAGGGCCATGTT[G/T]CAGGGAACTGTGCTG	25909
rs766023815	snp	A/G	3.01491e-05	0.00388248	intron-variant	AHCTF1	GRCh38.p7	1:246867362	TAGAACTATGAAAAT[A/G]AAAATTTAACTTCTG	25909
rs766026947	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246901298	GTGAGACGAGATCGT[A/G]CAAGTGCACTCCAGC	25909
rs766035109	snp	A/G			missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850268	CCTGTATTTTCAGAA[A/G]CATCTAAATTAGTAC	25909
rs766050848	in-del	-/TACTACTGA			downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838898	GTACATTGTTTACCT[-/TACTACTGA]TACTACTGATACTAA	25909
rs766057157	snp	A/G	1.64993e-05	0.00287218	intron-variant	AHCTF1	GRCh38.p7	1:246888381	AAATGATAGCACATT[A/G]CTGCAAACCTACATG	25909
rs766103945	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246858942	ACATCAAAAGAGCAA[C/T]GTAGGCCAGGACCGG	25909
rs766112046	snp	C/T	1.64969e-05	0.00287196	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246888221	CGTCTAATAGGTACA[C/T]ATCAAGTACTGCCTA	25909
rs766112113	in-del	-/A	3.29609e-05	0.00405948	splice-acceptor-variant	AHCTF1	GRCh38.p7	1:246899514	AAACAAGTGGCATCT[-/A]AAAAAAAAGATTTAA	25909
rs766133797	snp	G/T	1.65531e-05	0.00287686	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246891860	GCAAATAGCATTGCT[G/T]GATAGACTGTATAGT	25909
rs766150171	snp	A/G			synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851377	AGAGGGATATAACTC[A/G]TTAAATGAAAGATTC	25909
rs766154627	snp	C/T	1.65839e-05	0.00287953	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850666	AGCTTCAGAAATTTC[C/T]TTTGCCTTCCTAGTT	25909
rs766156618	snp	C/T	1.67581e-05	0.00289461	intron-variant	AHCTF1	GRCh38.p7	1:246855847	AGAAAAAGAAATACA[C/T]ACCTTAGTGTGTAAG	25909
rs766238300	snp	C/T	1.66994e-05	0.00288953	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246918350	GAGACCACTAGTCAC[C/T]TGAGCTCTTAAGTCT	25909
rs766243370	snp	C/G/T	0.000165334	0.00909074	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876965	CATAACATTAATCTT[C/G/T]AGAGTTTGGTTCAGC	25909
rs766244419	snp	C/T	3.29696e-05	0.00406001	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864014	CGAACTTGAGGGCAG[C/T]GAACGGGATACTAGG	25909
rs766260738	in-del	-/TGAC	3.55745e-05	0.00421734	intron-variant	AHCTF1	GRCh38.p7	1:246849574	TTTTAAGCTGAAGAG[-/TGAC]TGAGATGAAAAACTG	25909
rs766263546	snp	C/G	1.65029e-05	0.00287248	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246913375	TGAGTGCTTGCACTG[C/G]CTCCTCCATGATTAA	25909
rs766266032	snp	A/G	0.000149749	0.00865171	intron-variant	AHCTF1	GRCh38.p7	1:246900302	TACACATACAAATAC[A/G]AAGAGAAAGGAGAGA	25909
rs766279406	in-del	-/TATC			intron-variant	AHCTF1	GRCh38.p7	1:246849200	TTGAAATAATTTCTG[-/TATC]TATCTTAGTAAAAAG	25909
rs766282345	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246919289	CTAAAGGTGAGCAAG[A/C]ACAATACCCATTGTA	25909
rs766287409	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246869260	TAACTGTTCCCCCGC[A/G]TCTCTCCCTTTCCCC	25909
rs766292499	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246885821	CTACTTTAATCTGTG[C/T]TATATAGAGTTGGCT	25909
rs766295291	snp	A/C	2.4754e-05	0.00351801	intron-variant	AHCTF1	GRCh38.p7	1:246841012	TTCTGAAAAAAAAAG[A/C]TATGATCAAGTAAGA	25909
rs766307001	snp	C/T	1.65067e-05	0.00287282	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246890034	AGGGTAGTTGTAGCA[C/T]AACCTTGACAACTGC	25909
rs766350721	in-del	-/AA			intron-variant	AHCTF1	GRCh38.p7	1:246926048	AGACCCTGTCTTTAA[-/AA]AAAAAAAAAAAAAAA	25909
rs766418494	snp	A/G	8.3266e-05	0.00645183	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900162	TACTAATATATCCAA[A/G]ATGCCATGTGGAGAA	25909
rs766449025	snp	C/T	1.6574e-05	0.00287867	missense, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840822	TACAGCATTTTTCTG[C/T]GTAAAATTTGCTTTG	25909
rs766458120	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246865978	TTACCATAATCCATA[A/T]AAAGAATGCATCCTA	25909
rs766471858	snp	C/G/T	3.58425e-05	0.00423322	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876102	ATGGCTAATTTTCGA[C/G/T]GGACTCTAGGAAGGA	25909
rs766478498	snp	A/G	3.29538e-05	0.00405904	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849860	CTTTCAGTCTTTTTT[A/G]TAAGTTTTTTCTTAG	25909
rs766481808	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246920494	ATTATTAAACCAGCC[C/G]GGCGTGGTGGCTCAC	25909
rs766497607	snp	G/T	3.34029e-05	0.00408661	intron-variant	AHCTF1	GRCh38.p7	1:246900031	ACTTTTGTGCATTAC[G/T]TTTCTTAAGAGGTAA	25909
rs766507698	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246845825	AAAGAGAGCTCTGAT[C/T]TGCAGCATTTGCTGA	25909
rs766512918	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246893554	AACTGGACATGATAG[C/T]TTTTAATATTCATGA	25909
rs766524220	snp	C/G	6.6291e-05	0.00575683	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246887346	CATAATATCAAGTAG[C/G]AAATAAATGGTCTTT	25909
rs766533829	snp	C/T	6.59022e-05	0.00573993	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849783	GCTCATTTGTTTCTT[C/T]ATGTGTCATTTCATC	25909
rs766597402	snp	A/C	1.69911e-05	0.00291466	intron-variant	AHCTF1	GRCh38.p7	1:246903911	AAATAGAAAACAACA[A/C]AATGGTAATATAAAC	25909
rs766638956	snp	A/C/T	5.9818e-05	0.00546864	intron-variant	AHCTF1	GRCh38.p7	1:246876005	TCTTTTTTGATCCAA[A/C/T]AGATTATGATATTCT	25909
rs766639136	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246845175	AGTTCTATCAAATTC[C/T]GCTTTTCGAGCATGA	25909
rs766642670	snp	A/G	1.71114e-05	0.00292496	synonymous-codon, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843902	AAACTAATTCTTTCA[A/G]CTGTGCAGGAACCTC	25909
rs766659899	in-del	-/AAAT			utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839626	TATTATTTGGTAGAA[-/AAAT]AAATGCAGAAAGCAC	25909
rs766685381	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246927047	GCAGGGCGTGGTGAC[A/G]GGAACCTGTAGTCCC	25909
rs766688833	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246896041	ATCAGTATGACCCAT[A/C]AGAAGGGCTATAATC	25909
rs766695938	snp	C/G/T	5.58024e-05	0.00528192	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850482	ATGATTTTAATCTTT[C/G/T]TGATTCCCTACCTGT	25909
rs766698659	snp	C/G	1.64738e-05	0.00286995	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246907682	TACTAACTGGAAACA[C/G]AGATGGCGCCCTTGT	25909
rs766778496	snp	C/T	1.65737e-05	0.00287864	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246894689	CCTCTTTTGTGAGAA[C/T]CACTTTATTCCACGT	25909
rs766787059	snp	A/G	3.08228e-05	0.00392562	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867246	AATAAACTCTTACCT[A/G]GAAATTTTTTGTGAT	25909
rs766787443	snp	A/G	4.10282e-05	0.00452906	intron-variant	AHCTF1	GRCh38.p7	1:246885462	TTAACAGATACGATA[A/G]AGACTTTATAGTTTC	25909
rs766789283	in-del	-/TGATT			intron-variant	AHCTF1	GRCh38.p7	1:246908055	AACCATAAATAAAAC[-/TGATT]TATTTCTTTATTGAA	25909
rs766800016	snp	C/T	0.000881918	0.0209805	intron-variant	AHCTF1	GRCh38.p7	1:246916416	AGAAAAAAAAATTGC[C/T]TATTTTAATATTGTA	25909
rs766810830	snp	C/T	2.02677e-05	0.00318331	missense, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843814	TCATCTTCAAGCTTG[C/T]TCTTATTGGATGTGT	25909
rs766842451	snp	C/T	1.70342e-05	0.00291836	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877289	GCAAAAAATTCCAGG[C/T]TTCAACCATACACCT	25909
rs766863851	snp	C/T	1.67761e-05	0.00289617	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850369	ACTTTCCTGATTTTC[C/T]ACAGATCTTTTAATT	25909
rs766878377	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246855122	TCTAGAGTCAGATAA[A/C]AACTATGTCATAGTA	25909
rs766917479	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246912559	AAATACTCCTTTTCT[A/G]AAAATTAAGAGTAAA	25909
rs766925637	snp	A/G	1.64972e-05	0.00287199	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850225	AATACGCAGCTGCTT[A/G]TCACTGGATTTATCA	25909
rs766931539	snp	A/G	3.76541e-05	0.00433885	intron-variant	AHCTF1	GRCh38.p7	1:246890947	TTATAGATTAAGTAA[A/G]TATTTTACCTATGCC	25909
rs766971054	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246865747	ATCATCAAGACTTAA[C/T]AGTTTAAAGGTTCTG	25909
rs766989944	snp	C/T	1.64798e-05	0.00287047	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902629	CTCAAAGGGAACATG[C/T]CACCTGTCAGGTCCA	25909
rs766991103	snp	C/T	1.69703e-05	0.00291288	intron-variant	AHCTF1	GRCh38.p7	1:246913446	GATTTGCTTTTCTTC[C/T]GCAAAGTAAGAAAAT	25909
rs767000209	snp	A/G	1.88603e-05	0.00307079	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853111	TTTCTTGAGTATCAG[A/G]AGGGCTGTCAGAAAT	25909
rs767055835	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246911675	TTTTAGTAGAGACGG[C/G]GTTTCTCCATGTTGG	25909
rs767084936	snp	C/T	4.94572e-05	0.00497254	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851142	CAAGTTTTTCTTCAG[C/T]TGCTGTGTTAGCTGC	25909
rs767089304	in-del	-/AA			intron-variant	AHCTF1	GRCh38.p7	1:246870724	AGGGTATAAAACCTC[-/AA]AAAAAAAAAAAAAAA	25909
rs767098714	snp	A/C	1.6495e-05	0.0028718	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850110	GTATGGCAGACATAT[A/C]AAATTCTGCTTGAAC	25909
rs767118712	snp	C/T	5.10747e-05	0.00505319	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900465	ACTAGTGTCAGGCGA[C/T]AGAGCTGGAAGAAAA	25909
rs767129122	snp	A/G	1.65343e-05	0.00287521	intron-variant	AHCTF1	GRCh38.p7	1:246841021	AAAAAGATATGATCA[A/G]GTAAGAATAAACACA	25909
rs767153999	snp	A/G	1.64762e-05	0.00287016	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851273	CCATCTACTTCAGCA[A/G]TGTCACATTCAGCAG	25909
rs767223611	in-del	-/AAAT	1.7088e-05	0.00292296	intron-variant	AHCTF1	GRCh38.p7	1:246916111	TCAGTTTTGAAAGAG[-/AAAT]AAATGTCCAGGTATC	25909
rs767227067	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246876324	CATTTTTCCAAACCA[A/G]GAACTTCATCCACAT	25909
rs767227682	snp	C/G/T	4.99042e-05	0.004995	intron-variant	AHCTF1	GRCh38.p7	1:246898378	CAATCAATGCTCAAT[C/G/T]TGAATAATCAAATTT	25909
rs767247666	snp	C/G	1.64977e-05	0.00287203	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876990	TTCAGCTTCAAGGCA[C/G]GCACATAATTGGCAC	25909
rs767253974	snp	A/G	1.78401e-05	0.00298659	intron-variant	AHCTF1	GRCh38.p7	1:246888549	ATTAAGACTTATTTA[A/G]TATCACTGTTAATTA	25909
rs767274772	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246871195	TTAGGACAGTGGTTA[C/G]TACTTGCCTATTAGT	25909
rs767318310	snp	A/G	3.39225e-05	0.00411826	intron-variant	AHCTF1	GRCh38.p7	1:246855865	CTTAGTGTGTAAGAA[A/G]ATCCCATCTGCTTTA	25909
rs767334206	in-del	ACTAAGCACC/GATACTAAGCACCTTAGT			downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838991	TTACCTTACTACTAT[ACTAAGCACC/GATACTAAGCACCTTAGT]TTAACCAATGCTTTG	25909
rs767353815	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246887422	TACGTATATATTTAC[A/G]ATAGGTAGCAACAAA	25909
rs767374218	in-del	-/ATATAC			intron-variant	AHCTF1	GRCh38.p7	1:246846726	AAGATTTTGAAATAT[-/ATATAC]ATATACATATATATA	25909
rs767385500	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246892144	AACTCAAATCATCTA[-/T]TATCTAGAGCTTGTC	25909
rs767389363	in-del	-/TTTT			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932466	ACTTTTCTTTTTTTC[-/TTTT]TCTTTTTTTTGGAGA	25909
rs767389798	in-del	-/TTG	1.64768e-05	0.00287021	cds-indel, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849858	GACTTTCAGTCTTTT[-/TTG]TAAGTTTTTTCTTAG	25909
rs767415699	snp	C/T	1.65776e-05	0.00287898	intron-variant	AHCTF1	GRCh38.p7	1:246887202	TATGCTGTAAGTGAA[C/T]AGACTTACCTCATAG	25909
rs767423089	snp	A/C	1.89346e-05	0.00307684	intron-variant	AHCTF1	GRCh38.p7	1:246894625	AGTATTTTAATATTA[A/C]ATTCTGTCCTACATC	25909
rs767442042	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246886052	TAAGTTTAAACAAAA[A/C]AAGTGCAGTGGCTCA	25909
rs767470861	in-del	-/AATT	3.20067e-05	0.00400029	intron-variant	AHCTF1	GRCh38.p7	1:246853074	GATAAAGAAGTAAAA[-/AATT]AATTAATTTTTTTTA	25909
rs767478107	snp	C/T	0.000132468	0.00813735	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246891876	GATAGACTGTATAGT[C/T]TGTGGATCCATGAAA	25909
rs767575909	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246881973	GCATGAGCCACCGTG[C/T]CTGGCCTTTATTATT	25909
rs767598148	snp	C/G	1.71237e-05	0.00292602	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246862122	TCAGAAAATCCAGAA[C/G]TAGTAACTGACATGG	25909
rs767601519	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246927086	GGGAGGCTGAGGAGG[A/G]AGAATGGCGTGAACC	25909
rs767614421	snp	C/T	1.6566e-05	0.00287797	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246891001	AGAACCAAAGAACCA[C/T]TTGTGCATACTGACA	25909
rs767616942	snp	A/G	1.65436e-05	0.00287602	missense, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840939	GCTGGGCTAGCCAAG[A/G]GGGAAATCAGCCGAA	25909
rs767632674	snp	G/T	1.65037e-05	0.00287256	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246855744	CATTTATTGTCATTT[G/T]CTCTAATTGCAGGGG	25909
rs767668291	snp	G/T	4.96611e-05	0.00498278	missense, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840831	TTTCTGCGTAAAATT[G/T]GCTTTGGATAGGAAG	25909
rs767687977	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246927770	AGTACTTTGGGAGGC[A/C]GAGGCTGGCGGATCA	25909
rs767729543	in-del	-/TTT			intron-variant	AHCTF1	GRCh38.p7	1:246891445	AATGAAATTGGCTTG[-/TTT]TTGTTTTGAAATTGC	25909
rs767735464	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246847344	ATGACATAAGTAGGG[G/T]GACAAAAGCAGAATA	25909
rs767737594	snp	C/T	2.04288e-05	0.00319593	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876183	AAACGAGGATCACGA[C/T]CATTCTATTAAACAT	25909
rs767795810	snp	A/G	1.66081e-05	0.00288163	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861975	CCAGGAATCCATTTT[A/G]GGTGGACATCTTCTT	25909
rs767807860	snp	C/G	1.79842e-05	0.00299863	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853168	CACTTTCTTTTAGTA[C/G]ACCAACTTCTACTTC	25909
rs767815388	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246903244	AGCACCCCTCCGATC[C/T]CCTCAGGAATTCAGC	25909
rs767833484	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246914788	TACACCAACCATGCA[C/T]TCAACTGAGCAACCA	25909
rs767836813	snp	A/G	6.66112e-05	0.00577071	intron-variant	AHCTF1	GRCh38.p7	1:246900262	CTAAAAGAAAATTTA[A/G]AACATTACTAAGTCA	25909
rs767886013	snp	G/T	1.66485e-05	0.00288513	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900173	CCAAGATGCCATGTG[G/T]AGAAGTCCTACTTAC	25909
rs767901310	snp	C/T	1.69781e-05	0.00291355	intron-variant	AHCTF1	GRCh38.p7	1:246904060	ATTAACGAAGACACG[C/T]TAAATATATTAATAC	25909
rs767928092	snp	A/G	1.65061e-05	0.00287277	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246860999	AGTAGTTAGTGCAGT[A/G]GAAGAGCTTTTGGGC	25909
rs767928528	snp	A/T	1.64863e-05	0.00287104	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867723	TTCTCCAATTTTAGA[A/T]AACACATTGTTGATG	25909
rs767928956	in-del	-/TAAG	3.33225e-05	0.00408168	intron-variant	AHCTF1	GRCh38.p7	1:246900270	AATTTAAAACATTAC[-/TAAG]TAAGTCATTGGTCAG	25909
rs767939920	in-del	-/AAGATCGCTTAAGCCCAAGAGGTTGAGGCTACAGTGAGCCATGAC			intron-variant	AHCTF1	GRCh38.p7	1:246897887	GGGGGCTGGGGTGGG[lengthTooLong]AAGATCGCTTAAGCC	25909
rs767969005	snp	C/T	6.62252e-05	0.00575397	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246918307	CGTCTTCTCCAAGGG[C/T]TTGAAGAGTCACTTC	25909
rs767981565	snp	C/T	1.66286e-05	0.0028834	intron-variant	AHCTF1	GRCh38.p7	1:246867386	ACTTCTGATGTATCA[C/T]AAGGAGCACTGATAA	25909
rs768050688	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246889136	AAAATAATGAAGTTC[A/G]AAGACAGAGAGTTAA	25909
rs768058259	snp	A/G	3.29707e-05	0.00406008	intron-variant	AHCTF1	GRCh38.p7	1:246898159	CTGTAATAGAAAGCT[A/G]ATAACGTGATCCAAC	25909
rs768069639	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246902245	CACGGGTAAACTTCA[C/T]TCAAAGACTACTCAC	25909
rs768090998	snp	C/T	1.79544e-05	0.00299615	intron-variant	AHCTF1	GRCh38.p7	1:246885484	TATAGTTTCAAAAGA[C/T]GTACTTACCTATTAA	25909
rs768104236	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246915354	AAAAATTACTTCACC[A/G]TTGATTTCAAAGGAG	25909
rs768105437	snp	A/G	8.39328e-05	0.0064776	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877266	ATTCAACCTATTGCA[A/G]TGTTGCCGCAAAAAA	25909
rs768106016	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246928367	ACACTATGAATTCCT[A/G]AAAGGCAAAAATCAC	25909
rs768127230	in-del	-/GTAGCATAA	3.30066e-05	0.00406229	cds-indel, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246890028	AATTACAGGGTAGTT[-/GTAGCATAA]CCTTGACAACTGCAC	25909
rs768132394	snp	A/G	1.66718e-05	0.00288715	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246862051	CAGGTGATGGAGAGG[A/G]AGATGCTAAAGGTGT	25909
rs768146822	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246901549	GAATGGCATGAACCC[C/T]GGAGGCGGAGCTTGC	25909
rs768157294	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246927569	GAAACACCTACGTTC[A/G]GTACTGTACAAAATT	25909
rs768158889	snp	A/T	1.66543e-05	0.00288563	intron-variant	AHCTF1	GRCh38.p7	1:246890096	AAAAAGCTGGTAATA[A/T]TCCCCAAATATCTCA	25909
rs768164510	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246881057	CATTATGAAATGCAC[A/G]GTGGAGACCACAATA	25909
rs768172996	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246903763	GAATTGCTTGAATCC[A/G]GGTGGCGGAGGTTGC	25909
rs768181822	snp	G/T	1.71687e-05	0.00292986	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853217	CAGCGCTACTTCCTG[G/T]TTAAGCCTGCGCTCA	25909
rs768220585	in-del	-/ACA			intron-variant	AHCTF1	GRCh38.p7	1:246895451	GTAACAGTGATACAC[-/ACA]ACAATTTGGATGAAT	25909
rs768257985	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246908368	AGGGGGAAGCCTACC[C/T]TCCCCACCTACAAAA	25909
rs768264458	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246845579	TTTCACTTTTCGTAA[A/T]CTTCACCTAAGCTTT	25909
rs768272774	snp	G/T	1.79422e-05	0.00299513	intron-variant	AHCTF1	GRCh38.p7	1:246891087	AGTTAACATCAGTTG[G/T]TTACTTACAAAAAAA	25909
rs768283817	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246856186	TGGAATATTTTCTAT[A/G]AACTCAGTAGAGGCA	25909
rs768295753	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246889932	GAAACTTTGACTTCT[C/T]ACAGATGTAATTTCT	25909
rs768316855	snp	A/G	3.33139e-05	0.00408116	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900129	AGGAGGGACTCCTCT[A/G]TTTAAACTTCTCTCA	25909
rs768341840	snp	A/G	1.67697e-05	0.00289561	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916370	AAGTTGTGGACCACA[A/G]GCCAAGCAAGCAAGT	25909
rs768357436	in-del	-/AATA			utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839714	AGATAATCAATTATT[-/AATA]GTCCATTCATTACAC	25909
rs768362297	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246929929	TGGTGGCGTGCGCCT[A/G]TAATCCCAGCTACTC	25909
rs768395794	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246858095	CCCCCGAGTAGCTGG[C/G]ACTACAGATGCCCGC	25909
rs768401964	snp	C/T	3.29582e-05	0.00405931	intron-variant	AHCTF1	GRCh38.p7	1:246898187	AACCAAAAGAAACAA[C/T]AGAGTTAAAAATCAT	25909
rs768436703	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246878299	CTATTCAGTAGGCTA[A/C]GGTGGGAGGATTGCT	25909
rs768483433	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246844861	GCAATTATCAATATA[A/G]TTACAGACGAGCACA	25909
rs768488523	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246857257	TTGGGAGTATGTTTC[A/C]AATGGTCGTTAAAAA	25909
rs768493056	snp	G/T	1.70168e-05	0.00291687	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840780	TGACTTTACAAATAG[G/T]TGTACATTAAAATCT	25909
rs768496471	in-del	-/CT	3.47899e-05	0.00417058	intron-variant	AHCTF1	GRCh38.p7	1:246894646	GTCCTACATCTAGAC[-/CT]CTAATACTTACATAG	25909
rs768550046	in-del	-/CAGTCATT	1.65105e-05	0.00287315	intron-variant	AHCTF1	GRCh38.p7	1:246888273	TCAGTGGATCTTATA[-/CAGTCATT]CATTCATTCATGCTT	25909
rs768550375	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246856010	TCAGAAACAATGCTG[C/T]ACTTGTTTTACCCAT	25909
rs768553760	snp	A/T	1.64841e-05	0.00287085	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861034	AGGCCGTGAAAACAG[A/T]CTCTTCAAGGTCTTC	25909
rs768583957	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246915677	ACAGACCAAGTTCAA[C/T]TTATTCATCCTGGGA	25909
rs768604412	snp	C/G	3.30819e-05	0.00406692	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246857707	CTTCATAGACTGATG[C/G]TGCACAAAGAGAAGC	25909
rs768613394	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246843009	ATCAGTTTTATTTTT[G/T]AATGTTTCCACTGTC	25909
rs768616035	snp	C/T	3.29804e-05	0.00406068	intron-variant	AHCTF1	GRCh38.p7	1:246895939	TCCTAAACCATGCAT[C/T]ACAGAAAGGAAAGAA	25909
rs768627020	in-del	-/C			intron-variant	AHCTF1	GRCh38.p7	1:246871964	TCCTACTCCACAAGT[-/C]CCAGCCTCAGTGTTC	25909
rs768646743	snp	G/T	1.83893e-05	0.00303221	intron-variant	AHCTF1	GRCh38.p7	1:246877343	AGTTTTAGAAAAAGC[G/T]ATTTAAATGTACAAA	25909
rs768661982	snp	A/G	0.000167923	0.0091615	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867316	TCTGGAGCTGGGAGC[A/G]AATACACTATAGGAG	25909
rs768685968	snp	A/C/T	4.954e-05	0.00497674	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902560	CTGTCACCATGAGAT[A/C/T]GAAATTTCTCTATAC	25909
rs768704208	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246925033	AGATGGAAAAGGCCA[G/T]AATCACATTGTTACT	25909
rs768710998	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246876330	TCCAAACCAAGAACT[A/T]CATCCACATATCTAA	25909
rs768731649	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246875044	CAGGCCAACAACTTA[C/T]ATTATAGATAAACCA	25909
rs768746376	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246911007	AATCATAAATTACTT[C/T]TGTAATCAATAAAAT	25909
rs768790237	snp	A/G			synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849991	TGTAGATCTCCTTCT[A/G]ATGCTGGGAGCTTCT	25909
rs768792256	snp	C/T	1.65927e-05	0.00288029	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900361	TCTGGCATTTGTGCA[C/T]GATACCAACGATTTA	25909
rs768818251	snp	G/T	3.33525e-05	0.00408352	intron-variant	AHCTF1	GRCh38.p7	1:246855839	TTTCCTTTAGAAAAA[G/T]AAATACATACCTTAG	25909
rs768821089	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246883185	GTTTGATGGTTTAAA[C/T]ATTAAAACTTTTTCA	25909
rs768875739	snp	A/G	1.65157e-05	0.0028736	intron-variant	AHCTF1	GRCh38.p7	1:246877131	TTATCTTGAATTTCT[A/G]ACAAGTTTACATCGG	25909
rs768892121	snp	A/G	1.67593e-05	0.00289471	intron-variant	AHCTF1	GRCh38.p7	1:246913431	GAAAACATAATACGT[A/G]ATTTGCTTTTCTTCT	25909
rs768900228	snp	C/G	1.91944e-05	0.00309788	intron-variant	AHCTF1	GRCh38.p7	1:246900499	TAATTTTTAAAAACA[C/G]AATAAAGAATCTCAA	25909
rs768900701	snp	A/C	1.91122e-05	0.00309124	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876164	AGCCAGTGATCTCTC[A/C]CGCAAACGAGGATCA	25909
rs768907322	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246865295	ATGCTTTGGAGCCCA[C/G]AAATAAAAACTTGTA	25909
rs768913266	in-del	-/CTT	8.23988e-05	0.00641815	cds-indel, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851205	CTGGCTCAACTTCTC[-/CTT]CTTCACCTTCCAATA	25909
rs768921798	snp	C/T	1.83357e-05	0.00302779	intron-variant	AHCTF1	GRCh38.p7	1:246891967	TACAGTAAATCTAAA[C/T]AAATTAGAATCACAA	25909
rs768924275	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246900933	GAAAAAGAAAAGTGC[C/T]TGGATGGTGCCTGTG	25909
rs768931720	in-del	-/C			intron-variant	AHCTF1	GRCh38.p7	1:246868942	TCTGCCTCCCGGGTT[-/C]CACGCCATTCTCCTG	25909
rs768940782	snp	A/G	1.64762e-05	0.00287016	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246907616	ACCTACAGCAAGCTG[A/G]TTTGTCCTGCTTATG	25909
rs768974056	snp	C/T	1.65343e-05	0.00287521	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850824	CATCAACCTGGCTGA[C/T]ATTCATAGTCATTGT	25909
rs768993508	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246867884	AAGCATATGAAAGAA[C/T]GATTACACCCCCCCC	25909
rs769005035	snp	G/T	0.000163412	0.00903766	intron-variant, utr-variant-5-prime, upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246931296	CGACTGCCGGCGCAG[G/T]ACGCGAACCACCAGC	25909
rs769012159	in-del	-/TA			intron-variant	AHCTF1	GRCh38.p7	1:246889322	ATAGCGGCAGCACTT[-/TA]ACTACTCTTTGCGGT	25909
rs769018753	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246870759	CTAGGCTATTTAATT[A/T]CTCAGGGACAGGGGT	25909
rs769019506	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246894238	TCACTTTAATGTAAA[A/C]AGAAATAATTTTCTT	25909
rs769049702	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246871784	ACAGCTATTAGAGGC[A/G]GCAGTATAGCTACCT	25909
rs769058490	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246929740	GCGTGAAAGACACAA[C/T]GTTTTGCTTCCTCTT	25909
rs769093519	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246920013	CCGGGCGTGGAGGCA[C/T]ACGCTTGTAATTCCA	25909
rs769107595	snp	C/T	1.64749e-05	0.00287005	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849842	GAACGTTTTTGGCTT[C/T]GACTTTCAGTCTTTT	25909
rs769116967	snp	A/G	1.75286e-05	0.00296041	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876068	TGATGTTGACAGATG[A/G]TAAGGCTTAGCTCGT	25909
rs769136756	snp	A/C	1.91551e-05	0.0030947	intron-variant	AHCTF1	GRCh38.p7	1:246905680	AAATTAGTATATTTC[A/C]TATTTTTAAGTTATT	25909
rs769144566	in-del	-/AGAATA			intron-variant	AHCTF1	GRCh38.p7	1:246856249	TATGATAAATGACTC[-/AGAATA]AGAGACCAATGAAAC	25909
rs769148614	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246918880	ACCATCCTCCCTACA[G/T]AAAAAAGAAAAAGTG	25909
rs769148766	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246930279	TCAGCCTCCCAAGTA[A/G]GCGCGCGACTAGAGG	25909
rs769153631	snp	C/T			missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246918292	ATTCTAATGTTATTT[C/T]GTCTTCTCCAAGGGC	25909
rs769162657	snp	C/T	6.58989e-05	0.00573978	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849750	TGAAGGAAGCTGTGG[C/T]GAGCAATCTTTCTTC	25909
rs769184545	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246907272	CAAAACGTTGTAAAG[G/T]TACAAAGTCATGCTT	25909
rs769230889	snp	C/T			missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246903986	GCCAAACACTTTCTA[C/T]TACCAAAGGCCAGCT	25909
rs769249381	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246918523	CATATTGGCCAGATG[C/T]GGAGGCTCACGCCTT	25909
rs769258589	in-del	-/AA			intron-variant	AHCTF1	GRCh38.p7	1:246889389	CATACTATTTTATTT[-/AA]AGCTTTATACTGACT	25909
rs769269105	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246844729	AAGCTAACAGGAAGA[C/T]ATTCCATAGAAAAAT	25909
rs769274809	snp	C/T	2.86389e-05	0.003784	intron-variant	AHCTF1	GRCh38.p7	1:246853336	TTTTTACATTTAAAC[C/T]GAAAAATAAATCCAC	25909
rs769287506	in-del	-/A	1.70921e-05	0.00292331	intron-variant	AHCTF1	GRCh38.p7	1:246857647	GTTCATAATTTCATT[-/A]AACTTCTTTCTAAAA	25909
rs769295979	snp	A/G	3.34403e-05	0.00408889	intron-variant	AHCTF1	GRCh38.p7	1:246887181	TTCTAGTAATTCATG[A/G]AAGTTTATGCTGTAA	25909
rs769301786	snp	A/G	1.65523e-05	0.00287678	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246894712	TTCCACGTCCATTCA[A/G]GAACAAAGCGCAAAT	25909
rs769316985	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246903496	CTAATTTAAATTACT[C/T]CTACTACATTATGAA	25909
rs769319952	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246858314	CCCCCCTTAACCTCT[C/T]GCTTTTCACTTTTTG	25909
rs769341551	snp	A/G	1.64749e-05	0.00287005	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867669	AACATACCTATTGAA[A/G]GGTGTGGTGCTATTT	25909
rs769345120	snp	A/C	3.36089e-05	0.00409919	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246885565	GGCTTCATTGTCTGA[A/C]TATATCTGAGGGCTT	25909
rs769360009	snp	C/G/T	0.000146359	0.00855326	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867315	CTCTGGAGCTGGGAG[C/G/T]GAATACACTATAGGA	25909
rs769384220	in-del	-/TCAATCAA	3.34038e-05	0.00408666	intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842653	CAGAGCGAGACTGTC[-/TCAATCAA]TCAATCAATCAAGAA	25909
rs769396623	snp	C/G/T	4.96121e-05	0.00498036	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246891795	TCTCTCAGTGATCTC[C/G/T]CGGGCTTCTGATGCA	25909
rs769419285	snp	C/G	2.5944e-05	0.00360158	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850455	CTTCAACTGCTGGTT[C/G]CAACAGCTGAGATGA	25909
rs769420501	snp	A/G	3.31252e-05	0.00406958	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246860985	TGTTCAGTTACATTA[A/G]TAGTTAGTGCAGTGG	25909
rs769453707	snp	A/G	5.51293e-05	0.00524992	intron-variant	AHCTF1	GRCh38.p7	1:246891096	CAGTTGTTTACTTAC[A/G]AAAAAATCAAGATGC	25909
rs769485815	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246841407	TAGCAAAGATGCACA[A/G]AATTTCACAAACTTG	25909
rs769493097	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246857428	ATGCACAGCTGTGAG[C/T]GAAATCTTGGTCTTC	25909
rs769498450	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246904943	ATTTGAAGAATAAGA[C/G]AGCAGGGTACTGAGA	25909
rs769505894	snp	A/C	1.64982e-05	0.00287208	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861127	TTCCTTTGCTCACAT[A/C]CAGTTTCTCTAAACT	25909
rs769532757	snp	A/G	1.70904e-05	0.00292316	intron-variant	AHCTF1	GRCh38.p7	1:246916405	TTTTCCCTAGAAGAA[A/G]AAAAAATTGCCTATT	25909
rs769536393	snp	A/G	1.64958e-05	0.00287187	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246913369	AAATGCTGAGTGCTT[A/G]CACTGGCTCCTCCAT	25909
rs769538655	snp	A/G	5.12098e-05	0.00505987	intron-variant	AHCTF1	GRCh38.p7	1:246888522	TCCACTTCCCTCTGC[A/G]ATCAGGGAAAAATTA	25909
rs769571448	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246905361	AAATTAGCCAGGCAT[A/G]GTGACAGGCACCTGT	25909
rs769581467	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246875658	CACCATGCTGATCAG[G/T]CAGCAGCCATCAACA	25909
rs769620370	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246844463	CAGTGGCTCACAATT[C/G]TAATTCCAGCACTTT	25909
rs769671308	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246872432	GTCACACACAAAAAG[A/T]CAAATGAGGTGGTCA	25909
rs769686831	snp	A/G	1.65045e-05	0.00287263	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850100	CGTTTTCTAGGTATG[A/G]CAGACATATCAAATT	25909
rs769706438	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246847550	TTGCCCAGGCTGGAG[C/T]GCAGGGGCACACGAT	25909
rs769714758	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246925290	CTCAATACAATTTTG[C/G]AAAGATTTTCACAAA	25909
rs769738929	snp	C/T	3.29549e-05	0.00405911	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851239	CAAGGTAAAGTTGCT[C/T]TGAGCCACAAAAAGT	25909
rs769739683	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246930365	GTTGTTTGCAAACTC[A/G]TGACAGCTTGGTAGT	25909
rs769743319	snp	A/G	3.30136e-05	0.00406273	intron-variant	AHCTF1	GRCh38.p7	1:246888370	TTGTAGACTCTAAAT[A/G]ATAGCACATTACTGC	25909
rs769753380	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246901198	ATACAAAAATTAGCC[A/G]GGCATTGTGGCATGC	25909
rs769780387	in-del	-/A	1.64779e-05	0.00287031	intron-variant	AHCTF1	GRCh38.p7	1:246898194	AGAAACAATAGAGTT[-/A]AAAATCATCTCACTT	25909
rs769782209	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246877641	CAGGTTTTTAAGAAG[C/T]GACACTCAGTGGGAA	25909
rs769793322	snp	A/G/T	4.94624e-05	0.00497284	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849657	CTGGAGAAAATAAAG[A/G/T]CTCATTGTTTGGTTC	25909
rs769794584	snp	G/T	1.64746e-05	0.00287002	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246898213	ATCATCTCACTTGGC[G/T]TAAACTGGAAGGCTG	25909
rs769825671	in-del	-/T	1.74967e-05	0.00295771	intron-variant	AHCTF1	GRCh38.p7	1:246877312	TACACCTGAAAGCAG[-/T]TATTTATCAAAGTTT	25909
rs769825807	snp	C/G	4.94417e-05	0.00497176	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246895877	CAGTCAAAAGTCCCA[C/G]GGAACTAGTCTGAAT	25909
rs769826093	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246885693	ACTCTGGAAATAACA[C/T]GAAAAATGTTAAATA	25909
rs769851117	snp	C/G/T	1.68272e-05	0.00290057	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850376	TGATTTTCTACAGAT[C/G/T]TTTTAATTCTTCTAG	25909
rs769854747	snp	C/T	1.65048e-05	0.00287265	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850946	GACTGTTCCATTGTA[C/T]CTGAAGTAATTTCTT	25909
rs769866468	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246865326	GTTGCAGTACCTTCC[C/T]TGTCATTCTATCTAT	25909
rs769875584	snp	A/G	3.31318e-05	0.00406999	intron-variant	AHCTF1	GRCh38.p7	1:246905532	AAACAAAGTTTGTAT[A/G]AGACCTACCTATCTT	25909
rs769903839	snp	C/T	3.62516e-05	0.00425729	intron-variant	AHCTF1	GRCh38.p7	1:246857857	TTTATGCTAAATATT[C/T]AGTGATTACTGATAG	25909
rs769944202	snp	C/T	1.65154e-05	0.00287358	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246857738	TTCAGTTCCTTGAAC[C/T]GGGCTTAAGTGATTC	25909
rs769976161	snp	A/G	1.65392e-05	0.00287564	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246887334	GGGAAAGGAATACAT[A/G]ATATCAAGTAGCAAA	25909
rs770001250	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246871945	ATGACCCTGATCCCA[A/G]ACATCCTACTCCACA	25909
rs770009196	snp	C/T	1.69882e-05	0.00291441	intron-variant	AHCTF1	GRCh38.p7	1:246864139	CAGAATGCGCATTTA[C/T]TGAGTTATACTGAAA	25909
rs770028189	snp	C/T	9.89642e-05	0.00703365	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902573	ATCGAAATTTCTCTA[C/T]ACTCTGGCATCCCAA	25909
rs770029746	in-del	-/A	1.74251e-05	0.00295165	intron-variant	AHCTF1	GRCh38.p7	1:246860854	TTATAAACTTTATTG[-/A]GGGACATTAATAACA	25909
rs770031454	snp	C/G	1.65699e-05	0.00287831	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246894722	ATTCAAGAACAAAGC[C/G]CAAATTAGTGGCAGA	25909
rs770034623	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246884631	CTGTACTTCCAATCA[G/T]GCCATTTAGCTTTCT	25909
rs770082260	snp	C/T	5.0176e-05	0.00500854	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840797	GTACATTAAAATCTT[C/T]CCAAGAAATTACAGC	25909
rs770093915	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246873106	GTTCGACTTATTCCT[A/G]TAAGCCAGTCTCTGA	25909
rs770095238	in-del	-/AGT			intron-variant	AHCTF1	GRCh38.p7	1:246845222	TTTTTGTGGGTACAC[-/AGT]AGGTGTATATATAAA	25909
rs770121283	snp	A/G			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932182	AAATCGGGTCTCTCC[A/G]CCTCCGAGGAGCTGG	25909
rs770125274	in-del	-/TTC			intron-variant	AHCTF1	GRCh38.p7	1:246911385	GCTTTTGCTCATCAA[-/TTC]TTTTCATTTAAACTT	25909
rs770166834	in-del	-/TG			intron-variant	AHCTF1	GRCh38.p7	1:246901880	GAGCTCATGACAACA[-/TG]TGCTTTTCACATATT	25909
rs770170583	snp	A/G	4.95372e-05	0.00497656	missense, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840903	TCTGTAGTTTTTCTT[A/G]GTTTGCTCTTGACTC	25909
rs770188590	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246846992	TTTTGAAGAATATTT[A/C]AGATTAACTGAAGGC	25909
rs770208912	snp	C/T	3.33072e-05	0.00408075	intron-variant	AHCTF1	GRCh38.p7	1:246888145	ATAATTTTAGTAATA[C/T]ATGAAACACTGGATA	25909
rs770210034	snp	A/G/T	3.32156e-05	0.00407515	missense, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246842753	TGGCTTTCCCAGAGT[A/G/T]TCTACTGATTGTGCA	25909
rs770212670	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246914850	ATCCAAATGATCAAT[G/T]AGTGTCCATGTTTCC	25909
rs770214297	snp	C/T	4.17162e-05	0.00456688	intron-variant	AHCTF1	GRCh38.p7	1:246890940	TTAATACTTATAGAT[C/T]AAGTAAATATTTTAC	25909
rs770219573	snp	C/T	3.30983e-05	0.00406793	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849922	CACTAAAATGGATTT[C/T]CCTAAAGCTGGTTTT	25909
rs770220000	snp	C/G			missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246907568	TCTTTTCATGCTTTT[C/G]ATGTTCCAAAGTGCT	25909
rs770232662	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246912310	TGAAACCCCATCTCT[A/G]CTAAAAAAAAAAAAA	25909
rs770235460	snp	C/T	1.64743e-05	0.00287	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246907656	GTTGAAACAGCTGTT[C/T]CTGTTGGACTTACTA	25909
rs770260566	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246881328	TGTGAGGAACTGAGA[C/T]ATCCACCATTAGCGT	25909
rs770260735	snp	A/G	3.32662e-05	0.00407824	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900221	ACAGTGCAAAATAAG[A/G]GCAATTATGTAGATA	25909
rs770269173	snp	A/T	7.61992e-05	0.00617202	intron-variant	AHCTF1	GRCh38.p7	1:246862187	GGAATTACACCATTA[A/T]AAGTGCTTATAGGCC	25909
rs770277537	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246868532	AGTGCTGGGATAGAG[G/T]TGTGAGCCACCGGCC	25909
rs770313761	snp	C/T	1.69378e-05	0.00291009	intron-variant	AHCTF1	GRCh38.p7	1:246907781	CACAAATTAGACAAA[C/T]GAAGTTAAAAAACTA	25909
rs770318564	in-del	-/AAT			intron-variant	AHCTF1	GRCh38.p7	1:246871869	TTGAGGTTATTAAAA[-/AAT]AATAACAACCTAAAG	25909
rs770322398	snp	A/T	1.67178e-05	0.00289113	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246862061	AGAGGGAGATGCTAA[A/T]GGTGTTGATCGAAGA	25909
rs770357498	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246892788	AGGCATGTGCCACCC[A/T]GCCCAGCTAATTAAA	25909
rs770366664	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246849245	CTTCAAAACAATTTC[A/G]GGTTGTGGATATCAC	25909
rs770397897	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246897260	TGGAGGTTGCAGTGA[A/G]CCAAGATCACGTCAC	25909
rs770405647	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246906301	TGACAAACTGGCAGC[C/T]GGGCGTGGTAGCTCA	25909
rs770423744	snp	C/T	1.65822e-05	0.00287938	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850728	GAGTAGCAACATCTG[C/T]TGATGCTTCCTGTTG	25909
rs770442400	in-del	-/AA			intron-variant	AHCTF1	GRCh38.p7	1:246923109	TAATCAAATAATACC[-/AA]AAAAAAAAAAAAAAA	25909
rs770456149	snp	C/T	5.82021e-05	0.00539423	intron-variant	AHCTF1	GRCh38.p7	1:246918417	ATTATTATGACACAT[C/T]TGTAGACAATATACT	25909
rs770470708	snp	C/T	1.65236e-05	0.00287429	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246905551	CCTACCTATCTTGTG[C/T]AGACTGAACAGCCCA	25909
rs770470947	snp	C/T	1.65206e-05	0.00287403	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861160	GTGACCCCTCATCCA[C/T]TTCTTGATGCTCCTT	25909
rs770477433	in-del	-/CTGT			intron-variant	AHCTF1	GRCh38.p7	1:246854124	TAACACGGTGAAACC[-/CTGT]CTGTCTCCACTAAAA	25909
rs770485656	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246895423	GGGGTGTGTGTGTGT[A/G]TGTGTGTGAAGAGTA	25909
rs770489601	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246919831	TTAAAGAATTCTCAA[A/T]GTTAAAGCAACAAAG	25909
rs770504182	in-del	-/T			utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839197	ATTTAGAACAGGCAA[-/T]TTTGTTTGCTTATGA	25909
rs770529215	snp	A/T	3.6675e-05	0.00428208	intron-variant	AHCTF1	GRCh38.p7	1:246885708	TGAAAAATGTTAAAT[A/T]TAAATATAATCCTAT	25909
rs770537249	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246877748	GTAGATGTTTTTTGG[C/T]TGATTTGCAGCAAGA	25909
rs770552926	snp	C/G	1.78131e-05	0.00298433	intron-variant	AHCTF1	GRCh38.p7	1:246849566	TAACCAAATTTTAAG[C/G]TGAAGAGTGACTGAG	25909
rs770579070	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246867045	AGCAGTCTGAAATTA[C/T]TGAACAAAAATTTTA	25909
rs770582467	snp	C/T	0.000103313	0.0071865	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246885590	GGGCTTGTCTGTGCT[C/T]GCCCTGACTCATGAA	25909
rs770611406	in-del	-/AGA			intron-variant	AHCTF1	GRCh38.p7	1:246901743	GAATTGGTTGAGCCC[-/AGA]AGGTCAAGGCTGCAA	25909
rs770627319	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246894131	ATGACTTGGGCTCAA[A/G]AAGTCAAGGCTGCAC	25909
rs770635022	in-del	-/TACC	1.67461e-05	0.00289357	intron-variant	AHCTF1	GRCh38.p7	1:246913228	AAGTAAAGAACTGAT[-/TACC]TACCTGATGCTTCAA	25909
rs770636944	snp	C/T	1.65326e-05	0.00287507	intron-variant	AHCTF1	GRCh38.p7	1:246898347	AAAGTCTGTAACAGA[C/T]AAATTAGTAAGGCAT	25909
rs770647868	snp	C/G	1.70615e-05	0.00292069	intron-variant	AHCTF1	GRCh38.p7	1:246902499	ATCCAGCCTTCACAT[C/G]ACATATTTCAAGTAC	25909
rs770648988	snp	A/G	0.000151295	0.00869624	intron-variant	AHCTF1	GRCh38.p7	1:246904051	GAAACAGAAATTAAC[A/G]AAGACACGCTAAATA	25909
rs770650995	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246844598	ATGTGGTGGTGCACG[C/T]CTGTGGTGTCAGCTA	25909
rs770660332	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246879258	TACCATTTTTACCCA[C/T]GAGATGAAGAGACAA	25909
rs770662748	snp	C/G	2.67212e-05	0.00365512	intron-variant	AHCTF1	GRCh38.p7	1:246851468	TAAAGATAAGAGACT[C/G]GTTAAAGAATTTTAA	25909
rs770681220	snp	A/C/G	3.30443e-05	0.00406464	intron-variant	AHCTF1	GRCh38.p7	1:246877145	TGACAAGTTTACATC[A/C/G]GTAAGTAATTACCTG	25909
rs770741009	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246872243	TCCAATTTGTACAAA[A/G]TAATACTCAGATCGG	25909
rs770768048	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246926422	TCTCCAGACTTCATC[A/G]TGGTGCCTAGCACAA	25909
rs770776821	snp	A/G	1.67164e-05	0.00289101	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916166	AAGAACAACTGCTTT[A/G]ACTACTTTTGATATT	25909
rs770781092	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246852957	ACACTTATTTTTTGA[A/G]CCCATATTTTTATAA	25909
rs770799142	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246928048	TTCGGCCGGGTGCGG[C/T]GGCTCACGCCTGTAA	25909
rs770799337	in-del	-/AAGT			intron-variant	AHCTF1	GRCh38.p7	1:246863873	TCCTTGCTACTTGAA[-/AAGT]AAGAGCCATCTAGTT	25909
rs770804565	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246913660	AGAGCTTACTGATAC[A/G]CCAGGCATTGTGTTA	25909
rs770831159	snp	C/T	1.65625e-05	0.00287766	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850304	AATTTTCTGATCATT[C/T]TGCTAGGACTTGTTA	25909
rs770845244	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246920770	GCAAAACACTGTCTC[-/A]AAAAAAAAAAAAAAA	25909
rs770847163	snp	C/T	1.65425e-05	0.00287593	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851339	TCAATAGTATCAAAA[C/T]TGTACTGAAGCTTAA	25909
rs770863446	snp	A/G	1.64857e-05	0.00287099	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877052	ATTCTGAACGCTGGC[A/G]CTGGACTGCAAAAAT	25909
rs770866690	snp	C/T	6.73582e-05	0.00580298	intron-variant	AHCTF1	GRCh38.p7	1:246913437	ATAATACGTGATTTG[C/T]TTTTCTTCTGCAAAG	25909
rs770871250	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246888580	ATATCAAAGCAACCA[A/G]CATCAAAATATTAAA	25909
rs770875798	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246886953	TCTCTCTAATATTAA[C/T]GATCACTGTATCTGA	25909
rs770884177	snp	C/T	3.29832e-05	0.00406085	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850205	CTGACCCTTCTAACA[C/T]GTTTAATACGCAGCT	25909
rs770891984	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246854599	AGAAAGTTGCTTTTT[C/T]GATAATGATCATTTC	25909
rs770902178	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246868474	TGGCCAGACTGGTCT[C/G]AAACTCCGGGCCTCA	25909
rs770953764	snp	C/T	1.65051e-05	0.00287267	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246889989	ACGCTCAAACTTCTG[C/T]CGACGACTGGTGTAG	25909
rs770958397	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246872389	AGTGTAGACACCTTT[A/G]CTGGCTAAATAAAAG	25909
rs770965723	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246902051	GATGGAGAAACAGAG[C/G]TCTGAAATGTTAAGC	25909
rs770973551	snp	C/T	3.30371e-05	0.00406417	intron-variant	AHCTF1	GRCh38.p7	1:246888344	TAAGCATGTCTCCTC[C/T]CTCCCCAGCTTTGTA	25909
rs770976823	snp	C/T	1.65559e-05	0.00287709	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849942	AAGCTGGTTTTCCAA[C/T]ATCAACATTTTCACT	25909
rs770978831	snp	C/T			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933723	AGCTGGGACTACAGG[C/T]ATGGATATCATGCCT	25909
rs770999570	snp	A/G			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932571	CTTTTCATGCCAAAG[A/G]TGGGCTCCCAGACTT	25909
rs771006965	snp	C/T	1.75468e-05	0.00296194	intron-variant	AHCTF1	GRCh38.p7	1:246888536	CAATCAGGGAAAAAT[C/T]AAGACTTATTTAATA	25909
rs771069340	in-del	-/AAT			intron-variant	AHCTF1	GRCh38.p7	1:246896364	ATGCTCATACAACAG[-/AAT]ATTATACAGCCATAA	25909
rs771071299	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246873307	CTTTCTCCCTGTGCT[A/G]TTTAGTCCCTTTTAT	25909
rs771083456	snp	G/T	3.30066e-05	0.00406229	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851006	AAATTTTCTGCAATT[G/T]CTACTTTAATAGGTT	25909
rs771122251	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246879424	ATCCTTTCACCCTAG[A/G]ATTTTATTCTATAAA	25909
rs771130520	snp	C/G	3.29766e-05	0.00406045	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246907736	TGGTACTTCAGCTGG[C/G]ATACCAGTTAGAACT	25909
rs771131264	snp	G/T	1.66128e-05	0.00288204	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246860968	CTCCATCCTTTTCAG[G/T]TTGTTCAGTTACATT	25909
rs771151665	snp	A/T	1.65121e-05	0.00287329	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246888182	AAAAGGATACAATAG[A/T]GTGTTTGGCTGCTTC	25909
rs771156832	in-del	-/TG	1.66582e-05	0.00288597	intron-variant	AHCTF1	GRCh38.p7	1:246887192	CATGAAAGTTTATGC[-/TG]TAAGTGAATAGACTT	25909
rs771169699	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246911692	TTTCTCCATGTTGGT[C/T]AGGCTGGTCTCAAAC	25909
rs771227990	in-del	-/AAT			intron-variant	AHCTF1	GRCh38.p7	1:246862605	GATTTCTGCAAAGAA[-/AAT]AATACAAAATTCTTC	25909
rs771297386	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246841623	CTTTCTGTAAAATAA[C/T]TGCAGGATTTTAAAG	25909
rs771300929	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246927678	CAAAGGCTAGATAGG[C/G]AGAGCAGGAACGTTC	25909
rs771310818	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246869331	CCAACTAATAACCCT[A/G]CAAAGACCTCAAGTG	25909
rs771312651	snp	A/T	1.67444e-05	0.00289343	intron-variant	AHCTF1	GRCh38.p7	1:246891728	ATTCGTTTCTCTTAG[A/T]CAAGAAGTAAAATTT	25909
rs771345651	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246909891	ACCAGCAGTAACAAT[A/C]AAAAATGTCTTCTAA	25909
rs771350796	in-del	-/TATGTTTTAACAAACA	4.81012e-05	0.00490391	intron-variant	AHCTF1	GRCh38.p7	1:246843753	TGTAAAAAAAAAAAG[-/TATGTTTTAACAAACA]TACAAATAAAATCAT	25909
rs771352576	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246897322	CTGTCTCAAAAAAAA[A/T]AAAGGTAGTAACAAA	25909
rs771365960	snp	A/G	1.66418e-05	0.00288455	intron-variant	AHCTF1	GRCh38.p7	1:246900250	TATTCTCCTGACCTA[A/G]AAGAAAATTTAAAAC	25909
rs771386830	snp	A/G	4.96003e-05	0.00497973	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246891799	TCAGTGATCTCTCGG[A/G]CTTCTGATGCAAAAC	25909
rs771398603	snp	A/T	1.65151e-05	0.00287355	missense, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840921	TTGCTCTTGACTCCG[A/T]CAGCTGGGCTAGCCA	25909
rs771404535	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246928461	AATAAATTAGGATAA[C/G]AGGATACTGTATAGC	25909
rs771413639	snp	C/T	1.64917e-05	0.00287151	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246855805	CCAACACTGGTACCT[C/T]GGACTTCTGGGTGAA	25909
rs771517848	snp	G/T	2.04715e-05	0.00319927	intron-variant	AHCTF1	GRCh38.p7	1:246862195	ACCATTAAAAGTGCT[G/T]ATAGGCCGGGCGCGG	25909
rs771528634	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246878001	TCACTTGAGCATATC[C/T]ATAAAAATTATAATT	25909
rs771532467	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246882935	CTGAACTGCCTTTGA[C/T]CCTATTTCACAAAGT	25909
rs771559628	snp	C/T	3.54089e-05	0.00420752	intron-variant	AHCTF1	GRCh38.p7	1:246851488	AAGAATTTTAATACA[C/T]GTTTTAACTTGAAGC	25909
rs771564407	snp	A/C	3.45149e-05	0.00415406	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840773	ATTCTGATGACTTTA[A/C]AAATAGGTGTACATT	25909
rs771569343	snp	A/G	1.697e-05	0.00291285	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246862101	AGGATGGACTGAGGA[A/G]TGAACTCAGAAAATC	25909
rs771598958	snp	C/T	1.77798e-05	0.00298154	intron-variant	AHCTF1	GRCh38.p7	1:246899541	TTAAAAAATAATCCA[C/T]TTACATATATTTAAA	25909
rs771620173	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246898945	ATACAAAATATTAGC[C/T]GGGCGTGGTGGTGAG	25909
rs771649979	snp	G/T	1.73872e-05	0.00294844	intron-variant	AHCTF1	GRCh38.p7	1:246905669	ATATCTGAAACAAAT[G/T]AGTATATTTCATATT	25909
rs771665371	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246911464	TTAAGGTATAGTGTC[-/T]TATCTATGAAGATTC	25909
rs771665956	snp	C/T	3.52821e-05	0.00419998	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861202	TCAGGAAAAAAGATG[C/T]GGTCCTATCTTTGCT	25909
rs771733558	snp	G/T	1.89856e-05	0.00308098	synonymous-codon, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843839	ATGTGTTTTTTTGTC[G/T]GCTCCTTAAAGCAGG	25909
rs771756939	snp	A/C	1.82467e-05	0.00302043	intron-variant	AHCTF1	GRCh38.p7	1:246867833	AATGAAGAACGCTGG[A/C]ATTAAGTGCATCTCT	25909
rs771762552	snp	A/G	1.73766e-05	0.00294755	intron-variant	AHCTF1	GRCh38.p7	1:246860863	TTATTGAGGGACATT[A/G]ATAACAATTTTGAGT	25909
rs771784320	snp	A/C	1.66771e-05	0.00288761	intron-variant	AHCTF1	GRCh38.p7	1:246902686	AACCCCTGTAACATA[A/C]AATACACGCAAATAT	25909
rs771813404	snp	C/T	1.82774e-05	0.00302297	intron-variant	AHCTF1	GRCh38.p7	1:246864168	AAAAACAAAAGAATT[C/T]AGTATCCCATTTAAT	25909
rs771815317	snp	A/G			downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838782	AAGATCTATCCAGGC[A/G]GAATTAACTATACTT	25909
rs771819047	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246895763	ATTAAAATAACTAAG[-/A]AAAAAATATAACAAA	25909
rs771826196	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246914070	TATTATTTAAAGAAA[A/C]GTATACTTTAGCTAT	25909
rs771827895	in-del	-/CTG			intron-variant	AHCTF1	GRCh38.p7	1:246898576	ATGAACTGTATAACC[-/CTG]CTGTCTTCTCTAAAG	25909
rs771828269	in-del	-/ATG			intron-variant	AHCTF1	GRCh38.p7	1:246930316	CAATTCCCGGTTGAC[-/ATG]ATGTTTTAAAAATTT	25909
rs771831723	in-del	-/ATT	0.00010459	0.00723076	intron-variant	AHCTF1	GRCh38.p7	1:246861942	ATGTCTTTTCTCCCA[-/ATT]ATTATCAAACTTACC	25909
rs771873406	snp	A/G	1.66507e-05	0.00288532	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900170	TATCCAAGATGCCAT[A/G]TGGAGAAGTCCTACT	25909
rs771906906	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246869249	ACTCCACTGACTAAC[C/T]GTTCCCCCGCGTCTC	25909
rs771910866	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246844953	TCAAGTAACTTAAAC[C/T]TGTCTGTGCATCAGT	25909
rs771921644	snp	C/G	3.36276e-05	0.00410032	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916341	CGCTCTCCTGTTATA[C/G]AGTTTACTACCTCAA	25909
rs771923466	snp	A/G	1.67189e-05	0.00289122	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246894742	TTAGTGGCAGAATTT[A/G]GTTGTTCTTATTTGT	25909
rs771924254	snp	C/T	4.98915e-05	0.00499432	intron-variant	AHCTF1	GRCh38.p7	1:246842815	GTTAAGTATTAAACA[C/T]GAATCCAATTTTAAA	25909
rs771926650	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246902932	CTCATGCACTACTGG[C/T]TGGTATGTAAACTGG	25909
rs771930103	snp	A/C			utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839638	GAAAAATAAATGCAG[A/C]AAGCACACTGCATAT	25909
rs771935355	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246924243	ACATTAAAAGAACTA[C/T]TATAAATTTAACAAT	25909
rs771938324	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246860517	CTGTGCATTATGTCT[A/G]GGAACTAGTATACTG	25909
rs771978599	snp	C/T	1.64808e-05	0.00287057	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902600	CCAACAATTTGGTAT[C/T]ACTCGTCTGTCCCCT	25909
rs771979714	snp	A/G	1.66021e-05	0.0028811	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850319	CTGCTAGGACTTGTT[A/G]CCGTACTAACTTTTA	25909
rs771992145	snp	C/G	2.03415e-05	0.0031891	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867302	ATGCCTCAGGCAGCT[C/G]TGGAGCTGGGAGCGA	25909
rs771999516	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246874827	AAAAAGTTACAAAAA[A/C]ACCTGACCTCCGGCT	25909
rs772010384	snp	C/G	1.69126e-05	0.00290792	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916209	AGACAGAGAACACTC[C/G]CTTCTGTTTCTTCCA	25909
rs772017552	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246899763	ACACAGCAAAAAAAA[-/T]AAAAGCTACTATAAA	25909
rs772033834	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246857570	AAAACAGCCAACATT[A/G]CCAAAATGGAGATGT	25909
rs772044367	snp	C/T	1.64776e-05	0.00287028	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246863987	GATGGCCTGAGGCGA[C/T]CCTTTTAATTGCGAA	25909
rs772059330	snp	A/G/T	8.29502e-05	0.00643965	intron-variant	AHCTF1	GRCh38.p7	1:246890079	ATTTTTAAGAGTTGG[A/G/T]AAAAAAGCTGGTAAT	25909
rs772078783	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246910061	CTATGTGTCTCCTGA[C/T]GTGATACAATATGAA	25909
rs772092889	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246924603	CTCTCCACATCTTAG[A/T]CCCCTCCCCCAAAAA	25909
rs772094248	snp	C/T	1.6601e-05	0.00288101	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877235	CTTCATACATGTGCT[C/T]CAGTAACTCCTCTAT	25909
rs772118212	snp	C/T	1.65512e-05	0.00287669	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849950	TTTCCAACATCAACA[C/T]TTTCACTTTTAGCTG	25909
rs772119279	snp	A/T	1.76446e-05	0.00297018	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840980	AGGAGGTGACCAAGC[A/T]CTTTCTTTTTCTGTG	25909
rs772146323	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246923433	TAAATAAATAAATAC[A/T]TAAATAAATACATAA	25909
rs772147539	snp	G/T	1.65255e-05	0.00287445	intron-variant	AHCTF1	GRCh38.p7	1:246877154	TACATCGGTAAGTAA[G/T]TACCTGCTCAGTGTC	25909
rs772161616	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246921067	ATTGCACTCCAGCCT[A/G]GGCAACAAGAGTGAA	25909
rs772184798	snp	A/G	0.000313234	0.0125108	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877028	ATGGTGCACTAAAAG[A/G]AATTCATGATTCTGA	25909
rs772191744	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246862664	ACATAAAACTGCATC[C/T]ATCTTTCTAAAAGCA	25909
rs772207136	snp	C/T	0.00014928	0.00863815	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900342	AGAATCATACCTTAA[C/T]GAATCTGGCATTTGT	25909
rs772214474	snp	C/G	1.65307e-05	0.0028749	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850083	TTTTTCTTGGTCTAC[C/G]ACGTTTTCTAGGTAT	25909
rs772269675	snp	A/C	1.64928e-05	0.00287161	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851212	AACTTCTCCTTCTTC[A/C]CCTTCCAATATCAAG	25909
rs772278086	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246916022	GTAACACATTTACAT[-/A]AAAGTATACAAATTG	25909
rs772291127	snp	A/G	1.65097e-05	0.00287308	intron-variant	AHCTF1	GRCh38.p7	1:246888359	CCTCCCCAGCTTTGT[A/G]GACTCTAAATGATAG	25909
rs772316562	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246899084	ACAAGAGCGAAACTC[C/T]GTCTCAAAAAGAGAA	25909
rs772322671	snp	A/G	1.64866e-05	0.00287106	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246913311	CTGTCCAACATCAGT[A/G]ACCACAGCTGCCACT	25909
rs772425996	snp	A/C	6.89941e-05	0.00587301	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246885593	CTTGTCTGTGCTCGC[A/C]CTGACTCATGAATGC	25909
rs772439185	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246883028	GCTACAATAAGTGCT[A/G]TTTCAATAACATTAT	25909
rs772459402	snp	A/G	1.78321e-05	0.00298593	intron-variant	AHCTF1	GRCh38.p7	1:246907809	CTAGAAACAGCATTA[A/G]AAGCAAATATGTCAT	25909
rs772461108	in-del	-/AAAA	3.55878e-05	0.00421813	intron-variant	AHCTF1	GRCh38.p7	1:246843931	TCTATTTTTTTAGCT[-/AAAA]AAAGTTGAAAAAACT	25909
rs772463946	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246917307	TCAAGTACAGACTCC[A/G]AATTTCTGCTTGAGC	25909
rs772468806	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246884940	CAATTTGTCAACTCT[A/G]TCACTTCATTCTTCC	25909
rs772516311	snp	C/T	1.69117e-05	0.00290785	intron-variant	AHCTF1	GRCh38.p7	1:246857666	TTCTTTCTAAAAGTA[C/T]TTGAATTTCTCTCCA	25909
rs772523398	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246868343	CCAGGCTGGTCTTGA[A/T]CTCCTGACCTCATGT	25909
rs772525534	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246918605	AGTTCGAGGCTGCGC[C/T]TCCAGTGAGCTATGA	25909
rs772530229	snp	A/G/T			intron-variant	AHCTF1	GRCh38.p7	1:246906567	AGCCTGGGCAACAGA[A/G/T]TGAGACCCCACCCCC	25909
rs772541170	snp	A/T	1.67668e-05	0.00289537	intron-variant	AHCTF1	GRCh38.p7	1:246887167	TGTATTTTCTAAAAT[A/T]CTAGTAATTCATGAA	25909
rs772542522	snp	A/C/T	8.24034e-05	0.00641839	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849665	AATAAAGGCTCATTG[A/C/T]TTGGTTCAGAAAGGT	25909
rs772544290	in-del	-/TCTAAGA	1.65938e-05	0.00288039	intron-variant	AHCTF1	GRCh38.p7	1:246899401	ATAAATCAACTATAT[-/TCTAAGA]TCTAAGATCTGACTT	25909
rs772578229	snp	A/C	1.98687e-05	0.00315182	intron-variant	AHCTF1	GRCh38.p7	1:246918424	TGACACATTTGTAGA[A/C]AATATACTTGATTAT	25909
rs772590229	in-del	-/CTG	4.96093e-05	0.00498018	cds-indel, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850725	TAGGAGTAGCAACAT[-/CTG]CTGATGCTTCCTGTT	25909
rs772604185	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246870725	GGGTATAAAACCTCA[-/A]AAAAAAAAAAAAAAA	25909
rs772623853	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246858454	GCTCATGACGCATAC[G/T]CAGTAAGTAGCTGAG	25909
rs772635772	snp	G/T	3.33489e-05	0.0040833	intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842669	CAATCAATCAATCAA[G/T]CAAGAACAGAACAGA	25909
rs772645512	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246907897	AAGATTAGTGATAAC[-/A]AAAAAGTATGTTAAA	25909
rs772698155	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246870613	AATTTTACATTTAAA[A/G]GAGAAAAGTATAATA	25909
rs772707243	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246890467	ATGCAAGAAGCTGAA[A/G]GCTTTGCAAGTTATA	25909
rs772728498	snp	C/T	1.6543e-05	0.00287597	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246891835	AAGACTATATTAAGA[C/T]TGCTAAGAAGCAAAT	25909
rs772750447	snp	A/G	2.75099e-05	0.00370867	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850469	TCCAACAGCTGAGAT[A/G]ATTTTAATCTTTTTG	25909
rs772799244	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246892619	AGCCACTGTGCCCGA[C/T]CTAATTTGCTTTACT	25909
rs772807345	snp	C/T	3.45077e-05	0.00415363	synonymous-codon, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843885	CTGAGAAGATAAATC[C/T]GAAACTAATTCTTTC	25909
rs772810059	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246843257	TGTCTCCTCTAACCT[C/T]GGTCTATAAAGTATT	25909
rs772810319	snp	A/T	1.64741e-05	0.00286998	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246898217	TCTCACTTGGCTTAA[A/T]CTGGAAGGCTGAACA	25909
rs772853775	snp	A/C	1.65405e-05	0.00287576	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246918283	GAAGCACAGATTCTA[A/C]TGTTATTTCGTCTTC	25909
rs772855007	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246912397	CTGAGGCAGGAGAAT[C/T]GCTTGAACACGGGAG	25909
rs772879630	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246869881	CAAGATATAATTTAG[A/G]AATACATTTCATAAA	25909
rs772892565	snp	A/G	4.31295e-05	0.00464358	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850589	CTCCTAGGCGTAACA[A/G]AATTTTGAGGTATTT	25909
rs772893213	snp	A/G	0.000188251	0.0097	intron-variant	AHCTF1	GRCh38.p7	1:246885458	TTTATTAACAGATAC[A/G]ATAAAGACTTTATAG	25909
rs772905226	snp	C/T	2.40185e-05	0.00346536	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867338	CTATAGGAGATGGTT[C/T]TTCTATTTTAGAACT	25909
rs772940820	snp	A/T	3.19056e-05	0.00399397	intron-variant	AHCTF1	GRCh38.p7	1:246853343	ATTTAAACTGAAAAA[A/T]AAATCCACACACAAG	25909
rs772969822	snp	A/C	6.59968e-05	0.00574404	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246913372	TGCTGAGTGCTTGCA[A/C]TGGCTCCTCCATGAT	25909
rs772990777	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246879026	AAGCAGAACATTTTT[A/G]TATAAAGAAAAATAG	25909
rs773004278	snp	C/T	1.64844e-05	0.00287087	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877048	CATGATTCTGAACGC[C/T]GGCACTGGACTGCAA	25909
rs773026706	snp	A/G	3.32033e-05	0.00407438	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900371	GTGCATGATACCAAC[A/G]ATTTATATCAAAAAG	25909
rs773032679	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246899743	ACTCCAAGCACAGCT[A/G]AGAAACACAGCAAAA	25909
rs773045140	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246865377	AGGAGCGGTAGACCA[A/G]CACAGGTGATAATGG	25909
rs773063085	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246876532	TTACAGTTGATAAAA[G/T]CAAGACTCAGAGTGT	25909
rs773064606	snp	A/C/T	3.41625e-05	0.00413283	intron-variant	AHCTF1	GRCh38.p7	1:246903909	TAAAATAGAAAACAA[A/C/T]AAAATGGTAATATAA	25909
rs773188794	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246926267	CACATATTCCTTTAT[A/G]GCAACACAGGCTAAC	25909
rs773195156	snp	A/C/G	4.9504e-05	0.00497493	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850103	TTTCTAGGTATGGCA[A/C/G]ACATATCAAATTCTG	25909
rs773200330	snp	A/G	1.72142e-05	0.00293374	intron-variant	AHCTF1	GRCh38.p7	1:246888527	TTCCCTCTGCAATCA[A/G]GGAAAAATTAAGACT	25909
rs773234744	snp	A/G	1.6476e-05	0.00287014	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849772	TCTTTCTTCCTGCTC[A/G]TTTGTTTCTTTATGT	25909
rs773250325	snp	C/T	6.59055e-05	0.00574007	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851245	AAAGTTGCTTTGAGC[C/T]ACAAAAAGTTCCCCA	25909
rs773255225	in-del	-/ATATTTC	1.81138e-05	0.00300941	intron-variant	AHCTF1	GRCh38.p7	1:246905673	CTGAAACAAATTAGT[-/ATATTTC]ATATTTTTAAGTTAT	25909
rs773268034	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246871005	ACAAAAAGTGACTGC[A/G]CTCCCACTGTAGCCT	25909
rs773274163	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246886861	CCTATCACACTATTT[C/T]ATAAGATCTTCCCAT	25909
rs773286947	snp	G/T	4.96537e-05	0.00498241	intron-variant	AHCTF1	GRCh38.p7	1:246888165	AACACTGGATAAAAC[G/T]TAAAAGGATACAATA	25909
rs773290432	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246886083	TGCCTATAATCCCAG[A/C]ACTTTGGGAGGCTGA	25909
rs773297561	in-del	-/AGAT			intron-variant	AHCTF1	GRCh38.p7	1:246870571	TGATAAAGTGTAAAC[-/AGAT]AGAGGGTCTCCAGGG	25909
rs773302445	snp	A/G	8.26945e-05	0.00642965	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246887335	GGAAAGGAATACATA[A/G]TATCAAGTAGCAAAT	25909
rs773311351	snp	C/T	1.64741e-05	0.00286998	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246907658	TGAAACAGCTGTTCC[C/T]GTTGGACTTACTAAC	25909
rs773327390	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246920452	AATCACAGCTACATG[C/T]AACAATATGAATGAA	25909
rs773349922	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246902001	AATCCTCACAACTAC[C/T]CTTTGCAAAAGGTCT	25909
rs773350682	snp	C/T	1.65034e-05	0.00287253	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850980	TTCTTGTGTCTTTAA[C/T]TACATCTAGTAAATT	25909
rs773351685	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246854115	CCACCCTGGCTAACA[C/T]GGTGAAACCCTGTCT	25909
rs773359458	in-del	-/AA	2.48592e-05	0.00352548	intron-variant	AHCTF1	GRCh38.p7	1:246861305	TGCAGCCTGTAAAGT[-/AA]GATTTTGAAAAGAAA	25909
rs773359616	snp	G/T	1.66032e-05	0.0028812	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246894730	ACAAAGCGCAAATTA[G/T]TGGCAGAATTTGGTT	25909
rs773378669	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246877929	TATTTATTTATTTTT[-/A]TTTTTTTTAATGCCA	25909
rs773380841	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246930377	CTCGTGACAGCTTGG[C/T]AGTATGTTACTGAAG	25909
rs773403571	snp	C/T	1.64776e-05	0.00287028	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850871	GTCTTAAATGCAGAT[C/T]TGACCAATTTAGTGG	25909
rs773431464	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246849514	GGTTTGAGGGGGGAA[A/G]GGGAAAAATTCCCTA	25909
rs773449168	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246852671	TAAAAAAACCTTTCA[A/T]TTGAACCAGATCAGC	25909
rs773454962	snp	A/C/G	6.60593e-05	0.00574682	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246857739	TCAGTTCCTTGAACC[A/C/G]GGCTTAAGTGATTCA	25909
rs773457659	snp	C/T	3.32912e-05	0.00407976	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900231	ATAAGAGCAATTATG[C/T]AGATATTCTCCTGAC	25909
rs773471087	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246872224	CAAGGATCTAACAGG[C/T]GTCTCCAATTTGTAC	25909
rs773472072	snp	A/T	1.72689e-05	0.00293839	intron-variant	AHCTF1	GRCh38.p7	1:246916412	TAGAAGAAAAAAAAA[A/T]TGCCTATTTTAATAT	25909
rs773480305	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246859988	ATAATTTGGCAGGGC[A/G]CGGTGGCTCACGCCT	25909
rs773488271	snp	C/G	3.30229e-05	0.0040633	missense, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840904	CTGTAGTTTTTCTTG[C/G]TTTGCTCTTGACTCC	25909
rs773506033	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246860769	CCTCAGCCTCCCAAA[C/G]TGCTGAGATTAACTA	25909
rs773513235	snp	C/T	5.06376e-05	0.00503152	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853240	TGCGCTCAGAGACAA[C/T]AGGACCTTCAGAGAT	25909
rs773520062	snp	C/T	3.37137e-05	0.00410557	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877273	CTATTGCAATGTTGC[C/T]GCAAAAAATTCCAGG	25909
rs773523556	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246859025	TGCAGGAGCTGAAAT[A/T]GCCCCACTGTACTCC	25909
rs773553338	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246919504	GGATCACAAGGTTAG[A/G]AGATCAACACCATCC	25909
rs773570172	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246930250	GAGGCTGAAGCTCAA[A/C]CGTTCCCCCCGCCTC	25909
rs773575145	snp	A/C	2.01696e-05	0.0031756	intron-variant	AHCTF1	GRCh38.p7	1:246890942	AATACTTATAGATTA[A/C]GTAAATATTTTACCT	25909
rs773635038	snp	C/G	0.000452796	0.0150397	intron-variant, utr-variant-5-prime, upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246931376	CGAAGCCCGGCGCCC[C/G]CGAGCCTGCCGTACC	25909
rs773664465	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246844614	CTGTGGTGTCAGCTA[C/T]GTGGGAGGCTGAGGC	25909
rs773669188	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246914534	TCTAATTACTGTAAT[A/T]ATGTCTATAAATACT	25909
rs773672359	in-del	-/TG			intron-variant	AHCTF1	GRCh38.p7	1:246910049	AACTACTAGACACTA[-/TG]TGTCTCCTGATGTGA	25909
rs773716132	snp	C/T	4.98898e-05	0.00499424	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840809	CTTCCCAAGAAATTA[C/T]AGCATTTTTCTGCGT	25909
rs773784048	snp	G/T	3.34102e-05	0.00408705	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861181	GATGCTCCTTTTCAG[G/T]GCTGTTCAGGAAAAA	25909
rs773785342	snp	C/T	3.29516e-05	0.00405891	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849853	GCTTTGACTTTCAGT[C/T]TTTTTTGTAAGTTTT	25909
rs773787255	in-del	-/AT			intron-variant	AHCTF1	GRCh38.p7	1:246868355	TGAACTCCTGACCTC[-/AT]GTGATCCACCCGCCT	25909
rs773819879	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246879743	TGAGGCAGGAAAATC[A/G]GCTTGAACCCAGGAG	25909
rs773828178	snp	G/T	1.66579e-05	0.00288595	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900145	TTTAAACTTCTCTCA[G/T]GTACTAATATATCCA	25909
rs773838424	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246847065	GCCAAGGCGGGTGGA[C/T]TATCTGAGGTCAGGC	25909
rs773848576	snp	A/T	1.6476e-05	0.00287014	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851266	AAGTTCCCCATCTAC[A/T]TCAGCAATGTCACAT	25909
rs773863728	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246892951	ACACCTAATCTCTAA[C/T]ACTTTTAAAACACTT	25909
rs773869209	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246867903	TACACCCCCCCCCCC[-/A]CACACACACACACAC	25909
rs773882926	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246881862	ACCAAAAAAAAAAAC[-/A]AAAAAAAAAAGAAGA	25909
rs773886776	snp	C/G	1.96957e-05	0.00313807	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876174	CTCTCCCGCAAACGA[C/G]GATCACGATCATTCT	25909
rs773891099	snp	A/C	1.77241e-05	0.00297686	intron-variant	AHCTF1	GRCh38.p7	1:246849582	TGAAGAGTGACTGAG[A/C]TGAAAAACTGTTTTG	25909
rs773921863	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246865565	TTCGATCCAAACTTG[A/G]AAAACAGTTTGCTCA	25909
rs773936757	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246843354	ACAAGGAATTTGCCT[C/G]AATTATTCTTGTGTA	25909
rs773978044	snp	A/G	0.000143524	0.00847001	intron-variant	AHCTF1	GRCh38.p7	1:246867828	TGTAAAATGAAGAAC[A/G]CTGGAATTAAGTGCA	25909
rs773982016	snp	C/T	3.29734e-05	0.00406025	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861056	AAGGTCTTCCGGTGA[C/T]GGTGCATCCTGATAC	25909
rs774004801	snp	C/G	3.31055e-05	0.00406837	intron-variant	AHCTF1	GRCh38.p7	1:246898360	GATAAATTAGTAAGG[C/G]ATCAATCAATGCTCA	25909
rs774006467	in-del	-/AAGT	3.41099e-05	0.00412962	intron-variant	AHCTF1	GRCh38.p7	1:246913450	TGCTTTTCTTCTGCA[-/AAGT]AAGAAAATATAATTA	25909
rs774015441	snp	C/T	3.29652e-05	0.00405974	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849662	GAAAATAAAGGCTCA[C/T]TGTTTGGTTCAGAAA	25909
rs774016842	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246858695	CTGGGCATGGTGGCA[C/T]GTGCCTGTAATCCCA	25909
rs774032912	snp	C/G	1.6477e-05	0.00287024	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867702	AGGTTCTTTGCTTGC[C/G]CAAACTTCTCCAATT	25909
rs774038545	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246872849	TTTAAAAATACAAAC[G/T]CTTAAAACATGTGAA	25909
rs774063591	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246891733	TTTCTCTTAGTCAAG[-/A]AGTAAAATTTAATAA	25909
rs774095197	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246843521	ACTAGAATTTAAAAA[C/T]CCTTCCACAAACAGG	25909
rs774095825	snp	A/G	1.64806e-05	0.00287054	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902595	GCATCCCAACAATTT[A/G]GTATTACTCGTCTGT	25909
rs774115358	snp	C/T	1.65141e-05	0.00287346	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246905556	CTATCTTGTGTAGAC[C/T]GAACAGCCCACAAGT	25909
rs774116585	snp	A/T	1.67576e-05	0.00289457	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916191	GATATTCCAAGGTCA[A/T]AAAGACAGAGAACAC	25909
rs774128168	snp	A/G	3.2987e-05	0.00406108	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850211	CTTCTAACATGTTTA[A/G]TACGCAGCTGCTTGT	25909
rs774142521	snp	C/G/T	4.9464e-05	0.00497292	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864018	CTTGAGGGCAGTGAA[C/G/T]GGGATACTAGGTACA	25909
rs774147102	snp	A/G/T	5.10385e-05	0.00505144	intron-variant	AHCTF1	GRCh38.p7	1:246902502	CAGCCTTCACATGAC[A/G/T]TATTTCAAGTACTTT	25909
rs774156282	snp	A/G/T	5.72408e-05	0.00534955	intron-variant	AHCTF1	GRCh38.p7	1:246894619	AAGGTTAGTATTTTA[A/G/T]TATTAAATTCTGTCC	25909
rs774160147	snp	A/C	1.65625e-05	0.00287766	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850731	TAGCAACATCTGCTG[A/C]TGCTTCCTGTTGTGC	25909
rs774160350	in-del	-/AAG	0.000236752	0.0108775	intron-variant	AHCTF1	GRCh38.p7	1:246853064	ACTGAAAGACTGATA[-/AAG]AAGTAAAAAATTAAT	25909
rs774195900	snp	C/T	4.94605e-05	0.0049727	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877053	TTCTGAACGCTGGCA[C/T]TGGACTGCAAAAATT	25909
rs774205965	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246856427	AAAAGGTATTTGAAA[C/T]ATTTATAGATTTTAC	25909
rs774208924	in-del	-/T	1.66996e-05	0.00288956	intron-variant	AHCTF1	GRCh38.p7	1:246900035	TGTGCATTACTTTTC[-/T]TTAAGAGGTAATGTT	25909
rs774238789	snp	A/G	1.69928e-05	0.00291481	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246862103	GATGGACTGAGGAGT[A/G]AACTCAGAAAATCCA	25909
rs774260268	snp	A/G	3.31521e-05	0.00407123	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850312	GATCATTCTGCTAGG[A/G]CTTGTTACCGTACTA	25909
rs774282182	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246930456	GCGCTTGGCACACTT[A/C]AAACATCCCTTCAAG	25909
rs774340182	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246913865	TACTCTAGGATTCTA[C/T]GGCCTCTTCTCCTAA	25909
rs774352585	snp	A/G	1.66601e-05	0.00288614	stop-gained, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246842704	CATACTTGCTTGCTT[A/G]TTTTGTTTTTGACGT	25909
rs774405773	snp	C/G			utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839309	TTAAAAAAGTATTAA[C/G]TTGACATACGTTGCA	25909
rs774406381	snp	A/G	4.94597e-05	0.00497266	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851101	ATTTGCAATTTGTCC[A/G]TGATTATCATTTTCC	25909
rs774430728	snp	A/G	0.000220125	0.0104888	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876179	CCGCAAACGAGGATC[A/G]CGATCATTCTATTAA	25909
rs774455195	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246869922	TCACAGATAGTGATT[C/G]CTCTGAGAGATCCGA	25909
rs774461984	snp	G/T	1.66076e-05	0.00288158	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246860970	CCATCCTTTTCAGTT[G/T]GTTCAGTTACATTAG	25909
rs774473508	snp	A/G	1.65542e-05	0.00287695	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849943	AGCTGGTTTTCCAAC[A/G]TCAACATTTTCACTT	25909
rs774477322	snp	C/T	1.65037e-05	0.00287256	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246889990	CGCTCAAACTTCTGT[C/T]GACGACTGGTGTAGT	25909
rs774492793	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246888581	TATCAAAGCAACCAG[C/T]ATCAAAATATTAAAA	25909
rs774526938	snp	C/T	4.94319e-05	0.00497127	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849861	TTTCAGTCTTTTTTG[C/T]AAGTTTTTTCTTAGA	25909
rs774529895	snp	A/C/G	0.000103397	0.00718951	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246885591	GGCTTGTCTGTGCTC[A/C/G]CCCTGACTCATGAAT	25909
rs774554505	snp	C/T	1.65446e-05	0.00287612	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246918289	CAGATTCTAATGTTA[C/T]TTCGTCTTCTCCAAG	25909
rs774588884	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246896085	AAGCATGGTAAGGAC[A/G]TGTTAAAACTGGAAC	25909
rs774588969	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246897519	TGCAATCATGGTAAG[A/C]GCGTACTTACACAAA	25909
rs774592486	snp	A/G			missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861051	TCTTCAAGGTCTTCC[A/G]GTGACGGTGCATCCT	25909
rs774613906	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246927697	GCAGGAACGTTCTAC[C/T]GGCTTTGAATGAAGA	25909
rs774656306	snp	C/T	6.60131e-05	0.00574476	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851007	AATTTTCTGCAATTG[C/T]TACTTTAATAGGTTC	25909
rs774695420	in-del	-/AA			intron-variant	AHCTF1	GRCh38.p7	1:246903838	GCGAGACTCTGTCTC[-/AA]AAAAAAAAAAAAAAA	25909
rs774705813	in-del	-/AT	3.72696e-05	0.00431665	intron-variant	AHCTF1	GRCh38.p7	1:246843768	TATGTTTTAACAAAC[-/AT]ACAAATAAAATCATG	25909
rs774762218	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246928504	GGATACTAGCAGAGA[C/G]AAGAAATAGGCATGT	25909
rs774784059	snp	C/T	3.29478e-05	0.00405867	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246907686	AACTGGAAACACAGA[C/T]GGCGCCCTTGTCTCA	25909
rs774807322	snp	C/T	1.96311e-05	0.00313292	intron-variant	AHCTF1	GRCh38.p7	1:246918420	ATTATGACACATTTG[C/T]AGACAATATACTTGA	25909
rs774815569	in-del	-/AAATGCTATC			intron-variant	AHCTF1	GRCh38.p7	1:246875520	GAAGTTCTATGGCTA[-/AAATGCTATC]AAATGGTATCACATG	25909
rs774822433	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246903512	CTACTACATTATGAA[C/T]ACAATATTAACTTCA	25909
rs774852031	snp	G/T	8.26125e-05	0.00642646	missense, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840929	GACTCCGTCAGCTGG[G/T]CTAGCCAAGGGGGAA	25909
rs774852868	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246879709	GGTGCATGCCTGTAA[C/T]CCCAGCTACTTGCGA	25909
rs774867561	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246879959	AGCACCAAACTAAAG[C/T]GAAAAAAGTATACTG	25909
rs774889577	snp	C/T	1.69301e-05	0.00290942	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916212	CAGAGAACACTCCCT[C/T]CTGTTTCTTCCAATC	25909
rs774900170	snp	C/T			missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861036	GCCGTGAAAACAGTC[C/T]CTTCAAGGTCTTCCG	25909
rs774923048	snp	A/G	1.79194e-05	0.00299322	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850627	CTGAGATAGTCCTCT[A/G]ACATCAGAATAGATG	25909
rs774952115	in-del	-/TAAG			downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838911	CCTTACTACTGATAC[-/TAAG]TATCTTTCTGAGTAT	25909
rs774980326	snp	A/C	1.69129e-05	0.00290795	intron-variant	AHCTF1	GRCh38.p7	1:246855705	AAAAATGGAATAATC[A/C]TGAAGTCAAAATTAT	25909
rs774987774	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246928503	AGGATACTAGCAGAG[A/G]CAAGAAATAGGCATG	25909
rs775030950	snp	C/T	1.69123e-05	0.0029079	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853255	TAGGACCTTCAGAGA[C/T]AGTGAGCGAGGAGTT	25909
rs775038567	snp	A/C	1.70307e-05	0.00291806	intron-variant	AHCTF1	GRCh38.p7	1:246913448	TTTGCTTTTCTTCTG[A/C]AAAGTAAGAAAATAT	25909
rs775045527	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246869365	ATGTGAAAGGAGGAG[C/T]CACATGTCTAGGACT	25909
rs775050161	snp	C/T	1.66051e-05	0.00288137	intron-variant	AHCTF1	GRCh38.p7	1:246853040	GTGTCTTGAAACAAC[C/T]AAACCAAAACTGAAA	25909
rs775053557	snp	C/T	1.65941e-05	0.00288041	intron-variant	AHCTF1	GRCh38.p7	1:246900331	GAGAAAAAAAAAGAA[C/T]CATACCTTAACGAAT	25909
rs775061402	snp	G/T	3.69604e-05	0.0042987	intron-variant	AHCTF1	GRCh38.p7	1:246888563	AATATCACTGTTAAT[G/T]AATATCAAAGCAACC	25909
rs775073197	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246878070	TACAGTCTACAGAAA[C/T]ACCAGCAAAAATTGC	25909
rs775103193	snp	C/G/T	5.06311e-05	0.00503124	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851361	GAAGCTTAAGTGTTC[C/G/T]AGAGGGATATAACTC	25909
rs775105289	snp	A/C	1.86211e-05	0.00305126	intron-variant	AHCTF1	GRCh38.p7	1:246861913	TGTCAGAGCTAATAC[A/C]TTCTTATTAAAAAAT	25909
rs775132534	snp	C/T	1.6498e-05	0.00287206	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850226	ATACGCAGCTGCTTG[C/T]CACTGGATTTATCAT	25909
rs775142483	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246915255	GAATCGGTTGAACCC[A/G]GGACACAGAGGTTGC	25909
rs775185749	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246901826	GAGTGAGACCCCTGT[C/G]TCTAAATAAATAAAC	25909
rs775187221	snp	A/G			downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838614	AGAAGTGGGCGGGGC[A/G]GGGCGGGGGGAAGAC	25909
rs775198410	in-del	-/TCTA			intron-variant	AHCTF1	GRCh38.p7	1:246865333	TACCTTCCTTGTCAT[-/TCTA]TCTATCAAATGAGAG	25909
rs775217695	in-del	-/A	3.33244e-05	0.0040818	intron-variant	AHCTF1	GRCh38.p7	1:246887363	AATAAATGGTCTTTT[-/A]AAAAGCGGATTAAGG	25909
rs775223909	snp	A/G	1.66056e-05	0.00288141	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246887353	TCAAGTAGCAAATAA[A/G]TGGTCTTTTAAAAAG	25909
rs775251324	snp	A/G	1.6631e-05	0.00288362	intron-variant	AHCTF1	GRCh38.p7	1:246842818	AAGTATTAAACACGA[A/G]TCCAATTTTAAAACT	25909
rs775267549	snp	A/G	3.61317e-05	0.00425024	intron-variant	AHCTF1	GRCh38.p7	1:246899546	AAATAATCCACTTAC[A/G]TATATTTAAAATGGC	25909
rs775269480	in-del	-/T	0.000181547	0.00952577	intron-variant	AHCTF1	GRCh38.p7	1:246863875	TTGCTACTTGAAAAG[-/T]TAAGAGCCATCTAGT	25909
rs775276697	snp	C/T	3.30398e-05	0.00406434	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246857767	TCAATTCTGAAAATG[C/T]CTCTGCTGCAACTAA	25909
rs775285144	snp	A/G	1.64743e-05	0.00287	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849725	GTCCTGCTGCTGCGG[A/G]ATGATTTAGTGAAGG	25909
rs775292442	snp	A/G	1.73694e-05	0.00294693	intron-variant	AHCTF1	GRCh38.p7	1:246860864	TATTGAGGGACATTA[A/G]TAACAATTTTGAGTA	25909
rs775338645	in-del	-/AGTGAGCCGAGATTGC			intron-variant	AHCTF1	GRCh38.p7	1:246854240	GGAGGCGGAGCTTGC[-/AGTGAGCCGAGATTGC]ACCACTGCACTCTAG	25909
rs775353910	snp	C/T	3.29587e-05	0.00405934	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902604	CAATTTGGTATTACT[C/T]GTCTGTCCCCTCAAA	25909
rs775365662	snp	A/G	1.66776e-05	0.00288765	intron-variant	AHCTF1	GRCh38.p7	1:246902690	CCTGTAACATAAAAT[A/G]CACGCAAATATTAAT	25909
rs775368022	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246903037	CTCTAGAATAGTTCT[C/T]AGACTTTTAGCTTAT	25909
rs775377191	in-del	-/CAA			intron-variant	AHCTF1	GRCh38.p7	1:246920212	ACACACAAGGATATC[-/CAA]CAATAGCCAGCAGAA	25909
rs775402926	snp	A/C	1.84367e-05	0.00303612	synonymous-codon, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843849	TTGTCTGCTCCTTAA[A/C]GCAGGAGGTGAGATG	25909
rs775418333	in-del	-/C			intron-variant	AHCTF1	GRCh38.p7	1:246857498	TGTCTCTGTATATTT[-/C]CCGAAACTTTATAGT	25909
rs775419828	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246888707	TCAAGGTCAGGAGTT[C/T]GAGACCAGCCTGGGC	25909
rs775422745	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246921797	AACAAATACGAAATA[A/T]GTTTTTAGACAAAAA	25909
rs775427021	snp	C/T			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932883	GGGATTTTAAGAAGA[C/T]GCTCTTTTATCAGGA	25909
rs775438259	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246887675	TTCTAAAGATCTAGC[A/C]AAAGATGGCAGCTTA	25909
rs775474744	snp	C/G	1.79355e-05	0.00299456	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840981	GGAGGTGACCAAGCA[C/G]TTTCTTTTTCTGTGT	25909
rs775487838	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246847367	GCAGAATATATGCAC[A/G]TACATAAACTGCAGG	25909
rs775500195	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246909885	AGTAGCACCAGCAGT[A/G]ACAATCAAAAATGTC	25909
rs775516508	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246910927	GCTGCAGAACAATAT[A/T]TATGCTGTATGTTTG	25909
rs775527259	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246896795	ACCTATTAATTTCAT[C/T]CATTACAGGAGCAAA	25909
rs775565615	snp	C/G	1.65581e-05	0.00287728	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246918310	CTTCTCCAAGGGCTT[C/G]AAGAGTCACTTCTGG	25909
rs775570175	snp	G/T	1.648e-05	0.0028705	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246863997	GGCGATCCTTTTAAT[G/T]GCGAACTTGAGGGCA	25909
rs775600730	in-del	-/A	1.80468e-05	0.00300384	intron-variant	AHCTF1	GRCh38.p7	1:246843941	AGCTAAAAAAAGTTG[-/A]AAAAAACTGTATCTG	25909
rs775608939	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246897656	ATATGAAGTATACGT[A/G]TATTTAAACACAGAA	25909
rs775610326	snp	A/G	3.3066e-05	0.00406595	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864073	GAATAAACTCCGAAC[A/G]CTGAGAAGGCCGGGG	25909
rs775638442	snp	C/G	3.37211e-05	0.00410602	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246913318	ACATCAGTGACCACA[C/G]CTGCCACTCCAAAAA	25909
rs775643208	snp	A/G	1.65614e-05	0.00287757	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840944	GCTAGCCAAGGGGGA[A/G]ATCAGCCGAATTTCT	25909
rs775656563	snp	C/T	1.88724e-05	0.00307178	intron-variant	AHCTF1	GRCh38.p7	1:246867844	CTGGAATTAAGTGCA[C/T]CTCTAACAAACGGGA	25909
rs775674631	in-del	-/CAAAA			intron-variant	AHCTF1	GRCh38.p7	1:246930935	AATTTCCCCATCTCT[-/CAAAA]CAAAACACCCAAACC	25909
rs775677246	in-del	-/A	0.000503031	0.0158513	intron-variant	AHCTF1	GRCh38.p7	1:246916403	ATTTTTCCCTAGAAG[-/A]AAAAAAAATTGCCTA	25909
rs775719910	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246883089	ACTAACATAAATTAA[C/T]AGTTCAAAACAGGGC	25909
rs775726936	snp	C/T	1.66139e-05	0.00288213	intron-variant	AHCTF1	GRCh38.p7	1:246876945	TAAGACAACTTTAAT[C/T]GTACCATAACATTAA	25909
rs775729601	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246881522	GTAAATCAAGTCTTA[C/G]CAAAAAAATTTTTTT	25909
rs775747148	in-del	-/AGTG			intron-variant	AHCTF1	GRCh38.p7	1:246899958	CATATGTTAACTAAC[-/AGTG]AGATACAAACAGATA	25909
rs775760860	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246917353	AACTTCTAAATTTGA[A/G]ATGTCCATCAAGCAT	25909
rs775796909	snp	C/T	1.84391e-05	0.00303632	intron-variant	AHCTF1	GRCh38.p7	1:246905674	TGAAACAAATTAGTA[C/T]ATTTCATATTTTTAA	25909
rs775852735	snp	C/T	1.67638e-05	0.0028951	intron-variant	AHCTF1	GRCh38.p7	1:246887169	TATTTTCTAAAATTC[C/T]AGTAATTCATGAAAG	25909
rs775867832	snp	C/T	1.64789e-05	0.0028704	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851218	TCCTTCTTCACCTTC[C/T]AATATCAAGGTAAAG	25909
rs775899975	in-del	-/CTGATTTGACAT	3.32182e-05	0.00407529	cds-indel, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850746	ATGCTTCCTGTTGTG[-/CTGATTTGACAT]TCACGTTTTGGATAC	25909
rs775960328	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246915138	AGATCGAGAGCAGCC[G/T]GGCCAACAGGGTGAA	25909
rs775971498	snp	C/T	0.000200632	0.0100138	intron-variant	AHCTF1	GRCh38.p7	1:246902699	TAAAATACACGCAAA[C/T]ATTAATCTGATTCTA	25909
rs776006290	in-del	-/TAGA			utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839697	AAAGCAGTTCGTTTC[-/TAGA]TAGATAATCAATTAT	25909
rs776053931	snp	C/T	1.65348e-05	0.00287526	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850821	CGTCATCAACCTGGC[C/T]GACATTCATAGTCAT	25909
rs776059691	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246849112	ACAGTCCTTAGCTCG[-/T]GACAATGAAGGATGG	25909
rs776085266	snp	C/T	1.66021e-05	0.0028811	intron-variant	AHCTF1	GRCh38.p7	1:246855831	GTGAAGATTTTCCTT[C/T]AGAAAAAGAAATACA	25909
rs776100035	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246888841	TTGGAGCCCAGGAGT[A/T]TAAAGTGAGCTATAC	25909
rs776106976	snp	C/T	5.00271e-05	0.0050011	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850761	CTGATTTGACATTCA[C/T]GTTTTGGATACGTTG	25909
rs776111577	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246917056	TCATAGAGGTGACTA[C/T]CTGATTTAAATCAAG	25909
rs776158227	snp	C/T			missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246887357	GTAGCAAATAAATGG[C/T]CTTTTAAAAAGCGGA	25909
rs776164245	snp	A/T	1.71319e-05	0.00292672	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850640	CTGACATCAGAATAG[A/T]TGTTTTCAGAAGCTT	25909
rs776166461	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246915429	TTCTGGCCCCCTATT[C/G]TTCCTTCCCCTCATC	25909
rs776167403	snp	C/T	4.09996e-05	0.00452748	intron-variant	AHCTF1	GRCh38.p7	1:246853058	ACCAAAACTGAAAGA[C/T]TGATAAAGAAGTAAA	25909
rs776172749	snp	C/T	2.02603e-05	0.00318273	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850434	TAACTTCTTTTTTAG[C/T]AGTTTCTTCAACTGC	25909
rs776174769	snp	C/T	3.5478e-05	0.00421162	intron-variant	AHCTF1	GRCh38.p7	1:246843769	ATGTTTTAACAAACA[C/T]ACAAATAAAATCATG	25909
rs776183520	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246870616	TTTACATTTAAAAGA[G/T]AAAAGTATAATATGT	25909
rs776219616	snp	A/G	4.49226e-05	0.00473912	intron-variant	AHCTF1	GRCh38.p7	1:246867226	TGTGTCTCTAAGAAT[A/G]ATTTAATAAACTCTT	25909
rs776234961	snp	A/G	1.66624e-05	0.00288633	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850336	CGTACTAACTTTTAG[A/G]TCATTTATAATTTCA	25909
rs776260810	snp	C/T	1.68476e-05	0.00290233	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916392	CAAGCAAGTCCATTT[C/T]TCCCTAGAAGAAAAA	25909
rs776276508	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246925099	TTGATAAAACTAGTT[A/T]AATGATGAACTGAAG	25909
rs776331429	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246856238	CCTAGAAAAAGTATG[A/G]TAAATGACTCAGAAT	25909
rs776358251	snp	A/T	2.2186e-05	0.00333054	intron-variant	AHCTF1	GRCh38.p7	1:246876198	TCATTCTATTAAACA[A/T]CAAAATTGGTAAAAA	25909
rs776358501	snp	A/G	1.65113e-05	0.00287322	intron-variant	AHCTF1	GRCh38.p7	1:246888360	CTCCCCAGCTTTGTA[A/G]ACTCTAAATGATAGC	25909
rs776362997	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246880964	AATGCATGGGGGTTC[C/T]TGGCAATACAGCAAA	25909
rs776391663	snp	C/T	1.67119e-05	0.00289062	intron-variant	AHCTF1	GRCh38.p7	1:246890107	AATAATCCCCAAATA[C/T]CTCAACAATACATAT	25909
rs776393882	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246911051	AACCCTAAAGCTTAA[G/T]TTTTTGTGCTATAAA	25909
rs776411680	snp	A/C	1.64988e-05	0.00287213	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246888198	GTGTTTGGCTGCTTC[A/C]GTAACGCCGTCTAAT	25909
rs776461417	snp	C/T	2.20821e-05	0.00332274	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867326	GGAGCGAATACACTA[C/T]AGGAGATGGTTCTTC	25909
rs776487079	in-del	-/TTA			intron-variant	AHCTF1	GRCh38.p7	1:246848231	AGTCATCTACTTTAT[-/TTA]TTATTATTATTATTT	25909
rs776489117	snp	A/G	1.64982e-05	0.00287208	intron-variant	AHCTF1	GRCh38.p7	1:246895947	CATGCATTACAGAAA[A/G]GAAAGAAATGGAAAG	25909
rs776489369	snp	C/G	1.64784e-05	0.00287035	intron-variant	AHCTF1	GRCh38.p7	1:246898189	CCAAAAGAAACAATA[C/G]AGTTAAAAATCATCT	25909
rs776496158	snp	A/G	1.70249e-05	0.00291756	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916230	GTTTCTTCCAATCCT[A/G]TTAATAATCCAGTTC	25909
rs776530870	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246923758	GTGTGTGTGTGTGCG[C/T]GTAGCACACAGGAGC	25909
rs776540223	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246903188	AGAAAAGTCGGTTCT[A/G]GAGACAGGTATGTGA	25909
rs776540344	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246870084	GAATAACTTTTGAGG[C/G]CTTCAAGACTTCAGT	25909
rs776555445	snp	C/T	1.64841e-05	0.00287085	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851106	CAATTTGTCCATGAT[C/T]ATCATTTTCCCCACT	25909
rs776555868	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246875126	CGACTTCCTTACCAT[A/G]ACATGCGACCTATAT	25909
rs776556539	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246901698	TGGTGTGTGCCGGCA[G/T]TCCCAGTTACTTGGG	25909
rs776579708	snp	C/G	1.91676e-05	0.00309571	intron-variant	AHCTF1	GRCh38.p7	1:246894611	CATAAACCAAGGTTA[C/G]TATTTTAATATTAAA	25909
rs776593992	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246848561	TTCAAATATTAAACT[C/G]TAACTTAAATAGTCA	25909
rs776624928	in-del	-/A	1.65046e-05	0.00287264	intron-variant	AHCTF1	GRCh38.p7	1:246895962	GAAAGAAATGGAAAG[-/A]AAAGAGGGTGTGAGA	25909
rs776636117	snp	C/G			intron-variant, missense, utr-variant-5-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246931201	CCGGCCGCTTCCCTC[C/G]GGGAAAGGCCCGCCA	25909
rs776638582	snp	C/T	0.000116726	0.00763868	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850772	TTCACGTTTTGGATA[C/T]GTTGACCTCTCGTAC	25909
rs776665163	snp	A/G	1.66632e-05	0.0028864	synonymous-codon, splice-donor-variant, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246842696	CAGAAAGTCATACTT[A/G]CTTGCTTGTTTTGTT	25909
rs776684527	snp	A/T	1.6588e-05	0.00287988	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246860979	TCAGTTTGTTCAGTT[A/T]CATTAGTAGTTAGTG	25909
rs776737615	snp	A/G	1.67615e-05	0.0028949	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246860913	CCCATTTGTTTCTGT[A/G]GGTCTGAAGGAGTTA	25909
rs776751714	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246876338	AAGAACTTCATCCAC[A/C]TATCTAATTTTTTTA	25909
rs776751741	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246863292	AGAGAACCCAGGGAC[A/G]ATGGGGAGGGGTGAG	25909
rs776758772	snp	G/T	3.30409e-05	0.0040644	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246857721	GGTGCACAAAGAGAA[G/T]CTTCAGTTCCTTGAA	25909
rs776791923	snp	A/T	1.85441e-05	0.00304495	intron-variant	AHCTF1	GRCh38.p7	1:246861920	GCTAATACATTCTTA[A/T]TAAAAAATGTCTTTT	25909
rs776797004	snp	C/G	0.001386	0.0262884	intron-variant, missense, utr-variant-5-prime, upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246931315	CGAACCACCAGCGCC[C/G]CTCCGCCGCCATGTG	25909
rs776800372	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246858853	CTGCCTAATATTGTA[A/G]GAATAATCAGTGAAG	25909
rs776806795	snp	A/T	1.67066e-05	0.00289016	intron-variant	AHCTF1	GRCh38.p7	1:246887183	CTAGTAATTCATGAA[A/T]GTTTATGCTGTAAGT	25909
rs776807947	snp	C/T	1.67346e-05	0.00289258	intron-variant	AHCTF1	GRCh38.p7	1:246855845	TTAGAAAAAGAAATA[C/T]ATACCTTAGTGTGTA	25909
rs776810110	snp	C/T	6.61081e-05	0.00574888	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864066	CTTTGCTGAATAAAC[C/T]CCGAACACTGAGAAG	25909
rs776818511	snp	C/T	3.30022e-05	0.00406202	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246890008	CGACTGGTGTAGTAG[C/T]TCTGAATTACAGGGT	25909
rs776874783	in-del	-/AATT			intron-variant	AHCTF1	GRCh38.p7	1:246928004	ACTCCGCCACCAAAA[-/AATT]AATTAATTAATTAAA	25909
rs776894710	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246870848	ATTCTTGAAAATGGC[C/T]GGATTCTGTCACATA	25909
rs776905203	snp	C/T	1.64751e-05	0.00287007	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849848	TTTTGGCTTTGACTT[C/T]CAGTCTTTTTTGTAA	25909
rs776926702	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246929776	ATATCTGTACCAGCC[A/G]GGCGCGGTGGCTCAC	25909
rs776928750	snp	G/T	2.01266e-05	0.00317221	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840995	ACTTTCTTTTTCTGT[G/T]TTTCTGAAAAAAAAA	25909
rs776937884	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246903839	CGAGACTCTGTCTCA[-/A]AAAAAAAAAAAAAAA	25909
rs776939278	snp	C/T	1.66568e-05	0.00288585	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900130	GGAGGGACTCCTCTA[C/T]TTAAACTTCTCTCAT	25909
rs776963320	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246870147	CAAGAGAACTAGAAT[A/G]AGAAGCAGAGCCTAG	25909
rs776981157	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246894417	TCTACTAAAAAATAC[-/A]AAAAAAATTAGCCGA	25909
rs776985432	in-del	-/AAGAT	4.70572e-05	0.0048504	intron-variant	AHCTF1	GRCh38.p7	1:246851455	CACCTAAATGAATTA[-/AAGAT]AAGAGACTGGTTAAA	25909
rs777009869	snp	C/T	1.64912e-05	0.00287147	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850195	TTCTCTCCCTCTGAC[C/T]CTTCTAACATGTTTA	25909
rs777040366	in-del	-/TA	2.06499e-05	0.00321318	intron-variant	AHCTF1	GRCh38.p7	1:246843974	CTTTATATATGTGTG[-/TA]TATATATATAAACAC	25909
rs777048628	snp	C/T	3.30956e-05	0.00406776	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246891855	AAGAAGCAAATAGCA[C/T]TGCTGGATAGACTGT	25909
rs777073621	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246864649	GACCATCCTGGCTAA[C/T]AAGGTGAAACCCCGT	25909
rs777126355	snp	A/G	6.7906e-05	0.00582652	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840782	ACTTTACAAATAGGT[A/G]TACATTAAAATCTTC	25909
rs777132046	snp	C/T	1.8571e-05	0.00304715	intron-variant	AHCTF1	GRCh38.p7	1:246918403	TTTTAAAAGAAAACA[C/T]TATTATGACACATTT	25909
rs777147489	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246926559	ACATCGAAACACTCT[A/C]TTATTAGAAATAGGG	25909
rs777153406	snp	C/G	1.64749e-05	0.00287005	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849751	GAAGGAAGCTGTGGC[C/G]AGCAATCTTTCTTCC	25909
rs777178026	snp	C/T	2.01311e-05	0.00317256	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861256	GAACTGCACATTTTT[C/T]AGGTGTAGTAAATAC	25909
rs777183632	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246920101	GCCGAGATTGTGCAA[C/T]TGCACTCCAGCCTGA	25909
rs777188388	snp	G/T	2.08627e-05	0.00322969	intron-variant	AHCTF1	GRCh38.p7	1:246905684	TAGTATATTTCATAT[G/T]TTTAAGTTATTTTTT	25909
rs777199000	snp	C/T	2.89457e-05	0.00380421	intron-variant	AHCTF1	GRCh38.p7	1:246885700	AAATAACATGAAAAA[C/T]GTTAAATATAAATAT	25909
rs777201478	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246918553	TTAAGTCCCAGCTAC[C/T]TGGGAGGCTGAGGCA	25909
rs777204568	snp	C/T	6.59935e-05	0.0057439	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850836	TGACATTCATAGTCA[C/T]TGTGCTTGTTTCCTG	25909
rs777211448	snp	A/G	1.64982e-05	0.00287208	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850713	GCCCTGGCATCTTAG[A/G]AGTAGCAACATCTGC	25909
rs777223927	snp	C/T	6.67534e-05	0.00577687	intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842643	AGGGTGGGGACAGAG[C/T]GAGACTGTCTCAATC	25909
rs777255162	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246845581	TCACTTTTCGTAATC[G/T]TCACCTAAGCTTTCC	25909
rs777322500	snp	C/T	1.65045e-05	0.00287263	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246887317	GGAGTGTCTGTTTTG[C/T]TGGGAAAGGAATACA	25909
rs777334366	snp	C/T	1.66944e-05	0.0028891	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900422	TTCCCTGTCCATATA[C/T]ATTCACCTGCCAGGT	25909
rs777357927	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246870560	CAGTGTTGAAATGAT[A/G]AAGTGTAAACAGATA	25909
rs777373204	snp	A/C	1.65075e-05	0.00287289	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246889980	CCTTGATAAACGCTC[A/C]AACTTCTGTCGACGA	25909
rs777379821	snp	C/G	0.000142542	0.008441	intron-variant, missense, utr-variant-5-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246931219	GAAAGGCCCGCCAAC[C/G]AGTCCATCGCGTGGG	25909
rs777380264	snp	A/G	1.65614e-05	0.00287757	intron-variant	AHCTF1	GRCh38.p7	1:246905535	CAAAGTTTGTATGAG[A/G]CCTACCTATCTTGTG	25909
rs777383893	in-del	-/AA			intron-variant	AHCTF1	GRCh38.p7	1:246913948	CAAAAAAGATATTTT[-/AA]AAGTCCTCTTTATAC	25909
rs777389148	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246848934	ATGGGATCTATTCAG[A/C]CACACCAGTGTCTTA	25909
rs777391033	snp	A/G	1.68258e-05	0.00290045	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246885567	CTTCATTGTCTGAAT[A/G]TATCTGAGGGCTTGT	25909
rs777393086	in-del	-/CTT	6.61583e-05	0.00575107	cds-indel, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850002	TTCTAATGCTGGGAG[-/CTT]CTTTCTTCTTGGGGC	25909
rs777394908	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246845426	ATCTCTGCTCCCAGC[C/T]TGTAAATGGCAGAAA	25909
rs777395525	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246930161	TTTATTTTAGCAACA[A/G]GTTCTCGCTCTGTCA	25909
rs777416743	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246877659	CACTCAGTGGGAAGC[A/G]TGCGAAAGACTGAGA	25909
rs777439526	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246847341	CTCATGACATAAGTA[A/G]GGGGACAAAAGCAGA	25909
rs777440135	snp	C/T	6.69658e-05	0.00578605	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840795	GTGTACATTAAAATC[C/T]TCCCAAGAAATTACA	25909
rs777447877	in-del	-/C	3.33428e-05	0.00408293	intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842671	TCAATCAATCAATCA[-/C]AGAACAGAACAGAAA	25909
rs777469605	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246880489	GAATCACTTGAACCC[A/G]GGAGGTGGAGGTTAC	25909
rs777497040	snp	C/T	3.27327e-05	0.0040454	intron-variant	AHCTF1	GRCh38.p7	1:246861327	TGAAAAGAAAAAAAT[C/T]AGTAAATATCACAGT	25909
rs777582799	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246927977	TGCACTCCAGCCTGG[C/T]GACAGAGCAAGACTC	25909
rs777658602	in-del	-/TTATAGAT	2.4674e-05	0.00351232	intron-variant	AHCTF1	GRCh38.p7	1:246890932	TGTTTTAATTAATAC[-/TTATAGAT]TAAGTAAATATTTTA	25909
rs777668786	in-del	-/TTCT			intron-variant	AHCTF1	GRCh38.p7	1:246884147	GTTACCACATTTAGC[-/TTCT]TTATTTTGTTCTTAC	25909
rs777697550	snp	A/G			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932389	TGCCAGCTGGGGGCC[A/G]AGTGATAATCTTTCT	25909
rs777705950	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246902739	TCACTCTAAAATTAA[A/G]TATTCTCCAAATTTA	25909
rs777718699	snp	A/C	1.64741e-05	0.00286998	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849712	CTTGCTAGACCGAGT[A/C]CTGCTGCTGCGGGAT	25909
rs777775870	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246846131	GTATATAGCAGGCCC[G/T]TCTTAATATCTGCTG	25909
rs777790686	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246913648	TGATGTTGACTGAGA[A/G]CTTACTGATACGCCA	25909
rs777864976	snp	G/T	1.70542e-05	0.00292007	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850395	TAATTCTTCTAGGAG[G/T]CCTTTTTGTAACAGA	25909
rs777880388	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246883234	ATGTAATCAAATCAT[C/T]TGGGTGTTGGACTAT	25909
rs777888853	snp	A/C	1.71655e-05	0.00292958	intron-variant	AHCTF1	GRCh38.p7	1:246864149	ATTTATTGAGTTATA[A/C]TGAAAAAACAAAAGA	25909
rs777907891	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246877695	AGATGGAAACAAGCA[C/T]GCTGTGTCCATGAGG	25909
rs777928006	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246868420	GCCACTGCGCCTGGC[A/G]ATTTTTGTATTTTTA	25909
rs777935709	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246854026	AAAATCTGGCTGGGC[A/G]CAGTGGCTCACGCCT	25909
rs777997631	snp	A/G	3.38055e-05	0.00411116	intron-variant	AHCTF1	GRCh38.p7	1:246918229	ATTGTATTAGTAAAT[A/G]TTCAGTGACATTATG	25909
rs777998767	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246924068	TCCCCCTCCTATCTA[C/T]TGAGTACAGAAAGGA	25909
rs778023020	snp	C/G	1.65124e-05	0.00287331	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902657	CCAGGGTGTATCTTT[C/G]TTCACAGTATTCTAA	25909
rs778026421	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246915000	TCCTCGCTGACCCAA[C/T]CCAAGCAAGCCTTTT	25909
rs778039087	snp	A/T	1.73228e-05	0.00294297	missense, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843919	TGTGCAGGAACCTCT[A/T]TTTTTTTAGCTAAAA	25909
rs778050607	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246855565	GTCTGACAGCTTATA[C/T]ATCTCCTTAGAATAC	25909
rs778053682	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246874628	AACATTAACTTATCC[C/T]TACGTCTTGAACCTC	25909
rs778054784	in-del	-/TATC	1.6477e-05	0.00287024	intron-variant	AHCTF1	GRCh38.p7	1:246877317	CCTGAAAGCAGTATT[-/TATC]AAAGTTTAGTTTTAG	25909
rs778054918	snp	C/T	6.59141e-05	0.00574045	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246895892	GGGAACTAGTCTGAA[C/T]TGCTGCTGACAATAT	25909
rs778092310	snp	G/T	1.91889e-05	0.00309743	missense, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843835	TTGGATGTGTTTTTT[G/T]GTCTGCTCCTTAAAG	25909
rs778112639	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246841510	TCACGTGTGCTTTTA[C/T]TGAATTCAACCATGC	25909
rs778121719	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246847864	TATATTCCTCCAGGT[C/T]CTGAGGAGTGTATAA	25909
rs778132210	snp	C/T	3.2987e-05	0.00406108	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877000	AGGCAGGCACATAAT[C/T]GGCACGCTGCAAATG	25909
rs778139678	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246873171	TGTTAAGTAAATGTG[C/T]CCTTGCCATACTCTT	25909
rs778154947	snp	A/G	1.65979e-05	0.00288074	intron-variant	AHCTF1	GRCh38.p7	1:246900321	AGAAAGGAGAGAGAA[A/G]AAAAAAGAATCATAC	25909
rs778158536	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246893974	TTTGGAAGGCCCAGG[C/T]AGGAGGATCGCTTGA	25909
rs778160549	snp	C/T	3.29832e-05	0.00406085	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861016	AAGAGCTTTTGGGCT[C/T]AGAGGCCGTGAAAAC	25909
rs778162111	snp	A/C/G	3.30919e-05	0.00406756	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850009	GCTGGGAGCTTCTTT[A/C/G]TTCTTGGGGCTTCTC	25909
rs778182882	snp	C/T	1.65081e-05	0.00287293	intron-variant	AHCTF1	GRCh38.p7	1:246888269	ACCTTCAGTGGATCT[C/T]ATACAGTCATTCATT	25909
rs778202411	snp	C/T			downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838972	ATCTCTCTGAGTACA[C/T]TGTTTACCTTACTAC	25909
rs778202544	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246855662	GATTATTTTGTTCTA[A/C]GAACAGAAAACTCTT	25909
rs778203570	snp	A/G	1.69608e-05	0.00291206	intron-variant	AHCTF1	GRCh38.p7	1:246907782	ACAAATTAGACAAAT[A/G]AAGTTAAAAAACTAG	25909
rs778207893	snp	C/G	1.64906e-05	0.00287142	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246913280	AGTCATCCAAACATA[C/G]GTCAACAAGAAGGAT	25909
rs778213251	snp	G/T	3.29723e-05	0.00406018	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851155	AGTTGCTGTGTTAGC[G/T]GCTTTAGGTAACACA	25909
rs778215011	snp	C/G	1.65589e-05	0.00287736	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849939	CTAAAGCTGGTTTTC[C/G]AACATCAACATTTTC	25909
rs778216993	snp	A/C	1.92361e-05	0.00310124	intron-variant	AHCTF1	GRCh38.p7	1:246862188	GAATTACACCATTAA[A/C]AGTGCTTATAGGCCG	25909
rs778218281	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246922358	GAGCAAGACTCTGTC[C/T]CAAATAAAAGGGAAA	25909
rs778227594	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246863889	AGTAAGAGCCATCTA[A/G]TTTGATTGTGAACGC	25909
rs778254721	in-del	-/TTTA			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933125	AATTTTTTTATTTTA[-/TTTA]TTTATTTATTTATTT	25909
rs778270387	snp	C/T	1.64901e-05	0.00287137	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851088	CGGCAGATGGCAAAT[C/T]TGCAATTTGTCCATG	25909
rs778282058	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246909879	GTAGCAAGTAGCACC[A/T]GCAGTAACAATCAAA	25909
rs778295376	snp	A/G	1.66671e-05	0.00288674	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246905656	CCAATTGTATGTAAT[A/G]TCTGAAACAAATTAG	25909
rs778299314	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246906319	GCGTGGTAGCTCACA[C/T]CTGTAATCCCAGCAC	25909
rs778313672	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246871724	ATTTTTTTTTGAGGC[C/T]TCCTGACTGCAGACT	25909
rs778325584	snp	G/T	1.96412e-05	0.00313372	intron-variant	AHCTF1	GRCh38.p7	1:246876013	GATCCAATAGATTAT[G/T]ATATTCTTCAATGAA	25909
rs778328927	snp	C/T	4.94996e-05	0.00497467	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246888458	CACAACTTCTCAATT[C/T]GCTCTCCTAACTGAG	25909
rs778413892	snp	A/G	1.64901e-05	0.00287137	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246887271	AACTTGGCCCCAAGA[A/G]ATGGCAAATACAGTT	25909
rs778422886	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246872704	CTTCCCATCGCACTA[C/T]CATGGGTGCTGAAAG	25909
rs778443140	snp	C/G	3.29625e-05	0.00405958	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246907585	TGTTCCAAAGTGCTA[C/G]ATAGCCATCAGAAAA	25909
rs778461035	in-del	-/T	0.000121956	0.00780788	intron-variant	AHCTF1	GRCh38.p7	1:246853319	AGAAAAATGAGTGAA[-/T]TTTTTTACATTTAAA	25909
rs778461601	in-del	-/CTTTAAAAATGGAAAG			intron-variant	AHCTF1	GRCh38.p7	1:246863392	AAAAAAAAAACAAAA[-/CTTTAAAAATGGAAAG]GTTTAAAAAGGCCAC	25909
rs778469454	snp	G/T	3.32121e-05	0.00407492	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246894681	GTCAAATTCCTCTTT[G/T]GTGAGAACCACTTTA	25909
rs778476183	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246897300	GTCTGGGCAACAGAC[C/T]GAGATGCTGTCTCAA	25909
rs778481874	snp	C/T	1.64749e-05	0.00287005	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849807	TTTCATCTGTGCGTT[C/T]TTCTGATACTGAGTG	25909
rs778605979	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246896731	GTATGAAATATCTCA[A/G]TAAAGCTGATATTTT	25909
rs778606984	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246908485	CCTGTTCTGTAGACA[C/T]TGTGTTTCAGAGTGA	25909
rs778622677	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246927352	GTAGCAGCCAGCCAC[A/G]GCTGCATACGCTTGT	25909
rs778634742	snp	C/T	1.78404e-05	0.00298662	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853185	CCAACTTCTACTTCA[C/T]GATCTTCTTTTAAGT	25909
rs778646887	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246880206	AATAGCTTATTATCA[A/C]AAACAATATGTTATT	25909
rs778667802	snp	C/T	3.67667e-05	0.00428743	intron-variant	AHCTF1	GRCh38.p7	1:246885709	GAAAAATGTTAAATA[C/T]AAATATAATCCTATA	25909
rs778684218	in-del	-/C			intron-variant	AHCTF1	GRCh38.p7	1:246870723	GAGGGTATAAAACCT[-/C]AAAAAAAAAAAAAAA	25909
rs778765894	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246928041	AATACTGTTCGGCCG[G/T]GTGCGGTGGCTCACG	25909
rs778792987	snp	C/T	1.65938e-05	0.00288039	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877231	CAGACTTCATACATG[C/T]GCTTCAGTAACTCCT	25909
rs778802070	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246869616	TGGGAAATCTACTAT[A/G]CCTGTCTTCTATCAA	25909
rs778823379	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246882463	GGGAAAATAAACAAC[C/T]GTAATGAAAATTTAA	25909
rs778840802	snp	C/T	9.25318e-05	0.00680127	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876139	CATACTGGTCTAATA[C/T]AGAATTTCGAGCCAG	25909
rs778843387	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246889438	GCAGGATTAGAAAGC[A/G]TAACAAAGCTGCCAA	25909
rs778846926	snp	C/G	4.71665e-05	0.00485603	intron-variant	AHCTF1	GRCh38.p7	1:246861341	TTAGTAAATATCACA[C/G]TTAAGTCTAGTCCTA	25909
rs778882662	snp	C/T	2.87204e-05	0.00378937	intron-variant	AHCTF1	GRCh38.p7	1:246851470	AAGATAAGAGACTGG[C/T]TAAAGAATTTTAATA	25909
rs778902082	snp	A/G	1.65323e-05	0.00287505	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246888487	AGAAACCAGTCCATC[A/G]ATCATCAAGCAATCG	25909
rs778912850	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246875027	TTAAAACCATCTCCT[A/G]ACAGGCCAACAACTT	25909
rs778944314	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246902880	CTCTCAAAAATAATT[A/C]CCAACAAGTCTTCTA	25909
rs778956201	snp	C/T	1.66701e-05	0.002887	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900077	TACCAAAATTATAAG[C/T]GCTTGGATTAAAAAA	25909
rs778959386	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246858815	AAAAAAAAAAAAAAA[-/T]AAATACAAATTTCTA	25909
rs778980579	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246869243	GTACTTACTCCACTG[A/G]CTAACTGTTCCCCCG	25909
rs779012022	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246910913	TTAAGTCTGGGGAAG[A/C]TGCAGAACAATATTT	25909
rs779041561	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246874787	CTCCTTTAACATCTC[C/T]AGACACATATCCCTG	25909
rs779093632	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246841674	ATAGTTACCTAACTT[G/T]CCTGACAAAGAGGTA	25909
rs779094017	in-del	-/C	3.3657e-05	0.00410212	intron-variant	AHCTF1	GRCh38.p7	1:246905496	AGCGAGACTCTGTCT[-/C]CAAAAAAACAAAACA	25909
rs779101629	snp	C/T	8.24219e-05	0.00641905	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246913304	GAAGGATCTGTCCAA[C/T]ATCAGTGACCACAGC	25909
rs779102208	snp	A/G	1.6477e-05	0.00287024	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246898290	TTATAACCATCAGGA[A/G]TGAGTTCATTGAGTG	25909
rs779102324	snp	C/G	3.30295e-05	0.0040637	intron-variant	AHCTF1	GRCh38.p7	1:246888348	CATGTCTCCTCCCTC[C/G]CCAGCTTTGTAGACT	25909
rs779105377	snp	A/G	1.64844e-05	0.00287087	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851163	TGTTAGCTGCTTTAG[A/G]TAACACATCAGATGA	25909
rs779121555	in-del	-/GTGGTCTCTAACTAAAT			intron-variant	AHCTF1	GRCh38.p7	1:246872096	TCCCAAAAACCTAGG[-/GTGGTCTCTAACTAAAT]ATGGTCATAGATCAT	25909
rs779122758	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246929446	AAATACAGTGAAAAC[A/T]TTGGATTTAGAAGGA	25909
rs779139911	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246911873	GCATATTTAAGTTTT[G/T]TTCAGATGATTTTGG	25909
rs779145843	in-del	-/AAGAT	0.00053343	0.0163227	intron-variant	AHCTF1	GRCh38.p7	1:246891938	TCAAGAATAAAAGAA[-/AAGAT]AAGTTTCCATACAGT	25909
rs779151716	snp	C/G	1.64833e-05	0.00287078	intron-variant	AHCTF1	GRCh38.p7	1:246898171	GCTAATAACGTGATC[C/G]AACCAAAAGAAACAA	25909
rs779226636	snp	C/T			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932053	AGTTCTCGCGATGGT[C/T]CCGCGCTCTAGCGCC	25909
rs779243360	snp	A/C	1.68459e-05	0.00290219	intron-variant	AHCTF1	GRCh38.p7	1:246905490	CAACAGAGCGAGACT[A/C]TGTCTCCAAAAAAAC	25909
rs779247793	snp	A/T	1.6643e-05	0.00288465	synonymous-codon, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246842738	GATTCGTTTCGCTTT[A/T]GGCTTTCCCAGAGTT	25909
rs779264554	in-del	-/CT			intron-variant	AHCTF1	GRCh38.p7	1:246889284	CTCTTCTTTTTTCCC[-/CT]CTGATTTCCTTTTCT	25909
rs779268358	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246862574	CAATAAACATATCAA[G/T]AGAAATATTTATTCC	25909
rs779268815	snp	C/G	6.59152e-05	0.00574049	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246863953	GAGTTTCAAGCAAAT[C/G]TAATTCTGAAGCCCT	25909
rs779280036	in-del	-/TAAAAGTGAAAATGTTGA	1.64988e-05	0.00287213	cds-indel, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850219	TGTTTAATACGCAGC[-/TAAAAGTGAAAATGTTGA]TGCTTGTCACTGGAT	25909
rs779283511	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246896010	TTTAGAATTTAAAAA[A/T]TTTAAGGCTAAAAAA	25909
rs779296051	snp	G/T	1.64751e-05	0.00287007	intron-variant	AHCTF1	GRCh38.p7	1:246867633	GATTAACAAGCAGCA[G/T]GACTATGAAACGTGT	25909
rs779300922	snp	C/T	1.67153e-05	0.00289091	intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842653	CAGAGCGAGACTGTC[C/T]CAATCAATCAATCAA	25909
rs779316068	snp	A/G	1.64925e-05	0.00287158	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877006	GCACATAATTGGCAC[A/G]CTGCAAATGGTGCAC	25909
rs779324317	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246855090	GGAACAAAGGCATAA[C/T]AGTTGAGAGCATGGG	25909
rs779327424	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246898973	GAGCACCTGTAATCC[C/T]AGCTATTCAGGTGGC	25909
rs779358182	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246851888	ATCCCCGTAAGGTTG[A/T]AGAACAATTCACCTA	25909
rs779406638	snp	A/G	1.65111e-05	0.0028732	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864048	AAAGGAGATTTCATG[A/G]AGCTTTGCTGAATAA	25909
rs779421853	snp	C/T	1.67832e-05	0.00289677	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900449	AGGTAAAGACTGAAA[C/T]ACTAGTGTCAGGCGA	25909
rs779434747	snp	C/G	1.66527e-05	0.00288549	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900118	GGTGGATATGAAGGA[C/G]GGACTCCTCTATTTA	25909
rs779449978	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246849438	GTTAACCATACTGAA[A/T]AACTGAACTCAAACT	25909
rs779458999	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246857462	AAAAACAGAATCACC[A/G]GAGTTCTGCCTCAAT	25909
rs779504666	snp	C/T			missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867319	GGAGCTGGGAGCGAA[C/T]ACACTATAGGAGATG	25909
rs779507700	snp	C/T	1.66774e-05	0.00288763	intron-variant	AHCTF1	GRCh38.p7	1:246913423	GTTACCTAGAAAACA[C/T]AATACGTGATTTGCT	25909
rs779527555	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246927555	ACACAAACACACATG[A/C]AACACCTACGTTCAG	25909
rs779543619	snp	C/G	1.64817e-05	0.00287064	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246907729	TAATGTGTGGTACTT[C/G]AGCTGGGATACCAGT	25909
rs779549133	snp	A/C/T	3.41968e-05	0.00413488	intron-variant	AHCTF1	GRCh38.p7	1:246861948	TTTCTCCCAATTATT[A/C/T]TCAAACTTACCCCAG	25909
rs779553793	snp	A/C	1.89095e-05	0.0030748	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876159	TTTCGAGCCAGTGAT[A/C]TCTCCCGCAAACGAG	25909
rs779567378	snp	A/C	1.6638e-05	0.00288422	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900208	GACTCCAATGACCAC[A/C]GTGCAAAATAAGAGC	25909
rs779602859	snp	A/G	1.66579e-05	0.00288595	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246862044	GACCTTCCAGGTGAT[A/G]GAGAGGGAGATGCTA	25909
rs779606839	snp	C/T	3.44157e-05	0.00414809	intron-variant	AHCTF1	GRCh38.p7	1:246887409	AACAAAAACCTCCTA[C/T]GTATATATTTACAAT	25909
rs779613549	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246892856	TTGCTATATTGCTCA[A/G]GCTGGTCTTGAACTC	25909
rs779707462	snp	A/G	3.70617e-05	0.00430459	intron-variant	AHCTF1	GRCh38.p7	1:246843952	AGTTGAAAAAACTGT[A/G]TCTGTATCTTTATAT	25909
rs779735730	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246917003	CTCTTCTCCGCCTAT[C/T]AGTCATGTTTGGATT	25909
rs779736190	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246882780	GTGCATCATGGTTAA[C/T]TTGCACGTAAAACAG	25909
rs779738371	snp	A/G	1.64803e-05	0.00287052	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246907588	TCCAAAGTGCTAGAT[A/G]GCCATCAGAAAAACC	25909
rs779749038	snp	A/G	1.65094e-05	0.00287305	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849891	AGCTCATCACCATCG[A/G]AAGTTCCTCGTTTGG	25909
rs779757812	snp	A/C	1.6501e-05	0.00287232	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850928	GGTATTGTTTCATGA[A/C]TGGACTGTTCCATTG	25909
rs779761716	snp	A/C	3.44988e-05	0.0041531	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840774	TTCTGATGACTTTAC[A/C]AATAGGTGTACATTA	25909
rs779762323	snp	C/T	2.53926e-05	0.0035631	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850550	TCTAGTATGTCCTGA[C/T]TAACTTCTTTCTTTC	25909
rs779782678	snp	C/T	1.76375e-05	0.00296958	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876056	TCGAAAAACTGATGA[C/T]GTTGACAGATGATAA	25909
rs779796793	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246880977	TCTTGGCAATACAGC[A/C]AAGACAGACTGAAAA	25909
rs779836144	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246847087	AGGTCAGGCGTTTGA[A/G]ACTAGCTTGGCCAAC	25909
rs779910929	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246847547	CTGTTGCCCAGGCTG[G/T]AGTGCAGGGGCACAC	25909
rs779922668	snp	A/G	7.13827e-05	0.0059738	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853285	TTCCACCATCACCAA[A/G]GACATCAGCCATAGC	25909
rs779943622	in-del	-/GAAA			intron-variant	AHCTF1	GRCh38.p7	1:246877684	TGAGATCTATAGATG[-/GAAA]GAAACAAGCACGCTG	25909
rs779948316	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246844139	CCAAATGTGTAGGAC[A/G]ATTGAATGCTTCAAA	25909
rs779977730	snp	A/G	1.77596e-05	0.00297985	intron-variant	AHCTF1	GRCh38.p7	1:246862156	AACTTTTAGCTTTCT[A/G]TAGTAAAGAGCAAAT	25909
rs779991299	snp	A/C	1.65165e-05	0.00287367	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850266	TTCCTGTATTTTCAG[A/C]AGCATCTAAATTAGT	25909
rs779999268	snp	C/T	1.74622e-05	0.00295479	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850407	GAGTCCTTTTTGTAA[C/T]AGATGAAACCTTAAC	25909
rs780009140	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246842932	CTTTTAGTAGAAACC[G/T]TAGTTATGCAGGCCT	25909
rs780038506	snp	C/T	1.69651e-05	0.00291243	intron-variant	AHCTF1	GRCh38.p7	1:246916125	AGAAATGTCCAGGTA[C/T]CTTAAACAGTACCTA	25909
rs780077578	snp	A/C	1.76197e-05	0.00296809	intron-variant	AHCTF1	GRCh38.p7	1:246891077	TGTAAAGAAGAGTTA[A/C]CATCAGTTGTTTACT	25909
rs780090219	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246904686	TACTAAATCAACCCT[C/G]TAGTGAACTCAAGCA	25909
rs780121835	snp	C/G	1.81125e-05	0.00300931	intron-variant	AHCTF1	GRCh38.p7	1:246877335	CAAAGTTTAGTTTTA[C/G]AAAAAGCTATTTAAA	25909
rs780157059	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246924777	TAAGTCACAAAACCT[A/G]AAAAGTTATGTTTGA	25909
rs780171920	snp	A/C	3.33506e-05	0.0040834	intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842670	AATCAATCAATCAAT[A/C]AAGAACAGAACAGAA	25909
rs780201324	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246911994	GCTGGAGTGCAGTGG[C/T]GTGATCTCGGTTCAC	25909
rs780224423	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246887397	ATAAAATACAACAAC[-/A]AAAACCTCCTACGTA	25909
rs780228627	snp	A/C/T	0.000197868	0.0099447	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850179	CATCTGATGGACTAA[A/C/T]TTCTCTCCCTCTGAC	25909
rs780235960	in-del	-/T			utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840339	AAACAAAAAAATACA[-/T]TTTTCTGATTAGAAA	25909
rs780240138	snp	A/G	1.7598e-05	0.00296626	intron-variant	AHCTF1	GRCh38.p7	1:246900473	CAGGCGATAGAGCTG[A/G]AAGAAAAAGATAATT	25909
rs780245922	snp	G/T	1.64849e-05	0.00287092	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877035	ACTAAAAGGAATTCA[G/T]GATTCTGAACGCTGG	25909
rs780297258	snp	A/T	0.000132868	0.00814963	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246888506	ATCAAGCAATCGGGA[A/T]TCCACTTCCCTCTGC	25909
rs780302772	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246866372	AATGTCGGTAATAAC[A/G]ACTTTCATTTAAAAT	25909
rs780312818	snp	C/T	3.31148e-05	0.00406894	intron-variant	AHCTF1	GRCh38.p7	1:246889952	ATGTAATTTCTAAAA[C/T]TGTTTTACTATACCT	25909
rs780317212	snp	A/G	1.66824e-05	0.00288806	intron-variant	AHCTF1	GRCh38.p7	1:246900061	ATGTTAAGGAAATAC[A/G]TACCAAAATTATAAG	25909
rs780328113	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246869837	ACAACATCCATTCTG[C/T]AACCCTGGATCACAG	25909
rs780328299	snp	G/T	7.9818e-05	0.00631685	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851433	CTTCAAGCTTTTCTT[G/T]TTCAATCACCTAAAT	25909
rs780363517	snp	C/T	3.32745e-05	0.00407875	missense, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246842746	TCGCTTTTGGCTTTC[C/T]CAGAGTTTCTACTGA	25909
rs780379363	snp	C/T	4.9525e-05	0.00497595	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851328	AAAACTGTTGGTCAA[C/T]AGTATCAAAATTGTA	25909
rs780390071	snp	C/T	1.67089e-05	0.00289035	intron-variant	AHCTF1	GRCh38.p7	1:246857679	TATTTGAATTTCTCT[C/T]CATTAACTTACCCTT	25909
rs780404998	snp	A/G	1.64953e-05	0.00287182	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246887301	TGGGAAAGATTCAAT[A/G]GGAGTGTCTGTTTTG	25909
rs780423466	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246852248	CTTCCCAACTAAAAG[A/C]ACTGGAACTTTACTC	25909
rs780436531	snp	C/T	1.64988e-05	0.00287213	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861124	TGTTTCCTTTGCTCA[C/T]ATCCAGTTTCTCTAA	25909
rs780455875	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246885065	AATCTCAATTTGGCG[C/T]CCCTCCCTTTTATTC	25909
rs780496031	in-del	-/A	1.65016e-05	0.00287238	intron-variant	AHCTF1	GRCh38.p7	1:246877097	TAAAAAGAACAAAAT[-/A]AGATTGTAAACTACC	25909
rs780505403	snp	A/T	1.65902e-05	0.00288008	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864111	TGAACAACCAAATCT[A/T]GCAGTCTGTAATCAG	25909
rs780521481	snp	C/T	5.02685e-05	0.00501316	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246857811	TCTGCATCTTCTAAA[C/T]TGCCTATAAGTCATA	25909
rs780533964	snp	C/G			downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838706	AAGCAAGTCTTGATC[C/G]ACCTTTGACAAAGCC	25909
rs780553243	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246930198	CTGAGTGCAGCGGCG[C/G]GATCCTAGCTCACTG	25909
rs780564661	snp	C/G	1.65644e-05	0.00287783	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877214	TCAAGCCCATTTCCT[C/G]ACAGACTTCATACAT	25909
rs780573673	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246854888	CATATCGGGAGAAAT[A/G]GGCACAGAAAACAAA	25909
rs780623206	snp	A/G	4.49741e-05	0.00474184	intron-variant	AHCTF1	GRCh38.p7	1:246853313	AGCTGAAAGAAAAAT[A/G]AGTGAATTTTTTACA	25909
rs780626309	snp	A/C	1.6546e-05	0.00287624	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246891786	GAGCGTACCTCTCTC[A/C]GTGATCTCTCGGGCT	25909
rs780642779	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246930984	GTGGCAAAAGAAACC[A/G]TCCTGTTTCCCAGGT	25909
rs780676123	snp	C/T	1.64749e-05	0.00287005	intron-variant	AHCTF1	GRCh38.p7	1:246862181	GCAAATGGAATTACA[C/T]CATTAAAAGTGCTTA	25909
rs780691871	in-del	-/AAAT	1.66765e-05	0.00288756	intron-variant	AHCTF1	GRCh38.p7	1:246855839	TTCCTTTAGAAAAAG[-/AAAT]AAATACATACCTTAG	25909
rs780704727	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246884231	TGATTCTAGATTAAG[C/T]TATCTAAACATTTTT	25909
rs780715605	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246849290	AATGCAGCAGTACAT[C/G]GGAGATTAAAAATAT	25909
rs780728492	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246928405	TATTCCTGGGCATTC[A/G]ACAAGGTCACAGTGC	25909
rs780738143	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246882887	AAATGCAAAGATGCT[C/G]TTAATGAGGAAACTC	25909
rs780755393	snp	C/T	1.65269e-05	0.00287457	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902554	TCCTCCCTGTCACCA[C/T]GAGATCGAAATTTCT	25909
rs780758041	snp	C/T	1.651e-05	0.0028731	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246913260	TTCATTTTGATTGCA[C/T]GACAAGTCATCCAAA	25909
rs780784739	snp	C/G/T			intron-variant	AHCTF1	GRCh38.p7	1:246858279	CTTCTTCTTCTAATT[C/G/T]TCTGAACCTAGCTCA	25909
rs780790585	in-del	-/AAAAC	0.277778	0.248452	intron-variant	AHCTF1	GRCh38.p7	1:246905500	GACTCTGTCTCCAAA[-/AAAAC]AAAACAAAACAAAAC	25909
rs780802911	snp	A/C/G	3.29561e-05	0.00405921	synonymous-codon, missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246898298	ATCAGGAATGAGTTC[A/C/G]TTGAGTGATGGACCT	25909
rs780805476	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246888681	TGGGAGGCCAAGGCA[C/G]GAGGATCAACTCAAG	25909
rs780820447	snp	C/T	3.59848e-05	0.00424159	intron-variant	AHCTF1	GRCh38.p7	1:246891089	TTAACATCAGTTGTT[C/T]ACTTACAAAAAAATC	25909
rs780850591	snp	C/T			utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839527	CGTAACATCCATCAC[C/T]AACCTGACTAAAAGG	25909
rs780851394	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246898718	AAAGAGATTTGATAT[C/T]AAGTATAAATACAGC	25909
rs780870162	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246870419	CAGACAAAGACCTTG[C/T]CTCTTAAAAAAACAA	25909
rs780873479	snp	A/G	1.66358e-05	0.00288402	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900218	ACCACAGTGCAAAAT[A/G]AGAGCAATTATGTAG	25909
rs780881893	snp	C/T	1.65438e-05	0.00287605	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246918265	CTGCAGCAAACTTTC[C/T]ACGAAGCACAGATTC	25909
rs780896259	snp	A/G	1.67632e-05	0.00289505	missense, synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840964	GCCGAATTTCTATGG[A/G]AGGAGGTGACCAAGC	25909
rs780900382	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246863710	CCACACAGAACCCTA[A/T]ATTACCTTTAAGAAA	25909
rs780905653	snp	G/T	1.65408e-05	0.00287578	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849906	AAAGTTCCTCGTTTG[G/T]CACTAAAATGGATTT	25909
rs780913527	snp	A/G/T	3.39647e-05	0.00412085	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867808	AATGGTTTGGGTCTA[A/G/T]AAACTGTAAAATGAA	25909
rs780965250	snp	A/G	8.23703e-05	0.00641704	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849704	AAGATGGCCTTGCTA[A/G]ACCGAGTCCTGCTGC	25909
rs780970673	snp	A/T	1.99185e-05	0.00315577	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246885678	CAAAAGATCCAAACC[A/T]CTCTGGAAATAACAT	25909
rs780987965	snp	A/G/T			intron-variant	AHCTF1	GRCh38.p7	1:246857410	AGCAGAGGGCATGGA[A/G/T]GTATGCACAGCTGTG	25909
rs781001977	snp	A/T	1.6495e-05	0.0028718	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849650	TCTGACGCTGGAGAA[A/T]ATAAAGGCTCATTGT	25909
rs781015187	snp	C/T	1.67618e-05	0.00289493	intron-variant	AHCTF1	GRCh38.p7	1:246876900	AACCAAAAAAGCCTC[C/T]AGTTTTCCTTATTCT	25909
rs781031209	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246883764	GTATAGGAGCCTTAA[C/T]GTGCTAGTTTTCTGG	25909
rs781055463	snp	C/T	1.6492e-05	0.00287154	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850699	CTTCCTGACTGACTG[C/T]CCTGGCATCTTAGGA	25909
rs781085031	snp	A/T	3.29674e-05	0.00405988	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902641	ATGCCACCTGTCAGG[A/T]CCAGGGTGTATCTTT	25909
rs781110328	snp	G/T	2.23917e-05	0.00334594	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850578	TTCTCCTTCCTCTCC[G/T]AGGCGTAACAGAATT	25909
rs781125720	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246857610	AAGTGAAATCTAACA[C/T]GCACAGAATATTTTA	25909
rs781137876	snp	A/G	3.32801e-05	0.00407908	intron-variant	AHCTF1	GRCh38.p7	1:246905516	AAAACAAAACAAAAC[A/G]AAACAAAGTTTGTAT	25909
rs781164297	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246844303	GTCTGTGCCATAACT[A/G]CTGCTATTGCAGAGA	25909
rs781211089	in-del	-/AA			intron-variant	AHCTF1	GRCh38.p7	1:246888901	AGAGACCCTGTCTCT[-/AA]AAACAGAGAGAGAGG	25909
rs781233084	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246893828	TCCTAAGACCAAAAG[A/G]CAAGTTATAATCCTA	25909
rs781242042	snp	A/T	1.70359e-05	0.0029185	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916304	CTGTTCATTGACTCC[A/T]CTGAATCTGTAAGCA	25909
rs781300061	in-del	-/ACA	5.05072e-05	0.00502504	intron-variant	AHCTF1	GRCh38.p7	1:246887389	TAAGGACAATAAAAT[-/ACA]ACAACAAAAACCTCC	25909
rs781304733	in-del	-/TAAG			downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838834	TTACTACTATGATAC[-/TAAG]TATCTGAGTATTGTT	25909
rs781311198	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246867065	CAAAAATTTTAAGTA[G/T]ACTACTACCTGATGT	25909
rs781332869	snp	G/T	1.67172e-05	0.00289108	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916160	TCCAGGAAGAACAAC[G/T]GCTTTAACTACTTTT	25909
rs781346872	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246912165	AAAGAGCTACACTGA[C/T]ATTCTAGGCTTGCTT	25909
rs781354440	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246866686	GGCATATTAAGGACA[A/G]AGAATCAATACATGA	25909
rs781358603	in-del	-/TC	3.4132e-05	0.00413096	intron-variant	AHCTF1	GRCh38.p7	1:246857652	TAATTTCATTAAACT[-/TC]TTTCTAAAAGTATTT	25909
rs781445164	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246901837	CTGTCTCTAAATAAA[C/T]AAACAAATAAAAACT	25909
rs781446110	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246877396	TTCAAAGATACTTTG[C/T]AAAGTATCTTTATAA	25909
rs781454737	snp	C/T	1.65861e-05	0.00287972	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877227	CTGACAGACTTCATA[C/T]ATGTGCTTCAGTAAC	25909
rs781454927	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246853887	ATGTGGATACTAATA[A/G]AACAAAATGAAAAAT	25909
rs781481823	snp	A/G/T	3.34114e-05	0.00408715	intron-variant	AHCTF1	GRCh38.p7	1:246888132	CTCTTGAAATTTTAT[A/G/T]ATTTTAGTAATACAT	25909
rs781506108	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246880115	AGTTATTCACACTAC[-/T]TGGGTACTAAGAGGA	25909
rs781529581	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246860663	ACTCCCACCATGCCT[A/G]GCTAATTTTTAAATT	25909
rs781552719	in-del	-/AA			intron-variant	AHCTF1	GRCh38.p7	1:246930586	ACAAAAAAACAGTTT[-/AA]AAAAAAAAAAAAGGG	25909
rs781554840	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246923157	CGGTGGCCCATGCCT[A/G]TAATCCCAGCACTTT	25909
rs781572081	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246902456	AGGAGTATGAAATCT[A/T]GAAAATAACACCTGT	25909
rs781579285	snp	A/G	2.27033e-05	0.00336914	intron-variant	AHCTF1	GRCh38.p7	1:246851449	TTCAATCACCTAAAT[A/G]AATTAAAGATAAGAG	25909
rs781590768	snp	A/G	1.64885e-05	0.00287123	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246895857	TATCCATCTTCGGAT[A/G]TAACCAGTCAAAAGT	25909
rs781630719	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246849131	ATGAAGGATGGCCTC[-/A]ACTGAAGATGAGGGC	25909
rs781635057	snp	C/G	1.65004e-05	0.00287227	intron-variant	AHCTF1	GRCh38.p7	1:246888246	TGCCTATAAAACAAA[C/G]GGATAAAACCTTCAG	25909
rs781636571	snp	A/G	1.92978e-05	0.0031062	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876166	CCAGTGATCTCTCCC[A/G]CAAACGAGGATCACG	25909
rs781642189	snp	C/T	1.66732e-05	0.00288727	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246860944	CTTCTGATGCAAATA[C/T]ATCTTTATCTCCATC	25909
rs781647629	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246880568	GTGAGACTCCAGCTC[-/A]AAAAAAAAAAAAAAA	25909
rs781655475	snp	C/T			utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246931929	CCCCGCTCTGCGCAT[C/T]ACCCTGCGCCGACAA	25909
rs781664818	snp	A/G	1.6495e-05	0.0028718	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851074	TTGGTCACTAGTTAC[A/G]GCAGATGGCAAATTT	25909
rs781728209	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246871185	CCCCCATGTCTTAGG[A/G]CAGTGGTTACTACTT	25909
rs781739715	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246928302	GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	25909
rs781775779	in-del	-/A	1.64749e-05	0.00287005	intron-variant	AHCTF1	GRCh38.p7	1:246877306	TCAACCATACACCTG[-/A]AAGCAGTATTTATCA	25909
rs796066512	in-del	-/CT			intron-variant	AHCTF1	GRCh38.p7	1:246909437	AATTTGCATGCTGCT[-/CT]GAGTGGTATGATGAA	25909
rs796074494	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246925933	AGCCAGGTGTGGTGG[C/T]GCCTGCCTGTAGTCC	25909
rs796144096	in-del	-/CT			intron-variant	AHCTF1	GRCh38.p7	1:246903662	GTGAGACCCCCCCCC[-/CT]CCGTCTCTGCTAAAT	25909
rs796224739	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246920828	GGTGCCTCACGCCTA[-/T]TAATCCCAGCACTGT	25909
rs796268374	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246903854	AAAAAAAAAAAAAAA[-/A]GAATCACTTTTCAAT	25909
rs796366579	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246907847	TCAAGCTGCAAATGA[A/G]GTCAACTGAGTTAAA	25909
rs796387208	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246869040	TAGTAGAGACGGGGT[C/T]TCACCATGTTGGCCA	25909
rs796493119	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246923128	AAAAAAAAAAAAAAA[-/A]GATAGGCTGGGCACG	25909
rs796546047	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246902805	ACTGAAGAGAACCAA[C/T]CATGGAAAAAGGCTC	25909
rs796550402	snp	C/T			synonymous-codon, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843921	TGCAGGAACCTCTAT[C/T]TTTTTAGCTAAAAAA	25909
rs796574174	multinucleotide-polymorphism	AT/TG			intron-variant	AHCTF1	GRCh38.p7	1:246931052	ATTTTAAATCTCCTT[AT/TG]TCTGACCAATCGGGT	25909
rs796579076	in-del	C/GGG			intron-variant	AHCTF1	GRCh38.p7	1:246860195	ACCTGGTTGGGGGGG[C/GGG]CGGAGGTTGCAGTGA	25909
rs796596506	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246930052	GCAAGACCCCGTCTC[-/A]AAAAAAAAAAAAGAT	25909
rs796630102	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246903386	GGGTACCAATTAAGC[C/T]ACAAGCTTGAATCTA	25909
rs796635621	in-del	-/GG			intron-variant	AHCTF1	GRCh38.p7	1:246860189	TGCTTGAACCTGGTT[-/GG]GGGGGGGGCGGAGGT	25909
rs796659823	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246903890	AAAACAAAGACAACA[C/T]ATTTAAAATAGAAAA	25909
rs796682533	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246911643	CATGCGCCACCACAC[C/T]TGGCTAATTTTATAT	25909
rs796682817	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246903666	GACCCCCCCCCCTCC[G/T]TCTCTGCTAAATATA	25909
rs796683714	in-del	-/CACAC			intron-variant	AHCTF1	GRCh38.p7	1:246867904	ACACCCCCCCCCCCA[-/CACAC]ACACACACACACATT	25909
rs796711547	in-del	-/AAG			intron-variant	AHCTF1	GRCh38.p7	1:246843077	AGGCTCTCACTTTCT[-/AAG]AAGTAGACAACCAGA	25909
rs796736833	in-del	-/CTTA			intron-variant	AHCTF1	GRCh38.p7	1:246845969	GAACAACACATCTTA[-/CTTA]TTCCCTGGGTGATGT	25909
rs796773120	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246865519	TTCTCTTCTTTCTCT[A/G]TCTTGTTTGCATTTA	25909
rs796794431	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246899118	TATTTTTCAAAATTC[-/T]TTTTTTTTTTCCTGT	25909
rs796811689	in-del	-/AAAC			intron-variant	AHCTF1	GRCh38.p7	1:246854424	ACTGCAGAAACAGCA[-/AAAC]AAACCCCAAAATGGT	25909
rs796833739	in-del	-/AC			intron-variant	AHCTF1	GRCh38.p7	1:246847305	AAAAAAAAAAAACAA[-/AC]AAAAAAAAAACTGAA	25909
rs796835506	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246848411	TTTAGTAGTGTTAGC[C/T]AGGATGGTCTCGATC	25909
rs796836371	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246909661	AAGAGAAGCTGTAAA[C/G]TGCTTCCTTTAAATG	25909
rs796852549	in-del	AA/C			intron-variant	AHCTF1	GRCh38.p7	1:246930108	AGCATAAAAAGAAAA[AA/C]AAAAGTCTCAAAACT	25909
rs796888111	in-del	-/AA			intron-variant	AHCTF1	GRCh38.p7	1:246926047	TGAGACCCTGTCTTT[-/AA]AAAAAAAAAAAAAAA	25909
rs796909528	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246878043	TGACCCAATGATCCC[-/A]AATGCAAAGAATACA	25909
rs796973168	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246847858	GGTTACTATATTCCT[C/T]CAGGTCCTGAGGAGT	25909
rs797009254	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246903659	ATGGTGAGACCCCCC[C/T]CCCTCCGTCTCTGCT	25909
rs797010304	in-del	-/AA			intron-variant	AHCTF1	GRCh38.p7	1:246866500	AACATATGTCCATTA[-/AA]CTACACTCTGTACTT	25909
rs797012157	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246873342	GTGGCTGATGGTCTC[C/T]GGAAAGACAATTCAC	25909
rs797012234	multinucleotide-polymorphism	AAC/CAA			intron-variant	AHCTF1	GRCh38.p7	1:246847306	AAAAAAAAAACAAAC[AAC/CAA]AAAAAAACTGAAAAT	25909
rs797016082	in-del	-/TTTT			intron-variant	AHCTF1	GRCh38.p7	1:246868847	TGTGTGTGTTTTTTG[-/TTTT]TTTTTTTTTTTTGAG	25909

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