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
rs768197	snp	G/T	0.460477	0.134905	intron-variant	AHCTF1	GRCh38.p7	1:246923930	GAAACATGGCCCTCT[G/T]CTCAGGTCCTGTGGC	25909
rs903462	snp	C/G	0.49621	0.0433651	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932608	TAGAAAAAACAGCAC[C/G]GTGGAAAAAGCGTTT	25909
rs903464	snp	C/T	0.097727	0.198275	intron-variant	AHCTF1	GRCh38.p7	1:246907921	TGTTAAACTAGAAAA[C/T]TGCCATCCTTATCTA	25909
rs903465	snp	A/G	0.093417	0.194889	intron-variant	AHCTF1	GRCh38.p7	1:246908051	TAACAACCATAAATA[A/G]AACTGATTTATTTCT	25909
rs923972	snp	C/T	0.00478085	0.0486577	intron-variant	AHCTF1	GRCh38.p7	1:246916871	CTAAGGCTTAAACGA[C/T]TTAAACTAGAAGTTA	25909
rs967953	snp	A/C/G/T	0.0934559	0.195063	intron-variant	AHCTF1	GRCh38.p7	1:246894866	TCCCAAGTTGCCTCC[A/C/G/T]TGAAGTGTTGATGTT	25909
rs1039009	snp	A/C	0.461259	0.133677	intron-variant	AHCTF1	GRCh38.p7	1:246917156	GAAGCACAGAGTAGC[A/C]GCACTGGGTGGAAGA	25909
rs1039010	snp	A/G	0.434976	0.168179	intron-variant	AHCTF1	GRCh38.p7	1:246918081	AGGTTCACTGATAAC[A/G]TGTTTAAGAGCTTAT	25909
rs1047080	snp	A/G	0.233818	0.249476	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840729	AAATATCTAGTTTGG[A/G]AGAAAATAATTTATA	25909
rs1047085	snp	A/C	0	0	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840721	AGTTTGGAAGaaaat[A/C]atttatataaattat	25909
rs1053916	snp	A/G	0.0205511	0.0992634	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839173	CTAAATGAACTTTAC[A/G]TATATTTTAAATGAA	25909
rs1472275	snp	A/G	0.483053	0.0904792	intron-variant	AHCTF1	GRCh38.p7	1:246891228	GACCAAAGTAAACTA[A/G]ATACAAAGATGAATT	25909
rs1472276	snp	C/G	0.0782148	0.181884	intron-variant	AHCTF1	GRCh38.p7	1:246867173	Gtaatttttaattat[C/G]tttaacattttatag	25909
rs1472277	snp	A/G	0.0103295	0.0711199	intron-variant	AHCTF1	GRCh38.p7	1:246866950	TGTTAGTAGACCTCT[A/G]AATGAGGGTTGTTTT	25909
rs1612610	snp	G/T	0.460252	0.135255	intron-variant	AHCTF1	GRCh38.p7	1:246905224	TATGTATCAGGCCAG[G/T]CGTGGTGACTCACAC	25909
rs1613209	snp	A/G	0.485255	0.0845871	intron-variant	AHCTF1	GRCh38.p7	1:246871877	CTGTGTCTTTAGGTT[A/G]TTATTATTTTTTAAT	25909
rs1616541	snp	C/T	0.0154538	0.0865337	intron-variant	AHCTF1	GRCh38.p7	1:246871547	GTATACCTTGTTTTT[C/T]TGGGCCCCTTTCTGT	25909
rs1619941	snp	A/T	0.454784	0.1434	intron-variant	AHCTF1	GRCh38.p7	1:246929478	GACCTGAAATTTGAG[A/T]ATTTAAAAAAGGAAA	25909
rs1630829	snp	C/T	0.435694	0.167385	intron-variant	AHCTF1	GRCh38.p7	1:246860564	AACTCTCATGCTTTC[C/T]TTCTGAGATAGGGTC	25909
rs1691238	snp	A/G	0.108755	0.206276	intron-variant	AHCTF1	GRCh38.p7	1:246928140	CCCCATCTCTACTAA[A/G]AATACAAAAAAAATT	25909
rs1691239	snp	G/T	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246880178	ATTTACATGCTTCAG[G/T]GTTTAAGAGCTAAGA	25909
rs1691240	snp	A/C	0.460252	0.135255	intron-variant	AHCTF1	GRCh38.p7	1:246904579	GTATGGGAAGGAGAA[A/C]GGGCAGTTGGGGGAA	25909
rs1691241	snp	A/G	0.460365	0.13508	intron-variant	AHCTF1	GRCh38.p7	1:246904829	TTTACTTGGCTTCTA[A/G]CACACCACACCTTCC	25909
rs1691242	snp	A/G	0.46014	0.13543	intron-variant	AHCTF1	GRCh38.p7	1:246905365	TAGCCAGGCATGGTG[A/G]CAGGCACCTGTAGTC	25909
rs1691243	snp	C/T	0.0908922	0.192833	intron-variant	AHCTF1	GRCh38.p7	1:246906212	TTGACCAAGAGATGA[C/T]AGTGTTAGAGAAAGC	25909
rs1691251	snp	A/G	0.431177	0.172264	intron-variant	AHCTF1	GRCh38.p7	1:246864477	TGAATTTTAGTAAAT[A/G]GATTGCCAGGGAAGC	25909
rs1691252	snp	C/T	0.433818	0.169443	intron-variant	AHCTF1	GRCh38.p7	1:246900847	acctaaaacggatgc[C/T]tttgggcattaaggc	25909
rs1691253	snp	C/T	0.108048	0.20579	intron-variant	AHCTF1	GRCh38.p7	1:246901686	AGCCAGGTGTGGTGG[C/T]GTGTGCCGGCAGTCC	25909
rs1691254	snp	A/G	0.46014	0.13543	intron-variant	AHCTF1	GRCh38.p7	1:246901773	caaccagccaagatc[A/G]tgccaccacactctg	25909
rs1691255	snp	A/G	0.485933	0.0826777	intron-variant	AHCTF1	GRCh38.p7	1:246902170	GCGATGACACTAAAG[A/G]AGACAGAGAAAACAT	25909
rs1691256	snp	G/T	0.0970103	0.197722	intron-variant	AHCTF1	GRCh38.p7	1:246902296	GCCTGTTTTGAGAAC[G/T]AGATTAAAATAAAAG	25909
rs1691257	snp	A/C	0.00953873	0.0683987	intron-variant	AHCTF1	GRCh38.p7	1:246903806	ttgcaccactgcact[A/C]cagcctgggcgacag	25909
rs1779964	snp	A/G	0.476918	0.104919	intron-variant	AHCTF1	GRCh38.p7	1:246899907	ACATATAAATACTAA[A/G]TTTCTTGTGTGTATA	25909
rs1779965	snp	G/T	0.0973687	0.197999	intron-variant	AHCTF1	GRCh38.p7	1:246901978	TGGGTAAGTTCGCTG[G/T]GTGATTTAATCCTCA	25909
rs1779966	snp	C/T	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246903831	cgacagagcgagact[C/T]tgtctcaaaaaaaaa	25909
rs1779967	snp	A/T	0.465052	0.127485	intron-variant	AHCTF1	GRCh38.p7	1:246904790	GATCCCTTTTAATAA[A/T]TCCTATTACTAGTTC	25909
rs1779968	snp	A/T	0.453087	0.145793	intron-variant	AHCTF1	GRCh38.p7	1:246906395	CCAGTCTGACCAACA[A/T]GGTGAAAATCCGTCT	25909
rs1779969	snp	C/T	0.485731	0.0832509	intron-variant	AHCTF1	GRCh38.p7	1:246906647	TTGAGATACACTTCC[C/T]ATAAGATAAATTACT	25909
rs1779971	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246880211	taaCAAATAACATAT[G/T]GTTTTGGATAATAAG	25909
rs1779972	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246880205	ATAACATATGGTTTT[G/T]GATAATAAGCTATTT	25909
rs1779973	snp	C/G	0.00953873	0.0683987	intron-variant	AHCTF1	GRCh38.p7	1:246882638	AACCCACCTAACAAA[C/G]AGGAAAAATTATGCC	25909
rs1779975	snp	A/C	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246908936	CTTAATGAATGAAAC[A/C]ATTAGCTCAAAGTAA	25909
rs1779976	snp	A/C/G	0.00404816	0.0448079	intron-variant	AHCTF1	GRCh38.p7	1:246888139	AATTTTATAATTTTA[A/C/G]TAATACATGAAACAC	25909
rs1779977	snp	A/G	0.495174	0.0488838	intron-variant	AHCTF1	GRCh38.p7	1:246869776	cctgtacatcatcag[A/G]gctcctgggtgacca	25909
rs1779978	snp	A/T	0.467132	0.12391	intron-variant	AHCTF1	GRCh38.p7	1:246869579	ttaagggccttagga[A/T]ttttggaatggtgat	25909
rs1779979	snp	A/G	0.499713	0.0119774	intron-variant	AHCTF1	GRCh38.p7	1:246869138	ACAAAACACACGGCC[A/G]GGCGTGGTGGCTCAC	25909
rs1779980	snp	C/T	0.429837	0.173662	intron-variant	AHCTF1	GRCh38.p7	1:246869133	ACACACGGCCGGGCG[C/T]GGTGGCTCACGCCTG	25909
rs1779981	snp	A/G	0.11963	0.213316	intron-variant	AHCTF1	GRCh38.p7	1:246869001	aaaagttagccaggc[A/G]tggtggcgggcgcct	25909
rs1779982	snp	A/G	0.48666	0.0805725	intron-variant	AHCTF1	GRCh38.p7	1:246868937	GAATGGCGTGAACCC[A/G]GGAGGCAGAACTTGC	25909
rs1812703	snp	A/G	0.108048	0.20579	intron-variant	AHCTF1	GRCh38.p7	1:246925347	AAAAGCATTTTTTGG[A/G]AAATGAAATATAGTA	25909
rs1892116	snp	C/T	0.375598	0.21616			GRCh38.p7	1:246917020	GTCATGTTTGGATTT[C/T]ACCCTGCCTGCAATG	25909
rs2011875	snp	A/G	0.093777	0.195178	intron-variant	AHCTF1	GRCh38.p7	1:246908130	CTGATTCCGGGTCAG[A/G]GGGAAGAAAATACAT	25909
rs2029789	snp	A/T	0.375	0.216506	intron-variant	AHCTF1	GRCh38.p7	1:246930586	CCCTTTTTTTTTTTT[A/T]AACTGTTTTTTTGTG	25909
rs2047190	snp	C/T	0.0970103	0.197722	intron-variant	AHCTF1	GRCh38.p7	1:246926469	GTTTAATAAAGTTTT[C/T]CAAATTTAACAGCCT	25909
rs2047191	snp	A/G	0.386884	0.209196	intron-variant	AHCTF1	GRCh38.p7	1:246926788	ttgaacccgggaggc[A/G]gagattgcagtcagc	25909
rs2047192	snp	A/G	0.388964	0.20782	intron-variant	AHCTF1	GRCh38.p7	1:246926904	TATggccgggccgcg[A/G]tggcacacgcctgta	25909
rs2067915	snp	C/T	0.0588605	0.161139	intron-variant	AHCTF1	GRCh38.p7	1:246876670	GCAGTAGGAGTTACA[C/T]AGTACAAAGATCATT	25909
rs2067916	snp	A/G	0.329084	0.237162	intron-variant	AHCTF1	GRCh38.p7	1:246876646	GATCATTGTGTGGTA[A/G]AGGAAGACGTAGAGG	25909
rs2172796	snp	A/G	0.460702	0.134554	intron-variant	AHCTF1	GRCh38.p7	1:246924316	GCATTTCATACAATA[A/G]TCTCTATGAATTCTT	25909
rs2379094	snp	A/C	0.0652144	0.168387	intron-variant	AHCTF1	GRCh38.p7	1:246866902	TAATCTTGGGTAGCT[A/C]ATTGAAGCTTTCTTC	25909
rs2379188	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246908322	TTTTTTTTTTTTTTG[G/T]ATCCCTGTGAATTTT	25909
rs2493606	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246923325	gaggctgaggcatga[A/G]aactgcttgaaccta	25909
rs2642975	snp	A/T	0.4628	0.13121	intron-variant	AHCTF1	GRCh38.p7	1:246928884	TTTCAGAAATTTCTT[A/T]CCAACTTAATTCAAA	25909
rs2642976	snp	C/T	0.448836	0.15154	intron-variant	AHCTF1	GRCh38.p7	1:246929012	CTAGAAAAGGAGATA[C/T]ATAGTCAATTATCAG	25909
rs2642977	snp	C/T	0.462144	0.132269	intron-variant	AHCTF1	GRCh38.p7	1:246929076	TAGAGGTACATATGC[C/T]GTGAGATCCCAGTAA	25909
rs2642984	snp	G/T	0.474453	0.110094	intron-variant	AHCTF1	GRCh38.p7	1:246881390	GTGTCCTGAATAATT[G/T]TTTTTCCTAGTCTGT	25909
rs2642985	snp	A/T	0.0941369	0.195465	intron-variant	AHCTF1	GRCh38.p7	1:246880645	TCATAAATTAAGTTT[A/T]TCTTACTCCTGCTAG	25909
rs2642986	snp	C/T	0.116488	0.211364	intron-variant	AHCTF1	GRCh38.p7	1:246874984	GTTTCTTCCTAAACC[C/T]CATGTAAAATATTAG	25909
rs2642990	snp	C/T	0.491245	0.0655821	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246885532	TGAAGGATAACATCG[C/T]TACCACTGGACACTG	25909
rs2642991	snp	A/G	0.46014	0.13543	intron-variant	AHCTF1	GRCh38.p7	1:246886437	tacattgtattagat[A/G]ttataagtaatctac	25909
rs2800214	snp	C/T	0.461481	0.133325	intron-variant	AHCTF1	GRCh38.p7	1:246914396	CATGTGTTAAAAAGA[C/T]TAAAAGTTGTTTCAG	25909
rs2800215	snp	A/G	0.462472	0.13174	intron-variant	AHCTF1	GRCh38.p7	1:246928595	CTGGTTCAGTATTAA[A/G]CAAAACAAAATTCTT	25909
rs2800219	snp	A/C	0.460589	0.13473	intron-variant	AHCTF1	GRCh38.p7	1:246892125	AAGCCAAGAGTGAGA[A/C]TATGAACTCAAATCA	25909
rs2800220	snp	C/T	0.473909	0.111197	intron-variant	AHCTF1	GRCh38.p7	1:246894512	CGCGCCACTGCACTA[C/T]AGCCTGGCGACAGAG	25909
rs2800221	snp	C/T	0.460925	0.134204	intron-variant	AHCTF1	GRCh38.p7	1:246895403	TGAACAGACAATATG[C/T]GTTTGGGGTGTGTGT	25909
rs2800222	snp	C/G	0.434906	0.16979	intron-variant	AHCTF1	GRCh38.p7	1:246867935	TAAAATTTTTAGCTA[C/G]TATTACCACGTAATG	25909
rs2818888	snp	C/T	0.461037	0.134028	intron-variant	AHCTF1	GRCh38.p7	1:246925561	ctgatcatagcttac[C/T]gcaacctacaactcc	25909
rs2996543	snp	C/T	0.0115144	0.0749975	intron-variant	AHCTF1	GRCh38.p7	1:246927069	tgtagtcccaggtac[C/T]cgggaggctgaggag	25909
rs2996551	snp	G/T	0.00914312	0.0669923	downstream-variant-500B	AHCTF1	GRCh38.p7	1:246839056	TGCTACAAGGTCCGA[G/T]AATATCATTCATGCG	25909
rs2996552	snp	C/T	0.00835141	0.0640778	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839392	AGCTCTTTATTCATT[C/T]AACAAGTTCATTTAA	25909
rs3063899	in-del	-/TA			intron-variant	AHCTF1	GRCh38.p7	1:246899895	GAAACTTAGTATTTA[-/TA]TGTTTTATAAAGGAA	25909
rs3067058	in-del	-/ATTT			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933149	tttatttatttattt[-/ATTT]gagacggagtctcgc	25909
rs3104111	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246923215	aggtcaggagtttga[A/G]accagcctgactaac	25909
rs3122533	snp	A/T	0.00953873	0.0683987	intron-variant	AHCTF1	GRCh38.p7	1:246897148	GTGTAACTCTGTCTC[A/T]ACTAAAAATAAAAAA	25909
rs4011530	snp	C/T			synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850876	AAATGCAGATTTGAC[C/T]AATTTAGTGGGACAC	25909
rs4011531	in-del	-/TCTTA			intron-variant	AHCTF1	GRCh38.p7	1:246862720	AATTTAAGTAATTTA[-/TCTTA]CTAATTGGCACTTTT	25909
rs4130824	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246923824	CCCACACACATGAAG[A/G]ATGTTAGAATTCGA	25909
rs4971277	snp	A/G	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246927191	tcaaaaaaaaaaaaa[A/G]aaagaaaTAggccag	25909
rs4971284	snp	A/T	0.296619	0.245615	intron-variant	AHCTF1	GRCh38.p7	1:246843741	TATTAAAACATTTGT[A/T]AAAAAAAAAAGTATG	25909
rs4971285	snp	A/T	0.296619	0.245615	intron-variant	AHCTF1	GRCh38.p7	1:246843742	ATTAAAACATTTGTA[A/T]AAAAAAAAAGTATGT	25909
rs4971286	snp	A/G	0.344147	0.231595	intron-variant	AHCTF1	GRCh38.p7	1:246847141	aaaatacaaaaaaat[A/G]acccaggcgtggtgg	25909
rs4971287	snp	C/T	0.361894	0.223562	intron-variant	AHCTF1	GRCh38.p7	1:246868670	TTGGACATGTGCCTT[C/T]AACTGAAATAGGAGT	25909
rs4971289	snp	A/G	0.352504	0.228019	intron-variant	AHCTF1	GRCh38.p7	1:246869824	caggcatgaaaacac[A/G]acatccattctgtaa	25909
rs5021094	snp	G/T	0.426201	0.177351	intron-variant	AHCTF1	GRCh38.p7	1:246842858	AGACAAGGAATACTA[G/T]AGCCAAACACTGATG	25909
rs6426183	snp	C/T	0.303688	0.244167	intron-variant	AHCTF1	GRCh38.p7	1:246849422	ACAGGATTTAAGTCA[C/T]GTTAACCATACTGAA	25909
rs6426188	snp	A/C	0.463989	0.129263	intron-variant	AHCTF1	GRCh38.p7	1:246930108	AGCATAAAAAGAAAA[A/C]AAAAGTCTCAAAACT	25909
rs6659764	snp	C/G	0.0588605	0.161139	intron-variant	AHCTF1	GRCh38.p7	1:246889109	CAAACTACCATAAAG[C/G]CCAGCGTAGTGAAAA	25909
rs6672861	snp	C/T	0.298905	0.24517	intron-variant	AHCTF1	GRCh38.p7	1:246862436	agtgagccgagattg[C/T]gccactgcactccag	25909
rs6682729	snp	A/G	0.0364509	0.129988	intron-variant	AHCTF1	GRCh38.p7	1:246918524	atattggccagatgc[A/G]gaggctcacgccttt	25909
rs6685596	snp	A/G	0.312837	0.241974	intron-variant	AHCTF1	GRCh38.p7	1:246862467	cctgggcgacagagc[A/G]agactccgtctcaaa	25909
rs6686324	snp	C/T	0.0588605	0.161139	intron-variant	AHCTF1	GRCh38.p7	1:246902046	ttacagatggagaaa[C/T]agagctctgaaatgt	25909
rs6688227	snp	C/T	0.422	0.181428	intron-variant	AHCTF1	GRCh38.p7	1:246847432	CGATATACAGGAAAA[C/T]GTGAATGGTGATTCT	25909
rs6691158	snp	C/T	0.228253	0.249052	intron-variant	AHCTF1	GRCh38.p7	1:246869095	gtgatccgcccgcct[C/T]ggcctcccaaagtgc	25909
rs6694181	snp	C/T	0.0715223	0.175059	intron-variant	AHCTF1	GRCh38.p7	1:246869706	cctactgttgagaac[C/T]gttcagaaaaaaaaa	25909
rs6694693	snp	G/T	0.0115144	0.0749975	intron-variant	AHCTF1	GRCh38.p7	1:246924417	ATGCAAATTTGTGAT[G/T]TGCTCATTTCAGTAT	25909
rs6696656	snp	A/G	0.486984	0.079614	intron-variant	AHCTF1	GRCh38.p7	1:246922844	aaaaaatagccgggc[A/G]tggtggcaggcgcct	25909
rs6700546	snp	A/C	0.380138	0.213458	intron-variant	AHCTF1	GRCh38.p7	1:246847298	ccatctcaaaaaaaa[A/C]aaacaaacaaaaaaa	25909
rs7512439	snp	C/G	0.0652144	0.168387	intron-variant	AHCTF1	GRCh38.p7	1:246930291	gtaggcgcgcgacta[C/G]aggcgccaccaattc	25909
rs7516596	snp	C/G	0.0592355	0.161582	intron-variant	AHCTF1	GRCh38.p7	1:246926425	CCAGACTTCATCATG[C/G]TGCCTAGCACAAAGG	25909
rs7520969	snp	A/T	0.306679	0.24349	intron-variant	AHCTF1	GRCh38.p7	1:246845380	TAAAAAAAAGAAAAA[A/T]AGAGTTGATATCAGA	25909
rs7525627	snp	C/T	0.359364	0.22481	intron-variant	AHCTF1	GRCh38.p7	1:246856878	TTATGTATAAAGTAA[C/T]GAACCATTTATAATG	25909
rs7526386	snp	A/G	0.431177	0.172264	intron-variant	AHCTF1	GRCh38.p7	1:246858568	ggcacggaggctcat[A/G]cctgtaatcccagca	25909
rs7528980	snp	A/G	0.424503	0.179021	intron-variant	AHCTF1	GRCh38.p7	1:246845558	GCTACCTGAAAAAAC[A/G]ATTTATTTCACTTTT	25909
rs7529090	snp	A/G	0.429987	0.173507	intron-variant	AHCTF1	GRCh38.p7	1:246905930	TGTAACTGGTCCTAA[A/G]AGTCATATTCAATGC	25909
rs7530860	snp	A/G	0.429987	0.173507	intron-variant	AHCTF1	GRCh38.p7	1:246854882	TTCCAACATATCGGG[A/G]GAAATGGGCACAGAA	25909
rs7531694	snp	C/G	0.00953873	0.0683987	intron-variant	AHCTF1	GRCh38.p7	1:246906254	AGCCAGGTACTGCAG[C/G]TATTTCTTTAGGAGC	25909
rs7537256	snp	C/T	0.0592355	0.161582	intron-variant	AHCTF1	GRCh38.p7	1:246925939	gtgtggtggcgcctg[C/T]ctgtagtcccagcta	25909
rs7542895	snp	C/G	0.486398	0.0813386	intron-variant	AHCTF1	GRCh38.p7	1:246920627	tacaaaaaattagcc[C/G]agcgtggtggcgggc	25909
rs7543698	snp	A/G	0.0352966	0.128072	intron-variant	AHCTF1	GRCh38.p7	1:246915492	TCCCAAATGCTCCCT[A/G]TACTACTATTTTTCC	25909
rs7549408	snp	C/T	0.298905	0.24517	intron-variant	AHCTF1	GRCh38.p7	1:246845137	TCACAGTTCATGTTA[C/T]TTCAGCTACTGGGAT	25909
rs7549514	snp	G/T	0.433527	0.169758	intron-variant	AHCTF1	GRCh38.p7	1:246930163	TATTTTAGCAACAGG[G/T]TCTCGCTCTGTCACA	25909
rs7550035	snp	A/T	0.116838	0.211584	intron-variant	AHCTF1	GRCh38.p7	1:246870548	agacagaatctacAG[A/T]GTTGAAATGATAAAG	25909
rs7550911	snp	G/T	0.0592355	0.161582	intron-variant	AHCTF1	GRCh38.p7	1:246925740	atgggagaggacccc[G/T]catgaatgggttggt	25909
rs7551797	snp	C/T	0.330714	0.236612	intron-variant	AHCTF1	GRCh38.p7	1:246905483	gcctggacaacagag[C/T]gagactctgtctcca	25909
rs7551921	snp	C/G	0.403509	0.197319	intron-variant	AHCTF1	GRCh38.p7	1:246868988	tagctgggactacag[C/G]cgcccgccaccatgc	25909
rs7551928	snp	A/G	0.449091	0.151204	intron-variant	AHCTF1	GRCh38.p7	1:246869002	ggcgcccgccaccat[A/G]cctggctaacttttt	25909
rs7553684	snp	A/T	0.395818	0.203069	intron-variant	AHCTF1	GRCh38.p7	1:246902131	GGCTTAAAAAACCGA[A/T]GCAAAAAAAACTGCC	25909
rs7554747	snp	A/G	0.333491	0.235646	intron-variant	AHCTF1	GRCh38.p7	1:246869603	cccttaaaaatgatg[A/G]gaaatctactatgcc	25909
rs9729188	snp	C/T	0.0584853	0.160693	intron-variant	AHCTF1	GRCh38.p7	1:246907972	AAACACATTCAATTA[C/T]ATAATATTTAAAAAT	25909
rs9729306	snp	C/G	0.453331	0.145452	intron-variant	AHCTF1	GRCh38.p7	1:246882061	ggagtgcaatggcac[C/G]atctctgctcactgc	25909
rs9729316	snp	C/T	0.453453	0.145282	intron-variant	AHCTF1	GRCh38.p7	1:246882232	tcgatctcctgacct[C/T]gtgatccacccgcct	25909
rs9783081	snp	A/G	0.433673	0.1696	intron-variant	AHCTF1	GRCh38.p7	1:246853485	ATAAAACAGAAAAAG[A/G]TAAATTTCACATTTA	25909
rs9783101	snp	C/G	0.39979	0.200158	intron-variant	AHCTF1	GRCh38.p7	1:246854878	CCTCTTCCAACATAT[C/G]GGGAGAAATGGGCAC	25909
rs10157601	snp	C/T	0.0569829	0.158885	intron-variant	AHCTF1	GRCh38.p7	1:246898853	aacacttcgggaggc[C/T]gaggcaggcggatca	25909
rs10436931	snp	A/G	0.29278	0.246313	intron-variant	AHCTF1	GRCh38.p7	1:246893105	CATTATTCTCAAAGA[A/G]TAACAAAACTCAATT	25909
rs10558940	in-del	-/AA	0.438246	0.16451	intron-variant	AHCTF1	GRCh38.p7	1:246866499	TAACATATGTCCATT[-/AA]ACTACACTCTGTACT	25909
rs10571304	in-del	-/AAG	0.0825414	0.185628	intron-variant	AHCTF1	GRCh38.p7	1:246843080	CTCTCACTTTCTAAG[-/AAG]TAGACAACCAGAGAC	25909
rs10635304	in-del	-/TTTAC	0.430732	0.172731	intron-variant	AHCTF1	GRCh38.p7	1:246854962	TGATCGGCTTTTTAC[-/TTTAC]ATGTTAGACAATTCT	25909
rs10640263	in-del	-/GAG	0.460365	0.13508	intron-variant	AHCTF1	GRCh38.p7	1:246910784	GTCTTTTTCAGAGAA[-/GAG]GAGATTAGATTTTGC	25909
rs10657928	in-del	-/TATA/TATC/TATCTATC			intron-variant	AHCTF1	GRCh38.p7	1:246909079	ATCTATATATATCTA[-/TATA/TATC/TATCTATC]TATCTATCTATCTAT	25909
rs10666626	in-del	-/AAAATA/CAAATA	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246929411	ATAAAAATAAAAATA[-/AAAATA/CAAATA]CAGTGAAAACATTGG	25909
rs10682985	in-del	-/GGT/GTG	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246924869	AACCTAATATAAAGG[-/GGT/GTG]TGTGCATCAATAGGA	25909
rs10802450	snp	C/T	0.499954	0.00479211	intron-variant	AHCTF1	GRCh38.p7	1:246859779	GATGGGGTCTCCCTA[C/T]GTTGTCTAGGCTGGT	25909
rs10802451	snp	A/G	0.287085	0.247234	intron-variant	AHCTF1	GRCh38.p7	1:246864348	TTAAAAAGAGTTTGC[A/G]TCGTCCTCCTTCCCT	25909
rs10924861	snp	A/G	0.360842	0.224085	intron-variant	AHCTF1	GRCh38.p7	1:246865487	ATCAGGCTGCTAGAC[A/G]TTTCTTTTCTTCTAG	25909
rs10924862	snp	G/T	0.293807	0.246132	intron-variant	AHCTF1	GRCh38.p7	1:246872406	TGGCTAAATAAAAGG[G/T]ATACACCCTTGTCAC	25909
rs10924863	snp	A/G	0.347253	0.230308	intron-variant	AHCTF1	GRCh38.p7	1:246883476	CTTCTGATAAAAATG[A/G]AGTGTAAAGTATGCT	25909
rs10924865	snp	C/T	0.396	0.202938	intron-variant	AHCTF1	GRCh38.p7	1:246918602	AGAAGTTCGAGGCTG[C/T]GCCTCCAGTGAGCTA	25909
rs10924866	snp	C/T	0.325563	0.238307	intron-variant	AHCTF1	GRCh38.p7	1:246921569	CCTAATCAGAATCCC[C/T]CCAAAAATATAGTAC	25909
rs10924867	snp	A/G	0.325563	0.238307	intron-variant	AHCTF1	GRCh38.p7	1:246921651	GAGTCAGGAAGTCCA[A/G]TGAATCCTAGGAACT	25909
rs10924868	snp	A/G	0.340333	0.233109	intron-variant	AHCTF1	GRCh38.p7	1:246927978	GCACTCCAGCCTGGC[A/G]ACAGAGCAAGACTCC	25909
rs10924869	snp	A/G	0.336245	0.234652	intron-variant	AHCTF1	GRCh38.p7	1:246928077	AATCCCAAGGCAGGT[A/G]GATCACGAGGTCAGG	25909
rs10924871	snp	A/G	0.0569829	0.158885	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246931612	GCGCCGCCGCGGGCC[A/G]AGTCCACCGGGTCGC	25909
rs10924872	snp	C/T	0.100588	0.200439	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933569	ATGCCCAGCCTATTT[C/T]TATTTTTGTAGAGAC	25909
rs11340560	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246870740	AGGGTATAAAACCTC[-/A]AAAAAAAAAAAAAAA	25909
rs11370838	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246844821	TTTTTTTTTTTTTTT[-/T]AACTATAGGGCCCCC	25909
rs11396118	in-del	-/A	0.499793	0.0101816	intron-variant	AHCTF1	GRCh38.p7	1:246919703	CAAAAAAAAAAAAAA[-/A]TCCTCAAGAGAAGAA	25909
rs11436581	in-del	-/T	0.462582	0.131564	intron-variant	AHCTF1	GRCh38.p7	1:246892810	TAATTAAAAAAAAGA[-/T]TTTTTTTTTGGTTTT	25909
rs11576429	snp	C/T	0.343254	0.231956	intron-variant	AHCTF1	GRCh38.p7	1:246841927	cagagtagctgggac[C/T]acaggcacccaccac	25909
rs11580065	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246920812	taaaagcatccaggc[A/C]cggtgcctcacgcct	25909
rs11582097	snp	A/G	0.381113	0.21286	intron-variant	AHCTF1	GRCh38.p7	1:246871729	TTTTTGAGGCCTCCT[A/G]ACTGCAGACTATAAG	25909
rs11583611	snp	A/T	0.431325	0.172108	intron-variant	AHCTF1	GRCh38.p7	1:246877923	TACTGTTATTTATTT[A/T]TTTTTATTTTTTTTA	25909
rs11585265	snp	A/G	0.293551	0.246177	intron-variant	AHCTF1	GRCh38.p7	1:246903817	CACTCCAGCCTGGGC[A/G]ACAGAGCGAGACTCT	25909
rs11585741	snp	A/G	0.453331	0.145452	intron-variant	AHCTF1	GRCh38.p7	1:246881817	CACCCCAGCCTGGGT[A/G]ACAGAGCAAGGCTCC	25909
rs11800847	snp	G/T	0.00716266	0.059414	intron-variant	AHCTF1	GRCh38.p7	1:246858996	acttgggaggctgag[G/T]caagagaagaggttg	25909
rs11801219	snp	C/G	0.00716266	0.059414	intron-variant	AHCTF1	GRCh38.p7	1:246865259	AAGTGGCTCACCTGA[C/G]AATAACCAGAAAAGG	25909
rs11805223	snp	A/G	0.402277	0.198272	intron-variant	AHCTF1	GRCh38.p7	1:246894431	ACAAAAAAATTAGCC[A/G]AGCGTAGTGGCGGGC	25909
rs11806771	snp	C/T	0.350546	0.22889	intron-variant	AHCTF1	GRCh38.p7	1:246922839	tacaaaaaaaatagc[C/T]gggcgtggtggcagg	25909
rs12022495	snp	C/T	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246896702	gtacacttgaaatat[C/T]tgaactgcacggtgt	25909
rs12023594	snp	C/T	0.344226	0.231563	intron-variant	AHCTF1	GRCh38.p7	1:246898164	ATAGAAAGCTAATAA[C/T]GTGATCCAACCAAAA	25909
rs12023791	snp	C/G/T	0.00438332	0.0466095	intron-variant	AHCTF1	GRCh38.p7	1:246892926	actgggattacaagc[C/G/T]tgagccaccacaccT	25909
rs12024417	snp	C/T	0.0150606	0.0854603	intron-variant	AHCTF1	GRCh38.p7	1:246919601	acctgtagtctcacc[C/T]actcgggaggctgaa	25909
rs12029050	snp	C/T	0.336474	0.234568	intron-variant	AHCTF1	GRCh38.p7	1:246874801	CCAGACACATATCCC[C/T]GAACAACATTAAAAA	25909
rs12031687	snp	C/T	0.291235	0.246576	intron-variant	AHCTF1	GRCh38.p7	1:246841090	GAAAAACCTTAGGGA[C/T]TGCTTAGTGCTTTCA	25909
rs12032354	snp	A/C	0.338976	0.23363	intron-variant	AHCTF1	GRCh38.p7	1:246874715	ACAATACCAGCCATT[A/C]CAACCTATCCTGAGA	25909
rs12033144	snp	C/T	0.360421	0.224293	intron-variant	AHCTF1	GRCh38.p7	1:246912439	AGTGAGCAGGGATTA[C/T]GCCACTGCACTCCAG	25909
rs12033829	snp	C/T	0.378568	0.214407	intron-variant	AHCTF1	GRCh38.p7	1:246885076	GGCGCCCCTCCCTTT[C/T]ATTCAAGGTATTTAT	25909
rs12034769	snp	A/G	0.00716266	0.059414	intron-variant	AHCTF1	GRCh38.p7	1:246861600	CAAGACACACCCTCA[A/G]AAACATATAACTAGT	25909
rs12036689	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246926804	gagattgcagtcagc[C/T]gacactgcaccattg	25909
rs12037780	snp	A/G	0.318174	0.240525	intron-variant	AHCTF1	GRCh38.p7	1:246897921	GAGGTTGAGGCTACA[A/G]TGAGCCATGACCATG	25909
rs12048921	snp	C/T	0.292266	0.246401	intron-variant	AHCTF1	GRCh38.p7	1:246845535	TACATTCTATAACTC[C/T]CTTCTAGGCTACCTG	25909
rs12061420	snp	C/T	0.0592355	0.161582	intron-variant	AHCTF1	GRCh38.p7	1:246925126	GAAGTTAACACATTT[C/T]TCCTACTAAACTTAA	25909
rs12065654	snp	C/T	0.0592355	0.161582	intron-variant	AHCTF1	GRCh38.p7	1:246927674	TTTCCAAAGGCTAGA[C/T]AGGCAGAGCAGGAAC	25909
rs12067009	snp	C/T	0.0271762	0.113356	intron-variant	AHCTF1	GRCh38.p7	1:246874065	CTGACACAATCACCA[C/T]TAATATTTTATTATT	25909
rs12068067	snp	A/G	0.365439	0.221752	intron-variant	AHCTF1	GRCh38.p7	1:246862636	CAGAGCTTTTTATAC[A/G]TAAGTCTACGAAACA	25909
rs12072424	snp	A/T	0.0185938	0.0946107	intron-variant	AHCTF1	GRCh38.p7	1:246858812	ctcaaaaaaaaaaaa[A/T]aataaaTACAAATTT	25909
rs12081100	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246892415	aacctctacctccca[A/G]gttcaagggattctc	25909
rs12088097	snp	C/T	0.0607341	0.163335	intron-variant	AHCTF1	GRCh38.p7	1:246868031	gcagtggcatgatct[C/T]ggctcactgcaccct	25909
rs12093609	snp	C/G	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246847150	aaaaatgacccaggc[C/G]tggtggcaagcacct	25909
rs12093614	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246847181	gtaatcccagctact[G/T]gggaggctgaggcag	25909
rs12094061	snp	A/G	0.409891	0.192184	intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842237	CTTAATTTCCTTTTC[A/G]TAAAATTAAGGGTCT	25909
rs12096743	snp	A/C	0.0588605	0.161139	intron-variant	AHCTF1	GRCh38.p7	1:246894528	agcctggcgacagag[A/C]aagactcagtctcaa	25909
rs12097543	snp	G/T	0.0574049	0.161312	intron-variant	AHCTF1	GRCh38.p7	1:246855319	ACAAAAATGCTCATT[G/T]GATTAAAAAAAAAAT	25909
rs12121733	snp	C/G	0.308166	0.243139	intron-variant	AHCTF1	GRCh38.p7	1:246865910	CAAAAATCTATAGTG[C/G]TATTTAAAAAATTGA	25909
rs12123173	snp	C/T	0.0512217	0.151615	intron-variant	AHCTF1	GRCh38.p7	1:246853084	GTAAAAAATTAATTT[C/T]TTTTACATGAATTTC	25909
rs12126008	snp	A/G	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246927794	cggatcacaaggtca[A/G]gagacccagaccatc	25909
rs12126508	snp	A/T	0.157642	0.232314	intron-variant	AHCTF1	GRCh38.p7	1:246852495	TAGAATTTTTTTTTT[A/T]AAAAAACTAAGTCTT	25909
rs12127681	snp	A/C	0.29789	0.24537	intron-variant	AHCTF1	GRCh38.p7	1:246846583	ATCATCTCATTCTAG[A/C]AGGTGCCTATTTTTA	25909
rs12127941	snp	C/T	0.298398	0.245271	intron-variant	AHCTF1	GRCh38.p7	1:246841403	CAATTAGCAAAGATG[C/T]ACAGAATTTCACAAA	25909
rs12129503	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246918487	CAAAATAAAGAAAAA[C/G]TAAAATCTGGTTACa	25909
rs12131776	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246890853	TAAGGAGAAAAATAA[A/G]TGAGGTGGAAGAAAA	25909
rs12133947	snp	A/C	0.2776	0.248472	intron-variant	AHCTF1	GRCh38.p7	1:246852396	TTTTTATCCAAATTT[A/C]TATAAATAATTAGAA	25909
rs12134528	snp	C/T	0.19238	0.243269	intron-variant	AHCTF1	GRCh38.p7	1:246863902	TAGTTTGATTGTGAA[C/T]GCTAGATGCGTAAAT	25909
rs12239496	snp	C/T	0.00716266	0.059414	intron-variant	AHCTF1	GRCh38.p7	1:246848038	ATAGGTCTAACCACA[C/T]TTTTCTAACACTGTG	25909
rs12239497	snp	C/T	0.0850919	0.187897	intron-variant	AHCTF1	GRCh38.p7	1:246848110	AAATTTTCTGAGTGA[C/T]GAGGGGAGAGGAGGA	25909
rs12401831	snp	C/T	0.338523	0.233803	intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842560	gcactccagccttgg[C/T]gacagaccgagactc	25909
rs12401878	snp	C/T	0.343254	0.231956	intron-variant	AHCTF1	GRCh38.p7	1:246843012	AGTTTTATTTTTGAA[C/T]GTTTCCACTGTCTAC	25909
rs12409091	snp	C/T	0.324619	0.238604	intron-variant	AHCTF1	GRCh38.p7	1:246868945	TGCCTCCCGGGTTCA[C/T]GCCATTCTCCTGCCT	25909
rs12410563	snp	C/G	0.369481	0.219632	missense, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246842749	CTTTTGGCTTTCCCA[C/G]AGTTTCTACTGATTG	25909
rs12567737	snp	A/G	0.000798403	0.0199641	downstream-variant-500B	AHCTF1	GRCh38.p7	1:246839054	GTTGCTACAAGGTCC[A/G]AGAATATCATTCATG	25909
rs12691532	snp	C/G	0.338296	0.233889	intron-variant	AHCTF1	GRCh38.p7	1:246904560	GTTCAAAGGACAATG[C/G]GGAGTATGGGAAGGA	25909
rs12727818	snp	A/T	0.00716266	0.059414	intron-variant	AHCTF1	GRCh38.p7	1:246859748	gcccagctaattttt[A/T]tatattttttgtaga	25909
rs12727819	snp	A/T	0.00755907	0.0610114	intron-variant	AHCTF1	GRCh38.p7	1:246859749	cccagctaatttttt[A/T]atattttttgtagag	25909
rs12728345	snp	A/G	0.461259	0.133677	intron-variant	AHCTF1	GRCh38.p7	1:246869051	GGGTTTCACCATGTT[A/G]GCCAGGATGGTCTCG	25909
rs12728361	snp	A/G	0.372995	0.217652	intron-variant	AHCTF1	GRCh38.p7	1:246896958	CAGGGACAAAACAGA[A/G]ACGTCTGCTACTAAC	25909
rs12733729	snp	C/T			utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840096	TTTCCCTTTGTCAAA[C/T]CCTTTGATAAGGTTG	25909
rs12733852	snp	A/C			utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840136	AGTGAACCGGTCAAT[A/C]TAACCTGGATTAGTC	25909
rs12739487	snp	A/C	0.290201	0.246747	intron-variant	AHCTF1	GRCh38.p7	1:246899094	AACTCCGTCTCAAAA[A/C]GAGAAAAGTATTTTT	25909
rs12739603	snp	C/T	0.285519	0.247464	intron-variant	AHCTF1	GRCh38.p7	1:246899037	GAGGTTGCAATGAGC[C/T]GAGATGGTGTCACTG	25909
rs12748665	snp	A/C	0.373397	0.217424	intron-variant	AHCTF1	GRCh38.p7	1:246875954	TAGCGAAAGTAGCTA[A/C]ATTTAAGGTGGTTTC	25909
rs12752855	snp	C/T	0.371987	0.218218	intron-variant	AHCTF1	GRCh38.p7	1:246880159	GAATTCACTGTGTCA[C/T]CATTCTTAGCTCTTA	25909
rs13374054	snp	A/G	0.0241296	0.107157	intron-variant	AHCTF1	GRCh38.p7	1:246864132	CTGTAATCAGAATGC[A/G]CATTTATTGAGTTAT	25909
rs13375572	snp	C/G	0.0715223	0.175059	intron-variant	AHCTF1	GRCh38.p7	1:246858886	AATGCTATGAACATT[C/G]TTTTAACAGCTACCA	25909
rs28665436	snp	C/T	0.303187	0.244277	intron-variant	AHCTF1	GRCh38.p7	1:246848490	ACAGGCGTGAGCCAC[C/T]GTGACCGGCCAAGTC	25909
rs28805059	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246909111	TATCTATCTATCTAT[C/T]TATATATATATAAAA	25909
rs28833901	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246909115	TATCTATCTATTTAT[A/T]TATATATAAAATTCA	25909
rs34004609	in-del	-/G			frameshift-variant, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877054	CTGAACGCTGGCACT[-/G]GGACTGCAAAAATTT	25909
rs34044345	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246923145	ATAGGCTGGGCACGG[G/T]GGCCCATGCCTGTAA	25909
rs34071076	in-del	-/A	0.337386	0.23423	intron-variant	AHCTF1	GRCh38.p7	1:246877549	AAAAGCAAAGTAGAC[-/A]AAAAATTCAAAGAAG	25909
rs34076616	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246872097	CCCAAAAACCTAGGG[G/T]GGTCTCTAACTAAAT	25909
rs34085336	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246894183	TACTCCTGCCTGGGC[-/A]AAAAGTGAGACCATG	25909
rs34089730	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246909247	AACCTCGGCTCTACT[-/A]AAAAAAAAAAAAAAA	25909
rs34199129	in-del	-/T	0.457969	0.138741	intron-variant	AHCTF1	GRCh38.p7	1:246870076	TCTTTCATGAATAAC[-/T]TTTGAGGGCTTCAAG	25909
rs34313695	in-del	-/A	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246923004	AAAAAAAAAAAAAAA[-/A]GTATCAATAGTATTC	25909
rs34350306	in-del	-/C			intron-variant	AHCTF1	GRCh38.p7	1:246925314	CACAAAATCCAAAGT[-/C]CCAAAGGATAACACA	25909
rs34357403	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246878108	TAAGTATAAGAATAT[A/C]CAGTAAGAGCCAGGC	25909
rs34394403	in-del	-/G			intron-variant	AHCTF1	GRCh38.p7	1:246891702	ATCCATCTAAGACAT[-/G]GGGAAATGTTATTCG	25909
rs34402133	in-del	-/CTG	0.343254	0.231956	intron-variant	AHCTF1	GRCh38.p7	1:246842867	TAGAGCCAAACACTG[-/CTG]ATGAATTCAAACTCG	25909
rs34409924	in-del	-/G			intron-variant	AHCTF1	GRCh38.p7	1:246877144	TGACAAGTTTACATC[-/G]GGTAAGTAATTACCT	25909
rs34429575	in-del	-/G			intron-variant	AHCTF1	GRCh38.p7	1:246897608	CTGTATAGCATGTTA[-/G]CTGTGCTGAATACTG	25909
rs34445530	in-del	-/TTTAC			intron-variant	AHCTF1	GRCh38.p7	1:246854963	TGGGTGATCGGCTTT[-/TTTAC]TTACATGTTAGACAA	25909
rs34452579	in-del	-/C			intron-variant	AHCTF1	GRCh38.p7	1:246880176	TTCTTAGCTCTTAAA[-/C]CACTGAAGCATGTAA	25909
rs34452861	in-del	-/G			intron-variant	AHCTF1	GRCh38.p7	1:246926826	CACCATTGCACTCCA[-/G]GCCTGGGCAACAAGA	25909
rs34452947	in-del	-/C			intron-variant	AHCTF1	GRCh38.p7	1:246856173	TGTCAAGTATTCTGG[-/C]AATATTTTCTATGAA	25909
rs34479116	in-del	-/A	0.365646	0.221644	intron-variant	AHCTF1	GRCh38.p7	1:246879839	TCCCCCAACCCCGCC[-/A]AAAAAAAAAGGGAGA	25909
rs34538067	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246871241	CAAACCATGACTCAG[-/T]ACATTAATGGTCTAG	25909
rs34554106	in-del	-/G	0.464841	0.127841	intron-variant	AHCTF1	GRCh38.p7	1:246904191	TTTTATAAAAATGTA[-/G]TCCTTTGAAATAATA	25909
rs34589744	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246842897	TCGCCAAATGCAAAA[-/A]TTGACTCCTTTTCTC	25909
rs34595959	in-del	-/G			intron-variant	AHCTF1	GRCh38.p7	1:246919912	TGGGAGGCCAAGGCA[-/G]GGAGGATCATGAGCT	25909
rs34617990	in-del	-/T	0.452719	0.146304	intron-variant	AHCTF1	GRCh38.p7	1:246903663	TGAGACCCCCCCCCC[-/T]CCGTCTCTGCTAAAT	25909
rs34620309	in-del	-/C			utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839386	TGTTTAGCTCTTTAT[-/C]TCATTTAACAAGTTC	25909
rs34642893	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246857124	AAGGAGGCAGTGCAC[-/T]TTATCTATATTCCAA	25909
rs34733396	in-del	-/CTT	0.347473	0.230215	intron-variant	AHCTF1	GRCh38.p7	1:246884325	CAATCTATTATTAAA[-/CTT]CTTTTCTTCTGCCTG	25909
rs34851364	in-del	-/A			downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838628	GGGGCGGGGGGAAGA[-/A]CCTCATATAAGGTCA	25909
rs34945773	in-del	-/AA	0.433673	0.1696	intron-variant	AHCTF1	GRCh38.p7	1:246865761	TAGTTTAAAGGTTCT[-/AA]GAGAAATCTTTTTAA	25909
rs34997839	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246908323	AATTCACAGGGATAC[-/A]AAAAAAAAAAAAAAA	25909
rs35004695	snp	C/T	0.0110026	0.07335	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246890046	GCATAACCTTGACAA[C/T]TGCACAGAATCATCT	25909
rs35044246	snp	C/T	0.294832	0.245947	intron-variant	AHCTF1	GRCh38.p7	1:246922731	CTCACGCCTGTAATC[C/T]CAGCACTTTGGGAGG	25909
rs35048146	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246890079	ATTTTTAAGAGTTGG[-/A]AAAAAAGCTGGTAAT	25909
rs35049875	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246896742	TCAATAAAGCTGATA[-/T]TTTTGAAAATCACTG	25909
rs35080388	in-del	-/C			intron-variant	AHCTF1	GRCh38.p7	1:246885919	GGCTGGGCACGGTGG[-/C]CTCACGCCTGTAATC	25909
rs35083660	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246895028	AGGCCTAATTCCTTT[-/A]AAAAAAAAAAAGGTC	25909
rs35110822	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246908724	AACCCAGTCTCTACT[-/A]AAAAAAAAAAAAAAA	25909
rs35198488	in-del	-/GAG			intron-variant	AHCTF1	GRCh38.p7	1:246910785	TCTTTTTCAGAGAAG[-/GAG]AGATTAGATTTTGCC	25909
rs35199871	in-del	-/A			frameshift-variant, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246898322	GGACCTGATTTCTTT[-/A]AAAAAAGTCAAAGTC	25909
rs35224472	in-del	-/G			intron-variant	AHCTF1	GRCh38.p7	1:246919502	CGGATCACAAGGTTA[-/G]GGAGATCAACACCAT	25909
rs35320501	in-del	-/T/TTT	0.332337	0.236052	intron-variant	AHCTF1	GRCh38.p7	1:246911479	TATCTATGAAGATTC[-/T/TTT]TTTTTTTTTTTTTTT	25909
rs35341079	in-del	-/A			frameshift-variant, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246913329	CACAGCTGCCACTCC[-/A]AAAAGCCATCGCAGA	25909
rs35358938	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246871800	GCAGTATAGCTACCT[-/A]AAAGGGTAGCAGTGG	25909
rs35468864	snp	A/G	0.0240643	0.107019	utr-variant-5-prime, upstream-variant-2KB, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246931635	CGGGTCGCCAGGCCA[A/G]GCGCGAGCTCCTCCC	25909
rs35494760	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246931003	TGTTTCCCAGGTAGG[-/A]AAAAGGAAGGCAAAG	25909
rs35511835	in-del	-/AT	0.38934	0.207568	intron-variant	AHCTF1	GRCh38.p7	1:246899894	ATTCCTTTATAAAAC[-/AT]ATAAATACTAAGTTT	25909
rs35564406	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246875363	GTCCTCCTTACTTAG[-/A]AAGCCAAATAATAAA	25909
rs35646153	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246847477	TATATACTTCTATTT[-/T]AGAGTTTTCAGTAAG	25909
rs35687457	in-del	-/A	0.499539	0.0151687	intron-variant	AHCTF1	GRCh38.p7	1:246928323	GCGAGACTCCGTCTC[-/A]AAAAAAAAAAAAAAA	25909
rs35716055	snp	A/G	0.297382	0.245469	intron-variant	AHCTF1	GRCh38.p7	1:246901296	CAGTGAGACGAGATC[A/G]TGCAAGTGCACTCCA	25909
rs35764773	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246876784	AGAATTACGTGGTAA[-/T]TACCCTGTTCCCAAT	25909
rs35779626	in-del	-/C			intron-variant	AHCTF1	GRCh38.p7	1:246866107	AGGCTATACTGTCTA[-/C]CCAGTAATGCAAACT	25909
rs35790559	in-del	-/T			frameshift-variant, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861174	ATTTCTTGATGCTCC[-/T]TTTCAGGGCTGTTCA	25909
rs35829086	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246886565	TGACAAGAAAAATGT[-/A]CTGTACATGTTCAGT	25909
rs35881796	in-del	-/CT	0.284995	0.247539	intron-variant	AHCTF1	GRCh38.p7	1:246889285	CTCTTCTTTTTTCCC[-/CT]GATTTCCTTTTCTAA	25909
rs35946200	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246917702	TGGGAAGATGGCTAC[-/T]GAAGCTTATATTCAG	25909
rs35982364	in-del	-/A	0.375399	0.216275	intron-variant	AHCTF1	GRCh38.p7	1:246926047	TGAGACCCTGTCTTT[-/A]AAAAAAAAAAAAAAA	25909
rs36028619	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246863323	GGAGAAATAAAGCTT[C/T]TGGGTTTCAATCCAG	25909
rs36098218	in-del	-/C			intron-variant	AHCTF1	GRCh38.p7	1:246899679	AGAATAGATAACAAA[-/C]CCTATTACACAGCAA	25909
rs36102148	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246868630	AAAAAAAAAAAAAAA[-/A]GTTATTCTTTGTGTT	25909
rs41267533	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246867405	GAGCACTGATAACAA[A/G]TGGATGAGATGGGAG	25909
rs41267535	snp	C/G	6.61299e-05	0.00574983	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246891803	TGATCTCTCGGGCTT[C/G]TGATGCAAAACAGCT	25909
rs41267537	snp	A/T	0.0310518	0.120672	intron-variant	AHCTF1	GRCh38.p7	1:246898438	GTAAAATTTAAAGAT[A/T]GCAAGTGGAAATTAT	25909
rs41267539	snp	G/T	0.000255395	0.0112975	intron-variant	AHCTF1	GRCh38.p7	1:246931091	GAACCTCACGGCTGA[G/T]CCCCGAGTCCAACTT	25909
rs41304040	snp	C/T	0.303688	0.244167	intron-variant	AHCTF1	GRCh38.p7	1:246861389	ATACCCATACTTTCT[C/T]TGTTGTTTTTACCCA	25909
rs41304042	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246860702	GTAAAGACAGGGCCT[C/T]GCTATGTTGACCAGG	25909
rs41304151	snp	A/G	0.0527352	0.153579	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861024	TTGGGCTTAGAGGCC[A/G]TGAAAACAGTCTCTT	25909
rs41304153	snp	A/G/T	0.0116509	0.0754312	intron-variant	AHCTF1	GRCh38.p7	1:246857660	TTAAACTTCTTTCTA[A/G/T]AAGTATTTGAATTTC	25909
rs41305967	snp	C/T	0.00688882	0.0582834	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861097	TCTCATCGGATGTGA[C/T]TGAAACACTGCTGTT	25909
rs41308156	snp	A/G	0.0241408	0.10718	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849901	CATCGAAAGTTCCTC[A/G]TTTGGCACTAAAATG	25909
rs41308162	snp	C/G	0.194867	0.243845	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246857783	CTCTGCTGCAACTAA[C/G]AGATCCTTTGTTTCT	25909
rs41308196	snp	C/T	0.0116064	0.0752892	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246860986	GTTCAGTTACATTAG[C/T]AGTTAGTGCAGTGGA	25909
rs41310593	snp	A/T	0.098322	0.19873	intron-variant	AHCTF1	GRCh38.p7	1:246857836	GTCATACAAATAAGA[A/T]TATTATTTATGCTAA	25909
rs55701948	snp	A/G	0.124491	0.216211	intron-variant	AHCTF1	GRCh38.p7	1:246879233	ATAGTGAGACCAAAC[A/G]TATTAAAACTACCAT	25909
rs55703892	snp	A/G	0.111224	0.207945	intron-variant	AHCTF1	GRCh38.p7	1:246875482	GCAGAGGCAGGGTTT[A/G]AGAGGAGTGACTCAT	25909
rs55727006	snp	C/T	0.350327	0.228986	intron-variant	AHCTF1	GRCh38.p7	1:246862229	CTCACGCCTGTAATC[C/T]CTGCACTTTGGGAGG	25909
rs55783683	snp	C/T	0.287867	0.247116	intron-variant	AHCTF1	GRCh38.p7	1:246852874	GGGACTATGGGCACC[C/T]GCCACAGCACCCACC	25909
rs55794479	snp	A/C/G	1.64784e-05	0.00287035	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849678	TGTTTGGTTCAGAAA[A/C/G]GTCCGGCAACAAGAT	25909
rs55889824	snp	C/T	0.435119	0.16802	intron-variant	AHCTF1	GRCh38.p7	1:246908995	CCCTCTCATTATTTA[C/T]AGTTTCACTCTCCAA	25909
rs55998210	in-del	-/AAA	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246909421	AAAAAAAAAAAAAAA[-/AAA]TTTGCATGCTGCTCT	25909
rs56013703	in-del	-/CTAT/CTATCTAT	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246909110	TATCTATCTATCTAT[-/CTAT/CTATCTAT]TTATATATATATAAA	25909
rs56070865	snp	C/T	0.333722	0.235565	intron-variant	AHCTF1	GRCh38.p7	1:246847499	TTCAGTAAGTAGGCA[C/T]GTATTGTTTTTGTTT	25909
rs56086758	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246854317	AAAAAAAAAAAAAAA[-/A]TCTGTACATACTTCT	25909
rs56196643	snp	A/G	0.0448719	0.142907	intron-variant	AHCTF1	GRCh38.p7	1:246868771	CAGAGCAGCCAATAA[A/G]AAAGTACCACGTGAT	25909
rs56224319	in-del	-/AAG/AG/G	0.330482	0.236691	intron-variant	AHCTF1	GRCh38.p7	1:246930598	TTTAAAAAAAAAAAA[-/AAG/AG/G]GGGGGGGTCTCGCCA	25909
rs56242683	snp	C/T	0.0437281	0.141251	intron-variant	AHCTF1	GRCh38.p7	1:246868543	AGAGGTGTGAGCCAC[C/T]GGCCTGGCCTACATT	25909
rs56248647	snp	C/T			utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839336	TGCATCCATGTTTAT[C/T]GTGCTACTTGCGCAA	25909
rs56280494	snp	C/T			utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839994	TCCTTCACAGCAATA[C/T]TATAAAAATTTGTTC	25909
rs56354817	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246893711	TCAACTTCATCATTT[C/T]TATCAATATGTTAAA	25909
rs56791006	in-del	-/CT	0.0584853	0.160693	intron-variant	AHCTF1	GRCh38.p7	1:246909435	AAAATTTGCATGCTG[-/CT]CTGAGTGGTATGATG	25909
rs56797342	in-del	-/C			intron-variant	AHCTF1	GRCh38.p7	1:246847317	CAAACAAAAAAAAAA[-/C]TGAAAATGCTCATGA	25909
rs56869109	snp	C/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246856179	AGTATTCTGGAATAT[C/T]TTCTATGAACTCAGT	25909
rs57125777	snp	A/C	0.35894	0.225016	intron-variant	AHCTF1	GRCh38.p7	1:246847306	AAAAAAAAAAACAAA[A/C]AAAAAAAAAACTGAA	25909
rs57201275	snp	G/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246860052	AGATCACGAGGTCAG[G/T]AGTTCGAGACCAGCC	25909
rs57374813	snp	A/T	0.00835141	0.0640778	intron-variant	AHCTF1	GRCh38.p7	1:246916886	TTTAAACTAGAAGTT[A/T]TGGCAGTTATAAAAT	25909
rs57594834	in-del	-/G			intron-variant	AHCTF1	GRCh38.p7	1:246860189	TGCTTGAACCTGGTT[-/G]GGGGGGGGGCGGAGG	25909
rs57811947	in-del	-/ATGT			intron-variant	AHCTF1	GRCh38.p7	1:246884657	TTTCTCACAGTTACT[-/ATGT]GAGACTGTAATAATC	25909
rs58110440	in-del	-/AT			intron-variant	AHCTF1	GRCh38.p7	1:246846746	CATATACATATATAT[-/AT]TTTTTGGGGGGATGG	25909
rs58227848	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246847316	CAAACAAAAAAAAAA[-/A]CTGAAAATGCTCATG	25909
rs58383973	snp	A/G	0.00835141	0.0640778	intron-variant	AHCTF1	GRCh38.p7	1:246915775	TTTTAAAAATTGAAT[A/G]GTAATGAATACATTT	25909
rs58495791	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246847116	ACATGGCGAAACCCT[A/G]TCTCTACTAAAAATA	25909
rs58579338	in-del	-/CTTC/CTTT/CTTTC	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246857966	TAACACTTTCTTCTT[-/CTTC/CTTT/CTTTC]TTTTTTTTTTTGAGA	25909
rs58965522	snp	C/T	0.0209421	0.100162	intron-variant	AHCTF1	GRCh38.p7	1:246899308	AACTGATACTACTAG[C/T]TGATAATCTCATAAA	25909
rs59221281	in-del	-/CTTA	0.37138	0.218556	intron-variant	AHCTF1	GRCh38.p7	1:246845965	TCTAGAACAACACAT[-/CTTA]CTTATTCCCTGGGTG	25909
rs59476689	snp	G/T	0.0711525	0.174681	intron-variant	AHCTF1	GRCh38.p7	1:246853660	ACAGAATTACATGAG[G/T]AACATGCAATCTGGG	25909
rs59841568	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246847129	CTGTCTCTACTAAAA[A/G]TACAAAAAAATGACC	25909
rs59904791	snp	A/T	0.402277	0.198272	intron-variant	AHCTF1	GRCh38.p7	1:246909724	AATCATAATGTGTGC[A/T]GGGTTCAGTACTAGC	25909
rs59918343	in-del	-/GTGAGCCGAGATTGCA			intron-variant	AHCTF1	GRCh38.p7	1:246854241	GAGGCGGAGCTTGCA[-/GTGAGCCGAGATTGCA]CCACTGCACTCTAGC	25909
rs59968897	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246902067	TCTGAAATGTTAAGC[A/C]ATTTGTCAAAGGTCA	25909
rs60722674	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246847115	AACATGGCGAAACCC[C/T]GTCTCTACTAAAAAT	25909
rs61210171	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246847226	CTCAGGAGGCGGAGG[C/T]TGCAGTGAGCCAAGA	25909
rs61226215	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246860197	CCTGGTTGGGGGGGG[C/G]GCGGAGGTTGCAGTG	25909
rs61465631	in-del	-/AAG			intron-variant	AHCTF1	GRCh38.p7	1:246923086	AGGAGAATGAAGAAG[-/AAG]TTATTTAATCAAATA	25909
rs61562715	in-del	-/CAAATTTCTATAAATAATTAGAAGAGTTGGTTTTTTATC			intron-variant	AHCTF1	GRCh38.p7	1:246852389	AGTTGGTTTTTTATC[lengthTooLong]TTAAAATTTATTACA	25909
rs61734008	snp	A/G	0.00585232	0.0537765	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246855759	GCTCTAATTGCAGGG[A/G]TGTAGGTTTCAACAG	25909
rs61734012	snp	C/T	0.0082332	0.0636303	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877269	CAACCTATTGCAATG[C/T]TGCCGCAAAAAATTC	25909
rs61853988	snp	G/T	0.343254	0.231956	intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842205	CTTGTAAATGCCCGA[G/T]AATCTTTTCTGATGA	25909
rs61853990	snp	A/C	0.311123	0.242413	intron-variant	AHCTF1	GRCh38.p7	1:246848866	AACAAACAACACAAA[A/C]CCCCTACATTTTGTT	25909
rs61853992	snp	A/C	0.5	0	intron-variant	AHCTF1	GRCh38.p7	1:246855115	CATGGGCTCTAGAGT[A/C]AGATAACAACTATGT	25909
rs61853993	snp	A/C	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246859169	ATGCTTACTAAGTAA[A/C]GATATCGTAGTCCAA	25909
rs61853994	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246860234	GATCACGCCACTGCA[C/T]TCCAGCCTGGGCAAC	25909
rs61853995	snp	A/G	0.293294	0.246223	intron-variant	AHCTF1	GRCh38.p7	1:246861905	TTTTTACTTGTCAGA[A/G]CTAATACATTCTTAT	25909
rs61853996	snp	C/T	0.5	0	intron-variant	AHCTF1	GRCh38.p7	1:246862255	GGAGGCAGAGGCAGG[C/T]GGATCACCAGGTCAG	25909
rs61853997	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246864818	GCAGTCCGCAGTCCG[A/G]CCTGGGCGACAGAGC	25909
rs61853998	snp	A/G	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246865762	TAGTTTAAAGGTTCT[A/G]AGAAATCTTTTTAAG	25909
rs61854016	snp	A/C	0.0437281	0.141251	intron-variant	AHCTF1	GRCh38.p7	1:246873535	CATCACAGTGAAGGG[A/C]AAGAATCCGTCCCAA	25909
rs61854017	snp	C/G	0.00478085	0.0486577	intron-variant	AHCTF1	GRCh38.p7	1:246876409	AGCCTTGATTCTTCA[C/G]AATTAATAAAAACAA	25909
rs61854018	snp	A/T	0.0383715	0.133092	intron-variant	AHCTF1	GRCh38.p7	1:246878194	CTTGAGCCTAGGAGT[A/T]CAAGACCAACCTGGG	25909
rs61854019	snp	A/C	0.5	0	intron-variant	AHCTF1	GRCh38.p7	1:246879838	GTTCCCCCAACCCCG[A/C]CAAAAAAAAAGGGAG	25909
rs61854020	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246887421	CTACGTATATATTTA[C/T]AATAGGTAGCAACAA	25909
rs61854021	snp	A/G	0.435407	0.167703	intron-variant	AHCTF1	GRCh38.p7	1:246892144	GAACTCAAATCATCT[A/G]TATCTAGAGCTTGTC	25909
rs61854022	snp	C/T	0.399968	0.200024	intron-variant	AHCTF1	GRCh38.p7	1:246894029	GGCAATATAGTGAGA[C/T]CATGTCTCTACAAAA	25909
rs61854023	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246894215	CTCAAAAAAAAAAAT[A/T]ACTTTTATCACTTTA	25909
rs61854024	snp	C/G/T	0.00442647	0.0468369	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246894702	AACCACTTTATTCCA[C/G/T]GTCCATTCAAGAACA	25909
rs61854025	snp	A/G	6.61441e-05	0.00575045	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246899491	AAATGAACAACTCCC[A/G]AGTTTAACAAACAAG	25909
rs61854028	snp	A/C	0.5	0	intron-variant	AHCTF1	GRCh38.p7	1:246912481	AGCGAGACGCCGTCT[A/C]CAAAAAAAAAAAACA	25909
rs61854029	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246915114	AGGCAGGTGGATCAC[A/G]AGGTCAAGAGATCGA	25909
rs61854030	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246915132	GTCAAGAGATCGAGA[C/G]CAGCCTGGCCAACAG	25909
rs61854031	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246915135	AAGAGATCGAGAGCA[G/T]CCTGGCCAACAGGGT	25909
rs61854043	snp	C/T	0.5	0	intron-variant	AHCTF1	GRCh38.p7	1:246919922	AAGGCAGGAGGATCA[C/T]GAGCTCAAGAGATCG	25909
rs61854044	snp	C/T	0.399611	0.200291	intron-variant	AHCTF1	GRCh38.p7	1:246922611	GTTGCCCATGATGGT[C/T]TTGAACTCCTGGGTT	25909
rs61854046	snp	C/T	0.0236746	0.106192	intron-variant	AHCTF1	GRCh38.p7	1:246926998	GCTAACAAGGTGAAA[C/T]CCCGTCTCTACTAAA	25909
rs61854047	snp	A/C	0.5	0	intron-variant, missense, utr-variant-5-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246931184	AGGACAGGCTCAGCA[A/C]GCCGGCCGCTTCCCT	25909
rs61854048	snp	C/T	0.343477	0.231866	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932175	TACAAAAAAATCGGG[C/T]CTCTCCGCCTCCGAG	25909
rs66554661	in-del	-/TATC			intron-variant	AHCTF1	GRCh38.p7	1:246909080	TCTATCTATCTATCT[-/TATC]ATCTATCTATTTATA	25909
rs66680824	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246908339	AAAAAAAAAAAAAAA[-/A]GAGGGGTGGGGCAAG	25909
rs66688318	in-del	-/A	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246872070	AAAAAAAAAAAAAAA[-/A]GAACCTAGATTCCCA	25909
rs66787763	in-del	-/AA			intron-variant	AHCTF1	GRCh38.p7	1:246865762	AGTTTAAAGGTTCTG[-/AA]AGAAATCTTTTTAAG	25909
rs67647433	in-del	-/A	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246909267	AAAAAAAAAAAAAAA[-/A]TTGGCCGCACATGGT	25909
rs68194249	in-del	-/AAA			intron-variant	AHCTF1	GRCh38.p7	1:246920166	AAAAAAAAAAAAAAA[-/AAA]AAGAAAAGAAGCTCA	25909
rs71566675	in-del	-/T	0.5	0	intron-variant	AHCTF1	GRCh38.p7	1:246884078	CAAATGAAAAAAAAA[-/T]TTATATGCTGGTTTC	25909
rs71638371	snp	A/C	0.5	0	intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842582	CCGAGACTCTGTCTC[A/C]AAAAAAATAAATAAA	25909
rs71638372	snp	A/C	0.5	0	intron-variant	AHCTF1	GRCh38.p7	1:246853997	ACTTTATTGGATACA[A/C]CAATAAAATATTAAA	25909
rs71680437	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246843741	TATTAAAACATTTGT[-/A]AAAAAAAAAAGTATG	25909
rs71792894	in-del	-/CTGT	0.0592355	0.161582	intron-variant	AHCTF1	GRCh38.p7	1:246857318	TGGAAGGAAATAAAA[-/CTGT]CTGTCATCTCCCCTG	25909
rs72504914	in-del	-/GGT	0.486266	0.0817214	intron-variant	AHCTF1	GRCh38.p7	1:246924868	TAACCTAATATAAAG[-/GGT]GTGTGCATCAATAGG	25909
rs72764688	snp	C/T	0.0146672	0.084371	intron-variant	AHCTF1	GRCh38.p7	1:246842167	CTTCAGCAGTGAAAT[C/T]TAACAATGCCAGGGA	25909
rs72764701	snp	C/T	0.021333	0.101051	intron-variant	AHCTF1	GRCh38.p7	1:246861790	GCTTAGCCAATGGCC[C/T]TAGTGTTTCTTTCAG	25909
rs72766505	snp	G/T	0.0475351	0.146656	intron-variant	AHCTF1	GRCh38.p7	1:246866972	CTACTAACAAGCAGG[G/T]AACAAGGAAAGTAAG	25909
rs72766509	snp	C/T	0.0283406	0.115616	intron-variant	AHCTF1	GRCh38.p7	1:246874175	CTCCAGTTTCTAGTA[C/T]ATACAAGTAGACATG	25909
rs72766511	snp	C/T	0.0221141	0.102801	intron-variant	AHCTF1	GRCh38.p7	1:246875342	TTGGAGAATCCTCCC[C/T]GGTGTTGTCCTCCTT	25909
rs72766524	snp	A/G	0.0310518	0.120672	intron-variant	AHCTF1	GRCh38.p7	1:246903111	ATAAAAATGCAACAC[A/G]TAATTCAGGGCCTTT	25909
rs72766526	snp	G/T	0.0221141	0.102801	intron-variant	AHCTF1	GRCh38.p7	1:246904274	GTAGGAGATATCTTA[G/T]GTAGCAAAGACTGAT	25909
rs72766533	snp	C/T	0.00318978	0.0398085	intron-variant	AHCTF1	GRCh38.p7	1:246910693	GAGCAGATTCTCTCA[C/T]TGTTATAAAGGGGGA	25909
rs72766547	snp	A/G	0.0182019	0.0936463	intron-variant	AHCTF1	GRCh38.p7	1:246926524	TTTAAGACTTTTCCA[A/G]TTTAAGCACACTACA	25909
rs72766549	snp	C/T	0.077417	0.180873	intron-variant	AHCTF1	GRCh38.p7	1:246927261	GCCAAGGCGGGAGAA[C/T]GGCTGAGGTCAGGAG	25909
rs72766552	snp	C/T	0.0551013	0.156571	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932588	GGGCTCCCAGACTTC[C/T]GGGGAAACGCTTTTT	25909
rs73140260	snp	C/T	0.0115144	0.0749975	intron-variant	AHCTF1	GRCh38.p7	1:246846564	TCTTATCCCTTCCAA[C/T]CCCATCATCTCATTC	25909
rs73142224	snp	A/G	0.0193772	0.0965046	intron-variant	AHCTF1	GRCh38.p7	1:246848589	TCAACTACATGGCTG[A/G]GTGTGGTGGCTCACG	25909
rs73142235	snp	A/G	0.0596104	0.162024	intron-variant	AHCTF1	GRCh38.p7	1:246856780	CTAGATTTCTCAGGC[A/G]TAAAGCATGTGATTT	25909
rs73142239	snp	C/T	0.0115144	0.0749975	intron-variant	AHCTF1	GRCh38.p7	1:246858495	AATCTAGCTTCACTA[C/T]AGAGTTTGTGTTGTA	25909
rs73142243	snp	G/T	0.0707826	0.174302	intron-variant	AHCTF1	GRCh38.p7	1:246859596	TCTTTTTGAGACAGG[G/T]TCTCATTCTCTTGCC	25909
rs73142251	snp	A/G	0.0603597	0.1629	intron-variant	AHCTF1	GRCh38.p7	1:246865571	CCAAACTTGGAAAAC[A/G]GTTTGCTCACTTTTA	25909
rs73142253	snp	C/T	0.00914312	0.0669923	intron-variant	AHCTF1	GRCh38.p7	1:246866848	TAAACGTGCTGCATC[C/T]GAAGCAACACAAGAC	25909
rs73142256	snp	A/G	0.0659589	0.169201	intron-variant	AHCTF1	GRCh38.p7	1:246867034	CCTGTCCACTAAGCA[A/G]TCTGAAATTATTGAA	25909
rs73144220	snp	A/G	0.0923359	0.194016	intron-variant	AHCTF1	GRCh38.p7	1:246892280	AAAATCCTTCTTTAA[A/G]TCAAATTCTAATTTG	25909
rs73144222	snp	C/T	0.0588605	0.161139	intron-variant	AHCTF1	GRCh38.p7	1:246894255	GAAATAATTTTCTTT[C/T]GGGACATCTTCAAAT	25909
rs73144246	snp	A/T	0.107694	0.205546	intron-variant	AHCTF1	GRCh38.p7	1:246912873	CTGGGTAATTTCATA[A/T]TGGCTGATAAGGCTC	25909
rs73146606	snp	A/C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246923857	TGAAGTGAAATGAAG[A/C/G]GGGAAATAGATAACC	25909
rs73146640	snp	A/G	0.0711525	0.174681	intron-variant	AHCTF1	GRCh38.p7	1:246930961	ACCCAAACCAAAACA[A/G]TCAACCAGTGGCAAA	25909
rs74152741	snp	C/T	0.0832709	0.186283	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839512	TTTTCAACAAGGCAG[C/T]GTAACATCCATCACT	25909
rs74152745	snp	A/T	0.0850919	0.187897	intron-variant	AHCTF1	GRCh38.p7	1:246852752	TCATGAAAACCAGTT[A/T]ATTTATTTATTTATT	25909
rs74152747	snp	A/G	0.0839998	0.186933	intron-variant	AHCTF1	GRCh38.p7	1:246852875	GGACTATGGGCACCC[A/G]CCACAGCACCCACCT	25909
rs74152748	snp	C/T	0.307176	0.243374	intron-variant	AHCTF1	GRCh38.p7	1:246855975	CATTCTGAACAATAA[C/T]ATAAAATTTAAAAGT	25909
rs74152750	snp	A/C	0.295599	0.245806	intron-variant	AHCTF1	GRCh38.p7	1:246861521	ATTTTCAGAAGACTA[A/C]AACACAGAACAGGCT	25909
rs74152755	snp	A/G	0.0341408	0.126114	intron-variant	AHCTF1	GRCh38.p7	1:246872698	AAGCTCCTTCCCATC[A/G]CACTATCATGGGTGC	25909
rs74152756	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246878906	GCTTCTCTTACTAGA[C/T]GGTGGAATCATTGTA	25909
rs74163500	in-del	-/AAA	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246878425	AAAAAAAAAAAAAAA[-/AAA]TACAGTGAAACAATG	25909
rs74163502	in-del	-/TTTTT	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246892302	TTTTTTTTTTTTTTT[-/TTTTT]GGAGACAGCATCTTG	25909
rs74163703	in-del	-/CACA	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246898661	ACACACACACACACA[-/CACA]GGAAAACTCCTGCAG	25909
rs74163704	in-del	-/TA	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246899897	CCTTTATAAAACATA[-/TA]AATACTAAATTTCTT	25909
rs74163708	in-del	-/T	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246911500	TTTTTTTTTTTTTTT[-/T]GAGATGGAGTTTCAC	25909
rs74391332	snp	A/G	0.00716266	0.059414	intron-variant	AHCTF1	GRCh38.p7	1:246858371	TATATACATTAACTT[A/G]CTTAATCCTCAACAT	25909
rs74400921	snp	C/T	0.00795532	0.062565	intron-variant	AHCTF1	GRCh38.p7	1:246882418	TTTAAAACCCATTAT[C/T]TGTAAATTAAAACTT	25909
rs74407469	snp	A/G	0.077417	0.180873	intron-variant	AHCTF1	GRCh38.p7	1:246927771	GTACTTTGGGAGGCC[A/G]AGGCTGGCGGATCAC	25909
rs74456165	in-del	-/GTGT			intron-variant	AHCTF1	GRCh38.p7	1:246923741	TGTGTGCGTGCATGC[-/GTGT]GTGTGTGTGTGCGCG	25909
rs74473498	snp	C/T	0.0252325	0.109451	intron-variant	AHCTF1	GRCh38.p7	1:246909375	TGAGCCGAGATTGCG[C/T]CACTGCACTCCAGCC	25909
rs74564494	snp	C/T	0.0821764	0.185298	intron-variant	AHCTF1	GRCh38.p7	1:246868122	CATGGCCACCAAGCC[C/T]GGCTAATTTTTTTTT	25909
rs74715704	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246929491	AGTATTTAAAAAAGG[A/G]AAGATGGCACTCCAG	25909
rs74784719	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246885031	TCAATGTTGTCAACT[A/G]GCAACAAATATAACT	25909
rs74824937	snp	A/C	0.0165278	0.0893908	intron-variant	AHCTF1	GRCh38.p7	1:246878743	AGCAAATGGTACCCA[A/C]TGTTGGCAGATCAGG	25909
rs74951703	snp	C/T	0.404733	0.196361	intron-variant	AHCTF1	GRCh38.p7	1:246910570	CTTGAATTTGGGTGA[C/T]GGGTTTATGGGAACT	25909
rs74997643	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246896481	TATTTGACCCATTTA[C/T]ATGAAATGTCTAGAA	25909
rs75044729	snp	A/C	0.0718919	0.175435	intron-variant	AHCTF1	GRCh38.p7	1:246847317	CAAACAAAAAAAAAA[A/C]TGAAAATGCTCATGA	25909
rs75046282	snp	A/G	0.00716266	0.059414	intron-variant	AHCTF1	GRCh38.p7	1:246857483	CTGCCTCAATTTACC[A/G]TGTCTCTGTATATTT	25909
rs75082575	snp	A/C	0.5	0	intron-variant	AHCTF1	GRCh38.p7	1:246872053	GAACTATTAATGACA[A/C]AAAAAAAAAAAAAAA	25909
rs75099827	snp	A/G	0.0588605	0.161139	intron-variant	AHCTF1	GRCh38.p7	1:246895389	TTCTCAAATGGTTCT[A/G]AACAGACAATATGCG	25909
rs75100583	snp	C/T	0.00597247	0.0543191	intron-variant	AHCTF1	GRCh38.p7	1:246865163	AGGTCACTCTCTTCT[C/T]GATTTCCTAATAAAC	25909
rs75147128	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246914416	AGTTGTTTCAGGCTG[G/T]AACTTACTACAGACA	25909
rs75175259	snp	A/C	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246848862	CTCAAACAAACAACA[A/C]AAACCCCCTACATTT	25909
rs75206771	snp	A/C/T	0.00795532	0.062565	intron-variant	AHCTF1	GRCh38.p7	1:246910612	CTAACTATCTGAAGA[A/C/T]GTCTGAAATCTTCAA	25909
rs75217552	snp	A/G	0.0279526	0.114869	intron-variant	AHCTF1	GRCh38.p7	1:246920164	AAAAAAAAAAAAAAA[A/G]AAAAGAAAAGAAGCT	25909
rs75244123	snp	A/G	0.0360663	0.129354	intron-variant	AHCTF1	GRCh38.p7	1:246868735	CAAATCTTCTAAGAA[A/G]GGCTTACATTTCTTG	25909
rs75306832	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246922421	CAGTATTCTGTTGCG[C/G]TTTTTTGGGTTGTTT	25909
rs75319018	snp	A/G	0.00874735	0.0655527	intron-variant	AHCTF1	GRCh38.p7	1:246870444	AAACAAAAACAGACT[A/G]AAGATGTGATGAATT	25909
rs75328986	snp	A/C	0.5	0	intron-variant	AHCTF1	GRCh38.p7	1:246847309	AAAAAAAACAAACAA[A/C]AAAAAAACTGAAAAT	25909
rs75330127	snp	A/G	0.0130921	0.0798413	intron-variant	AHCTF1	GRCh38.p7	1:246864997	ACTACAAGGTTTTCC[A/G]TAATGTCCTAGTCCC	25909
rs75378536	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246913109	TACCTTTTTTTTTTT[A/T]ATAGATAGGAAGATA	25909
rs75379026	snp	A/G	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246930598	GTTTAAAAAAAAAAA[A/G]GGGGGGGTCTCGCCA	25909
rs75404843	snp	C/T	0.00795532	0.062565	intron-variant	AHCTF1	GRCh38.p7	1:246844279	TAATCCTATATGTAA[C/T]CTGAGCTAGTCTGTG	25909
rs75524158	snp	A/C	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246881850	CTCAAAAAAAAAAAC[A/C]AAAAAAAAAAACAAA	25909
rs75564165	snp	A/C	0.0115144	0.0749975	intron-variant	AHCTF1	GRCh38.p7	1:246841297	AATACTGCTGGATTA[A/C]AAGGACGGGCCGAGT	25909
rs75744500	snp	C/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246851623	AATCAGACTTTCTCA[C/T]TCAGTCAAAATAACT	25909
rs75810554	snp	A/G	0.0252325	0.109451	intron-variant	AHCTF1	GRCh38.p7	1:246920747	TGCACTCCAGCCTGG[A/G]TGACAGAGCAAAACA	25909
rs75856586	snp	C/G	0.108048	0.20579	intron-variant	AHCTF1	GRCh38.p7	1:246901317	GTGCACTCCAGCCTG[C/G]GCGACAGTGAGACCC	25909
rs75856974	snp	C/T	0.0119091	0.0762411	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932840	ATACTAAGTAGTAAG[C/T]AAAAGGATTATAACA	25909
rs75891732	snp	C/T	0.0162398	0.0886349	intron-variant	AHCTF1	GRCh38.p7	1:246921693	GAAATGACTCAACAA[C/T]AGTAGTAGAAACCGC	25909
rs75942303	snp	A/G	0.00755907	0.0610114	intron-variant	AHCTF1	GRCh38.p7	1:246900901	AGAAGGACTTATCCA[A/G]TTATAAGGTAAAGAG	25909
rs76041954	snp	C/T	0.0629771	0.165899	intron-variant	AHCTF1	GRCh38.p7	1:246918682	TAAAAACAAATGACA[C/T]GCATCTGGGACCAAG	25909
rs76119999	snp	A/G	0.000185401	0.00962634	intron-variant	AHCTF1	GRCh38.p7	1:246907512	GCTATATGCAAAAAA[A/G]CTACCTATAATCAAA	25909
rs76213609	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246844858	AAAGCAATTATCAAT[A/G]TAATTACAGACGAGC	25909
rs76243060	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246922423	GTATTCTGTTGCGGT[G/T]TTTTGGGTTGTTTTT	25909
rs76250599	snp	C/T	0.5	0	intron-variant	AHCTF1	GRCh38.p7	1:246846979	CAGGCTGGTTGGATT[C/T]TGAAGAATATTTAAG	25909
rs76289950	snp	A/G	0.077417	0.180873	intron-variant	AHCTF1	GRCh38.p7	1:246928258	CAGTGAGCCGACATC[A/G]CGCCACTGCACTGTA	25909
rs76320352	snp	C/T	0.00993419	0.0697739	intron-variant	AHCTF1	GRCh38.p7	1:246917087	TCAGTAACTATCTGA[C/T]TTATGCATGTTTTTA	25909
rs76330535	snp	C/T	0.00636936	0.0560724	intron-variant	AHCTF1	GRCh38.p7	1:246855020	GTATTACCTTAATCA[C/T]GGGACAAAAACTAGT	25909
rs76348162	snp	C/T	0.00422183	0.0457503	intron-variant	AHCTF1	GRCh38.p7	1:246877144	CTGACAAGTTTACAT[C/T]GGTAAGTAATTACCT	25909
rs76526962	snp	A/T	0.0126979	0.078662	intron-variant	AHCTF1	GRCh38.p7	1:246906770	CAAATTAACTTAGCT[A/T]CAAAGTATCAATATA	25909
rs76539569	snp	A/G	0.0592355	0.161582	intron-variant	AHCTF1	GRCh38.p7	1:246919727	AAAAAATCCTCAAGA[A/G]AAGAATTTATTATCA	25909
rs76559260	in-del	-/TTATA	0.398714	0.200958	intron-variant	AHCTF1	GRCh38.p7	1:246875041	TGACAGGCCAACAAC[-/TTATA]TTATAGATAAACCAG	25909
rs76579350	in-del	-/GG	0.185788	0.241613	intron-variant	AHCTF1	GRCh38.p7	1:246860197	TGCTTGAACCTGGTT[-/GG]GGGGGGGGCGGAGGT	25909
rs76581262	snp	C/G	0.0618563	0.164627	intron-variant	AHCTF1	GRCh38.p7	1:246878604	TTCTGAAGATATACA[C/G]TAAGAATGGTAATGA	25909
rs76803337	in-del	-/ACAA			intron-variant	AHCTF1	GRCh38.p7	1:246853776	TTTAGTGTTTAACAA[-/ACAA]CAACAAAACATCAAT	25909
rs76890750	snp	A/G	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246903853	AAAAAAAAAAAAAAA[A/G]AGAATCACTTTTCAA	25909
rs77050095	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246929489	TGAGTATTTAAAAAA[A/G]GAAAGATGGCACTCC	25909
rs77068184	snp	A/C	0.5	0	intron-variant	AHCTF1	GRCh38.p7	1:246880570	GAGACTCCAGCTCAA[A/C]AAAAAAAAAAAAAAA	25909
rs77098280	snp	A/C	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246881848	GTCTCAAAAAAAAAA[A/C]CCAAAAAAAAAAACA	25909
rs77164384	snp	C/T	0.00438332	0.0466095	intron-variant	AHCTF1	GRCh38.p7	1:246908089	AATTTAGAACTACTA[C/T]CTAAATACCTTCCTT	25909
rs77210882	snp	G/T	0.0111196	0.0737302	intron-variant	AHCTF1	GRCh38.p7	1:246871029	GTAGCCTTGCTTAAG[G/T]TGCCAAACCTTTTGA	25909
rs77241159	snp	A/C	0.0134861	0.0810011	intron-variant	AHCTF1	GRCh38.p7	1:246849061	TTTGGGGAGAGATCA[A/C]CCCTGTTGAGAAGCT	25909
rs77251069	snp	G/T	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246892327	TTTTTTTTTTTTTTT[G/T]TTTTGGAGACAGCAT	25909
rs77279727	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246909613	ACAGCCTCAAAGCAC[A/G]AGAGTGGTCATGCTG	25909
rs77343062	snp	C/T	0.5	0	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933432	CCACCGCGCCCGGCC[C/T]TATTTTTTATTTTTT	25909
rs77346208	snp	A/C	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246903839	CGAGACTCTGTCTCA[A/C]AAAAAAAAAAAAAAA	25909
rs77485059	snp	A/C/T	0.00496204	0.0495627	intron-variant	AHCTF1	GRCh38.p7	1:246904050	TGAAACAGAAATTAA[A/C/T]GAAGACACGCTAAAT	25909
rs77522965	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246922420	ACAGTATTCTGTTGC[G/T]GTTTTTTGGGTTGTT	25909
rs77580733	in-del	-/AT			downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838827	GTTTCCCTTACTACT[-/AT]GATACTAAGTATCTG	25909
rs77627517	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246903795	GTGAGCCAAGATTGC[A/G]CCACTGCACTCCAGC	25909
rs77637621	snp	C/G	0.0592355	0.161582	intron-variant	AHCTF1	GRCh38.p7	1:246903179	ATTAGGTTCAGAAAA[C/G]TCGGTTCTAGAGACA	25909
rs77651496	snp	A/C/T			intron-variant	AHCTF1	GRCh38.p7	1:246903663	TGAGACCCCCCCCCC[A/C/T]CCGTCTCTGCTAAAT	25909
rs77666704	in-del	-/TT			intron-variant	AHCTF1	GRCh38.p7	1:246913108	ATACCTTTTTTTTTT[-/TT]ATAGATAGGAAGATA	25909
rs77746851	snp	C/T	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246857967	TAACACTTTCTTCTT[C/T]TTTTTTTTTTGAGAT	25909
rs77823298	snp	G/T	0.0205511	0.0992634	intron-variant	AHCTF1	GRCh38.p7	1:246862850	AATTATGTATCAGAA[G/T]CCTCTGAAGATTTCG	25909
rs77855548	snp	A/T	0.0588605	0.161139	intron-variant	AHCTF1	GRCh38.p7	1:246931052	TATTTTAAATCTCCT[A/T]GATCTGACCAATCGG	25909
rs77886043	snp	A/G	0.298651	0.24522	intron-variant	AHCTF1	GRCh38.p7	1:246848270	CCGGGCTGGAATACA[A/G]TGGCACAATCTTGGA	25909
rs77945508	snp	C/T	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246899128	AATTCTTTTTTTTTT[C/T]CCTGTGCCAGGCACT	25909
rs77966128	snp	C/T	0.0107246	0.0724382	intron-variant	AHCTF1	GRCh38.p7	1:246913587	CTATACTAGGAATTA[C/T]ACCATTACTCAATAC	25909
rs77970420	snp	A/G	0.0383715	0.133092	intron-variant	AHCTF1	GRCh38.p7	1:246856084	AGTAGAAATGAAATG[A/G]TTTTAAAATGCCTGT	25909
rs78105842	snp	A/T	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246912325	ACTAAAAAAAAAAAA[A/T]TACAAAAATTAGCCA	25909
rs78140908	snp	G/T	0.5	0	downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838988	TGTTTACCTTACTAC[G/T]ATGATACTAAGCACC	25909
rs78228621	snp	A/T	0.5	0	intron-variant	AHCTF1	GRCh38.p7	1:246894213	GTCTCAAAAAAAAAA[A/T]TTACTTTTATCACTT	25909
rs78465670	snp	C/T	0.0741063	0.177655	intron-variant	AHCTF1	GRCh38.p7	1:246868891	GCTCTGTCACCCAGG[C/T]TGGAGTGCAGTGGTG	25909
rs78487876	in-del	-/A	0.380919	0.21298	intron-variant	AHCTF1	GRCh38.p7	1:246929491	AGTATTTAAAAAAGG[-/A]AAGATGGCACTCCAG	25909
rs78510255	snp	A/G	0.0711525	0.174681	intron-variant	AHCTF1	GRCh38.p7	1:246931000	TCCTGTTTCCCAGGT[A/G]GGAAAAAGGAAGGCA	25909
rs78518852	snp	A/G	0.0383715	0.133092	intron-variant	AHCTF1	GRCh38.p7	1:246880876	ATGCTAGGAAGAACA[A/G]TAAGAAAATTAATTT	25909
rs78528395	in-del	-/AAAA	0.422158	0.181278	intron-variant	AHCTF1	GRCh38.p7	1:246848862	AACAAACAACACAAA[-/AAAA]CCCCCTACATTTTGT	25909
rs78531048	snp	A/G	0.0111196	0.0737302	intron-variant	AHCTF1	GRCh38.p7	1:246866922	ACCCAAGATTAATCT[A/G]TAATTAAGTATAAAA	25909
rs78575465	snp	A/C	0.0130921	0.0798413	intron-variant	AHCTF1	GRCh38.p7	1:246924850	CAAAACAGATCCAAA[A/C]GTCTAACCTAATATA	25909
rs78575640	snp	C/T	0.00517822	0.0506191	intron-variant	AHCTF1	GRCh38.p7	1:246851522	CAGGTTTTTGATGAC[C/T]CTTGGCTGTGTGCCT	25909
rs78646281	snp	A/G/T	0.00222436	0.0332756	intron-variant	AHCTF1	GRCh38.p7	1:246843966	TATCTGTATCTTTAT[A/G/T]TATGTGTGTATATAT	25909
rs78735541	snp	A/G	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246892332	TTTTTTTTTTTTTTT[A/G]GAGACAGCATCTTGC	25909
rs78735882	in-del	-/G/GGG/GTG			intron-variant	AHCTF1	GRCh38.p7	1:246924867	CTAACCTAATATAAA[-/G/GGG/GTG]GGTGTGCATCAATAG	25909
rs78752151	snp	A/G	0.000112581	0.00750185	intron-variant	AHCTF1	GRCh38.p7	1:246853334	ATTTTTTACATTTAA[A/G]CTGAAAAATAAATCC	25909
rs78818563	snp	A/G	0.0228947	0.104514	intron-variant	AHCTF1	GRCh38.p7	1:246871101	AGCACTTACCCAAAT[A/G]CTAGGACCACTAAAA	25909
rs78841711	snp	C/G	0.0356815	0.128715	intron-variant	AHCTF1	GRCh38.p7	1:246901626	CTCAAAAAAACAAAA[C/G]AAAAAAAAACAAAAC	25909
rs78844199	snp	C/T	0.444444	0.157135	intron-variant	AHCTF1	GRCh38.p7	1:246918875	CCACCACCATCCTCC[C/T]TACAGAAAAAAGAAA	25909
rs78905536	snp	A/C	0.5	0	intron-variant	AHCTF1	GRCh38.p7	1:246903837	AGCGAGACTCTGTCT[A/C]AAAAAAAAAAAAAAA	25909
rs78952582	snp	C/T	0.00398564	0.0444627	intron-variant	AHCTF1	GRCh38.p7	1:246928738	AGTTCAACAATTATA[C/T]TGCAACATGTACCAA	25909
rs78998889	snp	A/C	0.5	0	intron-variant	AHCTF1	GRCh38.p7	1:246862480	GCAAGACTCCGTCTC[A/C]AAAAAAAAAAAAAGT	25909
rs79021188	snp	A/C	0.5	0	intron-variant	AHCTF1	GRCh38.p7	1:246903840	GAGACTCTGTCTCAA[A/C]AAAAAAAAAAAAAAG	25909
rs79053065	snp	A/G	0.0126979	0.078662	intron-variant	AHCTF1	GRCh38.p7	1:246872984	AACTGTTTGGACCAT[A/G]TATTATTAAGCACTC	25909
rs79067339	snp	C/T	0.384209	0.210922	intron-variant	AHCTF1	GRCh38.p7	1:246929550	GAGTGGAAACATCTC[C/T]TCCACAGAATGAGTC	25909
rs79212166	snp	C/T	0.0422008	0.138995	intron-variant	AHCTF1	GRCh38.p7	1:246888948	TGACCCTAGTTAGCA[C/T]GATGAGAACTACAGA	25909
rs79322666	snp	A/C	0.5	0	intron-variant	AHCTF1	GRCh38.p7	1:246897819	GACCCTGTCTCTACC[A/C]AAAAAAAAAAGGGCT	25909
rs79326084	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246853683	AATCTGGGCTTTGAT[A/G]CAACTAGGATAAAGA	25909
rs79369288	snp	C/G	0.302435	0.244439	intron-variant	AHCTF1	GRCh38.p7	1:246858257	AGCCACTGCACCCGG[C/G]CAACACCTTCTTCTT	25909
rs79453909	snp	C/T	0.00914312	0.0669923	intron-variant	AHCTF1	GRCh38.p7	1:246853988	AGTATACAAACTTTA[C/T]TGGATACAACAATAA	25909
rs79531849	snp	C/G	0.000399281	0.0141238	intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842640	AGTAGGGTGGGGACA[C/G]AGCGAGACTGTCTCA	25909
rs79618149	snp	A/G	0.0573587	0.15934	intron-variant	AHCTF1	GRCh38.p7	1:246879592	ACTTTGGGAGACCGA[A/G]ACAGGTGGATCAATC	25909
rs79709415	snp	A/C	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246880567	AGTGAGACTCCAGCT[A/C]AAAAAAAAAAAAAAA	25909
rs79921823	snp	A/C	0.5	0	intron-variant	AHCTF1	GRCh38.p7	1:246930573	ATCAGTGAAAGCTCA[A/C]AAAAAAACAGTTTAA	25909
rs80056231	snp	G/T	0.0588605	0.161139	intron-variant	AHCTF1	GRCh38.p7	1:246931053	ATTTTAAATCTCCTT[G/T]ATCTGACCAATCGGG	25909
rs80110842	snp	A/G	0.165853	0.235413	intron-variant	AHCTF1	GRCh38.p7	1:246846044	CAGAAGGAAGTAAAA[A/G]TACCTACACTTTACT	25909
rs80123663	snp	A/G	0.00517822	0.0506191	intron-variant	AHCTF1	GRCh38.p7	1:246887012	CCTTCTTTAAACAGT[A/G]AGAAACCTGGGGTTC	25909
rs80176342	snp	A/C	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246928304	CGAGACTCCGTCTCA[A/C]AAAAAAAAAAAAAAA	25909
rs80176396	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246878082	AAACACCAGCAAAAA[C/T]TGCAAAAGATTAAGT	25909
rs80254162	snp	C/T	0.0126979	0.078662	intron-variant	AHCTF1	GRCh38.p7	1:246874308	ACATTAACTATTAAA[C/T]GTCTCTATCTTCAGA	25909
rs80260655	snp	A/C	0.5	0	intron-variant	AHCTF1	GRCh38.p7	1:246912483	CGAGACGCCGTCTCC[A/C]AAAAAAAAAAACAAA	25909
rs80329222	snp	A/C	0.277867	0.248442	intron-variant	AHCTF1	GRCh38.p7	1:246847296	CTCCATCTCAAAAAA[A/C]AAAAACAAACAAAAA	25909
rs111306674	snp	C/T	0.00517822	0.0506191	intron-variant	AHCTF1	GRCh38.p7	1:246910314	AACTGTCAAATGCAA[C/T]TAATGTGCAGACTGT	25909
rs111386980	in-del	-/TTCT/TTCTT/TTT	0.0596104	0.162024	intron-variant	AHCTF1	GRCh38.p7	1:246857964	GCTAACACTTTCTTC[-/TTCT/TTCTT/TTT]TTTTTTTTTTTTTGA	25909
rs111449141	snp	A/G	0.0182019	0.0936463	intron-variant	AHCTF1	GRCh38.p7	1:246875590	AAATTGACATGGCCA[A/G]CTTCACTGTGTCATC	25909
rs111487016	snp	A/G	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246922477	GTCACCCAGGCTGGA[A/G]TGCAGTGGCATTATC	25909
rs111550056	snp	A/G	0.5	0	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840775	TCTGATGACTTTACA[A/G]ATAGGTGTACATTAA	25909
rs111560082	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246889377	TAGATGTCCTGCACA[C/T]ACTATTTTATTTAGC	25909
rs111560856	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246862340	AAAAAATTAGGCAGG[C/T]GGGGTGGCGGGCGCC	25909
rs111561029	snp	A/C/G/T	7.93106e-05	0.00629682	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876175	TCTCCCGCAAACGAG[A/C/G/T]ATCACGATCATTCTA	25909
rs111574615	in-del	-/TACA	0.00716266	0.059414	intron-variant	AHCTF1	GRCh38.p7	1:246864517	AAATATCCATTCACC[-/TACA]TACATGTAATATATA	25909
rs111639204	snp	A/G	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246910784	TGTCTTTTTCAGAGA[A/G]GAGATTAGATTTTGC	25909
rs111704204	snp	A/T	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246866496	GTTTAACATATGTCC[A/T]TTAAACTACACTCTG	25909
rs111707702	snp	A/C	0.299411	0.245069	intron-variant	AHCTF1	GRCh38.p7	1:246847297	TCCATCTCAAAAAAA[A/C]AAAACAAACAAAAAA	25909
rs111713548	snp	A/T	0.0170251	0.090679	intron-variant	AHCTF1	GRCh38.p7	1:246886823	GAATAAAAGCTTTAT[A/T]AAAAACCTGATACCT	25909
rs111742720	snp	A/C	0.5	0	intron-variant	AHCTF1	GRCh38.p7	1:246919605	GTAGTCTCACCTACT[A/C]GGGAGGCTGAAGCAG	25909
rs111745834	snp	C/T	0.5	0	intron-variant	AHCTF1	GRCh38.p7	1:246899606	GACTGCAAGGCAAGG[C/T]GTCAAATTATTACAT	25909
rs111766571	snp	A/G	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246856396	CAACAAATAGTATTT[A/G]AAAGTAAATTCAATA	25909
rs111792872	snp	A/G	0.0315348	0.121544	intron-variant	AHCTF1	GRCh38.p7	1:246853057	AACCAAAACTGAAAG[A/G]CTGATAAAGAAGTAA	25909
rs111800702	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246856341	ATTCTAATCTGACCT[C/T]TCTCAAAACCCAATT	25909
rs111816815	snp	C/T	0.305685	0.24372	intron-variant	AHCTF1	GRCh38.p7	1:246847624	CCTGCCTCAGCCTCC[C/T]AAGTAGCTGGGACCA	25909
rs111820215	in-del	-/AAAAAT/AAAAATAAAAAT/AAAAT	0.515779	0.113064	intron-variant	AHCTF1	GRCh38.p7	1:246929410	GAGACTCCGTCTCAA[-/AAAAAT/AAAAATAAAAAT/AAAAT]AAAAATAAAAATAAA	25909
rs111824048	in-del	-/C	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246847309	AAAAAAACAAACAAA[-/C]AAAAAAACTGAAAAT	25909
rs111836067	snp	C/T	0.00676609	0.0577691	intron-variant	AHCTF1	GRCh38.p7	1:246844461	TGCAGTGGCTCACAA[C/T]TGTAATTCCAGCACT	25909
rs111878868	snp	C/T	0.0588605	0.161139	intron-variant	AHCTF1	GRCh38.p7	1:246894467	AATGGCGTTTGAACC[C/T]GGGAGGTGGAGCCTG	25909
rs111882101	snp	C/T	0.0232847	0.105357	intron-variant	AHCTF1	GRCh38.p7	1:246857998	GGAGTCTTGCTGTGT[C/T]GCCCAGGCTGGAGTG	25909
rs111892942	snp	A/G	0.0162398	0.0886349	intron-variant	AHCTF1	GRCh38.p7	1:246915245	TAAGGCAGGAGAATC[A/G]GTTGAACCCGGGACA	25909
rs111926413	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246929169	ATCCCAGCACTTTGG[C/T]TGGCCGAGGTGGGCA	25909
rs111966101	snp	A/G	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246846864	TCAAGCCATCCTCAC[A/G]CCTCAGCCTCCCAAG	25909
rs111980491	snp	C/T	0.252421	0.249988	intron-variant	AHCTF1	GRCh38.p7	1:246922809	AACACGGTGAAACCC[C/T]GTCTCTACTAAAAAT	25909
rs111986753	snp	A/G	0.243061	0.249904	intron-variant	AHCTF1	GRCh38.p7	1:246869046	AGACGGGGTTTCACC[A/G]TGTTGGCCAGGATGG	25909
rs112063894	snp	A/G	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246847915	CCACTCCCTGCCAAT[A/G]AAATGTTTTTCATTT	25909
rs112161335	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246868152	TTTTTTTTTTGAGAC[A/G]GAGTCTTGCTCTGTA	25909
rs112172408	snp	A/C			missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246916372	GTTGTGGACCACAAG[A/C]CAAGCAAGCAAGTCC	25909
rs112185957	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246922102	CAGTGGCTCACGCCT[G/T]TAATCCCAGCACTTT	25909
rs112266039	snp	C/G			intron-variant	AHCTF1	GRCh38.p7	1:246884196	AACTACAATTTTGAT[C/G]TCATAAAAAATCTCA	25909
rs112314625	in-del	-/T	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246890105	GTAATAATCCCCAAA[-/T]ATCTCAACAATACAT	25909
rs112327310	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246929890	AACCCCGTCTCTACT[A/G]AAAATACAAAAATTA	25909
rs112419962	snp	C/T	0.00993419	0.0697739	intron-variant	AHCTF1	GRCh38.p7	1:246869889	AATTTAGAAATACAT[C/T]TCATAAAGCTATAGC	25909
rs112432982	snp	C/T	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246881961	CTGGGATTACAGGCA[C/T]GAGCCACCGTGCCTG	25909
rs112436963	snp	A/C	0.000368942	0.013577	intron-variant	AHCTF1	GRCh38.p7	1:246887164	ATGTGTATTTTCTAA[A/C]ATTCTAGTAATTCAT	25909
rs112457059	snp	C/T	0.5	0	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932500	CGGAGTCTTGCTCTG[C/T]TGCCCAGGCTGGAGT	25909
rs112484454	in-del	-/A	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246906412	TGAAAATCCGTCTCT[-/A]AAAAAAAAAAAATAC	25909
rs112496509	snp	A/C	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246868127	CCACCAAGCCCGGCT[A/C]ATTTTTTTTTTTTTT	25909
rs112498177	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246861458	ATTCTCTTCTAGTAC[A/G]TAAAAGTTAATGGTG	25909
rs112511665	in-del	-/AGAA	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246919360	CTGAGTCTCTTACTC[-/AGAA]AGACAACATTTTCTT	25909
rs112539534	snp	A/G	0.0592355	0.161582	intron-variant	AHCTF1	GRCh38.p7	1:246926609	ACCTGTCATCCCAGC[A/G]CTTCGGAAAGCTGAG	25909
rs112542991	snp	A/G	0.300673	0.244811	intron-variant	AHCTF1	GRCh38.p7	1:246869087	CTGACCTCGTGATCC[A/G]CCCGCCTTGGCCTCC	25909
rs112588849	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246869585	ATTCCAAAATTCCTA[A/C]GGCCCTTAAAAATGA	25909
rs112595233	in-del	-/GTT	0.5	0	intron-variant	AHCTF1	GRCh38.p7	1:246885343	ATGAACACTGTATTT[-/GTT]TCAATCTGAATTTGA	25909
rs112612636	snp	C/G	0.5	0	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246888478	TCCTAACTGAGAAAC[C/G]AGTCCATCAATCATC	25909
rs112613828	snp	A/G	0.5	0	intron-variant	AHCTF1	GRCh38.p7	1:246920353	AGGAAAAATCAAGTA[A/G]ATTTGAAAAAATTTC	25909
rs112636616	snp	A/G	0.5	0	intron-variant	AHCTF1	GRCh38.p7	1:246915882	GAGTATCAGAACATT[A/G]CATGTCATTGCTATT	25909
rs112684992	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246875571	CTCTAGTGGAAGGAA[A/G]AGTAAATTGACATGG	25909
rs112724110	snp	C/T	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246912925	TTATTCCAGCATTTA[C/T]TTAAGAATAGATCTT	25909
rs112802786	snp	A/G	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246865766	TTAAAGGTTCTGAGA[A/G]ATCTTTTTAAGGTAT	25909
rs112820496	snp	A/G	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246925526	CTGGGAAGCTCAGGC[A/G]GAAGGATCTCTTAAG	25909
rs112848017	snp	C/T	0.0729998	0.176553	intron-variant	AHCTF1	GRCh38.p7	1:246869005	GCCCGCCACCATGCC[C/T]GGCTAACTTTTTCTA	25909
rs112857397	in-del	-/A	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246858800	GCGAAACTCTGTCTC[-/A]AAAAAAAAAAAAAAT	25909
rs112900823	snp	C/T	0.0107246	0.0724382	intron-variant	AHCTF1	GRCh38.p7	1:246926374	TCTTCCTCCCTTTCA[C/T]ATCCAAGCTTCTAGA	25909
rs112922854	snp	A/C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246914556	ATAAATACTAAAGCA[A/C/T]ATTCAATTCCTCAGT	25909
rs112927817	snp	A/C/T	0.0150695	0.0854849	intron-variant	AHCTF1	GRCh38.p7	1:246852494	ATAGAATTTTTTTTT[A/C/T]AAAAAAACTAAGTCT	25909
rs112933647	snp	A/G			intron-variant	AHCTF1	GRCh38.p7	1:246862804	AGTGTTTCAGAAAAA[A/G]AATTTCGTCACACGA	25909
rs112962898	in-del	-/CATTTCTAT	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246900600	TGATTCATCAAAACG[-/CATTTCTAT]CATTTGTATGTAAGA	25909
rs113045510	snp	A/G	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246897717	TGGGCAAGGTGGCTC[A/G]TGCCTGTAATTTCAG	25909
rs113069655	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246882800	ACGTAAAACAGCCAC[A/G]CCACAGTTGTGATGG	25909
rs113072253	snp	C/T	0.15698	0.23205	intron-variant	AHCTF1	GRCh38.p7	1:246869012	ACCATGCCTGGCTAA[C/T]TTTTTCTATTTTTAG	25909
rs113113662	snp	C/T	0.5	0	intron-variant, downstream-variant-500B	AHCTF1	GRCh38.p7	1:246842194	GGGAGCCAGTGCTTG[C/T]AAATGCCCGATAATC	25909
rs113177866	snp	A/G	0.5	0	intron-variant, utr-variant-5-prime, upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246931266	GTCGCGGCCCCGGCC[A/G]TCCGTAAAGGGACCC	25909
rs113177890	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246887649	TACAAGAAACAAAGA[C/T]ATACGCAAATTTCTA	25909
rs113198494	snp	A/G	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246902368	ATAGCAATCTGGAGA[A/G]CAAGAAATATCTAGT	25909
rs113201284	in-del	-/ACAAAAA	0.413748	0.188909	intron-variant	AHCTF1	GRCh38.p7	1:246848707	GCTGTCTCTACAAAT[-/ACAAAAA]ATTAGCCAGGCCTGT	25909
rs113211697	in-del	-/AT	0.5	0	intron-variant	AHCTF1	GRCh38.p7	1:246913110	ACCTTTTTTTTTTTT[-/AT]AGATAGGAAGATATC	25909
rs113318350	snp	C/T	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246847848	CACTTTTGGTGGTTA[C/T]TATATTCCTCCAGGT	25909
rs113330099	snp	C/T	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246900673	AATTTTAAGGCCTTA[C/T]TAAAAAGTAGTCACT	25909
rs113331100	snp	C/T	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246922054	TTAGACTTTGTTACA[C/T]ATCCATGTTGAAAAC	25909
rs113355017	snp	C/T	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246849062	TTGGGGAGAGATCAC[C/T]CCTGTTGAGAAGCTC	25909
rs113415158	snp	A/T	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246862652	TAAGTCTACGAAACA[A/T]AAAACTGCATCCATC	25909
rs113479413	snp	A/G	0.5	0	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867305	CCTCAGGCAGCTCTG[A/G]AGCTGGGAGCGAATA	25909
rs113480627	snp	A/G	0.5	0	intron-variant	AHCTF1	GRCh38.p7	1:246888376	ACTCTAAATGATAGC[A/G]CATTACTGCAAACCT	25909
rs113481315	snp	C/T	0.0150606	0.0854603	intron-variant	AHCTF1	GRCh38.p7	1:246906711	GGAGAAACAAATAAA[C/T]TGACAACTTAAGGGC	25909
rs113491073	in-del	-/A	0.5	0	intron-variant	AHCTF1	GRCh38.p7	1:246869712	TTGAGAACTGTTCAG[-/A]AAAAAAAAAAAAGTC	25909
rs113507273	snp	C/T	0.00993419	0.0697739	intron-variant	AHCTF1	GRCh38.p7	1:246875533	TAAAATGCTATCAAA[C/T]GGTATCACATGCTAC	25909
rs113530301	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246878214	ACCAACCTGGGCAAC[A/G]TGGTGAGACCCTAAC	25909
rs113530654	snp	C/G	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246903694	ATACAAAAAAATTAG[C/G]CAGGCGTGGTGGCGG	25909
rs113617117	snp	A/T	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246864597	CTAGACTGACTTGGG[A/T]GGCCGAGGCGGGTGG	25909
rs113656994	snp	C/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246869086	CCTGACCTCGTGATC[C/T]GCCCGCCTTGGCCTC	25909
rs113703954	snp	A/G	0.5	0	intron-variant	AHCTF1	GRCh38.p7	1:246846525	CTAGTAAGTGGCAGA[A/G]ATGAGAGATCTCAAT	25909
rs113715626	snp	C/T	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246896990	TTATTACCTATAGTT[C/T]ATAGAAGTTCTACCA	25909
rs113767945	snp	A/C/T	0.00152939	0.0276115	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853227	TCCTGGTTAAGCCTG[A/C/T]GCTCAGAGACAATAG	25909
rs113926329	snp	C/T	0.0166325	0.0896639	intron-variant	AHCTF1	GRCh38.p7	1:246927102	AGAATGGCGTGAACC[C/T]GGGAGGCGGAGCTTG	25909
rs113929196	snp	A/C	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246870978	TTCGAAAAACTAAAA[A/C]CAACCAAGCAAACAA	25909
rs113949515	snp	C/T	0.0103295	0.0711199	intron-variant	AHCTF1	GRCh38.p7	1:246869661	ATGAAAACACATCTG[C/T]TGACAGCATGGTTTA	25909
rs113957278	snp	C/T	0.0221141	0.102801	intron-variant	AHCTF1	GRCh38.p7	1:246868930	GCTCACTGCAAGTTC[C/T]GCCTCCCGGGTTCAC	25909
rs114053005	snp	A/G	0.0134861	0.0810011	intron-variant	AHCTF1	GRCh38.p7	1:246857556	ACTAAACTTCTTTTA[A/G]AACAGCCAACATTAC	25909
rs114060363	snp	A/G	0.0352966	0.128072	intron-variant	AHCTF1	GRCh38.p7	1:246919871	TCACAGAGCCAGGCA[A/G]GGTGGCTCATGCCTG	25909
rs114075145	snp	C/T	0.00318978	0.0398085	intron-variant	AHCTF1	GRCh38.p7	1:246893321	CTAGAAAGCGCCATG[C/T]CTTCCTAACGAACTT	25909
rs114114245	snp	C/T	0.00517822	0.0506191	intron-variant	AHCTF1	GRCh38.p7	1:246864245	AGTCAAGTATATTAA[C/T]GTAATCCAAAGTGCT	25909
rs114177404	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246875578	GGAAGGAAGAGTAAA[G/T]TGACATGGCCAACTT	25909
rs114248509	snp	C/T	0.00517822	0.0506191	intron-variant	AHCTF1	GRCh38.p7	1:246841515	TGTGCTTTTATTGAA[C/T]TCAACCATGCCTACT	25909
rs114316927	snp	A/C	0.00716266	0.059414	intron-variant	AHCTF1	GRCh38.p7	1:246853543	GAAACATTAATATGA[A/C]GACCAACTGCTTCAA	25909
rs114321813	snp	C/T	0.00478085	0.0486577	intron-variant	AHCTF1	GRCh38.p7	1:246876855	TAATGCTAGGCACAG[C/T]GGTTACCAAACTGTA	25909
rs114419014	snp	A/T	0.0566069	0.158427	intron-variant	AHCTF1	GRCh38.p7	1:246915476	TAAATCAAGTCTAGT[A/T]TCCCAAATGCTCCCT	25909
rs114426926	snp	C/T	0.0134861	0.0810011	intron-variant	AHCTF1	GRCh38.p7	1:246856378	TGCTAATTTTGAAAA[C/T]TACAACAAATAGTAT	25909
rs114433508	snp	A/G	0.0263992	0.111815	intron-variant	AHCTF1	GRCh38.p7	1:246908610	CAAGAATCTTAGGCC[A/G]GGCACGGTGGCTCAC	25909
rs114463419	snp	C/T	0.0566069	0.158427	intron-variant	AHCTF1	GRCh38.p7	1:246884714	ACTGATTAGAGAACA[C/T]TAAAATCTGCAAAAG	25909
rs114581620	snp	C/T	0.00318978	0.0398085	intron-variant	AHCTF1	GRCh38.p7	1:246848977	TGTTTAAAGCACCCC[C/T]TATTAAAATTTTATT	25909
rs114583882	snp	A/G	0.00716266	0.059414	intron-variant	AHCTF1	GRCh38.p7	1:246861607	CACCCTCAAAAACAT[A/G]TAACTAGTTAGAAAC	25909
rs114629300	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246884828	TGAGGATGCAATAGG[A/G]CAAATGCAATGACAA	25909
rs114659015	snp	A/G	0.0130921	0.0798413	intron-variant	AHCTF1	GRCh38.p7	1:246851791	AAAAAAATTAACCGG[A/G]AAAAACAGAAACAAC	25909
rs114666220	snp	C/T	0.00597247	0.0543191	intron-variant	AHCTF1	GRCh38.p7	1:246847509	AGGCATGTATTGTTT[C/T]TGTTTTGAGACGTGG	25909
rs114685372	snp	A/C	0.0236746	0.106192	intron-variant	AHCTF1	GRCh38.p7	1:246892755	TCCTAGCTCAGCCTC[A/C]CAAGGAGCTGGGACT	25909
rs114713118	snp	C/T	0.00318978	0.0398085	intron-variant	AHCTF1	GRCh38.p7	1:246897436	AATTGCATTTTTCCA[C/T]ATAGCCATGTGTTGC	25909
rs114716257	snp	A/G	0.00795532	0.062565	intron-variant	AHCTF1	GRCh38.p7	1:246869660	GATGAAAACACATCT[A/G]TTGACAGCATGGTTT	25909
rs114745981	snp	C/T	0.0168055	0.0901129	intron-variant	AHCTF1	GRCh38.p7	1:246872921	TATTAACCTAGAGAC[C/T]GGGTTCACCTTAAGA	25909
rs114757176	snp	C/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246869241	GTGTACTTACTCCAC[C/T]GACTAACTGTTCCCC	25909
rs114761567	snp	C/G	0.00795532	0.062565	intron-variant	AHCTF1	GRCh38.p7	1:246843230	GCCATTTACTCTGTT[C/G]GGAGGAATGCCTGTC	25909
rs114766348	snp	C/T	0.0130921	0.0798413	intron-variant	AHCTF1	GRCh38.p7	1:246895666	TTTGTCAGATCATCA[C/T]ACTGTGGGCAAACGT	25909
rs114777821	snp	G/T	0.0189856	0.0955633	intron-variant	AHCTF1	GRCh38.p7	1:246882299	ACCGCACCTGGCCTA[G/T]TATTACTTTTAAACA	25909
rs114778821	snp	A/G	0.000133236	0.00816089	intron-variant, missense, utr-variant-5-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246931144	TGTGGCCAGGCCCAA[A/G]CGCATGTGGAACACA	25909
rs114799044	snp	A/G	0.0566069	0.158427	intron-variant	AHCTF1	GRCh38.p7	1:246887820	AGGTAGTATCACGCT[A/G]ACTTATAATGTATTC	25909
rs114875965	snp	A/G	0.00438332	0.0466095	intron-variant	AHCTF1	GRCh38.p7	1:246848207	GGCTCAAACTGTATC[A/G]GTACAACAAGTCATC	25909
rs114876655	snp	C/T	0.0228335	0.104381	intron-variant	AHCTF1	GRCh38.p7	1:246899949	TAAGTTATCCATATG[C/T]TAACTAACAGTGAGA	25909
rs114881438	snp	A/G	0.00517822	0.0506191	intron-variant	AHCTF1	GRCh38.p7	1:246885791	AAGACTCGTTTAAAT[A/G]TAAGCTGAAAAAATC	25909
rs114916491	snp	C/G	0.0232847	0.105357	intron-variant	AHCTF1	GRCh38.p7	1:246921774	TATATATTACTGAAA[C/G]GATCCTTAACAAATA	25909
rs114984756	snp	A/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246883634	ACTTTCTAGCAACCC[A/T]GAAGTCATTCTCTAT	25909
rs115056064	snp	C/T	0.00318978	0.0398085	intron-variant	AHCTF1	GRCh38.p7	1:246902900	CAAGTCTTCTAAAGT[C/T]ATTTAACACAGAAGC	25909
rs115067616	snp	A/G	0.00795532	0.062565	intron-variant	AHCTF1	GRCh38.p7	1:246925879	ATTTGACACCAGCCT[A/G]GGCCACATGGCGAAA	25909
rs115119240	snp	A/G	0.0221141	0.102801	intron-variant	AHCTF1	GRCh38.p7	1:246882481	AATGAAAATTTAAAG[A/G]TACTTAGAACAGAAT	25909
rs115125951	snp	C/T	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246879440	ATTTTATTCTATAAA[C/T]TGGCACATGTGCATT	25909
rs115134012	snp	C/T	0.0115144	0.0749975	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932093	GGAATTTTCAAACTC[C/T]CGGTGAAAGAAGGAG	25909
rs115153060	snp	A/G	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246861629	GTTAGAAACAACACA[A/G]TATAAGGTAAAAACA	25909
rs115162821	snp	G/T	0.00716266	0.059414	intron-variant	AHCTF1	GRCh38.p7	1:246857188	TGACACTCTCACCAA[G/T]CTGCTTGACCATACT	25909
rs115165967	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246853768	TTAAAATCCTTTAGT[A/G]TTTAACAACAACAAA	25909
rs115370486	snp	A/T	0.000870038	0.020839	intron-variant	AHCTF1	GRCh38.p7	1:246899548	ATAATCCACTTACAT[A/T]TATTTAAAATGGCAT	25909
rs115371557	snp	C/G	0.0115144	0.0749975	intron-variant	AHCTF1	GRCh38.p7	1:246871074	AAAAGGCAGGGAACA[C/G]CTAGCCAGGGGAGCA	25909
rs115409554	snp	C/T	0.0926964	0.194308	intron-variant	AHCTF1	GRCh38.p7	1:246891487	AAAATTTATGAGTTC[C/T]TTGAATAAAAAATAC	25909
rs115444277	snp	C/T	0.00755907	0.0610114	intron-variant	AHCTF1	GRCh38.p7	1:246872454	AGGTGGTCAGAGCTT[C/T]ACTCAAAGACATCAT	25909
rs115498568	snp	A/G	0.00636936	0.0560724	downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838947	CATTTACCTTACTAT[A/G]ATACTAAGTATCTCT	25909
rs115531817	snp	C/G	0.00795532	0.062565	intron-variant	AHCTF1	GRCh38.p7	1:246888895	GGCAACAGAGACCCT[C/G]TCTCTAAAAACAGAG	25909
rs115533290	snp	A/G	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246878618	ACTAAGAATGGTAAT[A/G]ATCAATCTGGCAGTT	25909
rs115548322	snp	C/T	0.0566069	0.158427	intron-variant	AHCTF1	GRCh38.p7	1:246885846	TTGGCTCTCAGTATC[C/T]ACAGGATCCATATCT	25909
rs115550883	snp	A/G	0.00755907	0.0610114	intron-variant	AHCTF1	GRCh38.p7	1:246916481	TACATACAACTATAT[A/G]TTCATTACATAAAAC	25909
rs115586890	snp	C/T	0.00478085	0.0486577	intron-variant	AHCTF1	GRCh38.p7	1:246879498	AAAATGGCTAAAGGT[C/T]GAAACAACCTAAATG	25909
rs115677671	snp	A/G	0.00478085	0.0486577	intron-variant	AHCTF1	GRCh38.p7	1:246890864	ATAAGTGAGGTGGAA[A/G]AAAAGAAACCCAAAG	25909
rs115712743	snp	C/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246917702	CTGGGAAGATGGCTA[C/T]GAAGCTTATATTCAG	25909
rs115734630	snp	C/T	0.0205511	0.0992634	intron-variant	AHCTF1	GRCh38.p7	1:246843358	GGAATTTGCCTGAAT[C/T]ATTCTTGTGTAATTT	25909
rs115790254	snp	C/T	0.112983	0.209108	intron-variant	AHCTF1	GRCh38.p7	1:246922236	ATGGCAGTATGTGCC[C/T]GTAGTCCCAGCTACT	25909
rs115821836	snp	A/G	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246897301	TCTGGGCAACAGACC[A/G]AGATGCTGTCTCAAA	25909
rs115893430	snp	C/T	0.0360663	0.129354	intron-variant	AHCTF1	GRCh38.p7	1:246911069	TTTGTGCTATAAAGT[C/T]CAACTGCTTCCAATT	25909
rs115894030	snp	A/G	0.0197687	0.0974348	intron-variant	AHCTF1	GRCh38.p7	1:246882909	AGGAAACTCAGGCTC[A/G]GAGAGGATAACTGAA	25909
rs115894418	snp	A/G	0.00636936	0.0560724	intron-variant	AHCTF1	GRCh38.p7	1:246855342	AAAAAAATTCCATAT[A/G]TTTGTTAATTTCCCT	25909
rs115896994	snp	A/C	0.0566069	0.158427	intron-variant	AHCTF1	GRCh38.p7	1:246920210	AAAACACACAAGGAT[A/C]TCCAATAGCCAGCAG	25909
rs115920770	snp	C/T	0.00359113	0.0422217	intron-variant	AHCTF1	GRCh38.p7	1:246891774	TGATAAAACAAAGAG[C/T]GTACCTCTCTCAGTG	25909
rs115955887	snp	A/C	0.0368353	0.130617	intron-variant	AHCTF1	GRCh38.p7	1:246901635	ACAAAACAAAAAAAA[A/C]CAAAACACCCTGTCA	25909
rs116023399	snp	A/C	0.0111196	0.0737302	intron-variant	AHCTF1	GRCh38.p7	1:246912710	ATTTCATTTTCTTTG[A/C]ATCTGAATAGAATTA	25909
rs116044324	snp	A/C	0.0205511	0.0992634	intron-variant	AHCTF1	GRCh38.p7	1:246841566	ACTGTGTAACAAATA[A/C]ATCTGAAATGGAGTG	25909
rs116084353	snp	C/T	0.0788843	0.182262	intron-variant	AHCTF1	GRCh38.p7	1:246868794	CACGTGATGAATGAG[C/T]ACAGGTCTACCTCAT	25909
rs116104791	snp	C/G	0.00450318	0.0472368	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246890053	CTTGACAACTGCACA[C/G]AATCATCTAGATTTT	25909
rs116105455	snp	C/T	0.02016	0.0983543	intron-variant	AHCTF1	GRCh38.p7	1:246885396	GACTGACTTTACTGA[C/T]TTAACGGCCAATTGT	25909
rs116163292	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246857969	ACACTTTCTTCTTTT[C/T]TTTTTTTTGAGATGG	25909
rs116210906	snp	A/G	0.0345262	0.126772	intron-variant	AHCTF1	GRCh38.p7	1:246918023	GATACAAAACACATG[A/G]GATTTTTAATAAGGA	25909
rs116252630	snp	G/T	0.0232847	0.105357	intron-variant	AHCTF1	GRCh38.p7	1:246883266	ATGCAGCTTAACTTC[G/T]CGGACTTTTAGTTCA	25909
rs116293629	snp	A/G	0.0205511	0.0992634	downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838678	GGACCAGGTCTTTGC[A/G]TGTTGTTCTGTCAAG	25909
rs116306131	snp	C/T	0.0126979	0.078662	intron-variant	AHCTF1	GRCh38.p7	1:246920914	AACATGGTGAATCCA[C/T]ATCTCTACTAATAAT	25909
rs116315911	snp	G/T	0.0614824	0.164198	intron-variant	AHCTF1	GRCh38.p7	1:246897648	GTAACACAATATGAA[G/T]TATACGTGTATTTAA	25909
rs116412197	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246843566	ACTGCTGGTAAAATA[C/T]GATCAGTAGCATACC	25909
rs116430711	snp	G/T	0.0130921	0.0798413	intron-variant	AHCTF1	GRCh38.p7	1:246910731	TATCACACTGTCCTA[G/T]AACAGGGCCCCCACC	25909
rs116432106	snp	A/G	0.0115144	0.0749975	intron-variant	AHCTF1	GRCh38.p7	1:246919872	CACAGAGCCAGGCAG[A/G]GTGGCTCATGCCTGT	25909
rs116442883	snp	G/T	0.0349115	0.127424	intron-variant	AHCTF1	GRCh38.p7	1:246881276	AAATTAAAACTCTTA[G/T]GTACCTAATATTCAA	25909
rs116554934	snp	A/G	0.00478085	0.0486577	intron-variant	AHCTF1	GRCh38.p7	1:246907063	GTAACACAAACCTAG[A/G]TGAGATAGCCTACTA	25909
rs116630006	snp	A/C	0.00557542	0.0525036	intron-variant	AHCTF1	GRCh38.p7	1:246844395	TTTGAACTACTTGTT[A/C]CAGCCAAAGGAACAG	25909
rs116631711	snp	A/C	0.00795532	0.062565	intron-variant	AHCTF1	GRCh38.p7	1:246888055	ATCCTGGGTTAACAC[A/C]TCTTCTTAAGAAAAC	25909
rs116663150	snp	C/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246875817	GCACACTTAGAAGTA[C/T]AGTGTAAACATTATG	25909
rs116706274	snp	A/T	0.0170251	0.090679	intron-variant	AHCTF1	GRCh38.p7	1:246870458	TAAAGATGTGATGAA[A/T]TGCTGTAATCTCATG	25909
rs116721005	snp	A/G	0.0637235	0.166737	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840107	CAAACCCTTTGATAA[A/G]GTTGCAAGTGAGCAG	25909
rs116757531	snp	C/T	0.0236746	0.106192	intron-variant	AHCTF1	GRCh38.p7	1:246887622	TTTTTATGAAGTCAG[C/T]AGCTCAGTAAATACA	25909
rs116790263	snp	C/T	0.0205511	0.0992634	intron-variant	AHCTF1	GRCh38.p7	1:246859487	TGACTCACTGTTTGA[C/T]CTTCAACACCTAGAA	25909
rs116829747	snp	A/T	0.00795532	0.062565	intron-variant	AHCTF1	GRCh38.p7	1:246914867	GTGTCCATGTTTCCT[A/T]CTGTATGTGTTCTGA	25909
rs116830294	snp	A/G	0.0217236	0.101931	intron-variant	AHCTF1	GRCh38.p7	1:246867989	TTTTCTTTTAGACCA[A/G]TCTTGCTGTGTCACT	25909
rs116831211	snp	A/G	0.0360663	0.129354	intron-variant	AHCTF1	GRCh38.p7	1:246922415	TATCAACAGTATTCT[A/G]TTGCGGTTTTTTGGG	25909
rs117071018	snp	A/G	0.00314033	0.0395007	intron-variant	AHCTF1	GRCh38.p7	1:246890064	CACAGAATCATCTAG[A/G]TTTTTAAGAGTTGGA	25909
rs117354341	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246913561	TGTGATCTGAATAAT[A/G]AAATCTTCAGCTATA	25909
rs117423076	snp	G/T	0.0103295	0.0711199	intron-variant	AHCTF1	GRCh38.p7	1:246875159	TGACATAGTAACTAA[G/T]TCTACACAACTGGGA	25909
rs117448044	snp	A/G	0.00398564	0.0444627	intron-variant	AHCTF1	GRCh38.p7	1:246851633	TCTCATTCAGTCAAA[A/G]TAACTACATTTTGAG	25909
rs117483369	snp	C/T	0.00398564	0.0444627	intron-variant	AHCTF1	GRCh38.p7	1:246890483	GCTTTGCAAGTTATA[C/T]TCTAAACAAATATAG	25909
rs118117923	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246910432	ACCAAAGAAGTGTTA[C/T]TGGCATTATGATTAT	25909
rs118170973	snp	A/C	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246893070	AACAGCTGAACTACC[A/C]AGTTAAACCCCCAAC	25909
rs137861865	snp	A/G	0.00597247	0.0543191	intron-variant	AHCTF1	GRCh38.p7	1:246854366	GTTAGGAATCTACCC[A/G]AAAGAAATACTGACA	25909
rs137866967	snp	A/G	0.0126979	0.078662	intron-variant	AHCTF1	GRCh38.p7	1:246926582	AAATAGGGGCCAGGC[A/G]CGGTGGCTCACACCT	25909
rs137895470	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246858955	AATGTAGGCCAGGAC[C/T]GGTGGCGCATGCCTG	25909
rs137993091	snp	A/G	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246881120	CCACTGATTTCTAGT[A/G]ACTGGAGTAAAGTAA	25909
rs138011766	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246859710	TGTCCTGAGTAGCTA[A/G]GAATACAAGTGCATG	25909
rs138016612	snp	C/T	0.0130921	0.0798413	intron-variant	AHCTF1	GRCh38.p7	1:246928080	CCCAAGGCAGGTGGA[C/T]CACGAGGTCAGGAGA	25909
rs138056791	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246843298	GTTTTCATCTCTTCA[A/G]TGAAACTGTGTATCT	25909
rs138061071	snp	C/T	0.000480542	0.0154932	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851345	GTATCAAAATTGTAC[C/T]GAAGCTTAAGTGTTC	25909
rs138070764	snp	C/G	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246899281	TACGTCTTCCGGCAG[C/G]CTGTCATTAGTAACT	25909
rs138162884	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246870316	CAGTCTCAGCCACTC[A/G]GAAAGCTGAGGCAGG	25909
rs138167920	snp	C/G	0.0123036	0.0774623	intron-variant	AHCTF1	GRCh38.p7	1:246889734	TTCCAGAAGTGTGGT[C/G]AAGACTCTCAACACC	25909
rs138211146	in-del	-/GAA	0.079617	0.182947	intron-variant	AHCTF1	GRCh38.p7	1:246923079	CAACCAAAGGAGAAT[-/GAA]GAAGAAGTTATTTAA	25909
rs138217683	snp	C/T	0.0734246	0.176978	intron-variant, utr-variant-5-prime, upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246931368	TTATGTAACGAAGCC[C/T]GGCGCCCGCGAGCCT	25909
rs138283580	snp	C/T	5.35585e-05	0.00517459	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876099	TCAATGGCTAATTTT[C/T]GATGGACTCTAGGAA	25909
rs138284466	snp	C/T	0.000525028	0.0161938	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849617	GAAAGAAAAGTACCT[C/T]TTGCTTTCCTTGGAA	25909
rs138324049	snp	C/T	0.000181382	0.00952145	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246887273	CTTGGCCCCAAGAAA[C/T]GGCAAATACAGTTGG	25909
rs138354298	snp	C/T	0.0248432	0.108648	intron-variant	AHCTF1	GRCh38.p7	1:246868372	GTGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC	25909
rs138359914	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246847307	AAAAAAAAAACAAAC[-/A]AAAAAAAAAACTGAA	25909
rs138371767	snp	A/G	0.00636936	0.0560724	intron-variant	AHCTF1	GRCh38.p7	1:246899832	AGTTCAAAATAAGTC[A/G]TAATTCCTTTATAAA	25909
rs138430276	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246904246	TCAACTAAATCGATG[C/T]TGTTTGCATACTGTA	25909
rs138431892	snp	C/T	0.021333	0.101051	intron-variant	AHCTF1	GRCh38.p7	1:246862474	GACAGAGCAAGACTC[C/T]GTCTCAAAAAAAAAA	25909
rs138440333	snp	C/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246846967	CACTAAGTTGCCCAG[C/G]CTGGTTGGATTTTGA	25909
rs138503360	snp	A/C	0.403509	0.197319	intron-variant	AHCTF1	GRCh38.p7	1:246911610	TGCCTCAGCCTCCTG[A/C]GTAGCTGGGATTAGA	25909
rs138554302	snp	C/T	3.29484e-05	0.00405871	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867679	TTGAAAGGTGTGGTG[C/T]TATTTATAGGTTCTT	25909
rs138568854	snp	C/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246890235	TACAGAGGCACAAGT[C/G]AGAAAATGATCTGTC	25909
rs138639898	snp	G/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246904151	CAAAACTAAAATCAC[G/T]GTGAAAAATTTAGTT	25909
rs138652795	snp	C/G	1.64933e-05	0.00287165	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246855806	CAACACTGGTACCTT[C/G]GACTTCTGGGTGAAG	25909
rs138721438	snp	C/T	0.000115868	0.00761056	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876958	ATCGTACCATAACAT[C/T]AATCTTCAGAGTTTG	25909
rs138732353	snp	A/G	0.000680594	0.0184346	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902535	CTAACCTTCATTCAC[A/G]CCTTCCTCCCTGTCA	25909
rs138743895	in-del	-/T	0.0162968	0.0887851	intron-variant	AHCTF1	GRCh38.p7	1:246905528	ACAAAACAAAGTTTG[-/T]TATGAGACCTACCTA	25909
rs138747278	snp	G/T	0.00102165	0.0225784	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246855764	AATTGCAGGGGTGTA[G/T]GTTTCAACAGATGTT	25909
rs138771252	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246926105	ACTCTCATCATGTGA[A/G]TATCCTGCTCTCCCT	25909
rs138777471	snp	C/T	9.2302e-05	0.00679283	intron-variant	AHCTF1	GRCh38.p7	1:246867399	CACAAGGAGCACTGA[C/T]AACAAGTGGATGAGA	25909
rs138782084	snp	A/G	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246859372	CTCTCCCATTTACTA[A/G]TGTTCCCCTGGCCCT	25909
rs138785134	snp	A/G	0.00795532	0.062565	intron-variant	AHCTF1	GRCh38.p7	1:246928036	AATTAAATACTGTTC[A/G]GCCGGGTGCGGTGGC	25909
rs138811688	in-del	-/A	0.0123036	0.0774623	intron-variant	AHCTF1	GRCh38.p7	1:246866323	AAAGGGGACTTGCAG[-/A]AAAAAAAAATCCGAA	25909
rs138844491	snp	C/G	0.000154675	0.00879282	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850639	TCTGACATCAGAATA[C/G]ATGTTTTCAGAAGCT	25909
rs138879376	snp	C/T	0.00036318	0.0134706	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840899	CACTTCTGTAGTTTT[C/T]CTTGGTTTGCTCTTG	25909
rs138981192	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246900976	AGGAATAGAGTAAGA[C/G]ACATCAACAGGAGAA	25909
rs139002829	snp	A/G			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932002	GGGCGGAGAGGGAGG[A/G]GAGAACCGGCGGGAG	25909
rs139003299	snp	A/G	0.00755907	0.0610114	intron-variant	AHCTF1	GRCh38.p7	1:246869123	TGCTGGATTACAGGC[A/G]TGAGCCACCACGCCC	25909
rs139015537	in-del	-/AA			intron-variant	AHCTF1	GRCh38.p7	1:246864888	AAAAAAAAAAAAAAA[-/AA]GACTAGACTGACAAC	25909
rs139036231	snp	C/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246871490	AACCCTTTCAGAACT[C/G]TCAAGTTAACAAAGC	25909
rs139055275	snp	C/T	6.65812e-05	0.00576942	synonymous-codon, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246842732	CGTCCTGATTCGTTT[C/T]GCTTTTGGCTTTCCC	25909
rs139084142	snp	C/T	0.0225045	0.103662	intron-variant	AHCTF1	GRCh38.p7	1:246913522	ATAGATTTAAGACTA[C/T]AGAGTAAATTTGCAT	25909
rs139104475	in-del	-/ACA			intron-variant	AHCTF1	GRCh38.p7	1:246867903	TACACCCCCCCCCCC[-/ACA]CACACACACACACAC	25909
rs139118312	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246869259	CTAACTGTTCCCCCG[C/T]GTCTCTCCCTTTCCC	25909
rs139187692	snp	C/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246896396	AAAGGGGATGAAGTA[C/T]TGATACTTGCTATAA	25909
rs139195625	snp	G/T	0.0528381	0.153711	intron-variant	AHCTF1	GRCh38.p7	1:246918663	ACAGAGCAAAATCCA[G/T]TCTTAAAAACAAATG	25909
rs139206093	snp	A/T	0.00478085	0.0486577	intron-variant	AHCTF1	GRCh38.p7	1:246880791	ATCCATTGCCAACAT[A/T]TAACAAATGTTTTAA	25909
rs139209531	snp	C/T	0.0123036	0.0774623	intron-variant	AHCTF1	GRCh38.p7	1:246897689	GGTACAGTAAAAATA[C/T]ATTATTACAGGCTGG	25909
rs139268547	snp	C/T	0.140919	0.224948	intron-variant	AHCTF1	GRCh38.p7	1:246927144	GATCGTGCCACTGCA[C/T]TCCAGCCTGGGCGAC	25909
rs139301849	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246883249	TTGGGTGTTGGACTA[C/T]TATGCAGCTTAACTT	25909
rs139374451	snp	C/T	0.0551013	0.156571	intron-variant	AHCTF1	GRCh38.p7	1:246928996	TTAAGGAGTTTACAA[C/T]CTAGAAAAGGAGATA	25909
rs139376112	snp	A/G	9.88745e-05	0.00703047	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902618	TCGTCTGTCCCCTCA[A/G]AGGGAACATGCCACC	25909
rs139377503	snp	C/T	0.000131872	0.00811902	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851105	GCAATTTGTCCATGA[C/T]TATCATTTTCCCCAC	25909
rs139497693	in-del	-/ACACACACACACAG			intron-variant	AHCTF1	GRCh38.p7	1:246898652	CACACACACACACAC[-/ACACACACACACAG]GAAAACTCCTGCAGT	25909
rs139518980	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246906974	ACACAGCCATGTGTC[A/G]CTTAACAAAAGGGGA	25909
rs139521241	snp	C/T	0.00914312	0.0669923	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932974	AGTGTCTCGCTCTGT[C/T]GCCCAGGCTGGAGTG	25909
rs139538819	snp	G/T	0.00438332	0.0466095	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839145	TAAAGACATTTATAC[G/T]TAAGTACATACATTC	25909
rs139612779	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246877978	ACCGACAGGATTATC[C/T]TGAAGGTTCACTTGA	25909
rs139625395	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246844897	GTTTAACCAGTCTGC[C/T]GGAGTAAATCCCAGC	25909
rs139627532	snp	A/T	0.00318978	0.0398085	intron-variant	AHCTF1	GRCh38.p7	1:246920356	AAAAATCAAGTAGAT[A/T]TGAAAAAATTTCTAA	25909
rs139662726	snp	C/T	0.0414363	0.137845	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839395	TCTTTATTCATTTAA[C/T]AAGTTCATTTAAATA	25909
rs139666427	snp	C/T	0.0182019	0.0936463	intron-variant	AHCTF1	GRCh38.p7	1:246901468	TCTCTACTAAATATA[C/T]AAAAAATTAGCTGGG	25909
rs139675122	snp	C/T	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246862907	TAGCATGTAAATTTA[C/T]TTAGTAGAGATAATT	25909
rs139678494	snp	A/G	0.000989935	0.0222258	intron-variant	AHCTF1	GRCh38.p7	1:246888373	TAGACTCTAAATGAT[A/G]GCACATTACTGCAAA	25909
rs139700015	snp	C/T	0.000248363	0.0111409	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246877211	CCATCAAGCCCATTT[C/T]CTGACAGACTTCATA	25909
rs139736452	snp	A/G	0.000748509	0.0193312	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246862039	GAGGAGACCTTCCAG[A/G]TGATGGAGAGGGAGA	25909
rs139833065	snp	A/G	0.0205511	0.0992634	intron-variant	AHCTF1	GRCh38.p7	1:246858078	CATTCTCCTGCCTCC[A/G]CCCCCCGAGTAGCTG	25909
rs139851612	snp	G/T			intron-variant	AHCTF1	GRCh38.p7	1:246892864	TTGCTCAGGCTGGTC[G/T]TGAACTCCTGGCCTC	25909
rs139868397	snp	A/G	0.0225638	0.103792	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864080	CTCCGAACACTGAGA[A/G]GGCCGGGGGACAGGC	25909
rs139900720	snp	A/G	1.77043e-05	0.0029752	intron-variant	AHCTF1	GRCh38.p7	1:246849585	AGAGTGACTGAGATG[A/G]AAAACTGTTTTGCAG	25909
rs139905601	snp	A/C	0.00636936	0.0560724	intron-variant	AHCTF1	GRCh38.p7	1:246923440	ATAAATACATAAATA[A/C]ATACATAAAATAATT	25909
rs139947110	snp	G/T	9.90328e-05	0.00703609	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850247	GATTTATCATCTTGC[G/T]TATTTCCTGTATTTT	25909
rs140112899	snp	C/T	0.00597247	0.0543191	intron-variant	AHCTF1	GRCh38.p7	1:246868481	ACTGGTCTCAAACTC[C/T]GGGCCTCAAGTGATC	25909
rs140125283	in-del	-/TAAA	0.0569829	0.158885	intron-variant	AHCTF1	GRCh38.p7	1:246867151	ATTCATTTAATAATT[-/TAAA]AGTCTATAAAATGTT	25909
rs140191724	snp	C/T	0.00716266	0.059414	intron-variant	AHCTF1	GRCh38.p7	1:246892096	AAAAAGTGCTTTCAA[C/T]ATAAAACTAGCAAAA	25909
rs140249572	snp	A/G	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246889626	ATTCCCAGGTGATTC[A/G]GGTGTAAGAAACCTG	25909
rs140249736	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933063	ACCTCAGCCCTCCAA[A/G]TAGCTGGGACTATGG	25909
rs140260985	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869538	TGTTAGTGGTTAATG[C/T]AGCTGATGACTTTAA	25909
rs140268617	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246917147	GGACAAGGAGAAGCA[C/T]AGAGTAGCCGCACTG	25909
rs140283773	snp	A/G	0.0566069	0.158427	intron-variant	AHCTF1	GRCh38.p7	1:246894409	AACCCCGTCTCTACT[A/G]AAAAATACAAAAAAA	25909
rs140339459	snp	A/T	0.000329544	0.0128321	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851302	AGTGTCTTTGTTATC[A/T]GCTAAGTCACAAAAC	25909
rs140356512	in-del	-/AT			intron-variant	AHCTF1	GRCh38.p7	1:246846738	TATATATACATATAC[-/AT]ATATATATTTTTTGG	25909
rs140385845	snp	C/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246872498	CTTACTCCAACCAAT[C/T]CAGAGTGACAACAGA	25909
rs140397173	snp	G/T	0.00478085	0.0486577	intron-variant	AHCTF1	GRCh38.p7	1:246903079	AGAATCTGACAAAAG[G/T]CTATGAGACTTCGCC	25909
rs140421518	snp	A/G	0.0707826	0.174302	intron-variant	AHCTF1	GRCh38.p7	1:246929988	ACCTGGGAGACGGAG[A/G]TTGCAGTGAGCCAAG	25909
rs140466849	snp	C/T			missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246894677	GTCTGTCAAATTCCT[C/T]TTTTGTGAGAACCAC	25909
rs140505021	snp	C/T	0.00557542	0.0525036	intron-variant	AHCTF1	GRCh38.p7	1:246870141	AAAGAGCAAGAGAAC[C/T]AGAATGAGAAGCAGA	25909
rs140585119	snp	A/G	6.59435e-05	0.00574172	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851147	TTTTCTTCAGTTGCT[A/G]TGTTAGCTGCTTTAG	25909
rs140597337	snp	C/T	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246841312	CAAGGACGGGCCGAG[C/T]ACCAGTTGTCAGCCC	25909
rs140602750	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246921437	ACTTAATACTCAACA[A/G]AAACAAACTCAAAGG	25909
rs140609930	snp	C/T	0.00874735	0.0655527	intron-variant	AHCTF1	GRCh38.p7	1:246875932	TCCAAGGCATGCCTG[C/T]ATGTGTTAGCGAAAG	25909
rs140610300	snp	C/T	0	0	intron-variant	AHCTF1	GRCh38.p7	1:246914773	ATATTCTCTCTTCCA[C/T]ACACCAACCATGCAT	25909
rs140613290	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246913795	TTCAAGCCATAAAAT[C/G]ATTACGCATAAAACG	25909
rs140742999	snp	C/T	0.0566069	0.158427	intron-variant	AHCTF1	GRCh38.p7	1:246927820	CCATCCTGGCCAACA[C/T]GGTGAAACCCTGTCT	25909
rs140774292	snp	C/T	0.00755907	0.0610114	intron-variant	AHCTF1	GRCh38.p7	1:246885348	ACACTGTATTTTCAA[C/T]CTGAATTTGATGCAG	25909
rs140782802	snp	C/T	8.25144e-05	0.00642265	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246889993	TCAAACTTCTGTCGA[C/T]GACTGGTGTAGTAGT	25909
rs140803492	snp	C/T	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246891337	CTTTCACCTCAGCTA[C/T]ACTTTCATTTAGCTA	25909
rs140831558	snp	G/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246898117	CTACTTCACCTATTT[G/T]TGCAGAAATTATCTA	25909
rs140851502	snp	C/T	0.000127137	0.00797199	intron-variant	AHCTF1	GRCh38.p7	1:246931084	TGAGCTGGAACCTCA[C/T]GGCTGAGCCCCGAGT	25909
rs140913748	snp	C/T	0.000153988	0.00877328	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850300	TCTCAATTTTCTGAT[C/T]ATTCTGCTAGGACTT	25909
rs140999106	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246910135	CATCTATAACCAGAG[A/C]TAATTTAATTTGCAG	25909
rs141030289	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246928681	AAATACACAAATTCC[C/T]GCAGTAACTGAATTC	25909
rs141067633	snp	C/T	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246860327	TATTTCTCATAGCTA[C/T]TGGAAGGACTTTCAA	25909
rs141076402	in-del	-/TTG	0.0588605	0.161139	intron-variant	AHCTF1	GRCh38.p7	1:246885341	CCATGAACACTGTAT[-/TTG]TTTCAATCTGAATTT	25909
rs141097043	snp	A/C	0.0162398	0.0886349	intron-variant	AHCTF1	GRCh38.p7	1:246880302	GGGTGTGGTGGCTCA[A/C]GCCTGTAATCCCAGC	25909
rs141147858	in-del	-/T			intron-variant	AHCTF1	GRCh38.p7	1:246858662	GTGAAACCCCGCCTC[-/T]TAATAATACAAAAAT	25909
rs141212789	snp	C/T	0.00755907	0.0610114	downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838863	TTGTTTCCCTTACTA[C/T]GATACTAAGTATCTT	25909
rs141244743	snp	C/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246870519	TTACAGATAGGCAAA[C/T]AAGTGGTTTCTTGAG	25909
rs141246553	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246880994	AGACAGACTGAAAAC[C/G]CATCCTGTGGCAAAC	25909
rs141282276	snp	C/T	0.00398564	0.0444627	intron-variant	AHCTF1	GRCh38.p7	1:246895501	GAGTAAAAAAGGTAA[C/T]CCAAAAAGGTTACAT	25909
rs141292322	snp	C/T	0.0119091	0.0762411	intron-variant	AHCTF1	GRCh38.p7	1:246875024	TTGTTAAAACCATCT[C/T]CTGACAGGCCAACAA	25909
rs141296664	snp	C/G/T	0.00914312	0.0669923	intron-variant	AHCTF1	GRCh38.p7	1:246882286	ACAGGCATGAGCCAC[C/G/T]GCACCTGGCCTATTA	25909
rs141361259	snp	A/G	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246844135	TAAGCCAAATGTGTA[A/G]GACGATTGAATGCTT	25909
rs141409693	snp	A/C	0.00218216	0.0329609	splice-donor-variant	AHCTF1	GRCh38.p7	1:246867243	TTTAATAAACTCTTA[A/C]CTAGAAATTTTTTGT	25909
rs141440710	snp	A/C	0.00517822	0.0506191	intron-variant	AHCTF1	GRCh38.p7	1:246914955	ATTTACCTGAATGGC[A/C]ATAGTCTACTTGTTT	25909
rs141450027	snp	A/C	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861188	CTTTTCAGGGCTGTT[A/C]AGGAAAAAAGATGTG	25909
rs141575447	in-del	-/AA			intron-variant	AHCTF1	GRCh38.p7	1:246865760	ATAGTTTAAAGGTTC[-/AA]TGAGAAATCTTTTTA	25909
rs141588111	snp	C/G	0.00398564	0.0444627	intron-variant	AHCTF1	GRCh38.p7	1:246904932	TCTCCAAGTATATTT[C/G]AAGAATAAGAGAGCA	25909
rs141660666	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246899667	TATTTTCATCCTAAG[A/T]ATAGATAACAAACCT	25909
rs141670552	in-del	-/TATG	0.400147	0.19989	intron-variant	AHCTF1	GRCh38.p7	1:246884656	CTTTCTCACAGTTAC[-/TATG]TGAGACTGTAATAAT	25909
rs141689938	snp	A/G	0.0182019	0.0936463	intron-variant	AHCTF1	GRCh38.p7	1:246872246	AATTTGTACAAAATA[A/G]TACTCAGATCGGGCT	25909
rs141764038	snp	A/C/T	0.150992	0.238404	intron-variant	AHCTF1	GRCh38.p7	1:246922961	GCACTCTAGCCTGGG[A/C/T]GACAGAGCGAGACTC	25909
rs141791876	snp	A/T	0.00953873	0.0683987	intron-variant	AHCTF1	GRCh38.p7	1:246926909	CCGGGCCGCGGTGGC[A/T]CACGCCTGTAATCCC	25909
rs141831225	snp	A/G	0.000347553	0.0131778	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246894703	ACCACTTTATTCCAC[A/G]TCCATTCAAGAACAA	25909
rs141845154	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246888867	TATACACATGCCACT[A/G]CACTGCAGCCTGGGC	25909
rs141851014	snp	C/T	0.0134861	0.0810011	intron-variant	AHCTF1	GRCh38.p7	1:246846121	ATGGCCTTAGGTATA[C/T]AGCAGGCCCTTCTTA	25909
rs141857631	snp	C/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246899853	CCTTTATAAAACATA[C/T]AAATACTAAATATCT	25909
rs141859428	snp	A/G	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246852598	AAGGATGCATGGGGC[A/G]GGGGTGTCAATCCTG	25909
rs141864056	snp	C/T	0.00755907	0.0610114	intron-variant	AHCTF1	GRCh38.p7	1:246928533	GTTAAACAATAAAAT[C/T]AATTTTTTAAAACTC	25909
rs141866586	snp	A/G	0.0505692	0.150756	intron-variant	AHCTF1	GRCh38.p7	1:246886440	ATTGTATTAGATGTT[A/G]TAAGTAATCTACAGA	25909
rs141990857	snp	C/T	0.000274661	0.0117156	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876171	GATCTCTCCCGCAAA[C/T]GAGGATCACGATCAT	25909
rs142087876	snp	C/T	0.0119091	0.0762411	intron-variant	AHCTF1	GRCh38.p7	1:246902766	TTTAAAGATTGTTCA[C/T]ACAATACAAAGAAAA	25909
rs142129636	snp	A/G	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246898253	AAATCTTGGGGAAAG[A/G]AGGCCAGCTACAAGA	25909
rs142153444	snp	A/G	0.0275645	0.114116	intron-variant	AHCTF1	GRCh38.p7	1:246873550	AAAGAATCCGTCCCA[A/G]TAATAAATATACTAG	25909
rs142177309	snp	C/G	0.0256215	0.110247	intron-variant	AHCTF1	GRCh38.p7	1:246869128	GATTACAGGCGTGAG[C/G]CACCACGCCCGGCCG	25909
rs142193362	snp	C/T	0.000153988	0.00877328	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246862022	AGTTTCTTTAAGTCG[C/T]TGAGGAGACCTTCCA	25909
rs142196581	snp	C/T	0.0111196	0.0737302	intron-variant	AHCTF1	GRCh38.p7	1:246903551	ATCGCTTTTCACAGC[C/T]AGGTGCGGTGGCTCA	25909
rs142240582	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246871514	ACAAAGCCTTTCTTC[A/G]TAAATCAGAGTAACA	25909
rs142265630	snp	C/T	0.00755907	0.0610114	intron-variant	AHCTF1	GRCh38.p7	1:246920823	AGGCACGGTGCCTCA[C/T]GCCTATAATCCCAGC	25909
rs142290498	in-del	-/AG	0.365646	0.221644	intron-variant	AHCTF1	GRCh38.p7	1:246862717	AAAAAAGTGCCAATT[-/AG]AGTAAGATAAATTAC	25909
rs142302349	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246857869	ATTTAGTGATTACTG[A/G]TAGTCTTGCATTATT	25909
rs142338484	snp	A/G/T	0.000774708	0.0196682	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246864019	TTGAGGGCAGTGAAC[A/G/T]GGATACTAGGTACAA	25909
rs142432026	snp	C/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246860343	TGGAAGGACTTTCAA[C/G]TCAGACTATGGCATC	25909
rs142569004	snp	C/T	1.65312e-05	0.00287495	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850082	ATTTTTCTTGGTCTA[C/T]CACGTTTTCTAGGTA	25909
rs142571678	snp	A/C	1.65685e-05	0.00287819	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850038	TCTCTTCCTTAACAG[A/C]CTTAGATCCTACATC	25909
rs142573086	snp	A/G	0.0138799	0.0821421	intron-variant	AHCTF1	GRCh38.p7	1:246925699	CCCAGTGTTGGAGGT[A/G]GGGCCTGGTAGGAGG	25909
rs142603415	snp	C/T	0.0066286	0.0571871	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850241	TCACTGGATTTATCA[C/T]CTTGCTTATTTCCTG	25909
rs142605416	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246887067	TCTAAAATAGTGCTT[A/G]GTAAAGGTACTGATT	25909
rs142609455	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246914664	AAGACAAAAATAAAC[A/G]TAATGAGTGTATACT	25909
rs142617351	snp	C/T	0.000511775	0.0159883	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246889975	CTATACCTTGATAAA[C/T]GCTCAAACTTCTGTC	25909
rs142622327	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246858420	AAAACTGAAGCCTAA[A/G]GTTATACTGCGTATC	25909
rs142641335	snp	A/G	0.00795532	0.062565	intron-variant	AHCTF1	GRCh38.p7	1:246869936	TCCTCTGAGAGATCC[A/G]AACAAAGTCCTTTGA	25909
rs142641898	snp	C/T	4.95642e-05	0.00497792	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849900	CCATCGAAAGTTCCT[C/T]GTTTGGCACTAAAAT	25909
rs142646495	snp	C/T	6.66322e-05	0.00577163	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246900406	AAATATACAGAAGGC[C/T]TTCCCTGTCCATATA	25909
rs142686289	snp	A/G	0.00236533	0.0343085	intron-variant	AHCTF1	GRCh38.p7	1:246918384	ATACTTCCACTGTAA[A/G]TATTTTTAAAAGAAA	25909
rs142720037	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246872644	AAAACATAAGGATCA[C/T]GCTAGCCAAACTATG	25909
rs142727111	snp	A/C/G	0.000645246	0.0179503	synonymous-codon, missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246876959	TCGTACCATAACATT[A/C/G]ATCTTCAGAGTTTGG	25909
rs142808731	in-del	-/TA	0.0383715	0.133092	intron-variant	AHCTF1	GRCh38.p7	1:246880225	CAATATGTTATTTGT[-/TA]TATATATATATAAAA	25909
rs142939758	in-del	-/AACCCCC			intron-variant	AHCTF1	GRCh38.p7	1:246896134	GAATGTAAAATGGAA[-/AACCCCC]CAGCCACTCTGCAAA	25909
rs142949133	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932736	ACCGCGGGTTTTCAT[C/T]GTGGAATTTCTTATT	25909
rs142973217	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932102	AAACTCTCGGTGAAA[A/G]AAGGAGGTGGGAGGG	25909
rs143001336	snp	C/T	2.08488e-05	0.00322861	intron-variant	AHCTF1	GRCh38.p7	1:246905685	AGTATATTTCATATT[C/T]TTAAGTTATTTTTTA	25909
rs143015692	snp	A/G	0.239037	0.24976	intron-variant	AHCTF1	GRCh38.p7	1:246868413	GGCGTGAGCCACTGC[A/G]CCTGGCAATTTTTGT	25909
rs143015709	snp	A/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246911961	TTCTTTGAGATGGAT[A/T]CTTGCTCTGTCGCCC	25909
rs143057343	snp	A/T			intron-variant	AHCTF1	GRCh38.p7	1:246896715	ATCTGAACTGCACGG[A/T]GTATGAAATATCTCA	25909
rs143060611	snp	A/C	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246889528	AAGCTAATGTTCACT[A/C]TCCTAAATTGGTCAT	25909
rs143078740	snp	C/T	0.030665	0.119967	intron-variant	AHCTF1	GRCh38.p7	1:246869100	CCGCCCGCCTTGGCC[C/T]CCCAAAGTGCTGGAT	25909
rs143171849	snp	C/T	0.00795532	0.062565	intron-variant	AHCTF1	GRCh38.p7	1:246895261	TTGATTTTTTATGAT[C/T]ACAAAGTGGTTTTGT	25909
rs143201658	snp	A/G	0.0126979	0.078662	intron-variant	AHCTF1	GRCh38.p7	1:246926901	GTGTATGGCCGGGCC[A/G]CGGTGGCACACGCCT	25909
rs143228130	snp	A/G	0.040671	0.13668	intron-variant	AHCTF1	GRCh38.p7	1:246845919	GATATTTAACAATTG[A/G]CTCTTACCAGCCAGT	25909
rs143229745	snp	C/T	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246864286	CAAAAAGTCAGAAAA[C/T]TATTCATCGCAAAAC	25909
rs143234124	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246932997	CTGGAGTGCAGTGGT[A/G]TAATCAAGGCTCACA	25909
rs143242697	snp	C/T			intron-variant	AHCTF1	GRCh38.p7	1:246904702	TAGTGAACTCAAGCA[C/T]GAAGCATGCAGTAAG	25909
rs143245095	snp	A/G	0.00084855	0.0205805	missense, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246842733	GTCCTGATTCGTTTC[A/G]CTTTTGGCTTTCCCA	25909
rs143290948	snp	A/C	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246868671	TGGACATGTGCCTTC[A/C]ACTGAAATAGGAGTT	25909
rs143303729	snp	C/T	0.00459057	0.0476887	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850190	CTAACTTCTCTCCCT[C/T]TGACCCTTCTAACAT	25909
rs143330344	snp	C/T	0.000837535	0.0204467	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853205	TTCTTTTAAGTTCAG[C/T]GCTACTTCCTGGTTA	25909
rs143336719	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246876314	CCTACATATCCATTT[C/T]TCCAAACCAAGAACT	25909
rs143342715	in-del	-/AAGATCGCTTAAGCCCAAGAGGTTGAGGCTACAGTGAGCCATGAC	0.410399	0.191761	intron-variant	AHCTF1	GRCh38.p7	1:246897888	GGGGGCTGGGGTGGG[lengthTooLong]CATGCCACTGCATTC	25909
rs143355150	snp	C/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246923658	CAAAGACATTACACA[C/T]GGCTAGAGTGAAGTG	25909
rs143410016	in-del	-/TC/TCTG/TCTTC/TTCT			intron-variant	AHCTF1	GRCh38.p7	1:246857965	CTAACACTTTCTTCT[-/TC/TCTG/TCTTC/TTCT]TTTTTTTTTTTTGAG	25909
rs143458956	snp	C/T	0.00279162	0.0372561	intron-variant	AHCTF1	GRCh38.p7	1:246913602	CACCATTACTCAATA[C/T]ATAGAAAAATCACGC	25909
rs143481519	snp	C/T	0.00438332	0.0466095	intron-variant	AHCTF1	GRCh38.p7	1:246927602	ACAGAATCCCAGCCT[C/T]TTATGACATGCCAGC	25909
rs143519690	snp	A/C/G	0.00557542	0.0525036	intron-variant	AHCTF1	GRCh38.p7	1:246843626	CAAAGGGGTGGATAC[A/C/G]ACCATTTTTGGCTTT	25909
rs143531926	snp	A/G	0.00517822	0.0506191	intron-variant	AHCTF1	GRCh38.p7	1:246847081	TATCTGAGGTCAGGC[A/G]TTTGAGACTAGCTTG	25909
rs143544844	snp	C/T	9.89071e-05	0.00703163	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851135	CTGCATACAAGTTTT[C/T]CTTCAGTTGCTGTGT	25909
rs143551247	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246899248	CATCTACATAAATTA[A/G]TTGCTAAAAACATAC	25909
rs143584393	snp	C/T	0.00755907	0.0610114	intron-variant	AHCTF1	GRCh38.p7	1:246861785	GTTTGGCTTAGCCAA[C/T]GGCCCTAGTGTTTCT	25909
rs143609888	in-del	-/TTTA			upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933122	CATTAATTTTTTTAT[-/TTTA]TTTATTTATTTATTT	25909
rs143648189	snp	A/C			intron-variant	AHCTF1	GRCh38.p7	1:246879506	TAAAGGTTGAAACAA[A/C]CTAAATGTTCATTAC	25909
rs143650145	snp	C/T	0.00676609	0.0577691	intron-variant	AHCTF1	GRCh38.p7	1:246879005	ACCAAAATCTAGAAA[C/T]GTTAAAAGCAGAACA	25909
rs143704658	in-del	-/ACACACACACACACAC			intron-variant	AHCTF1	GRCh38.p7	1:246898622	TGACATCTTGACAAA[-/ACACACACACACACAC]ACACACACACACACA	25909
rs143718823	snp	C/T	0.00148542	0.0272122	synonymous-codon, utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840884	AAGACCTGTTCCTGT[C/T]ACTTCTGTAGTTTTT	25909
rs143718915	snp	C/T	0.00716266	0.059414	intron-variant	AHCTF1	GRCh38.p7	1:246882666	GCCTATACAAAAGGA[C/T]TTTTTGGCTTTCTTG	25909
rs143797194	in-del	-/A			intron-variant	AHCTF1	GRCh38.p7	1:246895029	AGGCCTAATTCCTTT[-/A]AAAAAAAAAAGGTCA	25909
rs143813373	snp	C/T	0.00377385	0.0432745	synonymous-codon, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246842717	TTGTTTTGTTTTTGA[C/T]GTCCTGATTCGTTTC	25909
rs143835885	snp	A/T	0.000846308	0.0205533	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850402	TCTAGGAGTCCTTTT[A/T]GTAACAGATGAAACC	25909
rs143868238	snp	C/T	0.00716266	0.059414	intron-variant	AHCTF1	GRCh38.p7	1:246860241	CCACTGCACTCCAGC[C/T]TGGGCAACAGAGTGA	25909
rs143876978	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246869523	ACAGGGTGACTCTGC[C/T]GTTAGTGGTTAATGT	25909
rs143883846	snp	C/T	0.00772473	0.061666	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246891042	GAAACCACAAACTTA[C/T]TGCTTAAGTCTATCA	25909
rs143911818	snp	C/T	0.00517822	0.0506191	intron-variant	AHCTF1	GRCh38.p7	1:246862645	TTATACGTAAGTCTA[C/T]GAAACATAAAACTGC	25909
rs143918265	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246867438	CAGAGGGTTTTCATT[C/T]GTTTTACTTTGTACA	25909
rs143922986	snp	A/C	0.000134969	0.00821378	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246853246	CAGAGACAATAGGAC[A/C]TTCAGAGATAGTGAG	25909
rs143967117	in-del	-/ACAC	0.454311	0.144073	intron-variant	AHCTF1	GRCh38.p7	1:246898622	TGACATCTTGACAAA[-/ACAC]ACACACACACACACA	25909
rs143983840	snp	A/G	0.0558544	0.157504	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933204	AGTGGCACAATCTCG[A/G]CTCACTGCAACCTCC	25909
rs143991448	snp	C/T	0.00835141	0.0640778	intron-variant	AHCTF1	GRCh38.p7	1:246920077	GAACCCAGGAGGCAG[C/T]TGCAGTGAGCCGAGA	25909
rs144046700	snp	C/T	0.000379328	0.0137666	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246888210	TTCAGTAACGCCGTC[C/T]AATAGGTACATATCA	25909
rs144114580	snp	A/G	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246844837	AACTATAGGGCCCCC[A/G]TATTAAAAGCAATTA	25909
rs144204001	snp	C/T	0.367913	0.220446	intron-variant	AHCTF1	GRCh38.p7	1:246841911	ATTCTGCCTCAGCCT[C/T]CAGAGTAGCTGGGAC	25909
rs144251691	snp	A/G	0.00676609	0.0577691	intron-variant	AHCTF1	GRCh38.p7	1:246845154	TCAGCTACTGGGATA[A/G]TCAAGAGTTCTATCA	25909
rs144301715	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246890395	TGAAAAAATAAGATC[A/G]ACAATTATGTACAGT	25909
rs144318625	snp	A/C/T	0.000395299	0.0140534	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849722	CGAGTCCTGCTGCTG[A/C/T]GGGATGATTTAGTGA	25909
rs144319690	snp	A/T	1.64909e-05	0.00287144	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246851085	TTACGGCAGATGGCA[A/T]ATTTGCAATTTGTCC	25909
rs144381131	snp	C/T	0.00517822	0.0506191	intron-variant	AHCTF1	GRCh38.p7	1:246901572	GAGCTTGCAGTGAGC[C/T]GAGATCGTGCAACTG	25909
rs144439704	snp	A/G	0.0501905	0.150254	intron-variant	AHCTF1	GRCh38.p7	1:246922940	GTGAGCCGAGATTGC[A/G]CCACTGCACTCTAGC	25909
rs144446615	snp	C/T	1.65037e-05	0.00287256	intron-variant	AHCTF1	GRCh38.p7	1:246863882	CTTGAAAAGTAAGAG[C/T]CATCTAGTTTGATTG	25909
rs144461673	snp	A/C	0.00993419	0.0697739	intron-variant	AHCTF1	GRCh38.p7	1:246909707	TTGATTTAATAAGGA[A/C]AAATCATAATGTGTG	25909
rs144481579	snp	C/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246914242	GTTTGGTGATTTCTA[C/T]GCTAATACAGGTTGA	25909
rs144509730	snp	A/G	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246868813	GGTCTACCTCATTTT[A/G]TTGTGCTTTGCTTCA	25909
rs144544553	snp	C/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246857437	TGTGAGCGAAATCTT[C/G]GTCTTCAACAAAAAC	25909
rs144597398	snp	C/T	0.00636936	0.0560724	intron-variant	AHCTF1	GRCh38.p7	1:246859083	CTCAAATAAGTAAGG[C/T]AGTGTAAATTTCTAG	25909
rs144599339	snp	A/G	0.00881315	0.0657944	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246888412	CAGACTAGCAGGAGG[A/G]TATTTTCCTGTGCCT	25909
rs144607057	snp	C/T	0.00755907	0.0610114	intron-variant	AHCTF1	GRCh38.p7	1:246929274	ATTAGCCGAGTGTGG[C/T]GGCGCGTTCCTGTAG	25909
rs144631810	snp	C/T	0.00438332	0.0466095	intron-variant	AHCTF1	GRCh38.p7	1:246861497	TTCCCTAATTGGTAA[C/T]ATACCAGTATTTTCA	25909
rs144747230	snp	A/G	0.0088679	0.0659948	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246850762	TGATTTGACATTCAC[A/G]TTTTGGATACGTTGA	25909
rs144855018	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246863537	AGTAACAGTTTTGTC[A/G]AAGAATTTAAATAAA	25909
rs144863253	in-del	-/GGGCG	0.361684	0.223667	downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838605	GCAAGTTGTAGAAGT[-/GGGCG]GGGCGGGGCGGGGGG	25909
rs144894125	snp	C/T	0.00478085	0.0486577	intron-variant	AHCTF1	GRCh38.p7	1:246884371	TTACCCTCTTATCCG[C/T]AGAAGTACATGCTAT	25909
rs144969316	snp	C/T	0.0023933	0.0345097	intron-variant	AHCTF1	GRCh38.p7	1:246870556	TCTACAGTGTTGAAA[C/T]GATAAAGTGTAAACA	25909
rs144970789	snp	C/G	0.00398564	0.0444627	intron-variant	AHCTF1	GRCh38.p7	1:246929131	AGAGTACAGTGGGCT[C/G]GGTGCGGTGGTTCAC	25909
rs144971133	in-del	-/TA	0.00795532	0.062565	downstream-variant-500B	AHCTF1	GRCh38.p7	1:246838826	TGTTTCCCTTACTAC[-/TA]TGATACTAAGTATCT	25909
rs144994178	snp	C/T	0.000296721	0.0121767	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861050	CTCTTCAAGGTCTTC[C/T]GGTGACGGTGCATCC	25909
rs145003209	snp	A/G	0.0178098	0.0926698	intron-variant	AHCTF1	GRCh38.p7	1:246908840	GAGGCAGAGCTTGCC[A/G]TGAGCCAAGATTGAG	25909
rs145065480	snp	A/C/T	0.00159617	0.0282053	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246839223	TATGATCTACATTCA[A/C/T]GGAGGGGGGAAAAAA	25909
rs145090622	in-del	-/T	0.00318978	0.0398085	intron-variant	AHCTF1	GRCh38.p7	1:246879086	TCACAACAAGGTTGA[-/T]TTTCCCTAATGCATA	25909
rs145112684	snp	A/G	0.00438332	0.0466095	intron-variant	AHCTF1	GRCh38.p7	1:246912200	AATCAAGAATGTGCC[A/G]GGTGTGGTGGCTCAC	25909
rs145124901	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246866356	ATTGGTAGAAAAAAA[C/G]AATGTCGGTAATAAC	25909
rs145140945	snp	A/G	0.00199481	0.0315187	upstream-variant-2KB	AHCTF1	GRCh38.p7	1:246933924	GGAGGTTTGGGGTTC[A/G]TTGTCTTAATTATTT	25909
rs145146408	snp	C/G	0.0134861	0.0810011	intron-variant	AHCTF1	GRCh38.p7	1:246915187	ATACAAAAATTAGCT[C/G]GGCGTGGTGGTGCAC	25909
rs145149158	snp	A/T	0.0532157	0.154195	intron-variant	AHCTF1	GRCh38.p7	1:246883539	GCCTTTTGCAAAATT[A/T]TCAGTTCAAAAATTT	25909
rs145203002	snp	A/G	0.00398564	0.0444627	intron-variant	AHCTF1	GRCh38.p7	1:246845512	CAAAAGTATTTCTAC[A/G]AAAATTATACATTCT	25909
rs145223994	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246889712	GCAACTCGAGGAAGA[C/T]GACTATTTCCAGAAG	25909
rs145295081	snp	C/G	0.0119091	0.0762411	intron-variant	AHCTF1	GRCh38.p7	1:246889333	CACTTACTACTCTTT[C/G]CGGTTGTCCAATGAG	25909
rs145462531	snp	C/T	1.65479e-05	0.0028764	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246849959	TCAACATTTTCACTT[C/T]TAGCTGGGGTATTTC	25909
rs145510203	snp	A/G	1.64833e-05	0.00287078	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246905607	TTCTCAGGTTCTTGA[A/G]AAGTGACAGCATATA	25909
rs145530946	snp	C/T	0.0566069	0.158427	intron-variant	AHCTF1	GRCh38.p7	1:246894383	CGAGACCATCCTGGC[C/T]AACACGGTGAAACCC	25909
rs145531202	snp	A/C	0.0596104	0.162024	intron-variant	AHCTF1	GRCh38.p7	1:246930016	AAGATTGTGCCACTG[A/C]ACTCCAGCCTGGGCA	25909
rs145568373	snp	A/G	0.0115144	0.0749975	utr-variant-3-prime, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246840069	AATATCCATAAACAG[A/G]TTTATTTTACATTTC	25909
rs145576635	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246914243	TTTGGTGATTTCTAC[A/G]CTAATACAGGTTGAA	25909
rs145601846	snp	A/G	0.000798403	0.0199641	intron-variant	AHCTF1	GRCh38.p7	1:246889313	CTAATTGTGAATAGC[A/G]GCAGCACTTACTACT	25909
rs145616559	snp	A/C	0.00358779	0.0422022	intron-variant	AHCTF1	GRCh38.p7	1:246852996	TTATATAGCAGTCAA[A/C]TAAATGAACGTGTTA	25909
rs145616761	snp	C/T	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246892233	TCAATATTTAATGTG[C/T]CACTGGTCTAGAAAA	25909
rs145634607	snp	C/T	0.00438332	0.0466095	intron-variant	AHCTF1	GRCh38.p7	1:246910716	AAGGGGGAAAAATCA[C/T]ATCACACTGTCCTAG	25909
rs145641591	snp	A/C/G	0.00438332	0.0466095	intron-variant	AHCTF1	GRCh38.p7	1:246914846	CCTCATCCAAATGAT[A/C/G]AATGAGTGTCCATGT	25909
rs145649060	in-del	-/AA	0.0944967	0.195752	intron-variant	AHCTF1	GRCh38.p7	1:246924010	GAATATAAATCTGGC[-/AA]AAAGAGAGATCCGAG	25909
rs145670190	snp	A/G	0.00398564	0.0444627	intron-variant	AHCTF1	GRCh38.p7	1:246899098	CCGTCTCAAAAAGAG[A/G]AAAGTATTTTTCAAA	25909
rs145680709	snp	C/T	0.00199481	0.0315187	intron-variant	AHCTF1	GRCh38.p7	1:246924845	TTATCCAAAACAGAT[C/T]CAAAAGTCTAACCTA	25909
rs145681656	snp	A/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246858315	CCCCCTTAACCTCTC[A/G]CTTTTCACTTTTTGC	25909
rs145708659	snp	C/T	0.00716266	0.059414	intron-variant	AHCTF1	GRCh38.p7	1:246852194	AAATAACCTAGAAAT[C/T]AGGATTCCCACTTAC	25909
rs145750705	snp	C/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246910544	CACATATAGCAAATG[C/T]TGAAAATTAACTTGA	25909
rs145867818	in-del	-/CT	0.0205511	0.0992634	intron-variant	AHCTF1	GRCh38.p7	1:246925062	CTATGTTGTTTTCCC[-/CT]CTGACAGCCTTTTAT	25909
rs145980470	snp	C/T	0.00716266	0.059414	intron-variant	AHCTF1	GRCh38.p7	1:246901845	AAATAAATAAACAAA[C/T]AAAAACTTTAAAAAG	25909
rs145999407	snp	G/T	0.00438332	0.0466095	intron-variant	AHCTF1	GRCh38.p7	1:246887114	CAACTATTTTTAGTA[G/T]ACTGTATCATATCTT	25909
rs146002900	snp	G/T	0.00119737	0.0244387	intron-variant	AHCTF1	GRCh38.p7	1:246849516	TTTGAGGGGGGAAGG[G/T]GAAAAATTCCCTATA	25909
rs146052498	snp	C/T	0.000501866	0.0158329	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246867245	TAATAAACTCTTACC[C/T]AGAAATTTTTTGTGA	25909
rs146102598	snp	C/T	0.00159617	0.0282053	intron-variant	AHCTF1	GRCh38.p7	1:246924084	TGAGTACAGAAAGGA[C/T]TACATTCAGTTCCAA	25909
rs146126599	snp	A/G	0.0729998	0.176553	intron-variant	AHCTF1	GRCh38.p7	1:246868466	CACCATGTTGGCCAG[A/G]CTGGTCTCAAACTCC	25909
rs146143857	snp	A/G	0.0111196	0.0737302	intron-variant	AHCTF1	GRCh38.p7	1:246869121	AGTGCTGGATTACAG[A/G]CGTGAGCCACCACGC	25909
rs146242458	snp	C/T	0.0221141	0.102801	intron-variant	AHCTF1	GRCh38.p7	1:246926985	CGAGACCATCCTGGC[C/T]AACAAGGTGAAATCC	25909
rs146245760	snp	A/G	0.0123036	0.0774623	intron-variant	AHCTF1	GRCh38.p7	1:246882543	CTATGTGGGACATTC[A/G]ATATATACTTTTGTA	25909
rs146246798	snp	C/G	1.64795e-05	0.00287045	missense, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246902616	ACTCGTCTGTCCCCT[C/G]AAAGGGAACATGCCA	25909
rs146264026	snp	C/G	0.000399281	0.0141238	intron-variant	AHCTF1	GRCh38.p7	1:246886623	TTCTGATCTACAGTT[C/G]ATTGAAGCCACGGAT	25909
rs146287436	snp	A/G	8.23974e-05	0.00641809	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246895908	TGCTGCTGACAATAT[A/G]GCTTCTAACTGTTCT	25909
rs146398045	in-del	-/GGTACAGTGGGGTCTGAGAACGCCAA	0.00318978	0.0398085	intron-variant	AHCTF1	GRCh38.p7	1:246917434	TTAAGAAAGTAGCAT[-/GGTACAGTGGGGTCTGAGAACGCCAA]GGTTCCAAGATCCTT	25909
rs146417813	snp	C/T	0.00499005	0.0497003	missense, nc-transcript-variant, intron-variant	AHCTF1	GRCh38.p7	1:246843811	AGTTCATCTTCAAGC[C/T]TGTTCTTATTGGATG	25909
rs146464504	snp	A/G	0.00253883	0.0355383	synonymous-codon, nc-transcript-variant	AHCTF1	GRCh38.p7	1:246861203	CAGGAAAAAAGATGT[A/G]GTCCTATCTTTGCTC	25909

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