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

HLTF

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs2806	snp	A/T	0	0	utr-variant-3-prime	HLTF	GRCh38.p7	3:149031252	TGTAAACAATTGTTA[A/T]GTGTTTAGAATCAGA	6596
rs746671	snp	A/G	0.294064	0.246086	intron-variant	HLTF	GRCh38.p7	3:149071106	AACACAGTTTTTCCT[A/G]TAGTTTTTAGTTAAA	6596
rs751845	snp	C/T	0.407845	0.193868	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087266	CTCAGAGCGCCCCTC[C/T]GCAGTTCCTTGAGGA	6596
rs772813	snp	A/G	0.382279	0.212137	intron-variant	HLTF	GRCh38.p7	3:149077204	ctggagtgcaggggc[A/G]ctatcttggctcact	6596
rs772814	snp	C/T	0.294064	0.246086	intron-variant	HLTF	GRCh38.p7	3:149072136	AGTGAGTAGTGTAAT[C/T]CTAGAGTTGATTTAT	6596
rs772815	snp	C/T	0.294064	0.246086	intron-variant	HLTF	GRCh38.p7	3:149068981	aaacagttttgactt[C/T]gcattttcgtgaagg	6596
rs772816	snp	C/T	0.364193	0.222396	intron-variant, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149085892	GCGCTAGTAGAGATA[C/T]GCGCCACTTGCAAGG	6596
rs772817	snp	C/T	0.382279	0.212137	intron-variant	HLTF	GRCh38.p7	3:149083285	TTATTTTATAATTAA[C/T]GCATGTTCTTTTATT	6596
rs810082	snp	C/T			intron-variant	HLTF	GRCh38.p7	3:149079331	gctggtctcaaactt[C/T]ttttgacagtttgat	6596
rs812248	snp	A/G	0	0	intron-variant	HLTF	GRCh38.p7	3:149079245	cttcttatatgtgta[A/G]agtagtggtttccat	6596
rs812249	snp	A/G	0.406591	0.194883	synonymous-codon	HLTF	GRCh38.p7	3:149068321	GGGTAAAACTCTTAC[A/G]GCCATTGCAGTAATC	6596
rs812820	snp	C/G	0.293551	0.246177	intron-variant	HLTF	GRCh38.p7	3:149082414	tggagcgcagtggcg[C/G]gatctcggctcattg	6596
rs813853	snp	A/C	0	0	intron-variant	HLTF	GRCh38.p7	3:149079338	tgcccaggctggtct[A/C]aaacttcttttgaca	6596
rs975922	snp	A/C/G	0.0134861	0.0810011	utr-variant-3-prime	HLTF	GRCh38.p7	3:149030894	TTCAATGTGTGCCCT[A/C/G]TAACACAACATTGTC	6596
rs1017489	snp	C/T	0.475096	0.108775	intron-variant	HLTF	GRCh38.p7	3:149046303	AACTTTTAATTTCTA[C/T]ATAAATTGATCCAAG	6596
rs1042835	snp	A/G	0	0	missense	HLTF	GRCh38.p7	3:149074284	ACTTTTTGGGGAAAA[A/G]AAGAAAATAGAAAAG	6596
rs1081819	snp	A/T	0.409721	0.192325	intron-variant	HLTF	GRCh38.p7	3:149078323	cctggcctcaagaga[A/T]cctcacacttcagcc	6596
rs1272861	snp	A/C			intron-variant	HLTF	GRCh38.p7	3:149043608	TGTTGTCATTGTACC[A/C]CTGTATTTTGTATAA	6596
rs1350359	snp	A/T	0.409552	0.192466	intron-variant	HLTF	GRCh38.p7	3:149051236	AATATAAGGAAGTTT[A/T]AAAAAAAAAAAAAAG	6596
rs1457604	snp	C/T	0.29432	0.24604	intron-variant	HLTF	GRCh38.p7	3:149040348	ATGTGGTAAGTAGAA[C/T]GGATAAAGGAGGGAG	6596
rs1457605	snp	C/T	0.00874735	0.0655527	intron-variant	HLTF	GRCh38.p7	3:149043891	TTATTTAATTTAATA[C/T]ATGTAAAGTATTTAA	6596
rs1457606	snp	A/T	0.0894459	0.191631	intron-variant	HLTF	GRCh38.p7	3:149075097	TCTTAAATACAAAAA[A/T]CTTATTTTTCTCTTG	6596
rs1879170	snp	A/T	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149072065	CCCAAAAAATTAAGA[A/T]ATTGAAATTAAATTA	6596
rs1965258	snp	C/T	0.431769	0.17164	intron-variant	HLTF	GRCh38.p7	3:149051609	CTCATGCCTGTAATC[C/T]CGGCACTTTGGGAGG	6596
rs1965259	snp	C/T	0.00358779	0.0422022	intron-variant	HLTF	GRCh38.p7	3:149051740	GTGGTGATGGTGATG[C/T]GCACCTATAATTCCA	6596
rs2034905	snp	C/T	0.0345262	0.126772	intron-variant	HLTF	GRCh38.p7	3:149064459	GTTGTATTTAAAATG[C/T]AATATGCATGGATAA	6596
rs2034906	snp	A/G	0.382279	0.212137	intron-variant	HLTF	GRCh38.p7	3:149054135	TAAATTTGACAATTA[A/G]ACTATCACAAGTAGT	6596
rs2054197	snp	A/G	0.432357	0.171014	intron-variant	HLTF	GRCh38.p7	3:149045719	ATCTTGCTTGGACCA[A/G]AATTTCATACCTTCT	6596
rs2119341	snp	A/C			utr-variant-3-prime, intron-variant	HLTF	GRCh38.p7	3:149031773	AAAATTAATTCTTGT[A/C]TAGTCTGTATATATT	6596
rs2119342	snp	C/T	0.40733	0.194287	utr-variant-3-prime, intron-variant	HLTF	GRCh38.p7	3:149031834	AATCGGAGGCTTTGG[C/T]AAATAACTAAGTGTC	6596
rs2228257	snp	C/G	0.0133149	0.0804996	missense	HLTF	GRCh38.p7	3:149063507	GCATCTAGATGTAGT[C/G]AACAACCCAGTATTT	6596
rs2229361	snp	A/G	0.0594826	0.161874	missense	HLTF	GRCh38.p7	3:149040077	CAGAAGAATTAGCAC[A/G]TGACAGTGAGAAAAA	6596
rs2290725	snp	C/T	0.43424	0.168984	synonymous-codon	HLTF	GRCh38.p7	3:149041538	TTTACAAAATACATG[C/T]GCACAATGTGTTATC	6596
rs2290726	snp	A/C	0.432063	0.171327	intron-variant	HLTF	GRCh38.p7	3:149041773	TAGGGAAAGTCTCTC[A/C]TCATTTTCTGCCATA	6596
rs2305867	snp	C/G/T	0.000979748	0.0221119	intron-variant	HLTF	GRCh38.p7	3:149040172	CTATATAAGAAAGAA[C/G/T]GAAGTATGAGCAACA	6596
rs2305868	snp	A/G	0.0535406	0.154608	missense	HLTF	GRCh38.p7	3:149068298	CAGTAATCCTTACCA[A/G]CTTCCATGATGGCAG	6596
rs2607999	snp	A/C	0.410568	0.191619			GRCh38.p7	3:149087754	ACTAAAAATACAAAA[A/C]TTAGCTGGGCGTGGT	6596
rs2608003	snp	A/T	0.404384	0.196635			GRCh38.p7	3:149077284	ttatttttatttatt[A/T]atttatttatttatt	6596
rs2608004	snp	A/T	0.325799	0.238232			GRCh38.p7	3:149077268	atttatttatttatt[A/T]atttatttatttatt	6596
rs2877411	snp	C/T	0.134119	0.221521	intron-variant	HLTF	GRCh38.p7	3:149051695	GCGAAACCCTGCCTC[C/T]ACTAAAAATACAAAA	6596
rs3070552	in-del	-/GTCTA	0	0	intron-variant	HLTF	GRCh38.p7	3:149047213	AGTTGAACCACATTA[-/GTCTA]CATCTTGCAAAATGG	6596
rs3070582	in-del	-/AA	0	0	intron-variant	HLTF	GRCh38.p7	3:149083761	tacaaaaaaaaaaaa[-/AA]tacaaaaattagctg	6596
rs3182285	snp	A/G	0.424659	0.17887	utr-variant-3-prime	HLTF	GRCh38.p7	3:149030593	GTATGGGTTCTCCAT[A/G]TAGCAATACTTCAGT	6596
rs3213908	snp	A/G	0.0103356	0.0711407	utr-variant-3-prime, intron-variant	HLTF	GRCh38.p7	3:149031566	AATGAGTGTAGTACT[A/G]CTTAACTAAAATGGA	6596
rs3765075	snp	C/T			synonymous-codon	HLTF	GRCh38.p7	3:149059719	GGATATTTACTGACC[C/T]TTTTTCAACATTTTC	6596
rs3772565	snp	A/G	0.3744	0.216852	intron-variant	HLTF	GRCh38.p7	3:149053525	TTTACAGGAAGTATC[A/G]TGCTGGCATCTGCTT	6596
rs3816570	snp	C/G	0.487746	0.0773096	intron-variant	HLTF	GRCh38.p7	3:149042498	GCTGCCAATTGCAGT[C/G]TAAGTCAGATAGGAA	6596
rs3836276	in-del	-/T	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149040436	ATTGTTATTCATAGA[-/T]TTTTTTTTTTAAACT	6596
rs4681479	snp	A/C	0.496034	0.0443518	intron-variant	HLTF	GRCh38.p7	3:149052289	TCTTTTTAAAAAATT[A/C]TATGTTGTATGGAAA	6596
rs4681480	snp	G/T	0.405082	0.196086	intron-variant	HLTF	GRCh38.p7	3:149069858	tggaaaagttgtgtg[G/T]gacactatgaacata	6596
rs4974388	snp	C/G	0.431916	0.171483	intron-variant	HLTF	GRCh38.p7	3:149071154	TCTAGTCCCAAACTG[C/G]TACCAACATATTCCT	6596
rs6440581	snp	C/G	0.301429	0.244653	intron-variant	HLTF	GRCh38.p7	3:149044564	accatccacacatag[C/G]tgactttgaactcga	6596
rs6440583	snp	C/T	0.431473	0.171952	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087412	TGAGGAGGCTGCTGT[C/T]CCCGAAGCTGGCCTT	6596
rs6764352	snp	A/G	0.0480316	0.147428	intron-variant	HLTF	GRCh38.p7	3:149039038	CTGAAAAAATTTACA[A/G]AACTACTTACTGGAT	6596
rs6767681	snp	A/C			intron-variant	HLTF	GRCh38.p7	3:149032976	AAAAAAAAAAAAAAA[A/C]ACAAAAAACTATTCC	6596
rs6771107	snp	C/T	0.424193	0.179323	intron-variant	HLTF	GRCh38.p7	3:149062102	ATATTCTTCAATGCC[C/T]GTTTCCTCATAAGAA	6596
rs6772943	snp	A/C	0.0566069	0.158427	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087435	CTGGCCTTTTAATCG[A/C]ACAGGGCAGGAAGCT	6596
rs6783991	snp	A/G	0.0256215	0.110247	intron-variant	HLTF	GRCh38.p7	3:149049993	gcaaaactccatcGA[A/G]AGGGAGGGGGAGGGG	6596
rs6792312	snp	A/C	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149032978	AAAAAAAAAAAAAAA[A/C]AAAAAACTATTCCCA	6596
rs6792730	snp	A/C	0.29432	0.24604	intron-variant	HLTF	GRCh38.p7	3:149033468	ATTTTCAAAAAGGGT[A/C]ATCAGAACATTTTAC	6596
rs6796555	snp	C/T	0.495891	0.0451408	intron-variant	HLTF	GRCh38.p7	3:149079836	aacctcgtgatccac[C/T]caccttggcctccca	6596
rs6800063	snp	A/C	0	0	downstream-variant-500B	HLTF	GRCh38.p7	3:149029942	AAGCACTCTTGATTT[A/C]TGAACAAGAATTTCA	6596
rs6800629	snp	A/G	0.0275645	0.114116	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149088292	tcccagcactttggg[A/G]ggccgagttgggtgg	6596
rs6809084	snp	G/T	0.279991	0.248195	intron-variant	HLTF	GRCh38.p7	3:149037784	ACAGAAACAGCAGAG[G/T]GTTGCCTTTAGCCCA	6596
rs7611003	snp	C/G	0.00159617	0.0282053	intron-variant	HLTF	GRCh38.p7	3:149044215	AGCACTAAGATCAAT[C/G]TATAACACCTAGTGA	6596
rs7611297	snp	C/G	0.0577344	0.159793	intron-variant	HLTF	GRCh38.p7	3:149038739	gctgctctcaaactc[C/G]tgagctcaggcaatc	6596
rs7624263	snp	A/G	0.382473	0.212016	intron-variant	HLTF	GRCh38.p7	3:149066204	GGTATGCGCCACCAC[A/G]CCCAGCTAATTTTGT	6596
rs7625832	snp	C/T	0.431473	0.171952	intron-variant	HLTF	GRCh38.p7	3:149078741	gggtgcctgtagtcc[C/T]agttactcgggaagc	6596
rs7625894	snp	A/G	0.431916	0.171483	intron-variant	HLTF	GRCh38.p7	3:149054481	CCTCTGACATAAGAA[A/G]AATGGCGATGAGAGA	6596
rs7635712	snp	C/T	0.424503	0.179021	intron-variant	HLTF	GRCh38.p7	3:149052077	caggatcacttgaac[C/T]tgggaggtggaggtt	6596
rs7637603	snp	C/T	0.452103	0.147154	intron-variant	HLTF	GRCh38.p7	3:149054668	ATTCCAATGTCAATG[C/T]TTCAGAACAGAAAAG	6596
rs9289779	snp	G/T	0.372592	0.217879	intron-variant	HLTF	GRCh38.p7	3:149066822	ATAAAACATTAGGTT[G/T]CTCAGGGTGAGGAAT	6596
rs9683270	snp	A/G	0.432063	0.171327	intron-variant	HLTF	GRCh38.p7	3:149046756	CCCCAAAATAAAAAG[A/G]TAATATGGTAATTCA	6596
rs9822226	snp	A/G	0.406986	0.194565	intron-variant	HLTF	GRCh38.p7	3:149060303	AATGTAAACAATAAT[A/G]GTATTGCCAGGAAGA	6596
rs9834138	snp	A/C	0.489796	0.070696	intron-variant	HLTF	GRCh38.p7	3:149032971	TCAAAAAAAAAAAAA[A/C]AAAAAACAAAAAACT	6596
rs9835785	snp	C/T	0.382473	0.212016	intron-variant	HLTF	GRCh38.p7	3:149080928	ATGACAGACCACATG[C/T]ATTATGCAACAGTTG	6596
rs9850529	snp	A/G	0.406986	0.194565	intron-variant	HLTF	GRCh38.p7	3:149058824	TGTGACTTTGAAAAT[A/G]TTCTCTCTTGTATCA	6596
rs9864549	snp	A/C	0.3746	0.216737	intron-variant	HLTF	GRCh38.p7	3:149044028	TAGGCAAAATAATAC[A/C]AAGATTAAACTTACA	6596
rs10513347	snp	C/T	0.111224	0.207945	utr-variant-3-prime	HLTF	GRCh38.p7	3:149030729	CCTGCAGAAAGGTCT[C/T]GGTTTTGATGAAAAT	6596
rs10513348	snp	A/G	0.43221	0.171171	intron-variant	HLTF	GRCh38.p7	3:149038074	GATCCTAGACCACCT[A/G]TACCTCAATCACCTA	6596
rs10513349	snp	A/G	0.409382	0.192607	intron-variant	HLTF	GRCh38.p7	3:149065156	AAATGACACATTATT[A/G]TGAGAAAAATTCAAG	6596
rs10550068	in-del	-/G	0.5	0	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087584	TTTTTTCTTTTTTTT[-/G]TTTTTTCTTTTTTAT	6596
rs10651075	in-del	-/GTC			utr-variant-3-prime	HLTF	GRCh38.p7	3:149030478	AAGAAGCAAGCTGTC[-/GTC]CTCCCTTTACCTTCA	6596
rs10935740	snp	C/G	0.0255019	0.110003	intron-variant	HLTF	GRCh38.p7	3:149073333	TAAAGCTATAATTTA[C/G]AAAATAAAAAGAATA	6596
rs11306648	in-del	-/A	0.424659	0.17887	intron-variant	HLTF	GRCh38.p7	3:149033371	AATAATAAATTCAAT[-/A]AATCTCAAGATATCT	6596
rs11559143	snp	C/G	0	0	missense, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149084818	CACGCCTCTCATATC[C/G]AACTTTCTTTCCACG	6596
rs11710438	snp	A/G	0.495999	0.0445491	intron-variant	HLTF	GRCh38.p7	3:149067547	tcacagtgtcactga[A/G]ggtggagtgcaatag	6596
rs11715474	snp	G/T	0.495891	0.0451408	intron-variant	HLTF	GRCh38.p7	3:149084128	CATAAAATGCCACAA[G/T]TATGAAAATATAAAA	6596
rs11917715	snp	C/T	0	0	intron-variant	HLTF	GRCh38.p7	3:149078961	Caccaaacagcaatt[C/T]tagagtcaaaaggta	6596
rs11918527	snp	C/G/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149079080	ttgagattatacaat[C/G/T]taaggaacaaaaaaa	6596
rs11918628	snp	C/T	0	0	intron-variant	HLTF	GRCh38.p7	3:149079372	gggtaacgacagttt[C/T]taaaaaaaaaaaaaa	6596
rs11926206	snp	A/C	0.00952359	0.0683454	intron-variant	HLTF	GRCh38.p7	3:149079159	cacatacataagagt[A/C]ccataaggagaaaag	6596
rs12106722	snp	C/T	0.371177	0.218669	intron-variant	HLTF	GRCh38.p7	3:149065698	AGCCAGGCATGGTGG[C/T]GGGCACCTGTAATCC	6596
rs12152447	snp	A/G	0.0364509	0.129988	intron-variant	HLTF	GRCh38.p7	3:149078102	attatttaaaatgtc[A/G]atttttcaagaaaaa	6596
rs12488819	snp	C/T	0.45198	0.147323	intron-variant	HLTF	GRCh38.p7	3:149049329	CACTGAACTGTTCTA[C/T]CTCGGATTAAAACAT	6596
rs12488889	snp	G/T	0.431916	0.171483	intron-variant	HLTF	GRCh38.p7	3:149049370	TAGAAAATGGCAGTT[G/T]TAAGAATTACTTGAA	6596
rs12490157	snp	C/T	0.406986	0.194565	intron-variant	HLTF	GRCh38.p7	3:149036692	GAGGCTGAGGGAGGA[C/T]TGCTTGAGCTCAGGA	6596
rs12634247	snp	C/T	0.406986	0.194565	intron-variant	HLTF	GRCh38.p7	3:149043813	aggttgcttaaccta[C/T]gtcttgagcttcctc	6596
rs13062076	snp	A/C			intron-variant	HLTF	GRCh38.p7	3:149065646	actagcctggccaac[A/C]cagcaaaaccctgtc	6596
rs13062476	snp	A/G			intron-variant	HLTF	GRCh38.p7	3:149065639	gctcgagactagcct[A/G]gccaacacagcaaaa	6596
rs13078061	snp	A/C			intron-variant	HLTF	GRCh38.p7	3:149043397	AGACATCTAACATAC[A/C]CAGAGAGAAATAAAA	6596
rs13078559	snp	C/T	0.0391387	0.134304	intron-variant	HLTF	GRCh38.p7	3:149073669	ccactgtactctagc[C/T]tgggtgacagagcaa	6596
rs13082143	snp	A/C			intron-variant	HLTF	GRCh38.p7	3:149079365	ggcaaaagggtaacg[A/C]cagtttctaaaaaaa	6596
rs13084666	snp	C/T			intron-variant	HLTF	GRCh38.p7	3:149065638	agctcgagactagcc[C/T]ggccaacacagcaaa	6596
rs13087362	snp	A/C	0	0	intron-variant	HLTF	GRCh38.p7	3:149033025	TCTTTAGTATAATTC[A/C]CAACACTAACAAAGA	6596
rs13089226	snp	C/T	0.24019	0.249807	intron-variant	HLTF	GRCh38.p7	3:149080893	AGTATagtcataccc[C/T]gcataacaacatttc	6596
rs13090196	snp	C/G	0.448963	0.151372	intron-variant	HLTF	GRCh38.p7	3:149038147	ACTCCTAAGTCTCTA[C/G]GTTGAATGCAAAGGA	6596
rs13091100	snp	A/C	0	0	missense	HLTF	GRCh38.p7	3:149076028	TCTCGTTGTAATGCA[A/C]CCATTTCATTATTAT	6596
rs13095507	snp	A/C			intron-variant	HLTF	GRCh38.p7	3:149076064	TAATAAAAATGATAA[A/C]CAGATAATATTACAT	6596
rs13095513	snp	A/C			intron-variant	HLTF	GRCh38.p7	3:149076076	TAAACAGATAATATT[A/C]CATTATAAATAATAG	6596
rs13098422	snp	C/G	0.0391387	0.134304	intron-variant	HLTF	GRCh38.p7	3:149064160	TACCTAACTCATCTA[C/G]GTAGATGAGTTAGAC	6596
rs13099332	snp	A/G	0.424659	0.17887	intron-variant	HLTF	GRCh38.p7	3:149034651	AATGTATAGTTTTAA[A/G]GGAAACAAATATGTT	6596
rs13317754	snp	C/T	0.409212	0.192748	intron-variant	HLTF	GRCh38.p7	3:149049193	GCACACCTAATTTTA[C/T]AGATAAGAAAACTGA	6596
rs16861314	snp	C/T	0.0554779	0.157039	downstream-variant-500B	HLTF	GRCh38.p7	3:149029722	CAAAGCACACACTGC[C/T]GAAGATCATTAGTAC	6596
rs16861315	snp	C/T	0.0501905	0.150254	utr-variant-3-prime	HLTF	GRCh38.p7	3:149030579	TTATACTTAATCTCA[C/T]TGAAGTATTGCTATA	6596
rs16861342	snp	C/T	0.0349115	0.127424	intron-variant	HLTF	GRCh38.p7	3:149042881	TGGTCGGGGACATGA[C/T]TGTGACCTTTCCCTT	6596
rs16861365	snp	C/T	0.0178812	0.0928487	synonymous-codon	HLTF	GRCh38.p7	3:149050343	ATAAAAATTCAAGTG[C/T]ACATCTGATTTTATA	6596
rs16861379	snp	A/C	0.030278	0.119257	intron-variant	HLTF	GRCh38.p7	3:149070642	TTAATACTCTGCATA[A/C]CACAATATTTGTGAT	6596
rs16861399	snp	A/C	0.0345262	0.126772	intron-variant	HLTF	GRCh38.p7	3:149075648	CTAATATTTGAACCA[A/C]GGTCTATTTTCTCCA	6596
rs16861412	snp	C/T	0.0955749	0.196603	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149088188	AGAGTAAGAAAGTCA[C/T]GCTCACTAGACAAAG	6596
rs17786103	snp	C/T	0.0391387	0.134304	intron-variant	HLTF	GRCh38.p7	3:149074684	AACCACTGAGGGTAG[C/T]AACTCATTCTGCTTG	6596
rs34015521	in-del	-/G			intron-variant	HLTF	GRCh38.p7	3:149050990	AGTCTGATTAAACTG[-/G]AAAAGAGAAGATACC	6596
rs34016018	in-del	-/T			intron-variant	HLTF	GRCh38.p7	3:149047919	GCCATAAACACTTTT[-/T]AGAAGGAAAAGTTAA	6596
rs34064750	in-del	-/T			intron-variant	HLTF	GRCh38.p7	3:149034143	AGAACAGCACTTTTT[-/T]GGCCACAGAAGCATA	6596
rs34068820	in-del	-/G			upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087202	GGACGGGACCATTTT[-/G]CCCCGTGGGCACTTG	6596
rs34161408	in-del	-/T			intron-variant	HLTF	GRCh38.p7	3:149064003	GATTATAACTCCTTT[-/T]ATTCCAAGATGACCT	6596
rs34277949	in-del	-/T			intron-variant	HLTF	GRCh38.p7	3:149063600	CCCTCTTAAAACCTT[-/T]GGTTTTCTAATTACT	6596
rs34279621	in-del	-/C	0.431916	0.171483	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087733	CCGGGATTGCAGGAG[-/C]CCGCCACCACGCCCA	6596
rs34431669	in-del	-/G			intron-variant	HLTF	GRCh38.p7	3:149074579	GAGAAAATGGAATAA[-/G]AGCAGTTTTAAAAAT	6596
rs34471867	in-del	-/C			intron-variant	HLTF	GRCh38.p7	3:149083410	ACACTAGAGTTTACC[-/C]GAAGTCATAGAGATT	6596
rs34474865	snp	A/G	0.0933436	0.19483	synonymous-codon	HLTF	GRCh38.p7	3:149048879	CTTAGAATCAGAAAG[A/G]AGATGGGTTTTGACA	6596
rs34490329	snp	A/G	0.45235	0.146814	intron-variant	HLTF	GRCh38.p7	3:149045043	TTAAGGTTTCCTGTC[A/G]TAAAAAGTAAAAGCC	6596
rs34490564	in-del	-/C			intron-variant	HLTF	GRCh38.p7	3:149044725	GTAAACAGCAATTCC[-/C]AGCCTTCCACTTATG	6596
rs34529452	in-del	-/C			intron-variant	HLTF	GRCh38.p7	3:149050680	TTAATTAGAAGGCCC[-/C]TTTAATGCTGCATTA	6596
rs34599596	in-del	-/G			intron-variant	HLTF	GRCh38.p7	3:149038989	TTACCAAATAGTTTT[-/G]TTGTCTTATTTTTTT	6596
rs34622270	snp	A/G	0.00699464	0.0587231	missense	HLTF	GRCh38.p7	3:149041582	GATGAGGAATGTGCA[A/G]TTTGCCTGGATTCTT	6596
rs34957864	snp	C/T	0.0648419	0.167978	intron-variant, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149086082	AAGCCCCAGGCCCCC[C/T]ACAGTCGGTGACAGA	6596
rs35042588	snp	C/T	0.0298908	0.118541	intron-variant	HLTF	GRCh38.p7	3:149066129	TCGGCTCATTGAAAC[C/T]TCTACCTCCTGAGTT	6596
rs35063885	in-del	-/G			intron-variant	HLTF	GRCh38.p7	3:149078166	GGTCTATACACAGGG[-/G]AAAAAAAGCAATCAA	6596
rs35134202	in-del	-/A			intron-variant	HLTF	GRCh38.p7	3:149073737	AACGTGCATAACAAA[-/A]CTGCATTAAAAGCCT	6596
rs35142110	in-del	-/C			upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087315	CCAGAGTCTGAGGTG[-/C]ACCGGAAGGAGAATG	6596
rs35150289	snp	C/T	0.0399052	0.1355	intron-variant	HLTF	GRCh38.p7	3:149067887	GGTGGCTCACACCTA[C/T]AGCCCCAGCACTTTG	6596
rs35317937	in-del	-/A			intron-variant	HLTF	GRCh38.p7	3:149051236	AATATAAGGAAGTTT[-/A]AAAAAAAAAAAAAAG	6596
rs35334487	in-del	-/A	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149069159	CAGTTAAAAAAAAAA[-/A]GTTTTCCTTAAGAAT	6596
rs35350158	in-del	-/C			intron-variant	HLTF	GRCh38.p7	3:149046534	TAAGTTCTGTTCCCC[-/C]ATTTTTGTTCCAATC	6596
rs35581343	snp	A/G	0.0414363	0.137845	intron-variant	HLTF	GRCh38.p7	3:149071751	ATTTAATTAACTGGC[A/G]TTAATGTCAAACGGG	6596
rs35593819	in-del	-/C			intron-variant	HLTF	GRCh38.p7	3:149044372	ACACTAATTATTCCC[-/C]TGGCATGGTCATATC	6596
rs35612507	in-del	-/A			intron-variant	HLTF	GRCh38.p7	3:149050523	TCAGTCTAGACCAAA[-/A]TAATAACAATAAGAA	6596
rs35668449	in-del	-/C			intron-variant	HLTF	GRCh38.p7	3:149080703	TTAATTACAATTAGT[-/C]TAACTGTCGTTACAA	6596
rs35758525	snp	G/T	0.0391387	0.134304	intron-variant	HLTF	GRCh38.p7	3:149042592	ATGGCATGCCCTGAG[G/T]GGAAAATCAATACCT	6596
rs35805919	in-del	-/T	0.0399052	0.1355	intron-variant	HLTF	GRCh38.p7	3:149071052	CCATCTCAAAAAAAA[-/T]AAAAAAGAAAACTGA	6596
rs35839013	snp	C/T	0.432063	0.171327	intron-variant	HLTF	GRCh38.p7	3:149034363	TACGATATATCTATA[C/T]GGTTTTGTAGAGTAG	6596
rs35886147	snp	C/T	0.039522	0.134904	intron-variant	HLTF	GRCh38.p7	3:149067197	ATATGTATATATATA[C/T]ACACACACACACAAA	6596
rs35953851	in-del	-/A/G	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149043547	CTGAACTTCAGAGGG[-/A/G]AAAAAAAAAAAAAAA	6596
rs36031760	in-del	-/CG/CT/TC	0	0	intron-variant	HLTF	GRCh38.p7	3:149080412	AACCTCTCCCAGCAT[-/CG/CT/TC]GTCTACTGACTCAAG	6596
rs36037300	in-del	-/A/AA	0	0	intron-variant	HLTF	GRCh38.p7	3:149069472	AAACTCCATCTCAAG[-/A/AA]AAAAAAAAAAAAAAA	6596
rs41267867	snp	C/T	0.022722	0.104193	intron-variant	HLTF	GRCh38.p7	3:149048836	TTTAGAGATTTAAGG[C/T]TTTAGTAAGTTTAAT	6596
rs41267869	snp	C/T	0.00596214	0.0542727	intron-variant	HLTF	GRCh38.p7	3:149068234	GCGCACTTACTACTA[C/T]TTTACCTTCTTCAGT	6596
rs41267871	snp	A/G	0.170867	0.237146	intron-variant	HLTF	GRCh38.p7	3:149076067	TAAAAATGATAAACA[A/G]ATAATATTACATTAT	6596
rs55847638	snp	A/T			intron-variant	HLTF	GRCh38.p7	3:149061438	TAAAATAAAATAAAA[A/T]AAAATAAATTTGAAA	6596
rs56809507	in-del	-/AA	0	0	intron-variant	HLTF	GRCh38.p7	3:149057135	AAAAAAAAAAAAAAA[-/AA]TACAGAATGGGCCAG	6596
rs57089234	snp	C/T			intron-variant	HLTF	GRCh38.p7	3:149070428	GGCATAGTTATTTTT[C/T]TTTTAAAAATATGCT	6596
rs57323042	snp	C/T	0.202651	0.245475	intron-variant	HLTF	GRCh38.p7	3:149078615	GTAATCCCAGCACTT[C/T]GGGAGGCCGAGGTGG	6596
rs58642608	snp	C/T			intron-variant	HLTF	GRCh38.p7	3:149070427	TGGCATAGTTATTTT[C/T]CTTTTAAAAATATGC	6596
rs58937189	snp	A/G	0.487746	0.0773096	intron-variant	HLTF	GRCh38.p7	3:149043524	AGGGGAAAGTCAACA[A/G]AGAAGTTGCTGAACT	6596
rs59169553	snp	A/C	0.133777	0.221342	intron-variant	HLTF	GRCh38.p7	3:149043558	GAGGGAAAAAAAAAA[A/C]AAAAAAAAAAACCAG	6596
rs59371274	snp	A/G			intron-variant	HLTF	GRCh38.p7	3:149050003	ATCGAGAGGGAGGGG[A/G]AGGGGAGGAGTGGAG	6596
rs59657686	snp	A/G	0.0858192	0.188533	intron-variant	HLTF	GRCh38.p7	3:149066293	TCAGGTGATCTGCCC[A/G]CCTCAGCCTCCCAAA	6596
rs59996160	in-del	-/AAAAAA	0	0	intron-variant	HLTF	GRCh38.p7	3:149035678	AAAAAAAAAAAAAAA[-/AAAAAA]GGGGGTTTTAAGAGT	6596
rs60091976	in-del	-/GG			intron-variant	HLTF	GRCh38.p7	3:149055034	CTTTCCCACTTTGGG[-/GG]ACAAAAATAGCAAAG	6596
rs60974987	in-del	-/T			frameshift-variant	HLTF	GRCh38.p7	3:149048111	AAATGGTTTAAGTTT[-/T]AAAAAGGAAAGAAGA	6596
rs61044528	snp	A/C	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149032974	AAAAAAAAAAAAAAA[A/C]AAACAAAAAACTATT	6596
rs61750364	snp	A/G	0.00829723	0.0638731	missense	HLTF	GRCh38.p7	3:149040093	GTGCTAATTCTTCTG[A/G]AGGACATTCTAATAA	6596
rs61750365	snp	A/G	0.00556878	0.0524726	missense	HLTF	GRCh38.p7	3:149040122	AAATTATCTTCATGT[A/G]TATCATTTCTGCATA	6596
rs61750366	snp	A/C			missense, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149084786	CATCTGGAGGGATAA[A/C]ATCTTGGAATTCAAA	6596
rs61755303	snp	A/C/T	0.0124778	0.0779949	missense	HLTF	GRCh38.p7	3:149063459	AGCTAGACAATTCTG[A/C/T]CATGCGAAACTTACT	6596
rs61761956	snp	G/T	0.000626442	0.017687	missense	HLTF	GRCh38.p7	3:149064838	TTGTTTCCTCCAAGT[G/T]TCATAGAGTCATCGT	6596
rs62274646	snp	C/G	0.0197687	0.0974348	intron-variant	HLTF	GRCh38.p7	3:149036579	CAGGCATGAGCCTCC[C/G]CGCCAGGCCATATTA	6596
rs62274647	snp	A/G	0.449979	0.150028	intron-variant	HLTF	GRCh38.p7	3:149037372	TACTCAGGAGGCTGA[A/G]GCAGTGAACCGCTTG	6596
rs62274648	snp	A/C			intron-variant	HLTF	GRCh38.p7	3:149037968	GTTCTACCTTCATGC[A/C]TGTACTACACAACCA	6596
rs62278173	snp	G/T	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149062524	TGTGTAGATACTGAT[G/T]GTAGACAATACAACA	6596
rs62278174	snp	A/G	0.00358779	0.0422022	intron-variant	HLTF	GRCh38.p7	3:149074723	GAAATGCAAGAACTT[A/G]TGATTCACTAAGTTA	6596
rs62889662	in-del	-/A	0.483852	0.0883933	intron-variant	HLTF	GRCh38.p7	3:149081266	TATTGAAAACACACT[-/A]AAAAAAAAAAAACAA	6596
rs66525644	in-del	-/TG	0.338523	0.233803	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087583	CTTTTTTCTTTTTTT[-/TG]TTTTTTTTTCTTTTT	6596
rs67536612	in-del	-/GGCAGCA	0	0	intron-variant	HLTF	GRCh38.p7	3:149058353	AATTAAAGGAATAGT[-/GGCAGCA]GGCATGGTGGCACAT	6596
rs67848144	in-del	-/TAGTC			intron-variant	HLTF	GRCh38.p7	3:149047212	AAGTTGAACCACATT[-/TAGTC]ACATCTTGCAAAATG	6596
rs67952189	in-del	-/TT	0	0	intron-variant	HLTF	GRCh38.p7	3:149032974	GAATAGTTTTTTTTG[-/TT]TTTTTTTTTTTTTTT	6596
rs71135656	in-del	-/AAAAA/AAAAAAAAAAAA	0	0	intron-variant	HLTF	GRCh38.p7	3:149036307	GCGAGACTCCATCTC[-/AAAAA/AAAAAAAAAAAA]AAAAAAAAAACCTCA	6596
rs71135657	in-del	-/T	0	0	intron-variant	HLTF	GRCh38.p7	3:149037483	GTATTTTCTTTTTTC[-/T]TTTTTTTTTTTTTTT	6596
rs71135658	in-del	-/TTTA	0	0	intron-variant	HLTF	GRCh38.p7	3:149077294	CAACAAGCTATTATT[-/TTTA]TTTATTTATTTATTT	6596
rs71135659	in-del	-/TTTTTTTTTTTT	0	0	intron-variant	HLTF	GRCh38.p7	3:149079401	TATTTTTTTAAATAA[-/TTTTTTTTTTTT]TTTTTTTTTTTTTTT	6596
rs71304442	snp	C/T	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149042755	TATGGGCACAGCACT[C/T]TACACTCCAAGCACC	6596
rs71304443	snp	C/G	0.0391387	0.134304	intron-variant	HLTF	GRCh38.p7	3:149046519	CCTGTCCTTATTTTC[C/G]TAAGTTCTGTTCCCC	6596
rs71304444	snp	A/C	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149052505	ACAAAATAAGACATA[A/C]CAAATAATAAATGAA	6596
rs71304445	snp	A/G	0.0391387	0.134304	intron-variant	HLTF	GRCh38.p7	3:149057012	TACTCGGGAGGCTGA[A/G]GCAGGAGAATGGCGT	6596
rs71304446	snp	A/C	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149063320	CCGCCTCGGCCTCCC[A/C]AAGTGCTGGGATTAC	6596
rs71304447	snp	A/T	0.0941369	0.195465	intron-variant	HLTF	GRCh38.p7	3:149065076	TATCTCAAAAAAAAA[A/T]AAATAAATAAAACTA	6596
rs71304448	snp	A/G	0.0391387	0.134304	intron-variant	HLTF	GRCh38.p7	3:149070711	TTTAAAAGAAAACCT[A/G]TGAAAGACAGGTCAC	6596
rs71617497	in-del	-/C	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149083758	AAATACAAAAAAAAA[-/C]AAATACAAAAATTAG	6596
rs71617498	in-del	-/A	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149083929	AGAAAAAAAAAAAAA[-/A]TCCAATTCACTTAAG	6596
rs71708804	in-del	-/GTC			utr-variant-3-prime	HLTF	GRCh38.p7	3:149030476	CAAAGAAGCAAGCTG[-/GTC]TCCTCCCTTTACCTT	6596
rs71867923	in-del	-/A			intron-variant	HLTF	GRCh38.p7	3:149037468	CAAGACTCTGTCTCA[-/A]AAAAAAAAAAAAAAA	6596
rs72220245	in-del	-/TGCCTGC	0.039522	0.134904	intron-variant	HLTF	GRCh38.p7	3:149058349	AGGCATGTGCCACCA[-/TGCCTGC]TGCCACTATTCCTTT	6596
rs72586324	in-del	-/TC	0.495891	0.0451408	intron-variant	HLTF	GRCh38.p7	3:149080411	AAACCTCTCCCAGCA[-/TC]TGTCTACTGACTCAA	6596
rs73011401	snp	C/T	0.0138799	0.0821421	intron-variant	HLTF	GRCh38.p7	3:149044054	TTACAAGCTCTAAAC[C/T]AAAGTGCCAGAGTTA	6596
rs73013104	snp	G/T	0.225	0.256431	intron-variant	HLTF	GRCh38.p7	3:149045196	CATGTTCCCAACTGG[G/T]AGCATCTACACTTGC	6596
rs73013113	snp	C/G	0.0577344	0.159793	intron-variant	HLTF	GRCh38.p7	3:149063668	ACTCTATTTTCTCTA[C/G]TTTTTTCCTAATCTA	6596
rs73013120	snp	C/T	0.0894459	0.191631	intron-variant	HLTF	GRCh38.p7	3:149072516	TTTAAACTAGGTTAG[C/T]CCAATTTTATATCAA	6596
rs73013127	snp	C/T	0.0569829	0.158885	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149086761	TGCGACTGCGGTGCC[C/T]GCGGTGCCGGTGTTT	6596
rs73164909	snp	C/T	0.00517822	0.0506191	intron-variant	HLTF	GRCh38.p7	3:149038974	ATAACTATGAAGGTA[C/T]TTACCAAATAGTTTT	6596
rs73164926	snp	A/C/G	1.67916e-05	0.0028975	missense, stop-gained	HLTF	GRCh38.p7	3:149071437	GAAGCAGTGGTGTTT[A/C/G]AATAGCCTATAAATA	6596
rs73164928	snp	A/G	0.0236746	0.106192	intron-variant	HLTF	GRCh38.p7	3:149072626	AAATCAGAAGTAACC[A/G]GGGGCTTATCTACCA	6596
rs73164929	snp	C/T	0.0425829	0.139564	intron-variant	HLTF	GRCh38.p7	3:149077739	GCCCTAAACGCTCAC[C/T]TTTGCCTGAACTTGA	6596
rs73164930	snp	A/G			intron-variant	HLTF	GRCh38.p7	3:149080374	TTAAAAAATTCCTTG[A/G]AAATATACAAGAAAG	6596
rs73866943	snp	A/G	0.134802	0.221877	intron-variant	HLTF	GRCh38.p7	3:149062862	CCTTGACAAAATAGA[A/G]AAAAAGTAGTAGAAA	6596
rs73866945	snp	C/T	0.134119	0.221521	intron-variant	HLTF	GRCh38.p7	3:149063874	TGTTCAAATCTCAGA[C/T]GTCACCTTGTGTCAC	6596
rs73866946	snp	C/T	0.134802	0.221877	intron-variant	HLTF	GRCh38.p7	3:149065109	TGGCCTTCACCTTTT[C/T]GAAAGGAATACCGAA	6596
rs73866949	snp	A/C	0.0119091	0.0762411	intron-variant	HLTF	GRCh38.p7	3:149078916	CTTTCGACATGAAAA[A/C]GCATGTCTAAAAGCA	6596
rs74352455	snp	C/T	0.040671	0.13668	intron-variant	HLTF	GRCh38.p7	3:149058689	TTACTAAAGAGATCA[C/T]TATCTACCACAAGGA	6596
rs74360459	snp	C/T	0	0	intron-variant	HLTF	GRCh38.p7	3:149035284	AATTTGGTTTTTTTT[C/T]TCATTTTTAAAAGAA	6596
rs74362624	snp	A/G	0.139564	0.224285	intron-variant	HLTF	GRCh38.p7	3:149080240	AGGTTTCTTTTTGGA[A/G]TAATGAAAATGTTTT	6596
rs74394333	snp	A/T	0.00993419	0.0697739	intron-variant	HLTF	GRCh38.p7	3:149036767	AAAAAGAAAAAAAAA[A/T]TTAATGGTAAAAGAC	6596
rs74403158	snp	C/T	0.00755907	0.0610114	intron-variant	HLTF	GRCh38.p7	3:149037164	ACTTCATCCACAGTA[C/T]AAAGGCAAGAAAATA	6596
rs74447689	snp	A/T			intron-variant	HLTF	GRCh38.p7	3:149039273	ACAAACACTATTATT[A/T]TAAAAATAAAACAAA	6596
rs74629339	snp	C/T	0.0248432	0.108648	intron-variant	HLTF	GRCh38.p7	3:149055476	AGGAGATGGCAATAA[C/T]GTGCCTCCATGAAAA	6596
rs74739643	snp	A/G	0.0295035	0.117819	intron-variant	HLTF	GRCh38.p7	3:149064046	AAAGAAAATGAGAAG[A/G]TATCTTCCATAAAAA	6596
rs74812631	snp	C/T	0.0123036	0.0774623	intron-variant	HLTF	GRCh38.p7	3:149050836	TTGCCAGGTATCAAC[C/T]ACAATAGTGATGTAA	6596
rs74820266	snp	C/T	0.0100011	0.0700039	missense	HLTF	GRCh38.p7	3:149064862	TCATCGTTAACATTA[C/T]ATTCCTGGGTAAATA	6596
rs74865250	snp	G/T	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149077530	AGTGTTTTAACTTCA[G/T]GGCTACCTGAGGCAG	6596
rs74927267	snp	G/T	0.000862747	0.0207516	missense	HLTF	GRCh38.p7	3:149040062	CATTCCATATCAGAC[G/T]TTTTCTCACTGTCAC	6596
rs75019974	snp	C/T	0	0	intron-variant	HLTF	GRCh38.p7	3:149066061	CTTCTTTTTTTTTTT[C/T]CTGAGACAGAGTTTC	6596
rs75130084	snp	A/C	0.0158469	0.0875917	intron-variant	HLTF	GRCh38.p7	3:149077738	GGCCCTAAACGCTCA[A/C]CTTTGCCTGAACTTG	6596
rs75136918	snp	C/T	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149066062	TTCTTTTTTTTTTTT[C/T]TGAGACAGAGTTTCA	6596
rs75188919	snp	A/T	0.000399281	0.0141238	missense	HLTF	GRCh38.p7	3:149048940	GGATTTCGTATGGCA[A/T]GTCCTTCATCCAGGA	6596
rs75343158	snp	C/T	0.0422008	0.138995	intron-variant	HLTF	GRCh38.p7	3:149044073	GTGCCAGAGTTAATC[C/T]GTCCTGTCACTCACT	6596
rs75483592	snp	A/G	0.0114542	0.0748058	synonymous-codon, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149084826	GAAAGTTGGATATGA[A/G]AGGCGTGGAAAATTT	6596
rs75572145	snp	A/C	0.113334	0.209338	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149088548	AAAAAAATAAAAAGA[A/C]TTAAGATCTATGAAT	6596
rs75617527	snp	C/T	0.0505692	0.150756	intron-variant	HLTF	GRCh38.p7	3:149080118	GTATCATTTCATTTA[C/T]GTGAAATGTCAAGAG	6596
rs75682116	snp	A/G	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149067684	TTAAAACAATGTTGA[A/G]GGAAAAAAAAATAAT	6596
rs75788315	snp	A/C	0.00478085	0.0486577	intron-variant	HLTF	GRCh38.p7	3:149071145	ATAGTAAGATCTAGT[A/C]CCAAACTGGTACCAA	6596
rs75816746	snp	A/G	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149078989	GTACAATAACTGAAG[A/G]AAAAATTCACCAGAG	6596
rs75834493	snp	A/G	0.00358779	0.0422022	intron-variant	HLTF	GRCh38.p7	3:149046660	AAATGTTGTAAGAAT[A/G]CAAATATGGGTAAGA	6596
rs75934412	snp	C/G	0.134119	0.221521	intron-variant	HLTF	GRCh38.p7	3:149065685	ATAGACACAGATTAG[C/G]CAGGCATGGTGGCGG	6596
rs75965286	snp	A/G	2.64302e-05	0.00363516	intron-variant	HLTF	GRCh38.p7	3:149032383	ATGAACTTTAAAAAG[A/G]AAAAAAAAAGTTAAG	6596
rs75988131	snp	C/T	0.0349115	0.127424	intron-variant	HLTF	GRCh38.p7	3:149078938	CTAAAAGCATGGAGA[C/T]GATGTCTCACCAAAC	6596
rs75990373	snp	C/T	0.0456336	0.143994	intron-variant	HLTF	GRCh38.p7	3:149053447	GTGATGCTGGGTCCC[C/T]ATCACCTTCTGCCAA	6596
rs76044191	snp	A/G	0.00199481	0.0315187	intron-variant	HLTF	GRCh38.p7	3:149074155	CAAGAGAGAATAAAT[A/G]TTTCATAATCCCTGC	6596
rs76339830	snp	C/G	0.0158469	0.0875917	intron-variant	HLTF	GRCh38.p7	3:149033328	TGGAAACATTCGTTA[C/G]TTATAAAGAAAGATA	6596
rs76341895	snp	A/G	0.00398564	0.0444627	intron-variant	HLTF	GRCh38.p7	3:149052965	TGTATCATCCTCTCA[A/G]TAGAAAACGAAATAG	6596
rs76445146	snp	A/C	0.00874735	0.0655527	intron-variant	HLTF	GRCh38.p7	3:149038398	GTACTTAAATATTTA[A/C]ATGGACTATGATTCT	6596
rs76645455	snp	C/T	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149067716	ATAATAAAAAAAAAC[C/T]TGTATTTTCTTTGGA	6596
rs76743950	snp	A/C	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149071046	CAAGACTCCATCTCA[A/C]AAAAAAAAAAAAGAA	6596
rs76820644	snp	A/G	0.0130921	0.0798413	intron-variant	HLTF	GRCh38.p7	3:149056183	CAGCTAAGCCACTCC[A/G]ACTTCCAGCCCTGTC	6596
rs77124155	snp	C/T	0.5	0	intron-variant, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149085287	CCTGAGGTCAGGAAT[C/T]TGAGACCAACCTGGC	6596
rs77360323	snp	G/T	0.5	0	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087584	TTTTTTCTTTTTTTT[G/T]TTTTTTTTTCTTTTT	6596
rs77400372	snp	C/G	0.0422008	0.138995	intron-variant	HLTF	GRCh38.p7	3:149045412	ATATAAATTCCTCGA[C/G]TGCAGGCATTTTTGT	6596
rs77702256	snp	A/G	0.0622301	0.165053	intron-variant	HLTF	GRCh38.p7	3:149082494	AAAGAAATGAGACTC[A/G]TGGCTGCCTAGGGCA	6596
rs77740858	snp	C/T	0.0158469	0.0875917	intron-variant	HLTF	GRCh38.p7	3:149076412	GTACATTGCACAGAC[C/T]GACTTTTTAAATCCT	6596
rs78116525	snp	C/T	0.0486741	0.148216	intron-variant	HLTF	GRCh38.p7	3:149058606	CTTTGTTTATGGCAC[C/T]TTTTGATGCATGGAA	6596
rs78191481	snp	A/C	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149078856	AGCAAGACTCCGTCT[A/C]AAAAAAAAAAAAAAA	6596
rs78246157	snp	G/T	0.108048	0.20579	intron-variant	HLTF	GRCh38.p7	3:149078985	AAAGGTACAATAACT[G/T]AAGAAAAAATTCACC	6596
rs78312913	snp	C/G	0.00795532	0.062565	intron-variant	HLTF	GRCh38.p7	3:149080769	TGAGCCAAAATATTG[C/G]AGACTATAAAAACAA	6596
rs78333515	snp	A/T	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149066530	TTGAAAGAGTGACAA[A/T]TTTTTTTTTTTTTTT	6596
rs78415713	snp	C/T	0.0460142	0.144533	intron-variant	HLTF	GRCh38.p7	3:149038563	GCTGGAGTGCAGTGA[C/T]AGGAGCATGGCTCAC	6596
rs78433146	snp	A/G	0.00207669	0.0321564	intron-variant	HLTF	GRCh38.p7	3:149041441	ATTATATTAAAGACA[A/G]GTACACTACTCTATC	6596
rs78509339	snp	G/T	0.0345262	0.126772	intron-variant, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149086226	GCACAAATCGCCCAG[G/T]GAACGCAGAGGAACG	6596
rs78525660	snp	A/G	0.000979651	0.0221103	missense	HLTF	GRCh38.p7	3:149059789	AATGCCACATCTTCT[A/G]TAACCTTAGAAGATC	6596
rs78551114	snp	A/C	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149078858	CAAGACTCCGTCTCA[A/C]AAAAAAAAAAAAATA	6596
rs78569756	snp	C/T	0.0165278	0.0893908	intron-variant	HLTF	GRCh38.p7	3:149058605	ACTTTGTTTATGGCA[C/T]CTTTTGATGCATGGA	6596
rs78662523	snp	A/G	0.109108	0.206518	intron-variant	HLTF	GRCh38.p7	3:149061914	AACACAATGAAATAA[A/G]CAGCCAAAAGGCAAA	6596
rs78770696	snp	A/C	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149081267	ATTGAAAACACACTA[A/C]AAAAAAAAAAACAAA	6596
rs78884484	snp	A/G	0.139564	0.224285	intron-variant	HLTF	GRCh38.p7	3:149082690	TAAAGTAGAAAAAAA[A/G]TTAAAATAACAAGTA	6596
rs78955028	snp	C/T	0.0345262	0.126772	intron-variant	HLTF	GRCh38.p7	3:149045076	AGTCCTTGACATATG[C/T]GTTACATACCCCCAT	6596
rs78957066	snp	A/G	0.0170251	0.090679	intron-variant	HLTF	GRCh38.p7	3:149080134	GTGAAATGTCAAGAG[A/G]AGGTAAATCCATATA	6596
rs78965174	snp	C/T	0.134802	0.221877	intron-variant	HLTF	GRCh38.p7	3:149033026	CTTTAGTATAATTCA[C/T]AACACTAACAAAGAG	6596
rs79074995	snp	A/T	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149080050	ACACTAAAAAAAAAA[A/T]TCTATTTAACATAAA	6596
rs79303177	snp	C/T	0.0010433	0.0228158	intron-variant	HLTF	GRCh38.p7	3:149059395	AAATTAAACCTTTAA[C/T]TTAAATTAACCAAAA	6596
rs79393620	snp	A/G	0.0345262	0.126772	intron-variant	HLTF	GRCh38.p7	3:149038216	AAGACTACTAGAACC[A/G]TGATGGTAATCATTT	6596
rs79444203	snp	A/C	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149032975	AAAAAAAAAAAAAAA[A/C]AACAAAAAACTATTC	6596
rs79466282	snp	A/C	0.0205511	0.0992634	intron-variant	HLTF	GRCh38.p7	3:149034728	GGAGATGTACACATA[A/C]CTATAAATGTAGGTG	6596
rs79551442	snp	C/G	0.021333	0.101051	utr-variant-3-prime	HLTF	GRCh38.p7	3:149030713	TTATTCCACTATCAT[C/G]CCTGCAGAAAGGTCT	6596
rs79567952	snp	A/G	0.0182019	0.0936463	intron-variant	HLTF	GRCh38.p7	3:149056491	GAAGGTGAGCAAAGT[A/G]TCATACTGTATCTAC	6596
rs79738559	snp	A/T	0	0	intron-variant	HLTF	GRCh38.p7	3:149081268	TTGAAAACACACTAA[A/T]AAAAAAAAAACAAAA	6596
rs79764551	in-del	-/AA			intron-variant	HLTF	GRCh38.p7	3:149071062	AAAAAAAAAAAAGAA[-/AA]CTGAGGAACACATCT	6596
rs79794258	snp	C/G	0.00993419	0.0697739	intron-variant	HLTF	GRCh38.p7	3:149055075	CAAACCAAATCTTAT[C/G]TTAGCAATTGATTAT	6596
rs79808266	snp	A/C/T	0.00122089	0.0246773	synonymous-codon	HLTF	GRCh38.p7	3:149074267	CAACTGATCTGAAAC[A/C/T]GCTTTTCTATTTTCT	6596
rs79982077	in-del	-/AAAAAA			intron-variant	HLTF	GRCh38.p7	3:149043564	AAAAAAAAAAAAAAA[-/AAAAAA]CCAGGCTTCCCCACA	6596
rs79998012	snp	C/G	0.0452528	0.143452	intron-variant	HLTF	GRCh38.p7	3:149044501	CTATCTTCACAGTTA[C/G]ATCTCTTTCACTTTA	6596
rs80001066	snp	C/T	0.0345262	0.126772	intron-variant	HLTF	GRCh38.p7	3:149074737	TGTGATTCACTAAGT[C/T]ATTCTCAATAACTGA	6596
rs80082239	snp	A/C	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149032959	CAGAGCGACGTCTCA[A/C]AAAAAAAAAAAAAAA	6596
rs80082977	snp	A/C	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149071044	AGCAAGACTCCATCT[A/C]AAAAAAAAAAAAAAG	6596
rs80111164	snp	A/T	0	0	intron-variant	HLTF	GRCh38.p7	3:149083940	AAAGAAAAAAAAAAA[A/T]ATCCAATTCACTTAA	6596
rs80255020	snp	A/G	0.0174175	0.0916809	intron-variant, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149084356	AAATGAAAGAATAAA[A/G]TCCAGAAGATTCCAC	6596
rs80336605	snp	C/T	0.000692841	0.0185995	missense	HLTF	GRCh38.p7	3:149071341	TGTTATAGTATAAGT[C/T]ATTTCGCTGTTCCCA	6596
rs80349185	snp	A/T			utr-variant-3-prime, intron-variant	HLTF	GRCh38.p7	3:149031381	GAATTATAAAAATTT[A/T]TAAAGTTACTTCCAA	6596
rs111239765	snp	C/T	0.00643883	0.0563734	missense	HLTF	GRCh38.p7	3:149063464	GACAATTCTGACATG[C/T]GAAACTTACTCTTCT	6596
rs111289086	snp	A/G	0.0577344	0.159793	intron-variant	HLTF	GRCh38.p7	3:149082454	ACAGAGCGAGACTCC[A/G]TCTCAAAAAAAACAA	6596
rs111308670	in-del	-/AG	0.077417	0.180873	intron-variant	HLTF	GRCh38.p7	3:149070093	AGATTTTAACAAAAC[-/AG]GGTATAAAAAGCTCA	6596
rs111342204	snp	C/T	0.078151	0.181571	intron-variant	HLTF	GRCh38.p7	3:149083680	TTGGAGAGGCCAAGG[C/T]GGACGGATCACTTGA	6596
rs111353787	snp	C/T	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149066113	GTGCAACGGCACAAT[C/T]TCGGCTCATTGAAAC	6596
rs111381549	snp	A/T	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149081712	AAAATGGCACATTTT[A/T]TCAAAATTTGACAAT	6596
rs111402730	snp	C/T	0	0	intron-variant	HLTF	GRCh38.p7	3:149067900	TATAGCCCCAGCACT[C/T]TGGGAGGCTGAGGCA	6596
rs111441914	snp	A/G	0.0158469	0.0875917	intron-variant	HLTF	GRCh38.p7	3:149068109	TCTTATCAGCAACAC[A/G]TAAAAGACAGAGAGA	6596
rs111619107	snp	C/T	0.109108	0.206518	intron-variant, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149085422	TGAACCCGGGAGGCG[C/T]AGGTTGCAGCGAGCC	6596
rs111660642	snp	C/T	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149035256	ACCCAAAATAAGTAT[C/T]TGTTGATTAATCAAT	6596
rs111707454	snp	A/G	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149058387	ATTTGCATCTCCCCA[A/G]TAATTCTGAATCAGC	6596
rs111736311	snp	G/T	0.0193772	0.0965046	intron-variant	HLTF	GRCh38.p7	3:149046498	CATAGTTTAATCTTT[G/T]TATATCCTGTCCTTA	6596
rs111755636	snp	A/G	0.102014	0.201495	intron-variant	HLTF	GRCh38.p7	3:149046883	TTGAAATATAAATAC[A/G]ATTTCCTGGAGTTTA	6596
rs111789341	snp	A/G	0.0170251	0.090679	intron-variant	HLTF	GRCh38.p7	3:149075092	CTTGTCAAGAGAAAA[A/G]TAAGTTTTTTGTATT	6596
rs111876178	snp	C/T	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149078218	TATAGATGTTTGACA[C/T]AGTAGAAAAAGAATT	6596
rs111968083	snp	C/T	0	0	intron-variant	HLTF	GRCh38.p7	3:149047585	AGGCGGAGGTTGCAG[C/T]GAGCCAAGATCGCGC	6596
rs112020463	snp	A/G	1.85046e-05	0.00304171	synonymous-codon	HLTF	GRCh38.p7	3:149046208	TTTTCCTTTAATTTT[A/G]CTTGTCTTTGTTCTT	6596
rs112069451	snp	A/G	0	0	intron-variant	HLTF	GRCh38.p7	3:149056838	GAATGGGCCGGGCGC[A/G]GTGGCTCACGCCTGT	6596
rs112092174	in-del	-/A	0.00199481	0.0315187	intron-variant, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149085585	CTATTAATGTACCAG[-/A]AGTTGTTTATAATTT	6596
rs112095614	snp	A/G	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149075485	GGAGGCGGAGGTTGC[A/G]GTCAGCCGAGATCAC	6596
rs112110631	snp	A/T	0.0023933	0.0345097	intron-variant	HLTF	GRCh38.p7	3:149070036	GGTGTTATAAAATCA[A/T]ACATGGGTAAAATAT	6596
rs112118103	snp	C/G	0.108402	0.206034	intron-variant	HLTF	GRCh38.p7	3:149061294	TGGGTGCCTGTAGTC[C/G]CAGCTACTCGGGAGG	6596
rs112127156	snp	C/T	0.00159617	0.0282053	intron-variant	HLTF	GRCh38.p7	3:149042991	AAGGTAGGGGACACA[C/T]GGCAGTGAAAGAAAA	6596
rs112176054	snp	C/T	0.00279162	0.0372561	intron-variant	HLTF	GRCh38.p7	3:149047090	ATATTTACTAATCTC[C/T]TCTCTATTTCATTGT	6596
rs112285259	snp	A/G	0.0023933	0.0345097	intron-variant	HLTF	GRCh38.p7	3:149048494	AAGCAACTAGTTTAA[A/G]TTTACATTCTTTTCC	6596
rs112323948	snp	C/T	0.0562307	0.157967	intron-variant	HLTF	GRCh38.p7	3:149037460	GCGACAGAGCAAGAC[C/T]CTGTCTCAAAAAAAA	6596
rs112355613	in-del	-/TAGTC	0.301429	0.244653	intron-variant	HLTF	GRCh38.p7	3:149047211	AAAGTTGAACCACAT[-/TAGTC]TACATCTTGCAAAAT	6596
rs112446442	in-del	-/T	0	0	intron-variant	HLTF	GRCh38.p7	3:149065076	ATCTCAAAAAAAAAA[-/T]AAATAAATAAAACTA	6596
rs112491635	snp	A/T	0.0524604	0.153226	intron-variant	HLTF	GRCh38.p7	3:149056950	CCGTCTCTACTAAAA[A/T]TACAAAAAATTAGCC	6596
rs112520716	snp	C/T	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149063577	AGGTGTCTTAGAAAC[C/T]AGTATTATCCCTCTT	6596
rs112563223	snp	A/C	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149032967	CGTCTCAAAAAAAAA[A/C]AAAAAAAAAACAAAA	6596
rs112633508	snp	C/T	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149046017	ATCTAAATAATGTCA[C/T]TCAGTGAATGGGAAA	6596
rs112694673	snp	C/T	0.00358779	0.0422022	intron-variant	HLTF	GRCh38.p7	3:149055845	ATATAGCAGAGAAGA[C/T]AGTATGTCACTTCTG	6596
rs112726323	snp	A/C	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149070815	TTTGGGAGGCCAAGG[A/C]GGGCGGATCACTTGA	6596
rs112727652	snp	A/C	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149032977	AAAAAAAAAAAAAAA[A/C]CAAAAAACTATTCCC	6596
rs112819626	in-del	-/TTTAG	0.0509322	0.151235	intron-variant, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149084661	ATAATCAAAATTTAA[-/TTTAG]TTATCTACTATTATA	6596
rs112854938	snp	A/C	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149043013	GAAAGAAAACTCAGC[A/C]GAAAAATGTTGCCAC	6596
rs112974997	snp	C/T	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149047740	ATGTTTCCTGCTAAA[C/T]CTGTTAATGCTGGTT	6596
rs113098497	snp	A/G	0.113334	0.209338	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087722	CTCCGGAGTAGCCGG[A/G]ATTGCAGGAGCCCGC	6596
rs113123407	snp	A/T	0.039522	0.134904	intron-variant	HLTF	GRCh38.p7	3:149052149	ACAGAGCAAGACTGT[A/T]AAAAAAAAAAAAAAA	6596
rs113167303	snp	A/G	0.139564	0.224285	intron-variant, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149085972	CACTTGGGGACAAGG[A/G]CTGTCTTACTCGGCC	6596
rs113179265	snp	C/T	0	0	intron-variant	HLTF	GRCh38.p7	3:149067453	GTTTTATGGCTATAT[C/T]GTTTAACTGTTCCCT	6596
rs113180866	snp	C/T	0.109108	0.206518	intron-variant	HLTF	GRCh38.p7	3:149078071	AACAAACCACCCTGA[C/T]TTCCAGAGCTGCCAC	6596
rs113208202	snp	A/G	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149041407	AAATCCAAGTGCAAA[A/G]CTCCATATACTATCT	6596
rs113222666	snp	C/T	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149074161	AGAATAAATGTTTCA[C/T]AATCCCTGCATCTTA	6596
rs113344295	snp	A/G	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149037484	AAAAAAAAAAAAAAA[A/G]AAAAAAGAAAATACA	6596
rs113356030	snp	A/G	0.444444	0.157135	intron-variant	HLTF	GRCh38.p7	3:149072988	TGCATAAACAGGAAC[A/G]TGTGTGTTTTGTATG	6596
rs113393362	snp	G/T	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149042027	TATTGGATGTATTCC[G/T]AGCTGAGTCTCACAC	6596
rs113483340	snp	C/G	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149072270	TGTAAGTTTCAGCAA[C/G]ACTTGACCTTTATGG	6596
rs113483664	snp	C/T	0.110519	0.207473	intron-variant	HLTF	GRCh38.p7	3:149042559	ACAGAGCTGCCAAAA[C/T]ACAATTCTTTAAAAT	6596
rs113586374	snp	C/T	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149047675	ATAAATAAATAAAGC[C/T]ATATAAGATATGAAA	6596
rs113591205	snp	A/G	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149063983	TACATTGACCCCTTT[A/G]CCTAGATTATAACTC	6596
rs113656986	snp	C/T	0.0569829	0.158885	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087812	GGCTGGTCTTGAACT[C/T]CTGACCTCAGGTGAT	6596
rs113659904	snp	G/T	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149072451	ACTGCAATAAGGAAC[G/T]TGCCATGCACTATAG	6596
rs113660773	snp	A/G	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149071133	TGTTCTACAAAGATA[A/G]TAAGATCTAGTCCCA	6596
rs113677209	snp	G/T	0.000136839	0.00827047	intron-variant	HLTF	GRCh38.p7	3:149048171	TGGAGTACCTAGAAA[G/T]AACAGGAAACTGTTA	6596
rs113743362	snp	A/G	0.5	0	intron-variant	HLTF	GRCh38.p7	3:149071499	TCCTTTTTCACATGC[A/G]GATCCTGTGATTAAA	6596
rs113869632	snp	C/T	0.5	0	missense	HLTF	GRCh38.p7	3:149041639	TCTTCCTTATTAACT[C/T]CTTTCTCAGTTCTTC	6596
rs113954540	snp	A/T			intron-variant	HLTF	GRCh38.p7	3:149038740	CTGCTCTCAAACTCC[A/T]GAGCTCAGGCAATCC	6596
rs113966612	snp	C/T	0	0	intron-variant	HLTF	GRCh38.p7	3:149069696	TTTCATGCGACACCA[C/T]TTTTACTTGAATGAC	6596
rs113977520	snp	C/G	0	0	intron-variant	HLTF	GRCh38.p7	3:149083674	CAGCACTTGGAGAGG[C/G]CAAGGCGGACGGATC	6596
rs113982014	snp	A/G	0.5	0	missense	HLTF	GRCh38.p7	3:149064841	TTTCCTCCAAGTTTC[A/G]TAGAGTCATCGTTAA	6596
rs114001266	snp	C/T	0.00993419	0.0697739	intron-variant	HLTF	GRCh38.p7	3:149062276	ATTATTATTTCTATG[C/T]CCTTTAATCTGATCT	6596
rs114001482	snp	C/T	0.0349115	0.127424	intron-variant	HLTF	GRCh38.p7	3:149082180	GAAGACTTGTGTGGC[C/T]GGGCGCAGTGGCTCA	6596
rs114005934	snp	A/G	0.0287284	0.116357	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149088553	AATAAAAAGACTTAA[A/G]ATCTATGAATAATGA	6596
rs114045609	snp	C/T	0.0267878	0.112589	intron-variant	HLTF	GRCh38.p7	3:149075500	AGTCAGCCGAGATCA[C/T]ACAACTGCACTGCAG	6596
rs114134829	snp	A/G	0.00993419	0.0697739	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087282	GAGGGGCGCTCTGAG[A/G]CCCTCCATGGCTCTC	6596
rs114201035	snp	C/T	0.00318978	0.0398085	intron-variant	HLTF	GRCh38.p7	3:149038133	GGTCTAATCCTAGAA[C/T]TCCTAAGTCTCTACG	6596
rs114222688	snp	A/G	0.0138799	0.0821421	intron-variant	HLTF	GRCh38.p7	3:149051133	AGACTGATAGGACTT[A/G]GGGACTAATGAAATA	6596
rs114273913	snp	A/G	0.0217236	0.101931	intron-variant	HLTF	GRCh38.p7	3:149056807	TTTTGTTAACCAAAC[A/G]TGGATTAAAAATACA	6596
rs114322607	snp	C/T	0.011485	0.0749039	missense	HLTF	GRCh38.p7	3:149071340	GTGTTATAGTATAAG[C/T]CATTTCGCTGTTCCC	6596
rs114332582	snp	A/G	0.0138799	0.0821421	intron-variant	HLTF	GRCh38.p7	3:149041282	AATGATATAAACAGC[A/G]GAATTAAGATATTGA	6596
rs114381999	snp	A/G	0.0341408	0.126114	intron-variant	HLTF	GRCh38.p7	3:149056106	CAATGTTCAGATGAC[A/G]GCGGCCCCTGAAGAA	6596
rs114390725	snp	C/G	0.0341408	0.126114	intron-variant	HLTF	GRCh38.p7	3:149035776	TTTGACTTTAAAGCT[C/G]AGCTAAAAAAAGTAC	6596
rs114488839	snp	A/G	0.0134861	0.0810011	intron-variant	HLTF	GRCh38.p7	3:149041740	ATCTATCTTATAAGG[A/G]AAAGTTTCGCTTGCC	6596
rs114493889	snp	A/G/T	0.0111196	0.0737302	intron-variant	HLTF	GRCh38.p7	3:149043349	AAATGTAAAAGATCA[A/G/T]AAATAAAATGATACC	6596
rs114497838	snp	G/T	0.0452528	0.143452	intron-variant	HLTF	GRCh38.p7	3:149038877	ATTTCAGTAAAGTGC[G/T]TAAGAGAAAGCTCTT	6596
rs114574704	snp	A/G	0.0279526	0.114869	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087348	GCCCTGGGACCGTCA[A/G]CCTTGGACCAGCTGC	6596
rs114811100	snp	C/T	0.0162398	0.0886349	intron-variant	HLTF	GRCh38.p7	3:149045669	TTCACTTGTCTCTTA[C/T]TCATTCTGTTCCCTG	6596
rs114830634	snp	A/G	0.0341408	0.126114	intron-variant	HLTF	GRCh38.p7	3:149035840	ACTGTTTTAAGCTAA[A/G]AAATAAAATGATGGG	6596
rs114882190	snp	C/T	0.0345262	0.126772	intron-variant	HLTF	GRCh38.p7	3:149065272	CCATTGTCATCCTCT[C/T]TTTCTCTAGAATTTG	6596
rs114899652	snp	C/T	0.00993419	0.0697739	intron-variant	HLTF	GRCh38.p7	3:149058457	TCTATGGACTCCATA[C/T]GTACATCCTTTGACT	6596
rs114911279	snp	A/G	0.0158469	0.0875917	intron-variant	HLTF	GRCh38.p7	3:149034395	CAAATTCAGAGAAAG[A/G]AAGTAGAATGGTAGT	6596
rs114986110	snp	C/T	0.00279162	0.0372561	intron-variant	HLTF	GRCh38.p7	3:149062508	CAAATTTGCGATGAC[C/T]TGTGTAGATACTGAT	6596
rs115010561	snp	A/G	0.00517822	0.0506191	intron-variant	HLTF	GRCh38.p7	3:149068049	CTGGGCAACAGAGCC[A/G]CACCTTGTCTGAAAA	6596
rs115326021	snp	C/T	0.02016	0.0983543	intron-variant	HLTF	GRCh38.p7	3:149081260	TATGCTTATTGAAAA[C/T]ACACTAAAAAAAAAA	6596
rs115376930	snp	A/C	0.00993419	0.0697739	intron-variant	HLTF	GRCh38.p7	3:149057593	CCAAATCCCTGACAA[A/C]TACTGAGGGATGACT	6596
rs115425356	snp	C/G	0.0345262	0.126772	intron-variant	HLTF	GRCh38.p7	3:149072172	GCGAATGAACAGGTG[C/G]TTTAGTTGTTAGGAG	6596
rs115425991	snp	C/T	0.0352966	0.128072	intron-variant	HLTF	GRCh38.p7	3:149056267	TTTGTTACACAGTAA[C/T]AGGTAACTAATATAT	6596
rs115481794	snp	A/G	0.0391387	0.134304	intron-variant	HLTF	GRCh38.p7	3:149079028	CAGCAAATTTGAGCA[A/G]GCATAAGAAAAATCA	6596
rs115523058	snp	C/G	0.0452528	0.143452	intron-variant	HLTF	GRCh38.p7	3:149047162	CCCACTAATAGCTCT[C/G]AAATCTTCAGTCTAT	6596
rs115604932	snp	C/G	0.00159617	0.0282053	downstream-variant-500B	HLTF	GRCh38.p7	3:149029734	TGCCGAAGATCATTA[C/G]TACTCACTGGTAACA	6596
rs115625048	snp	A/C	0.0236746	0.106192	intron-variant	HLTF	GRCh38.p7	3:149074514	GGAAAAGAAATAGAA[A/C]CATAAACAATCAGAA	6596
rs115634563	snp	A/G	0.0217236	0.101931	intron-variant	HLTF	GRCh38.p7	3:149061268	ATAAATTTGATAGCC[A/G]GGCGTGGTGGTGGGT	6596
rs115640344	snp	A/C	0.0126979	0.078662	intron-variant	HLTF	GRCh38.p7	3:149049599	ATTGTGATAGAAAAC[A/C]ATTTTCCAGAATATT	6596
rs115678672	snp	A/G	0.0345262	0.126772	intron-variant	HLTF	GRCh38.p7	3:149067200	TGTATATATATACAC[A/G]CACACACACAAATTT	6596
rs115743986	snp	C/T	0.0248432	0.108648	intron-variant	HLTF	GRCh38.p7	3:149043889	TGTTATTTAATTTAA[C/T]ACATGTAAAGTATTT	6596
rs115803229	snp	A/G	0.0134861	0.0810011	intron-variant	HLTF	GRCh38.p7	3:149078479	TGCTTGAATGCAGGA[A/G]TTCAAGGTTACAGTG	6596
rs115959228	snp	C/T	0.0456336	0.143994	intron-variant	HLTF	GRCh38.p7	3:149066553	TTTTTTTTAATAAAT[C/T]CCTGGCTGGAAATCA	6596
rs115976491	snp	A/G	0.0345262	0.126772	intron-variant	HLTF	GRCh38.p7	3:149079162	ATACATAAGAGTACC[A/G]TAAGGAGAAAAGAGA	6596
rs116028561	snp	A/G	0.0345262	0.126772	intron-variant	HLTF	GRCh38.p7	3:149078936	GTCTAAAAGCATGGA[A/G]ACGATGTCTCACCAA	6596
rs116029935	snp	A/G	0.00358779	0.0422022	intron-variant, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149085493	GACTCCATGTCAAAA[A/G]AATAATTTAAAAAAT	6596
rs116119418	snp	C/T	0.0501905	0.150254	intron-variant	HLTF	GRCh38.p7	3:149047149	AATGATTTTATATCC[C/T]ACTAATAGCTCTCAA	6596
rs116162490	snp	C/G	0.0189856	0.0955633	intron-variant	HLTF	GRCh38.p7	3:149061277	ATAGCCGGGCGTGGT[C/G]GTGGGTGCCTGTAGT	6596
rs116181032	snp	A/T	0.0460142	0.144533	intron-variant	HLTF	GRCh38.p7	3:149072247	GTTTTATCACAAATA[A/T]GCTTATATGTAAGTT	6596
rs116193937	snp	C/T	0.0158469	0.0875917	intron-variant	HLTF	GRCh38.p7	3:149076294	TAAAAAATAGTCAAA[C/T]GTAAACTAGCAAATT	6596
rs116213243	snp	A/G	0.00676609	0.0577691	intron-variant	HLTF	GRCh38.p7	3:149034296	TTTATATATAATAAT[A/G]CTCATTATGGCACTG	6596
rs116280880	snp	A/T	0.0256215	0.110247	intron-variant	HLTF	GRCh38.p7	3:149032513	TAACTATTTAATAGA[A/T]CTGAACTTTGCTTTC	6596
rs116380751	snp	C/T	0.00597247	0.0543191	intron-variant	HLTF	GRCh38.p7	3:149041055	TGTGGCTAAGCCAAA[C/T]TGAGGTGTGCTGTAA	6596
rs116450854	snp	A/T	0.00199481	0.0315187	intron-variant	HLTF	GRCh38.p7	3:149038664	AGCACAAACCACTAC[A/T]CCAGAGTAACTTTTC	6596
rs116690824	snp	C/T	0.0103295	0.0711199	intron-variant	HLTF	GRCh38.p7	3:149038592	ACTGAAACTTCAACC[C/T]CCTGGGCCCAAGCAA	6596
rs116818539	snp	A/G	0.0341408	0.126114	intron-variant	HLTF	GRCh38.p7	3:149073515	CCTGGGCAACATGGT[A/G]AGATTCTGTCTCTAC	6596
rs117041763	snp	G/T	0.0115144	0.0749975	intron-variant	HLTF	GRCh38.p7	3:149050023	GAGGAGTGGAGAAAA[G/T]AAAAATACTCCTAAA	6596
rs117586729	snp	C/T	1.71876e-05	0.00293147	intron-variant	HLTF	GRCh38.p7	3:149041469	ATCAAACACTGAACC[C/T]GTACTGAGCAAAAAA	6596
rs117710151	snp	C/T	0.00318978	0.0398085	intron-variant	HLTF	GRCh38.p7	3:149065260	TTAATGAGGCTGCCA[C/T]TGTCATCCTCTCTTT	6596
rs118103872	snp	C/T	0.00318978	0.0398085	intron-variant	HLTF	GRCh38.p7	3:149055793	TTGTGTAATCTCCTC[C/T]CATACTCCACCAGGA	6596
rs137866464	snp	C/T	3.42877e-05	0.00414037	missense	HLTF	GRCh38.p7	3:149046159	GTGTAATGTGCTGAA[C/T]AAATACTTTACGTTC	6596
rs137933838	snp	C/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149058889	TGTGTAATTTAATTC[C/T]ATCTCAACCGAAATT	6596
rs137985485	snp	C/T	0.000248886	0.0111526	synonymous-codon	HLTF	GRCh38.p7	3:149060792	ACCTTTCATTTTCTG[C/T]GGCAATTCACTTGTT	6596
rs138020135	snp	A/G	0.0115144	0.0749975	intron-variant	HLTF	GRCh38.p7	3:149078763	TCGGGAAGCTGACAC[A/G]GGAGAATGATGTGAA	6596
rs138139773	snp	A/G	0.00755907	0.0610114	intron-variant	HLTF	GRCh38.p7	3:149065787	GTGAGCCAAGGTTGC[A/G]CCACTGCACTCCCTC	6596
rs138174505	snp	A/C	0.00993419	0.0697739	intron-variant	HLTF	GRCh38.p7	3:149069002	AAAACTGTTTTTATA[A/C]TACTACTAAGACAGA	6596
rs138196743	snp	C/T	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149040921	AAAATTCTACCCCAG[C/T]TGAATGACTGCTTAA	6596
rs138274556	snp	C/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149075355	GGAGTTCGAGACAGC[C/G]TGGCCAACATGGCAA	6596
rs138305266	snp	C/T	0.0158469	0.0875917	intron-variant	HLTF	GRCh38.p7	3:149079468	AATTTTTGTCCTATC[C/T]CATTAAAAAGTATAT	6596
rs138362499	snp	C/T	6.67045e-05	0.00577475	splice-acceptor-variant	HLTF	GRCh38.p7	3:149073324	ATTGAATCCTAAAGC[C/T]ATAATTTACAAAATA	6596
rs138495802	snp	A/G	0.00279162	0.0372561	intron-variant	HLTF	GRCh38.p7	3:149042689	CAAAAAAAGAGGGAA[A/G]GTAAACTGAATACAG	6596
rs138498353	snp	C/T	0.00874735	0.0655527	intron-variant	HLTF	GRCh38.p7	3:149076972	TTTAAAAATAGCTCA[C/T]GGCCAGGCACAGTAG	6596
rs138517401	snp	G/T	0.00159617	0.0282053	intron-variant	HLTF	GRCh38.p7	3:149047428	AAGAGGATAACCTGA[G/T]GTCAGAAGTTTGAGA	6596
rs138564813	snp	A/C	0.0271762	0.113356	intron-variant	HLTF	GRCh38.p7	3:149053939	AAGAAAGAACAGTTT[A/C]GTTGGAATAAAAAAA	6596
rs138594573	snp	C/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149058281	ATTTTGCCATGTTGC[C/T]CACCCCTGATCTTGA	6596
rs138658648	snp	A/G	0.000280456	0.0118385	missense	HLTF	GRCh38.p7	3:149060648	ATACACATACCTTTC[A/G]CCCTGCCTTTAGTTT	6596
rs138712215	snp	A/G	0.0134861	0.0810011	intron-variant	HLTF	GRCh38.p7	3:149077031	AGGTGGGAAGATCAC[A/G]AGGTCAAGAGATCAA	6596
rs138717471	snp	C/T	0.00158233	0.0280831	missense	HLTF	GRCh38.p7	3:149042177	CTACCTGAGGGGCCA[C/T]TGGAAGACACTGCAT	6596
rs138770187	snp	C/T	0.00119737	0.0244387	intron-variant	HLTF	GRCh38.p7	3:149084016	ATATGGAGATTTTAT[C/T]ACAAAGATTTTATTA	6596
rs138847655	snp	C/G	0.00119737	0.0244387	downstream-variant-500B	HLTF	GRCh38.p7	3:149030014	GACATTATTCTGTTA[C/G]AGTAATCTTCATGTA	6596
rs138867242	snp	G/T	0.0158469	0.0875917	intron-variant	HLTF	GRCh38.p7	3:149036196	GCAACAATGAAAAGG[G/T]AAGAATAACCAAAAA	6596
rs138910419	snp	A/C	0.0154538	0.0865337	intron-variant	HLTF	GRCh38.p7	3:149052642	GACTACCAAGGACTG[A/C]AGAAAGTATTAAACA	6596
rs139076774	snp	A/C	0.00199481	0.0315187	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087003	AACCGTGGGGACTTT[A/C]GCTCCAAATTTTCAT	6596
rs139180069	snp	A/T	0.00676609	0.0577691	intron-variant	HLTF	GRCh38.p7	3:149050526	GTCTAGACCAAAATA[A/T]TAACAATAAGAAAAA	6596
rs139276032	snp	C/T	0.00478085	0.0486577	intron-variant, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149085795	TACCAATTTGGACAA[C/T]GAAAAGTGAAGGGGA	6596
rs139289940	in-del	-/T			upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149086882	TCCTTCCTCTTATTT[-/T]CTTCTCATCTAATGT	6596
rs139300020	snp	A/G	8.24953e-05	0.0064219	missense	HLTF	GRCh38.p7	3:149068277	ACTCTTTCAATAGGA[A/G]GAGGTCTGCCATCAT	6596
rs139349759	snp	A/G	0.0023933	0.0345097	intron-variant	HLTF	GRCh38.p7	3:149071838	GATCACTTGAGCTCA[A/G]GAGTTTGAGACCAGC	6596
rs139352583	snp	A/C			intron-variant	HLTF	GRCh38.p7	3:149083748	AACCTAAAAAAAAAT[A/C]CAAAAAAAAAAAATA	6596
rs139354900	snp	C/T	0.00438332	0.0466095	intron-variant	HLTF	GRCh38.p7	3:149042000	ATAATTCCATTTCAT[C/T]GGTAAAAAAATTATT	6596
rs139358881	snp	C/T	8.26713e-05	0.00642875	missense	HLTF	GRCh38.p7	3:149074304	CCCCAAAAAGTCATA[C/T]GCAGAGGCATGGTAA	6596
rs139376640	in-del	-/G	0.0193772	0.0965046	intron-variant	HLTF	GRCh38.p7	3:149053153	CTTGAGAGCCAGGAA[-/G]GACGGTATCTTGTTC	6596
rs139489406	snp	C/G	0.00159617	0.0282053	utr-variant-5-prime, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149086493	GGTAAGTCGCCGCGA[C/G]TCCAGTCAGACGTCG	6596
rs139548011	snp	A/G	0.00159617	0.0282053	intron-variant	HLTF	GRCh38.p7	3:149070647	ACTCTGCATAACACA[A/G]TATTTGTGATGGAAT	6596
rs139580251	snp	A/G/T	0.00139395	0.0263638	intron-variant	HLTF	GRCh38.p7	3:149055288	GTTACATTTTTAAAG[A/G/T]GCTTAAAGACTTACA	6596
rs139653291	snp	C/T	0.00119737	0.0244387	intron-variant	HLTF	GRCh38.p7	3:149061084	ACCACCGTTATTGTT[C/T]TTTGAGACAGGGTCT	6596
rs139808349	snp	A/G	0.00716266	0.059414	intron-variant	HLTF	GRCh38.p7	3:149043703	TTAAGGCAACAGAAG[A/G]AATATAGCCTAACGG	6596
rs139827753	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149050112	ATTTTTCTATATATC[A/G]TTAAGTATCTAAAGA	6596
rs139926846	snp	A/G	0.00795532	0.062565	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087388	CTGGCAGGGCTGGTC[A/G]CTTTGCGTTGAGGAG	6596
rs139954914	in-del	-/AAAATAAAAT			intron-variant	HLTF	GRCh38.p7	3:149061414	ACACTCCATCTCAAA[-/AAAATAAAAT]AAAATAAAATAAAAT	6596
rs140070856	snp	C/T	0.00159617	0.0282053	intron-variant	HLTF	GRCh38.p7	3:149038422	TGATTCTGGTTTTGC[C/T]TATTACTAACTGTAT	6596
rs140073710	in-del	-/TTAAGAGTCAGTC			intron-variant	HLTF	GRCh38.p7	3:149035690	AAAAAAAAGGGGGTT[-/TTAAGAGTCAGTC]TTAAGAGTCAGTAAG	6596
rs140074102	snp	C/T	0.00119737	0.0244387	intron-variant	HLTF	GRCh38.p7	3:149035095	TCATTCATCTTTTTC[C/T]GACTGAAAGTTTTCT	6596
rs140126193	snp	A/T			intron-variant	HLTF	GRCh38.p7	3:149079426	AATTATTTAAAAAAA[A/T]AAAAATTTTTAAGTA	6596
rs140136313	snp	A/G	0.00199481	0.0315187	intron-variant	HLTF	GRCh38.p7	3:149067454	TTTTATGGCTATATC[A/G]TTTAACTGTTCCCTT	6596
rs140156548	snp	A/G	0.0088213	0.0658243	intron-variant	HLTF	GRCh38.p7	3:149071467	AAAAAGTCATAAAGC[A/G]AAATACATTAAGCCA	6596
rs140314385	snp	C/T	0.0023933	0.0345097	intron-variant	HLTF	GRCh38.p7	3:149058465	CTCCATATGTACATC[C/T]TTTGACTATTCTCCT	6596
rs140317783	snp	C/G	0.00112163	0.023655	stop-gained	HLTF	GRCh38.p7	3:149071333	TGTTATTGTGTTATA[C/G]TATAAGTCATTTCGC	6596
rs140329893	in-del	-/AAGAT	0.0345262	0.126772	intron-variant	HLTF	GRCh38.p7	3:149082895	CAGAAACAAGTGTAG[-/AAGAT]AAGTTATGGTTCTGG	6596
rs140350337	snp	C/T	0.000494527	0.0157168	missense	HLTF	GRCh38.p7	3:149060673	TAGTTTCAGACTGTA[C/T]ATTTTTCAGTTTGCC	6596
rs140360892	snp	C/T	0.0115144	0.0749975	intron-variant	HLTF	GRCh38.p7	3:149033816	AATGTGAAAATAAAG[C/T]CTTCTGTCCTAGGTA	6596
rs140417023	snp	C/T	0.00597247	0.0543191	intron-variant	HLTF	GRCh38.p7	3:149082906	GTAGAAGATAAGTTA[C/T]GGTTCTGGATGATAG	6596
rs140519523	snp	A/T	0.404559	0.196498	intron-variant	HLTF	GRCh38.p7	3:149077280	AATAAATAAATAAAT[A/T]AATAAATAAATAAAA	6596
rs140551459	snp	A/G			missense	HLTF	GRCh38.p7	3:149071356	CATTTCGCTGTTCCC[A/G]GAATGGTGGAAGTTC	6596
rs140636625	snp	A/G	0.0337553	0.125452	intron-variant	HLTF	GRCh38.p7	3:149036581	GGCATGAGCCTCCGC[A/G]CCAGGCCATATTACC	6596
rs140673177	snp	C/T			intron-variant	HLTF	GRCh38.p7	3:149058046	GTCAATACTTGGCAT[C/T]GTGAGATTTTTTAAT	6596
rs140692211	snp	C/G/T	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149077826	GTTGAAGGAATGCCC[C/G/T]AACATACAGAAGTTC	6596
rs140693755	snp	C/G	0.0158469	0.0875917	intron-variant	HLTF	GRCh38.p7	3:149062482	TTTGTTGATGAAATA[C/G]CTAGCAGAGACAAAT	6596
rs140716196	snp	C/T	0.00874735	0.0655527	intron-variant	HLTF	GRCh38.p7	3:149064313	CTCTTAAAATATTTT[C/T]AGTCTGCTCTAATCT	6596
rs140776452	snp	C/T	0.0005278	0.0162364	missense	HLTF	GRCh38.p7	3:149073268	TGCACTGGCATACTA[C/T]AGCTTGGTCCAGCTC	6596
rs140890038	snp	C/T	1.64917e-05	0.00287151	synonymous-codon	HLTF	GRCh38.p7	3:149064807	TTTGCTTAGTCCATC[C/T]GCCTTTTCACTGGTA	6596
rs140913707	snp	C/G	0.00597247	0.0543191	intron-variant	HLTF	GRCh38.p7	3:149080585	ATTATGCAAATCCTA[C/G]AAAATACATAACCAA	6596
rs140954450	snp	C/G/T	3.38119e-05	0.00411157	missense	HLTF	GRCh38.p7	3:149050236	ACAATACTTACTCCA[C/G/T]AGTCATGAGTTAAAA	6596
rs140966154	snp	C/T	0.00279162	0.0372561	intron-variant	HLTF	GRCh38.p7	3:149044849	ACAGAATCTAATCAT[C/T]TCTCACTCCCTTTAT	6596
rs140984097	snp	G/T	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149083318	GATATCTCAACATAG[G/T]GTTCCTGGAAAAAAA	6596
rs141025427	snp	A/G	0.00159617	0.0282053	intron-variant	HLTF	GRCh38.p7	3:149035559	GCTACTCAGGAGGCT[A/G]AGGCAGGAGAATGGC	6596
rs141065324	snp	C/T	0.00242277	0.0347205	intron-variant	HLTF	GRCh38.p7	3:149039015	TTTTTGAAAGAAGTA[C/T]TAAGATTCTGAAAAA	6596
rs141100561	snp	A/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149068939	TGGTCCACAGGCCAC[A/T]GGGGATGGGGAGGGT	6596
rs141143751	snp	C/G	0.0023933	0.0345097	intron-variant	HLTF	GRCh38.p7	3:149072814	AGAAATTCAGCATAA[C/G]TCATCCTAAATTACA	6596
rs141248314	snp	A/G	0.0345262	0.126772	intron-variant	HLTF	GRCh38.p7	3:149075291	CGGTGGCTCACGCCT[A/G]TAATCCCAGCATTTT	6596
rs141317988	snp	A/C	0.0150606	0.0854603	intron-variant	HLTF	GRCh38.p7	3:149079102	ACAAAAAAATGACAC[A/C]CAACAGAGCCTCAGA	6596
rs141342778	snp	C/T	0.00159617	0.0282053	intron-variant	HLTF	GRCh38.p7	3:149063051	GGGTCATGGTCATCT[C/T]TATCTCTCTCTTTTT	6596
rs141399797	snp	C/T	0.0252325	0.109451	intron-variant	HLTF	GRCh38.p7	3:149079248	GAAACCACTACTCTA[C/T]ACATATAAGAAGCTC	6596
rs141417571	snp	C/T	0.00438332	0.0466095	intron-variant	HLTF	GRCh38.p7	3:149066195	GAGATTACAGGTATG[C/T]GCCACCACACCCAGC	6596
rs141501286	snp	A/C	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149050178	TCTAGAAACCTGTGG[A/C]ATATTTCTTACATTC	6596
rs141520509	snp	C/T	0.00557542	0.0525036	intron-variant	HLTF	GRCh38.p7	3:149046515	ATATCCTGTCCTTAT[C/T]TTCGTAAGTTCTGTT	6596
rs141544440	snp	A/C/G			intron-variant	HLTF	GRCh38.p7	3:149054086	GATAATTCATGTCAC[A/C/G]GAAAAAAAGACTATA	6596
rs141557977	snp	A/G	0.00438332	0.0466095	intron-variant	HLTF	GRCh38.p7	3:149051659	TGAGGTCAGGAGTTC[A/G]AGACCAGCCTAGCCA	6596
rs141584615	in-del	-/A	0.0256215	0.110247	intron-variant	HLTF	GRCh38.p7	3:149080805	GGTCCCAGCAGCAAG[-/A]AAAAAACAGGACATA	6596
rs141615958	snp	A/G	1.6525e-05	0.00287441	missense	HLTF	GRCh38.p7	3:149042255	AGACCCAGGACATCT[A/G]CATAATGTGCCAGGA	6596
rs141642660	snp	A/G	1.69255e-05	0.00290903	synonymous-codon	HLTF	GRCh38.p7	3:149048159	AGAATTCTGGATTGG[A/G]GTACCTAGAAATAAC	6596
rs141704206	snp	C/T	0.00130162	0.0254778	synonymous-codon	HLTF	GRCh38.p7	3:149048882	CAAAACCCATCTTCT[C/T]TCTGATTCTAAGTCA	6596
rs141740731	snp	A/T	0.0271762	0.113356	intron-variant	HLTF	GRCh38.p7	3:149069292	CCTGGACCAACACGG[A/T]GAAACCCCGTCTCTA	6596
rs141788321	snp	A/T			intron-variant	HLTF	GRCh38.p7	3:149079415	AAAAAAAAAAAAATT[A/T]TTTAAAAAAATAAAA	6596
rs141810320	snp	G/T	0.00199481	0.0315187	intron-variant	HLTF	GRCh38.p7	3:149054956	AAGTTATTGTTGGTA[G/T]AGCTCTTAGAAAAGA	6596
rs141828887	snp	C/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149037152	CAAAGATTTCAAACT[C/T]CATCCACAGTACAAA	6596
rs141929036	snp	C/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149042712	GAATACAGAAACATA[C/T]AGGTGCACTGTATTT	6596
rs141964658	snp	C/T	0.00159617	0.0282053	utr-variant-3-prime	HLTF	GRCh38.p7	3:149030358	TAAACTTTTAAAATA[C/T]AACAACATCTAACAG	6596
rs142332055	snp	C/T	0.0341408	0.126114	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149088296	AGCACTTTGGGAGGC[C/T]GAGTTGGGTGGATCA	6596
rs142454558	snp	A/G	7.69181e-05	0.00620106	synonymous-codon	HLTF	GRCh38.p7	3:149071625	ATCATCTTCTTTTAA[A/G]TCTTCAAACAATTTG	6596
rs142473057	snp	A/G	0.00159617	0.0282053	intron-variant	HLTF	GRCh38.p7	3:149057988	TCCTTGGTAATTGGC[A/G]CTCCCATCAACAATG	6596
rs142492345	snp	A/C	0.0023933	0.0345097	intron-variant	HLTF	GRCh38.p7	3:149038698	TACTTTTTTTTGTAG[A/C]GATGGGGTTTTGCCA	6596
rs142536154	snp	A/G	0.00159617	0.0282053	downstream-variant-500B	HLTF	GRCh38.p7	3:149029783	TGTATTTCCAATTCT[A/G]GAGCTGTAATTTTAA	6596
rs142599572	snp	A/G	0.00438332	0.0466095	intron-variant	HLTF	GRCh38.p7	3:149044643	GGCATCCTATGATCA[A/G]TGTGTCCAAAACTGA	6596
rs142709617	snp	C/G/T	1.65116e-05	0.00287324	missense	HLTF	GRCh38.p7	3:149074241	GGACCCAATTTAAAT[C/G/T]CATGTTTCTTCAACT	6596
rs142727377	snp	A/G	0.0130921	0.0798413	intron-variant	HLTF	GRCh38.p7	3:149070816	TTGGGAGGCCAAGGC[A/G]GGCGGATCACTTGAA	6596
rs142806707	snp	G/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149060001	TCAACTCAGAGAAAC[G/T]ATGTAGTCATTCATG	6596
rs142925682	snp	A/G	5.80366e-05	0.00538655	missense	HLTF	GRCh38.p7	3:149039207	TGGAACCATCCAAAC[A/G]AGTAAACACAAATCC	6596
rs143125997	snp	C/T	0.00161543	0.0283744	missense	HLTF	GRCh38.p7	3:149042174	TACCTACCTGAGGGG[C/T]CATTGGAAGACACTG	6596
rs143181349	snp	A/G	0.00557542	0.0525036	intron-variant	HLTF	GRCh38.p7	3:149075195	CTAAAACACTGCAGG[A/G]CAAAATGAAATTCAC	6596
rs143183917	snp	A/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149086068	GGCCGAGATGCTTTA[A/G]GCCCCAGGCCCCCCA	6596
rs143223809	snp	A/G	0.0345262	0.126772	intron-variant	HLTF	GRCh38.p7	3:149037477	TGTCTCAAAAAAAAA[A/G]AAAAAAGAAAAAAGA	6596
rs143316474	snp	C/T	0.0134861	0.0810011	intron-variant	HLTF	GRCh38.p7	3:149047598	AGTGAGCCAAGATCG[C/T]GCCACTGCCCTCCAG	6596
rs143333066	snp	A/G	0.00795532	0.062565	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087642	CCAGGCTGGAGTGCA[A/G]TGGGGGTGATCTTGG	6596
rs143354201	snp	C/T	1.66106e-05	0.00288184	missense	HLTF	GRCh38.p7	3:149075963	GGCCAACTTGATTTC[C/T]ATTCACATTGTTTAC	6596
rs143355874	snp	A/C	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149042556	CAAACAGAGCTGCCA[A/C]AACACAATTCTTTAA	6596
rs143449509	snp	C/G	0.000132371	0.00813438	missense	HLTF	GRCh38.p7	3:149071300	GACATTTTCTGGTCG[C/G]TCCTTCTCAGAAAAA	6596
rs143482043	snp	C/T	0.00478085	0.0486577	intron-variant	HLTF	GRCh38.p7	3:149039940	CTAAAATGACAGGAA[C/T]GAAAGCAGAATTACG	6596
rs143507964	snp	A/T	0.00318978	0.0398085	intron-variant	HLTF	GRCh38.p7	3:149063847	ACAAATAGGTGCTGT[A/T]ATAAATTTACATGTT	6596
rs143599779	snp	C/T	0.00159617	0.0282053	intron-variant	HLTF	GRCh38.p7	3:149066104	CAGGCTGGAGTGCAA[C/T]GGCACAATCTCGGCT	6596
rs143631033	snp	A/G	0.000115413	0.00759562	synonymous-codon, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149084739	ACTTCCAAATAAAAC[A/G]GAATCTACTTCTTCA	6596
rs143646223	snp	A/G			synonymous-codon	HLTF	GRCh38.p7	3:149071357	ATTTCGCTGTTCCCA[A/G]AATGGTGGAAGTTCT	6596
rs143704793	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149036829	ATCATTATGTTTCTC[A/G]GACCTGACTTTTAAG	6596
rs144112168	in-del	-/G/T			upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087584	TTTTTTCTTTTTTTT[-/G/T]TTTTTTTTCTTTTTT	6596
rs144143268	snp	C/G	0.0267878	0.112589	intron-variant	HLTF	GRCh38.p7	3:149083165	CTGTTGCAGGAGAAC[C/G]GCTTGAACCTGGGAG	6596
rs144156348	snp	A/G	0.000272889	0.0116777	intron-variant	HLTF	GRCh38.p7	3:149059341	ATCATAACAAAGATC[A/G]CTAACATTTTAAAAT	6596
rs144164069	snp	C/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087317	CAGAGTCTGAGGTGA[C/G]CGGAAGGAGAATGCG	6596
rs144295287	snp	A/G	0.0414363	0.137845	intron-variant	HLTF	GRCh38.p7	3:149066105	AGGCTGGAGTGCAAC[A/G]GCACAATCTCGGCTC	6596
rs144301352	snp	G/T	0.00159617	0.0282053	intron-variant	HLTF	GRCh38.p7	3:149034481	TCAGTTTAAGATGAT[G/T]AAAAAGTTCTGGAGA	6596
rs144371728	snp	C/T	0.00159617	0.0282053	intron-variant	HLTF	GRCh38.p7	3:149055467	ATGTCAATAAGGAGA[C/T]GGCAATAATGTGCCT	6596
rs144381721	snp	A/G	0.000238916	0.0109271	missense	HLTF	GRCh38.p7	3:149032290	GCATTTGGTTTTTTA[A/G]TTCCAAAGGCTCCTG	6596
rs144462563	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149086992	TCCCTGTGGTGAACC[G/T]TGGGGACTTTCGCTC	6596
rs144482457	snp	A/C	0.00119737	0.0244387	intron-variant	HLTF	GRCh38.p7	3:149038496	TTCAGTAAAACAGAG[A/C]ATTTTTTTTCTTTTT	6596
rs144507215	snp	C/T	0.00557542	0.0525036	intron-variant	HLTF	GRCh38.p7	3:149062808	AAAACTTCTAAAATC[C/T]CAAAAAAAAGCAAAA	6596
rs144547303	snp	A/C	0.00557542	0.0525036	intron-variant	HLTF	GRCh38.p7	3:149066953	CAGGAAACTGATGTA[A/C]TGCCTTCTCTGAAAA	6596
rs144685464	snp	C/T	4.9933e-05	0.0049964	synonymous-codon	HLTF	GRCh38.p7	3:149050259	AGTTAAAATATTATA[C/T]GTAGTCAAAACAATA	6596
rs144696883	snp	A/G	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149053204	TTGATCATTGAAATC[A/G]TTTGGATGTTCATCT	6596
rs144726075	snp	G/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149070335	AGGTGAGAATTCAGC[G/T]GCCATCTATTCGGCC	6596
rs144732911	snp	A/G	0.0372196	0.131242	intron-variant	HLTF	GRCh38.p7	3:149035874	GGCACAGTGGCTCAC[A/G]CCTGTAATCCCAGCA	6596
rs144798918	snp	A/C	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149033095	TGATTTTAAAATACC[A/C]CAACTAGGAATGAAT	6596
rs144849497	snp	A/G	9.90148e-05	0.00703545	missense	HLTF	GRCh38.p7	3:149034928	CTCACTTTTGTGATG[A/G]TAACTTCTTGCTTCT	6596
rs144909724	snp	A/C	0.000132085	0.00812558	splice-donor-variant	HLTF	GRCh38.p7	3:149060642	TATAGTATACACATA[A/C]CTTTCGCCCTGCCTT	6596
rs144947575	snp	A/T	0.0166325	0.0896639	intron-variant	HLTF	GRCh38.p7	3:149067708	AAATAATAATAATAA[A/T]AAAAAACCTGTATTT	6596
rs145038700	snp	A/C	0.00557542	0.0525036	intron-variant	HLTF	GRCh38.p7	3:149050955	AAAACCAGACCTAGA[A/C]GATTTTCAGCAGAAA	6596
rs145045648	snp	A/G	0.00557542	0.0525036	intron-variant	HLTF	GRCh38.p7	3:149079107	AAAATGACACACAAC[A/G]GAGCCTCAGAAACTT	6596
rs145062543	snp	A/T	0.0399052	0.1355	intron-variant	HLTF	GRCh38.p7	3:149035523	ATTAGCCGGGAGAGG[A/T]GGCGGGCGCCTGTAG	6596
rs145065914	snp	A/G	0.0126979	0.078662	downstream-variant-500B	HLTF	GRCh38.p7	3:149029958	TGAACAAGAATTTCA[A/G]CCAGCTAAATTGAGC	6596
rs145066042	snp	C/T			intron-variant	HLTF	GRCh38.p7	3:149083684	AGAGGCCAAGGCGGA[C/T]GGATCACTTGAGCCC	6596
rs145129668	snp	A/G	0.00358779	0.0422022	intron-variant	HLTF	GRCh38.p7	3:149077486	AAACCTCCCTTGGGC[A/G]GATGTTTGTCAAAAC	6596
rs145168797	snp	C/T			intron-variant	HLTF	GRCh38.p7	3:149080736	AAGTAATTACTAGAA[C/T]TTTAAATAAAATATA	6596
rs145215821	snp	A/G	0.00199481	0.0315187	intron-variant	HLTF	GRCh38.p7	3:149057482	TTGCAAAACTCATGT[A/G]TATGGAAGGCCAACT	6596
rs145295234	in-del	-/GAG	0.0352966	0.128072	intron-variant	HLTF	GRCh38.p7	3:149060029	ATGGTAAGACTTGAG[-/GAG]AAGAAATGAAAGTAG	6596
rs145320966	snp	C/T	0.000164867	0.00907779	synonymous-codon	HLTF	GRCh38.p7	3:149060680	AGACTGTACATTTTT[C/T]AGTTTGCCTAAAAAT	6596
rs145340051	snp	C/T	0.00914312	0.0669923	intron-variant	HLTF	GRCh38.p7	3:149058774	TCTCTTTCAAAGATA[C/T]ACTTAGTTTGGTTAA	6596
rs145483464	snp	A/C	0.00517822	0.0506191	intron-variant	HLTF	GRCh38.p7	3:149061130	GATGGAGTACAGTGA[A/C]ACAATCAGAAGTCAC	6596
rs145550012	in-del	-/GTCTA			intron-variant	HLTF	GRCh38.p7	3:149047209	AAAAAGTTGAACCAC[-/GTCTA]ATTACATCTTGCAAA	6596
rs145604552	snp	A/G	0.00795532	0.062565	intron-variant	HLTF	GRCh38.p7	3:149078580	TTCAAAGACCTGGCC[A/G]GGCACAGTGGCTCAC	6596
rs145705282	snp	A/G	0.00795532	0.062565	intron-variant	HLTF	GRCh38.p7	3:149075347	TGAGGTCAGGAGTTC[A/G]AGACAGCCTGGCCAA	6596
rs145756285	snp	A/C	0.00716266	0.059414	intron-variant	HLTF	GRCh38.p7	3:149058091	AGGGTAAGAGCATCC[A/C]CCTATTCCTTTATTT	6596
rs145822193	in-del	-/TA			utr-variant-3-prime, intron-variant	HLTF	GRCh38.p7	3:149031419	TACATAAATAAAAAT[-/TA]TCTATTTATAGAAAT	6596
rs145870953	snp	G/T	0.00159617	0.0282053	intron-variant	HLTF	GRCh38.p7	3:149062332	CCAGGTTTATGATAA[G/T]TTCAAAGTTGTAACA	6596
rs145953454	snp	G/T	0.0115144	0.0749975	intron-variant	HLTF	GRCh38.p7	3:149043699	TATTTTAAGGCAACA[G/T]AAGAAATATAGCCTA	6596
rs145965013	snp	C/T	0.0185938	0.0946107	intron-variant	HLTF	GRCh38.p7	3:149049171	TTTATAAAATAAGTA[C/T]TTATTAGCACACCTA	6596
rs146155306	snp	A/T	0.0158469	0.0875917	intron-variant	HLTF	GRCh38.p7	3:149070841	CTTGAAGTCAGGAGT[A/T]CAAAACCAGCCTGGC	6596
rs146170189	snp	A/G	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149054088	TAATTCATGTCACGG[A/G]AAAAAAGACTATAAA	6596
rs146181227	snp	C/G	1.7105e-05	0.00292441	missense	HLTF	GRCh38.p7	3:149032317	CCTGCTGCAAGTTCT[C/G]TCTTTTTGTTTTGTA	6596
rs146224624	snp	A/G	3.37075e-05	0.00410519	missense	HLTF	GRCh38.p7	3:149046122	TTCACAGACTGATAA[A/G]TCTTTCTCTCTTCAT	6596
rs146278749	snp	A/G	0.00127194	0.0251863	intron-variant	HLTF	GRCh38.p7	3:149050221	ATCTGTTAAGTATCA[A/G]CAATACTTACTCCAT	6596
rs146496123	snp	C/T	0.0134861	0.0810011	intron-variant	HLTF	GRCh38.p7	3:149083232	CTCCAGCCTGGGCAA[C/T]GCAAGCAAGACTCCG	6596
rs146509171	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087333	CGGAAGGAGAATGCG[A/G]CCCTGGGACCGTCAA	6596
rs146619202	snp	C/T	0.00318978	0.0398085	intron-variant	HLTF	GRCh38.p7	3:149062900	GATTATTAAAATTTA[C/T]CAATTCATTTCTTTT	6596
rs146627106	snp	A/G	0.00874735	0.0655527	intron-variant	HLTF	GRCh38.p7	3:149067384	TTTTAACTAAAAAGA[A/G]TCATGAAAGTGATTA	6596
rs146749999	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149044066	AACCAAAGTGCCAGA[A/G]TTAATCTGTCCTGTC	6596
rs146900465	snp	A/G	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149085721	TACCCGCCTTCCGTC[A/G]CCGGTTTAAGCATAA	6596
rs146910943	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149088432	TAGCTACTTGGGAGG[C/G]TGAGGCAGGAGAATC	6596
rs146920692	snp	G/T	0.00159617	0.0282053	intron-variant	HLTF	GRCh38.p7	3:149073564	CAGAGCGTGATGGTG[G/T]GCGCCTGTAGTCCCA	6596
rs146997807	in-del	-/TAT	0.0452528	0.143452	intron-variant	HLTF	GRCh38.p7	3:149059185	ATAGCCTGCTATATC[-/TAT]CCCAACATGTAAAAT	6596
rs147161446	snp	C/T	0.00993419	0.0697739	intron-variant	HLTF	GRCh38.p7	3:149081527	TCATTAAGAAAAATT[C/T]AAGAGAGCCTGCCTT	6596
rs147298547	snp	A/T	3.29804e-05	0.00406068	synonymous-codon	HLTF	GRCh38.p7	3:149048942	ATTTCGTATGGCATG[A/T]CCTTCATCCAGGATC	6596
rs147311856	snp	A/G	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149080188	GTTGCCAGGGACTGA[A/G]GGGTAGAGATAATGG	6596
rs147320774	in-del	-/A			intron-variant	HLTF	GRCh38.p7	3:149079977	TTAATTGTAATCCCT[-/A]AAGCAATCATAAGTA	6596
rs147417179	snp	C/T	0.0123036	0.0774623	intron-variant	HLTF	GRCh38.p7	3:149060372	ACACATAGGTTTTAT[C/T]GAAGTCATTTTATAG	6596
rs147426957	snp	A/G	0.0142736	0.0832652	intron-variant	HLTF	GRCh38.p7	3:149065565	AAAAATCTGCCGGGC[A/G]CAGTGGCTCATGCCA	6596
rs147472587	snp	C/T	0.000153988	0.00877328	missense	HLTF	GRCh38.p7	3:149068266	GATTCTTTTTAACTC[C/T]TTCAATAGGAAGAGG	6596
rs147497749	snp	C/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149037945	GTTCAAAGTGAATTT[C/T]AGCCTCTGTTCTACC	6596
rs147573719	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149077646	AGTGTATTTCTGGAT[A/G]TCTAGAAGGCCGTAA	6596
rs147593347	snp	A/G	0.00874735	0.0655527	intron-variant	HLTF	GRCh38.p7	3:149033217	AACATTGTTTAAGAA[A/G]ACCCAATTACTGCAA	6596
rs147642409	snp	C/T	0.0138799	0.0821421	intron-variant	HLTF	GRCh38.p7	3:149074013	ATCCCCTCACTCTTA[C/T]TGTGTATATTTTTAT	6596
rs147683321	snp	A/G	2.16457e-05	0.00328974	missense	HLTF	GRCh38.p7	3:149039227	AACACAAATCCAGAG[A/G]CTCTAAAGGGGGGAA	6596
rs147746075	snp	A/G	0.0345262	0.126772	intron-variant	HLTF	GRCh38.p7	3:149051799	CACTTGAACCCAGGA[A/G]ACAGAGGTTGCAGTG	6596
rs147790252	snp	C/T	0.0130921	0.0798413	intron-variant	HLTF	GRCh38.p7	3:149072471	ATGCACTATAGGATA[C/T]TTTTATTATTATGCT	6596
rs147881841	in-del	-/T	0.0577344	0.159793	intron-variant	HLTF	GRCh38.p7	3:149062308	GTCCAATTAACAGTG[-/T]TGTGTTACCCAGGTT	6596
rs147885353	snp	A/G	0.00358779	0.0422022	intron-variant	HLTF	GRCh38.p7	3:149045374	TAATCATGTTTTTAA[A/G]TTATCTGTTTCTTCC	6596
rs147909210	snp	A/G	3.31082e-05	0.00406854	missense	HLTF	GRCh38.p7	3:149050305	AAGGCCGGTTCTCTA[A/G]TACGATCAGGACCAT	6596
rs147997683	snp	C/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149064122	CTTCAACCTTACTTC[C/T]TTCCTTCTACTGCTA	6596
rs148086460	snp	A/G	0.00159617	0.0282053	intron-variant, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149085036	ACTCTCGTTAAAGCA[A/G]GAATTGCAGTGAGTG	6596
rs148096237	snp	C/G			intron-variant	HLTF	GRCh38.p7	3:149036972	ATCAACTTTTTCATA[C/G]TAATTATTTTGGTAT	6596
rs148206552	snp	C/G/T	0.000115346	0.00759347	missense	HLTF	GRCh38.p7	3:149063462	TAGACAATTCTGACA[C/G/T]GCGAAACTTACTCTT	6596
rs148256506	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149075247	CAGTTTATAACCTCT[A/G]ATATAAACAAACACT	6596
rs148305963	snp	A/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149079152	ACCAACACACATACA[A/T]AAGAGTACCATAAGG	6596
rs148349852	snp	C/T	0.00636936	0.0560724	intron-variant	HLTF	GRCh38.p7	3:149048439	TATCAAGTACATCTG[C/T]TTATTTAGTTTTTAA	6596
rs148402481	snp	G/T	0.00199481	0.0315187	intron-variant	HLTF	GRCh38.p7	3:149054925	GTTCACTAACTGTTG[G/T]TATTGTTATAAAAAT	6596
rs148407918	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149038619	GCAATCAATCTTTCC[A/G]ACTTAGCCCTGCAAG	6596
rs148553300	snp	C/T	1.72383e-05	0.00293578	missense	HLTF	GRCh38.p7	3:149039161	GTGTTTTGAAAACAC[C/T]GAATTGATTCAACTC	6596
rs148566778	snp	C/T	0.000153988	0.00877328	missense, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149084830	GTTGGATATGAGAGG[C/T]GTGGAAAATTTCCAT	6596
rs148618088	snp	A/G	0.00874735	0.0655527	intron-variant	HLTF	GRCh38.p7	3:149081833	ACCAAGGCATAAAAG[A/G]GAGTTTAAGTATGTG	6596
rs148659725	snp	A/T	0.00557542	0.0525036	intron-variant	HLTF	GRCh38.p7	3:149051259	AAAAAAAGAAGGGAA[A/T]AGTGGGCATCCAAGT	6596
rs148726972	snp	A/G/T	1.65726e-05	0.00287855	missense	HLTF	GRCh38.p7	3:149071295	CCATGGACATTTTCT[A/G/T]GTCGGTCCTTCTCAG	6596
rs148778809	snp	A/G	0.0256215	0.110247	intron-variant	HLTF	GRCh38.p7	3:149032571	AGAATATGGCTGTAC[A/G]AATAGAAGTTACAGA	6596
rs148806371	in-del	-/GTC	0.365232	0.22186	utr-variant-3-prime	HLTF	GRCh38.p7	3:149030475	GCAAAGAAGCAAGCT[-/GTC]GTCCTCCCTTTACCT	6596
rs148855232	in-del	-/GTA	0.0607341	0.163335	intron-variant	HLTF	GRCh38.p7	3:149075713	TGTTTGATGGCTGGG[-/GTA]GTAGAAGTATGTAAA	6596
rs148878590	snp	A/C	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149078595	GGGCACAGTGGCTCA[A/C]GCCTGTAATCCCAGC	6596
rs148882615	snp	G/T	0.00279162	0.0372561	intron-variant	HLTF	GRCh38.p7	3:149044576	TAGCTGACTTTGAAC[G/T]CGACTCTCCTATCCA	6596
rs148916691	snp	C/T	0.000480662	0.0154952	missense	HLTF	GRCh38.p7	3:149050341	ACATAAAAATTCAAG[C/T]GTACATCTGATTTTA	6596
rs148931618	snp	C/T	0.000149523	0.00864517	missense, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149084684	CTATTATACTCACTA[C/T]TCCCGTGTAATAGCG	6596
rs149071512	snp	A/C	0.0107246	0.0724382	intron-variant	HLTF	GRCh38.p7	3:149067714	TAATAATAAAAAAAA[A/C]CCTGTATTTTCTTTG	6596
rs149074331	snp	C/T	1.65045e-05	0.00287263	missense	HLTF	GRCh38.p7	3:149042166	ATCAAATTTACCTAC[C/T]TGAGGGGCCATTGGA	6596
rs149115161	in-del	-/A	0.0345262	0.126772	intron-variant	HLTF	GRCh38.p7	3:149082723	CAAAGATAGTATCTC[-/A]ATTTTTATTATTTTT	6596
rs149134497	snp	A/G	0.00119737	0.0244387	intron-variant	HLTF	GRCh38.p7	3:149057605	CAAATACTGAGGGAT[A/G]ACTGTACTGTAATAA	6596
rs149143350	snp	C/T	0.00874735	0.0655527	intron-variant	HLTF	GRCh38.p7	3:149041320	CATCTTTTTATGTTG[C/T]AAATGTTGCATTAGA	6596
rs149269825	snp	A/C/G	0.000798403	0.0199641	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149086755	CAGGAGTGCGACTGC[A/C/G]GTGCCTGCGGTGCCG	6596
rs149363800	snp	A/T	0.404559	0.196498	intron-variant	HLTF	GRCh38.p7	3:149077276	AATAAATAAATAAAT[A/T]AATAAATAAATAAAT	6596
rs149388427	snp	C/T	0.00279162	0.0372561	intron-variant	HLTF	GRCh38.p7	3:149070249	TTTACAGCAACATAC[C/T]GTCGTAAGGACAAAT	6596
rs149449703	snp	A/G	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149058899	AATTCTATCTCAACC[A/G]AAATTTCCACATTTC	6596
rs149453804	in-del	-/AAAT			intron-variant	HLTF	GRCh38.p7	3:149075545	TGAGACTTCGTCTCA[-/AAAT]AAATAAATAAATAAA	6596
rs149505542	in-del	-/AT/T	9.08422e-05	0.00673891	intron-variant	HLTF	GRCh38.p7	3:149040018	TCAAATATTTGCACA[-/AT/T]TGAGTACTTTACCTT	6596
rs149616951	snp	A/G	0.00159617	0.0282053	intron-variant	HLTF	GRCh38.p7	3:149047557	TGAGACAGGAGAATC[A/G]CTTGAACCCAGGAGG	6596
rs149651192	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	HLTF	GRCh38.p7	3:149032037	GAACTTATTGCTATT[G/T]GAAGTTTCATTAAAA	6596
rs149700155	snp	C/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149072107	CACAAACTAGTCAAA[C/T]GCCAAAAAGGCACAT	6596
rs149753620	snp	C/T	0.00676609	0.0577691	intron-variant	HLTF	GRCh38.p7	3:149078497	CAAGGTTACAGTGAG[C/T]TATGATCACGCCACT	6596
rs149762869	snp	A/C	0.00993419	0.0697739	intron-variant	HLTF	GRCh38.p7	3:149061759	GAGAATTGCTTGAAC[A/C]CGGGAGGCAGAGGTT	6596
rs149813830	snp	G/T	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149067540	CAGGGTCTCACAGTG[G/T]CACTGAAGGTGGAGT	6596
rs149848386	snp	A/G	0.00172166	0.0292894	synonymous-codon	HLTF	GRCh38.p7	3:149032370	AGAGTCCTTTACAAT[A/G]AACTTTAAAAAGAAA	6596
rs149878755	snp	A/C	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149043560	GGGAAAAAAAAAAAA[A/C]AAAAAAAAACCAGGC	6596
rs150072566	snp	C/T	6.59489e-05	0.00574196	missense	HLTF	GRCh38.p7	3:149048935	CATTTGGATTTCGTA[C/T]GGCATGTCCTTCATC	6596
rs150121871	snp	A/G	0.000153988	0.00877328	synonymous-codon	HLTF	GRCh38.p7	3:149073297	TCTTCCAGAGCCCCA[A/G]CCACTTTCCAAATTG	6596
rs150128394	snp	A/G	0.0260105	0.111035	intron-variant	HLTF	GRCh38.p7	3:149069403	TTGAACCTGGGAGGC[A/G]GAGGGTGCAGTGAGC	6596
rs150218957	snp	A/T	0.00835141	0.0640778	intron-variant	HLTF	GRCh38.p7	3:149044862	ATTTCTCACTCCCTT[A/T]ATCACTACTATGGTA	6596
rs150268440	snp	A/G	0.00438332	0.0466095	intron-variant	HLTF	GRCh38.p7	3:149052607	AAGGGAGTTTCTGTA[A/G]TGAGTGGAAGCAAAA	6596
rs150382979	snp	C/G	0.00597247	0.0543191	intron-variant	HLTF	GRCh38.p7	3:149035146	ATCACAAATACTCTG[C/G]GGAAAAATCCACCCT	6596
rs150427092	snp	A/T	0.0158469	0.0875917	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149088111	GTTCAGCTTTTAGTA[A/T]GCCAGATTTTAAATA	6596
rs150436914	snp	C/T	0.0119091	0.0762411	intron-variant	HLTF	GRCh38.p7	3:149040738	TAAAAGTCAATACAG[C/T]GGGGTTACTTTTGGG	6596
rs150444896	snp	A/T	0.386504	0.209444	intron-variant	HLTF	GRCh38.p7	3:149077272	AATAAATAAATAAAT[A/T]AATAAATAAATAAAT	6596
rs150540969	snp	A/T	0.00119737	0.0244387	utr-variant-5-prime, nc-transcript-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149086458	ATTCCGAGCGCCGGA[A/T]CAGGAGCGCACGACT	6596
rs150582629	snp	A/T	0.00199481	0.0315187	intron-variant	HLTF	GRCh38.p7	3:149054982	AAAGACAGTTCCAAC[A/T]GTCAATCTGTAAATG	6596
rs150635589	snp	A/G	0.0345262	0.126772	intron-variant	HLTF	GRCh38.p7	3:149061284	GGCGTGGTGGTGGGT[A/G]CCTGTAGTCCCAGCT	6596
rs150749176	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149043208	GTGAAAGAAAACAGT[A/G]AATCATCAGAGAAAT	6596
rs150812492	snp	A/C	0.000399281	0.0141238	utr-variant-3-prime	HLTF	GRCh38.p7	3:149030427	CCAAACTTACTTATG[A/C]GTGTGTTTTAAAAAC	6596
rs150908880	snp	G/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149079334	AAACTGTCAAAAGAA[G/T]TTTGAGACCAGCCTG	6596
rs151012223	snp	C/T	0.00398564	0.0444627	intron-variant	HLTF	GRCh38.p7	3:149038759	CTCAGGCAATCCATT[C/T]ACCTTGGCCTCCCAA	6596
rs151046571	snp	A/G	6.59076e-05	0.00574016	missense	HLTF	GRCh38.p7	3:149055328	CTTAACACAGAAAGC[A/G]GACAGATGATCAGTG	6596
rs151066496	snp	C/T	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149044731	CAGCAATTCCAGCCT[C/T]CCACTTATGCAGGTA	6596
rs151153311	snp	C/G	0.000155474	0.00881549	intron-variant	HLTF	GRCh38.p7	3:149034885	TAAAAATCGTATCAA[C/G]CTAGTCTTAAAATAG	6596
rs151318815	snp	A/G			intron-variant	HLTF	GRCh38.p7	3:149058015	AATGCACGAATTCCT[A/G]TTGCTGCACAACTTT	6596
rs180808401	snp	C/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149074890	AAATATTCCAGATAC[C/T]TAAATTGAGATCACA	6596
rs180812038	snp	A/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149038220	CTACTAGAACCGTGA[A/T]GGTAATCATTTTGTC	6596
rs180827327	snp	A/G	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149048675	TTCCATAAATTATCA[A/G]TAAGTCAAATGTTGT	6596
rs180838374	snp	A/T	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149064271	AAGTAATAGCACCAA[A/T]TGTTATTTACAATTT	6596
rs180847034	snp	A/G			intron-variant	HLTF	GRCh38.p7	3:149084324	TTGAGAAGCTTAAAC[A/G]TAAGAAACATACGGA	6596
rs181075198	snp	C/T	0.00119737	0.0244387	intron-variant	HLTF	GRCh38.p7	3:149042566	TGCCAAAACACAATT[C/T]TTTAAAATGGATGGC	6596
rs181082301	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149069971	ATACATCAACATTTA[A/G]TAGGTCTGCCCAACT	6596
rs181107573	snp	C/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149034685	GAATAAAGTATAATT[C/T]CATTTATCTTTAAAA	6596
rs181114938	snp	A/G	0.0142736	0.0832652	intron-variant	HLTF	GRCh38.p7	3:149057315	CCTGTAGTCTCAGCT[A/G]CTTGGGAGGCTGAGA	6596
rs181117038	snp	C/T	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149079604	GGGTTTTCTTTGTTG[C/T]TGTTTTTTTGAGACA	6596
rs181270873	snp	A/G			intron-variant	HLTF	GRCh38.p7	3:149051211	TGACTACCTAGAATT[A/G]TGTGATAAAAATATA	6596
rs181275086	snp	A/T	0.000126654	0.00795683	intron-variant	HLTF	GRCh38.p7	3:149076055	TTATTAACCTAATAA[A/T]AATGATAAACAGATA	6596
rs181333966	snp	C/T	0.00716266	0.059414	intron-variant	HLTF	GRCh38.p7	3:149037685	AGTAGTATTCCTACA[C/T]GTATCTCAGTAGAAT	6596
rs181349599	snp	A/G	0.00279162	0.0372561	intron-variant	HLTF	GRCh38.p7	3:149083574	CAGAAATGCATATGA[A/G]AGCCAGAGAATATAT	6596
rs181468952	snp	C/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149062232	AACATGTGTGTCAGC[C/T]GTTGTTAAGTTTTTC	6596
rs181481391	snp	C/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149033823	AAATAAAGCCTTCTG[C/T]CCTAGGTAAGACCTT	6596
rs181494034	snp	A/G	0.0310518	0.120672	intron-variant	HLTF	GRCh38.p7	3:149057026	AGGCAGGAGAATGGC[A/G]TGAACCCCAGGGGGC	6596
rs181499385	snp	C/T	0.00279162	0.0372561	intron-variant	HLTF	GRCh38.p7	3:149078749	GTAGTCCCAGTTACT[C/T]GGGAAGCTGACACAG	6596
rs181712607	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149037328	GCAAAAATTAGCCAC[A/G]CGTGGTGGCAGGTGC	6596
rs181728901	snp	C/T	0.00119737	0.0244387	intron-variant	HLTF	GRCh38.p7	3:149050069	AATGCAACCCTTTCA[C/T]GCAAAAAGTCAAAAA	6596
rs181912043	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149032907	GGCGGAGCTTGCAGT[A/G]AGCCGACATTGCGCC	6596
rs181922280	snp	C/T	0.00318978	0.0398085	intron-variant	HLTF	GRCh38.p7	3:149056920	CGAGACCATCCTGGC[C/T]AACACGGTGAAACCC	6596
rs182192871	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149078416	TTAGCCAGGTATGGT[A/G]GTACATGCCTGTAGT	6596
rs182198536	snp	A/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149043272	AAAAAAAGACTAGTC[A/T]CTGATAAAAACATAG	6596
rs182199991	snp	A/T	0.0150606	0.0854603	intron-variant	HLTF	GRCh38.p7	3:149067693	TGTTGAGGGAAAAAA[A/T]AATAATAATAATAAA	6596
rs182208209	snp	A/C	0.00636936	0.0560724	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087753	CACCACGCCCAGCTA[A/C]TTTTTGTATTTTTAG	6596
rs182215535	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149075138	ATATGTATAAAATGC[A/G]GACTTAGCTATTTCA	6596
rs182394060	snp	C/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149045896	TTAAAAAATTACTTA[C/G]CTGGTGAATTATACT	6596
rs182401787	snp	G/T			intron-variant	HLTF	GRCh38.p7	3:149072599	CTCAGAAGAAATCAG[G/T]CCAGGTCTAAAAAAT	6596
rs182554723	snp	C/T	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149076642	TAGGTAAGAAAAATA[C/T]ATCCAGCCTTCAACT	6596
rs182817451	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149052298	AAAATTATATGTTGT[A/G]TGGAAATACAGAAAA	6596
rs183025453	snp	C/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149057786	ATTTTAACCAATTCA[C/T]AGCATCATACTGCAA	6596
rs183033434	snp	C/T	0.00478085	0.0486577	intron-variant	HLTF	GRCh38.p7	3:149081214	CATTATAAAATAAAG[C/T]CTTTGATGGGTCAAA	6596
rs183115500	snp	C/G/T	8.07143e-05	0.00635231	intron-variant	HLTF	GRCh38.p7	3:149039263	GAGACAAGTAACAAA[C/G/T]ACTATTATTATAAAA	6596
rs183127404	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087082	AATGGAACTTAGAGT[A/C]CCCTCCCCACCTCTT	6596
rs183145883	snp	A/T	0.00159617	0.0282053	intron-variant	HLTF	GRCh38.p7	3:149081641	TTTAAAAAAGTTTTT[A/T]AAAAGTTTAATGGAG	6596
rs183254213	snp	C/G	0.000399281	0.0141238	intron-variant, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149085289	TGAGGTCAGGAATTT[C/G]AGACCAACCTGGCCA	6596
rs183258999	snp	C/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149053656	AATGCCAAACCACCT[C/T]TCATTCCTTTAAATT	6596
rs183264687	snp	A/T	0.0433465	0.140692	intron-variant	HLTF	GRCh38.p7	3:149077288	AATAAATAAATAAAT[A/T]AATAAAAATAATAGC	6596
rs183385646	snp	A/G	0.0142736	0.0832652	intron-variant	HLTF	GRCh38.p7	3:149067186	TATACATATATATAT[A/G]TATATATATACACAC	6596
rs183401411	snp	C/T	1.65641e-05	0.00287781	missense	HLTF	GRCh38.p7	3:149071298	TGGACATTTTCTGGT[C/T]GGTCCTTCTCAGAAA	6596
rs183405816	snp	C/G	0.0577344	0.159793	intron-variant	HLTF	GRCh38.p7	3:149035607	GAGCCTGCAGTGAGC[C/G]GAGATCGCGCCACTG	6596
rs183479190	snp	A/C	0.000236766	0.0108778	intron-variant	HLTF	GRCh38.p7	3:149034897	CAACCTAGTCTTAAA[A/C]TAGTTTGTTTAAAAA	6596
rs183498510	snp	G/T	0.0023933	0.0345097	intron-variant	HLTF	GRCh38.p7	3:149057507	CCAACTTTTCATATA[G/T]ACTCGTCCTGCAGGG	6596
rs183502472	snp	A/C	0.00159649	0.0282165	intron-variant	HLTF	GRCh38.p7	3:149080548	TCTGCCACTGCCTAC[A/C]GGATGATCTTTTTTA	6596
rs183617086	snp	A/G	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149044403	TTACTGATACTCAGC[A/G]TTTCAATTTAAGAGA	6596
rs183672677	snp	C/T			intron-variant	HLTF	GRCh38.p7	3:149065807	TGCACTCCCTCTGTC[C/T]CAAAAAATAAAATTA	6596
rs183887134	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149038959	TTTTCACAGTTAATT[A/G]TAACTATGAAGGTAT	6596
rs184018816	snp	G/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149046870	TTTTTTCCCAACATT[G/T]AAATATAAATACAAT	6596
rs184046773	snp	C/T	0.000367426	0.0135491	missense	HLTF	GRCh38.p7	3:149048034	AGTACTTACCTAAGT[C/T]CTCCTTCATCTCCCA	6596
rs184050155	snp	C/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149074803	GAGACATTATGAGCA[C/T]TTATTTTCTCTTCAA	6596
rs184173809	snp	A/T	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149073647	TGCACTCAGCCACTG[A/T]TCGTGGCCACTGTAC	6596
rs184287821	snp	C/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149055708	GCAGTTTTCTGAATT[C/T]GTGTTATATTTAATT	6596
rs184297338	snp	C/G	0.00279162	0.0372561	intron-variant	HLTF	GRCh38.p7	3:149077911	AGCTAACCAAGTACA[C/G]ACTTCAGTGACCACA	6596
rs184353825	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime, intron-variant	HLTF	GRCh38.p7	3:149032103	ACCTCTTCACTAATA[C/T]AAAATATGCCCCTTT	6596
rs184363565	snp	A/C	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149082720	ATGCAAAGATAGTAT[A/C]TCAATTTTTATTATT	6596
rs184369761	snp	C/T	0.0158469	0.0875917	intron-variant	HLTF	GRCh38.p7	3:149078205	GTCCCCAAGAAAGTA[C/T]AGATGTTTGACATAG	6596
rs184488394	snp	C/T	0.00199481	0.0315187	intron-variant	HLTF	GRCh38.p7	3:149056344	AGTGATAATAAAGTG[C/T]TTTTACAAATTCTTG	6596
rs184532564	snp	C/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149047620	GCCCTCCAGCATGGA[C/T]GACAGAGCAAGACTC	6596
rs184597368	snp	C/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149033476	AAAGGGTCATCAGAA[C/T]ATTTTACCCTATCAG	6596
rs184608665	snp	C/T	0.00199481	0.0315187	intron-variant	HLTF	GRCh38.p7	3:149078506	AGTGAGCTATGATCA[C/T]GCCACTGCACTCCAG	6596
rs184614076	snp	A/C	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149058944	ATTAGGGTAAAGAAT[A/C]ATCCACCCAACATGC	6596
rs184731569	snp	C/T	0.00914312	0.0669923	intron-variant	HLTF	GRCh38.p7	3:149035971	AAACCCCATCTCTAC[C/T]AAAAATACAAAAAAT	6596
rs184816504	snp	A/C	0.00557542	0.0525036	intron-variant	HLTF	GRCh38.p7	3:149037134	GCCATAAAATACTGC[A/C]AACAAAGATTTCAAA	6596
rs184825200	snp	A/T	0.00159617	0.0282053	intron-variant	HLTF	GRCh38.p7	3:149060920	AAATAAGATATACAA[A/T]CATGTTTAATAAATG	6596
rs184836487	snp	C/G	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149082571	AGACGGATACAATCT[C/G]TATCTTGATTGGGGT	6596
rs185005443	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	HLTF	GRCh38.p7	3:149030821	TCACTGTTCCCTTTG[A/G]GCAAGAAAACGGCAC	6596
rs185037276	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149069712	TTTTACTTGAATGAC[A/G]ACTATCAATCACGAC	6596
rs185188127	snp	A/G	0.00517822	0.0506191	intron-variant	HLTF	GRCh38.p7	3:149037447	CACTCCAGCATGGGC[A/G]ACAGAGCAAGACTCT	6596
rs185310472	snp	A/G	0.0119091	0.0762411	intron-variant	HLTF	GRCh38.p7	3:149061959	ACAATAGGAAATTTC[A/G]TAAATTTTGTGTAGA	6596
rs185341981	snp	A/T	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149043059	TATGACCAAGGATAC[A/T]GTCACAATTTAACAC	6596
rs185348275	snp	C/T	0.00119737	0.0244387	intron-variant	HLTF	GRCh38.p7	3:149069976	TCAACATTTAGTAGG[C/T]CTGCCCAACTCAATG	6596
rs185383403	snp	A/G/T	0.0023933	0.0345097	intron-variant	HLTF	GRCh38.p7	3:149051216	ACCTAGAATTGTGTG[A/G/T]TAAAAATATAAGGAA	6596
rs185395954	snp	C/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149076286	TAATGTCTTAAAAAA[C/T]AGTCAAATGTAAACT	6596
rs185433798	snp	G/T	0.00199481	0.0315187	intron-variant	HLTF	GRCh38.p7	3:149068814	GCATTTTTCTTAAGT[G/T]GAAGTATGTAATTTT	6596
rs185551821	snp	C/T	0.00119737	0.0244387	intron-variant	HLTF	GRCh38.p7	3:149040915	TTTAAAAAAATTCTA[C/T]CCCAGCTGAATGACT	6596
rs185571086	snp	C/T	0.0126979	0.078662	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087921	CACATTTGTTCATTA[C/T]CGTAAATAAACTGTA	6596
rs185648014	snp	A/G	0.00119737	0.0244387	intron-variant	HLTF	GRCh38.p7	3:149078890	GTTCAAAGACCTAAA[A/G]CAAATCATTTCTTTC	6596
rs185656419	snp	C/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149044434	TCTCTTTTGAGTGCC[C/T]ACCATGTGCTAAATA	6596
rs185710515	snp	A/C	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149048698	AATGTTGTTATATCA[A/C]GGGCAATTATGAAGA	6596
rs185854939	snp	C/G			intron-variant	HLTF	GRCh38.p7	3:149074951	TGAAAGATTGAAAGA[C/G]TTTAGAAAAAGAAAA	6596
rs185906151	snp	C/T	0.00557542	0.0525036	intron-variant	HLTF	GRCh38.p7	3:149050847	CAACCACAATAGTGA[C/T]GTAACTAAAAATGAA	6596
rs185912834	snp	C/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149075296	GCTCACGCCTGTAAT[C/T]CCAGCATTTTGGGAG	6596
rs185993156	snp	A/G	0.00993419	0.0697739	intron-variant	HLTF	GRCh38.p7	3:149034764	AAAGGCCCCTTAAAC[A/G]GCATATATTAAATTA	6596
rs186013352	snp	A/G	0.00318978	0.0398085	intron-variant	HLTF	GRCh38.p7	3:149079652	GGCTGGAGTACAGTC[A/G]CACAATCTCGGCTCA	6596
rs186137659	snp	C/T	0.00199481	0.0315187	intron-variant	HLTF	GRCh38.p7	3:149057371	GTGGAGGTTGCAGTG[C/T]GCCGTGATCGCACCA	6596
rs186253476	snp	C/T			intron-variant	HLTF	GRCh38.p7	3:149062511	ATTTGCGATGACTTG[C/T]GTAGATACTGATGGT	6596
rs186413589	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149037767	ATCTTAAGTCTGAAT[A/G]CACAGAAACAGCAGA	6596
rs186424093	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149083782	AAATTAGCTGGGTAT[A/G]GTGGTGAACGCCAGC	6596
rs186474099	snp	A/G/T	0.00029912	0.012226	intron-variant	HLTF	GRCh38.p7	3:149040173	TATATAAGAAAGAAC[A/G/T]AAGTATGAGCAACAC	6596
rs186479315	snp	A/G	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149068066	ACCTTGTCTGAAAAC[A/G]TAAAAAGAATGTGAC	6596
rs186516566	snp	A/C	0.0193772	0.0965046	intron-variant	HLTF	GRCh38.p7	3:149057191	CCAGCACTTTGGAAG[A/C]CTGAGGCGGGTGGAT	6596
rs186570748	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149038287	AACTGACGCAAAGCA[A/G]GATCTCATTATTTGC	6596
rs186585684	snp	G/T	0.00953873	0.0683987	intron-variant	HLTF	GRCh38.p7	3:149065428	CCAATGTACATGAAT[G/T]GAAAACAATTTTATA	6596
rs186590938	snp	C/G	0.000798403	0.0199641	intron-variant, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149084513	CCCAACACTCTGGGA[C/G]GCTGAGGTGGGAGGG	6596
rs186713897	snp	C/T	3.24133e-05	0.00402562	intron-variant	HLTF	GRCh38.p7	3:149046285	TAAAACAAATAATTA[C/T]GTAACTTTTAATTTC	6596
rs186716015	snp	C/T	0.00119737	0.0244387	intron-variant	HLTF	GRCh38.p7	3:149073072	AAATGTTAACATATA[C/T]ATATTCTATTTATTC	6596
rs186720721	snp	C/T	0.0360663	0.129354	intron-variant	HLTF	GRCh38.p7	3:149036376	TCAGTGCAACCTCCA[C/T]CTCCTGGGTTCAAGC	6596
rs186723924	snp	A/G/T	0.00318978	0.0398085	intron-variant	HLTF	GRCh38.p7	3:149034043	TAACTATGAGAACTG[A/G/T]ACAGAAGATATAAAT	6596
rs186803978	snp	C/T	0.00196365	0.0312725	intron-variant	HLTF	GRCh38.p7	3:149039003	TTTTGTCTTATTTTT[C/T]TGAAAGAAGTACTAA	6596
rs186839426	snp	A/C/T	6.32216e-05	0.00562206	intron-variant, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149086291	GGCCGTTAGACCGAG[A/C/T]GCCCCACCCCCTCCG	6596
rs186913115	snp	C/T			intron-variant	HLTF	GRCh38.p7	3:149035690	AAAAAAAAAGGGGGT[C/T]TTAAGAGTCAGTAAG	6596
rs186948280	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149039294	ATAAAACAAAGTTAA[A/G]TAACTACAAATCTCT	6596
rs187028233	snp	G/T	0.00159617	0.0282053	intron-variant	HLTF	GRCh38.p7	3:149066023	ATGTTTATTCAAACA[G/T]AAAGGATGTCCTTTG	6596
rs187109097	snp	A/G	0.00119737	0.0244387	intron-variant	HLTF	GRCh38.p7	3:149070214	GCAATTATCTAAAAA[A/G]CTATTACAATACTCC	6596
rs187126485	snp	A/G	0.0023933	0.0345097	intron-variant	HLTF	GRCh38.p7	3:149077930	TCAGTGACCACACAC[A/G]ATAAAGGATAGACAT	6596
rs187273089	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149043288	CTGATAAAAACATAG[A/G]AAAGGATGTAGGAAA	6596
rs187581038	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	HLTF	GRCh38.p7	3:149030409	CATTTTTTAAACAAC[C/T]TGCCAAACTTACTTA	6596
rs187583224	snp	C/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149054889	CTTAAAAGAGGTTAA[C/G]GACAAACCAAATAAA	6596
rs187592121	snp	G/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149077408	TTATTCTCCTGAAGT[G/T]CCCCGGAAGACCCCA	6596
rs187678904	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149081916	ACACATCATACCACC[A/G]AACCCCAATTCCAGA	6596
rs187688589	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149076770	AATGGTAGAATGAGG[A/G]CTTTCAAAAATTCCT	6596
rs187819846	snp	A/G	0.00118663	0.0243291	intron-variant	HLTF	GRCh38.p7	3:149035005	ATTCCAGGCCTAACA[A/G]GAACATGGATGAGTT	6596
rs187825682	snp	A/G	0.00676609	0.0577691	intron-variant	HLTF	GRCh38.p7	3:149057602	TGACAAATACTGAGG[A/G]ATGACTGTACTGTAA	6596
rs187833920	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149080925	GCAATGACAGACCAC[A/G]TGCATTATGCAACAG	6596
rs187928401	snp	C/T	0.000399281	0.0141238	utr-variant-3-prime	HLTF	GRCh38.p7	3:149030873	GTGAGAGATTTGGCA[C/T]ATACCTTCAATGTGT	6596
rs187955330	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149058977	ATATTTTCTATTCCT[A/G]ATTATCTGATTCTTG	6596
rs188147587	snp	A/C	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149043098	AAAACAATTCCTCCA[A/C]AAAAAAAAAATCTTA	6596
rs188150029	snp	A/C	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149070019	CTAAATGAGCAATGC[A/C]TGGTGTTATAAAATC	6596
rs188185794	snp	C/T	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149058309	TGAACTCATGGGCCT[C/T]GGCCTCCCAAAGTGC	6596
rs188213322	snp	C/T			upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087088	ACTTAGAGTCCCCTC[C/T]CCACCTCTTTTTGTT	6596
rs188221120	snp	A/G			intron-variant	HLTF	GRCh38.p7	3:149055960	GGAGCCAGCTGCCAC[A/G]ATGTGAGGCCACTCA	6596
rs188395067	snp	C/T	0.0023933	0.0345097	intron-variant	HLTF	GRCh38.p7	3:149074872	TTAGAATATCAAGAT[C/T]CTAAATATTCCAGAT	6596
rs188405481	snp	C/T	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149038125	GCTTCCTGGGTCTAA[C/T]CCTAGAACTCCTAAG	6596
rs188412129	snp	C/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149063920	ACTAAACACTGTTCG[C/G]CTCCCCTACCCATTT	6596
rs188467234	snp	A/T			intron-variant	HLTF	GRCh38.p7	3:149035639	ACTCCAGACTGGGCG[A/T]CAGCGAGACTCCGTC	6596
rs188482845	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149081481	GTAGAAAAACCGAAT[A/G]TAAGAGTAATTATTA	6596
rs188648536	snp	C/G	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149042354	CTTCCTATTCTAAAA[C/G]AGCAGAGTAAAATGG	6596
rs188659509	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149069919	ATAACATCAGTGGTA[A/G]TATTAATGAATGTAA	6596
rs188730548	snp	C/G	0.0126979	0.078662	intron-variant	HLTF	GRCh38.p7	3:149073844	TCTTGCCAAGCAATC[C/G]TTTTCATTCGCTATC	6596
rs188901352	snp	C/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149047709	TAATGCATATTAGAT[C/G]CTCAAAGGATATACG	6596
rs188972367	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149052534	AATAACATATTCAAG[A/G]CAGAGGAAAAGGGGA	6596
rs188999943	snp	C/T	0.00159617	0.0282053	intron-variant	HLTF	GRCh38.p7	3:149047012	TCCAGCAAAAATATA[C/T]AAACACATACAAAAG	6596
rs189014823	snp	C/T	0.00358779	0.0422022	intron-variant	HLTF	GRCh38.p7	3:149056787	TGATGCACTTACATG[C/T]AAATTTTTGTTAACC	6596
rs189046103	snp	C/T	0	0	intron-variant	HLTF	GRCh38.p7	3:149033728	ATAATAAGCTTAGAC[C/T]CATGTCACAAATCAT	6596
rs189058651	snp	C/T	0.00119737	0.0244387	intron-variant	HLTF	GRCh38.p7	3:149078701	TCTCTACTAAAAATA[C/T]AAAAAATTAGCCGGG	6596
rs189276124	snp	A/G	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149048396	ACACACTAGCCAAGA[A/G]AAAGACTGGAAAATT	6596
rs189283252	snp	A/G	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149037199	AGACCGGCTGGGCGC[A/G]GTGGCTCATGCCTGT	6596
rs189285592	snp	A/G	0.00119737	0.0244387	intron-variant	HLTF	GRCh38.p7	3:149032657	GGCAAAATGACTTCA[A/G]CATTGTATTAAAAAG	6596
rs189295713	snp	A/G	0.00159617	0.0282053	intron-variant	HLTF	GRCh38.p7	3:149061343	GTGAAGCCAGGAGAC[A/G]GAGTTTCCAGTGAGC	6596
rs189303232	snp	C/T	0.00199481	0.0315187	intron-variant	HLTF	GRCh38.p7	3:149082671	TACGTAAACCACATC[C/T]CAATAAAGTAGAAAA	6596
rs189303990	snp	A/G	0.0126979	0.078662	intron-variant	HLTF	GRCh38.p7	3:149078210	CAAGAAAGTATAGAT[A/G]TTTGACATAGTAGAA	6596
rs189309447	snp	A/G	0.00398564	0.0444627	intron-variant	HLTF	GRCh38.p7	3:149083830	AGGCTGAATTGGGAG[A/G]ATTGCTTGAGTCTGG	6596
rs189715732	snp	A/C	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149034866	TGCATTACTTGCTTA[A/C]TTGTAAAAATCGTAT	6596
rs189839229	snp	A/G	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149062147	ATATAATCCTCATAG[A/G]ATAAAATGTTACTAC	6596
rs190078323	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149040997	GACCTACCTTATCCA[A/G]CACAATAGCCAATAA	6596
rs190080140	snp	C/T	0.00199481	0.0315187	intron-variant	HLTF	GRCh38.p7	3:149037667	AACTAAAATTTATAT[C/T]TCAGTAGTATTCCTA	6596
rs190101505	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149083511	AAAATAATTATCGAA[A/G]GCAATGTAAGTTTTG	6596
rs190121584	snp	A/C	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149045275	TTACCTATATATCAT[A/C]TTCTCAGTGAGGTCT	6596
rs190337105	snp	C/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149069237	AGCACTTTGGGAGGC[C/T]GAAGCAGGTGGATCA	6596
rs190364135	snp	A/G	0.00119737	0.0244387	intron-variant	HLTF	GRCh38.p7	3:149050860	GATGTAACTAAAAAT[A/G]AAGAACAAATAATCA	6596
rs190376182	snp	A/C/T	0.00159617	0.0282053	intron-variant	HLTF	GRCh38.p7	3:149075785	CAGTGATAGAAATTG[A/C/T]TAGCATACCTTTATA	6596
rs190379515	snp	A/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149075072	CTGCATTGCCAGATT[A/T]CCCACTTGTCAAGAG	6596
rs190456614	snp	C/G			intron-variant, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149085953	ATACAGATAAGCTGT[C/G]AGCCACTTGGGGACA	6596
rs190624487	snp	C/T	0.00159617	0.0282053	intron-variant	HLTF	GRCh38.p7	3:149049961	CACACCATTATATTC[C/T]AGCCTGGGCAACAAG	6596
rs190659860	snp	A/G	0.00478085	0.0486577	intron-variant	HLTF	GRCh38.p7	3:149057456	ACAAACAAAAAAACA[A/G]TATCTGCTGATTGCA	6596
rs190779152	snp	A/G	0.00318978	0.0398085	intron-variant	HLTF	GRCh38.p7	3:149035515	TAGAAAAAATTAGCC[A/G]GGAGAGGTGGCGGGC	6596
rs190793406	snp	A/G	0.00953873	0.0683987	intron-variant	HLTF	GRCh38.p7	3:149057700	CTGAAACTGTAGAAC[A/G]TGAAACTGCAGATAA	6596
rs190799874	snp	A/T	0.00597247	0.0543191	intron-variant	HLTF	GRCh38.p7	3:149081012	TTATACAATATTTTT[A/T]CTGTACTTTTTTCAT	6596
rs190919697	snp	A/G			intron-variant	HLTF	GRCh38.p7	3:149079871	GCTGGGATTACAGGC[A/G]TGAGCCACCATGCCC	6596
rs190924119	snp	G/T	0.00478085	0.0486577	intron-variant	HLTF	GRCh38.p7	3:149051511	ACAGAATACCGGTAT[G/T]TAAGGAGAAGACTTG	6596
rs191039247	snp	C/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149038910	TCCACATTTACTAAG[C/T]TTTTGTTATTTATTT	6596
rs191043191	snp	A/G	0.00159617	0.0282053	intron-variant	HLTF	GRCh38.p7	3:149065514	AATGTGGTTGAAAAG[A/G]TTCATCCTCTTTAAA	6596
rs191054136	snp	A/C	0.00119737	0.0244387	intron-variant, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149084559	GTTATTTTTTGCGTA[A/C]AAATATTTAACTAAC	6596
rs191174288	snp	C/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149034555	AATGCATCTAAACTG[C/T]ATACTTCAAAATGGT	6596
rs191179665	snp	C/T	0.00159617	0.0282053	intron-variant	HLTF	GRCh38.p7	3:149076368	CCAACCCTTATTGAG[C/T]GCTTACTATGTGCCA	6596
rs191183377	snp	C/T	0.000170407	0.009229	intron-variant	HLTF	GRCh38.p7	3:149073190	TGCAACATTTAAAAT[C/T]CACTTTTAGATTACA	6596
rs191186227	snp	C/T	0.00279162	0.0372561	intron-variant	HLTF	GRCh38.p7	3:149079571	AATAGGATGGAGCTG[C/T]GAGCAAAGGTTTTTT	6596
rs191191460	snp	A/G	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149036920	CTGCTAAAACGTTCT[A/G]TAAATTTTTAAAAAC	6596
rs191199639	snp	A/G	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149060277	TTTGATTATTTTCAC[A/G]TCTGTATAATAATGT	6596
rs191207694	snp	A/G	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149082142	TGAAGTTCTAGAATA[A/G]GCAAAACTTATTTAT	6596
rs191421242	snp	G/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149057244	CATCTTGGCTAACAT[G/T]GTGAAACCCGTCTCT	6596
rs191436273	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149039971	ATTTTGATATACTGT[A/G]TATATTTCCTTATAT	6596
rs191450363	snp	A/G			intron-variant	HLTF	GRCh38.p7	3:149067645	GTAGGTGGAACTACA[A/G]GTGCCAGTCACTATG	6596
rs191458316	snp	A/C	0.00358779	0.0422022	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087135	TTCCTTTCTTGGTGC[A/C]GGAAACCCATCACAT	6596
rs191468984	snp	C/T			intron-variant	HLTF	GRCh38.p7	3:149066760	TTCTATCAAATCTGG[C/T]AACCTAAAACTTCAG	6596
rs191712038	snp	C/G	6.75847e-05	0.00581273	missense	HLTF	GRCh38.p7	3:149039146	GGAGATCCTGCTTCA[C/G]TGTTTTGAAAACACT	6596
rs191725399	snp	A/G	0.00279162	0.0372561	intron-variant	HLTF	GRCh38.p7	3:149044021	CAAGGAATAGGCAAA[A/G]TAATACAAAGATTAA	6596
rs191734134	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149086962	TAGAGCTACCGGCGA[C/G]ATACTTTACTTCATT	6596
rs191825695	snp	C/G	0.00279162	0.0372561	intron-variant	HLTF	GRCh38.p7	3:149047880	AAACAAGCATCACTA[C/G]GTTCTGAAAGACAAA	6596
rs191833930	snp	C/T	0.0138799	0.0821421	intron-variant	HLTF	GRCh38.p7	3:149074797	CAAAGTGAGACATTA[C/T]GAGCATTTATTTTCT	6596
rs191991066	snp	C/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149076921	TAAACAGCTGAATAT[C/T]AGTACTTCAGTCCCA	6596
rs192025509	snp	A/C	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149070928	CACATGCCTGTAATC[A/C]CAGCTATTTGGAAGT	6596
rs192055103	snp	A/G	0.000399281	0.0141238	utr-variant-3-prime	HLTF	GRCh38.p7	3:149030487	AGCTGTCCTCCCTTT[A/G]CCTTCATAGTGAGTT	6596
rs192061066	snp	C/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149054947	TATAAAAATAAGTTA[C/T]TGTTGGTATAGCTCT	6596
rs192073396	snp	A/T	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149077527	GAAAGTGTTTTAACT[A/T]CATGGCTACCTGAGG	6596
rs192292641	snp	A/G	0.00119737	0.0244387	intron-variant	HLTF	GRCh38.p7	3:149061359	GAGTTTCCAGTGAGC[A/G]GAGATTGCGCCACTG	6596
rs192305062	snp	A/T	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149082719	TATGCAAAGATAGTA[A/T]CTCAATTTTTATTAT	6596
rs192315744	snp	C/T	0.00557542	0.0525036	intron-variant	HLTF	GRCh38.p7	3:149052973	CCTCTCAATAGAAAA[C/T]GAAATAGGTGTTATT	6596
rs192505954	snp	A/G	0.0023933	0.0345097	intron-variant	HLTF	GRCh38.p7	3:149056048	GTAATGAGGTCTGCT[A/G]ACAACTATGTGAGTG	6596
rs192546415	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149068134	GAGAGACCATTCATC[A/G]CATTTCTGAAAACAC	6596
rs192558762	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087821	TGAACTCCTGACCTC[A/T]GGTGATCCGCCCGCC	6596
rs192623414	snp	A/T	0.00119737	0.0244387	intron-variant	HLTF	GRCh38.p7	3:149046503	TTTAATCTTTTTATA[A/T]CCTGTCCTTATTTTC	6596
rs192727306	snp	A/C			intron-variant	HLTF	GRCh38.p7	3:149035883	GCTCACGCCTGTAAT[A/C]CCAGCACTTTGGGAG	6596
rs192731163	snp	A/C	0.0142736	0.0832652	intron-variant	HLTF	GRCh38.p7	3:149081502	GTAATTATTAAGCCA[A/C]GAAACACAATCATTA	6596
rs192804350	snp	G/T	0.00199481	0.0315187	utr-variant-3-prime, intron-variant	HLTF	GRCh38.p7	3:149031379	CTGAATTATAAAAAT[G/T]TATAAAGTTACTTCC	6596
rs192811225	snp	A/G	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149078140	AGACATGCAAAAAAA[A/G]TAAGAAAGTATGGTC	6596
rs192868718	snp	A/T	0.00119737	0.0244387	intron-variant	HLTF	GRCh38.p7	3:149069556	ACTTCAGTACAAATC[A/T]TTTTAATATTCTGTG	6596
rs192930144	snp	A/T	0.00119737	0.0244387	intron-variant	HLTF	GRCh38.p7	3:149058746	ATTCACAGAGTTTTG[A/T]TTCTATTCTGCTTCT	6596
rs192989352	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149047498	AATACAAAAATTAGC[A/G]GGGCATGCTGGCGCA	6596
rs193071182	snp	C/T	0.00398564	0.0444627	intron-variant	HLTF	GRCh38.p7	3:149041755	AAAAGTTTCGCTTGC[C/T]AGTAGGGAAAGTCTC	6596
rs193109806	snp	A/G			intron-variant	HLTF	GRCh38.p7	3:149040736	TTTAAAAGTCAATAC[A/G]GTGGGGTTACTTTTG	6596
rs193199171	snp	C/T	0.00601722	0.0545197	intron-variant	HLTF	GRCh38.p7	3:149074166	AAATGTTTCATAATC[C/T]CTGCATCTTACAATA	6596
rs199552856	snp	A/C	0.000365821	0.0135195	intron-variant	HLTF	GRCh38.p7	3:149039551	ATATAAAATCCTTTT[A/C]CTGAAAGTGAAAAAC	6596
rs199589670	snp	A/G			intron-variant	HLTF	GRCh38.p7	3:149083928	GGTCTCAAAAAAAAA[A/G]AAAAAAAAAAAAATC	6596
rs199624620	snp	A/G			intron-variant	HLTF	GRCh38.p7	3:149069169	CAGTTAAAAAAAAAA[A/G]TTTTCCTTAAGAATG	6596
rs199656698	snp	C/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149060773	ATCAAATCTATTACA[C/T]GTTACCTTTCATTTT	6596
rs199658833	snp	A/G			intron-variant	HLTF	GRCh38.p7	3:149052650	AGGACTGAAGAAAGT[A/G]TTAAACATGAAATAA	6596
rs199662968	snp	C/T	4.96282e-05	0.00498113	missense	HLTF	GRCh38.p7	3:149073310	CAACCACTTTCCAAA[C/T]TGAATCCTAAAGCTA	6596
rs199668603	snp	C/T			intron-variant	HLTF	GRCh38.p7	3:149073025	ACAAATGTTCACGTA[C/T]GGATTTATTCCTTAT	6596
rs199737245	snp	C/G			utr-variant-3-prime	HLTF	GRCh38.p7	3:149030479	AAGAAGCAAGCTGTC[C/G]TCCCTTTACCTTCAT	6596
rs199760392	in-del	-/TTG			upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149087582	TCTTTTTTCTTTTTT[-/TTG]TTTTTTTTTCTTTTT	6596
rs199836978	snp	A/G	0.000138406	0.00831768	intron-variant	HLTF	GRCh38.p7	3:149071457	GCCTATAAATAAAAA[A/G]TCATAAAGCGAAATA	6596
rs199860917	snp	C/G			intron-variant	HLTF	GRCh38.p7	3:149079514	TTGATAGGTATACTA[C/G]ATATATAAAGATATA	6596
rs199872618	snp	A/G	0.000239808	0.0109474	intron-variant	HLTF	GRCh38.p7	3:149041472	AAACACTGAACCTGT[A/G]CTGAGCAAAAAACTA	6596
rs199873117	in-del	-/CCTGGGTTCAAG	0.0341408	0.126114	intron-variant	HLTF	GRCh38.p7	3:149036379	GTGCAACCTCCACCT[-/CCTGGGTTCAAG]CGATTCTCCTGCCTC	6596
rs199891685	snp	G/T			intron-variant	HLTF	GRCh38.p7	3:149037116	CAAATATTTTTTATA[G/T]TAGCCATAAAATACT	6596
rs199927201	in-del	-/ACCT	0.0345262	0.126772	intron-variant	HLTF	GRCh38.p7	3:149080399	AGAAAGCTGCTTCAA[-/ACCT]CTCCCAGCATGTCTA	6596
rs199962239	snp	A/C			intron-variant	HLTF	GRCh38.p7	3:149079517	ATAGGTATACTACAT[A/C]TATAAAGATATAACT	6596
rs199971777	snp	A/C	1.69289e-05	0.00290933	intron-variant	HLTF	GRCh38.p7	3:149075869	TAAAACTAAATTCTG[A/C]AAGTACATTACCCTT	6596
rs199988419	in-del	-/ACTT	0.031825	0.122064	utr-variant-3-prime	HLTF	GRCh38.p7	3:149030415	TAAACAACTTGCCAA[-/ACTT]ACTTACTTATGAGTG	6596
rs200026463	snp	C/T	5.25555e-05	0.00512591	intron-variant	HLTF	GRCh38.p7	3:149048191	GGAAACTGTTATAAC[C/T]CTTTAACCAGAGTAT	6596
rs200083068	snp	C/G	1.64836e-05	0.0028708	missense	HLTF	GRCh38.p7	3:149063437	ATAGTTTACCTTTTG[C/G]GGCGGGAGCTAGACA	6596
rs200230104	snp	A/G	0.00358779	0.0422022	intron-variant	HLTF	GRCh38.p7	3:149060587	AGATACAAATCAATG[A/G]AGCTGTACTTTAATA	6596
rs200309642	in-del	-/T	0.0123036	0.0774623	intron-variant	HLTF	GRCh38.p7	3:149044486	TTCACCAGCCATTGC[-/T]TATCTTCACAGTTAG	6596
rs200400145	snp	C/G	0.000365195	0.0135079	missense	HLTF	GRCh38.p7	3:149032356	ATATTTTCTTCAACA[C/G]AGTCCTTTACAATGA	6596
rs200461348	in-del	-/A			intron-variant	HLTF	GRCh38.p7	3:149054691	AGAAAAGCAATCTGG[-/A]AAAAAAAAAATTTCT	6596
rs200484610	snp	A/T			intron-variant	HLTF	GRCh38.p7	3:149078872	AAAAAAAAAAAAAAA[A/T]AAGTTCAAAGACCTA	6596
rs200515493	snp	C/T	0.000399281	0.0141238	missense	HLTF	GRCh38.p7	3:149074326	GCATGGTAAAAGCAT[C/T]GTTTGCACCAAAAGG	6596
rs200644941	snp	A/T			intron-variant	HLTF	GRCh38.p7	3:149079515	TGATAGGTATACTAC[A/T]TATATAAAGATATAA	6596
rs200667438	snp	C/T			intron-variant	HLTF	GRCh38.p7	3:149079511	TTGTTGATAGGTATA[C/T]TACATATATAAAGAT	6596
rs200736972	snp	A/G	0.000399281	0.0141238	missense	HLTF	GRCh38.p7	3:149060794	CTTTCATTTTCTGCG[A/G]CAATTCACTTGTTTC	6596
rs200744635	in-del	-/AAAAAAC			intron-variant	HLTF	GRCh38.p7	3:149036138	AGACTACATCTCAAA[-/AAAAAAC]AAAAAACAAAAAACA	6596
rs200776697	snp	C/T	0.000399281	0.0141238	synonymous-codon	HLTF	GRCh38.p7	3:149039673	TCTTAAGTCAGTCAA[C/T]GCGTGCATTAGCGCA	6596
rs200783692	snp	A/G	0.000283562	0.0119038	stop-gained	HLTF	GRCh38.p7	3:149076017	GGTTATTAGGATCTC[A/G]TTGTAATGCAACCAT	6596
rs200840947	in-del	-/T	0.00318978	0.0398085	intron-variant, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149085388	AGCTACTCGGGAGGC[-/T]TGAGGCAGGAGAATC	6596
rs200841482	snp	C/T	0.000150252	0.00866621	intron-variant	HLTF	GRCh38.p7	3:149060908	CAACCCAAAGCAAAA[C/T]AAGATATACAAACAT	6596
rs200887794	snp	A/G	6.59217e-05	0.00574078	missense	HLTF	GRCh38.p7	3:149063441	TTTACCTTTTGGGGC[A/G]GGAGCTAGACAATTC	6596
rs200923474	snp	A/C/T	3.51724e-05	0.00419347	intron-variant	HLTF	GRCh38.p7	3:149041715	GCAAGGTTTGTAATA[A/C/T]GACAAGTTAATCTAT	6596
rs200936969	snp	A/T	1.70449e-05	0.00291928	missense	HLTF	GRCh38.p7	3:149032278	TTCATTTCGTCAGCA[A/T]TTGGTTTTTTAGTTC	6596
rs200974169	in-del	-/AT			intron-variant	HLTF	GRCh38.p7	3:149080410	CAAACCTCTCCCAGC[-/AT]ATGTCTACTGACTCA	6596
rs201083285	snp	A/C			intron-variant	HLTF	GRCh38.p7	3:149081264	CTTATTGAAAACACA[A/C]TAAAAAAAAAAAAAC	6596
rs201128683	snp	A/G	0.000399281	0.0141238	missense	HLTF	GRCh38.p7	3:149059729	TGACCCTTTTTCAAC[A/G]TTTTCTTTTTTGTTG	6596
rs201163851	snp	A/T	1.64996e-05	0.0028722	synonymous-codon	HLTF	GRCh38.p7	3:149075922	CATGATATAGGCCAA[A/T]GCACCTGCAAGCTCT	6596
rs201168554	snp	C/T	3.43071e-05	0.00414154	intron-variant	HLTF	GRCh38.p7	3:149047990	AGCTACTAACAGTTA[C/T]TTGTAACTAATATTA	6596
rs201177848	in-del	-/A			intron-variant	HLTF	GRCh38.p7	3:149040508	TTAGTACTATTCTTT[-/A]AAAAAAAAATCCATC	6596
rs201188971	snp	A/C			intron-variant	HLTF	GRCh38.p7	3:149043096	ATAAAACAATTCCTC[A/C]AAAAAAAAAAAATCT	6596
rs201252374	snp	C/G/T	3.30247e-05	0.00406343	intron-variant	HLTF	GRCh38.p7	3:149063529	TCTAGATGCGTCTAT[C/G/T]TCAAAGAAAAATGCA	6596
rs201331636	snp	A/T			intron-variant	HLTF	GRCh38.p7	3:149079513	GTTGATAGGTATACT[A/T]CATATATAAAGATAT	6596
rs201380908	snp	C/T	0.000148408	0.0086129	missense	HLTF	GRCh38.p7	3:149064842	TTCCTCCAAGTTTCA[C/T]AGAGTCATCGTTAAC	6596
rs201438103	in-del	-/T	0.0126979	0.078662	utr-variant-3-prime	HLTF	GRCh38.p7	3:149030292	TTTCATTCCAGTGGC[-/T]TTTTTTATATATTTA	6596
rs201482213	snp	C/T			intron-variant	HLTF	GRCh38.p7	3:149079516	GATAGGTATACTACA[C/T]ATATAAAGATATAAC	6596
rs201519643	in-del	-/TTACT			intron-variant	HLTF	GRCh38.p7	3:149072775	ATTGATCTGCATTAA[-/TTACT]TTATATACTTTTTTT	6596
rs201520168	snp	C/T	1.67002e-05	0.00288961	missense	HLTF	GRCh38.p7	3:149041495	AAAAACTAACCTGCT[C/T]ATTCTGAATGACTTG	6596
rs201547822	snp	C/T	0.000429773	0.0146527	synonymous-codon	HLTF	GRCh38.p7	3:149073234	GCACACCTGTTCAGT[C/T]GTCATCTGTACTGCA	6596
rs201554369	in-del	-/AAATAAAT			intron-variant	HLTF	GRCh38.p7	3:149077248	CGAGACTTCATCTCA[-/AAATAAAT]AAATAAATAAATAAA	6596
rs201587496	in-del	-/T			intron-variant	HLTF	GRCh38.p7	3:149051232	AAAAATATAAGGAAG[-/T]TTTAAAAAAAAAAAA	6596
rs201648572	snp	C/T	0.000247498	0.0111215	missense	HLTF	GRCh38.p7	3:149075918	TGTCCATGATATAGG[C/T]CAAAGCACCTGCAAG	6596
rs201653124	snp	A/T	0.000281268	0.0118556	missense	HLTF	GRCh38.p7	3:149060784	TACATGTTACCTTTC[A/T]TTTTCTGCGGCAATT	6596
rs201714042	in-del	-/A	0.0146672	0.084371	intron-variant	HLTF	GRCh38.p7	3:149033669	TTGGAATTTTCAAAG[-/A]AAAAAAATGATGTGA	6596
rs201715409	snp	A/G			intron-variant	HLTF	GRCh38.p7	3:149041824	TTTGAAATTTAAGAA[A/G]CATTCAGAAGCCAAA	6596
rs201738138	snp	A/G	0.000399281	0.0141238	missense	HLTF	GRCh38.p7	3:149039647	AAACTTTTTATGTTG[A/G]GATTCTTCTTTCTTA	6596
rs201754257	snp	C/G	4.97146e-05	0.00498546	missense	HLTF	GRCh38.p7	3:149039113	CCACCTGCTTTTAAG[C/G]ACAGAAGCATTATAG	6596
rs201772207	snp	A/G			intron-variant	HLTF	GRCh38.p7	3:149073343	ATTTACAAAATAAAA[A/G]GAATAAAGCCATCAA	6596
rs201773782	snp	C/G	0.000399281	0.0141238	missense	HLTF	GRCh38.p7	3:149060850	ATGTACTGGACAGCA[C/G]TTTTTCTTCTAAAAT	6596
rs201932854	in-del	-/AC			intron-variant	HLTF	GRCh38.p7	3:149032977	AAAAAAAAAAAAAAA[-/AC]AAAAAACTATTCCCA	6596
rs201937197	in-del	-/G			intron-variant	HLTF	GRCh38.p7	3:149043544	TTGCTGAACTTCAGA[-/G]GGGAAAAAAAAAAAA	6596
rs201963102	snp	C/T	1.64781e-05	0.00287033	missense	HLTF	GRCh38.p7	3:149063456	GGGAGCTAGACAATT[C/T]TGACATGCGAAACTT	6596
rs201978472	snp	C/T	0.000480522	0.0154929	missense	HLTF	GRCh38.p7	3:149046257	ATTAGGGACTGTAAA[C/T]GCCTAATCAGAATAA	6596
rs202070384	snp	A/C	6.66356e-05	0.00577177	intron-variant	HLTF	GRCh38.p7	3:149074203	TAATATTAAGTGAAA[A/C]CCTAAACTTACTTTT	6596
rs202075733	in-del	-/A			intron-variant	HLTF	GRCh38.p7	3:149043108	TCCAAAAAAAAAAAA[-/A]TCTTAAAGCAAAGAC	6596
rs202199103	snp	A/G	1.64817e-05	0.00287064	stop-gained	HLTF	GRCh38.p7	3:149048914	GTACAGCTTTTGTCT[A/G]CTGAGCATTTGGATT	6596
rs202233141	snp	C/T			intron-variant	HLTF	GRCh38.p7	3:149062581	GAAGATAAATGAAGT[C/T]TGTAAAGTTAACAGA	6596
rs202243174	snp	C/G	1.6477e-05	0.00287024	missense	HLTF	GRCh38.p7	3:149055329	TTAACACAGAAAGCG[C/G]ACAGATGATCAGTGT	6596
rs367600539	in-del	-/AAAAT	0.121921	0.214699	intron-variant	HLTF	GRCh38.p7	3:149061413	ACACTCCATCTCAAA[-/AAAAT]AAAATAAAATAAAAT	6596
rs367624366	in-del	-/AA			intron-variant	HLTF	GRCh38.p7	3:149083750	CTAAAAAAAAATACA[-/AA]AAAAAAAAAAATACA	6596
rs367633765	in-del	-/TATC	0.00321801	0.0399831	utr-variant-3-prime, intron-variant	HLTF	GRCh38.p7	3:149031419	TACATAAATAAAAAT[-/TATC]TATTTATAGAAATAT	6596
rs367673340	snp	A/T	3.30289e-05	0.00406366	intron-variant	HLTF	GRCh38.p7	3:149042155	GATATGAAGCAATCA[A/T]ATTTACCTACCTGAG	6596
rs367685462	snp	G/T	6.6189e-05	0.0057524	missense	HLTF	GRCh38.p7	3:149068253	ACCTTCTTCAGTAGA[G/T]TCTTTTTAACTCTTT	6596
rs367748171	snp	A/G	0.00119737	0.0244387	intron-variant	HLTF	GRCh38.p7	3:149054260	CAAGAGTATGACAGT[A/G]AAGGAAAGCAGAAGA	6596
rs367764908	snp	A/C	6.81919e-05	0.00583878	intron-variant	HLTF	GRCh38.p7	3:149071449	TTTCAATAGCCTATA[A/C]ATAAAAAGTCATAAA	6596
rs367774332	snp	A/G	3.74069e-05	0.00432459	intron-variant	HLTF	GRCh38.p7	3:149040008	AAAACAAATACTCAA[A/G]TATTTGCACATGAGT	6596
rs367798903	snp	A/G			utr-variant-3-prime, intron-variant	HLTF	GRCh38.p7	3:149032021	GCCACAGTATATAAC[A/G]GAACTTATTGCTATT	6596
rs367849095	snp	A/G	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149071764	GCGTTAATGTCAAAC[A/G]GGCCAGGAGTGGTGG	6596
rs367854433	snp	A/C			intron-variant	HLTF	GRCh38.p7	3:149055957	GGTGGAGCCAGCTGC[A/C]ACGATGTGAGGCCAC	6596
rs367867563	snp	C/T	1.79961e-05	0.00299962	missense	HLTF	GRCh38.p7	3:149039665	TTCTTCTTTCTTAAG[C/T]CAGTCAATGCGTGCA	6596
rs367885239	snp	A/T			intron-variant	HLTF	GRCh38.p7	3:149061413	GACACTCCATCTCAA[A/T]AAAATAAAATAAAAT	6596
rs367887879	snp	C/T	0.00119737	0.0244387	intron-variant	HLTF	GRCh38.p7	3:149045930	ATTTCATTCACTTTA[C/T]TGATTTGTAAAAAAC	6596
rs367890191	snp	A/G	8.2991e-05	0.00644117	synonymous-codon	HLTF	GRCh38.p7	3:149050267	TATTATACGTAGTCA[A/G]AACAATATCCTGTTT	6596
rs367961560	in-del	-/C			intron-variant	HLTF	GRCh38.p7	3:149032978	AAAAAAAAAAAAAAA[-/C]AAAAAACTATTCCCA	6596
rs367993357	in-del	-/A			intron-variant	HLTF	GRCh38.p7	3:149065067	TTCACGGGTTATCTC[-/A]AAAAAAAAAAAATAA	6596
rs368279070	snp	A/T			intron-variant	HLTF	GRCh38.p7	3:149080062	AAAATCTATTTAACA[A/T]AAAAATGAGTATTGG	6596
rs368297561	snp	C/G	4.97088e-05	0.00498517	synonymous-codon	HLTF	GRCh38.p7	3:149039112	TCCACCTGCTTTTAA[C/G]GACAGAAGCATTATA	6596
rs368326544	in-del	-/AA			intron-variant	HLTF	GRCh38.p7	3:149032978	AAAAAAAAAAAAAAC[-/AA]AAAAAACTATTCCCA	6596
rs368373271	snp	C/T	0.00013187	0.00811895	missense	HLTF	GRCh38.p7	3:149041540	TACAAAATACATGTG[C/T]ACAATGTGTTATCAC	6596
rs368380305	snp	A/G			intron-variant	HLTF	GRCh38.p7	3:149061700	AACTAGCCAGGTGTG[A/G]TGGTGCGTGCCTGTA	6596
rs368389009	snp	A/G	5.46762e-05	0.0052283	intron-variant, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149084653	GCCAGAAATATAATC[A/G]AAATTTAATTATCTA	6596
rs368412837	snp	A/G	1.73631e-05	0.00294639	intron-variant	HLTF	GRCh38.p7	3:149042324	AATATTATTAAGTCC[A/G]CTAAACAATAATAAC	6596
rs368480768	in-del	-/G			upstream-variant-2KB, intron-variant	HLTF, HLTF-AS1	GRCh38.p7	3:149088460	TCGCTTGAACCAGGG[-/G]AGACATGGGTTGCAG	6596
rs368487159	snp	C/T	3.16912e-05	0.00398053	intron-variant, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149086295	GTTAGACCGAGCGCC[C/T]CACCCCCTCCGCCCC	6596
rs368708723	snp	A/C	0.0115144	0.0749975	intron-variant	HLTF	GRCh38.p7	3:149079522	TATACTACATATATA[A/C]AGATATAACTTGGAT	6596
rs368784035	snp	C/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149045407	TTAAAATATAAATTC[C/T]TCGAGTGCAGGCATT	6596
rs368845681	snp	C/T			intron-variant	HLTF	GRCh38.p7	3:149075162	TATTTCAATAATTAG[C/T]ACTGAACGAAAAAAT	6596
rs368896251	snp	A/C			intron-variant	HLTF	GRCh38.p7	3:149051970	ACCAGCCTGATCAAC[A/C]TGGTGAAACCCCATC	6596
rs368929197	snp	A/T			intron-variant	HLTF	GRCh38.p7	3:149041340	GTTGCATTAGAAGAA[A/T]TATATCACCTATTAA	6596
rs368999558	snp	C/T			intron-variant	HLTF	GRCh38.p7	3:149056905	ACGAGGTCAGGAGCT[C/T]GAGACCATCCTGGCT	6596
rs368999731	snp	C/T			intron-variant	HLTF	GRCh38.p7	3:149068169	TCTTGGTAGTTTTTT[C/T]TAATGATGAAATTTA	6596
rs369064202	snp	C/T	3.49742e-05	0.00418161	intron-variant	HLTF	GRCh38.p7	3:149071466	TAAAAAGTCATAAAG[C/T]GAAATACATTAAGCC	6596
rs369084592	snp	C/T	0.000882987	0.0209932	intron-variant	HLTF	GRCh38.p7	3:149055449	TGTTTTTCTGAAATA[C/T]ATATGTCAATAAGGA	6596
rs369113248	snp	G/T			intron-variant	HLTF	GRCh38.p7	3:149063722	AAGTACCTTCAAATT[G/T]TTATGACCCAGTCTT	6596
rs369183381	snp	A/G/T	0.000174046	0.0093271	intron-variant	HLTF	GRCh38.p7	3:149034878	TTAATTGTAAAAATC[A/G/T]TATCAACCTAGTCTT	6596
rs369266458	snp	C/T			intron-variant	HLTF	GRCh38.p7	3:149048418	TGGAAAATTCAACTT[C/T]CTCCTTATCAAGTAC	6596
rs369282626	snp	C/G/T	0.00159617	0.0282053	intron-variant	HLTF	GRCh38.p7	3:149064713	ATTAGGCTGAAAAAA[C/G/T]GCAAATCAAATATTG	6596
rs369343569	snp	A/G			intron-variant	HLTF	GRCh38.p7	3:149058489	TTCTCCTATTGGGTG[A/G]TCTTTTTCCAATTGT	6596
rs369349908	snp	A/G			intron-variant	HLTF	GRCh38.p7	3:149073924	GGGTTTCCAGATGTT[A/G]CCATTAGGGAAAATT	6596
rs369556490	snp	C/T			intron-variant	HLTF	GRCh38.p7	3:149045827	GCAAGCAAAATCTTC[C/T]GGCTAGCAATTGAGA	6596
rs369557633	snp	C/T	1.65976e-05	0.00288072	intron-variant	HLTF	GRCh38.p7	3:149040162	TAGCATGTGGCTATA[C/T]AAGAAAGAACGAAGT	6596
rs369594108	in-del	-/TAG			intron-variant	HLTF	GRCh38.p7	3:149075717	TGATGGCTGGGGTAG[-/TAG]AAGTATGTAAAAGGA	6596
rs369603637	snp	C/G	0.000798403	0.0199641	intron-variant	HLTF	GRCh38.p7	3:149068187	ATGATGAAATTTAAA[C/G]ATTTCACAATAAACT	6596
rs369613821	snp	A/G			intron-variant	HLTF	GRCh38.p7	3:149042703	AGGTAAACTGAATAC[A/G]GAAACATACAGGTGC	6596
rs369631758	in-del	-/TAGTT			intron-variant, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149084663	AATCAAAATTTAATT[-/TAGTT]ATCTACTATTATACT	6596
rs369671613	snp	G/T	1.75807e-05	0.0029648	missense	HLTF	GRCh38.p7	3:149046182	TTACGTTCTGGTAAC[G/T]CCAAAACAGGTTTTC	6596
rs369746600	in-del	-/GAAA			intron-variant	HLTF	GRCh38.p7	3:149081188	TTTAAAATAGAAAAA[-/GAAA]TAAACCACATTATAA	6596
rs369776457	snp	A/G			intron-variant	HLTF	GRCh38.p7	3:149043717	GAAATATAGCCTAAC[A/G]GCTAAGAGTACAAAT	6596
rs369777437	snp	C/T	0.00119737	0.0244387	intron-variant	HLTF	GRCh38.p7	3:149073929	TCCAGATGTTACCAT[C/T]AGGGAAAATTAGGGG	6596
rs369781578	snp	A/C			intron-variant	HLTF	GRCh38.p7	3:149051576	ATAATTAAAAATATT[A/C]CAGGCCAGGTGCAGT	6596
rs369843526	in-del	-/TTAGT			intron-variant, upstream-variant-2KB	HLTF, HLTF-AS1	GRCh38.p7	3:149084662	TAATCAAAATTTAAT[-/TTAGT]TATCTACTATTATAC	6596
rs369846997	snp	A/G	1.66208e-05	0.00288273	synonymous-codon	HLTF	GRCh38.p7	3:149075964	GCCAACTTGATTTCC[A/G]TTCACATTGTTTACT	6596
rs369853612	snp	A/T			intron-variant	HLTF	GRCh38.p7	3:149051175	TAATAATAATAAGAC[A/T]AAGATGCTCTGATAC	6596
rs370061396	snp	A/C			intron-variant	HLTF	GRCh38.p7	3:149065125	GAAAGGAATACCGAA[A/C]GCAAATCTCAATTAT	6596
rs370072347	snp	C/G			intron-variant	HLTF	GRCh38.p7	3:149039425	AATCTTTAAATTCTT[C/G]TGCTGCCAGGAAGTA	6596
rs370072942	snp	C/T	0.00318978	0.0398085	intron-variant	HLTF	GRCh38.p7	3:149067195	ATATATGTATATATA[C/T]ACACACACACACACA	6596
rs370092302	snp	C/T	9.93723e-05	0.00704814	intron-variant	HLTF	GRCh38.p7	3:149071684	AGCAACAAGAAACAA[C/T]GTAAAACAAACTAAT	6596
rs370131290	snp	A/C			intron-variant	HLTF	GRCh38.p7	3:149035910	GGAGGCCGAGGCAGG[A/C]AGATCACGAGTTCAG	6596
rs370204976	snp	C/T			intron-variant	HLTF	GRCh38.p7	3:149037327	TGCAAAAATTAGCCA[C/T]GCGTGGTGGCAGGTG	6596
rs370277058	snp	C/T	0.00318978	0.0398085	intron-variant	HLTF	GRCh38.p7	3:149032684	AAAGGCCATTCTGGC[C/T]GGGCACGGTGGCTCA	6596
rs370282686	snp	A/G			intron-variant	HLTF	GRCh38.p7	3:149065320	ATATATAATAGTACA[A/G]GTCCCAGAGTGTCCT	6596
rs370314679	snp	A/T			intron-variant	HLTF	GRCh38.p7	3:149033987	GATTTCAAGTCAGAC[A/T]GTATCAGGGAGTCCT	6596
rs370321290	snp	G/T			intron-variant	HLTF	GRCh38.p7	3:149083228	TGCACTCCAGCCTGG[G/T]CAATGCAAGCAAGAC	6596
rs370376213	snp	A/G	0.000151437	0.00870033	intron-variant	HLTF	GRCh38.p7	3:149068221	GGTTTCACATAAAGC[A/G]CACTTACTACTACTT	6596
rs370406256	snp	C/T	0.000399281	0.0141238	intron-variant	HLTF	GRCh38.p7	3:149065288	TTTCTCTAGAATTTG[C/T]AGGGCAAATAACTCT	6596
rs370415771	snp	A/T	3.29614e-05	0.00405951	missense	HLTF	GRCh38.p7	3:149041544	AAATACATGTGCACA[A/T]TGTGTTATCACAGGA	6596
rs370435111	snp	A/T			intron-variant	HLTF	GRCh38.p7	3:149059621	GTCTCTATTTTCTAA[A/T]CTTCTTGTAATATGG	6596
rs370529938	snp	A/T	3.30104e-05	0.00406252	intron-variant	HLTF	GRCh38.p7	3:149060761	ACACATTATCAAATC[A/T]AATCTATTACATGTT	6596
rs370532985	snp	A/G	0.000153988	0.00877327	intron-variant	HLTF	GRCh38.p7	3:149050409	TATTTTTAACAATGA[A/G]CAGATTTGTGTCAGA	6596

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