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

HCK

SNP - dbSNP
dbSNP	Type	Alleles	Het	Se(het)	Fxn-class	Gene Name	Assembly	Chr-pos	Sequence	Entrez Gene
rs173355	snp	C/T	0.363985	0.222503	intron-variant	HCK	GRCh38.p7	20:32078334	acaggtgtgagccac[C/T]gcgcccagccGGGGG	3055
rs242598	snp	C/T	0.499984	0.00279548	intron-variant	HCK	GRCh38.p7	20:32076386	GGGGGCTCTTAGCTG[C/T]TTCTCTCTCCTTCTT	3055
rs242599	snp	A/G	0.306431	0.243548	intron-variant	HCK	GRCh38.p7	20:32076571	AAAACGCAGGGTGTA[A/G]ACAACATGAATGGGG	3055
rs242600	snp	A/G	0.405603	0.195673	intron-variant	HCK	GRCh38.p7	20:32077760	CGAACTCCTGAACTC[A/G]TGATCCTCCTGCCTT	3055
rs242601	snp	G/T	0.491834	0.0633738	intron-variant	HCK	GRCh38.p7	20:32078031	CAGTTGGTttttttt[G/T]tttgtttgtttgttt	3055
rs242602	snp	C/T	0.496034	0.0443518	intron-variant	HCK	GRCh38.p7	20:32079145	CCAAATATCTCAATA[C/T]TCAGGAAGAATGAAG	3055
rs242603	snp	C/T	0.499831	0.00918375	intron-variant	HCK	GRCh38.p7	20:32079256	ATTCAACTCCATATA[C/T]GCGGAGGAGGATTGG	3055
rs242604	snp	C/T	0.499839	0.00898417	intron-variant	HCK	GRCh38.p7	20:32080448	gcgatccacccctct[C/T]gccctcccaaagtgc	3055
rs242605	snp	C/G	0.318415	0.240457	intron-variant	HCK	GRCh38.p7	20:32080741	ggcctcgaacttctg[C/G]actcaagcaatctgc	3055
rs242606	snp	A/G	0.499913	0.00658888	intron-variant	HCK	GRCh38.p7	20:32080830	TTTTTTTAAATACCC[A/G]TAACAGACCAAGTAG	3055
rs242607	snp	C/T	0.36928	0.219709	intron-variant	HCK	GRCh38.p7	20:32084072	CAGGGGTGACATCCC[C/T]ACCACGATGGGCCCA	3055
rs242608	snp	C/T	0.392881	0.205147	intron-variant	HCK	GRCh38.p7	20:32085033	AACTTAAGAACAACA[C/T]TGCCTGCTTTGCAGG	3055
rs242609	snp	C/T	0.299158	0.245119	intron-variant	HCK	GRCh38.p7	20:32085621	AAATATCATATAAGA[C/T]GCTAGACTCCTACTA	3055
rs242610	snp	C/T	0.4628	0.13121	intron-variant	HCK	GRCh38.p7	20:32085889	gtggacgaggctggg[C/T]catgtagggcctggg	3055
rs242611	snp	A/G	0.499693	0.0123764	intron-variant	HCK	GRCh38.p7	20:32086175	caggcgcccacaact[A/G]cgcctggctaatttt	3055
rs242612	snp	A/T	0.493827	0.0552116	intron-variant	HCK	GRCh38.p7	20:32087646	taatttctaaaaaaa[A/T]tttttttttttttga	3055
rs242613	snp	A/G	0.499866	0.0081858	intron-variant	HCK	GRCh38.p7	20:32087728	ctcaatgcaagctcc[A/G]cctaccaggttcacg	3055
rs242614	snp	A/G	0.302936	0.244331	intron-variant	HCK	GRCh38.p7	20:32087873	ggtctcaatctcctg[A/G]ccttgtgatccgccc	3055
rs242615	snp	C/G	0.499908	0.00678851	intron-variant	HCK	GRCh38.p7	20:32088011	aactcctgggttcaa[C/G]tgatcctcccaaagc	3055
rs381619	snp	C/T	0.274929	0.248754	intron-variant	HCK	GRCh38.p7	20:32076080	gtaatcccagcactt[C/T]gggaggccaaggcac	3055
rs442268	snp	A/T	0.391954	0.205789	intron-variant	HCK	GRCh38.p7	20:32076078	ctgtaatcccagcac[A/T]tcgggaggccaaggc	3055
rs885495	snp	C/T	0.5	0	intron-variant	HCK	GRCh38.p7	20:32059297	TCCTTCCTTCCTTCC[C/T]TCCCTCCCTCCTTTC	3055
rs910185	snp	A/G	0.0856613	0.188395	intron-variant	HCK	GRCh38.p7	20:32086815	GGCCAAAGGTGCTGC[A/G]TGCTGGGGCTGGGGG	3055
rs926687	snp	G/T	0.499713	0.0119774	intron-variant	HCK	GRCh38.p7	20:32092422	GGTTCATCTTCAACC[G/T]CTTTTGTCCAAACCC	3055
rs926688	snp	G/T	0.499703	0.0121769	intron-variant	HCK	GRCh38.p7	20:32092535	CCACGCAGTCTGTTA[G/T]TCACTCAGCAGCCAT	3055
rs980367	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32093508	gtgtgtgtgtgtgtg[G/T]gtgtgtgtgtgtgtg	3055
rs980368	snp	A/G	0.499928	0.00598999	intron-variant	HCK	GRCh38.p7	20:32093740	GCCCTCCCGACACAA[A/G]AGGGAGGGCTGGTGC	3055
rs1004910	snp	A/C	0.205417	0.245993	upstream-variant-2KB	HCK	GRCh38.p7	20:32051627	CCCAGGGGTCTATAC[A/C]GCCGGTCCAAAGATT	3055
rs1883882	snp	C/T	0.00676609	0.0577691	intron-variant	HCK	GRCh38.p7	20:32082498	AATACAAAAATTAGC[C/T]GGGCGTAGTGGCGGG	3055
rs1987960	snp	C/T	0.0134861	0.0810011	intron-variant	HCK	GRCh38.p7	20:32062031	tgcaacctctgactc[C/T]ggggttcaagcgatt	3055
rs2001413	snp	C/G	0.334147	0.239924	intron-variant	HCK	GRCh38.p7	20:32061199	GTCAGGAGTTCAAGA[C/G]CAGCCTGGCCAACAT	3055
rs2223785	snp	C/T	0.122064	0.214785	intron-variant	HCK	GRCh38.p7	20:32088513	CAAAAGTAATTGTGG[C/T]TTTTGCCATTAAATA	3055
rs2227967	snp	C/T	0.00186575	0.030486	synonymous-codon	HCK	GRCh38.p7	20:32073771	CGAGGCCATTCACCA[C/T]GAAGACCTCAGCTTC	3055
rs2269052	snp	A/G	0.117188	0.211804	intron-variant	HCK	GRCh38.p7	20:32091179	CATCCCTGCCCCATC[A/G]AGCTCCTGTGAAAAT	3055
rs2297303	snp	A/T	0.0652144	0.168387	intron-variant	HCK	GRCh38.p7	20:32073449	GAGGCATAAATCCCA[A/T]ACAGTCAAACCCCTG	3055
rs2297304	snp	A/G	0.455144	0.142885	intron-variant	HCK	GRCh38.p7	20:32073494	AATTTCCTCTGAAGT[A/G]CTTTGCGCAGGCTAT	3055
rs2297305	snp	A/G	0.222035	0.248431	intron-variant	HCK	GRCh38.p7	20:32073501	TCTGAAGTGCTTTGC[A/G]CAGGCTATTGTGTTT	3055
rs3073296	in-del	-/CTTT/TT	0	0	intron-variant	HCK	GRCh38.p7	20:32059420	TCTCTTTCTTTCTTT[-/CTTT/TT]TTTCTTTCTTTCTTT	3055
rs3073297	in-del	-/GT			intron-variant	HCK	GRCh38.p7	20:32093491	AGTATCCTAGGGTTC[-/GT]GTGTGTGTGTGTGTG	3055
rs3746601	snp	A/C	0.499885	0.00758699	intron-variant	HCK	GRCh38.p7	20:32075002	CTTTGGTTGGTTACA[A/C]GTGCATTCTCTGCCT	3055
rs3746602	snp	A/G	0.495407	0.0477027	intron-variant	HCK	GRCh38.p7	20:32075034	CCCTGCAAGGAAGAG[A/G]GCTGGTGAGAGCGGG	3055
rs3746603	snp	A/G	0.0617873	0.164548	intron-variant	HCK	GRCh38.p7	20:32079887	CTAAAGGTGACACCA[A/G]CCCTCCCCACCTTGT	3055
rs3787366	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32062683	AAAGTTTTGAGCTCT[A/G]TGAGAAAGAAGCTGA	3055
rs3787367	snp	A/G	0.332337	0.236052	intron-variant	HCK	GRCh38.p7	20:32064574	gttgagacttgccta[A/G]catcacacaatgagc	3055
rs3833316	in-del	-/A	0.146314	0.227484	intron-variant	HCK	GRCh38.p7	20:32058231	TCAGTTCCCAAATCC[-/A]AAAAAAAAATGGAAC	3055
rs3833317	in-del	-/G	0.112983	0.209108	intron-variant	HCK	GRCh38.p7	20:32098879	GGAGGCCACGTATCA[-/G]GGAAATTGCAGGTCT	3055
rs3838038	in-del	-/TAAAAAAAA			intron-variant	HCK	GRCh38.p7	20:32072563	GAGACCCTGTCTCTT[-/TAAAAAAAA]AAAAAAAAAAAAAAA	3055
rs4359727	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32054716	GAGGCTGAGGCAGGA[A/G]AATGGCGTGAACCCT	3055
rs4911541	snp	C/T	0.489608	0.0713316	intron-variant	HCK	GRCh38.p7	20:32060775	agactcccatagcat[C/T]aaatgtgcaagaaat	3055
rs4911542	snp	C/T	0.484421	0.0868729	intron-variant	HCK	GRCh38.p7	20:32061022	agagtcttgctctgt[C/T]gcccaggctggagtg	3055
rs5841096	in-del	-/A	0.499527	0.0153681	intron-variant	HCK	GRCh38.p7	20:32091810	GACCTCTTCTCTATT[-/A]AAAAAAAAAAAAATT	3055
rs5841098	in-del	-/T	0.491421	0.0649309	intron-variant	HCK	GRCh38.p7	20:32099903	TGTCCTTTCTCCACC[-/T]TTTTTTTTTTTTTTA	3055
rs6058519	snp	A/C			upstream-variant-2KB	HCK	GRCh38.p7	20:32050638	gtctgatcttggaag[A/C]taagcaggatcaagc	3055
rs6058520	snp	C/T	0.00953873	0.0683987	intron-variant	HCK	GRCh38.p7	20:32054898	ATTTGCCCCATCTTA[C/T]CATTAAGTTGTCAAA	3055
rs6058522	snp	C/T	0.318656	0.240388	intron-variant	HCK	GRCh38.p7	20:32058156	GACcccgagtctgag[C/T]gccagctctgccaaa	3055
rs6058523	snp	A/G	0.301177	0.244706	intron-variant	HCK	GRCh38.p7	20:32062500	GGCATCTCAGAGCCA[A/G]CCCTATGGCTCAGCC	3055
rs6058524	snp	C/T	0	0	synonymous-codon	HCK	GRCh38.p7	20:32084006	ATCCCCCCGAAGCAC[C/T]TTCAGCACTCTGCAG	3055
rs6058525	snp	A/G	0	0	intron-variant	HCK	GRCh38.p7	20:32094751	AGAAAGAAAGAAAGA[A/G]AGAAAGAAAGAAGGA	3055
rs6061134	snp	C/G	0.5	0	intron-variant	HCK	GRCh38.p7	20:32052792	CTTCTTGGGGGGGGG[C/G]GGGGatttttttttt	3055
rs6061135	snp	G/T	0	0	intron-variant	HCK	GRCh38.p7	20:32054625	TCCTGGCTAACACGG[G/T]GAAACCCCGTCTCTA	3055
rs6061136	snp	G/T	0.15665	0.231917	intron-variant	HCK	GRCh38.p7	20:32056662	gtttatattttatta[G/T]tattattattaccat	3055
rs6061137	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32057308	CTTTTTTATAGAAAA[A/G]GAACATGAAGggctg	3055
rs6061138	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32057391	gatcatctgagctca[A/G]gagttcgagaccagc	3055
rs6061139	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32057503	tactcaggaggctga[A/G]gtgggaggatcgtct	3055
rs6061140	snp	A/G	0	0	intron-variant	HCK	GRCh38.p7	20:32057535	agcacagaaggtgaa[A/G]gttgcagtgatctga	3055
rs6061141	snp	C/T	0	0	intron-variant	HCK	GRCh38.p7	20:32057993	CTAGGACGTGCGCTC[C/T]TGACTCTCCCTTCGA	3055
rs6061142	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32058386	aaaatgcaaaaatta[G/T]ccgggcgtggtggcg	3055
rs6061143	snp	C/T	0.0452528	0.143452	intron-variant	HCK	GRCh38.p7	20:32059584	gcagtgatgctatca[C/T]ggctcatgcagcccc	3055
rs6061144	snp	A/G	0.00477324	0.0486193	intron-variant	HCK	GRCh38.p7	20:32060120	AAACTTCCACTCAGC[A/G]GCAGCCAAGGAAAGA	3055
rs6061145	snp	A/G	0	0	intron-variant	HCK	GRCh38.p7	20:32063918	TGCCTTGCTGCTGCA[A/G]GCCTTTTTTTCCAGC	3055
rs6061146	snp	A/G	0	0	intron-variant	HCK	GRCh38.p7	20:32065835	agtgggagaaagctg[A/G]ttctccaaaggaaaa	3055
rs6061147	snp	G/T	0	0	intron-variant	HCK	GRCh38.p7	20:32066330	TTTTTTTTTTTTTTT[G/T]TGACAGAGTCTTGCT	3055
rs6061148	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32066331	TTTTTTTTTTTTTTT[A/T]GACAGAGTCTTGCTC	3055
rs6061151	snp	A/G	0	0	intron-variant	HCK	GRCh38.p7	20:32071533	TGCATGGAGCTGGCA[A/G]GGGAGTTAAGACCGG	3055
rs6061152	snp	C/T	0.292523	0.246357	intron-variant	HCK	GRCh38.p7	20:32072818	GACCGAAGGCCGAGG[C/T]CACAGCTCAAGAAAC	3055
rs6061153	snp	G/T	0.5	0	intron-variant	HCK	GRCh38.p7	20:32074444	GCACAGCAGGAACTG[G/T]TGTAAGGATCCCTAC	3055
rs6061154	snp	C/G	0.311859	0.242226	intron-variant	HCK	GRCh38.p7	20:32074471	CTACCCTAATCATGG[C/G]CACATGCTGGGGCTG	3055
rs6061156	snp	C/T	0	0	synonymous-codon	HCK	GRCh38.p7	20:32086632	TCCCCCTCCAGCCAC[C/T]TACAACAAGCACACC	3055
rs6087815	snp	A/G	0.396694	0.202437	intron-variant	HCK	GRCh38.p7	20:32078880	AAAAAAAAAAAAAAA[A/G]GGGGGGAATGATAAA	3055
rs6087816	snp	A/G	0.220843	0.248294	intron-variant	HCK	GRCh38.p7	20:32101041	agagatgaagggtgc[A/G]ttctccaaagactct	3055
rs6089157	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32059513	tctctctctctctct[C/T]ttttttttctttttc	3055
rs6089158	snp	A/T	0.235854	0.249599	intron-variant	HCK	GRCh38.p7	20:32063767	GGGCAAGACTCTTTG[A/T]TGTTTAAAGGGAAAT	3055
rs6089159	snp	G/T	0.360632	0.224189	intron-variant	HCK	GRCh38.p7	20:32064035	TTGAGATAGAGTCTC[G/T]CTCTGTCACCCAGGC	3055
rs6089160	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32066031	cccctgtgaggttga[A/G]gctgctggttctcac	3055
rs6089161	snp	A/G	0	0	intron-variant	HCK	GRCh38.p7	20:32066108	ACCACTTTGTCACAA[A/G]GCACTCTGCAGAGAG	3055
rs6089162	snp	C/G	0	0	intron-variant	HCK	GRCh38.p7	20:32066148	TACATAAACCTCTTT[C/G]TTCCACCATTCTCTC	3055
rs6089163	snp	C/T	0.384976	0.210431	intron-variant	HCK	GRCh38.p7	20:32068260	tggagatggcaccac[C/T]gtactccagcctggg	3055
rs6089164	snp	A/G	0.332337	0.236052	intron-variant	HCK	GRCh38.p7	20:32069816	CATCTAAGCCTAGGA[A/G]TTTGGGGTTTTTTTC	3055
rs6089165	snp	C/T	1.64846e-05	0.0028709	missense	HCK	GRCh38.p7	20:32071718	ATACATTCTCAAAAA[C/T]TGAAACCAGCGCCAG	3055
rs6089166	snp	G/T	0.010341	0.0711587	missense	HCK	GRCh38.p7	20:32073782	ACCACGAAGACCTCA[G/T]CTTCCAGAAGGGGGA	3055
rs6089167	snp	G/T	0	0	intron-variant	HCK	GRCh38.p7	20:32075080	tgcatcctcggcaca[G/T]gctggcatgcagtca	3055
rs6089168	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32076273	agaggttgcagtgag[C/T]tgaaatatcatgcca	3055
rs6089170	snp	C/T	0.499853	0.008585	intron-variant	HCK	GRCh38.p7	20:32089405	GTTAAGTGGCTTGCA[C/T]AAGTTACTGTGCTAA	3055
rs6089171	snp	C/T	0.282632	0.247861	intron-variant	HCK	GRCh38.p7	20:32094968	GATGCCACTTGGTTT[C/T]GTTTTTGTGAAATTC	3055
rs6089174	snp	A/T	0.499703	0.0121769	intron-variant	HCK	GRCh38.p7	20:32096985	acgttataactcgat[A/T]aaaaaaAATTTAgac	3055
rs6089175	snp	A/T	0.499703	0.0121769	intron-variant	HCK	GRCh38.p7	20:32097026	ggctcatgactataa[A/T]cctagcactttggga	3055
rs6089177	snp	C/T	0.0912534	0.193131	intron-variant	HCK	GRCh38.p7	20:32100937	TCAGCAACTCAGCAG[C/T]TGTCAGGACTCTGGG	3055
rs6119756	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32059419	CTTCTTTCTCTCTCT[C/T]TCTTTCTTTCTTTTT	3055
rs6119757	snp	C/T	0.0107246	0.0724382	intron-variant	HCK	GRCh38.p7	20:32061453	gcacagcagctgagc[C/T]gctgatcaatttctc	3055
rs6119758	snp	A/G	0.290718	0.246662	intron-variant	HCK	GRCh38.p7	20:32061858	ttacccaccttggag[A/G]ggacttgggctttta	3055
rs6119760	snp	C/T	0	0	intron-variant	HCK	GRCh38.p7	20:32077207	GAGCACAACTGGGAC[C/T]TTGGGAATCAGGGCG	3055
rs6119761	snp	C/T	0.223522	0.248594	intron-variant	HCK	GRCh38.p7	20:32077833	ccggACAcctccttc[C/T]tttttataccacagg	3055
rs6119762	snp	C/T	0	0	intron-variant	HCK	GRCh38.p7	20:32092652	ccctcctctcctgac[C/T]tacaaggcagttcat	3055
rs6121325	snp	G/T	0.157311	0.232183	intron-variant	HCK	GRCh38.p7	20:32053536	ccagctactcgggag[G/T]ctgaggcacgagaat	3055
rs6121326	snp	G/T	0.165289	0.235211	intron-variant	HCK	GRCh38.p7	20:32054537	AAAGCCCGGACGCGG[G/T]GGCTCACGCCTGTAA	3055
rs6121327	snp	A/G	0.102014	0.201495	intron-variant	HCK	GRCh38.p7	20:32055712	tatgatttttaaagc[A/G]aacaattcagtggta	3055
rs6121328	snp	C/T	0.14933	0.228835	intron-variant	HCK	GRCh38.p7	20:32055792	AACATTTCCATCACC[C/T]CTGAAAAAGGAAACT	3055
rs6121329	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32059409	tccttcctttcttct[C/T]tctctctctctcttt	3055
rs6121330	snp	C/T	0.255782	0.249933	intron-variant	HCK	GRCh38.p7	20:32061727	gcaatgccccagagg[C/T]ataagcacagttggt	3055
rs6121331	snp	C/G	0.24134	0.24985	intron-variant	HCK	GRCh38.p7	20:32062299	GCAGATTCAAACCCA[C/G]CTCTATCTGACTTCA	3055
rs6121334	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32075367	cccagctaatttttt[C/T]cttttttgtattttt	3055
rs6121335	snp	C/T	0.272241	0.249009	intron-variant	HCK	GRCh38.p7	20:32082793	GAGCTGAAAGACTTA[C/T]GTGTTTCTGCTCTAT	3055
rs6121336	snp	C/T	0	0	intron-variant	HCK	GRCh38.p7	20:32084126	TGTGGCCCCTGAGAC[C/T]TGCTGTGTCCTTCTT	3055
rs6121337	snp	C/T	0.499703	0.0121769	intron-variant	HCK	GRCh38.p7	20:32094196	AGTCTCACTCAGAGA[C/T]TTTGAGGAGATTTTA	3055
rs6121338	snp	A/G	0.494484	0.0522255	intron-variant	HCK	GRCh38.p7	20:32098429	tgaggtcaggagttc[A/G]aggcttcagtgaact	3055
rs6142598	snp	A/G	0	0	intron-variant	HCK	GRCh38.p7	20:32053758	GGCCCCGTgttctca[A/G]actttagcctacatc	3055
rs6142599	snp	A/G	0	0	intron-variant	HCK	GRCh38.p7	20:32053822	ctgggccgaatccta[A/G]agtttctgattcagt	3055
rs6142601	snp	A/C	0.00398564	0.0444627	intron-variant	HCK	GRCh38.p7	20:32057439	accctgtctctacaa[A/C]aagtacaaaaattag	3055
rs6142602	snp	A/G	0	0	intron-variant	HCK	GRCh38.p7	20:32061620	TTGCCAGGGTGATGA[A/G]GGAAGGTTGCTCTGA	3055
rs6142603	snp	C/T	0	0	intron-variant	HCK	GRCh38.p7	20:32072012	GCTTGGCCCCTCAGC[C/T]TGAGCTCCACCAAAC	3055
rs6142604	snp	A/G	0	0	intron-variant	HCK	GRCh38.p7	20:32072783	GGGAGGGGTCAAGCA[A/G]CATCCCCCGGTACAT	3055
rs6142605	snp	C/G	0	0	intron-variant	HCK	GRCh38.p7	20:32083841	AGAGTGCTAATGCAA[C/G]GTGGCAGGCCTCCAA	3055
rs6142606	snp	G/T	0	0	intron-variant	HCK	GRCh38.p7	20:32087107	TCACAGTGAGCCTTA[G/T]AGGCCAGGGTGTGGC	3055
rs6142607	snp	A/G	0.0115144	0.0749975	intron-variant	HCK	GRCh38.p7	20:32094768	gaaagaaagaaggaa[A/G]gaaagaaagagagag	3055
rs6579320	snp	C/T	0.212425	0.24716	intron-variant	HCK	GRCh38.p7	20:32061271	acaggcgtgagccac[C/T]gcgcccagctgccgt	3055
rs6579321	snp	A/T	0.0372196	0.131242	intron-variant	HCK	GRCh38.p7	20:32068326	aagtaaatgaaaatt[A/T]aaaaaaaataaaaac	3055
rs7260985	snp	C/T	0.0345262	0.126772	intron-variant	HCK	GRCh38.p7	20:32093482	GCTCTTCATAGTATC[C/T]TAGGGTTCGTGTGTG	3055
rs7263906	snp	A/G	0.0189856	0.0955633	intron-variant	HCK	GRCh38.p7	20:32056184	tcaattcctttgggt[A/G]tatacctgaagtaga	3055
rs7264792	snp	C/G/T			intron-variant	HCK	GRCh38.p7	20:32070884	ggaagaggaagaaga[C/G/T]gaagaaagaggagga	3055
rs7264938	snp	A/G	0.00902341	0.0665604	intron-variant	HCK	GRCh38.p7	20:32073408	ATGTGTCCTGCAGAG[A/G]ACTCCGCTAGGTTCT	3055
rs7265833	snp	A/G	0.0456336	0.143994	intron-variant	HCK	GRCh38.p7	20:32061763	gaagaagagcaagga[A/G]ggctccagtggaatg	3055
rs7266178	snp	A/G	0.16028	0.233346	intron-variant	HCK	GRCh38.p7	20:32057679	gcaagttagtagcaC[A/G]ATCTCTCTCAGCCTC	3055
rs7267655	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32070878	ggaagaggaagagga[A/G]gaagacgaagaaaga	3055
rs7268039	snp	A/G	0.00478085	0.0486577	intron-variant	HCK	GRCh38.p7	20:32062855	CCAAGGCACTGCTCA[A/G]GGAATTGGCTCCTGT	3055
rs7269735	snp	C/T	0.0524604	0.153226	intron-variant	HCK	GRCh38.p7	20:32065213	attctgctACATTGG[C/T]GGATCTCAAATTTTA	3055
rs7270725	snp	C/T	0	0	intron-variant	HCK	GRCh38.p7	20:32073466	CAGTCAAACCCCTGT[C/T]GAGAATCCCCAAAAT	3055
rs7275160	snp	C/G	0.0418186	0.138422	intron-variant	HCK	GRCh38.p7	20:32068754	tgagacctgcccccc[C/G]tctctgccccctgtc	3055
rs7347740	snp	A/G	0	0	intron-variant	HCK	GRCh38.p7	20:32090311	TCTGTCCAGAAGCAG[A/G]GGTAGATTCAGAGCC	3055
rs7354349	snp	A/G	0.231775	0.249335	intron-variant	HCK	GRCh38.p7	20:32070774	cttctcttcttcacA[A/G]TTTAGAAAAGTGCCC	3055
rs7354524	snp	G/T	0	0	intron-variant	HCK	GRCh38.p7	20:32060728	TACTTAACTTCAGCA[G/T]ACCCTGAGAtagttc	3055
rs7509404	snp	C/T	0.20111	0.245173	intron-variant	HCK	GRCh38.p7	20:32059518	ctctctctctttttt[C/T]tttctttttcttttt	3055
rs8114692	snp	G/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32061464	gagccgctgatcaat[G/T]tctccagtcgtactc	3055
rs8121958	snp	C/G	0	0	intron-variant	HCK	GRCh38.p7	20:32086453	ggaagtggtgaaccc[C/G]cctttcaacccacag	3055
rs8122892	snp	G/T	0.0352966	0.128072	intron-variant	HCK	GRCh38.p7	20:32101120	cccatcagctcccat[G/T]ggcccaaactgggtc	3055
rs9679931	snp	A/G	0.0444908	0.142359	intron-variant	HCK	GRCh38.p7	20:32097905	AACTATgccaggtgc[A/G]gtggctcacacctat	3055
rs10557922	in-del	-/TTT			intron-variant	HCK	GRCh38.p7	20:32059519	TCTCTCTCTTTTTTT[-/TTT]CTTTTTCTTTTTGAG	3055
rs10599801	in-del	-/ATC	0.211819	0.247067	intron-variant	HCK	GRCh38.p7	20:32089311	ACAGAGTAGGTAATT[-/ATC]ATCCCATTTTACAGA	3055
rs10719271	in-del	-/T	0.155325	0.23138	intron-variant	HCK	GRCh38.p7	20:32068390	GTAAAATGAAAATAA[-/T]TTTTTTTTAAAAAAG	3055
rs11167298	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32093491	AGTATCCTAGGGTTC[C/G]tgtgtgtgtgtgtgt	3055
rs11267532	in-del	-/GGAAGAAGAAAGGAA	0	0	intron-variant	HCK	GRCh38.p7	20:32060909	GAAGGAAGAAAGGAA[-/GGAAGAAGAAAGGAA]TAAAAGGAGGACGTG	3055
rs11269818	in-del	-/GAAGAAAGGAAGGAA			intron-variant	HCK	GRCh38.p7	20:32060898	AAAAAGAAAAGGAAG[-/GAAGAAAGGAAGGAA]GAAGAAAGGAATAAA	3055
rs11272727	in-del	-/CTTC/CTTCCTTC/CTTCCTTCCTTC/CTTCCTTCCTTCCTTC	0.405603	0.195673	intron-variant	HCK	GRCh38.p7	20:32059279	CTGTAATGTTTTAAT[lengthTooLong]CTTCCTTCCTTCCTT	3055
rs11472244	in-del	-/A/AA/AAG/AG	0	0	intron-variant	HCK	GRCh38.p7	20:32058544	CAAAAAAAAAAAAAA[-/A/AA/AAG/AG]GGGGGAGAACTGAGG	3055
rs11480270	in-del	-/AA			intron-variant	HCK	GRCh38.p7	20:32058543	AGCAAGACTCTGTCA[-/AA]AAAAAAAAAAAAAGG	3055
rs11480322	in-del	-/A			downstream-variant-500B	HCK	GRCh38.p7	20:32102122	AAAAAAAAAAAAAAA[-/A]GATGAAGAAGAAGAA	3055
rs11482239	in-del	-/T/TT/TTTTT	0.499424	0.0169631	intron-variant	HCK	GRCh38.p7	20:32067531	CCTGATGCTTTTACT[-/T/TT/TTTTT]TTTTTTTTTTTTTTT	3055
rs11696958	snp	C/T	0.00470586	0.0482782	intron-variant	HCK	GRCh38.p7	20:32067812	GTCATAGCtgagatg[C/T]gctctaacagtaaaa	3055
rs11697159	snp	A/C	0.030665	0.119967	intron-variant	HCK	GRCh38.p7	20:32093651	CTAGAGAATCCCCCA[A/C]ACTGGCCCAGGCCTC	3055
rs11697528	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32058365	ggtgaaaccccgtct[C/T]tactaaaaatgcaaa	3055
rs11699670	snp	A/G	0.00763348	0.0613063	intron-variant	HCK	GRCh38.p7	20:32052622	CGGAACGTCGGGGGA[A/G]CCGCGGGTAGCCCGG	3055
rs11906504	snp	C/G	0	0	intron-variant	HCK	GRCh38.p7	20:32089246	cagtgtgggagggga[C/G]tgaccaaggacacaa	3055
rs12329552	snp	C/G	0	0	intron-variant	HCK	GRCh38.p7	20:32093485	CTTCATAGTATCCTA[C/G]GGTTCgtgtgtgtgt	3055
rs12481708	snp	C/T	0.0854556	0.188216	intron-variant	HCK	GRCh38.p7	20:32098620	CCTCCCTTTTCCCAT[C/T]GCCCAGGATGAGAGG	3055
rs13038345	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32096424	atcatttgaacccgg[C/G]aggcagaggttgcag	3055
rs13043040	snp	G/T			upstream-variant-2KB	HCK	GRCh38.p7	20:32052005	GTGGAGCGGAAGGGA[G/T]GGGGGTTCGCATCCT	3055
rs17093775	snp	A/G	0.0119091	0.0762411	upstream-variant-2KB	HCK	GRCh38.p7	20:32051561	ATCTTTGAAGACTGT[A/G]GCAGGAATCCCTTGA	3055
rs17093784	snp	A/G			upstream-variant-2KB	HCK	GRCh38.p7	20:32051693	GCAGGAGCAGGAGCG[A/G]TATTGGAACCCTGGG	3055
rs17093788	snp	A/G	0.0834294	0.189812	intron-variant	HCK	GRCh38.p7	20:32062769	GGACAGTAGTCACTC[A/G]GGGATAAAGACAGTT	3055
rs17093790	snp	C/G	0.0360663	0.129354	intron-variant	HCK	GRCh38.p7	20:32063723	CTTGAGTGCAAATCA[C/G]AATCCCTTATAAGAA	3055
rs17093799	snp	A/T	0.0139853	0.0824443	intron-variant	HCK	GRCh38.p7	20:32066875	CTTTTTGAGTCTTGC[A/T]GTGCTCTGTGTATGG	3055
rs17093805	snp	A/G	0.0248432	0.108648	intron-variant	HCK	GRCh38.p7	20:32069320	ATGTACATTGATCAC[A/G]TAAGTGAAGCATACA	3055
rs17093809	snp	C/T	0.0341408	0.126114	intron-variant	HCK	GRCh38.p7	20:32074116	TGGACCAGGCCCCAT[C/T]GAGTCGACCTTGCAT	3055
rs17093810	snp	C/T	0.0926964	0.194308	intron-variant	HCK	GRCh38.p7	20:32075623	GAGCTCTCCATAACC[C/T]ATCGTTCTTGGCTGT	3055
rs17093812	snp	C/G	0.0341408	0.126114	intron-variant	HCK	GRCh38.p7	20:32081300	TTCTGTGCTGCAAGG[C/G]TGGATTCATGCTGAT	3055
rs17093823	snp	A/G	0.0916144	0.193427	intron-variant	HCK	GRCh38.p7	20:32088973	GTGGTTCTTCTGCTC[A/G]TCATGGTAAAGTGAG	3055
rs17093827	snp	A/G	0.0748431	0.178382	intron-variant	HCK	GRCh38.p7	20:32093292	TGCAGGGGCTTTGCC[A/G]GGCTCATCACCTGTT	3055
rs17093828	snp	A/C/G	0.000153988	0.00877328	missense	HCK	GRCh38.p7	20:32101443	GTCCGGAGGAGCGGC[A/C/G]GACCTTCGAATACAT	3055
rs17259459	snp	C/T	0.28578	0.247426	intron-variant	HCK	GRCh38.p7	20:32090749	TGCTTACACCTGGGC[C/T]CAATAAACCTACTCG	3055
rs17379736	snp	C/G	0.0333695	0.124785	intron-variant	HCK	GRCh38.p7	20:32059984	CCTGTGTTACTGAGG[C/G]TTTGAGGATTCCATT	3055
rs28712323	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32068335	AAAATTAAAAAAAAA[A/T]AAAAACTAAAAATAA	3055
rs34007778	in-del	-/T			intron-variant	HCK	GRCh38.p7	20:32099482	CTGCCTCAGCCTCCT[-/T]GAGTAACTGGGATTA	3055
rs34022054	in-del	-/G			intron-variant	HCK	GRCh38.p7	20:32081808	AGCTTTTGGCTTGGG[-/G]CTGGTCCATCCTGCA	3055
rs34099113	in-del	-/G			intron-variant	HCK	GRCh38.p7	20:32097353	GGAGGCTGAGGTGGG[-/G]AGGATCACGAGGTCA	3055
rs34143132	in-del	-/C			intron-variant	HCK	GRCh38.p7	20:32056241	TCTGTGGCCGGGTGC[-/C]GGTGGCTCACGCCTG	3055
rs34188764	in-del	-/G			intron-variant	HCK	GRCh38.p7	20:32068921	GCACTCCAGCCTGGG[-/G]TGACAGAGCGAGACT	3055
rs34422885	in-del	-/G			intron-variant	HCK	GRCh38.p7	20:32067690	GCACTGAGGAACGCA[-/G]GGTGTGAGCACCAGC	3055
rs34436416	snp	A/G	0.027392	0.113779	synonymous-codon	HCK	GRCh38.p7	20:32086785	CATGAACTCCGTGAT[A/G]ATGTAGATGGGCTCC	3055
rs34507358	in-del	-/T	0.181659	0.240478	intron-variant	HCK	GRCh38.p7	20:32053998	TTCTCTTTATGGTCC[-/T]TTTTTTTTTAGGGGA	3055
rs34513177	snp	A/G	0.0213812	0.10116	synonymous-codon	HCK	GRCh38.p7	20:32073327	GTTGCTGTTGTGGCT[A/G]TTAGGCCCCTGTGGG	3055
rs34711233	in-del	-/G			intron-variant	HCK	GRCh38.p7	20:32095618	CAGCTGGTGGTGGGG[-/G]AGTTGGGAGAAATGA	3055
rs34774796	snp	A/G	0.0492801	0.149035	synonymous-codon	HCK	GRCh38.p7	20:32071734	CACAGGACAGTGTGG[A/G]CTGGCGCTGGTTTCA	3055
rs34881114	in-del	-/G			intron-variant	HCK	GRCh38.p7	20:32100476	GGAGGTGAGAGAGAG[-/G]AGAATAAAGGATGAT	3055
rs35088805	snp	C/G	0.5	0	intron-variant	HCK	GRCh38.p7	20:32078882	AAAAAAAAAAAAAGG[C/G]GGGGAATGATAAAGG	3055
rs35091816	in-del	-/A			intron-variant	HCK	GRCh38.p7	20:32081123	CCCATTACAATAGAT[-/A]CTTATCCACAAGCCT	3055
rs35228115	in-del	-/G			intron-variant	HCK	GRCh38.p7	20:32088958	CTGGGTTCAGCTGGG[-/G]TGGTTCTTCTGCTCG	3055
rs35263404	in-del	-/C			intron-variant	HCK	GRCh38.p7	20:32094555	ATGGTGGCACATGCC[-/C]TGTATGCCTGTAGTT	3055
rs35305942	snp	A/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32068000	ATGTAAAAATTTTTT[A/T]AAAAATGAAAAATAG	3055
rs35315557	in-del	-/G			intron-variant	HCK	GRCh38.p7	20:32081341	ATGGCAAGAACAGGC[-/G]CTGGAAAACATCGCG	3055
rs35316298	in-del	-/C			intron-variant	HCK	GRCh38.p7	20:32100430	CTGGTGCTACGTTTC[-/C]AAAAGGAGAAAAGAT	3055
rs35526857	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32092117	GAAGCCGGCCGGTGG[G/T]GCTTTGATTGTTCTG	3055
rs35710845	in-del	-/C			intron-variant	HCK	GRCh38.p7	20:32068222	GAATCACTTGAACCC[-/C]TGGAGGCAGAGGTTG	3055
rs35802892	in-del	-/G			intron-variant	HCK	GRCh38.p7	20:32087136	CATGGGTGGTGGGGG[-/G]TGCCACTCTCCCGCA	3055
rs35827345	in-del	-/C			intron-variant	HCK	GRCh38.p7	20:32066303	GTGCCCTCCAGTGAC[-/C]TTTTTTTTTTTTTTT	3055
rs35904270	in-del	-/C			intron-variant	HCK	GRCh38.p7	20:32087162	CGCATCAGCCACCTT[-/C]CCCTGTACTTGCCAA	3055
rs35974379	snp	C/T	0	0	intron-variant	HCK	GRCh38.p7	20:32099262	CCTCACCTTTCCTGT[C/T]TTAGTTAAAGGCACC	3055
rs36019250	in-del	-/A			intron-variant	HCK	GRCh38.p7	20:32066013	CTGCATTTCTTACAG[-/A]CTCCCCTGTGAGGTT	3055
rs36060537	in-del	-/T			intron-variant	HCK	GRCh38.p7	20:32066626	CCCCAGTGACCTTTT[-/T]ATGAGGAGCCACAGA	3055
rs41303795	snp	C/G			utr-variant-5-prime	HCK	GRCh38.p7	20:32052349	CACCAAAGCCCCTCA[C/G]AGCGTCGCCCCCGCC	3055
rs55722810	snp	A/T	0.034565	0.126847	missense	HCK	GRCh38.p7	20:32073802	CAGAAGGGGGACCAG[A/T]TGGTGGTCCTAGAGG	3055
rs55726906	snp	A/C	0.0345262	0.126772	intron-variant	HCK	GRCh38.p7	20:32058335	TCAGGAGTTCAAGAC[A/C]AGCCTGGCCAACATG	3055
rs55905450	in-del	-/AA			intron-variant	HCK	GRCh38.p7	20:32096520	AAAAAAAAAAAAAAA[-/AA]GATAGGTGCTTGCTC	3055
rs56029200	snp	A/G	0.00655677	0.0568805	missense	HCK	GRCh38.p7	20:32071729	AAAACTGAAACCAGC[A/G]CCAGCCCACACTGTC	3055
rs56097656	snp	A/C	0.00358779	0.0422022	intron-variant	HCK	GRCh38.p7	20:32075305	CTCAGTTGATCCTCC[A/C]ACCTCAGCCTCCCAA	3055
rs56390911	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32059515	TCTCTCTCTCTCTTT[C/T]TTTTTTCTTTTTCTT	3055
rs56660439	in-del	-/CATC			intron-variant	HCK	GRCh38.p7	20:32075742	ATCCATCCATCCATC[-/CATC]ATCCAACAGATACCT	3055
rs57144947	snp	A/G	0.3746	0.216737	intron-variant	HCK	GRCh38.p7	20:32089255	AGGGGACTGACCAAG[A/G]ACACAAATCCCAGGG	3055
rs57242437	snp	A/G	0.152334	0.230133	intron-variant	HCK	GRCh38.p7	20:32053726	ATGTATGTTAACATT[A/G]CCCTAGCTAGACATA	3055
rs57701871	snp	A/G	0.0146672	0.084371	upstream-variant-2KB	HCK	GRCh38.p7	20:32051580	GGAATCCCTTGATAG[A/G]TGGGGTTAGGATCTC	3055
rs58517209	in-del	-/TG/TGTGTGTGTA/TGTGTGTGTG/TGTGTGTGTGCG			intron-variant	HCK	GRCh38.p7	20:32093523	GTGTGTGTGTGTGTG[lengthTooLong]CATGTGCACGTGTGT	3055
rs58620860	in-del	-/TTT			intron-variant	HCK	GRCh38.p7	20:32064019	TTTTTTTTTTTTTTT[-/TTT]GAGATAGAGTCTCTC	3055
rs58663849	snp	C/T	0.00676609	0.0577691	intron-variant	HCK	GRCh38.p7	20:32081315	GTGGATTCATGCTGA[C/T]TGGGTGCATGGATGG	3055
rs58814478	snp	A/G	0.0456336	0.143994	intron-variant	HCK	GRCh38.p7	20:32063228	ATATATCCATTACAC[A/G]AATGTGTATGGGGGG	3055
rs58948864	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32067419	CTGGCAACCACCATT[C/T]TACTTTTTGTATCTC	3055
rs58976342	in-del	-/C			intron-variant	HCK	GRCh38.p7	20:32052792	CTTCTTGGGGGGGGG[-/C]GGGGATTTTTTTTTT	3055
rs59047893	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32086419	GACGTTAAGCCACTT[C/G]CCCTAGTGTGCACAG	3055
rs59055761	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32086418	AGACGTTAAGCCACT[G/T]GCCCTAGTGTGCACA	3055
rs59388669	snp	A/C	0.021333	0.101051	intron-variant	HCK	GRCh38.p7	20:32083637	GGAGGCGTGAGAACT[A/C]TTCCCATTTTACAGA	3055
rs59489790	snp	C/T	0.0414363	0.137845	intron-variant	HCK	GRCh38.p7	20:32072338	TGTTGTAAGCCTTTA[C/T]GGTTATTAACACCCT	3055
rs59995765	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32054189	CCACCTTGTATCACT[C/T]TCAGTCCTGTTTCTC	3055
rs60000242	snp	A/C	0.227959	0.249026	intron-variant	HCK	GRCh38.p7	20:32074044	GAGATGAACAGGTGA[A/C]GCTTTCTCAGGGAAG	3055
rs60044994	in-del	-/GA/T/TTTGA/TTTTTGA/TTTTTTGA	0	0	intron-variant	HCK	GRCh38.p7	20:32066331	TTTTTTTTTTTTTTT[-/GA/T/TTTGA/TTTTTGA/TTTTTTGA]GACAGAGTCTTGCTC	3055
rs60349531	in-del	-/CACA			intron-variant	HCK	GRCh38.p7	20:32058637	ACACACACACACACA[-/CACA]TACACACACTAGTCC	3055
rs60740993	in-del	-/CACACA/CATACA	0	0	intron-variant	HCK	GRCh38.p7	20:32058640	ACACACACACACACA[-/CACACA/CATACA]TACACACACTAGTCC	3055
rs60766411	snp	C/G	0.00835141	0.0640778	intron-variant	HCK	GRCh38.p7	20:32073489	CCCAAAATTTCCTCT[C/G]AAGTGCTTTGCGCAG	3055
rs60782500	snp	A/G	0.0345262	0.126772	intron-variant	HCK	GRCh38.p7	20:32094293	AGAGCAGCTTTGTGC[A/G]TAACAGACAAAAATG	3055
rs60902201	snp	C/T	0.0944967	0.195752	intron-variant	HCK	GRCh38.p7	20:32085310	TCAAGGTCAGCAGTT[C/T]GAGAAAAACCTGGAT	3055
rs61456149	in-del	-/T			intron-variant	HCK	GRCh38.p7	20:32055068	TACAACGAACAATAT[-/T]GACAGGAGCATCCTG	3055
rs62204979	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32086145	CTGCCTCAGCCTCCC[C/T]AGTAGCTGGGACTAC	3055
rs62204981	snp	C/T	0.5	0	intron-variant	HCK	GRCh38.p7	20:32093141	GTAGAGACGGGGTTT[C/T]GCCATGTTGGCCAGG	3055
rs62204982	snp	A/G	0.0759472	0.179459	intron-variant	HCK	GRCh38.p7	20:32093228	GGGATTACAAGTGTA[A/G]GCCACCATGCCCGGC	3055
rs62204983	snp	A/G	0.139225	0.224118	intron-variant	HCK	GRCh38.p7	20:32096358	AAAAATTAGCTGGGC[A/G]TGGTGGCAGGTGCCT	3055
rs62207270	snp	A/T	0.110872	0.20771	intron-variant	HCK	GRCh38.p7	20:32053772	AGACTTTAGCCTACA[A/T]CAGCATCACCTGGAC	3055
rs62207271	snp	C/T	0.110872	0.20771	intron-variant	HCK	GRCh38.p7	20:32053995	GTTTTCTCTTTATGG[C/T]CCTTTTTTTTTTAGG	3055
rs62207272	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32058606	TCCTTTTATGTCAAA[A/C]CACACACACACACAC	3055
rs62207273	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32073020	CAGGAGAATCACTTG[A/G]ACCCGAGAGGTGGAG	3055
rs62207274	snp	C/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32073056	GGTGAGCTGAGATCA[C/T]GCCACTGCACTCCAG	3055
rs66527980	in-del	-/TGTTT	0.499745	0.0112903	intron-variant	HCK	GRCh38.p7	20:32077512	GCAGCACCTTGTTCC[-/TGTTT]TGTTTTGTTTTGTTT	3055
rs71185377	in-del	-/TTCTTTCT	0	0	intron-variant	HCK	GRCh38.p7	20:32094748	TCTTTCCTTCTTTCT[-/TTCTTTCT]TTCTTTCTTTCTTTC	3055
rs71185378	in-del	-/TTCTTTCT	0	0	intron-variant	HCK	GRCh38.p7	20:32094800	TCTTTCTTTCTTTCT[-/TTCTTTCT]TTCTTTCTTTCTCTT	3055
rs71336556	in-del	-/G	0.5	0	intron-variant	HCK	GRCh38.p7	20:32076810	CGCATATCTGGCCAG[-/G]TGTGGTGGCTCACAC	3055
rs71336559	in-del	-/T	0.5	0	intron-variant	HCK	GRCh38.p7	20:32099375	TTTTTTTTTTTTTTT[-/T]GAGACGGAGTCTCCC	3055
rs71708551	in-del	-/GC			intron-variant	HCK	GRCh38.p7	20:32052791	CCTTCTTGGGGGGGG[-/GC]GGGGATTTTTTTTTT	3055
rs73104632	snp	C/T	0.00159617	0.0282053	upstream-variant-2KB	HCK	GRCh38.p7	20:32051956	GAGACTGGGGTAGGA[C/T]GCTGGGCGGTGGGAT	3055
rs73104645	snp	G/T	0.0225045	0.103662	intron-variant	HCK	GRCh38.p7	20:32069216	ATGAGGTAGAACCCT[G/T]GCCACCCTTTCTCAG	3055
rs73104662	snp	A/C	0.0356815	0.128715	intron-variant	HCK	GRCh38.p7	20:32089830	GGCCTCTAGGCCGAG[A/C]CTGAAGGATGAATAG	3055
rs73247012	snp	C/T	0.00318978	0.0398085	upstream-variant-2KB	HCK	GRCh38.p7	20:32051100	AGACGCGGTAGAATT[C/T]TTGTAGTTTTGGAGA	3055
rs73247023	snp	C/T	0.00318978	0.0398085	intron-variant	HCK	GRCh38.p7	20:32058465	GGAACCCGGGAGGCA[C/T]GGTTGCAGTGAGCCA	3055
rs73247031	snp	A/G	0.0626037	0.165477	intron-variant	HCK	GRCh38.p7	20:32066941	AGTCGGTTCTTCTTT[A/G]GAGTATTCTTGACTT	3055
rs73247033	snp	A/G	0.0482946	0.147699	intron-variant	HCK	GRCh38.p7	20:32069399	ATCAGTGGGTGCCCA[A/G]AGAGGTAGAGTGAGC	3055
rs73247040	snp	A/G	0.0178098	0.0926698	intron-variant	HCK	GRCh38.p7	20:32070111	AAGTCTGCAAGCTCT[A/G]CCTCCAAAATGTCCC	3055
rs73247043	snp	C/G	0.0178098	0.0926698	intron-variant	HCK	GRCh38.p7	20:32071873	TCCCAAGGTTGGGCA[C/G]GGTGAGCTTGGGGTG	3055
rs73247045	snp	A/G	0.0414363	0.137845	intron-variant	HCK	GRCh38.p7	20:32072067	TCCGGCCTGGGCAGA[A/G]GCAAAAGCAGTGCTG	3055
rs73247052	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32074081	TAGGGCTCCTGCGAT[C/T]AAGCCACCGGCTTTA	3055
rs73247053	snp	A/G	0.0182019	0.0936463	intron-variant	HCK	GRCh38.p7	20:32074285	CTATTCTCAGCCCCA[A/G]CTGAACCATTCTGAG	3055
rs73248931	snp	G/T	0.097727	0.198275	intron-variant	HCK	GRCh38.p7	20:32080174	TCTTCACTGACTTGT[G/T]TTTTCATTTGTTTTG	3055
rs73248938	snp	C/T	0.0966517	0.197444	intron-variant	HCK	GRCh38.p7	20:32087054	AGAAGGGAATGGGGC[C/T]AGAATACTCCTGGGC	3055
rs73248948	snp	A/T	0.0456336	0.143994	intron-variant	HCK	GRCh38.p7	20:32091867	GCATGCACCTATAGT[A/T]CCAGCTGCTTGGGAA	3055
rs73248962	snp	C/T	0.212122	0.247114	intron-variant	HCK	GRCh38.p7	20:32099595	ACTGCTGACCTTAGG[C/T]GATGCGCCTGCCTCG	3055
rs73613746	snp	C/T	0.00874735	0.0655527	intron-variant	HCK	GRCh38.p7	20:32055878	TGCTTTTTGCCTCTA[C/T]GGACTAATTTATTCA	3055
rs73613747	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32056712	ACGAATCTTAATCTC[A/T]TTCAAACCAGGCTGC	3055
rs73906723	snp	A/T	0.00358779	0.0422022	intron-variant	HCK	GRCh38.p7	20:32065404	AGCAAAATTGATAAT[A/T]TATTTGCTCGTGGAC	3055
rs73906725	snp	C/T	0.0349115	0.127424	intron-variant	HCK	GRCh38.p7	20:32067607	ACATAAAGTATGGCA[C/T]GCCAGGCATGCAGCC	3055
rs73906726	snp	A/G	0.000650089	0.0180173	intron-variant	HCK	GRCh38.p7	20:32069791	TCTTTTTTCATTTTT[A/G]AAAGTAACTCATCTA	3055
rs73906727	snp	C/T	0.0337553	0.125452	intron-variant	HCK	GRCh38.p7	20:32072557	TACAGGGAGACCCTG[C/T]CTCTTTAAAAAAAAA	3055
rs73906729	snp	C/T	0.0011724	0.0241832	intron-variant	HCK	GRCh38.p7	20:32073373	GAGGGTAAGTATCTA[C/T]GAGCAGATGCAGTGG	3055
rs73906730	snp	A/G	0.0337553	0.125452	intron-variant	HCK	GRCh38.p7	20:32079623	ACCTTCTCTCCCCCA[A/G]AAAATCTTTGAGTAA	3055
rs73906731	snp	A/C	0.031825	0.122064	intron-variant	HCK	GRCh38.p7	20:32079985	GCTGAAAAACCCAAC[A/C]AGGTGCTGTGGCTGC	3055
rs73906733	snp	C/G	0.0726307	0.176182	intron-variant	HCK	GRCh38.p7	20:32083316	ACATATTCCCAGGTT[C/G]CAGGGTTTAGGGCAT	3055
rs73906735	snp	A/G	0.00358779	0.0422022	intron-variant	HCK	GRCh38.p7	20:32089134	AGACAGAGCTGGACC[A/G]GGGGCCAAGCCTTCA	3055
rs73906736	snp	A/T	0.00731097	0.060017	intron-variant	HCK	GRCh38.p7	20:32099162	GCATCAGCTCAGGGC[A/T]GCTACCAGGGCCCAG	3055
rs74183468	snp	A/G	0.00438332	0.0466095	intron-variant	HCK	GRCh38.p7	20:32065913	CAAAAGAGGTTCTCT[A/G]GCCTTCTTGGCTAGA	3055
rs74183469	snp	A/G	0.5	0	intron-variant	HCK	GRCh38.p7	20:32077583	CCAGGCTGGAGTGCA[A/G]TGGTGTGATCTCGGC	3055
rs74502037	snp	A/C	0.0558544	0.157504	intron-variant	HCK	GRCh38.p7	20:32091091	ACATCACAGAGCTGC[A/C]GCGCTCAAGCTGAGT	3055
rs74566007	snp	A/G	0.0337553	0.125452	intron-variant	HCK	GRCh38.p7	20:32085499	AGCCTGGGAGACAGA[A/G]TGAGACTCTGTCTAA	3055
rs74633596	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32091826	AAAAAAAAAAAAATT[C/T]TTTTTAAATTTAATC	3055
rs74638193	snp	C/T	0.0437281	0.141251	intron-variant	HCK	GRCh38.p7	20:32064997	ATTAGATGAGAAATG[C/T]GTATGCAGAAGTTTT	3055
rs74654967	snp	A/G	0.00659994	0.057065	intron-variant	HCK	GRCh38.p7	20:32088666	GCCTAACGAGGAAAC[A/G]GGGAAGGGAAACAGG	3055
rs74795366	snp	G/T	0.0165278	0.0893908	intron-variant	HCK	GRCh38.p7	20:32100769	CCACCTGAATGTTTT[G/T]TCTTGAGGGTGCACT	3055
rs74829661	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32095535	CTGCTGGGATTACAG[A/G]TGTGAGCCACCATGC	3055
rs75018364	snp	C/T	0.00835141	0.0640778	intron-variant	HCK	GRCh38.p7	20:32093146	GACGGGGTTTCGCCA[C/T]GTTGGCCAGGCTGGT	3055
rs75084400	snp	C/T	0.00168231	0.0289538	synonymous-codon	HCK	GRCh38.p7	20:32099116	GGAGATCGTCACCTA[C/T]GGCCGGATCCCTTAC	3055
rs75091625	snp	A/G	0.0158469	0.0875917	intron-variant	HCK	GRCh38.p7	20:32100334	GGTGGCAGCCAGTGA[A/G]GAGGCCACAGCAGTG	3055
rs75119412	snp	C/G/T	0.00318978	0.0398085	intron-variant	HCK	GRCh38.p7	20:32090016	ATGCCAAGGGCAGGG[C/G/T]TCATTTGAGTATGCA	3055
rs75163777	snp	A/G	0.0509478	0.151255	intron-variant	HCK	GRCh38.p7	20:32062908	CCCCATTGCTGAGCT[A/G]TTCTGAGAAGGGAAA	3055
rs75181892	snp	A/C	0	0	intron-variant	HCK	GRCh38.p7	20:32096505	ACTCCGTCTCAAAAA[A/C]AAAAAAAAAAAAAAA	3055
rs75238070	in-del	-/GAA			intron-variant	HCK	GRCh38.p7	20:32060910	AAGGAAGAAAGGAAG[-/GAA]GAAGAAAGGAATAAA	3055
rs75263112	snp	C/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32090348	CAGAAAGGAGCCCAC[C/G]TGGGGCTTTGGTCTT	3055
rs75265826	snp	C/T	0.00600906	0.0544832	intron-variant	HCK	GRCh38.p7	20:32101303	CCGTTTCTAATTCCA[C/T]GGCTCCTTTTCAGGG	3055
rs75337347	snp	A/G	0.0103295	0.0711199	intron-variant	HCK	GRCh38.p7	20:32059968	TGTAAAAGGATCAGC[A/G]CCTGTGTTACTGAGG	3055
rs75479947	snp	A/G	0.00557542	0.0525036	intron-variant	HCK	GRCh38.p7	20:32063476	CAGCCTTGTACTCCT[A/G]GGCTCAAAGCAATCC	3055
rs75506866	snp	A/T	0.5	0	intron-variant	HCK	GRCh38.p7	20:32054475	AAGCGAAACTCCACC[A/T]AAAAAAAAAAAAAAA	3055
rs75517018	snp	C/T	0.0437281	0.141251	intron-variant	HCK	GRCh38.p7	20:32067644	TCACTGTGCATGACA[C/T]TCCTACTGTGTGCCA	3055
rs75577237	snp	C/T	0.5	0	intron-variant	HCK	GRCh38.p7	20:32070564	TTTAGACCGCAGGTT[C/T]TGTATCCCTTTCTCT	3055
rs75725903	snp	A/G	0.00318978	0.0398085	intron-variant	HCK	GRCh38.p7	20:32092675	CAGTTCATGATTGGC[A/G]GCCTCCCTCTCAACT	3055
rs75736658	snp	G/T	0	0	intron-variant	HCK	GRCh38.p7	20:32087660	ATTTTTTTTTTTTTT[G/T]AGACAGAGTCTCACT	3055
rs75747523	snp	A/G	0.100944	0.200705	intron-variant	HCK	GRCh38.p7	20:32054101	AATTAACAAATAATA[A/G]CATTTTGTTGTGTTT	3055
rs75936112	snp	A/C	0	0	intron-variant	HCK	GRCh38.p7	20:32067856	GTGAAGGCTTAGTAC[A/C]AAAAAAAATGTAAAG	3055
rs76011311	snp	A/C	0.0839998	0.186933	intron-variant	HCK	GRCh38.p7	20:32072333	AGCACTGTTGTAAGC[A/C]TTTACGGTTATTAAC	3055
rs76170030	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32095529	CCCAAACTGCTGGGA[G/T]TACAGGTGTGAGCCA	3055
rs76175734	snp	A/G	0.0158469	0.0875917	intron-variant	HCK	GRCh38.p7	20:32089827	AGTGGCCTCTAGGCC[A/G]AGCCTGAAGGATGAA	3055
rs76198155	snp	A/G	0.5	0	intron-variant	HCK	GRCh38.p7	20:32056518	GAGACTCCTTCTCAG[A/G]AAAAAAAAAAACAGT	3055
rs76365699	snp	C/G	0.0209421	0.100162	intron-variant	HCK	GRCh38.p7	20:32074890	ATCCTTCCAGTCAGG[C/G]AAGAGAGGCTAAAGT	3055
rs76379542	snp	C/T	0.0490639	0.148744	intron-variant	HCK	GRCh38.p7	20:32101289	TTTCCCAACTGCTTC[C/T]GTTTCTAATTCCACG	3055
rs76386673	snp	A/T	0.103794	0.20279	intron-variant	HCK	GRCh38.p7	20:32095176	GAACACAGATGACCC[A/T]TAAAAACATTTTGTT	3055
rs76556319	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32060633	ATATCCTATTGGTCA[G/T]ATGGATAATAAACAA	3055
rs76650041	snp	C/G	0.031825	0.122064	intron-variant	HCK	GRCh38.p7	20:32055992	TCCACATGGTGGCAA[C/G]TATTAGTACTTTATT	3055
rs76687355	snp	A/G	0.133093	0.220981	intron-variant	HCK	GRCh38.p7	20:32057877	GGTACTTTCAGAGGC[A/G]TGGGTAATGATGCAG	3055
rs76702896	snp	A/G	0.00358779	0.0422022	intron-variant	HCK	GRCh38.p7	20:32077073	TGGACAACAGAGCGA[A/G]ACTCTATCTCAAAAA	3055
rs76711076	in-del	-/CAAAA			intron-variant	HCK	GRCh38.p7	20:32096499	AGCGAGACTCCGTCT[-/CAAAA]AAAAAAAAAAAAAAA	3055
rs76743099	snp	C/T	0.0670745	0.170406	upstream-variant-2KB	HCK	GRCh38.p7	20:32051643	GTATAGACCCCTGGG[C/T]ATTAAAACTCTTAGG	3055
rs76745534	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32090746	CAGTGCTTACACCTG[G/T]GCCCAATAAACCTAC	3055
rs76838786	snp	A/G	0.00676609	0.0577691	intron-variant	HCK	GRCh38.p7	20:32090342	CAGGGACAGAAAGGA[A/G]CCCACCTGGGGCTTT	3055
rs77236395	snp	A/G	0.0437281	0.141251	intron-variant	HCK	GRCh38.p7	20:32084655	ACCCAAGGCAGAGGG[A/G]GAGATTTAAATAATA	3055
rs77678831	snp	C/G	0.0494327	0.149241	intron-variant	HCK	GRCh38.p7	20:32079131	TTGAACTTTTCCACC[C/G]AAATATCTCAATATT	3055
rs77791474	snp	A/G	0.00358779	0.0422022	intron-variant	HCK	GRCh38.p7	20:32078789	TTGAACCCGAGAAGC[A/G]GAGGTTTCAGTGAGC	3055
rs77889465	snp	A/C	0.0916144	0.193427	intron-variant	HCK	GRCh38.p7	20:32077115	AATAACAAATGAATA[A/C]ACATATGTGTCCTTT	3055
rs77911312	in-del	-/TTG			intron-variant	HCK	GRCh38.p7	20:32067551	TTTTTTTTTTTTTTT[-/TTG]CCCCGTCTTATGGTG	3055
rs78035105	snp	A/C	0.5	0	intron-variant	HCK	GRCh38.p7	20:32067855	TGTGAAGGCTTAGTA[A/C]AAAAAAAAATGTAAA	3055
rs78139418	snp	A/G	0.0410537	0.137264	intron-variant	HCK	GRCh38.p7	20:32071547	AGGGGAGTTAAGACC[A/G]GGAAGGCCAGTGGGA	3055
rs78160522	snp	A/G	0.00358779	0.0422022	intron-variant	HCK	GRCh38.p7	20:32082660	CACACAAAAAATAAA[A/G]TTTAAACTTCCCAAA	3055
rs78428608	snp	C/T	0.0166325	0.0896639	intron-variant	HCK	GRCh38.p7	20:32084907	GCAGCTTGGAGATTT[C/T]CAGGCAACTGATGAA	3055
rs78612195	snp	C/T	0.00318978	0.0398085	intron-variant	HCK	GRCh38.p7	20:32072276	GCTAGGAGAGGTATT[C/T]ACCAACTTCTTTTAT	3055
rs78937021	snp	C/G	0.152334	0.230133	intron-variant	HCK	GRCh38.p7	20:32055047	AAGTTGTTCCTAGGC[C/G]TTCACTACAACGAAC	3055
rs78943459	snp	A/G	0.0232847	0.105357	intron-variant	HCK	GRCh38.p7	20:32087381	CAATCATAACTCCTG[A/G]GCTCAAGTGATCCTC	3055
rs79007598	snp	A/G	0.0150606	0.0854603	intron-variant	HCK	GRCh38.p7	20:32063683	AACCTGGTATCAGGG[A/G]GGTCTTTGCCATCAG	3055
rs79052786	snp	C/T	0.0509478	0.151255	intron-variant	HCK	GRCh38.p7	20:32063903	TCTATTTCTTGGGTT[C/T]GCCTTGCTGCTGCAG	3055
rs79331306	snp	A/T	0	0	intron-variant	HCK	GRCh38.p7	20:32070941	AGGAGGAGGGGAAGG[A/T]GGAGGAGGGGGAAGG	3055
rs79345290	snp	A/G	0.193653	0.243567	intron-variant	HCK	GRCh38.p7	20:32091626	CCTCATCCCCATTTC[A/G]TCCCCACCCCCCACT	3055
rs79430376	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32072863	GGCACAGTGGCTCAC[A/T]CCTGTAATCCCAGCA	3055
rs79432199	snp	C/T	0.0998734	0.199905	intron-variant	HCK	GRCh38.p7	20:32057013	ACCCGCAGCGATTAT[C/T]TTTAATTAGTTGCTA	3055
rs79465460	snp	A/G	0.0240643	0.107019	intron-variant	HCK	GRCh38.p7	20:32090331	GATTCAGAGCCCAGG[A/G]ACAGAAAGGAGCCCA	3055
rs79541727	snp	C/T	0.0103295	0.0711199	intron-variant	HCK	GRCh38.p7	20:32070239	TCCCTCCCCTGCTCC[C/T]CACTGTCCACGCCTC	3055
rs79678843	snp	C/T	0.0494327	0.149241	intron-variant	HCK	GRCh38.p7	20:32071570	CAGTGGGAGCCAGCC[C/T]GGGGGCAGGGGACCT	3055
rs80029162	snp	C/T	0.5	0	intron-variant	HCK	GRCh38.p7	20:32059301	TCCTTCCTTCCCTCC[C/T]TCCCTCCTTTCTTTT	3055
rs80138575	snp	C/G/T	0.000622466	0.017631	missense	HCK	GRCh38.p7	20:32084421	TCTGCCAGAAACTGT[C/G/T]GGTGCCCTGCATGTC	3055
rs80236822	snp	C/T	0.0998734	0.199905	intron-variant	HCK	GRCh38.p7	20:32057098	AGAAGAGTTAGCAGC[C/T]CTGAGACTAGAACCC	3055
rs80345938	in-del	-/AAA			intron-variant	HCK	GRCh38.p7	20:32058529	ACAGCAAGACTCTGT[-/AAA]CAAAAAAAAAAAAAA	3055
rs111226194	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32097433	AAATACAAAAAATTA[G/T]CCAGGCGTGGTGGCG	3055
rs111353278	in-del	-/TA	0.0693013	0.172766	intron-variant	HCK	GRCh38.p7	20:32096905	TGGTGATTACAAGGG[-/TA]TATATATATATATAT	3055
rs111471428	snp	C/T	0.5	0	intron-variant	HCK	GRCh38.p7	20:32060330	AGTTCAAGCAATTCT[C/T]CTGCCTTAGCCTCCC	3055
rs111702470	snp	C/T	0.5	0	upstream-variant-2KB	HCK	GRCh38.p7	20:32050681	TGGATGGGAGACCCC[C/T]TCAAAATAGTTAGCA	3055
rs111835850	snp	C/T	0.5	0	intron-variant	HCK	GRCh38.p7	20:32059434	CTCTTTCTTTCTTTT[C/T]TCTTTCTTTCTTTCT	3055
rs111942775	snp	C/T	0.0236746	0.106192	intron-variant	HCK	GRCh38.p7	20:32079296	TAACAAAACTCAGGC[C/T]CTTCACAGGCTTCCA	3055
rs111995106	snp	G/T	0.5	0	intron-variant	HCK	GRCh38.p7	20:32081039	GGCTGCAGCGAGCCA[G/T]AATGGAGCCACTAGA	3055
rs112056599	snp	C/G	0.5	0	intron-variant	HCK	GRCh38.p7	20:32090831	CTTAGGAGTCACACA[C/G]AGTTTTGTTTTGATC	3055
rs112063342	snp	C/T	0.0607341	0.163335	intron-variant	HCK	GRCh38.p7	20:32061233	GTGATTCGCCCGCCT[C/T]GGCCTCCCAAAGTGC	3055
rs112064933	in-del	-/TATTT	0.5	0	intron-variant	HCK	GRCh38.p7	20:32098034	TTTTCTATTTTTTTA[-/TATTT]TATTTTATTTTATTT	3055
rs112101801	snp	C/T	0.0182019	0.0936463	intron-variant	HCK	GRCh38.p7	20:32087170	GCCACCTTCCCTGTA[C/T]TTGCCAAAGCCCTGG	3055
rs112127642	in-del	-/A	0.5	0	intron-variant	HCK	GRCh38.p7	20:32094829	AAGAAAGAAAGAAAG[-/A]AAAGAAAGAAAGAAA	3055
rs112141547	snp	A/G	0.5	0	intron-variant	HCK	GRCh38.p7	20:32083810	GACGGTGCCAGCGGT[A/G]GCCTTACAGGGTGTC	3055
rs112210927	snp	C/T	0.5	0	intron-variant	HCK	GRCh38.p7	20:32074227	GCTGAAGCCCGAGAA[C/T]GGGAGTGGTCATGCC	3055
rs112254129	snp	G/T	0.0232847	0.105357	intron-variant	HCK	GRCh38.p7	20:32065436	GGAAAAATCCTGAGG[G/T]GTATAGGCCTCAGGC	3055
rs112331783	snp	C/T	0.0970103	0.197722	intron-variant	HCK	GRCh38.p7	20:32077686	CATGCGCCACCATAC[C/T]TAGCTAATTTTGTAT	3055
rs112496266	snp	G/T	0.5	0	intron-variant	HCK	GRCh38.p7	20:32077538	GTTTTGTTTTGTTTT[G/T]TTTTTTAGGTGGAGT	3055
rs112517886	snp	C/G	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32086167	TGGGACTACAGGCGC[C/G]CACAACTGCGCCTGG	3055
rs112571861	snp	A/G	0.0287284	0.116357	intron-variant	HCK	GRCh38.p7	20:32087919	CATGCTGGAATTACA[A/G]GCGTGAGCAACTGCG	3055
rs112610391	snp	C/T	4.95282e-05	0.00497611	synonymous-codon	HCK	GRCh38.p7	20:32071752	ACACTGTCCTGTGTA[C/T]GTGCCGGATCCCACA	3055
rs112666039	snp	A/G	0.5	0	intron-variant	HCK	GRCh38.p7	20:32061285	CTGCGCCCAGCTGCC[A/G]TGCCATTCTAAGGAA	3055
rs112680409	snp	A/G	0.0170251	0.090679	intron-variant	HCK	GRCh38.p7	20:32080619	CCATCTCAGTCTCCC[A/G]AGTAGCTGGGACTAC	3055
rs112796504	snp	C/T	0.5	0	intron-variant	HCK	GRCh38.p7	20:32059509	CTTCTCTCTCTCTCT[C/T]TCTTTTTTTTTTCTT	3055
rs112798247	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32097430	TAAAAATACAAAAAA[C/T]TAGCCAGGCGTGGTG	3055
rs112934778	snp	A/C	0.5	0	intron-variant	HCK	GRCh38.p7	20:32090280	CCAAGGGAGGAAAAG[A/C]GGTTCTGGGCCTTCA	3055
rs112981959	snp	G/T	0.5	0	intron-variant	HCK	GRCh38.p7	20:32074328	CAGGACCCTGCCATG[G/T]GTATAGCTAATAAGA	3055
rs112987706	in-del	-/T	0	0	intron-variant	HCK	GRCh38.p7	20:32096985	ACGTTATAACTCGAT[-/T]AAAAAAAATTTAGAC	3055
rs113011250	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32066334	TTTTTTTTTTTTTGA[C/G]AGAGTCTTGCTCTGT	3055
rs113028755	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32063005	GGGTTCCTCATTCTC[C/T]CCTTCCCCTTCATCG	3055
rs113037125	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32059360	TCCCCCCTTCTCCTC[C/T]TCCTCTTCCTCCTCC	3055
rs113217881	snp	A/T	0.5	0	intron-variant	HCK	GRCh38.p7	20:32072563	GAGACCCTGTCTCTT[A/T]AAAAAAAAAAAAAAA	3055
rs113219740	in-del	-/C	0.5	0	intron-variant	HCK	GRCh38.p7	20:32075741	CATCCATCCATCCAT[-/C]CATCCAACAGATACC	3055
rs113242783	snp	A/T	0.0019509	0.0311712	intron-variant	HCK	GRCh38.p7	20:32069800	ATTTTTAAAAGTAAC[A/T]CATCTAAGCCTAGGA	3055
rs113353931	snp	C/T	0.5	0	intron-variant	HCK	GRCh38.p7	20:32074074	GCCTTTCTAGGGCTC[C/T]TGCGATTAAGCCACC	3055
rs113357682	snp	C/T	0.00318978	0.0398085	intron-variant	HCK	GRCh38.p7	20:32058222	TTCTGAGCCTCAGTT[C/T]CCAAATCCAAAAAAA	3055
rs113436292	snp	C/T	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32076801	ATCTAAATACGCATA[C/T]CTGGCCAGGTGTGGT	3055
rs113466159	snp	C/T	0.0322114	0.122752	intron-variant	HCK	GRCh38.p7	20:32099609	GTGATGCGCCTGCCT[C/T]GGCCTCCCAAAGTGC	3055
rs113478993	snp	A/G	0.222928	0.24853	intron-variant	HCK	GRCh38.p7	20:32080587	CAACTTCTGCCTCCT[A/G]GGCTCAAATGATTCT	3055
rs113494732	snp	C/T	0.00438332	0.0466095	intron-variant	HCK	GRCh38.p7	20:32070403	CACCCTCTTCCCTGC[C/T]CATGAGCTTCAGCTA	3055
rs113614715	snp	A/G			downstream-variant-500B	HCK	GRCh38.p7	20:32102125	GAGACCCTGTTTAAA[A/G]AAAAAAAAAAAAGAT	3055
rs113655359	snp	A/C	0.00154041	0.0277098	intron-variant	HCK	GRCh38.p7	20:32086601	AGTGGGCTCTGACCA[A/C]CTTCCCTGCTCTCTA	3055
rs113703726	snp	C/T	0.0379877	0.132479	intron-variant	HCK	GRCh38.p7	20:32055657	TTTTTAGAAATATTT[C/T]AATCGAGGTGAAATT	3055
rs113740430	snp	A/G	0.0150606	0.0854603	upstream-variant-2KB	HCK	GRCh38.p7	20:32052051	AAGCCTCCTATGGAT[A/G]GTGCTAATATTTTTT	3055
rs113743904	in-del	-/A	0	0	intron-variant	HCK	GRCh38.p7	20:32091983	GCCCTGTCTCAAAAG[-/A]AAAAAAAAAAGAAGA	3055
rs113881144	snp	C/T	0.227369	0.248974	intron-variant	HCK	GRCh38.p7	20:32080347	GGGATTACAAGTGCT[C/T]GCCACCATGCCCAGC	3055
rs113884718	snp	A/G	0.0170251	0.090679	intron-variant	HCK	GRCh38.p7	20:32064216	CACCATGTTGGACAA[A/G]CTCCTGACCTCTGGT	3055
rs113954151	snp	A/G	0.444444	0.157135	intron-variant	HCK	GRCh38.p7	20:32071414	GTCCTTGGTACCCAC[A/G]ACAATGACAGCTTGT	3055
rs114250687	snp	A/G	0.0387552	0.1337	intron-variant	HCK	GRCh38.p7	20:32075809	ATGGGGCTCCCTGCT[A/G]GAGATGTTCTCTGTA	3055
rs114502178	snp	C/T	0.0248432	0.108648	intron-variant	HCK	GRCh38.p7	20:32071980	CAAAGAAGTCATCTC[C/T]CTTTCCTGCAGCCCA	3055
rs114505022	snp	A/G	0.00483779	0.0489437	missense	HCK	GRCh38.p7	20:32093878	ATTGCAGAAGGCATG[A/G]CCTTCATCGAGCAGA	3055
rs114698088	snp	A/G	0.0252325	0.109451	intron-variant	HCK	GRCh38.p7	20:32080714	ATGGGGTTTTGCCAT[A/G]TTGCCTAGGCTGGCC	3055
rs114705778	snp	A/G	0.0130921	0.0798413	intron-variant	HCK	GRCh38.p7	20:32063102	TACCACTGACTAGCC[A/G]GGGGACCCACTCTCC	3055
rs114785130	snp	A/G	0.0364509	0.129988	intron-variant	HCK	GRCh38.p7	20:32064841	ATTTCACTCAGCAGA[A/G]GCTGAGGCGGTGAGG	3055
rs114810008	snp	A/G	0.0178098	0.0926698	intron-variant	HCK	GRCh38.p7	20:32077844	CTTCCTTTTTATACC[A/G]CAGGGCGTCTGTCCT	3055
rs114979752	snp	A/C	0.00112321	0.0236715	intron-variant	HCK	GRCh38.p7	20:32073290	CACATTGGTCAGATT[A/C]ATTCTCTTCTCTCAT	3055
rs114981530	snp	A/G	0.0349115	0.127424	intron-variant	HCK	GRCh38.p7	20:32065483	GCTCAATTTATCTTC[A/G]GGAATTACTTTATCT	3055
rs114992393	snp	A/C	0.00755907	0.0610114	intron-variant	HCK	GRCh38.p7	20:32070023	TTCTTCCACTTTTAC[A/C]ATTATGTTTTGACTC	3055
rs114995233	snp	C/T	0.0115144	0.0749975	intron-variant	HCK	GRCh38.p7	20:32055268	TGCTGATCTCCCAGC[C/T]GTCTCTGGATCAATG	3055
rs115099684	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32091823	TTAAAAAAAAAAAAA[A/T]TTCTTTTTAAATTTA	3055
rs115133498	snp	A/G	0.00597247	0.0543191	intron-variant	HCK	GRCh38.p7	20:32074228	CTGAAGCCCGAGAAC[A/G]GGAGTGGTCATGCCT	3055
rs115232410	snp	C/T	0.0182019	0.0936463	intron-variant	HCK	GRCh38.p7	20:32075648	GGCTGTGGGTTCTTC[C/T]TGTGTCTAGCTTGAC	3055
rs115477395	snp	A/G	0.0248432	0.108648	intron-variant	HCK	GRCh38.p7	20:32095832	GAGGTCAGAATTGCA[A/G]TCACCTTTAGTTTCT	3055
rs115501610	snp	C/T	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32072806	CGGTACATCCAAGAC[C/T]GAAGGCCGAGGTCAC	3055
rs115570200	snp	A/G	0.0111196	0.0737302	intron-variant	HCK	GRCh38.p7	20:32067506	CTCAACTCGGTCATA[A/G]AGCAGGAATGTCCTG	3055
rs116034076	snp	A/G	0.0111196	0.0737302	intron-variant	HCK	GRCh38.p7	20:32063450	ACAGGGTCTCGATAT[A/G]TTGTCAGGACCAGCC	3055
rs116038017	snp	C/T	0.02016	0.0983543	intron-variant	HCK	GRCh38.p7	20:32066105	CAAACCACTTTGTCA[C/T]AAGGCACTCTGCAGA	3055
rs116085060	snp	C/T	0.0494327	0.149241	intron-variant	HCK	GRCh38.p7	20:32076567	GTGGAAAACGCAGGG[C/T]GTAGACAACATGAAT	3055
rs116190471	snp	C/T	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32064508	TTCTTTCAGAGAACT[C/T]CTAATCCAACATCTC	3055
rs116282079	snp	A/G	0.0225045	0.103662	intron-variant	HCK	GRCh38.p7	20:32061884	TTTTACTCCAAGTGA[A/G]ACGGAAACCCTGGGT	3055
rs116483029	snp	C/T	0.0244538	0.107838	intron-variant	HCK	GRCh38.p7	20:32079519	TTAAAGGAAGTTCCC[C/T]CACTCCAAATTGCAT	3055
rs116591956	snp	A/C	0.0197687	0.0974348	intron-variant	HCK	GRCh38.p7	20:32063137	GGCTTCCATTTCCCT[A/C]TCTGAAAAATAACTT	3055
rs116647719	snp	A/G	0.0248432	0.108648	intron-variant	HCK	GRCh38.p7	20:32093241	TAAGCCACCATGCCC[A/G]GCCTGTTTTATCTTT	3055
rs116757447	snp	A/G	0.00278811	0.0372328	intron-variant	HCK	GRCh38.p7	20:32073374	AGGGTAAGTATCTAC[A/G]AGCAGATGCAGTGGA	3055
rs116785851	snp	C/T	0.0387552	0.1337	intron-variant	HCK	GRCh38.p7	20:32085349	GAAATCCCGTCTCTA[C/T]GAAAAAATACAACAA	3055
rs117351131	snp	A/G	0.00795532	0.062565	intron-variant	HCK	GRCh38.p7	20:32059219	GGGAAAGAGGTGGCC[A/G]TGGAGGGCTTATAGA	3055
rs117529687	snp	A/G	0.00398564	0.0444627	intron-variant	HCK	GRCh38.p7	20:32091325	TGGACCCCAAGCAGC[A/G]CTTTTGGAGCTCCAG	3055
rs117681170	snp	C/G	0.0252325	0.109451	intron-variant	HCK	GRCh38.p7	20:32098170	CTCCTGTCTCAGCCT[C/G]TAGCTGGAACTACAG	3055
rs117694768	snp	C/T	0.0240643	0.107019	intron-variant	HCK	GRCh38.p7	20:32087627	ATGCACTACCACACC[C/T]AGCTAATTTCTAAAA	3055
rs117769099	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32082162	TTCAGTTTCCTCATC[C/T]GTAAATGAGGATGAT	3055
rs117811737	snp	A/T	0.0919752	0.193722	intron-variant	HCK	GRCh38.p7	20:32063430	GCTAATTTTTTTGGG[A/T]AGAGACAGGGTCTCG	3055
rs117911133	snp	G/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32061625	AGGGTGATGAGGGAA[G/T]GTTGCTCTGAGAAGG	3055
rs117948101	snp	A/T	0.0926964	0.194308	intron-variant	HCK	GRCh38.p7	20:32080692	TCTTTCTTTCTTTTT[A/T]GTAGAGATGGGGTTT	3055
rs118156741	snp	C/T	0.0103295	0.0711199	intron-variant	HCK	GRCh38.p7	20:32092523	AATAAGAATCCTCCA[C/T]GCAGTCTGTTAGTCA	3055
rs137871205	snp	C/T	1.65146e-05	0.0028735	missense	HCK	GRCh38.p7	20:32099120	ATCGTCACCTACGGC[C/T]GGATCCCTTACCCAG	3055
rs137871550	snp	A/G	0.000412742	0.0143597	intron-variant	HCK	GRCh38.p7	20:32088564	TCCCCTCTCCCCCAT[A/G]TAGGAAGCTTGCTGG	3055
rs137937160	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32092399	GTGCTGCTTTCTGGG[C/T]ATCTGAGGGTTCATC	3055
rs137939037	snp	C/G	0.00279162	0.0372561	intron-variant	HCK	GRCh38.p7	20:32053894	CTGCTGCTGCTGATC[C/G]AAGGAGGACACTTTG	3055
rs138051525	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32071500	GATGGAGTGGGTTCC[A/G]TGTGGGGAGGATAAG	3055
rs138053980	snp	C/T	0.00676609	0.0577691	intron-variant	HCK	GRCh38.p7	20:32099546	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT	3055
rs138082119	snp	A/G	0.00874735	0.0655527	intron-variant	HCK	GRCh38.p7	20:32061077	CAACCTCCGCCTCCC[A/G]GGTTCAAGCAATTCT	3055
rs138094245	snp	C/G/T	0.000199845	0.00999424	missense	HCK	GRCh38.p7	20:32071781	CATCCACCATCAAGC[C/G/T]GGTGAGTAGGGGAGG	3055
rs138257227	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32053290	CTGTTTTCACAACTG[C/T]AGGATGGGGAGAGTA	3055
rs138265969	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32073072	GCCACTGCACTCCAG[C/T]CTGGGTGACAGAGTG	3055
rs138308088	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32083855	AGGTGGCAGGCCTCC[A/G]AGATGCCATTCTGAG	3055
rs138328433	snp	A/G	0.00636936	0.0560724	intron-variant	HCK	GRCh38.p7	20:32075341	TGGGACTACAAGTGC[A/G]CATCACCATGCCCAG	3055
rs138396759	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32059433	TCTCTTTCTTTCTTT[C/T]TTCTTTCTTTCTTTC	3055
rs138439763	snp	A/G	0.00318978	0.0398085	intron-variant	HCK	GRCh38.p7	20:32078790	TGAACCCGAGAAGCA[A/G]AGGTTTCAGTGAGCC	3055
rs138471544	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32083627	GATCAGGTAGGGAGG[C/T]GTGAGAACTATTCCC	3055
rs138648125	snp	A/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32094091	GTTGATACTTGTGAG[A/T]GCGATTGGTAAAATG	3055
rs138697586	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32078481	GGAGTTAGACTGCCT[A/G]GCTTCAAATCCTGCC	3055
rs138700944	snp	A/C	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32062892	AATACTTTTTCCCCA[A/C]CCCCATTGCTGAGCT	3055
rs138733283	snp	C/T	0.00716266	0.059414	intron-variant	HCK	GRCh38.p7	20:32087884	CCTGACCTTGTGATC[C/T]GCCCGCCTCAGCCTC	3055
rs138754176	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32067349	TAACTCATTTCATCT[A/G]AAACTCTACACCCAT	3055
rs138807863	snp	A/G	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32100251	TATTGCTATGTTGCC[A/G]GGCTGGTGATTTCCA	3055
rs138876987	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32084313	AGATCCAGTGGACCA[G/T]GTAGGGCGGCCTCCA	3055
rs139002310	in-del	-/AC	0.0333695	0.124785	intron-variant	HCK	GRCh38.p7	20:32097721	AGGGAGAAAACATAT[-/AC]ACACACACACACTCT	3055
rs139063926	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32068733	AGACCAGCCTGAGCA[A/G]CATTGTGAGACCTGC	3055
rs139063978	snp	C/G	0.00597247	0.0543191	intron-variant	HCK	GRCh38.p7	20:32076734	CTAACAGGTTCTTGG[C/G]TGAGGCAGCTGCTGC	3055
rs139128043	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32055374	AGTGTTCAAGAAAAT[A/G]GAAGCATGAACCTTT	3055
rs139129406	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32072517	CATGAGCTATGATCA[C/T]GCCACTGCACTCCAG	3055
rs139198176	snp	C/T	0.00597247	0.0543191	intron-variant	HCK	GRCh38.p7	20:32060493	GGTGATCCGCCTGCC[C/T]CAGCTTCCCAAAGTG	3055
rs139349926	snp	C/T	0.00075039	0.0193554	synonymous-codon	HCK	GRCh38.p7	20:32079855	GGGCTCCTTCATGAT[C/T]CGGGATAGCGAGACC	3055
rs139360896	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32067573	GTCTTATGGTGCTCA[A/G]ACACTTTTACTTCCT	3055
rs139422056	snp	A/G	0.0023933	0.0345097	intron-variant	HCK	GRCh38.p7	20:32095721	TCTGAAAGCCACGGA[A/G]TTATACACTTTAAAT	3055
rs139444548	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32080150	AAGAAACATCCAGCT[A/G]AAGCTTGATCTTCAC	3055
rs139451043	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32073841	CCCATCCCACTCCCC[C/T]TAAGACAGACCTGCC	3055
rs139562019	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32085958	AAGATTAAAGTGGGC[A/G]GTGTATGTGTGTGAC	3055
rs139623106	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32089929	TGAAGGAGTTCAGCC[C/T]ACTCAGCAGGAGCCC	3055
rs139661210	snp	C/G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32076512	CAACCATGGAGGAGG[C/G/T]GTGGCTGGCATTATT	3055
rs139771538	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32085347	GTGAAATCCCGTCTC[G/T]ACGAAAAAATACAAC	3055
rs139900926	snp	A/C	0.0399052	0.1355	intron-variant	HCK	GRCh38.p7	20:32061196	ACCATGTTGGCCAGG[A/C]TGGTCTTGAACTCCT	3055
rs139932512	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32073587	CACACCCAGCATGGT[A/G]AGACGCCTACTTATA	3055
rs139992734	snp	C/G	0.00318978	0.0398085	intron-variant	HCK	GRCh38.p7	20:32061897	GAGACGGAAACCCTG[C/G]GTGGGGGTTGAGCAG	3055
rs140081700	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32059365	CCTTCTCCTCCTCCT[C/T]TTCCTCCTCCTCCAC	3055
rs140130723	snp	G/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32064842	TTTCACTCAGCAGAG[G/T]CTGAGGCGGTGAGGA	3055
rs140200054	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32069231	TGCCACCCTTTCTCA[A/G]AGATGGCCTTGGATT	3055
rs140374401	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32067412	CCAGCCCCTGGCAAC[C/G]ACCATTCTACTTTTT	3055
rs140392783	snp	G/T	4.95209e-05	0.00497574	missense	HCK	GRCh38.p7	20:32099006	TTCAACCCTGCAGGG[G/T]CCAAGTTCCCCATCA	3055
rs140430181	snp	A/C	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32071170	CTGAGCCTGACACTG[A/C]ACTGAGTATTTCCCC	3055
rs140438579	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32059654	TGAGTAGCTGGGATC[A/G]CAGGCACATGCCACC	3055
rs140468269	in-del	-/T	0.104859	0.203554	intron-variant	HCK	GRCh38.p7	20:32092948	TTACTTTGTTTTATC[-/T]TTTTTTTTCTTTTTG	3055
rs140490409	snp	C/G	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32083329	TTCCAGGGTTTAGGG[C/G]ATGACTATCTTGAGG	3055
rs140539414	snp	C/T	0.0232847	0.105357	intron-variant	HCK	GRCh38.p7	20:32087788	CTGGGACTACAGGTG[C/T]CTGCCACCATGCCTG	3055
rs140551218	snp	A/G	0.0115144	0.0749975	intron-variant	HCK	GRCh38.p7	20:32086262	CTGACCTTGTGATCC[A/G]CCCACCTCGGCCCCC	3055
rs140643709	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32059293	ATCTTCCTTCCTTCC[C/T]TCCCTCCCTCCCTCC	3055
rs140676686	snp	G/T	0.00676609	0.0577691	intron-variant	HCK	GRCh38.p7	20:32064382	TTGGAGTCAACTCTA[G/T]CCCAATCCATAAACT	3055
rs140779915	snp	C/G/T	0.00239393	0.0345281	intron-variant	HCK	GRCh38.p7	20:32066554	CTGACCTCAAGTGAT[C/G/T]CACCCACATCAGCCT	3055
rs140843812	snp	C/T	0.00676609	0.0577691	intron-variant	HCK	GRCh38.p7	20:32070445	TTTCAGTGCCTCCAA[C/T]TTCTCTCTAAGCACA	3055
rs140850435	snp	A/G	0.00391504	0.0440703	synonymous-codon	HCK	GRCh38.p7	20:32074623	CCTCATGTCCCTCAG[A/G]TCCGGGGAGTGGTGG	3055
rs140863550	in-del	-/TCTT	0.386123	0.209692	intron-variant	HCK	GRCh38.p7	20:32059419	TTCTTTCTCTCTCTC[-/TCTT]TCTTTCTTTCTTTTT	3055
rs140947730	in-del	-/CAGG	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32063524	AAAGTGCTGGGATTA[-/CAGG]CATGAGCCCCTGCAC	3055
rs140968392	snp	A/G	0.0244538	0.107838	intron-variant	HCK	GRCh38.p7	20:32078096	CTGGAGTGCAGTGGC[A/G]TGATCTCGGCTCACT	3055
rs140996615	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32053836	AGAGTTTCTGATTCA[A/G]TAGCTCTGTGCAGGA	3055
rs141032157	snp	A/G	0.00557542	0.0525036	intron-variant	HCK	GRCh38.p7	20:32057863	ACTGGGAGTTTGAAG[A/G]TACTTTCAGAGGCGT	3055
rs141150727	snp	C/T	0.00078469	0.0197921	synonymous-codon	HCK	GRCh38.p7	20:32073750	CGTGGTTGCCCTGTA[C/T]GATTACGAGGCCATT	3055
rs141245875	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32091648	CCCCCCACTATTCTA[A/G]ACAAAATCAGAGTCT	3055
rs141265857	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32056236	TCTATCTCTGTGGCC[A/G]GGTGCGGTGGCTCAC	3055
rs141363017	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32099215	CAACATGTCCATTCA[A/G]ACTGAGTTCTTGATC	3055
rs141447152	snp	A/T	0.0138799	0.0821421	intron-variant	HCK	GRCh38.p7	20:32087455	CCACACTCAGCTAAT[A/T]TTATTTATTTATTTA	3055
rs141469844	in-del	-/G	0.0926964	0.194308	intron-variant	HCK	GRCh38.p7	20:32081598	TCTACTTGACCCTCA[-/G]GCTATCTGAATTGGC	3055
rs141552134	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32075981	ATTATGGGTTTGGGA[C/T]GCTTGCCTGTTAAAA	3055
rs141629066	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32092619	AATATCTCCCCAACA[C/T]GCTCAGAATAAAATC	3055
rs141638027	snp	C/G	0.000395818	0.0140624	missense	HCK	GRCh38.p7	20:32071744	GCCAGCCCACACTGT[C/G]CTGTGTACGTGCCGG	3055
rs141677926	snp	A/G	1.67396e-05	0.00289301	splice-donor-variant	HCK	GRCh38.p7	20:32084544	GGGAAGTCTGGATGG[A/G]TAAGGACCCAGGGCC	3055
rs141743150	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32063096	TTGACCTACCACTGA[C/G]TAGCCGGGGGACCCA	3055
rs141901266	snp	A/C	0.0437281	0.141251	intron-variant	HCK	GRCh38.p7	20:32068099	GTTGGGAGTTCAAGA[A/C]CAGCCTGACCAACGT	3055
rs142016443	snp	A/G/T	0.0237284	0.106681	intron-variant	HCK	GRCh38.p7	20:32073188	GGCATGTCCCCTGCC[A/G/T]TATGTGGGCCTCCTC	3055
rs142066643	snp	A/G			utr-variant-3-prime	HCK	GRCh38.p7	20:32101543	ACCAGGGCAGGGCCA[A/G]GGGGTGCCCAGGTGG	3055
rs142086248	snp	A/G	0.0023933	0.0345097	intron-variant	HCK	GRCh38.p7	20:32060755	GTTCAAGTCCTTTGA[A/G]AAGCAGACTCCCATA	3055
rs142126874	in-del	-/TATTTATTTATTTATT			intron-variant	HCK	GRCh38.p7	20:32095858	TTTCTGTTAGCCTAA[-/TATTTATTTATTTATT]TATTTATTTATTTAT	3055
rs142160189	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32089354	GAAGCATAGAGCAGA[A/G]GTAAAGTACAGATGT	3055
rs142264240	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32078599	CAGTGGCTCATACCT[A/G]TAATCCCATCACTTT	3055
rs142491977	snp	A/G	0.000153988	0.00877328	missense	HCK	GRCh38.p7	20:32101406	GAGCTCTACAACATC[A/G]TGATGCGCTGCTGGA	3055
rs142517188	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32097001	AAAAAAAATTTAGAC[C/T]GGGCACAGTGGCTCA	3055
rs142614864	snp	C/T	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32058924	TGTCCACCCTGTTCT[C/T]GCTCCTGTCTTTTGT	3055
rs142623249	snp	A/C/T	0.0205846	0.0995907	intron-variant	HCK	GRCh38.p7	20:32061140	AAGCATGCGCCACCA[A/C/T]GCCCAGCTAATTTTT	3055
rs142683546	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32062563	AGTGTGTTGCTCTGT[C/T]GCTCGCCATCGTGTG	3055
rs142693218	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32085305	ATCAATCAAGGTCAG[C/T]AGTTCGAGAAAAACC	3055
rs142718266	snp	A/G	0.00358779	0.0422022	intron-variant	HCK	GRCh38.p7	20:32074498	GCTGACATAGTCACA[A/G]CCCTGTCCTTCACCC	3055
rs142790668	snp	A/G	0.0111196	0.0737302	intron-variant	HCK	GRCh38.p7	20:32061274	GGCGTGAGCCACTGC[A/G]CCCAGCTGCCGTGCC	3055
rs142888866	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32094747	AGAAAGAAAGAAAGA[A/G]AGAAAGAAAGAAAGA	3055
rs142918435	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32064892	GGACGGCAGTGGCCC[A/G]AGGAAGTATCTTTAC	3055
rs142951686	snp	A/T	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32078847	GGGTGACAGAGCAAG[A/T]CTCAGTCTCAAAAAA	3055
rs142986284	in-del	-/TTT	0.20111	0.245173	intron-variant	HCK	GRCh38.p7	20:32059512	CTCTCTCTCTCTCTC[-/TTT]TTTTTTTCTTTTTCT	3055
rs143027777	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32098754	GGGGTATCAGCTGAA[C/T]CAACGAGGAGGATTC	3055
rs143179466	snp	A/G	0.00597247	0.0543191	intron-variant	HCK	GRCh38.p7	20:32070545	CACTGGCTCCTTTGT[A/G]TCATTTAGACCGCAG	3055
rs143242352	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32074019	CTTACTGAGAGTGCA[C/T]GTCCAGCCTGAGATG	3055
rs143308587	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32067808	TGGAGTCATAGCTGA[A/G]ATGTGCTCTAACAGT	3055
rs143312395	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32072403	ATACATTCTTCTTGA[A/G]AATAAAAACACAGGC	3055
rs143375861	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32087492	TATTTTTAGAGACAG[A/G]GTTGCCCTCTGCCTA	3055
rs143450216	snp	C/T	0.00597247	0.0543191	intron-variant	HCK	GRCh38.p7	20:32062306	CAAACCCAGCTCTAT[C/T]TGACTTCAAATCTCA	3055
rs143482626	snp	A/G	0.00676609	0.0577691	intron-variant	HCK	GRCh38.p7	20:32058457	GAATTGCTGGAACCC[A/G]GGAGGCACGGTTGCA	3055
rs143554297	snp	C/G	0.00398564	0.0444627	intron-variant	HCK	GRCh38.p7	20:32067509	AACTCGGTCATAGAG[C/G]AGGAATGTCCTGATG	3055
rs143576683	snp	A/G	0.0134861	0.0810011	intron-variant	HCK	GRCh38.p7	20:32056817	TAAACTCTTCTAGAA[A/G]GTAAATTCTACAAGA	3055
rs143643871	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32059493	TTCTTCTTCTTTCTT[A/G]CTTCTCTCTCTCTCT	3055
rs143693784	snp	C/G	0.0023933	0.0345097	upstream-variant-2KB	HCK	GRCh38.p7	20:32051265	CCCCTCCCCCGACCA[C/G]CTCCCCCAGCTTGGG	3055
rs143761381	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32095873	TATTTATTTATTTAT[A/T]TATTTATTTATTTAT	3055
rs143765697	snp	C/G	0.00279162	0.0372561	intron-variant	HCK	GRCh38.p7	20:32090915	TTTCCCCCACTGGGA[C/G]CACTGGGAGCCACTC	3055
rs143800485	snp	A/G	0.0998734	0.199905	intron-variant	HCK	GRCh38.p7	20:32057457	GTACAAAAATTAGCT[A/G]GGTGTGGTGGCACAT	3055
rs143943816	snp	C/T	0.00438332	0.0466095	intron-variant	HCK	GRCh38.p7	20:32084788	GGGAAGCAGGTGTCA[C/T]GGATGAGGAATCCCT	3055
rs144123944	snp	G/T	0.00557542	0.0525036	intron-variant	HCK	GRCh38.p7	20:32088764	GGTAAAATGTATTGA[G/T]AGCTCAGTATAAAAC	3055
rs144206178	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32086303	AGATTACAGGCGTGA[A/G]CCACTTAGAGCTATT	3055
rs144246321	snp	A/G	0.0919752	0.193722	intron-variant	HCK	GRCh38.p7	20:32064065	CTGGAGTGCAATGGC[A/G]CAATCTCGGCTCACT	3055
rs144261849	snp	A/T	0.00398564	0.0444627	intron-variant	HCK	GRCh38.p7	20:32089932	AGGAGTTCAGCCTAC[A/T]CAGCAGGAGCCCAGG	3055
rs144313088	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32084059	GTGAGTCCCACCCCA[A/G]GGGTGACATCCCCAC	3055
rs144348771	snp	C/T	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32069348	ACAAGGTGCTCAACG[C/T]GCATGGATTGGAAAT	3055
rs144393224	snp	C/T	1.65168e-05	0.00287369	stop-gained	HCK	GRCh38.p7	20:32083998	TTCTACATATCCCCC[C/T]GAAGCACCTTCAGCA	3055
rs144486157	snp	A/C	0.0123036	0.0774623	intron-variant	HCK	GRCh38.p7	20:32077381	AGCAACCAGTTTCTC[A/C]TGAGTCCTCCCAGAT	3055
rs144550500	snp	A/C	0.0252325	0.109451	intron-variant	HCK	GRCh38.p7	20:32080280	CTCGGCTCACTGCAA[A/C]CTCCACCTCCCAGGT	3055
rs144591702	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32058900	GAGAGGTGAGGGAAC[C/T]GGGGTATTTGTCCAC	3055
rs144688047	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32100407	TCGTGACTGGCATAC[A/G]TTGATGAACTGGTGC	3055
rs144688972	snp	A/G	0.000351332	0.0132493	synonymous-codon	HCK	GRCh38.p7	20:32101432	CTGGAAAAACCGTCC[A/G]GAGGAGCGGCCGACC	3055
rs144868485	snp	G/T	0.00318978	0.0398085	intron-variant	HCK	GRCh38.p7	20:32062694	CTCTATGAGAAAGAA[G/T]CTGAGGCTCAGTAAA	3055
rs144900300	snp	C/T	0.0460142	0.144533	intron-variant	HCK	GRCh38.p7	20:32061962	TTTTTTTTTTTGAGA[C/T]GGACTCTCACTCTGT	3055
rs144911828	snp	A/G	0.0275645	0.114116	intron-variant	HCK	GRCh38.p7	20:32066464	TTACAGGTGTGCGCC[A/G]CCACACCTGGCTAAT	3055
rs144930136	snp	A/C	0.00517822	0.0506191	intron-variant	HCK	GRCh38.p7	20:32067293	CAGTGGTATTCAATC[A/C]ATTCAGCATGTTGTG	3055
rs144959021	snp	A/G	0.00517822	0.0506191	intron-variant	HCK	GRCh38.p7	20:32064387	GTCAACTCTATCCCA[A/G]TCCATAAACTGAGAC	3055
rs144976144	snp	C/G	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32081070	CTCCAGCCTGGGCAA[C/G]AGAGCAAGACCCCAT	3055
rs145177360	snp	A/G	0.0134861	0.0810011	upstream-variant-2KB	HCK	GRCh38.p7	20:32051909	TAGACGGGCGGGTTC[A/G]AATCCCTAGGAGTGG	3055
rs145242092	in-del	-/AGC	0.0494327	0.149241	intron-variant	HCK	GRCh38.p7	20:32064653	GCAGGTTTCTGCTTA[-/AGC]AGCATAGAAGCTCCC	3055
rs145246383	snp	G/T	0.00358779	0.0422022	intron-variant	HCK	GRCh38.p7	20:32081063	CACTAGACTCCAGCC[G/T]GGGCAACAGAGCAAG	3055
rs145282137	snp	C/T	0.00597247	0.0543191	intron-variant	HCK	GRCh38.p7	20:32085454	AGGAGGTGGAAGTTG[C/T]AGGGAACCGAGATCG	3055
rs145348032	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32058641	ACACACACACACACA[C/T]ACACACACTAGTCCA	3055
rs145351518	in-del	-/TG	0.103438	0.202533	intron-variant	HCK	GRCh38.p7	20:32055178	TGTCACACTCCCCTT[-/TG]TGTGTGAGAGGAGTA	3055
rs145407551	snp	A/G	0.0103295	0.0711199	intron-variant	HCK	GRCh38.p7	20:32060376	CAGGCACCCACTACC[A/G]CGCCCAGCTAATTTT	3055
rs145436208	snp	A/G	6.7104e-05	0.00579202	synonymous-codon	HCK	GRCh38.p7	20:32086707	GGCCTTCCTGGCAGA[A/G]GCCAACGTGATGAAA	3055
rs145449353	in-del	-/TTTT			intron-variant	HCK	GRCh38.p7	20:32064018	TTTTTTTTTTTTTTT[-/TTTT]GAGATAGAGTCTCTC	3055
rs145509465	snp	C/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32062100	ATGCGCCACCATGCC[C/T]GCCTAATTTTTGTAT	3055
rs145543439	snp	C/G	0.00597247	0.0543191	intron-variant	HCK	GRCh38.p7	20:32099542	TTTGTATTTTTAGTA[C/G]AGACGGGGTTTCACC	3055
rs145545151	snp	A/G	0.00716266	0.059414	upstream-variant-2KB	HCK	GRCh38.p7	20:32050446	TCTGTTTTTATAAAA[A/G]GCACATACAGACTAG	3055
rs145632103	snp	C/T	3.29777e-05	0.00406051	missense	HCK	GRCh38.p7	20:32093980	GACTTTGGCCTGGCC[C/T]GGGTCATTGAGGACA	3055
rs145693889	snp	A/G	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32100588	GTTGACTTAAATATA[A/G]AGACATCCAAGTAAA	3055
rs145738671	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32094764	GAAAGAAAGAAAGAA[A/G]GAAAGAAAGAAAGAG	3055
rs145833354	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32060955	CTTGGACTGCCATGC[C/T]GTATTTTTTTTTTGT	3055
rs145864344	snp	A/G	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32090716	TCATGAAATCTCACC[A/G]CCTTTATCAACCCGC	3055
rs145895392	snp	C/T	0.00398564	0.0444627	intron-variant	HCK	GRCh38.p7	20:32062088	GGGATTACAGGCATG[C/T]GCCACCATGCCCGCC	3055
rs145919024	snp	G/T	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32083404	GGACTGGATTTCTGG[G/T]TTTTTTTCCAGAAAA	3055
rs145967888	snp	C/T	0.00755907	0.0610114	intron-variant	HCK	GRCh38.p7	20:32074778	AAAGCCAGCCTTGTT[C/T]GCAACTCAGGACGTC	3055
rs146000608	snp	C/T	0.13446	0.221699	intron-variant	HCK	GRCh38.p7	20:32061157	CCCAGCTAATTTTTG[C/T]ATTTTTAGTAGAGAC	3055
rs146205781	snp	A/C	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32076706	TCCACTGTCAGATTC[A/C]GAATGTGCATTTCTA	3055
rs146249289	snp	C/T	0.00438332	0.0466095	intron-variant	HCK	GRCh38.p7	20:32094428	CTCACGCCTGTAATC[C/T]CAGCACTTTAGGAGG	3055
rs146350710	snp	C/T	0.000399281	0.0141238	synonymous-codon	HCK	GRCh38.p7	20:32073735	CTCTGAGGACATCAT[C/T]GTGGTTGCCCTGTAT	3055
rs146372860	snp	C/G/T	3.29538e-05	0.00405904	missense, stop-gained	HCK	GRCh38.p7	20:32074645	GAGTGGTGGAAGGCT[C/G/T]GATCCCTGGCCACCC	3055
rs146551076	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32090216	GCTGGGCAGCAGTCA[C/T]CGACCAGGGCAAGAG	3055
rs146570583	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32055949	GTGTCTAGCTTCTTC[C/T]ACTTAACATAATGTT	3055
rs146578227	in-del	-/AAAAGA			intron-variant	HCK	GRCh38.p7	20:32094700	AAAAGAAAAGAAAAG[-/AAAAGA]AAAGAAAGAAAGAAA	3055
rs146651984	snp	C/T	0.00279162	0.0372561	intron-variant	HCK	GRCh38.p7	20:32070597	CAGGCCTTCCCCAAA[C/T]GCCCTGCCTAAAAGA	3055
rs146670822	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32074090	TGCGATTAAGCCACC[A/G]GCTTTACCTGTGGAC	3055
rs146774165	snp	C/T	0.00716266	0.059414	intron-variant	HCK	GRCh38.p7	20:32057138	GTGCTCTTCAGACAA[C/T]CTCAGTGGAGCTGGG	3055
rs146786846	snp	C/T	0.00597247	0.0543191	intron-variant	HCK	GRCh38.p7	20:32060492	AGGTGATCCGCCTGC[C/T]TCAGCTTCCCAAAGT	3055
rs146791805	snp	C/T	0.0209421	0.100162	intron-variant	HCK	GRCh38.p7	20:32059617	CCTCCTGCGCTCAAG[C/T]GATCCTCCCACCTCA	3055
rs146805025	in-del	-/TTC/TTCA/TTTC			intron-variant	HCK	GRCh38.p7	20:32059422	TTTCTCTCTCTCTCT[-/TTC/TTCA/TTTC]TTCTTTCTTTTTTCT	3055
rs146953797	snp	A/G	0.0146672	0.084371	intron-variant	HCK	GRCh38.p7	20:32092113	TTGAGAAGCCGGCCG[A/G]TGGTGCTTTGATTGT	3055
rs146970146	snp	A/G	0.0162398	0.0886349	intron-variant	HCK	GRCh38.p7	20:32097222	GAGGTTGAGGCTGCA[A/G]TGAGCCAAGATCATG	3055
rs146970405	snp	A/C	0.00279162	0.0372561	intron-variant	HCK	GRCh38.p7	20:32058031	CCCTGAGTTCCAGGC[A/C]TCACCCTGAAATCCT	3055
rs146996549	snp	A/G/T	0.000153988	0.00877328	missense	HCK	GRCh38.p7	20:32071753	CACTGTCCTGTGTAC[A/G/T]TGCCGGATCCCACAT	3055
rs147052999	snp	C/T	0.0185938	0.0946107	intron-variant	HCK	GRCh38.p7	20:32075340	CTGGGACTACAAGTG[C/T]GCATCACCATGCCCA	3055
rs147074745	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32077873	CTGTAGATGTCCTAC[C/T]GTCCATTTAACCTCT	3055
rs147110347	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32083813	GGTGCCAGCGGTAGC[C/T]TTACAGGGTGTCAGA	3055
rs147230209	snp	A/G	0.0123036	0.0774623	intron-variant	HCK	GRCh38.p7	20:32054566	AATCCCAGCACTTTG[A/G]GAGGCTGAGCCGGGC	3055
rs147265361	snp	A/C	0.00318978	0.0398085	intron-variant	HCK	GRCh38.p7	20:32062509	GAGCCAGCCCTATGG[A/C]TCAGCCAGGCAAATG	3055
rs147325498	snp	C/T	0.00398564	0.0444627	intron-variant	HCK	GRCh38.p7	20:32100621	AAGCACTTGAGTTCA[C/T]GAGTTTGGAGTTTGA	3055
rs147341816	snp	A/G	0.00835141	0.0640778	intron-variant	HCK	GRCh38.p7	20:32085318	AGCAGTTCGAGAAAA[A/G]CCTGGATAGTATAGT	3055
rs147358493	snp	C/T	0.00874735	0.0655527	intron-variant	HCK	GRCh38.p7	20:32088154	CAGGTGATCCTCTCA[C/T]CTCGGTCTCCTAAAG	3055
rs147374574	snp	A/G	0.00716266	0.059414	intron-variant	HCK	GRCh38.p7	20:32053573	AACCTGGGAGGTGGA[A/G]GTTGCGGTGAGCCGA	3055
rs147458167	snp	C/T	0.0364509	0.129988	intron-variant	HCK	GRCh38.p7	20:32073040	GAGAGGTGGAGGTTT[C/T]GGTGAGCTGAGATCA	3055
rs147546066	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32068852	AGGAGGCTGAGGTGG[A/G]AGGATCACTTGATCC	3055
rs147586921	snp	A/G	0.00438332	0.0466095	intron-variant	HCK	GRCh38.p7	20:32097568	CTGGGCAAACAGAGC[A/G]AGACCCTGTCTCAAA	3055
rs147712671	snp	C/G	0.00597247	0.0543191	intron-variant	HCK	GRCh38.p7	20:32091046	ACAGAGAAGAAAAGT[C/G]AGGTACAGAGAGATG	3055
rs147811714	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32075260	TGCAGTAGCACCATC[A/G]CAGCTCACTTCAGCC	3055
rs147876395	snp	A/G	1.67902e-05	0.00289738	synonymous-codon	HCK	GRCh38.p7	20:32084422	CTGCCAGAAACTGTC[A/G]GTGCCCTGCATGTCT	3055
rs147906206	snp	C/G	0.000659348	0.0181449	missense	HCK	GRCh38.p7	20:32071735	GAAACCAGCGCCAGC[C/G]CACACTGTCCTGTGT	3055
rs147933931	snp	A/G	0.00358779	0.0422022	intron-variant	HCK	GRCh38.p7	20:32062003	GGACTGCAGTGGTGC[A/G]ACCTCGGCTCCCTGC	3055
rs147950255	snp	A/G	0.0189856	0.0955633	intron-variant	HCK	GRCh38.p7	20:32064669	AGCATAGAAGCTCCC[A/G]GAAAACCATCTCCAG	3055
rs148027194	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32067757	TGCATGTTTGCATAT[A/G]GTGGCTCTGAGCCAC	3055
rs148149505	snp	G/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32057810	CACCAACCACATGTT[G/T]GTCCCCACCCCATTT	3055
rs148201037	snp	C/G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32084961	TGTGCCCAGCACTGT[C/G/T]AGGGTCTTGTGGGAA	3055
rs148202112	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32060994	TTCTGTTTTATTTTG[G/T]TTTTTTTGAGACAGA	3055
rs148264751	snp	A/G	0.000214332	0.0103499	missense	HCK	GRCh38.p7	20:32073335	GGCCTAATAGCCACA[A/G]CAGCAACACACCAGG	3055
rs148271123	in-del	-/AC/ACAC/ACACAC			intron-variant	HCK	GRCh38.p7	20:32058605	TCCTTTTATGTCAAA[-/AC/ACAC/ACACAC]ACACACACACACACA	3055
rs148430914	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32079494	ACTTGTTAATGCTGT[A/G]TTATTTTTCTTAAAG	3055
rs148462106	snp	A/G	0.0103295	0.0711199	intron-variant	HCK	GRCh38.p7	20:32058901	AGAGGTGAGGGAACC[A/G]GGGTATTTGTCCACC	3055
rs148504189	snp	A/G	0.00716266	0.059414	intron-variant	HCK	GRCh38.p7	20:32100418	ATACGTTGATGAACT[A/G]GTGCTACGTTTCAAA	3055
rs148520337	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32061273	AGGCGTGAGCCACTG[C/T]GCCCAGCTGCCGTGC	3055
rs148691315	snp	A/C	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32077112	AAAAATAACAAATGA[A/C]TACACATATGTGTCC	3055
rs148760942	snp	A/C	0.00129954	0.0254575	intron-variant	HCK	GRCh38.p7	20:32069777	GTAAATAAAAGGAAT[A/C]TTTTTTCATTTTTAA	3055
rs148820354	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32074279	TCTCCCCTATTCTCA[A/G]CCCCAGCTGAACCAT	3055
rs148830301	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32065058	GACCTCAGGCCAAGC[C/T]TGAGAAGCAAGGCCT	3055
rs148834847	snp	A/G	0.0189856	0.0955633	intron-variant	HCK	GRCh38.p7	20:32062146	GGTTTCACCATGTTG[A/G]TCAGGCTGGTCTCCA	3055
rs148955373	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	HCK	GRCh38.p7	20:32050925	TCATTCACAGGACAG[A/T]CCCCCGCAACAAAGA	3055
rs149013056	snp	C/T	0.0119091	0.0762411	intron-variant	HCK	GRCh38.p7	20:32057397	CTGAGCTCAGGAGTT[C/T]GAGACCAGCCTGGGT	3055
rs149047829	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32097899	AAGGATAACTATGCC[A/C]GGTGCGGTGGCTCAC	3055
rs149121640	snp	A/G	0.000115427	0.00759606	missense	HCK	GRCh38.p7	20:32073320	TTTCTTCCCCACAGG[A/G]GCCTAATAGCCACAA	3055
rs149170942	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32081183	ATGAGGTAGGATGAG[A/G]TCGCCAGAAGAGACT	3055
rs149203169	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32060486	GACCTCAGGTGATCC[A/G]CCTGCCTCAGCTTCC	3055
rs149327631	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32058794	GAACAGGAGGTAGTC[A/C]TTAAAGGTGTCTTCT	3055
rs149369737	snp	A/G	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32100394	AGGGTGGTGGCATTC[A/G]TGACTGGCATACGTT	3055
rs149487671	snp	C/T	0.00475932	0.048549	synonymous-codon	HCK	GRCh38.p7	20:32084401	TCCAGAGGGGAACGA[C/T]GGGCTCTGCCAGAAA	3055
rs149546072	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32088720	ATATTTACTGACCAC[A/C]TACTATGATGATAGC	3055
rs149562095	snp	C/T	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32075618	TCAAGGAGCTCTCCA[C/T]AACCCATCGTTCTTG	3055
rs149620250	snp	C/T			synonymous-codon	HCK	GRCh38.p7	20:32083919	TTTGTCCGTGCGAGA[C/T]TACGACCCTCGGCAG	3055
rs149806714	snp	A/C	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32085978	ATGTGTGTGACATAA[A/C]CTGAGTAGTGTTTTA	3055
rs149822623	snp	C/T	0.00676609	0.0577691	intron-variant	HCK	GRCh38.p7	20:32073591	CCCAGCATGGTGAGA[C/T]GCCTACTTATACTTG	3055
rs149859280	snp	C/T	0.00676609	0.0577691	intron-variant	HCK	GRCh38.p7	20:32090367	GGCTTTGGTCTTCAC[C/T]TCCAGACTCAGAGAG	3055
rs149874978	snp	A/C/T	0.00875054	0.0656008	intron-variant	HCK	GRCh38.p7	20:32076795	CCACTGATCTAAATA[A/C/T]GCATATCTGGCCAGG	3055
rs150009044	in-del	-/GTGG			intron-variant	HCK	GRCh38.p7	20:32093508	TGTGTGTGTGTGTGT[-/GTGG]GTGTGTGTGTGTGTG	3055
rs150017973	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32055466	ATTAACATAATTAGT[A/G]TAATGCTACACATAG	3055
rs150026806	snp	C/T	3.29701e-05	0.00406005	synonymous-codon	HCK	GRCh38.p7	20:32083910	AAGCTACTCTTTGTC[C/T]GTGCGAGACTACGAC	3055
rs150049488	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32069282	TGAGACCCCTCCCTC[A/G]GGACCCTGTGGCCAT	3055
rs150053196	snp	A/G	0.0368353	0.130617	intron-variant	HCK	GRCh38.p7	20:32096172	TGGGATTACAGATGC[A/G]AGCCACTGTGCCAGT	3055
rs150069066	snp	G/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32059873	TACTAGGTGGTAAAA[G/T]GTCATTTTAAAAATA	3055
rs150178388	snp	G/T	0.00279162	0.0372561	intron-variant	HCK	GRCh38.p7	20:32093626	AGTGCTCTCTGGAAG[G/T]CTTGGAATTCTAGAG	3055
rs150245476	snp	G/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32084253	CGTCACACTCTGCTT[G/T]CTTGGGAATGTCTCT	3055
rs150315881	snp	A/C	0.0275645	0.114116	intron-variant	HCK	GRCh38.p7	20:32066378	GTGCAGTGGCACGAT[A/C]TTGGCTCACTGCAAC	3055
rs150367794	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32071396	TAAACATCCATCACG[C/T]TGGTCCTTGGTACCC	3055
rs150388534	snp	A/G	0.0023933	0.0345097	intron-variant	HCK	GRCh38.p7	20:32061023	GAGTCTTGCTCTGTT[A/G]CCCAGGCTGGAGTGC	3055
rs150457303	snp	A/G	0.00279162	0.0372561	intron-variant	HCK	GRCh38.p7	20:32053200	GTGAGAGACAGGCTA[A/G]TGGGTAGCGGAGGGG	3055
rs150515325	snp	A/G	0.0023933	0.0345097	intron-variant	HCK	GRCh38.p7	20:32080045	CTGGGGAGGGTTGAG[A/G]CTCTGTGCCTGGCTC	3055
rs150687506	snp	A/G	0.00398564	0.0444627	intron-variant	HCK	GRCh38.p7	20:32073266	ACACAGACCTTCCAC[A/G]GGTCCCCACACATTG	3055
rs150760216	snp	C/T	0.00398564	0.0444627	intron-variant	HCK	GRCh38.p7	20:32089594	ATAATGTTCACAAAT[C/T]GCAAAAACACTGCTG	3055
rs150862806	snp	A/G	0.00438332	0.0466095	intron-variant	HCK	GRCh38.p7	20:32063354	ACCTCCCAGGCTCAA[A/G]TGATCCTCCCACCTC	3055
rs151026457	snp	G/T	0.00279162	0.0372561	intron-variant	HCK	GRCh38.p7	20:32061367	CCCCCAGACATGGGT[G/T]GGCTTCGGTCTCCCT	3055
rs151045621	snp	A/C/G	0.00156507	0.0279304	missense	HCK	GRCh38.p7	20:32071703	TCCAGGTCGGAGGCA[A/C/G]TACATTCTCAAAAAC	3055
rs151054795	snp	C/T	6.59348e-05	0.00574135	missense	HCK	GRCh38.p7	20:32088628	CATTGCCAAAACTCA[C/T]TGACTTCTCAGCCCA	3055
rs151061044	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32077974	TTCTCCCTTGTGCAA[A/G]GTCTATGGGATAACT	3055
rs151236075	snp	C/T	0.00517822	0.0506191	intron-variant	HCK	GRCh38.p7	20:32095372	GCGATTCTTGTGCCT[C/T]AGCCTTCTGAGTAGC	3055
rs151257501	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32083245	TGGAATAATCTCCCC[A/G]TCTCCAGATCCTTAA	3055
rs180770907	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32062570	TGCTCTGTCGCTCGC[C/T]ATCGTGTGAGCCAGG	3055
rs180804717	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32100400	GTGGCATTCGTGACT[A/G]GCATACGTTGATGAA	3055
rs180823818	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32083704	ATGGCCAAGGTCTCA[C/T]GGGTGGATGTGGTAG	3055
rs180943454	snp	C/G	0.00358779	0.0422022	intron-variant	HCK	GRCh38.p7	20:32096253	CCTGTAATACCAGCA[C/G]TTTGGGAGGCCAAGG	3055
rs180964213	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32080330	CAGCCTTCCAAGTAG[C/T]TGGGATTACAAGTGC	3055
rs181079478	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32087387	TAACTCCTGGGCTCA[A/G]GTGATCCTCCCACCC	3055
rs181086742	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32058828	CCCAGTTACCACTGC[A/G]GGCACCTGGAGCTCA	3055
rs181147151	snp	A/G	0.0023933	0.0345097	intron-variant	HCK	GRCh38.p7	20:32068261	GGAGATGGCACCACC[A/G]TACTCCAGCCTGGGC	3055
rs181212241	snp	C/T	0.0023933	0.0345097	intron-variant	HCK	GRCh38.p7	20:32084801	CATGGATGAGGAATC[C/T]CTCCCTCATACGGAG	3055
rs181224568	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32100498	AAGGATGATTACCCT[A/G]GCTTTGCACCACAGG	3055
rs181301173	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	HCK	GRCh38.p7	20:32051750	GTTAGAATCCACTGA[A/G]GTGAGAGTTCGGATC	3055
rs181314683	snp	C/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32073523	ATTGTGTTTCTAGAA[C/T]GCTGTTTAGTAACAT	3055
rs181374537	snp	C/T	0.0023933	0.0345097	intron-variant	HCK	GRCh38.p7	20:32064064	GCTGGAGTGCAATGG[C/T]GCAATCTCGGCTCAC	3055
rs181412607	snp	C/T	0.00874735	0.0655527	intron-variant	HCK	GRCh38.p7	20:32090598	TCCATAGGATTCAGT[C/T]GGAAGAGCTCTACAG	3055
rs181532658	snp	A/G	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32057325	AACATGAAGGGCTGG[A/G]TGCGGTGGCTCACCC	3055
rs181535628	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32078920	TCCATAGAGCTGTTG[G/T]GTGGATAGCAAGATA	3055
rs181577847	snp	G/T	8.24463e-05	0.00642	missense	HCK	GRCh38.p7	20:32093920	CACCGAGACCTCCGA[G/T]CTGCCAACATCTTGG	3055
rs181700206	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32091450	CAAAAGTGCCTCCTC[C/T]AAAGCACATGGTAAA	3055
rs181720208	snp	C/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32087742	CACCTACCAGGTTCA[C/T]GCCATTCTCCTGCCT	3055
rs181819688	snp	C/G	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32052925	GCCAGCTTGGGGAAG[C/G]GGGTAGTTGGGCGGA	3055
rs181823796	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32074121	CAGGCCCCATCGAGT[C/T]GACCTTGCATTTGGA	3055
rs181863786	snp	A/G	0.00318978	0.0398085	intron-variant	HCK	GRCh38.p7	20:32069097	CCGGGGCAGTGTCAC[A/G]TCTGCCAGTAAACAG	3055
rs181897135	snp	A/T	0.0174175	0.0916809	intron-variant	HCK	GRCh38.p7	20:32068001	TGTAAAAATTTTTTT[A/T]AAAATGAAAAATAGG	3055
rs181987462	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32100156	CAAACGATCCTCCAG[C/G]CTTGGCCTCCCAAAA	3055
rs181994186	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32061764	AAGAAGAGCAAGGAG[G/T]GCTCCAGTGGAATGA	3055
rs182123702	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32079153	CTCAATATTCAGGAA[G/T]AATGAAGAAAATGTC	3055
rs182240878	snp	C/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32083221	TACACTGGGGCTACC[C/T]GGATCATCTGGAATA	3055
rs182262778	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32065943	AATGTTCACATGAAT[A/C]GCCTGGGAACCTTGT	3055
rs182274477	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32085933	CTGGCATTTATTTAA[C/G]AGCAGTGTTAAGATT	3055
rs182431300	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32094742	AAGAAAGAAAGAAAG[A/G]AAGAAAGAAAGAAAG	3055
rs182432721	snp	G/T	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32058004	GCTCCTGACTCTCCC[G/T]TCGAGTCACCTCCCT	3055
rs182533168	snp	A/T	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32092368	AAAGAGCTCAAGCCC[A/T]GTTTGTAAACCAAAA	3055
rs182544176	snp	A/G	0.000324517	0.0127339	intron-variant, utr-variant-5-prime	HCK	GRCh38.p7	20:32054250	TTACAGTCCTTCCAG[A/G]ATGTGCCTCTGAAAA	3055
rs182560681	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32053900	CTGCTGATCCAAGGA[A/G]GACACTTTGAGAACC	3055
rs182597901	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32075722	CATCCATCCATCCAT[C/T]CATCCATCCATCCAT	3055
rs182715825	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32070375	CTACAGGATATGGTG[A/G]CCTTGTCACAACCAC	3055
rs182734932	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32071569	CCAGTGGGAGCCAGC[C/T]CGGGGGCAGGGGACC	3055
rs182845541	snp	A/G	0.00318978	0.0398085	intron-variant	HCK	GRCh38.p7	20:32059745	GGTCTTAAATTCCTC[A/G]GCTCAAACGATCCTC	3055
rs182852728	snp	A/G	0.00016475	0.00907457	missense	HCK	GRCh38.p7	20:32074661	GATCCCTGGCCACCC[A/G]GAAGGAGGGCTACAT	3055
rs182854790	snp	A/T	0.00557542	0.0525036	intron-variant	HCK	GRCh38.p7	20:32081371	GTAGCTCAAACTGGC[A/T]TCGATTGAGGCTCAT	3055
rs182860586	snp	C/T			upstream-variant-2KB	HCK	GRCh38.p7	20:32050199	AGGACGATAAGGGGA[C/T]GTGTATGAGGATGTC	3055
rs182869393	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32096972	TATTATTTCATGTAC[A/G]TTATAACTCGATTAA	3055
rs182955378	snp	A/G	8.25117e-05	0.00642254	intron-variant	HCK	GRCh38.p7	20:32088658	AGGTGAGAGCCTAAC[A/G]AGGAAACGGGGAAGG	3055
rs182978462	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32076785	AGCTTGGGAACCACT[C/G]ATCTAAATACGCATA	3055
rs183255618	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32088914	CTTGAAACAACAGCA[A/G]TTGTTATTTCTCATG	3055
rs183324585	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32092946	TTGTTACTTTGTTTT[A/G]TCTTTTTTTTCTTTT	3055
rs183386953	snp	C/G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32069473	GCTGACCAAAACACA[C/G/T]GAAATGTGATATAAT	3055
rs183456603	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32087972	TAGAGACAAGGTCTC[A/G]CCATCTTGCCCCAGC	3055
rs183460221	snp	A/G	0.0023933	0.0345097	intron-variant	HCK	GRCh38.p7	20:32068159	AAAAATTAGCCAGGC[A/G]TAGTGGCACATGCCT	3055
rs183465478	snp	A/G	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32086861	ATACTGGTCAATTGC[A/G]GGCCCAAGGGTGGCT	3055
rs183573240	snp	C/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32064923	CAGGGATCAGCAGTT[C/T]TGAGTGGGTGTGCAA	3055
rs183585741	snp	C/T	0.00279162	0.0372561	downstream-variant-500B	HCK	GRCh38.p7	20:32102060	CCCAGGAGGTCGAGG[C/T]CACAGTGAGCTATGA	3055
rs183806453	snp	C/T	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32085198	AAAATCCATGTATTT[C/T]GACTGTATTTATTGC	3055
rs183892364	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32061127	TAGCTAGGATTACAA[A/G]CATGCGCCACCACGC	3055
rs183949714	snp	C/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32098082	AGACGGAGTCTGACT[C/G]TATCATCCAGGCTGG	3055
rs183975238	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32081490	ACTGCTTGACTCAAA[C/T]AAGCCAAGTATATTG	3055
rs184089554	snp	C/G	0.000453034	0.0150437	intron-variant	HCK	GRCh38.p7	20:32093827	TCTTGGCGTAGGCCA[C/G]GTCTGAGGACAAAGG	3055
rs184099313	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32097446	TAGCCAGGCGTGGTG[A/G]CGGGCACCTGTAGTC	3055
rs184116804	snp	A/G	0.00318978	0.0398085	intron-variant	HCK	GRCh38.p7	20:32093316	ACCTGTTCAAGCAAC[A/G]TGTCTGGCACCCACA	3055
rs184127693	snp	G/T	0.00557542	0.0525036	intron-variant	HCK	GRCh38.p7	20:32061036	TTGCCCAGGCTGGAG[G/T]GCAGTGGCGCAGTCT	3055
rs184135101	snp	C/T	0.0158469	0.0875917	intron-variant	HCK	GRCh38.p7	20:32056394	TGTGGTGGGCGCCTG[C/T]AGTCCCAGCTACTCG	3055
rs184233137	snp	A/T	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32057214	TTGCCAGGCCCACTT[A/T]CCTCATCCGCAGAAC	3055
rs184238085	snp	G/T	0.00318978	0.0398085	intron-variant	HCK	GRCh38.p7	20:32078799	GAAGCAGAGGTTTCA[G/T]TGAGCCCAGATCACA	3055
rs184284107	snp	C/T	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32077803	TGCTGGGATTACAGG[C/T]GTGAGCCACTGCTCC	3055
rs184382529	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32099851	CCTATTCTCCACTTG[A/C]AGCCAGAAGGATAAT	3055
rs184537004	snp	A/C	0.000379147	0.0137633	missense	HCK	GRCh38.p7	20:32073330	ACAGGGGCCTAATAG[A/C]CACAACAGCAACACA	3055
rs184658269	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	HCK	GRCh38.p7	20:32051469	AGGGCCGGGCCAGAA[A/G]GGAGGGGTCGGAGTG	3055
rs184676234	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32090265	AGAGGGGAAAACAAA[A/C]CAAGGGAGGAAAAGA	3055
rs184718329	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32094513	AGGAAGACCTAGTCT[C/T]TACAAAAATTTAAGA	3055
rs184720453	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32078954	GTTAACTTCCTCCCC[A/G]GTTGATAACAGAGGA	3055
rs184757074	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32072955	AAAATACAAAATTAG[C/T]CAGGCATGGTGGCAT	3055
rs184762602	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32089979	TGAGACCCTGCCTGG[A/G]CCTCAGCTGGGCCTG	3055
rs184789138	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	HCK	GRCh38.p7	20:32050715	TAGGCTAAAGAGAAG[A/G]AAAAAAGGCCCATAC	3055
rs184829317	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32086317	AGCCACTTAGAGCTA[C/T]TTTTAAATCCTTGCA	3055
rs184980079	snp	G/T	0.0494327	0.149241	intron-variant	HCK	GRCh38.p7	20:32066351	GAGTCTTGCTCTGTT[G/T]CCCAGGCTGGAGTGC	3055
rs185016898	snp	A/G	0.00557542	0.0525036	intron-variant	HCK	GRCh38.p7	20:32061212	TGGTCTTGAACTCCT[A/G]ACCTTGTGATTCGCC	3055
rs185085671	snp	A/C	0.00557542	0.0525036	intron-variant	HCK	GRCh38.p7	20:32082649	TCTGACACACACACA[A/C]AAAAAATAAAGTTTA	3055
rs185165863	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32088258	AATCCCATTTAGTGC[A/G]ATTTGAAACCTCAAG	3055
rs185220836	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32062699	TGAGAAAGAAGCTGA[A/G]GCTCAGTAAAGGGAA	3055
rs185229488	snp	A/G	0.00279162	0.0372561	intron-variant	HCK	GRCh38.p7	20:32083839	TCAGAGTGCTAATGC[A/G]AGGTGGCAGGCCTCC	3055
rs185250795	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32100448	AAGGAGAAAAGATCT[A/G]ACTTGCTGACTTAGG	3055
rs185289983	snp	C/T	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32067842	ATCCACACTGAGATG[C/T]GAAGGCTTAGTACAA	3055
rs185375515	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32080993	ACTCAGAAGGGTGAG[A/G]CCAGATGATCTCTTG	3055
rs185402060	snp	G/T	0	0	intron-variant	HCK	GRCh38.p7	20:32096827	TTAAGTAAGGGGGTA[G/T]TAACTGGAAGGACGC	3055
rs185418864	snp	A/G	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32059564	TCTGTCTCCCAGGCT[A/G]GAGTGCAGTGATGCT	3055
rs185469906	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32086495	CTAAGCCCATGATTT[C/T]GCTTCCCTCTCTGAG	3055
rs185491141	snp	C/T	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32083244	CTGGAATAATCTCCC[C/T]GTCTCCAGATCCTTA	3055
rs185598792	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32100193	GATTACAGACACACA[C/T]CACCATGCCCAGCTA	3055
rs185756481	snp	A/G	0.0107246	0.0724382	intron-variant	HCK	GRCh38.p7	20:32061983	CTCACTCTGTTGCCC[A/G]GGCTGGACTGCAGTG	3055
rs185819084	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32094869	GAAAGAAAGAGGCAC[A/G]AGCCAATGCTAAATG	3055
rs185904737	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime	HCK	GRCh38.p7	20:32052329	AGGACGAGAAACGCC[C/G]GCGGCACCAAAGCCC	3055
rs185915003	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32073605	ACGCCTACTTATACT[C/T]GGAACCACATATCGA	3055
rs185921631	snp	G/T	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32090653	CTCCCTGATACTCTT[G/T]GGAAGCAAACCCAAG	3055
rs185961479	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32079267	TATATGCGGAGGAGG[A/T]TTGGTTGTAAAGCTA	3055
rs185981301	snp	C/T	0.00277172	0.0371238	intron-variant	HCK	GRCh38.p7	20:32074734	GGAGTAAGTATCCTA[C/T]TTCCTACCTTCCAGA	3055
rs186118711	snp	C/G	0.00279162	0.0372561	intron-variant	HCK	GRCh38.p7	20:32092525	TAAGAATCCTCCACG[C/G]AGTCTGTTAGTCACT	3055
rs186252870	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32053994	GGTTTTCTCTTTATG[G/T]TCCTTTTTTTTTTAG	3055
rs186255936	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32069308	GCCATCTTGAATATG[C/T]ACATTGATCACGTAA	3055
rs186299533	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32087396	GGCTCAAGTGATCCT[C/T]CCACCCCAGCCCCCC	3055
rs186361342	snp	A/G	0.00517822	0.0506191	intron-variant	HCK	GRCh38.p7	20:32091550	GTTAACTGTTCATCT[A/G]AGGACTCATAAATTT	3055
rs186396225	snp	A/G	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32074397	GACCCAGGGCTCTGG[A/G]CTGTGGACAGGGAGA	3055
rs186439907	snp	A/C/G	0.00159649	0.0282165	intron-variant	HCK	GRCh38.p7	20:32068753	GTGAGACCTGCCCCC[A/C/G]CTCTCTGCCCCCTGT	3055
rs186590248	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32100906	ACTCCCAATCTTCCA[C/T]TGGTGACTGGTTAGT	3055
rs186631426	snp	C/T	0.00398564	0.0444627	intron-variant	HCK	GRCh38.p7	20:32064367	CTCTACAGCCAGGGG[C/T]TGGAGTCAACTCTAT	3055
rs186828891	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32066088	GCATTTCTAAACTCA[C/T]TCAAACCACTTTGTC	3055
rs186833714	snp	C/T	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32086209	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCGTGT	3055
rs186859057	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32084917	GATTTCCAGGCAACT[A/G]ATGAACAGGTTATTC	3055
rs187130221	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32053746	AGCTAGACATATGGC[C/T]CCGTGTTCTCAGACT	3055
rs187143930	snp	C/G	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32061194	TCACCATGTTGGCCA[C/G]GCTGGTCTTGAACTC	3055
rs187147856	snp	A/G	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32087858	CGTGTTAGCCAGGAT[A/G]GTCTCAATCTCCTGA	3055
rs187161062	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32057784	CCTTTCTAAACAAAC[A/C]CCACCACATGCACCA	3055
rs187172318	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32099444	CTCACTGCAACCTCC[A/G]CCTCCCAGGTTCAAG	3055
rs187175231	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32082503	AAAAATTAGCCGGGC[A/G]TAGTGGCGGGCGTCT	3055
rs187275349	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32093007	TGGAGGACAGTGGCA[C/T]GATCTCGGCTCACTG	3055
rs187364972	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32072112	AGTAATGATAGCAGC[C/T]GAAGTGACAATGTAA	3055
rs187366574	snp	A/T	0.00597247	0.0543191	intron-variant	HCK	GRCh38.p7	20:32096993	ACTCGATTAAAAAAA[A/T]TTTAGACCGGGCACA	3055
rs187372607	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32089031	AGAATGTCCAAGACA[C/T]GGCTCAGCCTCCAGG	3055
rs187419656	snp	C/T	0.00318978	0.0398085	upstream-variant-2KB	HCK	GRCh38.p7	20:32050292	AATGGATAAATAAAA[C/T]GTGAAGGATGTAAAC	3055
rs187482769	snp	A/G	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32061045	CTGGAGTGCAGTGGC[A/G]CAGTCTTGGCTCACT	3055
rs187723246	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32093179	CGAACTCCTGGCCTC[A/C]AGTGATCCGCCCACC	3055
rs187744020	snp	A/G	0.00279162	0.0372561	intron-variant	HCK	GRCh38.p7	20:32081592	GTGGCCTTCTACTTG[A/G]CCCTCAGCTATCTGA	3055
rs187805966	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32064967	TTCTGCTCTCAGAGC[A/G]TGCTTTTGAAGCACA	3055
rs187891326	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32093624	AAAGTGCTCTCTGGA[A/C]GTCTTGGAATTCTAG	3055
rs187962706	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32088895	ACCATCCAAGTCCTA[A/G]TAGCTTGAAACAACA	3055
rs188188295	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32070601	CCTTCCCCAAATGCC[C/T]TGCCTAAAAGAGCCA	3055
rs188232418	snp	C/T	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32068254	GGTGAGTGGAGATGG[C/T]ACCACCGTACTCCAG	3055
rs188241037	snp	G/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32087121	AGAGGCCAGGGTGTG[G/T]CATGGGTGGTGGGGG	3055
rs188246708	snp	G/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32066506	TCGGTAGAGTCAGGG[G/T]TTCATCATATTGGCC	3055
rs188392580	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32086373	CATTTCCACTTTACA[G/T]ATGAGGAAGCTGAGG	3055
rs188412565	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32081374	GCTCAAACTGGCATC[G/T]ATTGAGGCTCATTGC	3055
rs188690454	snp	C/G	0.00676609	0.0577691	intron-variant	HCK	GRCh38.p7	20:32060093	TGGCCACCATGTCCT[C/G]TCTGGAGGGGGAAAC	3055
rs188695714	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32085746	GCAGGGTGGGGTGAG[A/G]GGAGGGAACAGCATG	3055
rs188751535	snp	A/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32055416	TAACCAATATTTTCA[A/T]GTATCTTTATGTAGT	3055
rs188809839	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32057222	CCCACTTTCCTCATC[C/T]GCAGAACCCTCCACA	3055
rs188818230	snp	C/T	0.00279162	0.0372561	intron-variant	HCK	GRCh38.p7	20:32078906	ATAAAGGTGACAACT[C/T]CATAGAGCTGTTGGG	3055
rs188820246	snp	C/T	6.76865e-05	0.0058171	synonymous-codon	HCK	GRCh38.p7	20:32093874	GCAGATTGCAGAAGG[C/T]ATGGCCTTCATCGAG	3055
rs188898660	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32097527	GGAACTTGCAGTGAG[C/T]TGAGATGACACCACT	3055
rs189041036	snp	A/C	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32077306	ATGTGGGGAAGCATG[A/C]AGAAGAGTGAAAAGT	3055
rs189122473	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32091300	CTGGGCCAAGTAACA[A/G]GTAAGTGCGTGGACC	3055
rs189152516	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32052886	TACGGTTCCCGGTGG[A/G]GGCCGGGTCACGCCG	3055
rs189163110	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32073618	CTTGGAACCACATAT[C/T]GATGGGTGCGGAGCT	3055
rs189188215	snp	C/T	0.0154538	0.0865337	intron-variant	HCK	GRCh38.p7	20:32078280	TCGAACTCCTGACCT[C/T]GTGATCCACCCGCCT	3055
rs189330656	snp	C/G	0.0130921	0.0798413	upstream-variant-2KB	HCK	GRCh38.p7	20:32051088	ACGGGAATAGAGAGA[C/G]GCGGTAGAATTCTTG	3055
rs189455902	snp	C/T	0.00279162	0.0372561	intron-variant	HCK	GRCh38.p7	20:32073265	AACACAGACCTTCCA[C/T]GGGTCCCCACACATT	3055
rs189459640	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32056594	CATTTTACATTCCCA[C/T]CGTAATATACAAGGG	3055
rs189463375	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32089985	CCTGCCTGGGCCTCA[G/T]CTGGGCCTGCTGGAG	3055
rs189470002	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32061996	CCAGGCTGGACTGCA[A/G]TGGTGCGACCTCGGC	3055
rs189525192	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	HCK	GRCh38.p7	20:32051506	AAAAGAGATCACGAT[A/G]CTTCCGGGGTAGGGT	3055
rs189541370	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32090559	TTTCTTTTGTCTCCC[C/T]CACCCCCATATAACC	3055
rs189703749	snp	C/T	0	0	intron-variant	HCK	GRCh38.p7	20:32069040	TGCAGTATCTCTAGG[C/T]TTGTGGGCCAGAGGA	3055
rs189776313	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32088459	TTAAATCTACTACTA[C/T]GAAAAATCTTCACCA	3055
rs189806870	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32058758	AGAGACCCTCCTAGG[A/G]GAGTAAGGAAGTGAG	3055
rs189914037	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32100478	GAGGTGAGAGAGAGA[A/G]AATAAAGGATGATTA	3055
rs189936344	snp	C/T	0.00478085	0.0486577	intron-variant	HCK	GRCh38.p7	20:32063670	TCTCTTCTACCAAAA[C/T]CTGGTATCAGGGAGG	3055
rs189947820	snp	C/T	1.64974e-05	0.00287201	missense	HCK	GRCh38.p7	20:32084483	GCCTGGGAGATCCCT[C/T]GGGAATCCCTCAAGC	3055
rs189963501	snp	C/T	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32087617	CACTACAGGCATGCA[C/T]TACCACACCCAGCTA	3055
rs190066062	snp	C/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32083102	AGAGGCTACAGCATT[C/T]CTTGGCTCATAGTCC	3055
rs190203543	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32094557	TGGTGGCACATGCCT[A/G]TATGCCTGTAGTTGT	3055
rs190257225	snp	C/G	0.00795532	0.062565	intron-variant	HCK	GRCh38.p7	20:32061350	AGTCTCTTGACAGAG[C/G]TCCCCCAGACATGGG	3055
rs190260185	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32096956	ATTAAAGATTTGTGC[A/G]TATTATTTCATGTAC	3055
rs190281266	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32059628	CAAGCGATCCTCCCA[C/T]CTCAGCCTCCTGAGT	3055
rs190287724	snp	A/G	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32081323	ATGCTGATTGGGTGC[A/G]TGGATGGCAAGAACA	3055
rs190303223	snp	C/T	0.00358779	0.0422022	intron-variant	HCK	GRCh38.p7	20:32100024	CCCGCTTCAGCCTCC[C/T]GAGTATCTGGGACCA	3055
rs190353411	snp	A/C/T	0.00279162	0.0372561	intron-variant	HCK	GRCh38.p7	20:32057876	AGGTACTTTCAGAGG[A/C/T]GTGGGTAATGATGCA	3055
rs190520700	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32100276	TTTCCATTTTTAAGC[A/G]ATGCTTTCAGCATGG	3055
rs190612176	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32078995	CAAAGAGGAAGGCAA[C/T]TTGCTCAAAGTCACA	3055
rs190742687	snp	C/T	0.00279162	0.0372561	intron-variant	HCK	GRCh38.p7	20:32083466	AAGTATACTATGGTC[C/T]CTTGGCTTTTTGTAG	3055
rs190834038	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32079397	AGCTGGTTAAGACTG[C/T]TGTCTGTTTCCACTC	3055
rs190873809	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32069373	GGAAATCACAAGACT[C/T]ACAGCTGCAGATCAG	3055
rs190883557	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32087892	TGTGATCCGCCCGCC[C/T]CAGCCTCCCACCATG	3055
rs190989184	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32092594	GTCACGCTCCTGCTC[A/G]AAGGCCTCTAATATC	3055
rs191099530	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32069908	AGAAGAAAATGGCAA[C/T]TGTGCAGAGATGAGA	3055
rs191115740	snp	C/G	0.00636936	0.0560724	intron-variant	HCK	GRCh38.p7	20:32095717	ATATTCTGAAAGCCA[C/G]GGAATTATACACTTT	3055
rs191209672	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32092298	TTCCTGGTGGTGTGA[C/T]CTGGAACAAGTGGTT	3055
rs191225343	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32085873	TGATGAGGCTAGAGG[A/G]GTGGACGAGGCTGGG	3055
rs191230105	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32075514	GGCCCATCCCTCATT[C/T]GATTCATTCGACAAG	3055
rs191364844	snp	A/G	0.0023933	0.0345097	intron-variant	HCK	GRCh38.p7	20:32061117	GCCTCCTGAGTAGCT[A/G]GGATTACAAGCATGC	3055
rs191373207	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32082431	TGGATCACCTGAGCT[C/G]AGGAGTTGGAGACCA	3055
rs191627825	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32066189	CCCCATCCCCTGTTC[C/T]CAAACTCACCCGAAT	3055
rs191653729	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32085088	CCCAGTGTGGGGCAG[A/C]CTGCTGTGTTAATAC	3055
rs191674110	snp	C/T	0.0115144	0.0749975	intron-variant	HCK	GRCh38.p7	20:32086254	TCGATCTCCTGACCT[C/T]GTGATCCGCCCACCT	3055
rs191678939	snp	A/C/G	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32057166	GGGGGCTGCCCTGGG[A/C/G]GCTACACCTGGGCTG	3055
rs191762055	snp	A/G	0.00229276	0.0337805	intron-variant	HCK	GRCh38.p7	20:32101290	TTCCCAACTGCTTCC[A/G]TTTCTAATTCCACGG	3055
rs191790392	snp	A/C	0.00517822	0.0506191	intron-variant	HCK	GRCh38.p7	20:32060444	CAGGCTTGTCTCAAA[A/C]TCCTGACATCAGGTG	3055
rs191797546	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32099497	TGAGTAACTGGGATT[A/G]CAAGCATCCACCACC	3055
rs191813878	snp	A/G	0.0119091	0.0762411	intron-variant	HCK	GRCh38.p7	20:32097370	GGATCACGAGGTCAG[A/G]AGATCGAGACCATCC	3055
rs191914993	snp	G/T	0.00517822	0.0506191	intron-variant	HCK	GRCh38.p7	20:32061203	TGGCCAGGCTGGTCT[G/T]GAACTCCTGACCTTG	3055
rs191927102	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32082524	GCGGGCGTCTGTAAT[C/T]CCAGCTACTCAGGAG	3055
rs191935714	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32064684	AGAAAACCATCTCCA[A/G]CCCACTGGATGGATG	3055
rs191996680	snp	A/C	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32093097	TTACAGGCGTGCACC[A/C]CCATGCTCATCTTCT	3055
rs192022132	snp	A/G	0.00597247	0.0543191	intron-variant	HCK	GRCh38.p7	20:32076778	GGGACCCAGCTTGGG[A/G]ACCACTGATCTAAAT	3055
rs192061621	snp	G/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32074479	ATCATGGCCACATGC[G/T]GGGGCTGACATAGTC	3055
rs192101133	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32081466	TTTACTAATACATTT[A/C]GGTTCACAACTGCTT	3055
rs192169540	snp	G/T	0.137187	0.223099	intron-variant	HCK	GRCh38.p7	20:32054615	ATCGAGACCATCCTG[G/T]CTAACACGGGGAAAC	3055
rs192316782	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	HCK	GRCh38.p7	20:32050649	GAAGCTAAGCAGGAT[C/T]AAGCCTGGTTAGTAC	3055
rs192377887	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32072279	AGGAGAGGTATTTAC[C/T]AACTTCTTTTATGTT	3055
rs192384732	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32089388	AACTGAGCCCCAGTG[C/T]GGTTAAGTGGCTTGC	3055
rs192416656	snp	C/T	0.00358779	0.0422022	intron-variant	HCK	GRCh38.p7	20:32053879	CCATCCCCGGTGATG[C/T]TGCTGCTGCTGATCC	3055
rs192532887	snp	A/G	0.000397693	0.0140957	intron-variant	HCK	GRCh38.p7	20:32086827	TGCGTGCTGGGGCTG[A/G]GGGTGCAGGCTGTGG	3055
rs192624958	snp	A/C	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32093764	CTGGTGCAGACATTT[A/C]GCATTTTCTTCACTT	3055
rs192673819	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32097814	CAGGTCTCAACAAAT[C/T]CCAAAGAACATATAT	3055
rs192803402	snp	A/C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32071194	TTTCCCCACTGTAGG[A/C/T]CATATTATTGTCCCC	3055
rs192857058	snp	C/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32086479	CACAGTTGTCTGAGG[C/G]CTAAGCCCATGATTT	3055
rs192859052	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32078374	TTAGTCTTACATAGT[G/T]GAATATTTTACCATG	3055
rs192990886	snp	C/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32088909	AGTAGCTTGAAACAA[C/T]AGCAATTGTTATTTC	3055
rs193083838	snp	A/T	0.00318978	0.0398085	intron-variant	HCK	GRCh38.p7	20:32066626	CCCCAGTGACCTTTT[A/T]ATGAGGAGCCACAGA	3055
rs193141179	snp	A/C	0.0023933	0.0345097	intron-variant	HCK	GRCh38.p7	20:32077711	TTGTATTTTTAATAG[A/C]GACAGGGTTTCTCCA	3055
rs193290576	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32055927	GAAGCATACTATGTG[A/G]CTTTCTGTGTCTAGC	3055
rs193297807	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32093188	GGCCTCAAGTGATCC[A/G]CCCACCTCGGCCTCC	3055
rs199531584	snp	A/G	8.87997e-05	0.00666273	missense	HCK	GRCh38.p7	20:32084402	CCAGAGGGGAACGAC[A/G]GGCTCTGCCAGAAAC	3055
rs199570263	snp	C/T	0.000610365	0.0174588	intron-variant	HCK	GRCh38.p7	20:32088657	CAGGTGAGAGCCTAA[C/T]GAGGAAACGGGGAAG	3055
rs199596214	in-del	-/T	0.237593	0.249692	intron-variant	HCK	GRCh38.p7	20:32072561	GGGAGACCCTGTCTC[-/T]TTAAAAAAAAAAAAA	3055
rs199684278	in-del	-/AAAAAAAAAAAA			intron-variant	HCK	GRCh38.p7	20:32072564	AGACCCTGTCTCTTT[-/AAAAAAAAAAAA]AAAAAAAAAAAAAAA	3055
rs199725229	snp	C/G	9.89185e-05	0.00703203	missense	HCK	GRCh38.p7	20:32074711	CGCGTTGACTCTCTG[C/G]AGACAGAGGAGTAAG	3055
rs199778544	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32094748	GAAAGAAAGAAAGAA[A/G]GAAAGAAAGAAAGAA	3055
rs199815006	snp	G/T	1.8247e-05	0.00302046	missense	HCK	GRCh38.p7	20:32079779	TTTCCATCAGGTGGT[G/T]TTTCAAGGGCATCAG	3055
rs199854883	snp	A/G	1.64776e-05	0.00287028	missense	HCK	GRCh38.p7	20:32083921	TGTCCGTGCGAGACT[A/G]CGACCCTCGGCAGGG	3055
rs199878298	snp	A/G/T	0.00011852	0.00769731	intron-variant	HCK	GRCh38.p7	20:32071613	TCAGAAGACTTCCCC[A/G/T]CATGAGGCTCTTGGT	3055
rs199888400	in-del	-/AAAGAAAGAAAGAAAGAAAGAAAG			intron-variant	HCK	GRCh38.p7	20:32094706	AAAGAAAAGAAAAGA[-/AAAGAAAGAAAGAAAGAAAGAAAG]AAAGAAAGAAAGAAA	3055
rs199899476	in-del	-/A	0.0193772	0.0965046	intron-variant	HCK	GRCh38.p7	20:32088887	TATAACAAACCATCC[-/A]AGTCCTAGTAGCTTG	3055
rs199988882	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32094785	AAAGAAAGAGAGAGA[A/G]AGAGAAAGAAAGAAA	3055
rs200005064	snp	C/T	1.65345e-05	0.00287524	missense	HCK	GRCh38.p7	20:32101397	TGCCCAGAGGAGCTC[C/T]ACAACATCATGATGC	3055
rs200057522	in-del	-/AGAAAGAAAGAAAGAAAGAA			intron-variant	HCK	GRCh38.p7	20:32094788	GAAAGAGAGAGAAAG[-/AGAAAGAAAGAAAGAAAGAA]AGAAAGAAAGAAAGA	3055
rs200151553	in-del	-/ATTT			intron-variant	HCK	GRCh38.p7	20:32095906	TTTATTTATTTATTT[-/ATTT]TGAGACGGAGTCTCG	3055
rs200178250	snp	C/T	0.000324102	0.0127258	missense	HCK	GRCh38.p7	20:32086664	AGGTGGCAGTGAAGA[C/T]GATGAAGCCAGGGAG	3055
rs200244202	snp	A/C/G	0.000363268	0.0134728	intron-variant	HCK	GRCh38.p7	20:32083849	AATGCAAGGTGGCAG[A/C/G]CCTCCAAGATGCCAT	3055
rs200284342	in-del	-/G			intron-variant	HCK	GRCh38.p7	20:32052782	CAGGTTCCCCTTCTT[-/G]GGGGGGGGGCGGGGA	3055
rs200298183	in-del	-/TTCC/TTCCTTCCTTCCTTCC	0	0	intron-variant	HCK	GRCh38.p7	20:32059296	TCCTTCCTTCCTTCC[-/TTCC/TTCCTTCCTTCCTTCC]CTCCCTCCCTCCTTT	3055
rs200306034	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32076966	TGGCGGGCTCCTGTA[A/G]TCCCAGCTACTCAGA	3055
rs200374213	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32086853	TGTGGCCTATACTGG[C/T]CAATTGCGGGCCCAA	3055
rs200519132	snp	A/G	0.000214184	0.0103463	missense	HCK	GRCh38.p7	20:32074646	AGTGGTGGAAGGCTC[A/G]ATCCCTGGCCACCCG	3055
rs200576977	in-del	-/AC			intron-variant	HCK	GRCh38.p7	20:32082638	CACAGCGAGACTCTG[-/AC]ACACACACACAAAAA	3055
rs200650194	in-del	-/A			intron-variant	HCK	GRCh38.p7	20:32076077	CTGTAATCCCAGCAC[-/A]TTCGGGAGGCCAAGG	3055
rs200671784	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32094868	AGAAAGAAAGAGGCA[G/T]AAGCCAATGCTAAAT	3055
rs200693880	snp	A/G	0.00299549	0.0385846	intron-variant	HCK	GRCh38.p7	20:32084377	CTCTCAATTGACCAG[A/G]GACTCTGTTCCAGAG	3055
rs200851178	in-del	-/AGAAAGAA			intron-variant	HCK	GRCh38.p7	20:32094788	GAAAGAGAGAGAAAG[-/AGAAAGAA]AGAAAGAAAGAAAGA	3055
rs200859654	in-del	-/GGC			intron-variant	HCK	GRCh38.p7	20:32052790	CCCTTCTTGGGGGGG[-/GGC]GGGGATTTTTTTTTT	3055
rs200860869	in-del	-/A	0.0228947	0.104514	intron-variant	HCK	GRCh38.p7	20:32059944	AGCTTTGTCAATTAT[-/A]AAAAAAAATGTAAAA	3055
rs200867413	snp	A/T			missense	HCK	GRCh38.p7	20:32084537	CAGTTTGGGGAAGTC[A/T]GGATGGGTAAGGACC	3055
rs200896933	snp	C/G	0.000263813	0.011482	missense	HCK	GRCh38.p7	20:32083977	CGGACCCTGGACAAC[C/G]GGGGCTTCTACATAT	3055
rs200964135	in-del	-/T			intron-variant	HCK	GRCh38.p7	20:32095887	TTATTTATTTATTTA[-/T]TTTATTTATTTATTT	3055
rs201030771	in-del	-/AAGAAAGAAAG			intron-variant	HCK	GRCh38.p7	20:32094711	AAAGAAAAGAAAAGA[-/AAGAAAGAAAG]AAAGAAAGAAAGAAA	3055
rs201042885	in-del	-/ACACACAC			intron-variant	HCK	GRCh38.p7	20:32058606	TCCTTTTATGTCAAA[-/ACACACAC]ACACACACACACACA	3055
rs201054651	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32063995	CCATCTCTACTTCTT[C/T]TTTTTTTTTTTTTTT	3055
rs201087116	snp	C/G	0.000263974	0.0114855	missense	HCK	GRCh38.p7	20:32073358	ACACCAGGAATCAGG[C/G]AGGGTAAGTATCTAC	3055
rs201117750	snp	A/G	0.000233193	0.0107955	intron-variant	HCK	GRCh38.p7	20:32098979	TCCCCAGCCTTCCCC[A/G]ACTCTGCTCTGTTCA	3055
rs201220050	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32099907	CTTTCTCCACCTTTT[A/T]TTTTTTTTTTAAGAC	3055
rs201242919	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32087508	GTTGCCCTCTGCCTA[C/T]CCAGGCTGGAGTGCA	3055
rs201280171	snp	A/G			upstream-variant-2KB	HCK	GRCh38.p7	20:32051663	AAACTCTTAGGCGGC[A/G]GGAGGTTAGATCGCG	3055
rs201319909	in-del	-/A	0.0372196	0.131242	intron-variant	HCK	GRCh38.p7	20:32076326	GAGCGATACTCTGTC[-/A]AAAAAAAAACAATTA	3055
rs201349302	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32059436	CTTTCTTTCTTTTTT[C/T]TTTCTTTCTTTCTTT	3055
rs201451674	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32090290	AAAAGAGGTTCTGGG[C/T]CTTCATCTGTCCAGA	3055
rs201487019	snp	A/G	5.45172e-05	0.00522069	synonymous-codon	HCK	GRCh38.p7	20:32101486	GGATGACTTCTACAC[A/G]GCCACAGAGAGCCAG	3055
rs201489491	in-del	-/G			intron-variant	HCK	GRCh38.p7	20:32078031	CAGTTGGTTTTTTTT[-/G]TTTGTTTGTTTGTTT	3055
rs201530129	in-del	-/AAAAT	0.0166325	0.0896639	intron-variant	HCK	GRCh38.p7	20:32068409	TTTTTAAAAAAGGAA[-/AAAAT]AAAATAAAATAAAAT	3055
rs201573109	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32086829	CGTGCTGGGGCTGGG[C/G]GTGCAGGCTGTGGCC	3055
rs201577924	snp	A/C	0.000251141	0.011203	intron-variant	HCK	GRCh38.p7	20:32098971	CTCACTACTCCCCAG[A/C]CTTCCCCGACTCTGC	3055
rs201619397	in-del	-/T			intron-variant	HCK	GRCh38.p7	20:32078023	CAGGGAGACAGTTGG[-/T]TTTTTTTGTTTGTTT	3055
rs201640035	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	HCK	GRCh38.p7	20:32102255	GCTCCTGTAACAAAT[A/G]ACCACATATCTGGTA	3055
rs201699346	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32078678	CCTGGCCAACATGGT[A/G]AAACCCCGTCTCTAC	3055
rs201741015	in-del	-/AAAGAAAGAAAGAAAGAAAG			intron-variant	HCK	GRCh38.p7	20:32094706	AAAGAAAAGAAAAGA[-/AAAGAAAGAAAGAAAGAAAG]AAAGAAAGAAAGAAA	3055
rs201763257	in-del	-/A			intron-variant	HCK	GRCh38.p7	20:32067855	GTGAAGGCTTAGTAC[-/A]AAAAAAAAATGTAAA	3055
rs201789923	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32097904	TAACTATGCCAGGTG[C/T]GGTGGCTCACACCTA	3055
rs201839186	in-del	-/CTC			intron-variant	HCK	GRCh38.p7	20:32059509	CTTCTCTCTCTCTCT[-/CTC]TTTTTTTTTTCTTTT	3055
rs201853810	in-del	-/A			intron-variant	HCK	GRCh38.p7	20:32094709	AGAAAAGAAAAGAAA[-/A]GAAAGAAAGAAAGAA	3055
rs201935506	in-del	-/A			intron-variant	HCK	GRCh38.p7	20:32087638	ACCCAGCTAATTTCT[-/A]AAAAAAATTTTTTTT	3055
rs201979534	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32088561	TCCTCCCCTCTCCCC[C/T]ATATAGGAAGCTTGC	3055
rs202001086	snp	A/G	1.65192e-05	0.00287391	missense	HCK	GRCh38.p7	20:32083999	TCTACATATCCCCCC[A/G]AAGCACCTTCAGCAC	3055
rs202002898	snp	C/T	0.00010082	0.00709928	synonymous-codon	HCK	GRCh38.p7	20:32086713	CCTGGCAGAGGCCAA[C/T]GTGATGAAAACTCTG	3055
rs202045401	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32059519	TCTCTCTCTTTTTTT[C/T]TTCTTTTTCTTTTTG	3055
rs202049705	snp	A/G	1.65244e-05	0.00287436	synonymous-codon	HCK	GRCh38.p7	20:32071758	TCCTGTGTACGTGCC[A/G]GATCCCACATCCACC	3055
rs202147830	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32099917	CTTTTTTTTTTTTTT[A/T]AAGACAAGGTCTCAC	3055
rs202169601	snp	C/T	0.000329527	0.0128318	missense	HCK	GRCh38.p7	20:32099055	CCATCAACTTTGGCT[C/T]CTTCACCATCAAGTC	3055
rs202179840	snp	A/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32073396	TGCAGTGGAGTCATG[A/T]GTCCTGCAGAGGACT	3055
rs207477531	snp	A/C/T			intron-variant	HCK	GRCh38.p7	20:32085957	TAAGATTAAAGTGGG[A/C/T]GGTGTATGTGTGTGA	3055
rs367544269	snp	C/T	0.0023933	0.0345097	intron-variant	HCK	GRCh38.p7	20:32059546	TTTGAGACAGGGTCT[C/T]GCTCTGTCTCCCAGG	3055
rs367548562	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32092150	TAGTCAGACGCCCTC[A/T]CTTCCAGAATAATTT	3055
rs367698836	in-del	-/ATAA	0.0908466	0.195289	intron-variant	HCK	GRCh38.p7	20:32097585	ACCCTGTCTCAAAAC[-/ATAA]ATAAATAAATAAATA	3055
rs367796631	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32057561	TCTGAGACTGCACCA[C/T]TGTACTCCAGCCTGG	3055
rs367801192	snp	A/T	0.0178098	0.0926698	intron-variant	HCK	GRCh38.p7	20:32086117	CTCCGTCTCCTGGGT[A/T]CACACCATTCTCCTG	3055
rs367842803	snp	C/T	0.000153988	0.00877328	intron-variant	HCK	GRCh38.p7	20:32074593	ATGATCCTTCTGTCC[C/T]TAACACCTTTACTCC	3055
rs367891102	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32065888	GGGACAGATGCTGAG[A/G]AGGCAGGAGCAAAAG	3055
rs367924247	in-del	-/AA			intron-variant	HCK	GRCh38.p7	20:32094794	GAGAGAAAGAGAAAG[-/AA]AGAAAGAAAGAAAGA	3055
rs367936044	snp	A/G	0.000118718	0.00770355	intron-variant	HCK	GRCh38.p7	20:32084571	GGCCACAGCCCACAG[A/G]GCCAGAGGGTGGAGG	3055
rs367955528	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32099418	GCTGGAGTGCAGTGA[C/T]GTGATCTCGGCTCAC	3055
rs367974826	in-del	-/CTC			intron-variant	HCK	GRCh38.p7	20:32091803	ATAGTGGGACCTCTT[-/CTC]TATTAAAAAAAAAAA	3055
rs367979772	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32076859	GGGAAGCCGAGGGAG[A/G]TGGAACACTTGAGGT	3055
rs368008295	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32071938	CTCGACTCTCCGGGA[C/T]GCAGCGCCAGCCAGC	3055
rs368022390	snp	C/G	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32058104	CAGCCTCATCTCTAC[C/G]ATAGAAATGAAGAAC	3055
rs368037561	snp	C/T			downstream-variant-500B	HCK	GRCh38.p7	20:32102022	AGTGCTTTGGGAGAC[C/T]GAGGAGCGGGGGATT	3055
rs368094209	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32092242	GCAGGATGCACTGGA[C/T]TGGGAGTCCTCAGAC	3055
rs368194350	in-del	-/AA/AAA			intron-variant	HCK	GRCh38.p7	20:32078856	GCAAGACTCAGTCTC[-/AA/AAA]AAAAAAAAAAAAAAA	3055
rs368348216	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	HCK	GRCh38.p7	20:32050909	GCTGTTAAACATCCT[A/G]TCATTCACAGGACAG	3055
rs368360006	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32070961	GAGGGGGAAGGAAGA[A/G]GAGGGGGAGCAGGAA	3055
rs368395419	snp	A/G	0.00279162	0.0372561	intron-variant	HCK	GRCh38.p7	20:32054609	CAGGAGATCGAGACC[A/G]TCCTGGCTAACACGG	3055
rs368452902	snp	A/T			upstream-variant-2KB	HCK	GRCh38.p7	20:32050452	TTTATAAAAAGCACA[A/T]ACAGACTAGGTGCAA	3055
rs368536611	in-del	-/A			intron-variant	HCK	GRCh38.p7	20:32094833	AAGAAAGAAAGAAAG[-/A]AAAGAAAGAAAGAAA	3055
rs368573899	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32070265	GCCTCACTCAGCCAC[C/T]GGTGGGATTATTTAA	3055
rs368583419	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32074993	ACCTGGTTTCTTTGG[C/T]TGGTTACACGTGCAT	3055
rs368660132	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32086221	AGACGGGGTTTCACC[A/G]TGTTAGCCAGGATGG	3055
rs368723410	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32061748	CACAGTTGGTGAGTT[C/G]AAGAAGAGCAAGGAG	3055
rs368724701	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32086278	CCCACCTCGGCCCCC[C/G]AAAGTGCTGAGATTA	3055
rs368796550	snp	A/C/G	1.65781e-05	0.00287902	intron-variant	HCK	GRCh38.p7	20:32099141	CCTTACCCAGGTAGG[A/C/G]AAGGGGCATCAGCTC	3055
rs368809621	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32093732	GCCCTGGGGCCCTCC[C/T]GACACAAAAGGGAGG	3055
rs368867229	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32065413	GATAATTTATTTGCT[C/T]GTGGACTGGAAAAAT	3055
rs369025763	snp	G/T	1.68547e-05	0.00290294	synonymous-codon	HCK	GRCh38.p7	20:32084419	GCTCTGCCAGAAACT[G/T]TCGGTGCCCTGCATG	3055
rs369134516	snp	A/C	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32066894	CTCTGTGTATGGTTT[A/C]ATATTATAAGCTCCT	3055
rs369171323	snp	C/T	0.000153988	0.00877328	intron-variant	HCK	GRCh38.p7	20:32079889	AAAGGTGACACCAGC[C/T]CTCCCCACCTTGTCC	3055
rs369207649	snp	C/T	0.000132214	0.00812954	intron-variant	HCK	GRCh38.p7	20:32088559	GTTCCTCCCCTCTCC[C/T]CCATATAGGAAGCTT	3055
rs369240467	in-del	-/TA			intron-variant	HCK	GRCh38.p7	20:32096906	TGGTGATTACAAGGG[-/TA]TATATATATATATAA	3055
rs369269936	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32059313	TCCCTCCCTCCTTTC[C/T]TTTCTTTTCTTTCTT	3055
rs369294499	snp	A/C	0.000153988	0.00877328	missense	HCK	GRCh38.p7	20:32073347	ACAACAGCAACACAC[A/C]AGGAATCAGGGAGGG	3055
rs369307656	in-del	-/A	0.365646	0.221644	intron-variant	HCK	GRCh38.p7	20:32056517	GAGACTCCTTCTCAG[-/A]AAAAAAAAAAAACAG	3055
rs369313038	snp	C/T	0.000115336	0.00759305	synonymous-codon	HCK	GRCh38.p7	20:32083943	TCGGCAGGGAGATAC[C/T]GTGAAACATTACAAG	3055
rs369319334	in-del	-/T			intron-variant	HCK	GRCh38.p7	20:32060968	CCGTATTTTTTTTTT[-/T]GTAGTTGTTGTTCTG	3055
rs369369487	snp	A/G	0.00011618	0.00762078	missense	HCK	GRCh38.p7	20:32101353	TCCGAGCTCTGGAGC[A/G]TGGATACCGGATGCC	3055
rs369369524	snp	G/T			upstream-variant-2KB	HCK	GRCh38.p7	20:32051606	ATCTCTGAAGGGCAG[G/T]GTTGGAATCTTTGGA	3055
rs369398165	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32056554	TATCTTTAACTTTTT[A/G]AGGAACTGCTATGCT	3055
rs369401817	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32059217	TGGGGAAAGAGGTGG[C/T]CATGGAGGGCTTATA	3055
rs369414030	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32076095	CGGGAGGCCAAGGCA[C/T]GCAGATCACCTGAGG	3055
rs369414224	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32097758	ACACAAACACACACA[C/T]AGAACATTTTCAAAA	3055
rs369465470	snp	C/G/T			intron-variant	HCK	GRCh38.p7	20:32054534	AAAAAAGCCCGGACG[C/G/T]GGGGGCTCACGCCTG	3055
rs369481790	snp	A/G	9.71487e-05	0.00696885	intron-variant	HCK	GRCh38.p7	20:32073683	TGGATGCACTTAGAC[A/G]AAACCTCACCCTCTG	3055
rs369542343	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32059404	TCTCTTCCTTCCTTT[C/T]TTCTTTCTCTCTCTC	3055
rs369611440	snp	C/T	4.95299e-05	0.00497619	missense	HCK	GRCh38.p7	20:32071754	ACTGTCCTGTGTACG[C/T]GCCGGATCCCACATC	3055
rs369673215	snp	C/T	0.00755907	0.0610114	intron-variant	HCK	GRCh38.p7	20:32093182	ACTCCTGGCCTCAAG[C/T]GATCCGCCCACCTCG	3055
rs369736937	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32062002	TGGACTGCAGTGGTG[C/T]GACCTCGGCTCCCTG	3055
rs369813714	snp	A/G	3.44169e-05	0.00414816	intron-variant	HCK	GRCh38.p7	20:32084592	AGGGTGGAGGGGAGA[A/G]GGAGGCCACTTGCTT	3055
rs369873781	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32077814	CAGGCGTGAGCCACT[A/G]CTCCCGGACACCTCC	3055
rs369877137	snp	C/T	6.58321e-05	0.00573687	intron-variant	HCK	GRCh38.p7	20:32079758	GTTCACATTTGTCCC[C/T]TCCCTTTTCCATCAG	3055
rs369898770	snp	A/G	0.00016954	0.00920551	synonymous-codon	HCK	GRCh38.p7	20:32101444	TCCGGAGGAGCGGCC[A/G]ACCTTCGAATACATC	3055
rs369900759	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32057976	CTCTGGATGGCACTG[A/C]GCTAGGACGTGCGCT	3055
rs369903832	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32067909	TTTATTATATGTTAA[C/T]AATTTTGATATATTG	3055
rs369904410	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32082768	TCACAAATAGCAAAA[C/T]GGTGGTCATGAGCTG	3055
rs369945538	snp	C/T	0.000198138	0.00995136	intron-variant	HCK	GRCh38.p7	20:32088665	AGCCTAACGAGGAAA[C/T]GGGGAAGGGAAACAG	3055
rs370030252	snp	C/T	0.000165503	0.00909527	intron-variant	HCK	GRCh38.p7	20:32073273	CCTTCCACGGGTCCC[C/T]ACACATTGGTCAGAT	3055

Page 1 | 2