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
rs370053581	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32097447	AGCCAGGCGTGGTGG[C/T]GGGCACCTGTAGTCC	3055
rs370119506	snp	A/G	0.000161987	0.00899818	intron-variant	HCK	GRCh38.p7	20:32073850	CTCCCCCTAAGACAG[A/G]CCTGCCTCCTCTACT	3055
rs370137944	snp	C/G	0.000437904	0.0147905	intron-variant	HCK	GRCh38.p7	20:32073256	GTCCTTCTCAACACA[C/G]ACCTTCCACGGGTCC	3055
rs370167095	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32064023	TTTTTTTTTTTTTTG[A/T]GATAGAGTCTCTCTC	3055
rs370210736	in-del	-/GAC			intron-variant	HCK	GRCh38.p7	20:32081826	GTCCATCCTGCAGAC[-/GAC]AAGGGCAGAGAAATC	3055
rs370294567	in-del	-/A			intron-variant	HCK	GRCh38.p7	20:32094790	AAGAGAGAGAAAGAG[-/A]AAGAAAGAAAGAAAG	3055
rs370380247	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32068930	GCCTGGGTGACAGAG[C/T]GAGACTGTCTCTGAG	3055
rs370473046	snp	A/C	1.65097e-05	0.00287308	missense	HCK	GRCh38.p7	20:32084504	TCCCTCAAGCTGGAG[A/C]AGAAACTTGGAGCTG	3055
rs370474555	snp	A/G	3.33723e-05	0.00408473	intron-variant	HCK	GRCh38.p7	20:32094023	CTCGGGAAGGTAGGG[A/G]ACGCTGCCAAGCAGC	3055
rs370528332	in-del	-/A			intron-variant	HCK	GRCh38.p7	20:32094700	AAAAGAAAAGAAAAG[-/A]AAAGAAAAGAAAGAA	3055
rs370735691	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32057996	GGACGTGCGCTCCTG[A/G]CTCTCCCTTCGAGTC	3055
rs370780396	snp	C/T	0.000159212	0.0089208	synonymous-codon	HCK	GRCh38.p7	20:32086638	TCCAGCCACCTACAA[C/T]AAGCACACCAAGGTG	3055
rs370853719	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32094739	AGAAAGAAAGAAAGA[A/G]AGAAAGAAAGAAAGA	3055
rs370956856	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32085206	TGTATTTCGACTGTA[C/T]TTATTGCGATTCTGC	3055
rs371010534	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32052834	GAAAAAGAAGGAAGG[C/G]ATGGGGCTTCACAGA	3055
rs371157821	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32094760	GAAAGAAAGAAAGAA[A/G]GAAGGAAAGAAAGAA	3055
rs371191707	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32055058	AGGCGTTCACTACAA[C/T]GAACAATATTGACAG	3055
rs371194110	snp	A/T	0.000153988	0.00877328	intron-variant	HCK	GRCh38.p7	20:32093820	GGGGCCATCTTGGCG[A/T]AGGCCAGGTCTGAGG	3055
rs371195805	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32096941	TGCAGCAAAATGGAT[A/G]TTAAAGATTTGTGCA	3055
rs371206615	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32061548	GGTTAGGGGCATGAA[C/G]ACTAGCTGGGAACAG	3055
rs371207239	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32075526	ATTTGATTCATTCGA[C/T]AAGCACATGCTCATG	3055
rs371260834	snp	C/G	1.8145e-05	0.00301201	intron-variant	HCK	GRCh38.p7	20:32086851	GCTGTGGCCTATACT[C/G]GTCAATTGCGGGCCC	3055
rs371280728	snp	C/T	8.23866e-05	0.00641767	synonymous-codon	HCK	GRCh38.p7	20:32099074	CACCATCAAGTCAGA[C/T]GTCTGGTCCTTTGGT	3055
rs371303968	snp	A/G			upstream-variant-2KB	HCK	GRCh38.p7	20:32050457	AAAAAGCACATACAG[A/G]CTAGGTGCAATGACT	3055
rs371304588	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32072796	CAGCATCCCCCGGTA[C/T]ATCCAAGACCGAAGG	3055
rs371368691	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32090174	GGTCTGTTGCTAAAT[C/T]ATCATCTTCAAACTA	3055
rs371397974	in-del	-/AAAGAAAGAAAGAAAGAA			intron-variant	HCK	GRCh38.p7	20:32094794	GAGAGAAAGAGAAAG[-/AAAGAAAGAAAGAAAGAA]AGAAAGAAAGAAAGA	3055
rs371490082	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32064602	AGCTTATAGCAGAGA[C/T]GGGACCACAATCCAG	3055
rs371503935	snp	C/G	0.000121063	0.00777926	intron-variant	HCK	GRCh38.p7	20:32084382	AATTGACCAGGGACT[C/G]TGTTCCAGAGGGGAA	3055
rs371600600	snp	A/T	0.000153988	0.00877328	intron-variant	HCK	GRCh38.p7	20:32073378	TAAGTATCTACGAGC[A/T]GATGCAGTGGAGTCA	3055
rs371687714	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32082769	CACAAATAGCAAAAC[A/G]GTGGTCATGAGCTGA	3055
rs371695854	snp	A/G			upstream-variant-2KB	HCK	GRCh38.p7	20:32051148	ACAGCATTTAGGGTG[A/G]TAGCCCCTGTCTTTT	3055
rs371761519	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32087338	GGACAGGAACTTGCT[C/T]TGTTACTCAGGCTGG	3055
rs371789368	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32094889	AATGCTAAATGCACC[A/G]AAATGGGTAACTCTC	3055
rs371853614	in-del	-/GAGA			intron-variant	HCK	GRCh38.p7	20:32100476	AGGAGGTGAGAGAGA[-/GAGA]ATAAAGGATGATTAC	3055
rs371916148	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32071112	AATATAAAAATGGCA[A/T]TTTATCATCTGATAA	3055
rs372017012	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32071239	GACCTGAGAGGTGGG[C/T]AGGGGCAGGAAAGTG	3055
rs372166561	snp	C/T	0.000153988	0.00877328	missense	HCK	GRCh38.p7	20:32086802	TCACGGAGTTCATGG[C/T]CAAAGGTGCTGCGTG	3055
rs372214356	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32095401	GCTGGGATTACAGGC[G/T]CACACCACCATACCC	3055
rs372233490	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32065479	AGGTGCTCAATTTAT[C/T]TTCAGGAATTACTTT	3055
rs372242617	snp	A/C	1.69163e-05	0.00290824	intron-variant	HCK	GRCh38.p7	20:32071621	CTTCCCCGCATGAGG[A/C]TCTTGGTAACTGGGG	3055
rs372243836	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32086240	TAGCCAGGATGGTCT[C/T]GATCTCCTGACCTTG	3055
rs372463603	snp	A/G	9.82367e-05	0.00700776	intron-variant	HCK	GRCh38.p7	20:32073863	AGACCTGCCTCCTCT[A/G]CTCAACTATGTGCTC	3055
rs372571266	snp	A/T	0.000153988	0.00877328	intron-variant	HCK	GRCh38.p7	20:32073278	CACGGGTCCCCACAC[A/T]TTGGTCAGATTCATT	3055
rs372585955	in-del	-/TAGT			upstream-variant-2KB	HCK	GRCh38.p7	20:32050688	GAGACCCCCTCAAAA[-/TAGT]TAGCACTGTAGGCTA	3055
rs372621598	snp	A/C	4.97979e-05	0.00498964	missense	HCK	GRCh38.p7	20:32071774	GATCCCACATCCACC[A/C]TCAAGCCGGTGAGTA	3055
rs372761182	snp	A/C/G	0.00014829	0.00860965	missense	HCK	GRCh38.p7	20:32083923	TCCGTGCGAGACTAC[A/C/G]ACCCTCGGCAGGGAG	3055
rs372875659	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32080812	GGATTGTTTTTGTTT[G/T]GGTTTTTTTAAATAC	3055
rs372933291	snp	C/T	1.98022e-05	0.00314654	intron-variant	HCK	GRCh38.p7	20:32079767	TGTCCCCTCCCTTTT[C/T]CATCAGGTGGTTTTT	3055
rs372985105	in-del	C/TTCCTTCCT			intron-variant	HCK	GRCh38.p7	20:32059297	TCCTTCCTTCCTTCC[C/TTCCTTCCT]TCCCTCCCTCCTTTC	3055
rs373021851	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32068071	GGAGGCCAAGGAGGA[C/T]GGATCACCTGAGGTT	3055
rs373118182	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32083731	GTAGAGCCTGGATGA[G/T]AGCCCAGGATGCCTG	3055
rs373188975	snp	C/T	0.000153988	0.00877328	intron-variant	HCK	GRCh38.p7	20:32093846	TGAGGACAAAGGTGT[C/T]TCTGTTTGGGGTGCA	3055
rs373209595	snp	A/G	8.83275e-05	0.00664499	missense	HCK	GRCh38.p7	20:32073763	TATGATTACGAGGCC[A/G]TTCACCACGAAGACC	3055
rs373284340	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32061008	GTTTTTTTTGAGACA[A/G]AGTCTTGCTCTGTTG	3055
rs373288312	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32099323	CTGGGGGCTTCCTTG[A/G]CCCTTCCTTCTCTCT	3055
rs373319468	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32094969	ATGCCACTTGGTTTC[A/G]TTTTTGTGAAATTCT	3055
rs373540492	in-del	-/TTCTTGGCTAGAATGTTCA	0.0023933	0.0345097	intron-variant	HCK	GRCh38.p7	20:32065917	AGAGGTTCTCTAGCC[-/TTCTTGGCTAGAATGTTCA]CATGAATCGCCTGGG	3055
rs373544558	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32060647	AGATGGATAATAAAC[A/G]AATCAACAGGTAATA	3055
rs373551816	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32053623	AGCCTGGGCGACAGA[A/G]AGAGACTCTGTCTCA	3055
rs373562575	in-del	-/TATC	0.00318978	0.0398085	intron-variant	HCK	GRCh38.p7	20:32066969	CTTTCCCCCAATCTT[-/TATC]TATTCAGATCCTCCC	3055
rs373638157	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32059399	CTTCTTCTCTTCCTT[C/T]CTTTCTTCTTTCTCT	3055
rs373680308	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32064407	TAAACTGAGACTAGG[G/T]GCGGAGTAATTCCCA	3055
rs373716108	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32092128	GTGGTGCTTTGATTG[G/T]TCTGTCTAGTCAGAC	3055
rs373755730	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32053760	CCCCGTGTTCTCAGA[A/C]TTTAGCCTACATCAG	3055
rs373891936	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32060302	CTTGGCTCACTGCAA[C/T]CTCTGCCTCTTGAGT	3055
rs374132672	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32080415	TGTTGGCCAGTATGG[C/T]CTCGATCTCCTGACC	3055
rs374136464	snp	A/G	0.00318978	0.0398085	intron-variant	HCK	GRCh38.p7	20:32061204	GGCCAGGCTGGTCTT[A/G]AACTCCTGACCTTGT	3055
rs374166042	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32078754	CCCAGCTGCTTGGGA[A/G]GCTGAGGCAAAATAA	3055
rs374183117	snp	A/G	1.67798e-05	0.00289648	intron-variant	HCK	GRCh38.p7	20:32099187	GCCCAGTCTGGCAAT[A/G]GGCTCATCTCAACAA	3055
rs374222917	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32080116	GAACTAGTGCCAGGT[A/G]GCTTAGGCCCTGAAA	3055
rs374360915	snp	A/G	4.9552e-05	0.0049773	missense	HCK	GRCh38.p7	20:32099121	TCGTCACCTACGGCC[A/G]GATCCCTTACCCAGG	3055
rs374731326	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32064850	AGCAGAGGCTGAGGC[A/G]GTGAGGAGCAGGTTT	3055
rs374876463	in-del	-/TTAG			upstream-variant-2KB	HCK	GRCh38.p7	20:32050691	ACCCCCTCAAAATAG[-/TTAG]CACTGTAGGCTAAAG	3055
rs374949285	snp	C/T	0.000101538	0.00712452	intron-variant	HCK	GRCh38.p7	20:32084564	GACCCAGGGCCACAG[C/T]CCACAGGGCCAGAGG	3055
rs374983027	in-del	-/A			intron-variant	HCK	GRCh38.p7	20:32094705	AAAAGAAAAGAAAAG[-/A]AAAGAAAGAAAGAAA	3055
rs375001341	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32059310	CCCTCCCTCCCTCCT[C/T]TCTTTTCTTTTCTTT	3055
rs375053312	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32055345	GCCTTACTCACTATG[C/G]CTGGCACTTAATAAG	3055
rs375093291	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32100044	ATCTGGGACCATAGG[C/T]ACATGCCACCATGTC	3055
rs375246831	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32060429	TTTCACCATGTTGGC[C/T]AGGCTTGTCTCAAAC	3055
rs375249670	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32083003	GATCAGTAGTCTGAC[C/G]TCACTGGGCTCAAGA	3055
rs375313782	snp	C/T	0.000115345	0.00759337	missense	HCK	GRCh38.p7	20:32074696	AGCAACTATGTCGCC[C/T]GCGTTGACTCTCTGG	3055
rs375537109	snp	C/T	0.000131944	0.00812123	synonymous-codon	HCK	GRCh38.p7	20:32071695	CAAGTTCCTCCAGGT[C/T]GGAGGCAATACATTC	3055
rs375537405	snp	C/T	0.000153988	0.00877328	intron-variant	HCK	GRCh38.p7	20:32084387	ACCAGGGACTCTGTT[C/T]CAGAGGGGAACGACG	3055
rs375586107	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32059012	TGGGCAGAGCAGGCA[A/C]CAATAGCCACAGAGA	3055
rs375602398	snp	A/C			upstream-variant-2KB	HCK	GRCh38.p7	20:32050842	GAGACATTTTGTTGT[A/C]ACAACTAGGGAGGAG	3055
rs375602821	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32097511	GTGAAAGCCGGGAGG[C/T]GGAACTTGCAGTGAG	3055
rs375681715	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32086210	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCGTGTT	3055
rs375705652	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32067072	ACTTACTAACATACA[C/T]GTAGGCACATAAATT	3055
rs375764907	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32064021	TTTTTTTTTTTTTTT[G/T]GAGATAGAGTCTCTC	3055
rs375765839	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32058401	GCCGGGCGTGGTGGC[A/G]GGCGCCTGTAATTTC	3055
rs375797407	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32066563	AGTGATCCACCCACA[C/T]CAGCCTCCTAAAGTG	3055
rs375847090	snp	C/T	0.000155988	0.00883005	synonymous-codon	HCK	GRCh38.p7	20:32073786	CGAAGACCTCAGCTT[C/T]CAGAAGGGGGACCAG	3055
rs375871167	snp	A/G	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32085350	AAATCCCGTCTCTAC[A/G]AAAAAATACAACAAT	3055
rs375976906	in-del	C/TTTT			intron-variant	HCK	GRCh38.p7	20:32059515	TCTCTCTCTCTCTTT[C/TTTT]TTTCTTTTTCTTTTT	3055
rs376025420	snp	A/C/G/T	0.000164768	0.00907538	synonymous-codon, missense	HCK	GRCh38.p7	20:32083929	CGAGACTACGACCCT[A/C/G/T]GGCAGGGAGATACCG	3055
rs376062257	snp	G/T	1.86995e-05	0.00305767	synonymous-codon	HCK	GRCh38.p7	20:32084395	CTCTGTTCCAGAGGG[G/T]AACGACGGGCTCTGC	3055
rs376090706	in-del	-/TATTCAGTAG			intron-variant	HCK	GRCh38.p7	20:32090464	GGTGACATGAAATGT[-/TATTCAGTAG]CTGCATATATACAAA	3055
rs376121418	snp	C/T	0.000153988	0.00877328	intron-variant	HCK	GRCh38.p7	20:32073369	CAGGGAGGGTAAGTA[C/T]CTACGAGCAGATGCA	3055
rs376155882	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32089826	AAGTGGCCTCTAGGC[C/T]GAGCCTGAAGGATGA	3055
rs376203273	snp	C/T	0.000153988	0.00877328	intron-variant	HCK	GRCh38.p7	20:32101311	AATTCCACGGCTCCT[C/T]TTCAGGGATGTCAAA	3055
rs376227592	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32063385	AGCCTCCCAAGTAGC[C/T]GGGAATACAGGCACA	3055
rs376235567	in-del	-/GTGT			intron-variant	HCK	GRCh38.p7	20:32093490	AGTATCCTAGGGTTC[-/GTGT]GTGTGTGTGTGTGTG	3055
rs376270766	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	HCK	GRCh38.p7	20:32051456	CGCGGAGTTGGGGAG[A/G]GCCGGGCCAGAAGGG	3055
rs376281952	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32089082	ACCACCCAATCACCC[A/G]GCCTGAGCTTCTTCA	3055
rs376291473	in-del	-/ATGA			upstream-variant-2KB	HCK	GRCh38.p7	20:32051024	TTTGCTGAATGAATT[-/ATGA]ATGAATGAATGAAGA	3055
rs376295387	snp	A/C	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32093737	GGGGCCCTCCCGACA[A/C]AAAAGGGAGGGCTGG	3055
rs376306607	snp	A/C/G	0.000135726	0.00823699	intron-variant	HCK	GRCh38.p7	20:32084078	TGACATCCCCACCAC[A/C/G]ATGGGCCCACAGACT	3055
rs376333365	in-del	-/GTTTT			intron-variant	HCK	GRCh38.p7	20:32077538	GTTTTGTTTTGTTTT[-/GTTTT]TTAGGTGGAGTTTCT	3055
rs376354017	snp	C/T			synonymous-codon	HCK	GRCh38.p7	20:32093901	CGAGCAGAGGAACTA[C/T]ATCCACCGAGACCTC	3055
rs376386946	snp	C/T	4.95782e-05	0.00497862	intron-variant	HCK	GRCh38.p7	20:32073377	GTAAGTATCTACGAG[C/T]AGATGCAGTGGAGTC	3055
rs376481023	in-del	-/GGGA			intron-variant	HCK	GRCh38.p7	20:32071000	GGAGGGAGGGAGGGA[-/GGGA]AGGAGTTATAAGCAA	3055
rs376493351	snp	C/G	1.68309e-05	0.00290089	intron-variant	HCK	GRCh38.p7	20:32084557	GGGTAAGGACCCAGG[C/G]CCACAGCCCACAGGG	3055
rs376549403	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32078193	GCTCCTGCCACCATG[C/T]TCGGCTAATTTTTTT	3055
rs376736324	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32062141	GATGGGGTTTCACCA[C/T]GTTGGTCAGGCTGGT	3055
rs376739879	snp	C/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32085191	TAAGTTTAAAATCCA[C/T]GTATTTCGACTGTAT	3055
rs376775108	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32095503	CTCAAGTGATCCGCC[C/T]GCCTTGGCCTCCCAA	3055
rs376837308	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32096389	GTAGTCCCAGCTACT[C/T]GGGAGGCTGAGGCAG	3055
rs376863762	snp	C/T	0.00023826	0.0109121	intron-variant	HCK	GRCh38.p7	20:32084350	AACCTCTGGCTGGCT[C/T]GGTGCTTGTTGCTCT	3055
rs376911985	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32066112	CTTTGTCACAAGGCA[C/T]TCTGCAGAGAGGCCC	3055
rs376948711	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32059403	TTCTCTTCCTTCCTT[C/T]CTTCTTTCTCTCTCT	3055
rs376957755	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32069319	TATGTACATTGATCA[C/T]GTAAGTGAAGCATAC	3055
rs377101411	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32086396	AGCTGAGGAAGCCAC[A/G]GCTCAGAGACGTTAA	3055
rs377107739	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32093285	TACCACCTGCAGGGG[C/T]TTTGCCGGGCTCATC	3055
rs377117578	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32065702	ATGCCTACAACTGAA[C/T]CAATCTCTGTAGCCA	3055
rs377138478	snp	C/T	0.000153988	0.00877328	intron-variant	HCK	GRCh38.p7	20:32074772	ATGAGCAAAGCCAGC[C/T]TTGTTTGCAACTCAG	3055
rs377179319	in-del	-/G			intron-variant	HCK	GRCh38.p7	20:32078880	AAAAAAAAAAAAAAA[-/G]GGGGGGAATGATAAA	3055
rs377239025	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32072301	TTTTATGTTTATACA[A/G]AGCTGACTATGAACC	3055
rs377275768	snp	A/G	8.72167e-05	0.00660308	intron-variant	HCK	GRCh38.p7	20:32071833	ACGGATGCTGCCCCA[A/G]CATTGCCCTAACAGC	3055
rs377335962	snp	C/T	0.00358779	0.0422022	intron-variant	HCK	GRCh38.p7	20:32063696	GGAGGTCTTTGCCAT[C/T]AGCCATTTGCACTTG	3055
rs377379867	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32078732	TGTAGTGGTGGGTGC[C/T]TGTAATCCCAGCTGC	3055
rs377392775	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32060464	GACATCAGGTGATCC[A/G]CCTGCTGACCTCAGG	3055
rs377404532	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32073041	AGAGGTGGAGGTTTC[A/G]GTGAGCTGAGATCAC	3055
rs377420054	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32082833	TAGGGTGGTGCAAAA[A/G]TAATTTCAGTTTTTT	3055
rs377461587	snp	A/G	5.49234e-05	0.0052401	intron-variant	HCK	GRCh38.p7	20:32093819	TGGGGCCATCTTGGC[A/G]TAGGCCAGGTCTGAG	3055
rs377468533	snp	C/T	4.97558e-05	0.00498753	missense	HCK	GRCh38.p7	20:32094005	AGGACAACGAGTACA[C/T]GGCTCGGGAAGGTAG	3055
rs377570647	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32065339	AATATGCAAGAATCA[A/G]TGGAGACTTTTTGAG	3055
rs377685507	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32085880	GCTAGAGGGGTGGAC[A/G]AGGCTGGGTCATGTA	3055
rs386813702	in-del	CTCTTTTTTT/TTC			intron-variant	HCK	GRCh38.p7	20:32059509	CTTCTCTCTCTCTCT[CTCTTTTTTT/TTC]TTTCTTTTTCTTTTT	3055
rs386813703	multinucleotide-polymorphism	GA/TT			intron-variant	HCK	GRCh38.p7	20:32066330	TTTTTTTTTTTTTTT[GA/TT]GACAGAGTCTTGCTC	3055
rs386813704	multinucleotide-polymorphism	ATT/TTC			intron-variant	HCK	GRCh38.p7	20:32076078	CTGTAATCCCAGCAC[ATT/TTC]GGGAGGCCAAGGCAC	3055
rs397760261	in-del	-/T	0	0	intron-variant	HCK	GRCh38.p7	20:32067552	TTTTTTTTTTTTTTT[-/T]GCCCCGTCTTATGGT	3055
rs397799329	in-del	-/T			intron-variant	HCK	GRCh38.p7	20:32052807	GGGGATTTTTTTTTT[-/T]AATTTAAAAAAGAAA	3055
rs397817031	in-del	-/A	0	0	intron-variant	HCK	GRCh38.p7	20:32058240	AAATCCAAAAAAAAA[-/A]TGGAACTGAGGCTGG	3055
rs397817661	in-del	-/G			intron-variant	HCK	GRCh38.p7	20:32098881	AGGCCACGTATCAGG[-/G]AAATTGCAGGTCTGC	3055
rs397829726	in-del	-/TG	0	0	intron-variant	HCK	GRCh38.p7	20:32093522	GTGTGTGTGTGTGTG[-/TG]CATGTGCACGTGTGT	3055
rs397831380	in-del	-/A			downstream-variant-500B	HCK	GRCh38.p7	20:32102137	AAAAAAAAAAAAAAA[-/A]GATGAAGAAGAAGAA	3055
rs397838502	in-del	-/CTTT			intron-variant	HCK	GRCh38.p7	20:32059432	tctctttctttcttt[-/CTTT]tttctttctttcttt	3055
rs397838503	in-del	-/GT			intron-variant	HCK	GRCh38.p7	20:32093521	tgtgtgtgtgtgtgt[-/GT]gcatgtgcacgtgtg	3055
rs397864786	in-del	-/A			intron-variant	HCK	GRCh38.p7	20:32091823	TTAAAAAAAAAAAAA[-/A]TTCTTTTTAAATTTA	3055
rs397864978	in-del	-/T			intron-variant	HCK	GRCh38.p7	20:32054007	TGGTCCTTTTTTTTT[-/T]AGGGGAGGGGGTGAC	3055
rs527424675	in-del	-/A			intron-variant	HCK	GRCh38.p7	20:32096521	AAAAAAAAAAAAAAA[-/A]GATAGGTGCTTGCTC	3055
rs527429600	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32074976	GTTTTACTAGCAAAA[C/T]GACCTGGTTTCTTTG	3055
rs527440666	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32068830	GTAACTGTAGTCCCA[A/G]CTACTAAGGAGGCTG	3055
rs527465738	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32074461	GTAAGGATCCCTACC[A/C]TAATCATGGCCACAT	3055
rs527499733	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32058433	GCTACTTGGGAAGCC[A/G]AGGCAGGAGAATTGC	3055
rs527549394	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32052784	AGGTTCCCCTTCTTG[A/G]GGGGGGGCGGGGATT	3055
rs527611238	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32079756	AGGTTCACATTTGTC[C/G]CCTCCCTTTTCCATC	3055
rs527653536	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32094412	TGGCCAGGCTCAGTG[C/G]CTCACGCCTGTAATC	3055
rs527655431	in-del	-/A	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32068398	AAATAATTTTTTTTT[-/A]AAAAAAGGAAAAAAT	3055
rs527681304	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32087585	GATCCTCCCGACTTA[C/G]TCTCCCCAGTAGCTG	3055
rs527749397	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32074198	CACCATCATGGGTAT[A/G]GTGTCCAGGATGTGC	3055
rs527813411	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32072456	TACTCCCAGCATTTT[C/G]GGAGGCTGAGGCAGG	3055
rs527845905	snp	A/G	0.00398564	0.0444627	intron-variant	HCK	GRCh38.p7	20:32061141	AGCATGCGCCACCAC[A/G]CCCAGCTAATTTTTG	3055
rs527891311	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32067178	CATGGCCCCTCCTAT[A/G]TTTACCACTCCCTAG	3055
rs527997368	snp	A/C	0.00478085	0.0486577	intron-variant	HCK	GRCh38.p7	20:32082651	TGACACACACACACA[A/C]AAAATAAAGTTTAAA	3055
rs528072073	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32073049	AGGTTTCGGTGAGCT[A/G]AGATCACGCCACTGC	3055
rs528113839	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32078964	TCCCCAGTTGATAAC[A/G]GAGGAACCAAAGGCC	3055
rs528152539	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32085935	GGCATTTATTTAAGA[A/G]CAGTGTTAAGATTAA	3055
rs528240120	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32101219	AGCTTGCAAGGTGAG[A/G]TGGGGAGTGATGCCT	3055
rs528253478	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32053307	GGATGGGGAGAGTAA[C/T]AGTACCTCCTTCACA	3055
rs528256831	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32092421	GGGTTCATCTTCAAC[C/T]GCTTTTGTCCAAACC	3055
rs528277066	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32093058	CAAGCAATTCTCGTG[A/C]CTCAACCTCCTGAGC	3055
rs528288446	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32069634	GATAATTTTTCAAAT[G/T]AATGATCCAGCACTC	3055
rs528384082	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32052517	AGGGGACCGGGAATA[A/C]CCGGCCCGCGAGGGG	3055
rs528392608	snp	A/G	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32060354	GCCTCCCAAGTAGCT[A/G]GGATTACAGGCACCC	3055
rs528428332	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32059631	GCGATCCTCCCACCT[C/T]AGCCTCCTGAGTAGC	3055
rs528456351	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32089520	TAACCAAATCTCTTA[A/G]AGACCATGACCCAAG	3055
rs528506421	snp	C/T	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32064506	TCTTCTTTCAGAGAA[C/T]TTCTAATCCAACATC	3055
rs528612118	snp	C/T	0.00318978	0.0398085	intron-variant	HCK	GRCh38.p7	20:32077879	ATGTCCTACCGTCCA[C/T]TTAACCTCTGCCCTA	3055
rs528786885	in-del	-/C			intron-variant	HCK	GRCh38.p7	20:32092871	TTTGCTAAAATCTCA[-/C]CCCCTCAAAGCAGGT	3055
rs528852738	in-del	-/A	0.498253	0.0295011	downstream-variant-500B	HCK	GRCh38.p7	20:32102121	AGTGAGACCCTGTTT[-/A]AAAAAAAAAAAAAAA	3055
rs528874049	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32073911	GAACCTGATAGATGG[A/G]CTATCTTATCCTGGG	3055
rs528935522	snp	A/G	0.000256032	0.0113115	missense	HCK	GRCh38.p7	20:32079829	CAACTGCTGGCTCCC[A/G]GCAACATGCTGGGCT	3055
rs529087706	snp	C/G	0.000296667	0.0121756	missense	HCK	GRCh38.p7	20:32074708	GCCCGCGTTGACTCT[C/G]TGGAGACAGAGGAGT	3055
rs529114003	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32086041	GTTTGTTTGTTTGAG[A/G]CAGAGTCTCGCTCTG	3055
rs529147453	snp	C/T	0.000490065	0.0156458	intron-variant	HCK	GRCh38.p7	20:32101286	TCATTTCCCAACTGC[C/T]TCCGTTTCTAATTCC	3055
rs529220422	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32093142	TAGAGACGGGGTTTC[C/G]CCATGTTGGCCAGGC	3055
rs529239628	snp	A/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32053374	CGGGCAGGGTGGCAC[A/T]CGCCTGTAATCTCAG	3055
rs529244686	snp	A/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32060358	CCCAAGTAGCTGGGA[A/T]TACAGGCACCCACTA	3055
rs529263175	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32095500	GACCTCAAGTGATCC[A/G]CCCGCCTTGGCCTCC	3055
rs529274774	in-del	-/AAAAAAAAAAAAAAAAAAA			intron-variant	HCK	GRCh38.p7	20:32054506	AAAAAAAAAAAAAAA[-/AAAAAAAAAAAAAAAAAAA]GCCCGGACGCGGGGG	3055
rs529280474	snp	C/T	0	0	intron-variant	HCK	GRCh38.p7	20:32066182	ACCTTCACCCCATCC[C/T]CTGTTCCCAAACTCA	3055
rs529370062	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32056494	GCACTCTAGCCTGGG[C/T]GACAGAGCGAGACTC	3055
rs529392364	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32072908	GAGTTCTAGACCAGC[C/T]GGGCCAACATGGTGA	3055
rs529430013	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32065329	GTGACCCAAGAATAT[A/G]CAAGAATCAGTGGAG	3055
rs529437550	in-del	-/TGTTT	0.00389407	0.043953	intron-variant	HCK	GRCh38.p7	20:32077516	ACCTTGTTCCTGTTT[-/TGTTT]TGTTTTGTTTTGTTT	3055
rs529463691	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32078094	GGCTGGAGTGCAGTG[A/G]CGTGATCTCGGCTCA	3055
rs529573118	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32068827	TTTGTAACTGTAGTC[A/C]CAGCTACTAAGGAGG	3055
rs529661768	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32091324	GTGGACCCCAAGCAG[C/T]GCTTTTGGAGCTCCA	3055
rs529773571	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	HCK	GRCh38.p7	20:32051050	AATGAAGAAATGACT[A/G]TGGTCCTGATCAGCT	3055
rs529775630	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32059026	ACCAATAGCCACAGA[A/G]AAATCTCTCAGACAA	3055
rs529811198	snp	A/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32098344	CCAAAAAAATTTTTT[A/T]AATTAGCTTGGCATA	3055
rs529812478	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32058388	AATGCAAAAATTAGC[C/T]GGGCGTGGTGGCGGG	3055
rs529820198	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32064359	AGATCCACCTCTACA[A/G]CCAGGGGTTGGAGTC	3055
rs529847002	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32099343	TCCTTCTCTCTCACT[C/T]CTATGACTTTTTTTT	3055
rs529896360	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32053875	ACTTCCATCCCCGGT[G/T]ATGCTGCTGCTGCTG	3055
rs530050843	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32070816	GCTGTGTAAATGGAT[A/G]AATGAATTACCAAAC	3055
rs530099357	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32076669	ATCACCTGGATTGCC[A/G]GCTAACAAGTGCTTT	3055
rs530282123	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32097192	GGCTGAGGCGGGAGA[A/G]TCGCTTGAGCCCAGG	3055
rs530307131	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32086220	GAGACGGGGTTTCAC[C/T]GTGTTAGCCAGGATG	3055
rs530358849	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32096390	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	3055
rs530366152	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32088320	GTCCTGTGAAGGCAT[G/T]ATCCCAGCCATCCAG	3055
rs530412157	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32057753	TATACCACAAGTCAT[C/G]AAGCAATCACTTCTG	3055
rs530454140	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32057061	AGCTCACATAATCTG[G/T]ATTTCTGTCTCCTAA	3055
rs530514515	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32078173	CCGAGTAGCTGGGAC[C/T]ACAGGCTCCTGCCAC	3055
rs530545429	snp	A/G	0.00170503	0.029148	intron-variant	HCK	GRCh38.p7	20:32052498	CCAGGTGAGTGCCGC[A/G]CACAGGGGACCGGGA	3055
rs530553104	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32085240	ATGCAAGGCCGGGCA[C/T]AGTGGCTCACGCCTG	3055
rs530582107	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32059609	AGCCCCAACCTCCTG[C/T]GCTCAAGCGATCCTC	3055
rs530723943	snp	C/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32093711	GATGGAGGAATGCCA[C/T]CCTGAGCCCTGGGGC	3055
rs530730344	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32064916	TCTTTACCAGGGATC[A/G]GCAGTTTTGAGTGGG	3055
rs530824378	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32077226	GGAATCAGGGCGGGA[C/T]GGAATCTTGGTTTCT	3055
rs530902469	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32063727	AGTGCAAATCACAAT[C/T]CCTTATAAGAATTCC	3055
rs530942294	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32070993	GAAGGGAGGGAGGGA[A/G]GGAGGGAAGGAGTTA	3055
rs531109039	snp	C/G	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32097261	CTCCAGCCTGTGTAA[C/G]AGAGCAAGACTTTGT	3055
rs531123464	snp	C/T	0.000132048	0.00812444	synonymous-codon	HCK	GRCh38.p7	20:32083988	CAACGGGGGCTTCTA[C/T]ATATCCCCCCGAAGC	3055
rs531143993	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32098097	CTATCATCCAGGCTG[G/T]AGTGCAGTGGTGTGA	3055
rs531220884	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	HCK	GRCh38.p7	20:32050891	TGGGTAGAGCCCAGG[A/G]ATGCTGTTAAACATC	3055
rs531278381	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32080101	CAGCTTAGGTCAGTG[G/T]AACTAGTGCCAGGTG	3055
rs531345185	snp	C/G	0.00318978	0.0398085	intron-variant	HCK	GRCh38.p7	20:32062390	CCAAGAAGGTTCACA[C/G]TTGCTCTGGAATTCT	3055
rs531348375	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32069979	CTCAGCAAATGTGTG[G/T]GCACATTTTGAGAAA	3055
rs531456882	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32074487	CACATGCTGGGGCTG[A/G]CATAGTCACAGCCCT	3055
rs531549014	snp	C/T	0.0170251	0.090679	intron-variant	HCK	GRCh38.p7	20:32080584	CTGCAACTTCTGCCT[C/T]CTGGGCTCAAATGAT	3055
rs531588419	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32082011	ACACCCCATCCAGCA[C/G]CAACCAAGCCAGTCT	3055
rs531633156	snp	A/G	0.00318978	0.0398085	intron-variant	HCK	GRCh38.p7	20:32059608	CAGCCCCAACCTCCT[A/G]CGCTCAAGCGATCCT	3055
rs531739593	snp	A/G/T	0.000811863	0.0201316	intron-variant	HCK	GRCh38.p7	20:32088687	GGGAAACAGGAATTC[A/G/T]ATTTTTTTACTTGCC	3055
rs531777278	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32055648	AGTTCAAAATTTTTA[G/T]AAATATTTTAATCGA	3055
rs531814819	snp	A/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32061206	CCAGGCTGGTCTTGA[A/T]CTCCTGACCTTGTGA	3055
rs531840916	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32094497	CCAGCCTGGGCAACA[C/T]AGGAAGACCTAGTCT	3055
rs531876555	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32095086	CAATTGATGAACAGA[C/T]GAACAAAATGTGATA	3055
rs531899730	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32061563	GACTAGCTGGGAACA[A/G]GCTAGACAGTGATGG	3055
rs531985542	snp	C/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32058329	CTGAGGTCAGGAGTT[C/T]AAGACCAGCCTGGCC	3055
rs532014401	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32099234	GAGTTCTTGATCCTC[A/G]CCCCCAACCTTCCCT	3055
rs532100464	snp	C/G	0.000399281	0.0141238	upstream-variant-2KB	HCK	GRCh38.p7	20:32050928	TTCACAGGACAGTCC[C/G]CCGCAACAAAGAATT	3055
rs532109929	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32057875	AAGGTACTTTCAGAG[A/G]CGTGGGTAATGATGC	3055
rs532115591	snp	A/C	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32063634	CTCACCTACTCTAAT[A/C]GGTCTAGTACCATCT	3055
rs532129599	in-del	-/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32060694	CCAGGTCCTTTTTTA[-/T]TTTTTCTTTTCTTTT	3055
rs532180555	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32070727	TCTGTCTCCCATTCG[A/G]CTGCAGTTGAGGTCC	3055
rs532485678	snp	G/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32075810	TGGGGCTCCCTGCTG[G/T]AGATGTTCTCTGTAT	3055
rs532526261	snp	A/C	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32089664	CAGCTCCTCTCACCC[A/C]CAGCCTAAGCAGTTT	3055
rs532562462	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32095270	GGCAATCTTTTTTTT[G/T]TCTTTGAGATGGAGT	3055
rs532574503	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32082258	TAGTTATAATTCATT[A/G]TAATGAATATTATTC	3055
rs532655070	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32096821	GTCACCTTAAGTAAG[C/G]GGGTATTAACTGGAA	3055
rs532707026	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32056986	TCAGCTGCCCTCCCC[A/G]AACACCCCTCCACCC	3055
rs532740587	snp	G/T	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32096214	TTTTAAAGAGACGGG[G/T]GCGGCCGGGCACAGT	3055
rs532840131	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32074077	TTTCTAGGGCTCCTG[C/T]GATTAAGCCACCGGC	3055
rs532972532	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32068056	AATCCCAGTACTTTG[A/G]GAGGCCAAGGAGGAC	3055
rs532996242	snp	A/G	0.00279162	0.0372561	intron-variant	HCK	GRCh38.p7	20:32080992	TACTCAGAAGGGTGA[A/G]GCCAGATGATCTCTT	3055
rs533050593	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32076739	AGGTTCTTGGGTGAG[A/G]CAGCTGCTGCTGCTG	3055
rs533095544	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32094249	AGATTTTAGAGGGAG[C/T]GGGCAAATATATGTC	3055
rs533142944	snp	A/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32054110	ATAATAGCATTTTGT[A/T]GTGTTTGTTTTGAGA	3055
rs533155438	snp	A/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32093697	AACCTGAATGGGTTG[A/T]TGGAGGAATGCCACC	3055
rs533287729	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32055075	AACAATATTGACAGG[A/C]GCATCCTGGATGTGT	3055
rs533293671	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32074958	TTAATCCCTTCTGAA[A/C]ATGTTTTACTAGCAA	3055
rs533306995	in-del	-/TTTATTTATTTATTTAT	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32095884	TTATTTATTTATTTA[-/TTTATTTATTTATTTAT]TTATTTTGAGACGGA	3055
rs533326848	snp	A/C	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32066302	TTGTGCCCTCCAGTG[A/C]CTTTTTTTTTTTTTT	3055
rs533501739	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32096074	TTTGTATTTTTAGTA[C/G]AGACAGGGTTTCACC	3055
rs533511199	snp	A/G	0.00358779	0.0422022	intron-variant	HCK	GRCh38.p7	20:32094743	AGAAAGAAAGAAAGA[A/G]AGAAAGAAAGAAAGA	3055
rs533521238	in-del	-/AGGG	0.0452881	0.143503	intron-variant	HCK	GRCh38.p7	20:32070983	AGCAGGAAGGAAGGG[-/AGGG]AGGGAGGGAGGGAGG	3055
rs533598444	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32075063	GGGACTTTGTCTGCT[C/T]CTGCATCCTCGGCAC	3055
rs533768902	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32067599	TTCCTACTACATAAA[A/G]TATGGCACGCCAGGC	3055
rs533782314	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32055841	TACCCCCCATTCCCC[C/T]GGCCCCTGGCAACCA	3055
rs533804364	snp	C/T	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32073594	AGCATGGTGAGACGC[C/T]TACTTATACTTGGAA	3055
rs533963718	snp	A/G	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32086909	CTTGAGATGGCCCCA[A/G]TCTGGCCAGGAGCTC	3055
rs533972208	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32068100	TTGGGAGTTCAAGAC[A/C]AGCCTGACCAACGTG	3055
rs534090502	snp	A/G	0.0023933	0.0345097	utr-variant-3-prime	HCK	GRCh38.p7	20:32101675	TGGGTAGGTTGGACT[A/G]GAAAATCTCTTTTTG	3055
rs534136035	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32053062	ACACTGCATGCATGC[C/T]CTGTCTCTTTCCTCC	3055
rs534270649	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32059997	GGCTTTGAGGATTCC[A/C]TTTGTGGAGGACAGG	3055
rs534305242	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32065622	TCCTTATAGAAAGAG[A/G]GTGCTTTTTCCCTAA	3055
rs534341694	snp	G/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32072625	AGTTTAGGTGTCACT[G/T]CCCCCTTGCATGGAC	3055
rs534642140	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32091478	AAATGTCACATAAGT[A/G]TTTAAGTATCATCTT	3055
rs534671021	snp	C/G	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32072004	CAGCCCAGGCTTGGC[C/G]CCTCAGCCTGAGCTC	3055
rs534745253	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32087306	CCCCTGCCATTTTTT[A/G]TTTGTTTGTTTTTTA	3055
rs534805765	snp	A/G	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32077676	GGATTACAGGCATGC[A/G]CCACCATACCTAGCT	3055
rs534845473	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32084857	TGAGATAACCAGAGA[C/T]CTTTTCAGATGATGA	3055
rs534892626	snp	A/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32071162	TGTTTGCTCTGAGCC[A/T]GACACTGCACTGAGT	3055
rs534899838	in-del	-/GCCCCAGACCACACT	0.00358779	0.0422022	intron-variant	HCK	GRCh38.p7	20:32053037	CCCCCAAACCTCCTG[-/GCCCCAGACCACACT]GCATGCATGCCCTGT	3055
rs534934370	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32094198	TCTCACTCAGAGATT[C/T]TGAGGAGATTTTAGA	3055
rs534936010	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32062933	GGGAAAGTTCCTGTA[A/C]CTGAACAGCCTTAAG	3055
rs534985888	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32059259	CCAAGAGTGTCTTAA[A/G]TGTATCTGTAATGTT	3055
rs535005815	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32060853	GGACAGGAGAGCCAT[C/G]AGATAGTGGGGTACC	3055
rs535081793	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32060582	GAAATCTGGGGGCAT[C/T]CAGCAGACTAAATGG	3055
rs535174840	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32063950	AGAAACCAAGGGCTG[A/G]CTCTCGTTGGCCAGA	3055
rs535282544	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32076421	GCTTTGCCCTGGGTC[A/G]TCCCATGCTCTGTTT	3055
rs535317958	in-del	-/T	0.0107246	0.0724382	intron-variant	HCK	GRCh38.p7	20:32060993	TTCTGTTTTATTTTG[-/T]TTTTTTTTGAGACAG	3055
rs535415901	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32070140	CCCCAAACCTGTCCA[A/G]TGCTTACCTCCTCTC	3055
rs535416180	in-del	-/ACA	0.0023933	0.0345097	intron-variant	HCK	GRCh38.p7	20:32085358	TCTCTACGAAAAAAT[-/ACA]ACAATTAGCCAGGCG	3055
rs535438200	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32067054	AGGTTGCTTTTTATA[C/T]GAACTTACTAACATA	3055
rs535490430	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32065755	CTCTGATTGGCCAGG[C/G]CTGTGTCAAGTTGCC	3055
rs535490629	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32094736	GAAAGAAAGAAAGAA[A/G]GAAAGAAAGAAAGAA	3055
rs535499281	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32073161	CTGCCCCTAATGTGC[C/T]GTGTGGTGCCAGGCA	3055
rs535577345	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32099703	GTTTTGGCCACTCGA[C/T]TCCAAAACATATCCC	3055
rs535587649	snp	G/T	0.0023933	0.0345097	intron-variant	HCK	GRCh38.p7	20:32061096	TCAAGCAATTCTCCT[G/T]CCTCAGCCTCCTGAG	3055
rs535637888	snp	A/T	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32072776	TGTTGAGGGGAGGGG[A/T]CAAGCAGCATCCCCC	3055
rs535704439	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32071281	GCTGGTGGGGTGGAG[A/G]GGCCAAGGATCAGCT	3055
rs535813164	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32052629	TCGGGGGAGCCGCGG[A/G]TAGCCCGGGGGATGA	3055
rs535838966	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32076806	AATACGCATATCTGG[C/G]CAGGTGTGGTGGCTC	3055
rs535872810	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32076483	CCCTGGGTCACCTCA[G/T]GTAGTCCTTGCAGCA	3055
rs535898005	snp	A/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32084182	TTTGGATGCTTCTGA[A/T]GGCTTAGGACTGTTG	3055
rs536011073	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	HCK	GRCh38.p7	20:32050438	GAACATTATCTGTTT[C/T]TATAAAAAGCACATA	3055
rs536052498	snp	A/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32057885	CAGAGGCGTGGGTAA[A/T]GATGCAGAAGCAGCC	3055
rs536056229	in-del	-/AGGG	0.00163399	0.0285363	intron-variant	HCK	GRCh38.p7	20:32070980	GGGGAGCAGGAAGGA[-/AGGG]AGGGAGGGAGGGAGG	3055
rs536114541	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32085370	AATACAACAATTAGC[C/G]AGGCGTGGTGGTGGG	3055
rs536193799	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32057419	AGCCTGGGTAACATG[A/G]CAAAACCCTGTCTCT	3055
rs536338102	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32064409	AACTGAGACTAGGGG[C/T]GGAGTAATTCCCAAA	3055
rs536343268	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32090125	AAATGTGTTTTCACT[C/G]CTATGGGCCAGGTCC	3055
rs536410611	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32097483	ACTTGGGAGACTGAG[G/T]CAGGAGAATGGCGTG	3055
rs536479719	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32097829	TCCAAAGAACATATA[G/T]TCTATAGACCATGTT	3055
rs536550240	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32087846	ACGGTGTTTCACCGT[C/G]TTAGCCAGGATGGTC	3055
rs536571734	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32096903	TGATGGTGATTACAA[A/G]GGTATATATATATAT	3055
rs536674529	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32077618	TGCAACCTCCGCCTC[A/C]CGGGTTCAAGCGATT	3055
rs536711284	snp	C/T	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32084754	AGACCAGTCCTGTAG[C/T]GGTCAAAAACTTCCT	3055
rs536831957	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32056881	CTTCTAACACCTGGC[A/G]CCTGGCACATAGTAG	3055
rs536947832	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32095358	CCTCCCAGGTTCAAG[A/C]GATTCTTGTGCCTCA	3055
rs536962602	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32080731	TGCCTAGGCTGGCCT[C/T]GAACTTCTGGACTCA	3055
rs536989789	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32058432	AGCTACTTGGGAAGC[C/T]GAGGCAGGAGAATTG	3055
rs537048009	in-del	-/C			intron-variant	HCK	GRCh38.p7	20:32054887	AGAGGAGCATATTTG[-/C]CCCCATCTTATCATT	3055
rs537109754	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32081074	AGCCTGGGCAACAGA[A/G]CAAGACCCCATCTCT	3055
rs537110982	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32076960	GTGTGATGGCGGGCT[C/G]CTGTAATCCCAGCTA	3055
rs537239589	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32076219	TAGTCCCAGCTACTC[A/G]GGAGGCTGAGGCAGG	3055
rs537330340	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32097552	ACCACTGCACTCCAG[C/T]CTGGGCAAACAGAGC	3055
rs537369170	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32090243	AGAGCCACTCTGCCC[A/G]TTTCACAGAGGGGAA	3055
rs537394320	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	HCK	GRCh38.p7	20:32050518	CAAGGCAGGAGGTTC[A/G]GTTGAGCCCCGGAGT	3055
rs537411811	snp	A/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32096674	GCCCAGCTAATTTTT[A/T]AATTATTTGTAGAGA	3055
rs537451507	snp	C/T	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32084235	GATGTAGAGGTGGCA[C/T]CCCGTCACACTCTGC	3055
rs537456060	snp	A/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32063278	TTCTTTTTTTGAAAC[A/T]TTCTTGCTCTGTAAC	3055
rs537460480	in-del	-/A	0.0023933	0.0345097	intron-variant	HCK	GRCh38.p7	20:32085296	GCAAGTGGATCAATC[-/A]AAGGTCAGCAGTTCG	3055
rs537501816	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32063393	AAGTAGCTGGGAATA[A/C]AGGCACATGCCGCCA	3055
rs537573913	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32095538	CTGGGATTACAGGTG[C/T]GAGCCACCATGCCCG	3055
rs537624184	snp	A/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32055863	TGGCAACCACCAATC[A/T]GCTTTTTGCCTCTAC	3055
rs537662932	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32061311	AGGAAAGTTTGTCAA[A/G]GCTGTTAAGGAGCCC	3055
rs537668401	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32068959	AGAAAACAAATCACA[C/T]TTTATTGTGCAAAAA	3055
rs537677526	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32075508	GCACCTGGCCCATCC[C/T]TCATTTGATTCATTC	3055
rs537697748	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32068242	GGCAGAGGTTGCGGT[A/G]AGTGGAGATGGCACC	3055
rs537713186	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32082598	AGTGAGCCAAGATTG[C/T]GCCACTGCACTCCAG	3055
rs537838055	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32074222	GATGTGCTGAAGCCC[A/G]AGAACGGGAGTGGTC	3055
rs537874864	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32073619	TTGGAACCACATATC[A/G]ATGGGTGCGGAGCTG	3055
rs537918269	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32080102	AGCTTAGGTCAGTGG[A/G]ACTAGTGCCAGGTGG	3055
rs537954864	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32087116	GCCTTAGAGGCCAGG[G/T]TGTGGCATGGGTGGT	3055
rs537984693	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32056485	CGAGCCACTGCACTC[C/T]AGCCTGGGCGACAGA	3055
rs538051897	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32054581	GGAGGCTGAGCCGGG[A/C]GGATCACGAGGTCAG	3055
rs538054330	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32075384	TTTTTTGTATTTTTG[A/G]TAGAGAGGGGGTCTC	3055
rs538185486	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32053781	CCTACATCAGCATCA[C/T]CTGGACTGCTTGTGA	3055
rs538244691	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32083463	AAAAAGTATACTATG[A/G]TCTCTTGGCTTTTTG	3055
rs538264449	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32080605	CTCAAATGATTCTCC[C/T]ATCTCAGTCTCCCGA	3055
rs538351585	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	HCK	GRCh38.p7	20:32050188	AATTCTAATGTAGGA[C/T]GATAAGGGGACGTGT	3055
rs538384514	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32097376	CGAGGTCAGGAGATC[A/G]AGACCATCCTGGCTA	3055
rs538401851	snp	C/T	9.16112e-05	0.00676736	intron-variant	HCK	GRCh38.p7	20:32093818	GTGGGGCCATCTTGG[C/T]GTAGGCCAGGTCTGA	3055
rs538418559	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32057333	GGGCTGGGTGCGGTG[A/G]CTCACCCTGTAATCC	3055
rs538455346	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32062505	CTCAGAGCCAGCCCT[A/G]TGGCTCAGCCAGGCA	3055
rs538462539	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32056619	CAAGGGTTTCAATTG[A/G]CTTCACATCCTTGCC	3055
rs538563066	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32093258	CCTGTTTTATCTTTT[C/T]TTTATGGTACTTACC	3055
rs538570196	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32061085	GCCTCCCGGGTTCAA[A/G]CAATTCTCCTTCCTC	3055
rs538593378	snp	A/G	0.00358779	0.0422022	intron-variant	HCK	GRCh38.p7	20:32061887	TACTCCAAGTGAGAC[A/G]GAAACCCTGGGTGGG	3055
rs538596746	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32093717	GGAATGCCACCCTGA[A/G]CCCTGGGGCCCTCCC	3055
rs538603258	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32069483	ACACACGAAATGTGA[C/T]ATAATTTTATGTCAT	3055
rs538633922	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32069070	AATTGCAAACTGTGC[C/T]TGCTTCATGATCCGG	3055
rs538641192	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32068115	CAGCCTGACCAACGT[C/G]GTGAAACCCTGTCTC	3055
rs538718492	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32096784	TAGGATTACAGGCAT[A/G]AGCCACTATGCACAG	3055
rs539220891	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32092194	CCAGCTGCAGTCTGC[C/T]GGAGCACTGGAGTGC	3055
rs539233694	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32088416	TTCTCTTTCTCAAAC[A/G]CTAGGAATTGCAAAC	3055
rs539310896	snp	C/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32087132	TGTGGCATGGGTGGT[C/G]GGGGTGCCACTCTCC	3055
rs539316205	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32079297	AACAAAACTCAGGCC[C/T]TTCACAGGCTTCCAA	3055
rs539369021	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32094618	ACTTGAGTCTAGGAA[A/G]CTGAAGCTGCAGTAA	3055
rs539418813	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32061229	CCTTGTGATTCGCCC[A/G]CCTTGGCCTCCCAAA	3055
rs539471777	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32070521	CACTCTTCCCTCAGA[C/G]TGTCCCCTCACTGGC	3055
rs539483292	snp	A/G	0	0	intron-variant	HCK	GRCh38.p7	20:32085407	TAATCCCACCTACTC[A/G]GGAGGCTAAGGCAGG	3055
rs539582841	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32066090	ATTTCTAAACTCACT[C/T]AAACCACTTTGTCAC	3055
rs539588903	snp	G/T	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32052842	AGGAAGGGATGGGGC[G/T]TCACAGAACCCGGGA	3055
rs539604874	snp	A/G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32073524	TTGTGTTTCTAGAAC[A/G/T]CTGTTTAGTAACATG	3055
rs539625987	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32059932	AACTGAGACCTGGAG[C/G]TTTGTCAATTATAAA	3055
rs539628446	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32066525	ATCATATTGGCCAGG[C/T]TTGTCTCGAACTCCT	3055
rs539642709	snp	C/T	2.26088e-05	0.00336213	intron-variant	HCK	GRCh38.p7	20:32079919	CTCCCTGCCGAGGTG[C/T]CCCAGCTGGGGCTGG	3055
rs539741028	in-del	-/A			intron-variant	HCK	GRCh38.p7	20:32069000	GGAATTCCCTATTTT[-/A]AAAAAAAGCGAACTT	3055
rs539826760	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32053436	TGAGGTCTAGAGTTT[C/G]AGACCAGCCTGGCCA	3055
rs539935046	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32093472	GAAGGTGAAAGCTCT[C/T]CATAGTATCCTAGGG	3055
rs540039565	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32059471	TTTCCCTTCCTCCTC[C/T]TCCTCCTTCTTCTTC	3055
rs540216736	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32093187	TGGCCTCAAGTGATC[C/T]GCCCACCTCGGCCTC	3055
rs540264890	snp	C/T	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32087221	GCAGTTCTGCCCCCA[C/T]CCCCGCCCTGCCACA	3055
rs540297893	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32078686	ACATGGTAAAACCCC[A/G]TCTCTACTAAAAATA	3055
rs540334989	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32085468	GCAGGGAACCGAGAT[C/T]GCACCACTGCACTCC	3055
rs540342845	snp	A/G	5.01165e-05	0.00500557	intron-variant	HCK	GRCh38.p7	20:32094026	GGGAAGGTAGGGAAC[A/G]CTGCCAAGCAGCCCC	3055
rs540376056	snp	A/G	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32054723	AGGCAGGAGAATGGC[A/G]TGAACCCTGGAGGTG	3055
rs540414527	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32053992	ATGGTTTTCTCTTTA[C/T]GGTCCTTTTTTTTTT	3055
rs540468721	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32085144	GGAGCGAAGACAACT[C/T]ACAGGGATGCAAACA	3055
rs540483266	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32068493	TTGTGGCTCACATGA[C/G]ATTTCTGGGCCTAGT	3055
rs540546478	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32095152	GGAATGAAGTACTAC[A/G]CCAGGCTAGAACACA	3055
rs540553414	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32100016	ATGATCCTCCCGCTT[C/T]AGCCTCCCGAGTATC	3055
rs540574965	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime	HCK	GRCh38.p7	20:32052279	GGGAGCACATCAGAG[C/G]CTTAGAGGCGAGTGG	3055
rs540590047	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32091875	CTATAGTACCAGCTG[C/T]TTGGGAAGCTGAGGT	3055
rs540684367	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32064297	CCGCGCCCATCCACC[A/C]ATCTCTGCTTCTATT	3055
rs540864576	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32071557	AGACCGGGAAGGCCA[C/G]TGGGAGCCAGCCCGG	3055
rs540880646	snp	A/G	0.00279162	0.0372561	intron-variant	HCK	GRCh38.p7	20:32052605	GGGGCAGCGAGGGGA[A/G]ACGGAACGTCGGGGG	3055
rs541006700	snp	A/G	0.000798403	0.0199641	upstream-variant-2KB	HCK	GRCh38.p7	20:32051475	GGGCCAGAAGGGAGG[A/G]GTCGGAGTGGTGGGG	3055
rs541041586	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32064770	GTCTCTGAGTTTTCC[A/C]CAGCCAGCATGGTAA	3055
rs541068033	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32099235	AGTTCTTGATCCTCA[C/T]CCCCAACCTTCCCTC	3055
rs541069595	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32058663	ACTAGTCCATCATGG[C/T]GTATATGTCTTAGTT	3055
rs541069607	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32088337	TCCCAGCCATCCAGG[A/C]TCAGGGGCTGTCTCA	3055
rs541074749	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	HCK	GRCh38.p7	20:32050607	ATGCCATACCACACC[A/G]AACACATCTGATCTT	3055
rs541184994	snp	A/G	0.00478085	0.0486577	intron-variant	HCK	GRCh38.p7	20:32097783	TCAAAACTTGACCAT[A/G]TACTCAGTCATAAAG	3055
rs541194801	snp	C/G	0.0023933	0.0345097	intron-variant	HCK	GRCh38.p7	20:32072080	GAAGCAAAAGCAGTG[C/G]TGAGAAACGAGTGAA	3055
rs541259742	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32077056	GCCACTGCACTCCAG[C/T]CTGGACAACAGAGCG	3055
rs541289632	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32076609	ATTTGCAGACAAAGG[C/T]AAAATAACCTAGATG	3055
rs541340422	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32083833	AGGGTGTCAGAGTGC[C/T]AATGCAAGGTGGCAG	3055
rs541400523	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32053148	AAGTCTTTCTTGCAA[A/G]GATGCAGGAAATTGG	3055
rs541443092	snp	G/T	0.000568666	0.0168526	utr-variant-5-prime	HCK	GRCh38.p7	20:32052390	GAAAGTCAGTTTCCC[G/T]GCACTGGCACCCCGG	3055
rs541481429	snp	C/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32083161	TCCATCTTCACCTCT[C/T]CCACTTTGACCTTCC	3055
rs541516010	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32059588	TGATGCTATCATGGC[C/T]CATGCAGCCCCAACC	3055
rs541557251	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32089676	CCCCCAGCCTAAGCA[A/G]TTTTTTCACTTCTGT	3055
rs541583624	snp	A/C	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32058095	CAGGAATCCCAGCCT[A/C]ATCTCTACCATAGAA	3055
rs541585183	snp	G/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32091724	GGCATGACAGCTCAG[G/T]CCTGTAATCCCAGCA	3055
rs541624925	snp	A/G	0.00279162	0.0372561	intron-variant	HCK	GRCh38.p7	20:32057624	AAAGAAAAGGAATGT[A/G]AAGCCTAGAGAGGGT	3055
rs541647134	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32064880	TCAGGTTCCCAGGGA[C/T]GGCAGTGGCCCGAGG	3055
rs541663238	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32062711	TGAGGCTCAGTAAAG[A/G]GAAGACGTGAGAAGT	3055
rs541670192	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32057003	ACACCCCTCCACCCG[C/T]AGCGATTATTTTTAA	3055
rs541822765	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32060070	GAAAAGTGGCCCTGG[G/T]GGTGAACTGGCCACC	3055
rs541906170	snp	A/C/T	0.000164884	0.00907852	synonymous-codon	HCK	GRCh38.p7	20:32099107	CCTGCTGATGGAGAT[A/C/T]GTCACCTACGGCCGG	3055
rs541960373	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32100084	TTTATTTTTTTAATT[C/T]TTTTGTAGAGACTTG	3055
rs542191004	in-del	-/AAAAAAAAAAAAAAAAAAAAAAA			intron-variant	HCK	GRCh38.p7	20:32054502	AAAAAAAAAAAAAAA[-/AAAAAAAAAAAAAAAAAAAAAAA]GCCCGGACGCGGGGG	3055
rs542318075	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32082787	GGTCATGAGCTGAAA[A/G]ACTTATGTGTTTCTG	3055
rs542320208	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32089280	CCAGGGACCCCCTCA[A/G]TGTAACAGTCTGGCC	3055
rs542382998	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	HCK	GRCh38.p7	20:32051274	CGACCACCTCCCCCA[A/G]CTTGGGAGTCCTCTG	3055
rs542417240	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32089500	GTGGGAAGATGAGTA[C/T]TAAATAACCAAATCT	3055
rs542417648	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	HCK	GRCh38.p7	20:32050793	TCATGGTTCTTCCCC[C/T]CTTCCCCACCAGGGG	3055
rs542453226	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32081980	AATCCCACCCTGCTG[C/G]TTCCTGGATCCTGCC	3055
rs542471243	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32055517	TTGCTTAGTATTACA[C/T]TGTAGCATTTTCCAG	3055
rs542588526	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32056699	GGGTACAGAAAGCAC[A/G]AATCTTAATCTCATT	3055
rs542601193	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32062783	CGGGGATAAAGACAG[C/T]TCATTCAGAAGACAG	3055
rs542700793	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32077791	GGCCTCCCAAAGTGC[C/T]GGGATTACAGGCGTG	3055
rs542703853	snp	C/T	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32095024	ACATTCATGGCAGCA[C/T]TCTTCCTAATAGCCA	3055
rs542739655	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32058006	TCCTGACTCTCCCTT[C/T]GAGTCACCTCCCTGA	3055
rs542883592	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32067970	ACTTGTTTCTTTTTA[C/T]TTTAAGAAACCTGGA	3055
rs542999281	snp	A/C	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32064128	CCAGCCTCAGCCTCC[A/C]AAGTAGCTGGGATTA	3055
rs543036305	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32063598	TGCCATCAGCTTAAT[A/G]AGGTCCATATTCCTC	3055
rs543073008	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32070682	TAACTCAATTTGCCC[C/T]GTTATTTATTTGTTG	3055
rs543090260	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32083137	CTGACATCTGTCCAA[A/G]CTCTTGTTTCCATCT	3055
rs543120943	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32094167	ATCCTTCTGGATAAT[G/T]TCCTGAACTTCAGAG	3055
rs543197248	snp	A/C	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32068341	AAAAAAAAATAAAAA[A/C]TAAAAATAAATTTAA	3055
rs543251690	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32076560	TTGCTAAGTGGAAAA[C/T]GCAGGGTGTAGACAA	3055
rs543271799	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32074298	CAGCTGAACCATTCT[A/G]AGTCTCTATAGGCAC	3055
rs543312336	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32080843	CCGTAACAGACCAAG[C/T]AGGGGAGGCCAACAC	3055
rs543313055	snp	A/G	0.00597247	0.0543191	intron-variant	HCK	GRCh38.p7	20:32061189	GGGTTTCACCATGTT[A/G]GCCAGGCTGGTCTTG	3055
rs543384083	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32085532	AATAATAATAAAATT[A/G]AAAAGAATTTGACAA	3055
rs543390248	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32058277	TGGCTCACACCTGTA[A/G]TCCCAGCACTTTGGG	3055
rs543468588	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32057515	TGAGGTGGGAGGATC[A/G]TCTGAGCACAGAAGG	3055
rs543675255	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32082865	CACTACTTTTGAAGG[C/T]AAAAACTGCAATTAC	3055
rs543683894	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32061615	TGTCTTTGCCAGGGT[G/T]ATGAGGGAAGGTTGC	3055
rs543715557	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32058140	GTACAGTACAGTAGA[C/T]GACCCCGAGTCTGAG	3055
rs543730401	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32089592	AAATAATGTTCACAA[A/G]TCGCAAAAACACTGC	3055
rs543852805	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32056926	ACTGATGGGACAAAC[A/G]CAATGAATGTTGGAC	3055
rs543892429	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32094780	GAAAGAAAGAAAGAG[A/G]GAGAAAGAGAAAGAA	3055
rs543898983	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32057537	CACAGAAGGTGAAGG[C/T]TGCAGTGATCTGAGA	3055
rs543948898	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32096171	CTGGGATTACAGATG[C/T]GAGCCACTGTGCCAG	3055
rs543954404	snp	C/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32094178	TAATGTCCTGAACTT[C/T]AGAGTCTCACTCAGA	3055
rs544093060	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32074829	CTGGCACATACTCTT[C/T]CCAGGGCTCTGGGCT	3055
rs544134151	snp	G/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32054015	TTTTTTTTAGGGGAG[G/T]GGGTGACAGGTTAAA	3055
rs544224815	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32074319	CTATAGGCACAGGAC[C/T]CTGCCATGGGTATAG	3055
rs544226995	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32066885	CTTGCAGTGCTCTGT[A/G]TATGGTTTAATATTA	3055
rs544232139	snp	A/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32080924	GAGACCCCATCTGTA[A/T]GAAAAATTTTAAAAA	3055
rs544266934	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32099313	AGCCTGAAATCTGGG[C/G]GCTTCCTTGGCCCTT	3055
rs544674412	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32075524	TCATTTGATTCATTC[A/G]ACAAGCACATGCTCA	3055
rs544675752	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32081567	CATTGATTAAAGGCA[C/T]GTTCCTCATGTGGCC	3055
rs544908787	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32092760	GCTGTTCCATGAACA[C/T]CCAAGCTCTTACCTA	3055
rs545019845	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32074914	CTAAAGTGGGTCCCA[A/G]CTGTGACTCTGTCTT	3055
rs545020716	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32061198	CATGTTGGCCAGGCT[C/G]GTCTTGAACTCCTGA	3055
rs545049614	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32073899	TGCTTCCATAAAGAA[C/T]CTGATAGATGGGCTA	3055
rs545055783	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32055086	CAGGAGCATCCTGGA[C/T]GTGTAGCTTTCGGCC	3055
rs545061413	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32067797	TTGAGCACAGATGGA[A/G]TCATAGCTGAGATGT	3055
rs545081328	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32081186	AGGTAGGATGAGGTC[A/G]CCAGAAGAGACTCAA	3055
rs545191346	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32067037	CAATTATTATTGTAA[A/G]CAGGTTGCTTTTTAT	3055
rs545305506	snp	G/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32094933	CAAAATGAAAGAAAT[G/T]AGACCAAAAAAAAAG	3055
rs545313688	snp	A/G	0.00358779	0.0422022	upstream-variant-2KB	HCK	GRCh38.p7	20:32051260	CTCCTCCCCTCCCCC[A/G]ACCACCTCCCCCAGC	3055
rs545330483	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32055898	TAATTTATTCAGGAT[A/G]TTTAACATAAATAGA	3055
rs545348257	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32079720	GCATCCTGTGTAGGC[C/T]GGACAGGACTGCATG	3055
rs545724081	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32086502	CATGATTTCGCTTCC[C/T]TCTCTGAGAGTTGAG	3055
rs545865009	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32085076	ATGCAGTGCCAGCCC[A/C]GTGTGGGGCAGCCTG	3055
rs545878098	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32072195	TACCAACCATAATTG[C/T]GTGAGTATAAGACCA	3055
rs545900069	snp	A/G	0.000798403	0.0199641	downstream-variant-500B	HCK	GRCh38.p7	20:32102159	GAAGAAGAAAGAAAG[A/G]AAAGGAAAGAAAATT	3055
rs545946589	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32091112	CAAGCTGAGTTGGTC[C/T]AGCTCCAGAGCCATT	3055
rs546003588	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32060158	TCTCCCAGCAGAAGC[A/G]AGCAAATGTGCATCA	3055
rs546044356	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32066046	GGCTGCTGGTTCTCA[C/T]GCTAGCCACACTCTG	3055
rs546067777	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32098136	CACTGCAACCTCCAT[C/T]CCCTGGGTTCAAGTG	3055
rs546252680	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32077268	TTGAAATAGGCAATA[C/T]TTTCAAATGTTTCAA	3055
rs546287799	snp	G/T	0.000165006	0.00908161	missense	HCK	GRCh38.p7	20:32084497	TCGGGAATCCCTCAA[G/T]CTGGAGAAGAAACTT	3055
rs546500695	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32101260	CCACAGGGCCTGCCA[C/T]CCCTGGGCTCTCATT	3055
rs546574158	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32062008	GCAGTGGTGCGACCT[C/T]GGCTCCCTGCAACCT	3055
rs546660596	snp	C/T	1.73063e-05	0.00294157	missense	HCK	GRCh38.p7	20:32079796	TTCAAGGGCATCAGC[C/T]GGAAGGACGCAGAGC	3055
rs546783926	snp	C/T	0.000280785	0.0118454	missense	HCK	GRCh38.p7	20:32071757	GTCCTGTGTACGTGC[C/T]GGATCCCACATCCAC	3055
rs546831596	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32053349	AGGATTAATTGGGTA[C/G]TGAAGGGGCCGGGCA	3055
rs546860629	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32069772	TCCTTGTAAATAAAA[G/T]GAATCTTTTTTCATT	3055
rs546868228	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32084597	GGAGGGGAGAGGGAG[G/T]CCACTTGCTTCCAGG	3055
rs546868717	snp	A/G	0.00788942	0.0623095	intron-variant	HCK	GRCh38.p7	20:32052537	CCCGCGAGGGGTCCC[A/G]GGAGGCGGAGGGAGC	3055
rs546904969	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32084108	TCCTAGTCACGGATG[C/T]ACTGTGGCCCCTGAG	3055
rs547001410	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32065029	TACAGTCCTTCACAT[C/T]CCTAGTCACATAGGA	3055
rs547006020	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32059634	ATCCTCCCACCTCAG[C/T]CTCCTGAGTAGCTGG	3055
rs547043071	snp	A/C	0.00398564	0.0444627	intron-variant	HCK	GRCh38.p7	20:32059350	CTTCTTTCCTTCCCC[A/C]CTTCTCCTCCTCCTC	3055
rs547100514	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	HCK	GRCh38.p7	20:32050942	CCCCGCAACAAAGAA[A/T]TACCTGGCCCAAATG	3055
rs547123272	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32090689	CCAACCTCATGGCAC[A/C]CTATCTGGGGGTCAT	3055
rs547184260	snp	A/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32098337	TACCTGGCCAAAAAA[A/T]TTTTTTTAATTAGCT	3055
rs547185914	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32063635	TCACCTACTCTAATA[A/G]GTCTAGTACCATCTT	3055
rs547255773	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32091283	AAAGCAAGGCAAAAA[A/G]GCTGGGCCAAGTAAC	3055
rs547340954	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32070142	CCAAACCTGTCCAAT[A/G]CTTACCTCCTCTCTG	3055
rs547463786	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32070549	GGCTCCTTTGTGTCA[C/T]TTAGACCGCAGGTTC	3055
rs547479108	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32090092	ACTTTCAGAGCCTGG[A/C]ATGCCAGAGGCATAT	3055
rs547524368	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32073207	GTGGGCCTCCTCCCA[C/T]GACATGCAGGGCTAG	3055
rs547659518	snp	A/G			intron-variant, utr-variant-5-prime	HCK	GRCh38.p7	20:32054227	CCAGGGGCAACCGCT[A/G]TCATGAGTTACAGTC	3055
rs547673661	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32069535	TTTAATTTCCCAGAA[C/G]TGTAATACACATTTA	3055
rs547688644	snp	C/T	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32061172	TATTTTTAGTAGAGA[C/T]GGGGTTTCACCATGT	3055
rs547926869	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32084658	CAAGGCAGAGGGGGA[G/T]ATTTAAATAATAGCC	3055
rs548070738	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32056191	CTTTGGGTATATACC[G/T]GAAGTAGAGTTACTG	3055
rs548077750	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32095271	GCAATCTTTTTTTTT[C/T]CTTTGAGATGGAGTC	3055
rs548096120	snp	C/T	0.0154538	0.0865337	intron-variant	HCK	GRCh38.p7	20:32086562	GGGTCTGCAGCTGGG[C/T]CTTCTAGGGTGGTAC	3055
rs548114605	snp	A/C/G	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32058389	ATGCAAAAATTAGCC[A/C/G]GGCGTGGTGGCGGGC	3055
rs548244557	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32090725	CTCACCGCCTTTATC[A/G]ACCCGCAGTGCTTAC	3055
rs548283876	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32099407	CTGTCACCCAGGCTG[C/G]AGTGCAGTGACGTGA	3055
rs548358231	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32059037	CAGAGAAATCTCTCA[A/G]ACAAAGAGATGAAGG	3055
rs548447525	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32096579	AGATCATAGCTCACT[A/G]TAGCCTCCAACTCTT	3055
rs548467434	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32063206	GGTCCATAGAGAGTA[C/G]AACATAATATATCCA	3055
rs548483710	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32097194	CTGAGGCGGGAGAAT[C/T]GCTTGAGCCCAGGAG	3055
rs548485989	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32060004	AGGATTCCATTTGTG[C/G]AGGACAGGTTTGGGG	3055
rs548504210	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32070895	AAGACGAAGAAAGAG[A/G]AGGAGGAGGGAGGAC	3055
rs548549562	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32089859	AGAAGTTCAGTAGAT[C/G]AAGAGAAAAGGTAAA	3055
rs548616379	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32077180	AAACTGCTAACAGAG[A/G]TTGCCTCTGGGGAGC	3055
rs548642443	snp	C/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32070295	AAGTGCAAATTGAAT[C/G]CCATCATTCTCCTGC	3055
rs548677146	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32076169	CTCTACTAAAAATAC[A/C]AAAAAAATTAGCTGG	3055
rs548681421	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32075074	TGCTTCTGCATCCTC[A/G]GCACAGGCTGGCATG	3055
rs548767298	snp	C/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32069346	ATACAAGGTGCTCAA[C/T]GCGCATGGATTGGAA	3055
rs548848021	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32056985	TTCAGCTGCCCTCCC[C/T]GAACACCCCTCCACC	3055
rs548873385	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32084140	CCTGCTGTGTCCTTC[C/T]TGGCCATCCCCTAGA	3055
rs549029570	snp	A/G	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32056445	GGCATGAACCCGGGA[A/G]GCGGAGCTTGCAGTG	3055
rs549311082	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32087590	TCCCGACTTAGTCTC[C/T]CCAGTAGCTGGCACT	3055
rs549347168	in-del	-/AG	0.00398564	0.0444627	intron-variant	HCK	GRCh38.p7	20:32092968	TTTTCTTTTTGAGAC[-/AG]AGTCTTGCTCTGTCG	3055
rs549407612	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32097331	ATGCCTGTAATTCCA[C/G]CACTTTGGGAGGCTG	3055
rs549417167	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32066404	GCAACCTCTGCTTCC[C/T]GGGTTCAAGCGATTC	3055
rs549468411	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32094418	GGCTCAGTGGCTCAC[A/G]CCTGTAATCCCAGCA	3055
rs549471146	snp	C/T	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32096690	AATTATTTGTAGAGA[C/T]AGTGTCTCACTGTGT	3055
rs549489811	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32056047	ATTGTATGGATATTC[C/T]ACAGTTTATTTACCC	3055
rs549532781	snp	A/C	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32057817	CACATGTTGGTCCCC[A/C]CCCCATTTCTCCAGT	3055
rs549560846	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32062441	AGAGTAACATTGAAC[A/C]TGCTATGAGTTTTAT	3055
rs549621688	snp	A/G	0.00318978	0.0398085	intron-variant	HCK	GRCh38.p7	20:32067223	TTCATTCTTAAAACT[A/G]TGGTAAAATATGCAT	3055
rs549638938	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32069039	TTGCAGTATCTCTAG[G/T]CTTGTGGGCCAGAGG	3055
rs549855492	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32089837	AGGCCGAGCCTGAAG[A/G]ATGAATAGAAGTTCA	3055
rs550070978	snp	A/G	0.00478085	0.0486577	intron-variant	HCK	GRCh38.p7	20:32077550	TTTGTTTTTTAGGTG[A/G]AGTTTCTCTCTTGTT	3055
rs550098323	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32056124	TGAAAATAATACTGC[C/T]ATGAGCATGCATGTG	3055
rs550283516	snp	C/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32088197	AGGAGTGAGCCTCGT[C/G]CCTAGCCACTCTGCC	3055
rs550438419	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32094527	TCTACAAAAATTTAA[C/G]AAATTAGCCAGGCAT	3055
rs550475150	snp	A/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32093632	CTCTGGAAGTCTTGG[A/T]ATTCTAGAGAATCCC	3055
rs550586198	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32086051	TTGAGACAGAGTCTC[A/G]CTCTGTCACCCAGGC	3055
rs550604392	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32072972	AGGCATGGTGGCATG[C/T]GCCTGTAATCCCAGC	3055
rs550631872	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32067375	CCCATTGAACACCAC[C/T]AACTCCTCACTTCCC	3055
rs550663144	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32062192	TGATCTGCCCGCTTC[A/G]GCCTCCCAAAGTGCT	3055
rs550836795	snp	A/C	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32071891	TGAGCTTGGGGTGAA[A/C]GGGAGCTGACTGGCC	3055
rs550873910	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32077596	CAATGGTGTGATCTC[A/G]GCTCACTGCAACCTC	3055
rs550981322	snp	C/G	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32060374	TACAGGCACCCACTA[C/G]CACGCCCAGCTAATT	3055
rs550984858	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32053382	GTGGCACACGCCTGT[A/G]ATCTCAGCTTTTTGG	3055
rs551023717	snp	C/T	0.0023933	0.0345097	intron-variant	HCK	GRCh38.p7	20:32052781	TCCAGGTTCCCCTTC[C/T]TGGGGGGGGGCGGGG	3055
rs551207418	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32080477	GCTGAGATTACAGGC[A/G]TGAGCCACTGCGCCT	3055
rs551366068	snp	C/T	2.41118e-05	0.00347208	intron-variant	HCK	GRCh38.p7	20:32079925	GCCGAGGTGCCCCAG[C/T]TGGGGCTGGCCACCA	3055
rs551394140	snp	A/C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32061676	AAGGAAGTGATGGAG[A/C/G]CTTTCTGGGTGAAGA	3055
rs551427937	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32068080	GGAGGACGGATCACC[C/T]GAGGTTGGGAGTTCA	3055
rs551557712	snp	C/T	0.00358779	0.0422022	intron-variant	HCK	GRCh38.p7	20:32060485	TGACCTCAGGTGATC[C/T]GCCTGCCTCAGCTTC	3055
rs551909798	snp	C/T	0.0023933	0.0345097	intron-variant	HCK	GRCh38.p7	20:32099514	AAGCATCCACCACCA[C/T]GCCTGGCTAATTTTT	3055
rs552020524	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32073024	AGAATCACTTGAACC[C/T]GAGAGGTGGAGGTTT	3055
rs552045060	snp	A/C	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32060664	ATCAACAGGTAATAC[A/C]TTAGGTGCATTAGTC	3055
rs552106047	snp	G/T	0.000399281	0.0141238	upstream-variant-2KB	HCK	GRCh38.p7	20:32051668	CTTAGGCGGCGGGAG[G/T]TTAGATCGCGCAGGA	3055
rs552281266	snp	A/G	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32092373	GCTCAAGCCCAGTTT[A/G]TAAACCAAAAGTGCT	3055
rs552283374	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32085249	CGGGCACAGTGGCTC[A/G]CGCCTGTAATCCCAG	3055
rs552398309	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32076736	AACAGGTTCTTGGGT[A/G]AGGCAGCTGCTGCTG	3055
rs552444124	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32091385	AGCTGGGGCCACTTA[C/T]CTATTTCTCTGGGCT	3055
rs552468446	snp	A/C	0.00398564	0.0444627	intron-variant	HCK	GRCh38.p7	20:32090581	CATATAACCTTGAGG[A/C]ATCCATAGGATTCAG	3055
rs552540034	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32062951	GAACAGCCTTAAGCC[C/T]TGGGCCCCCAGCGGT	3055
rs552541171	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32058452	CAGGAGAATTGCTGG[A/G]ACCCGGGAGGCACGG	3055
rs552674337	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32071004	GGGAGGGAGGGAAGG[A/G]GTTATAAGCAATTTA	3055
rs552783767	snp	G/T	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32076229	TACTCGGGAGGCTGA[G/T]GCAGGAGAATCACTT	3055
rs552805065	snp	C/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32072054	AGCATCTCAGGCCTC[C/T]GGCCTGGGCAGAAGC	3055
rs552839309	snp	A/G/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32060356	CTCCCAAGTAGCTGG[A/G/T]ATTACAGGCACCCAC	3055
rs552971359	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32065731	CAGGGGGCCAGAGGA[C/T]ATGGGATTCTCTGAT	3055
rs552979233	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32094265	GGGCAAATATATGTC[C/G]AAATTAAGGGTAAGA	3055
rs552994331	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32061011	TTTTTTGAGACAGAG[C/T]CTTGCTCTGTTGCCC	3055
rs553008481	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32072694	ATGGAATATAAATCA[C/T]TGGTGGGCCTGTGAT	3055
rs553118264	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32078281	CGAACTCCTGACCTC[A/G]TGATCCACCCGCCTC	3055
rs553129651	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32090916	TTCCCCCACTGGGAG[C/T]ACTGGGAGCCACTCT	3055
rs553268399	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32076427	CCCTGGGTCATCCCA[C/T]GCTCTGTTTCTCCAC	3055
rs553393562	snp	G/T	0.00358779	0.0422022	upstream-variant-2KB	HCK	GRCh38.p7	20:32051776	GGATCCTTCCACTGG[G/T]CAGATTAGAATCTTT	3055
rs553467268	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32058711	AGACCCTAGGCAAGG[C/T]TTCAAATGCAAATAG	3055
rs553587308	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32081673	GCAGCTCAGTGAATG[A/C]CTGGGCTTTGTCTCT	3055
rs553643271	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32069848	TTAAACCACAAATAC[A/C]TGTTTATTTTAACAA	3055
rs553680372	snp	C/T	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32075597	AAATAAGATATATCC[C/T]TACCCTCAAGGAGCT	3055
rs553708165	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32072031	GCTCCACCAAACAGG[G/T]GTGAGTGAGCATCTC	3055
rs553788174	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32061431	GAGAGCAGTGATGGA[A/C]TTCAGAGCACAGCAG	3055
rs553820332	in-del	-/T	0.00358779	0.0422022	intron-variant	HCK	GRCh38.p7	20:32095262	CCAGAAGAGGCAATC[-/T]TTTTTTTTTCTTTGA	3055
rs553919503	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32069083	GCTTGCTTCATGATC[C/T]GGGGCAGTGTCACGT	3055
rs554140646	snp	A/G	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32094643	CAGTAAGCCATGATC[A/G]TGCCACTGCACCCAG	3055
rs554194058	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32070637	GTTGTTCCCCACAGC[A/C]TCCTCTCTTATTGTC	3055
rs554260040	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32074292	CAGCCCCAGCTGAAC[A/C]ATTCTGAGTCTCTAT	3055
rs554370276	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32057977	TCTGGATGGCACTGC[A/G]CTAGGACGTGCGCTC	3055
rs554447287	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32075706	CATCCATCCATCCAT[C/T]CATCCATCCATCCAT	3055
rs554497650	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32087844	AGACGGTGTTTCACC[A/G]TGTTAGCCAGGATGG	3055
rs554497707	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32080234	AGATGGAGTCTCACT[C/T]TGTCGCCAGGCTGGA	3055
rs554506667	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32090148	CCAGGTCCTCTGGGA[C/G]ACAATAGACTGGTCT	3055
rs554534418	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32087156	ACTCTCCCGCATCAG[C/T]CACCTTCCCTGTACT	3055
rs554542410	in-del	-/TCAT			intron-variant	HCK	GRCh38.p7	20:32075706	CATCCATCCATCCAT[-/TCAT]CCATCCATCCATCCA	3055
rs554636171	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32084228	TGGCCAAGATGTAGA[G/T]GTGGCACCCCGTCAC	3055
rs554816076	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32057940	GGTCTTGGCCCCGGC[C/T]GTGGTCCCACATGCT	3055
rs554838611	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32085373	ACAACAATTAGCCAG[G/T]CGTGGTGGTGGGAGC	3055
rs554850965	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32089536	AGACCATGACCCAAG[C/T]GGTCCTGGCTGAGTC	3055
rs554905981	snp	A/G	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32097512	TGAAAGCCGGGAGGC[A/G]GAACTTGCAGTGAGC	3055
rs554975326	snp	A/G			upstream-variant-2KB	HCK	GRCh38.p7	20:32050961	CTGGCCCAAATGTCA[A/G]TAGTGCCAAATTTAA	3055
rs554982876	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32078292	CCTCGTGATCCACCC[A/G]CCTCGGCCTCCCAAA	3055
rs554987957	snp	C/T	3.33039e-05	0.00408055	intron-variant	HCK	GRCh38.p7	20:32088543	AGTAAAAGTAGTAAA[C/T]GTTCCTCCCCTCTCC	3055
rs555056167	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32069116	GCCAGTAAACAGAAA[C/T]AGTTGTGGTTAATGT	3055
rs555077351	snp	C/T	0.00340715	0.0411335	intron-variant	HCK	GRCh38.p7	20:32069780	AATAAAAGGAATCTT[C/T]TTTCATTTTTAAAAG	3055
rs555114247	snp	G/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32075405	AGGGGGTCTCTCTGT[G/T]TTGCCCAGGCTGGTC	3055
rs555287891	snp	C/T	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32081445	ATTTCATGTGCTAAG[C/T]GCACCTTTACTAATA	3055
rs555311023	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32068113	ACCAGCCTGACCAAC[A/G]TGGTGAAACCCTGTC	3055
rs555312302	snp	C/T	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32054571	CAGCACTTTGGGAGG[C/T]TGAGCCGGGCGGATC	3055
rs555326648	snp	A/G	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32080850	AGACCAAGTAGGGGA[A/G]GCCAACACAGGAGGA	3055
rs555442420	snp	A/G	0.0107246	0.0724382	intron-variant	HCK	GRCh38.p7	20:32094750	AAGAAAGAAAGAAAG[A/G]AAGAAAGAAAGAAGG	3055
rs555471526	snp	A/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32055861	CCTGGCAACCACCAA[A/T]CTGCTTTTTGCCTCT	3055
rs555504710	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32054767	GCCGAGATCGTGCCA[C/T]TGCACTCTAGCCTGG	3055
rs555568266	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32086921	CCAATCTGGCCAGGA[A/G]CTCTTCCAACAAGTA	3055
rs555608525	snp	A/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32053100	AATTCTCCGCCTCCG[A/T]ATTCGTTTCCTCATC	3055
rs555647359	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32060020	AGGACAGGTTTGGGG[G/T]CAGCTGATCTCTCAG	3055
rs555712417	in-del	-/TATT	0.0418038	0.138399	intron-variant	HCK	GRCh38.p7	20:32095861	TGTTAGCCTAATATT[-/TATT]TATTTATTTATTTAT	3055
rs555782474	snp	A/G	8.23852e-05	0.00641762	missense	HCK	GRCh38.p7	20:32099075	ACCATCAAGTCAGAC[A/G]TCTGGTCCTTTGGTA	3055
rs555782880	snp	A/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32089200	GCTTGCTAATGGCCC[A/T]TTGGCCAAGTCACAT	3055
rs555786385	snp	A/G	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32092717	CACTCTCTCTGTGGC[A/G]TCTTCTGCTGGCCAC	3055
rs555807509	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32095676	GGAAATGTGATGAAA[A/G]TATTCTAAAATCCAC	3055
rs555964284	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32093240	GTAAGCCACCATGCC[C/T]GGCCTGTTTTATCTT	3055
rs555971008	snp	A/G	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32094853	AAAGAAAGAAAGAAA[A/G]GAAAGAAAGAGGCAC	3055
rs555995868	snp	G/T	0.000399281	0.0141238	utr-variant-3-prime	HCK	GRCh38.p7	20:32101818	ATAGTGAAATGAATA[G/T]TTAAATAAAAGATAT	3055
rs556046669	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32068253	CGGTGAGTGGAGATG[A/G]CACCACCGTACTCCA	3055
rs556059644	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32100898	AATCTATTACTCCCA[A/G]TCTTCCATTGGTGAC	3055
rs556081339	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32081523	TAATATGTGACCTCA[C/T]GGTACCCTGAAGCAA	3055
rs556117098	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32061882	GCTTTTACTCCAAGT[G/T]AGACGGAAACCCTGG	3055
rs556182991	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32067655	GACACTCCTACTGTG[C/T]GCCAGGAGACACTGG	3055
rs556221818	snp	C/G	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32073646	GCTGTTCCAGGTGCC[C/G]GGTGAGGGTCACCAA	3055
rs556335018	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32064423	GCGGAGTAATTCCCA[A/C]AGGAAAATTGGAGAA	3055
rs556398571	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32061326	GGCTGTTAAGGAGCC[C/T]TTGGCCAAAGTCTCT	3055
rs556571921	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32073592	CCAGCATGGTGAGAC[A/G]CCTACTTATACTTGG	3055
rs556639923	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32080142	TGAAAACAAAGAAAC[A/G]TCCAGCTGAAGCTTG	3055
rs556676663	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32087119	TTAGAGGCCAGGGTG[C/T]GGCATGGGTGGTGGG	3055
rs556708241	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32067269	CTAATCATTTGCAAG[C/T]GTACACTTCAGTGGT	3055
rs556742251	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32075390	GTATTTTTGGTAGAG[A/C]GGGGGTCTCTCTGTG	3055
rs556777337	in-del	-/TCAGGTGATCCGCCTGCTGACC	0.0023933	0.0345097	intron-variant	HCK	GRCh38.p7	20:32060453	CTCAAACTCCTGACA[-/TCAGGTGATCCGCCTGCTGACC]TCAGGTGATCCGCCT	3055
rs556863352	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32093261	GTTTTATCTTTTCTT[C/T]ATGGTACTTACCACC	3055
rs556909984	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32053789	AGCATCACCTGGACT[A/G]CTTGTGAAAACAGAT	3055
rs557003013	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32099738	CTCACCACTTTGAAC[A/C]CCACAGTCTCCACTG	3055
rs557026438	snp	A/C	0.00557542	0.0525036	downstream-variant-500B	HCK	GRCh38.p7	20:32102088	TGATCGTGCCACTGC[A/C]CTCTAGCCTGAGCGA	3055
rs557105757	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32073162	TGCCCCTAATGTGCC[A/G]TGTGGTGCCAGGCAT	3055
rs557160696	snp	A/G	1.64901e-05	0.00287137	missense	HCK	GRCh38.p7	20:32099108	CTGCTGATGGAGATC[A/G]TCACCTACGGCCGGA	3055
rs557203114	in-del	-/T			intron-variant	HCK	GRCh38.p7	20:32061936	GCGATCTGACTTACC[-/T]TTTTTTTTTTTTTTT	3055
rs557207147	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32078337	GGTGTGAGCCACCGC[A/G]CCCAGCCGGGGGAGA	3055
rs557241082	snp	A/C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32072788	GGGTCAAGCAGCATC[A/C/T]CCCGGTACATCCAAG	3055
rs557304715	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32058827	GCCCAGTTACCACTG[C/T]GGGCACCTGGAGCTC	3055
rs557344020	snp	C/G	0.00318978	0.0398085	intron-variant	HCK	GRCh38.p7	20:32064102	TCCACCTCCCAGGTT[C/G]AAGCAATTCTCCAGC	3055
rs557480806	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32091940	CAGTAAGCTGTGATC[C/T]CACCACTGTACTCCG	3055
rs557527867	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32059366	CTTCTCCTCCTCCTC[C/T]TCCTCCTCCTCCACT	3055
rs557529325	snp	A/C	0.000399281	0.0141238	downstream-variant-500B	HCK	GRCh38.p7	20:32102165	GAAAGAAAGGAAAGG[A/C]AAGAAAATTGGGGTT	3055
rs557585255	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	HCK	GRCh38.p7	20:32051329	CCTTCGGGCAGGGAA[A/C]TTTGCATGGCCATGG	3055
rs557770250	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32054674	AGCCGGGCATGGTGG[C/T]GGGCGCCTGTAGTCC	3055
rs557783049	snp	A/C	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32072800	ATCCCCCGGTACATC[A/C]AAGACCGAAGGCCGA	3055
rs557822814	snp	C/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32085428	CTAAGGCAGGAGAAT[C/T]GTTTGAACCCAGGAG	3055
rs557823654	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32078482	GAGTTAGACTGCCTA[C/G]CTTCAAATCCTGCCT	3055
rs557962624	snp	A/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32091807	TGGGACCTCTTCTCT[A/T]TTAAAAAAAAAAAAA	3055
rs558038110	snp	C/T	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32064686	AAAACCATCTCCAGC[C/T]CACTGGATGGATGCT	3055
rs558065208	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32099995	GCCTCGACTTCCTAG[A/G]CTCAAATGATCCTCC	3055
rs558103823	snp	A/G	0.000399281	0.0141238	utr-variant-5-prime	HCK	GRCh38.p7	20:32052194	ACTTGGGGCGGAGTT[A/G]GCCTCGCTCAGGGCG	3055
rs558177046	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32064164	GCCTGCCACCAAGCC[C/T]GGCTAATTTTTTGTA	3055
rs558255967	in-del	-/TATT	0.0181913	0.0936201	intron-variant	HCK	GRCh38.p7	20:32095858	TTTCTGTTAGCCTAA[-/TATT]TATTTATTTATTTAT	3055
rs558541895	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32088118	GCGATGTTGCCCAGG[C/G]TGGTCTCAAACTCTT	3055
rs558569285	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32071939	TCGACTCTCCGGGAC[A/G]CAGCGCCAGCCAGCA	3055
rs558602758	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32077620	CAACCTCCGCCTCCC[A/G]GGTTCAAGCGATTCT	3055
rs558625870	snp	A/G			utr-variant-5-prime	HCK	GRCh38.p7	20:32052316	ACTCAGACAGTGCAG[A/G]ACGAGAAACGCCCGC	3055
rs558648114	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32057328	ATGAAGGGCTGGGTG[C/T]GGTGGCTCACCCTGT	3055
rs558742570	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32084239	TAGAGGTGGCACCCC[A/G]TCACACTCTGCTTGC	3055
rs558777809	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	HCK	GRCh38.p7	20:32051115	CTTGTAGTTTTGGAG[A/G]TTTTGGAGGTGTGTT	3055
rs558778156	snp	A/C/T			intron-variant	HCK	GRCh38.p7	20:32069824	CCTAGGAGTTTGGGG[A/C/T]TTTTTTCCTTAAACC	3055
rs558786149	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32098700	GTCCCCAAAGACCTG[C/T]GACCTCTGGGATTCC	3055
rs558807668	snp	A/G	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32083738	CTGGATGAGAGCCCA[A/G]GATGCCTGGCTCCCA	3055
rs558984659	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32057556	AGTGATCTGAGACTG[C/T]ACCACTGTACTCCAG	3055
rs559002471	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32058989	GCACTTTCGGCTTGC[C/T]AAGCCCATGGGCAGA	3055
rs559006089	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32082599	GTGAGCCAAGATTGC[A/G]CCACTGCACTCCAGC	3055
rs559039924	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32058376	GTCTCTACTAAAAAT[A/G]CAAAAATTAGCCGGG	3055
rs559064893	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32063328	CATGACTACAACTCA[C/T]TGTAGCCTCAACCTC	3055
rs559224149	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32074851	CTCTGGGCTTGGCTG[A/G]CTCCTTCTCTTCCTT	3055
rs559239374	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32069806	AAAAGTAACTCATCT[A/G]AGCCTAGGAGTTTGG	3055
rs559377909	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32070812	CTTGGCTGTGTAAAT[C/G]GATGAATGAATTACC	3055
rs559413973	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32064356	CACAGATCCACCTCT[A/G]CAGCCAGGGGTTGGA	3055
rs559681014	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32077009	AGATTTGCTTGATCT[G/T]GGAGGCAGAGGTTGC	3055
rs559709229	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32076610	TTTGCAGACAAAGGC[A/G]AAATAACCTAGATGG	3055
rs559783324	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32083201	CTAACAAGAACTCAA[A/G]GGATTACACTGGGGC	3055
rs559878289	snp	A/G	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32081033	GTTCAAGGCTGCAGC[A/G]AGCCATAATGGAGCC	3055
rs559888544	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32055262	TTGCTCTGCTGATCT[A/C]CCAGCCGTCTCTGGA	3055
rs559917072	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32087975	AGACAAGGTCTCGCC[A/G]TCTTGCCCCAGCTGG	3055
rs560149128	snp	A/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32094955	AAAAAAAAGAGTAGA[A/T]GCCACTTGGTTTCGT	3055
rs560182042	snp	G/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32068757	GACCTGCCCCCCCTC[G/T]CTGCCCCCTGTCTCT	3055
rs560220733	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32074454	AACTGTTGTAAGGAT[C/T]CCTACCCTAATCATG	3055
rs560231281	snp	A/G	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32061047	GGAGTGCAGTGGCGC[A/G]GTCTTGGCTCACTGC	3055
rs560330929	snp	C/T	0.0140414	0.0826048	intron-variant	HCK	GRCh38.p7	20:32052508	GCCGCGCACAGGGGA[C/T]CGGGAATACCCGGCC	3055
rs560401398	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32067814	CATAGCTGAGATGTG[C/T]TCTAACAGTAAAATC	3055
rs560436282	snp	C/T	0.000351185	0.0132465	synonymous-codon	HCK	GRCh38.p7	20:32073756	TGCCCTGTATGATTA[C/T]GAGGCCATTCACCAC	3055
rs560447333	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32062591	GTGAGCCAGGGCCCA[C/T]GCAGCCTCTTGGGGT	3055
rs560560151	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32094379	TATAATACCACGCAG[C/T]GATGAAAAAGCACAA	3055
rs560602375	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32055837	CAATTACCCCCCATT[C/G]CCCCGGCCCCTGGCA	3055
rs560636633	snp	C/T	0.00318978	0.0398085	intron-variant	HCK	GRCh38.p7	20:32069944	AAGCACTTCCTTATG[C/T]GGTTGTCACAGCCTG	3055
rs560672848	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32082696	TGACATTGTACTATT[A/G]TCATGGTAAAGAACA	3055
rs560686185	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32067103	CATTTTAGAAGAGTG[A/G]TTTGATGTACATGTT	3055
rs560710202	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32075003	TTTGGTTGGTTACAC[A/G]TGCATTCTCTGCCTG	3055
rs560771692	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32062838	TGCTGGGCTCTGCAC[A/C]CCCAAGGCACTGCTC	3055
rs560794810	snp	A/T	2.29166e-05	0.00338493	intron-variant	HCK	GRCh38.p7	20:32079754	CCAGGTTCACATTTG[A/T]CCCCTCCCTTTTCCA	3055
rs560846291	in-del	-/A/AA/AAA	0.381891	0.212379	intron-variant	HCK	GRCh38.p7	20:32058530	CAGCAAGACTCTGTC[-/A/AA/AAA]AAAAAAAAAAAAAAG	3055
rs560951399	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32080063	CTGTGCCTGGCTCTG[C/T]CCTTCTTATCCACCA	3055
rs560990543	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32088671	ACGAGGAAACGGGGA[A/G]GGGAAACAGGAATTC	3055
rs561017612	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32055999	GGTGGCAACTATTAG[C/T]ACTTTATTCCCTTTG	3055
rs561023167	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32082010	CACACCCCATCCAGC[A/C]GCAACCAAGCCAGTC	3055
rs561234783	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32061522	CCTCATGGCCACCAC[A/G]TTTAAGAGGTGGTTA	3055
rs561256943	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32095070	ACTCTTTAATGTCCA[C/T]CAATTGATGAACAGA	3055
rs561293689	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32095912	TTATTTATTTTGAGA[C/T]GGAGTCTCGCTCTGC	3055
rs561306530	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32088104	ATAGATGGGGTCTTG[C/T]GATGTTGCCCAGGCT	3055
rs561356700	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32076096	GGGAGGCCAAGGCAC[A/G]CAGATCACCTGAGGT	3055
rs561362629	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32053928	ACCACTGGGGTAGCC[C/T]ATGCCTGGCACAGAG	3055
rs561370489	snp	A/T	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32068398	AAAATAATTTTTTTT[A/T]AAAAAAGGAAAAAAT	3055
rs561459026	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32088009	CAAACTCCTGGGTTC[A/G]ACTGATCCTCCCAAA	3055
rs561550171	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32074300	GCTGAACCATTCTGA[G/T]TCTCTATAGGCACAG	3055
rs561592783	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32094081	AGTGTTGAGAGTTGA[G/T]ACTTGTGAGAGCGAT	3055
rs561601148	snp	C/T	4.6134e-05	0.00480259	intron-variant	HCK	GRCh38.p7	20:32101276	CCCTGGGCTCTCATT[C/T]CCCAACTGCTTCCGT	3055
rs561612764	snp	A/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32067993	AACCTGGATGTAAAA[A/T]TTTTTTTAAAAATGA	3055
rs561626848	snp	C/T	0.00438332	0.0466095	intron-variant	HCK	GRCh38.p7	20:32087287	GTTTCACAACCATTT[C/T]CAACCCCTGCCATTT	3055
rs561630206	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32080302	CTCCCAGGTTTGAGC[A/G]ATTCTCCTGCCTCAG	3055
rs561723698	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32093098	TACAGGCGTGCACCA[C/T]CATGCTCATCTTCTT	3055
rs561764073	snp	C/T	0.00010244	0.00715607	synonymous-codon	HCK	GRCh38.p7	20:32079828	CCAACTGCTGGCTCC[C/T]GGCAACATGCTGGGC	3055
rs561764080	snp	G/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32072454	TGTACTCCCAGCATT[G/T]TGGGAGGCTGAGGCA	3055
rs561831849	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32072857	TGGCTGGGCACAGTG[A/G]CTCACTCCTGTAATC	3055
rs561850507	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32066655	GAACAAATTCTCTTT[C/T]GAATTTATACTCAAA	3055
rs561857553	snp	A/C	0.000399281	0.0141238	missense	HCK	GRCh38.p7	20:32086694	GCATGTCGGTGGAGG[A/C]CTTCCTGGCAGAGGC	3055
rs561870969	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32078700	CGTCTCTACTAAAAA[C/T]ACAAAAATTAGCTAG	3055
rs561942274	snp	A/C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32053351	GATTAATTGGGTACT[A/C/G]AAGGGGCCGGGCAGG	3055
rs562032011	snp	A/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32060357	TCCCAAGTAGCTGGG[A/T]TTACAGGCACCCACT	3055
rs562042990	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32068806	AAGATTAGCCAGGCA[C/T]GGTAGTTTGTAACTG	3055
rs562066964	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32066126	ACTCTGCAGAGAGGC[C/T]CTGGGCTACATAAAC	3055
rs562080175	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32084634	TTATGGCAAAGCGGG[A/G]ATGCTACCCAAGGCA	3055
rs562302524	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32074325	GCACAGGACCCTGCC[A/G]TGGGTATAGCTAATA	3055
rs562370705	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32091933	CAGGTTGCAGTAAGC[C/T]GTGATCCCACCACTG	3055
rs562405289	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32085155	AACTTACAGGGATGC[A/G]AACAACTCAGCCAGA	3055
rs562438641	snp	A/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32080934	CTGTATGAAAAATTT[A/T]AAAAATTAGCCAAGC	3055
rs562526060	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32059191	CCAAATGCTGGCAGA[A/G]GATATCTGGGTGGGG	3055
rs562619694	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32074879	CTTCAGGTTTCATCC[C/T]TCCAGTCAGGGAAGA	3055
rs562632948	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32080418	TGGCCAGTATGGTCT[C/T]GATCTCCTGACCTTG	3055
rs562638546	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32093712	ATGGAGGAATGCCAC[C/T]CTGAGCCCTGGGGCC	3055
rs562663984	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32066200	GTTCCCAAACTCACC[C/T]GAATAATATCAGCAC	3055
rs562666523	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32053776	TTTAGCCTACATCAG[C/T]ATCACCTGGACTGCT	3055
rs562670320	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32066790	TAAATCTAGTACTCA[A/G]TGGTAGTAGCAGTCC	3055
rs562686159	snp	C/T	0.00318978	0.0398085	intron-variant	HCK	GRCh38.p7	20:32079566	AAACAGGATTCACTT[C/T]GGGTAAAATGTCTAT	3055
rs562701521	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32072970	CCAGGCATGGTGGCA[C/T]GCGCCTGTAATCCCA	3055
rs562757434	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32069140	TTAATGTTTCTGCAG[C/T]GCTTACTGCATGCTG	3055
rs562856900	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32071578	GCCAGCCCGGGGGCA[A/G]GGGACCTGGAATGCC	3055
rs562899281	snp	A/C	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32079657	TGATGCTGCAGGAAG[A/C]CAGACCCTCTGTATC	3055
rs563015170	snp	C/G	0.000399281	0.0141238	utr-variant-5-prime, synonymous-codon	HCK	GRCh38.p7	20:32052454	AAGCTGCGAGGATCC[C/G]GGCTGCCCGCGAGAC	3055
rs563106635	snp	A/G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32085199	AAATCCATGTATTTC[A/G/T]ACTGTATTTATTGCG	3055
rs563228768	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32085662	ACGGTTCTGGATTGG[A/C]GCTTCCTGGAAGCCA	3055
rs563266625	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32100964	TGGGTTCCTGTCTCT[A/G]TGATGGTCTTCTCCA	3055
rs563302787	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32092865	CAGATCTTTGCTAAA[A/G]TCTCACCCCCTCAAA	3055
rs563327448	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32100096	ATTTTTTTGTAGAGA[C/G]TTGGTCTCACTACGT	3055
rs563385310	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32059056	AAGAGATGAAGGTGC[C/G]GGCAGCTGGAAGTCC	3055
rs563408110	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32091061	GAGGTACAGAGAGAT[A/G]ACACAACTTGCTTGA	3055
rs563595564	snp	G/T	1.68889e-05	0.00290588	intron-variant	HCK	GRCh38.p7	20:32071624	CCCCGCATGAGGCTC[G/T]TGGTAACTGGGGCTC	3055
rs563632010	snp	A/C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32077221	CCTTGGGAATCAGGG[A/C/T]GGGATGGAATCTTGG	3055
rs563686096	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32061387	TCGGTCTCCCTGCCA[A/C]ACTCAGTCATTGGCT	3055
rs563747636	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32089102	GAGCTTCTTCACGGC[A/G]CAGCAGCTGGGTTCC	3055
rs563759695	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32090473	AAATGTTATTCAGTA[A/G]CTGCATATATACAAA	3055
rs563768460	snp	C/T	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32076712	GTCAGATTCCGAATG[C/T]GCATTTCTAACAGGT	3055
rs563800077	snp	A/G	9.97191e-05	0.00706043	missense	HCK	GRCh38.p7	20:32084432	CTGTCGGTGCCCTGC[A/G]TGTCTTCCAAGCCCC	3055
rs563834445	snp	A/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32057808	TGCACCAACCACATG[A/T]TGGTCCCCACCCCAT	3055
rs563906812	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	HCK	GRCh38.p7	20:32050822	GGACATTTTACAAAT[A/G]TCTGGAGACATTTTG	3055
rs563923711	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32093328	AACATGTCTGGCACC[A/C]ACAAGACACTCAGTG	3055
rs564163501	snp	C/T	0.00201816	0.0317019	intron-variant	HCK	GRCh38.p7	20:32052509	CCGCGCACAGGGGAC[C/T]GGGAATACCCGGCCC	3055
rs564168565	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32093008	GGAGGACAGTGGCAC[A/G]ATCTCGGCTCACTGC	3055
rs564211304	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32053303	TGCAGGATGGGGAGA[G/T]TAATAGTACCTCCTT	3055
rs564229534	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32099767	TGCATCCAGGCCAGC[A/G]TCATCTCCCATAGAT	3055
rs564305567	snp	C/T	0.000399281	0.0141238	synonymous-codon	HCK	GRCh38.p7	20:32084518	GAAGAAACTTGGAGC[C/T]GGGCAGTTTGGGGAA	3055
rs564312893	snp	C/G	0.00318978	0.0398085	intron-variant	HCK	GRCh38.p7	20:32060314	CAACCTCTGCCTCTT[C/G]AGTTCAAGCAATTCT	3055
rs564451804	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32077304	AAATGTGGGGAAGCA[C/T]GCAGAAGAGTGAAAA	3055
rs564460820	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32072239	GAACAACAGCAAGAG[C/T]TGTAAAAAGAGAAGC	3055
rs564490372	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32069265	AATGAACACAGGTCT[A/T]CTGAGACCCCTCCCT	3055
rs564556715	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32064040	ATAGAGTCTCTCTCT[C/G]TCACCCAGGCTGGAG	3055
rs564616574	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32063617	TCCATATTCCTCCCA[C/T]CCTCACCTACTCTAA	3055
rs564655748	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32062903	CCCACCCCCATTGCT[C/G]AGCTGTTCTGAGAAG	3055
rs564655845	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32070690	TTTGCCCTGTTATTT[A/G]TTTGTTGGCCTGTTT	3055
rs564673525	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32067783	GCCACAGACGGCTGT[G/T]GAGCACAGATGGAGT	3055
rs564692532	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32070088	TAAATTAATTCAATA[C/T]AGCAGCAAAGTCTGC	3055
rs564750211	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32098162	AAGTGATTCTCCTGT[A/C]TCAGCCTGTAGCTGG	3055
rs564768389	snp	G/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32058306	GGAGGACAAAGCAGG[G/T]GGATCACCTGAGGTC	3055
rs564773740	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	HCK	GRCh38.p7	20:32051460	GAGTTGGGGAGGGCC[A/G]GGCCAGAAGGGAGGG	3055
rs564830950	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32072097	GAGAAACGAGTGAAC[A/C]GTAATGATAGCAGCT	3055
rs564929214	in-del	-/TT			intron-variant	HCK	GRCh38.p7	20:32056150	ATGTGCATACATGTA[-/TT]TGTTTGAGCACCTGT	3055
rs565063559	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32090067	ACCACAAAGTGTAAC[A/G]AAAGACTCTACTTTC	3055
rs565063572	snp	C/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32082888	GCAATTACTTTTGCA[C/G]CAGCCTAATATGTAT	3055
rs565250565	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32082184	GAGGATGATGATATT[A/G]TAAAACCCTTACCCC	3055
rs565346030	snp	C/T	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32083595	AGGCATTACTTCTTT[C/T]AGCCGTCAGGCAATA	3055
rs565415777	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	HCK	GRCh38.p7	20:32051049	GAATGAAGAAATGAC[C/T]GTGGTCCTGATCAGC	3055
rs565454990	snp	A/G	0.00119737	0.0244387	upstream-variant-2KB	HCK	GRCh38.p7	20:32050381	TGGGGGTGGCGGGAG[A/G]GAATGTACAAAAGTG	3055
rs565522430	snp	A/G	0.00279162	0.0372561	intron-variant	HCK	GRCh38.p7	20:32056149	CATGTGCATACATGT[A/G]TTTGTTTGAGCACCT	3055
rs565526417	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32062032	GCAACCTCTGACTCT[A/G]GGGTTCAAGCGATTC	3055
rs565538838	snp	C/T	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32081353	AGGCCTGGAAAACAT[C/T]GCGTAGCTCAAACTG	3055
rs565560661	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32069223	AGAACCCTTGCCACC[C/T]TTTCTCAGAGATGGC	3055
rs565562685	snp	A/G	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32061624	CAGGGTGATGAGGGA[A/G]GGTTGCTCTGAGAAG	3055
rs565591753	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32090101	GCCTGGAATGCCAGA[A/G]GCATATGGAAATGTG	3055
rs565623052	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32057402	CTCAGGAGTTCGAGA[C/G]CAGCCTGGGTAACAT	3055
rs565660508	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32090715	GTCATGAAATCTCAC[C/T]GCCTTTATCAACCCG	3055
rs565674865	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32070758	TGAGGGCGTGAACTT[C/G]CTTCTCTTCTTCACA	3055
rs565699493	snp	A/G	0.00358779	0.0422022	downstream-variant-500B	HCK	GRCh38.p7	20:32102102	CACTCTAGCCTGAGC[A/G]ACACAGTGAGACCCT	3055
rs565722041	snp	A/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32098338	ACCTGGCCAAAAAAA[A/T]TTTTTTAATTAGCTT	3055
rs565751025	snp	A/G	0.00318978	0.0398085	intron-variant	HCK	GRCh38.p7	20:32097473	AGTCCCAGCTACTTG[A/G]GAGACTGAGGCAGGA	3055
rs565856499	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32062532	GGCAAATGATCAAAG[C/T]CCTGAGTTCTCCTTT	3055
rs565896550	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32069609	ACATTATAAATCTGT[A/G]CTTAATTATGATAAT	3055
rs565992602	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32070162	CCTCCTCTCTGCCCC[C/G]ACACTACCCTGGGCC	3055
rs566153635	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32088478	AAATCTTCACCACAC[A/G]CTAAAGTACTAGATT	3055
rs566192796	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32095320	GAGTGCAGTGGCTCA[A/G]TCTCAGCTCACTGCA	3055
rs566215859	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32082437	ACCTGAGCTCAGGAG[C/T]TGGAGACCAGCCTGG	3055
rs566237933	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32056688	ACCATTCTAATGGGT[A/G]CAGAAAGCACGAATC	3055
rs566289393	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32088951	TGGGTTGCCTGGGTT[C/T]AGCTGGGTGGTTCTT	3055
rs566299253	snp	A/G			missense	HCK	GRCh38.p7	20:32083980	ACCCTGGACAACGGG[A/G]GCTTCTACATATCCC	3055
rs566329756	snp	C/T	0.00358779	0.0422022	intron-variant	HCK	GRCh38.p7	20:32080488	AGGCGTGAGCCACTG[C/T]GCCTGGCCTGTTTTG	3055
rs566395193	snp	C/T	0.00676609	0.0577691	intron-variant	HCK	GRCh38.p7	20:32056212	AGAGTTACTGGGTCA[C/T]ATAAAAGTTCTATCT	3055
rs566428336	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32055797	TTCCATCACCCCTGA[A/G]AAAGGAAACTTTGTA	3055
rs566468005	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32079970	AATGCCCTGGGAAAG[A/G]CTGAAAAACCCAACC	3055
rs566477221	snp	A/G	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32094724	GAAAGAAAGAAAGAA[A/G]GAAAGAAAGAAAGAA	3055
rs566532626	in-del	-/A			intron-variant	HCK	GRCh38.p7	20:32056349	AACCTCGTCTCTACT[-/A]AAAAAAATACAAAAA	3055
rs566564919	snp	C/T	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32061255	CCAAAGTGCTGGGAT[C/T]ACAGGCGTGAGCCAC	3055
rs566811452	snp	A/G	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32066375	GGAGTGCAGTGGCAC[A/G]ATCTTGGCTCACTGC	3055
rs566829021	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32054542	CCGGACGCGGGGGCT[A/C]ACGCCTGTAATCCCA	3055
rs566904915	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32095380	TGTGCCTCAGCCTTC[C/T]GAGTAGCTGGGATTA	3055
rs566908243	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32093197	TGATCCGCCCACCTC[A/G]GCCTCCCAAAGTGCT	3055
rs566941460	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32096664	GTGCTACCATGCCCA[A/G]CTAATTTTTTAATTA	3055
rs567079931	snp	C/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32068916	ACCACTGCACTCCAG[C/G]CTGGGTGACAGAGCG	3055
rs567235368	snp	C/T	0.000581497	0.0170414	intron-variant	HCK	GRCh38.p7	20:32088547	AAAGTAGTAAATGTT[C/T]CTCCCCTCTCCCCCA	3055
rs567236143	snp	C/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32056464	GAGCTTGCAGTGAGC[C/G]GAGATCGAGCCACTG	3055
rs567254923	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32074166	TGAGTTTGCCACCTC[A/G]GATCTCCTACAGCCT	3055
rs567325785	snp	C/T	0.00318978	0.0398085	intron-variant	HCK	GRCh38.p7	20:32063363	GCTCAAGTGATCCTC[C/T]CACCTCAGCCTCCCA	3055
rs567329099	snp	A/C	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32080085	TATCCACCATAGCTG[A/C]CAGCTTAGGTCAGTG	3055
rs567523911	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32080600	CTGGGCTCAAATGAT[C/T]CTCCCATCTCAGTCT	3055
rs567564706	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32054577	TTTGGGAGGCTGAGC[C/T]GGGCGGATCACGAGG	3055
rs567584856	snp	C/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32081154	CATTCCTCCTTTCCT[C/G]CCTCCATAAGGAAAT	3055
rs567635247	snp	A/G	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32091189	CCATCGAGCTCCTGT[A/G]AAAATCAGTAGCATA	3055
rs567911030	in-del	-/G			intron-variant	HCK	GRCh38.p7	20:32060078	CCCTGGTGGTGAACT[-/G]GGCCACCATGTCCTG	3055
rs567968678	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32060564	TAGCTATTGTTTAGA[C/T]GGGAAATCTGGGGGC	3055
rs568002083	snp	A/G	0.000399281	0.0141238	downstream-variant-500B	HCK	GRCh38.p7	20:32102030	GGGAGACCGAGGAGC[A/G]GGGGATTGCTTGAGC	3055
rs568011551	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32066435	TCCTACCTCAGCCTC[C/T]CAAGTAGCTGGGATT	3055
rs568194417	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32072731	AAACTTAGTCGGAAA[A/G]CACTGATCTGGACCG	3055
rs568232770	snp	C/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32078296	GTGATCCACCCGCCT[C/T]GGCCTCCCAAAGTGC	3055
rs568275694	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32072746	ACACTGATCTGGACC[G/T]ACCCCTTCACTGTGT	3055
rs568298863	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32092483	CCCTGTGTTTTCATC[A/G]GAGGCTTCTAGGGCT	3055
rs568378824	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32091614	CCACCCTGGCAACCT[C/T]ATCCCCATTTCGTCC	3055
rs568382060	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32097160	TGGTGTGAGCCTGTG[G/T]TCCCTGCTACTCAGG	3055
rs568414015	snp	A/G	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32077547	TGTTTTGTTTTTTAG[A/G]TGGAGTTTCTCTCTT	3055
rs568513394	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	HCK	GRCh38.p7	20:32051850	AATCCTTTGGCGGGG[C/T]GGGGTTAGTATCTTG	3055
rs568600746	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32071849	CATTGCCCTAACAGC[C/T]TCCTGTCTTCCCAAG	3055
rs568781691	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32070405	CCCTCTTCCCTGCCC[A/G]TGAGCTTCAGCTACA	3055
rs568825485	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32068017	AAAATGAAAAATAGG[C/T]CAGGCGCAGTGGCTC	3055
rs569067652	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32065435	TGGAAAAATCCTGAG[A/G]TGTATAGGCCTCAGG	3055
rs569202732	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32053404	GCTTTTTGGGAGGCC[A/G]AGGCAGGTGGATCTC	3055
rs569204929	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32064682	CCAGAAAACCATCTC[C/T]AGCCCACTGGATGGA	3055
rs569238607	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32071934	CTGACTCGACTCTCC[A/G]GGACGCAGCGCCAGC	3055
rs569319024	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32052786	GTTCCCCTTCTTGGG[C/G]GGGGGCGGGGATTTT	3055
rs569355320	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32059895	TTAAAAATAAAATAC[A/G]TACCCTTCAAAAAAT	3055
rs569408158	snp	A/G			upstream-variant-2KB	HCK	GRCh38.p7	20:32051455	CCGCGGAGTTGGGGA[A/G]GGCCGGGCCAGAAGG	3055
rs569482301	snp	G/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32078163	CCTCAGCCTCCCGAG[G/T]AGCTGGGACTACAGG	3055
rs569563741	snp	C/T	0.000798403	0.0199641	upstream-variant-2KB	HCK	GRCh38.p7	20:32051098	AGAGACGCGGTAGAA[C/T]TCTTGTAGTTTTGGA	3055
rs569602207	snp	C/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32077611	GGCTCACTGCAACCT[C/T]CGCCTCCCGGGTTCA	3055
rs569639257	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32084751	TTGAGACCAGTCCTG[C/T]AGTGGTCAAAAACTT	3055
rs569666396	snp	A/C	0.00318978	0.0398085	intron-variant	HCK	GRCh38.p7	20:32067596	TACTTCCTACTACAT[A/C]AAGTATGGCACGCCA	3055
rs569693969	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32084231	CCAAGATGTAGAGGT[A/G]GCACCCCGTCACACT	3055
rs569724927	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32091335	GCAGCGCTTTTGGAG[A/C]TCCAGCCCTGGCTCC	3055
rs569727884	snp	A/G	0.00159617	0.0282053	intron-variant	HCK	GRCh38.p7	20:32071289	GGTGGAGGGGCCAAG[A/G]ATCAGCTGAGGCTTT	3055
rs569776434	snp	C/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32091347	GAGCTCCAGCCCTGG[C/T]TCCGCAACTTGCAAG	3055
rs569848523	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32098547	GGTGGGAGGAAGGGC[A/G]GGTAAAGGGAGAGAC	3055
rs569874351	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32057951	CGGCTGTGGTCCCAC[A/G]TGCTGCATCCTCTGG	3055
rs569885144	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32099469	TTCAAGCGATTCTCC[C/T]GCCTCAGCCTCCTGA	3055
rs569885219	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32090730	CGCCTTTATCAACCC[A/G]CAGTGCTTACACCTG	3055
rs569919696	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32058405	GGCGTGGTGGCGGGC[A/G]CCTGTAATTTCAGCT	3055
rs570021203	snp	G/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32070901	AAGAAAGAGGAGGAG[G/T]AGGGAGGACAGAGGA	3055
rs570039666	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32083306	ATGTAAGGTAACATA[A/T]TCCCAGGTTCCAGGG	3055
rs570194774	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32076176	AAAAATACAAAAAAA[A/C]TTAGCTGGGTGTGGT	3055
rs570209966	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32089101	TGAGCTTCTTCACGG[C/T]GCAGCAGCTGGGTTC	3055
rs570233416	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32075478	AAAATGCTGGGATTA[C/T]AGGCCTGAACCACTG	3055
rs570282345	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32059618	CTCCTGCGCTCAAGC[A/G]ATCCTCCCACCTCAG	3055
rs570296263	snp	A/G	0.00199481	0.0315187	intron-variant	HCK	GRCh38.p7	20:32084157	GGCCATCCCCTAGAC[A/G]GATAGTTGCTTTGGA	3055
rs570391281	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32072609	CTGCTTAGAATGCCA[C/T]AGTTTAGGTGTCACT	3055
rs570429845	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32078196	CCTGCCACCATGCTC[A/G]GCTAATTTTTTTTTT	3055
rs570491859	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32061070	CTCACTGCAACCTCC[A/G]CCTCCCGGGTTCAAG	3055
rs570492032	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32077675	GGGATTACAGGCATG[C/T]GCCACCATACCTAGC	3055
rs570621891	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32069474	CTGACCAAAACACAC[A/G]AAATGTGATATAATT	3055
rs570668945	snp	A/T	0.000399281	0.0141238	upstream-variant-2KB	HCK	GRCh38.p7	20:32051227	TCCACTTGGGGCCTC[A/T]GTCACCCTCCAGCCC	3055
rs570684213	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32096448	GTTGCAGCAATGAGC[C/T]GAGATTGTGCCATTG	3055
rs570701453	snp	C/T	0.00119737	0.0244387	upstream-variant-2KB	HCK	GRCh38.p7	20:32051744	GGCAGGGTTAGAATC[C/T]ACTGAAGTGAGAGTT	3055
rs570713481	snp	C/G	1.66363e-05	0.00288407	missense	HCK	GRCh38.p7	20:32084042	GGTGGACCACTACAA[C/G]AGTGAGTCCCACCCC	3055
rs570768279	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32098722	TGGGATTCCACTCTT[C/T]GGAGTTGCAGTTAAC	3055
rs570773644	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32059220	GGAAAGAGGTGGCCA[C/T]GGAGGGCTTATAGAA	3055
rs570808280	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32091122	TGGTCCAGCTCCAGA[A/G]CCATTTAGCTATTAC	3055
rs570816340	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32064455	TGTTGTTAGAAGAAG[A/G]GGGGAATGGATTCTA	3055
rs570921197	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32070475	ATGCCAGCCTCAGGG[A/C]CTTTGCATTTGCTGT	3055
rs570954641	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32071094	GACCTCATCTTGTTA[C/T]TTAATATAAAAATGG	3055
rs571119374	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32061976	ACGGACTCTCACTCT[C/G]TTGCCCAGGCTGGAC	3055
rs571251450	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32054050	AGAAAAGTGAAGATA[A/G]TAATATATTAGATGT	3055
rs571302078	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32096738	AACTCCTGGACTTAC[A/G]TGATCCTCCTGCCTC	3055
rs571356359	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32081340	GGATGGCAAGAACAG[G/T]CCTGGAAAACATCGC	3055
rs571519619	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32074517	TGTCCTTCACCCTAC[C/T]GGCTTTCTGGAGGCA	3055
rs571545934	snp	C/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32075275	ACAGCTCACTTCAGC[C/T]TCAGCCTCCCTGGGC	3055
rs571556436	snp	C/T			upstream-variant-2KB	HCK	GRCh38.p7	20:32050880	TAGACAACTAGTGGG[C/T]AGAGCCCAGGAATGC	3055
rs571586080	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32055500	ATTTTTATCCTATTT[A/G]TTTGCTTAGTATTAC	3055
rs571679872	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32076481	ATCCCTGGGTCACCT[C/T]ATGTAGTCCTTGCAG	3055
rs571719085	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32075607	TATCCCTACCCTCAA[A/G]GAGCTCTCCATAACC	3055
rs571824525	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32055696	TTTATAAAATTAACT[A/G]TATGATTTTTAAAGC	3055
rs571850378	snp	A/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32061073	ACTGCAACCTCCGCC[A/T]CCCGGGTTCAAGCAA	3055
rs571853432	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32094590	CTACTCAGGAGGTTA[A/G]GGTGAGAGGATCACT	3055
rs571891609	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32095246	CCCTTCTATGAAATG[C/T]CCAGAAGAGGCAATC	3055
rs571892375	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32081921	AGATGGGGCATGTTG[A/G]GAATTTTAGCCGATT	3055
rs571910734	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32055412	ACAATAACCAATATT[G/T]TCATGTATCTTTATG	3055
rs571910801	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32085342	GTATAGTGAAATCCC[A/G]TCTCTACGAAAAAAT	3055
rs571920065	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32069879	GATAAGTATAACTGA[C/G]TTCTAACTGCTTTAG	3055
rs571972137	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32082521	GTGGCGGGCGTCTGT[A/G]ATCCCAGCTACTCAG	3055
rs571985663	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32061228	ACCTTGTGATTCGCC[C/T]GCCTTGGCCTCCCAA	3055
rs572031135	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32056676	AGTATTATTATTACC[A/G]TTCTAATGGGTACAG	3055
rs572067942	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32055954	TAGCTTCTTCCACTT[A/G]ACATAATGTTTTCCA	3055
rs572159768	snp	G/T	4.34509e-05	0.00466085	utr-variant-5-prime, stop-gained	HCK	GRCh38.p7	20:32052446	GGGCGCTCAAGCTGC[G/T]AGGATCCGGGCTGCC	3055
rs572184582	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32096853	GACGCAGAAAGGAGC[A/G]TTCTGAAATGCTGAA	3055
rs572268870	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32069831	GTTTGGGGTTTTTTT[C/T]CTTAAACCACAAATA	3055
rs572291224	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32095729	CCACGGAATTATACA[A/C]TTTAAATGGGTGAAA	3055
rs572418141	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32072055	GCATCTCAGGCCTCC[A/G]GCCTGGGCAGAAGCA	3055
rs572483693	in-del	-/GCTGCT	0.00358779	0.0422022	intron-variant	HCK	GRCh38.p7	20:32076741	TTCTTGGGTGAGGCA[-/GCTGCT]GCTGCTGCTGCTGCT	3055
rs572499974	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32069086	TGCTTCATGATCCGG[A/G]GCAGTGTCACGTCTG	3055
rs572522046	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32074293	AGCCCCAGCTGAACC[A/G]TTCTGAGTCTCTATA	3055
rs572650398	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32070759	GAGGGCGTGAACTTG[C/T]TTCTCTTCTTCACAG	3055
rs572765775	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32089619	CTGCTGAAAACCTAA[C/T]TTTCTTTCTCATGTT	3055
rs572823994	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32087845	GACGGTGTTTCACCG[C/T]GTTAGCCAGGATGGT	3055
rs572824039	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32080239	GAGTCTCACTCTGTC[A/G]CCAGGCTGGAGTGCA	3055
rs572914210	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32078568	AATTTCATCATCCAT[A/G]AAATGGGGCCAGGAG	3055
rs572933301	snp	A/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32093403	GGCATGAGGAAGATA[A/T]GAGAGGTATAGCAGA	3055
rs572966555	snp	G/T	0.00318978	0.0398085	intron-variant	HCK	GRCh38.p7	20:32054698	GTAGTCCCAGCTACT[G/T]GGGAGGCTGAGGCAG	3055
rs573033404	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32060925	GAAGAAGAAAGGAAT[A/G]AAAGGAGGACGTGTC	3055
rs573086986	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32085134	GTTCCAAATGGGAGC[A/G]AAGACAACTTACAGG	3055
rs573090198	snp	C/G	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32073222	CGACATGCAGGGCTA[C/G]GGTAAGATGCTCTTG	3055
rs573126005	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32066092	TTCTAAACTCACTCA[A/G]ACCACTTTGTCACAA	3055
rs573165734	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32095151	TGGAATGAAGTACTA[A/C]GCCAGGCTAGAACAC	3055
rs573371533	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32092648	TCCACCCTCCTCTCC[C/T]GACCTACAAGGCAGT	3055
rs573473300	snp	C/T	0.000399281	0.0141238	utr-variant-5-prime	HCK	GRCh38.p7	20:32052201	GCGGAGTTAGCCTCG[C/T]TCAGGGCGCGGCTAA	3055
rs573520477	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32100012	TCAAATGATCCTCCC[A/G]CTTCAGCCTCCCGAG	3055
rs573537499	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32080920	TAGTGAGACCCCATC[C/T]GTATGAAAAATTTTA	3055
rs573635492	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32087376	AGGTGCAATCATAAC[C/T]CCTGGGCTCAAGTGA	3055
rs573804312	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32055862	CTGGCAACCACCAAT[C/T]TGCTTTTTGCCTCTA	3055
rs573840666	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32079569	CAGGATTCACTTCGG[A/G]TAAAATGTCTATTTT	3055
rs573843046	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32054866	CAATTCTGACAATGG[A/G]GATAGCAGAGGAGCA	3055
rs573877678	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32078715	TACAAAAATTAGCTA[A/G]GTGTAGTGGTGGGTG	3055
rs573884734	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32067617	TGGCACGCCAGGCAT[A/G]CAGCCATTCACTCAC	3055
rs573913803	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32061003	ATTTTGTTTTTTTTG[A/G]GACAGAGTCTTGCTC	3055
rs573949826	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32066868	AGTAACCCTTTTTGA[A/G]TCTTGCAGTGCTCTG	3055
rs573961428	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32071066	AAACTAGATTGTTTG[A/T]GCCATGTTATGTGAC	3055
rs574014056	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32053137	ACGGGGCTATGAAGT[C/T]TTTCTTGCAAGGATG	3055
rs574057204	snp	A/C/T	0.000798403	0.0199641	utr-variant-5-prime	HCK	GRCh38.p7	20:32052387	CTAGAAAGTCAGTTT[A/C/T]CCGGCACTGGCACCC	3055
rs574115777	in-del	-/ATTTATTTATTTATTT			intron-variant	HCK	GRCh38.p7	20:32095891	TTTATTTATTTATTT[-/ATTTATTTATTTATTT]TGAGACGGAGTCTCG	3055
rs574196255	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32085602	GGTGAGATTTGAAAG[C/T]CAAAAATATCATATA	3055
rs574301251	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32075196	CGTCCCTCATTTGTT[G/T]TTTTGTTTTGTTTTG	3055
rs574304681	snp	C/T	0.00279162	0.0372561	intron-variant	HCK	GRCh38.p7	20:32099274	TGTCTTAGTTAAAGG[C/T]ACCTCCATCCATCTA	3055
rs574308428	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32060041	GATCTCTCAGTACCA[C/T]GGCAGGTTAAAGTGA	3055
rs574318857	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32092718	ACTCTCTCTGTGGCA[C/T]CTTCTGCTGGCCACA	3055
rs574324237	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32077065	CTCCAGCCTGGACAA[C/G]AGAGCGAGACTCTAT	3055
rs574443036	snp	A/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32065747	ATGGGATTCTCTGAT[A/T]GGCCAGGCCTGTGTC	3055
rs574688103	snp	G/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32084916	AGATTTCCAGGCAAC[G/T]GATGAACAGGTTATT	3055
rs574755456	snp	C/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32090972	AAACACTCTACTAAG[C/T]CCTTGATGTAGGCTT	3055
rs574824267	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32067053	CAGGTTGCTTTTTAT[A/G]CGAACTTACTAACAT	3055
rs575044293	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32089276	AATCCCAGGGACCCC[C/G]TCAATGTAACAGTCT	3055
rs575044564	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32058146	TACAGTAGACGACCC[C/T]GAGTCTGAGTGCCAG	3055
rs575112303	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32070599	GGCCTTCCCCAAATG[C/T]CCTGCCTAAAAGAGC	3055
rs575238320	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32060734	ACTTCAGCATACCCT[A/G]AGATAGTTCAAGTCC	3055
rs575280618	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32067461	TTAGTATGTGGCTTC[C/G]GAATGTAATTGTGTG	3055
rs575286660	snp	A/G	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32053206	GACAGGCTAGTGGGT[A/G]GCGGAGGGGGCTTCT	3055
rs575323232	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32060146	AAAGACTGCTCCTCT[C/T]CCAGCAGAAGCGAGC	3055
rs575335218	snp	A/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32101015	ATAAGTATCTCACAG[A/T]GTTCAAAGGAAGAGA	3055
rs575380354	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32091668	AATCAGAGTCTCTTC[C/G]AAGTTTTTACTGAAA	3055
rs575411598	in-del	-/A			intron-variant	HCK	GRCh38.p7	20:32065508	TTATCTCCATACCTC[-/A]GCTCTGTTGTCCTCT	3055
rs575439818	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32066510	TAGAGTCAGGGTTTC[A/C]TCATATTGGCCAGGC	3055
rs575441212	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32099790	CCATAGATGGTGCAG[C/T]GGCATCCTCATCAGT	3055
rs575516771	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32072791	TCAAGCAGCATCCCC[A/C]GGTACATCCAAGACC	3055
rs575528985	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32085374	CAACAATTAGCCAGG[C/T]GTGGTGGTGGGAGCC	3055
rs575562013	snp	G/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32064116	TCAAGCAATTCTCCA[G/T]CCTCAGCCTCCCAAG	3055
rs575573219	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32077804	GCTGGGATTACAGGC[A/G]TGAGCCACTGCTCCC	3055
rs575599129	snp	G/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32071361	GTTACATTTCTGTTA[G/T]CCTCATGCCATCCTC	3055
rs575635918	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32070679	CATTAACTCAATTTG[A/C]CCTGTTATTTATTTG	3055
rs575708938	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32059396	TTTCTTCTTCTCTTC[C/G]TTCCTTTCTTCTTTC	3055
rs575860587	snp	A/C	0.000399281	0.0141238	upstream-variant-2KB	HCK	GRCh38.p7	20:32051421	ACCGCTGACCACAGA[A/C]CTGCCTGGAAGTCTC	3055
rs575875420	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32058269	GGGCACGGTGGCTCA[C/T]ACCTGTAATCCCAGC	3055
rs575915141	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32063577	CCTTTTAAGGCATGG[C/T]TTCAGTGCCATCAGC	3055
rs575918932	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	HCK	GRCh38.p7	20:32050482	ATGACTCACACCTAT[A/G]ATCCCAGTACTTTGG	3055
rs575954001	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32076868	AGGGAGGTGGAACAC[C/T]TGAGGTCAGGAGTTC	3055
rs576131264	snp	A/C	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32076537	ATTATTTCTCAAAGG[A/C]AACATAATTGCTAAG	3055
rs576142394	snp	C/T	0.000399281	0.0141238	upstream-variant-2KB	HCK	GRCh38.p7	20:32050528	GGTTCAGTTGAGCCC[C/T]GGAGTTCAAGACTAG	3055
rs576165984	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32083683	ATAGAGAGGTGACAT[A/G]GTCACATGGCCAAGG	3055
rs576173658	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32082809	GTGTTTCTGCTCTAT[G/T]TGATAATATAGGGTG	3055
rs576200430	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32066127	CTCTGCAGAGAGGCC[A/C]TGGGCTACATAAACC	3055
rs576206544	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32061178	TAGTAGAGACGGGGT[C/T]TCACCATGTTGGCCA	3055
rs576240532	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32057985	GCACTGCGCTAGGAC[A/G]TGCGCTCCTGACTCT	3055
rs576286471	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32090235	CCAGGGCAAGAGCCA[C/T]TCTGCCCGTTTCACA	3055
rs576303870	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32089553	GTCCTGGCTGAGTCA[A/G]AAGAGCACAGTATCT	3055
rs576393699	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32064752	TCTGAGAGCACAGGC[C/T]GAGTCTCTGAGTTTT	3055
rs576396138	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32058904	GGTGAGGGAACCGGG[G/T]TATTTGTCCACCCTG	3055
rs576457942	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32056897	CCTGGCACATAGTAG[G/T]GCCTCAAAAAAACAC	3055
rs576475998	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32096109	TGGCCAGGCTGGTCT[C/T]GAACTGATGACCTCA	3055
rs576510104	snp	C/G/T	0.000798403	0.0199641	upstream-variant-2KB	HCK	GRCh38.p7	20:32051259	ACTCCTCCCCTCCCC[C/G/T]GACCACCTCCCCCAG	3055
rs576514200	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32096970	CATATTATTTCATGT[A/G]CGTTATAACTCGATT	3055
rs576713207	snp	C/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32068605	TTTACACAAATTTGA[C/G]TCCTGCCAGTGTATC	3055
rs576850833	snp	A/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32074308	ATTCTGAGTCTCTAT[A/T]GGCACAGGACCCTGC	3055
rs576918535	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32088257	CAATCCCATTTAGTG[C/T]GATTTGAAACCTCAA	3055
rs576945381	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32077051	ATCACGCCACTGCAC[C/T]CCAGCCTGGACAACA	3055
rs576972254	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32081482	GGTTCACAACTGCTT[A/G]ACTCAAATAAGCCAA	3055
rs577124781	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	HCK	GRCh38.p7	20:32050536	TGAGCCCCGGAGTTC[A/G]AGACTAGCCTGGGCA	3055
rs577144478	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32097690	ATCAAGAAAAGTCTG[C/T]AGATCCAAAGGAGGA	3055
rs577195710	snp	A/G	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32082618	CTGCACTCCAGCCTG[A/G]ATGACACAGCGAGAC	3055
rs577253613	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32055053	TTCCTAGGCGTTCAC[C/T]ACAACGAACAATATT	3055
rs577259302	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32083798	CCCAGGTGTCAGGAC[A/G]GTGCCAGCGGTAGCC	3055
rs577259458	snp	G/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32090759	TGGGCCCAATAAACC[G/T]ACTCGTTATTCATTC	3055
rs577270836	snp	C/T	4.94931e-05	0.00497434	intron-variant	HCK	GRCh38.p7	20:32088654	GCCCAGGTGAGAGCC[C/T]AACGAGGAAACGGGG	3055
rs577296581	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32057576	CTGTACTCCAGCCTG[A/G]GTGACAGAGCAAGAC	3055
rs577315295	snp	A/G	0.000399281	0.0141238	upstream-variant-2KB	HCK	GRCh38.p7	20:32051901	GGGGTTCTTAGACGG[A/G]CGGGTTCGAATCCCT	3055
rs577322755	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32090275	ACAAACCAAGGGAGG[A/G]AAAGAGGTTCTGGGC	3055
rs577403051	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32087971	CTAGAGACAAGGTCT[C/T]GCCATCTTGCCCCAG	3055
rs577427532	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32095683	TGATGAAAGTATTCT[A/G]AAATCCACAACTTTG	3055
rs577506626	snp	C/T	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32075523	CTCATTTGATTCATT[C/T]GACAAGCACATGCTC	3055
rs577578628	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32081558	ATTTGGGGACATTGA[C/T]TAAAGGCATGTTCCT	3055
rs577652073	snp	C/T	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32069306	TGGCCATCTTGAATA[C/T]GTACATTGATCACGT	3055
rs577718022	snp	A/G	0.000399281	0.0141238	intron-variant	HCK	GRCh38.p7	20:32056596	TTTTACATTCCCACC[A/G]TAATATACAAGGGTT	3055
rs577848200	snp	C/T	0.000798403	0.0199641	intron-variant	HCK	GRCh38.p7	20:32055891	TACGGACTAATTTAT[C/T]CAGGATATTTAACAT	3055
rs577898153	in-del	-/T	0.111224	0.207945	intron-variant	HCK	GRCh38.p7	20:32099350	TCTCACTCCTATGAC[-/T]TTTTTTTTTTTTTTT	3055
rs578120375	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32085304	GATCAATCAAGGTCA[A/G]CAGTTCGAGAAAAAC	3055
rs578136198	snp	A/G	0.00119737	0.0244387	intron-variant	HCK	GRCh38.p7	20:32079660	TGCTGCAGGAAGCCA[A/G]ACCCTCTGTATCCTG	3055
rs578174332	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32075393	TTTTTGGTAGAGAGG[G/T]GGTCTCTCTGTGTTG	3055
rs745324001	snp	A/G	3.30028e-05	0.00406205	synonymous-codon	HCK	GRCh38.p7	20:32073360	ACCAGGAATCAGGGA[A/G]GGTAAGTATCTACGA	3055
rs745367271	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32075186	CCTGGCCAGTCGTCC[C/T]TCATTTGTTGTTTTG	3055
rs745406191	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32065626	TATAGAAAGAGGGTG[C/T]TTTTTCCCTAATTTT	3055
rs745414519	snp	A/G	1.81929e-05	0.00301598	intron-variant	HCK	GRCh38.p7	20:32093822	GGCCATCTTGGCGTA[A/G]GCCAGGTCTGAGGAC	3055
rs745459712	snp	A/G			upstream-variant-2KB	HCK	GRCh38.p7	20:32050671	GGTTAGTACTTGGAT[A/G]GGAGACCCCCTCAAA	3055
rs745511823	snp	A/G	3.42091e-05	0.00413562	intron-variant	HCK	GRCh38.p7	20:32071820	TCCCTGGGGGCTGAC[A/G]GATGCTGCCCCAACA	3055
rs745558831	snp	A/G			missense	HCK	GRCh38.p7	20:32073757	GCCCTGTATGATTAC[A/G]AGGCCATTCACCACG	3055
rs745576083	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32101065	AGACTCTCCTCTAAG[C/T]GGGAGGAAAAACCTT	3055
rs745663743	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32089729	GTCTGGGAAAACAGA[A/G]TGTAAGGACGGGGTG	3055
rs745669661	snp	G/T	1.64966e-05	0.00287194	missense	HCK	GRCh38.p7	20:32083983	CTGGACAACGGGGGC[G/T]TCTACATATCCCCCC	3055
rs745672750	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32091287	CAAGGCAAAAAAGCT[A/G]GGCCAAGTAACAGGT	3055
rs745791291	snp	A/G	1.64784e-05	0.00287035	missense	HCK	GRCh38.p7	20:32093954	CTGCATCCCTGGTGT[A/G]TAAGATTGCTGACTT	3055
rs745803245	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32090932	ACTGGGAGCCACTCT[A/T]TAAATAAATACTTAA	3055
rs745873052	in-del	-/G			intron-variant	HCK	GRCh38.p7	20:32080302	CTCCCAGGTTTGAGC[-/G]ATTCTCCTGCCTCAG	3055
rs745899437	snp	C/G	1.68482e-05	0.00290238	missense	HCK	GRCh38.p7	20:32086692	GAGCATGTCGGTGGA[C/G]GCCTTCCTGGCAGAG	3055
rs745960202	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32083268	ATCCTTAACTTAATC[A/C]CATCTCTAAAGTACC	3055
rs745997826	snp	A/G	1.79011e-05	0.00299169	missense	HCK	GRCh38.p7	20:32086800	CATCACGGAGTTCAT[A/G]GCCAAAGGTGCTGCG	3055
rs746016330	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32071439	GCTTGTCAGCCCTGG[G/T]CCAGTGCTGTGGCAC	3055
rs746088932	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32070672	CACTTTTCATTAACT[C/T]AATTTGCCCTGTTAT	3055
rs746152363	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32056869	AAACCACTGTATCTT[C/G]TAACACCTGGCACCT	3055
rs746177618	in-del	-/CAC	1.64789e-05	0.0028704	cds-indel	HCK	GRCh38.p7	20:32099059	CAACTTTGGCTCCTT[-/CAC]CATCAAGTCAGACGT	3055
rs746215798	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32061898	AGACGGAAACCCTGG[A/G]TGGGGGTTGAGCAGA	3055
rs746315342	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32062423	AATTGACCAAGTGTC[C/T]CAAGAGTAACATTGA	3055
rs746368765	snp	C/T	3.29527e-05	0.00405898	missense	HCK	GRCh38.p7	20:32074660	CGATCCCTGGCCACC[C/T]GGAAGGAGGGCTACA	3055
rs746441853	snp	A/G	1.75637e-05	0.00296337	synonymous-codon	HCK	GRCh38.p7	20:32084404	AGAGGGGAACGACGG[A/G]CTCTGCCAGAAACTG	3055
rs746519685	snp	A/G	1.70368e-05	0.00291858	intron-variant	HCK	GRCh38.p7	20:32071814	CCAGTTTCCCTGGGG[A/G]CTGACGGATGCTGCC	3055
rs746543303	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32076513	AACCATGGAGGAGGC[A/G]TGGCTGGCATTATTT	3055
rs746596541	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32077288	AAATGTTTCAAAATG[C/T]AAATGTGGGGAAGCA	3055
rs746617419	in-del	-/T	1.65799e-05	0.00287918	intron-variant	HCK	GRCh38.p7	20:32088688	GAAACAGGAATTCGA[-/T]TTTTTTTACTTGCCA	3055
rs746647795	snp	A/G	3.31675e-05	0.00407218	missense	HCK	GRCh38.p7	20:32101355	CGAGCTCTGGAGCGT[A/G]GATACCGGATGCCTC	3055
rs746704341	in-del	-/CA	1.65433e-05	0.002876	intron-variant	HCK	GRCh38.p7	20:32073277	CACGGGTCCCCACAC[-/CA]ATTGGTCAGATTCAT	3055
rs746721029	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32065277	ACTACAGATTCCAGG[A/G]CCTCACTCCCAGATA	3055
rs746775844	snp	C/T	1.8239e-05	0.0030198	intron-variant	HCK	GRCh38.p7	20:32093815	TGGGTGGGGCCATCT[C/T]GGCGTAGGCCAGGTC	3055
rs746828466	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32055409	GGAACAATAACCAAT[A/G]TTTTCATGTATCTTT	3055
rs746858136	snp	A/G	2.18902e-05	0.00330827	intron-variant	HCK	GRCh38.p7	20:32079913	CTTGTCCTCCCTGCC[A/G]AGGTGCCCCAGCTGG	3055
rs746909915	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32088388	ATCAAAAAGTCACTT[C/G]ACTAAAACTCAATTC	3055
rs746972386	in-del	-/T			downstream-variant-500B	HCK	GRCh38.p7	20:32102192	GTTCAATGCTTGAGG[-/T]TTTTCTAACTGCCCT	3055
rs747035016	snp	C/T	2.21031e-05	0.00332431	utr-variant-3-prime	HCK	GRCh38.p7	20:32101529	CCATGATAGGGAGGA[C/T]CAGGGCAGGGCCAGG	3055
rs747054128	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32092920	CAAAAAAGCTCTCTA[C/G]AGGTCATATTTTGTT	3055
rs747107038	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32093858	TGTCTCTGTTTGGGG[C/T]GCAGATTGCAGAAGG	3055
rs747159241	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32064780	TTTCCACAGCCAGCA[A/T]GGTAACCCTGGGAAG	3055
rs747192481	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32093300	CTTTGCCGGGCTCAT[C/T]ACCTGTTCAAGCAAC	3055
rs747304023	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32069422	GAGTGAGCTGCCCTA[C/T]CTCACACAGTGCTGC	3055
rs747355853	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32057636	TGTGAAGCCTAGAGA[A/G]GGTAATTGACTTTCC	3055
rs747399117	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32073157	GGCTCTGCCCCTAAT[A/G]TGCCGTGTGGTGCCA	3055
rs747400899	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32086452	GGGAAGTGGTGAACC[C/T]GCCTTTCAACCCACA	3055
rs747481287	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32061000	TTTATTTTGTTTTTT[C/T]TGAGACAGAGTCTTG	3055
rs747503111	snp	A/C	1.70284e-05	0.00291786	stop-gained	HCK	GRCh38.p7	20:32086685	AGCCAGGGAGCATGT[A/C]GGTGGAGGCCTTCCT	3055
rs747584152	in-del	-/CATC			intron-variant	HCK	GRCh38.p7	20:32075706	ATCCATCCATCCATT[-/CATC]CATCCATCCATCCAT	3055
rs747595004	in-del	-/T	1.67262e-05	0.00289185	intron-variant	HCK	GRCh38.p7	20:32071652	CTCACCTCCCTTCTG[-/T]CTGCTGCAGGATGGG	3055
rs747621818	snp	C/G	3.31367e-05	0.00407029	missense	HCK	GRCh38.p7	20:32084021	CTTCAGCACTCTGCA[C/G]GAGCTGGTGGACCAC	3055
rs747622941	snp	A/C			synonymous-codon	HCK	GRCh38.p7	20:32093973	GATTGCTGACTTTGG[A/C]CTGGCCCGGGTCATT	3055
rs747629985	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32056298	GCGGGCGGATCACGA[C/G]GTCAGGAGATGGAGA	3055
rs747662259	snp	C/T	3.43572e-05	0.00414456	intron-variant	HCK	GRCh38.p7	20:32084093	GATGGGCCCACAGAC[C/T]CCTAGTCACGGATGC	3055
rs747667542	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32088034	CCCAAAGCTTTGGGA[A/T]TATAGGCATGAACCA	3055
rs747806782	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32062701	AGAAAGAAGCTGAGG[A/C]TCAGTAAAGGGAAGA	3055
rs747810761	in-del	-/A			intron-variant	HCK	GRCh38.p7	20:32057350	TCACCCTGTAATCCC[-/A]GCACTTTGGGAGGCC	3055
rs747850415	snp	A/G	1.65564e-05	0.00287714	intron-variant	HCK	GRCh38.p7	20:32098995	ACTCTGCTCTGTTCA[A/G]CCCTGCAGGGGCCAA	3055
rs747881046	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32076227	GCTACTCGGGAGGCT[A/G]AGGCAGGAGAATCAC	3055
rs747886135	snp	A/G/T			intron-variant	HCK	GRCh38.p7	20:32073414	CCTGCAGAGGACTCC[A/G/T]CTAGGTTCTCCCTTA	3055
rs747975444	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32068106	GTTCAAGACCAGCCT[A/G]ACCAACGTGGTGAAA	3055
rs747978102	snp	C/G	1.64814e-05	0.00287061	missense	HCK	GRCh38.p7	20:32088601	TGAAAAGTGATGAGG[C/G]CAGCAAGCAGCCATT	3055
rs748071984	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32096217	TAAAGAGACGGGTGC[A/G]GCCGGGCACAGTGGC	3055
rs748174092	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32055131	TCTTGAGGAAAACAC[A/C]AAAAGGCTGGATGGC	3055
rs748194379	snp	A/G	1.78487e-05	0.00298731	missense	HCK	GRCh38.p7	20:32079865	ATGATCCGGGATAGC[A/G]AGACCACTAAAGGTG	3055
rs748203790	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32060577	GACGGGAAATCTGGG[C/G]GCATCCAGCAGACTA	3055
rs748354614	snp	C/T	9.96363e-05	0.00705749	intron-variant	HCK	GRCh38.p7	20:32088695	GGAATTCGATTTTTT[C/T]ACTTGCCAAATATTT	3055
rs748486342	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32098222	TAATTTTGTATTTTT[A/C]GTAGAGATGGAGTTG	3055
rs748511319	snp	A/T			upstream-variant-2KB	HCK	GRCh38.p7	20:32050449	GTTTTTATAAAAAGC[A/T]CATACAGACTAGGTG	3055
rs748541374	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32099747	TTGAACCCCACAGTC[C/T]CCACTGCATCCAGGC	3055
rs748590150	snp	A/G	2.02727e-05	0.0031837	synonymous-codon	HCK	GRCh38.p7	20:32101516	GTACCAACAGCAGCC[A/G]TGATAGGGAGGACCA	3055
rs748652118	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32073189	GCATGTCCCCTGCCG[C/T]ATGTGGGCCTCCTCC	3055
rs748674781	snp	C/T	1.66854e-05	0.00288833	missense	HCK	GRCh38.p7	20:32084427	AGAAACTGTCGGTGC[C/T]CTGCATGTCTTCCAA	3055
rs748720737	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32054755	AGCTTGCAGTGAGCC[A/G]AGATCGTGCCACTGC	3055
rs748744998	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32100145	ACTTCCAGGCTCAAA[C/T]GATCCTCCAGCCTTG	3055
rs748800258	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32101281	GGCTCTCATTTCCCA[A/G]CTGCTTCCGTTTCTA	3055
rs748835530	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32054415	GGGGAAGCAGAAGTC[A/G]CAGTGAGCCGAGATC	3055
rs748856407	snp	C/T	5.00496e-05	0.00500223	intron-variant	HCK	GRCh38.p7	20:32098978	CTCCCCAGCCTTCCC[C/T]GACTCTGCTCTGTTC	3055
rs748995586	in-del	-/AAATACCA			intron-variant	HCK	GRCh38.p7	20:32076803	TAAATACGCATATCT[-/AAATACCA]GGCCAGGTGTGGTGG	3055
rs749050407	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32091130	CTCCAGAGCCATTTA[A/G]CTATTACCCTCTGCT	3055
rs749075140	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32069175	CTTTTACACTCATCA[A/G]CTTGCTCAGTGCTCA	3055
rs749106557	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32092510	GGCTCCTGGTGTGAA[C/T]AAGAATCCTCCACGC	3055
rs749110895	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32077482	TGTTCCATGCCTCTC[A/G]TTCAGACCTTCCATG	3055
rs749130721	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32091625	ACCTCATCCCCATTT[C/T]GTCCCCACCCCCCAC	3055
rs749258466	snp	A/G	1.64762e-05	0.00287016	synonymous-codon	HCK	GRCh38.p7	20:32074680	GGAGGGCTACATCCC[A/G]AGCAACTATGTCGCC	3055
rs749323511	snp	C/T	3.29902e-05	0.00406128	synonymous-codon	HCK	GRCh38.p7	20:32088572	CCCCCATATAGGAAG[C/T]TTGCTGGACTTTCTG	3055
rs749459965	snp	C/T	3.60581e-05	0.00424591	intron-variant	HCK	GRCh38.p7	20:32086814	TGGCCAAAGGTGCTG[C/T]GTGCTGGGGCTGGGG	3055
rs749578325	snp	G/T	1.65611e-05	0.00287755	missense	HCK	GRCh38.p7	20:32101362	TGGAGCGTGGATACC[G/T]GATGCCTCGCCCAGA	3055
rs749691379	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32063497	AAAGCAATCCTCCCA[A/C]CTCAGCCTCCAAAAG	3055
rs749743665	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32098071	TTTTATTTTTGAGAC[A/G]GAGTCTGACTCTATC	3055
rs749785459	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32083373	CCTACCACAGCATGT[A/T]CACATTTCAATAACT	3055
rs749795196	snp	C/T			synonymous-codon	HCK	GRCh38.p7	20:32084407	GGGGAACGACGGGCT[C/T]TGCCAGAAACTGTCG	3055
rs749819847	snp	G/T	1.67329e-05	0.00289243	intron-variant	HCK	GRCh38.p7	20:32099180	TACCAGGGCCCAGTC[G/T]GGCAATGGGCTCATC	3055
rs749879033	in-del	-/G			intron-variant	HCK	GRCh38.p7	20:32074315	GTCTCTATAGGCACA[-/G]GACCCTGCCATGGGT	3055
rs749879087	snp	C/T	3.99289e-05	0.00446798	intron-variant	HCK	GRCh38.p7	20:32086610	TGACCACCTTCCCTG[C/T]TCTCTATCCCCCTCC	3055
rs749924758	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32079206	AAATTCTTTCCAATC[A/T]CACATTGTAGCTTAG	3055
rs749967035	snp	A/G	8.81795e-05	0.00663943	synonymous-codon	HCK	GRCh38.p7	20:32073738	TGAGGACATCATCGT[A/G]GTTGCCCTGTATGAT	3055
rs749967117	snp	C/G	1.70185e-05	0.00291701	missense	HCK	GRCh38.p7	20:32086731	GATGAAAACTCTGCA[C/G]CATGACAAGCTGGTC	3055
rs749981992	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32063520	TCCAAAAGTGCTGGG[A/T]TTACAGGCATGAGCC	3055
rs750027955	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32080529	GACAGGGTCTCACTC[C/T]GTTGCCCAGGCTGGT	3055
rs750150796	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32068938	GACAGAGCGAGACTG[A/T]CTCTGAGAAAACAAA	3055
rs750178879	snp	C/T	1.67539e-05	0.00289425	intron-variant	HCK	GRCh38.p7	20:32098968	ACCCTCACTACTCCC[C/T]AGCCTTCCCCGACTC	3055
rs750251926	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32072665	GTTTCACATACATAA[C/T]AGAGCCTTTATTTAT	3055
rs750266748	snp	C/T	1.64787e-05	0.00287038	synonymous-codon	HCK	GRCh38.p7	20:32099093	TGGTCCTTTGGTATC[C/T]TGCTGATGGAGATCG	3055
rs750305790	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32077717	TTTTAATAGAGACAG[A/G]GTTTCTCCATGTTGG	3055
rs750320415	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32060398	GCTAATTTTTGTATT[G/T]TTGGTTGAGACAGGG	3055
rs750337605	snp	A/G	1.64871e-05	0.00287111	intron-variant	HCK	GRCh38.p7	20:32074612	CACCTTTACTCCCTC[A/G]TGTCCCTCAGATCCG	3055
rs750423950	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32092222	TGCTGGGTTATTTAG[A/C]GGCAGCAGGATGCAC	3055
rs750529660	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32097667	AACCAGAAGAAGATA[A/C]GCAGGAAATCAAGAA	3055
rs750602420	snp	A/G			missense	HCK	GRCh38.p7	20:32099118	AGATCGTCACCTACG[A/G]CCGGATCCCTTACCC	3055
rs750668741	snp	C/T	1.99986e-05	0.0031621	intron-variant	HCK	GRCh38.p7	20:32084383	ATTGACCAGGGACTC[C/T]GTTCCAGAGGGGAAC	3055
rs750677312	snp	C/T			upstream-variant-2KB	HCK	GRCh38.p7	20:32050997	CCTGCATTCCCCAGC[C/T]CCCAGGACAGCTTTG	3055
rs750690335	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32085279	GCACTTTGGGAGGCC[A/G]AGGCAAGTGGATCAA	3055
rs750723033	in-del	-/TA			intron-variant	HCK	GRCh38.p7	20:32096907	GTGATTACAAGGGTA[-/TA]TATATATATATATAA	3055
rs750728003	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32057741	TTTTTCTTTTTTTAT[A/G]CCACAAGTCATCAAG	3055
rs750744039	snp	A/G	1.65403e-05	0.00287574	intron-variant	HCK	GRCh38.p7	20:32088683	GGAAGGGAAACAGGA[A/G]TTCGATTTTTTTACT	3055
rs750756963	snp	C/T	1.65012e-05	0.00287234	intron-variant	HCK	GRCh38.p7	20:32074727	AGACAGAGGAGTAAG[C/T]ATCCTATTTCCTACC	3055
rs750974549	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32087266	GGGGAATTTTTTTAG[C/G]CCACTGTTTCACAAC	3055
rs751000888	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32077099	AAAAAATAATAATAA[A/T]AATAACAAATGAATA	3055
rs751055530	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32090683	GGGTGCCCAACCTCA[C/T]GGCACCCTATCTGGG	3055
rs751084503	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32060325	TCTTGAGTTCAAGCA[A/G]TTCTCCTGCCTTAGC	3055
rs751099785	snp	A/T	3.29989e-05	0.00406182	missense	HCK	GRCh38.p7	20:32084489	GAGATCCCTCGGGAA[A/T]CCCTCAAGCTGGAGA	3055
rs751157398	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32092112	CTTGAGAAGCCGGCC[A/G]GTGGTGCTTTGATTG	3055
rs751196141	in-del	-/TAAAAAAAAAA			intron-variant	HCK	GRCh38.p7	20:32072563	GAGACCCTGTCTCTT[-/TAAAAAAAAAA]AAAAAAAAAAAAAAA	3055
rs751350806	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32077609	TCGGCTCACTGCAAC[C/T]TCCGCCTCCCGGGTT	3055
rs751356172	snp	G/T	0.000197742	0.00994143	missense	HCK	GRCh38.p7	20:32093938	GCCAACATCTTGGTC[G/T]CTGCATCCCTGGTGT	3055
rs751384881	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32085077	TGCAGTGCCAGCCCA[G/T]TGTGGGGCAGCCTGC	3055
rs751423614	snp	A/T	4.98691e-05	0.0049932	intron-variant	HCK	GRCh38.p7	20:32086588	GGTACGGGAGACCAG[A/T]GGGCTCTGACCACCT	3055
rs751505417	snp	C/T	9.132e-05	0.0067566	intron-variant	HCK	GRCh38.p7	20:32073713	GTGTGTCTCCCTTCC[C/T]AGCAGGCTCTGAGGA	3055
rs751511413	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32072339	GTTGTAAGCCTTTAC[A/G]GTTATTAACACCCTA	3055
rs751547264	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32074987	AAAACGACCTGGTTT[C/T]TTTGGTTGGTTACAC	3055
rs751576419	snp	C/T	1.64863e-05	0.00287104	missense	HCK	GRCh38.p7	20:32083969	ACAAGATCCGGACCC[C/T]GGACAACGGGGGCTT	3055
rs751606575	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32057917	GTGCTTAAGTGTAAA[C/T]GTGCCCTGGTCTTGG	3055
rs751666211	snp	A/C	1.66899e-05	0.00288871	intron-variant	HCK	GRCh38.p7	20:32084054	CAAGAGTGAGTCCCA[A/C]CCCAGGGGTGACATC	3055
rs751666345	snp	A/G	0.000162694	0.0090178	intron-variant	HCK	GRCh38.p7	20:32069651	ATGATCCAGCACTCC[A/G]AGAGTCTGAATGTGT	3055
rs751702180	in-del	-/GC	3.43371e-05	0.00414335	frameshift-variant	HCK	GRCh38.p7	20:32079842	CCGGCAACATGCTGG[-/GC]TCCTTCATGATCCGG	3055
rs751722828	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32075677	ACTCTAAAAATATAC[C/T]TCAGTCATCCATCCA	3055
rs751778482	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32095404	GGGATTACAGGCGCA[C/T]ACCACCATACCCAGC	3055
rs751843166	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32069916	ATGGCAATTGTGCAG[A/G]GATGAGAAAAGCAAG	3055
rs751900396	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32064706	GGATGGATGCTCAGG[C/T]AGGCCCCGGCCTCTC	3055
rs751902493	snp	C/T	1.75779e-05	0.00296457	missense	HCK	GRCh38.p7	20:32086774	GTGGTCACCAAGGAG[C/T]CCATCTACATCATCA	3055
rs751990347	snp	C/G	1.65669e-05	0.00287805	intron-variant	HCK	GRCh38.p7	20:32088552	AGTAAATGTTCCTCC[C/G]CTCTCCCCCATATAG	3055
rs752034838	snp	A/C	3.30628e-05	0.00406575	synonymous-codon	HCK	GRCh38.p7	20:32071680	GGGGTGCATGAAGTC[A/C]AAGTTCCTCCAGGTC	3055
rs752154859	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32088876	ATCTATTTTGGTATA[A/G]CAAACCATCCAAGTC	3055
rs752161765	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32074791	TTTGCAACTCAGGAC[A/G]TCTGCACACACTGTA	3055
rs752221323	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32071340	GCCCACCCAACAGCT[C/T]TACCTGTTACATTTC	3055
rs752251751	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32086535	GAGCAGGAAAGACTT[G/T]CTGGAGGAGGCGGGT	3055
rs752270685	in-del	-/TTT			intron-variant	HCK	GRCh38.p7	20:32059516	CTCTCTCTCTCTTTT[-/TTT]TTTCTTTTTCTTTTT	3055
rs752297827	snp	A/C	3.33233e-05	0.00408173	missense	HCK	GRCh38.p7	20:32101344	CTGAAGTGATCCGAG[A/C]TCTGGAGCGTGGATA	3055
rs752347191	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32089109	TTCACGGCGCAGCAG[A/C]TGGGTTCCAAGACAG	3055
rs752366272	in-del	-/ACAT			intron-variant	HCK	GRCh38.p7	20:32058638	CACACACACACACAC[-/ACAT]ACACACACTAGTCCA	3055
rs752380921	snp	A/G	1.65051e-05	0.00287267	synonymous-codon	HCK	GRCh38.p7	20:32084461	CCAGAAGCCTTGGGA[A/G]AAAGATGCCTGGGAG	3055
rs752400964	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32059479	CCTCCTCCTCCTCCT[C/T]CTTCTTCTTTCTTGC	3055
rs752447291	snp	A/G	1.70632e-05	0.00292084	missense	HCK	GRCh38.p7	20:32079812	GGAAGGACGCAGAGC[A/G]CCAACTGCTGGCTCC	3055
rs752486781	snp	C/G	1.66935e-05	0.00288903	intron-variant	HCK	GRCh38.p7	20:32071785	CACCATCAAGCCGGT[C/G]AGTAGGGGAGGTCCC	3055
rs752510078	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32097185	CTCAGGAGGCTGAGG[C/T]GGGAGAATCGCTTGA	3055
rs752563370	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32095082	CCATCAATTGATGAA[C/T]AGACGAACAAAATGT	3055
rs752568964	snp	C/T	1.67318e-05	0.00289234	missense	HCK	GRCh38.p7	20:32101431	GCTGGAAAAACCGTC[C/T]GGAGGAGCGGCCGAC	3055
rs752616514	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32082709	TTATCATGGTAAAGA[A/C]CACTGAGACAGAGGG	3055
rs752652010	snp	A/G	0.000486421	0.0155876	intron-variant	HCK	GRCh38.p7	20:32054183	GTCTCCCCACCTTGT[A/G]TCACTCTCAGTCCTG	3055
rs752678082	snp	A/G	0.000363115	0.0134694	missense	HCK	GRCh38.p7	20:32084399	GTTCCAGAGGGGAAC[A/G]ACGGGCTCTGCCAGA	3055
rs752703448	in-del	-/T	1.66452e-05	0.00288484	intron-variant	HCK	GRCh38.p7	20:32088545	TAAAAGTAGTAAATG[-/T]TCCTCCCCTCTCCCC	3055
rs752705173	snp	A/G	1.6492e-05	0.00287154	synonymous-codon	HCK	GRCh38.p7	20:32093919	CCACCGAGACCTCCG[A/G]GCTGCCAACATCTTG	3055
rs752708227	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32093033	CACTGCAGCCTCTGC[C/T]TCCTGGGTCCAAGCA	3055
rs752736365	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32070463	CTCTCTAAGCACATG[A/C]CAGCCTCAGGGCCTT	3055
rs752794859	snp	A/G	0.000100956	0.00710406	intron-variant	HCK	GRCh38.p7	20:32094044	GCCAAGCAGCCCCAC[A/G]TTGCCCATTTGGATG	3055
rs752797290	snp	C/T	1.65081e-05	0.00287293	intron-variant	HCK	GRCh38.p7	20:32083876	CCATTCTGAGGGGTT[C/T]CTCTTTGGTCAATTC	3055
rs752867725	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32056305	GATCACGAGGTCAGG[A/C]GATGGAGATCATCCC	3055
rs752916957	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32054069	TATATTAGATGTCCC[A/G]AGAATCCACCATCCA	3055
rs752947777	in-del	-/AGAA			intron-variant	HCK	GRCh38.p7	20:32094793	GAGAGAAAGAGAAAG[-/AGAA]AAAGAAAGAAAGAAA	3055
rs753014975	in-del	-/TATTTATTTATTTATT			intron-variant	HCK	GRCh38.p7	20:32095862	TGTTAGCCTAATATT[-/TATTTATTTATTTATT]TATTTATTTATTTAT	3055
rs753094338	snp	A/G			upstream-variant-2KB	HCK	GRCh38.p7	20:32051371	AGAGAGGAACTTTGC[A/G]TGGTGTCTGAATGGA	3055
rs753146662	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32068595	ACAATCACATTTTAC[A/C]CAAATTTGACTCCTG	3055
rs753175110	snp	A/C/T	3.29637e-05	0.00405968	synonymous-codon, missense	HCK	GRCh38.p7	20:32083962	AAACATTACAAGATC[A/C/T]GGACCCTGGACAACG	3055
rs753182831	in-del	-/T			intron-variant	HCK	GRCh38.p7	20:32095176	GAACACAGATGACCC[-/T]TAAAAACATTTTGTT	3055
rs753220986	in-del	-/TTCTTGGCTAGAATGTTCA			intron-variant	HCK	GRCh38.p7	20:32065916	AGAGGTTCTCTAGCC[-/TTCTTGGCTAGAATGTTCA]TTCTTGGCTAGAATG	3055
rs753306784	snp	C/G			downstream-variant-500B	HCK	GRCh38.p7	20:32102074	GCCACAGTGAGCTAT[C/G]ATCGTGCCACTGCAC	3055
rs753308383	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32086297	GTGCTGAGATTACAG[G/T]CGTGAGCCACTTAGA	3055
rs753309526	snp	C/T	0.000162167	0.00900316	intron-variant	HCK	GRCh38.p7	20:32054188	CCCACCTTGTATCAC[C/T]CTCAGTCCTGTTTCT	3055
rs753328251	snp	C/T	3.36112e-05	0.00409932	intron-variant	HCK	GRCh38.p7	20:32088522	TTGTGGTTTTTGCCA[C/T]TAAATAGTAAAAGTA	3055
rs753346015	in-del	-/AAAA			intron-variant	HCK	GRCh38.p7	20:32094705	AAAAGAAAAGAAAAG[-/AAAA]GAAAGAAAGAAAGAA	3055
rs753422243	snp	A/G	0.000131833	0.00811782	missense	HCK	GRCh38.p7	20:32074699	AACTATGTCGCCCGC[A/G]TTGACTCTCTGGAGA	3055
rs753427437	snp	A/G	1.73631e-05	0.00294639	synonymous-codon	HCK	GRCh38.p7	20:32086758	GGTCAAACTTCATGC[A/G]GTGGTCACCAAGGAG	3055
rs753434688	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32082635	TGACACAGCGAGACT[C/G]TGACACACACACACA	3055
rs753592493	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32056182	TTTCAATTCCTTTGG[G/T]TATATACCTGAAGTA	3055
rs753597053	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32061173	ATTTTTAGTAGAGAC[A/G]GGGTTTCACCATGTT	3055
rs753654022	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32083697	TAGTCACATGGCCAA[G/T]GTCTCACGGGTGGAT	3055
rs753754489	in-del	-/GGCCTTCCT	1.68525e-05	0.00290275	cds-indel	HCK	GRCh38.p7	20:32086692	GAGCATGTCGGTGGA[-/GGCCTTCCT]GGCAGAGGCCAACGT	3055
rs753818592	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32093581	TCCTGGAGAAATAGT[C/T]CCATTGCTTTTTCCC	3055
rs753879646	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32094960	AAAGAGTAGATGCCA[A/C]TTGGTTTCGTTTTTG	3055
rs753928014	snp	C/T			upstream-variant-2KB	HCK	GRCh38.p7	20:32051116	TTGTAGTTTTGGAGA[C/T]TTTGGAGGTGTGTTA	3055
rs754061875	snp	G/T	3.3264e-05	0.0040781	missense	HCK	GRCh38.p7	20:32071779	CACATCCACCATCAA[G/T]CCGGTGAGTAGGGGA	3055
rs754174252	snp	C/T	0.000280688	0.0118434	intron-variant	HCK	GRCh38.p7	20:32083853	CAAGGTGGCAGGCCT[C/T]CAAGATGCCATTCTG	3055
rs754229021	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32077168	GTCTGAATCAAGAAA[C/T]TGCTAACAGAGGTTG	3055
rs754236202	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32065145	TCACATACCCAGTCA[C/G]TGGCAGAACTGCTAT	3055
rs754280289	snp	G/T	1.72955e-05	0.00294065	missense	HCK	GRCh38.p7	20:32101464	TCGAATACATCCAGA[G/T]TGTGCTGGATGACTT	3055
rs754283922	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32078344	GCCACCGCGCCCAGC[C/T]GGGGGAGACAGTTCT	3055
rs754289993	in-del	-/TT			intron-variant	HCK	GRCh38.p7	20:32063993	GCCCATCTCTACTTC[-/TT]TTTTTTTTTTTTTTT	3055
rs754364530	snp	A/G	1.66574e-05	0.0028859	synonymous-codon	HCK	GRCh38.p7	20:32093889	CATGGCCTTCATCGA[A/G]CAGAGGAACTACATC	3055
rs754463243	snp	C/T			upstream-variant-2KB	HCK	GRCh38.p7	20:32050326	GACTACACGTACAGC[C/T]GCTACCTTTGGCAAC	3055
rs754535151	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32070354	AATCCAAAGTCCTTA[C/G]TGGCCCTACAGGATA	3055
rs754569688	snp	G/T			synonymous-codon	HCK	GRCh38.p7	20:32083931	AGACTACGACCCTCG[G/T]CAGGGAGATACCGTG	3055
rs754573109	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32056208	AAGTAGAGTTACTGG[A/G]TCATATAAAAGTTCT	3055
rs754616174	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32087931	ACAGGCGTGAGCAAC[C/T]GCGCCCAGCTTCTAA	3055
rs754741818	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32095920	TTTGAGACGGAGTCT[C/T]GCTCTGCTGCCCAGG	3055
rs754800488	snp	A/C	0.000111035	0.00745018	missense	HCK	GRCh38.p7	20:32084397	CTGTTCCAGAGGGGA[A/C]CGACGGGCTCTGCCA	3055
rs754823296	in-del	-/CAATCTG			intron-variant	HCK	GRCh38.p7	20:32055858	GCCCCTGGCAACCAC[-/CAATCTG]CTTTTTGCCTCTACG	3055
rs754825319	in-del	-/TGCA	5.42716e-05	0.00520892	intron-variant	HCK	GRCh38.p7	20:32086830	TGCTGGGGCTGGGGG[-/TGCA]TGCAGGCTGTGGCCT	3055
rs754926961	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32060714	TCTTTTCTTTTTCAT[A/G]CTTAACTTCAGCATA	3055
rs754972134	snp	A/G	1.73643e-05	0.0029465	synonymous-codon	HCK	GRCh38.p7	20:32101318	CGGCTCCTTTTCAGG[A/G]ATGTCAAACCCTGAA	3055
rs754997982	snp	A/C	1.69743e-05	0.00291322	intron-variant	HCK	GRCh38.p7	20:32084079	GACATCCCCACCACG[A/C]TGGGCCCACAGACTC	3055
rs755024531	in-del	-/G	0.000617856	0.0175655	utr-variant-5-prime, frameshift-variant	HCK	GRCh38.p7	20:32052426	AGGGGCTGCCGAGCT[-/G]GGGGGGGCGCTCAAG	3055
rs755112668	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32090705	CTATCTGGGGGTCAT[A/G]AAATCTCACCGCCTT	3055
rs755143804	snp	A/C/G	3.51137e-05	0.00418997	missense	HCK	GRCh38.p7	20:32079857	GCTCCTTCATGATCC[A/C/G]GGATAGCGAGACCAC	3055
rs755187545	snp	C/T	1.64841e-05	0.00287085	missense	HCK	GRCh38.p7	20:32088586	GCTTGCTGGACTTTC[C/T]GAAAAGTGATGAGGG	3055
rs755265774	snp	C/T			utr-variant-3-prime	HCK	GRCh38.p7	20:32101585	TGGCTCCAGCACCAT[C/T]CGCCAGGGCCCACAC	3055
rs755268256	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32053997	TTTCTCTTTATGGTC[C/T]TTTTTTTTTTAGGGG	3055
rs755269188	snp	A/T	1.79326e-05	0.00299432	missense	HCK	GRCh38.p7	20:32101481	GTGCTGGATGACTTC[A/T]ACACGGCCACAGAGA	3055
rs755426787	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32067055	GGTTGCTTTTTATAC[A/G]AACTTACTAACATAC	3055
rs755445120	snp	C/T	1.65111e-05	0.0028732	intron-variant	HCK	GRCh38.p7	20:32083861	CAGGCCTCCAAGATG[C/T]CATTCTGAGGGGTTT	3055
rs755493137	snp	A/G			upstream-variant-2KB	HCK	GRCh38.p7	20:32050371	ACAACAGTGATGGGG[A/G]TGGCGGGAGGGAATG	3055
rs755625300	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32093380	TGAATTTTCCCTACC[C/T]AGGCTGGGGCATGAG	3055
rs755627824	in-del	-/T			intron-variant	HCK	GRCh38.p7	20:32074338	CATGGGTATAGCTAA[-/T]TAAGACCAAAGCTGC	3055
rs755689155	snp	C/T	3.29669e-05	0.00405984	intron-variant	HCK	GRCh38.p7	20:32074617	TTACTCCCTCATGTC[C/T]CTCAGATCCGGGGAG	3055
rs755704505	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32069022	AGCGAACTTCTCCAG[G/T]GTTGCAGTATCTCTA	3055
rs755743429	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32101193	TCTGTCTTTCACAGT[A/G]GAAGGGGCTCAGCTT	3055
rs755859309	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32072735	TTAGTCGGAAAACAC[C/T]GATCTGGACCGACCC	3055
rs755870026	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32060410	ATTTTTGGTTGAGAC[A/G]GGGTTTCACCATGTT	3055
rs755928099	snp	C/T	6.7807e-05	0.00582227	intron-variant	HCK	GRCh38.p7	20:32084077	GTGACATCCCCACCA[C/T]GATGGGCCCACAGAC	3055
rs756078606	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32097958	AAGATGGGAGGATCA[C/T]TTGAGCCCAGGAGTT	3055
rs756104229	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32064881	CAGGTTCCCAGGGAC[A/G]GCAGTGGCCCGAGGA	3055
rs756150238	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32092385	TTTGTAAACCAAAAG[C/T]GCTGCTTTCTGGGCA	3055
rs756152529	snp	C/G	3.34835e-05	0.00409153	intron-variant	HCK	GRCh38.p7	20:32098970	CCTCACTACTCCCCA[C/G]CCTTCCCCGACTCTG	3055
rs756271404	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32099291	CCTCCATCCATCTAA[C/T]GTCTTAAGCCTGAAA	3055
rs756291215	snp	C/T			upstream-variant-2KB	HCK	GRCh38.p7	20:32050450	TTTTTATAAAAAGCA[C/T]ATACAGACTAGGTGC	3055
rs756302449	snp	G/T	6.59565e-05	0.00574229	missense	HCK	GRCh38.p7	20:32071700	TCCTCCAGGTCGGAG[G/T]CAATACATTCTCAAA	3055
rs756377281	in-del	-/AGCCACAAC			cds-indel	HCK	GRCh38.p7	20:32073328	CCACAGGGGCCTAAT[-/AGCCACAAC]AGCAACACACCAGGA	3055
rs756438966	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32088979	CTTCTGCTCGTCATG[G/T]TAAAGTGAGGTGCAG	3055
rs756466886	in-del	-/AAAGAAAGAAAGAAAGAAAGAA			intron-variant	HCK	GRCh38.p7	20:32094794	GAGAGAAAGAGAAAG[-/AAAGAAAGAAAGAAAGAAAGAA]AGAAAGAAAGAAAGA	3055
rs756551982	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32077111	TAAAAATAACAAATG[A/C]ATACACATATGTGTC	3055
rs756690016	snp	A/C/T	6.60507e-05	0.00574646	intron-variant	HCK	GRCh38.p7	20:32074731	AGAGGAGTAAGTATC[A/C/T]TATTTCCTACCTTCC	3055
rs756750910	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32060353	AGCCTCCCAAGTAGC[C/T]GGGATTACAGGCACC	3055
rs756780282	snp	G/T	1.64988e-05	0.00287213	missense	HCK	GRCh38.p7	20:32073357	CACACCAGGAATCAG[G/T]GAGGGTAAGTATCTA	3055
rs756825979	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32077307	TGTGGGGAAGCATGC[A/C]GAAGAGTGAAAAGTC	3055
rs756829825	snp	C/G	1.65233e-05	0.00287426	intron-variant	HCK	GRCh38.p7	20:32086590	TACGGGAGACCAGTG[C/G]GCTCTGACCACCTTC	3055
rs756848531	snp	C/G	1.65773e-05	0.00287895	missense	HCK	GRCh38.p7	20:32101356	GAGCTCTGGAGCGTG[C/G]ATACCGGATGCCTCG	3055
rs756879148	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32065332	ACCCAAGAATATGCA[A/C]GAATCAGTGGAGACT	3055
rs756902885	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32063382	CTCAGCCTCCCAAGT[A/G]GCTGGGAATACAGGC	3055
rs756922460	in-del	-/G			intron-variant	HCK	GRCh38.p7	20:32061784	CAGTGGAATGATCAA[-/G]GGAGAGTTAGAAGGA	3055
rs756931424	in-del	-/C			intron-variant	HCK	GRCh38.p7	20:32072670	ACATACATAACAGAG[-/C]CTTTATTTATGGAAT	3055
rs756936393	snp	A/G	1.70513e-05	0.00291982	missense	HCK	GRCh38.p7	20:32101451	GAGCGGCCGACCTTC[A/G]AATACATCCAGAGTG	3055
rs756987398	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32084355	CTGGCTGGCTCGGTG[C/T]TTGTTGCTCTCAATT	3055
rs757041171	snp	C/T	1.64787e-05	0.00287038	synonymous-codon	HCK	GRCh38.p7	20:32093946	CTTGGTCTCTGCATC[C/T]CTGGTGTGTAAGATT	3055
rs757062375	snp	A/G	1.70078e-05	0.0029161	intron-variant	HCK	GRCh38.p7	20:32094067	TTTGGATGCTTGTGA[A/G]TGTTGAGAGTTGATA	3055
rs757077065	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32054092	ACCATCCAGAATTAA[C/T]AAATAATAGCATTTT	3055
rs757121486	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32057935	GCCCTGGTCTTGGCC[A/C]CGGCTGTGGTCCCAC	3055
rs757137573	snp	A/G	4.94531e-05	0.00497234	missense	HCK	GRCh38.p7	20:32083911	AGCTACTCTTTGTCC[A/G]TGCGAGACTACGACC	3055
rs757231454	snp	A/G	8.95616e-05	0.00669125	synonymous-codon	HCK	GRCh38.p7	20:32073726	CCCAGCAGGCTCTGA[A/G]GACATCATCGTGGTT	3055
rs757275636	snp	C/T	0.000162536	0.0090134	intron-variant	HCK	GRCh38.p7	20:32069656	CCAGCACTCCAAGAG[C/T]CTGAATGTGTTCCTT	3055
rs757281852	in-del	-/A			upstream-variant-2KB	HCK	GRCh38.p7	20:32050752	ATATACCAAAAACAT[-/A]AGAGTAGGGTCATTG	3055
rs757363569	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32062294	AGAATGCAGATTCAA[A/G]CCCAGCTCTATCTGA	3055
rs757364712	snp	C/T	1.65045e-05	0.00287263	missense	HCK	GRCh38.p7	20:32071687	ATGAAGTCCAAGTTC[C/T]TCCAGGTCGGAGGCA	3055
rs757365555	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32075836	TGTATGGTGGATGAG[A/G]TTGATGAGTAAAAAG	3055
rs757414462	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32073187	AGGCATGTCCCCTGC[C/T]GTATGTGGGCCTCCT	3055
rs757420741	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32063306	AACCCAGGCTGGAGT[A/G]CAGTGGCATGACTAC	3055
rs757421259	snp	C/T	1.64882e-05	0.00287121	synonymous-codon	HCK	GRCh38.p7	20:32083973	GATCCGGACCCTGGA[C/T]AACGGGGGCTTCTAC	3055
rs757505157	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32084867	AGAGACCTTTTCAGA[C/T]GATGAAAATTAAGAA	3055
rs757544220	snp	A/T	1.6477e-05	0.00287024	synonymous-codon	HCK	GRCh38.p7	20:32074647	GTGGTGGAAGGCTCG[A/T]TCCCTGGCCACCCGG	3055
rs757644023	in-del	-/AAG			intron-variant	HCK	GRCh38.p7	20:32094726	AGAAAGAAAGAAAGA[-/AAG]AAGAAAGAAAGAAAG	3055
rs757660320	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32071003	AGGGAGGGAGGGAAG[A/G]AGTTATAAGCAATTT	3055
rs757678615	snp	A/T	1.65425e-05	0.00287593	intron-variant	HCK	GRCh38.p7	20:32088556	AATGTTCCTCCCCTC[A/T]CCCCCATATAGGAAG	3055
rs757805734	in-del	-/AT	1.65315e-05	0.00287498	intron-variant	HCK	GRCh38.p7	20:32088562	CCTCCCCTCTCCCCC[-/AT]ATAGGAAGCTTGCTG	3055
rs757809567	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32074925	CCCAGCTGTGACTCT[A/G]TCTTGTGGAAACCTG	3055
rs757813928	snp	C/T	4.98186e-05	0.00499067	missense	HCK	GRCh38.p7	20:32101352	ATCCGAGCTCTGGAG[C/T]GTGGATACCGGATGC	3055
rs757866724	snp	C/T	3.55999e-05	0.00421885	missense	HCK	GRCh38.p7	20:32086790	CCATCTACATCATCA[C/T]GGAGTTCATGGCCAA	3055
rs757876882	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32059305	TCCTTCCCTCCCTCC[C/T]TCCTTTCTTTTCTTT	3055
rs757942181	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32071451	TGGGCCAGTGCTGTG[A/G]CACGTGGACATGGGG	3055
rs758013775	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32061375	CATGGGTGGGCTTCG[A/G]TCTCCCTGCCACACT	3055
rs758017555	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32090346	GACAGAAAGGAGCCC[A/C]CCTGGGGCTTTGGTC	3055
rs758196213	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32082762	CACAGCTCACAAATA[A/G]CAAAACGGTGGTCAT	3055
rs758222198	snp	C/G	1.64879e-05	0.00287118	missense	HCK	GRCh38.p7	20:32073329	CACAGGGGCCTAATA[C/G]CCACAACAGCAACAC	3055
rs758226147	in-del	-/ACAC			intron-variant	HCK	GRCh38.p7	20:32100186	ATGCTGGGATTACAG[-/ACAC]ACACCACCATGCCCA	3055
rs758386305	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32070490	CCTTTGCATTTGCTG[C/T]TCCCTCTGCCTGGAA	3055
rs758417058	snp	A/G	1.6853e-05	0.0029028	intron-variant	HCK	GRCh38.p7	20:32071802	GTAGGGGAGGTCCCA[A/G]TTTCCCTGGGGGCTG	3055
rs758453485	snp	A/C	1.64933e-05	0.00287165	missense	HCK	GRCh38.p7	20:32083898	GGTCAATTCAGGAAG[A/C]TACTCTTTGTCCGTG	3055
rs758508228	snp	A/G			missense	HCK	GRCh38.p7	20:32074666	CTGGCCACCCGGAAG[A/G]AGGGCTACATCCCAA	3055
rs758555670	snp	A/G	1.66153e-05	0.00288225	intron-variant	HCK	GRCh38.p7	20:32088696	GAATTCGATTTTTTT[A/G]CTTGCCAAATATTTA	3055
rs758631239	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32062094	ACAGGCATGCGCCAC[C/G]ATGCCCGCCTAATTT	3055
rs758658186	snp	A/G	1.78551e-05	0.00298784	synonymous-codon	HCK	GRCh38.p7	20:32086665	GGTGGCAGTGAAGAC[A/G]ATGAAGCCAGGGAGC	3055
rs758715744	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32067639	TTCACTCACTGTGCA[C/T]GACACTCCTACTGTG	3055
rs758750083	snp	A/C/T	1.80564e-05	0.00300466	missense	HCK	GRCh38.p7	20:32073769	TACGAGGCCATTCAC[A/C/T]ACGAAGACCTCAGCT	3055
rs758766153	in-del	-/CATCCATCCATT			intron-variant	HCK	GRCh38.p7	20:32075695	AGTCATCCATCCATC[-/CATCCATCCATT]CATCCATCCATCCAT	3055
rs758769250	snp	A/G			upstream-variant-2KB	HCK	GRCh38.p7	20:32051413	GAAGAGAAACCGCTG[A/G]CCACAGACCTGCCTG	3055
rs758769729	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32099782	GTCATCTCCCATAGA[C/T]GGTGCAGCGGCATCC	3055
rs758823917	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32069579	TGCTGGTTTCAGTTT[A/T]AAATGCATGCAAGTA	3055
rs758853779	snp	A/G	1.7516e-05	0.00295934	synonymous-codon	HCK	GRCh38.p7	20:32086770	TGCGGTGGTCACCAA[A/G]GAGCCCATCTACATC	3055
rs758896067	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32053860	TGCAGGACAATGAGA[A/G]CTTCCATCCCCGGTG	3055
rs758924811	snp	C/T	1.648e-05	0.0028705	missense	HCK	GRCh38.p7	20:32074700	ACTATGTCGCCCGCG[C/T]TGACTCTCTGGAGAC	3055
rs758944350	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32086407	CCACGGCTCAGAGAC[A/G]TTAAGCCACTTGCCC	3055
rs759094815	in-del	-/AAGAAAG			intron-variant	HCK	GRCh38.p7	20:32094711	AAAGAAAAGAAAAGA[-/AAGAAAG]AAAGAAAGAAAGAAA	3055
rs759131196	snp	C/G	1.71138e-05	0.00292516	missense	HCK	GRCh38.p7	20:32079806	TCAGCCGGAAGGACG[C/G]AGAGCGCCAACTGCT	3055
rs759210197	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32074505	TAGTCACAGCCCTGT[C/T]CTTCACCCTACTGGC	3055
rs759226436	snp	C/T	1.6666e-05	0.00288664	missense	HCK	GRCh38.p7	20:32101427	CGCTGCTGGAAAAAC[C/T]GTCCGGAGGAGCGGC	3055
rs759247467	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32071147	GCAGTTTTTCTGTAG[C/T]GTTTGCTCTGAGCCT	3055
rs759250700	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32084819	CCCTCATACGGAGTG[A/G]GGACTGCCTAACAGT	3055
rs759268910	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32057757	CCACAAGTCATCAAG[C/G]AATCACTTCTGCCTT	3055
rs759301060	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32071943	CTCTCCGGGACGCAG[C/T]GCCAGCCAGCATGCA	3055
rs759338196	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32088481	TCTTCACCACACACT[A/G]AAGTACTAGATTGGT	3055
rs759387397	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32075488	GATTATAGGCCTGAA[C/T]CACTGCACCTGGCCC	3055
rs759440492	snp	C/T	3.39841e-05	0.004122	utr-variant-3-prime	HCK	GRCh38.p7	20:32101570	GTGGTGGCTGCAAGG[C/T]GGCTCCAGCACCATC	3055
rs759472997	snp	G/T	1.65168e-05	0.00287369	missense	HCK	GRCh38.p7	20:32084452	TTCCAAGCCCCAGAA[G/T]CCTTGGGAGAAAGAT	3055
rs759517308	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32064105	ACCTCCCAGGTTCAA[G/T]CAATTCTCCAGCCTC	3055
rs759520283	snp	A/C	0.00077607	0.0196833	intron-variant	HCK	GRCh38.p7	20:32088562	CCTCCCCTCTCCCCC[A/C]TATAGGAAGCTTGCT	3055
rs759525887	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32086363	CAAAGCTTACCATTT[C/T]CACTTTACAGATGAG	3055
rs759549487	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32069602	TGCAAGTACATTATA[A/C]ATCTGTGCTTAATTA	3055
rs759587085	in-del	-/TTC			intron-variant	HCK	GRCh38.p7	20:32059520	CTCTCTCTTTTTTTT[-/TTC]TTTTTCTTTTTGAGA	3055
rs759652787	snp	C/T	0.000183085	0.00956602	intron-variant	HCK	GRCh38.p7	20:32073413	TCCTGCAGAGGACTC[C/T]GCTAGGTTCTCCCTT	3055
rs759657585	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32087194	GCCCTGGGAGAGGGA[C/G]CTGGCAAAGCAGCAG	3055
rs759660073	in-del	-/A			intron-variant	HCK	GRCh38.p7	20:32089152	GGCCAAGCCTTCATG[-/A]GCAGGCTCTCATTAA	3055
rs759670290	snp	A/G	1.65209e-05	0.00287405	missense	HCK	GRCh38.p7	20:32093909	GGAACTACATCCACC[A/G]AGACCTCCGAGCTGC	3055
rs759676096	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32055552	TTAAAATGTTCTTAA[A/T]TTTTTAGTGGCTGCA	3055
rs759781577	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32077432	AAGACATCTCTTCCC[A/G]CTTATCTCACACAAG	3055
rs759824952	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32096975	TATTTCATGTACGTT[A/T]TAACTCGATTAAAAA	3055
rs759842107	snp	C/T	1.65064e-05	0.00287279	missense	HCK	GRCh38.p7	20:32099007	TCAACCCTGCAGGGG[C/T]CAAGTTCCCCATCAA	3055
rs759846487	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32092091	CGCCACCCACTTGCC[C/T]CAGACCTTGAGAAGC	3055
rs759855298	snp	A/G	1.70831e-05	0.00292254	intron-variant	HCK	GRCh38.p7	20:32084582	ACAGGGCCAGAGGGT[A/G]GAGGGGAGAGGGAGG	3055
rs759855346	snp	G/T	1.64901e-05	0.00287137	synonymous-codon	HCK	GRCh38.p7	20:32073321	TTCTTCCCCACAGGG[G/T]CCTAATAGCCACAAC	3055
rs759860294	snp	C/T	1.66225e-05	0.00288287	synonymous-codon	HCK	GRCh38.p7	20:32084039	GCTGGTGGACCACTA[C/T]AAGAGTGAGTCCCAC	3055
rs760019905	in-del	-/T	1.65151e-05	0.00287355	intron-variant	HCK	GRCh38.p7	20:32073371	GGGAGGGTAAGTATC[-/T]ACGAGCAGATGCAGT	3055
rs760040311	snp	A/C	1.67441e-05	0.0028934	intron-variant	HCK	GRCh38.p7	20:32094032	GTAGGGAACGCTGCC[A/C]AGCAGCCCCACGTTG	3055
rs760080976	snp	A/T	1.72255e-05	0.0029347	missense	HCK	GRCh38.p7	20:32086749	TGACAAGCTGGTCAA[A/T]CTTCATGCGGTGGTC	3055
rs760127106	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32068486	CTTATATTTGTGGCT[C/T]ACATGACATTTCTGG	3055
rs760132266	in-del	-/T			intron-variant	HCK	GRCh38.p7	20:32091235	AGCATCAAACAGTGG[-/T]TAACTACCAGCATTA	3055
rs760226040	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32067045	ATTGTAAACAGGTTG[C/T]TTTTTATACGAACTT	3055
rs760302271	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32094266	GGCAAATATATGTCG[A/C]AATTAAGGGTAAGAG	3055
rs760325727	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32094582	AGTTGTGGCTACTCA[A/G]GAGGTTAGGGTGAGA	3055
rs760349590	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32082327	CTTGCCTGGCATGTA[C/T]GGTAAGCTATTATTC	3055
rs760389981	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32069775	TTGTAAATAAAAGGA[A/C]TCTTTTTTCATTTTT	3055
rs760472522	snp	A/G	4.97006e-05	0.00498476	missense	HCK	GRCh38.p7	20:32101413	ACAACATCATGATGC[A/G]CTGCTGGAAAAACCG	3055
rs760490096	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32059610	GCCCCAACCTCCTGC[A/G]CTCAAGCGATCCTCC	3055
rs760588334	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32074334	CCTGCCATGGGTATA[A/G]CTAATAAGACCAAAG	3055
rs760621105	snp	A/C/G	6.59146e-05	0.00574052	missense	HCK	GRCh38.p7	20:32074697	GCAACTATGTCGCCC[A/C/G]CGTTGACTCTCTGGA	3055
rs760643361	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32075343	GGACTACAAGTGCGC[A/C]TCACCATGCCCAGCT	3055
rs760643369	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32061787	TGGAATGATCAAGGG[A/G]GAGTTAGAAGGAGAC	3055
rs760711224	snp	A/G	1.65418e-05	0.00287587	intron-variant	HCK	GRCh38.p7	20:32073281	GGGTCCCCACACATT[A/G]GTCAGATTCATTCTC	3055
rs760742002	in-del	-/T			intron-variant	HCK	GRCh38.p7	20:32092836	TATGCGACACACTTA[-/T]TATTATCATCATTCA	3055
rs760765497	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32078048	TTGTTTGTTTGTTTG[C/T]TTTTGAGACAGAGTC	3055
rs760767412	in-del	-/C			intron-variant	HCK	GRCh38.p7	20:32059440	CTTTCTTTTTTCTTT[-/C]TTTCTTTCTTTCTTC	3055
rs760767518	snp	G/T	1.66153e-05	0.00288225	missense	HCK	GRCh38.p7	20:32071775	ATCCCACATCCACCA[G/T]CAAGCCGGTGAGTAG	3055
rs760789501	snp	C/T	1.66109e-05	0.00288187	missense	HCK	GRCh38.p7	20:32084433	TGTCGGTGCCCTGCA[C/T]GTCTTCCAAGCCCCA	3055
rs760818636	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32066821	CACCCTGGGCTTCTG[A/G]TTCAATAATCTTTCC	3055
rs760965711	snp	C/T	1.94165e-05	0.00311575	intron-variant	HCK	GRCh38.p7	20:32084388	CCAGGGACTCTGTTC[C/T]AGAGGGGAACGACGG	3055
rs760968939	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32094800	AAGAGAAAGAAAGAA[A/G]GAAAGAAAGAAAGAA	3055
rs760973634	snp	C/T			upstream-variant-2KB	HCK	GRCh38.p7	20:32051071	CTGATCAGCTGGTAG[C/T]AACGGGAATAGAGAG	3055
rs760982143	snp	A/G	1.65414e-05	0.00287583	missense	HCK	GRCh38.p7	20:32101403	GAGGAGCTCTACAAC[A/G]TCATGATGCGCTGCT	3055
rs761097449	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32090036	TTGAGTATGCAAATT[C/T]AGGGGCCCAGAGGAC	3055
rs761150504	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32091638	TTCGTCCCCACCCCC[C/T]ACTATTCTAAACAAA	3055
rs761230865	snp	A/G	1.65337e-05	0.00287517	intron-variant	HCK	GRCh38.p7	20:32073384	TCTACGAGCAGATGC[A/G]GTGGAGTCATGTGTC	3055
rs761247402	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32061132	AGGATTACAAGCATG[C/T]GCCACCACGCCCAGC	3055
rs761329822	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32055813	AAAGGAAACTTTGTA[A/C]CCATTAAGCAATTAC	3055
rs761472558	snp	C/T	1.65021e-05	0.00287241	intron-variant	HCK	GRCh38.p7	20:32074600	TTCTGTCCCTAACAC[C/T]TTTACTCCCTCATGT	3055
rs761475931	in-del	-/CA			intron-variant	HCK	GRCh38.p7	20:32093524	GTGTGTGTGTGTGTG[-/CA]TGTGCACGTGTGTGT	3055
rs761525114	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32061592	GGGAGTTGGGGGGCA[A/G]AGGATCCTGTCTTTG	3055
rs761538701	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32098878	GGGAGGCCACGTATC[A/G]GGGAAATTGCAGGTC	3055
rs761611372	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32069347	TACAAGGTGCTCAAC[A/G]CGCATGGATTGGAAA	3055
rs761659379	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32100275	ATTTCCATTTTTAAG[C/T]GATGCTTTCAGCATG	3055
rs761682366	in-del	-/TTTG			intron-variant	HCK	GRCh38.p7	20:32086019	TATTTGTTTGGGTTT[-/TTTG]TTTGTTTGTTTGTTT	3055
rs761714339	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32085940	TTATTTAAGAGCAGT[A/G]TTAAGATTAAAGTGG	3055
rs761716878	snp	A/G/T	4.94338e-05	0.00497141	missense	HCK	GRCh38.p7	20:32074693	CCAAGCAACTATGTC[A/G/T]CCCGCGTTGACTCTC	3055
rs761753487	snp	C/G	1.69126e-05	0.00290792	missense	HCK	GRCh38.p7	20:32086724	CCAACGTGATGAAAA[C/G]TCTGCAGCATGACAA	3055
rs761799394	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32091261	CATTAGTCCTTGCTC[C/T]AGAAGAAAAGCAAGG	3055
rs761837983	snp	C/G	4.09324e-05	0.00452378	intron-variant	HCK	GRCh38.p7	20:32084380	TCAATTGACCAGGGA[C/G]TCTGTTCCAGAGGGG	3055
rs761901150	snp	A/G	1.67072e-05	0.00289021	intron-variant	HCK	GRCh38.p7	20:32084058	AGTGAGTCCCACCCC[A/G]GGGGTGACATCCCCA	3055
rs761928699	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32094777	AAGGAAAGAAAGAAA[A/G]AGAGAGAAAGAGAAA	3055
rs761992006	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32077020	ATCTGGGAGGCAGAG[G/T]TTGCAGTGAGCCGAG	3055
rs762048612	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32083767	CACAGCCCACTCAGA[C/T]CCTCGGGCACTTCTG	3055
rs762116893	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32064714	GCTCAGGCAGGCCCC[A/G]GCCTCTCCCCCTTGA	3055
rs762145919	in-del	-/G	3.70343e-05	0.004303	frameshift-variant	HCK	GRCh38.p7	20:32079877	AGCGAGACCACTAAA[-/G]GTGACACCAGCCCTC	3055
rs762293541	snp	C/G	3.3089e-05	0.00406736	synonymous-codon	HCK	GRCh38.p7	20:32071764	GTACGTGCCGGATCC[C/G]ACATCCACCATCAAG	3055
rs762339235	snp	C/G	1.65162e-05	0.00287365	intron-variant	HCK	GRCh38.p7	20:32088668	CTAACGAGGAAACGG[C/G]GAAGGGAAACAGGAA	3055
rs762352870	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32058451	GCAGGAGAATTGCTG[G/T]AACCCGGGAGGCACG	3055
rs762356091	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32074366	TGCAAGTCCAGGGAA[A/C]AGGAGTGGAGCCAGA	3055
rs762502447	in-del	-/AAGAAAGAAAGAAAGAAA			intron-variant	HCK	GRCh38.p7	20:32094795	AGAGAAAGAGAAAGA[-/AAGAAAGAAAGAAAGAAA]GAAAGAAAGAAAGAA	3055
rs762509306	snp	A/C/G	4.89479e-05	0.00494692	intron-variant	HCK	GRCh38.p7	20:32079928	GAGGTGCCCCAGCTG[A/C/G]GGCTGGCCACCACCC	3055
rs762528074	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32085741	ATGAAGCAGGGTGGG[G/T]TGAGGGGAGGGAACA	3055
rs762602289	snp	C/T	0.000103546	0.00719462	intron-variant	HCK	GRCh38.p7	20:32086577	CCTTCTAGGGTGGTA[C/T]GGGAGACCAGTGGGC	3055
rs762618358	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32063276	GCTTCTTTTTTTGAA[A/G]CATTCTTGCTCTGTA	3055
rs762705057	snp	A/C	1.70394e-05	0.0029188	missense	HCK	GRCh38.p7	20:32079817	GACGCAGAGCGCCAA[A/C]TGCTGGCTCCCGGCA	3055
rs762710921	snp	A/G	1.80592e-05	0.00300487	intron-variant	HCK	GRCh38.p7	20:32093832	GCGTAGGCCAGGTCT[A/G]AGGACAAAGGTGTCT	3055
rs762753793	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32086612	ACCACCTTCCCTGCT[C/G]TCTATCCCCCTCCAG	3055
rs762820738	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32064559	GAGGCTCAGAGACAA[A/G]TTGAGACTTGCCTAA	3055
rs762841725	in-del	-/C			intron-variant	HCK	GRCh38.p7	20:32084115	ACGGATGCACTGTGG[-/C]CCCCTGAGACCTGCT	3055
rs762847959	snp	G/T			upstream-variant-2KB	HCK	GRCh38.p7	20:32050761	AAACATAAGAGTAGG[G/T]TCATTGTCTTTCTCA	3055
rs762975518	in-del	-/G	1.65921e-05	0.00288024	intron-variant	HCK	GRCh38.p7	20:32074766	AGAGGCATGAGCAAA[-/G]CCAGCCTTGTTTGCA	3055
rs762994176	snp	C/T	1.69381e-05	0.00291011	intron-variant	HCK	GRCh38.p7	20:32094058	CGTTGCCCATTTGGA[C/T]GCTTGTGAGTGTTGA	3055
rs763023518	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32065990	ATTTGGGAAGTGGGG[A/G]CTGAGATTCTGCATT	3055
rs763044769	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32089845	CCTGAAGGATGAATA[A/G]AAGTTCAGTAGATGA	3055
rs763047058	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32057074	TGGATTTCTGTCTCC[C/T]AAAACATTAGAAGAG	3055
rs763083879	snp	C/T	1.64792e-05	0.00287042	synonymous-codon	HCK	GRCh38.p7	20:32099047	TCCTGAAGCCATCAA[C/T]TTTGGCTCCTTCACC	3055
rs763177625	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32094334	CCAAATGTCCATAGC[A/C]GGAGGATGGATTGTG	3055
rs763221373	snp	C/T	2.5665e-05	0.00358216	intron-variant	HCK	GRCh38.p7	20:32073852	CCCCCTAAGACAGAC[C/T]TGCCTCCTCTACTCA	3055
rs763245498	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32075611	CCTACCCTCAAGGAG[C/T]TCTCCATAACCCATC	3055
rs763261159	snp	C/T	4.50653e-05	0.00474665	intron-variant	HCK	GRCh38.p7	20:32084363	CTCGGTGCTTGTTGC[C/T]CTCAATTGACCAGGG	3055
rs763328887	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32080449	CGATCCACCCCTCTT[A/G]CCCTCCCAAAGTGCT	3055
rs763334713	snp	C/T	1.67492e-05	0.00289384	intron-variant	HCK	GRCh38.p7	20:32071649	GGGCTCACCTCCCTT[C/T]TGTCTGCTGCAGGAT	3055
rs763493477	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32070782	CTTCACAGTTTAGAA[A/G]AGTGCCCAGTAAATC	3055
rs763611293	snp	A/G	1.6819e-05	0.00289987	synonymous-codon	HCK	GRCh38.p7	20:32101438	AAACCGTCCGGAGGA[A/G]CGGCCGACCTTCGAA	3055
rs763621856	snp	C/T			utr-variant-3-prime	HCK	GRCh38.p7	20:32101771	TGGTTGGATTTTAGT[C/T]ACAGCTGTGATTTGG	3055
rs763657773	in-del	-/GAAGAAAGGAAGGAA			intron-variant	HCK	GRCh38.p7	20:32060897	AAAAAGAAAAGGAAG[-/GAAGAAAGGAAGGAA]GAAGAAAGGAAGGAA	3055
rs763667494	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32092108	AGACCTTGAGAAGCC[A/G]GCCGGTGGTGCTTTG	3055
rs763733467	in-del	-/G			intron-variant	HCK	GRCh38.p7	20:32063574	GTCCTTTTAAGGCAT[-/G]GGCTTCAGTGCCATC	3055
rs763769368	snp	C/T	1.70539e-05	0.00292005	missense	HCK	GRCh38.p7	20:32079827	GCCAACTGCTGGCTC[C/T]CGGCAACATGCTGGG	3055
rs763775232	snp	A/G	3.4715e-05	0.00416609	intron-variant	HCK	GRCh38.p7	20:32093859	GTCTCTGTTTGGGGT[A/G]CAGATTGCAGAAGGC	3055
rs763835782	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32084232	CAAGATGTAGAGGTG[C/G]CACCCCGTCACACTC	3055
rs763864817	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32097211	CTTGAGCCCAGGAGG[C/T]TGAGGCTGCAGTGAG	3055
rs763893178	snp	A/G	3.29973e-05	0.00406172	missense	HCK	GRCh38.p7	20:32084484	CCTGGGAGATCCCTC[A/G]GGAATCCCTCAAGCT	3055
rs763917853	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32077497	GTTCAGACCTTCCAT[A/G]CAGCACCTTGTTCCT	3055
rs763940941	snp	G/T	3.59376e-05	0.00423881	intron-variant	HCK	GRCh38.p7	20:32073702	CCTCACCCTCTGTGT[G/T]TCTCCCTTCCCAGCA	3055
rs763960186	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32071483	AGCCCAGAGGTGGCA[A/C]GGATGGAGTGGGTTC	3055
rs763977375	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32098621	CTCCCTTTTCCCATC[A/G]CCCAGGATGAGAGGA	3055
rs764138133	snp	A/G	1.65482e-05	0.00287643	intron-variant	HCK	GRCh38.p7	20:32086578	CTTCTAGGGTGGTAC[A/G]GGAGACCAGTGGGCT	3055
rs764149571	snp	A/G	1.64825e-05	0.00287071	missense	HCK	GRCh38.p7	20:32083963	AACATTACAAGATCC[A/G]GACCCTGGACAACGG	3055
rs764219331	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32095435	TAATTTTTGTATTTT[G/T]AGTAGATAACAGGGT	3055
rs764256093	snp	A/C/T	0.00011598	0.00761432	intron-variant	HCK	GRCh38.p7	20:32088686	AGGGAAACAGGAATT[A/C/T]GATTTTTTTACTTGC	3055
rs764259434	snp	A/G/T	3.39445e-05	0.00411962	intron-variant	HCK	GRCh38.p7	20:32094063	CCCATTTGGATGCTT[A/G/T]TGAGTGTTGAGAGTT	3055
rs764268909	in-del	-/C	1.70772e-05	0.00292204	frameshift-variant	HCK	GRCh38.p7	20:32079811	CGGAAGGACGCAGAG[-/C]GCCAACTGCTGGCTC	3055
rs764274011	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32058260	ACTGAGGCTGGGCAC[A/G]GTGGCTCACACCTGT	3055
rs764399840	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32063277	CTTCTTTTTTTGAAA[C/G]ATTCTTGCTCTGTAA	3055
rs764435953	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32076923	ATACCCTGCCTCTAC[C/T]AAAAATACAAAAATT	3055
rs764494222	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32072855	CCTGGCTGGGCACAG[A/T]GGCTCACTCCTGTAA	3055
rs764495034	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32069823	GCCTAGGAGTTTGGG[G/T]TTTTTTTCCTTAAAC	3055
rs764513438	snp	A/C	1.66399e-05	0.00288438	missense	HCK	GRCh38.p7	20:32084043	GTGGACCACTACAAG[A/C]GTGAGTCCCACCCCA	3055
rs764518186	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32082163	TCAGTTTCCTCATCC[G/T]TAAATGAGGATGATG	3055
rs764605203	snp	A/G	1.65364e-05	0.0028754	synonymous-codon	HCK	GRCh38.p7	20:32071677	GATGGGGTGCATGAA[A/G]TCCAAGTTCCTCCAG	3055
rs764653552	snp	A/G	1.70895e-05	0.00292309	missense	HCK	GRCh38.p7	20:32079808	AGCCGGAAGGACGCA[A/G]AGCGCCAACTGCTGG	3055
rs764782432	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32096494	GATAGAGCGAGACTC[C/T]GTCTCAAAAAAAAAA	3055
rs764873794	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32075562	TCAAGCCCTGTGCCA[C/G]CCTAAGGGGCTGTGG	3055
rs764944547	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32062067	GCCTCAGCCTCCTAA[G/T]TAGCTGGGATTACAG	3055
rs764993677	snp	C/T	1.64819e-05	0.00287066	synonymous-codon	HCK	GRCh38.p7	20:32074704	TGTCGCCCGCGTTGA[C/T]TCTCTGGAGACAGAG	3055
rs764999063	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32063197	GTATGATGAGGTCCA[C/T]AGAGAGTAGAACATA	3055
rs765034186	snp	C/T	1.69095e-05	0.00290765	missense	HCK	GRCh38.p7	20:32101329	CAGGGATGTCAAACC[C/T]TGAAGTGATCCGAGC	3055
rs765050113	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32095076	TAATGTCCATCAATT[A/G]ATGAACAGACGAACA	3055
rs765114593	snp	C/G	1.65157e-05	0.0028736	missense	HCK	GRCh38.p7	20:32084453	TCCAAGCCCCAGAAG[C/G]CTTGGGAGAAAGATG	3055
rs765116536	in-del	-/C			intron-variant	HCK	GRCh38.p7	20:32060330	AGTTCAAGCAATTCT[-/C]CTGCCTTAGCCTCCC	3055
rs765166630	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32053764	GTGTTCTCAGACTTT[A/T]GCCTACATCAGCATC	3055
rs765204750	in-del	-/T			intron-variant	HCK	GRCh38.p7	20:32069865	TTTATTTTAACAAGA[-/T]TAAGTATAACTGAGT	3055
rs765221826	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32086276	CGCCCACCTCGGCCC[C/G]CCAAAGTGCTGAGAT	3055
rs765234843	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32097082	CCCAGGAGTTCAAGA[C/T]CAGCCTGGGCAATAT	3055
rs765257294	snp	C/T	1.67058e-05	0.00289009	missense	HCK	GRCh38.p7	20:32101430	TGCTGGAAAAACCGT[C/T]CGGAGGAGCGGCCGA	3055
rs765313394	snp	C/T	3.3e-05	0.00406189	stop-gained	HCK	GRCh38.p7	20:32093917	ATCCACCGAGACCTC[C/T]GAGCTGCCAACATCT	3055
rs765313919	snp	A/G	1.71941e-05	0.00293202	intron-variant	HCK	GRCh38.p7	20:32084590	AGAGGGTGGAGGGGA[A/G]AGGGAGGCCACTTGC	3055
rs765394752	snp	C/T			downstream-variant-500B	HCK	GRCh38.p7	20:32102073	GGCCACAGTGAGCTA[C/T]GATCGTGCCACTGCA	3055
rs765424624	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32093013	ACAGTGGCACGATCT[C/G]GGCTCACTGCAGCCT	3055
rs765493289	snp	A/G	3.2975e-05	0.00406035	missense	HCK	GRCh38.p7	20:32073325	TCCCCACAGGGGCCT[A/G]ATAGCCACAACAGCA	3055
rs765581370	snp	C/T	9.81306e-05	0.00700398	intron-variant	HCK	GRCh38.p7	20:32073668	GGTCACCAAGGGCTG[C/T]GGATGCACTTAGACG	3055
rs765637073	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32067486	TGTGTGTCCAGTCTC[C/T]CCTTCTCAACTCGGT	3055
rs765690104	snp	A/C	1.67742e-05	0.002896	intron-variant	HCK	GRCh38.p7	20:32094035	GGGAACGCTGCCAAG[A/C]AGCCCCACGTTGCCC	3055
rs765707316	in-del	-/AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA			intron-variant	HCK	GRCh38.p7	20:32054481	AAACTCCACCTAAAA[lengthTooLong]AAAAAAGCCCGGACG	3055
rs765715998	snp	A/G	3.29549e-05	0.00405911	missense	HCK	GRCh38.p7	20:32083944	CGGCAGGGAGATACC[A/G]TGAAACATTACAAGA	3055
rs765737953	snp	C/T	1.65113e-05	0.00287322	intron-variant	HCK	GRCh38.p7	20:32083862	AGGCCTCCAAGATGC[C/T]ATTCTGAGGGGTTTC	3055
rs765757405	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32068533	CATGGACATTTCTGA[C/T]GCCCAGTCCACACCA	3055
rs765791760	snp	A/G	1.68185e-05	0.00289982	intron-variant	HCK	GRCh38.p7	20:32088521	ATTGTGGTTTTTGCC[A/G]TTAAATAGTAAAAGT	3055
rs765796296	in-del	-/T	0.000193293	0.00982899	intron-variant	HCK	GRCh38.p7	20:32073842	CCATCCCACTCCCCC[-/T]AAGACAGACCTGCCT	3055
rs765847910	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32100812	GCAACACACAATAGA[C/T]GCTGAATCCATTAGG	3055
rs765861376	snp	C/G/T	3.29681e-05	0.00405995	intron-variant	HCK	GRCh38.p7	20:32074618	TACTCCCTCATGTCC[C/G/T]TCAGATCCGGGGAGT	3055
rs765971970	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32094705	AAAAGAAAAGAAAAG[A/G]AAAGAAAGAAAGAAA	3055
rs765973158	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32070136	TGTCCCCCAAACCTG[C/T]CCAATGCTTACCTCC	3055
rs766002196	snp	G/T	1.68869e-05	0.00290571	intron-variant	HCK	GRCh38.p7	20:32071625	CCCGCATGAGGCTCT[G/T]GGTAACTGGGGCTCA	3055
rs766022386	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32082359	TTCAACAGTATAAAC[C/T]GGCCAGGTGAGGTGA	3055
rs766075852	in-del	-/ACC	4.78549e-05	0.00489134	intron-variant	HCK	GRCh38.p7	20:32086596	GACCAGTGGGCTCTG[-/ACC]ACCACCTTCCCTGCT	3055
rs766086098	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32087191	AAAGCCCTGGGAGAG[A/G]GAGCTGGCAAAGCAG	3055
rs766094857	snp	C/T	1.72457e-05	0.00293642	missense	HCK	GRCh38.p7	20:32086750	GACAAGCTGGTCAAA[C/T]TTCATGCGGTGGTCA	3055
rs766143125	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32061264	TGGGATTACAGGCGT[C/G]AGCCACTGCGCCCAG	3055
rs766155333	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32083772	CCCACTCAGACCCTC[A/G]GGCACTTCTGCCCAG	3055
rs766298820	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32066929	ATCCTTTTTGGAAGT[C/T]GGTTCTTCTTTGGAG	3055
rs766390696	in-del	-/TTTTTTT			intron-variant	HCK	GRCh38.p7	20:32059512	CTCTCTCTCTCTCTC[-/TTTTTTT]TTTCTTTTTCTTTTT	3055
rs766421808	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32093400	TGGGGCATGAGGAAG[A/T]TATGAGAGGTATAGC	3055
rs766443048	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32077052	TCACGCCACTGCACT[C/G]CAGCCTGGACAACAG	3055
rs766526014	in-del	-/AG			frameshift-variant	HCK	GRCh38.p7	20:32074716	TGACTCTCTGGAGAC[-/AG]AGGAGTAAGTATCCT	3055
rs766537093	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32068295	AAGAGCAAAACTCCA[A/T]CTCAAAAAAATAAAT	3055
rs766560741	snp	A/C	1.66125e-05	0.00288201	missense	HCK	GRCh38.p7	20:32071777	CCCACATCCACCATC[A/C]AGCCGGTGAGTAGGG	3055
rs766669962	snp	A/G	1.87749e-05	0.00306384	missense	HCK	GRCh38.p7	20:32084394	ACTCTGTTCCAGAGG[A/G]GAACGACGGGCTCTG	3055
rs766674230	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32053531	TAATCCCAGCTACTC[C/G]GGAGGCTGAGGCACG	3055
rs766719988	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32090057	CCCAGAGGACACCAC[A/G]AAGTGTAACAAAAGA	3055
rs766758121	snp	C/T	1.6582e-05	0.00287936	synonymous-codon	HCK	GRCh38.p7	20:32084437	GGTGCCCTGCATGTC[C/T]TCCAAGCCCCAGAAG	3055
rs766772966	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32091683	CAAGTTTTTACTGAA[A/T]AATTTGGGTCTCTGG	3055
rs766773063	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32094330	GTATCCAAATGTCCA[C/T]AGCAGGAGGATGGAT	3055
rs766818107	in-del	-/ATAA			intron-variant	HCK	GRCh38.p7	20:32097589	TGTCTCAAAACATAA[-/ATAA]ATAAATAAATAAATA	3055
rs766844170	snp	C/T	3.34308e-05	0.00408831	synonymous-codon	HCK	GRCh38.p7	20:32093886	AGGCATGGCCTTCAT[C/T]GAGCAGAGGAACTAC	3055
rs767031405	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32092185	AGACTGCACCCAGCT[A/G]CAGTCTGCCGGAGCA	3055
rs767091271	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32080507	TGGCCTGTTTTGTTT[C/T]GTTTGAGACAGGGTC	3055
rs767257227	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32080261	TGGAGTGCAGTGGTG[C/G]GATCTCGGCTCACTG	3055
rs767291366	snp	A/G	1.74579e-05	0.00295443	missense	HCK	GRCh38.p7	20:32073736	TCTGAGGACATCATC[A/G]TGGTTGCCCTGTATG	3055
rs767337119	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32085956	TTAAGATTAAAGTGG[A/G]CGGTGTATGTGTGTG	3055
rs767360249	snp	C/T			upstream-variant-2KB	HCK	GRCh38.p7	20:32050967	CAAATGTCAATAGTG[C/T]CAAATTTAAGAACCC	3055
rs767376085	snp	G/T	1.69223e-05	0.00290876	synonymous-codon	HCK	GRCh38.p7	20:32086725	CAACGTGATGAAAAC[G/T]CTGCAGCATGACAAG	3055
rs767463993	snp	C/G	1.64955e-05	0.00287184	intron-variant	HCK	GRCh38.p7	20:32074607	CCTAACACCTTTACT[C/G]CCTCATGTCCCTCAG	3055
rs767493923	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32077026	GAGGCAGAGGTTGCA[A/G]TGAGCCGAGATCACG	3055
rs767515804	snp	A/G	1.65512e-05	0.00287669	intron-variant	HCK	GRCh38.p7	20:32073397	GCAGTGGAGTCATGT[A/G]TCCTGCAGAGGACTC	3055
rs767598085	snp	C/T	1.64776e-05	0.00287028	synonymous-codon	HCK	GRCh38.p7	20:32099077	CATCAAGTCAGACGT[C/T]TGGTCCTTTGGTATC	3055
rs767679917	snp	A/G	1.67253e-05	0.00289178	intron-variant	HCK	GRCh38.p7	20:32084060	TGAGTCCCACCCCAG[A/G]GGTGACATCCCCACC	3055
rs767689694	in-del	-/AAG			intron-variant	HCK	GRCh38.p7	20:32094811	GAAAGAAAGAAAGAA[-/AAG]AGAAAGAAAGAAAGA	3055
rs767710388	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32056087	CAGATGGAAATTCAG[A/G]TTGTTTCCACATTTT	3055
rs767756739	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32064848	TCAGCAGAGGCTGAG[A/G]CGGTGAGGAGCAGGT	3055
rs767831018	snp	C/T	4.49206e-05	0.00473902	intron-variant	HCK	GRCh38.p7	20:32101285	CTCATTTCCCAACTG[C/T]TTCCGTTTCTAATTC	3055
rs767851708	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32071014	GAAGGAGTTATAAGC[A/G]ATTTATAAATTGATA	3055
rs767863383	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32099403	CCCTCTGTCACCCAG[C/G]CTGGAGTGCAGTGAC	3055
rs767879937	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32066532	TGGCCAGGCTTGTCT[C/T]GAACTCCTGACCTCA	3055
rs767919503	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32089991	TGGGCCTCAGCTGGG[C/T]CTGCTGGAGATGCCA	3055
rs767949384	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32053577	TGGGAGGTGGAGGTT[C/G]CGGTGAGCCGAGATC	3055
rs767954647	snp	C/T	0.000149309	0.00863901	missense	HCK	GRCh38.p7	20:32071772	CGGATCCCACATCCA[C/T]CATCAAGCCGGTGAG	3055
rs767983967	snp	A/G	1.65302e-05	0.00287486	intron-variant	HCK	GRCh38.p7	20:32088677	AAACGGGGAAGGGAA[A/G]CAGGAATTCGATTTT	3055
rs768003529	snp	A/G			upstream-variant-2KB	HCK	GRCh38.p7	20:32051810	GGCAAGTTGAGTTTA[A/G]AAATCCTTCAGAGGT	3055
rs768025373	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32088924	CAGCAATTGTTATTT[C/T]TCATGATCCTGTGGG	3055
rs768155510	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32075949	TCTCTTCTGCCTCCT[C/T]TTTCTAGCTAGATGG	3055
rs768160079	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32055033	GTGGATAAATACTCA[A/T]GTTGTTCCTAGGCGT	3055
rs768182335	snp	C/G	9.9231e-05	0.00704313	intron-variant	HCK	GRCh38.p7	20:32088557	ATGTTCCTCCCCTCT[C/G]CCCCATATAGGAAGC	3055
rs768193568	in-del	-/CGGAGGCGTGACGTGCGAGCCACACCCAGGC			intron-variant	HCK	GRCh38.p7	20:32052937	AAGGGGGTAGTTGGG[lengthTooLong]CGGCTGCAGCTGGTC	3055
rs768249690	snp	A/C	1.64768e-05	0.00287021	missense	HCK	GRCh38.p7	20:32083926	GTGCGAGACTACGAC[A/C]CTCGGCAGGGAGATA	3055
rs768261788	in-del	-/CATT			intron-variant	HCK	GRCh38.p7	20:32075703	ATCCATCCATCCATC[-/CATT]CATCCATCCATCCAT	3055
rs768268733	snp	A/C	0.000255232	0.0112938	intron-variant	HCK	GRCh38.p7	20:32052494	GCGCCCAGGTGAGTG[A/C]CGCGCACAGGGGACC	3055
rs768339548	snp	C/T	1.65296e-05	0.00287481	missense	HCK	GRCh38.p7	20:32084005	TATCCCCCCGAAGCA[C/T]CTTCAGCACTCTGCA	3055
rs768354456	in-del	-/AG			intron-variant	HCK	GRCh38.p7	20:32078058	GTTTGTTTTTGAGAC[-/AG]AGTCTCGCTCTGTTG	3055
rs768447790	snp	A/G	1.65946e-05	0.00288046	missense	HCK	GRCh38.p7	20:32094007	GACAACGAGTACACG[A/G]CTCGGGAAGGTAGGG	3055
rs768449147	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32067973	TGTTTCTTTTTACTT[C/T]AAGAAACCTGGATGT	3055
rs768558698	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32066157	CTCTTTCTTCCACCA[C/T]TCTCTCCCCACCTTC	3055
rs768594909	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32100250	GTATTGCTATGTTGC[C/T]GGGCTGGTGATTTCC	3055
rs768596176	snp	A/T	9.91391e-05	0.00703987	intron-variant	HCK	GRCh38.p7	20:32074735	GAGTAAGTATCCTAT[A/T]TCCTACCTTCCAGAA	3055
rs768608013	snp	A/G			upstream-variant-2KB	HCK	GRCh38.p7	20:32050809	CTTCCCCACCAGGGG[A/G]CATTTTACAAATGTC	3055
rs768633614	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32079301	AAACTCAGGCCCTTC[A/T]CAGGCTTCCAAGGTC	3055
rs768793369	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32058182	CCAAAGACAGGTTGT[C/G]ATGCACTAGGCAAAT	3055
rs768812477	in-del	-/ATAA			intron-variant	HCK	GRCh38.p7	20:32097586	ACCCTGTCTCAAAAC[-/ATAA]ATAAATAAATAAATA	3055
rs768947666	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32083628	ATCAGGTAGGGAGGC[A/G]TGAGAACTATTCCCA	3055
rs768951484	snp	A/G	1.64768e-05	0.00287021	missense	HCK	GRCh38.p7	20:32074682	AGGGCTACATCCCAA[A/G]CAACTATGTCGCCCG	3055
rs768980393	snp	A/G	1.67419e-05	0.00289321	intron-variant	HCK	GRCh38.p7	20:32099181	ACCAGGGCCCAGTCT[A/G]GCAATGGGCTCATCT	3055
rs769065441	snp	G/T	1.70997e-05	0.00292396	intron-variant	HCK	GRCh38.p7	20:32071821	CCCTGGGGGCTGACG[G/T]ATGCTGCCCCAACAT	3055
rs769127863	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32065686	AGTGAGGAGGACGTA[C/T]ATGCCTACAACTGAA	3055
rs769134157	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32096755	GATCCTCCTGCCTCA[A/G]GCTCTGAAAGTGCTA	3055
rs769158026	in-del	-/GAA			intron-variant	HCK	GRCh38.p7	20:32094713	AGAAAAGAAAAGAAA[-/GAA]AGAAAGAAAGAAAGA	3055
rs769171417	snp	A/G	2.19957e-05	0.00331623	intron-variant	HCK	GRCh38.p7	20:32084368	TGCTTGTTGCTCTCA[A/G]TTGACCAGGGACTCT	3055
rs769187707	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32070787	CAGTTTAGAAAAGTG[C/T]CCAGTAAATCTTGGC	3055
rs769189442	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32098084	ACGGAGTCTGACTCT[A/G]TCATCCAGGCTGGAG	3055
rs769231384	snp	A/T	4.96652e-05	0.00498298	missense	HCK	GRCh38.p7	20:32101364	GAGCGTGGATACCGG[A/T]TGCCTCGCCCAGAGA	3055
rs769233277	snp	A/G	0.000167729	0.00915622	intron-variant	HCK	GRCh38.p7	20:32084549	GTCTGGATGGGTAAG[A/G]ACCCAGGGCCACAGC	3055
rs769418755	snp	A/G			upstream-variant-2KB	HCK	GRCh38.p7	20:32051522	CTTCCGGGGTAGGGT[A/G]AGGCCTTTCCAGGGT	3055
rs769428440	snp	A/C	1.82131e-05	0.00301765	intron-variant	HCK	GRCh38.p7	20:32093824	CCATCTTGGCGTAGG[A/C]CAGGTCTGAGGACAA	3055
rs769441202	snp	A/G	1.65132e-05	0.00287339	intron-variant	HCK	GRCh38.p7	20:32073368	TCAGGGAGGGTAAGT[A/G]TCTACGAGCAGATGC	3055
rs769479536	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32084831	GTGGGGACTGCCTAA[C/T]AGTTTGGGATTGAGA	3055
rs769647255	snp	C/T	3.29549e-05	0.00405911	synonymous-codon	HCK	GRCh38.p7	20:32083922	GTCCGTGCGAGACTA[C/T]GACCCTCGGCAGGGA	3055
rs769651388	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32077410	ATGCTTCCTCCTTAT[A/G]TAAGAAAAGACATCT	3055
rs769679228	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32076707	CCACTGTCAGATTCC[A/G]AATGTGCATTTCTAA	3055
rs769707140	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32089738	AACAGAGTGTAAGGA[C/T]GGGGTGGTATTAGAG	3055
rs769711436	snp	C/G	6.82788e-05	0.00584249	intron-variant	HCK	GRCh38.p7	20:32079920	TCCCTGCCGAGGTGC[C/G]CCAGCTGGGGCTGGC	3055
rs769733884	snp	A/G	1.79965e-05	0.00299965	intron-variant	HCK	GRCh38.p7	20:32086810	TTCATGGCCAAAGGT[A/G]CTGCGTGCTGGGGCT	3055
rs769801370	snp	A/G	0.000162404	0.00900974	intron-variant	HCK	GRCh38.p7	20:32069755	CCACCAGAAGAGGTA[A/G]ATCCTTGTAAATAAA	3055
rs769881933	in-del	-/GG			intron-variant	HCK	GRCh38.p7	20:32094775	GAAGGAAAGAAAGAA[-/GG]AGAGAGAGAAAGAGA	3055
rs769921999	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32070674	CTTTTCATTAACTCA[A/G]TTTGCCCTGTTATTT	3055
rs769965732	in-del	-/GCATGTGCAC			intron-variant	HCK	GRCh38.p7	20:32093523	TGTGTGTGTGTGTGT[-/GCATGTGCAC]GTGTGTGTGTATGTG	3055
rs770080800	snp	A/C	1.68097e-05	0.00289906	synonymous-codon	HCK	GRCh38.p7	20:32086695	CATGTCGGTGGAGGC[A/C]TTCCTGGCAGAGGCC	3055
rs770136614	snp	C/T	1.66977e-05	0.00288939	intron-variant	HCK	GRCh38.p7	20:32099173	GGGCTGCTACCAGGG[C/T]CCAGTCTGGCAATGG	3055
rs770169744	in-del	-/AG	1.68383e-05	0.00290153	frameshift-variant	HCK	GRCh38.p7	20:32101332	GATGTCAAACCCTGA[-/AG]AGTGATCCGAGCTCT	3055
rs770193145	snp	A/G	1.6625e-05	0.00288309	missense	HCK	GRCh38.p7	20:32084040	CTGGTGGACCACTAC[A/G]AGAGTGAGTCCCACC	3055
rs770332822	snp	A/G	1.64977e-05	0.00287203	synonymous-codon	HCK	GRCh38.p7	20:32099011	CCCTGCAGGGGCCAA[A/G]TTCCCCATCAAGTGG	3055
rs770353048	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32062469	TATATGTGGTTGAAT[A/G]AGTGTTTGGAACACA	3055
rs770361896	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32072496	TGAGCCCAGGAGTTC[A/G]AACTGCATGAGCTAT	3055
rs770387420	in-del	-/TGT			intron-variant	HCK	GRCh38.p7	20:32057806	CATGCACCAACCACA[-/TGT]TGGTCCCCACCCCAT	3055
rs770450499	snp	A/C/T	0.000171203	0.00925064	intron-variant	HCK	GRCh38.p7	20:32071819	TTCCCTGGGGGCTGA[A/C/T]GGATGCTGCCCCAAC	3055
rs770517156	snp	A/G	7.11415e-05	0.0059637	intron-variant	HCK	GRCh38.p7	20:32084351	ACCTCTGGCTGGCTC[A/G]GTGCTTGTTGCTCTC	3055
rs770523793	snp	A/G	1.64999e-05	0.00287222	missense	HCK	GRCh38.p7	20:32071747	AGCCCACACTGTCCT[A/G]TGTACGTGCCGGATC	3055
rs770557816	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32096852	GGACGCAGAAAGGAG[C/T]GTTCTGAAATGCTGA	3055
rs770671364	in-del	-/T	1.65799e-05	0.00287918	intron-variant	HCK	GRCh38.p7	20:32088689	GAAACAGGAATTCGA[-/T]TTTTTTACTTGCCAA	3055
rs770686517	snp	A/G	4.40373e-05	0.0046922	intron-variant	HCK	GRCh38.p7	20:32079915	TGTCCTCCCTGCCGA[A/G]GTGCCCCAGCTGGGG	3055
rs770733393	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32098301	CTCCCAAAGTGCTGG[A/G]ATTACAGGCACAAGC	3055
rs770798401	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32055442	GTAGTCTTTTCTATG[C/T]ACTTTTAAATTAACA	3055
rs770812190	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32088428	AACACTAGGAATTGC[A/G]AACAAATATTCGTAT	3055
rs770828626	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32056843	CAAGAGCACAAACAT[A/G]TTTGTCCTATAAACC	3055
rs770907123	in-del	-/T			intron-variant	HCK	GRCh38.p7	20:32052797	GGGGGGGGGCGGGGA[-/T]TTTTTTTTTTAATTT	3055
rs770919464	in-del	-/C			intron-variant	HCK	GRCh38.p7	20:32083853	CAAGGTGGCAGGCCT[-/C]CAAGATGCCATTCTG	3055
rs770931769	snp	A/G			synonymous-codon	HCK	GRCh38.p7	20:32094006	GGACAACGAGTACAC[A/G]GCTCGGGAAGGTAGG	3055
rs770973323	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32081236	CTGCTGAAAATGCTC[A/C]TTGGAAGCTTTTGGA	3055
rs771075347	snp	A/G			utr-variant-3-prime	HCK	GRCh38.p7	20:32101755	TTTCTATTTCCTGGA[A/G]TGGTTGGATTTTAGT	3055
rs771131947	snp	A/G	1.69815e-05	0.00291384	intron-variant	HCK	GRCh38.p7	20:32084572	GCCACAGCCCACAGG[A/G]CCAGAGGGTGGAGGG	3055
rs771165715	in-del	-/G	1.6537e-05	0.00287545	intron-variant	HCK	GRCh38.p7	20:32073279	CGGGTCCCCACACAT[-/G]TGGTCAGATTCATTC	3055
rs771236044	snp	C/T	1.65512e-05	0.00287669	missense	HCK	GRCh38.p7	20:32101407	AGCTCTACAACATCA[C/T]GATGCGCTGCTGGAA	3055
rs771313242	snp	C/T	8.35527e-05	0.00646292	intron-variant	HCK	GRCh38.p7	20:32094025	CGGGAAGGTAGGGAA[C/T]GCTGCCAAGCAGCCC	3055
rs771326061	snp	A/G	2.23751e-05	0.00334471	utr-variant-3-prime	HCK	GRCh38.p7	20:32101531	ATGATAGGGAGGACC[A/G]GGGCAGGGCCAGGGG	3055
rs771451299	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32093070	GTGCCTCAACCTCCT[C/G]AGCAGATGGGATTAC	3055
rs771466260	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32082457	GACCAGCCTGGCCAG[C/T]ATGGTGAAACTCCAT	3055
rs771481116	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32073912	AACCTGATAGATGGG[A/C]TATCTTATCCTGGGT	3055
rs771503154	snp	A/G	0.000178763	0.00945249	missense	HCK	GRCh38.p7	20:32073772	GAGGCCATTCACCAC[A/G]AAGACCTCAGCTTCC	3055
rs771503854	snp	A/G	1.69775e-05	0.0029135	synonymous-codon	HCK	GRCh38.p7	20:32086686	GCCAGGGAGCATGTC[A/G]GTGGAGGCCTTCCTG	3055
rs771506527	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32074205	ATGGGTATAGTGTCC[A/G]GGATGTGCTGAAGCC	3055
rs771508108	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32088191	AATTACAGGAGTGAG[C/T]CTCGTGCCTAGCCAC	3055
rs771532432	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32055947	CTGTGTCTAGCTTCT[A/T]CCACTTAACATAATG	3055
rs771533097	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32094094	GATACTTGTGAGAGC[A/G]ATTGGTAAAATGCAA	3055
rs771555859	snp	C/T	1.6525e-05	0.00287441	intron-variant	HCK	GRCh38.p7	20:32099001	CTCTGTTCAACCCTG[C/T]AGGGGCCAAGTTCCC	3055
rs771582924	snp	A/G	7.1547e-05	0.00598067	intron-variant	HCK	GRCh38.p7	20:32084346	GAGCAACCTCTGGCT[A/G]GCTCGGTGCTTGTTG	3055
rs771623063	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32096223	GACGGGTGCGGCCGG[A/G]CACAGTGGCTCACAC	3055
rs771623991	in-del	-/TG	1.70551e-05	0.00292015	intron-variant	HCK	GRCh38.p7	20:32071816	AGTTTCCCTGGGGGC[-/TG]ACGGATGCTGCCCCA	3055
rs771624713	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32075280	TCACTTCAGCCTCAG[C/T]CTCCCTGGGCTCAGT	3055
rs771645978	snp	A/C	0.000149201	0.00863586	missense	HCK	GRCh38.p7	20:32084025	AGCACTCTGCAGGAG[A/C]TGGTGGACCACTACA	3055
rs771666516	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32069349	CAAGGTGCTCAACGC[A/G]CATGGATTGGAAATC	3055
rs771685649	in-del	-/G			intron-variant	HCK	GRCh38.p7	20:32056726	CATTCAAACCAGGCT[-/G]CCCTCTGAGGGCTCT	3055
rs771722059	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32062718	CAGTAAAGGGAAGAC[A/G]TGAGAAGTCAGGAGT	3055
rs771840311	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32080885	TTAAGCCCAAAAGTT[C/T]GAGACCAGCCTGGGC	3055
rs771849634	snp	C/G	3.2963e-05	0.00405961	missense	HCK	GRCh38.p7	20:32088605	AAGTGATGAGGGCAG[C/G]AAGCAGCCATTGCCA	3055
rs771940422	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32101304	CGTTTCTAATTCCAC[G/T]GCTCCTTTTCAGGGA	3055
rs772046066	snp	A/G	1.81148e-05	0.0030095	intron-variant	HCK	GRCh38.p7	20:32086842	GGGGTGCAGGCTGTG[A/G]CCTATACTGGTCAAT	3055
rs772057874	snp	A/G			upstream-variant-2KB	HCK	GRCh38.p7	20:32051990	GAGGTGTTAGGGAAA[A/G]TGGAGCGGAAGGGAT	3055
rs772112910	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32055304	TCTTTCAGGCCTCAT[A/G]TTCTCTGCTGTAAGG	3055
rs772224008	snp	C/T	2.00066e-05	0.00316274	intron-variant	HCK	GRCh38.p7	20:32079766	TTGTCCCCTCCCTTT[C/T]CCATCAGGTGGTTTT	3055
rs772274365	snp	A/G	3.30611e-05	0.00406565	synonymous-codon	HCK	GRCh38.p7	20:32101390	AGAGAACTGCCCAGA[A/G]GAGCTCTACAACATC	3055
rs772281719	snp	A/G			upstream-variant-2KB	HCK	GRCh38.p7	20:32050460	AAGCACATACAGACT[A/G]GGTGCAATGACTCAC	3055
rs772313600	snp	C/T	1.82138e-05	0.00301771	synonymous-codon	HCK	GRCh38.p7	20:32079873	GGATAGCGAGACCAC[C/T]AAAGGTGACACCAGC	3055
rs772376584	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32071904	AAAGGGAGCTGACTG[A/G]CCACCAACAGTGTCC	3055
rs772401418	snp	A/C	1.66322e-05	0.00288371	stop-gained	HCK	GRCh38.p7	20:32084431	ACTGTCGGTGCCCTG[A/C]ATGTCTTCCAAGCCC	3055
rs772485133	snp	G/T	1.65589e-05	0.00287736	intron-variant	HCK	GRCh38.p7	20:32073268	ACAGACCTTCCACGG[G/T]TCCCCACACATTGGT	3055
rs772501678	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32078460	GTGATTCAGAGCTTG[G/T]GTTCTGGAGTTAGAC	3055
rs772638936	snp	A/G	0.000149725	0.00865101	utr-variant-3-prime	HCK	GRCh38.p7	20:32101522	ACAGCAGCCATGATA[A/G]GGAGGACCAGGGCAG	3055
rs772657364	snp	C/T	1.68803e-05	0.00290515	intron-variant	HCK	GRCh38.p7	20:32084561	AAGGACCCAGGGCCA[C/T]AGCCCACAGGGCCAG	3055
rs772689471	in-del	-/ATCCACCATCAA	1.71228e-05	0.00292594	intron-variant	HCK	GRCh38.p7	20:32071819	TCCCTGGGGGCTGAC[-/ATCCACCATCAA]GGATGCTGCCCCAAC	3055
rs772708437	snp	A/C/G			intron-variant	HCK	GRCh38.p7	20:32094779	GGAAAGAAAGAAAGA[A/C/G]AGAGAAAGAGAAAGA	3055
rs772801541	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32082230	CATTAAATAAATAAT[A/C]TTATAATTTATATAG	3055
rs772827550	in-del	-/AAAGAAAAGAAAAG			intron-variant	HCK	GRCh38.p7	20:32094696	TGTCAAAAGAAAAGA[-/AAAGAAAAGAAAAG]AAAGAAAGAAAGAAA	3055
rs772900757	snp	A/G	9.95603e-05	0.0070548	synonymous-codon	HCK	GRCh38.p7	20:32084030	TCTGCAGGAGCTGGT[A/G]GACCACTACAAGAGT	3055
rs772909371	snp	A/G	9.92474e-05	0.00704371	missense	HCK	GRCh38.p7	20:32101371	GATACCGGATGCCTC[A/G]CCCAGAGAACTGCCC	3055
rs772929348	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32094516	AAGACCTAGTCTCTA[A/C]AAAAATTTAAGAAAT	3055
rs772959210	in-del	-/ATTTTTTTT			intron-variant	HCK	GRCh38.p7	20:32052797	TGGGGGGGGGCGGGG[-/ATTTTTTTT]TTAATTTAAAAAAGA	3055
rs773080080	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32086890	CTTGGACATGGTTCT[C/T]GCCCTTGAGATGGCC	3055
rs773102455	snp	C/T	1.81289e-05	0.00301067	intron-variant	HCK	GRCh38.p7	20:32086849	AGGCTGTGGCCTATA[C/T]TGGTCAATTGCGGGC	3055
rs773130419	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32077876	TAGATGTCCTACCGT[A/C]CATTTAACCTCTGCC	3055
rs773176904	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32055362	TGGCACTTAATAAGT[A/G]TTCAAGAAAATGGAA	3055
rs773190531	snp	A/C	1.64825e-05	0.00287071	missense	HCK	GRCh38.p7	20:32088621	AAGCAGCCATTGCCA[A/C]AACTCATTGACTTCT	3055
rs773196746	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32074273	GCCCACTCTCCCCTA[C/T]TCTCAGCCCCAGCTG	3055
rs773313287	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32092826	AGAATATTCTTATGC[A/G]ACACACTTATTATTA	3055
rs773529828	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32100362	GTGGCCCAGGCAGAG[A/G]TGATGATGGTCTGGA	3055
rs773601301	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32071925	AACAGTGTCCTGACT[C/T]GACTCTCCGGGACGC	3055
rs773662053	snp	C/T	1.65367e-05	0.00287543	intron-variant	HCK	GRCh38.p7	20:32073383	ATCTACGAGCAGATG[C/T]AGTGGAGTCATGTGT	3055
rs773728350	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32059195	ATGCTGGCAGAGGAT[A/G]TCTGGGTGGGGAAAG	3055
rs773800506	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32076668	CATCACCTGGATTGC[C/T]GGCTAACAAGTGCTT	3055
rs773813020	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32073064	GAGATCACGCCACTG[C/T]ACTCCAGCCTGGGTG	3055
rs773818337	snp	A/T			missense	HCK	GRCh38.p7	20:32086780	ACCAAGGAGCCCATC[A/T]ACATCATCACGGAGT	3055
rs773856142	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32053600	CCGAGATCGCGCCAC[C/T]GCACTCCAGCCTGGG	3055
rs773883094	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32061374	ACATGGGTGGGCTTC[A/G]GTCTCCCTGCCACAC	3055
rs773888581	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32078559	CTGTTCCTCAATTTC[A/G]TCATCCATAAAATGG	3055
rs774033506	snp	C/T	1.66139e-05	0.00288213	missense	HCK	GRCh38.p7	20:32094010	AACGAGTACACGGCT[C/T]GGGAAGGTAGGGAAC	3055
rs774117953	snp	C/G			upstream-variant-2KB	HCK	GRCh38.p7	20:32050931	ACAGGACAGTCCCCC[C/G]CAACAAAGAATTACC	3055
rs774123100	snp	C/T	1.65162e-05	0.00287365	intron-variant	HCK	GRCh38.p7	20:32083843	AGTGCTAATGCAAGG[C/T]GGCAGGCCTCCAAGA	3055
rs774137091	snp	A/G	1.80843e-05	0.00300696	intron-variant	HCK	GRCh38.p7	20:32086826	CTGCGTGCTGGGGCT[A/G]GGGGTGCAGGCTGTG	3055
rs774151457	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32098837	TTAGCCATCTGTCCT[C/T]AGGATGGATGTCCCT	3055
rs774199270	snp	C/T	9.83913e-05	0.00701327	intron-variant	HCK	GRCh38.p7	20:32073864	GACCTGCCTCCTCTA[C/T]TCAACTATGTGCTCT	3055
rs774332986	snp	A/G	1.68071e-05	0.00289884	missense	HCK	GRCh38.p7	20:32086714	CTGGCAGAGGCCAAC[A/G]TGATGAAAACTCTGC	3055
rs774356393	snp	C/G			upstream-variant-2KB	HCK	GRCh38.p7	20:32051954	TGGAGACTGGGGTAG[C/G]ACGCTGGGCGGTGGG	3055
rs774387667	snp	C/T	4.94319e-05	0.00497127	synonymous-codon	HCK	GRCh38.p7	20:32074692	CCCAAGCAACTATGT[C/T]GCCCGCGTTGACTCT	3055
rs774398584	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32058214	TCTTCCCTTTCTGAG[C/T]CTCAGTTCCCAAATC	3055
rs774557287	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32061224	CCTGACCTTGTGATT[C/T]GCCCGCCTTGGCCTC	3055
rs774572397	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32091231	CAGTGAGCATCAAAC[A/C]GTGGTAACTACCAGC	3055
rs774659315	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32076955	GCCAGGTGTGATGGC[A/G]GGCTCCTGTAATCCC	3055
rs774699694	snp	C/T	0.000165426	0.00909316	missense	HCK	GRCh38.p7	20:32101370	GGATACCGGATGCCT[C/T]GCCCAGAGAACTGCC	3055
rs774710914	snp	C/T	1.71982e-05	0.00293237	intron-variant	HCK	GRCh38.p7	20:32071826	GGGGCTGACGGATGC[C/T]GCCCCAACATTGCCC	3055
rs774742110	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32083687	AGAGGTGACATAGTC[A/T]CATGGCCAAGGTCTC	3055
rs774785497	snp	C/G	1.67075e-05	0.00289023	missense	HCK	GRCh38.p7	20:32084426	CAGAAACTGTCGGTG[C/G]CCTGCATGTCTTCCA	3055
rs774814991	snp	A/G	4.11811e-05	0.00453749	intron-variant	HCK	GRCh38.p7	20:32084379	CTCAATTGACCAGGG[A/G]CTCTGTTCCAGAGGG	3055
rs774823528	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32052983	CGGCTGCAGCTGGTC[C/G]GCTCTCTGCCCCTCC	3055
rs774876760	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32070825	ATGGATGAATGAATT[A/G]CCAAACAACTCAGAG	3055
rs774891911	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32100109	GACTTGGTCTCACTA[C/T]GTTGTGCAGCCTGGT	3055
rs774946996	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32085697	AAAATGGAAACCCAA[A/G]CAATTATAAAATTGA	3055
rs775025268	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32074248	TGGTCATGCCTGGTC[A/G]GACTCCCAAGCCCAC	3055
rs775233682	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32072163	CAAAAATACAGTAAC[A/G]ATTGTCATACTAATA	3055
rs775451607	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32077449	TTATCTCACACAAGT[A/G]GTAGATACCACACAC	3055
rs775535327	in-del	-/AAAGAA			intron-variant	HCK	GRCh38.p7	20:32094798	GAAAGAGAAAGAAAG[-/AAAGAA]AGAAAGAAAGAAAGA	3055
rs775556498	snp	A/G	1.67787e-05	0.00289639	synonymous-codon	HCK	GRCh38.p7	20:32086701	GGTGGAGGCCTTCCT[A/G]GCAGAGGCCAACGTG	3055
rs775557931	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32098556	AAGGGCGGGTAAAGG[A/G]AGAGACACATAGTGA	3055
rs775569426	in-del	-/GAGGAA			intron-variant	HCK	GRCh38.p7	20:32070861	CAGAGAGAAAGAGAG[-/GAGGAA]GAGGAAGAGGAAGAA	3055
rs775573405	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32062809	GACAGTCAGGGAACC[C/T]GAGGAGAGGGAGCTG	3055
rs775597846	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32091488	TAAGTGTTTAAGTAT[A/C]ATCTTATAAATAAGC	3055
rs775629271	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32079348	CCGTGGTCTTGTATG[C/T]TTGTGAAACCTGCAA	3055
rs775629437	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32057929	AAATGTGCCCTGGTC[G/T]TGGCCCCGGCTGTGG	3055
rs775722601	snp	A/G	1.64768e-05	0.00287021	synonymous-codon	HCK	GRCh38.p7	20:32074668	GGCCACCCGGAAGGA[A/G]GGCTACATCCCAAGC	3055
rs775726005	snp	A/C	1.64727e-05	0.00286986	intron-variant	HCK	GRCh38.p7	20:32071637	TCTTGGTAACTGGGG[A/C]TCACCTCCCTTCTGT	3055
rs775829045	snp	C/T	3.78251e-05	0.00434869	intron-variant	HCK	GRCh38.p7	20:32073682	GTGGATGCACTTAGA[C/T]GAAACCTCACCCTCT	3055
rs775833338	snp	G/T	6.84861e-05	0.00585136	intron-variant	HCK	GRCh38.p7	20:32084361	GGCTCGGTGCTTGTT[G/T]CTCTCAATTGACCAG	3055
rs775893073	snp	C/T			utr-variant-3-prime	HCK	GRCh38.p7	20:32101730	TTCTCAGGAAGCCCC[C/T]AAGTTGATATTTCTA	3055
rs775912662	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32089751	GACGGGGTGGTATTA[G/T]AGTGCATAGCTAGAG	3055
rs775916901	snp	A/G	9.35935e-05	0.00684018	missense	HCK	GRCh38.p7	20:32073818	TGGTGGTCCTAGAGG[A/G]GTGAGTCCCCATCCC	3055
rs775919396	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32081389	GATTGAGGCTCATTG[A/C]CTCAAAGGAATGAAC	3055
rs775939943	snp	C/T	1.64792e-05	0.00287042	missense	HCK	GRCh38.p7	20:32099043	CAGCTCCTGAAGCCA[C/T]CAACTTTGGCTCCTT	3055
rs775994792	in-del	-/G	4.94275e-05	0.00497105	frameshift-variant	HCK	GRCh38.p7	20:32074668	GGCCACCCGGAAGGA[-/G]GGCTACATCCCAAGC	3055
rs776038055	snp	A/G	3.32557e-05	0.00407759	missense	HCK	GRCh38.p7	20:32084041	TGGTGGACCACTACA[A/G]GAGTGAGTCCCACCC	3055
rs776039655	snp	C/G	1.66921e-05	0.00288891	intron-variant	HCK	GRCh38.p7	20:32099174	GGCTGCTACCAGGGC[C/G]CAGTCTGGCAATGGG	3055
rs776103404	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32064066	TGGAGTGCAATGGCG[C/G]AATCTCGGCTCACTG	3055
rs776260121	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32088439	TTGCAAACAAATATT[C/T]GTATTTAAATCTACT	3055
rs776270826	snp	A/G			upstream-variant-2KB	HCK	GRCh38.p7	20:32050699	AAAATAGTTAGCACT[A/G]TAGGCTAAAGAGAAG	3055
rs776278560	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32056866	TATAAACCACTGTAT[C/T]TTCTAACACCTGGCA	3055
rs776296661	in-del	-/ACTGCATGAGCTAGGATC			intron-variant	HCK	GRCh38.p7	20:32072497	AGCCCAGGAGTTCGA[-/ACTGCATGAGCTAGGATC]ACTGCATGAGCTATG	3055
rs776337933	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32062717	TCAGTAAAGGGAAGA[C/T]GTGAGAAGTCAGGAG	3055
rs776381696	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32075450	TCAAGTGATCTTCTC[A/G]CCTCAGCCTCCCAAA	3055
rs776412545	snp	A/G	1.71787e-05	0.00293071	missense	HCK	GRCh38.p7	20:32079802	GGCATCAGCCGGAAG[A/G]ACGCAGAGCGCCAAC	3055
rs776510508	in-del	-/GGAAAGAAAGAAAGAGAGAGAAAG			intron-variant	HCK	GRCh38.p7	20:32094764	GAAAGAAAGAAAGAA[-/GGAAAGAAAGAAAGAGAGAGAAAG]AGAAAGAAAGAAAGA	3055
rs776537763	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32088498	AGTACTAGATTGGTG[A/C]AAAAGTAATTGTGGT	3055
rs776554447	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32062964	CCCTGGGCCCCCAGC[G/T]GTCTGCCTTCTTGAG	3055
rs776580530	in-del	-/A			intron-variant	HCK	GRCh38.p7	20:32094761	AAGAAAGAAAGAAAG[-/A]AAGGAAAGAAAGAAA	3055
rs776632454	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32082510	AGCCGGGCGTAGTGG[C/T]GGGCGTCTGTAATCC	3055
rs776669153	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32081277	TCAGGTGACCAGCTT[C/T]CTGGAATTTCTGTGC	3055
rs776683669	snp	C/T	1.64846e-05	0.0028709	utr-variant-3-prime	HCK	GRCh38.p7	20:32101540	AGGACCAGGGCAGGG[C/T]CAGGGGGTGCCCAGG	3055
rs776701171	snp	G/T	2.20924e-05	0.00332351	intron-variant	HCK	GRCh38.p7	20:32079916	GTCCTCCCTGCCGAG[G/T]TGCCCCAGCTGGGGC	3055
rs776706589	in-del	-/GG			intron-variant	HCK	GRCh38.p7	20:32052805	GCGGGGATTTTTTTT[-/GG]TTAATTTAAAAAAGA	3055
rs776733202	in-del	-/A			intron-variant	HCK	GRCh38.p7	20:32094708	AGAAAAGAAAAGAAA[-/A]GAAAGAAAGAAAGAA	3055
rs776821504	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32055953	CTAGCTTCTTCCACT[G/T]AACATAATGTTTTCC	3055
rs776892739	snp	A/G	1.64773e-05	0.00287026	missense	HCK	GRCh38.p7	20:32083930	GAGACTACGACCCTC[A/G]GCAGGGAGATACCGT	3055
rs776922531	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32055541	TTTCCAGGTCATTAA[A/G]ATGTTCTTAAATTTT	3055
rs776931907	snp	G/T			downstream-variant-500B	HCK	GRCh38.p7	20:32101933	TCAGAAATGGTGAAG[G/T]ACTCTCCCGGGGACC	3055
rs776964661	snp	C/T	3.31312e-05	0.00406995	synonymous-codon	HCK	GRCh38.p7	20:32084440	GCCCTGCATGTCTTC[C/T]AAGCCCCAGAAGCCT	3055
rs776971672	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32087192	AAGCCCTGGGAGAGG[A/G]AGCTGGCAAAGCAGC	3055
rs777036034	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32057831	CACCCCATTTCTCCA[A/G]TTTCCTCCCCCACAG	3055
rs777054556	snp	A/C	1.7e-05	0.00291543	intron-variant	HCK	GRCh38.p7	20:32084573	CCACAGCCCACAGGG[A/C]CAGAGGGTGGAGGGG	3055
rs777067785	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32093089	AGATGGGATTACAGG[C/T]GTGCACCACCATGCT	3055
rs777100029	in-del	-/T	1.65418e-05	0.00287587	intron-variant	HCK	GRCh38.p7	20:32073281	GGTCCCCACACATTG[-/T]GTCAGATTCATTCTC	3055
rs777188396	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32080268	CAGTGGTGCGATCTC[A/G]GCTCACTGCAACCTC	3055
rs777190424	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32094096	TACTTGTGAGAGCGA[C/T]TGGTAAAATGCAAGG	3055
rs777232752	snp	A/G	9.08802e-05	0.00674031	missense	HCK	GRCh38.p7	20:32073793	CTCAGCTTCCAGAAG[A/G]GGGACCAGATGGTGG	3055
rs777237655	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32096280	AAGGCAGGCGGATCA[C/T]AAGGTCAGGAGTTTG	3055
rs777245931	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32089382	TGTGGAAACTGAGCC[C/G]CAGTGTGGTTAAGTG	3055
rs777358849	snp	G/T	9.55155e-05	0.00691004	intron-variant	HCK	GRCh38.p7	20:32084347	AGCAACCTCTGGCTG[G/T]CTCGGTGCTTGTTGC	3055
rs777379623	in-del	-/G			intron-variant	HCK	GRCh38.p7	20:32057047	TTTAAACTCAGGAGA[-/G]CTCACATAATCTGGA	3055
rs777381549	in-del	-/TA	1.64977e-05	0.00287203	intron-variant	HCK	GRCh38.p7	20:32088654	GCCCAGGTGAGAGCC[-/TA]ACGAGGAAACGGGGA	3055
rs777491659	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32063806	CTCAAAACTGGCTCA[A/G]GCAGAAGAAGGAGGT	3055
rs777545892	snp	C/T	3.6505e-05	0.00427214	intron-variant	HCK	GRCh38.p7	20:32093812	TTTTGGGTGGGGCCA[C/T]CTTGGCGTAGGCCAG	3055
rs777575698	in-del	-/TTTC			intron-variant	HCK	GRCh38.p7	20:32074984	AGCAAAACGACCTGG[-/TTTC]TTTGGTTGGTTACAC	3055
rs777578874	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32073467	AGTCAAACCCCTGTC[A/G]AGAATCCCCAAAATT	3055
rs777728818	snp	A/G	1.69398e-05	0.00291026	intron-variant	HCK	GRCh38.p7	20:32071812	TCCCAGTTTCCCTGG[A/G]GGCTGACGGATGCTG	3055
rs777757009	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32062187	TCAGGTGATCTGCCC[A/G]CTTCAGCCTCCCAAA	3055
rs777860896	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32080952	AAATTAGCCAAGCAT[A/G]GTGGTGCACATCTGT	3055
rs777874382	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32056663	TTTATATTTTATTAG[C/T]ATTATTATTACCATT	3055
rs777924357	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32093755	AAGGGAGGGCTGGTG[C/T]AGACATTTCGCATTT	3055
rs777975741	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32095212	AAAGCCAACATGAAG[A/C]CCACATGTTGTATAA	3055
rs777999649	snp	A/C	1.64827e-05	0.00287073	missense	HCK	GRCh38.p7	20:32093928	CCTCCGAGCTGCCAA[A/C]ATCTTGGTCTCTGCA	3055
rs778010407	snp	G/T	5.26524e-05	0.00513063	missense	HCK	GRCh38.p7	20:32086773	GGTGGTCACCAAGGA[G/T]CCCATCTACATCATC	3055
rs778012775	snp	C/T	1.64904e-05	0.00287139	missense	HCK	GRCh38.p7	20:32083903	ATTCAGGAAGCTACT[C/T]TTTGTCCGTGCGAGA	3055
rs778030654	snp	G/T	2.13993e-05	0.00327096	utr-variant-3-prime	HCK	GRCh38.p7	20:32101523	CAGCAGCCATGATAG[G/T]GAGGACCAGGGCAGG	3055
rs778188795	snp	C/T	0.000162615	0.0090156	intron-variant	HCK	GRCh38.p7	20:32054317	GGATTGTTTTGTGTG[C/T]TTTAAAAATGCTATC	3055
rs778261953	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32082199	ATAAAACCCTTACCC[C/T]ATGAGGTTATTCATT	3055
rs778281134	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32055104	GTAGCTTTCGGCCCA[G/T]GTACAGGTGGTTCTT	3055
rs778386238	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32086422	GTTAAGCCACTTGCC[A/C]TAGTGTGCACAGCTG	3055
rs778408622	snp	A/C	1.71158e-05	0.00292534	missense	HCK	GRCh38.p7	20:32086681	ATGAAGCCAGGGAGC[A/C]TGTCGGTGGAGGCCT	3055
rs778424995	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32057175	CCTGGGGGCTACACC[C/T]GGGCTGTCCAGCTTG	3055
rs778437586	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32073626	CACATATCGATGGGT[A/G]CGGAGCTGTTCCAGG	3055
rs778470257	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32073241	AAGATGCTCTTGGGT[A/G]TCCTTCTCAACACAG	3055
rs778487476	snp	A/G	4.97451e-05	0.00498699	intron-variant	HCK	GRCh38.p7	20:32098990	CCCCGACTCTGCTCT[A/G]TTCAACCCTGCAGGG	3055
rs778488179	snp	A/G	6.60273e-05	0.00574537	missense	HCK	GRCh38.p7	20:32099117	GAGATCGTCACCTAC[A/G]GCCGGATCCCTTACC	3055
rs778562208	in-del	-/A	0.000324675	0.012737	intron-variant, utr-variant-5-prime	HCK	GRCh38.p7	20:32069694	TTCCAAAAGACAAAC[-/A]AAGCAAAACCGCTCA	3055
rs778570551	snp	C/T	1.65575e-05	0.00287724	missense	HCK	GRCh38.p7	20:32084017	GCACCTTCAGCACTC[C/T]GCAGGAGCTGGTGGA	3055
rs778637119	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32075127	GTTGAATGAAGCACA[C/T]GGTCTTGCCAAGGAG	3055
rs778667680	in-del	-/AA			intron-variant	HCK	GRCh38.p7	20:32100861	AACAAAATAACAGAC[-/AA]AGAGTAACTGAAATA	3055
rs778749451	snp	C/T					GRCh38.p7	20:32096210	ATTTTTTTAAAGAGA[C/T]GGGTGCGGCCGGGCA	3055
rs778749743	snp	A/G					GRCh38.p7	20:32099846	TACAGCCTATTCTCC[A/G]CTTGCAGCCAGAAGG	3055
rs778833919	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32079335	AGAAGGATCTTCCCC[A/G]TGGTCTTGTATGCTT	3055
rs778936221	in-del	-/ATTAA	1.68516e-05	0.00290268	intron-variant	HCK	GRCh38.p7	20:32088521	ATTGTGGTTTTTGCC[-/ATTAA]ATAGTAAAAGTAGTA	3055
rs778946589	snp	C/T	1.69738e-05	0.00291317	intron-variant	HCK	GRCh38.p7	20:32084080	ACATCCCCACCACGA[C/T]GGGCCCACAGACTCC	3055
rs779000296	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32060565	AGCTATTGTTTAGAC[A/G]GGAAATCTGGGGGCA	3055
rs779034005	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32072807	GGTACATCCAAGACC[A/G]AAGGCCGAGGTCACA	3055
rs779034625	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32064286	GGCATGAGCCACCGC[A/G]CCCATCCACCCATCT	3055
rs779036282	snp	C/T	1.84174e-05	0.00303453	synonymous-codon	HCK	GRCh38.p7	20:32084398	TGTTCCAGAGGGGAA[C/T]GACGGGCTCTGCCAG	3055
rs779059256	snp	A/G	1.64806e-05	0.00287054	synonymous-codon	HCK	GRCh38.p7	20:32088599	TCTGAAAAGTGATGA[A/G]GGCAGCAAGCAGCCA	3055
rs779067912	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32092572	CTTTAAATGTACATC[A/T]GAACATGTCACGCTC	3055
rs779095106	in-del	-/GTGTGTGTGT			intron-variant	HCK	GRCh38.p7	20:32093492	TATCCTAGGGTTCGT[-/GTGTGTGTGT]GTGTGTGTGTGTGTG	3055
rs779140311	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32065235	CAAATTTTAGTGTAT[A/G]TACTAATTTCCTGTA	3055
rs779172321	snp	C/T	4.97715e-05	0.00498831	intron-variant	HCK	GRCh38.p7	20:32088689	GAAACAGGAATTCGA[C/T]TTTTTTACTTGCCAA	3055
rs779229097	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32087927	AATTACAGGCGTGAG[C/G]AACTGCGCCCAGCTT	3055
rs779235798	snp	A/G	0.000346275	0.0131536	missense	HCK	GRCh38.p7	20:32071696	AAGTTCCTCCAGGTC[A/G]GAGGCAATACATTCT	3055
rs779244165	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32084620	CTTCCAGGAACACCT[C/T]ATGGCAAAGCGGGAA	3055
rs779420656	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32067803	ACAGATGGAGTCATA[A/G]CTGAGATGTGCTCTA	3055
rs779481676	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32085375	AACAATTAGCCAGGC[A/G]TGGTGGTGGGAGCCT	3055
rs779482916	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32078160	CTGCCTCAGCCTCCC[A/G]AGTAGCTGGGACTAC	3055
rs779515819	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32099666	CCTGGCCTCACCCCT[A/G]TGACATCTGAGCAGT	3055
rs779524680	snp	C/T	2.05295e-05	0.0032038	missense	HCK	GRCh38.p7	20:32086646	CCTACAACAAGCACA[C/T]CAAGGTGGCAGTGAA	3055
rs779613959	in-del	-/AGAAAGAAAGAA			intron-variant	HCK	GRCh38.p7	20:32094788	GAAAGAGAGAGAAAG[-/AGAAAGAAAGAA]AGAAAGAAAGAAAGA	3055
rs779696834	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32101201	TCACAGTGGAAGGGG[C/T]TCAGCTTGCAAGGTG	3055
rs779718524	snp	C/T	9.92113e-05	0.00704243	synonymous-codon	HCK	GRCh38.p7	20:32093997	GGTCATTGAGGACAA[C/T]GAGTACACGGCTCGG	3055
rs779780341	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32054117	CATTTTGTTGTGTTT[C/G]TTTTGAGATTTTAAA	3055
rs779822485	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32060428	GTTTCACCATGTTGG[C/T]CAGGCTTGTCTCAAA	3055
rs779823172	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32086529	TGAGATGAGCAGGAA[A/G]GACTTTCTGGAGGAG	3055
rs779862834	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32079258	TCAACTCCATATATG[C/T]GGAGGAGGATTGGTT	3055
rs779972147	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32093568	CTGGAAGAATAGGTC[C/T]TGGAGAAATAGTCCC	3055
rs780059808	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32069117	CCAGTAAACAGAAAT[A/T]GTTGTGGTTAATGTT	3055
rs780157389	snp	A/G			missense	HCK	GRCh38.p7	20:32084403	CAGAGGGGAACGACG[A/G]GCTCTGCCAGAAACT	3055
rs780211762	snp	C/T	1.64866e-05	0.00287106	synonymous-codon	HCK	GRCh38.p7	20:32071728	AAAAACTGAAACCAG[C/T]GCCAGCCCACACTGT	3055
rs780272384	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32058037	GTTCCAGGCATCACC[C/T]TGAAATCCTTTGGCC	3055
rs780365765	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32095792	TGTTAAAGAAAGAAA[C/G]AGGCAAAATTTATTT	3055
rs780392818	snp	C/T	1.80013e-05	0.00300006	intron-variant	HCK	GRCh38.p7	20:32086811	TCATGGCCAAAGGTG[C/T]TGCGTGCTGGGGCTG	3055
rs780405467	snp	C/T	1.65644e-05	0.00287783	missense	HCK	GRCh38.p7	20:32101361	CTGGAGCGTGGATAC[C/T]GGATGCCTCGCCCAG	3055
rs780553654	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32077378	AGAAGCAACCAGTTT[C/T]TCGTGAGTCCTCCCA	3055
rs780610816	in-del	-/G			intron-variant	HCK	GRCh38.p7	20:32064925	GGGATCAGCAGTTTT[-/G]AGTGGGTGTGCAACC	3055
rs780660187	snp	A/C	1.70755e-05	0.00292189	synonymous-codon	HCK	GRCh38.p7	20:32079831	ACTGCTGGCTCCCGG[A/C]AACATGCTGGGCTCC	3055
rs780674488	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32097985	AGTTTTGAGAACAGG[C/T]TGGGTAACATAATAA	3055
rs780741453	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32101147	GGTCCCAGGCCCATG[G/T]CCTAGCTGCAAGTGA	3055
rs780777361	snp	A/C	1.70915e-05	0.00292326	missense	HCK	GRCh38.p7	20:32101453	GCGGCCGACCTTCGA[A/C]TACATCCAGAGTGTG	3055
rs780785338	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32065538	TCTGGTGGCTTCACT[C/T]TAAAGCAGCTTTTAC	3055
rs780838582	snp	G/T			intron-variant	HCK	GRCh38.p7	20:32067688	TAAGCACTGAGGAAC[G/T]CAGGTGTGAGCACCA	3055
rs780858491	snp	A/C			intron-variant	HCK	GRCh38.p7	20:32079168	GAATGAAGAAAATGT[A/C]CCAGGATATAATCCT	3055
rs780859955	snp	A/G	1.648e-05	0.0028705	missense	HCK	GRCh38.p7	20:32083915	ACTCTTTGTCCGTGC[A/G]AGACTACGACCCTCG	3055
rs780861004	snp	C/T	1.65026e-05	0.00287246	synonymous-codon	HCK	GRCh38.p7	20:32084498	CGGGAATCCCTCAAG[C/T]TGGAGAAGAAACTTG	3055
rs780964979	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32099870	CAGAAGGATAATTCT[A/G]AACTTTAAATCAGAT	3055
rs780997096	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32090902	CTCTGAGTGCCACTT[A/T]CCCCCACTGGGAGCA	3055
rs781030111	snp	C/T	8.46848e-05	0.00650655	intron-variant	HCK	GRCh38.p7	20:32071612	ATCAGAAGACTTCCC[C/T]GCATGAGGCTCTTGG	3055
rs781056918	snp	A/G	1.68221e-05	0.00290014	intron-variant	HCK	GRCh38.p7	20:32098953	ACCTTAGCAGAGCCA[A/G]CCCTCACTACTCCCC	3055
rs781062471	snp	A/G	3.2956e-05	0.00405918	missense	HCK	GRCh38.p7	20:32093950	GTCTCTGCATCCCTG[A/G]TGTGTAAGATTGCTG	3055
rs781081441	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32057944	TTGGCCCCGGCTGTG[A/G]TCCCACATGCTGCAT	3055
rs781193250	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32091176	TGTCATCCCTGCCCC[A/G]TCGAGCTCCTGTGAA	3055
rs781217155	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32095541	GGATTACAGGTGTGA[A/G]CCACCATGCCCGGCC	3055
rs781275682	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32070572	GCAGGTTCTGTATCC[C/T]TTTCTCTGACAGGCC	3055
rs781342888	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32083227	GGGGCTACCTGGATC[A/T]TCTGGAATAATCTCC	3055
rs781342975	snp	C/G			intron-variant	HCK	GRCh38.p7	20:32097624	AATGTAATGACTAAA[C/G]GAATAAAAGTAGAAT	3055
rs781359812	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32087215	AAAGCAGCAGTTCTG[C/T]CCCCACCCCCGCCCT	3055
rs781386576	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32087888	ACCTTGTGATCCGCC[C/T]GCCTCAGCCTCCCAC	3055
rs781413220	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32093765	TGGTGCAGACATTTC[A/G]CATTTTCTTCACTTG	3055
rs781421982	snp	A/G	3.38949e-05	0.00411659	missense	HCK	GRCh38.p7	20:32086687	CCAGGGAGCATGTCG[A/G]TGGAGGCCTTCCTGG	3055
rs781437224	snp	A/G	0.000131744	0.00811508	intron-variant, utr-variant-5-prime	HCK	GRCh38.p7	20:32069705	AAACAAAGCAAAACC[A/G]CTCAAGTCTTGAGGT	3055
rs781528952	in-del	-/C	1.67795e-05	0.00289646	intron-variant	HCK	GRCh38.p7	20:32098965	CCAACCCTCACTACT[-/C]CCCAGCCTTCCCCGA	3055
rs781674698	snp	A/T			intron-variant	HCK	GRCh38.p7	20:32073996	ACCTGGATGAAGGGG[A/T]TTGTGCACTTACTGA	3055
rs781676406	snp	A/C	1.64936e-05	0.00287168	missense	HCK	GRCh38.p7	20:32074721	CTCTGGAGACAGAGG[A/C]GTAAGTATCCTATTT	3055
rs781743797	snp	A/G	1.78245e-05	0.00298529	synonymous-codon	HCK	GRCh38.p7	20:32086791	CATCTACATCATCAC[A/G]GAGTTCATGGCCAAA	3055
rs781773764	snp	C/T	1.64768e-05	0.00287021	missense	HCK	GRCh38.p7	20:32074649	GGTGGAAGGCTCGAT[C/T]CCTGGCCACCCGGAA	3055
rs796506384	snp	C/T			intron-variant	HCK	GRCh38.p7	20:32061052	GCAGTGGCGCAGTCT[C/T]GGCTCACTGCAACCT	3055
rs796748700	snp	A/G			intron-variant	HCK	GRCh38.p7	20:32071240	ACCTGAGAGGTGGGT[A/G]GGGGCAGGAAAGTGG	3055

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