chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46185324561853246GA47GENIChomozygous112670633
46185326761853268TC49GENIChomozygous112670635
46185361361853614AC52GENICpossibly homozygous112670637
46185462361854624GA62GENIChomozygous112670639
46185486061854861AG60GENIChomozygous112670641
46185723861857239CT44GENIChomozygous112670643
46185748161857482CT38GENIChomozygous112670645
46185817061858171CG56GENIChomozygous112670647
46185894461858945CT53GENIChomozygous112670649
46185987461859875GA48GENIChomozygous112670651
46185756861857569T39GENIChomozygous128040364
46186020861860209T32GENICheterozygous128040365
46186021261860219TGTTGTG32GENICheterozygous128040366
46186106461861065CA49GENIChomozygous112670653
46186131661861317CA46GENIChomozygous112670655
46186235361862354TC48GENIChomozygous112670657
46186326961863270CT39GENIChomozygous112670659
46186353261863545GAAAAAAAGAAAA41GENICpossibly homozygous128040367
46186375761863758CG43GENIChomozygous112670661
46186409761864098TC53GENIChomozygous112670663
46186635261866353GA48GENIChomozygous112670666
46186675761866758CT56GENIChomozygous112670668
46186707461867075CT48GENIChomozygous112670670
46186740861867409G46GENIChomozygous128040368
46186747961867480TC27GENIChomozygous112670672
46187016561870251GTTTCTACCCATGGTCAGCTGGTTCACCTTTTCAGTTTTGTGGATGAAGCAGAATATCATTGTAAGAGCAGGAGATAGAAGAAGCT28GENIChomozygous128040369
46187057061870571CT44GENIChomozygous112670676
46187076361870764GA61GENIChomozygous112670678
46187094661870947CG42GENIChomozygous112670680
46187113061871131TA50GENIChomozygous112670682
46187636961876370AT42GENIChomozygous112670686
46187723261877233AG51GENIChomozygous112670688
46187739261877393AG52GENIChomozygous112670690
46187788761877888CT44GENIChomozygous112670692
46187826361878264AC46GENIChomozygous112670694
46187874361878744TA49GENIChomozygous112670696
46187081161870811C56GENIChomozygous128040370
46187969361879693G40GENIChomozygous128040371