chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
185703818857038188CACACTGC25GENICpossibly homozygous129541358
185703822357038224CT22GENICpossibly homozygous110544299
185703928357039283AG25GENIChomozygous129541359
185703987457039875GA23GENIChomozygous110363599
185704044257040443AG18GENIChomozygous110363601
185704211357042114AG6GENIChomozygous110363603
185704242157042422TC24GENIChomozygous110544301
185704323957043240GA20GENIChomozygous110544307
185704272357042724CT17GENIChomozygous110544303
185704318057043181CT15GENIChomozygous110544305
185704318957043190TA15GENIChomozygous110363611
185704324857043249TA21GENIChomozygous110544309
185704331257043312C21GENIChomozygous129541360
185704331757043318CT22GENIChomozygous110544311
185704333557043336CT24GENIChomozygous110544313
185704337257043373AT20GENIChomozygous110363616
185704488057044881TA20GENIChomozygous110544315
185704816457048165AG9GENIChomozygous110363636
185704342657043427TA17GENIChomozygous110813814
185704695357046955AG15GENICpossibly homozygous131206499
185704775257047753GA7GENIChomozygous110363630
185704778157047782TC8GENIChomozygous110363632
185704859557048596AG16GENIChomozygous110363638
185704934457049345TC21GENIChomozygous110544317
185704941257049412A21GENIChomozygous129541364
185704949057049491CT23GENIChomozygous110363640
185705004857050049GC14GENIChomozygous110544319