chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191138972811389728ACGTACCAG12GENIChomozygous129584417
191138973311389733T16GENIChomozygous129584418
191138983511389836CG11GENIChomozygous109636570
191138984211389842G11GENIChomozygous129584419
191138991011389911A11GENIChomozygous129584420
191138992911389929T13GENIChomozygous129584421
191138993511389936TG14GENIChomozygous109636572
191138995411389955TG16GENIChomozygous109636574
191138995811389959C16GENIChomozygous129584422
191138999011389992TC20GENIChomozygous129584423
191139002911390029C24GENIChomozygous129584424
191139006211390063A23GENIChomozygous129584425
191139009911390099T22GENIChomozygous129584426
191139010711390107T23GENIChomozygous129584427
191139014811390148G18GENIChomozygous129584428
191139016511390166A19GENIChomozygous129584429
191139019211390192G14GENIChomozygous129584430
191139348111393482CT21GENICpossibly homozygous109764841
191139428911394290TC9GENIChomozygous119596655
191139803911398040AT9GENICheterozygous131221970
191141164611411647AG18GENIChomozygous109636578
191141269711412698CT23GENIChomozygous109636581
191141537611415377CG34GENIChomozygous109636583
191141539211415393CA32GENIChomozygous109636585
191141557611415577AG16GENIChomozygous109636587