chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
87174989971749900GA18GENIChomozygous118149845
87175563171755632C14GENICheterozygous132993769
87176333571763335AAG14GENIChomozygous132993776
87177142871771429CT23GENIChomozygous117965833
87177683771776838AG14GENIChomozygous117965841
87176135171761351A16GENICpossibly homozygous130769677
87176480171764802T12GENIChomozygous130769678
87176811171768111T22GENICheterozygous135191928
87176811271768112T17GENICpossibly homozygous135191929
87177695971776959TATG10GENICheterozygous135191930
87177580171775802A14GENICheterozygous132122734
87177743471777435CT13GENIChomozygous118149849
87177906771779068A20GENIChomozygous132993783
87178452171784522TG21GENIChomozygous118149851
87177928571779286TG21GENIChomozygous118176660