chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122632268626322687AT20GENIChomozygous50147542
122632333726323338T-15GENIChomozygous50927733
122632397026323971TC18GENIChomozygous50147550
122632540326325404CG25GENIChomozygous50147554
122632562626325634TTTTTTTT--------11GENICheterozygous50614685
122632622526326226TC21GENIChomozygous50147558
122632641526326416AG25GENIChomozygous50147560
122632690526326906AC18GENIChomozygous50147562
122632730426327306GG--21GENIChomozygous50298891
122632859626328597GT22GENIChomozygous50147564
122632944026329441TC17GENIChomozygous50147566
122632963426329635AAT22GENICpossibly homozygous50298893
122632985626329857GA33GENIChomozygous50298895
122633237526332376GA13GENIChomozygous50298897
122633274426332745CT24GENIChomozygous50298899
122633331526333316GA13GENIChomozygous50298901
122633345326333454GA16GENIChomozygous50147572
122633416726334168TC12GENIChomozygous50147576
122633475026334757GACCTGT-------30GENIChomozygous50298903
122633482526334826CA25GENIChomozygous50147578
122633520626335218TGTGTGTGTGTG------------8GENIChomozygous50927736
122633601726336018TTACAC33GENIChomozygous50147580
122632553326325534CCT8GENICheterozygous50597929