chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
176946968869469689AG14GENIChomozygous878642073
176946971669469717GT5GENIChomozygous878642074
176947430569474306TC5GENIChomozygous878642076
176947444769474448TC22GENICpossibly homozygous878642077
176947612869476129TC9GENIChomozygous878642078
176947813969478140AG16GENIChomozygous878642079
176947815569478156AG18GENIChomozygous878642080
176947839969478400TC12GENIChomozygous878642081
176948118969481190TC4GENIChomozygous878427745
176948119069481191GA4GENIChomozygous878427744
176948145669481457GA7GENIChomozygous879184038
176948812469488125AC11GENIChomozygous878642082
176948884469488845CA10GENIChomozygous878642083
176948884869488849AT10GENIChomozygous878642084
176948967769489678AG14GENIChomozygous878642085
176949135269491353AG15GENIChomozygous878642086
176949388569493886TC11GENICheterozygous878642087
176949390669493907GA12GENICheterozygous878642088
176949559169495592CT21GENIChomozygous878642089