chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1019760410197605CT44GENIChomozygous108224077
X1019780710197808TC48GENIChomozygous108224079
X1019856710198568AG31GENIChomozygous108224081
X1020291910202920CT55GENIChomozygous108224083
X1020345210203453TC35GENIChomozygous108224085
X1020448110204482GA42GENIChomozygous108224087
X1020465010204651GA48GENIChomozygous108224089
X1020655510206556GT45GENIChomozygous108224091
X1020907510209076AG47GENIChomozygous108224093
X1020926710209268GA40GENIChomozygous108224095
X1020968110209682GA31GENIChomozygous108224097
X1020981110209812GA32GENIChomozygous108224099
X1021000110210002CT24GENIChomozygous108224101
X1021082810210829GA41GENIChomozygous108224103
X1021084410210845CG34GENICpossibly homozygous108224105
X1021193410211935AT36GENIChomozygous108224107
X1021201410212015TA51GENIChomozygous108224109
X1021215110212152CT36GENIChomozygous108224112
X1021311610213117TC48GENIChomozygous108224114
X1021560910215610CT41GENIChomozygous108224116
X1021717610217177AG35GENICheterozygous108366665
X1021777110217772AG63GENIChomozygous108224118
X1021506010215061AT9GENICpossibly homozygous108630591
X1021507410215075AT6GENIChomozygous119903036