chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1019760410197605CT8GENIChomozygous108224077
X1019780710197808TC8GENIChomozygous108224079
X1019856710198568AG3GENIChomozygous108224081
X1020291910202920CT15GENIChomozygous108224083
X1020345210203453TC4GENIChomozygous108224085
X1020448110204482GA14GENIChomozygous108224087
X1020465010204651GA9GENIChomozygous108224089
X1020655510206556GT9GENIChomozygous108224091
X1020907510209076AG16GENIChomozygous108224093
X1020926710209268GA9GENIChomozygous108224095
X1020968110209682GA7GENIChomozygous108224097
X1020981110209812GA9GENIChomozygous108224099
X1021000110210002CT12GENIChomozygous108224101
X1021082810210829GA11GENIChomozygous108224103
X1021084410210845CG10GENIChomozygous108224105
X1021193410211935AT16GENIChomozygous108224107
X1021201410212015TA7GENIChomozygous108224109
X1021215110212152CT11GENIChomozygous108224112
X1021311610213117TC12GENIChomozygous108224114
X1021560910215610CT12GENIChomozygous108224116
X1021717610217177AG6GENIChomozygous108366665
X1021777110217772AG6GENIChomozygous108224118