chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1019760410197605CT23GENIChomozygous108224077
X1019780710197808TC36GENIChomozygous108224079
X1019856710198568AG28GENIChomozygous108224081
X1020291910202920CT23GENIChomozygous108224083
X1020345210203453TC23GENIChomozygous108224085
X1020448110204482GA16GENIChomozygous108224087
X1020465010204651GA25GENIChomozygous108224089
X1020655510206556GT28GENIChomozygous108224091
X1020907510209076AG24GENIChomozygous108224093
X1020926710209268GA28GENICpossibly homozygous108224095
X1020968110209682GA34GENIChomozygous108224097
X1020981110209812GA31GENIChomozygous108224099
X1021000110210002CT32GENIChomozygous108224101
X1021082810210829GA21GENIChomozygous108224103
X1021084410210845CG22GENIChomozygous108224105
X1021193410211935AT23GENIChomozygous108224107
X1021201410212015TA21GENIChomozygous108224109
X1021215110212152CT27GENIChomozygous108224112
X1021311610213117TC26GENIChomozygous108224114
X1021560910215610CT24GENIChomozygous108224116
X1021777110217772AG32GENIChomozygous108224118
X1021780910217809A32GENIChomozygous129719530
X1020017810200179T20GENIChomozygous129719527
X1021496310214965GT11GENIChomozygous129719528
X1021503010215032GT13GENIChomozygous129719529
X1020819110208205GTGTGTGTGTGTGC14GENICheterozygous132370129
X1021717610217177AG22GENIChomozygous108366665