chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1019760410197605CT23GENIChomozygous108224077
X1019780710197808TC28GENIChomozygous108224079
X1019856710198568AG41GENIChomozygous108224081
X1020291910202920CT19GENIChomozygous108224083
X1020345210203453TC23GENIChomozygous108224085
X1020448110204482GA31GENIChomozygous108224087
X1020465010204651GA29GENIChomozygous108224089
X1020655510206556GT18GENIChomozygous108224091
X1020907510209076AG15GENIChomozygous108224093
X1020926710209268GA24GENIChomozygous108224095
X1020968110209682GA27GENIChomozygous108224097
X1020981110209812GA22GENIChomozygous108224099
X1021000110210002CT35GENIChomozygous108224101
X1021082810210829GA20GENIChomozygous108224103
X1021084410210845CG18GENIChomozygous108224105
X1021193410211935AT20GENICpossibly homozygous108224107
X1021201410212015TA23GENIChomozygous108224109
X1021215110212152CT33GENIChomozygous108224112
X1021311610213117TC26GENIChomozygous108224114
X1021560910215610CT20GENIChomozygous108224116
X1021777110217772AG25GENIChomozygous108224118
X1020017810200179T36GENIChomozygous129719527
X1021496310214965GT18GENIChomozygous129719528
X1021503010215032GT15GENIChomozygous129719529
X1021780910217809A21GENIChomozygous129719530
X1021717610217177AG30GENIChomozygous108366665