chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1019760410197605CT11GENIChomozygous108224077
X1019780710197808TC11GENIChomozygous108224079
X1019856710198568AG9GENIChomozygous108224081
X1020017810200179T5GENIChomozygous129719527
X1020291910202920CT5GENIChomozygous108224083
X1020345210203453TC7GENIChomozygous108224085
X1020448110204482GA7GENIChomozygous108224087
X1020465010204651GA8GENIChomozygous108224089
X1020655510206556GT9GENIChomozygous108224091
X1020907510209076AG13GENIChomozygous108224093
X1020926710209268GA7GENIChomozygous108224095
X1020968110209682GA13GENIChomozygous108224097
X1020981110209812GA6GENIChomozygous108224099
X1021000110210002CT5GENIChomozygous108224101
X1021082810210829GA7GENIChomozygous108224103
X1021084410210845CG6GENIChomozygous108224105
X1021193410211935AT7GENIChomozygous108224107
X1021201410212015TA5GENIChomozygous108224109
X1021215110212152CT11GENIChomozygous108224112
X1021311610213117TC15GENIChomozygous108224114
X1021496310214965GT7GENICpossibly homozygous129719528
X1021503010215032GT8GENIChomozygous129719529
X1021560910215610CT7GENIChomozygous108224116
X1021777110217772AG7GENIChomozygous108224118
X1021780910217809A5GENIChomozygous129719530
X1021717610217177AG9GENIChomozygous108366665