chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X4496484044964845CTTGA5GENIChomozygous134468807
X4496530744965308CG8GENIChomozygous108672640
X4496567044965670T11GENICpossibly homozygous132778917
X4496689544966896T7GENIChomozygous134468808
X4496942244969423TC15GENIChomozygous108489579
X4497315244973152T10GENIChomozygous134468809
X4497386444973864T8GENIChomozygous132778919
X4497482044974821CT12GENIChomozygous108489585
X4497583944975839A9GENIChomozygous134468810
X4497645344976454CT6GENIChomozygous108672642
X4497645744976458CT6GENIChomozygous108672643
X4497747844977479A7GENIChomozygous132778921
X4497936344979364AG10GENIChomozygous108489591
X4497941544979416CT16GENIChomozygous108672644
X4497973944979740CT8GENIChomozygous108489593
X4498261044982614AGAC14GENICpossibly homozygous132778922
X4498265644982658AC15GENIChomozygous134468811
X4498267444982676AC19GENIChomozygous134468812
X4498618844986188A6GENIChomozygous134468813
X4498266544982666GC16GENIChomozygous120050189
X4498179644981797AC8GENIChomozygous108489597