chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X4256026042560261AG10GENIChomozygous108486720
X4258245442582455CT9GENIChomozygous108486774
X4258662142586622AG16GENIChomozygous108486778
X4259053042590531GA5GENIChomozygous120049590
X4258166242581663CT9GENIChomozygous108672152
X4258362642583627AG20GENIChomozygous108672153
X4259306642593067AG8GENICpossibly homozygous108672155
X4259341542593416GA9GENIChomozygous108672156
X4259422942594230AC10GENIChomozygous108672157
X4259707442597075GA20GENIChomozygous108486786
X4259721042597211CG10GENIChomozygous108672158
X4259734542597346CT8GENIChomozygous108672159
X4259887242598873CG11GENICpossibly homozygous108256997
X4259219842592199GT12GENIChomozygous108256991
X4259243042592431CA9GENIChomozygous119917552
X4259964742599648CA17GENIChomozygous120049591
X4260575642605757CA10GENIChomozygous108486788
X4260699342606994CA30GENICheterozygous119996051
X4260699742606998TC33GENICheterozygous119996053
X4261023742610238GA9GENIChomozygous108672162