chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X4256026042560261AG15GENICpossibly homozygous108486720
X4256489242564893TG7GENICpossibly homozygous108705962
X4257483842574839AG17GENICpossibly homozygous108486758
X4257838242578383CT10GENIChomozygous108486768
X4256961542569616AG11GENIChomozygous108731825
X4258245442582455CT15GENICpossibly homozygous108486774
X4258289142582892AG19GENICheterozygous108705964
X4258662142586622AG16GENIChomozygous108486778
X4258819242588193CT11GENIChomozygous108705966
X4259053342590534TC10GENIChomozygous108705968
X4259306642593067AG9GENICpossibly homozygous108672155
X4259707442597075GA13GENIChomozygous108486786
X4259721042597211CG17GENIChomozygous108672158
X4259817642598177CA8GENIChomozygous108705970
X4259887242598873CG9GENIChomozygous108256997
X4259246542592466TG9GENIChomozygous108256993
X4259246742592468GA8GENIChomozygous108256995
X4260575642605757CA9GENICpossibly homozygous108486788