chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X114928688114928689GA18GENICpossibly homozygous671612147
X114933406114933407TC27GENICpossibly homozygous671612148
X114934944114934945AC5GENIChomozygous671612149
X114935731114935733TC--22GENIChomozygous769092783
X114935946114935947CT24GENIChomozygous671612150
X114937245114937246GC16GENICheterozygous671612151
X114937462114937463TC14GENIChomozygous671612152
X114937956114937957GA14GENIChomozygous671612153
X114938530114938531TG13GENICpossibly homozygous671612154
X114939476114939477GA15GENIChomozygous671612155
X114939824114939825AG11GENIChomozygous671612156
X114940907114940908AT6GENICheterozygous671612157
X114941746114941747CA14GENIChomozygous671612158
X114941989114941990CT16GENICpossibly homozygous671612159
X114943654114943655CT17GENICpossibly homozygous671612160
X114943983114943991AAAAAAAG--------2GENIChomozygous769092784
X114946807114946810AAG---4GENICheterozygous769092785