chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2859436428594365GC19GENIChomozygous108249213
X2859440428594405GC17GENIChomozygous108249215
X2859578728595788TG20GENIChomozygous108249217
X2859898328598984AG4GENICheterozygous119912691
X2859945928599460TG15GENIChomozygous119912692
X2859969228599693CT11GENIChomozygous108377955
X2859979928599800CA17GENIChomozygous108682712
X2859987628599877CA11GENIChomozygous119912694
X2860000128600002CA9GENIChomozygous119912695
X2860001428600015CA8GENIChomozygous119912697
X2860027228600273CA11GENIChomozygous108608145
X2860205828602059GA17GENIChomozygous108249219
X2860326628603267CG14GENIChomozygous119912698
X2860343528603436GT26GENIChomozygous108249221
X2860560328605604TA11GENIChomozygous119912700
X2860563628605637CA5GENIChomozygous119912701
X2860574228605743CT5GENIChomozygous119912702
X2860576728605768CA10GENIChomozygous108441615
X2860645928606460CG21GENICpossibly homozygous108249223
X2860871328608714TC27GENIChomozygous108249225
X2861133728611338GA18GENIChomozygous119912704
X2861369128613692GT11GENIChomozygous108249227
X2861421228614213CA11GENIChomozygous108249229
X2861473828614739AG11GENIChomozygous108249231
X2861510228615103AG12GENIChomozygous108249233
X2861515728615158TC18GENIChomozygous108249235
X2861558628615587CT12GENIChomozygous108249243
X2861522928615230TC17GENIChomozygous108595689
X2861523028615231AG17GENIChomozygous108671873
X2861668328616684GA2GENIChomozygous108682714
X2861681728616818AG18GENIChomozygous108249249