chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1584868315848684TC28GENIChomozygous45097676
X1584951315849514GA25GENIChomozygous45097677
X1585058515850586TTG16GENIChomozygous45097678
X1585137715851378T-24GENICpossibly homozygous45097679
X1585403615854037AG21GENIChomozygous45097681
X1585606215856063GGT14GENICpossibly homozygous45097682
X1585827515858278GTT---27GENIChomozygous45097684
X1585901615859019CCT---4GENICheterozygous45097687
X1586349015863491T-25GENICheterozygous45097688
X1586374715863748T-31GENIChomozygous45097689
X1586576415865765CA31GENIChomozygous45097690
X1586693815866939GGT24GENIChomozygous45097691
X1586708015867081GGTTTA14GENIChomozygous45097692
X1586847515868476A-20GENIChomozygous45097693
X1586848415868485T-21GENIChomozygous45097694
X1587086415870865TC46GENIChomozygous45097695
X1587141015871411GA13GENIChomozygous45097696
X1586348915863491TT--25GENICheterozygous45252119
X1585027315850287ACACACACACACAC--------------8GENIChomozygous45501250