chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2551615525516156CT8GENIChomozygous62926710
X2553550325535504TC9GENIChomozygous63032799
X2553636825536369AT11GENIChomozygous63032800
X2552025025520251CA6GENICheterozygous63145702
X2552183425521835TC6GENICheterozygous63145703
X2553740125537402AC9GENICheterozygous63032802
X2553765125537652AC8GENICpossibly homozygous62926725
X2553846225538463TA21GENICpossibly homozygous63032803
X2553911125539112TC8GENIChomozygous62926727
X2553917925539180TC14GENIChomozygous62926728
X2553964325539644GA14GENIChomozygous63032804
X2554060925540610GA15GENIChomozygous63032805
X2554237525542376AG3GENIChomozygous63145704
X2554251025542511TC6GENIChomozygous62926732
X2554255725542558CT6GENIChomozygous63032806
X2554261525542616CG8GENIChomozygous63032807
X2554284125542842GT7GENIChomozygous62926733
X2554352725543528GA11GENICpossibly homozygous63032808
X2554421225544213TC16GENIChomozygous63032809
X2554447825544479AT7GENIChomozygous62926735
X2554470725544708AG5GENIChomozygous63032811
X2554482725544828CT10GENIChomozygous63032812
X2554637125546372TC5GENIChomozygous62926738
X2554674825546749CT4GENIChomozygous62926739
X2554708225547083TC10GENIChomozygous63145705