chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2551615525516156CT15GENIChomozygous62926710
X2553636825536369AT18GENIChomozygous63032800
X2552084125520842TG20GENIChomozygous63032797
X2553550325535504TC13GENIChomozygous63032799
X2553708925537090GA18GENICpossibly homozygous63032801
X2553846225538463TA24GENIChomozygous63032803
X2553911125539112TC7GENIChomozygous62926727
X2553917925539180TC15GENIChomozygous62926728
X2553964325539644GA23GENIChomozygous63032804
X2553998325539984AG9GENICheterozygous62926730
X2554060925540610GA20GENIChomozygous63032805
X2554251025542511TC8GENIChomozygous62926732
X2554255725542558CT4GENIChomozygous63032806
X2554261525542616CG26GENIChomozygous63032807
X2554284125542842GT21GENIChomozygous62926733
X2554352725543528GA20GENIChomozygous63032808
X2554421225544213TC20GENIChomozygous63032809
X2554430325544304TC15GENIChomozygous63032810
X2554447825544479AT12GENIChomozygous62926735
X2554470725544708AG15GENIChomozygous63032811
X2554482725544828CT12GENIChomozygous63032812
X2554637125546372TC23GENIChomozygous62926738
X2554674825546749CT15GENIChomozygous62926739
X2554708225547083TC20GENIChomozygous63145705