chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1114046511140466TG15GENIChomozygous108225743
X1114053811140539CG24GENIChomozygous108225745
X1114127711141278GT17GENIChomozygous108225747
X1114128011141281GT17GENIChomozygous108225749
X1114144011141441TC12GENIChomozygous108225751
X1114213711142138TC15GENIChomozygous108225753
X1114328511143286GA20GENIChomozygous108225755
X1114485011144851CG11GENIChomozygous108225764
X1114441911144420GA16GENIChomozygous108225757
X1114472811144729CA14GENIChomozygous108225759
X1114477311144774TC12GENIChomozygous108225762
X1114506311145064GA15GENIChomozygous108225766
X1114514111145142GA10GENIChomozygous108225768
X1114535011145351CT9GENIChomozygous108225770
X1114569811145699TC11GENIChomozygous108225772
X1114602511146026CA10GENIChomozygous108225774
X1114684211146843GA22GENIChomozygous108225776
X1114750211147503CT21GENIChomozygous108225778
X1114769511147696CA12GENIChomozygous108225780
X1114783111147832CG8GENIChomozygous108225782
X1114849211148493CA16GENIChomozygous108225784
X1114968411149685CT15GENIChomozygous108225786
X1115033711150338AC6GENIChomozygous108225788
X1116218611162187TC24GENIChomozygous108225790
X1116354611163547AT17GENIChomozygous108225792
X1116369511163696GC23GENIChomozygous108225794
X1116400911164010TC7GENIChomozygous108225796
X1114641611146417CG10GENIChomozygous108671515
X1114702011147021GA3GENIChomozygous108630612
X1114702211147023TC3GENIChomozygous108630614