chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X107494476107494477AG11GENIChomozygous108411951
X107494507107494508GC14GENIChomozygous108529392
X107494929107494930AG12GENIChomozygous108529394
X107495190107495191AG14GENIChomozygous108529396
X107496640107496641CG16GENIChomozygous108529398
X107497515107497516GA10GENICpossibly homozygous108411953
X107499098107499099CT11GENIChomozygous108529400
X107502793107502794CT11GENIChomozygous108411955
X107504845107504846TC12GENIChomozygous108529402
X107507332107507333AG19GENIChomozygous108529404
X107508463107508464TC18GENIChomozygous108411961
X107499994107499995CA7GENIChomozygous119945163