chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1265887865265887866CT12GENIChomozygous108637433
1265889955265889956CG30GENIChomozygous108637436
1265890847265890848CT15GENIChomozygous108637437
1265891099265891100TC16GENIChomozygous109218285
1265890363265890364A20GENIChomozygous127508969
1265889820265889820ATGTATCCATGTATCT15GENIChomozygous127508968
1265889219265889219C20GENIChomozygous127508966
1265889539265889540A20GENICpossibly homozygous127508967
1265891092265891092CCAC15GENIChomozygous127508970
1265891407265891408GT13GENIChomozygous108637438
1265891496265891504AGAAAGAG16GENIChomozygous127508971