chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10106837729106837730GT13GENICpossibly homozygous118012652
10106837742106837743GT12GENIChomozygous118012653
10106837755106837756GT12GENIChomozygous118012654
10106837853106837854GT11GENICpossibly homozygous116961714
10106837950106837951TC5GENIChomozygous118012655
10106837990106837991CA10GENIChomozygous117089129
10106838007106838008TA11GENIChomozygous118012656