chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8130482717130482718GT21GENICpossibly homozygous116725612
8130489015130489016CT12GENIChomozygous116725613
8130489149130489150AG18GENIChomozygous116725614
8130489393130489394TG22GENICheterozygous116725615
8130489394130489395AG19GENICheterozygous117930727
8130489458130489459AG9GENIChomozygous116725616
8130490264130490265GA20GENIChomozygous116725617