chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123595908235959083GT59GENICpossibly homozygous139137129
123596236635962367AG79GENICpossibly homozygous142336644
123596398735963988AG58GENICpossibly homozygous139137130
123596486635964867AG91GENIChomozygous139137132
123596607635966077TA45GENIChomozygous139137133
123596681435966815GA64GENIChomozygous139137134
123596764135967642G19GENIChomozygous144914711
123596766635967667TG11GENICheterozygous154738055
123596766635967667T11GENICheterozygous403325989