chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101492044914920450A10GENICpossibly homozygous403277084
101492044914920450AT10GENICheterozygous403277085
101492045114920452A10GENICpossibly homozygous403277086
101492045114920452AT10GENICheterozygous403277087
101492045914920460T10GENICpossibly homozygous403631781
101492045914920460TA10GENICheterozygous403631782
101493348814933489CT21GENIChomozygous138726759
101493257514932581ACACAG13GENIChomozygous138669266