chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101390722213907223CG50GENIChomozygous142218314
101390822613908227TC56GENICpossibly homozygous142218315
101390915313909153GCAGTTTATTGTGTGTGGGCACACGTAT41GENIChomozygous142196879
101390958713909588GA48GENIChomozygous142218316
101391016013910161AG70GENIChomozygous142218317
101391124413911245AG65GENIChomozygous142218318
101391197313911974TC48GENIChomozygous142218319
101391124413911245A65GENICheterozygous403276910