chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106562177865621779CT30GENICpossibly homozygous116793111
106562372065623721TG29GENIChomozygous116793113
106562938265629383GT20GENIChomozygous116793115
106563017865630179TC43GENIChomozygous116619052
106563107165631072AG34GENIChomozygous116793117