chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46760894767608948CA11GENICpossibly homozygous784854156
46761180167611802CT18GENIChomozygous784854157
46761335867613359GA22GENIChomozygous784854158
46761474867614749CT19GENIChomozygous784854159
46761505367615054GA27GENIChomozygous784854160
46761509067615091TC25GENIChomozygous784854161
46761538967615390CT23GENIChomozygous784854162
46761586667615867GA26GENICpossibly homozygous784854163