chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
46760894767608948CA17GENICpossibly homozygous793579262
46761180167611802CT35GENIChomozygous793579263
46761335867613359GA34GENIChomozygous793579264
46761474867614749CT41GENICpossibly homozygous793579265
46761505367615054GA41GENICpossibly homozygous793579266
46761509067615091TC40GENIChomozygous793579267
46761538967615390CT32GENIChomozygous793579268
46761586667615867GA36GENIChomozygous793579269