chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122149796621497967TA22GENICpossibly homozygous143532262
122150398121503982AG28GENIChomozygous139109476
122150526221505263AG34GENIChomozygous139109479
122150903521509036GA29GENIChomozygous139109489
122151009421510095C17GENICpossibly homozygous139046737