chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
173398112533981126CT17GENICpossibly homozygous140101818
173398136233981363TG25GENIChomozygous140101819
173398200733982008GA36GENIChomozygous140101820
173398218833982189GA35GENIChomozygous140101821