chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4115571005115571006AC17GENICpossibly homozygous112816034
4115606435115606436AT13GENIChomozygous112816082
4115606455115606456TC9GENIChomozygous112816084
4115606620115606621GT9GENIChomozygous112816086
4115606675115606676GT6GENIChomozygous112816088
4115665847115665848AT34GENICheterozygous112816176