chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1115329995115329996CG29GENICpossibly homozygous60808801
1115330208115330209AG18GENICpossibly homozygous61746691
1115330509115330510CT20GENIChomozygous60808803
1115330611115330612CT15GENICpossibly homozygous60808804
1115330964115330965AG22GENIChomozygous60808805