chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120889180120889181CT54GENICpossibly homozygous54085079
7120889437120889438GGTT21GENIChomozygous54085080
7120892043120892044CCAA39GENIChomozygous54085081
7120892056120892059AAC---36GENIChomozygous54085082
7120892430120892431CT45GENIChomozygous54085083
7120892769120892770GA56GENIChomozygous54085084
7120893276120893277GA38GENIChomozygous54085085
7120893284120893285CT40GENIChomozygous54085086
7120893574120893575GA40GENIChomozygous54085087
7120893824120893825CA49GENIChomozygous54085088
7120893886120893887TTC38GENIChomozygous54085089