chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101903966519039666AAGT10GENICpossibly homozygous52119038
101903993019039931AG17GENICpossibly homozygous51338177
101904020019040201CA12GENICheterozygous52119040
101904151619041517AG12GENICheterozygous51338186