chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X2663930826639309CT16GENIChomozygous62928295
X2663932526639326GA15GENICpossibly homozygous62928296
X2663940726639408GA15GENICheterozygous62928298
X2664025826640259GA14GENIChomozygous62928299
X2664185926641860CA11GENIChomozygous62928300
X2664216726642168TC9GENIChomozygous62928301