chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122418434424184346TG--32GENIChomozygous50292679
122418466824184670TC--14GENICpossibly homozygous50132098
122418467124184672CCTG15GENICpossibly homozygous50292681
122418467324184674CG21GENICpossibly homozygous50132100
122418496824184970TG--18GENIChomozygous50292683
122418499524184999GTGC----18GENICheterozygous50132110
122418559324185594CT28GENIChomozygous50292685
122418563424185635CCAAAAAA15GENIChomozygous50132114
122418564924185650GA31GENICheterozygous50292687
122418647224186473CT45GENIChomozygous50292689