chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
116671425266714253GA56GENICpossibly homozygous781684835
116671647966716480TC48GENIChomozygous781684836
116671668466716685GA69GENIChomozygous781684837
116671730866717309TA53GENICpossibly homozygous781684838
116671751166717512CG14GENIChomozygous781684839
116671755366717554CA32GENIChomozygous781684840
116671760366717604GC42GENIChomozygous781684841
116671771366717714GA45GENIChomozygous781684842
116671894366718944AG53GENIChomozygous781684843
116672098466720985TA37GENIChomozygous781684844
116672232466722325CT75GENIChomozygous781684845
116672350966723510TC54GENIChomozygous781684846
116672411266724113AC62GENIChomozygous781684847
116672422866724229TC70GENIChomozygous781684848
116672543466725435TC60GENIChomozygous781684849
116672636166726362TC59GENIChomozygous781684850
116672675466726755GC51GENIChomozygous781684851
116672734666727347AG48GENIChomozygous781684852
116672886966728870AC40GENICpossibly homozygous781684853
116672908866729089AT78GENICpossibly homozygous781684854
116672959066729591AT98GENICpossibly homozygous781684855
116672969766729698TC71GENIChomozygous781684856
116673084166730842GA40GENICpossibly homozygous781684857