chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4159077448159077449TC11GENICpossibly homozygous57000490
4159077781159077782AG5GENIChomozygous57000491
4159077928159077929AG10GENIChomozygous57000492
4159078137159078138GA18GENIChomozygous57000493
4159078305159078306CCAAACA3GENIChomozygous57000494