chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1101205910101205911AC19GENIChomozygous108900029
1101205918101205919TC19GENICpossibly homozygous108900031
1101205985101205986TC15GENIChomozygous108900033
1101209497101209498GA21GENIChomozygous108900035