chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7117067534117067535CT38GENICpossibly homozygous116301969
7117067840117067841CT36GENIChomozygous115846207
7117069670117069671TA37GENIChomozygous115846209
7117070620117070621AC25GENICpossibly homozygous115846211