chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5161024754161024755AG21GENIChomozygous55816867
5161024834161024835G-15GENICpossibly homozygous55816868
5161025139161025140GA13GENIChomozygous55816869
5161025148161025149C-11GENIChomozygous55816870
5161025784161025785GA23GENIChomozygous55816871
5161026345161026346CT19GENICpossibly homozygous55816874
5161026388161026389AC12GENICpossibly homozygous55816875
5161026563161026564CCCACTTT6GENIChomozygous55816876
5161026610161026611GA9GENIChomozygous55816877