chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71177043311770434CT31GENIChomozygous790006627
71177196711771968TC18GENIChomozygous790006628
71177197011771971GA19GENICpossibly homozygous790006629
71177263311772634GA30GENIChomozygous790006630
71177348211773483GA23GENIChomozygous790006631
71177377311773774GA31GENIChomozygous790006632
71177412511774126AC38GENIChomozygous790006633
71177432011774321CT38GENIChomozygous790006634