chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
28330672983306730GT14GENIChomozygous136174862
28330789383307894CT12GENIChomozygous136174863
28330794083307941AG18GENIChomozygous136174864
28330832783308328GA13GENIChomozygous136174865
28330842383308424CG21GENIChomozygous136174866
28330853483308534ATAGGACTCTTTCAAAA27GENIChomozygous135921070
28330863383308634AT24GENICpossibly homozygous136174867
28330901883309019TC20GENIChomozygous136174868
28330908783309088AC19GENIChomozygous136174869
28330915883309159AG19GENIChomozygous136174870
28330965883309659GC14GENIChomozygous136174871