chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97886334678863347AG34GENIChomozygous799552865
97886351778863518TC26GENIChomozygous799552866
97886936678869367AG33GENIChomozygous799552867
97887017378870174AG29GENIChomozygous799552868
97887169478871695TA31GENIChomozygous799552869
97887298178872982CG28GENIChomozygous799552870
97887557078875571TC18GENIChomozygous799552871
97887574478875745TA26GENIChomozygous799552872
97887575478875755GC14GENIChomozygous799552873
97887575978875760GA14GENIChomozygous799552874
97887576178875762CT14GENIChomozygous799552875
97887576678875767CA16GENIChomozygous799552876