chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5136760194136760195GT9GENIChomozygous114020706
5136760251136760252CA5GENIChomozygous114020708
5136760512136760513GC4GENIChomozygous114020711
5136761130136761131CT26GENIChomozygous114020713
5136761915136761916TC11GENIChomozygous114020715
5136762034136762035GA19GENIChomozygous114020717
5136762178136762179GT20GENIChomozygous114020719
5136762353136762354CT17GENIChomozygous114020721
5136762975136762976TC13GENIChomozygous114020723
5136763371136763372GC16GENIChomozygous114020725
5136763429136763430GT21GENICpossibly homozygous114020727
5136764472136764473GA17GENIChomozygous114020729