chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5136759879136759880GA17GENIChomozygous114020704
5136760194136760195GT12GENIChomozygous114020706
5136760251136760252CA8GENIChomozygous114020708
5136761130136761131CT29GENIChomozygous114020713
5136762034136762035GA29GENIChomozygous114020717
5136762178136762179GT29GENIChomozygous114020719
5136762353136762354CT24GENIChomozygous114020721
5136762975136762976TC8GENIChomozygous114020723
5136763371136763372GC15GENIChomozygous114020725
5136763429136763430GT20GENICpossibly homozygous114020727
5136764472136764473GA28GENIChomozygous114020729