chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5136760251136760252CA28GENIChomozygous114020708
5136760270136760271TC23GENIChomozygous114020709
5136760512136760513GC27GENIChomozygous114020711
5136761130136761131CT23GENIChomozygous114020713
5136761915136761916TC31GENIChomozygous114020715
5136762034136762035GA26GENIChomozygous114020717
5136762081136762082G26GENIChomozygous134206133
5136762178136762179GT22GENIChomozygous114020719
5136762353136762354CT31GENIChomozygous114020721
5136762890136762891CT29GENIChomozygous114443327
5136762975136762976TC26GENIChomozygous114020723
5136763371136763372GC28GENIChomozygous114020725
5136763429136763430GT26GENICpossibly homozygous114020727
5136764472136764473GA32GENIChomozygous114020729
5136764520136764521CT32GENIChomozygous114443329