chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
19064726190647262AG29GENIChomozygous516191758
19064868490648685AG32GENIChomozygous516191759
19064886290648863AT17GENICpossibly homozygous519172828
19064895090648951AG20GENIChomozygous516191760
19064937890649379CT18GENIChomozygous519172829
19064941190649412GC20GENIChomozygous519172830
19064948690649487GA21GENIChomozygous519172831
19064957690649577CT26GENIChomozygous519172832
19065228590652286CT30GENICpossibly homozygous519172833
19065250290652503GA15GENIChomozygous519172834
19065287190652872CT29GENIChomozygous519172835