chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
139184266691842667CT33GENICpossibly homozygous114577970
139184287391842874TC42GENIChomozygous114693448
139184412291844123GC42GENIChomozygous114577972
139184610591846106AG18GENIChomozygous114577974
139184703391847034GT31GENIChomozygous114577976
139184758591847586GA36GENIChomozygous114577978
139184795691847957CA41GENIChomozygous114577980
139184801891848019TA43GENIChomozygous114577982
139184820191848202TC35GENIChomozygous114577984
139184872591848726CT33GENIChomozygous114577986
139184879991848800AG25GENIChomozygous114577988
139185100191851002TC23GENIChomozygous114577990