chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
136976519269765193TC34GENIChomozygous973649674
136976519369765194GA34GENIChomozygous973649675
136976526269765263CT30GENIChomozygous973649676
136976647269766473CT19GENIChomozygous973649677
136976668969766690GT17GENIChomozygous973649678
136976905969769060GA25GENIChomozygous973649679
136976977769769778GT18GENIChomozygous973649680
136977149369771494AG18GENIChomozygous973649681
136977246169772462AT30GENICpossibly homozygous973649682
136977270069772701AG19GENIChomozygous973649683
136977413269774133CG22GENIChomozygous973649684
136977422769774228AG22GENIChomozygous973649685
136977440469774405TC24GENIChomozygous973649686
136978009569780096TG8GENIChomozygous973649687