chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
137025966370259664TC28GENIChomozygous959055917
137026731570267316CT32GENICpossibly homozygous959055918
137026814470268145GA22GENIChomozygous959055919
137026850270268503CA22GENIChomozygous959055920
137027185070271851TC18GENIChomozygous959055921
137027550870275509AT27GENIChomozygous959055922
137027600370276004GA22GENIChomozygous959055923
137027612970276130TC16GENIChomozygous959055924
137027954770279548TC19GENIChomozygous959055925
137028235070282351CG19GENIChomozygous959055926
137028476270284763CT31GENIChomozygous959055927
137029326670293267CT20GENIChomozygous959055928
137029651570296516CT17GENIChomozygous959055929
137030672170306722TC20GENIChomozygous959055930