chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
58258926182589262GC28GENICpossibly homozygous55505738
58258926382589264GC29GENICheterozygous55505740
58258960482589605GC35GENICpossibly homozygous55505742
58259181482591815CT22GENIChomozygous55505744
58259588182595882TG19GENICheterozygous55505746
58259949482599498TATC----18GENIChomozygous55505748
58260063282600633CT18GENIChomozygous55505750