chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
154110103741101038CT13GENICpossibly homozygous804824939
154110104241101043AC12GENIChomozygous804824940
154110104341101044AT11GENIChomozygous804824941
154110111741101118GC24GENIChomozygous804824942
154110119341101194GC22GENIChomozygous804824943
154110120441101205CG20GENIChomozygous804824944
154110283541102836TC45GENICheterozygous804824945
154110632641106327AG15GENICheterozygous804824946
154114954341149544GA53GENICheterozygous804824947
154117250441172505CT15GENIChomozygous804824948