chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
154110103741101038CT8GENIChomozygous795874267
154110111741101118GC13GENICpossibly homozygous795874268
154110119341101194GC18GENIChomozygous795874269
154110120441101205CG18GENICpossibly homozygous795874270
154110283541102836TC38GENICheterozygous795874271
154110289241102893TC34GENICheterozygous795874272
154110290141102902CG32GENICheterozygous795874273
154112372641123727GA41GENICheterozygous795874274
154114954341149544GA66GENICheterozygous795874275
154117250441172505CT25GENIChomozygous795874276