chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
74794279247942793CT32GENIChomozygous54379520
74794300447943005CT22GENIChomozygous54379522
74794335547943356A-15GENIChomozygous54898034
74794357847943579TA16GENICpossibly homozygous54379528
74794362247943623TG18GENIChomozygous54898036
74794687347946874AG23GENIChomozygous53911316
74794712047947121AG17GENICpossibly homozygous53911317
74794732847947329GT7GENICpossibly homozygous53911318
74794770647947707TTTGTC20GENIChomozygous53911320
74794858847948589GA18GENIChomozygous53911322
74794876547948766GGTA7GENIChomozygous55859443