chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
191067440310674404CA22GENIChomozygous109634736
191067549110675492TC17GENIChomozygous109634738
191067576310675764GA17GENIChomozygous109634741
191067638610676387TG16GENIChomozygous109764632
191067651810676519TG15GENIChomozygous109634743
191067669010676691AG16GENIChomozygous109634745
191067778110677782CT24GENIChomozygous109634749
191067793410677935AG18GENIChomozygous109634751
191067834210678343GA5GENIChomozygous109634753
191067868910678690CT19GENIChomozygous109634755
191067953410679535CT23GENIChomozygous109634757
191068018410680185TC18GENIChomozygous109634759
191068071410680715AG12GENIChomozygous109634761
191068075010680751TC12GENIChomozygous109634763