chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8117680721117680722CT22GENIChomozygous950357435
8117681922117681923GA8GENIChomozygous950357436
8117682434117682435TC24GENIChomozygous950357437
8117682613117682614AT16GENIChomozygous950357438
8117684025117684026CT21GENIChomozygous950357439
8117684752117684753GA19GENIChomozygous950357440
8117685491117685492CT14GENIChomozygous950357441
8117686654117686655GA16GENIChomozygous950357442
8117686792117686793TC21GENICpossibly homozygous950357443
8117687057117687058TC16GENIChomozygous950357444
8117687957117687958TC14GENIChomozygous950357445
8117690138117690139AG12GENIChomozygous950357446