chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
123790478937904790TG52GENIChomozygous115321958
123790479037904791AG53GENICpossibly homozygous115321960
123790483937904840TC44GENIChomozygous115321962
123790518837905189AG45GENIChomozygous115321964
123790547837905479TC54GENIChomozygous115321966
123790572937905730TC66GENICpossibly homozygous115321968
123790580437905805GA72GENIChomozygous115321970