chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101406023214060233GA25GENIChomozygous51622683
101406069314060694TG10GENICheterozygous51622684
101406205414062055GT12GENICheterozygous51622687
101406218914062190CT21GENIChomozygous51622688
101406239014062391AG17GENICpossibly homozygous51622689
101406257014062571AG10GENICheterozygous51622690
101406342814063429C-12GENIChomozygous51622691