chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77888887778888878GGTT11GENICheterozygous53986264
77893668778936688GGGT11GENICpossibly homozygous53986622
77894374878943749AAC35GENIChomozygous53986642
77894375478943755GC36GENIChomozygous54984467
77894374978943750AT35GENIChomozygous54984463
77894375278943753TG36GENIChomozygous54984465
77894375578943756TA38GENIChomozygous54984469
77894375978943760AC37GENIChomozygous54206132
77894376378943764A-40GENIChomozygous53986644