chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
97130654771306548TA19GENIChomozygous117718006
97130689971306900CA18GENIChomozygous117718008
97130748771307488AG13GENIChomozygous117718010
97130812371308124CA13GENIChomozygous117718012
97131076771310768CT11GENIChomozygous117718014
97131322371313224GA7GENIChomozygous117718016
97131346771313468GC4GENIChomozygous117718018