chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101306609713066098GT9GENIChomozygous116735578
101306640713066408TC18GENIChomozygous116735579
101306736313067364AG9GENIChomozygous116735580
101306759313067594GA28GENIChomozygous116735581
101306842713068428CA10GENIChomozygous116735582
101306926113069262TA18GENIChomozygous116735583
101307020413070205GC34GENIChomozygous116735584
101307047313070474CG21GENIChomozygous116735585
101307049513070496TC21GENIChomozygous116735586
101307058813070589AG16GENIChomozygous116735587
101307153013071531GA14GENIChomozygous116735588
101307176013071761TC20GENIChomozygous116735589