chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101306162213061623AG12GENIChomozygous116975829
101306700513067006TC21GENIChomozygous117982113
101306706913067070GA23GENIChomozygous118029980
101306609713066098GT14GENIChomozygous116735578
101306640713066408TC23GENIChomozygous116735579
101306736313067364AG28GENIChomozygous116735580
101306759313067594GA18GENIChomozygous116735581
101306842713068428CA26GENIChomozygous116735582
101306674713066748TG29GENIChomozygous117120327
101306926113069262TA18GENIChomozygous116735583
101307020413070205GC20GENIChomozygous116735584
101307047313070474CG16GENIChomozygous116735585
101307049513070496TC18GENIChomozygous116735586
101307058813070589AG21GENIChomozygous116735587
101307153013071531GA22GENIChomozygous116735588
101307176013071761TC28GENIChomozygous116735589