chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101306162213061623AG6GENIChomozygous116975829
101306674713066748TG23GENIChomozygous117120327
101306700513067006TC13GENICpossibly homozygous117982113
101306706913067070GA9GENIChomozygous118029980
101306759313067594GA12GENIChomozygous116735581
101306609713066098GT9GENIChomozygous116735578
101306640713066408TC17GENIChomozygous116735579
101306736313067364AG15GENIChomozygous116735580
101306842713068428CA18GENIChomozygous116735582
101306926113069262TA18GENIChomozygous116735583
101307020413070205GC14GENIChomozygous116735584
101307047313070474CG19GENIChomozygous116735585
101307049513070496TC16GENIChomozygous116735586
101307058813070589AG13GENIChomozygous116735587
101307153013071531GA12GENIChomozygous116735588
101307176013071761TC16GENIChomozygous116735589