chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101306276113062762GA38GENIChomozygous116994575
101306609713066098GT14GENIChomozygous116735578
101306640713066408TC23GENIChomozygous116735579
101306736313067364AG56GENICpossibly homozygous116735580
101306759313067594GA23GENIChomozygous116735581
101306824713068248CT43GENIChomozygous116994578
101306983213069833AC46GENIChomozygous116994579
101307020413070205GC71GENIChomozygous116735584
101307047313070474CG76GENIChomozygous116735585
101307049513070496TC81GENIChomozygous116735586
101307058813070589AG84GENIChomozygous116735587
101307163413071635TC33GENIChomozygous116994580