chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10108877114108877115CT53GENIChomozygous502975716
10108877194108877195CT65GENIChomozygous502975717
10108877595108877596TG53GENIChomozygous502975718
10108877657108877658AG59GENIChomozygous502975719
10108877702108877703AT43GENIChomozygous502975720
10108877811108877812GA41GENICheterozygous505934138
10108877927108877928CT24GENICheterozygous502975721
10108878363108878364TG42GENICheterozygous505934139
10108878538108878539CCTT16GENIChomozygous684431512
10108878562108878563CCTT11GENICpossibly homozygous684431514
10108878644108878645TC34GENICpossibly homozygous502975722