chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10108877114108877115CT35GENIChomozygous521103043
10108877194108877195CT41GENIChomozygous521103044
10108877595108877596TG39GENIChomozygous521103045
10108877657108877658AG37GENIChomozygous521103046
10108877702108877703AT35GENIChomozygous521103047
10108877811108877812GA29GENICheterozygous523787346
10108877927108877928CT10GENICheterozygous521103048
10108878538108878539CCTT12GENIChomozygous691146218
10108878562108878563CCTT10GENIChomozygous691146220
10108878644108878645TC35GENICpossibly homozygous521103049