chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10108877114108877115CT42GENIChomozygous525391985
10108877194108877195CT34GENIChomozygous525391986
10108877595108877596TG31GENIChomozygous525391987
10108877657108877658AG31GENIChomozygous525391988
10108877702108877703AT33GENIChomozygous525391989
10108877811108877812GA29GENICheterozygous528165837
10108877927108877928CT19GENICheterozygous525391990
10108878538108878539CCTT16GENICpossibly homozygous692819204
10108878562108878563CCTT12GENIChomozygous692819206
10108878644108878645TC40GENICpossibly homozygous525391991