chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108861160688611607A17GENIChomozygous130394149
108861306188613062C58GENIChomozygous128843434
108861501488615015TC30GENIChomozygous116950072
108861812588618126GA64GENIChomozygous116901748
108861306788613068CA58GENIChomozygous116674239
108861778188617782AG63GENIChomozygous116674241
108861475188614752AT9GENIChomozygous132151650
108861475388614754AT7GENIChomozygous132151651
108861543188615432GT70GENIChomozygous116901742
108861603188616032AG51GENIChomozygous116901744
108861740488617405GA56GENIChomozygous116901746
108861865788618658AG68GENIChomozygous116901750