chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108861160688611607A18GENIChomozygous130394149
108861306188613062C59GENIChomozygous128843434
108861501488615015TC33GENIChomozygous116950072
108861812588618126GA58GENIChomozygous116901748
108861306788613068CA60GENIChomozygous116674239
108861778188617782AG60GENIChomozygous116674241
108861475188614752AT7GENICpossibly homozygous132151650
108861475388614754AT6GENICheterozygous132151651
108861543188615432GT59GENIChomozygous116901742
108861603188616032AG63GENIChomozygous116901744
108861740488617405GA54GENIChomozygous116901746
108861865788618658AG66GENIChomozygous116901750