chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
474501477450148GA49GENICpossibly homozygous112481757
474504907450491TG53GENIChomozygous112481759
474514687451469AC37GENIChomozygous112481761
474521807452181AG30GENICpossibly homozygous112996483