chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6105596686105596687CT19GENIChomozygous54611730
6105598886105598887GA27GENIChomozygous55047389
6105600153105600154CT19GENIChomozygous54611735
6105600710105600711CG18GENIChomozygous55047390
6105600855105600856GGA23GENICpossibly homozygous54611736
6105601727105601728GA17GENIChomozygous54611737
6105601872105601873GA26GENIChomozygous55047391
6105602073105602074GC28GENIChomozygous54611738
6105603063105603064AT31GENIChomozygous54611739
6105603133105603134TC22GENIChomozygous54611740