chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6135107589135107590TC13GENIChomozygous54737647
6135107925135107926CT13GENIChomozygous54737649
6135108127135108128TG11GENICheterozygous54737651
6135108389135108390TA19GENIChomozygous54737653
6135109092135109093A-8GENIChomozygous54737655
6135109435135109436GA13GENIChomozygous54737657
6135110229135110231CT--17GENICpossibly homozygous54737659
6135110348135110349AG18INTERGENIChomozygous54737661
6135110432135110433AG15INTERGENIChomozygous54737663
6135111294135111295CA20INTERGENIChomozygous54737665
6135111843135111844TA3INTERGENIChomozygous54737667
6135111969135111970CCTTTT1INTERGENIChomozygous55434950
6135112645135112646A-10INTERGENIChomozygous54737675