chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6135107589135107590TC9GENICheterozygous54737647
6135107925135107926CT7GENIChomozygous54737649
6135108127135108128TG6GENICheterozygous54737651
6135108389135108390TA24GENICpossibly homozygous54737653
6135109092135109093A-5GENIChomozygous54737655
6135109435135109436GA19GENIChomozygous54737657
6135110229135110231CT--14GENIChomozygous54737659
6135110348135110349AG18INTERGENIChomozygous54737661
6135110432135110433AG18INTERGENIChomozygous54737663
6135111294135111295CA18INTERGENICpossibly homozygous54737665
6135111843135111844TA6INTERGENICheterozygous54737667
6135112645135112646A-15INTERGENIChomozygous54737675