chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6135107589135107590TC11GENIChomozygous54737647
6135107925135107926CT9GENIChomozygous54737649
6135108127135108128TG3GENICheterozygous54737651
6135108389135108390TA15GENICpossibly homozygous54737653
6135109092135109093A-7GENIChomozygous54737655
6135109435135109436GA11GENIChomozygous54737657
6135110229135110231CT--18GENICpossibly homozygous54737659
6135110348135110349AG22INTERGENICpossibly homozygous54737661
6135110432135110433AG18INTERGENIChomozygous54737663
6135111294135111295CA14INTERGENIChomozygous54737665
6135111843135111844TA7INTERGENICheterozygous54737667
6135112645135112646A-10INTERGENIChomozygous54737675