chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6135107589135107590TC11GENIChomozygous54737647
6135107925135107926CT10GENICpossibly homozygous54737649
6135108127135108128TG12GENICheterozygous54737651
6135108389135108390TA16GENIChomozygous54737653
6135109092135109093A-7GENIChomozygous54737655
6135109435135109436GA15GENICpossibly homozygous54737657
6135110229135110231CT--23GENICpossibly homozygous54737659
6135110348135110349AG20INTERGENICheterozygous54737661
6135110432135110433AG17INTERGENIChomozygous54737663
6135111294135111295CA18INTERGENICpossibly homozygous54737665
6135111843135111844TA3INTERGENIChomozygous54737667
6135112645135112646A-17INTERGENIChomozygous54737675