chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6135107589135107590TC14GENIChomozygous54737647
6135107925135107926CT9GENIChomozygous54737649
6135108127135108128TG6GENICheterozygous54737651
6135108389135108390TA13GENIChomozygous54737653
6135109092135109093A-8GENIChomozygous54737655
6135109435135109436GA9GENIChomozygous54737657
6135110229135110231CT--16GENICpossibly homozygous54737659
6135110348135110349AG15INTERGENICpossibly homozygous54737661
6135110432135110433AG15INTERGENIChomozygous54737663
6135111294135111295CA17INTERGENIChomozygous54737665
6135111843135111844TA4INTERGENICheterozygous54737667
6135111969135111970CCTTTTT1INTERGENIChomozygous54737669
6135112645135112646A-10INTERGENIChomozygous54737675