chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
6135107589135107590TC18GENIChomozygous54737647
6135107925135107926CT21GENICpossibly homozygous54737649
6135108127135108128TG29GENIChomozygous54737651
6135108389135108390TA29GENIChomozygous54737653
6135109092135109093A-16GENIChomozygous54737655
6135109435135109436GA23GENIChomozygous54737657
6135110229135110231CT--25GENIChomozygous54737659
6135110348135110349AG31INTERGENICpossibly homozygous54737661
6135110432135110433AG21INTERGENIChomozygous54737663
6135111294135111295CA18INTERGENIChomozygous54737665
6135111843135111844TA13INTERGENIChomozygous54737667
6135111969135111970CCTTTTT7INTERGENIChomozygous54737669
6135111981135111982CT25INTERGENICheterozygous54737671
6135111986135111987CT25INTERGENICheterozygous54737673
6135112645135112646A-28INTERGENIChomozygous54737675