chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71231731712317318TC21GENIChomozygous53790714
71231857712318580TTG---5GENICheterozygous53790716
71232044312320444GA18GENIChomozygous53790717
71232090912320910TC22GENIChomozygous53790718
71232214012322142GT--25GENIChomozygous54954858
71232293512322936GGCTGT12GENIChomozygous53790720
71232639912326400GA23GENIChomozygous53790721
71232643412326435AAG17GENIChomozygous53790722
71232680412326805GA28GENIChomozygous53790724
71232914012329141GA19GENIChomozygous53790726
71233139912331400AG22GENIChomozygous53790727
71233332112333322GC33GENIChomozygous53790728
71233355212333553CT24GENIChomozygous53790729
71233528412335285CT21GENIChomozygous53790733
71233701812337019GA37GENIChomozygous53790737
71233832112338322AAT18GENICpossibly homozygous53790738