chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71231731712317318TC29GENIChomozygous53790714
71231857612318580TTTG----20GENICheterozygous53790715
71231857712318580TTG---20GENICpossibly homozygous53790716
71232044312320444GA31GENIChomozygous53790717
71232090912320910TC29GENIChomozygous53790718
71232213012322134GTGT----16GENICheterozygous54558095
71232213212322134GT--16GENICheterozygous53790719
71232293512322936GGCTGT23GENIChomozygous53790720
71232639912326400GA30GENIChomozygous53790721
71232643412326435AAG22GENIChomozygous53790722
71232643512326436GGC21GENICpossibly homozygous53790723
71232680412326805GA39GENIChomozygous53790724
71232797712327978CT15GENIChomozygous53790725
71232914012329141GA26GENIChomozygous53790726
71233139912331400AG25GENIChomozygous53790727
71233332112333322GC27GENIChomozygous53790728
71233355212333553CT22GENIChomozygous53790729
71233519512335196C-46GENICheterozygous53790731
71233528412335285CT47GENICpossibly homozygous53790733
71233562312335624T-38GENICheterozygous53790735
71233564312335645CA--34GENICheterozygous53790736
71233566712335668CT43GENICheterozygous54301818
71233701812337019GA34GENIChomozygous53790737
71233832112338322AAT14GENICpossibly homozygous53790738