chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122417202624172028TT--15GENIChomozygous50131985
122417319124173192CT31GENIChomozygous50131987
122417483724174839GC--34GENICheterozygous50131995
122417483824174839CCGT26GENIChomozygous50292656
122417492124174925GAGA----24GENIChomozygous50292658
122417505524175059GAGA----18GENIChomozygous50132003
122417547024175471CT22GENIChomozygous50292660
122417615524176156CT11GENICpossibly homozygous50292662
122417616624176167TTC6GENIChomozygous50132007
122417629724176298TG16GENICheterozygous50132017
122417630124176302TG17GENICheterozygous50132019
122417665324176654TC28GENICpossibly homozygous50292663
122417669824176699GT28GENIChomozygous50292665
122417682424176825AG41GENIChomozygous50132021