chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
124905051249050520TTTTTTTA--------8GENICpossibly homozygous50455731
124905051449050515TTC19GENIChomozygous50230908
124905051549050516TTTTC19GENICheterozygous50230910
124905052349050524AC17GENICpossibly homozygous50230912
124905052749050528AC16GENIChomozygous50230914
124905053149050532AC16GENICheterozygous50230916
124905053549050536AC17GENICheterozygous50230918
124905175649051760TTTT----14GENICheterozygous50470669
124905236449052365AT59GENICpossibly homozygous50230932
124905238449052394TGAGTGTGTG----------37GENIChomozygous50491773
124905276849052769TC46GENIChomozygous50230934
124905571649055717TTG11GENICheterozygous50343654
124905614649056147CA26GENIChomozygous50230942