chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
154657770146577702G7GENIChomozygous130440784
154657771046577711C7GENIChomozygous130440785
154657773246577733A9GENIChomozygous129252626
154657773646577737C8GENIChomozygous129252627
154657775146577752G8GENIChomozygous129252628
154657778046577781A8GENIChomozygous129252629
154657780546577806T10GENIChomozygous129252630
154657780846577809AC10GENIChomozygous112679879
154657781546577816AT11GENIChomozygous112679881
154657782446577824G12GENIChomozygous129252631
154657783146577831G12GENIChomozygous129252632
154657784146577842AT16GENIChomozygous112679883
154657784246577843CA16GENIChomozygous112679885
154657786346577864G18GENIChomozygous129252633
154657788446577885A16GENIChomozygous129252634
154657789346577894T19GENIChomozygous129252635
154657793246577933TA19GENIChomozygous112500331
154657796146577962A19GENIChomozygous129252636
154657797146577971C17GENIChomozygous129252637
154657808646578087CT14GENICpossibly homozygous119035025
154657941546579416A7GENIChomozygous129252640
154657943746579437G7GENIChomozygous129252641
154657944146579441G7GENIChomozygous129252642
154657944646579446G6GENIChomozygous129252643
154657946146579461G6GENIChomozygous129252644
154657946546579465G7GENIChomozygous129252645
154657947846579479A7GENIChomozygous129252646
154658075946580760G25GENIChomozygous129252650
154657950746579507G8GENIChomozygous129252647
154657952846579529A12GENIChomozygous129252648
154657953346579533A11GENIChomozygous129252649
154657950346579504CG8GENIChomozygous129315793
154657950446579505TC8GENIChomozygous129315794
154658078246580783G25GENIChomozygous129252651
154658079146580792G25GENIChomozygous129252652