chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
34302699643027006TGTGTGTGTT----------10GENICheterozygous60425947
34302733543027336CG16GENICheterozygous59098767
34302764243027643GA11GENICheterozygous59098769
34302898643028987CT19GENICheterozygous59098771
34302953143029532CT16GENICheterozygous58736367
34302993943029940CT18GENICheterozygous59098773
34302994643029947AG18GENICheterozygous58124013
34302995743029958AG15GENICheterozygous59098775
34303017143030172CT17GENICheterozygous58124014
34303094843030949AG15GENICheterozygous59098777
34303111143031112GA21GENICheterozygous59098779
34303140943031410AT12GENICheterozygous58124016
34303241243032413A-16GENICheterozygous59098781
34303545443035455CT14GENICheterozygous59098783
34303640143036402TA19GENICheterozygous59098785
34303665143036652CCA13GENICheterozygous60425948
34303701343037014CA15GENICheterozygous59098787
34303701743037018CT14GENICheterozygous59098789
34303706443037065GT11GENICheterozygous59098791
34303777943037780AG19GENICheterozygous58124018
34303997543039976CA19GENICheterozygous58736373
34304011143040112AG16GENICheterozygous58736375
34304016143040162GA12GENICheterozygous58736379
34304016643040168CT--11GENICheterozygous58736381
34304016843040169GA11GENICheterozygous58736383
34304017143040172AC11GENICheterozygous58736385
34304017743040178TC10GENICheterozygous58736387
34304082643040827C-14GENICheterozygous58736389
34304089843040899GA19GENICheterozygous58736391
34304122743041228AG13GENICheterozygous58736394
34304136143041362TC20GENICheterozygous59098793
34304187043041872AA--8GENICheterozygous60425949
34304187343041883AAGAAGAAGA----------8GENICheterozygous60425950
34304189443041895GA10GENICheterozygous60425951
34304190443041907AGG---6GENICheterozygous59674465
34304195743041958AG11GENICheterozygous58736396
34304436543044366AG20GENICheterozygous58736400
34304473643044737GA19GENICheterozygous59098795