chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103891976838919769GA45GENIChomozygous116762768
103891981538919816TA48GENIChomozygous116565853
103892002838920029GA65GENIChomozygous116762770
103892076838920769GT50GENIChomozygous116762772
103892117338921174GA39GENIChomozygous116762774
103892171838921719TC41GENIChomozygous116762776
103892257738922578AT44GENICpossibly homozygous116565859
103892260538922606TA46GENIChomozygous116565861
103892266538922666CA52GENIChomozygous116762778
103892330638923307CT41GENIChomozygous116762780
103892374838923749TC35GENIChomozygous116762782
103892375438923755CT37GENIChomozygous116762784
103892402038924021TC61GENIChomozygous116762786
103892544438925445CT53GENIChomozygous116565863
103893085138930852GA44GENIChomozygous116762788
103892087238920872TA45GENIChomozygous128808653
103892158638921587CT30GENIChomozygous117057479
103892186438921865A22GENIChomozygous131091501
103893408538934086TC37GENIChomozygous116762790
103893448338934484GA64GENIChomozygous116762792
103893644338936471TTCTTGCACTCTAATTCTAGGACTCTAA63GENIChomozygous131091502
103893858338938584TA52GENIChomozygous116762794