chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
71096448610964486GTG29GENIChomozygous128435235
71096605010966051A59GENIChomozygous128435236
71096642410966425A46GENIChomozygous128435237
71096683410966835T68GENIChomozygous128435238
71098063910980639C33GENIChomozygous128435239
71098075210980753G20GENIChomozygous128435240
71098076410980765G18GENIChomozygous128435241
71096625110966252TC48GENIChomozygous115567740
71096636410966365TC56GENIChomozygous115567742
71096670310966704AG61GENIChomozygous115567744
71096723010967231GA66GENIChomozygous115567746
71098343210983433GA65GENIChomozygous115567748
71098408410984097TGTCTCCCACCCC49GENIChomozygous128435242
71098460410984605T59GENICpossibly homozygous128435243
71098487110984871GCAG42GENIChomozygous128435244
71098487910984880C36GENIChomozygous128435245
71098488610984887CT34GENIChomozygous116003364
71098488810984889CG35GENIChomozygous115567750
71098489510984896AG38GENIChomozygous115567751
71098489710984898CG35GENIChomozygous115567753
71098527510985275CAGC61GENIChomozygous128435246
71098604910986049GGGACTTT51GENIChomozygous128435247
71098630510986306GA67GENIChomozygous115567755
71098648010986481GA50GENIChomozygous115567757
71098487310984874AG38GENIChomozygous118306871
71098487610984877CG38GENIChomozygous118306872
71098487710984878CG38GENIChomozygous118306873