chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7142026296142026297GA21INTERGENIChomozygous54267722
7142029521142029535ACACACACACATAT--------------11INTERGENICheterozygous54160329
7142029797142029798TC14INTERGENIChomozygous54160331
7142030245142030246AG13INTERGENIChomozygous54267733
7142030491142030492GA12INTERGENIChomozygous54267736
7142033903142033904GT14INTERGENIChomozygous54267739
7142034035142034036GA12INTERGENIChomozygous54267742
7142035705142035706CG16INTERGENIChomozygous54267745
7142038194142038195A-8INTERGENIChomozygous54267748
7142039530142039531AG10INTERGENIChomozygous54160344
7142039747142039748CT10INTERGENIChomozygous54267752
7142039872142039873C-10INTERGENIChomozygous54160348
7142044003142044004CT11INTERGENIChomozygous54160355
7142044300142044301TC8INTERGENIChomozygous54160356
7142044326142044327GA10INTERGENIChomozygous54160357
7142044436142044437TTCTTC15INTERGENIChomozygous54160359
7142045863142045864CT13INTERGENIChomozygous54267756
7142050660142050661AT15INTERGENICpossibly homozygous54160375
7142052746142052747CA10INTERGENIChomozygous54267769
7142053429142053430AG13INTERGENIChomozygous54160384
7142055539142055540TC11INTERGENIChomozygous54160394
7142057262142057263TC20GENIChomozygous54267772
7142057706142057707AG20GENIChomozygous54160408
7142060290142060291GA12GENIChomozygous54267775
7142062180142062181C-13GENIChomozygous54160426
7142062184142062185AAT13GENIChomozygous54160427