chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55606888156068882AG55GENIChomozygous137474821
55606891956068921GG55GENIChomozygous137309704
55606901556069016CT69GENIChomozygous137474822
55606931356069314GT51GENIChomozygous137474823
55606944556069445A39GENIChomozygous137309705
55606946856069469CT46GENIChomozygous137474824
55606982556069826TA55GENIChomozygous137474826
55607015656070157T32GENIChomozygous137309706
55607094156070942GA27GENIChomozygous137474827
55607135356071354TC54GENIChomozygous137474828
55607169456071695CA48GENICpossibly homozygous137474829
55607175656071757TC43GENIChomozygous137474830
55607213756072138CT49GENIChomozygous137474831
55607245056072451TC50GENIChomozygous137474832
55607281856072819TC50GENIChomozygous137474835
55607378256073783CT39GENIChomozygous141726704
55607308856073089TC54GENICpossibly homozygous141726701
55607336056073361CA45GENIChomozygous141726702
55607336556073366CT45GENIChomozygous141726703
55607388256073883CT44GENIChomozygous137474838
55607419156074192A50GENIChomozygous141682347
55607571856075719CT56GENIChomozygous141726705
55607656156076562TC56GENIChomozygous137474839
55607867056078670A48GENIChomozygous141682348