chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
56207154562071546GC31GENIChomozygous113830611
56207165562071656GC22GENICpossibly homozygous113830613
56207185762071858GC9GENICpossibly homozygous113830615
56207233362072334GC4GENIChomozygous113830617
56207357962073580GT24GENIChomozygous113830619
56207437362074374TC33GENIChomozygous113830621
56207652362076524TC39GENIChomozygous113830623
56207956162079562TC10GENICpossibly homozygous113830625
56207957362079574TG12GENICpossibly homozygous113830627
56207978362079784CT36GENIChomozygous113830629
56208144562081446AG28GENIChomozygous113830631
56208261762082618TC14GENIChomozygous113830633
56208882762088828TA57GENIChomozygous113830635
56209021962090220GA52GENICpossibly homozygous113830637
56209156362091564TC41GENIChomozygous113830639
56209194562091946CG53GENIChomozygous113830641
56209249362092494GA43GENIChomozygous113830643
56209270662092707TC35GENICheterozygous113830645
56209376762093768CT51GENICpossibly homozygous113830647