chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
101080915910809160T40GENICpossibly homozygous128789536
101080984410809844T14GENICheterozygous132142963
101081045510810455T39GENIChomozygous128789537
101081630810816309TC58GENICpossibly homozygous116493789
101081499110814992GA63GENIChomozygous116493785
101081243110812432AC77GENIChomozygous116858616
101081609410816095GA63GENICpossibly homozygous116858618
101081329910813300AG60GENIChomozygous116493783
101081529410815295TC52GENIChomozygous116493787
101081745510817456GT62GENIChomozygous116493791
101081754210817543AC65GENIChomozygous116493793
101081754210817542C62GENIChomozygous128789538
101081770810817709CA53GENIChomozygous116493795
101081887110818872TC67GENIChomozygous116734092
101082180610821807CG58GENIChomozygous116858620
101082333410823335TA59GENIChomozygous116734096
101082340110823402C63GENIChomozygous132142964
101082358810823589GA68GENIChomozygous116493799
101082449410824495CT59GENIChomozygous116858622
101082606110826062TC60GENIChomozygous116734097
101082643910826440TC72GENIChomozygous116858624
101082644110826442CT72GENIChomozygous116493801
101082789110827892AC87GENIChomozygous116858626
101082938610829387GA66GENIChomozygous116858628
101082241210822413AC51GENIChomozygous118079141
101081987810819879CG1GENIChomozygous132332158
101081988410819885TG1GENIChomozygous132332159
101081995410819955AG1GENIChomozygous118073741