chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2149321799149321800AG9GENIChomozygous110051459
2149323155149323156AG23GENIChomozygous110051460
2149323504149323505AG24GENIChomozygous110051461
2149324328149324329TG24GENICpossibly homozygous110051462
2149324642149324643TA12GENIChomozygous110051463
2149324650149324651TC10GENIChomozygous110051464
2149324677149324678TA21GENICheterozygous110051465
2149324679149324680AG19GENICheterozygous110051466
2149324685149324686TC16GENICheterozygous110051467
2149324751149324752GA18GENIChomozygous110051468
2149324763149324764TG21GENICpossibly homozygous110051469
2149324897149324898GA7GENIChomozygous110051472
2149324909149324910TG12GENICheterozygous110051473
2149325076149325077GA40GENICheterozygous110051475
2149325086149325087GT49GENICheterozygous110051476
2149325094149325095CT51GENICheterozygous110051477
2149325148149325149TC32GENIChomozygous110051478
2149325158149325159TC30GENICheterozygous110596750
2149325267149325268GT14GENICheterozygous110051480
2149325407149325408GT23GENICpossibly homozygous110051484
2149325589149325590GT38GENICheterozygous110596758
2149325616149325617GA22GENICpossibly homozygous110596760
2149325686149325687GA34GENICheterozygous110596762
2149325756149325757GA26GENICheterozygous110596764
2149325791149325792GA17GENICheterozygous110051485
2149325826149325827GA27GENICpossibly homozygous110051486
2149326475149326476GT18GENIChomozygous110051487