chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5131837546131837547GA36GENICpossibly homozygous114141757
5131844777131844778GA29GENIChomozygous114009087
5131845402131845403CT23GENIChomozygous114009088
5131845727131845728CA28GENIChomozygous114009089
5131846180131846181TG23GENIChomozygous114009090
5131847859131847860GA21GENIChomozygous114141758
5131850089131850090AT12GENIChomozygous114009101
5131850416131850417TC11GENICpossibly homozygous114141760
5131853410131853411AG36GENIChomozygous114009103
5131853511131853512TG33GENIChomozygous114009104
5131853678131853679TC42GENIChomozygous114009105
5131855380131855381CG21GENICheterozygous114009107
5131859483131859484TC19GENIChomozygous114009108
5131859936131859937GA33GENIChomozygous114009109
5131862290131862291CG25GENIChomozygous114009111