chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5131841339131841340AG23GENIChomozygous114009084
5131842186131842187AC27GENIChomozygous114009085
5131842813131842814GA25GENIChomozygous114009086
5131844777131844778GA20GENIChomozygous114009087
5131845402131845403CT19GENIChomozygous114009088
5131845727131845728CA28GENIChomozygous114009089
5131846180131846181TG29GENIChomozygous114009090
5131849672131849673CT15GENIChomozygous114009100
5131850089131850090AT10GENIChomozygous114009101
5131852932131852933CA36GENIChomozygous114009102
5131853410131853411AG36GENIChomozygous114009103
5131853511131853512TG25GENIChomozygous114009104
5131853678131853679TC20GENIChomozygous114009105
5131854297131854298CA27GENIChomozygous114009106
5131855380131855381CG23GENIChomozygous114009107
5131859483131859484TC25GENIChomozygous114009108
5131859936131859937GA18GENIChomozygous114009109
5131861443131861444GT25GENIChomozygous114009110
5131862290131862291CG15GENIChomozygous114009111
5131864052131864053CT39GENIChomozygous114009112