chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5131841339131841340AG42GENIChomozygous794023960
5131842186131842187AC39GENIChomozygous794023961
5131842813131842814GA51GENIChomozygous794023962
5131844777131844778GA40GENIChomozygous794023963
5131845402131845403CT29GENIChomozygous794023964
5131845727131845728CA44GENIChomozygous794023965
5131846180131846181TG25GENIChomozygous794023966
5131848908131848909TG40GENIChomozygous794023967
5131849672131849673CT43GENIChomozygous794023968
5131850089131850090AT33GENIChomozygous794023969
5131852932131852933CA43GENIChomozygous794023970
5131853410131853411AG60GENIChomozygous794023971
5131853511131853512TG32GENIChomozygous794023972
5131853678131853679TC35GENIChomozygous794023973
5131854297131854298CA43GENIChomozygous794023974
5131855380131855381CG47GENIChomozygous794023975
5131859483131859484TC36GENICpossibly homozygous794023976
5131859936131859937GA41GENIChomozygous794023977
5131861443131861444GT51GENIChomozygous794023978
5131862290131862291CG51GENIChomozygous794023979
5131864052131864053CT39GENICpossibly homozygous794023980