chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
139851525898515259CT55GENIChomozygous114436911
139851756098517561TC30GENIChomozygous114436913
139851763298517633CG17GENICheterozygous131926846
139851811598518116GA41GENIChomozygous118467141
139851879598518796TC54GENIChomozygous114436915
139851960298519603AG29GENIChomozygous118467142
139852012198520122CT40GENIChomozygous114436917
139852031898520319CT16GENIChomozygous115155158
139852042098520421AG25GENIChomozygous115155160
139852190198521902AG52GENIChomozygous114436921
139852331598523316CT59GENIChomozygous114436923
139852354498523545TC42GENIChomozygous118467144
139852373598523736AG51GENIChomozygous114436925
139852512098525121AG39GENIChomozygous114436927
139852780398527804TC52GENIChomozygous114436929
139852828598528286GA37GENIChomozygous114436931
139852966998529670TC45GENIChomozygous114436933
139852973998529740GC43GENIChomozygous114436935
139852180098521800T56GENICpossibly homozygous129089403
139852244998522449C50GENIChomozygous129089404
139852360098523601G30GENIChomozygous129089405
139852451098524510G43GENIChomozygous129089406
139852526998525271CT13GENICheterozygous129089407
139852293598522936TC44GENIChomozygous114650519
139853197698531977TC59GENIChomozygous118467147
139853197898531979TC58GENIChomozygous118467148
139853259298532592T44GENICpossibly homozygous129089408
139853292398532924AG21GENIChomozygous114650521
139853333498533335TC47GENIChomozygous114436937
139853392998533930TC80GENIChomozygous114436939
139853786998537870CT61GENIChomozygous114436941