chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
113554672935546730AG46GENICheterozygous118143498
113554673735546738GA42GENICheterozygous118143499
113554887335548874GA24GENICpossibly homozygous116109708
113554900435549005GC25GENIChomozygous115823866
113555025835550259GA55GENIChomozygous115823868
113555075535550756CT69GENIChomozygous115823870
113555365935553660AG56GENIChomozygous115823872
113555638935556390GT45GENIChomozygous116109709
113555651935556520CG46GENIChomozygous116360529
113555681235556813TA13GENIChomozygous118143501
113555683935556840TC13GENIChomozygous118143503
113555698235556983TC45GENIChomozygous115961899
113555703135557032TG24GENIChomozygous115961900
113555724335557244CT28GENIChomozygous118143504
113556329935563300TA164GENICheterozygous118180232
113556332135563322CA161GENICheterozygous118180233
113556336135563362TG131GENICheterozygous118180234
113556450935564510TA56GENIChomozygous115823874
113556514935565150TC53GENIChomozygous115823876
113556782935567830CT49GENICheterozygous118180235
113557029535570296CT61GENIChomozygous115823878
113557507935575080TC65GENIChomozygous115823880
113558479335584794GA52GENIChomozygous115823882
113558494835584949TC61GENIChomozygous115823884
113558632635586327AG49GENIChomozygous115823886
113558707935587080GA62GENICpossibly homozygous115823888
113558784035587841TG74GENIChomozygous115823890
113558798135587982AT70GENICpossibly homozygous115823892
113558818735588188GA54GENIChomozygous115823894