chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
117071114470711145AT22GENIChomozygous115899600
117072906870729069T5GENIChomozygous128921266
117072900770729007A11GENIChomozygous128921263
117072904970729056ACCTAGG5GENIChomozygous128921264
117072906470729064T5GENIChomozygous128921265
117072907670729077C5GENIChomozygous128921267
117072907970729080GA4GENIChomozygous115899602
117072908170729082AG3GENIChomozygous115899604
117072908370729083C3GENIChomozygous128921268
117072909370729094TG2GENIChomozygous116050670
117072937070729371CG16GENIChomozygous116321775
117073093170730931T21GENICheterozygous132417503
117073265970732660G1GENIChomozygous128921270
117073267170732671G2GENIChomozygous128921271
117073268370732684T2GENIChomozygous128921272
117073432870734329T13GENIChomozygous128921279
117073436370734364TA15GENIChomozygous115899606
117073436470734365AT15GENIChomozygous115899608
117073441270734413CT18GENIChomozygous115899610
117073441370734414TC18GENIChomozygous115899612
117073443970734439T14GENIChomozygous128921280
117073677370736774G11GENIChomozygous128921281
117073678870736789A19GENICheterozygous128921282
117073695170736952TC8GENIChomozygous115899614
117073695270736953CT8GENIChomozygous115899616
117073714870737149C2GENIChomozygous128921283
117073715270737152A2GENIChomozygous128921284
117073716070737160C2GENIChomozygous128921285
117074780270747803AG13GENIChomozygous116050672
117074780470747805GT13GENIChomozygous116050674
117074785470747855T8GENIChomozygous128921287
117074787570747876A6GENIChomozygous128921288
117074788170747882CA6GENIChomozygous118163799
117074789770747897A5GENIChomozygous128921289
117074797070747971C5GENIChomozygous128921291
117074797370747974CT5GENIChomozygous116411351
117074802970748030TG6GENIChomozygous123523986
117074803070748031GT6GENIChomozygous123523987
117074803470748036TC6GENIChomozygous128921292
117074807570748076G6GENIChomozygous128921293
117074808070748080T5GENIChomozygous128921294
117073706270737063TC5GENIChomozygous116420874