chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
33619551436195515AC59GENIChomozygous111544202
33619608236196083TC55GENIChomozygous111544203
33619611836196119AG53GENIChomozygous111544204
33619614836196149GA55GENIChomozygous111544205
33619623936196240CG43GENIChomozygous111544206
33619643636196437AG47GENIChomozygous111544207
33619645536196456TG47GENIChomozygous111544208
33619654736196548TC51GENIChomozygous111544209
33619766736197668AG50GENIChomozygous111544210
33619775636197757CA63GENIChomozygous111544211
33619793236197933AG61GENIChomozygous111544212
33619952536199526GC30GENIChomozygous111544213
33619957036199571TC52GENICheterozygous111544215
33619964636199647AG60GENICheterozygous111544216
33619964836199649AT62GENICheterozygous111544217
33619967836199679TC54GENICheterozygous111902813
33619968336199684TA54GENICheterozygous111902815
33619970136199702CT52GENICheterozygous111902817
33619971436199715AG49GENICheterozygous111902819
33619976136199762AT51GENIChomozygous111544218
33619992136199922TG52GENIChomozygous111544219
33620048536200486GA58GENIChomozygous111544220
33620118636201187TC45GENIChomozygous111544221
33620171236201713GA17GENICheterozygous112417489
33620279136202792AG44GENIChomozygous111544222
33620463636204637CA45GENIChomozygous111544223
33620512536205126GC56GENIChomozygous111544224
33620614136206142CT53GENIChomozygous111544225