chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
115862420558624206CG19INTERGENIChomozygous50958876
115863829658638297TTTCTC6INTERGENICheterozygous50793166
115864081158640812TC38GENICheterozygous50793169
115864082858640829GA37GENICheterozygous50793170
115864083158640832TC34GENICheterozygous50793171
115864091958640920GA27GENICheterozygous50958878
115864103058641031GA28GENICheterozygous50793172
115864104558641046TC22GENICheterozygous50881834
115865351558653516GGCA4INTERGENICheterozygous50793198
115866255658662557TG15INTERGENICheterozygous50793216
115866324258663243GA16GENICheterozygous50793221
115866324558663246TC17GENICheterozygous50793223
115866329458663295GA27GENICheterozygous50793224
115866330358663304CG30GENICheterozygous50793226
115866333358663334GA30GENICheterozygous50793229
115866485258664853TC39INTERGENICheterozygous50958880
115866516758665168CT33INTERGENICheterozygous50958882
115866517058665171CA34INTERGENICheterozygous50793232
115866517658665177GA36INTERGENICheterozygous50793233
115866522158665222TG34INTERGENICheterozygous50793235
115867180958671810CCA13INTERGENICheterozygous50793286
115867282258672823AAG9INTERGENIChomozygous50793287
115868689058686891CG12INTERGENIChomozygous50793292
115869180658691807AAC15INTERGENIChomozygous50793295
115869182958691830TTC16INTERGENIChomozygous50793297