<HashMap><database>GEO</database><file_versions><headers><Content-Type>application/xml</Content-Type></headers><body><files><Other>ftp://ftp.ncbi.nlm.nih.gov/geo/series/GSE338nnn/GSE338774/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><species>Mus musculus</species><gds_type>Genome binding/occupancy profiling by high throughput sequencing</gds_type><full_dataset_link>https://www.ncbi.nlm.nih.gov/geo/query/acc.cgi?acc=GSE338774</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>The Histone Demethylase KDM6B Restrains Hypermetabolic LYVE1+ Perivascular Macrophages and Preserves Adipogenic Balance [ATAC-Seq]</name><description>We employed ATAC sequencing to study chromatin accessibility in bone marrow-derived macrophages from wild-type and macrophage-specific KDM6B knockout mice following stimulation with LPS and IFNγ. This study was designed to identify genotype-dependent changes in accessible chromatin regions associated with inflammatory macrophage activation.</description><dates><publication>2026/09/01</publication></dates><accession>GSE338774</accession><cross_references><GSM>GSM9881319</GSM><GSM>GSM9881318</GSM><GSM>GSM9881317</GSM><GSM>GSM9881327</GSM><GSM>GSM9881316</GSM><GSM>GSM9881315</GSM><GSM>GSM9881326</GSM><GSM>GSM9881325</GSM><GSM>GSM9881314</GSM><GSM>GSM9881324</GSM><GSM>GSM9881313</GSM><GSM>GSM9881312</GSM><GSM>GSM9881323</GSM><GSM>GSM9881322</GSM><GSM>GSM9881321</GSM><GSM>GSM9881320</GSM><GPL>24247</GPL><GSE>338774</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>