<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/GSE342nnn/GSE342565/</Other></files><type>primary</type></body><statusCodeValue>200</statusCodeValue><statusCode>OK</statusCode></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=GSE342565</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Chromatin accessibility profiling of high endothelial cells (HECs) from mouse peripheral lymph node and Peyer's patch by ATAC-seq</name><description>High endothelial venules (HEVs) are specialized blood vessels that mediate lymphocyte entry into secondary lymphoid organs. We performed ATAC-seq on high endothelial cells (HECs) isolated by flow cytometry from mouse peripheral lymph nodes (PLNs, identified by PNAd expression using the MECA-79 antibody) and Peyer's patches (PPs, identified by MAdCAM-1 expression using the MECA-367 antibody) to characterize genome-wide chromatin accessibility and identify HEC-specific cis-regulatory elements.</description><dates><publication>2026/08/06</publication></dates><accession>GSE342565</accession><cross_references><GSM>GSM9932940</GSM><GSM>GSM9932939</GSM><GPL>37305</GPL><GSE>342565</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>