<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/GSE310nnn/GSE310014/</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=GSE310014</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>MBD3 regulates thymic Treg precursor cell development by modulating CD25 expression [ChIP-seq]</name><description>ChIP-seq was performed in wild-type (WT) thymocytes to profile MBD3 occupancy and histone modifications, including H3K27ac and H3K4me1. These data reveal direct binding of MBD3 to Treg-specific regulatory regions and co-localization with activating histone marks. In Mbd3 conditional knockout (CKO) thymocytes, these regulatory regions exhibit altered chromatin modifications, correlating with impaired thymic Treg differentiation. These ChIP-seq datasets provide a multi-omic view of how MBD3 binding and associated histone modifications contribute to thymic Treg lineage specification.</description><dates><publication>2026/09/29</publication></dates><accession>GSE310014</accession><cross_references><GSM>GSM9286488</GSM><GSM>GSM9286477</GSM><GSM>GSM9286478</GSM><GSM>GSM9286479</GSM><GSM>GSM9286484</GSM><GSM>GSM9286485</GSM><GSM>GSM9286486</GSM><GSM>GSM9286487</GSM><GSM>GSM9286476</GSM><GSM>GSM9286480</GSM><GSM>GSM9286481</GSM><GSM>GSM9286482</GSM><GSM>GSM9286483</GSM><GPL>25723</GPL><GPL>34290</GPL><GSE>310014</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>