<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/GSE214nnn/GSE214526/</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=GSE214526</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Histone chaperon ASF1B recruits distinct epigenetic factors in regulation of histone variant H3.3 during the fetal and adult erythropoiesis [ATAC-seq]</name><description>To determine ASF1B function in chromatin accessbility, ATAC Seq was performed in both WT and ASF1B KO mouse liver. Loss of ASF1B caused generally decresed of chrmoatin accessbility on the promoters.</description><dates><publication>2026/05/15</publication></dates><accession>GSE214526</accession><cross_references><GSM>GSM6610527</GSM><GSM>GSM6610528</GSM><GSM>GSM6610529</GSM><GSM>GSM6610530</GSM><GPL>21626</GPL><GSE>214526</GSE><taxon>Mus musculus</taxon><PMID>[42100853]</PMID></cross_references></HashMap>