<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/GSE331nnn/GSE331039/</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=GSE331039</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>Impact of Peg3 deletion in mouse trophoblast stem cells on H3K9me3 profiles</name><description>Peg3 is an imprinted gene that in itself is a KRAB zinc finger protein. We established knockout trophoblast stem cell lines (TSCs) in which we ablated the majority of the zinc finger motifs of the PEG3 coding region using CRISPR-Cas9-mediated deletion. We then profiled wild-type (WT) and knockout (KO) TSC lines for the genome-wide distribution of the epigenetic repressive mark H3K9me3 by ChIP-seq.</description><dates><publication>2026/06/19</publication></dates><accession>GSE331039</accession><cross_references><GSM>GSM9737981</GSM><GSM>GSM9737992</GSM><GSM>GSM9737991</GSM><GSM>GSM9737990</GSM><GSM>GSM9737989</GSM><GSM>GSM9737988</GSM><GSM>GSM9737987</GSM><GSM>GSM9737986</GSM><GSM>GSM9737985</GSM><GSM>GSM9737984</GSM><GSM>GSM9737983</GSM><GSM>GSM9737982</GSM><GPL>30172</GPL><GSE>331039</GSE><taxon>Mus musculus</taxon></cross_references></HashMap>