<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/GSE96nnn/GSE96933/</Other></files><type>primary</type></body><statusCode>OK</statusCode><statusCodeValue>200</statusCodeValue></file_versions><scores/><additional><omics_type>Genomics</omics_type><species>Homo sapiens</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=GSE96933</full_dataset_link><repository>GEO</repository><entry_type>GSE</entry_type></additional><is_claimable>false</is_claimable><name>ChIP-seq for SMARCE1 and SMARCC1 in non-invasive and invasive HMLE-Twist-ER cells</name><description>We find that in invasive HMLE-Twist-ER cells, SMARCE1 binds to ILF3 and is localized to ILF motifs. In contrast, ILF motifs were not enriched at SMARCE1-bound sites in noninvasive HMLE-Twist-ER cells or at SMARCC1-bound sites.</description><dates><publication>2017/03/23</publication></dates><accession>GSE96933</accession><cross_references><GSM>GSM2546250</GSM><GSM>GSM2546249</GSM><GSM>GSM2546254</GSM><GSM>GSM2546253</GSM><GSM>GSM2546252</GSM><GSM>GSM2546251</GSM><GPL>11154</GPL><SRA>SRP102316</SRA><GSE>96933</GSE><taxon>Homo sapiens</taxon><PMID>[28377514]</PMID></cross_references></HashMap>