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EWS/FLI cDNA constructs including various deletions of the FLI portion were virally transduced into cells and we sought to determine the ATAC profile of each. Overall design: Endogenous EWS/FLI was knocked-down in the Ewing sarcoma A673 cell line and EWS/FLI cDNA constructs were expressed in these cells. Cells were collected after 8 days and antibody-directed micrococcal nuclease was used to determine the binding locations of these EWS/FLI protein constructs. Two biological replicates for each sample were used to construct cDNA libraries each library was submitted twice to acheive sufficient read-depth and combined for analysis.</long_description><repository>ENA</repository></additional><is_claimable>false</is_claimable><name>The FLI portion of EWS/FLI contributes a transcriptional regulatory function that is distinct from its DNA-binding function in Ewing sarcoma [CUT&amp;RUN]</name><description>The FLI portion of EWS/FLI contributes a transcriptional regulatory function that is distinct from its DNA-binding function in Ewing sarcoma [CUT&amp;RUN]</description><dates><last_updated>2025-09-24</last_updated><first_public>2021-06-16</first_public></dates><accession>PRJNA674798</accession><cross_references><GEO>GSE160896</GEO><taxon>9606</taxon></cross_references></HashMap>