Figure 1.
Overview of Smarca4FLAG mouse generation and SMARCA4 binding site mapping in vivo. A knock-in mouse strain carrying a FLAG epitope at the carboxy terminus of SMARCA4 was engineered and used to perform ChIP-seq from a panel of embryonic tissues. For each ChIP-seq data set, the total number of identified enriched SMARCA4 regions is indicated near the corresponding coverage map (schematics).
