Bigwig files for Med8 ChIP-seq on Col-0 (wild-type) and med18 (lacking Mediator subunit 18) plants.

The raw sequencing reads were processed using the nf-core/chipseq pipeline for initial quality control and alignment. Peak calling was performed with the narrow peak option, applying a maximum false discovery rate (FDR) of 0.001. The Arabidopsis TAIR10 genome was used as the reference. The resulting BAM files were then normalized for library size using the bamCoverage tool from the deepTools suite, with normalization performed using the reads per genome coverage (RPGC) option to generate normalized bigWig files.