[galaxy-user] Chip-Seq, Encode Peaks and Galaxy

From Encode download page, i got some files corresponding to peaks of these hsitone modifications and would like to know if there is a way to create a

Hi everyone, I have a list of genomic regions with some variants and would like to study the correlation between theses variants and epigenomics marks such as histone modifications. pipeline using galaxy to map my variants, depending on genomic regions to the information I have from the histone modification peaks. Is there someone who can point me to a step by step to do things to start using Galaxy ? Thank you Rad