The data come from an H3K27ac ChIP-seq experiment which was aligned to the human reference genome (hg19), aligned read counts were used to produce the coverage data; looking at these data in a genome browser was used to produce the labels.
data("Mono27ac")
A list of 2 data.tables: coverage has 4 columns (chrom, chromStart, chromEnd, count=number of aligned reads at each position on chrom:chromStart-chromEnd); labels has 4 columns (chrom, chromStart, chromEnd, annotation=label at chrom:chromStart-chromEnd).