Additional data file 3.

PCR primers were designed for nine regions in selected clusters and six negative regions without enrichment in CpG islands. Data are relative fold enrichments, calculated by determining the apparent immunoprecipitation efficiency and normalized to the level observed at a control region (mean ± standard deviation, n = 2).

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Kubosaki et al. Genome Biology 2009 10:R41   doi:10.1186/gb-2009-10-4-r41