Genomic responses to hepatitis B virus (HBV) infection in primary human hepatocytes.

In two of them (Xu et al 2013 and Ding et al 2012), DMPs were slightly more distant to HBV integration sites compared to a randomly generated list of genomic locations (Figure 5C ), although these differences did not reach statistical significance.

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Taking together all differentially expressed genes across all time points, we found a highly significant enrichment in HNF4A targets, using the ChEA database (overlap of 1045 differentially expressed genes to 6083 genes in the HNF4 dataset) ( Table S2 ).

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