Fig. 4
From: Enhancer prediction in the human genome by probabilistic modelling of the chromatin feature patterns
The unique and overlapping genome-wide enhancer predictions obtained by different methods in cell line K562. In comparisons a and c, the PREPRINT predictions were obtained by the ML approach whereas in comparisons b and d, the PREPRINT predictions were obtained by the Bayesian approach. The overlap between the PREPRINT, RFECS and ChromHMM predictions were quantified as the number of enhancers. In each comparison, the number of enhancers predicted by PREPRINT and RFECS was equal. The numbers were: a 15531, b 15786, c 35089, and d 35089. Inside every region or intersection, the number of enhancers in the given the set is indicated together with the percentage of validated enhancers in the set. The areas of the intersection sets are not proportional to the number of overlapping regions due to the asymmetry of overlaps