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. Author manuscript; available in PMC: 2021 Mar 27.
Published in final edited form as: Circ Res. 2020 Feb 17;126(7):875–888. doi: 10.1161/CIRCRESAHA.119.316075

Figure 1. Genome-wide identification of artery and vein enhancers.

Figure 1.

A, Volcano plot of HUAEC/HUVEC RNAseq. Red and blue indicates significantly-enriched HUAEC- and HUVEC-specific genes, respectively (log2 fold change >= 1, or <=−1, padj <=0.01). Grey indicates genes that are not significantly changed. Selected artery- and vein-specific genes are noted. B, Binding affinity heat map showing normalized read density (score) of replicate acEP300 and H3K27ac ChIP-seq samples from HUAEC and HUVEC. Only features with FDR<0.01 are shown. C, Pie charts showing distribution of HUAEC, HUVEC and common elements at inter/intragenic regions, transcriptional start sites (TSS) or heterochromatin/centromeric regions. D, Proportion of indicated elements concordant to DNAseI hypersensitivity I sites (DHS) from human microvascular endothelial cells (HMVEC) or T helper cells (Th1). E,F, Plots showing relationship between fold-enrichment in HUAEC or HUVEC and number of flanking E, artery-specific, or F, vein-specific enhancers. r and P values from Pearson Correlation are shown. H, I, Selected over-represented sites in H, vein-specific or I, artery-specific enhancers. Also see Online Tables V and VI.