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[Preprint]. 2024 Jan 18:2024.01.06.573649. [Version 2] doi: 10.1101/2024.01.06.573649

Figure 6: Effects of Phf6 loss on chromatin accessibility in LIC-e cells.

Figure 6:

A, Volcano plot showing differentially accessible regions in LIC-e cells from cKO+Hoxa9 compared Ctrl+Hoxa9. (n = 3 biological replicates)

B, Representative signal profile (left) and metagene plots (right) showing genome-wide intensity of ATAC signal in Ctrl+Hoxa9 and cKO+Hoxa9 LIC-e cells.

C, HOMER analysis for regions of decreased chromatin accessibility in cKO+Hoxa9 LIC-e cells, showing enrichment of AP-1, HOX, GATA, SPI1, and MAF motifs.

D, Representative metagene plots at regions of decreased chromatin accessibility in cKO+Hoxa9 LIC-e, show ChIP-Seq signal for select proteins whose motifs are seen to be enriched through HOMER in (C).

E, HOMER analysis for regions of increased chromatin accessibility in cKO+Hoxa9 LIC-e cells showing enrichment of NF-kB and IRF motifs.

F, Representative metagene plots at regions of increased chromatin accessibility in cKO+Hoxa9 LIC-e, show ChIP-Seq signal for select proteins whose motifs are seen to be enriched through HOMER in (E).

Publicly available ChIP-Seq datasets in leukemia or myeloid cells were used in metagene heatmaps (Table S3). All plots were centered around ATAC-Seq peaks. SeqPlots was used to draw all metagene plots.