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. 2018 Apr 18;4(4):eaar8187. doi: 10.1126/sciadv.aar8187

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Copyright © 2018 The Authors, some rights reserved; exclusive licensee American Association for the Advancement of Science. No claim to original U.S. Government Works. Distributed under a Creative Commons Attribution NonCommercial License 4.0 (CC BY-NC).

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Fig. 3 — The data under analysis were generated with 1000 nuclei per assay using samples from mouse M3. (A) SurfaceChIP-seq signals around Snap25 gene for all four cell populations. (B) H3K4me3, H3K27ac, and H3K27me3 coverage in intergenic regions relative to intragenic regions (genebody). The pair-wise comparisons of H3K4me3, H3K27ac, and H3K27me3 for four cell populations show significant difference (P < 0.01), except PNeuN+/CNeuN+ and CNeuN+/CNeuN− on H3K4me3 mark and PNeuN+/CNeuN+ on H3K27ac mark. (C) Distributions of differentially marked regions in various genomic features.