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. 2021 Jul 22;11:403. doi: 10.1038/s41398-021-01493-6

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© The Author(s) 2021

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

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Fig. 5 — A Motifs overrepresented among ATRA-independent (allele effect without interaction) SNPs (left columns) or among ATRA-dependent (interaction) SNPs (right column). The heatmap is shown in halves for visibility. TFs identified as ATRA-upregulated in human neuroblastoma lines [104] are in bold font. B TFs implicated by ATRA-interacting SNPs significantly overlap TFs enriched in serotonergic neurons. Plot generated using the cell-specific expression analysis (CSEA) tool (http://genetics.wustl.edu/jdlab/csea-tool-2/) [32]. 5HT serotonin, ACh acetylcholine, ODC oligodendrocyte, OPC oligodendrocyte progenitor.