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. 2017 Nov 30;7:1263. doi: 10.1038/s41398-017-0010-9

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© The Author(s) 2017

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. 2 — Regional association plot representing the –log₁₀ P-values for an association between haplotypes in the Generation Scotland: Scottish Family Health Study cohort and Major Depressive Disorder within the 107.4–107.6 Mb region on chromosome 6. The start and end position (using build GRCh37) of haplotypes represent the outermost SNP positions within the windows examined. The warmth of colour represents the r ² with the genome-wide significant haplotype located between 108,338,267 and 108,454,437 bp