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. 2015 May 20;5:10442. doi: 10.1038/srep10442

Figure 1. Genome-wide P-values (–log10P, y-axis) plotted against their respective chromosomal positions (x-axis).

Figure 1

Known regions attaining genome-wide significance (i.e. P = 5.0 × 10−8) are labelled with their chromosomal location. Variants in grey lie in novel regions that reach the significance threshold level (P = 1.0 × 10−7) required for variants to be analysed further in this study. Variants in black lie in novel regions attaining genome-wide significance.