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. 2021 Jan 12;11:504. doi: 10.1038/s41598-020-79990-9

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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 licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence 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 licence, visit http://creativecommons.org/licenses/by/4.0/.

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Study design and systematic identification of transcribed single nucleotide polymorphisms (SNPs) suitable for allelic expression analysis of Parkinson’s disease (PD) risk loci. PD genome-wide associated risk SNPs were taken from Nalls et al.⁵ and proxy SNPs were identified in the HaploReg database v4.1. Adapted from Locke et al.¹⁹. Ct cycle threshold.