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ajmgb32168-sm-0001-SupFig-S1.docx169K

Figure S1. Venn diagram showing the breakdown of the sample by Illumina genotyping platform.

ajmgb32168-sm-0001-SupFig-S2.tiff66KSupporting Information.
ajmgb32168-sm-0001-SupFig-S3.tif10477KSupporting Information.
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ajmgb32168-sm-0001-SupFig-S8.tiff65KSupporting Information.
ajmgb32168-sm-0001-SupFig-S9.tif10480KSupporting Information.
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ajmgb32168-sm-0001-SupFig-S11.tiff64KSupporting Information.
ajmgb32168-sm-0001-SupFig-S12.tif10480KSupporting Information.
ajmgb32168-sm-0001-SupFig-S13.tif10480KSupporting Information.
ajmgb32168-sm-0001-SupData.docx100KSupporting Information
ajmgb32168-sm-0001-SupTab-S1.docx45K

Table S1. Correlation between the six variables analysed. All correlations were significant with P < 0.01.

ajmgb32168-sm-0001-SupTab-S2.docx46K

Table S2. Power to detect variants with sample size used in present study explaining different proportions of the phenotypic variance in a phenotype with total heritability of 30%. Calculations assume that causal variant is directly genotyped or is tagged by a SNP in complete LD and with the same minor allele frequency.

ajmgb32168-sm-0001-SupTab-S3.docx77K

Table S3. Results from ingenuity pathway analysis of sleep traits showing the number of genes with P < 0.05 from gene-based test and top functions and pathways.

ajmgb32168-sm-0001-SupTab-S4.docx136K

Table S4. SNPs in or near candidate genes for sleep/wake regulation with P < 0.001.

ajmgb32168-sm-0001-SupTab-S5.docx62K

Table S5. SNPs listed as most strongly associated from Gottlieb et al that show nominal association with sleep traits analysed out of 34 SNPs genotyped or imputed in present sample.

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