Human Whole Blood mQTL Atlas (CRIC)
Systematic integrated analysis of genetic and epigenetic varition in diabetic kidney disease
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Human Blood mQTL:
This table provides 12,354,191 significant SNP~CpG pairs identified by a false discovery rate (FDR) threshold of <0.05 (Storey’s q method) based on beta distribution-adjusted empirical p-values from FastQTL permutation.
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Human Blood MWAS with eGFR:
This table provides association between blood CpG methylation and kidney function maker eGFRcrea. P value was calculated by the mixed-effect model analysis using lmer in the lme4 package.
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Human Blood MWAS with eGFR slope:
This table provides association between blood CpG methylation and kidney function maker eGFRcrea slope. P value was calculated by the mixed-effect model analysis using lmer in the lme4 package.
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Human Blood MWAS with Hemoglobin A1c:
This table provides association between blood CpG methylation and kidney function maker Hemoglobin A1c. P value was calculated by the mixed-effect model analysis using lmer in the lme4 package.
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Human Blood MWAS with Albuminuria:
This table provides association between blood CpG methylation and kidney function maker Albuminuria. P value was calculated by the mixed-effect model analysis using lmer in the lme4 package.