Skip to main content
Log in

12 Impact of functional information on understanding variation

  • Thread
  • Published:

From Nature

View current issue Submit your manuscript

ENCODE provides an initial interpretation of many human variants and plausible leads for the role of many variants identified in genome-wide association studies

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Figure 10: Comparison of genome-wide-association-study-identified loci with ENCODE data.
Figure 2: Individual variation of the binding sites for 15 Drosophila and 36 human TFs selected for this study.
Figure 5: Allelic Effects
Supplementary Figure S2: Web-based Interface
Figure 4: TNFAIP3-associated SNV
Figure 7: Genetic variation in regulatory DNA linked to mutation rate.
Figure 1: Schematic overview of the functional SNP approach.
Figure 2: Proportions of associations for different types of functional data.
Figure 3: Overview of enrichment for different combinations of assays.
Figure 4: Phenotype level overview of the overlap between associations and ChIP-seq binding.
Figure 6: Functional information and linkage disequilibrium patterns support the implication of rs1333047 in coronary artery disease.
Figure 2: Characteristics of regulatory variation among individuals.
Figure 3: Significant variation of diversity between 732 cis-regulatory motifs.
Figure 6: Genome-wide distribution of population structure in regulatory DNA.

Rights and permissions

Reprints and permissions

About this article

Check for updates. Verify currency and authenticity via CrossMark

Cite this article

12 Impact of functional information on understanding variation. Nature (2019). https://doi.org/10.1038/nature28181

Download citation

  • Published:

  • DOI: https://doi.org/10.1038/nature28181

  • Springer Nature Limited

Navigation