Figure 2 shows the PPARG genomic information displayed using the HapMap Genome Browser (step 6). Multiple types of information can be visualised and downloaded by using the combobox under ‘Reports & Analysis’ and the controls under the plot window. Useful features to look at are copy number variations (CNVs) and results from previously published GWA studies by default presented as separate tracks in the plot. By clicking on the question mark beside the ‘GWA studies (NHGRI Catalog)’ label it is possible to get directly linked to published GWA studies.
