Seventeen genes with the strong evidence for association with Crohn's Disease risk in WTCCC and one or both of Non-Jewish and Jewish dbGap GWASs, with chromosomal locations, numbers of SNPs, approximate p-values, and Bayes factors.

**indicates genes in the chromosomal locations where the WTCCC single-SNP analysis showed strong evidence.+indicates chromosomal locations are those with three or more genes in the 195 genes (see Table S1) showing strong evidence in our WTCCC logic-regression-based analysis, but without strong or moderate evidence in the single-SNP analysis of WTCCC.

指示WTCCC单核苷酸分析中显示出强烈证据的染色质位置中的基因。+表示的染色质位置包含195个基因中的三个或更多基因，这些基因在我们的基于WTCCC逻辑回归分析中显示出强烈证据，但在WTCCC的单核苷酸分析中并未显示出强烈或中等的证据（参见表S1）。