Analysis of transcription factor binding sites in the DNA sequences surrounding SNPs rs4495224 and rs7720838 applying the program TFsearch.

Note:#Nucleotides in the genomic sequences according with the consensus sequences are underlined and the polymorphic nucleotide is marked in bold.‡Predicted binding scores differing more than 5 points between CD risk alleles and protective alleles are depicted in bold. Scores differing 10 points and more are depicted in bold italic. Binding score threshold for each allele was set to 75.0. Nucleotide codes: K = G or T, M = A or C, R = A or G, S = C or G, W = A or T, Y = C or T, N = A, G, C or T.