A table of Human loci associated with Crohn's Disease. Cytogenetic bands are defined using data from UCSC genome browser, protein coding and non-coding genes were extracted from EnsEMBL v84. Hits were defined by taking the index variant as described in the listed publication. Starting at the variant of interest, the hit is extended out ±0.1cM. These hits are then merged together to form regions of the genome that are of interest to this disease.

The alleles shown are major allele > minor allele, with the odds ratio being defined for the risk allele. Other signals located in the same region as the primary signal have a pale yellow background and are shown in italics