| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:51030580-51030910 | Common:5; Rare:209; Clinvar:4; Clinvar (benign):8 | ||||
| chr18:51197351-51198119 | Rare:392 | ||||
| chr18:54224446-54224807 | Common:2; Rare:181 | ||||
| chr18:54269424-54269634 | Common:5; Rare:173 | ||||
| chr18:54357856-54357965 | Common:5; Rare:33 | ||||
| chr18:54357869-54357973 | Common:4; Rare:29 | ||||
| chr18:54358051-54358453 | Common:3; Rare:80 | ||||
| chr18:54959347-54959563 | Common:3; Rare:95 | ||||
| chr18:56651129-56651417 | Common:6; Rare:107 | ||||
| chr18:56651430-56651820 | Common:9; Rare:154 | ||||
| chr18:57435115-57435415 | Rare:156 | ||||
| chr18:57586451-57587251 | Common:2; Rare:239; Clinvar (benign):1 | ||||
| chr18:57621710-57621977 | Common:6; Rare:184 | ||||
| chr18:58043942-58044435 | Common:9; Rare:331 | ||||
| chr18:58221381-58221590 | Common:1; Rare:38 |