| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:55585998-55586185 | Common:1; Rare:53 | ||||
| chr18:55588108-55588294 | Rare:44; Clinvar:3; Clinvar (benign):1 | ||||
| chr18:55588609-55588726 | Rare:19 | ||||
| chr18:56651133-56651421 | Common:4; Rare:77 | ||||
| chr18:56651507-56651705 | Common:4; Rare:44 | ||||
| chr18:57621713-57621920 | Common:2; Rare:77 | ||||
| chr18:57621926-57622016 | Common:1; Rare:31 | ||||
| chr18:58045395-58045946 | Common:6; Rare:132 | ||||
| chr18:58864799-58864907 | Rare:18 | ||||
| chr18:59139718-59139976 | Common:2; Rare:68 | ||||
| chr18:59697370-59697734 | Common:1; Rare:116; Clinvar:1 | ||||
| chr18:62186938-62187334 | Common:5; Rare:108 | ||||
| chr18:63367151-63367328 | Common:1; Rare:61 | ||||
| chr18:63422377-63422716 | Common:2; Rare:100 | ||||
| chr18:68714987-68715296 | Common:7; Rare:132 |