| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:55321670-55321916 | Rare:53 | ||||
| chr18:55322322-55322593 | Rare:58 | ||||
| chr18:55401684-55401995 | Rare:57 | ||||
| chr18:55588120-55588183 | Rare:17; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:55589757-55589968 | Common:2; Rare:68 | ||||
| chr18:56651124-56651421 | Common:4; Rare:78 | ||||
| chr18:56651608-56651714 | Common:4; Rare:25 | ||||
| chr18:57586554-57587015 | Common:1; Rare:114; Clinvar (benign):1 | ||||
| chr18:57621706-57621981 | Common:3; Rare:96 | ||||
| chr18:57803340-57803452 | Common:1; Rare:28 | ||||
| chr18:57803587-57803866 | Rare:55 | ||||
| chr18:58045408-58045747 | Common:5; Rare:85 | ||||
| chr18:59139727-59140035 | Common:3; Rare:83 | ||||
| chr18:59697589-59697852 | Common:2; Rare:69 | ||||
| chr18:59899849-59899997 | Common:3; Rare:44 |