| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:23525766-23525835 | Rare:17 | ||||
| chr18:23563742-23563810 | Common:2; Rare:13 | ||||
| chr18:23907567-23907842 | Rare:76; Clinvar (pathogenic):1 | ||||
| chr18:24161287-24161574 | Common:1; Rare:72 | ||||
| chr18:24171260-24171493 | Common:1; Rare:40 | ||||
| chr18:24190053-24190339 | Common:1; Rare:53 | ||||
| chr18:24291803-24291951 | Common:1; Rare:21 | ||||
| chr18:25089313-25089519 | Rare:44 | ||||
| chr18:25100410-25100587 | Common:2; Rare:24 | ||||
| chr18:25100696-25100807 | Common:1; Rare:25 | ||||
| chr18:25137387-25137626 | Common:2; Rare:39 | ||||
| chr18:25148837-25149034 | Common:3; Rare:37 | ||||
| chr18:25150821-25150869 | Rare:10 | ||||
| chr18:25160944-25161202 | Common:1; Rare:42 | ||||
| chr18:25174206-25174284 | Rare:16 |