| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:29629760-29629850 | Rare:16 | ||||
| chr18:29724182-29724308 | Common:1; Rare:35 | ||||
| chr18:30419459-30419615 | Common:1; Rare:56 | ||||
| chr18:30838740-30838869 | Common:1; Rare:31 | ||||
| chr18:31401627-31401724 | Rare:20 | ||||
| chr18:31556946-31557012 | Rare:13 | ||||
| chr18:31724109-31724215 | Common:1; Rare:16 | ||||
| chr18:32111686-32111846 | Common:2; Rare:33 | ||||
| chr18:32140550-32140645 | Rare:15 | ||||
| chr18:32511571-32511681 | Common:2; Rare:36 | ||||
| chr18:32833364-32833470 | Rare:10 | ||||
| chr18:34820546-34820823 | Common:2; Rare:52; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:35271164-35271377 | Common:2; Rare:53 | ||||
| chr18:35376159-35376411 | Common:1; Rare:43 | ||||
| chr18:35683187-35683598 | Rare:85 |