| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr18:50374877-50375137 | Common:3; Rare:84 | ||||
| chr18:50879000-50879299 | Common:4; Rare:97 | ||||
| chr18:51030017-51030233 | Rare:72 | ||||
| chr18:51196881-51196957 | Common:1; Rare:27 | ||||
| chr18:54357875-54358080 | Common:7; Rare:55 | ||||
| chr18:54828286-54828489 | Rare:45 | ||||
| chr18:55302517-55302815 | Common:1; Rare:46 | ||||
| chr18:55321576-55321938 | Rare:81 | ||||
| chr18:55322216-55322544 | Common:1; Rare:62 | ||||
| chr18:55401611-55401825 | Rare:45 | ||||
| chr18:55401978-55402177 | Common:1; Rare:34 | ||||
| chr18:55588095-55588261 | Rare:38; Clinvar:1; Clinvar (benign):1 | ||||
| chr18:55589586-55589904 | Rare:82 | ||||
| chr18:56651122-56651382 | Common:3; Rare:64 | ||||
| chr18:57802990-57803122 | Common:2; Rare:34; Clinvar:2; Clinvar (benign):2 |