| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43777114-43777409 | Rare:65 | ||||
| chr15:43824641-43824805 | Common:2; Rare:43 | ||||
| chr15:44427563-44427660 | Rare:29 | ||||
| chr15:44536886-44537187 | Common:1; Rare:105 | ||||
| chr15:44711300-44711612 | Rare:92; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44728869-44729138 | Common:1; Rare:53 | ||||
| chr15:45023052-45023246 | Common:3; Rare:52 | ||||
| chr15:45378542-45378680 | Common:3; Rare:35; Clinvar (benign):1 | ||||
| chr15:45587262-45587273 | Rare:2 | ||||
| chr15:45587321-45587474 | Rare:47; Clinvar:4 | ||||
| chr15:45587553-45587763 | Common:1; Rare:72 | ||||
| chr15:48878059-48878163 | Rare:36 | ||||
| chr15:49046441-49046605 | Common:2; Rare:55 | ||||
| chr15:49155574-49155832 | Common:2; Rare:90 | ||||
| chr15:49169971-49170269 | Rare:69 |