| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40105417-40105531 | Common:1; Rare:19 | ||||
| chr15:40115908-40116038 | Common:1; Rare:31 | ||||
| chr15:40308594-40308622 | Rare:7 | ||||
| chr15:40471765-40471829 | Rare:15; Clinvar (benign):1 | ||||
| chr15:40511105-40511490 | Common:1; Rare:65 | ||||
| chr15:40511794-40511864 | Rare:19 | ||||
| chr15:40543840-40543904 | Common:1; Rare:8 | ||||
| chr15:40553685-40553727 | Rare:2 | ||||
| chr15:40554113-40554376 | Common:1; Rare:42 | ||||
| chr15:40558158-40558312 | Rare:21 | ||||
| chr15:40693843-40694084 | Common:2; Rare:60 | ||||
| chr15:40847411-40847591 | Common:1; Rare:46 | ||||
| chr15:40872248-40872406 | Rare:29 | ||||
| chr15:40940070-40940136 | Rare:9 | ||||
| chr15:40941639-40942185 | Common:2; Rare:158 |