| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40845958-40846211 | Rare:64 | ||||
| chr15:40865725-40866432 | Common:12; Rare:265 | ||||
| chr15:40906542-40907756 | Common:10; Rare:390 | ||||
| chr15:40941150-40941690 | Common:5; Rare:161 | ||||
| chr15:40941710-40942210 | Common:6; Rare:313 | ||||
| chr15:41283748-41284104 | Common:6; Rare:240 | ||||
| chr15:41585570-41586140 | Common:3; Rare:105 | ||||
| chr15:41589270-41589990 | Rare:122 | ||||
| chr15:41661730-41662100 | Common:2; Rare:148 | ||||
| chr15:41862780-41863120 | Common:4; Rare:159 | ||||
| chr15:41925025-41925260 | Common:6; Rare:43 | ||||
| chr15:41928132-41928378 | Rare:47 | ||||
| chr15:42119025-42119219 | Common:3; Rare:34 | ||||
| chr15:42270594-42271040 | Common:3; Rare:163 | ||||
| chr15:42392410-42392810 | Common:4; Rare:109; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):5 |