| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40470653-40471110 | Common:2; Rare:126 | ||||
| chr15:40564574-40564690 | Rare:20 | ||||
| chr15:40564955-40565280 | Common:3; Rare:65 | ||||
| chr15:40569134-40569404 | Common:3; Rare:67 | ||||
| chr15:40569728-40569849 | Common:1; Rare:34 | ||||
| chr15:40593906-40594043 | Common:1; Rare:63 | ||||
| chr15:40594206-40594407 | Common:1; Rare:47; Clinvar (benign):1 | ||||
| chr15:40594501-40594617 | Common:1; Rare:31 | ||||
| chr15:40594638-40594829 | Common:2; Rare:52 | ||||
| chr15:40694555-40695251 | Common:2; Rare:204 | ||||
| chr15:40755162-40755604 | Common:4; Rare:138 | ||||
| chr15:40763921-40764140 | Rare:60 | ||||
| chr15:40769766-40770006 | Rare:48 | ||||
| chr15:40806990-40807234 | Common:1; Rare:60 | ||||
| chr15:40807354-40807815 | Common:5; Rare:146 |