| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40569201-40569332 | Common:3; Rare:23 | ||||
| chr15:40695056-40695200 | Rare:40 | ||||
| chr15:40755220-40755424 | Common:2; Rare:66 | ||||
| chr15:40763921-40764087 | Rare:44 | ||||
| chr15:40806807-40807119 | Common:4; Rare:54 | ||||
| chr15:40807436-40807761 | Common:4; Rare:107 | ||||
| chr15:40894361-40894477 | Rare:41 | ||||
| chr15:41231206-41231379 | Rare:57 | ||||
| chr15:41402427-41402558 | Common:4; Rare:47; Clinvar:1; Clinvar (benign):1 | ||||
| chr15:41416976-41417202 | Common:3; Rare:101 | ||||
| chr15:41544243-41544339 | Rare:39 | ||||
| chr15:41621419-41621552 | Common:1; Rare:30 | ||||
| chr15:41621971-41622068 | Common:1; Rare:26 | ||||
| chr15:41660302-41660493 | Rare:62 | ||||
| chr15:42208248-42208404 | Rare:52 |