| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40002406-40002631 | Common:1; Rare:26 | ||||
| chr15:40039095-40039350 | Rare:198 | ||||
| chr15:40106457-40106800 | Common:8; Rare:113 | ||||
| chr15:40160754-40161146 | Common:9; Rare:154 | ||||
| chr15:40358000-40358300 | Common:9; Rare:118 | ||||
| chr15:40382784-40383010 | Common:1; Rare:117 | ||||
| chr15:40405565-40405839 | Common:4; Rare:157; Clinvar:1; Clinvar (benign):8; Clinvar (pathogenic):6 | ||||
| chr15:40440783-40441213 | Rare:201 | ||||
| chr15:40470700-40471110 | Rare:177 | ||||
| chr15:40564983-40565273 | Common:6; Rare:104 | ||||
| chr15:40594206-40594308 | Rare:25 | ||||
| chr15:40649900-40650310 | Common:4; Rare:80 | ||||
| chr15:40694490-40694870 | Rare:191 | ||||
| chr15:40695050-40695239 | Common:4; Rare:110 | ||||
| chr15:40755189-40755407 | Common:6; Rare:139 |