| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:45114170-45114326 | Common:2; Rare:28 | ||||
| chr15:45378481-45378766 | Common:4; Rare:75; Clinvar:2; Clinvar (benign):4 | ||||
| chr15:45522568-45522672 | Rare:26 | ||||
| chr15:45587090-45587273 | Rare:33 | ||||
| chr15:45587288-45587628 | Common:1; Rare:115; Clinvar:7; Clinvar (benign):3 | ||||
| chr15:45634668-45634835 | Common:1; Rare:41 | ||||
| chr15:47717174-47717474 | Common:1; Rare:61 | ||||
| chr15:48331367-48331465 | Rare:32 | ||||
| chr15:48645310-48645415 | Common:1; Rare:32 | ||||
| chr15:48645668-48645908 | Common:2; Rare:77; Clinvar (benign):1 | ||||
| chr15:48878017-48878308 | Rare:106 | ||||
| chr15:49155543-49155842 | Common:2; Rare:98 | ||||
| chr15:49620769-49621121 | Common:6; Rare:133 | ||||
| chr15:50354703-50355018 | Rare:94 | ||||
| chr15:50355074-50355501 | Common:3; Rare:168 |