| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:35546139-35546269 | Common:1; Rare:45 | ||||
| chr15:36579536-36579673 | Common:2; Rare:29 | ||||
| chr15:37100423-37100781 | Common:1; Rare:119 | ||||
| chr15:37101295-37101499 | Common:25; Rare:78 | ||||
| chr15:39580843-39581236 | Common:2; Rare:109 | ||||
| chr15:39588214-39588699 | Common:3; Rare:113; Clinvar (benign):2 | ||||
| chr15:39592997-39593668 | Common:3; Rare:149; Clinvar (benign):1 | ||||
| chr15:40039050-40039329 | Rare:119 | ||||
| chr15:40405609-40405830 | Common:2; Rare:66; Clinvar (benign):3; Clinvar (pathogenic):3 | ||||
| chr15:40695081-40695180 | Rare:26 | ||||
| chr15:40755202-40755346 | Common:2; Rare:50 | ||||
| chr15:40807049-40807125 | Rare:20 | ||||
| chr15:40807421-40807767 | Common:4; Rare:117 | ||||
| chr15:40953221-40953475 | Common:1; Rare:69 | ||||
| chr15:41402450-41402554 | Common:2; Rare:34 |