| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:37101280-37101411 | Common:23; Rare:58 | ||||
| chr15:39588711-39589022 | Common:1; Rare:84 | ||||
| chr15:39592762-39593476 | Common:3; Rare:156; Clinvar (benign):1 | ||||
| chr15:39782779-39782919 | Rare:40 | ||||
| chr15:39920880-39921031 | Common:3; Rare:59 | ||||
| chr15:40020645-40020984 | Common:4; Rare:70; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr15:40038848-40039354 | Common:2; Rare:179 | ||||
| chr15:40340838-40340997 | Common:2; Rare:55 | ||||
| chr15:40695050-40695258 | Common:2; Rare:63 | ||||
| chr15:40807050-40807158 | Common:1; Rare:36 | ||||
| chr15:40807372-40807833 | Common:5; Rare:150 | ||||
| chr15:40953228-40953477 | Common:1; Rare:69 | ||||
| chr15:41115982-41116038 | Rare:20 | ||||
| chr15:41402401-41402563 | Common:4; Rare:64; Clinvar:2; Clinvar (benign):1 | ||||
| chr15:41416995-41417282 | Common:2; Rare:110 |