| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40694637-40694802 | Rare:43 | ||||
| chr15:40695006-40695443 | Common:4; Rare:128; Clinvar:1 | ||||
| chr15:40695483-40695570 | Common:2; Rare:25 | ||||
| chr15:40755205-40755357 | Common:2; Rare:50 | ||||
| chr15:40763762-40764105 | Common:3; Rare:79 | ||||
| chr15:40807050-40807125 | Rare:20 | ||||
| chr15:40807436-40807767 | Common:4; Rare:109 | ||||
| chr15:40894354-40894477 | Rare:45 | ||||
| chr15:41115982-41116109 | Rare:38 | ||||
| chr15:41230639-41230890 | Rare:74 | ||||
| chr15:41231132-41231371 | Rare:84 | ||||
| chr15:41402376-41402558 | Common:4; Rare:67; Clinvar:2; Clinvar (benign):1 | ||||
| chr15:41416959-41417311 | Common:4; Rare:128 | ||||
| chr15:41474566-41474689 | Rare:34 | ||||
| chr15:41477343-41477499 | Common:1; Rare:35 |