| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:40350787-40351089 | Common:2; Rare:65 | ||||
| chr15:40694595-40694777 | Rare:47 | ||||
| chr15:40695050-40695214 | Rare:47 | ||||
| chr15:40763802-40764119 | Common:3; Rare:76 | ||||
| chr15:40770200-40770258 | Rare:11 | ||||
| chr15:40806901-40807149 | Common:2; Rare:59 | ||||
| chr15:40807388-40807805 | Common:5; Rare:136 | ||||
| chr15:40809148-40809351 | Rare:56 | ||||
| chr15:40828662-40828925 | Rare:41 | ||||
| chr15:40843757-40844092 | Common:5; Rare:95 | ||||
| chr15:40844255-40844530 | Rare:76 | ||||
| chr15:40853687-40853731 | Common:1; Rare:12 | ||||
| chr15:40855952-40856333 | Common:4; Rare:103 | ||||
| chr15:41231206-41231514 | Rare:94; Clinvar (pathogenic):1 | ||||
| chr15:41402450-41402558 | Common:2; Rare:35 |