| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:29822500-29822602 | Common:2; Rare:34 | ||||
| chr15:30991538-30991565 | Rare:8 | ||||
| chr15:30991569-30991789 | Common:4; Rare:77 | ||||
| chr15:31326740-31326901 | Rare:64 | ||||
| chr15:32615090-32615210 | Common:3; Rare:34 | ||||
| chr15:32615380-32615534 | Common:3; Rare:40 | ||||
| chr15:32684203-32684453 | Common:1; Rare:53 | ||||
| chr15:33068171-33068447 | Common:2; Rare:66 | ||||
| chr15:34039030-34039347 | Common:4; Rare:96 | ||||
| chr15:34101661-34102123 | Common:2; Rare:119 | ||||
| chr15:34145645-34145829 | Common:3; Rare:24 | ||||
| chr15:34224904-34225198 | Rare:99 | ||||
| chr15:34238433-34238715 | Rare:50 | ||||
| chr15:34240757-34240945 | Rare:50; Clinvar:1; Clinvar (benign):1 | ||||
| chr15:34318586-34318947 | Common:2; Rare:86; Clinvar (benign):2 |