| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43824573-43824803 | Common:2; Rare:67 | ||||
| chr15:44288386-44288785 | Common:39; Rare:229 | ||||
| chr15:44427433-44427722 | Common:1; Rare:70 | ||||
| chr15:44536663-44537192 | Common:1; Rare:160 | ||||
| chr15:44663562-44663816 | Rare:129; Clinvar:11; Clinvar (benign):6 | ||||
| chr15:44711336-44711611 | Rare:84; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44712616-44712855 | Rare:61 | ||||
| chr15:45129850-45130017 | Rare:37 | ||||
| chr15:45378456-45378552 | Common:1; Rare:29; Clinvar:1; Clinvar (benign):6 | ||||
| chr15:45522545-45522661 | Rare:28 | ||||
| chr15:45587093-45587265 | Rare:32 | ||||
| chr15:45587304-45587470 | Rare:49; Clinvar:6 | ||||
| chr15:45587703-45587831 | Common:1; Rare:30 | ||||
| chr15:45634872-45635084 | Rare:57 | ||||
| chr15:47718183-47718282 | Rare:22 |