| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:44288231-44288395 | Rare:26 | ||||
| chr15:44288611-44288789 | Common:1; Rare:51 | ||||
| chr15:44289120-44289283 | Common:1; Rare:44 | ||||
| chr15:44426847-44427312 | Common:1; Rare:127 | ||||
| chr15:44427427-44427732 | Common:1; Rare:74 | ||||
| chr15:44427749-44427950 | Common:2; Rare:55 | ||||
| chr15:44536388-44536927 | Common:1; Rare:117 | ||||
| chr15:44537003-44537266 | Common:2; Rare:103 | ||||
| chr15:44537369-44537418 | Rare:12 | ||||
| chr15:44537597-44537817 | Common:1; Rare:51 | ||||
| chr15:44663096-44663271 | Common:1; Rare:42 | ||||
| chr15:44663437-44663896 | Rare:203; Clinvar:15; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr15:44711250-44711623 | Rare:102; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44711839-44711944 | Rare:22 | ||||
| chr15:44712081-44712171 | Common:1; Rare:10 |