| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:30903787-30903958 | Rare:77 | ||||
| chr15:30991504-30991789 | Common:8; Rare:175 | ||||
| chr15:31326340-31326910 | Common:8; Rare:489 | ||||
| chr15:31327910-31328240 | Common:1; Rare:215 | ||||
| chr15:32615073-32615535 | Common:10; Rare:211 | ||||
| chr15:34038408-34038711 | Common:12; Rare:148 | ||||
| chr15:34039036-34039347 | Common:4; Rare:94 | ||||
| chr15:34101779-34102133 | Common:2; Rare:143 | ||||
| chr15:34224856-34225139 | Rare:143 | ||||
| chr15:34318757-34318933 | Common:2; Rare:40 | ||||
| chr15:34343079-34343280 | Common:4; Rare:57; Clinvar:2; Clinvar (benign):1 | ||||
| chr15:34367120-34367360 | Common:4; Rare:199 | ||||
| chr15:34582803-34582912 | Rare:35 | ||||
| chr15:34583534-34583733 | Common:6; Rare:118 | ||||
| chr15:34588438-34588595 | Rare:84 |