| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43371039-43371127 | Rare:19 | ||||
| chr15:43510590-43510979 | Rare:128 | ||||
| chr15:43517462-43517678 | Common:2; Rare:54 | ||||
| chr15:43648715-43649022 | Common:3; Rare:132 | ||||
| chr15:43746271-43746464 | Common:1; Rare:72 | ||||
| chr15:43776961-43777112 | Rare:44 | ||||
| chr15:43777116-43777409 | Rare:65 | ||||
| chr15:44288366-44288785 | Common:39; Rare:231 | ||||
| chr15:44536670-44537418 | Common:3; Rare:244 | ||||
| chr15:44711341-44711611 | Rare:83; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44711849-44712020 | Rare:33 | ||||
| chr15:45114149-45114326 | Common:2; Rare:36 | ||||
| chr15:45200492-45200656 | Common:1; Rare:46 | ||||
| chr15:45201096-45201151 | Common:1; Rare:26 | ||||
| chr15:45378482-45378717 | Common:3; Rare:63; Clinvar:1; Clinvar (benign):3 |