| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43371021-43371121 | Rare:22 | ||||
| chr15:43510688-43511067 | Rare:142 | ||||
| chr15:43648709-43649030 | Common:3; Rare:136 | ||||
| chr15:43746275-43746704 | Common:2; Rare:172 | ||||
| chr15:43776933-43777100 | Common:1; Rare:51 | ||||
| chr15:43777114-43777409 | Rare:65 | ||||
| chr15:43792669-43793083 | Rare:121 | ||||
| chr15:43824586-43824805 | Common:2; Rare:62 | ||||
| chr15:44288396-44288785 | Common:39; Rare:228 | ||||
| chr15:44536663-44537401 | Common:3; Rare:242 | ||||
| chr15:44575358-44575534 | Rare:38 | ||||
| chr15:44598043-44598225 | Rare:34 | ||||
| chr15:44663532-44663827 | Rare:143; Clinvar:13; Clinvar (benign):6 | ||||
| chr15:44711257-44711627 | Rare:102; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44711849-44711977 | Rare:25 |