| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:23038870-23039264 | Common:5; Rare:117 | ||||
| chr15:23039305-23039346 | Common:1; Rare:15 | ||||
| chr15:23039471-23039835 | Common:1; Rare:151 | ||||
| chr15:23039986-23040026 | Common:1; Rare:14 | ||||
| chr15:23565389-23565778 | Common:2; Rare:111 | ||||
| chr15:23565880-23566008 | Rare:59 | ||||
| chr15:23566045-23566401 | Rare:153; Clinvar (pathogenic):1 | ||||
| chr15:24954971-24955062 | Rare:48 | ||||
| chr15:25438159-25438295 | Rare:41 | ||||
| chr15:25438396-25438822 | Common:2; Rare:117; Clinvar (benign):1 | ||||
| chr15:25438902-25439342 | Common:3; Rare:155 | ||||
| chr15:28098948-28099029 | Rare:16 | ||||
| chr15:28099295-28099546 | Common:2; Rare:88; Clinvar:1 | ||||
| chr15:29269573-29269952 | Common:5; Rare:169 | ||||
| chr15:29821445-29821778 | Rare:103 |