| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:41095644-41095786 | Rare:35 | ||||
| chr15:41299153-41299401 | Common:1; Rare:58 | ||||
| chr15:41301232-41301532 | Rare:56 | ||||
| chr15:41303758-41303783 | Rare:2 | ||||
| chr15:41304890-41305121 | Rare:37 | ||||
| chr15:41306266-41306482 | Common:1; Rare:46 | ||||
| chr15:41385665-41385853 | Rare:41 | ||||
| chr15:41418827-41418841 | Rare:3 | ||||
| chr15:41784812-41785206 | Common:2; Rare:62 | ||||
| chr15:42168106-42168371 | Common:1; Rare:41 | ||||
| chr15:42233959-42234098 | Rare:27 | ||||
| chr15:42287529-42287559 | Rare:7 | ||||
| chr15:42295401-42295564 | Common:1; Rare:33 | ||||
| chr15:42329067-42329364 | Common:1; Rare:74 | ||||
| chr15:42390014-42390228 | Common:2; Rare:65; Clinvar:6; Clinvar (benign):4; Clinvar (pathogenic):1 |