| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:43371043-43371117 | Rare:17 | ||||
| chr15:43510835-43510954 | Rare:33 | ||||
| chr15:43648751-43649021 | Common:3; Rare:118 | ||||
| chr15:43746261-43746459 | Common:2; Rare:73 | ||||
| chr15:43776961-43777071 | Rare:27 | ||||
| chr15:43777114-43777410 | Rare:65 | ||||
| chr15:44536863-44537401 | Common:3; Rare:198 | ||||
| chr15:44663543-44663694 | Rare:89; Clinvar:12; Clinvar (benign):6 | ||||
| chr15:44711346-44711611 | Rare:80; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:45252010-45252242 | Common:2; Rare:52 | ||||
| chr15:45378384-45378743 | Common:4; Rare:101; Clinvar:4; Clinvar (benign):11 | ||||
| chr15:45397278-45397482 | Rare:38 | ||||
| chr15:45402181-45402347 | Common:2; Rare:50 | ||||
| chr15:45587309-45587468 | Rare:46; Clinvar:4 | ||||
| chr15:48331367-48331453 | Rare:27 |