| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:74202939-74203150 | Common:1; Rare:45 | ||||
| chr15:74203169-74203357 | Common:1; Rare:27 | ||||
| chr15:74461077-74461319 | Common:1; Rare:74 | ||||
| chr15:74540966-74541278 | Common:4; Rare:111 | ||||
| chr15:74615671-74615902 | Common:3; Rare:71 | ||||
| chr15:74695932-74696064 | Rare:44 | ||||
| chr15:74889842-74890087 | Rare:75; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr15:74995314-74995616 | Common:5; Rare:110 | ||||
| chr15:75347341-75347631 | Rare:78 | ||||
| chr15:75368572-75368651 | Rare:37 | ||||
| chr15:75455764-75455980 | Rare:67 | ||||
| chr15:75578759-75578819 | Rare:21 | ||||
| chr15:75640181-75640399 | Common:1; Rare:69 | ||||
| chr15:75647864-75647925 | Rare:10 | ||||
| chr15:75648279-75648375 | Common:1; Rare:24 |