| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:41402438-41402538 | Common:3; Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
| chr15:41416978-41417313 | Common:3; Rare:120 | ||||
| chr15:41827906-41828186 | Common:4; Rare:107 | ||||
| chr15:41972506-41972817 | Common:2; Rare:91 | ||||
| chr15:42273045-42273275 | Common:1; Rare:98 | ||||
| chr15:42273384-42273633 | Common:1; Rare:92 | ||||
| chr15:42409801-42409951 | Common:2; Rare:66; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr15:42491002-42491214 | Common:1; Rare:67 | ||||
| chr15:42495508-42495694 | Common:2; Rare:56 | ||||
| chr15:42548713-42548875 | Common:2; Rare:90 | ||||
| chr15:42575520-42575707 | Common:1; Rare:67 | ||||
| chr15:42737107-42737353 | Common:1; Rare:82; Clinvar:1 | ||||
| chr15:43106018-43106231 | Rare:67 | ||||
| chr15:43330535-43330772 | Common:1; Rare:81 | ||||
| chr15:43371030-43371152 | Common:1; Rare:29 |