| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr15:42273400-42273653 | Rare:93 | ||||
| chr15:42457091-42457393 | Common:1; Rare:65 | ||||
| chr15:42491005-42491252 | Common:1; Rare:72 | ||||
| chr15:42495508-42495708 | Common:2; Rare:61 | ||||
| chr15:42548702-42548875 | Common:2; Rare:92 | ||||
| chr15:43330611-43330711 | Rare:33 | ||||
| chr15:43371030-43371196 | Common:1; Rare:38 | ||||
| chr15:43510671-43511108 | Rare:169 | ||||
| chr15:43777116-43777403 | Rare:65 | ||||
| chr15:43824655-43824889 | Common:2; Rare:60 | ||||
| chr15:44427269-44427653 | Common:1; Rare:96 | ||||
| chr15:44536852-44537215 | Common:2; Rare:129 | ||||
| chr15:44711318-44711612 | Rare:88; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr15:44728849-44729140 | Common:1; Rare:57 | ||||
| chr15:45378477-45378721 | Common:4; Rare:63; Clinvar:1; Clinvar (benign):4 |