| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:45215993-45216163 | Rare:57 | ||||
| chr12:46371289-46371669 | Common:2; Rare:158 | ||||
| chr12:46372656-46372975 | Rare:130 | ||||
| chr12:47705962-47706088 | Rare:57 | ||||
| chr12:47820564-47820813 | Rare:35 | ||||
| chr12:48105845-48105936 | Rare:21 | ||||
| chr12:48105994-48106132 | Common:1; Rare:40 | ||||
| chr12:48925424-48925711 | Common:2; Rare:74 | ||||
| chr12:49018739-49018927 | Common:1; Rare:76 | ||||
| chr12:49131341-49131605 | Common:2; Rare:104 | ||||
| chr12:49188506-49188607 | Common:2; Rare:15 | ||||
| chr12:49188980-49189281 | Rare:82; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264781-49265092 | Common:4; Rare:111 | ||||
| chr12:49568104-49568190 | Common:2; Rare:28 | ||||
| chr12:49741350-49741606 | Rare:76 |