| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:46371460-46371583 | Rare:61 | ||||
| chr12:46372594-46372965 | Rare:142 | ||||
| chr12:47079511-47079629 | Common:1; Rare:24 | ||||
| chr12:47705978-47706124 | Rare:65 | ||||
| chr12:47758121-47758223 | Rare:15 | ||||
| chr12:47758691-47759058 | Common:2; Rare:65 | ||||
| chr12:47820561-47820804 | Rare:33 | ||||
| chr12:48105994-48106208 | Common:2; Rare:71 | ||||
| chr12:48350763-48350963 | Rare:69 | ||||
| chr12:48716628-48716945 | Common:4; Rare:97 | ||||
| chr12:48957353-48957750 | Common:5; Rare:99 | ||||
| chr12:49018733-49018947 | Common:1; Rare:88 | ||||
| chr12:49131299-49131626 | Common:2; Rare:129 | ||||
| chr12:49188482-49188621 | Common:2; Rare:18 | ||||
| chr12:49188981-49189175 | Rare:58; Clinvar:2; Clinvar (benign):2 |