| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48925490-48925609 | Rare:20 | ||||
| chr12:48939677-48940028 | Common:2; Rare:82 | ||||
| chr12:48957404-48957581 | Common:1; Rare:52 | ||||
| chr12:49018736-49018895 | Rare:66 | ||||
| chr12:49131299-49131626 | Common:2; Rare:129 | ||||
| chr12:49188482-49188651 | Common:2; Rare:22 | ||||
| chr12:49188981-49189237 | Rare:69; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264775-49265083 | Common:4; Rare:107 | ||||
| chr12:49323017-49323308 | Common:2; Rare:71 | ||||
| chr12:49367263-49367548 | Common:1; Rare:77 | ||||
| chr12:49568066-49568412 | Common:2; Rare:87 | ||||
| chr12:49623290-49623571 | Common:1; Rare:78 | ||||
| chr12:49828359-49828553 | Common:1; Rare:71 | ||||
| chr12:49843095-49843187 | Common:1; Rare:33 | ||||
| chr12:50085046-50085364 | Common:1; Rare:84 |