| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49060203-49060413 | Rare:57 | ||||
| chr12:49069642-49069699 | Common:1; Rare:10 | ||||
| chr12:49069703-49070366 | Common:2; Rare:167 | ||||
| chr12:49110200-49110357 | Common:2; Rare:35 | ||||
| chr12:49110598-49111096 | Rare:120 | ||||
| chr12:49130213-49130484 | Common:1; Rare:110 | ||||
| chr12:49130699-49131070 | Common:5; Rare:136 | ||||
| chr12:49131270-49132001 | Common:2; Rare:231 | ||||
| chr12:49188298-49188697 | Common:2; Rare:89 | ||||
| chr12:49188761-49188808 | Rare:9 | ||||
| chr12:49188948-49189285 | Rare:92; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264741-49265382 | Common:6; Rare:216 | ||||
| chr12:49265533-49265717 | Common:1; Rare:36 | ||||
| chr12:49322785-49323353 | Common:5; Rare:141 | ||||
| chr12:49366518-49366661 | Rare:32 |