| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48865845-48866013 | Rare:42 | ||||
| chr12:48925508-48925598 | Rare:16 | ||||
| chr12:48957417-48957592 | Common:1; Rare:51 | ||||
| chr12:49018741-49018928 | Common:1; Rare:74 | ||||
| chr12:49069934-49070144 | Common:2; Rare:54 | ||||
| chr12:49110663-49110783 | Rare:23 | ||||
| chr12:49110843-49111045 | Rare:48 | ||||
| chr12:49130739-49130912 | Common:4; Rare:67 | ||||
| chr12:49131282-49131642 | Common:2; Rare:143 | ||||
| chr12:49188981-49189274 | Rare:81; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49322980-49323323 | Common:3; Rare:79 | ||||
| chr12:49367194-49367524 | Common:1; Rare:91 | ||||
| chr12:49568086-49568205 | Common:2; Rare:46 | ||||
| chr12:49741369-49741598 | Rare:69 | ||||
| chr12:49843092-49843192 | Common:1; Rare:35 |