| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48106064-48106117 | Common:1; Rare:16 | ||||
| chr12:48106121-48106149 | Common:1; Rare:12 | ||||
| chr12:48119149-48119379 | Common:2; Rare:44; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:48716660-48717008 | Common:4; Rare:104 | ||||
| chr12:48814677-48814875 | Rare:35 | ||||
| chr12:48852127-48852394 | Common:2; Rare:69 | ||||
| chr12:48957384-48957581 | Common:2; Rare:56 | ||||
| chr12:49018741-49018888 | Rare:60 | ||||
| chr12:49069996-49070144 | Common:2; Rare:33 | ||||
| chr12:49131301-49131621 | Common:2; Rare:126 | ||||
| chr12:49188981-49189274 | Rare:81; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264749-49265092 | Common:5; Rare:120 | ||||
| chr12:49322980-49323303 | Common:3; Rare:74 | ||||
| chr12:49367214-49367548 | Common:1; Rare:93 | ||||
| chr12:49568104-49568211 | Common:2; Rare:36 |