| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:110614036-110614223 | Rare:61; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:110689381-110689512 | Rare:31 | ||||
| chr12:110689610-110689957 | Common:1; Rare:53 | ||||
| chr12:110704925-110705086 | Common:2; Rare:35 | ||||
| chr12:110742662-110742705 | Common:1; Rare:7; Clinvar:1 | ||||
| chr12:110742783-110743178 | Common:3; Rare:147 | ||||
| chr12:110846871-110847053 | Common:2; Rare:39 | ||||
| chr12:111369019-111369261 | Common:1; Rare:65 | ||||
| chr12:111598845-111598929 | Rare:27 | ||||
| chr12:111599290-111599635 | Common:2; Rare:115 | ||||
| chr12:111685667-111686168 | Rare:183 | ||||
| chr12:111766847-111766992 | Rare:47 | ||||
| chr12:111841860-111842241 | Common:3; Rare:105 | ||||
| chr12:112013110-112013603 | Common:1; Rare:189 | ||||
| chr12:112108716-112108845 | Rare:35 |