| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:124914819-124915048 | Common:3; Rare:94 | ||||
| chr12:124980420-124980515 | Common:3; Rare:28 | ||||
| chr12:128824016-128824111 | Common:1; Rare:32 | ||||
| chr12:130871735-130872126 | Common:4; Rare:162 | ||||
| chr12:131710779-131711113 | Rare:92 | ||||
| chr12:131929016-131929301 | Common:10; Rare:87; Clinvar:1 | ||||
| chr12:132144339-132144519 | Common:1; Rare:74 | ||||
| chr12:132687269-132687791 | Common:5; Rare:188; Clinvar:12; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr12:132710528-132711042 | Common:5; Rare:162 | ||||
| chr12:132829048-132829247 | Rare:91 | ||||
| chr12:132887548-132887845 | Rare:87 | ||||
| chr12:132956250-132956435 | Common:1; Rare:39 | ||||
| chr12:132986269-132986500 | Rare:58 | ||||
| chr12:133080146-133080459 | Common:7; Rare:100 | ||||
| chr12:133130226-133130662 | Common:7; Rare:147 |