| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:131918320-131918532 | Common:1; Rare:65 | ||||
| chr12:131928984-131929296 | Common:10; Rare:92; Clinvar:1 | ||||
| chr12:132687303-132687713 | Common:4; Rare:151; Clinvar:7; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132710564-132711005 | Common:5; Rare:146 | ||||
| chr12:132887545-132887845 | Rare:89 | ||||
| chr12:132956265-132956410 | Common:1; Rare:33 | ||||
| chr12:132986269-132986428 | Rare:35 | ||||
| chr12:133037220-133037536 | Common:4; Rare:64 | ||||
| chr12:133080603-133080943 | Common:1; Rare:106 | ||||
| chr12:133130238-133130642 | Common:7; Rare:130 | ||||
| chr13:19659107-19659275 | Rare:46 | ||||
| chr13:19782918-19783090 | Common:2; Rare:62 | ||||
| chr13:19863448-19863657 | Common:3; Rare:68 | ||||
| chr13:19958384-19958747 | Common:5; Rare:159 | ||||
| chr13:21140384-21140681 | Rare:124 |