| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123659571-123659872 | Common:5; Rare:78 | ||||
| chr12:123972561-123972660 | Common:3; Rare:31 | ||||
| chr12:128823966-128824089 | Rare:36 | ||||
| chr12:131929074-131929336 | Common:9; Rare:80; Clinvar:1 | ||||
| chr12:132144309-132144489 | Rare:73 | ||||
| chr12:132687332-132687659 | Common:2; Rare:116; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:132761807-132762154 | Common:3; Rare:119 | ||||
| chr12:132956260-132956413 | Common:1; Rare:34 | ||||
| chr13:19863635-19863964 | Common:3; Rare:125 | ||||
| chr13:21140381-21140618 | Rare:108 | ||||
| chr13:21176550-21176697 | Common:1; Rare:72 | ||||
| chr13:23579236-23579488 | Common:4; Rare:79 | ||||
| chr13:23889268-23889484 | Common:1; Rare:76 | ||||
| chr13:28658786-28659184 | Common:1; Rare:136; Clinvar (pathogenic):1 | ||||
| chr13:30306812-30307204 | Common:7; Rare:105 |