| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123633597-123633851 | Common:1; Rare:123; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972553-123972646 | Common:3; Rare:29 | ||||
| chr12:123972972-123973328 | Common:2; Rare:116 | ||||
| chr12:124422625-124422808 | Common:2; Rare:46 | ||||
| chr12:124913848-124914238 | Common:9; Rare:147 | ||||
| chr12:124914562-124914993 | Common:8; Rare:167 | ||||
| chr12:125065148-125065543 | Common:2; Rare:130 | ||||
| chr12:128824016-128824089 | Rare:18 | ||||
| chr12:130871723-130872126 | Common:4; Rare:168 | ||||
| chr12:131710795-131711119 | Rare:87 | ||||
| chr12:131929021-131929296 | Common:10; Rare:83; Clinvar:1 | ||||
| chr12:132144315-132144503 | Common:1; Rare:77 | ||||
| chr12:132687295-132687737 | Common:4; Rare:163; Clinvar:11; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132710564-132710842 | Common:4; Rare:101 | ||||
| chr12:132829048-132829241 | Rare:88 |