| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:124914585-124914993 | Common:8; Rare:159 | ||||
| chr12:124917675-124917812 | Rare:43 | ||||
| chr12:125065301-125065495 | Common:2; Rare:69 | ||||
| chr12:130871755-130872126 | Common:4; Rare:148 | ||||
| chr12:130953760-130954004 | Rare:47 | ||||
| chr12:131710788-131711113 | Rare:87 | ||||
| chr12:131929021-131929296 | Common:10; Rare:83; Clinvar:1 | ||||
| chr12:132687303-132687656 | Common:2; Rare:131; Clinvar:7; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132710564-132710993 | Common:5; Rare:143 | ||||
| chr12:132829048-132829247 | Rare:91 | ||||
| chr12:132887548-132887880 | Rare:99 | ||||
| chr12:132956280-132956442 | Common:1; Rare:30 | ||||
| chr12:132986226-132986428 | Rare:45 | ||||
| chr12:133037198-133037574 | Common:5; Rare:86 | ||||
| chr12:133080143-133080459 | Common:7; Rare:100 |