| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:124989010-124989262 | Common:4; Rare:73 | ||||
| chr12:130506895-130507123 | Common:2; Rare:45 | ||||
| chr12:130871755-130872126 | Common:4; Rare:148 | ||||
| chr12:130872321-130872628 | Common:1; Rare:116 | ||||
| chr12:131710788-131711125 | Rare:93 | ||||
| chr12:131929208-131929301 | Rare:34; Clinvar:1 | ||||
| chr12:131949674-131949971 | Common:2; Rare:93 | ||||
| chr12:132084094-132084303 | Common:6; Rare:73 | ||||
| chr12:132687298-132687439 | Rare:60; Clinvar:9; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132710594-132710859 | Common:4; Rare:102 | ||||
| chr12:132828814-132829154 | Common:4; Rare:115 | ||||
| chr12:132887553-132887860 | Rare:91 | ||||
| chr12:132956252-132956383 | Common:1; Rare:31 | ||||
| chr12:132986258-132986466 | Rare:52 | ||||
| chr12:133037220-133037545 | Common:4; Rare:67 |