| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108561154-108561459 | Common:4; Rare:72 | ||||
| chr12:109477293-109477631 | Common:3; Rare:76 | ||||
| chr12:109573491-109573852 | Common:3; Rare:100; Clinvar:4; Clinvar (benign):3 | ||||
| chr12:111766859-111767036 | Rare:56 | ||||
| chr12:111841928-111842266 | Common:2; Rare:94 | ||||
| chr12:112013137-112013468 | Common:1; Rare:116 | ||||
| chr12:113185447-113185595 | Common:7; Rare:60 | ||||
| chr12:118135961-118136204 | Common:2; Rare:72 | ||||
| chr12:118372846-118373189 | Common:2; Rare:93 | ||||
| chr12:119668094-119668195 | Common:1; Rare:20 | ||||
| chr12:120116703-120116933 | Common:3; Rare:72 | ||||
| chr12:120201078-120201354 | Common:2; Rare:88 | ||||
| chr12:120446269-120446477 | Common:1; Rare:78 | ||||
| chr12:120495864-120496139 | Common:4; Rare:88 | ||||
| chr12:121399916-121400147 | Common:3; Rare:85 |