| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120194685-120194804 | Rare:43 | ||||
| chr12:120201081-120201385 | Common:2; Rare:96 | ||||
| chr12:120361811-120362005 | Rare:43 | ||||
| chr12:120437863-120437988 | Common:2; Rare:34 | ||||
| chr12:120438012-120438229 | Rare:94; Clinvar (benign):2 | ||||
| chr12:120446340-120446491 | Common:2; Rare:69 | ||||
| chr12:120469542-120470071 | Common:4; Rare:165 | ||||
| chr12:120495859-120496228 | Common:7; Rare:125 | ||||
| chr12:120529094-120529391 | Common:2; Rare:83 | ||||
| chr12:120581353-120581596 | Common:2; Rare:85 | ||||
| chr12:120725718-120725879 | Rare:52; Clinvar:1 | ||||
| chr12:121296669-121296886 | Common:1; Rare:66 | ||||
| chr12:121399830-121400173 | Common:5; Rare:130 | ||||
| chr12:121536062-121536413 | Common:1; Rare:69 | ||||
| chr12:121537034-121537168 | Rare:29 |