| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:118190459-118190614 | Common:1; Rare:31 | ||||
| chr12:118372846-118373165 | Common:2; Rare:83 | ||||
| chr12:118376243-118376561 | Common:1; Rare:86 | ||||
| chr12:118981402-118981547 | Rare:44 | ||||
| chr12:119178831-119179083 | Common:1; Rare:39; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:119667684-119668026 | Common:2; Rare:91 | ||||
| chr12:120116607-120116955 | Common:5; Rare:100 | ||||
| chr12:120194693-120194786 | Rare:34 | ||||
| chr12:120201081-120201366 | Common:2; Rare:90 | ||||
| chr12:120437881-120438235 | Common:2; Rare:137; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr12:120446353-120446474 | Common:1; Rare:55 | ||||
| chr12:120469635-120469901 | Common:3; Rare:94 | ||||
| chr12:120495828-120496550 | Common:8; Rare:235 | ||||
| chr12:120529113-120529185 | Common:2; Rare:27 | ||||
| chr12:120534183-120534377 | Common:1; Rare:49 |