| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123233077-123233517 | Common:3; Rare:152; Clinvar:1 | ||||
| chr12:123364703-123364948 | Common:4; Rare:112 | ||||
| chr12:123383776-123384196 | Rare:94 | ||||
| chr12:123436413-123436839 | Common:2; Rare:93 | ||||
| chr12:123458125-123458209 | Rare:27 | ||||
| chr12:123584295-123584813 | Common:9; Rare:173 | ||||
| chr12:123602062-123602175 | Common:3; Rare:44 | ||||
| chr12:123633545-123633875 | Common:2; Rare:157; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972534-123972676 | Common:3; Rare:45 | ||||
| chr12:123972892-123973310 | Common:2; Rare:129 | ||||
| chr12:124423019-124423354 | Common:2; Rare:83 | ||||
| chr12:124518230-124518383 | Common:2; Rare:40 | ||||
| chr12:124786454-124786789 | Common:3; Rare:89 | ||||
| chr12:124914081-124914251 | Common:5; Rare:65 | ||||
| chr12:128823397-128823500 | Rare:30 |