| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122980590-122980743 | Common:1; Rare:51 | ||||
| chr12:123233113-123233494 | Common:2; Rare:123; Clinvar:1 | ||||
| chr12:123364824-123364962 | Common:2; Rare:52 | ||||
| chr12:123436437-123436536 | Rare:15 | ||||
| chr12:123584278-123584616 | Common:6; Rare:113 | ||||
| chr12:123602018-123602139 | Common:3; Rare:37 | ||||
| chr12:123633607-123633845 | Common:1; Rare:114; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972575-123972893 | Common:6; Rare:112 | ||||
| chr12:124914092-124914219 | Common:5; Rare:52 | ||||
| chr12:124914804-124914993 | Common:2; Rare:65 | ||||
| chr12:132144345-132144486 | Rare:59 | ||||
| chr12:132687332-132687726 | Common:4; Rare:139; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:132887551-132887843 | Rare:85 | ||||
| chr12:132956250-132956421 | Common:1; Rare:37 | ||||
| chr12:132986140-132986414 | Rare:70 |