| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123436522-123436788 | Common:1; Rare:63 | ||||
| chr12:123533289-123533411 | Common:1; Rare:26 | ||||
| chr12:123584307-123584813 | Common:9; Rare:170 | ||||
| chr12:123602018-123602184 | Common:3; Rare:59 | ||||
| chr12:123616449-123616551 | Common:1; Rare:23 | ||||
| chr12:123617685-123617864 | Common:2; Rare:53 | ||||
| chr12:123633587-123633868 | Common:2; Rare:139; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972543-123972656 | Common:3; Rare:34 | ||||
| chr12:124388777-124388934 | Common:3; Rare:54 | ||||
| chr12:124430613-124431055 | Common:3; Rare:143 | ||||
| chr12:124518516-124518759 | Common:1; Rare:65 | ||||
| chr12:124914092-124914143 | Rare:26 | ||||
| chr12:124914819-124915066 | Common:3; Rare:103 | ||||
| chr12:128853311-128853561 | Common:4; Rare:55 | ||||
| chr12:130839171-130839477 | Common:2; Rare:100 |