| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123633620-123633845 | Common:1; Rare:105; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972545-123972899 | Common:6; Rare:120 | ||||
| chr12:123972993-123973312 | Common:2; Rare:103 | ||||
| chr12:124422636-124422955 | Common:4; Rare:80 | ||||
| chr12:124863842-124864112 | Common:1; Rare:77 | ||||
| chr12:124914092-124914143 | Rare:26 | ||||
| chr12:124914814-124914993 | Common:2; Rare:61 | ||||
| chr12:124917166-124917444 | Rare:69 | ||||
| chr12:128824011-128824095 | Rare:26 | ||||
| chr12:130827528-130827694 | Rare:34 | ||||
| chr12:130839129-130839386 | Common:2; Rare:91 | ||||
| chr12:130871755-130872110 | Common:4; Rare:142 | ||||
| chr12:131710776-131711113 | Rare:94 | ||||
| chr12:131929018-131929322 | Common:10; Rare:95; Clinvar:1 | ||||
| chr12:131949604-131949975 | Common:2; Rare:113 |