| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55709758-55709985 | Common:1; Rare:32 | ||||
| chr12:55718946-55719115 | Common:1; Rare:28 | ||||
| chr12:57165854-57166207 | Common:1; Rare:82 | ||||
| chr12:57179797-57180096 | Rare:86 | ||||
| chr12:57195771-57196170 | Common:3; Rare:109 | ||||
| chr12:57211478-57211815 | Common:1; Rare:96 | ||||
| chr12:57936139-57936211 | Common:2; Rare:26 | ||||
| chr12:62603444-62603618 | Common:1; Rare:64 | ||||
| chr12:64694614-64694865 | Rare:57 | ||||
| chr12:101748451-101748577 | Rare:23 | ||||
| chr12:101935831-101935956 | Rare:23 | ||||
| chr12:102475641-102475953 | Common:1; Rare:75; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:108792804-108792860 | Rare:25 | ||||
| chr12:113273421-113273638 | Common:1; Rare:49 | ||||
| chr12:113291548-113291677 | Common:1; Rare:28 |