| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:106357924-106358164 | Common:4; Rare:107 | ||||
| chr12:106774082-106774381 | Common:3; Rare:78 | ||||
| chr12:106774547-106774714 | Common:1; Rare:53 | ||||
| chr12:106955496-106955907 | Common:1; Rare:153 | ||||
| chr12:106987049-106987286 | Common:4; Rare:67 | ||||
| chr12:107093510-107093626 | Rare:46 | ||||
| chr12:107685679-107685935 | Common:1; Rare:81 | ||||
| chr12:108561141-108561202 | Rare:31 | ||||
| chr12:108562380-108562733 | Common:9; Rare:142; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108826141-108826699 | Common:3; Rare:123 | ||||
| chr12:108827382-108827410 | Rare:10 | ||||
| chr12:108827469-108827604 | Rare:16 | ||||
| chr12:108827677-108827861 | Common:2; Rare:46 | ||||
| chr12:109052453-109052660 | Common:3; Rare:61 | ||||
| chr12:109093624-109093903 | Common:2; Rare:62 |