| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:104287204-104287430 | Rare:59 | ||||
| chr12:105107612-105107846 | Common:1; Rare:101; Clinvar:1 | ||||
| chr12:105236047-105236363 | Common:3; Rare:142 | ||||
| chr12:107093477-107093623 | Rare:55 | ||||
| chr12:107685709-107685899 | Rare:68 | ||||
| chr12:108561141-108561461 | Common:4; Rare:78 | ||||
| chr12:108562324-108562686 | Common:10; Rare:137; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:109097841-109098287 | Common:5; Rare:135 | ||||
| chr12:109477272-109477650 | Common:3; Rare:97 | ||||
| chr12:109573478-109573852 | Common:3; Rare:110; Clinvar:5; Clinvar (benign):5 | ||||
| chr12:109880361-109880675 | Common:1; Rare:94 | ||||
| chr12:109900204-109900356 | Rare:62 | ||||
| chr12:109996257-109996439 | Common:2; Rare:54 | ||||
| chr12:110450253-110450443 | Common:2; Rare:72 | ||||
| chr12:110468714-110468909 | Rare:52 |