| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:106987027-106987329 | Common:5; Rare:86 | ||||
| chr12:107093499-107093629 | Rare:51 | ||||
| chr12:107093777-107094004 | Common:2; Rare:66 | ||||
| chr12:107685614-107685948 | Common:2; Rare:107 | ||||
| chr12:107686007-107686108 | Rare:34 | ||||
| chr12:107760569-107760649 | Rare:14 | ||||
| chr12:107760843-107761025 | Common:2; Rare:69 | ||||
| chr12:107761032-107761374 | Common:6; Rare:130 | ||||
| chr12:108320620-108320854 | Rare:45 | ||||
| chr12:108514909-108515396 | Common:2; Rare:144 | ||||
| chr12:108561058-108561584 | Common:5; Rare:143 | ||||
| chr12:108562306-108562706 | Common:12; Rare:148; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108562779-108562873 | Common:1; Rare:16 | ||||
| chr12:108568018-108568102 | Common:1; Rare:15 | ||||
| chr12:108631759-108631921 | Rare:32 |