| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:106774536-106774688 | Rare:45 | ||||
| chr12:106955635-106955916 | Rare:102 | ||||
| chr12:106956656-106956932 | Rare:51 | ||||
| chr12:107093510-107093642 | Rare:50 | ||||
| chr12:107685717-107685895 | Rare:63 | ||||
| chr12:107761097-107761399 | Common:6; Rare:106 | ||||
| chr12:108561150-108561443 | Common:3; Rare:69 | ||||
| chr12:108562399-108562658 | Common:8; Rare:109; Clinvar:2; Clinvar (benign):3 | ||||
| chr12:109477259-109477656 | Common:3; Rare:105 | ||||
| chr12:109573443-109573821 | Common:3; Rare:121; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109880361-109880673 | Common:1; Rare:94 | ||||
| chr12:109900081-109900336 | Rare:71 | ||||
| chr12:109996299-109996439 | Common:2; Rare:39 | ||||
| chr12:109999118-109999211 | Rare:13 | ||||
| chr12:110450254-110450443 | Common:2; Rare:71 |