| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108561020-108561498 | Common:6; Rare:138 | ||||
| chr12:108562434-108562732 | Common:9; Rare:128; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108731433-108731837 | Common:3; Rare:130 | ||||
| chr12:108857528-108857850 | Common:3; Rare:154 | ||||
| chr12:109052413-109052693 | Common:3; Rare:84 | ||||
| chr12:109097547-109097682 | Rare:51; Clinvar:2 | ||||
| chr12:109097983-109098213 | Common:4; Rare:75 | ||||
| chr12:109154557-109154707 | Common:1; Rare:38 | ||||
| chr12:109477281-109477649 | Common:3; Rare:90 | ||||
| chr12:109573466-109573860 | Common:3; Rare:119; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr12:109880468-109880673 | Rare:52 | ||||
| chr12:109900159-109900420 | Rare:78 | ||||
| chr12:109996273-109996436 | Common:2; Rare:47 | ||||
| chr12:109999118-109999438 | Rare:68 | ||||
| chr12:110124123-110124474 | Common:2; Rare:110 |