| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:105107612-105107802 | Common:1; Rare:90; Clinvar:1 | ||||
| chr12:105236072-105236294 | Common:2; Rare:102 | ||||
| chr12:106774120-106774376 | Common:3; Rare:61 | ||||
| chr12:106955502-106955880 | Common:1; Rare:135 | ||||
| chr12:107093503-107093626 | Rare:48 | ||||
| chr12:107685737-107685902 | Rare:58 | ||||
| chr12:108515044-108515313 | Common:1; Rare:81 | ||||
| chr12:108562408-108562695 | Common:9; Rare:121; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:108633872-108634095 | Rare:41 | ||||
| chr12:109052470-109052659 | Common:3; Rare:55 | ||||
| chr12:109093401-109093667 | Common:2; Rare:100 | ||||
| chr12:109097867-109098221 | Common:5; Rare:110 | ||||
| chr12:109154557-109154713 | Common:1; Rare:40 | ||||
| chr12:109477281-109477643 | Common:3; Rare:89 | ||||
| chr12:109573430-109573813 | Common:3; Rare:126; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 |