| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:105107641-105107789 | Common:1; Rare:70 | ||||
| chr12:105236049-105236304 | Common:2; Rare:112 | ||||
| chr12:107093510-107093617 | Rare:43 | ||||
| chr12:107685678-107685877 | Common:1; Rare:70 | ||||
| chr12:108561150-108561443 | Common:3; Rare:69 | ||||
| chr12:108731991-108732246 | Common:2; Rare:72 | ||||
| chr12:109097902-109098204 | Common:4; Rare:95 | ||||
| chr12:109477287-109477643 | Common:3; Rare:87 | ||||
| chr12:109573443-109573813 | Common:3; Rare:120; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109880381-109880662 | Common:1; Rare:86 | ||||
| chr12:109900216-109900336 | Rare:50 | ||||
| chr12:109999136-109999213 | Rare:12 | ||||
| chr12:110468671-110468909 | Rare:59 | ||||
| chr12:110502062-110502324 | Common:1; Rare:93 | ||||
| chr12:110614008-110614178 | Rare:51; Clinvar:2; Clinvar (benign):2 |