| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109154528-109154768 | Common:2; Rare:60 | ||||
| chr12:109477260-109477664 | Common:3; Rare:108 | ||||
| chr12:109573443-109573863 | Common:3; Rare:134; Clinvar:6; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr12:109880271-109880665 | Common:1; Rare:126 | ||||
| chr12:109900209-109900385 | Rare:67 | ||||
| chr12:109996218-109996439 | Common:2; Rare:65 | ||||
| chr12:109999117-109999217 | Rare:15 | ||||
| chr12:110281003-110281164 | Common:1; Rare:66 | ||||
| chr12:110468721-110468915 | Rare:54 | ||||
| chr12:110502051-110502332 | Common:1; Rare:102 | ||||
| chr12:110614017-110614363 | Rare:112; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:110742709-110743036 | Common:2; Rare:115 | ||||
| chr12:111685718-111686138 | Rare:149 | ||||
| chr12:111766853-111767014 | Rare:54 | ||||
| chr12:111841854-111842047 | Common:2; Rare:57 |