| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:106955482-106955960 | Common:1; Rare:179 | ||||
| chr12:108633792-108634043 | Rare:52 | ||||
| chr12:109052552-109052659 | Common:2; Rare:36 | ||||
| chr12:109477293-109477443 | Common:3; Rare:51 | ||||
| chr12:109573483-109573854 | Common:3; Rare:106; Clinvar:4; Clinvar (benign):5 | ||||
| chr12:109996212-109996424 | Common:2; Rare:63 | ||||
| chr12:110468648-110468878 | Rare:59 | ||||
| chr12:110502055-110502324 | Common:1; Rare:97 | ||||
| chr12:111685766-111686134 | Rare:137 | ||||
| chr12:111841894-111842299 | Common:3; Rare:116 | ||||
| chr12:112013119-112013463 | Common:1; Rare:122 | ||||
| chr12:112978424-112978580 | Rare:20 | ||||
| chr12:113185436-113185769 | Common:8; Rare:121 | ||||
| chr12:116559406-116559593 | Common:3; Rare:32 | ||||
| chr12:118135983-118136232 | Common:2; Rare:71 |