| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:108816212-108816528 | Common:2; Rare:60 | ||||
| chr12:109585787-109586083 | Common:2; Rare:53 | ||||
| chr12:109941483-109941495 | Rare:3 | ||||
| chr12:110013026-110013226 | Rare:50 | ||||
| chr12:110282601-110282796 | Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:110339281-110339599 | Rare:62 | ||||
| chr12:110356171-110356249 | Rare:19 | ||||
| chr12:110496922-110497059 | Common:1; Rare:26 | ||||
| chr12:110497752-110497962 | Rare:37 | ||||
| chr12:110650674-110650693 | Common:1; Rare:2 | ||||
| chr12:111581189-111581432 | Rare:47 | ||||
| chr12:111839813-111839899 | Rare:12 | ||||
| chr12:111865863-111866156 | Rare:61 | ||||
| chr12:111868480-111868789 | Common:2; Rare:44 | ||||
| chr12:112019490-112019825 | Rare:69 |