| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55728961-55729123 | Rare:29 | ||||
| chr12:55729657-55729790 | Rare:29 | ||||
| chr12:55829534-55829793 | Rare:84 | ||||
| chr12:55830525-55830885 | Common:1; Rare:102 | ||||
| chr12:55966031-55966178 | Common:1; Rare:32 | ||||
| chr12:55966716-55966843 | Rare:32 | ||||
| chr12:56041658-56041961 | Common:3; Rare:77; Clinvar (benign):1 | ||||
| chr12:56116532-56116704 | Common:2; Rare:73 | ||||
| chr12:56152481-56152620 | Rare:41 | ||||
| chr12:56158237-56158403 | Rare:58 | ||||
| chr12:56221856-56222019 | Common:1; Rare:38 | ||||
| chr12:56224061-56224459 | Common:2; Rare:112 | ||||
| chr12:56315862-56316116 | Common:1; Rare:65 | ||||
| chr12:56333948-56334155 | Rare:60 | ||||
| chr12:56360088-56360438 | Common:3; Rare:81 |