| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:55973684-55973959 | Common:2; Rare:76 | ||||
| chr12:56041571-56042037 | Common:4; Rare:96; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:56104201-56104956 | Common:5; Rare:234 | ||||
| chr12:56110186-56110475 | Rare:61 | ||||
| chr12:56116482-56116752 | Common:3; Rare:104 | ||||
| chr12:56116998-56117209 | Common:4; Rare:61 | ||||
| chr12:56128447-56128661 | Rare:64 | ||||
| chr12:56152210-56152502 | Common:2; Rare:81 | ||||
| chr12:56152505-56152655 | Rare:40 | ||||
| chr12:56157008-56157459 | Common:1; Rare:94 | ||||
| chr12:56158211-56158475 | Rare:100 | ||||
| chr12:56158616-56158714 | Rare:26 | ||||
| chr12:56161144-56161579 | Common:1; Rare:106 | ||||
| chr12:56189445-56189749 | Common:1; Rare:99 | ||||
| chr12:56221635-56221758 | Rare:30 |