| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109999093-109999259 | Rare:29 | ||||
| chr12:110281024-110281250 | Rare:81 | ||||
| chr12:110449718-110449872 | Rare:26 | ||||
| chr12:110450253-110450437 | Common:2; Rare:70 | ||||
| chr12:110502058-110502331 | Common:1; Rare:99 | ||||
| chr12:110613973-110614187 | Rare:61; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:110689087-110689208 | Common:1; Rare:29 | ||||
| chr12:110689314-110689494 | Rare:40 | ||||
| chr12:110742762-110743191 | Common:3; Rare:154 | ||||
| chr12:111368973-111369285 | Common:1; Rare:81 | ||||
| chr12:111434705-111434960 | Common:2; Rare:47 | ||||
| chr12:111599316-111599620 | Common:2; Rare:98 | ||||
| chr12:111685718-111686120 | Rare:142 | ||||
| chr12:111766693-111766992 | Rare:83 | ||||
| chr12:111841887-111842249 | Common:3; Rare:99 |