| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109154557-109154818 | Common:3; Rare:61 | ||||
| chr12:109477258-109477666 | Common:3; Rare:109 | ||||
| chr12:109573355-109573845 | Common:5; Rare:162; Clinvar:8; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
| chr12:109880370-109880675 | Common:1; Rare:93 | ||||
| chr12:109914278-109914558 | Common:1; Rare:65 | ||||
| chr12:110468226-110468484 | Common:3; Rare:73 | ||||
| chr12:110468716-110468909 | Rare:52 | ||||
| chr12:110502037-110502198 | Common:1; Rare:58 | ||||
| chr12:110614017-110614250 | Rare:75; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:110742783-110743118 | Common:3; Rare:128 | ||||
| chr12:111369025-111369282 | Common:1; Rare:70 | ||||
| chr12:111597830-111597927 | Rare:17 | ||||
| chr12:111599286-111599639 | Common:2; Rare:120 | ||||
| chr12:111685731-111686168 | Rare:156 | ||||
| chr12:111766819-111767091 | Rare:87 |