| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109097589-109097629 | Rare:13; Clinvar:1 | ||||
| chr12:109098361-109098377 | Rare:7 | ||||
| chr12:109154528-109154691 | Common:1; Rare:42 | ||||
| chr12:109477287-109477656 | Common:3; Rare:91 | ||||
| chr12:109573479-109573837 | Common:3; Rare:104; Clinvar:5; Clinvar (benign):5 | ||||
| chr12:109880370-109880662 | Common:1; Rare:90 | ||||
| chr12:109900207-109900343 | Rare:57 | ||||
| chr12:109996309-109996431 | Common:2; Rare:32 | ||||
| chr12:110468702-110468909 | Rare:54 | ||||
| chr12:110502058-110502331 | Common:1; Rare:99 | ||||
| chr12:110614052-110614191 | Rare:44; Clinvar:1; Clinvar (benign):2 | ||||
| chr12:111685717-111686090 | Rare:134 | ||||
| chr12:111766863-111766997 | Rare:43 | ||||
| chr12:111841879-111842243 | Common:3; Rare:100 | ||||
| chr12:112013125-112013468 | Common:1; Rare:121 |