| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109097846-109098242 | Common:5; Rare:126 | ||||
| chr12:109098324-109098435 | Rare:47 | ||||
| chr12:109154528-109154707 | Common:1; Rare:45 | ||||
| chr12:109477260-109477643 | Common:3; Rare:100 | ||||
| chr12:109573430-109573813 | Common:3; Rare:126; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109880274-109880651 | Common:1; Rare:122 | ||||
| chr12:110468715-110468909 | Rare:52 | ||||
| chr12:110502058-110502244 | Common:1; Rare:66 | ||||
| chr12:110613957-110614257 | Rare:97; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:111685765-111686110 | Rare:129 | ||||
| chr12:111841877-111842028 | Common:2; Rare:44 | ||||
| chr12:112013129-112013478 | Common:1; Rare:124 | ||||
| chr12:112108761-112108884 | Common:1; Rare:30 | ||||
| chr12:113185440-113185748 | Common:7; Rare:113 | ||||
| chr12:114683240-114683456 | Common:2; Rare:52; Clinvar:4; Clinvar (benign):3 |