| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120710332-120710488 | Common:3; Rare:50 | ||||
| chr12:120903362-120903790 | Common:5; Rare:193 | ||||
| chr12:120904101-120904460 | Common:9; Rare:233 | ||||
| chr12:120978345-120978799 | Common:3; Rare:197; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr12:121296662-121296923 | Common:2; Rare:148 | ||||
| chr12:121352332-121352651 | Common:6; Rare:226 | ||||
| chr12:121399833-121400176 | Common:10; Rare:235 | ||||
| chr12:121536880-121537360 | Common:8; Rare:176 | ||||
| chr12:121580219-121580539 | Rare:164 | ||||
| chr12:121580956-121581163 | Rare:52 | ||||
| chr12:121626197-121626633 | Common:4; Rare:299 | ||||
| chr12:121712645-121712853 | Common:5; Rare:144 | ||||
| chr12:121793902-121794185 | Common:5; Rare:124 | ||||
| chr12:121799938-121800389 | Common:8; Rare:321 | ||||
| chr12:121802895-121803308 | Common:1; Rare:190 |