| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6851845-6852238 | Common:2; Rare:108 | ||||
| chr12:6852396-6852688 | Common:1; Rare:69 | ||||
| chr12:6867332-6867606 | Common:2; Rare:129; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6867979-6868145 | Common:3; Rare:67 | ||||
| chr12:6873226-6873656 | Common:5; Rare:126 | ||||
| chr12:6904678-6904935 | Common:1; Rare:59 | ||||
| chr12:6914350-6914544 | Rare:42 | ||||
| chr12:6924364-6924518 | Common:1; Rare:38 | ||||
| chr12:6928333-6928476 | Common:2; Rare:33 | ||||
| chr12:6937367-6937728 | Common:2; Rare:98 | ||||
| chr12:6937796-6938270 | Common:2; Rare:177; Clinvar (benign):1 | ||||
| chr12:6943480-6944174 | Common:18; Rare:524; Clinvar:6; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:6944580-6944850 | Common:3; Rare:97; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:6946241-6946588 | Common:1; Rare:85 | ||||
| chr12:6951227-6951588 | Rare:103 |