| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6200208-6200446 | Common:3; Rare:71 | ||||
| chr12:6312735-6312915 | Common:2; Rare:23 | ||||
| chr12:6341843-6342177 | Rare:71; Clinvar:1; Clinvar (benign):3 | ||||
| chr12:6363336-6363477 | Common:2; Rare:55; Clinvar (benign):1 | ||||
| chr12:6377155-6377194 | Rare:8 | ||||
| chr12:6444301-6444405 | Common:1; Rare:18 | ||||
| chr12:6444791-6445003 | Rare:37 | ||||
| chr12:6451155-6451302 | Common:1; Rare:35 | ||||
| chr12:6451383-6451749 | Common:2; Rare:87; Clinvar (benign):1 | ||||
| chr12:6451938-6452263 | Common:3; Rare:64 | ||||
| chr12:6470571-6470927 | Common:4; Rare:114 | ||||
| chr12:6470928-6471190 | Common:6; Rare:80 | ||||
| chr12:6493194-6493532 | Common:9; Rare:93 | ||||
| chr12:6493724-6494224 | Common:3; Rare:140 | ||||
| chr12:6494239-6494468 | Common:6; Rare:46 |