| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr6:127343323-127343639 | Common:2; Rare:75 | ||||
| chr6:132401443-132401579 | Common:1; Rare:40 | ||||
| chr6:134177810-134178052 | Rare:45 | ||||
| chr6:135054766-135055017 | Common:6; Rare:77 | ||||
| chr6:135497604-135497886 | Common:4; Rare:104; Clinvar:1; Clinvar (benign):2 | ||||
| chr6:138107410-138107540 | Common:1; Rare:35 | ||||
| chr6:138773701-138773813 | Common:3; Rare:57 | ||||
| chr6:139374412-139374513 | Common:3; Rare:36 | ||||
| chr6:142147212-142147334 | Rare:66 | ||||
| chr6:143060707-143061038 | Common:8; Rare:114 | ||||
| chr6:143450650-143450961 | Common:1; Rare:115; Clinvar:4; Clinvar (benign):1 | ||||
| chr6:143843179-143843477 | Common:2; Rare:100 | ||||
| chr6:144285130-144285513 | Common:3; Rare:104 | ||||
| chr6:145814624-145814927 | Common:1; Rare:126 | ||||
| chr6:146544031-146544058 | Rare:9 |