| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74147855-74148140 | Common:1; Rare:75; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74178779-74179047 | Common:3; Rare:74 | ||||
| chr2:74198578-74198654 | Rare:55 | ||||
| chr2:74421579-74421781 | Rare:69 | ||||
| chr2:74440419-74440685 | Rare:69 | ||||
| chr2:74441875-74442026 | Common:2; Rare:27 | ||||
| chr2:74458072-74458322 | Common:1; Rare:77 | ||||
| chr2:74465367-74465455 | Common:1; Rare:21 | ||||
| chr2:74483000-74483113 | Rare:47 | ||||
| chr2:74507273-74507538 | Rare:74 | ||||
| chr2:74529653-74529957 | Rare:92; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74530465-74530638 | Common:2; Rare:54; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74552613-74552774 | Rare:40 | ||||
| chr2:74553892-74554142 | Rare:48 | ||||
| chr2:74576938-74577078 | Rare:16 |