| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74002576-74002721 | Common:2; Rare:59 | ||||
| chr2:74147835-74148151 | Common:3; Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74198425-74198637 | Rare:81 | ||||
| chr2:74421590-74421771 | Rare:63 | ||||
| chr2:74440419-74440679 | Rare:69 | ||||
| chr2:74454828-74455138 | Rare:83 | ||||
| chr2:74458128-74458498 | Common:1; Rare:111 | ||||
| chr2:74482964-74483121 | Common:1; Rare:64 | ||||
| chr2:74507652-74507823 | Rare:38 | ||||
| chr2:74529654-74530006 | Rare:109; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:74530515-74530616 | Common:1; Rare:36; Clinvar:2 | ||||
| chr2:74835133-74835281 | Rare:36 | ||||
| chr2:74958498-74958701 | Common:4; Rare:75 | ||||
| chr2:74958876-74959032 | Rare:59 | ||||
| chr2:75646624-75646836 | Rare:60 |