| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:73828801-73829037 | Common:1; Rare:54 | ||||
| chr2:73926722-73926934 | Common:2; Rare:111; Clinvar:7; Clinvar (benign):3 | ||||
| chr2:74147830-74148143 | Common:2; Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
| chr2:74178779-74179017 | Common:2; Rare:64 | ||||
| chr2:74198424-74198648 | Rare:91 | ||||
| chr2:74391795-74392140 | Common:2; Rare:162 | ||||
| chr2:74421582-74421768 | Rare:65 | ||||
| chr2:74439940-74440105 | Rare:34 | ||||
| chr2:74440425-74440915 | Rare:109 | ||||
| chr2:74454865-74455138 | Rare:75 | ||||
| chr2:74458350-74458509 | Rare:52 | ||||
| chr2:74465350-74465487 | Common:1; Rare:41; Clinvar:1 | ||||
| chr2:74482982-74483113 | Rare:51 | ||||
| chr2:74483251-74483387 | Common:1; Rare:55 | ||||
| chr2:74502961-74503154 | Rare:42 |