| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:26244568-26244965 | Common:2; Rare:147; Clinvar:6; Clinvar (benign):9 | ||||
| chr2:26345781-26346182 | Common:1; Rare:120 | ||||
| chr2:26764210-26764337 | Rare:52 | ||||
| chr2:27032867-27033000 | Rare:47 | ||||
| chr2:27051546-27051673 | Rare:36 | ||||
| chr2:27071566-27071884 | Common:1; Rare:97 | ||||
| chr2:27086535-27086773 | Common:3; Rare:74 | ||||
| chr2:27211742-27212078 | Common:3; Rare:116 | ||||
| chr2:27212257-27212398 | Common:2; Rare:75 | ||||
| chr2:27323066-27323154 | Rare:20 | ||||
| chr2:27356750-27357032 | Rare:74 | ||||
| chr2:27370272-27370650 | Common:1; Rare:153 | ||||
| chr2:27489705-27489996 | Common:1; Rare:70 | ||||
| chr2:27582973-27583101 | Rare:49 | ||||
| chr2:27628981-27629073 | Common:1; Rare:45 |