| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:24123272-24123522 | Common:1; Rare:67 | ||||
| chr2:24360470-24360667 | Common:3; Rare:73 | ||||
| chr2:24793140-24793156 | Rare:6 | ||||
| chr2:24971908-24972148 | Common:1; Rare:76 | ||||
| chr2:26244573-26244975 | Common:2; Rare:149; Clinvar:6; Clinvar (benign):9 | ||||
| chr2:26345781-26346160 | Common:1; Rare:116 | ||||
| chr2:27032852-27033049 | Rare:75 | ||||
| chr2:27078529-27078950 | Common:3; Rare:101 | ||||
| chr2:27086754-27086757 | Rare:1 | ||||
| chr2:27211768-27212163 | Common:4; Rare:139 | ||||
| chr2:27212232-27212372 | Common:1; Rare:72 | ||||
| chr2:27217076-27217504 | Common:1; Rare:131 | ||||
| chr2:27356170-27356287 | Rare:28 | ||||
| chr2:27356737-27356801 | Rare:14 | ||||
| chr2:27356968-27357188 | Common:2; Rare:80 |