| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:85327009-85327891 | Common:10; Rare:425 | ||||
| chr2:85327906-85328500 | Common:32; Rare:763 | ||||
| chr2:85353787-85354187 | Common:2; Rare:72 | ||||
| chr2:85354483-85354963 | Common:9; Rare:731 | ||||
| chr2:85401181-85401838 | Common:6; Rare:569 | ||||
| chr2:85409810-85409973 | Rare:34 | ||||
| chr2:85409953-85410618 | Rare:261 | ||||
| chr2:85413481-85414269 | Common:9; Rare:271 | ||||
| chr2:85418337-85418994 | Common:27; Rare:558 | ||||
| chr2:85419112-85419512 | Common:6; Rare:68 | ||||
| chr2:85420695-85421081 | Common:9; Rare:195 | ||||
| chr2:85421147-85421569 | Common:4; Rare:196 | ||||
| chr2:85421580-85422070 | Common:5; Rare:163 | ||||
| chr2:85538372-85538940 | Common:6; Rare:396 | ||||
| chr2:85538960-85539353 | Common:17; Rare:724; Clinvar (benign):13 |