| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:27134621-27134696 | Rare:32 | ||||
| chr2:27139392-27139503 | Common:1; Rare:18 | ||||
| chr2:27211394-27211427 | Rare:9 | ||||
| chr2:27211730-27212103 | Common:3; Rare:128 | ||||
| chr2:27212175-27212437 | Common:2; Rare:133 | ||||
| chr2:27217296-27217544 | Rare:107 | ||||
| chr2:27263031-27263350 | Common:1; Rare:74 | ||||
| chr2:27275309-27275490 | Common:1; Rare:57 | ||||
| chr2:27323039-27323149 | Rare:30; Clinvar (benign):1 | ||||
| chr2:27325683-27325979 | Rare:63 | ||||
| chr2:27328547-27328631 | Rare:26 | ||||
| chr2:27335351-27335600 | Common:1; Rare:65 | ||||
| chr2:27356162-27356307 | Common:1; Rare:32 | ||||
| chr2:27356750-27356855 | Rare:27 | ||||
| chr2:27356957-27357232 | Common:2; Rare:96 |