| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:190957119-190957371 | Common:1; Rare:40 | ||||
| chr2:190959962-190960044 | Rare:18 | ||||
| chr2:190960960-190961020 | Rare:6 | ||||
| chr2:190965550-190965653 | Rare:27 | ||||
| chr2:190971120-190971214 | Common:1; Rare:12 | ||||
| chr2:190973548-190973571 | Rare:5 | ||||
| chr2:190975986-190976082 | Common:1; Rare:16 | ||||
| chr2:190980242-190980618 | Common:1; Rare:93; Clinvar (benign):1 | ||||
| chr2:190980619-190980707 | Rare:14 | ||||
| chr2:190984618-190984724 | Rare:13 | ||||
| chr2:191012797-191012799 | |||||
| chr2:191012834-191012923 | Rare:10 | ||||
| chr2:191174036-191174136 | Rare:14 | ||||
| chr2:191363858-191364274 | Rare:100 | ||||
| chr2:191385697-191385958 | Common:2; Rare:52 |