| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:3519510-3519659 | Common:1; Rare:38 | ||||
| chr2:3558294-3558471 | Common:5; Rare:67 | ||||
| chr2:3575107-3575358 | Common:2; Rare:73; Clinvar:3; Clinvar (benign):5 | ||||
| chr2:9423442-9423676 | Rare:73 | ||||
| chr2:9474504-9474600 | Common:6; Rare:51 | ||||
| chr2:9555730-9555916 | Common:2; Rare:58 | ||||
| chr2:9630950-9631316 | Common:3; Rare:118 | ||||
| chr2:10689942-10690018 | Common:1; Rare:22 | ||||
| chr2:11466135-11466168 | Rare:6 | ||||
| chr2:11746499-11746648 | Common:1; Rare:46; Clinvar:2 | ||||
| chr2:17753721-17753903 | Common:2; Rare:66 | ||||
| chr2:19990062-19990211 | Rare:38 | ||||
| chr2:20350822-20351058 | Common:1; Rare:95 | ||||
| chr2:20446893-20447086 | Common:2; Rare:69 | ||||
| chr2:20823055-20823140 | Rare:36 |