| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:48489237-48489541 | Common:3; Rare:115 | ||||
| chr22:50085238-50085495 | Common:3; Rare:52; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:50244954-50245070 | Common:2; Rare:45 | ||||
| chr22:50562887-50563055 | Common:3; Rare:46 | ||||
| chr22:50582365-50582465 | Rare:45 | ||||
| chr22:50601517-50601868 | Common:4; Rare:83 | ||||
| chr22:50628087-50628276 | Common:9; Rare:92; Clinvar:3; Clinvar (benign):1 | ||||
| chr22:50783581-50783904 | Common:2; Rare:106 | ||||
| chr3:196237-196519 | Common:1; Rare:63 | ||||
| chr3:196528-196614 | Rare:20 | ||||
| chr3:196702-197071 | Common:2; Rare:121 | ||||
| chr3:197093-197358 | Common:3; Rare:86 | ||||
| chr3:197680-197815 | Rare:55 | ||||
| chr3:197830-198058 | Common:3; Rare:70 | ||||
| chr3:382176-382554 | Common:2; Rare:128 |