| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:143018432-143018583 | Common:1; Rare:43 | ||||
| chr8:143541443-143541643 | Common:2; Rare:61 | ||||
| chr8:143558259-143558366 | Common:1; Rare:41 | ||||
| chr8:143597362-143597388 | Rare:11 | ||||
| chr8:143617479-143617761 | Common:2; Rare:107 | ||||
| chr8:143635893-143636058 | Common:2; Rare:72 | ||||
| chr8:143927068-143927287 | Common:5; Rare:72; Clinvar:5; Clinvar (benign):4 | ||||
| chr8:143939536-143939752 | Common:3; Rare:68 | ||||
| chr8:144078556-144078699 | Common:1; Rare:43 | ||||
| chr8:144413552-144413707 | Rare:47; Clinvar:1 | ||||
| chr8:145052220-145052504 | Common:10; Rare:85 | ||||
| chr9:504391-504730 | Common:4; Rare:166 | ||||
| chr9:2844036-2844349 | Common:5; Rare:120 | ||||
| chr9:4679437-4679721 | Common:1; Rare:124 | ||||
| chr9:6015612-6015719 | Rare:47 |