| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144792342-144792577 | Common:3; Rare:91 | ||||
| chr8:144798782-144798924 | Common:1; Rare:46 | ||||
| chr8:144827235-144827603 | Common:2; Rare:94 | ||||
| chr8:144852967-144853131 | Rare:60 | ||||
| chr8:144853473-144853591 | Common:2; Rare:32 | ||||
| chr8:144901397-144901727 | Common:1; Rare:94 | ||||
| chr8:144950593-144950910 | Common:4; Rare:100 | ||||
| chr8:145052102-145052504 | Common:11; Rare:102 | ||||
| chr9:214678-214906 | Common:4; Rare:129; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:215122-215226 | Common:1; Rare:53 | ||||
| chr9:470142-470379 | Common:15; Rare:104 | ||||
| chr9:504407-504745 | Common:4; Rare:165 | ||||
| chr9:706925-707178 | Common:3; Rare:86 | ||||
| chr9:2015066-2015393 | Common:3; Rare:94 | ||||
| chr9:2017387-2017475 | Common:1; Rare:27 |