| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144902066-144902280 | Common:2; Rare:46 | ||||
| chr8:144950593-144950910 | Common:4; Rare:100 | ||||
| chr8:145052139-145052504 | Common:11; Rare:94 | ||||
| chr9:178948-179322 | Common:6; Rare:64 | ||||
| chr9:215076-215201 | Common:3; Rare:72; Clinvar (benign):1 | ||||
| chr9:504391-504742 | Common:4; Rare:169 | ||||
| chr9:2015054-2015392 | Common:3; Rare:99 | ||||
| chr9:2016964-2017101 | Rare:34 | ||||
| chr9:2017492-2017718 | Rare:69 | ||||
| chr9:2844047-2844352 | Common:5; Rare:117 | ||||
| chr9:3525960-3526119 | Common:1; Rare:74 | ||||
| chr9:3526371-3526541 | Common:5; Rare:86 | ||||
| chr9:4490102-4490239 | Common:2; Rare:31 | ||||
| chr9:4490326-4490561 | Common:1; Rare:78; Clinvar:3 | ||||
| chr9:4662262-4662354 | Common:1; Rare:37 |