| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:126804874-126805046 | Rare:53 | ||||
| chr9:127424275-127424440 | Common:1; Rare:52 | ||||
| chr9:127451267-127451562 | Common:3; Rare:122; Clinvar (benign):1 | ||||
| chr9:127854587-127854866 | Rare:60; Clinvar:6 | ||||
| chr9:127877651-127877791 | Rare:31 | ||||
| chr9:127937824-127937922 | Common:1; Rare:27; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:128191750-128191878 | Common:1; Rare:33 | ||||
| chr9:128275919-128276302 | Common:5; Rare:172 | ||||
| chr9:128322410-128322621 | Common:1; Rare:61 | ||||
| chr9:128322746-128322880 | Common:2; Rare:63; Clinvar (benign):5 | ||||
| chr9:128371159-128371399 | Common:1; Rare:88 | ||||
| chr9:128552394-128552611 | Rare:81; Clinvar:1 | ||||
| chr9:128656635-128656816 | Common:2; Rare:83; Clinvar (pathogenic):1 | ||||
| chr9:128724073-128724472 | Common:3; Rare:132 | ||||
| chr9:128787148-128787336 | Common:3; Rare:61 |