| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128371178-128371426 | Rare:183 | ||||
| chr9:128428732-128428983 | Common:1; Rare:138 | ||||
| chr9:128455852-128456193 | Common:3; Rare:186 | ||||
| chr9:128504598-128504806 | Rare:195; Clinvar:10 | ||||
| chr9:128552388-128552617 | Rare:165; Clinvar:2 | ||||
| chr9:128656635-128657022 | Common:4; Rare:210; Clinvar (pathogenic):2 | ||||
| chr9:128683533-128683904 | Rare:128 | ||||
| chr9:128684770-128685160 | Rare:134 | ||||
| chr9:128688907-128689334 | Rare:321 | ||||
| chr9:128702247-128702553 | Common:2; Rare:68 | ||||
| chr9:128702733-128702921 | Rare:83 | ||||
| chr9:128724079-128724472 | Common:5; Rare:251 | ||||
| chr9:128771815-128772060 | Common:2; Rare:126 | ||||
| chr9:128787040-128787381 | Common:7; Rare:176 | ||||
| chr9:128818262-128818569 | Common:6; Rare:153 |