| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:105244343-105244652 | Common:1; Rare:113 | ||||
| chr9:105447955-105448181 | Common:2; Rare:84 | ||||
| chr9:105448201-105448439 | Common:2; Rare:51 | ||||
| chr9:105557992-105558186 | Rare:63; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:105558204-105558604 | Common:1; Rare:116 | ||||
| chr9:105694348-105694661 | Common:4; Rare:132 | ||||
| chr9:106862498-106862662 | Common:3; Rare:53 | ||||
| chr9:106862969-106863203 | Rare:78 | ||||
| chr9:106863376-106863646 | Common:1; Rare:54 | ||||
| chr9:107282838-107283368 | Common:3; Rare:178 | ||||
| chr9:107283480-107283609 | Common:3; Rare:27 | ||||
| chr9:107283910-107284430 | Common:4; Rare:138 | ||||
| chr9:107489762-107490002 | Common:3; Rare:96 | ||||
| chr9:107490085-107490485 | Common:2; Rare:141 | ||||
| chr9:108933571-108933723 | Rare:37 |