| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35665142-35665345 | Common:3; Rare:72 | ||||
| chr9:35732037-35732334 | Common:2; Rare:77 | ||||
| chr9:35732365-35732683 | Common:3; Rare:81 | ||||
| chr9:35748969-35749361 | Common:2; Rare:146 | ||||
| chr9:35814983-35815293 | Rare:79 | ||||
| chr9:35906092-35906267 | Rare:40 | ||||
| chr9:36190725-36191278 | Common:3; Rare:169 | ||||
| chr9:36258404-36258630 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:36400841-36400975 | Common:3; Rare:63 | ||||
| chr9:36572771-36572967 | Rare:54 | ||||
| chr9:37120202-37120626 | Common:2; Rare:131 | ||||
| chr9:37422580-37422768 | Common:2; Rare:94; Clinvar:1 | ||||
| chr9:37485728-37486030 | Common:3; Rare:106 | ||||
| chr9:37592401-37592698 | Common:3; Rare:102 | ||||
| chr9:37784882-37785160 | Common:1; Rare:124; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):3 |