| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35732373-35732716 | Common:3; Rare:85 | ||||
| chr9:35748882-35749371 | Common:3; Rare:160 | ||||
| chr9:35792578-35792764 | Rare:53; Clinvar:3; Clinvar (pathogenic):2 | ||||
| chr9:35814963-35815231 | Rare:72 | ||||
| chr9:36036759-36036980 | Common:3; Rare:72 | ||||
| chr9:36190731-36191272 | Common:3; Rare:168 | ||||
| chr9:36258343-36258639 | Common:2; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:37422617-37422820 | Common:2; Rare:95; Clinvar:1 | ||||
| chr9:37485731-37486030 | Common:3; Rare:103 | ||||
| chr9:37592492-37592693 | Common:2; Rare:70 | ||||
| chr9:37785004-37785149 | Common:1; Rare:71; Clinvar:1; Clinvar (benign):3 | ||||
| chr9:37800689-37800842 | Common:1; Rare:48 | ||||
| chr9:37904067-37904222 | Rare:52 | ||||
| chr9:43127192-43127376 | Rare:49 | ||||
| chr9:69173922-69174332 | Common:6; Rare:129 |