| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128684776-128685119 | Rare:59 | ||||
| chr9:128689451-128689651 | Rare:73 | ||||
| chr9:128690609-128690940 | Common:2; Rare:97 | ||||
| chr9:128690958-128691225 | Common:3; Rare:91 | ||||
| chr9:128692635-128692685 | Common:1; Rare:12 | ||||
| chr9:128692693-128692982 | Rare:55 | ||||
| chr9:128724086-128724459 | Common:2; Rare:123 | ||||
| chr9:128771581-128771605 | Rare:9 | ||||
| chr9:128881902-128882213 | Common:2; Rare:104 | ||||
| chr9:128882513-128882634 | Common:1; Rare:30 | ||||
| chr9:128947523-128947740 | Common:2; Rare:98; Clinvar:6; Clinvar (benign):2 | ||||
| chr9:129011480-129011677 | Rare:48 | ||||
| chr9:129110660-129110962 | Common:4; Rare:69 | ||||
| chr9:129139335-129139552 | Common:2; Rare:52 | ||||
| chr9:129141479-129142058 | Common:8; Rare:171 |