| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128826093-128827121 | Common:18; Rare:658 | ||||
| chr9:128829651-128830151 | Common:4; Rare:303 | ||||
| chr9:128881871-128882229 | Common:4; Rare:224 | ||||
| chr9:128920774-128920986 | Common:3; Rare:58 | ||||
| chr9:128922004-128922324 | Common:1; Rare:114 | ||||
| chr9:128947520-128947761 | Common:4; Rare:210; Clinvar:12; Clinvar (benign):4 | ||||
| chr9:129080567-129081376 | Common:8; Rare:521 | ||||
| chr9:129110609-129110978 | Common:9; Rare:137 | ||||
| chr9:129139906-129140179 | Rare:111 | ||||
| chr9:129608732-129608952 | Common:3; Rare:42 | ||||
| chr9:129803056-129803223 | Common:4; Rare:122 | ||||
| chr9:129824075-129824198 | Common:2; Rare:44; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:129835210-129835502 | Common:6; Rare:221 | ||||
| chr9:130043070-130043314 | Common:4; Rare:139 | ||||
| chr9:130053430-130053740 | Common:2; Rare:117 |