| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128771854-128771980 | Rare:35 | ||||
| chr9:128787162-128787332 | Common:3; Rare:58 | ||||
| chr9:128881901-128882206 | Common:2; Rare:100 | ||||
| chr9:128882526-128882654 | Common:1; Rare:28 | ||||
| chr9:128947593-128947725 | Common:1; Rare:57; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:129110646-129110941 | Common:2; Rare:64 | ||||
| chr9:129111240-129111603 | Common:2; Rare:104 | ||||
| chr9:129139945-129140129 | Rare:38 | ||||
| chr9:129626113-129626209 | Rare:37 | ||||
| chr9:129803053-129803245 | Common:2; Rare:72 | ||||
| chr9:129824098-129824282 | Common:3; Rare:49; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:129835112-129835492 | Common:3; Rare:147 | ||||
| chr9:130043097-130043296 | Common:2; Rare:62 | ||||
| chr9:130053556-130053741 | Rare:42 | ||||
| chr9:130053854-130053979 | Common:1; Rare:52 |