| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128504605-128504798 | Rare:90; Clinvar:5 | ||||
| chr9:128552408-128552611 | Rare:79; Clinvar:1 | ||||
| chr9:128630070-128630343 | Common:4; Rare:69; Clinvar (benign):3 | ||||
| chr9:128656652-128657002 | Common:2; Rare:115; Clinvar (pathogenic):1 | ||||
| chr9:128724089-128724467 | Common:2; Rare:125 | ||||
| chr9:128771854-128771980 | Rare:35 | ||||
| chr9:128881907-128882197 | Common:2; Rare:96 | ||||
| chr9:128882526-128882634 | Common:1; Rare:26 | ||||
| chr9:128921958-128922324 | Common:1; Rare:80 | ||||
| chr9:128947593-128947722 | Common:1; Rare:55; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:129110698-129111029 | Common:5; Rare:102 | ||||
| chr9:129139948-129140132 | Rare:36 | ||||
| chr9:129824098-129824299 | Common:3; Rare:53; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:129835168-129835492 | Common:3; Rare:127 | ||||
| chr9:130043113-130043296 | Common:2; Rare:59 |