| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:125261691-125261860 | Common:1; Rare:65 | ||||
| chr9:125707070-125707370 | Common:2; Rare:95 | ||||
| chr9:126804922-126805080 | Common:3; Rare:53 | ||||
| chr9:127122502-127122659 | Common:1; Rare:36 | ||||
| chr9:127122662-127122994 | Common:3; Rare:91 | ||||
| chr9:127424294-127424485 | Common:1; Rare:60 | ||||
| chr9:127451257-127451557 | Common:3; Rare:127; Clinvar (benign):1 | ||||
| chr9:127569069-127569339 | Common:4; Rare:60 | ||||
| chr9:127579008-127579221 | Common:3; Rare:36 | ||||
| chr9:127612246-127612431 | Common:1; Rare:64; Clinvar:3; Clinvar (benign):3 | ||||
| chr9:127897327-127897560 | Common:1; Rare:54 | ||||
| chr9:127899518-127899872 | Common:3; Rare:102 | ||||
| chr9:128169143-128169489 | Common:1; Rare:85; Clinvar:1 | ||||
| chr9:128191457-128191642 | Rare:56 | ||||
| chr9:128191748-128191848 | Common:1; Rare:27 |