| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:125261691-125261848 | Common:1; Rare:62 | ||||
| chr9:125707147-125707364 | Common:2; Rare:72 | ||||
| chr9:126804928-126805070 | Common:3; Rare:43 | ||||
| chr9:127424337-127424440 | Common:1; Rare:30 | ||||
| chr9:127451257-127451520 | Common:2; Rare:116 | ||||
| chr9:127452074-127452235 | Common:1; Rare:20 | ||||
| chr9:127578998-127579278 | Common:4; Rare:58 | ||||
| chr9:127877645-127877785 | Rare:34 | ||||
| chr9:128091267-128091462 | Rare:39 | ||||
| chr9:128159996-128160423 | Common:3; Rare:103 | ||||
| chr9:128275919-128276307 | Common:5; Rare:173 | ||||
| chr9:128322410-128322924 | Common:5; Rare:176; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr9:128371193-128371423 | Rare:90 | ||||
| chr9:128552401-128552611 | Rare:81; Clinvar:1 | ||||
| chr9:128656646-128656774 | Common:2; Rare:61; Clinvar (pathogenic):1 |