| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:122264527-122264703 | Common:2; Rare:38 | ||||
| chr9:122264713-122264945 | Common:3; Rare:67 | ||||
| chr9:122828131-122828315 | Common:1; Rare:67 | ||||
| chr9:122913268-122913351 | Common:2; Rare:16 | ||||
| chr9:122931482-122931673 | Common:3; Rare:34 | ||||
| chr9:123929928-123930247 | Rare:96 | ||||
| chr9:124261269-124261470 | Rare:31 | ||||
| chr9:124861908-124862136 | Common:1; Rare:95 | ||||
| chr9:124940962-124941168 | Common:3; Rare:72 | ||||
| chr9:125189715-125190027 | Common:1; Rare:141 | ||||
| chr9:125241245-125241637 | Common:2; Rare:115 | ||||
| chr9:126804924-126805064 | Common:1; Rare:43 | ||||
| chr9:127424106-127424440 | Common:1; Rare:92 | ||||
| chr9:127451280-127451565 | Common:3; Rare:119; Clinvar (benign):1 | ||||
| chr9:127612047-127612323 | Common:1; Rare:106; Clinvar:4; Clinvar (benign):2 |