| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:20658219-20658369 | Common:3; Rare:61 | ||||
| chr9:20684115-20684282 | Common:2; Rare:64 | ||||
| chr9:21335351-21335526 | Common:2; Rare:67 | ||||
| chr9:21802522-21802677 | Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:26892731-26892895 | Common:1; Rare:79 | ||||
| chr9:26947089-26947298 | Common:1; Rare:77 | ||||
| chr9:26956182-26956470 | Common:2; Rare:96 | ||||
| chr9:26976376-26976534 | Rare:33 | ||||
| chr9:27573723-27573978 | Common:2; Rare:81; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:32384449-32384703 | Common:1; Rare:87 | ||||
| chr9:32552558-32552632 | Common:1; Rare:14; Clinvar:2 | ||||
| chr9:32573064-32573231 | Common:3; Rare:59 | ||||
| chr9:33001568-33001718 | Common:2; Rare:82; Clinvar (benign):3 | ||||
| chr9:33025049-33025378 | Common:7; Rare:134 | ||||
| chr9:33076601-33076810 | Common:2; Rare:73 |