| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:28212807-28213332 | Rare:176 | ||||
| chr9:31030585-31031139 | Common:10; Rare:163 | ||||
| chr9:32550829-32551213 | Common:1; Rare:147; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:33044164-33044582 | Common:2; Rare:129 | ||||
| chr9:33160979-33161379 | Common:1; Rare:84 | ||||
| chr9:33375328-33375526 | Rare:36 | ||||
| chr9:33448299-33448699 | Common:1; Rare:112 | ||||
| chr9:33510919-33511111 | Common:1; Rare:51 | ||||
| chr9:33511132-33511238 | Rare:38 | ||||
| chr9:33523425-33523643 | Common:1; Rare:39 | ||||
| chr9:33560017-33560581 | Rare:147 | ||||
| chr9:33677039-33677306 | Common:7; Rare:72 | ||||
| chr9:33816669-33816827 | Common:1; Rare:35 | ||||
| chr9:33818280-33818445 | Common:1; Rare:31 | ||||
| chr9:34072420-34072760 | Common:1; Rare:50 |