| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:35732373-35732684 | Common:3; Rare:79 | ||||
| chr9:35748994-35749361 | Common:2; Rare:140 | ||||
| chr9:35812244-35812310 | Rare:24 | ||||
| chr9:35814983-35815251 | Rare:71 | ||||
| chr9:36190715-36190994 | Common:1; Rare:93 | ||||
| chr9:36258386-36258580 | Common:2; Rare:42; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:36572772-36572939 | Rare:47 | ||||
| chr9:37120174-37120626 | Common:2; Rare:141 | ||||
| chr9:37422617-37422749 | Common:2; Rare:71 | ||||
| chr9:37485737-37486024 | Common:3; Rare:102 | ||||
| chr9:37592474-37592661 | Common:2; Rare:68 | ||||
| chr9:37784947-37785141 | Common:1; Rare:93; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr9:37800682-37800794 | Common:1; Rare:34 | ||||
| chr9:37904076-37904463 | Common:3; Rare:127 | ||||
| chr9:42129324-42129376 | Common:1; Rare:5 |