| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:14791386-14791587 | Common:2; Rare:38 | ||||
| chr9:14993148-14993318 | Common:5; Rare:73 | ||||
| chr9:15469266-15469395 | Rare:38 | ||||
| chr9:15469944-15470224 | Rare:84 | ||||
| chr9:15479616-15479913 | Common:2; Rare:89 | ||||
| chr9:25677352-25677666 | Common:3; Rare:121 | ||||
| chr9:26989866-26990192 | Common:1; Rare:60 | ||||
| chr9:29214015-29214336 | Common:3; Rare:88 | ||||
| chr9:32550829-32551156 | Common:1; Rare:130; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:34557663-34557904 | Rare:61 | ||||
| chr9:35604021-35604177 | Common:3; Rare:41 | ||||
| chr9:35684247-35684794 | Rare:133; Clinvar:4; Clinvar (benign):5 | ||||
| chr9:36353005-36353246 | Rare:65 | ||||
| chr9:38437573-38437698 | Common:1; Rare:25 | ||||
| chr9:39464458-39464657 | Common:1; Rare:50 |