| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:27573709-27573972 | Common:2; Rare:85; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:32384491-32384728 | Common:1; Rare:89 | ||||
| chr9:32552532-32552663 | Common:1; Rare:22; Clinvar:2 | ||||
| chr9:33001539-33001751 | Common:3; Rare:105; Clinvar (benign):4 | ||||
| chr9:33025071-33025382 | Common:7; Rare:127 | ||||
| chr9:33076583-33076865 | Common:2; Rare:91 | ||||
| chr9:33166856-33166956 | Rare:39 | ||||
| chr9:33167109-33167509 | Common:1; Rare:139; Clinvar:6 | ||||
| chr9:33264712-33265139 | Rare:119 | ||||
| chr9:33290394-33290595 | Common:2; Rare:77 | ||||
| chr9:33402458-33402650 | Rare:32 | ||||
| chr9:33817627-33817934 | Common:1; Rare:87 | ||||
| chr9:34048870-34048957 | Rare:33 | ||||
| chr9:34126555-34126855 | Common:1; Rare:89 | ||||
| chr9:34329213-34329606 | Rare:122 |