| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127954081-127954248 | Rare:24 | ||||
| chr9:128094459-128094660 | Common:2; Rare:26 | ||||
| chr9:128109585-128109664 | Rare:13 | ||||
| chr9:128109925-128110015 | Rare:19 | ||||
| chr9:128110244-128110303 | Rare:19 | ||||
| chr9:128113469-128113744 | Common:3; Rare:58 | ||||
| chr9:128113872-128114089 | Common:1; Rare:40 | ||||
| chr9:128114284-128114567 | Rare:63 | ||||
| chr9:128115116-128115501 | Common:5; Rare:71 | ||||
| chr9:128257818-128258049 | Common:1; Rare:71 | ||||
| chr9:128588568-128588943 | Common:1; Rare:96; Clinvar (benign):6 | ||||
| chr9:128684429-128684555 | Rare:26 | ||||
| chr9:128693634-128694037 | Rare:103; Clinvar:1 | ||||
| chr9:129488487-129488869 | Common:2; Rare:101 | ||||
| chr9:130690061-130690310 | Common:1; Rare:45 |