| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127937832-127937981 | Common:2; Rare:36; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:128160008-128160419 | Common:2; Rare:97 | ||||
| chr9:128191474-128191657 | Rare:57 | ||||
| chr9:128191753-128191857 | Common:1; Rare:25 | ||||
| chr9:128204202-128204232 | Rare:14 | ||||
| chr9:128275909-128276327 | Common:5; Rare:187 | ||||
| chr9:128322410-128322485 | Rare:30 | ||||
| chr9:128322711-128322887 | Common:2; Rare:78; Clinvar (benign):5 | ||||
| chr9:128371195-128371401 | Rare:78 | ||||
| chr9:128552408-128552597 | Rare:73; Clinvar:1 | ||||
| chr9:128683406-128683470 | Rare:7 | ||||
| chr9:128724095-128724472 | Common:3; Rare:123 | ||||
| chr9:128881929-128882202 | Common:2; Rare:93 | ||||
| chr9:128921982-128922333 | Common:2; Rare:80 | ||||
| chr9:128947528-128947745 | Common:2; Rare:102; Clinvar:6; Clinvar (benign):2 |