| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127424267-127424406 | Rare:49 | ||||
| chr9:127451282-127451520 | Common:2; Rare:105 | ||||
| chr9:127937816-127937992 | Common:2; Rare:47; Clinvar:4; Clinvar (benign):2 | ||||
| chr9:128160036-128160383 | Common:2; Rare:85 | ||||
| chr9:128191793-128191826 | Rare:6 | ||||
| chr9:128275946-128276293 | Common:4; Rare:163 | ||||
| chr9:128322417-128322535 | Common:1; Rare:38 | ||||
| chr9:128322739-128322860 | Common:2; Rare:45; Clinvar (benign):5 | ||||
| chr9:128683659-128683890 | Rare:58 | ||||
| chr9:128724095-128724485 | Common:4; Rare:128 | ||||
| chr9:128947601-128947716 | Common:1; Rare:53; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:129753034-129753174 | Rare:36 | ||||
| chr9:129824098-129824191 | Common:2; Rare:30; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:129835237-129835475 | Common:2; Rare:89 | ||||
| chr9:130053867-130053924 | Common:1; Rare:20 |