| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:127854686-127854877 | Rare:36; Clinvar:4 | ||||
| chr9:127877631-127877728 | Rare:27 | ||||
| chr9:127937816-127937923 | Common:1; Rare:31; Clinvar:3; Clinvar (benign):1 | ||||
| chr9:128160008-128160401 | Common:2; Rare:93 | ||||
| chr9:128191775-128191857 | Common:1; Rare:17 | ||||
| chr9:128275918-128276307 | Common:5; Rare:173 | ||||
| chr9:128322410-128322485 | Rare:30 | ||||
| chr9:128322751-128322880 | Common:2; Rare:62; Clinvar (benign):5 | ||||
| chr9:128371175-128371404 | Common:1; Rare:87 | ||||
| chr9:128504601-128504782 | Rare:84; Clinvar:5 | ||||
| chr9:128552394-128552624 | Rare:90; Clinvar:2 | ||||
| chr9:128689534-128689648 | Rare:46 | ||||
| chr9:128724095-128724427 | Common:1; Rare:109 | ||||
| chr9:128771866-128771980 | Rare:30 | ||||
| chr9:128921958-128922314 | Common:1; Rare:77 |