| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:96523401-96523727 | Common:3; Rare:89 | ||||
| chr9:96686888-96687087 | Common:3; Rare:56 | ||||
| chr9:97238247-97238504 | Common:5; Rare:75 | ||||
| chr9:97238670-97238950 | Common:2; Rare:62 | ||||
| chr9:97502828-97502954 | Common:1; Rare:18 | ||||
| chr9:97662861-97663040 | Rare:52 | ||||
| chr9:97689535-97689725 | Rare:63; Clinvar:1; Clinvar (pathogenic):5 | ||||
| chr9:97786493-97786748 | Common:2; Rare:47 | ||||
| chr9:97787537-97787838 | Common:2; Rare:50 | ||||
| chr9:97817452-97817755 | Common:2; Rare:38 | ||||
| chr9:97819445-97819716 | Common:4; Rare:45 | ||||
| chr9:97851917-97852098 | Common:5; Rare:43 | ||||
| chr9:97852169-97852328 | Common:2; Rare:42 | ||||
| chr9:97852452-97852680 | Rare:54 | ||||
| chr9:97854875-97855117 | Common:1; Rare:75 |