| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:36036800-36036990 | Common:2; Rare:64 | ||||
| chr9:36190656-36191074 | Common:2; Rare:127 | ||||
| chr9:36258409-36258580 | Common:2; Rare:38; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:37465271-37465597 | Common:3; Rare:104 | ||||
| chr9:37800707-37800794 | Rare:25 | ||||
| chr9:37903701-37903771 | Rare:17 | ||||
| chr9:37904059-37904217 | Rare:54 | ||||
| chr9:38392593-38392785 | Common:1; Rare:50 | ||||
| chr9:65675682-65675964 | Common:1; Rare:70 | ||||
| chr9:69173949-69174250 | Common:6; Rare:94 | ||||
| chr9:69759930-69760143 | Common:3; Rare:95 | ||||
| chr9:70258864-70259071 | Common:2; Rare:97 | ||||
| chr9:70414309-70414477 | Rare:31 | ||||
| chr9:71911173-71911510 | Common:3; Rare:96 | ||||
| chr9:73151713-73151921 | Rare:40 |