| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:37120136-37120598 | Common:2; Rare:143 | ||||
| chr9:37422617-37422735 | Common:2; Rare:63 | ||||
| chr9:37485728-37486037 | Common:3; Rare:109 | ||||
| chr9:37592461-37592649 | Common:2; Rare:72 | ||||
| chr9:37650725-37651028 | Common:1; Rare:92 | ||||
| chr9:37784995-37785149 | Common:1; Rare:75; Clinvar:1; Clinvar (benign):3 | ||||
| chr9:37800689-37800822 | Common:1; Rare:40 | ||||
| chr9:37904061-37904237 | Common:2; Rare:57 | ||||
| chr9:38392504-38392777 | Common:2; Rare:75 | ||||
| chr9:68356354-68356635 | Common:7; Rare:49 | ||||
| chr9:68779949-68780076 | Common:1; Rare:39 | ||||
| chr9:69035677-69035809 | Common:1; Rare:35; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:69759934-69760157 | Common:3; Rare:97 | ||||
| chr9:70258824-70259081 | Common:4; Rare:120 | ||||
| chr9:71768467-71768605 | Rare:34 |