| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:33934367-33934386 | Common:1; Rare:1 | ||||
| chr9:34048827-34048992 | Common:2; Rare:73 | ||||
| chr9:34049185-34049293 | Common:1; Rare:27 | ||||
| chr9:34126361-34126482 | Rare:50 | ||||
| chr9:34178974-34179247 | Common:1; Rare:68 | ||||
| chr9:34329198-34329603 | Rare:127 | ||||
| chr9:34637715-34638125 | Common:3; Rare:108 | ||||
| chr9:34652015-34652231 | Rare:60 | ||||
| chr9:34665363-34665665 | Rare:96 | ||||
| chr9:34666009-34666178 | Common:1; Rare:38 | ||||
| chr9:35071413-35071522 | Common:1; Rare:29 | ||||
| chr9:35072342-35072466 | Rare:34; Clinvar:1 | ||||
| chr9:35072535-35072737 | Rare:55; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:35075278-35075563 | Rare:71; Clinvar:5; Clinvar (benign):2 | ||||
| chr9:35103017-35103232 | Common:1; Rare:87 |