| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:89310910-89311200 | Common:2; Rare:85 | ||||
| chr9:89318368-89318548 | Common:5; Rare:80 | ||||
| chr9:90801701-90801982 | Common:2; Rare:78 | ||||
| chr9:92115378-92115492 | Common:1; Rare:31; Clinvar:1 | ||||
| chr9:92293660-92293940 | Common:5; Rare:94 | ||||
| chr9:92325317-92325930 | Common:8; Rare:154 | ||||
| chr9:92964183-92964323 | Rare:24 | ||||
| chr9:93029764-93029996 | Common:1; Rare:53 | ||||
| chr9:93453528-93453690 | Rare:37 | ||||
| chr9:94030693-94030854 | Common:1; Rare:47 | ||||
| chr9:94259196-94259328 | Rare:39 | ||||
| chr9:95875977-95876080 | Common:4; Rare:51; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:96566791-96566991 | Common:1; Rare:63 | ||||
| chr9:96655302-96655434 | Rare:33 | ||||
| chr9:96778038-96778154 | Rare:36 |