| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:92325632-92325973 | Common:3; Rare:103 | ||||
| chr9:92535978-92536122 | Rare:19 | ||||
| chr9:93451511-93451688 | Common:3; Rare:54 | ||||
| chr9:95875453-95875684 | Rare:76 | ||||
| chr9:97633302-97633448 | Rare:37 | ||||
| chr9:97633544-97633828 | Common:3; Rare:87 | ||||
| chr9:98943579-98943885 | Common:4; Rare:84 | ||||
| chr9:99221916-99222329 | Common:2; Rare:156; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:99906589-99906690 | Rare:50 | ||||
| chr9:100098974-100099319 | Common:2; Rare:96; Clinvar:2 | ||||
| chr9:100352881-100353081 | Rare:69 | ||||
| chr9:101028565-101028829 | Common:2; Rare:85 | ||||
| chr9:101398565-101398910 | Common:1; Rare:118 | ||||
| chr9:104747585-104747776 | Rare:54 | ||||
| chr9:105558038-105558142 | Rare:34 |