| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:92393102-92393380 | Common:1; Rare:66 | ||||
| chr9:92404494-92404637 | Rare:37 | ||||
| chr9:92404641-92404798 | Rare:26 | ||||
| chr9:92424298-92424430 | Rare:23 | ||||
| chr9:92424433-92424776 | Common:2; Rare:49 | ||||
| chr9:92482459-92482678 | Rare:30 | ||||
| chr9:92535960-92536166 | Rare:31 | ||||
| chr9:92670001-92670351 | Common:1; Rare:109 | ||||
| chr9:92764762-92765006 | Common:1; Rare:84; Clinvar (benign):2 | ||||
| chr9:93134207-93134367 | Common:2; Rare:57 | ||||
| chr9:93451445-93451702 | Common:3; Rare:70 | ||||
| chr9:93452292-93452387 | Rare:15 | ||||
| chr9:93452927-93453046 | Rare:27 | ||||
| chr9:93453546-93453687 | Rare:31 | ||||
| chr9:94259289-94259345 | Common:1; Rare:18 |