| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:90997639-90997799 | Rare:41 | ||||
| chr9:91424596-91424720 | Common:1; Rare:30 | ||||
| chr9:92650837-92651066 | Common:2; Rare:43 | ||||
| chr9:92668981-92669233 | Common:3; Rare:47 | ||||
| chr9:94347452-94347494 | Rare:6 | ||||
| chr9:95032630-95032884 | Common:1; Rare:45 | ||||
| chr9:95038148-95038209 | Rare:17 | ||||
| chr9:95058507-95058718 | Rare:38 | ||||
| chr9:95075872-95076107 | Common:1; Rare:39 | ||||
| chr9:95083128-95083259 | Common:1; Rare:28 | ||||
| chr9:95092741-95092930 | Common:4; Rare:42 | ||||
| chr9:95106901-95107193 | Common:1; Rare:74; Clinvar:6; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr9:95117249-95117311 | Rare:10; Clinvar (benign):2 | ||||
| chr9:95426780-95426954 | Common:3; Rare:62 | ||||
| chr9:97238366-97238468 | Common:1; Rare:27 |