| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:128160008-128160429 | Common:2; Rare:99 | ||||
| chr9:128191768-128191847 | Common:1; Rare:20 | ||||
| chr9:128204212-128204381 | Rare:37 | ||||
| chr9:128275900-128276288 | Common:4; Rare:169 | ||||
| chr9:128322410-128322485 | Rare:30 | ||||
| chr9:128322731-128322906 | Common:2; Rare:85; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr9:128371187-128371383 | Rare:66 | ||||
| chr9:128552394-128552622 | Rare:88; Clinvar:1 | ||||
| chr9:128630123-128630348 | Common:3; Rare:59; Clinvar (benign):3 | ||||
| chr9:128683616-128683897 | Rare:66 | ||||
| chr9:128724102-128724464 | Common:2; Rare:116 | ||||
| chr9:128881929-128882202 | Common:2; Rare:93 | ||||
| chr9:128921956-128922320 | Common:1; Rare:78 | ||||
| chr9:128947598-128947734 | Common:1; Rare:63; Clinvar:4; Clinvar (benign):1 | ||||
| chr9:129080975-129081125 | Common:2; Rare:47 |