| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:19127399-19127692 | Common:6; Rare:85 | ||||
| chr9:19230618-19230825 | Common:2; Rare:108 | ||||
| chr9:19380191-19380345 | Common:4; Rare:76 | ||||
| chr9:20684101-20684284 | Common:3; Rare:73 | ||||
| chr9:21031586-21031691 | Common:1; Rare:45 | ||||
| chr9:21802467-21802700 | Common:3; Rare:74; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:21994766-21995104 | Common:1; Rare:70 | ||||
| chr9:26892731-26892835 | Rare:57 | ||||
| chr9:26947146-26947298 | Rare:52 | ||||
| chr9:26956255-26956481 | Common:2; Rare:84 | ||||
| chr9:32384524-32384721 | Common:1; Rare:77 | ||||
| chr9:32573064-32573226 | Common:3; Rare:58 | ||||
| chr9:33001538-33001713 | Common:1; Rare:100; Clinvar (benign):4 | ||||
| chr9:33025049-33025407 | Common:7; Rare:139 | ||||
| chr9:33166862-33166956 | Rare:38 |