| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:15423031-15423106 | Common:1; Rare:36 | ||||
| chr9:19049324-19049677 | Common:2; Rare:143 | ||||
| chr9:19102863-19103030 | Common:1; Rare:67 | ||||
| chr9:19127401-19127581 | Common:2; Rare:53 | ||||
| chr9:19230349-19230849 | Common:8; Rare:211 | ||||
| chr9:19380190-19380330 | Common:4; Rare:71 | ||||
| chr9:19408710-19409017 | Common:5; Rare:113 | ||||
| chr9:20684094-20684283 | Common:3; Rare:76 | ||||
| chr9:22009153-22009476 | Common:1; Rare:112 | ||||
| chr9:26892731-26892887 | Common:1; Rare:77 | ||||
| chr9:26946992-26947281 | Common:1; Rare:114 | ||||
| chr9:26956255-26956459 | Common:2; Rare:76 | ||||
| chr9:27529738-27529819 | Common:1; Rare:31 | ||||
| chr9:27573430-27573535 | Common:5; Rare:58 | ||||
| chr9:27573709-27573975 | Common:2; Rare:86; Clinvar:5; Clinvar (benign):1 |