| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:5628938-5629235 | Common:1; Rare:140 | ||||
| chr9:15422562-15422880 | Common:1; Rare:136 | ||||
| chr9:19102874-19103042 | Common:2; Rare:72 | ||||
| chr9:19380191-19380373 | Common:4; Rare:88 | ||||
| chr9:20684058-20684282 | Common:3; Rare:90 | ||||
| chr9:21802323-21802696 | Common:3; Rare:98; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:21994329-21994575 | Rare:77; Clinvar:2; Clinvar (benign):6 | ||||
| chr9:26947128-26947287 | Rare:59 | ||||
| chr9:27573430-27573533 | Common:5; Rare:56 | ||||
| chr9:33025100-33025301 | Common:5; Rare:81 | ||||
| chr9:33473838-33474143 | Common:4; Rare:94 | ||||
| chr9:33750548-33750710 | Rare:47 | ||||
| chr9:34126662-34126786 | Rare:42 | ||||
| chr9:34178834-34179061 | Common:1; Rare:59 | ||||
| chr9:34612090-34612223 | Common:8; Rare:43 |