| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:100099424-100099708 | Rare:63 | ||||
| chr9:100352844-100353155 | Rare:113 | ||||
| chr9:100426614-100426719 | Rare:19 | ||||
| chr9:100427610-100427980 | Rare:83 | ||||
| chr9:100472891-100473211 | Common:1; Rare:83 | ||||
| chr9:101028576-101028783 | Common:2; Rare:65 | ||||
| chr9:101398551-101398927 | Common:1; Rare:132 | ||||
| chr9:101486960-101487380 | Common:3; Rare:101 | ||||
| chr9:101533662-101533976 | Common:2; Rare:92 | ||||
| chr9:104093871-104094330 | Common:5; Rare:122 | ||||
| chr9:104094509-104094650 | Common:3; Rare:47 | ||||
| chr9:104747535-104747757 | Rare:57 | ||||
| chr9:104747810-104748150 | Common:6; Rare:124 | ||||
| chr9:104764004-104764198 | Common:2; Rare:45 | ||||
| chr9:104928154-104928601 | Common:13; Rare:202; Clinvar:1; Clinvar (benign):3 |