| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:104788535-104788592 | Rare:17 | ||||
| chr9:121289122-121289410 | Common:1; Rare:68 | ||||
| chr9:121302653-121303065 | Common:2; Rare:97; Clinvar (benign):4 | ||||
| chr9:121304041-121304244 | Rare:31 | ||||
| chr9:121304503-121304791 | Common:1; Rare:51 | ||||
| chr9:121309767-121309958 | Common:2; Rare:32 | ||||
| chr9:121316787-121317230 | Common:1; Rare:112; Clinvar:1 | ||||
| chr9:121318176-121319052 | Common:4; Rare:204; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:121319079-121319116 | Rare:11 | ||||
| chr9:121331325-121331446 | Rare:23 | ||||
| chr9:121332952-121333220 | Common:3; Rare:47 | ||||
| chr9:121463297-121463519 | Common:1; Rare:38 | ||||
| chr9:121498832-121499024 | Common:1; Rare:29 | ||||
| chr9:121499650-121499836 | Rare:56 | ||||
| chr9:124355108-124355312 | Common:2; Rare:56 |