| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:99105962-99105984 | Rare:7 | ||||
| chr9:99112335-99112595 | Rare:50 | ||||
| chr9:99819876-99820181 | Common:2; Rare:90 | ||||
| chr9:99987972-99988173 | Common:1; Rare:38 | ||||
| chr9:100004156-100004274 | Rare:18 | ||||
| chr9:100049493-100049605 | Common:2; Rare:15 | ||||
| chr9:100292120-100292406 | Rare:58; Clinvar:2 | ||||
| chr9:100296682-100296969 | Common:2; Rare:51; Clinvar:3; Clinvar (benign):2 | ||||
| chr9:100303425-100303638 | Common:6; Rare:51 | ||||
| chr9:100305498-100305629 | Rare:16 | ||||
| chr9:100305963-100306247 | Common:2; Rare:55 | ||||
| chr9:100984808-100985102 | Rare:41 | ||||
| chr9:101486335-101486409 | Common:2; Rare:20 | ||||
| chr9:104785583-104785877 | Common:1; Rare:69; Clinvar (benign):1 | ||||
| chr9:107637718-107638011 | Common:1; Rare:68 |