| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:19049328-19049469 | Rare:65 | ||||
| chr9:19102857-19103049 | Common:2; Rare:81 | ||||
| chr9:19380165-19380377 | Common:6; Rare:105 | ||||
| chr9:20622446-20622667 | Rare:77 | ||||
| chr9:20684088-20684282 | Common:3; Rare:76 | ||||
| chr9:21031596-21031743 | Common:1; Rare:54 | ||||
| chr9:21335300-21335504 | Common:4; Rare:66 | ||||
| chr9:21802515-21802700 | Common:1; Rare:58; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:21994218-21994452 | Rare:90; Clinvar:13; Clinvar (benign):13; Clinvar (pathogenic):2 | ||||
| chr9:21994595-21994736 | Common:1; Rare:37 | ||||
| chr9:22008789-22009152 | Common:1; Rare:131 | ||||
| chr9:22009174-22009482 | Common:1; Rare:108 | ||||
| chr9:26892338-26892490 | Rare:66 | ||||
| chr9:26892719-26892895 | Common:1; Rare:85 | ||||
| chr9:26947024-26947300 | Common:1; Rare:102 |