| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:99221592-99221660 | Rare:31; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:99221890-99222357 | Common:2; Rare:187; Clinvar:3; Clinvar (benign):3 | ||||
| chr9:99906570-99906694 | Rare:63 | ||||
| chr9:100098951-100099341 | Common:4; Rare:111; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:100352860-100353071 | Rare:72 | ||||
| chr9:101398526-101398998 | Common:1; Rare:155 | ||||
| chr9:101435706-101435939 | Common:2; Rare:49; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr9:101487015-101487088 | Rare:23 | ||||
| chr9:101533748-101533907 | Rare:52 | ||||
| chr9:104094431-104094603 | Common:2; Rare:46 | ||||
| chr9:104747582-104747776 | Rare:57 | ||||
| chr9:105447959-105448153 | Common:2; Rare:72 | ||||
| chr9:105557855-105558170 | Rare:78; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:106862782-106863106 | Rare:91 | ||||
| chr9:106863109-106863186 | Rare:20 |