| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:99906570-99906718 | Rare:69 | ||||
| chr9:100098966-100099337 | Common:4; Rare:106; Clinvar:2; Clinvar (benign):1 | ||||
| chr9:100352854-100353078 | Rare:79 | ||||
| chr9:100427066-100427384 | Common:3; Rare:110 | ||||
| chr9:101398503-101398910 | Common:1; Rare:145 | ||||
| chr9:101487043-101487185 | Common:1; Rare:43 | ||||
| chr9:101533671-101533907 | Common:2; Rare:76 | ||||
| chr9:104093977-104094345 | Common:3; Rare:91 | ||||
| chr9:104094522-104094650 | Common:2; Rare:42 | ||||
| chr9:104747559-104747799 | Common:1; Rare:71 | ||||
| chr9:104927941-104927996 | Rare:11; Clinvar:4 | ||||
| chr9:105447955-105448126 | Common:2; Rare:65 | ||||
| chr9:105558033-105558170 | Rare:45; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:106862960-106863180 | Rare:74 | ||||
| chr9:106863542-106863648 | Rare:19 |