| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:101533700-101533899 | Rare:58 | ||||
| chr9:104093985-104094327 | Common:3; Rare:80 | ||||
| chr9:104094522-104094603 | Common:1; Rare:26 | ||||
| chr9:104747644-104747779 | Rare:40 | ||||
| chr9:105447966-105448135 | Common:2; Rare:62 | ||||
| chr9:105558086-105558170 | Rare:20; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:106862685-106862735 | Rare:9 | ||||
| chr9:106862971-106863180 | Rare:72 | ||||
| chr9:106863322-106863630 | Common:1; Rare:67 | ||||
| chr9:108933951-108934493 | Common:8; Rare:215; Clinvar:7; Clinvar (benign):2 | ||||
| chr9:110048518-110048736 | Common:1; Rare:68 | ||||
| chr9:110125345-110125553 | Rare:42 | ||||
| chr9:110256416-110256725 | Common:5; Rare:109 | ||||
| chr9:111038686-111039035 | Common:6; Rare:80 | ||||
| chr9:111484173-111484469 | Common:1; Rare:147 |