| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:98255344-98255683 | Common:1; Rare:96 | ||||
| chr9:98255693-98255957 | Common:3; Rare:84 | ||||
| chr9:99221898-99222357 | Common:2; Rare:182; Clinvar:2; Clinvar (benign):3 | ||||
| chr9:99906570-99906711 | Rare:67 | ||||
| chr9:100098966-100099314 | Common:3; Rare:99; Clinvar:2 | ||||
| chr9:100352831-100353081 | Rare:90 | ||||
| chr9:101398511-101398910 | Common:1; Rare:141 | ||||
| chr9:101487037-101487176 | Common:1; Rare:40 | ||||
| chr9:101533724-101533914 | Rare:60 | ||||
| chr9:104093985-104094371 | Common:5; Rare:98 | ||||
| chr9:104747544-104747788 | Common:1; Rare:71 | ||||
| chr9:104764057-104764207 | Common:2; Rare:33 | ||||
| chr9:104928141-104928536 | Common:6; Rare:102; Clinvar:1; Clinvar (benign):2 | ||||
| chr9:105558027-105558163 | Rare:48; Clinvar (benign):1 | ||||
| chr9:106862978-106863201 | Rare:74 |