| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:98056565-98056777 | Common:1; Rare:72 | ||||
| chr9:98255600-98255915 | Common:3; Rare:98 | ||||
| chr9:99221898-99222365 | Common:2; Rare:188; Clinvar:3; Clinvar (benign):3 | ||||
| chr9:99821682-99821893 | Rare:70 | ||||
| chr9:99906563-99906717 | Rare:69 | ||||
| chr9:100098966-100099323 | Common:3; Rare:103; Clinvar:2 | ||||
| chr9:100352858-100353107 | Rare:92 | ||||
| chr9:101028527-101028776 | Common:2; Rare:75 | ||||
| chr9:101398570-101398910 | Common:1; Rare:114 | ||||
| chr9:101487097-101487185 | Common:1; Rare:20 | ||||
| chr9:101533706-101533914 | Rare:64 | ||||
| chr9:104093976-104094371 | Common:5; Rare:104 | ||||
| chr9:104094481-104094627 | Common:2; Rare:49 | ||||
| chr9:104747601-104747821 | Common:1; Rare:72 | ||||
| chr9:105447959-105448144 | Common:2; Rare:66 |