| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:97922171-97922327 | Common:1; Rare:56 | ||||
| chr9:97922456-97922622 | Common:4; Rare:79 | ||||
| chr9:97984494-97984601 | Common:1; Rare:55 | ||||
| chr9:98056521-98056798 | Common:2; Rare:95 | ||||
| chr9:98119175-98119419 | Common:1; Rare:57 | ||||
| chr9:98192611-98192891 | Common:6; Rare:76 | ||||
| chr9:98255340-98255476 | Common:1; Rare:44 | ||||
| chr9:98255534-98255854 | Common:3; Rare:99 | ||||
| chr9:98943287-98943585 | Rare:52 | ||||
| chr9:98943708-98943968 | Common:4; Rare:77 | ||||
| chr9:99221887-99222360 | Common:2; Rare:190; Clinvar:3; Clinvar (benign):3 | ||||
| chr9:99222368-99222575 | Common:2; Rare:82 | ||||
| chr9:99821693-99822319 | Rare:169 | ||||
| chr9:99906574-99906717 | Rare:67 | ||||
| chr9:100098959-100099337 | Common:4; Rare:107; Clinvar:2; Clinvar (benign):1 |