| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:95082207-95082542 | Common:2; Rare:83 | ||||
| chr9:95083272-95083510 | Common:4; Rare:89 | ||||
| chr9:97645383-97645645 | Rare:32 | ||||
| chr9:97660790-97661054 | Common:2; Rare:53 | ||||
| chr9:97661814-97662083 | Common:2; Rare:38 | ||||
| chr9:97662740-97663046 | Rare:64 | ||||
| chr9:97687097-97687432 | Common:1; Rare:77; Clinvar:2; Clinvar (pathogenic):4 | ||||
| chr9:98219401-98219599 | Common:1; Rare:27 | ||||
| chr9:99819882-99820089 | Common:1; Rare:65 | ||||
| chr9:104841759-104841989 | Common:3; Rare:33 | ||||
| chr9:106859964-106860176 | Common:1; Rare:51 | ||||
| chr9:107637721-107637978 | Rare:53 | ||||
| chr9:110446019-110446203 | Common:1; Rare:38 | ||||
| chr9:112754900-112754986 | Common:2; Rare:14 | ||||
| chr9:113171582-113171879 | Common:6; Rare:74 |