| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:88523587-88523848 | Common:2; Rare:93 | ||||
| chr4:88592306-88592520 | Common:1; Rare:63 | ||||
| chr4:88823134-88823389 | Common:3; Rare:42 | ||||
| chr4:89111349-89111585 | Common:4; Rare:91 | ||||
| chr4:94451760-94452002 | Common:3; Rare:83 | ||||
| chr4:94757733-94757993 | Common:4; Rare:64 | ||||
| chr4:95548921-95549149 | Common:2; Rare:48 | ||||
| chr4:95549202-95549343 | Common:1; Rare:25 | ||||
| chr4:98143450-98143638 | Common:1; Rare:48 | ||||
| chr4:98261279-98261519 | Common:1; Rare:83 | ||||
| chr4:98929108-98929365 | Common:3; Rare:64 | ||||
| chr4:99088696-99088891 | Common:6; Rare:90 | ||||
| chr4:99563612-99563772 | Common:2; Rare:42 | ||||
| chr4:99563931-99564127 | Common:2; Rare:68; Clinvar:1; Clinvar (benign):2 | ||||
| chr4:99894352-99894620 | Common:3; Rare:93 |