| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:94207990-94208023 | Rare:10 | ||||
| chr4:94451703-94452002 | Common:4; Rare:95 | ||||
| chr4:94454546-94454854 | Common:2; Rare:54 | ||||
| chr4:95548921-95549114 | Common:1; Rare:43 | ||||
| chr4:98143450-98143642 | Common:1; Rare:49 | ||||
| chr4:98261142-98261534 | Common:1; Rare:130 | ||||
| chr4:98658609-98658913 | Common:2; Rare:82 | ||||
| chr4:98929093-98929397 | Common:3; Rare:76 | ||||
| chr4:98995356-98995790 | Common:6; Rare:147 | ||||
| chr4:99088696-99088891 | Common:6; Rare:90 | ||||
| chr4:99352980-99353163 | Common:2; Rare:40 | ||||
| chr4:99563598-99563763 | Common:2; Rare:46 | ||||
| chr4:99563922-99564173 | Common:2; Rare:82; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:99894339-99894625 | Common:3; Rare:97 | ||||
| chr4:99946519-99946792 | Rare:103 |