| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:177442376-177442554 | Rare:105; Clinvar:2 | ||||
| chr4:182143869-182143976 | Rare:27 | ||||
| chr4:182144418-182144700 | Common:3; Rare:88 | ||||
| chr4:182917287-182917514 | Common:3; Rare:82 | ||||
| chr4:183444309-183444815 | Common:2; Rare:214 | ||||
| chr4:183504523-183504809 | Common:2; Rare:94 | ||||
| chr4:183505788-183506110 | Common:1; Rare:116 | ||||
| chr4:183659080-183659401 | Common:1; Rare:104 | ||||
| chr4:183905225-183905417 | Common:1; Rare:44 | ||||
| chr4:184474512-184474796 | Rare:63 | ||||
| chr4:184649399-184649835 | Common:4; Rare:142 | ||||
| chr4:184734032-184734447 | Common:10; Rare:161 | ||||
| chr4:185142967-185143337 | Common:4; Rare:106; Clinvar:1; Clinvar (benign):3 | ||||
| chr4:185203890-185204096 | Rare:66 | ||||
| chr4:185396581-185396858 | Rare:89 |