| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:174522423-174522613 | Rare:62; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr4:174829210-174829419 | Common:1; Rare:44 | ||||
| chr4:175788053-175788204 | Rare:23 | ||||
| chr4:175812196-175812893 | Common:11; Rare:159 | ||||
| chr4:175812994-175813206 | Rare:40 | ||||
| chr4:176065714-176066078 | Common:7; Rare:109 | ||||
| chr4:176195554-176195694 | Common:1; Rare:51 | ||||
| chr4:176319670-176320064 | Common:5; Rare:125 | ||||
| chr4:177442376-177442530 | Rare:93; Clinvar:2 | ||||
| chr4:182143918-182143982 | Rare:16 | ||||
| chr4:182144435-182144734 | Common:3; Rare:97 | ||||
| chr4:183444309-183444711 | Common:2; Rare:173 | ||||
| chr4:183504522-183504803 | Common:1; Rare:94 | ||||
| chr4:183659049-183659417 | Common:1; Rare:113 | ||||
| chr4:183960107-183960302 | Common:2; Rare:36 |