| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:158671830-158672132 | Common:4; Rare:82 | ||||
| chr4:158672208-158672383 | Common:1; Rare:39; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:158723316-158723463 | Common:2; Rare:66 | ||||
| chr4:165112825-165113013 | Common:1; Rare:56 | ||||
| chr4:168318739-168318834 | Rare:20 | ||||
| chr4:168480458-168480618 | Rare:21 | ||||
| chr4:169010237-169010474 | Common:1; Rare:72 | ||||
| chr4:169270939-169271152 | Common:1; Rare:72 | ||||
| chr4:169620391-169620702 | Common:2; Rare:107 | ||||
| chr4:173369802-173369935 | Common:1; Rare:45 | ||||
| chr4:173370690-173370962 | Common:2; Rare:68 | ||||
| chr4:174283618-174283932 | Common:1; Rare:59 | ||||
| chr4:177442371-177442526 | Rare:93; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr4:182917319-182917514 | Common:3; Rare:76 | ||||
| chr4:183659090-183659401 | Common:1; Rare:103 |