| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:153466109-153466381 | Common:3; Rare:106 | ||||
| chr4:154550304-154550505 | Common:2; Rare:69 | ||||
| chr4:158172365-158172778 | Rare:69 | ||||
| chr4:158173021-158173186 | Rare:28 | ||||
| chr4:158210315-158210355 | Rare:7 | ||||
| chr4:158210363-158210599 | Common:3; Rare:58 | ||||
| chr4:158671825-158672359 | Common:5; Rare:135; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:158723319-158723463 | Common:2; Rare:66 | ||||
| chr4:158805825-158805872 | Common:1; Rare:8 | ||||
| chr4:162163790-162164137 | Common:2; Rare:81 | ||||
| chr4:162164290-162164357 | Rare:18 | ||||
| chr4:163166849-163167001 | Common:2; Rare:51 | ||||
| chr4:163494421-163494792 | Common:3; Rare:149 | ||||
| chr4:164956836-164956999 | Common:2; Rare:56 | ||||
| chr4:165112818-165112990 | Common:1; Rare:51 |