| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:152679870-152680112 | Rare:84 | ||||
| chr4:152779730-152780172 | Common:2; Rare:113 | ||||
| chr4:152936149-152936391 | Common:4; Rare:64 | ||||
| chr4:152936836-152937089 | Common:2; Rare:44 | ||||
| chr4:153788687-153788737 | Common:2; Rare:13 | ||||
| chr4:153789081-153789205 | Rare:21 | ||||
| chr4:156970958-156971190 | Rare:35 | ||||
| chr4:158173012-158173172 | Rare:27 | ||||
| chr4:158671830-158672171 | Common:4; Rare:91; Clinvar:1 | ||||
| chr4:158672215-158672359 | Common:1; Rare:32; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:158723214-158723463 | Common:2; Rare:107 | ||||
| chr4:163166832-163166964 | Common:2; Rare:42 | ||||
| chr4:165327418-165327880 | Common:2; Rare:129 | ||||
| chr4:165378938-165379087 | Common:2; Rare:40 | ||||
| chr4:169010227-169010443 | Common:1; Rare:65 |