| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:152779674-152780156 | Common:4; Rare:207 | ||||
| chr4:152936000-152936392 | Common:8; Rare:138 | ||||
| chr4:153344508-153344745 | Common:8; Rare:142 | ||||
| chr4:153345030-153345400 | Common:7; Rare:110 | ||||
| chr4:153466203-153466386 | Common:6; Rare:144 | ||||
| chr4:154550347-154550530 | Rare:112 | ||||
| chr4:158671825-158672316 | Common:9; Rare:199; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:158723348-158723471 | Rare:99 | ||||
| chr4:158768822-158769001 | Common:1; Rare:60 | ||||
| chr4:159103450-159104130 | Common:8; Rare:290 | ||||
| chr4:159229150-159229442 | Common:2; Rare:84 | ||||
| chr4:163166779-163166986 | Common:5; Rare:109 | ||||
| chr4:163494081-163494257 | Common:6; Rare:30 | ||||
| chr4:163494538-163494794 | Common:5; Rare:171 | ||||
| chr4:165112795-165112898 | Rare:41 |