| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:155376770-155377040 | Rare:68 | ||||
| chr4:155758870-155759091 | Common:1; Rare:53 | ||||
| chr4:156971797-156971972 | Common:1; Rare:67 | ||||
| chr4:157220452-157220589 | Common:4; Rare:41 | ||||
| chr4:158172371-158172594 | Rare:33 | ||||
| chr4:158173023-158173064 | Rare:11 | ||||
| chr4:158201427-158201622 | Common:3; Rare:31 | ||||
| chr4:158210380-158210459 | Common:1; Rare:16 | ||||
| chr4:158671809-158672173 | Common:4; Rare:100; Clinvar:1 | ||||
| chr4:158672203-158672359 | Common:1; Rare:33; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:158723131-158723439 | Common:2; Rare:132 | ||||
| chr4:158723443-158723465 | Rare:6 | ||||
| chr4:159035160-159035302 | Common:1; Rare:26 | ||||
| chr4:163166826-163166988 | Common:2; Rare:58 | ||||
| chr4:163332586-163332652 | Rare:9 |