| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:153152116-153152352 | Common:1; Rare:56 | ||||
| chr4:153152995-153153147 | Rare:26 | ||||
| chr4:153153323-153153475 | Common:4; Rare:42 | ||||
| chr4:153204292-153204502 | Common:1; Rare:43 | ||||
| chr4:153257248-153257591 | Common:2; Rare:61 | ||||
| chr4:153344562-153344729 | Common:4; Rare:48 | ||||
| chr4:153759877-153760096 | Common:2; Rare:47 | ||||
| chr4:154550366-154550492 | Rare:39 | ||||
| chr4:155376771-155376993 | Rare:56 | ||||
| chr4:156971067-156971183 | Rare:19 | ||||
| chr4:157220503-157220937 | Common:5; Rare:118 | ||||
| chr4:157221552-157221722 | Common:3; Rare:45 | ||||
| chr4:158172360-158172711 | Rare:58 | ||||
| chr4:158210352-158210497 | Common:1; Rare:30 | ||||
| chr4:158671849-158672432 | Common:5; Rare:152; Clinvar:3; Clinvar (benign):2 |