| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:158172360-158172845 | Common:1; Rare:77 | ||||
| chr4:158172986-158172995 | Rare:1 | ||||
| chr4:158173002-158173240 | Rare:37 | ||||
| chr4:158210210-158210497 | Common:1; Rare:64 | ||||
| chr4:158671849-158672402 | Common:5; Rare:139; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:163166768-163166941 | Common:3; Rare:52 | ||||
| chr4:164977607-164977738 | Rare:35 | ||||
| chr4:165112824-165112990 | Common:1; Rare:50 | ||||
| chr4:165327346-165327769 | Common:3; Rare:130 | ||||
| chr4:165874809-165874958 | Common:1; Rare:48 | ||||
| chr4:168480415-168480522 | Common:1; Rare:20 | ||||
| chr4:168894452-168894650 | Rare:52; Clinvar:1; Clinvar (benign):3 | ||||
| chr4:169010233-169010421 | Common:1; Rare:56 | ||||
| chr4:169270864-169271172 | Common:2; Rare:95 | ||||
| chr4:169612268-169612431 | Rare:38; Clinvar:1 |