| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:88523587-88523865 | Common:2; Rare:95 | ||||
| chr4:88592294-88592550 | Common:1; Rare:80 | ||||
| chr4:88697594-88697947 | Common:3; Rare:148 | ||||
| chr4:88759090-88759277 | Common:1; Rare:32 | ||||
| chr4:88759447-88759711 | Rare:45 | ||||
| chr4:88823182-88823482 | Common:2; Rare:59 | ||||
| chr4:89057119-89057273 | Common:1; Rare:32 | ||||
| chr4:89111393-89111534 | Common:2; Rare:50 | ||||
| chr4:89307758-89307977 | Common:1; Rare:71 | ||||
| chr4:89836144-89836320 | Common:3; Rare:43 | ||||
| chr4:89836836-89837539 | Common:5; Rare:207; Clinvar:5; Clinvar (benign):1 | ||||
| chr4:92303947-92304314 | Rare:101 | ||||
| chr4:92304427-92304659 | Common:1; Rare:37 | ||||
| chr4:94451792-94451986 | Common:3; Rare:61 | ||||
| chr4:94757745-94757987 | Common:4; Rare:54 |