| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:88284534-88284711 | Common:1; Rare:33 | ||||
| chr4:88592312-88592520 | Common:1; Rare:61 | ||||
| chr4:88759435-88759525 | Rare:17 | ||||
| chr4:88823158-88823338 | Common:2; Rare:30 | ||||
| chr4:89111332-89111588 | Common:4; Rare:98 | ||||
| chr4:89836131-89836247 | Common:4; Rare:29 | ||||
| chr4:89836844-89837245 | Common:3; Rare:124; Clinvar:5; Clinvar (benign):1 | ||||
| chr4:90127294-90127595 | Common:1; Rare:99 | ||||
| chr4:95548928-95549114 | Common:1; Rare:40 | ||||
| chr4:95549189-95549343 | Common:1; Rare:27 | ||||
| chr4:98143459-98143638 | Common:1; Rare:44 | ||||
| chr4:98261194-98261519 | Common:1; Rare:107 | ||||
| chr4:98657626-98657680 | Rare:7 | ||||
| chr4:98929093-98929365 | Common:3; Rare:70 | ||||
| chr4:98995515-98995783 | Common:5; Rare:88 |