| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15469796-15469912 | Common:1; Rare:23 | ||||
| chr4:15655223-15655491 | Common:2; Rare:106 | ||||
| chr4:15681560-15681898 | Common:4; Rare:119 | ||||
| chr4:15778115-15778445 | Rare:72 | ||||
| chr4:16898513-16898886 | Common:14; Rare:66 | ||||
| chr4:17512061-17512180 | Common:3; Rare:55; Clinvar:2; Clinvar (benign):3 | ||||
| chr4:17614548-17614651 | Common:2; Rare:44 | ||||
| chr4:17781311-17781396 | Common:2; Rare:17 | ||||
| chr4:17810639-17811086 | Common:4; Rare:138 | ||||
| chr4:20700270-20700502 | Common:1; Rare:101 | ||||
| chr4:20983907-20983988 | Rare:17 | ||||
| chr4:21303908-21304136 | Common:17; Rare:69 | ||||
| chr4:23890034-23890299 | Common:1; Rare:44 | ||||
| chr4:24584248-24584352 | Rare:37 | ||||
| chr4:24584459-24584710 | Common:1; Rare:81 |