| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:107989675-107990059 | Common:6; Rare:161; Clinvar:5; Clinvar (benign):5 | ||||
| chr4:108620378-108620636 | Common:6; Rare:130 | ||||
| chr4:109433779-109433930 | Common:1; Rare:49 | ||||
| chr4:110476460-110477056 | Common:4; Rare:233 | ||||
| chr4:110623067-110623343 | Common:2; Rare:69 | ||||
| chr4:112285851-112285959 | Rare:33 | ||||
| chr4:112636893-112637181 | Rare:76 | ||||
| chr4:112637322-112637632 | Common:3; Rare:86 | ||||
| chr4:113761080-113761373 | Common:1; Rare:72 | ||||
| chr4:114598306-114598455 | Common:1; Rare:34 | ||||
| chr4:114598502-114598917 | Common:9; Rare:114 | ||||
| chr4:114598919-114599001 | Common:1; Rare:17 | ||||
| chr4:119212510-119212816 | Common:4; Rare:80 | ||||
| chr4:119300463-119300928 | Common:2; Rare:208 | ||||
| chr4:119627960-119628138 | Common:2; Rare:38 |