| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:151408874-151409184 | Common:5; Rare:100 | ||||
| chr4:152779730-152779993 | Common:1; Rare:72 | ||||
| chr4:154743832-154744000 | Rare:64 | ||||
| chr4:158671856-158672139 | Common:4; Rare:70 | ||||
| chr4:158672198-158672313 | Common:1; Rare:23; Clinvar:1; Clinvar (benign):1 | ||||
| chr4:165327372-165327759 | Common:3; Rare:117 | ||||
| chr4:169010227-169010459 | Common:1; Rare:69 | ||||
| chr4:173369802-173369943 | Common:1; Rare:48 | ||||
| chr4:173370643-173370962 | Common:2; Rare:79 | ||||
| chr4:174283658-174283965 | Common:1; Rare:59 | ||||
| chr4:177442377-177442562 | Rare:108; Clinvar:2 | ||||
| chr4:182143790-182143937 | Common:2; Rare:37 | ||||
| chr4:183659122-183659387 | Common:1; Rare:88 | ||||
| chr4:184649406-184649796 | Common:4; Rare:126 | ||||
| chr4:185143173-185143275 | Common:1; Rare:33; Clinvar (benign):2 |