| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:176319713-176320096 | Common:10; Rare:243 | ||||
| chr4:176320370-176320830 | Common:1; Rare:158 | ||||
| chr4:177309702-177309936 | Common:2; Rare:73 | ||||
| chr4:177441970-177442250 | Common:2; Rare:114; Clinvar (benign):2 | ||||
| chr4:177442377-177442574 | Rare:213; Clinvar:4 | ||||
| chr4:182143610-182144020 | Common:2; Rare:133 | ||||
| chr4:182144120-182144310 | Common:9; Rare:58 | ||||
| chr4:182144330-182144730 | Common:8; Rare:221 | ||||
| chr4:182448787-182449062 | Common:2; Rare:97 | ||||
| chr4:182916686-182917086 | Common:5; Rare:139 | ||||
| chr4:182917239-182917569 | Common:8; Rare:184 | ||||
| chr4:183098991-183099302 | Common:6; Rare:199 | ||||
| chr4:183444299-183444776 | Common:4; Rare:368 | ||||
| chr4:183504396-183504785 | Common:2; Rare:218 | ||||
| chr4:183505018-183505120 | Rare:29 |