| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:134201757-134201973 | Rare:48 | ||||
| chr4:138242144-138242668 | Common:2; Rare:171 | ||||
| chr4:139015462-139015802 | Common:4; Rare:220 | ||||
| chr4:139083600-139083790 | Rare:50 | ||||
| chr4:139084192-139084760 | Common:9; Rare:345 | ||||
| chr4:139177146-139177456 | Rare:157 | ||||
| chr4:139301214-139301593 | Common:7; Rare:172 | ||||
| chr4:139302270-139302700 | Common:4; Rare:114 | ||||
| chr4:139453620-139454201 | Common:10; Rare:306; Clinvar:19; Clinvar (benign):8 | ||||
| chr4:139556133-139556750 | Common:1; Rare:187 | ||||
| chr4:139556770-139557020 | Rare:58 | ||||
| chr4:139606677-139606971 | Rare:97 | ||||
| chr4:139665741-139666029 | Common:4; Rare:127 | ||||
| chr4:140153950-140154950 | Common:9; Rare:362 | ||||
| chr4:140373384-140373709 | Common:5; Rare:259 |