| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:177309707-177309896 | Common:1; Rare:53 | ||||
| chr4:177442136-177442220 | Rare:34 | ||||
| chr4:177442248-177442554 | Common:1; Rare:161; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
| chr4:182448743-182449095 | Common:2; Rare:117 | ||||
| chr4:182917319-182917547 | Common:4; Rare:79 | ||||
| chr4:183098980-183099134 | Common:1; Rare:54 | ||||
| chr4:183444298-183444724 | Common:2; Rare:182 | ||||
| chr4:183504522-183504810 | Common:2; Rare:94 | ||||
| chr4:183505778-183506116 | Common:1; Rare:118 | ||||
| chr4:183506318-183506419 | Common:2; Rare:31 | ||||
| chr4:183659049-183659439 | Common:1; Rare:118 | ||||
| chr4:184474519-184474823 | Rare:71 | ||||
| chr4:184649386-184649826 | Common:5; Rare:142 | ||||
| chr4:184714065-184714127 | Common:1; Rare:11 | ||||
| chr4:184733422-184733502 | Common:1; Rare:19 |