| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:174283612-174284053 | Common:1; Rare:98 | ||||
| chr4:174284205-174284449 | Common:2; Rare:55 | ||||
| chr4:174829164-174829413 | Common:1; Rare:55 | ||||
| chr4:175812339-175812489 | Rare:38 | ||||
| chr4:175812413-175812942 | Rare:151 | ||||
| chr4:175970820-175971140 | Common:3; Rare:78 | ||||
| chr4:176002327-176002493 | Rare:44 | ||||
| chr4:176065703-176065880 | Common:2; Rare:54 | ||||
| chr4:176066237-176066474 | Common:1; Rare:35 | ||||
| chr4:176195544-176195765 | Common:3; Rare:92 | ||||
| chr4:176319667-176320031 | Common:4; Rare:112 | ||||
| chr4:176792322-176792722 | Common:2; Rare:144 | ||||
| chr4:177309620-177309990 | Common:4; Rare:101 | ||||
| chr4:177441830-177442290 | Common:4; Rare:126; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr4:177442364-177442584 | Rare:125; Clinvar:2; Clinvar (pathogenic):1 |