| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:41990389-41990580 | Common:1; Rare:69 | ||||
| chr4:44678352-44678481 | Rare:40 | ||||
| chr4:44678593-44678731 | Rare:64 | ||||
| chr4:44726492-44726642 | Common:2; Rare:53 | ||||
| chr4:46123945-46124226 | Common:3; Rare:57 | ||||
| chr4:46993453-46993688 | Common:2; Rare:62 | ||||
| chr4:47463635-47463754 | Common:1; Rare:41 | ||||
| chr4:47485210-47485401 | Common:2; Rare:61 | ||||
| chr4:48016634-48016784 | Common:1; Rare:44 | ||||
| chr4:48269801-48269971 | Common:1; Rare:37 | ||||
| chr4:48341333-48341560 | Common:1; Rare:95 | ||||
| chr4:51842826-51843230 | Common:1; Rare:123 | ||||
| chr4:52038240-52038402 | Rare:61; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr4:53365987-53366222 | Rare:54 | ||||
| chr4:53377434-53377754 | Common:4; Rare:103 |