| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:44678593-44678706 | Rare:52 | ||||
| chr4:44726498-44726659 | Common:1; Rare:61 | ||||
| chr4:46123954-46124194 | Common:3; Rare:48 | ||||
| chr4:46389914-46390110 | Common:3; Rare:50 | ||||
| chr4:46993448-46993901 | Common:2; Rare:112 | ||||
| chr4:47463647-47463785 | Common:1; Rare:45 | ||||
| chr4:47485204-47485353 | Common:1; Rare:55 | ||||
| chr4:48341271-48341581 | Common:1; Rare:127 | ||||
| chr4:48830938-48831258 | Common:1; Rare:92 | ||||
| chr4:48906704-48906869 | Rare:40 | ||||
| chr4:51842793-51843247 | Common:1; Rare:135 | ||||
| chr4:52038240-52038417 | Rare:67; Clinvar:7; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr4:52659161-52659439 | Common:1; Rare:93 | ||||
| chr4:52862144-52862322 | Common:7; Rare:82 | ||||
| chr4:53365990-53366121 | Rare:24 |