| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:54232940-54233150 | Common:5; Rare:50 | ||||
| chr4:54267280-54267661 | Common:3; Rare:108; Clinvar:28; Clinvar (benign):20 | ||||
| chr4:55875728-55875904 | Common:1; Rare:22 | ||||
| chr4:55947920-55948158 | Common:2; Rare:40 | ||||
| chr4:56410292-56410517 | Common:1; Rare:43 | ||||
| chr4:56446544-56446749 | Rare:43 | ||||
| chr4:56976924-56977024 | Common:1; Rare:33 | ||||
| chr4:57025227-57025526 | Common:1; Rare:48 | ||||
| chr4:57109801-57109829 | Rare:6 | ||||
| chr4:61203100-61203408 | Rare:64 | ||||
| chr4:68733905-68734294 | Common:3; Rare:76 | ||||
| chr4:68734485-68734511 | Rare:5 | ||||
| chr4:68736209-68736235 | Rare:4 | ||||
| chr4:68736332-68736559 | Common:2; Rare:46 | ||||
| chr4:71186552-71186770 | Common:1; Rare:57 |