| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:56467542-56467684 | Common:2; Rare:62; Clinvar (benign):4 | ||||
| chr4:56977574-56977785 | Common:1; Rare:81 | ||||
| chr4:65670433-65670606 | Rare:42 | ||||
| chr4:67545400-67545764 | Common:2; Rare:90 | ||||
| chr4:67701105-67701379 | Common:4; Rare:129 | ||||
| chr4:68349861-68350210 | Common:1; Rare:115 | ||||
| chr4:70688450-70688574 | Common:2; Rare:34 | ||||
| chr4:70902164-70902324 | Common:2; Rare:60 | ||||
| chr4:70993498-70993830 | Common:5; Rare:103 | ||||
| chr4:72569188-72569315 | Common:1; Rare:41 | ||||
| chr4:73069703-73069946 | Common:1; Rare:102 | ||||
| chr4:73258561-73258905 | Common:1; Rare:102 | ||||
| chr4:73259117-73259241 | Rare:27 | ||||
| chr4:73450405-73450508 | Rare:20 | ||||
| chr4:73450781-73450930 | Rare:28 |