| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:71186552-71186790 | Common:1; Rare:62 | ||||
| chr4:71186823-71187176 | Common:3; Rare:78 | ||||
| chr4:73069229-73069543 | Common:1; Rare:131; Clinvar (benign):1 | ||||
| chr4:73069579-73070200 | Common:4; Rare:212 | ||||
| chr4:73258696-73258977 | Rare:89 | ||||
| chr4:73259061-73259383 | Common:3; Rare:89 | ||||
| chr4:73620355-73620520 | Rare:56 | ||||
| chr4:74157767-74158466 | Common:2; Rare:262 | ||||
| chr4:74158509-74158650 | Common:1; Rare:20 | ||||
| chr4:74365055-74365165 | Common:1; Rare:27 | ||||
| chr4:74444893-74445173 | Common:1; Rare:58 | ||||
| chr4:74932898-74933154 | Common:1; Rare:79 | ||||
| chr4:74933309-74933557 | Common:1; Rare:76 | ||||
| chr4:75514210-75514612 | Common:1; Rare:135 | ||||
| chr4:75514624-75514801 | Rare:51 |