| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:663604-663736 | Rare:41 | ||||
| chr4:674228-674596 | Common:3; Rare:174 | ||||
| chr4:678554-678972 | Common:2; Rare:127 | ||||
| chr4:681142-681225 | Rare:30 | ||||
| chr4:705577-705963 | Common:1; Rare:131 | ||||
| chr4:730462-730727 | Rare:74 | ||||
| chr4:804787-804975 | Common:2; Rare:65 | ||||
| chr4:872706-872854 | Common:1; Rare:40 | ||||
| chr4:932090-932523 | Common:2; Rare:166 | ||||
| chr4:986930-987150 | Common:2; Rare:71; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:1113497-1113703 | Common:4; Rare:84 | ||||
| chr4:1249988-1250147 | Common:3; Rare:28 | ||||
| chr4:1289650-1289931 | Common:1; Rare:97 | ||||
| chr4:1309390-1309637 | Common:3; Rare:68 | ||||
| chr4:1346979-1347213 | Common:3; Rare:68 |