| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:499141-499298 | Common:2; Rare:58 | ||||
| chr4:663624-663753 | Rare:46 | ||||
| chr4:673369-673594 | Rare:81 | ||||
| chr4:673821-673949 | Common:1; Rare:51 | ||||
| chr4:674210-674636 | Common:4; Rare:190 | ||||
| chr4:681128-681245 | Rare:46 | ||||
| chr4:687270-687485 | Rare:61 | ||||
| chr4:730858-730982 | Rare:21 | ||||
| chr4:932239-932497 | Common:2; Rare:98 | ||||
| chr4:986901-987223 | Common:4; Rare:109; Clinvar:4; Clinvar (benign):3 | ||||
| chr4:993804-993939 | Common:3; Rare:38 | ||||
| chr4:1113524-1113647 | Common:2; Rare:47 | ||||
| chr4:1289662-1289925 | Common:1; Rare:86 | ||||
| chr4:1309390-1309621 | Common:3; Rare:62 | ||||
| chr4:1346824-1347096 | Common:4; Rare:77 |