| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:674209-674596 | Common:4; Rare:180 | ||||
| chr4:705578-705961 | Common:1; Rare:130 | ||||
| chr4:932048-932497 | Common:2; Rare:158 | ||||
| chr4:986928-987120 | Common:1; Rare:61; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:1171138-1171333 | Rare:84 | ||||
| chr4:1172628-1173057 | Common:4; Rare:74 | ||||
| chr4:1289665-1289934 | Common:1; Rare:91 | ||||
| chr4:1309403-1309639 | Common:3; Rare:63 | ||||
| chr4:1346816-1347233 | Common:6; Rare:126 | ||||
| chr4:1712316-1712405 | Common:1; Rare:30 | ||||
| chr4:1712696-1712878 | Common:1; Rare:49 | ||||
| chr4:1721331-1721638 | Common:6; Rare:92 | ||||
| chr4:2041902-2042072 | Common:1; Rare:64 | ||||
| chr4:2261727-2261916 | Common:1; Rare:64 | ||||
| chr4:2468878-2469212 | Common:5; Rare:139 |