| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:37977192-37977463 | Rare:68 | ||||
| chr4:39458857-39459112 | Common:3; Rare:147; Clinvar (benign):5 | ||||
| chr4:39527383-39527775 | Common:2; Rare:103 | ||||
| chr4:39638847-39639140 | Common:1; Rare:109 | ||||
| chr4:39697936-39698185 | Common:2; Rare:108 | ||||
| chr4:40056662-40056935 | Common:4; Rare:90 | ||||
| chr4:41990402-41990580 | Common:1; Rare:65 | ||||
| chr4:44678233-44678448 | Common:2; Rare:65 | ||||
| chr4:44678598-44678689 | Rare:42 | ||||
| chr4:44726547-44726642 | Rare:38 | ||||
| chr4:47485174-47485340 | Common:1; Rare:61 | ||||
| chr4:47914544-47914837 | Common:1; Rare:86 | ||||
| chr4:48016598-48016795 | Common:1; Rare:58 | ||||
| chr4:48341178-48341483 | Common:1; Rare:127 | ||||
| chr4:56387423-56387535 | Rare:38 |