| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:39182204-39182510 | Rare:62; Clinvar:1 | ||||
| chr4:39458878-39459121 | Common:2; Rare:137; Clinvar:1; Clinvar (benign):5 | ||||
| chr4:39527383-39527763 | Common:2; Rare:96 | ||||
| chr4:39527952-39528021 | Rare:18 | ||||
| chr4:39638834-39639142 | Common:1; Rare:112 | ||||
| chr4:39697997-39698192 | Common:1; Rare:75 | ||||
| chr4:41256787-41256994 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:41360705-41360835 | Common:1; Rare:37 | ||||
| chr4:41990225-41990580 | Common:2; Rare:92 | ||||
| chr4:42656935-42657295 | Common:7; Rare:124 | ||||
| chr4:44678376-44678496 | Rare:42 | ||||
| chr4:44678614-44678751 | Rare:62 | ||||
| chr4:44726487-44726642 | Common:2; Rare:54 | ||||
| chr4:47485211-47485353 | Common:1; Rare:51 | ||||
| chr4:48269838-48270021 | Common:1; Rare:34 |