| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:39638841-39639147 | Common:1; Rare:112 | ||||
| chr4:39697911-39698188 | Common:2; Rare:117 | ||||
| chr4:41990412-41990566 | Common:1; Rare:58 | ||||
| chr4:44726547-44726642 | Rare:38 | ||||
| chr4:47485166-47485401 | Common:2; Rare:75 | ||||
| chr4:48016561-48016794 | Common:2; Rare:67 | ||||
| chr4:48269802-48269989 | Common:1; Rare:39 | ||||
| chr4:48341243-48341581 | Common:2; Rare:138 | ||||
| chr4:48780101-48780582 | Common:3; Rare:150 | ||||
| chr4:48830891-48831199 | Common:1; Rare:96 | ||||
| chr4:52038246-52038431 | Rare:66; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr4:52862171-52862322 | Common:5; Rare:66 | ||||
| chr4:53365980-53366222 | Rare:56 | ||||
| chr4:54228932-54229335 | Common:1; Rare:84; Clinvar (benign):4 | ||||
| chr4:55546816-55547011 | Common:2; Rare:68 |