| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:39527336-39527754 | Common:4; Rare:103 | ||||
| chr4:39638829-39639154 | Common:1; Rare:119 | ||||
| chr4:39697936-39698188 | Common:2; Rare:108 | ||||
| chr4:40629862-40630191 | Common:2; Rare:65 | ||||
| chr4:41256728-41256994 | Common:3; Rare:86; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:41935023-41935208 | Common:3; Rare:56 | ||||
| chr4:41990388-41990572 | Common:1; Rare:66 | ||||
| chr4:44678352-44678486 | Rare:44 | ||||
| chr4:44726547-44726631 | Rare:36 | ||||
| chr4:47485157-47485340 | Common:1; Rare:67 | ||||
| chr4:48016624-48016775 | Common:1; Rare:42 | ||||
| chr4:48269802-48269972 | Common:1; Rare:36 | ||||
| chr4:48780202-48780626 | Common:3; Rare:131 | ||||
| chr4:48830960-48831223 | Rare:78 | ||||
| chr4:52659234-52659422 | Common:1; Rare:63 |