| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:37977173-37977459 | Rare:68 | ||||
| chr4:38664211-38664306 | Rare:32 | ||||
| chr4:38867700-38867833 | Common:1; Rare:52 | ||||
| chr4:39182202-39182548 | Rare:75; Clinvar:2 | ||||
| chr4:39458868-39459065 | Common:3; Rare:105 | ||||
| chr4:39527383-39527780 | Common:2; Rare:106 | ||||
| chr4:39527944-39528059 | Rare:28 | ||||
| chr4:39638742-39639140 | Common:1; Rare:135 | ||||
| chr4:39697997-39698192 | Common:1; Rare:75 | ||||
| chr4:40056605-40056935 | Common:4; Rare:102 | ||||
| chr4:40629705-40629978 | Common:1; Rare:65 | ||||
| chr4:40630571-40630886 | Common:2; Rare:72 | ||||
| chr4:41256785-41256971 | Common:2; Rare:61; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:41360699-41360842 | Common:1; Rare:41 | ||||
| chr4:41935008-41935294 | Common:3; Rare:77 |