| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15479146-15479283 | Rare:35 | ||||
| chr4:15655289-15655475 | Common:1; Rare:83 | ||||
| chr4:15681554-15681672 | Rare:33 | ||||
| chr4:15681694-15681869 | Common:2; Rare:69 | ||||
| chr4:17614527-17614670 | Common:2; Rare:63 | ||||
| chr4:17810580-17811149 | Common:5; Rare:165 | ||||
| chr4:18021640-18021776 | Rare:86 | ||||
| chr4:20700280-20700493 | Common:1; Rare:94 | ||||
| chr4:20983872-20984003 | Common:1; Rare:25 | ||||
| chr4:21303908-21304171 | Common:17; Rare:75 | ||||
| chr4:23890030-23890171 | Rare:22 | ||||
| chr4:24584416-24584725 | Common:1; Rare:94 | ||||
| chr4:25160399-25160727 | Common:3; Rare:92; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25376955-25377302 | Common:4; Rare:104 | ||||
| chr4:25914051-25914321 | Common:2; Rare:115 |