| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:13627675-13627869 | Common:1; Rare:59 | ||||
| chr4:15339840-15340007 | Rare:39 | ||||
| chr4:15374267-15374603 | Common:4; Rare:59 | ||||
| chr4:15427848-15428059 | Rare:28 | ||||
| chr4:15469640-15469907 | Common:1; Rare:55 | ||||
| chr4:15478575-15478806 | Common:2; Rare:40; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr4:15479088-15479296 | Rare:52 | ||||
| chr4:15655203-15655499 | Common:2; Rare:111 | ||||
| chr4:15681478-15681893 | Common:4; Rare:146 | ||||
| chr4:15703011-15703134 | Common:1; Rare:27 | ||||
| chr4:15778485-15778502 | Rare:5 | ||||
| chr4:16898395-16898807 | Common:1; Rare:77 | ||||
| chr4:17577307-17577572 | Rare:121 | ||||
| chr4:17614548-17614660 | Common:2; Rare:49 | ||||
| chr4:17810558-17811061 | Common:4; Rare:151 |