| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:4248169-4248317 | Common:4; Rare:61 | ||||
| chr4:4290042-4290312 | Common:5; Rare:101 | ||||
| chr4:4541970-4542171 | Common:1; Rare:85 | ||||
| chr4:6640518-6640720 | Common:2; Rare:86 | ||||
| chr4:6986999-6987303 | Common:2; Rare:99 | ||||
| chr4:7068011-7068382 | Common:7; Rare:129 | ||||
| chr4:8440702-8440780 | Rare:30 | ||||
| chr4:10106500-10106707 | Common:1; Rare:58 | ||||
| chr4:10116687-10117054 | Common:7; Rare:167 | ||||
| chr4:13627418-13627612 | Rare:59 | ||||
| chr4:15478508-15478806 | Common:2; Rare:62; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr4:15681422-15681879 | Common:4; Rare:153 | ||||
| chr4:17577316-17577567 | Rare:117 | ||||
| chr4:17614532-17614666 | Common:2; Rare:54 | ||||
| chr4:17810681-17811091 | Common:4; Rare:125 |