| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:13627598-13627917 | Common:2; Rare:172 | ||||
| chr4:15001995-15002556 | Common:3; Rare:281 | ||||
| chr4:15002640-15002950 | Common:3; Rare:172 | ||||
| chr4:15003019-15003212 | Common:3; Rare:169 | ||||
| chr4:15004307-15004456 | Rare:56 | ||||
| chr4:15469786-15469896 | Common:1; Rare:24 | ||||
| chr4:15655258-15655521 | Common:3; Rare:198 | ||||
| chr4:15659840-15660110 | Common:1; Rare:57 | ||||
| chr4:15681400-15681881 | Common:7; Rare:311 | ||||
| chr4:16226459-16226709 | Common:6; Rare:177 | ||||
| chr4:17512042-17512294 | Common:3; Rare:95; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr4:17577274-17577544 | Common:1; Rare:217 | ||||
| chr4:17614512-17614678 | Common:4; Rare:123 | ||||
| chr4:17810652-17811085 | Common:8; Rare:257 | ||||
| chr4:18021701-18021960 | Common:2; Rare:139 |