| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:17512021-17512314 | Common:3; Rare:111; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr4:17576988-17577204 | Common:10; Rare:169 | ||||
| chr4:17577116-17577611 | Common:8; Rare:455 | ||||
| chr4:17613802-17614475 | Common:8; Rare:153 | ||||
| chr4:17614495-17614728 | Common:7; Rare:242 | ||||
| chr4:17810607-17811066 | Common:12; Rare:396 | ||||
| chr4:18021578-18021967 | Common:4; Rare:339 | ||||
| chr4:18022060-18022430 | Common:5; Rare:103 | ||||
| chr4:20700200-20700529 | Common:3; Rare:300 | ||||
| chr4:22515070-22515580 | Common:9; Rare:195 | ||||
| chr4:22515927-22516291 | Common:13; Rare:274 | ||||
| chr4:22516320-22516710 | Common:2; Rare:80 | ||||
| chr4:24583728-24583842 | Rare:25 | ||||
| chr4:24584178-24584799 | Common:3; Rare:484 | ||||
| chr4:24912310-24912680 | Common:3; Rare:181 |