| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:83010034-83010698 | Common:4; Rare:205 | ||||
| chr4:83010673-83010933 | Rare:126 | ||||
| chr4:83010890-83011290 | Rare:89 | ||||
| chr4:83012199-83012651 | Common:2; Rare:177 | ||||
| chr4:83012810-83013395 | Common:14; Rare:793 | ||||
| chr4:83034104-83034816 | Common:22; Rare:167 | ||||
| chr4:83034730-83035555 | Common:12; Rare:827 | ||||
| chr4:83284068-83284468 | Common:3; Rare:75 | ||||
| chr4:83284408-83284601 | Common:4; Rare:135; Clinvar:8; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr4:83284520-83284970 | Common:10; Rare:450; Clinvar:9; Clinvar (benign):27; Clinvar (pathogenic):6 | ||||
| chr4:83285009-83285409 | Rare:94 | ||||
| chr4:83454623-83455669 | Common:3; Rare:485 | ||||
| chr4:83455692-83456585 | Common:23; Rare:1154 | ||||
| chr4:83461261-83461661 | Common:3; Rare:74 | ||||
| chr4:83484560-83484690 | Common:2; Rare:36 |