| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:16226446-16227607 | Common:24; Rare:926 | ||||
| chr4:17511700-17511980 | Common:4; Rare:87; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr4:17512022-17512422 | Common:14; Rare:397; Clinvar:9; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr4:17576930-17577202 | Common:5; Rare:249 | ||||
| chr4:17577204-17577994 | Common:7; Rare:745 | ||||
| chr4:17613906-17614340 | Common:5; Rare:129 | ||||
| chr4:17614330-17614830 | Common:17; Rare:593 | ||||
| chr4:17614857-17615381 | Common:1; Rare:209 | ||||
| chr4:17810521-17811121 | Common:26; Rare:953 | ||||
| chr4:17811200-17811687 | Common:8; Rare:172 | ||||
| chr4:18020610-18022599 | Common:44; Rare:1755 | ||||
| chr4:20699943-20700664 | Common:7; Rare:713 | ||||
| chr4:22515230-22515660 | Common:4; Rare:130 | ||||
| chr4:22515960-22516360 | Common:5; Rare:124 | ||||
| chr4:24583783-24584250 | Common:4; Rare:229 |