| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:56977581-56977757 | Common:1; Rare:66 | ||||
| chr4:67545461-67545748 | Common:2; Rare:73 | ||||
| chr4:67701121-67701358 | Common:4; Rare:111 | ||||
| chr4:68349966-68350209 | Common:1; Rare:88 | ||||
| chr4:70688406-70688567 | Common:2; Rare:45 | ||||
| chr4:73069703-73069832 | Rare:62 | ||||
| chr4:75514273-75514502 | Common:1; Rare:78 | ||||
| chr4:75673106-75673239 | Rare:34 | ||||
| chr4:75724375-75724721 | Common:1; Rare:95 | ||||
| chr4:76148357-76148587 | Common:4; Rare:72 | ||||
| chr4:76949559-76949859 | Common:1; Rare:94 | ||||
| chr4:77862618-77862877 | Common:3; Rare:90 | ||||
| chr4:82373928-82374317 | Common:3; Rare:117 | ||||
| chr4:82429363-82429585 | Rare:139; Clinvar:10; Clinvar (benign):4 | ||||
| chr4:82900488-82900741 | Rare:72 |