| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:47485157-47485340 | Common:1; Rare:67 | ||||
| chr4:48906722-48906871 | Rare:32 | ||||
| chr4:52038255-52038431 | Rare:62; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
| chr4:55546801-55546894 | Rare:26 | ||||
| chr4:56387423-56387528 | Rare:35 | ||||
| chr4:56435458-56435791 | Common:5; Rare:114 | ||||
| chr4:56436018-56436312 | Rare:106 | ||||
| chr4:56467521-56467674 | Common:2; Rare:65; Clinvar (benign):4 | ||||
| chr4:56977597-56977753 | Common:1; Rare:55 | ||||
| chr4:67545442-67545742 | Common:2; Rare:76 | ||||
| chr4:67701115-67701395 | Common:4; Rare:130 | ||||
| chr4:68349966-68350252 | Common:2; Rare:100 | ||||
| chr4:70688463-70688563 | Common:2; Rare:24 | ||||
| chr4:70839232-70839417 | Common:2; Rare:78 | ||||
| chr4:70902181-70902402 | Common:5; Rare:77 |