| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:55395833-55395968 | Common:1; Rare:34; Clinvar:2 | ||||
| chr4:56387427-56387547 | Rare:44 | ||||
| chr4:56435551-56435758 | Common:3; Rare:70 | ||||
| chr4:56467521-56467679 | Common:2; Rare:68; Clinvar (benign):4 | ||||
| chr4:56977343-56977739 | Common:3; Rare:146 | ||||
| chr4:67545442-67545742 | Common:2; Rare:76 | ||||
| chr4:67701117-67701358 | Common:4; Rare:114 | ||||
| chr4:68349966-68350209 | Common:1; Rare:88 | ||||
| chr4:70688203-70688567 | Common:2; Rare:92 | ||||
| chr4:70993339-70993657 | Common:5; Rare:91 | ||||
| chr4:71186558-71186815 | Common:1; Rare:72 | ||||
| chr4:71186981-71187401 | Common:3; Rare:116 | ||||
| chr4:73258496-73258887 | Common:1; Rare:107 | ||||
| chr4:73259124-73259205 | Rare:17 | ||||
| chr4:73620393-73620644 | Common:2; Rare:70 |