| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:75673059-75673665 | Common:1; Rare:211 | ||||
| chr4:75724370-75724730 | Common:1; Rare:100 | ||||
| chr4:76148357-76148586 | Common:4; Rare:71 | ||||
| chr4:76251675-76251740 | Rare:18 | ||||
| chr4:76949549-76949918 | Common:2; Rare:123 | ||||
| chr4:77020362-77020580 | Rare:53 | ||||
| chr4:77075961-77076136 | Common:4; Rare:85 | ||||
| chr4:77076301-77076424 | Common:2; Rare:63 | ||||
| chr4:77156683-77156939 | Common:2; Rare:67 | ||||
| chr4:77157141-77157373 | Common:5; Rare:93 | ||||
| chr4:77158011-77158183 | Common:1; Rare:62 | ||||
| chr4:77862650-77862872 | Common:3; Rare:83 | ||||
| chr4:78939239-78939471 | Common:1; Rare:95 | ||||
| chr4:80072644-80072747 | Rare:30 | ||||
| chr4:80072749-80072851 | Common:1; Rare:26; Clinvar (benign):1 |