| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:56387423-56387528 | Rare:35 | ||||
| chr4:56435467-56435973 | Common:6; Rare:166 | ||||
| chr4:56467521-56467684 | Common:2; Rare:69; Clinvar (benign):4 | ||||
| chr4:56977581-56977771 | Common:1; Rare:70 | ||||
| chr4:57110095-57110230 | Rare:46 | ||||
| chr4:57110383-57110569 | Common:2; Rare:57 | ||||
| chr4:67545442-67545742 | Common:2; Rare:76 | ||||
| chr4:67701111-67701362 | Common:4; Rare:118 | ||||
| chr4:68349952-68350224 | Common:2; Rare:99 | ||||
| chr4:70688176-70688599 | Common:2; Rare:106 | ||||
| chr4:70902185-70902387 | Common:5; Rare:71 | ||||
| chr4:70993452-70993825 | Common:6; Rare:119 | ||||
| chr4:73069640-73069886 | Common:1; Rare:116 | ||||
| chr4:74038687-74038861 | Rare:48 | ||||
| chr4:74157821-74158179 | Common:2; Rare:150 |