| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:74157893-74158195 | Common:1; Rare:138 | ||||
| chr4:75514273-75514492 | Common:1; Rare:72 | ||||
| chr4:75673332-75673654 | Common:1; Rare:130 | ||||
| chr4:75724363-75724810 | Common:2; Rare:132 | ||||
| chr4:76148357-76148561 | Common:3; Rare:66 | ||||
| chr4:76251562-76251739 | Rare:43 | ||||
| chr4:76586074-76586306 | Common:2; Rare:42 | ||||
| chr4:76949549-76949889 | Common:2; Rare:114 | ||||
| chr4:77075965-77076122 | Common:3; Rare:80 | ||||
| chr4:77862650-77862870 | Common:3; Rare:80 | ||||
| chr4:78057452-78057604 | Common:2; Rare:35 | ||||
| chr4:78939255-78939515 | Common:2; Rare:107 | ||||
| chr4:80072599-80072631 | Rare:7 | ||||
| chr4:80072637-80072886 | Common:3; Rare:65; Clinvar (benign):3 | ||||
| chr4:81471797-81472038 | Common:1; Rare:70 |