| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:89111405-89111588 | Common:2; Rare:70 | ||||
| chr4:98261161-98261500 | Common:1; Rare:104 | ||||
| chr4:98657621-98657845 | Rare:40 | ||||
| chr4:98658537-98658922 | Common:2; Rare:110 | ||||
| chr4:99088690-99088900 | Common:7; Rare:100 | ||||
| chr4:99563690-99563756 | Rare:20 | ||||
| chr4:99564004-99564140 | Common:2; Rare:47; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:99950267-99950515 | Rare:46 | ||||
| chr4:101346920-101347109 | Common:1; Rare:46 | ||||
| chr4:101347498-101347824 | Common:5; Rare:101 | ||||
| chr4:102501289-102501454 | Common:1; Rare:26 | ||||
| chr4:102826779-102826958 | Rare:54 | ||||
| chr4:102827067-102827336 | Common:2; Rare:102 | ||||
| chr4:102827481-102827857 | Common:4; Rare:122 | ||||
| chr4:102827963-102828148 | Common:1; Rare:64 |