| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:94488754-94489038 | Common:2; Rare:44 | ||||
| chr4:98143459-98143649 | Common:1; Rare:47 | ||||
| chr4:98261142-98261556 | Common:1; Rare:143 | ||||
| chr4:98929031-98929382 | Common:3; Rare:103 | ||||
| chr4:98995313-98995810 | Common:6; Rare:169 | ||||
| chr4:99088687-99088891 | Common:6; Rare:98 | ||||
| chr4:99563586-99563806 | Common:2; Rare:66 | ||||
| chr4:99563956-99564162 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:99894342-99894620 | Common:3; Rare:97 | ||||
| chr4:99946519-99946759 | Rare:89 | ||||
| chr4:99950223-99950537 | Rare:76 | ||||
| chr4:100190421-100190606 | Common:3; Rare:39 | ||||
| chr4:101347528-101347830 | Common:5; Rare:93 | ||||
| chr4:102344887-102345119 | Common:2; Rare:53 | ||||
| chr4:102345301-102345669 | Common:1; Rare:84 |