| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:95548960-95549129 | Common:2; Rare:40 | ||||
| chr4:98261194-98261493 | Common:1; Rare:95 | ||||
| chr4:98929101-98929376 | Common:3; Rare:70 | ||||
| chr4:98995515-98995790 | Common:5; Rare:90 | ||||
| chr4:99088689-99088884 | Common:6; Rare:93 | ||||
| chr4:99563637-99563775 | Common:2; Rare:34 | ||||
| chr4:99563970-99564173 | Common:2; Rare:65; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:99946564-99946813 | Rare:89 | ||||
| chr4:99950254-99950499 | Rare:47 | ||||
| chr4:101347528-101347807 | Common:5; Rare:85 | ||||
| chr4:102345468-102345665 | Rare:51 | ||||
| chr4:102760916-102761046 | Rare:45; Clinvar:1 | ||||
| chr4:102825759-102825860 | Rare:27 | ||||
| chr4:102826695-102826989 | Rare:81 | ||||
| chr4:102827110-102827425 | Common:1; Rare:117 |