| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:107989689-107989941 | Common:5; Rare:113; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108168842-108169080 | Common:2; Rare:50 | ||||
| chr4:108620380-108620647 | Common:6; Rare:135 | ||||
| chr4:109302705-109303044 | Common:5; Rare:95 | ||||
| chr4:109433756-109433822 | Common:1; Rare:26 | ||||
| chr4:109815464-109815798 | Common:1; Rare:89 | ||||
| chr4:110365293-110365702 | Common:4; Rare:62 | ||||
| chr4:112231587-112231831 | Common:2; Rare:75 | ||||
| chr4:112285823-112285993 | Rare:53 | ||||
| chr4:112636879-112637204 | Common:2; Rare:88 | ||||
| chr4:112637390-112637570 | Common:3; Rare:47 | ||||
| chr4:113116760-113117057 | Common:1; Rare:46 | ||||
| chr4:113335600-113335900 | Rare:61; Clinvar:1 | ||||
| chr4:113979582-113979817 | Common:6; Rare:56 | ||||
| chr4:114598619-114598981 | Common:10; Rare:97 |