| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:107989679-107989963 | Common:6; Rare:122; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620388-108620647 | Common:6; Rare:131 | ||||
| chr4:109433502-109433655 | Common:1; Rare:43 | ||||
| chr4:109433757-109433815 | Rare:24 | ||||
| chr4:109815415-109815553 | Rare:40 | ||||
| chr4:110476155-110476279 | Rare:23 | ||||
| chr4:112231597-112231890 | Common:2; Rare:89 | ||||
| chr4:112285738-112285961 | Rare:70 | ||||
| chr4:112636888-112637187 | Common:1; Rare:82 | ||||
| chr4:112637448-112637597 | Common:2; Rare:43 | ||||
| chr4:113049467-113049786 | Common:1; Rare:70; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:113293329-113293447 | Common:1; Rare:29; Clinvar (benign):1 | ||||
| chr4:113761102-113761243 | Common:1; Rare:39 | ||||
| chr4:113979569-113979706 | Common:1; Rare:33 | ||||
| chr4:118685272-118685475 | Common:3; Rare:66 |