| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:107989689-107989913 | Common:5; Rare:107; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108620393-108620647 | Common:6; Rare:128 | ||||
| chr4:109433757-109433957 | Common:1; Rare:66 | ||||
| chr4:109703406-109703606 | Common:1; Rare:64 | ||||
| chr4:109815475-109815538 | Rare:19 | ||||
| chr4:110198504-110198691 | Rare:55 | ||||
| chr4:112231395-112231930 | Common:3; Rare:154 | ||||
| chr4:112636879-112637182 | Common:1; Rare:82 | ||||
| chr4:112637319-112637570 | Common:3; Rare:77 | ||||
| chr4:112817973-112818244 | Rare:44 | ||||
| chr4:113049467-113049773 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):2 | ||||
| chr4:117085521-117085586 | Common:1; Rare:18 | ||||
| chr4:118685291-118685446 | Common:3; Rare:51 | ||||
| chr4:119212408-119212738 | Common:3; Rare:99 | ||||
| chr4:119627308-119627609 | Rare:84 |