| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:107989726-107990047 | Common:5; Rare:140; Clinvar:5; Clinvar (benign):5 | ||||
| chr4:108620393-108620676 | Common:6; Rare:137 | ||||
| chr4:108650564-108650791 | Rare:78 | ||||
| chr4:109433759-109433998 | Common:1; Rare:83 | ||||
| chr4:109560068-109560442 | Common:5; Rare:108 | ||||
| chr4:109730001-109730218 | Common:3; Rare:52 | ||||
| chr4:112231421-112231858 | Common:2; Rare:134 | ||||
| chr4:112285761-112285892 | Rare:42 | ||||
| chr4:112285894-112285961 | Rare:18 | ||||
| chr4:112636838-112637237 | Common:2; Rare:108 | ||||
| chr4:112637360-112637573 | Common:3; Rare:59 | ||||
| chr4:113761068-113761276 | Common:1; Rare:60 | ||||
| chr4:113979582-113979661 | Common:1; Rare:20 | ||||
| chr4:113979672-113979817 | Common:5; Rare:33 | ||||
| chr4:118685319-118685571 | Common:2; Rare:72 |