| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:106316173-106316613 | Common:5; Rare:140 | ||||
| chr4:107720181-107720505 | Common:7; Rare:130 | ||||
| chr4:107989663-107989949 | Common:6; Rare:122; Clinvar:4; Clinvar (benign):5 | ||||
| chr4:108167901-108168141 | Common:1; Rare:59 | ||||
| chr4:108620380-108620760 | Common:6; Rare:158 | ||||
| chr4:109560076-109560414 | Common:5; Rare:98 | ||||
| chr4:109703400-109703608 | Common:1; Rare:65 | ||||
| chr4:109730045-109730244 | Common:2; Rare:48 | ||||
| chr4:109815464-109815544 | Rare:25 | ||||
| chr4:110198535-110198787 | Rare:74 | ||||
| chr4:110622732-110622951 | Common:3; Rare:41 | ||||
| chr4:110623067-110623324 | Common:2; Rare:66 | ||||
| chr4:112231572-112231876 | Common:2; Rare:98 | ||||
| chr4:112285818-112285998 | Rare:56 | ||||
| chr4:112636853-112637184 | Common:1; Rare:93 |