| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:98747330-98747750 | Common:1; Rare:73 | ||||
| chr4:98928249-98928365 | Rare:30 | ||||
| chr4:99467915-99468315 | Common:5; Rare:94 | ||||
| chr4:99948887-99949287 | Common:3; Rare:186 | ||||
| chr4:100022202-100023143 | Common:15; Rare:305 | ||||
| chr4:102344215-102344615 | Common:2; Rare:176; Clinvar (pathogenic):2 | ||||
| chr4:103075613-103075780 | Common:1; Rare:31 | ||||
| chr4:103255686-103255907 | Common:6; Rare:64 | ||||
| chr4:103256117-103256517 | Common:10; Rare:165 | ||||
| chr4:103306931-103307105 | Common:2; Rare:43 | ||||
| chr4:103363483-103363883 | Common:5; Rare:76 | ||||
| chr4:103364147-103364476 | Common:2; Rare:51 | ||||
| chr4:103996110-103996460 | Common:3; Rare:59 | ||||
| chr4:104420919-104421043 | Rare:25 | ||||
| chr4:104424248-104424648 | Common:3; Rare:124 |