| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:47485198-47485358 | Common:1; Rare:58 | ||||
| chr4:47914503-47914847 | Common:1; Rare:106 | ||||
| chr4:48016645-48016795 | Common:1; Rare:45 | ||||
| chr4:48269816-48269981 | Common:1; Rare:31 | ||||
| chr4:48341103-48341487 | Common:1; Rare:152 | ||||
| chr4:48780236-48780626 | Common:2; Rare:120 | ||||
| chr4:48830886-48831249 | Common:1; Rare:104 | ||||
| chr4:48906657-48906871 | Rare:45 | ||||
| chr4:51842813-51843224 | Common:1; Rare:124 | ||||
| chr4:53377559-53377710 | Common:1; Rare:54 | ||||
| chr4:55346169-55346347 | Common:3; Rare:62; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:55948720-55948988 | Common:2; Rare:55 | ||||
| chr4:56387414-56387519 | Rare:35 | ||||
| chr4:56435467-56435973 | Common:6; Rare:166 | ||||
| chr4:56436048-56436315 | Rare:100 |