| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:53987844-53987889 | Rare:11 | ||||
| chr4:54003550-54003689 | Common:1; Rare:18 | ||||
| chr4:54024552-54024612 | Rare:12 | ||||
| chr4:54034119-54034176 | Common:1; Rare:14 | ||||
| chr4:55328203-55328212 | Rare:1 | ||||
| chr4:55397619-55397895 | Rare:64 | ||||
| chr4:55398133-55398290 | Rare:30 | ||||
| chr4:55400091-55400131 | Rare:2 | ||||
| chr4:55412417-55412432 | Rare:2 | ||||
| chr4:55419404-55419485 | Rare:12 | ||||
| chr4:55425290-55425420 | Common:3; Rare:40; Clinvar (benign):4 | ||||
| chr4:55609376-55609659 | Common:2; Rare:43 | ||||
| chr4:55609676-55609982 | Common:2; Rare:54 | ||||
| chr4:55948009-55948261 | Common:1; Rare:42 | ||||
| chr4:56402857-56403073 | Rare:47 |