| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:128287671-128287911 | Common:1; Rare:104; Clinvar:1 | ||||
| chr4:128809505-128809834 | Common:1; Rare:105 | ||||
| chr4:128811409-128811729 | Common:2; Rare:82 | ||||
| chr4:129093458-129093756 | Common:1; Rare:87 | ||||
| chr4:138241788-138242036 | Rare:71 | ||||
| chr4:138242135-138242573 | Common:2; Rare:89 | ||||
| chr4:138242585-138242646 | Rare:12 | ||||
| chr4:139015411-139015802 | Common:2; Rare:129 | ||||
| chr4:139074024-139074056 | Rare:4 | ||||
| chr4:139084162-139084471 | Common:4; Rare:133 | ||||
| chr4:139301223-139301549 | Common:4; Rare:94 | ||||
| chr4:139302452-139302573 | Common:1; Rare:25 | ||||
| chr4:139351194-139351562 | Rare:75 | ||||
| chr4:139453770-139454160 | Common:3; Rare:95; Clinvar:10; Clinvar (benign):3 | ||||
| chr4:139556102-139556606 | Rare:105 |