| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:134648685-134648816 | Rare:37 | ||||
| chr5:134738418-134738615 | Rare:75 | ||||
| chr5:135399123-135399325 | Rare:56 | ||||
| chr5:137735707-137735928 | Common:1; Rare:43; Clinvar (benign):2 | ||||
| chr5:137880335-137880675 | Common:1; Rare:57 | ||||
| chr5:137889314-137889457 | Common:1; Rare:49 | ||||
| chr5:138465674-138465929 | Common:1; Rare:97 | ||||
| chr5:138543104-138543513 | Common:2; Rare:126 | ||||
| chr5:138753255-138753507 | Common:2; Rare:87 | ||||
| chr5:138930244-138930654 | Common:1; Rare:81; Clinvar (benign):1 | ||||
| chr5:139198274-139198555 | Rare:92; Clinvar (benign):1 | ||||
| chr5:139273953-139274142 | Rare:85 | ||||
| chr5:139404007-139404388 | Common:2; Rare:109 | ||||
| chr5:139561112-139561409 | Common:1; Rare:118 | ||||
| chr5:139561728-139561800 | Rare:30 |