| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:138213285-138213633 | Rare:157 | ||||
| chr5:138331731-138332151 | Common:4; Rare:211 | ||||
| chr5:138337689-138338267 | Common:7; Rare:326 | ||||
| chr5:138352251-138352918 | Common:6; Rare:257 | ||||
| chr5:138464930-138465290 | Common:1; Rare:84 | ||||
| chr5:138542909-138543589 | Common:6; Rare:373 | ||||
| chr5:138574845-138575245 | Common:10; Rare:186 | ||||
| chr5:138575307-138575497 | Common:2; Rare:176 | ||||
| chr5:138575630-138575930 | Rare:94 | ||||
| chr5:138753271-138753514 | Common:4; Rare:138 | ||||
| chr5:139198241-139198567 | Rare:202; Clinvar (benign):2 | ||||
| chr5:139273956-139274192 | Rare:187 | ||||
| chr5:139341565-139341938 | Common:2; Rare:150 | ||||
| chr5:139383268-139383445 | Rare:67 | ||||
| chr5:139388160-139388580 | Common:4; Rare:130 |