| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:10258077-10258148 | Rare:19; Clinvar:1 | ||||
| chr5:10307719-10308037 | Common:1; Rare:62 | ||||
| chr5:10353587-10353958 | Common:3; Rare:139 | ||||
| chr5:10354040-10354355 | Rare:111 | ||||
| chr5:10564167-10564347 | Common:1; Rare:60 | ||||
| chr5:10761185-10761464 | Common:13; Rare:85 | ||||
| chr5:11588826-11589047 | Common:3; Rare:41 | ||||
| chr5:14143110-14143351 | Rare:81 | ||||
| chr5:14581643-14581920 | Common:1; Rare:118 | ||||
| chr5:14664570-14664747 | Common:4; Rare:81 | ||||
| chr5:14871776-14871810 | Rare:10 | ||||
| chr5:15500039-15500202 | Rare:56 | ||||
| chr5:16465702-16465902 | Rare:39 | ||||
| chr5:16616973-16616999 | Common:1; Rare:13; Clinvar (benign):3 | ||||
| chr5:16737687-16737999 | Common:3; Rare:73 |