| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:151080993-151081154 | Common:1; Rare:55 | ||||
| chr5:154038887-154038999 | Rare:34 | ||||
| chr5:154754991-154755318 | Common:4; Rare:99 | ||||
| chr5:154938186-154938303 | Rare:35 | ||||
| chr5:159263191-159263333 | Common:1; Rare:44 | ||||
| chr5:160419037-160419260 | Common:4; Rare:85 | ||||
| chr5:163460069-163460150 | Common:1; Rare:34 | ||||
| chr5:163460360-163460659 | Common:5; Rare:66 | ||||
| chr5:172958767-172958890 | Rare:36 | ||||
| chr5:176388550-176388806 | Common:4; Rare:98 | ||||
| chr5:177022635-177022741 | Rare:39 | ||||
| chr5:177516917-177517012 | Rare:44; Clinvar (pathogenic):1 | ||||
| chr5:179559546-179559805 | Common:1; Rare:74 | ||||
| chr5:179623650-179623976 | Common:4; Rare:109 | ||||
| chr5:179698588-179698605 | Rare:3 |