| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:149551369-149551624 | Rare:59 | ||||
| chr5:150155817-150156150 | Common:2; Rare:89 | ||||
| chr5:150449683-150449795 | Common:4; Rare:41 | ||||
| chr5:150701038-150701110 | Common:2; Rare:25 | ||||
| chr5:151080929-151081182 | Common:1; Rare:79 | ||||
| chr5:154038884-154038989 | Common:1; Rare:33 | ||||
| chr5:154858475-154858655 | Common:1; Rare:57 | ||||
| chr5:159263191-159263317 | Common:1; Rare:39 | ||||
| chr5:160419053-160419260 | Common:4; Rare:75 | ||||
| chr5:163460332-163460663 | Common:5; Rare:74 | ||||
| chr5:169583597-169583819 | Common:6; Rare:72 | ||||
| chr5:173328412-173328605 | Rare:36 | ||||
| chr5:176388563-176388806 | Common:4; Rare:92 | ||||
| chr5:177022635-177022724 | Rare:28 | ||||
| chr5:177516938-177517093 | Rare:52; Clinvar (pathogenic):1 |