| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:172771175-172771332 | Common:4; Rare:67 | ||||
| chr5:172834162-172834371 | Common:1; Rare:46 | ||||
| chr5:173057082-173057361 | Common:2; Rare:75 | ||||
| chr5:173144870-173145115 | Common:2; Rare:54 | ||||
| chr5:173888992-173889044 | Rare:5 | ||||
| chr5:176388981-176389198 | Rare:63 | ||||
| chr5:176448194-176448368 | Common:1; Rare:54 | ||||
| chr5:176537816-176538163 | Common:1; Rare:112 | ||||
| chr5:177006669-177006848 | Common:1; Rare:62 | ||||
| chr5:177022622-177022751 | Rare:50 | ||||
| chr5:177133483-177133815 | Rare:120 | ||||
| chr5:177303654-177303962 | Common:4; Rare:132 | ||||
| chr5:177351640-177351724 | Rare:20 | ||||
| chr5:177516889-177517084 | Common:2; Rare:77; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:177553375-177553517 | Rare:30 |