| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:176361733-176361896 | Common:1; Rare:50 | ||||
| chr5:176388569-176388816 | Common:4; Rare:99 | ||||
| chr5:176448049-176448410 | Common:1; Rare:116 | ||||
| chr5:176542599-176542875 | Rare:63 | ||||
| chr5:176543506-176543621 | Rare:36 | ||||
| chr5:176549208-176549405 | Rare:50 | ||||
| chr5:177006427-177006472 | Rare:14 | ||||
| chr5:177006641-177006935 | Common:2; Rare:97 | ||||
| chr5:177022572-177022807 | Common:1; Rare:95 | ||||
| chr5:177133474-177133847 | Rare:138 | ||||
| chr5:177303665-177303868 | Common:4; Rare:98 | ||||
| chr5:177370668-177370897 | Common:1; Rare:79 | ||||
| chr5:177371031-177371117 | Common:19; Rare:86 | ||||
| chr5:177403173-177403214 | Rare:7 | ||||
| chr5:177516818-177517081 | Common:2; Rare:110; Clinvar:1; Clinvar (pathogenic):1 |