| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:176388479-176388822 | Common:4; Rare:136 | ||||
| chr5:176448207-176448440 | Common:1; Rare:88 | ||||
| chr5:176537849-176538108 | Common:1; Rare:80 | ||||
| chr5:176543493-176543581 | Rare:28 | ||||
| chr5:177022635-177022746 | Rare:40 | ||||
| chr5:177133453-177133869 | Rare:149 | ||||
| chr5:177303639-177304077 | Common:4; Rare:162 | ||||
| chr5:177351617-177351772 | Rare:46 | ||||
| chr5:177351790-177352014 | Rare:54 | ||||
| chr5:177367202-177367390 | Common:1; Rare:44 | ||||
| chr5:177370531-177370997 | Common:1; Rare:159 | ||||
| chr5:177371007-177371209 | Common:20; Rare:141 | ||||
| chr5:177497540-177497761 | Common:1; Rare:81 | ||||
| chr5:177516872-177517093 | Common:2; Rare:89; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:177600033-177600234 | Common:4; Rare:70; Clinvar (benign):5 |