| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:176361620-176361906 | Common:1; Rare:75 | ||||
| chr5:176388569-176388971 | Common:5; Rare:153 | ||||
| chr5:176388995-176389417 | Common:2; Rare:140 | ||||
| chr5:176448136-176448434 | Common:1; Rare:106 | ||||
| chr5:176537849-176538127 | Common:1; Rare:89 | ||||
| chr5:177006301-177006378 | Common:1; Rare:17 | ||||
| chr5:177006543-177006850 | Common:3; Rare:89 | ||||
| chr5:177022618-177022742 | Rare:47 | ||||
| chr5:177133436-177133853 | Rare:151 | ||||
| chr5:177134038-177134167 | Common:1; Rare:39 | ||||
| chr5:177303644-177304075 | Common:4; Rare:162 | ||||
| chr5:177351640-177351958 | Rare:81 | ||||
| chr5:177367009-177367350 | Common:2; Rare:81 | ||||
| chr5:177370927-177371111 | Common:18; Rare:122 | ||||
| chr5:177516891-177517093 | Common:2; Rare:80; Clinvar:1; Clinvar (pathogenic):1 |