| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:176537835-176538161 | Common:1; Rare:106 | ||||
| chr5:177006560-177006850 | Common:3; Rare:86 | ||||
| chr5:177022579-177022760 | Common:1; Rare:73 | ||||
| chr5:177303655-177303816 | Common:4; Rare:76 | ||||
| chr5:177308055-177308124 | Common:1; Rare:10 | ||||
| chr5:177351643-177351731 | Rare:23 | ||||
| chr5:177497594-177497798 | Common:1; Rare:73 | ||||
| chr5:177516881-177517090 | Common:2; Rare:84; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:178130882-178131047 | Rare:44 | ||||
| chr5:178232555-178232885 | Common:4; Rare:107 | ||||
| chr5:179023641-179023870 | Common:3; Rare:69 | ||||
| chr5:179550675-179550874 | Rare:82 | ||||
| chr5:179559556-179559813 | Common:1; Rare:75 | ||||
| chr5:179617542-179617920 | Rare:92 | ||||
| chr5:179698671-179699098 | Common:4; Rare:137 |