| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:172959370-172959475 | Common:1; Rare:38 | ||||
| chr5:173056148-173056429 | Common:1; Rare:79 | ||||
| chr5:173057121-173057394 | Common:1; Rare:73 | ||||
| chr5:173328374-173328506 | Rare:26 | ||||
| chr5:175968189-175968428 | Common:2; Rare:41 | ||||
| chr5:176388535-176388806 | Common:4; Rare:105 | ||||
| chr5:177006329-177006542 | Rare:61 | ||||
| chr5:177006697-177006951 | Common:2; Rare:83 | ||||
| chr5:177022600-177022741 | Common:1; Rare:58 | ||||
| chr5:177133448-177133853 | Rare:145 | ||||
| chr5:177303678-177304059 | Common:3; Rare:144 | ||||
| chr5:177497599-177497886 | Common:1; Rare:98 | ||||
| chr5:177516932-177517068 | Rare:48; Clinvar (pathogenic):1 | ||||
| chr5:178130872-178131039 | Rare:44 | ||||
| chr5:178153809-178153972 | Rare:55; Clinvar:5; Clinvar (benign):1 |