| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:172959136-172959482 | Common:5; Rare:88 | ||||
| chr5:173056137-173056407 | Common:1; Rare:73 | ||||
| chr5:175478409-175478609 | Common:1; Rare:73 | ||||
| chr5:176361746-176361940 | Common:2; Rare:52 | ||||
| chr5:176388536-176388827 | Common:4; Rare:118 | ||||
| chr5:176448217-176448410 | Common:1; Rare:71 | ||||
| chr5:176610007-176610227 | Common:1; Rare:89 | ||||
| chr5:177006561-177006828 | Common:3; Rare:83 | ||||
| chr5:177022622-177022732 | Rare:38 | ||||
| chr5:177133438-177133804 | Rare:129 | ||||
| chr5:177303672-177304003 | Common:4; Rare:133 | ||||
| chr5:177460435-177460704 | Common:1; Rare:90 | ||||
| chr5:177516881-177517084 | Common:2; Rare:81; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:178130746-178131020 | Common:2; Rare:79 | ||||
| chr5:178153813-178154110 | Rare:90; Clinvar:5; Clinvar (benign):1 |