| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177133423-177133853 | Rare:154 | ||||
| chr5:177303678-177304059 | Common:3; Rare:144 | ||||
| chr5:177460431-177460673 | Common:1; Rare:76 | ||||
| chr5:177473436-177473775 | Common:1; Rare:116 | ||||
| chr5:177516881-177517093 | Common:2; Rare:85; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:177592051-177592214 | Common:1; Rare:57 | ||||
| chr5:177600021-177600213 | Common:4; Rare:64; Clinvar (benign):5 | ||||
| chr5:178130823-178131033 | Rare:60 | ||||
| chr5:178153813-178154170 | Rare:100; Clinvar:5; Clinvar (benign):1 | ||||
| chr5:178204339-178204534 | Common:3; Rare:68 | ||||
| chr5:178626992-178627235 | Common:7; Rare:88 | ||||
| chr5:178859857-178860065 | Common:3; Rare:58 | ||||
| chr5:178895866-178895948 | Rare:30 | ||||
| chr5:178940929-178941242 | Common:1; Rare:84 | ||||
| chr5:179023652-179023867 | Common:2; Rare:67 |