| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:177022557-177022741 | Common:1; Rare:74 | ||||
| chr5:177133448-177133844 | Rare:141 | ||||
| chr5:177303691-177304003 | Common:3; Rare:125 | ||||
| chr5:177311874-177311981 | Common:1; Rare:29 | ||||
| chr5:177351643-177351716 | Rare:20 | ||||
| chr5:177357764-177357933 | Rare:39 | ||||
| chr5:177425910-177426036 | Rare:27 | ||||
| chr5:177497591-177497865 | Common:1; Rare:99 | ||||
| chr5:177509777-177509921 | Common:1; Rare:60 | ||||
| chr5:177510371-177510498 | Common:2; Rare:32 | ||||
| chr5:177510859-177510948 | Common:2; Rare:21 | ||||
| chr5:177516880-177517100 | Common:2; Rare:85; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr5:177600014-177600151 | Common:3; Rare:39 | ||||
| chr5:178113353-178113670 | Common:5; Rare:101 | ||||
| chr5:178130823-178131039 | Rare:60 |