| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:16508787-16509089 | Common:4; Rare:53 | ||||
| chr5:31532037-31532374 | Common:3; Rare:97 | ||||
| chr5:32173837-32173977 | Rare:52 | ||||
| chr5:32174251-32174416 | Common:1; Rare:61 | ||||
| chr5:32710572-32710660 | Common:1; Rare:21 | ||||
| chr5:33440632-33441125 | Common:7; Rare:140 | ||||
| chr5:33461009-33461289 | Common:4; Rare:81 | ||||
| chr5:34008006-34008317 | Common:2; Rare:107; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:34656158-34656425 | Common:3; Rare:66 | ||||
| chr5:34915483-34915766 | Common:1; Rare:79 | ||||
| chr5:35047843-35048256 | Common:4; Rare:96 | ||||
| chr5:35856803-35856931 | Rare:19 | ||||
| chr5:36151838-36152161 | Rare:89 | ||||
| chr5:36241575-36241909 | Common:5; Rare:115; Clinvar:1; Clinvar (benign):5 | ||||
| chr5:36876636-36876889 | Common:1; Rare:74; Clinvar:1; Clinvar (benign):1 |