| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:443095-443284 | Common:9; Rare:88 | ||||
| chr5:612191-612351 | Rare:64 | ||||
| chr5:892698-892969 | Common:5; Rare:100 | ||||
| chr5:1345019-1345210 | Common:1; Rare:65 | ||||
| chr5:1799784-1799977 | Common:7; Rare:93 | ||||
| chr5:1801349-1801504 | Common:1; Rare:88; Clinvar:3; Clinvar (benign):2 | ||||
| chr5:5422337-5422722 | Common:2; Rare:130 | ||||
| chr5:6378134-6378198 | Rare:15 | ||||
| chr5:6378446-6378595 | Rare:64 | ||||
| chr5:6632996-6633460 | Common:8; Rare:151; Clinvar:9; Clinvar (benign):4 | ||||
| chr5:7868984-7869212 | Common:2; Rare:119; Clinvar (benign):1 | ||||
| chr5:9546069-9546307 | Common:6; Rare:53 | ||||
| chr5:10249862-10250183 | Common:16; Rare:148 | ||||
| chr5:10250187-10250357 | Common:3; Rare:89; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:10353576-10353916 | Common:3; Rare:130 |