| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:218134-218361 | Common:3; Rare:90; Clinvar:5; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr5:892614-892923 | Common:5; Rare:101 | ||||
| chr5:1799795-1799986 | Common:4; Rare:91 | ||||
| chr5:1801366-1801447 | Common:1; Rare:45; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:7868987-7869200 | Common:2; Rare:109; Clinvar (benign):1 | ||||
| chr5:9546049-9546376 | Common:7; Rare:75 | ||||
| chr5:10249874-10250170 | Common:16; Rare:141 | ||||
| chr5:10353609-10353907 | Common:3; Rare:105 | ||||
| chr5:16465717-16465855 | Rare:24 | ||||
| chr5:31532052-31532341 | Common:3; Rare:82 | ||||
| chr5:33440632-33441125 | Common:7; Rare:140 | ||||
| chr5:34915472-34915741 | Common:1; Rare:65 | ||||
| chr5:36151874-36152120 | Rare:68 | ||||
| chr5:36606470-36606619 | Rare:24 | ||||
| chr5:36876650-36876889 | Common:1; Rare:72; Clinvar:1; Clinvar (benign):1 |