| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:218104-218403 | Common:4; Rare:121; Clinvar:11; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr5:443084-443176 | Common:3; Rare:43 | ||||
| chr5:612177-612354 | Rare:72 | ||||
| chr5:892743-892990 | Common:2; Rare:100 | ||||
| chr5:1799786-1799949 | Common:7; Rare:82 | ||||
| chr5:1801300-1801447 | Common:4; Rare:71; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:7868986-7869204 | Common:2; Rare:112; Clinvar (benign):1 | ||||
| chr5:10249856-10250398 | Common:19; Rare:255; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:10353590-10353896 | Common:3; Rare:113 | ||||
| chr5:16465715-16465895 | Rare:32 | ||||
| chr5:31532052-31532367 | Common:3; Rare:94 | ||||
| chr5:33440624-33441095 | Common:7; Rare:129 | ||||
| chr5:34656144-34656470 | Common:3; Rare:85 | ||||
| chr5:34915218-34915355 | Rare:38 | ||||
| chr5:34915461-34915761 | Common:1; Rare:81 |