| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:443080-443280 | Common:10; Rare:93 | ||||
| chr5:892629-892929 | Common:5; Rare:101 | ||||
| chr5:1799785-1799993 | Common:7; Rare:98 | ||||
| chr5:1801300-1801460 | Common:4; Rare:80; Clinvar:3; Clinvar (benign):1 | ||||
| chr5:6378492-6378650 | Rare:70 | ||||
| chr5:7868991-7869200 | Common:2; Rare:106; Clinvar (benign):1 | ||||
| chr5:9546033-9546372 | Common:8; Rare:79 | ||||
| chr5:10250190-10250377 | Common:3; Rare:98; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:10353597-10353905 | Common:3; Rare:111 | ||||
| chr5:16465529-16465895 | Rare:101 | ||||
| chr5:31532052-31532319 | Common:2; Rare:72 | ||||
| chr5:31935947-31936162 | Rare:43 | ||||
| chr5:32174277-32174532 | Common:4; Rare:82 | ||||
| chr5:33440624-33441044 | Common:4; Rare:109 | ||||
| chr5:34656083-34656426 | Common:4; Rare:96 |