| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:50666752-50666967 | Common:1; Rare:52 | ||||
| chr5:50667760-50667957 | Common:1; Rare:63 | ||||
| chr5:53109725-53109897 | Common:1; Rare:87; Clinvar:2 | ||||
| chr5:54310496-54310709 | Rare:65 | ||||
| chr5:55160090-55160250 | Rare:49 | ||||
| chr5:55307617-55307838 | Common:3; Rare:74 | ||||
| chr5:55307902-55308029 | Common:2; Rare:52 | ||||
| chr5:57173671-57174146 | Common:1; Rare:162 | ||||
| chr5:58455463-58455619 | Common:1; Rare:35 | ||||
| chr5:58457079-58457183 | Common:1; Rare:38 | ||||
| chr5:58457340-58457556 | Common:1; Rare:46 | ||||
| chr5:58459681-58460012 | Common:1; Rare:116 | ||||
| chr5:60700129-60700228 | Common:1; Rare:30 | ||||
| chr5:60945011-60945341 | Common:6; Rare:129; Clinvar:5; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr5:61162218-61162535 | Common:1; Rare:73 |