| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:38445460-38445673 | Rare:50 | ||||
| chr5:38556452-38556841 | Common:3; Rare:133 | ||||
| chr5:38557204-38557433 | Rare:61 | ||||
| chr5:38557458-38557488 | Rare:6 | ||||
| chr5:38845706-38846220 | Common:2; Rare:126 | ||||
| chr5:39074333-39074486 | Common:1; Rare:73 | ||||
| chr5:39219525-39219843 | Common:1; Rare:62 | ||||
| chr5:39425010-39425322 | Common:2; Rare:67 | ||||
| chr5:40679159-40679450 | Common:3; Rare:56 | ||||
| chr5:40679698-40679960 | Common:1; Rare:59 | ||||
| chr5:40798152-40798401 | Common:1; Rare:94 | ||||
| chr5:40835173-40835374 | Common:2; Rare:81 | ||||
| chr5:41870364-41870561 | Common:1; Rare:65; Clinvar:2; Clinvar (benign):1 | ||||
| chr5:41904003-41904391 | Common:2; Rare:124 | ||||
| chr5:41925136-41925411 | Common:2; Rare:97 |