| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:1801629-1801755 | Rare:26 | ||||
| chr5:5422180-5422693 | Common:3; Rare:171 | ||||
| chr5:6378476-6378694 | Rare:92 | ||||
| chr5:6632930-6633367 | Common:10; Rare:141; Clinvar:10; Clinvar (benign):6 | ||||
| chr5:7851028-7851219 | Common:2; Rare:38 | ||||
| chr5:7868991-7869204 | Common:2; Rare:109; Clinvar (benign):1 | ||||
| chr5:7869624-7869677 | Common:1; Rare:18 | ||||
| chr5:10249856-10250404 | Common:19; Rare:256; Clinvar:4; Clinvar (benign):2 | ||||
| chr5:10250751-10250834 | Rare:23 | ||||
| chr5:10353553-10353975 | Common:4; Rare:161 | ||||
| chr5:10441775-10442286 | Common:1; Rare:138 | ||||
| chr5:10761074-10761423 | Common:13; Rare:118 | ||||
| chr5:14387457-14387752 | Common:2; Rare:86 | ||||
| chr5:14581643-14581846 | Rare:82 | ||||
| chr5:14664517-14664973 | Common:5; Rare:181 |