| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:40798167-40798401 | Common:1; Rare:88 | ||||
| chr5:41925240-41925310 | Rare:21 | ||||
| chr5:43121404-43121643 | Common:1; Rare:93 | ||||
| chr5:43483853-43483913 | Common:1; Rare:22 | ||||
| chr5:43603072-43603260 | Rare:46 | ||||
| chr5:44808721-44808955 | Common:2; Rare:77 | ||||
| chr5:51383261-51383448 | Common:2; Rare:68 | ||||
| chr5:53109719-53109949 | Common:1; Rare:112; Clinvar:3 | ||||
| chr5:54310517-54310711 | Rare:61 | ||||
| chr5:55307651-55308016 | Common:4; Rare:121 | ||||
| chr5:56952109-56952315 | Rare:76 | ||||
| chr5:57173514-57173867 | Common:3; Rare:136 | ||||
| chr5:60945031-60945233 | Common:4; Rare:77; Clinvar:3; Clinvar (benign):4 | ||||
| chr5:61162398-61162558 | Common:1; Rare:48 | ||||
| chr5:62306353-62306475 | Rare:33; Clinvar (benign):2 |