| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:34915508-34915741 | Common:1; Rare:49 | ||||
| chr5:36151881-36152120 | Rare:66 | ||||
| chr5:43067450-43067489 | Rare:8 | ||||
| chr5:43603102-43603212 | Rare:26 | ||||
| chr5:53109725-53109860 | Rare:71; Clinvar:2 | ||||
| chr5:55307657-55307797 | Common:3; Rare:48 | ||||
| chr5:58460063-58460228 | Common:4; Rare:62 | ||||
| chr5:60945056-60945238 | Common:4; Rare:64; Clinvar:2; Clinvar (benign):4 | ||||
| chr5:61162356-61162673 | Common:1; Rare:80 | ||||
| chr5:64768603-64768965 | Common:4; Rare:93 | ||||
| chr5:65563124-65563302 | Common:3; Rare:61 | ||||
| chr5:69369473-69369828 | Common:1; Rare:144 | ||||
| chr5:73498382-73498492 | Common:1; Rare:32 | ||||
| chr5:73565665-73565756 | Common:1; Rare:40 | ||||
| chr5:74767110-74767330 | Common:2; Rare:64 |