| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:53962560-53962851 | Common:1; Rare:44 | ||||
| chr5:54022626-54022844 | Common:2; Rare:30 | ||||
| chr5:55431952-55432075 | Rare:29 | ||||
| chr5:57235842-57236056 | Common:1; Rare:58 | ||||
| chr5:58937057-58937340 | Common:8; Rare:45 | ||||
| chr5:62397621-62397810 | Common:1; Rare:50 | ||||
| chr5:63961165-63961314 | Common:2; Rare:49 | ||||
| chr5:65210643-65210911 | Common:1; Rare:43 | ||||
| chr5:65585848-65586134 | Common:2; Rare:65 | ||||
| chr5:65925533-65925829 | Rare:118 | ||||
| chr5:66029575-66029793 | Common:4; Rare:54 | ||||
| chr5:68922293-68922736 | Common:1; Rare:76 | ||||
| chr5:71635019-71635229 | Common:1; Rare:57; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr5:72108230-72108346 | Rare:29 | ||||
| chr5:72108918-72109176 | Rare:47 |