| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:43602886-43603266 | Rare:94 | ||||
| chr5:44389404-44389614 | Rare:28 | ||||
| chr5:44808693-44808976 | Common:2; Rare:91 | ||||
| chr5:50665733-50665912 | Common:1; Rare:25 | ||||
| chr5:50666896-50666972 | Common:1; Rare:24 | ||||
| chr5:52787531-52788022 | Common:6; Rare:105 | ||||
| chr5:52788214-52788493 | Common:1; Rare:80 | ||||
| chr5:53109711-53109891 | Common:1; Rare:92; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr5:54310513-54310711 | Rare:63 | ||||
| chr5:55307620-55308035 | Common:5; Rare:145 | ||||
| chr5:58460038-58460228 | Common:5; Rare:76 | ||||
| chr5:59275539-59275901 | Common:1; Rare:55 | ||||
| chr5:59768115-59768204 | Rare:17 | ||||
| chr5:59768370-59768451 | Rare:19 | ||||
| chr5:60488014-60488397 | Common:1; Rare:67 |