| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:50441357-50441555 | Common:3; Rare:55 | ||||
| chr5:50665776-50665933 | Common:1; Rare:21 | ||||
| chr5:50667422-50667563 | Rare:40 | ||||
| chr5:52787841-52787950 | Common:1; Rare:18 | ||||
| chr5:53109714-53109899 | Common:1; Rare:96; Clinvar:4 | ||||
| chr5:54310421-54310711 | Common:1; Rare:84 | ||||
| chr5:55307651-55308049 | Common:5; Rare:141 | ||||
| chr5:55994863-55995203 | Rare:127 | ||||
| chr5:56952095-56952321 | Rare:83 | ||||
| chr5:57173540-57173893 | Common:3; Rare:133 | ||||
| chr5:58460043-58460182 | Common:4; Rare:59 | ||||
| chr5:59768437-59768595 | Rare:50 | ||||
| chr5:60700049-60700237 | Common:1; Rare:71 | ||||
| chr5:60844149-60844464 | Common:5; Rare:103 | ||||
| chr5:60945026-60945235 | Common:5; Rare:80; Clinvar:3; Clinvar (benign):5 |