| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:50188784-50188994 | Rare:57; Clinvar:1; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr17:50345926-50346161 | Common:4; Rare:78 | ||||
| chr17:50373160-50373259 | Common:3; Rare:43 | ||||
| chr17:50534396-50534627 | Common:1; Rare:60 | ||||
| chr17:50719461-50719823 | Rare:118 | ||||
| chr17:50866300-50866774 | Common:4; Rare:140 | ||||
| chr17:51166686-51166955 | Rare:78 | ||||
| chr17:51260113-51260610 | Common:3; Rare:189 | ||||
| chr17:51260899-51260978 | Common:1; Rare:36 | ||||
| chr17:54968595-54968799 | Common:3; Rare:95 | ||||
| chr17:56833913-56834214 | Common:3; Rare:102 | ||||
| chr17:56913496-56913706 | Rare:61 | ||||
| chr17:56913978-56914186 | Common:1; Rare:58 | ||||
| chr17:56978034-56978235 | Common:3; Rare:93 | ||||
| chr17:57084959-57085359 | Common:1; Rare:129 |