| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:51166304-51166497 | Common:1; Rare:42 | ||||
| chr17:51260277-51260581 | Common:3; Rare:115 | ||||
| chr17:54968611-54968799 | Common:3; Rare:90 | ||||
| chr17:56914029-56914176 | Rare:35 | ||||
| chr17:56978034-56978168 | Common:3; Rare:70 | ||||
| chr17:57084959-57085390 | Common:2; Rare:134 | ||||
| chr17:57085649-57085969 | Common:1; Rare:82 | ||||
| chr17:57849938-57850274 | Common:1; Rare:114 | ||||
| chr17:57988122-57988524 | Common:5; Rare:118 | ||||
| chr17:58692528-58692650 | Common:1; Rare:64; Clinvar:5; Clinvar (benign):16 | ||||
| chr17:59106701-59106972 | Common:2; Rare:90; Clinvar:4; Clinvar (benign):2 | ||||
| chr17:59154979-59155517 | Common:2; Rare:140 | ||||
| chr17:59331476-59331822 | Common:2; Rare:112 | ||||
| chr17:59619538-59620104 | Common:3; Rare:198 | ||||
| chr17:59707397-59707742 | Common:3; Rare:93; Clinvar (benign):3 |