| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:59565431-59565781 | Common:3; Rare:275 | ||||
| chr17:59565820-59566360 | Common:1; Rare:185 | ||||
| chr17:59619409-59620129 | Common:8; Rare:429 | ||||
| chr17:59685047-59685914 | Common:2; Rare:210 | ||||
| chr17:59688533-59689372 | Rare:220 | ||||
| chr17:59707272-59707982 | Common:13; Rare:395; Clinvar (benign):18 | ||||
| chr17:59837230-59838142 | Common:8; Rare:241 | ||||
| chr17:59838151-59839005 | Common:1; Rare:249 | ||||
| chr17:59892594-59893320 | Common:2; Rare:341 | ||||
| chr17:59893446-59893971 | Common:1; Rare:153 | ||||
| chr17:59958938-59959338 | Common:2; Rare:84 | ||||
| chr17:59962157-59962928 | Rare:314 | ||||
| chr17:59964000-59964270 | Rare:49 | ||||
| chr17:59964634-59965193 | Common:6; Rare:451 | ||||
| chr17:60078280-60079099 | Common:19; Rare:591 |