| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:57256253-57256684 | Common:1; Rare:93 | ||||
| chr17:57849995-57850396 | Common:1; Rare:123 | ||||
| chr17:57893041-57893322 | Common:1; Rare:47 | ||||
| chr17:57903277-57903613 | Common:1; Rare:44 | ||||
| chr17:57955263-57955476 | Rare:46 | ||||
| chr17:57987884-57988000 | Common:2; Rare:36 | ||||
| chr17:57988109-57988577 | Common:6; Rare:140 | ||||
| chr17:58006201-58006365 | Rare:40 | ||||
| chr17:58006497-58006805 | Common:1; Rare:94 | ||||
| chr17:58007015-58007944 | Common:3; Rare:281 | ||||
| chr17:58083079-58083515 | Common:6; Rare:166 | ||||
| chr17:58083902-58084120 | Rare:60 | ||||
| chr17:58219132-58219431 | Common:2; Rare:112; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:58352115-58352513 | Common:6; Rare:145 | ||||
| chr17:58417496-58417841 | Common:1; Rare:64 |