| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:56960894-56961181 | Common:3; Rare:92 | ||||
| chr17:56978020-56978192 | Common:3; Rare:85 | ||||
| chr17:57084902-57085295 | Common:1; Rare:123 | ||||
| chr17:57085504-57085675 | Common:1; Rare:44 | ||||
| chr17:57256272-57256662 | Common:1; Rare:85 | ||||
| chr17:57849987-57850343 | Common:1; Rare:117 | ||||
| chr17:57868122-57868281 | Common:1; Rare:51 | ||||
| chr17:57987592-57987804 | Common:1; Rare:65 | ||||
| chr17:57988218-57988611 | Common:5; Rare:118 | ||||
| chr17:58007138-58007445 | Common:1; Rare:148 | ||||
| chr17:58007533-58007871 | Common:1; Rare:73 | ||||
| chr17:58083217-58083445 | Common:1; Rare:82 | ||||
| chr17:58219132-58219504 | Common:2; Rare:139; Clinvar:7; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
| chr17:58352113-58352506 | Common:6; Rare:145 | ||||
| chr17:58353031-58353156 | Common:1; Rare:23 |