| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:58352976-58353376 | Common:3; Rare:117 | ||||
| chr17:58415087-58415487 | Common:2; Rare:102; Clinvar (benign):2 | ||||
| chr17:58415540-58416131 | Common:1; Rare:171 | ||||
| chr17:58417477-58417686 | Common:1; Rare:39 | ||||
| chr17:58492656-58492908 | Rare:65 | ||||
| chr17:58513835-58514357 | Rare:161 | ||||
| chr17:58514499-58514899 | Rare:243 | ||||
| chr17:58517826-58518421 | Common:3; Rare:541 | ||||
| chr17:58692300-58693110 | Common:17; Rare:1122; Clinvar:175; Clinvar (benign):172; Clinvar (pathogenic):6 | ||||
| chr17:58693109-58693509 | Common:2; Rare:92 | ||||
| chr17:58755610-58756090 | Rare:235 | ||||
| chr17:59106194-59106594 | Common:2; Rare:170 | ||||
| chr17:59106633-59107266 | Common:18; Rare:1011; Clinvar:35; Clinvar (benign):22 | ||||
| chr17:59107199-59107599 | Common:2; Rare:107 | ||||
| chr17:59154606-59155020 | Common:1; Rare:137 |