| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:58417407-58417666 | Rare:87 | ||||
| chr17:58513860-58514210 | Rare:93 | ||||
| chr17:58514485-58514797 | Rare:118 | ||||
| chr17:58517743-58518594 | Common:2; Rare:326 | ||||
| chr17:58692360-58692802 | Common:8; Rare:467; Clinvar:85; Clinvar (benign):81; Clinvar (pathogenic):5 | ||||
| chr17:58692916-58693429 | Common:2; Rare:165 | ||||
| chr17:58755600-58755910 | Common:1; Rare:111 | ||||
| chr17:58756120-58756520 | Common:3; Rare:111 | ||||
| chr17:59106065-59106562 | Common:3; Rare:174 | ||||
| chr17:59106592-59107497 | Common:10; Rare:443; Clinvar:13; Clinvar (benign):8 | ||||
| chr17:59154834-59155039 | Rare:104 | ||||
| chr17:59155091-59155858 | Common:4; Rare:443 | ||||
| chr17:59209400-59210252 | Common:15; Rare:581 | ||||
| chr17:59220270-59220717 | Common:11; Rare:260 | ||||
| chr17:59331428-59331817 | Common:7; Rare:323 |