| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:57988121-57988524 | Common:6; Rare:184 | ||||
| chr17:58006581-58006751 | Rare:98 | ||||
| chr17:58007074-58007446 | Common:2; Rare:285 | ||||
| chr17:58007520-58007820 | Common:2; Rare:113 | ||||
| chr17:58083146-58083507 | Common:10; Rare:242 | ||||
| chr17:58219216-58219372 | Common:2; Rare:110; Clinvar:4; Clinvar (benign):7 | ||||
| chr17:58352070-58352495 | Common:7; Rare:226 | ||||
| chr17:58415780-58416270 | Common:2; Rare:147 | ||||
| chr17:58417420-58417725 | Common:1; Rare:63 | ||||
| chr17:58514571-58514732 | Rare:61 | ||||
| chr17:58518237-58518357 | Rare:20 | ||||
| chr17:58692528-58692718 | Common:2; Rare:179; Clinvar:42; Clinvar (benign):41 | ||||
| chr17:59106612-59107074 | Common:6; Rare:250; Clinvar:12; Clinvar (benign):8 | ||||
| chr17:59155115-59155802 | Common:4; Rare:340 | ||||
| chr17:59209670-59210132 | Common:5; Rare:247 |