| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:58219142-58219476 | Common:2; Rare:127; Clinvar:7; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:58352115-58352506 | Common:6; Rare:144 | ||||
| chr17:58352519-58352695 | Common:1; Rare:38 | ||||
| chr17:58353029-58353106 | Common:1; Rare:13 | ||||
| chr17:58415437-58415576 | Common:1; Rare:39; Clinvar (benign):1 | ||||
| chr17:58417459-58417726 | Common:1; Rare:55 | ||||
| chr17:58514003-58514139 | Rare:25 | ||||
| chr17:58514195-58514406 | Rare:43 | ||||
| chr17:58514419-58514504 | Common:1; Rare:17 | ||||
| chr17:58514555-58514720 | Rare:39 | ||||
| chr17:58517614-58517793 | Rare:38 | ||||
| chr17:58517833-58518498 | Common:1; Rare:141 | ||||
| chr17:58692466-58692957 | Common:4; Rare:216; Clinvar:36; Clinvar (benign):34; Clinvar (pathogenic):3 | ||||
| chr17:59106219-59106520 | Common:1; Rare:87 | ||||
| chr17:59106613-59107428 | Common:5; Rare:224; Clinvar:6; Clinvar (benign):4 |