| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8152362-8152556 | Common:2; Rare:45 | ||||
| chr17:8248042-8248122 | Common:2; Rare:39; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:10630090-10630469 | Common:3; Rare:118; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:10657225-10657642 | Common:4; Rare:122 | ||||
| chr17:10697494-10697653 | Common:3; Rare:67; Clinvar:3; Clinvar (benign):2 | ||||
| chr17:14069395-14069587 | Common:2; Rare:76; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:15262478-15262605 | Rare:31 | ||||
| chr17:15651859-15652006 | Rare:20 | ||||
| chr17:15999600-16000028 | Common:3; Rare:182; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr17:16217115-16217227 | Rare:28 | ||||
| chr17:17496393-17496535 | Rare:35 | ||||
| chr17:17507049-17507254 | Common:4; Rare:64 | ||||
| chr17:17591595-17591926 | Common:1; Rare:94 | ||||
| chr17:18258686-18258815 | Common:1; Rare:40 | ||||
| chr17:18314944-18315293 | Rare:103 |