| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:8481352-8481543 | Rare:52 | ||||
| chr17:8965673-8965891 | Common:2; Rare:57 | ||||
| chr17:10697417-10697654 | Common:3; Rare:105; Clinvar:5; Clinvar (benign):5 | ||||
| chr17:10729531-10729833 | Common:3; Rare:114 | ||||
| chr17:13017898-13018284 | Common:6; Rare:131; Clinvar (benign):2 | ||||
| chr17:14069394-14069593 | Common:2; Rare:78; Clinvar:4; Clinvar (benign):3 | ||||
| chr17:14300806-14301126 | Common:3; Rare:86 | ||||
| chr17:15563441-15563739 | Common:1; Rare:101 | ||||
| chr17:15699458-15699773 | Common:4; Rare:86 | ||||
| chr17:15999595-15999981 | Common:3; Rare:176; Clinvar:5; Clinvar (benign):10; Clinvar (pathogenic):2 | ||||
| chr17:16215532-16215614 | Rare:34 | ||||
| chr17:16217152-16217251 | Rare:39; Clinvar:1 | ||||
| chr17:16380567-16380814 | Common:4; Rare:62 | ||||
| chr17:16381018-16381170 | Common:3; Rare:77 | ||||
| chr17:17237133-17237429 | Common:4; Rare:89; Clinvar (benign):2 |