| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:7931869-7932248 | Common:5; Rare:100 | ||||
| chr17:8176331-8176471 | Rare:43 | ||||
| chr17:8248042-8248159 | Common:3; Rare:51; Clinvar:2; Clinvar (benign):2 | ||||
| chr17:8249203-8249325 | Common:1; Rare:36 | ||||
| chr17:10697475-10697654 | Common:3; Rare:83; Clinvar:5; Clinvar (benign):3 | ||||
| chr17:14069393-14069549 | Common:2; Rare:52; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:15699566-15699773 | Common:3; Rare:59 | ||||
| chr17:15999586-15999970 | Common:3; Rare:177; Clinvar:5; Clinvar (benign):9; Clinvar (pathogenic):2 | ||||
| chr17:17591573-17591926 | Common:2; Rare:103 | ||||
| chr17:18183685-18183853 | Rare:77 | ||||
| chr17:18260333-18260662 | Rare:88 | ||||
| chr17:18314928-18315297 | Common:1; Rare:106 | ||||
| chr17:18682211-18682322 | Common:4; Rare:14 | ||||
| chr17:19977804-19977974 | Common:1; Rare:58 | ||||
| chr17:21214140-21214316 | Common:2; Rare:70 |