| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:16217037-16217327 | Rare:90; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr17:16353377-16353655 | Rare:90 | ||||
| chr17:16380557-16380799 | Common:4; Rare:66 | ||||
| chr17:16380996-16381419 | Common:4; Rare:177 | ||||
| chr17:16492088-16492383 | Common:3; Rare:101 | ||||
| chr17:16569085-16569376 | Common:1; Rare:89 | ||||
| chr17:16653375-16653417 | Common:1; Rare:9 | ||||
| chr17:16653505-16653642 | Rare:43 | ||||
| chr17:16653740-16653870 | Rare:45 | ||||
| chr17:17042080-17042570 | Common:20; Rare:160 | ||||
| chr17:17205936-17206014 | Rare:29 | ||||
| chr17:17206153-17206616 | Common:4; Rare:172 | ||||
| chr17:17237122-17237422 | Common:4; Rare:92; Clinvar (benign):2 | ||||
| chr17:17237647-17237761 | Rare:37 | ||||
| chr17:17280665-17280980 | Common:4; Rare:128 |