| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:9645038-9645177 | Common:2; Rare:26 | ||||
| chr17:9959420-9959600 | Common:1; Rare:38 | ||||
| chr17:10026245-10026417 | Rare:28 | ||||
| chr17:10697481-10697654 | Common:3; Rare:78; Clinvar:5; Clinvar (benign):2 | ||||
| chr17:11997444-11997594 | Rare:50 | ||||
| chr17:14069384-14069580 | Common:2; Rare:75; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:15260787-15261009 | Common:2; Rare:67; Clinvar (benign):1 | ||||
| chr17:15563435-15563745 | Common:1; Rare:104 | ||||
| chr17:15684257-15684348 | Common:2; Rare:36 | ||||
| chr17:15699500-15699791 | Common:3; Rare:76 | ||||
| chr17:15999590-16000222 | Common:4; Rare:261; Clinvar:7; Clinvar (benign):15; Clinvar (pathogenic):2 | ||||
| chr17:16217094-16217249 | Rare:52; Clinvar:1 | ||||
| chr17:16380561-16380829 | Common:4; Rare:74 | ||||
| chr17:16381019-16381184 | Common:3; Rare:80 | ||||
| chr17:16415479-16415571 | Rare:17 |