| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:15999590-16000028 | Common:3; Rare:185; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
| chr17:17237393-17237688 | Common:4; Rare:67 | ||||
| chr17:17281182-17281379 | Rare:78 | ||||
| chr17:17591589-17591943 | Common:2; Rare:101 | ||||
| chr17:17592117-17592195 | Common:1; Rare:29 | ||||
| chr17:17823591-17823852 | Common:5; Rare:115 | ||||
| chr17:18039081-18039410 | Common:3; Rare:84; Clinvar:1; Clinvar (benign):1 | ||||
| chr17:18087771-18087985 | Rare:54 | ||||
| chr17:18183685-18183925 | Rare:109 | ||||
| chr17:18225329-18225661 | Common:4; Rare:104 | ||||
| chr17:18254590-18254824 | Rare:79 | ||||
| chr17:18258661-18258795 | Common:1; Rare:46 | ||||
| chr17:18314944-18315326 | Rare:111 | ||||
| chr17:18682211-18682459 | Common:7; Rare:26 | ||||
| chr17:18856149-18856375 | Common:1; Rare:41 |