| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:12020674-12020958 | Common:2; Rare:123 | ||||
| chr17:12665776-12666191 | Common:3; Rare:91 | ||||
| chr17:12666623-12666856 | Rare:34 | ||||
| chr17:13017941-13018263 | Common:5; Rare:97; Clinvar (benign):2 | ||||
| chr17:14069333-14069648 | Common:3; Rare:118; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr17:14300830-14301134 | Common:3; Rare:85 | ||||
| chr17:15260787-15260928 | Rare:50 | ||||
| chr17:15262443-15262657 | Rare:48 | ||||
| chr17:15563435-15563754 | Common:1; Rare:104 | ||||
| chr17:15699631-15699773 | Common:1; Rare:42 | ||||
| chr17:15999586-16000059 | Common:3; Rare:201; Clinvar:6; Clinvar (benign):13; Clinvar (pathogenic):2 | ||||
| chr17:16039714-16039790 | Rare:14 | ||||
| chr17:16040454-16040761 | Common:2; Rare:53 | ||||
| chr17:16057722-16058130 | Rare:103 | ||||
| chr17:16215530-16215657 | Common:1; Rare:52 |