| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:6651553-6651672 | Common:1; Rare:42 | ||||
| chr17:7012301-7012758 | Rare:150 | ||||
| chr17:7013101-7013456 | Common:1; Rare:95 | ||||
| chr17:7115020-7115063 | Rare:10 | ||||
| chr17:7219795-7219971 | Common:3; Rare:82; Clinvar:5; Clinvar (benign):2 | ||||
| chr17:7223901-7224240 | Rare:126; Clinvar:8; Clinvar (benign):6; Clinvar (pathogenic):10 | ||||
| chr17:7224255-7224333 | Rare:17; Clinvar:1 | ||||
| chr17:7224338-7224999 | Common:5; Rare:243; Clinvar:20; Clinvar (benign):26; Clinvar (pathogenic):7 | ||||
| chr17:7234236-7234615 | Rare:171 | ||||
| chr17:7238533-7238667 | Common:2; Rare:12 | ||||
| chr17:7241733-7241939 | Common:2; Rare:40 | ||||
| chr17:7241998-7242233 | Common:1; Rare:53 | ||||
| chr17:7242234-7242510 | Common:1; Rare:89 | ||||
| chr17:7242889-7243159 | Common:2; Rare:122 | ||||
| chr17:7251955-7252321 | Common:1; Rare:146 |