| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:41583092-41583474 | Common:5; Rare:135; Clinvar:8; Clinvar (benign):1; Clinvar (pathogenic):4 | ||||
| chr17:41586296-41586908 | Common:8; Rare:230; Clinvar:7; Clinvar (benign):7; Clinvar (pathogenic):4 | ||||
| chr17:41586925-41587192 | Common:3; Rare:57 | ||||
| chr17:41612156-41612812 | Common:3; Rare:233; Clinvar:1; Clinvar (pathogenic):2 | ||||
| chr17:41612862-41613163 | Common:1; Rare:50 | ||||
| chr17:41624741-41624938 | Rare:51 | ||||
| chr17:41688640-41689077 | Common:3; Rare:174 | ||||
| chr17:41689350-41689569 | Common:1; Rare:75 | ||||
| chr17:41772193-41772520 | Common:1; Rare:59 | ||||
| chr17:41785192-41785393 | Common:1; Rare:43 | ||||
| chr17:41785922-41786152 | Rare:43 | ||||
| chr17:41786564-41786850 | Common:4; Rare:76; Clinvar:3; Clinvar (benign):4 | ||||
| chr17:41786911-41787128 | Rare:48 | ||||
| chr17:41918878-41919260 | Common:2; Rare:141; Clinvar:1 | ||||
| chr17:41966595-41966837 | Common:1; Rare:85 |