| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:77287757-77287958 | Rare:22 | ||||
| chr17:77319464-77319619 | Common:3; Rare:43; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:77319891-77320192 | Common:2; Rare:71; Clinvar:2; Clinvar (benign):3 | ||||
| chr17:77373797-77373919 | Rare:32 | ||||
| chr17:77453825-77454039 | Common:1; Rare:50 | ||||
| chr17:78121079-78121398 | Common:4; Rare:61; Clinvar:1 | ||||
| chr17:78126618-78126729 | Rare:41; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr17:78130623-78130821 | Rare:38 | ||||
| chr17:78168453-78168687 | Common:2; Rare:63 | ||||
| chr17:78187045-78187391 | Common:3; Rare:114 | ||||
| chr17:78360173-78360469 | Common:2; Rare:84 | ||||
| chr17:78378616-78378742 | Common:1; Rare:53 | ||||
| chr17:78678954-78679141 | Rare:40 | ||||
| chr17:78782203-78782577 | Common:9; Rare:122 | ||||
| chr17:78840745-78841124 | Common:2; Rare:140 |