| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:76737317-76737687 | Common:4; Rare:130 | ||||
| chr17:76737845-76738089 | Common:3; Rare:70 | ||||
| chr17:77088597-77088762 | Common:1; Rare:44 | ||||
| chr17:77127731-77127877 | Rare:26 | ||||
| chr17:77129954-77130110 | Rare:26 | ||||
| chr17:77140666-77141058 | Common:2; Rare:136 | ||||
| chr17:77185309-77185332 | Rare:3 | ||||
| chr17:77319388-77319674 | Common:3; Rare:75; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:77319691-77319961 | Common:1; Rare:66; Clinvar (benign):1 | ||||
| chr17:77320074-77320329 | Common:1; Rare:67; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:77323144-77323431 | Common:1; Rare:60 | ||||
| chr17:77323579-77323732 | Common:3; Rare:27 | ||||
| chr17:78128706-78129018 | Common:7; Rare:74 | ||||
| chr17:78187042-78187380 | Common:3; Rare:109 | ||||
| chr17:78378596-78378687 | Common:1; Rare:38 |