| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:75667136-75667411 | Common:4; Rare:95 | ||||
| chr17:75784553-75784875 | Common:2; Rare:145 | ||||
| chr17:75904879-75905218 | Common:4; Rare:93 | ||||
| chr17:75979091-75979271 | Rare:51; Clinvar:4 | ||||
| chr17:76103696-76103867 | Common:5; Rare:60 | ||||
| chr17:76353888-76353976 | Rare:24 | ||||
| chr17:76726491-76726886 | Common:5; Rare:146 | ||||
| chr17:76737309-76737537 | Common:3; Rare:91 | ||||
| chr17:76737883-76738084 | Common:3; Rare:58 | ||||
| chr17:77319348-77319561 | Common:3; Rare:59; Clinvar (benign):3 | ||||
| chr17:77320131-77320324 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:78187018-78187364 | Common:3; Rare:116 | ||||
| chr17:78378400-78378709 | Common:2; Rare:97 | ||||
| chr17:78782255-78782587 | Common:9; Rare:107 | ||||
| chr17:78840745-78841016 | Common:2; Rare:98 |