| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:74872913-74873048 | Common:2; Rare:57; Clinvar (pathogenic):1 | ||||
| chr17:74873349-74873741 | Common:6; Rare:129 | ||||
| chr17:74972660-74972857 | Common:2; Rare:56 | ||||
| chr17:75012368-75012738 | Common:2; Rare:88 | ||||
| chr17:75012877-75013148 | Common:3; Rare:73 | ||||
| chr17:75046387-75046560 | Rare:38 | ||||
| chr17:75046895-75047301 | Common:2; Rare:132 | ||||
| chr17:75087559-75088210 | Common:6; Rare:134 | ||||
| chr17:75088246-75088416 | Common:1; Rare:31 | ||||
| chr17:75088576-75088613 | Rare:10 | ||||
| chr17:75089063-75089191 | Rare:20 | ||||
| chr17:75093797-75094129 | Common:1; Rare:81 | ||||
| chr17:75109803-75110032 | Common:3; Rare:67 | ||||
| chr17:75110489-75110561 | Rare:27 | ||||
| chr17:75130597-75130906 | Common:1; Rare:110 |