| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:28043323-28043723 | Common:6; Rare:68 | ||||
| chr17:28318829-28319258 | Common:21; Rare:864 | ||||
| chr17:28319350-28319470 | Common:4; Rare:60 | ||||
| chr17:28335334-28335884 | Common:7; Rare:662 | ||||
| chr17:28335937-28336622 | Common:4; Rare:222 | ||||
| chr17:28357312-28357795 | Common:44; Rare:1006; Clinvar (pathogenic):6 | ||||
| chr17:28384251-28384850 | Rare:417 | ||||
| chr17:28405225-28406410 | Common:5; Rare:712; Clinvar:12; Clinvar (benign):3; Clinvar (pathogenic):10 | ||||
| chr17:28551983-28552918 | Common:2; Rare:402; Clinvar:12; Clinvar (benign):4 | ||||
| chr17:28570272-28571218 | Rare:367; Clinvar (pathogenic):1 | ||||
| chr17:28571376-28571776 | Rare:495 | ||||
| chr17:28571866-28572132 | Rare:42 | ||||
| chr17:28576840-28577270 | Common:14; Rare:474 | ||||
| chr17:28577490-28577890 | Common:3; Rare:88 | ||||
| chr17:28598540-28598940 | Rare:115 |