| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:28728594-28729113 | Common:2; Rare:153; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr17:28743430-28743687 | Rare:38 | ||||
| chr17:28743714-28744086 | Common:4; Rare:98 | ||||
| chr17:28744383-28744518 | Common:1; Rare:36 | ||||
| chr17:28811652-28811842 | Common:1; Rare:30 | ||||
| chr17:28812073-28812221 | Rare:29 | ||||
| chr17:28812385-28812716 | Common:1; Rare:89 | ||||
| chr17:28842337-28842386 | Rare:10 | ||||
| chr17:28842724-28842965 | Common:1; Rare:81 | ||||
| chr17:28854600-28855257 | Common:2; Rare:171 | ||||
| chr17:28896998-28897426 | Rare:98 | ||||
| chr17:28897600-28897963 | Common:2; Rare:106 | ||||
| chr17:28902248-28902524 | Rare:51 | ||||
| chr17:28949420-28949553 | Rare:19 | ||||
| chr17:28949661-28949956 | Common:3; Rare:58 |