| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:63137040-63137072 | Rare:5 | ||||
| chr17:63162265-63162430 | Common:1; Rare:33 | ||||
| chr17:63188604-63188620 | Rare:3 | ||||
| chr17:63331979-63332125 | Rare:27 | ||||
| chr17:63756235-63756572 | Common:1; Rare:86; Clinvar (pathogenic):1 | ||||
| chr17:63799521-63799568 | Rare:11 | ||||
| chr17:64145694-64146006 | Common:2; Rare:102 | ||||
| chr17:64146185-64146446 | Common:2; Rare:113 | ||||
| chr17:64489387-64489665 | Common:1; Rare:53 | ||||
| chr17:64513502-64513715 | Rare:45 | ||||
| chr17:64522531-64522759 | Common:1; Rare:67 | ||||
| chr17:64531828-64531860 | Rare:4 | ||||
| chr17:64556490-64556715 | Rare:34 | ||||
| chr17:64557601-64557928 | Rare:83 | ||||
| chr17:64592698-64592941 | Common:1; Rare:38 |