| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1771522-1771759 | Rare:60 | ||||
| chr17:1776377-1776660 | Common:6; Rare:90; Clinvar:2 | ||||
| chr17:1829792-1830062 | Common:8; Rare:113 | ||||
| chr17:2303715-2303980 | Common:2; Rare:102 | ||||
| chr17:2336423-2336528 | Rare:39 | ||||
| chr17:2337322-2337609 | Common:1; Rare:85 | ||||
| chr17:2511796-2511975 | Common:2; Rare:53 | ||||
| chr17:2593486-2593658 | Common:2; Rare:64 | ||||
| chr17:2593863-2593984 | Common:1; Rare:34; Clinvar:1; Clinvar (benign):3 | ||||
| chr17:2711762-2712031 | Common:2; Rare:75 | ||||
| chr17:3530246-3530324 | Common:4; Rare:18 | ||||
| chr17:3636241-3636517 | Common:4; Rare:78; Clinvar (benign):1 | ||||
| chr17:3636662-3636772 | Common:1; Rare:28; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:3668533-3668829 | Common:3; Rare:118 | ||||
| chr17:3723767-3723917 | Common:1; Rare:84 |