| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:31318239-31318451 | Rare:73 | ||||
| chr17:31318456-31318757 | Rare:98; Clinvar (benign):1 | ||||
| chr17:31320442-31320575 | Rare:24 | ||||
| chr17:31487751-31488165 | Rare:131 | ||||
| chr17:31901600-31901987 | Common:3; Rare:113 | ||||
| chr17:31936671-31937078 | Common:2; Rare:114 | ||||
| chr17:32007218-32007487 | Rare:83 | ||||
| chr17:32142072-32142187 | Common:1; Rare:27 | ||||
| chr17:32142310-32142735 | Common:8; Rare:162 | ||||
| chr17:32341820-32342058 | Common:2; Rare:60 | ||||
| chr17:32342059-32342312 | Rare:64 | ||||
| chr17:32349954-32350223 | Rare:124 | ||||
| chr17:32350565-32350856 | Rare:73 | ||||
| chr17:32444212-32444579 | Common:1; Rare:128 | ||||
| chr17:32445270-32445328 | Common:1; Rare:3 |