| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:30477283-30477449 | Rare:51 | ||||
| chr17:30824635-30824914 | Common:3; Rare:114 | ||||
| chr17:30831900-30832020 | Rare:41 | ||||
| chr17:30906200-30906354 | Common:1; Rare:46 | ||||
| chr17:31321608-31321858 | Common:3; Rare:40 | ||||
| chr17:31901647-31901787 | Common:1; Rare:51 | ||||
| chr17:31936782-31937014 | Rare:57 | ||||
| chr17:32142327-32142621 | Common:8; Rare:126 | ||||
| chr17:32341904-32342006 | Rare:27 | ||||
| chr17:32342121-32342262 | Rare:41 | ||||
| chr17:32350002-32350198 | Rare:101 | ||||
| chr17:34961458-34961585 | Common:1; Rare:62 | ||||
| chr17:34980378-34980604 | Common:4; Rare:65 | ||||
| chr17:35119805-35120013 | Common:1; Rare:58; Clinvar:2; Clinvar (benign):1 | ||||
| chr17:35578531-35578721 | Common:1; Rare:49; Clinvar (benign):1 |