| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:1716223-1716533 | Common:3; Rare:92 | ||||
| chr17:1776359-1776549 | Common:6; Rare:44 | ||||
| chr17:1829780-1830071 | Common:8; Rare:122 | ||||
| chr17:2214297-2214572 | Common:1; Rare:52 | ||||
| chr17:2303728-2304004 | Common:2; Rare:103 | ||||
| chr17:2336430-2336507 | Rare:25 | ||||
| chr17:2511820-2511966 | Common:2; Rare:40 | ||||
| chr17:2593840-2593984 | Common:1; Rare:41; Clinvar:3; Clinvar (benign):3 | ||||
| chr17:3636261-3636505 | Common:4; Rare:60; Clinvar (benign):1 | ||||
| chr17:3668552-3668837 | Common:2; Rare:112 | ||||
| chr17:3723757-3723925 | Common:1; Rare:93 | ||||
| chr17:3892955-3893265 | Common:3; Rare:105 | ||||
| chr17:4143011-4143244 | Rare:76 | ||||
| chr17:4143605-4143740 | Common:4; Rare:77 | ||||
| chr17:4263937-4264024 | Rare:38 |