| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:16486762-16486923 | Rare:28 | ||||
| chr17:17805866-17806065 | Common:2; Rare:40 | ||||
| chr17:17836180-17836435 | Common:3; Rare:68 | ||||
| chr17:18329279-18329495 | Rare:76 | ||||
| chr17:27551925-27552191 | Rare:53 | ||||
| chr17:28344106-28344411 | Common:2; Rare:84 | ||||
| chr17:28478306-28478404 | Rare:18 | ||||
| chr17:28496228-28496587 | Rare:81 | ||||
| chr17:28574209-28574329 | Rare:29 | ||||
| chr17:28748703-28749278 | Rare:149 | ||||
| chr17:29099661-29099951 | Common:1; Rare:54 | ||||
| chr17:29178225-29178409 | Rare:34 | ||||
| chr17:29507692-29507987 | Rare:42 | ||||
| chr17:30222856-30223142 | Common:5; Rare:51; Clinvar (benign):2 | ||||
| chr17:30326733-30326944 | Common:2; Rare:34 |