| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:16215375-16215671 | Common:3; Rare:175 | ||||
| chr17:16217109-16217243 | Rare:74; Clinvar:2 | ||||
| chr17:16353060-16353360 | Rare:141 | ||||
| chr17:16353378-16353813 | Rare:115 | ||||
| chr17:16380570-16381465 | Common:12; Rare:422 | ||||
| chr17:17042212-17042539 | Common:39; Rare:217 | ||||
| chr17:17237124-17237740 | Common:16; Rare:328; Clinvar (benign):4 | ||||
| chr17:17280610-17280940 | Common:8; Rare:194 | ||||
| chr17:17281166-17281395 | Rare:162 | ||||
| chr17:17303218-17303387 | Common:3; Rare:113 | ||||
| chr17:17303750-17304100 | Common:2; Rare:181 | ||||
| chr17:17476868-17477113 | Common:6; Rare:121 | ||||
| chr17:17496365-17496553 | Rare:87 | ||||
| chr17:17591250-17591510 | Common:2; Rare:138 | ||||
| chr17:17591569-17591960 | Common:4; Rare:217 |