| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:48625854-48625950 | Rare:36 | ||||
| chr17:48944736-48944918 | Common:2; Rare:69 | ||||
| chr17:48997458-48997482 | Rare:4 | ||||
| chr17:49414833-49415147 | Common:2; Rare:80 | ||||
| chr17:49788546-49788724 | Common:1; Rare:55 | ||||
| chr17:50373168-50373249 | Common:3; Rare:33 | ||||
| chr17:50719518-50719652 | Rare:56 | ||||
| chr17:51153301-51153643 | Common:1; Rare:88 | ||||
| chr17:51260232-51260598 | Common:3; Rare:142 | ||||
| chr17:54968595-54968793 | Common:3; Rare:94 | ||||
| chr17:56914029-56914177 | Rare:36 | ||||
| chr17:57084980-57085321 | Rare:114 | ||||
| chr17:57849995-57850292 | Common:1; Rare:98 | ||||
| chr17:57988175-57988519 | Common:5; Rare:101 | ||||
| chr17:58219201-58219339 | Common:1; Rare:51; Clinvar:2; Clinvar (benign):5 |