| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:68601361-68601522 | Common:2; Rare:38 | ||||
| chr17:69327050-69327353 | Common:2; Rare:96 | ||||
| chr17:70169293-70169539 | Common:1; Rare:70 | ||||
| chr17:72120793-72121044 | Rare:65 | ||||
| chr17:73192817-73193099 | Common:15; Rare:118; Clinvar:3; Clinvar (benign):1 | ||||
| chr17:73232220-73232707 | Common:3; Rare:176 | ||||
| chr17:73311959-73312225 | Rare:70 | ||||
| chr17:74213328-74213583 | Common:4; Rare:57 | ||||
| chr17:74274177-74274328 | Common:2; Rare:29; Clinvar (benign):2 | ||||
| chr17:74431274-74431408 | Rare:34 | ||||
| chr17:74431909-74432141 | Common:1; Rare:91 | ||||
| chr17:74466578-74466705 | Rare:38 | ||||
| chr17:74546015-74546172 | Rare:25 | ||||
| chr17:74748421-74748689 | Common:4; Rare:100 | ||||
| chr17:74776290-74776543 | Common:4; Rare:80 |