| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:41812593-41813067 | Common:3; Rare:109; Clinvar:6 | ||||
| chr17:41818171-41818475 | Common:1; Rare:107; Clinvar:5; Clinvar (benign):2 | ||||
| chr17:41930508-41930645 | Rare:40 | ||||
| chr17:41966614-41966845 | Common:1; Rare:82 | ||||
| chr17:42017382-42017483 | Rare:46 | ||||
| chr17:42154937-42155223 | Common:3; Rare:70 | ||||
| chr17:42388566-42388887 | Common:1; Rare:81 | ||||
| chr17:42423064-42423399 | Common:1; Rare:97; Clinvar:2 | ||||
| chr17:42458738-42458914 | Common:1; Rare:70 | ||||
| chr17:42566957-42567159 | Common:3; Rare:71 | ||||
| chr17:42577671-42577845 | Rare:86 | ||||
| chr17:42609307-42609730 | Common:8; Rare:178; Clinvar (benign):2 | ||||
| chr17:42682470-42682588 | Rare:30 | ||||
| chr17:42773369-42773510 | Rare:42 | ||||
| chr17:42833351-42833479 | Rare:48 |