| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:48908300-48908455 | Common:1; Rare:38 | ||||
| chr17:48944660-48944928 | Common:2; Rare:87 | ||||
| chr17:48996963-48997203 | Rare:57 | ||||
| chr17:49013751-49013857 | Rare:27 | ||||
| chr17:49210456-49210712 | Common:1; Rare:45 | ||||
| chr17:49230698-49230894 | Common:3; Rare:53 | ||||
| chr17:49362370-49362492 | Rare:29 | ||||
| chr17:49414828-49415110 | Common:1; Rare:66 | ||||
| chr17:49677961-49678266 | Rare:74 | ||||
| chr17:49707871-49708106 | Rare:107 | ||||
| chr17:49708119-49708387 | Common:1; Rare:92 | ||||
| chr17:49788546-49788845 | Common:1; Rare:101 | ||||
| chr17:49789121-49789365 | Common:3; Rare:64 | ||||
| chr17:50165980-50166019 | Rare:16; Clinvar:1; Clinvar (benign):2 | ||||
| chr17:50172224-50172389 | Common:2; Rare:42 |