| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr17:45148159-45148478 | Common:1; Rare:93 | ||||
| chr17:47189254-47189568 | Rare:81 | ||||
| chr17:47941368-47941607 | Rare:48; Clinvar:1 | ||||
| chr17:48048069-48048405 | Rare:86 | ||||
| chr17:48944773-48944918 | Common:2; Rare:47 | ||||
| chr17:49210567-49210712 | Rare:21 | ||||
| chr17:49414845-49415145 | Common:2; Rare:76 | ||||
| chr17:49788462-49788718 | Common:1; Rare:81 | ||||
| chr17:50188740-50189017 | Rare:72; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):4 | ||||
| chr17:50189167-50189540 | Rare:81; Clinvar:5; Clinvar (benign):2 | ||||
| chr17:50192473-50192694 | Common:1; Rare:49; Clinvar:3; Clinvar (benign):6 | ||||
| chr17:50192797-50193048 | Common:2; Rare:79; Clinvar:1; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr17:50194136-50194449 | Common:1; Rare:80; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr17:50194571-50194831 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr17:50195029-50195667 | Common:1; Rare:180; Clinvar:3; Clinvar (benign):7; Clinvar (pathogenic):1 |