Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:65100666-65100906 | Rare:76 | ||||
chr17:65183830-65184096 | Common:3; Rare:48 | ||||
chr17:68101465-68101739 | Common:6; Rare:114 | ||||
chr17:68523745-68524122 | Common:3; Rare:101; Clinvar:2; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
chr17:71081070-71081299 | Common:2; Rare:49 | ||||
chr17:74794967-74795015 | Rare:13 | ||||
chr17:75220903-75221176 | Common:3; Rare:51 | ||||
chr17:75235428-75235710 | Common:1; Rare:94; Clinvar (pathogenic):1 | ||||
chr17:75257887-75258190 | Common:1; Rare:69 | ||||
chr17:75787989-75788003 | Rare:1 | ||||
chr17:75895205-75895362 | Rare:27 | ||||
chr17:76132506-76132785 | Common:6; Rare:72 | ||||
chr17:76557564-76557857 | Common:2; Rare:93 | ||||
chr17:76561190-76561401 | Common:2; Rare:62 | ||||
chr17:76563539-76563704 | Rare:29 |