Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:5002418-5002842 | Common:1; Rare:139; Clinvar:3; Clinvar (benign):1 | ||||
chr17:5003344-5003689 | Common:2; Rare:109 | ||||
chr17:5378037-5378227 | Common:1; Rare:44 | ||||
chr17:7311014-7311651 | Common:1; Rare:157 | ||||
chr17:7578216-7578469 | Rare:79 | ||||
chr17:8189627-8189927 | Rare:108 | ||||
chr17:8190040-8190204 | Rare:65 | ||||
chr17:8222534-8222623 | Rare:17 | ||||
chr17:10494567-10495320 | Common:1; Rare:216 | ||||
chr17:10497067-10497454 | Common:2; Rare:110 | ||||
chr17:10505810-10506056 | Common:2; Rare:79 | ||||
chr17:10515924-10516343 | Rare:144 | ||||
chr17:10523116-10523286 | Common:1; Rare:52; Clinvar:2 | ||||
chr17:10523494-10523888 | Rare:108; Clinvar:3 | ||||
chr17:10533283-10533634 | Rare:105; Clinvar:6; Clinvar (benign):3; Clinvar (pathogenic):3 |