Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:48944773-48944895 | Common:1; Rare:40 | ||||
chr17:49210182-49210432 | Common:2; Rare:39 | ||||
chr17:49210522-49210721 | Rare:33 | ||||
chr17:49788576-49788778 | Common:1; Rare:68 | ||||
chr17:50165823-50166071 | Common:2; Rare:66; Clinvar:3; Clinvar (benign):3 | ||||
chr17:50166367-50166465 | Common:1; Rare:16 | ||||
chr17:50194810-50195084 | Common:1; Rare:55; Clinvar (pathogenic):2 | ||||
chr17:50345779-50346143 | Common:4; Rare:101 | ||||
chr17:50373151-50373235 | Common:2; Rare:39 | ||||
chr17:50719467-50719768 | Rare:112 | ||||
chr17:50866309-50866560 | Common:3; Rare:84 | ||||
chr17:51120642-51120983 | Rare:139 | ||||
chr17:51166681-51166955 | Rare:80 | ||||
chr17:51260139-51260607 | Common:3; Rare:178 | ||||
chr17:51260904-51260978 | Common:1; Rare:33 |