Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:39637057-39637174 | Common:2; Rare:33 | ||||
chr17:39688023-39688098 | Rare:23 | ||||
chr17:40443366-40443454 | Rare:21 | ||||
chr17:41688850-41689069 | Common:2; Rare:108 | ||||
chr17:41812895-41813013 | Rare:32 | ||||
chr17:41966603-41966845 | Common:1; Rare:86 | ||||
chr17:42017409-42017584 | Common:1; Rare:59 | ||||
chr17:42423144-42423434 | Common:1; Rare:75; Clinvar:2 | ||||
chr17:42536066-42536299 | Common:3; Rare:69; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):2 | ||||
chr17:42577671-42577825 | Rare:72 | ||||
chr17:42609253-42609715 | Common:9; Rare:194; Clinvar (benign):1 | ||||
chr17:43125345-43125601 | Rare:53; Clinvar:3; Clinvar (benign):2 | ||||
chr17:44004357-44004623 | Rare:51 | ||||
chr17:44070620-44070940 | Common:3; Rare:109; Clinvar:4; Clinvar (benign):2 | ||||
chr17:44123636-44123886 | Common:3; Rare:65 |