Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:45161482-45161916 | Common:1; Rare:115 | ||||
chr17:45425607-45425840 | Common:1; Rare:42 | ||||
chr17:45431923-45432040 | Common:2; Rare:19 | ||||
chr17:45490693-45490898 | Common:1; Rare:69 | ||||
chr17:45894247-45894570 | Common:2; Rare:99; Clinvar:4; Clinvar (benign):1 | ||||
chr17:46192766-46193019 | Common:3; Rare:65; Clinvar (benign):2 | ||||
chr17:46193432-46193611 | Common:3; Rare:53 | ||||
chr17:46922869-46923187 | Common:3; Rare:89; Clinvar:1; Clinvar (benign):7 | ||||
chr17:47188824-47189048 | Common:1; Rare:42 | ||||
chr17:47189077-47189151 | Rare:20 | ||||
chr17:47189159-47189598 | Common:1; Rare:118 | ||||
chr17:47253821-47253947 | Common:2; Rare:40; Clinvar:1; Clinvar (benign):4 | ||||
chr17:47323695-47323780 | Rare:25 | ||||
chr17:47323801-47323880 | Common:2; Rare:37 | ||||
chr17:47323885-47324044 | Common:1; Rare:55 |