Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:7311096-7311437 | Rare:88 | ||||
chr17:8186723-8186863 | Common:2; Rare:65 | ||||
chr17:17752308-17752485 | Common:1; Rare:61 | ||||
chr17:21286432-21286622 | Common:1; Rare:35 | ||||
chr17:42422718-42422778 | Rare:23; Clinvar:1; Clinvar (pathogenic):1 | ||||
chr17:50189883-50190355 | Common:2; Rare:139; Clinvar:5; Clinvar (benign):5 | ||||
chr17:50199217-50199430 | Rare:68; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr17:64145707-64145975 | Common:2; Rare:78 | ||||
chr17:64837137-64837274 | Rare:34 | ||||
chr17:64975558-64975721 | Common:1; Rare:57 | ||||
chr17:76557661-76557815 | Common:1; Rare:56 | ||||
chr18:5238025-5238135 | Common:1; Rare:45 | ||||
chr19:4363868-4364127 | Common:2; Rare:85 | ||||
chr19:21569235-21569430 | Common:7; Rare:54 | ||||
chr19:27793343-27793498 | Common:3; Rare:39 |