Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr3:48473289-48473370 | Rare:11 | ||||
chr3:48556789-48557173 | Common:1; Rare:86 | ||||
chr3:48609336-48609785 | Common:1; Rare:153 | ||||
chr3:48662860-48663056 | Rare:43 | ||||
chr3:48847762-48848005 | Common:1; Rare:76 | ||||
chr3:48918748-48918912 | Common:2; Rare:92 | ||||
chr3:48989730-48989921 | Rare:50 | ||||
chr3:49006629-49006722 | Rare:23 | ||||
chr3:49006991-49007438 | Common:2; Rare:156 | ||||
chr3:49007507-49007612 | Rare:26 | ||||
chr3:49014486-49014647 | Common:1; Rare:50 | ||||
chr3:49018365-49018625 | Rare:101 | ||||
chr3:49021502-49021710 | Rare:52; Clinvar:1 | ||||
chr3:49022026-49022185 | Rare:58; Clinvar (pathogenic):1 | ||||
chr3:49029357-49029570 | Common:2; Rare:157 |