Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:177022642-177022741 | Rare:37 | ||||
chr5:177133453-177133853 | Rare:145 | ||||
chr5:177303691-177303975 | Common:3; Rare:119 | ||||
chr5:177516932-177517084 | Rare:52; Clinvar (pathogenic):1 | ||||
chr5:178130868-178131039 | Rare:44 | ||||
chr5:178153682-178153947 | Rare:96; Clinvar:7; Clinvar (benign):1 | ||||
chr5:178940996-178941233 | Common:1; Rare:63 | ||||
chr5:179550792-179550849 | Rare:19 | ||||
chr5:179698551-179699072 | Common:3; Rare:185 | ||||
chr5:179806859-179807063 | Common:3; Rare:81 | ||||
chr5:179820848-179821117 | Common:2; Rare:105; Clinvar:7; Clinvar (benign):2 | ||||
chr5:179858796-179859063 | Rare:142 | ||||
chr5:179907828-179908015 | Common:2; Rare:97 | ||||
chr5:180071562-180071835 | Common:3; Rare:101 | ||||
chr5:180353291-180353512 | Common:9; Rare:100 |