Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:88663094-88663339 | Common:6; Rare:93 | ||||
chr16:88856937-88857156 | Common:4; Rare:97; Clinvar (benign):2 | ||||
chr16:89508262-89508411 | Common:1; Rare:84 | ||||
chr16:89560532-89560724 | Rare:85 | ||||
chr16:89657660-89658082 | Common:3; Rare:225 | ||||
chr16:89686898-89686975 | Rare:35 | ||||
chr16:89816625-89816749 | Common:1; Rare:55; Clinvar:1; Clinvar (benign):1 | ||||
chr16:89873490-89873654 | Common:1; Rare:81 | ||||
chr16:89923224-89923355 | Rare:52 | ||||
chr16:90022552-90022703 | Rare:59 | ||||
chr17:752276-752347 | Rare:16 | ||||
chr17:1400133-1400452 | Common:3; Rare:131 | ||||
chr17:1485743-1486065 | Common:4; Rare:107 | ||||
chr17:1516628-1516978 | Common:1; Rare:125 | ||||
chr17:1684813-1685057 | Common:2; Rare:75; Clinvar:2; Clinvar (benign):1 |