Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:69339541-69339856 | Common:1; Rare:136; Clinvar:1; Clinvar (benign):1 | ||||
chr16:69726443-69726806 | Common:3; Rare:95 | ||||
chr16:70289440-70289802 | Common:3; Rare:146; Clinvar:1 | ||||
chr16:70346779-70346940 | Common:1; Rare:82 | ||||
chr16:70454480-70454612 | Common:1; Rare:43 | ||||
chr16:70523517-70523852 | Common:3; Rare:113; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr16:72093539-72093934 | Rare:101 | ||||
chr16:74296725-74296898 | Rare:73 | ||||
chr16:74666857-74667003 | Rare:54 | ||||
chr16:75433459-75433795 | Common:4; Rare:96 | ||||
chr16:75647632-75647863 | Common:4; Rare:113; Clinvar:4 | ||||
chr16:77722284-77722549 | Common:4; Rare:80 | ||||
chr16:81006452-81006559 | Rare:32 | ||||
chr16:81006809-81007263 | Common:4; Rare:154 | ||||
chr16:82170171-82170344 | Common:3; Rare:93 |