Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:66934377-66934494 | Rare:43 | ||||
chr16:67226883-67227163 | Common:1; Rare:102 | ||||
chr16:67481136-67481384 | Common:1; Rare:79 | ||||
chr16:67660227-67660364 | Rare:80; Clinvar:2; Clinvar (benign):2 | ||||
chr16:68023223-68023296 | Common:1; Rare:15 | ||||
chr16:68310934-68311019 | Rare:36 | ||||
chr16:69339559-69339807 | Rare:97; Clinvar (benign):1 | ||||
chr16:70523539-70523855 | Common:3; Rare:100 | ||||
chr16:72093610-72093929 | Rare:73 | ||||
chr16:74666857-74667166 | Common:4; Rare:99 | ||||
chr16:75433420-75433821 | Common:4; Rare:119 | ||||
chr16:75647635-75647733 | Common:1; Rare:50; Clinvar:3 | ||||
chr16:81006809-81007272 | Common:4; Rare:157 | ||||
chr16:84116791-84117066 | Common:3; Rare:110 | ||||
chr16:85799538-85799748 | Common:2; Rare:62 |