Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:4734193-4734320 | Common:1; Rare:48 | ||||
chr16:5097738-5097988 | Common:4; Rare:91 | ||||
chr16:8797630-8797877 | Rare:96; Clinvar:2; Clinvar (benign):2 | ||||
chr16:11414586-11414756 | Common:1; Rare:42 | ||||
chr16:11851517-11851645 | Rare:61 | ||||
chr16:11976648-11976772 | Rare:47 | ||||
chr16:15643031-15643267 | Rare:73 | ||||
chr16:18801449-18801841 | Common:4; Rare:137 | ||||
chr16:18926108-18926213 | Common:2; Rare:46 | ||||
chr16:19067401-19067667 | Common:5; Rare:93 | ||||
chr16:20806337-20806510 | Rare:60 | ||||
chr16:20900226-20900792 | Common:3; Rare:126 | ||||
chr16:20900794-20900868 | Common:1; Rare:24 | ||||
chr16:21599359-21599716 | Common:4; Rare:127 | ||||
chr16:21953003-21953391 | Common:1; Rare:92; Clinvar (benign):1 |