Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:44643793-44643929 | Rare:40 | ||||
chr19:45322819-45323103 | Common:1; Rare:57 | ||||
chr19:45323126-45323164 | Rare:11 | ||||
chr19:45406290-45406649 | Common:1; Rare:77 | ||||
chr19:45467890-45468000 | Rare:30 | ||||
chr19:45507228-45507535 | Common:1; Rare:84 | ||||
chr19:45692381-45692678 | Common:1; Rare:62 | ||||
chr19:45730860-45731114 | Common:1; Rare:59 | ||||
chr19:45769206-45769520 | Common:1; Rare:132 | ||||
chr19:46296798-46297069 | Common:4; Rare:108 | ||||
chr19:46346941-46347205 | Common:3; Rare:92 | ||||
chr19:46600913-46601434 | Common:6; Rare:179; Clinvar (benign):3 | ||||
chr19:47112152-47112339 | Rare:54 | ||||
chr19:47256472-47256585 | Rare:42 | ||||
chr19:47484169-47484415 | Common:2; Rare:77 |