Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:6374311-6374582 | Common:1; Rare:103 | ||||
chr19:6707074-6707429 | Common:2; Rare:111; Clinvar:1; Clinvar (benign):4 | ||||
chr19:6718078-6718413 | Common:1; Rare:83; Clinvar:2; Clinvar (benign):1 | ||||
chr19:9407022-9407132 | Common:2; Rare:40 | ||||
chr19:11059578-11059863 | Common:2; Rare:76; Clinvar:11; Clinvar (benign):10 | ||||
chr19:13777882-13778075 | Rare:49 | ||||
chr19:14565950-14566083 | Common:1; Rare:54 | ||||
chr19:14622010-14622327 | Common:1; Rare:16 | ||||
chr19:16283532-16283820 | Common:1; Rare:68 | ||||
chr19:18194587-18195000 | Common:1; Rare:144 | ||||
chr19:18279621-18279794 | Rare:68 | ||||
chr19:18280047-18280177 | Common:6; Rare:47 | ||||
chr19:18280179-18280292 | Common:2; Rare:42 | ||||
chr19:19776378-19776596 | Common:2; Rare:60 | ||||
chr19:23274199-23274351 | Common:1; Rare:39 |