Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:54115635-54115792 | Common:1; Rare:34; Clinvar:4 | ||||
chr19:54200577-54200891 | Common:2; Rare:100 | ||||
chr19:54449039-54449258 | Common:2; Rare:65 | ||||
chr19:55385738-55385982 | Common:6; Rare:83 | ||||
chr19:55461584-55461980 | Common:5; Rare:111 | ||||
chr19:55654804-55655103 | Rare:109 | ||||
chr19:57435127-57435349 | Common:6; Rare:46 | ||||
chr19:58183329-58183417 | Rare:31 | ||||
chr19:58228820-58228955 | Common:1; Rare:56 | ||||
chr19:58326859-58326996 | Common:1; Rare:30 | ||||
chr19:58327239-58327361 | Rare:24 | ||||
chr19:58499181-58499523 | Common:3; Rare:104; Clinvar:3; Clinvar (benign):1 | ||||
chr19:58519787-58519886 | Rare:26 | ||||
chr19:58554939-58555183 | Common:1; Rare:81 | ||||
chr2:264565-264966 | Common:4; Rare:147 |