Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:45507228-45507516 | Common:1; Rare:74 | ||||
chr19:45692523-45692673 | Rare:31 | ||||
chr19:45730869-45731052 | Common:1; Rare:39 | ||||
chr19:46600913-46600976 | Common:1; Rare:22 | ||||
chr19:46600978-46601402 | Common:4; Rare:141 | ||||
chr19:46787270-46787450 | Common:1; Rare:46 | ||||
chr19:47256472-47256571 | Rare:34 | ||||
chr19:48170275-48170669 | Common:2; Rare:109 | ||||
chr19:48325400-48325595 | Common:2; Rare:44 | ||||
chr19:48445866-48446005 | Rare:47 | ||||
chr19:48619139-48619428 | Rare:92 | ||||
chr19:48624178-48624417 | Common:1; Rare:69 | ||||
chr19:48900197-48900372 | Common:1; Rare:61 | ||||
chr19:48965017-48965609 | Common:1; Rare:166; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):7 | ||||
chr19:48993296-48993579 | Common:2; Rare:116; Clinvar:1; Clinvar (benign):1 |