Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:48255486-48255720 | Common:3; Rare:43 | ||||
chr19:48390887-48390976 | Rare:7 | ||||
chr19:48445909-48446161 | Common:1; Rare:105 | ||||
chr19:48619139-48619435 | Rare:96 | ||||
chr19:48619476-48619598 | Rare:40 | ||||
chr19:48624201-48624391 | Common:1; Rare:57 | ||||
chr19:48810988-48811129 | Rare:50 | ||||
chr19:48965485-48965609 | Rare:41; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr19:48993234-48993508 | Common:3; Rare:124; Clinvar:3; Clinvar (benign):3 | ||||
chr19:48993553-48993914 | Common:5; Rare:94 | ||||
chr19:49085126-49085492 | Common:3; Rare:146 | ||||
chr19:49154824-49155529 | Common:7; Rare:202 | ||||
chr19:49157643-49157850 | Rare:62; Clinvar:1 | ||||
chr19:49362375-49362477 | Rare:31 | ||||
chr19:49453094-49453318 | Common:1; Rare:70 |