Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:49453094-49453313 | Common:1; Rare:70 | ||||
chr19:49513088-49513468 | Common:1; Rare:80 | ||||
chr19:49580537-49580683 | Rare:46 | ||||
chr19:49665760-49666027 | Common:3; Rare:131; Clinvar (pathogenic):1 | ||||
chr19:49877299-49877723 | Common:1; Rare:110 | ||||
chr19:49929404-49929619 | Common:4; Rare:74 | ||||
chr19:50476383-50476548 | Rare:77 | ||||
chr19:50511070-50511548 | Common:4; Rare:154 | ||||
chr19:52397701-52397880 | Common:3; Rare:53 | ||||
chr19:54115246-54115441 | Common:1; Rare:50; Clinvar (benign):1 | ||||
chr19:54115625-54115792 | Common:1; Rare:41; Clinvar:4 | ||||
chr19:54189333-54189671 | Common:3; Rare:114 | ||||
chr19:55643403-55643666 | Common:3; Rare:84 | ||||
chr19:55654732-55655081 | Rare:116 | ||||
chr19:56478079-56478215 | Rare:56 |