Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:49513050-49513433 | Common:1; Rare:79 | ||||
chr19:49580527-49580650 | Rare:43 | ||||
chr19:49665752-49665997 | Common:3; Rare:115; Clinvar (pathogenic):1 | ||||
chr19:49808805-49808997 | Common:1; Rare:64 | ||||
chr19:49813258-49813346 | Rare:38 | ||||
chr19:49850996-49851027 | Rare:13 | ||||
chr19:49851051-49851150 | Rare:38 | ||||
chr19:49867495-49867681 | Common:3; Rare:52; Clinvar:1; Clinvar (benign):2 | ||||
chr19:49877264-49877724 | Common:2; Rare:116 | ||||
chr19:49877899-49878136 | Common:2; Rare:76 | ||||
chr19:49929423-49929832 | Common:7; Rare:140 | ||||
chr19:50476213-50476563 | Common:1; Rare:161 | ||||
chr19:50511206-50511511 | Common:3; Rare:91 | ||||
chr19:50804592-50804906 | Common:6; Rare:94 | ||||
chr19:51366271-51366551 | Common:5; Rare:85; Clinvar (benign):2 |