Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:49665611-49666020 | Common:6; Rare:191; Clinvar (pathogenic):1 | ||||
chr19:49851058-49851120 | Rare:24 | ||||
chr19:49867518-49867689 | Common:3; Rare:48; Clinvar:1 | ||||
chr19:49877299-49877742 | Common:1; Rare:120 | ||||
chr19:50377595-50377863 | Common:1; Rare:101 | ||||
chr19:50476238-50476550 | Rare:146 | ||||
chr19:50511185-50511295 | Rare:38 | ||||
chr19:51124962-51125123 | Rare:56 | ||||
chr19:51366333-51366530 | Common:5; Rare:51; Clinvar (benign):2 | ||||
chr19:51751825-51751987 | Common:2; Rare:35 | ||||
chr19:51887866-51888130 | Rare:89 | ||||
chr19:52008182-52008359 | Rare:52 | ||||
chr19:52028336-52028477 | Common:3; Rare:29 | ||||
chr19:52095710-52096051 | Common:3; Rare:68 | ||||
chr19:52269431-52269603 | Common:1; Rare:60 |