Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:51751842-51751997 | Common:2; Rare:33 | ||||
chr19:52008182-52008369 | Common:1; Rare:56 | ||||
chr19:52028336-52028684 | Common:3; Rare:66 | ||||
chr19:52048641-52048697 | Rare:10 | ||||
chr19:52397711-52397907 | Common:5; Rare:63 | ||||
chr19:52735004-52735155 | Common:2; Rare:44 | ||||
chr19:52786726-52786861 | Common:8; Rare:39 | ||||
chr19:53132863-53132955 | Common:4; Rare:39 | ||||
chr19:53254795-53255020 | Common:2; Rare:76 | ||||
chr19:53867682-53867942 | Common:1; Rare:68 | ||||
chr19:53869369-53869726 | Common:2; Rare:93 | ||||
chr19:54102674-54102951 | Common:4; Rare:79 | ||||
chr19:54115289-54115417 | Common:1; Rare:26; Clinvar (benign):1 | ||||
chr19:54115628-54115797 | Common:1; Rare:43; Clinvar:4 | ||||
chr19:54159677-54160079 | Rare:137 |