Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:50464196-50464426 | Common:3; Rare:55 | ||||
chr19:50476242-50476542 | Rare:140 | ||||
chr19:50804582-50804915 | Common:6; Rare:102 | ||||
chr19:51366301-51366595 | Common:8; Rare:91; Clinvar (benign):2 | ||||
chr19:51751858-51751987 | Common:2; Rare:28 | ||||
chr19:51887883-51888068 | Rare:65 | ||||
chr19:52008154-52008349 | Rare:56 | ||||
chr19:52028336-52028451 | Common:3; Rare:25 | ||||
chr19:52048642-52048697 | Rare:9 | ||||
chr19:52397750-52397879 | Common:2; Rare:38 | ||||
chr19:53254814-53255019 | Common:1; Rare:69 | ||||
chr19:53538052-53538169 | Common:3; Rare:57 | ||||
chr19:54115625-54115797 | Common:1; Rare:44; Clinvar:4 | ||||
chr19:54449028-54449229 | Common:2; Rare:57 | ||||
chr19:54449428-54449461 | Rare:10 |