Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:49877268-49877714 | Common:2; Rare:109 | ||||
chr19:49877863-49878173 | Common:4; Rare:101 | ||||
chr19:49929080-49929258 | Common:3; Rare:58 | ||||
chr19:49929395-49929594 | Common:4; Rare:68 | ||||
chr19:50025347-50025689 | Common:5; Rare:104 | ||||
chr19:50476433-50476561 | Rare:55 | ||||
chr19:50511029-50511567 | Common:4; Rare:172 | ||||
chr19:50723169-50723421 | Common:2; Rare:56 | ||||
chr19:50723652-50723763 | Rare:25 | ||||
chr19:51366273-51366589 | Common:8; Rare:98; Clinvar (benign):2 | ||||
chr19:51751840-51751988 | Common:2; Rare:32 | ||||
chr19:51887883-51888052 | Rare:61 | ||||
chr19:52397725-52397878 | Common:3; Rare:46 | ||||
chr19:54115265-54115411 | Common:1; Rare:34; Clinvar (benign):1 | ||||
chr19:54115615-54115790 | Common:2; Rare:42; Clinvar:5 |