Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:37467186-37467519 | Common:2; Rare:96 | ||||
chr19:37594760-37594910 | Rare:41 | ||||
chr19:37655436-37655603 | Common:3; Rare:69 | ||||
chr19:37779569-37779662 | Rare:21 | ||||
chr19:38253198-38253594 | Common:2; Rare:69 | ||||
chr19:38256107-38256396 | Rare:75 | ||||
chr19:38264351-38264787 | Common:5; Rare:110 | ||||
chr19:38264800-38265013 | Rare:68 | ||||
chr19:38336300-38336472 | Common:2; Rare:35 | ||||
chr19:38389662-38389838 | Rare:24 | ||||
chr19:38727879-38728022 | Rare:51; Clinvar (benign):2 | ||||
chr19:38899561-38900079 | Rare:154 | ||||
chr19:38930738-38930987 | Common:2; Rare:67; Clinvar:2; Clinvar (benign):3 | ||||
chr19:39386716-39386913 | Rare:49 | ||||
chr19:39389127-39389351 | Rare:45 |