Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:35637169-35637485 | Common:1; Rare:83 | ||||
chr19:35755857-35756006 | Rare:41 | ||||
chr19:35776569-35776717 | Common:2; Rare:20 | ||||
chr19:36065778-36066006 | Rare:51; Clinvar (pathogenic):2 | ||||
chr19:36142205-36142343 | Common:1; Rare:56 | ||||
chr19:36255307-36255408 | Common:3; Rare:28 | ||||
chr19:36266526-36266702 | Common:6; Rare:98 | ||||
chr19:36331697-36331975 | Common:1; Rare:68 | ||||
chr19:36775663-36775890 | Common:4; Rare:62 | ||||
chr19:36797259-36797596 | Common:1; Rare:72 | ||||
chr19:36797704-36797785 | Rare:22 | ||||
chr19:36915181-36915319 | Rare:36 | ||||
chr19:37010036-37010172 | Common:1; Rare:35 | ||||
chr19:37056943-37057104 | Common:1; Rare:51 | ||||
chr19:37059156-37059461 | Common:2; Rare:81 |