Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:38852324-38852508 | Rare:44 | ||||
chr19:38899561-38899928 | Rare:100 | ||||
chr19:38930742-38931002 | Common:3; Rare:69; Clinvar:2; Clinvar (benign):3 | ||||
chr19:39342393-39342518 | Common:2; Rare:42 | ||||
chr19:39390850-39391011 | Rare:53 | ||||
chr19:39391019-39391418 | Common:1; Rare:158 | ||||
chr19:39406684-39406873 | Rare:69 | ||||
chr19:39846335-39846470 | Common:1; Rare:60 | ||||
chr19:39970964-39971196 | Common:2; Rare:60 | ||||
chr19:39996956-39997101 | Common:4; Rare:50 | ||||
chr19:40056160-40056342 | Rare:32 | ||||
chr19:40348388-40348724 | Common:4; Rare:110 | ||||
chr19:40377835-40378041 | Common:2; Rare:84; Clinvar (benign):1 | ||||
chr19:40425987-40426147 | Common:1; Rare:46 | ||||
chr19:40751064-40751220 | Common:1; Rare:40 |