Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:39515643-39515720 | Common:1; Rare:26 | ||||
chr19:39846308-39846478 | Common:1; Rare:81 | ||||
chr19:39970918-39971214 | Common:4; Rare:82 | ||||
chr19:39996925-39997157 | Common:5; Rare:67 | ||||
chr19:40056137-40056268 | Rare:17 | ||||
chr19:40090865-40090999 | Common:1; Rare:37 | ||||
chr19:40191374-40191656 | Common:2; Rare:65 | ||||
chr19:40257039-40257309 | Rare:58; Clinvar (pathogenic):1 | ||||
chr19:40265238-40265451 | Rare:47 | ||||
chr19:40266204-40266532 | Common:1; Rare:60 | ||||
chr19:40285186-40285537 | Common:1; Rare:121 | ||||
chr19:40348347-40348746 | Common:4; Rare:129 | ||||
chr19:40366407-40366678 | Rare:75 | ||||
chr19:40377793-40378144 | Common:2; Rare:122; Clinvar (benign):1 | ||||
chr19:40413354-40413521 | Rare:48 |