Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:36331486-36331602 | Rare:27 | ||||
chr19:36331615-36331980 | Common:2; Rare:90 | ||||
chr19:36776138-36776327 | Common:2; Rare:38 | ||||
chr19:36797445-36797587 | Common:1; Rare:32 | ||||
chr19:36901898-36902056 | Common:4; Rare:26 | ||||
chr19:37737049-37737303 | Common:1; Rare:55 | ||||
chr19:38709979-38710291 | Common:1; Rare:79; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr19:38755039-38755227 | Common:7; Rare:40 | ||||
chr19:39352510-39352768 | Common:2; Rare:48 | ||||
chr19:39539189-39539337 | Rare:29 | ||||
chr19:39796057-39796171 | Rare:26 | ||||
chr19:39824539-39824799 | Common:2; Rare:73 | ||||
chr19:39972201-39972494 | Common:1; Rare:78 | ||||
chr19:39974311-39974816 | Common:7; Rare:132 | ||||
chr19:39979954-39980151 | Rare:47 |