Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:93740953-93741161 | Rare:73 | ||||
chr8:93754765-93754937 | Common:1; Rare:62; Clinvar (benign):4 | ||||
chr8:93916628-93917048 | Common:4; Rare:150; Clinvar:1; Clinvar (benign):1 | ||||
chr8:93917521-93917890 | Common:1; Rare:115 | ||||
chr8:94436926-94437098 | Rare:37 | ||||
chr8:94553436-94553668 | Common:3; Rare:85 | ||||
chr8:94640739-94641012 | Common:2; Rare:64 | ||||
chr8:94642748-94643091 | Common:4; Rare:65 | ||||
chr8:94719745-94719964 | Common:1; Rare:61 | ||||
chr8:94823149-94823312 | Common:1; Rare:48 | ||||
chr8:94895194-94895377 | Rare:59 | ||||
chr8:94949357-94949544 | Common:1; Rare:56 | ||||
chr8:95024915-95025189 | Common:2; Rare:104; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
chr8:96235510-96235669 | Common:1; Rare:84; Clinvar (benign):2 | ||||
chr8:96261544-96261981 | Common:6; Rare:147 |