Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:28846315-28846696 | Common:2; Rare:116; Clinvar:3; Clinvar (benign):2 | ||||
chr16:28863308-28863565 | Common:1; Rare:54 | ||||
chr16:28925159-28925371 | Rare:66 | ||||
chr16:29745897-29746233 | Common:2; Rare:64 | ||||
chr16:29805482-29805768 | Common:2; Rare:136 | ||||
chr16:29926185-29926332 | Common:3; Rare:52 | ||||
chr16:29961965-29962163 | Common:1; Rare:64 | ||||
chr16:29995596-29995722 | Rare:58 | ||||
chr16:29996064-29996333 | Common:2; Rare:101 | ||||
chr16:30065560-30065881 | Rare:107 | ||||
chr16:30075942-30076088 | Common:1; Rare:47 | ||||
chr16:30184025-30184264 | Common:1; Rare:43 | ||||
chr16:30186610-30186954 | Common:1; Rare:106; Clinvar (benign):2 | ||||
chr16:30186959-30187486 | Common:1; Rare:169; Clinvar:1; Clinvar (benign):1 | ||||
chr16:30355219-30355446 | Common:2; Rare:82 |