Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:58578858-58579288 | Common:5; Rare:123 | ||||
chr11:58579418-58579610 | Common:3; Rare:79 | ||||
chr11:58622552-58622688 | Rare:33 | ||||
chr11:58905091-58905155 | Rare:11 | ||||
chr11:58905274-58905410 | Common:1; Rare:32 | ||||
chr11:59142627-59142973 | Common:1; Rare:69 | ||||
chr11:60873184-60873411 | Rare:86; Clinvar (pathogenic):1 | ||||
chr11:60902423-60902643 | Rare:44 | ||||
chr11:60906372-60906646 | Common:1; Rare:77 | ||||
chr11:60914020-60914267 | Common:1; Rare:64 | ||||
chr11:60924366-60924648 | Common:3; Rare:80 | ||||
chr11:61161402-61161757 | Common:1; Rare:102 | ||||
chr11:61332153-61332436 | Rare:69 | ||||
chr11:61333014-61333276 | Common:1; Rare:95 | ||||
chr11:61361756-61361973 | Common:1; Rare:54 |