Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:65429170-65430102 | Common:9; Rare:171 | ||||
chr11:65430104-65430453 | Rare:63 | ||||
chr11:65430455-65430963 | Common:2; Rare:72 | ||||
chr11:65437758-65438021 | Rare:48 | ||||
chr11:65438026-65438253 | Rare:38 | ||||
chr11:65438488-65438881 | Common:3; Rare:69 | ||||
chr11:65441376-65441626 | Rare:41 | ||||
chr11:65441633-65442621 | Rare:171 | ||||
chr11:65442648-65443382 | Common:5; Rare:127 | ||||
chr11:65443385-65444244 | Common:4; Rare:153 | ||||
chr11:65446170-65446446 | Rare:52 | ||||
chr11:65497451-65497843 | Common:1; Rare:175 | ||||
chr11:65498557-65498734 | Common:2; Rare:109 | ||||
chr11:65526000-65526276 | Rare:94; Clinvar (pathogenic):1 | ||||
chr11:65629386-65629630 | Rare:71 |