Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:62054510-62054820 | Common:3; Rare:45 | ||||
chr11:62082125-62082291 | Rare:40 | ||||
chr11:62171289-62171457 | Rare:30 | ||||
chr11:62311130-62311530 | Common:4; Rare:99 | ||||
chr11:62472380-62472750 | Common:3; Rare:58 | ||||
chr11:62500382-62500559 | Rare:39 | ||||
chr11:62508341-62508482 | Common:2; Rare:32 | ||||
chr11:62508645-62508803 | Rare:33 | ||||
chr11:62539187-62539587 | Common:2; Rare:110 | ||||
chr11:62553486-62553715 | Rare:47 | ||||
chr11:62614304-62614704 | Common:6; Rare:160; Clinvar:1; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
chr11:62673078-62673192 | Rare:20 | ||||
chr11:62680840-62681100 | Rare:50 | ||||
chr11:62786609-62786761 | Rare:44 | ||||
chr11:62906063-62906206 | Common:1; Rare:37 |