Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:49633956-49634031 | Common:1; Rare:32; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr14:49789497-49789758 | Rare:58 | ||||
chr14:49862626-49863025 | Common:1; Rare:181 | ||||
chr14:51599890-51600265 | Common:1; Rare:69 | ||||
chr14:52872804-52873133 | Common:2; Rare:77 | ||||
chr14:61721668-61721817 | Common:1; Rare:26 | ||||
chr14:61740673-61740799 | Rare:28 | ||||
chr14:68040967-68041158 | Rare:25 | ||||
chr14:68547633-68547938 | Common:1; Rare:36 | ||||
chr14:68795239-68795347 | Common:3; Rare:29 | ||||
chr14:68925657-68925776 | Common:3; Rare:23 | ||||
chr14:68937994-68938282 | Common:3; Rare:47 | ||||
chr14:68951062-68951373 | Common:1; Rare:80 | ||||
chr14:69682776-69683073 | Common:2; Rare:54 | ||||
chr14:73712953-73713246 | Common:1; Rare:116 |