Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:73247208-73247334 | Rare:74 | ||||
chr10:73730462-73730595 | Rare:35 | ||||
chr10:79067413-79067502 | Common:1; Rare:24 | ||||
chr10:79221365-79221388 | Rare:4 | ||||
chr10:79242540-79242721 | Rare:40 | ||||
chr10:87342308-87342414 | Common:2; Rare:33 | ||||
chr10:88939505-88939866 | Common:1; Rare:64; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr10:95503051-95503204 | Rare:17 | ||||
chr10:96090194-96090286 | Common:1; Rare:36 | ||||
chr10:96750513-96750548 | Rare:7 | ||||
chr10:100373311-100373546 | Common:1; Rare:48 | ||||
chr10:110209172-110209425 | Common:2; Rare:58 | ||||
chr10:111076244-111076412 | Rare:35 | ||||
chr11:1175914-1176245 | Common:3; Rare:53 | ||||
chr11:9758177-9758326 | Rare:43 |