Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:48966257-48966745 | Common:1; Rare:168; Clinvar:4; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
chr19:49829858-49830157 | Common:1; Rare:113; Clinvar:5; Clinvar (benign):4 | ||||
chr19:50500714-50500966 | Common:1; Rare:52 | ||||
chr19:51726258-51726461 | Common:2; Rare:35 | ||||
chr19:55540279-55540588 | Common:1; Rare:66 | ||||
chr2:10868996-10869290 | Common:5; Rare:57 | ||||
chr2:20447729-20447961 | Rare:69 | ||||
chr2:20448025-20448125 | Rare:45 | ||||
chr2:20448385-20448820 | Common:2; Rare:109 | ||||
chr2:23617996-23618215 | Rare:46 | ||||
chr2:27716709-27716804 | Rare:23 | ||||
chr2:28736212-28736369 | Rare:25 | ||||
chr2:29015854-29016071 | Common:1; Rare:39 | ||||
chr2:36548280-36548562 | Common:1; Rare:82 | ||||
chr2:47906476-47906815 | Common:2; Rare:121 |