Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:1876149-1876293 | Common:1; Rare:57 | ||||
chr19:2065043-2065169 | Rare:29 | ||||
chr19:3977213-3977455 | Common:2; Rare:79; Clinvar (benign):2 | ||||
chr19:4365592-4365760 | Rare:55 | ||||
chr19:4513619-4513785 | Rare:62 | ||||
chr19:6712363-6712562 | Rare:54; Clinvar (benign):2 | ||||
chr19:6744707-6744876 | Common:1; Rare:54 | ||||
chr19:7198149-7198412 | Common:4; Rare:89 | ||||
chr19:8371103-8371384 | Common:2; Rare:97 | ||||
chr19:10009481-10009551 | Common:1; Rare:24 | ||||
chr19:12673002-12673279 | Rare:101 | ||||
chr19:12675253-12675556 | Common:2; Rare:72 | ||||
chr19:12793558-12793737 | Common:3; Rare:44 | ||||
chr19:15239485-15239694 | Common:1; Rare:94 | ||||
chr19:16283686-16283824 | Rare:32 |