Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:43174236-43174536 | Rare:41 | ||||
chr8:43174542-43174740 | Common:1; Rare:28 | ||||
chr8:43176025-43176246 | Common:3; Rare:29 | ||||
chr8:43197680-43197930 | Common:2; Rare:73; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):3 | ||||
chr8:47395267-47395506 | Rare:38 | ||||
chr8:47459014-47459170 | Rare:28 | ||||
chr8:47480449-47480712 | Common:3; Rare:50 | ||||
chr8:47512224-47512498 | Rare:53 | ||||
chr8:47736699-47737087 | Common:3; Rare:103 | ||||
chr8:47737123-47737305 | Common:1; Rare:46 | ||||
chr8:47737387-47737872 | Common:4; Rare:157 | ||||
chr8:47738138-47738504 | Common:2; Rare:109 | ||||
chr8:47774295-47774540 | Common:1; Rare:56; Clinvar (benign):1 | ||||
chr8:47974537-47974770 | Rare:65 | ||||
chr8:48430274-48430540 | Common:2; Rare:60 |