Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:100088909-100089117 | Rare:76; Clinvar:1; Clinvar (benign):2 | ||||
chr13:102596785-102597039 | Common:1; Rare:119 | ||||
chr13:102773733-102773898 | Common:1; Rare:74 | ||||
chr13:102798998-102799134 | Rare:30 | ||||
chr13:102845952-102846157 | Common:3; Rare:47; Clinvar:4; Clinvar (benign):1 | ||||
chr13:106568069-106568267 | Rare:61 | ||||
chr13:108218339-108218520 | Rare:71 | ||||
chr13:110561672-110561843 | Common:5; Rare:62 | ||||
chr13:110615517-110615581 | Rare:23 | ||||
chr13:110712986-110713266 | Common:2; Rare:125 | ||||
chr13:110715810-110715855 | Rare:37 | ||||
chr13:111153619-111153720 | Common:2; Rare:43 | ||||
chr13:113208625-113208741 | Rare:68 | ||||
chr13:113863856-113864166 | Common:2; Rare:75 | ||||
chr13:114281318-114281637 | Common:4; Rare:119 |