Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:97976385-97976720 | Common:1; Rare:123 | ||||
chr13:98577963-98578256 | Common:1; Rare:66 | ||||
chr13:99200668-99200921 | Common:6; Rare:119 | ||||
chr13:100088859-100089134 | Rare:105; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr13:100674745-100675070 | Common:3; Rare:135 | ||||
chr13:101416345-101416721 | Rare:76 | ||||
chr13:101916465-101916742 | Rare:105; Clinvar (benign):2 | ||||
chr13:102596785-102597117 | Common:1; Rare:137; Clinvar (benign):1 | ||||
chr13:102773736-102773834 | Rare:48 | ||||
chr13:102798939-102799180 | Common:1; Rare:49 | ||||
chr13:102845639-102846245 | Common:11; Rare:157; Clinvar:4; Clinvar (benign):6 | ||||
chr13:106567577-106568210 | Rare:187 | ||||
chr13:107866630-107866999 | Common:3; Rare:94 | ||||
chr13:107867003-107867297 | Rare:89 | ||||
chr13:108215334-108215732 | Common:5; Rare:79 |