Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:95577408-95577602 | Common:5; Rare:58 | ||||
chr6:96897791-96898083 | Common:4; Rare:108; Clinvar:4; Clinvar (benign):1 | ||||
chr6:99425234-99425452 | Common:2; Rare:64 | ||||
chr6:100881173-100881489 | Common:6; Rare:116 | ||||
chr6:106325551-106325906 | Common:1; Rare:118 | ||||
chr6:106629443-106629638 | Common:3; Rare:41 | ||||
chr6:107957233-107957368 | Rare:31 | ||||
chr6:107958075-107958409 | Common:2; Rare:100; Clinvar:2; Clinvar (benign):3 | ||||
chr6:108074661-108074848 | Rare:60; Clinvar:1 | ||||
chr6:108294806-108295085 | Common:1; Rare:74 | ||||
chr6:108560729-108560960 | Rare:96 | ||||
chr6:109382066-109382111 | Common:1; Rare:11 | ||||
chr6:109382266-109382838 | Common:6; Rare:199; Clinvar (benign):2 | ||||
chr6:109440552-109440856 | Common:1; Rare:109 | ||||
chr6:109483129-109483242 | Rare:52 |