Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:1533492-1533694 | Common:1; Rare:39 | ||||
chr16:1782510-1782886 | Common:4; Rare:122 | ||||
chr16:1943152-1943520 | Common:1; Rare:116 | ||||
chr16:1964814-1965066 | Common:6; Rare:111 | ||||
chr16:1971878-1972110 | Common:3; Rare:67 | ||||
chr16:2047727-2048050 | Rare:161; Clinvar:2; Clinvar (benign):1 | ||||
chr16:2155350-2155494 | Rare:43 | ||||
chr16:2155519-2155815 | Common:1; Rare:89 | ||||
chr16:2223311-2223620 | Rare:121 | ||||
chr16:2268072-2268186 | Common:1; Rare:53 | ||||
chr16:2429126-2429484 | Common:3; Rare:118 | ||||
chr16:2459980-2460145 | Common:1; Rare:47 | ||||
chr16:2682350-2682603 | Rare:116 | ||||
chr16:2776997-2777392 | Common:2; Rare:145 | ||||
chr16:2911735-2912051 | Common:5; Rare:107 |