Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:1827129-1827241 | Common:1; Rare:50 | ||||
chr16:1964810-1964978 | Common:5; Rare:75 | ||||
chr16:1971913-1972103 | Common:1; Rare:54 | ||||
chr16:2047727-2048050 | Rare:161; Clinvar:2; Clinvar (benign):1 | ||||
chr16:2205673-2205835 | Common:4; Rare:78 | ||||
chr16:2268072-2268227 | Common:1; Rare:63 | ||||
chr16:2268393-2268503 | Rare:40 | ||||
chr16:2474993-2475151 | Rare:51 | ||||
chr16:2513650-2514007 | Rare:121 | ||||
chr16:2518973-2519240 | Rare:68 | ||||
chr16:2537729-2538055 | Common:4; Rare:127 | ||||
chr16:2682350-2682633 | Rare:133 | ||||
chr16:2752598-2752846 | Common:2; Rare:109 | ||||
chr16:2776993-2777388 | Common:2; Rare:145 | ||||
chr16:3112403-3112603 | Rare:53 |