Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:1971913-1972110 | Common:1; Rare:57 | ||||
chr16:1984527-1984723 | Common:1; Rare:46 | ||||
chr16:2009637-2009891 | Common:15; Rare:101 | ||||
chr16:2047737-2048050 | Rare:154; Clinvar:2; Clinvar (benign):1 | ||||
chr16:2251546-2251587 | Rare:16 | ||||
chr16:2267779-2267885 | Rare:37 | ||||
chr16:2268050-2268178 | Common:1; Rare:69 | ||||
chr16:2268358-2268520 | Common:2; Rare:57 | ||||
chr16:2459976-2460133 | Rare:41 | ||||
chr16:2475003-2475149 | Rare:49 | ||||
chr16:2513648-2514045 | Rare:150 | ||||
chr16:2537684-2538132 | Common:4; Rare:169 | ||||
chr16:2682343-2682693 | Rare:162 | ||||
chr16:2752588-2752846 | Common:2; Rare:114 | ||||
chr16:2770320-2770665 | Common:2; Rare:163 |