Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:2474913-2475154 | Rare:77; Clinvar (benign):1 | ||||
chr16:2519364-2519635 | Common:1; Rare:98 | ||||
chr16:2519874-2520456 | Common:10; Rare:272 | ||||
chr16:2682350-2682702 | Rare:161 | ||||
chr16:2721042-2721215 | Rare:38 | ||||
chr16:2751938-2752054 | Rare:41 | ||||
chr16:2752241-2752515 | Common:1; Rare:79 | ||||
chr16:2752567-2753082 | Common:3; Rare:255 | ||||
chr16:2756983-2757216 | Common:1; Rare:71 | ||||
chr16:2758519-2758722 | Rare:59 | ||||
chr16:2777073-2777420 | Common:4; Rare:134 | ||||
chr16:2857578-2857608 | Rare:9 | ||||
chr16:2858166-2858310 | Rare:34 | ||||
chr16:2882658-2882863 | Common:2; Rare:51 | ||||
chr16:2911716-2912062 | Common:6; Rare:116 |