Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:17540445-17540749 | Common:1; Rare:71 | ||||
chr2:17753721-17754159 | Common:3; Rare:141; Clinvar (benign):1 | ||||
chr2:19901652-19901746 | Common:1; Rare:47 | ||||
chr2:19901957-19902049 | Rare:31 | ||||
chr2:19990062-19990211 | Rare:38 | ||||
chr2:20051545-20051870 | Common:1; Rare:85 | ||||
chr2:20350835-20351083 | Common:2; Rare:107 | ||||
chr2:20446843-20447074 | Common:3; Rare:93 | ||||
chr2:20651061-20651248 | Rare:56 | ||||
chr2:20823055-20823188 | Common:1; Rare:48 | ||||
chr2:23927058-23927330 | Common:3; Rare:95 | ||||
chr2:23940388-23940542 | Common:3; Rare:59 | ||||
chr2:24049592-24049865 | Common:2; Rare:82 | ||||
chr2:24076219-24076747 | Common:1; Rare:131 | ||||
chr2:24123272-24123514 | Common:1; Rare:65 |