Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:113690913-113691140 | Common:10; Rare:39 | ||||
chr1:113694453-113694469 | Rare:3 | ||||
chr1:113706594-113706824 | Common:3; Rare:46 | ||||
chr1:113740188-113740383 | Rare:44 | ||||
chr1:113746848-113746902 | Rare:10 | ||||
chr1:113747407-113747424 | Rare:3 | ||||
chr1:113747751-113747873 | Rare:17 | ||||
chr1:113755318-113755565 | Common:1; Rare:51 | ||||
chr1:114510279-114510459 | Common:1; Rare:45 | ||||
chr1:114541852-114541915 | Rare:14 | ||||
chr1:114572890-114573110 | Common:1; Rare:49 | ||||
chr1:114711317-114711428 | Common:1; Rare:23 | ||||
chr1:114713712-114713885 | Rare:41; Clinvar:1; Clinvar (benign):3 | ||||
chr1:114719528-114719825 | Rare:77 | ||||
chr1:114726952-114727168 | Common:1; Rare:52 |