Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:19990092-19990211 | Rare:29 | ||||
chr2:26033788-26034142 | Common:3; Rare:123 | ||||
chr2:26244602-26244949 | Common:2; Rare:125; Clinvar:5; Clinvar (benign):6 | ||||
chr2:27212266-27212364 | Common:1; Rare:50 | ||||
chr2:27323067-27323115 | Rare:10 | ||||
chr2:27370317-27370632 | Common:1; Rare:124 | ||||
chr2:27663607-27663921 | Rare:114 | ||||
chr2:37084328-37084527 | Common:3; Rare:70 | ||||
chr2:37231570-37231703 | Common:3; Rare:71; Clinvar (benign):3 | ||||
chr2:38875906-38876010 | Common:1; Rare:26 | ||||
chr2:39437087-39437442 | Common:4; Rare:125 | ||||
chr2:46617037-46617252 | Common:6; Rare:80 | ||||
chr2:46915740-46915908 | Common:1; Rare:51; Clinvar:2; Clinvar (benign):1 | ||||
chr2:53786933-53787080 | Rare:57 | ||||
chr2:53970788-53971126 | Common:10; Rare:113 |