Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:27663661-27663911 | Rare:92 | ||||
chr2:27890425-27890815 | Rare:99 | ||||
chr2:28751686-28751859 | Common:2; Rare:97 | ||||
chr2:28870278-28870418 | Rare:48 | ||||
chr2:37084351-37084561 | Common:2; Rare:82 | ||||
chr2:37231563-37231689 | Common:4; Rare:65; Clinvar (benign):3 | ||||
chr2:38875902-38876049 | Common:1; Rare:50 | ||||
chr2:46616991-46617275 | Common:7; Rare:126 | ||||
chr2:46915733-46915869 | Common:1; Rare:34; Clinvar:2; Clinvar (benign):1 | ||||
chr2:53786944-53787090 | Rare:60 | ||||
chr2:53970788-53971126 | Common:10; Rare:113 | ||||
chr2:60881418-60881566 | Common:1; Rare:48 | ||||
chr2:61017434-61017731 | Common:1; Rare:83; Clinvar:1 | ||||
chr2:61144921-61145149 | Common:2; Rare:78 | ||||
chr2:61888574-61888714 | Common:1; Rare:57 |