Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:206085152-206085327 | Common:1; Rare:55 | ||||
chr2:215367861-215368217 | Common:2; Rare:95 | ||||
chr2:215433582-215433833 | Common:1; Rare:54 | ||||
chr2:218277044-218277289 | Common:1; Rare:53 | ||||
chr2:218402634-218402714 | Rare:25 | ||||
chr2:218403023-218403278 | Common:4; Rare:91 | ||||
chr2:218429298-218429673 | Common:4; Rare:128; Clinvar (benign):1 | ||||
chr2:219001977-219002132 | Common:2; Rare:32 | ||||
chr2:219071191-219071448 | Rare:43 | ||||
chr2:219113107-219113244 | Rare:26 | ||||
chr2:222646132-222646222 | Common:2; Rare:17 | ||||
chr2:226799174-226799222 | Common:1; Rare:8 | ||||
chr2:231412425-231412580 | Common:2; Rare:26 | ||||
chr2:232790841-232791027 | Rare:42 | ||||
chr2:233012352-233012665 | Common:5; Rare:57 |