Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:178438711-178438907 | Common:1; Rare:46 | ||||
chr2:188996176-188996469 | Common:12; Rare:65; Clinvar:3; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr2:191846502-191846581 | Common:2; Rare:33 | ||||
chr2:200477575-200477696 | Rare:26 | ||||
chr2:202037235-202037525 | Rare:48 | ||||
chr2:202376066-202376209 | Rare:72 | ||||
chr2:206084430-206084670 | Common:1; Rare:54 | ||||
chr2:207163586-207163710 | Rare:18 | ||||
chr2:215408106-215408427 | Common:1; Rare:88 | ||||
chr2:215433550-215433820 | Common:1; Rare:55 | ||||
chr2:216692160-216692373 | Common:3; Rare:52 | ||||
chr2:217826580-217826838 | Common:5; Rare:51 | ||||
chr2:217829849-217829990 | Common:2; Rare:41 | ||||
chr2:217847238-217847790 | Common:3; Rare:138 | ||||
chr2:217910079-217910379 | Common:2; Rare:48 |