Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:235650592-235650716 | Rare:38 | ||||
chr1:236065065-236065326 | Common:2; Rare:104; Clinvar (pathogenic):1 | ||||
chr1:236281888-236282258 | Common:7; Rare:113 | ||||
chr1:236523889-236524045 | Common:2; Rare:41 | ||||
chr1:236524506-236524581 | Rare:17 | ||||
chr1:236604389-236604672 | Common:5; Rare:83 | ||||
chr1:236686388-236686517 | Rare:53 | ||||
chr1:236795060-236795408 | Common:6; Rare:141; Clinvar:3 | ||||
chr1:239386540-239386689 | Rare:21 | ||||
chr1:241357147-241357258 | Rare:26 | ||||
chr1:241519670-241519988 | Common:2; Rare:100; Clinvar:11; Clinvar (benign):8; Clinvar (pathogenic):3 | ||||
chr1:241639659-241639870 | Common:3; Rare:52 | ||||
chr1:241639961-241639999 | Rare:11 | ||||
chr1:241640243-241640577 | Common:7; Rare:124 | ||||
chr1:241848092-241848356 | Common:2; Rare:51 |