Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:160493798-160493962 | Common:1; Rare:41 | ||||
chr2:161307991-161308301 | Rare:71 | ||||
chr2:161308359-161308603 | Common:2; Rare:58 | ||||
chr2:162074203-162074321 | Common:1; Rare:37 | ||||
chr2:162318654-162318841 | Common:1; Rare:39 | ||||
chr2:162343870-162344218 | Common:1; Rare:114 | ||||
chr2:163735994-163736137 | Rare:26 | ||||
chr2:163736166-163736181 | Rare:3 | ||||
chr2:163736186-163736421 | Common:3; Rare:95 | ||||
chr2:165794074-165794421 | Common:2; Rare:93; Clinvar:6; Clinvar (benign):1 | ||||
chr2:165794706-165794945 | Rare:45 | ||||
chr2:165953707-165953892 | Common:1; Rare:83; Clinvar:9; Clinvar (benign):2 | ||||
chr2:168247409-168247778 | Common:5; Rare:146 | ||||
chr2:168455932-168456319 | Common:2; Rare:117 | ||||
chr2:168456628-168456793 | Rare:57 |