Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:197498780-197498928 | Common:1; Rare:44; Clinvar (benign):3 | ||||
chr2:204515097-204515316 | Common:1; Rare:46 | ||||
chr2:206452762-206453083 | Common:2; Rare:66 | ||||
chr2:207163366-207163509 | Rare:25 | ||||
chr2:209425023-209425122 | Rare:25 | ||||
chr2:209426505-209426642 | Rare:19 | ||||
chr2:209578483-209578604 | Common:1; Rare:26 | ||||
chr2:209581134-209581261 | Rare:19 | ||||
chr2:209730106-209730263 | Rare:38 | ||||
chr2:216114758-216115052 | Common:5; Rare:113 | ||||
chr2:216372695-216372860 | Rare:28 | ||||
chr2:216636394-216636478 | Rare:9 | ||||
chr2:217328702-217328772 | Rare:10 | ||||
chr2:218665991-218666161 | Rare:46 | ||||
chr2:219302306-219302815 | Common:1; Rare:158 |