Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:10398716-10399118 | Common:2; Rare:146 | ||||
chr1:11189162-11189361 | Common:1; Rare:44 | ||||
chr1:11262496-11262817 | Common:2; Rare:97 | ||||
chr1:11805935-11806258 | Common:2; Rare:88; Clinvar:1 | ||||
chr1:11934561-11934754 | Common:2; Rare:65; Clinvar:5; Clinvar (benign):1 | ||||
chr1:11980125-11980467 | Common:6; Rare:113; Clinvar:1; Clinvar (benign):4 | ||||
chr1:12019251-12019533 | Common:5; Rare:97 | ||||
chr1:12616378-12616726 | Common:4; Rare:65 | ||||
chr1:12617416-12617583 | Rare:26 | ||||
chr1:12618117-12618449 | Common:2; Rare:71 | ||||
chr1:15526600-15526905 | Common:2; Rare:97 | ||||
chr1:15758752-15758811 | Common:1; Rare:12 | ||||
chr1:16352410-16352569 | Common:2; Rare:89 | ||||
chr1:17439725-17439875 | Rare:52 | ||||
chr1:19210071-19210520 | Rare:148 |