Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:55069105-55069136 | Rare:16 | ||||
chr1:55071522-55071582 | Common:1; Rare:13 | ||||
chr1:55159071-55159248 | Rare:22 | ||||
chr1:58497397-58497612 | Rare:38 | ||||
chr1:58576681-58576851 | Common:1; Rare:54; Clinvar (benign):1 | ||||
chr1:58576858-58577101 | Rare:89; Clinvar:2 | ||||
chr1:58671860-58672133 | Common:3; Rare:53 | ||||
chr1:58931865-58932003 | Common:2; Rare:26 | ||||
chr1:59333654-59333882 | Common:1; Rare:48 | ||||
chr1:59672962-59673147 | Rare:24 | ||||
chr1:59821773-59821921 | Rare:39 | ||||
chr1:59863625-59863751 | Rare:20 | ||||
chr1:61113683-61113967 | Common:1; Rare:49 | ||||
chr1:61146839-61147141 | Rare:51 | ||||
chr1:61293181-61293273 | Common:1; Rare:13 |