Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:51878638-51878961 | Common:1; Rare:94 | ||||
chr1:51990690-51990771 | Common:1; Rare:24 | ||||
chr1:52055114-52055256 | Common:1; Rare:37 | ||||
chr1:52056163-52056338 | Rare:55 | ||||
chr1:52404415-52404626 | Common:1; Rare:62 | ||||
chr1:52553069-52553361 | Common:4; Rare:81 | ||||
chr1:53220590-53220755 | Common:2; Rare:67 | ||||
chr1:53238460-53238695 | Common:2; Rare:88 | ||||
chr1:53946253-53946385 | Rare:50 | ||||
chr1:54053165-54053319 | Rare:57 | ||||
chr1:54053384-54053609 | Common:3; Rare:70 | ||||
chr1:54199993-54200215 | Rare:54 | ||||
chr1:54887159-54887461 | Common:3; Rare:95; Clinvar:2; Clinvar (benign):1 | ||||
chr1:57424014-57424293 | Common:4; Rare:78 | ||||
chr1:58784058-58784410 | Common:1; Rare:88 |