Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:52553014-52553386 | Common:4; Rare:109 | ||||
chr1:52698334-52698458 | Common:2; Rare:38 | ||||
chr1:53220586-53220677 | Common:1; Rare:40 | ||||
chr1:53238460-53238592 | Rare:59 | ||||
chr1:53946260-53946487 | Rare:82 | ||||
chr1:54053266-54053637 | Common:6; Rare:116 | ||||
chr1:54199993-54200204 | Rare:43 | ||||
chr1:54715746-54715894 | Common:2; Rare:47 | ||||
chr1:54887168-54887385 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
chr1:58546712-58546850 | Common:4; Rare:69 | ||||
chr1:58700055-58700174 | Common:4; Rare:49 | ||||
chr1:58784001-58784384 | Common:1; Rare:101 | ||||
chr1:59814910-59815024 | Rare:38 | ||||
chr1:61077003-61077243 | Common:3; Rare:63 | ||||
chr1:61725020-61725180 | Rare:80 |