Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:52698334-52698464 | Common:2; Rare:39 | ||||
chr1:53220291-53220410 | Rare:63 | ||||
chr1:53220573-53220654 | Common:1; Rare:50 | ||||
chr1:53238460-53238592 | Rare:59 | ||||
chr1:53945565-53946045 | Common:7; Rare:121 | ||||
chr1:53946260-53946438 | Rare:66 | ||||
chr1:54053190-54053671 | Common:6; Rare:158 | ||||
chr1:54199995-54200207 | Rare:45 | ||||
chr1:54887142-54887418 | Common:3; Rare:95; Clinvar:3; Clinvar (benign):1 | ||||
chr1:56645264-56645384 | Common:1; Rare:51 | ||||
chr1:58700059-58700187 | Common:4; Rare:50 | ||||
chr1:58784020-58784257 | Rare:57 | ||||
chr1:59814902-59815024 | Rare:38 | ||||
chr1:60865267-60865341 | Rare:13 | ||||
chr1:61076913-61077243 | Common:3; Rare:94 |