Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:92298945-92299076 | Common:1; Rare:66; Clinvar:1; Clinvar (benign):1 | ||||
chr1:92961428-92961592 | Rare:64 | ||||
chr1:93180366-93180721 | Common:1; Rare:157 | ||||
chr1:93345794-93345904 | Common:3; Rare:43 | ||||
chr1:93879144-93879279 | Common:1; Rare:46 | ||||
chr1:94541751-94542006 | Rare:72 | ||||
chr1:94820264-94820382 | Common:2; Rare:33 | ||||
chr1:94903121-94903445 | Common:1; Rare:65 | ||||
chr1:94927022-94927481 | Common:3; Rare:153 | ||||
chr1:95233945-95234231 | Common:5; Rare:83 | ||||
chr1:98661609-98661869 | Common:2; Rare:93 | ||||
chr1:99850029-99850132 | Rare:38 | ||||
chr1:99969907-99970062 | Rare:38 | ||||
chr1:100037984-100038160 | Common:1; Rare:72 | ||||
chr1:100132924-100133216 | Common:2; Rare:106 |