Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:93180224-93180751 | Common:2; Rare:209 | ||||
chr1:93345820-93345946 | Common:2; Rare:45 | ||||
chr1:93447968-93448168 | Common:2; Rare:73 | ||||
chr1:93879136-93879308 | Common:3; Rare:62 | ||||
chr1:94418185-94418480 | Common:2; Rare:107 | ||||
chr1:94541755-94541998 | Rare:72 | ||||
chr1:94927041-94927449 | Common:1; Rare:135 | ||||
chr1:95072866-95073003 | Common:1; Rare:54; Clinvar (benign):1 | ||||
chr1:95117294-95117408 | Rare:35 | ||||
chr1:95233945-95234251 | Common:5; Rare:95 | ||||
chr1:96721593-96721827 | Common:2; Rare:103 | ||||
chr1:99646015-99646341 | Rare:68 | ||||
chr1:99849997-99850130 | Common:1; Rare:49 | ||||
chr1:99969916-99970069 | Rare:43 | ||||
chr1:100037990-100038148 | Common:1; Rare:67 |