Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:89822211-89822530 | Rare:134 | ||||
chr1:89843030-89843485 | Common:4; Rare:237 | ||||
chr1:89994960-89995403 | Common:6; Rare:330 | ||||
chr1:91021690-91021870 | Rare:55 | ||||
chr1:91021912-91022360 | Rare:254 | ||||
chr1:91404430-91404704 | Common:2; Rare:77 | ||||
chr1:91500708-91501166 | Common:6; Rare:280 | ||||
chr1:91501240-91501680 | Common:2; Rare:201 | ||||
chr1:91886082-91886500 | Rare:358 | ||||
chr1:92029450-92030110 | Common:6; Rare:333 | ||||
chr1:92030270-92030690 | Common:18; Rare:141 | ||||
chr1:92080165-92080452 | Common:3; Rare:101 | ||||
chr1:92080620-92081160 | Common:3; Rare:185 | ||||
chr1:92298809-92299118 | Common:3; Rare:293; Clinvar:5; Clinvar (benign):5 | ||||
chr1:92485857-92486215 | Common:1; Rare:88 |