Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:130342642-130342930 | Common:5; Rare:90 | ||||
chr2:130355728-130356071 | Common:3; Rare:92 | ||||
chr2:131093373-131093559 | Common:1; Rare:86 | ||||
chr2:131105193-131105365 | Common:1; Rare:78 | ||||
chr2:131492378-131492449 | Common:1; Rare:25 | ||||
chr2:131492779-131492945 | Common:4; Rare:58 | ||||
chr2:131493013-131493115 | Common:1; Rare:30 | ||||
chr2:134918588-134918933 | Common:1; Rare:148 | ||||
chr2:135052192-135052305 | Common:1; Rare:44; Clinvar (benign):1 | ||||
chr2:135531170-135531514 | Common:1; Rare:72 | ||||
chr2:135742631-135742750 | Rare:29 | ||||
chr2:135985404-135985692 | Common:4; Rare:126; Clinvar (benign):1 | ||||
chr2:136118044-136118328 | Rare:77 | ||||
chr2:138501613-138501866 | Common:3; Rare:113 | ||||
chr2:143129257-143129428 | Common:1; Rare:37 |