Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:131093358-131093539 | Common:1; Rare:84 | ||||
chr2:131105192-131105385 | Common:2; Rare:88 | ||||
chr2:131492321-131492570 | Common:8; Rare:99 | ||||
chr2:131492754-131492959 | Common:4; Rare:66 | ||||
chr2:131492999-131493097 | Common:2; Rare:27 | ||||
chr2:132416658-132416858 | Common:1; Rare:57 | ||||
chr2:134918580-134918863 | Common:1; Rare:111 | ||||
chr2:135531172-135531514 | Common:1; Rare:72 | ||||
chr2:135741566-135742011 | Common:5; Rare:150 | ||||
chr2:135985063-135985212 | Common:1; Rare:41 | ||||
chr2:135985388-135985720 | Common:4; Rare:136; Clinvar (benign):1 | ||||
chr2:136118101-136118328 | Rare:59 | ||||
chr2:137964095-137964589 | Common:2; Rare:88 | ||||
chr2:138501639-138502077 | Common:4; Rare:156 | ||||
chr2:142130251-142130578 | Common:2; Rare:70 |