Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:130182116-130182396 | Common:2; Rare:108 | ||||
chr2:130342129-130342265 | Rare:55 | ||||
chr2:130342642-130342935 | Common:5; Rare:92 | ||||
chr2:130346088-130346381 | Common:2; Rare:115 | ||||
chr2:130355760-130356065 | Common:3; Rare:83 | ||||
chr2:130372596-130372760 | Common:1; Rare:51 | ||||
chr2:131105193-131105385 | Common:2; Rare:88 | ||||
chr2:131492292-131492519 | Common:6; Rare:105 | ||||
chr2:131493047-131493100 | Common:1; Rare:15 | ||||
chr2:134918604-134918911 | Common:1; Rare:130 | ||||
chr2:135531172-135531514 | Common:1; Rare:72 | ||||
chr2:137964085-137964436 | Common:2; Rare:47 | ||||
chr2:138501675-138501932 | Common:1; Rare:93 | ||||
chr2:148020682-148021096 | Common:2; Rare:97; Clinvar (benign):2 | ||||
chr2:148021502-148021675 | Rare:35 |