Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:128091031-128091349 | Common:8; Rare:105 | ||||
chr2:130181553-130181780 | Common:3; Rare:100 | ||||
chr2:130341548-130341754 | Rare:63 | ||||
chr2:130342118-130342306 | Rare:76; Clinvar:1 | ||||
chr2:130342640-130342932 | Common:5; Rare:91 | ||||
chr2:130372551-130372787 | Common:1; Rare:65 | ||||
chr2:131105193-131105375 | Common:1; Rare:84 | ||||
chr2:131492749-131493097 | Common:8; Rare:105 | ||||
chr2:134918601-134918857 | Common:1; Rare:100 | ||||
chr2:135531167-135531532 | Common:1; Rare:77 | ||||
chr2:135984951-135985199 | Common:1; Rare:59 | ||||
chr2:135985441-135985660 | Common:4; Rare:101; Clinvar (benign):1 | ||||
chr2:138501647-138501845 | Common:3; Rare:88 | ||||
chr2:143129011-143129433 | Common:2; Rare:94 | ||||
chr2:144332449-144332712 | Rare:104 |