Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:127650417-127650672 | Common:5; Rare:66 | ||||
chr2:127811099-127811258 | Rare:52 | ||||
chr2:127885866-127885982 | Rare:27 | ||||
chr2:128091058-128091339 | Common:8; Rare:94 | ||||
chr2:130181553-130181760 | Common:2; Rare:94 | ||||
chr2:130182072-130182318 | Common:2; Rare:92 | ||||
chr2:130342111-130342281 | Rare:72; Clinvar:1 | ||||
chr2:131093397-131093533 | Common:1; Rare:62 | ||||
chr2:131105192-131105351 | Common:1; Rare:67 | ||||
chr2:131492749-131493097 | Common:8; Rare:105 | ||||
chr2:134918627-134918863 | Common:1; Rare:97 | ||||
chr2:135531167-135531521 | Common:1; Rare:76 | ||||
chr2:135741617-135741944 | Common:3; Rare:119 | ||||
chr2:135985407-135985647 | Common:4; Rare:111; Clinvar (benign):1 | ||||
chr2:138501661-138501931 | Common:1; Rare:104 |