Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:200864215-200864252 | Rare:10 | ||||
chr2:200889005-200889471 | Common:3; Rare:150 | ||||
chr2:200963576-200963816 | Common:1; Rare:63 | ||||
chr2:201071620-201072012 | Rare:79 | ||||
chr2:201115933-201116223 | Common:2; Rare:50 | ||||
chr2:201260414-201260609 | Rare:44 | ||||
chr2:201451450-201451749 | Rare:66 | ||||
chr2:201780746-201780965 | Common:3; Rare:55; Clinvar:1; Clinvar (benign):2 | ||||
chr2:202238550-202238685 | Common:1; Rare:43 | ||||
chr2:202265806-202265848 | Rare:12 | ||||
chr2:203238944-203239021 | Rare:27 | ||||
chr2:203328175-203328411 | Common:2; Rare:90 | ||||
chr2:206085905-206086139 | Common:2; Rare:57 | ||||
chr2:206159343-206159903 | Common:4; Rare:150; Clinvar (benign):1 | ||||
chr2:206765283-206765668 | Common:3; Rare:105; Clinvar:4; Clinvar (benign):5 |