Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:189784276-189784507 | Common:3; Rare:75; Clinvar:7; Clinvar (benign):1 | ||||
chr2:190880623-190880859 | Common:4; Rare:80 | ||||
chr2:191014143-191014333 | Common:1; Rare:61; Clinvar:2; Clinvar (benign):2 | ||||
chr2:191677858-191678180 | Common:4; Rare:93 | ||||
chr2:197434995-197435192 | Rare:66 | ||||
chr2:197453247-197453554 | Rare:103 | ||||
chr2:197499792-197500424 | Common:2; Rare:240; Clinvar:1; Clinvar (benign):2 | ||||
chr2:200306277-200306575 | Common:5; Rare:75 | ||||
chr2:200509913-200510087 | Common:1; Rare:66 | ||||
chr2:200609068-200609240 | Rare:47 | ||||
chr2:200811399-200811596 | Common:1; Rare:69 | ||||
chr2:200889003-200889439 | Common:3; Rare:141 | ||||
chr2:201071625-201071831 | Rare:49 | ||||
chr2:201642637-201642770 | Rare:68 | ||||
chr2:202912141-202912281 | Common:1; Rare:50 |