Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr2:178451090-178451267 | Common:5; Rare:53; Clinvar:4; Clinvar (benign):3 | ||||
chr2:178478514-178478676 | Common:1; Rare:54 | ||||
chr2:179264508-179264857 | Common:4; Rare:130 | ||||
chr2:180980266-180980545 | Common:1; Rare:87 | ||||
chr2:181891616-181892096 | Common:4; Rare:201 | ||||
chr2:182426662-182426863 | Rare:33 | ||||
chr2:182715935-182716328 | Common:3; Rare:137 | ||||
chr2:186486024-186486354 | Common:3; Rare:94 | ||||
chr2:186590243-186590335 | Rare:29 | ||||
chr2:187554267-187554525 | Rare:52 | ||||
chr2:188974240-188974284 | Rare:13 | ||||
chr2:188974292-188974568 | Rare:70; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr2:189007497-189007930 | Common:1; Rare:99; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):10 | ||||
chr2:189007935-189008053 | Rare:43; Clinvar (benign):1; Clinvar (pathogenic):5 | ||||
chr2:189441086-189441511 | Common:2; Rare:130 |