Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr12:55974103-55974650 | Common:4; Rare:146 | ||||
chr12:55996644-55997044 | Common:2; Rare:102 | ||||
chr12:55996996-55997375 | Common:8; Rare:504; Clinvar:12 | ||||
chr12:56006791-56007191 | Common:1; Rare:76 | ||||
chr12:56007160-56007557 | Common:4; Rare:218 | ||||
chr12:56007591-56007991 | Common:4; Rare:166 | ||||
chr12:56020426-56020642 | Rare:30 | ||||
chr12:56020730-56021112 | Rare:254 | ||||
chr12:56021060-56022184 | Common:47; Rare:742 | ||||
chr12:56041535-56042252 | Common:27; Rare:755; Clinvar:9; Clinvar (benign):19 | ||||
chr12:56042276-56042676 | Common:1; Rare:180; Clinvar (benign):2 | ||||
chr12:56079213-56079613 | Rare:110 | ||||
chr12:56079628-56080340 | Common:20; Rare:543 | ||||
chr12:56082437-56083343 | Common:5; Rare:179 | ||||
chr12:56104063-56104812 | Common:29; Rare:1144 |