Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr11:134224513-134224722 | Rare:88 | ||||
chr11:134253290-134253608 | Common:2; Rare:117; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr11:134331705-134332023 | Common:10; Rare:68 | ||||
chr11:134387423-134387612 | Rare:45 | ||||
chr12:66622-66866 | Rare:60 | ||||
chr12:389087-389398 | Common:6; Rare:155 | ||||
chr12:389481-389703 | Common:6; Rare:99 | ||||
chr12:752079-752156 | Rare:9 | ||||
chr12:752283-752597 | Common:1; Rare:89 | ||||
chr12:949540-949893 | Common:6; Rare:109 | ||||
chr12:991038-991371 | Common:6; Rare:134 | ||||
chr12:2004394-2004669 | Common:2; Rare:96 | ||||
chr12:2053270-2053360 | Rare:19; Clinvar:1 | ||||
chr12:2795016-2795238 | Rare:87 | ||||
chr12:2795826-2796005 | Common:1; Rare:50 |