Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:10411988-10412255 | Common:2; Rare:46 | ||||
chr1:10470241-10470412 | Common:1; Rare:11 | ||||
chr1:10537437-10537460 | Rare:5 | ||||
chr1:10539047-10539262 | Common:1; Rare:31 | ||||
chr1:10990934-10991083 | Common:3; Rare:30 | ||||
chr1:11075484-11075762 | Common:2; Rare:44 | ||||
chr1:11087566-11087864 | Rare:79 | ||||
chr1:11109646-11109989 | Common:1; Rare:59 | ||||
chr1:11119802-11120042 | Common:3; Rare:39 | ||||
chr1:11199348-11199585 | Rare:49; Clinvar (benign):1 | ||||
chr1:11257122-11257372 | Common:4; Rare:49 | ||||
chr1:11282583-11282842 | Rare:49 | ||||
chr1:11954805-11954842 | Rare:9 | ||||
chr1:11966728-11967090 | Common:1; Rare:90; Clinvar:7; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:12184225-12184545 | Common:1; Rare:59 |