Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:235329285-235329311 | Rare:6 | ||||
chr1:235367159-235367802 | Common:2; Rare:126; Clinvar:2; Clinvar (benign):2 | ||||
chr1:235503768-235503802 | Rare:5 | ||||
chr1:235503804-235503869 | Common:1; Rare:10 | ||||
chr1:235504018-235504249 | Common:2; Rare:67; Clinvar:3; Clinvar (benign):3 | ||||
chr1:235504361-235504870 | Common:6; Rare:152 | ||||
chr1:235504881-235504941 | Rare:9 | ||||
chr1:235504955-235505234 | Common:1; Rare:62 | ||||
chr1:235649959-235650410 | Common:5; Rare:105 | ||||
chr1:235650536-235650703 | Rare:49 | ||||
chr1:235651016-235651160 | Rare:29 | ||||
chr1:235866838-235867257 | Common:3; Rare:130 | ||||
chr1:236065045-236065453 | Common:4; Rare:138; Clinvar (pathogenic):1 | ||||
chr1:236142485-236142577 | Rare:31 | ||||
chr1:236281909-236282175 | Common:6; Rare:79 |