Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149636458-149636760 | Common:6; Rare:91 | ||||
chr1:149793788-149794007 | Common:1; Rare:37 | ||||
chr1:150477543-150477784 | Common:1; Rare:53 | ||||
chr1:150512330-150512809 | Common:5; Rare:135; Clinvar (benign):1 | ||||
chr1:150556002-150556325 | Rare:97; Clinvar:3 | ||||
chr1:150559038-150559341 | Rare:108; Clinvar:2 | ||||
chr1:150561304-150561666 | Common:1; Rare:92 | ||||
chr1:151046490-151046712 | Common:1; Rare:64 | ||||
chr1:152032338-152032591 | Rare:32 | ||||
chr1:152880432-152880648 | Rare:48 | ||||
chr1:152964668-152964724 | Rare:12 | ||||
chr1:152983837-152984125 | Common:3; Rare:53 | ||||
chr1:152985779-152985947 | Common:2; Rare:30 | ||||
chr1:153003809-153004028 | Common:2; Rare:51 | ||||
chr1:153032867-153033104 | Common:4; Rare:57 |