Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:207320160-207321240 | Common:18; Rare:257 | ||||
chr1:207321230-207321821 | Common:18; Rare:845 | ||||
chr1:207322137-207322537 | Rare:298 | ||||
chr1:207454030-207454488 | Common:4; Rare:213; Clinvar:3 | ||||
chr1:207454484-207454960 | Common:7; Rare:220 | ||||
chr1:207496010-207496410 | Rare:131 | ||||
chr1:207644830-207645234 | Common:10; Rare:464 | ||||
chr1:207645394-207645943 | Common:5; Rare:157 | ||||
chr1:207751696-207752238 | Common:10; Rare:732; Clinvar:3 | ||||
chr1:209651202-209651660 | Common:9; Rare:150 | ||||
chr1:209675080-209675518 | Common:12; Rare:450 | ||||
chr1:209675893-209676293 | Common:3; Rare:101 | ||||
chr1:209784331-209784869 | Common:13; Rare:602 | ||||
chr1:209806120-209806407 | Common:20; Rare:332; Clinvar:8; Clinvar (benign):8 | ||||
chr1:209806429-209806537 | Common:1; Rare:20 |