Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:166876229-166876492 | Rare:82 | ||||
chr1:167220586-167220925 | Common:1; Rare:97 | ||||
chr1:167935888-167936261 | Common:1; Rare:102 | ||||
chr1:167936544-167936697 | Rare:52 | ||||
chr1:167936840-167936961 | Rare:53 | ||||
chr1:167937044-167937082 | Rare:10 | ||||
chr1:168178836-168179196 | Common:3; Rare:115 | ||||
chr1:168225706-168226118 | Common:4; Rare:135 | ||||
chr1:169367745-169368256 | Common:3; Rare:104 | ||||
chr1:169427460-169427534 | Rare:19 | ||||
chr1:169485685-169486206 | Common:2; Rare:154; Clinvar:6; Clinvar (benign):4 | ||||
chr1:169794690-169795107 | Common:3; Rare:91 | ||||
chr1:169893655-169893748 | Rare:31 | ||||
chr1:169893870-169894004 | Common:1; Rare:41 | ||||
chr1:169894263-169894407 | Common:2; Rare:49 |