Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:167937491-167937666 | Rare:45 | ||||
chr1:168178714-168179178 | Common:4; Rare:134 | ||||
chr1:168225854-168226086 | Common:3; Rare:83 | ||||
chr1:169106037-169106338 | Common:4; Rare:91 | ||||
chr1:169107828-169107981 | Common:1; Rare:32 | ||||
chr1:169367722-169368271 | Common:3; Rare:118 | ||||
chr1:169427347-169427534 | Common:2; Rare:41 | ||||
chr1:169485726-169486206 | Common:2; Rare:134; Clinvar:6; Clinvar (benign):4 | ||||
chr1:169794678-169794716 | Rare:11 | ||||
chr1:169794872-169795094 | Common:3; Rare:57 | ||||
chr1:170074395-170074752 | Common:2; Rare:118 | ||||
chr1:170532018-170532201 | Common:1; Rare:76; Clinvar:1 | ||||
chr1:171485262-171485598 | Rare:107 | ||||
chr1:171741867-171742191 | Common:3; Rare:99 | ||||
chr1:171781284-171781728 | Common:5; Rare:121 |