Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:167376540-167376773 | Common:1; Rare:44 | ||||
chr1:167396453-167396498 | Common:1; Rare:11 | ||||
chr1:167728059-167728208 | Common:6; Rare:21 | ||||
chr1:167820284-167820400 | Rare:31 | ||||
chr1:167977025-167977206 | Rare:29 | ||||
chr1:167977230-167977239 | Rare:2 | ||||
chr1:168031557-168031700 | Common:1; Rare:23 | ||||
chr1:168033566-168033624 | Common:3; Rare:10 | ||||
chr1:168179975-168180075 | Rare:11 | ||||
chr1:168239477-168239753 | Rare:40 | ||||
chr1:168319762-168319994 | Rare:38 | ||||
chr1:168380743-168381015 | Common:3; Rare:43 | ||||
chr1:169111160-169111351 | Common:1; Rare:47 | ||||
chr1:169129780-169130055 | Common:7; Rare:44; Clinvar (benign):1 | ||||
chr1:169160834-169161051 | Common:1; Rare:32 |