Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:159712076-159712301 | Common:1; Rare:36 | ||||
chr1:159752160-159752485 | Common:3; Rare:70 | ||||
chr1:159753643-159753826 | Common:2; Rare:32 | ||||
chr1:159991549-159991805 | Common:1; Rare:52 | ||||
chr1:160030930-160031032 | Rare:32 | ||||
chr1:160292010-160292435 | Common:1; Rare:79 | ||||
chr1:160344172-160344307 | Rare:24 | ||||
chr1:160999705-161000196 | Common:2; Rare:121 | ||||
chr1:161013929-161014159 | Rare:34 | ||||
chr1:161530853-161531107 | Common:6; Rare:93 | ||||
chr1:167454986-167455098 | Rare:23 | ||||
chr1:171092363-171092696 | Rare:70 | ||||
chr1:171103595-171103972 | Common:2; Rare:111; Clinvar:4; Clinvar (pathogenic):3 | ||||
chr1:171110520-171110826 | Common:1; Rare:61; Clinvar:1 | ||||
chr1:171214005-171214176 | Common:1; Rare:32 |