Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:177164684-177164766 | Rare:23 | ||||
chr1:178725123-178725341 | Common:10; Rare:80 | ||||
chr1:178871027-178871046 | Rare:1 | ||||
chr1:178871059-178871177 | Rare:20 | ||||
chr1:179293672-179293858 | Common:2; Rare:64 | ||||
chr1:179877766-179877930 | Rare:31 | ||||
chr1:179882155-179882308 | Common:1; Rare:30 | ||||
chr1:179882478-179882908 | Rare:212; Clinvar:9; Clinvar (benign):2 | ||||
chr1:180502376-180502678 | Common:1; Rare:108 | ||||
chr1:181482558-181482974 | Common:2; Rare:131 | ||||
chr1:181483272-181483357 | Common:1; Rare:20 | ||||
chr1:181483606-181483634 | Rare:2 | ||||
chr1:182391744-182392073 | Common:4; Rare:120; Clinvar:5; Clinvar (benign):4 | ||||
chr1:182604381-182604550 | Rare:39 | ||||
chr1:182671754-182671999 | Common:3; Rare:54 |