Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:171741922-171742347 | Common:3; Rare:123 | ||||
chr1:171841401-171841624 | Common:2; Rare:64 | ||||
chr1:173477169-173477416 | Common:2; Rare:87 | ||||
chr1:173714874-173715048 | Common:1; Rare:40 | ||||
chr1:173824402-173824708 | Rare:56; Clinvar:1 | ||||
chr1:173867981-173868385 | Common:2; Rare:133 | ||||
chr1:174159274-174159618 | Common:4; Rare:116 | ||||
chr1:174799512-174799824 | Rare:63 | ||||
chr1:174999337-174999471 | Rare:37 | ||||
chr1:174999829-175000156 | Common:3; Rare:115 | ||||
chr1:175023409-175023617 | Common:1; Rare:56 | ||||
chr1:178725114-178725356 | Common:10; Rare:86 | ||||
chr1:179877766-179877866 | Rare:22 | ||||
chr1:179882158-179882308 | Common:1; Rare:29 | ||||
chr1:179882488-179882871 | Rare:183; Clinvar:8; Clinvar (benign):2 |