Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:173205613-173205797 | Rare:36 | ||||
chr1:173207073-173207144 | Rare:23 | ||||
chr1:173477158-173477484 | Common:4; Rare:117 | ||||
chr1:173714861-173715026 | Common:1; Rare:38 | ||||
chr1:173824397-173824732 | Rare:60; Clinvar:2 | ||||
chr1:173824864-173824990 | Rare:28 | ||||
chr1:173867962-173868163 | Rare:80 | ||||
chr1:174999268-174999468 | Common:1; Rare:59 | ||||
chr1:174999617-175000183 | Common:3; Rare:192 | ||||
chr1:175023405-175023612 | Common:1; Rare:58 | ||||
chr1:178725114-178725309 | Common:10; Rare:76 | ||||
chr1:179143052-179143238 | Rare:34 | ||||
chr1:179877766-179877896 | Rare:27 | ||||
chr1:179882155-179882324 | Common:1; Rare:33 | ||||
chr1:179882499-179882884 | Rare:192; Clinvar:9; Clinvar (benign):2 |