Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:173824240-173824838 | Rare:110; Clinvar:2 | ||||
chr1:173867958-173868204 | Common:1; Rare:93 | ||||
chr1:174022358-174022483 | Rare:32 | ||||
chr1:174159340-174159560 | Common:2; Rare:82 | ||||
chr1:174999308-174999472 | Common:1; Rare:47 | ||||
chr1:174999648-175000193 | Common:3; Rare:180 | ||||
chr1:175023404-175023614 | Common:1; Rare:58 | ||||
chr1:178725098-178725316 | Common:10; Rare:84 | ||||
chr1:179293603-179293909 | Common:3; Rare:100 | ||||
chr1:179877770-179877884 | Rare:24 | ||||
chr1:179882488-179882855 | Rare:175; Clinvar:7; Clinvar (benign):2 | ||||
chr1:179954494-179954814 | Common:2; Rare:78 | ||||
chr1:180502487-180502648 | Common:1; Rare:63 | ||||
chr1:181088532-181088704 | Rare:61 | ||||
chr1:182391746-182392045 | Common:4; Rare:103; Clinvar:4; Clinvar (benign):4 |