Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:169367770-169368250 | Common:3; Rare:92 | ||||
chr1:169794890-169795045 | Common:3; Rare:31 | ||||
chr1:170074480-170074762 | Common:1; Rare:78 | ||||
chr1:170663029-170663153 | Rare:33 | ||||
chr1:171742034-171742191 | Common:1; Rare:47 | ||||
chr1:173477136-173477407 | Common:4; Rare:100 | ||||
chr1:173714874-173715017 | Common:1; Rare:36 | ||||
chr1:173824331-173824708 | Rare:75; Clinvar:1 | ||||
chr1:173867975-173868148 | Rare:67 | ||||
chr1:174999343-174999471 | Rare:35 | ||||
chr1:174999644-175000149 | Common:3; Rare:160 | ||||
chr1:179143052-179143136 | Rare:19 | ||||
chr1:179882024-179882324 | Common:2; Rare:69 | ||||
chr1:179882509-179882828 | Rare:151; Clinvar:7; Clinvar (benign):2 | ||||
chr1:179883007-179883133 | Common:3; Rare:51 |