Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:171741959-171742367 | Common:3; Rare:117 | ||||
chr1:171781405-171781718 | Common:4; Rare:78 | ||||
chr1:173477002-173477433 | Common:5; Rare:148 | ||||
chr1:173714876-173714986 | Rare:27 | ||||
chr1:173824234-173824721 | Rare:101; Clinvar:2 | ||||
chr1:173867975-173868140 | Rare:66 | ||||
chr1:174799673-174799791 | Rare:24 | ||||
chr1:174999648-175000152 | Common:3; Rare:161 | ||||
chr1:178725131-178725320 | Common:10; Rare:72 | ||||
chr1:179882487-179882862 | Rare:179; Clinvar:7; Clinvar (benign):2 | ||||
chr1:179883021-179883168 | Common:3; Rare:55 | ||||
chr1:180502529-180502658 | Rare:57 | ||||
chr1:181088494-181088701 | Rare:67 | ||||
chr1:182604383-182604509 | Rare:26 | ||||
chr1:182789642-182789776 | Common:2; Rare:43 |