Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:171781420-171781695 | Common:2; Rare:59 | ||||
chr1:171841401-171841588 | Common:2; Rare:56 | ||||
chr1:173477169-173477425 | Common:2; Rare:93 | ||||
chr1:173714842-173714941 | Rare:21 | ||||
chr1:173824390-173824702 | Rare:57; Clinvar:1 | ||||
chr1:173867975-173868389 | Common:2; Rare:138 | ||||
chr1:174999344-174999471 | Rare:35 | ||||
chr1:174999621-175000156 | Common:3; Rare:177 | ||||
chr1:177164684-177164821 | Rare:32 | ||||
chr1:178725114-178725340 | Common:10; Rare:82 | ||||
chr1:178871059-178871366 | Rare:56 | ||||
chr1:179877740-179877872 | Rare:30 | ||||
chr1:179882172-179882313 | Rare:27 | ||||
chr1:179882478-179882868 | Rare:183; Clinvar:8; Clinvar (benign):2 | ||||
chr1:180502376-180502643 | Common:1; Rare:95 |