Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:167935957-167936249 | Common:1; Rare:89 | ||||
chr1:167936544-167936727 | Rare:62 | ||||
chr1:168225816-168226050 | Common:2; Rare:81 | ||||
chr1:169367784-169368246 | Common:3; Rare:84 | ||||
chr1:169794855-169795110 | Common:3; Rare:66 | ||||
chr1:173477011-173477414 | Common:5; Rare:137 | ||||
chr1:173824137-173824702 | Rare:124; Clinvar:1 | ||||
chr1:174999354-174999486 | Common:1; Rare:36 | ||||
chr1:174999620-175000140 | Common:2; Rare:163 | ||||
chr1:175023409-175023667 | Common:1; Rare:73 | ||||
chr1:178725006-178725316 | Common:10; Rare:106 | ||||
chr1:179293672-179293898 | Common:3; Rare:69 | ||||
chr1:179882472-179882870 | Rare:185; Clinvar:8; Clinvar (benign):2 | ||||
chr1:180502399-180502715 | Common:1; Rare:115 | ||||
chr1:183186125-183186344 | Common:3; Rare:48; Clinvar:2; Clinvar (benign):3 |