Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26695804-26696161 | Common:1; Rare:108 | ||||
chr1:26696198-26696442 | Common:1; Rare:71; Clinvar:1 | ||||
chr1:26696451-26696677 | Common:2; Rare:75; Clinvar:2; Clinvar (benign):6 | ||||
chr1:26696700-26696797 | Rare:46; Clinvar:1; Clinvar (benign):2 | ||||
chr1:26696887-26697228 | Rare:145; Clinvar:2 | ||||
chr1:26787430-26787734 | Common:1; Rare:79 | ||||
chr1:26787790-26788060 | Common:3; Rare:87; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26788099-26788356 | Rare:67 | ||||
chr1:26788621-26788794 | Common:1; Rare:30 | ||||
chr1:26789162-26789280 | Rare:22 | ||||
chr1:26826564-26827068 | Rare:141 | ||||
chr1:26862821-26863258 | Rare:98 | ||||
chr1:26863403-26863484 | Rare:24 | ||||
chr1:26863520-26863768 | Common:1; Rare:72 | ||||
chr1:26889371-26889721 | Rare:85 |