Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:161202029-161202512 | Common:3; Rare:143; Clinvar:5; Clinvar (benign):10 | ||||
chr1:161202579-161202747 | Common:2; Rare:32 | ||||
chr1:161223590-161223796 | Rare:33; Clinvar:1 | ||||
chr1:161224126-161224641 | Common:3; Rare:108 | ||||
chr1:161225607-161225675 | Rare:11 | ||||
chr1:161225678-161226139 | Common:10; Rare:81 | ||||
chr1:161226319-161226525 | Common:1; Rare:55 | ||||
chr1:161226714-161226749 | Rare:2 | ||||
chr1:161258573-161258778 | Common:2; Rare:40 | ||||
chr1:161313735-161313783 | Rare:8 | ||||
chr1:161314156-161314467 | Common:4; Rare:111; Clinvar:10; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
chr1:161314804-161314947 | Rare:36 | ||||
chr1:161726087-161726317 | Common:1; Rare:81 | ||||
chr1:161726328-161726652 | Common:1; Rare:93 | ||||
chr1:161749586-161749937 | Common:1; Rare:122 |