Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:173351928-173352003 | Rare:8 | ||||
chr1:173418327-173418616 | Common:3; Rare:51 | ||||
chr1:173720188-173720208 | |||||
chr1:173720274-173720564 | Common:2; Rare:57 | ||||
chr1:173769479-173769692 | Common:1; Rare:33 | ||||
chr1:173797636-173797688 | Rare:5 | ||||
chr1:173798228-173798389 | Common:1; Rare:22 | ||||
chr1:173836714-173836980 | Common:2; Rare:49; Clinvar:1; Clinvar (benign):1 | ||||
chr1:173853168-173853484 | Rare:73; Clinvar (benign):1 | ||||
chr1:173856113-173856297 | Common:1; Rare:34 | ||||
chr1:173863924-173863996 | Rare:18 | ||||
chr1:173864057-173864139 | Rare:28 | ||||
chr1:173864205-173864758 | Rare:154 | ||||
chr1:173864817-173864841 | Rare:11 | ||||
chr1:173865202-173865598 | Common:5; Rare:116 |