Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:10694429-10694574 | Rare:43 | ||||
chr1:10694750-10694886 | Rare:40 | ||||
chr1:10796632-10796862 | Common:2; Rare:65 | ||||
chr1:11012209-11012421 | Rare:53 | ||||
chr1:11012587-11012737 | Common:1; Rare:45; Clinvar:4; Clinvar (benign):1 | ||||
chr1:11012997-11013122 | Rare:44 | ||||
chr1:11013246-11013454 | Common:2; Rare:64 | ||||
chr1:11059928-11060394 | Common:3; Rare:147 | ||||
chr1:11099341-11099494 | Rare:38 | ||||
chr1:11099758-11100058 | Common:4; Rare:116 | ||||
chr1:11262440-11262928 | Common:3; Rare:141 | ||||
chr1:11272868-11273338 | Common:2; Rare:132; Clinvar:1; Clinvar (benign):2 | ||||
chr1:11273391-11273526 | Common:1; Rare:37; Clinvar:1; Clinvar (benign):1 | ||||
chr1:11273616-11273722 | Rare:28 | ||||
chr1:11273934-11274001 | Rare:22; Clinvar (benign):2 |