Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:243255776-243256157 | Common:1; Rare:114; Clinvar:4; Clinvar (benign):1 | ||||
chr1:244451752-244452214 | Common:1; Rare:156 | ||||
chr1:244835088-244835339 | Rare:96 | ||||
chr1:244835575-244835752 | Common:2; Rare:80; Clinvar (benign):5 | ||||
chr1:244863961-244864686 | Common:1; Rare:245; Clinvar:3; Clinvar (benign):6 | ||||
chr1:244970021-244970438 | Common:5; Rare:182 | ||||
chr1:246566163-246566624 | Common:3; Rare:152 | ||||
chr1:246566971-246567058 | Rare:24 | ||||
chr1:247104301-247104527 | Common:2; Rare:70 | ||||
chr1:247331590-247332054 | Rare:119 | ||||
chr1:248825854-248826070 | Common:3; Rare:59 | ||||
chr1:248838032-248838444 | Common:3; Rare:132 | ||||
chr1:248858919-248859168 | Rare:96 | ||||
chr10:134685-134829 | Rare:39 | ||||
chr10:135393-135556 | Rare:35 |