Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:244451775-244452219 | Common:1; Rare:149 | ||||
chr1:244835573-244835765 | Common:2; Rare:86; Clinvar:1; Clinvar (benign):5 | ||||
chr1:244862957-244863292 | Common:4; Rare:135 | ||||
chr1:244863616-244864127 | Common:1; Rare:171; Clinvar:8; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
chr1:244864130-244864185 | Rare:20; Clinvar (benign):2 | ||||
chr1:244864249-244864607 | Rare:126 | ||||
chr1:244970160-244970439 | Common:5; Rare:129 | ||||
chr1:246566118-246566641 | Common:3; Rare:168 | ||||
chr1:246566947-246567286 | Common:1; Rare:73 | ||||
chr1:247104301-247104512 | Common:2; Rare:66 | ||||
chr1:247331669-247332054 | Rare:110 | ||||
chr1:248825817-248825978 | Common:2; Rare:38 | ||||
chr1:248838208-248838542 | Common:2; Rare:95 | ||||
chr1:248906049-248906299 | Common:2; Rare:96 | ||||
chr10:134670-134864 | Rare:56 |