Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:208181085-208181175 | Rare:16 | ||||
chr1:211382676-211382854 | Common:1; Rare:67 | ||||
chr1:212187940-212188156 | Common:1; Rare:32 | ||||
chr1:212665639-212665722 | Rare:19 | ||||
chr1:220147210-220147518 | Common:1; Rare:71; Clinvar (benign):2 | ||||
chr1:220253391-220253551 | Common:2; Rare:33 | ||||
chr1:220690597-220690654 | Rare:23 | ||||
chr1:220880011-220880096 | Rare:28 | ||||
chr1:221845760-221846080 | Common:1; Rare:76 | ||||
chr1:222711479-222711595 | Rare:23 | ||||
chr1:223992554-223992818 | Common:4; Rare:97 | ||||
chr1:225853714-225853883 | Common:2; Rare:55 | ||||
chr1:226675006-226675224 | Rare:33 | ||||
chr1:226680100-226680325 | Common:2; Rare:49 | ||||
chr1:229563755-229563913 | Common:1; Rare:17 |