Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:91021963-91022410 | Common:1; Rare:109 | ||||
chr1:91500568-91500881 | Common:2; Rare:74 | ||||
chr1:91885878-91886306 | Common:1; Rare:162 | ||||
chr1:92029910-92030059 | Rare:39 | ||||
chr1:92298934-92299076 | Common:1; Rare:71; Clinvar:2; Clinvar (benign):1 | ||||
chr1:92784624-92784862 | Common:2; Rare:66 | ||||
chr1:92832000-92832113 | Rare:75; Clinvar:6; Clinvar (benign):5 | ||||
chr1:92961411-92961574 | Rare:61 | ||||
chr1:93179721-93179954 | Common:1; Rare:47 | ||||
chr1:93180062-93180180 | Rare:41 | ||||
chr1:93180184-93180694 | Common:1; Rare:194 | ||||
chr1:93345766-93345971 | Common:4; Rare:84 | ||||
chr1:93447996-93448154 | Common:2; Rare:58 | ||||
chr1:93847211-93847286 | Common:1; Rare:19 | ||||
chr1:93879128-93879248 | Common:1; Rare:40 |