Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:174999621-175000177 | Common:3; Rare:186 | ||||
chr1:179143045-179143258 | Rare:42 | ||||
chr1:179882106-179882308 | Common:1; Rare:37 | ||||
chr1:181088570-181088704 | Rare:44 | ||||
chr1:182391776-182392016 | Common:3; Rare:76; Clinvar:3; Clinvar (benign):3 | ||||
chr1:182839041-182839413 | Common:1; Rare:125 | ||||
chr1:183635666-183636094 | Common:4; Rare:123 | ||||
chr1:184051601-184051782 | Common:3; Rare:69 | ||||
chr1:185156929-185157200 | Rare:69 | ||||
chr1:186375123-186375430 | Rare:84 | ||||
chr1:186375678-186375914 | Common:1; Rare:60 | ||||
chr1:186680417-186680681 | Common:2; Rare:57 | ||||
chr1:193059292-193059689 | Rare:189 | ||||
chr1:193121737-193122060 | Common:1; Rare:121; Clinvar:3 | ||||
chr1:197902559-197902652 | Common:1; Rare:31 |