Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:1013346-1013535 | Common:3; Rare:58 | ||||
chr1:1308489-1308634 | Common:7; Rare:79 | ||||
chr1:1324594-1324863 | Common:3; Rare:141 | ||||
chr1:1574518-1574978 | Common:1; Rare:208 | ||||
chr1:1658926-1659058 | Common:2; Rare:48 | ||||
chr1:1724269-1724484 | Common:3; Rare:78 | ||||
chr1:1890875-1891180 | Rare:117 | ||||
chr1:2391540-2391922 | Common:2; Rare:139 | ||||
chr1:5992404-5992654 | Common:3; Rare:80; Clinvar:6 | ||||
chr1:6208680-6208944 | Common:1; Rare:81 | ||||
chr1:7771146-7771363 | Common:4; Rare:90 | ||||
chr1:7961455-7961767 | Common:4; Rare:107; Clinvar:2; Clinvar (benign):3 | ||||
chr1:8878578-8878860 | Rare:148 | ||||
chr1:9943292-9943488 | Common:2; Rare:46 | ||||
chr1:10032763-10032965 | Rare:53 |