Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:2391488-2391884 | Common:2; Rare:144 | ||||
chr1:2412279-2412345 | Rare:24 | ||||
chr1:2412428-2412849 | Common:2; Rare:169; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):3 | ||||
chr1:2412999-2413126 | Rare:34 | ||||
chr1:2413336-2413372 | Rare:4 | ||||
chr1:2413770-2413946 | Rare:48 | ||||
chr1:2526147-2526386 | Common:1; Rare:63 | ||||
chr1:2526533-2526756 | Common:4; Rare:88 | ||||
chr1:2586317-2586523 | Common:1; Rare:64 | ||||
chr1:2586563-2586876 | Common:3; Rare:80 | ||||
chr1:3068861-3069270 | Common:3; Rare:99; Clinvar (benign):2 | ||||
chr1:3069708-3069822 | Rare:27 | ||||
chr1:3453903-3454067 | Rare:35 | ||||
chr1:3454326-3454764 | Common:1; Rare:117 | ||||
chr1:3454869-3455211 | Common:2; Rare:80 |