Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:925602-925753 | Common:1; Rare:43 | ||||
chr1:1013359-1013549 | Common:4; Rare:61 | ||||
chr1:1231895-1232270 | Rare:129; Clinvar (benign):2 | ||||
chr1:1307817-1308003 | Rare:38 | ||||
chr1:1324598-1324827 | Common:3; Rare:128 | ||||
chr1:1358474-1358638 | Rare:72 | ||||
chr1:1399308-1399584 | Common:1; Rare:122 | ||||
chr1:1407186-1407373 | Common:1; Rare:87 | ||||
chr1:1890823-1891164 | Rare:124 | ||||
chr1:2391543-2391914 | Common:2; Rare:138 | ||||
chr1:2556332-2556408 | Rare:30 | ||||
chr1:3625103-3625265 | Common:1; Rare:32 | ||||
chr1:3796472-3796609 | Common:2; Rare:48 | ||||
chr1:3857203-3857315 | Common:1; Rare:37 | ||||
chr1:3900184-3900406 | Common:12; Rare:112 |