Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:25819885-25820013 | Common:2; Rare:38 | ||||
chr1:25906392-25906608 | Rare:83 | ||||
chr1:26110852-26111211 | Common:4; Rare:109 | ||||
chr1:26279907-26280158 | Rare:143 | ||||
chr1:26432091-26432414 | Common:5; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472304-26472551 | Common:4; Rare:90 | ||||
chr1:26890266-26890377 | Common:1; Rare:44 | ||||
chr1:26900435-26900547 | Rare:37 | ||||
chr1:26921485-26921815 | Common:3; Rare:95 | ||||
chr1:27322088-27322327 | Common:1; Rare:93 | ||||
chr1:27725690-27725985 | Common:2; Rare:83 | ||||
chr1:27772891-27773291 | Common:1; Rare:126 | ||||
chr1:27830706-27830831 | Common:1; Rare:40 | ||||
chr1:27914513-27914908 | Common:1; Rare:146 | ||||
chr1:28235963-28236209 | Common:3; Rare:79 |