Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:109548478-109548714 | Common:4; Rare:93 | ||||
chr1:109619777-109619886 | Rare:22 | ||||
chr1:109625705-109626031 | Rare:79; Clinvar (benign):1 | ||||
chr1:109656049-109656362 | Common:3; Rare:78 | ||||
chr1:109667927-109668101 | Common:1; Rare:52 | ||||
chr1:109984576-109984805 | Common:1; Rare:54 | ||||
chr1:110339149-110339506 | Common:2; Rare:117 | ||||
chr1:110390973-110391124 | Rare:31 | ||||
chr1:110406319-110406542 | Rare:57 | ||||
chr1:110407360-110407418 | Rare:21 | ||||
chr1:110407541-110407856 | Common:4; Rare:133 | ||||
chr1:110963784-110964037 | Rare:85 | ||||
chr1:111139792-111139870 | Rare:12 | ||||
chr1:111140021-111140287 | Common:3; Rare:89 | ||||
chr1:111619523-111619929 | Common:2; Rare:121 |