Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26473086-26473261 | Rare:84 | ||||
chr1:26787859-26787974 | Common:1; Rare:40; Clinvar (benign):1 | ||||
chr1:26900444-26900471 | Rare:11 | ||||
chr1:26921543-26921825 | Common:3; Rare:88 | ||||
chr1:27366946-27367016 | Rare:11 | ||||
chr1:27725762-27726067 | Common:4; Rare:87 | ||||
chr1:27914506-27914747 | Common:1; Rare:93 | ||||
chr1:28236054-28236259 | Common:1; Rare:73 | ||||
chr1:28505861-28506067 | Common:1; Rare:90 | ||||
chr1:28552801-28553113 | Common:2; Rare:106 | ||||
chr1:28643002-28643278 | Rare:97 | ||||
chr1:28736713-28737133 | Common:4; Rare:142 | ||||
chr1:29230857-29231042 | Rare:71; Clinvar:1 | ||||
chr1:31296720-31297099 | Common:5; Rare:129 | ||||
chr1:31413087-31413269 | Common:3; Rare:48 |