Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:145927364-145927657 | Common:1; Rare:76; Clinvar (pathogenic):1 | ||||
chr1:145958007-145958212 | Rare:48 | ||||
chr1:145964587-145964767 | Rare:40 | ||||
chr1:145994016-145994286 | Rare:108 | ||||
chr1:145996389-145996808 | Common:1; Rare:148 | ||||
chr1:146228928-146229205 | Common:3; Rare:66 | ||||
chr1:146938297-146938480 | Common:2; Rare:61 | ||||
chr1:147172420-147172830 | Common:1; Rare:105 | ||||
chr1:147242615-147242798 | Common:3; Rare:91 | ||||
chr1:147270607-147270849 | Common:1; Rare:52 | ||||
chr1:147541264-147541561 | Common:1; Rare:47 | ||||
chr1:147600083-147600251 | Rare:73 | ||||
chr1:147908238-147908333 | Rare:44 | ||||
chr1:147928274-147928472 | Common:2; Rare:73 | ||||
chr1:148152294-148152334 | Common:1; Rare:15 |