Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:144460882-144461585 | Common:13; Rare:414 | ||||
chr1:145823872-145824373 | Rare:162 | ||||
chr1:145858290-145858570 | Common:1; Rare:45 | ||||
chr1:145858697-145858826 | Rare:28 | ||||
chr1:145858983-145859213 | Rare:66 | ||||
chr1:145859761-145859977 | Common:3; Rare:72 | ||||
chr1:145885720-145886120 | Common:1; Rare:128 | ||||
chr1:145918658-145918844 | Common:1; Rare:52; Clinvar:1 | ||||
chr1:145918869-145919040 | Common:1; Rare:41 | ||||
chr1:145926745-145927408 | Common:3; Rare:265; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr1:145927482-145927691 | Rare:55 | ||||
chr1:145957932-145958251 | Rare:80 | ||||
chr1:145964385-145964749 | Rare:74 | ||||
chr1:145996526-145996918 | Common:2; Rare:150 | ||||
chr1:147172488-147172805 | Common:1; Rare:81 |