Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:10348529-10348734 | Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
chr1:12598410-12598464 | Rare:11 | ||||
chr1:12618637-12618832 | Common:1; Rare:41 | ||||
chr1:12619006-12619236 | Rare:46 | ||||
chr1:15603579-15603713 | Common:3; Rare:40 | ||||
chr1:15789879-15790034 | Rare:31 | ||||
chr1:15800172-15800412 | Common:1; Rare:41 | ||||
chr1:15800634-15800734 | Rare:29 | ||||
chr1:15835805-15836095 | Common:6; Rare:135 | ||||
chr1:16447752-16447873 | Common:1; Rare:34 | ||||
chr1:16499214-16499423 | Common:1; Rare:96 | ||||
chr1:16618404-16618564 | Common:4; Rare:4 | ||||
chr1:16644653-16644792 | Common:1; Rare:2 | ||||
chr1:20755078-20755330 | Rare:57 | ||||
chr1:20783587-20783671 | Rare:18 |