Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:26432073-26432445 | Common:5; Rare:95; Clinvar:2; Clinvar (benign):1 | ||||
chr1:26472213-26472563 | Common:4; Rare:122 | ||||
chr1:26472743-26472910 | Common:1; Rare:55 | ||||
chr1:26473025-26473270 | Common:1; Rare:132 | ||||
chr1:26529971-26530076 | Rare:31 | ||||
chr1:26530575-26530719 | Rare:23 | ||||
chr1:26530753-26530774 | Rare:5 | ||||
chr1:26542287-26542619 | Common:1; Rare:57 | ||||
chr1:26543247-26543361 | Rare:27 | ||||
chr1:26545682-26545930 | Common:1; Rare:55 | ||||
chr1:26695563-26696125 | Common:1; Rare:180 | ||||
chr1:26786970-26787065 | Rare:24 | ||||
chr1:26787374-26787689 | Common:1; Rare:82 | ||||
chr1:26787835-26788381 | Common:3; Rare:157; Clinvar:2; Clinvar (benign):2 | ||||
chr1:26788618-26788681 | Rare:12 |