Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:54886943-54886988 | Rare:15 | ||||
chr1:54887073-54887298 | Common:1; Rare:86; Clinvar:4; Clinvar (benign):1 | ||||
chr1:56645269-56645384 | Common:1; Rare:46 | ||||
chr1:58546706-58546774 | Common:4; Rare:33 | ||||
chr1:58546783-58546833 | Rare:24 | ||||
chr1:58784001-58784257 | Rare:61 | ||||
chr1:59296508-59297096 | Common:14; Rare:164 | ||||
chr1:62436948-62437102 | Common:1; Rare:38 | ||||
chr1:62688266-62688541 | Common:1; Rare:106 | ||||
chr1:62784047-62784185 | Rare:54 | ||||
chr1:63367526-63367675 | Rare:44; Clinvar (benign):1 | ||||
chr1:63523204-63523559 | Common:3; Rare:93 | ||||
chr1:63593109-63593453 | Rare:108; Clinvar (benign):1 | ||||
chr1:63773818-63774048 | Rare:50 | ||||
chr1:64841302-64841606 | Rare:71; Clinvar:2 |