Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:62688271-62688499 | Common:1; Rare:95 | ||||
chr1:63523204-63523581 | Common:3; Rare:99 | ||||
chr1:63593116-63593460 | Rare:111; Clinvar (benign):1 | ||||
chr1:64841302-64841636 | Rare:76; Clinvar:2 | ||||
chr1:64846708-64846826 | Rare:39 | ||||
chr1:66533274-66533624 | Common:2; Rare:52 | ||||
chr1:66924810-66925083 | Rare:110 | ||||
chr1:66925194-66925518 | Common:2; Rare:101 | ||||
chr1:67053936-67054107 | Rare:73 | ||||
chr1:67430151-67430555 | Rare:148 | ||||
chr1:67833343-67833662 | Common:5; Rare:105 | ||||
chr1:68232507-68232681 | Rare:36 | ||||
chr1:70205536-70205778 | Rare:77 | ||||
chr1:70221306-70221614 | Rare:123 | ||||
chr1:70354659-70354856 | Rare:66 |