Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:128843846-128844096 | Rare:76; Clinvar:3; Clinvar (benign):6 | ||||
chr7:128848557-128848982 | Common:2; Rare:132; Clinvar:19; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
chr7:128851225-128851628 | Common:3; Rare:103; Clinvar:14; Clinvar (benign):11 | ||||
chr7:128852586-128853030 | Common:4; Rare:132; Clinvar:15; Clinvar (benign):11 | ||||
chr7:128854574-128854912 | Rare:88; Clinvar:9; Clinvar (benign):11; Clinvar (pathogenic):2 | ||||
chr7:129410521-129410821 | Common:2; Rare:46 | ||||
chr7:130912208-130912224 | Common:1; Rare:2 | ||||
chr7:130913129-130913508 | Common:1; Rare:70 | ||||
chr7:131106344-131106565 | Common:1; Rare:45 | ||||
chr7:131107937-131108162 | Common:1; Rare:38 | ||||
chr7:134432377-134432578 | Rare:66 | ||||
chr7:143836672-143836984 | Common:1; Rare:12 | ||||
chr7:152436515-152436853 | Rare:118 | ||||
chr7:153748035-153748333 | Common:3; Rare:55 | ||||
chr7:154928302-154928520 | Common:4; Rare:53 |