Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:158671880-158672132 | Common:3; Rare:59 | ||||
chr4:158672229-158672313 | Rare:19; Clinvar:1 | ||||
chr4:174283612-174283938 | Common:1; Rare:64 | ||||
chr4:177442384-177442514 | Rare:76; Clinvar:2 | ||||
chr4:183659122-183659337 | Common:1; Rare:67 | ||||
chr4:184474540-184474829 | Rare:71 | ||||
chr4:184649436-184649756 | Common:4; Rare:105 | ||||
chr4:189940613-189940958 | Common:9; Rare:119 | ||||
chr5:218125-218390 | Common:3; Rare:112; Clinvar:11; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
chr5:892732-892941 | Common:2; Rare:81 | ||||
chr5:1799795-1799977 | Common:4; Rare:89 | ||||
chr5:1801374-1801420 | Common:1; Rare:18; Clinvar (benign):1 | ||||
chr5:7869020-7869204 | Common:2; Rare:90; Clinvar (benign):1 | ||||
chr5:10353600-10353896 | Common:3; Rare:106 | ||||
chr5:16465749-16465813 | Rare:15 |